Geochemistry and Geochronology of the Jinghong Ophiolites: Implications for the Tectonic Evolution of the Eastern Paleo-Tethys

The Jinghong mafic–ultramafic complex, exposed in the eastern margin of the Lancangjiang tectonic belt, is related to the subduction of the Paleo-Tethys Ocean. Its petrogenesis plays a key role in constraining the tectonic evolution of the eastern Paleo-Tethys Ocean in southwestern China. In this study, we present petrological, geochemical and geochronological results of the Jinghong complex rocks, in order to decipher their origin and tectonic significance. The Jinghong mafic–ultramafic complex was composed of peridotite, gabbro, basalt and minor plagiogranite. Whole-rock geochemical data of the mafic rocks indicate that they have both MORB and IAB affinities and plot in the back-arc basin basalt (BABB) field in the FeO*/MgO vs. TiO2 diagram. Combined with their trace element characteristics, it can be concluded that the Jinghong mafic–ultramafic complex represents an ophiolite suite that was formed in a back-arc ocean basin. Precise LA-ICP-MS zircon U-Pb dating yielded weighted mean 206Pb/238U ages of 298.4 ± 1.7 Ma, 294.3 ± 1.6 Ma, and 292.8 ± 2.0 Ma for gabbroic rocks from this complex, which indicates that the Jinghong ophiolites were formed during the early Permian (298–293 Ma). We propose that during subduction of the main Paleo-Tethys Ocean, a back-arc ocean basin was formed at the east of the Lancangjiang tectonic belt.     

Late Mesozoic Ore‐forming Events in the Ningwu Ore District,Middle‐Lower Yangtze River Polymetallic Ore Belt,East China: Evidence from Zircon U‐Pb Geochronology and Hf Isotopic Compositions of the Granodioritic Stocks

Late Mesozoic volcanic-subvolcanic rocks and related iron deposits, known as porphyry iron deposits in China, are widespread in the Ningwu ore district (Cretaceous basin) of the middle–lower Yangtze River polymetallic ore belt, East China. Two types of Late Mesozoic magmatic rocks are exposed: one is dioritic rocks closely related to iron mineralization as the hosted rock, and the other one is granodioritic (-granitic) rocks that cut the ore bodies. To understand the age of the iron mineralization and the ore-forming event, detailed zircon U-Pb dating and Hf isotope measurement were performed on granodioritic stocks in the Washan, Gaocun-Nanshan, Dongshan and Heshangqiao iron deposits in the basin. Four emplacement and crystallization (typically for zircons) ages of granodioritic rocks were measured as 126.1±0.5 Ma, 126.8±0.5 Ma, 127.3±0.5 Ma and 126.3±0.4 Ma, respectively in these four deposits, with the LA-MC-ICP-MS zircon U-Pb method. Based on the above results combined with previous dating, it is inferred that the iron deposits in the Ningwu Cretaceous basin occurred in a very short period of 131–127 Ma. In situ zircon Hf compositions of εHf(t) of the granodiorite are mainly from ?3 to ?8 and their corresponding 176Hf/177Hf ratio are from 0.28245 to 0.28265, indicating similar characteristics of dioritic rocks in the basin. We infer that granodioritic rocks occurring in the Ningwu ore district have an original relationship with dioritic rocks. These new results provide significant evidence for further study of this ore district so as to understand the ore-forming event in the study area.     

Geochronology and Significance of Granites Associated with Gold Deposits in the Jidong Area, China

The Jidong area is located on the north margin of the North China craton. It is a nucleus composed of the oldest rocks in China. Precambrian metamorphic rocks with various Phanerozoic granitoids invaded are widespread. Gold deposits here have close spatial relations to granitoids. Some deposits occur within them and others in the outer zone of the contact belt of the intrusion, extending thousands of metres. There have been controversial views in regard to the relations of the deposits to the intrusions although traditional techniques have been used to date the intrusions. In order to solve such a problem, the SHRIMP technique was adopted to date the U-Pb ages of zircon collected from the Yuerya intrusion which hosts the large-sized Yuerya Au deposit and Qingshankou intrusion 2 km away from the Jinchangyu (larger-sized) Au deposit. Analysis shows that the ages of 175±1 Ma and 174±3 Ma for Yuerya intrusion and the age of 199±2 Ma for Qingshankou granite indicate the Early Yanshanian stage of the Meso-     

Late Jurassic Cu-Mo Mineralization at the Zhashui-Shanyang District, South Qinling, China: Constraints from Re-Os Molybdenite and Laser Ablation-Inductively Coupled Plasma Mass Spectrometry U-Pb Zircon Dating

The Zhashui-Shanyang district is one of the most important sulfide deposits in the Qinling Orogen where the formation of porphyry-skarn Cu-Mo deposits has a close genetic link with the Yanshannian magmatism. Laser Ablation-Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS) U-Pb zircon dating of two granodiorite intrusions (Xiaohekou and Lengshuigou deposits) was investigated in the Zhashui-Shanyang district and the rock-forming ages obtained from 148.3±2.8?to 152.6±1.2?Ma, averaging 150.5 Ma, accompanied by a younger disturbance age of 144.3±1.7?Ma in the Lengshuigou intrusion, which is in excellent agreement with published sensitive high resolution ion micro-probe (SHRIMP) zircon date on the later monzodiorite porphyry phase in the Lenshuigou deposit. Two samples were selected for molybdenite ICP-MS Re-Os isotopic analyses from the Lengshuigou granodiorite porphyry, yielding Re-Os model ages from 149.2±2.7 Ma to 150.6±3.4 Ma, with a weighted mean age of 149.7±2.1 Ma. These mineralization ages overlap rock-forming ages of the host intrusions within the error range. This implies that the mineralization occurred in the Late Jurassic, which belongs to the tectonic phase B event of the Yanshan Movement, not Cretaceous as previously thought. Therefore, the Late Jurassic mineralization of the Zhashui-Shanyang district could be connected to the large-scale Yanshan molybdenum metallogenic period, the geodynamic regime of which is attributable to the far field response of convergence of surrounding plates, perhaps the approximately westward subduction of the Izanagi plate beneath the Eurasian continent.     

Extensional Setting of Hainan Island in Mesoproterozoic: Evidence from Granitic Intrusions in the Baoban Group

The Mesoproterozoic Baoban Group is the oldest basement in Hainan Island and has played an important role in Columbia (Nuna) supercontinent reconstructions. The Mesoproterozoic granitic intrusions in the Baoban Group are the most widely-exposed Precambrian magmatic rocks and are the key to understanding the tectonic settings of Hainan Island and its relationship with the South China Block and the Columbia supercontinent. New LA-ICP-MS zircon U-Pb dating on three mylonitic granite samples from the Tuwaishan and Baoban areas yield ages ranging from 1447 Ma to 1437 Ma, representing the absolute timing of the emplacement of the granitic intrusions. Combined with previously published geochronological data for rocks from the Baoban Group and regional mafic intrusions, it is concluded that the Baoban Group formed at 1460–1430 Ma, coeval with the emplacement of the granitic and mafic intrusions. New in-situ zircon Lu-Hf isotope analyses for the three mylonitic granite samples yielded positive εHf(t) values, ranging from +0.49 to +8.27, with model ages (TCDM) ranging from 2181 Ma to 1687 Ma, suggesting that the granitic intrusions originated from a mixed source of Paleoproterozoic crust with juvenile crust. New zircon trace element data show characteristics of high Th/U values of 0.24–1.50, steep slopes from LREE to HREE and negative Pr, Eu anomalies with positive Ce, Sm anomalies, representing typical magmatic zircons formed in continental crust. Compared with available magmatic and detrital zircon ages from Precambrian rocks in the Cathaysia Block, Yangtze Block and western Laurentia, it is inferred that Hainan Island was separated from both the Cathaysia Block and the Yangtze Block, instead being connected with western Laurentia in the Columbia supercontinent. Considering the decreasing tendency of basin deposition time along the western margin of Laurentia, it is proposed that Hainan Island was located to the north or northwest of the Belt-Purcell Supergroup, along the western margin of Laurentia, during the breakup of the Columbia supercontinent.     

Provenance of Conglomerate and Sandstone from Early Permian Shoushangou Formation in Xi Ujimqin, Inner Mongolia: Implications for Understanding Paleo-Asian Ocean Subduction

During the Late Carboniferous to Early Permian, a rift was formed by post-collisional extension after ocean closure or an island arc-related basin formed by Paleo-Asian Ocean (PAO) subduction in the Xi Ujimqin area. Nevertheless, the closure time of the PAO is still under debate. Thus, to identify the origin of the PAO, the geochemistry and U-Pb age of zircons were analyzed for the extra-large deep marine, polymict clastic boulders and sandstones in the Shoushangou Formation within the basin. The analyses revealed magmatic activity and tectonic evolution. The conglomerates include megaclasts of granite (298.8 ± 9.1?Ma) and granodiorite porphyry (297.1 ± 3.1?Ma), which were deposited by muddy debris flow. Results of this study demonstrated that the boulders of granitoids have the geochemistry of typical I-type granite, characterized by low Zr + Nb + Ce + Y and low Ga/Al values. The granitoid boulders were formed in island arc setting, indicating the presence of arc magmatism in the area that is composed of the Late Carboniferous to Early Permian subduction-related granitoid in southern Xi Ujimqin. Multiple diagrams for determining sedimentary provenance using major and trace elements indicate that Shoushangou sediments originated from continental island arc-related felsic rocks. Detrital zircon U-Pb age cluster of 330–280?Ma was obtained, indicating input from granite, ophiolite, Xilin Gol complex, and Carboniferous sources to the south. The basin was geographically developed behind the arc during the Early Permian period because the outcropped intrusive rocks in the Late Carboniferous to Early Permian form a volcanic arc. The comprehensive analyses of source areas suggest that Shoushangou sediments developed in a backarc basin in response to the northward subduction of the PAO. The backarc basin and intrusive rocks, in addition to previously published Late Carboniferous to Early Permian magmatic rocks of arc unit in Xilin Gol, confirm the presence of an Early Permian trench-arc-basin system in the region, represented by the Baolidao arc and Xi Ujimqin backarc basin. This study highlights the importance and potential of combined geochemical and geochronological studies of conglomerates and sandstone for reconstructing the geodynamic setting of a basin.     

Zircon U-Pb geochronology of Early Jurassic-Late cretaceous volcanic rocks in North Yellow Sea BasinEI北大核心CSCD

The X-drilling cores of the North Yellow Sea basin reveal two sets of Mesozoic clastic rocks, which are the dark rocks in lower part and the red rocks in upper part, respectively. There are two layers of volcanic rocks at the bottom and the upper part of the dark rock unit. The volcanic rocks at the bottom part are trachytic dacite while rocks at the upper part are clastic dacite. The zircon grains from the upper and lower units of volcanic rocks are euhedral-subhedral columnar crystals and show oscillatory zoning on cathodoluminescence images. 22 tests of zircons in the trachytic dacite from the bottom part yield an age of 141-151 Ma, with weighted mean 206Pb/238U age of 145±2 Ma. Whereas 18 tests of zircons from the sample at the upper part give 206Pb/238U ages around 139-149 Ma with weighted mean 206Pb/238U age of 141±2 Ma, which implies that the X well volcanic rocks belong to Late Jurassic-Early Cretaceous. Comparing with the age and geochemical characteristics of the Mesozoic igneous rocks in Shandong peninsula, we suggest that the igneous rocks from both the North Yellow Sea basin and Jiaolai basin were formed under same dynamic setting, i.e., the subduction related volcano arc and back-arc extension. ©, 2015, Science Press. All right reserved.     

Switching from advancing to retreating subduction in the Neoproterozoic Tarim Craton,NW China: Implications for Rodinia breakup

Geodynamic drivers for the supercontinent cycle are generally attributed to either top-down(subduction-related)or bottom-up(mantle-related)processes.Compiled geochemical data and U-Pb ages and Hf isotopic signatures for magmatic and detrital zircons from the Tarim Craton reveal a distinct change in subduction style during the Neoproterozoic.The subduction cycle is recorded in increasing and decreasing intensity of subduction-related magmatic rocks and time-equivalent sedimentary successions,and converse trends ofεHf(t)values and corresponding changes in crustal incubation time.These trends are consistent with a switch from advancing to retreating subduction.The switch likely occurred at ca.760 Ma when zirconεHf(t)values increase and crustal incubation times decrease following a transitional shift between 800 Ma and 760 Ma.A switch at this time is consistent with Rodinia breakup and may have resulted in the late Neoproterozoic Tarim rift basin.The long-lived(ca.500 Ma)subduction recorded in the Tarim Craton suggests the predominance of a top-down process for Rodinia breakup on this part of its margin.     

~(40)Ar/~(39)Ar Age and Geological Significance of Lamprophyres in Pishan on the SW Margin of the Tarim Terrane, NW China

The dike swarm of lamprophyres at Pishan on the SW margin of the Tarim terrane is composed of ultra-potassic lamprophyres that have intruded into the Proterozoic hornblende schists. 40Ar/39Ar dating data suggest that the isochron ages for phlogopite and whole rock separates of the lamprophyres are 231.7±0.3 Ma and 228.5±0.3 Ma, respectively. Geochemical data indicate that the dikes were derived from a subduction-related or metasomatized mantle. During the Middle-Late Triassic the western Kunlun area entered the post-orogeny period, and thus the occurrence of the dike swarm in the study area may have been controlled by underplating.     

Abstracts of Acta Geologica Sinica (Chinese Edition)Vol. 76, No. 3,2002

At the end of the Oligocene, the "long-range effect" of the India-Eurasia collision terminated the link between the Tarim basin and the Paiaeo-Mediterranean and the Tarim basin started a development of continental basin. A very thick continental sequence mainly of fluvial-lacustrine facies deposited in the western Tarim basin in the Neogene. This sequence, composed mainly of clastic rocks with intercalation of evaporites, and of varying thickness with maximum of 6050 m, is classified into the     

Thermochemistry of glasses and liquids in the systems CaMgSi2O6-CaAl2Si2O8-NaAlSi3O8, SiO2-CaAl2Si2O8-NaAlSi3O8 and SiO2-Al2O3-CaO-Na2O

Enthalpies of solution in 2PbO· B₂O₃ at 712°C have been measured for glasses in the systems albite anorthite diopside, NaAlO₂-SiO₂, Ca_0.5AlO₂-SiO₂ and albite-anorthite-quartz. The systems albite-anorthite and diopside-anorthite show substantial negative enthalpies of mixing, albite-diopside shows significant positive heats of mixing. For compositions up to NaAlO₂ = 0.42 (which includes the subsystem albite-silica) the system NaAlO₂-SiO₂ shows essentially zero heats of mixing. A negative ternary excess heat of mixing is found in the plagioclase-rich portion of the albite-anorthite-diopside system. The join Si₄O₈-CaAl₂Si₂O₈ shows small but significant heats of mixing. In albite-anorthite-quartz. ternary glasses, the ternary excess enthalpy of mixing is positive.Based on available heat capacity data and appropriate consideration of the glass transition, the enthalpy of the crystal-glass transition (vitrification) is a serious underestimate of the enthalpy of the crystal-liquid transition (fusion) especially when the melting point, T_f, is many hundreds of degrees higher than the glass transition temperature, T_g. On the other hand, the same heat capacity data suggest that the enthalpies of mixing in albite-anorthite-diopside liquids are calculated to be quite similar to those in the glasses. The enthalpies of mixing observed in general support the structural models proposed by Taylor and Brown (1979a, b) and others for the structure of aluminosilicate glasses.     

Thermochemical study of glasses in the system NaAlSi3O8-KAlSi3O8-Si4O8 and the join Na1.6Al1.6Si2.4O8-K1.6Al1.6Si2.4O8

Enthalpies of solution in 2PbO · B₂O₃ at 981 K have been measured for glasses in the system albite-orthoclase-silica and along the join Na_1.6Al_1.6Si_2.4O₈-K_1.6Al_1.6Si_2.4O₈. The join KAlSi₃O₈-Si₄O₈ shows zero heat of mixing similar to that found previously for NaAlSi₃O₈-Si₄O₈ glasses. Albite-orthoclase glasses show negative heats of mixing symmetric about Ab₅₀Or₅₀ (W_n = ? 2.4 ± 0.8 kcal). Negative heats of (Na, K) mixing are also found at $\text{Si}\text{(Si + Al)}\text{= 0.6.}$ Ternary excess enthalpies of mixing in the glassy system Ab-Or-4Q are positive but rarely exceed 1 kcal mol^?1.Using earlier studies of the thermodynamic properties of the crystals, the present calorimetric data and the “two-lattice” entropy model, the albite-orthoclase phase diagram is calculated in good agreement with experimental data. Attempts to calculate albite-silica and orthoclase-silica phase diagrams reveal complexities probably related to significant (but unknown) mutual solid solubility between cristobalite and alkali feldspar and to the very small heat and entropy of fusion of SiO₂.     

Alkali-free tourmaline in the system MgO-Al2O3-B2O3-SiO2-H2O

An end member of the tourmaline series with a structural formula □(Mg₂Al)Al₆(BO₃)₃[Si₆O₁₈](OH)₄ has been synthesized in the system MgO-Al₂O₃-B₂O₃-SiO₂-H₂O where it represents the only phase with a tourmaline structure. Our experiments provide no evidence for the substitutions Al → Mg + H, Mg → 2H, B + H → Si, and AlAl → MgSi and we were not able to synthesize a phase “Mg-aluminobuergerite” characterized by Mg in the (3a)-site and a strong (OH)-deficiency reported by Rosenberg and Foit (1975). The alkali-free tourmaline has a vacant (3a)-site and is related to dravite by the □ + Al for Na + Mg substitution. It is stable from at least 300°C to about 800°C at low fluid pressures and 100% excess B₂O₃, and can be synthesized up to a pressure of 20 kbars. At higher temperatures the tourmaline decomposes into grandidierite or a boron-bearing phase possibly related to mullite (“B-mullite”), quartz, and unidentified solid phases, or the tourmaline melts incongruently into corundum + liquid, depending on pressure. In the absence of excess B₂O₃ tourmaline stability is lowered by about 60°C. Tourmaline may coexist with the other MgO-Al₂O₃-B₂O₃-SiO₂-H₂O phases forsterite, enstatite, chlorite, talc, quartz, grandidierite, corundum, spinel, “B-mullite,” cordierite, and sinhalite depending on the prevailing PTX-conditions.The (3a)-vacant tourmaline has the space group R3m with $\text{a =15.90}\text{A}\text{?}$, $\text{c = 7.115}\text{A}\text{?}$, and $\text{V = 1557.0}\text{A}\text{?}{}^3$. However, these values vary at room temperature with the pressure-temperature conditions of synthesis by $\text{±0.015}\text{A}\text{?}\text{in a}$, $\text{±0.010}\text{A}\text{?}\text{in c}$, and $\text{±4.0}\text{A}\text{?}{}^3\text{in V}$, probably as a result of MgAl order/disorder relations in the octahedral positions. Despite these variations intensity calculations support the assumed structural formula. Refractive indices are n_o = 1.631(2), n_E = 1.610(2), Δn = 0.021. The infrared spectrum is intermediate between those of dravite and elbaite. The common alkali and calcium deficiencies of natural tourmalines may at least partly be explained by miscibilities towards (3a)-vacant end members. The apparent absence of (3a)-vacant tourmaline in nature is probably due to the lack of fluids that carry boron but no Na or Ca.     

Thermochemistry of glasses along joins of pyroxene stoichiometry in the system Ca2Si2O6-Mg2Si2O6-Al4O6

Enthalpies of solution in 2PbO · B₂O₃ at 974 K have been measured for glasses along the joins Ca₂Si₂O₆ (Wo)-Mg₂Si₂O₆ (En) and Mg₂Si₂O₆-MgAl₂SiO₆ (MgTs). Heats of mixing are symmetric and negative for Wo-En with W_H = ?31.0 ± 3.6 kJ mol^?. Negative heats of mixing were also found for the En-MgTs glasses (W_H = ?33.4 ± 3.7 kJ mol^?).Enthalpies of vitrification of pyroxenes and pyroxenoids generally increase with decreasing alumina content and with decreasing basicity of the divalent cation.Heats of mixing along several glassy joins show systematic trends. When only non-tetrahedral cations mix (outside the aluminosilicate framework), small exothermic heats of mixing are seen. When both nontetrahedral and framework cations mix (on separate sublattices, presumably), the enthalpies of mixing are substantially more negative. Maximum enthalpy stabilization near compositions with Al/Si ≈ 1 is suggested.     

A model for silicate melt viscosity in the system CaMgSi2O6-CaAl2Si2O8-NaAlSi3O8

Five hundred eighty-five viscosity measurements on 40 melt compositions from the ternary system CaMgSi₂O₆ (Di)-CaAl₂Si₂O₈ (An)-NaAlSi₃O₈ (Ab) have been compiled to create an experimental database spanning a wide range of temperatures (660-2175°C). The melts within this ternary system show near-Arrhenian to strongly non-Arrhenian properties, and in this regard are comparable to natural melts. The database is used to produce a chemical model for the compositional and temperature dependence of melt viscosity in the Di-An-Ab system. We use the Vogel-Fulcher-Tammann equation (VFT: log η = A + B/(T − C)) to account for the temperature dependence of melt viscosity. We also assume that all silicate melts converge to a common viscosity at high temperature. Thus, A is independent of composition, and all compositional dependence resides in the parameters B and C. The best estimate for A is −5.06, which implies a high-temperature limit to viscosity of 10^-5.06 Pa s. The compositional dependence of B and C is expressed by 12 coefficients (b_i=1,2.6, c_j=1,2..6) representing linear (e.g., b_i=1:3) and higher order, nonlinear (e.g., b_i=4:6) contributions. Our results suggest a near-linear compositional dependence for B (<10% nonlinear) and C (<7% nonlinear). We use the model to predict model VFT functions and to demonstrate the systematic variations in viscosity due to changes in melt composition. Despite the near linear compositional dependence of B and C, the model reproduces the pronounced nonlinearities shown by the original data, including the crossing of VFT functions for different melt compositions. We also calculate values of T_g for melts across the Di-An-Ab ternary system and show that intermediate melt compositions have T_g values that are depressed by up to 100°C relative to the end-members Di-An-Ab. Our non-Arrhenian viscosity model accurately reproduces the original database, allows for continuous variations in rheological properties, and has a demonstrated capacity for extrapolation beyond the original data.     

A hydrofluoric acid solution calorimetric investigation of glasses in the systems NaAlSi3O8-KAlSi3O8 and NaAlSi3O8-Si4O8

Glasses in the systems NaAlSi₃O₈-KAlSi₃O₈ and NaAlSi₃O₈-Si₄O₈ have been studied by means of hydrofluoric acid solution calorimetry at 50°C. Results indicate small negative enthalpies of mixing in the former system and small positive departures from ideality in the latter.     

Thermochemistry of synthetic clinopyroxenes on the join CaMgSi2O6-Mg2Si2O6

Enthalpies of solution of synthetic clinopyroxenes on the join CaMgSi₂O₆-Mg₂Si₂O₆ have been measured in a melt of composition Pb₂B₂O₅ at 970 K. Most of the measurements were made on samples crystallized at 1600°–1700°C and 30 kbar pressure, which covered the range 0–78 mole per cent Mg₂Si₂O₆, and whose X-ray patterns could be satisfactorily indexed on the diopside (C2/c) structure. For the reaction: Mg₂Si₂O₆→-Mg₂Si₂O₆ enstatite diopside the present data, in conjunction with previous and new measurements on Mg₂Si₂O₆ enstatite, determine ΔH° ~ 2 kcal and W_H (regular solution parameter) ~ 7 kcal. These values are in good agreement with those deduced by Saxena and Nehru (1975) from a study of high temperature, high pressure phase equilibrium data under the assumption that the excess entropy of mixing is small, but, in light of the recent theoretical treatment of Navrotsky and Loucks (1977, Phys. Chem. Min.1, 109–127), the meanings of these parameters may be ambiguous.Heat of solution measurements on Ca-rich binary diopsides made by annealing glasses at 1358°C in air gave slighter higher values than the higher temperature high pressure samples. This may be evidence for some (Ca, Mg) disorder of the sort postulated by Navrotsky and Loucks (1977, Phys. Chem. Min.1, 109–127), although no differences in heat of solution dependent on synthesis temperature in the range 1350°–1700°C could be found in stoichiometric CaMgSi₂O₆.     

莱河矿(Fe0.52+Fe1.03+SiO4)的超结构

莱河矿于1976年在中国辽宁省的磁铁矿床中首次被发现,许多人对它进行过研究。该矿物为黑色、不透明,化学式为Fe_0.58²⁺Fe_1.0³⁺Mg_0.03Si_0.96O₄,虽然它的晶体结构近似于橄榄石,但已确定为单斜晶系,空间群为P2₁/b。本文作者利用X射线、电子探针、高分解能透过电子显微镜对该矿物进行了系统的研究,发现它具有假双晶、超结构和显微条纹结构。     

Structure of mineral glasses—I. The feldspar glasses NaAlSi3O8, KAlSi3O8, CaAl2Si2O8

The short range distribution of interatomic distances in three feldspar glasses has been determined by X-ray radial distribution analysis. The resulting radial distribution functions (RDF's) are interpreted by comparison with RDF's calculated for various quasi-crystalline models of the glass structure.The experimental RDF's of the alkali feldspar glasses were found to be inconsistent with the four-membered rings of tetrahedra associated with crystalline feldspars; the structures of these glasses are probably based on interconnected six-membered rings of the type found in tridymite, nepheline, or kalsilite. In contrast, the RDF of calcic feldspar glass is consistent with a four-membered ring structure of the type found in crystalline anorthite. T-O bond lengths (T = Si,Al) increase from 1.60 Å in SiO₂ glass [J. H. Konnert and J. Karle (1973) Acta Cryst.A29, 702–710] to 1.63 Å in the alkali feldspar glasses to 1.66 Å in the calcic feldspar glass due to the substitution of Al for Si in the tetrahedra] sites. The T-O-T bond angles inferred from the RDF peak positions are 151° in SiO₂ glass (see reference above), 146° in the alkali feldspar glasses, and 143° in the calcic feldspar glass. Detail in the RDF at distances greater than 5 Å suggests that the alkali feldspar glasses have a higher degree of long range order than the calcic feldspar glasses.Assuming that the structural details of our feldspar glasses are similar to those of the melts, the observed structural differences between the alkali feldspar and calcic feldspar glasses helps explain the differences in crystallization kinetics of anhydrous feldspar composition melts. Structural interpretations of some thermodynamic and rheologic phenomena associated with feldspar melts are also presented based on these results.     

六氟化硫法测量33S/32S、34S/32S和36S/32S的方法研究

六氟化硫法是测量硫同位素组成的新方法。与传统的二氧化硫法相比，六氯化硫法有灵敏度高，准确度高，能同时测定扩δ³³S、δ³⁴S和δ³⁶S的优越性。本文介绍了国内第一台同位素分析用的六氟化硫制样装置，并报导了对硫化银、黄铁矿、黄铜矿、陨硫铁、方铅矿和闪锌矿等天然硫化物用六氟化硫法进行硫同位素测定的结果。结果表明，我们的装置和方法达到了国际上现有的水平，并在操作的方便性、可靠性及样品适用范围方面有所改进。