三块普通球粒陨石岩石矿物学特征及其复合球粒研究

普通球粒陨石数量约占球粒陨石的80%,对其开展研究有助于揭示早期太阳系的演化。本文使用扫描电镜和电子探针对三块普通球粒陨石的岩石学、矿物学和地球化学特征进行了分析，重点讨论了复合球粒的成因。研究表明，三块陨石均具典型的球粒陨石结构，其中GRV 050191与GRV 051993分别为LL3型和H3型陨石，球粒结构清晰且丰富；NWA 15005为H5型陨石，球粒可分辨，基质出现重结晶。GRV 050191与GRV 051993中矿物成分变化较大，橄榄石有成分环带，NWA 15005中矿物成分均一。根据陨石岩石矿物学特征，GRV 050191、GRV 051993和NWA 15005冲击变质程度分别为S2、S1和S3,风化程度为W1、W1和W2。复合球粒是由两个或多个球粒熔融形成的，本次研究发现的3个复合球粒，其中2个属于包封型复合球粒(CPC-1和CPC-3),1个为伴生型复合球粒(CPC-2)。SiO₂-FeO-MgO相图数据表明，复合球粒形成温度窗口约为100℃。根据复合球粒中橄榄石的FeO含量变化推测越早形成的球粒，其FeO含量越低，橄榄石化学成分变化趋势表明...     

我国普通球粒陨石岩石学,化学组成及分类的研究

对69个普通球粒陨石进行了岩石学及化学组成的研究,在此基础上提出橄榄石成分(mol％Fa)-铁纹石中钴含量两维分类参数,69个球粒陨石包括25个H、20个L、17个LL、2个介于H与L之间及5个介于L与LL之间的类型。根据矿物学的分类参数及化学组成的研究,普通球粒陨石母体至少有5个,即H、H/L、L、L/LL及LL,而不是3个(H、L及LL)。每群球粒陨石的不同岩石类型之间化学成分无重大的变化,表明球粒陨石的变质作用是在封闭体系的条件下发生的。本文给出了普通球粒陨石不同化学群和不同岩石类型的平均化学成分。     

南极格罗夫山陨石的磁化率

我国在南极格罗夫山发现并收集到大量南极陨石,需要一种无损、快速简单的分类方法。陨石磁化率(χ)的主要贡献是其中的铁镍金属,因而有可能成为一种简便有效的分类参数。同时,磁化率是陨石的一个重要物理参数。我们在国内首次开展陨石磁化率的研究,通过对模拟陨石磁化率样品的测量,证明可以通过不同取向的测量平均,将样品的大小和形状等几何因素的影响减小在仪器的测量精度范围之内。完成了首批613块南格格罗夫山陨石的磁化率测量,除普通球粒陨石外,还包括火星陨石、灶神星陨石、碳质球粒陨石、中铁陨石、橄榄陨铁、橄辉无球粒陨石等特殊类型。根据质量磁化率,可以划分大部分H、L、LL群陨石。特别重要的是,磁化率对于划分非平衡的普通球粒陨石化学群提供了更为可靠的参数。格罗夫山H群陨石的磁化率分布与南极其他地区的陨石十分相似,二者相对降落型陨石均向低质量磁化率方向平移0.2（logχ, 10^-9m³/kg）,反映了风化作用对南极陨石磁化率的平均影响程度;格罗夫山L群陨石的质量磁化率分布同样较降落型陨石偏低0.2左右,但南极其他地区的陨石与沙漠陨石的磁化率分布相似,二者均更为离散和偏低,可能反映了不同的风化程度。     

南极格罗夫山6块非平衡型普通球粒陨石的矿物-岩石学特征

主要报导了南极格罗夫山新回收的6块非平衡型普通球粒陨石的岩石学和矿物化学特征.它们都保存了原始的矿物-岩石学特征,包括非常清晰的球粒结构、基质不透明、橄榄石和低钙辉石颗粒具有明显的成分环带、以及颗粒之间极不均匀的化学组成等.这6块陨石包括3块高铁群(H3)和3块低铁群(L3)群.根据非平衡型普通球粒陨石中橄榄石成分Fa变化的PMD(相对标准偏差)值与陨石热变质程度的相关性,进一步划分岩石类型亚类:CRV 020016为H3.7型、GRV 020162为H3.5型、GRV 020166为H3.4型、GRV 020106为L3.7型、GRV 020164为L3.7型、GRV 020165为L3.7型.全部6块陨石的冲击变质程度很低,为S1-S2;样品比较新鲜,风化作用划分为W1-W2.     

我国球粒陨石稀有气体的研究

对43个球粒陨石进行了稀有气体分析,其中34个为我国球粒陨石,9个为国外球粒陨石。43个球粒陨石包括17个H、15个L、6个LL、3个L/LL、1个EH3及1个CV3-an化学群。给出了43个球粒陨石的宇宙射线暴露年龄及气体保存年龄,在此基础上讨论了二者(T_3/T_(21)与T_4/T_(40))之间的关系,划分出~3He_c和~4He_r同步丟失及~4He_r单独丢失两种类型的球粒陨石。     

南极三块（L3）陨石球粒结构类型及其矿物学物征

我国第16次南极考察队回收到6块稀少种类陨石-L3型,GRV99001,GRV99019,GRV99020,GRV99021, GRV99022,GRV99026。本文对其中3块陨石进行研究,研究它们的球粒结构和矿物化学成分．它们虽然都属于非平衡普通球粒陨石(L3),但它们的亚类不同,GRV 99001为L3．4,GRV99026为L3．5,GRV99019为L3．6．它们的球粒结构和球粒内的矿物晶体完整性和矿物组合变化比较大,橄榄石和辉石以高镁为特征．这三块陨石的球粒结构种类比较多,有班状的、炉条状的、扇形的和隐晶质的等．在GRV99001陨石中班状结构的球粒内能见到一个或两个以上完整的单晶橄榄石构成的球粒,也能见到多个细小的或是破碎橄榄石,被包裹在辉石晶体内．而在GRV99019和GRV99026陨石中只能见到多个细小单晶体或是破碎的橄榄石晶体．GRV99001陨石的炉条状结构,好象是由一条带状长石矿物,穿插在单个橄榄石晶体中构成．扇形和伞形结构的球粒,以一个点为中心,向外放射呈扇形．如GRV99019陨石中扇形结构球粒,它们是以辉石为主,陨硫铁充填在低钙辉石缝隙中,形成扇形．另一种是以多个点为中心,如GRV99001陨石,它们是由橄榄石、低钙辉石和长石质的玻璃,构成多个小伞形,形状类似三维立体的球,裂缝中也充填有金属矿物．隐晶质的球粒在GRV99026陨石中有两种,一种是在一厘米等于 100un时呈现隐晶质矿物,而放大到一厘米等于5un时,就可以清楚看到两种低钙辉石矿物,在低钙辉石中还有金属矿物．另一种隐晶质结构球粒由极细小破碎的橄榄石和辉石矿物构成．这三块陨石中的橄榄石和辉石都以高镁为特征．班状结构球粒,在GRV99001陨石中橄榄石的MgO-33．37-51．21,辉石为35．9-36．61;GRV99019陨石中橄榄石23．33-56．58,辉石 21．38-33．07;GRV99026陨石中橄榄石45．91-52．63,辉石34．48-37．35．扇形结构球粒,在GRV99001陨石中橄榄石29．94 -46．22,辉石28．17-30．36;GRV99019陨石中橄榄石29．17-34．38,辉石23．11-27．79．炉条状结构的球粒,在GRV99001 陨石中橄榄石51．84-56．03．隐晶质结构球粒,在GRV99026陨石中辉石20．17-21．54,橄榄石30．84-32．66．由此看出矿物晶体完整性越好镁的含量越高．     

风化作用对普通球粒陨石物理性质的影响

陨石的物理性质在陨石母体的演化过程中起到了重要作用。地球上的风化作用也会对陨石的一些物理性质造成显著影响。为了探讨风化对普通球粒陨石物理性质的影响,本文以库姆塔格普通球粒陨石为研究对象,使用密度仪、磁化率仪、热导仪、分光光度计等测量了其不同部位的物质性质,如颗粒密度,体积密度、孔隙度、磁化率、热导率、反射光谱强度等。研究结果表明:H型普通球粒陨石的颗粒密度、孔隙度、磁化率以及反射光谱强度会随着风化程度的加深而降低,而热导率和体密度受风化作用的影响相对较小。     

六个中国普通球粒陨石的组成和各相元素分布

本文运用INAA测定了6个中国普通球粒陨石磁性相21个元素和非磁相20个元素的含量。5个H群球粒陨石的组成没有显示出明显的差异,但其元素丰度明显地不同于另一个L群的肇东球粒陨石。相对于CI,磁性相中Ga归一化的元素丰度可以作为普通球粒陨石分群的指示剂。根据普通球粒陨石各相元素丰度建立的模式成分和组成与全岩分析结果一致。     

陨石分类研究进展及其地学意义

近40年来陨石分类学经历了3个发展阶段，60－70年代，由根据陨石的矿物结构的分类方法发展为球粒陨石的化学一岩石学分类法和铁陨石的化学群分类法；70－80年代，提出了分异型陨石和未分异型陨石的概念，球粒陨石被认为是未分异型陨石，而其它陨石（铁陨石，石铁陨石和无球粒陨石）大多被划入分异型陨石，80－90年代以来，陨石氧同位素组成成为了陨石成因分类的一个主要依据，使陨石分类学进入了一个新的成因分类阶段，作者对80－90年代以来新确立的R群，K小群，CR群和CK群球粒陨石，以及根据氧同位素划分出的原始型无球粒陨石系列：A－L无球粒陨石，Winonaites无球粒陨石和Brachinites无球粒陨石进行了介绍，笔者对陨石研究和陨石分类学的发展在估算地球整体成分，探讨地球成因和早期演化历史方面的重要意义进行了说明，并建议地球科学家应对陨石学和陨石分类的发展现状给以关注。     

我国首批回收的四块南极陨石类型的确定

中国第15次南极考察队于1999年元月在格罗夫山实施首次考察时回收了四块陨石，填补了我国南极陨石回收的空白。根据国际陨石协会命名委员会新回收陨石的命名原则，这些陨石已分别命名为GRV98001，GRV98002，GRV98003和GRV98004。根据初步岩石、矿物以及全岩化学分析，这四块陨石分别属于石质球粒陨石（GRV98001），L5型球粒陨石（GRV98002），H4型球粒陨石（GRV98004）和极细粒八面体缺陨石（GRV98003）。     

Classification of 24 New Ordinary Chondrites from the Grove Mountains, Antarctica

Petrography and mineral chemistry of 24 ordinary chondrites from the Grove Mountains, Antarctica, have been studied in order to identify their chemical-petrographic types. These samples were selected from a total of 4448 Grove Mountains (GRV) meteorites collected during the 19th Chinese Antarctic Research Expedition so as to make an estimation of the large GRV meteorite collection. The chemical-petrographic types of these meteorites are presented below: 1 H3,2 H4, 4 H5, 2 H6, 1 L4, 7 L5, 5 L6, 1 LL4 and 1 LL6. The new data weaken the previous report that unequilibrated ordinary chondrites are unusually abundant in the Grove Mountains region. However, this work confirms significant differences in distribution patterns of chemical-petrographic types between the Grove Mountains and other     

Bulk compositions of metallic Fe-Ni of chondrites： Constraints on fractionation of siderophile and chalcophile elements

Bulk compositions of metallic Fe-Ni from two equilibrated ordinary chondrites, Jilin (H5) and Anlong (H5), and two unequilibrated ones, GRV 9919 (L3) and GRV 021603 (H3), were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). The CI-, Co-normalized abundances of siderophile and chalcophile elements of metallic Fe-Ni from the unequilibrated ordinary chondrites correlate with 50% condensation temperatures (i.e., volatility) of the elements. The refractory siderophile elements (i.e., platinum group elements, Re), Au, Ni and Co show a flat pattern (1.01×CI Co-normalized), while moderate elements (As, Cu, Ag, Ga, Ge, Zn) decrease with volatility from 0.63×CI (Co-normalized, As) to 0.05×CI (Co-normalized, Zn). Cr and Mn show deficit relative to the trend, probably due to their main partition in silicates and sulfides (nonmagnetic). Metallic Fe-Ni from the equilibrated ordinary chondrites shows similar patterns, except for strong deficit of Cr, Mn, Ag and Zn. It is indicated that these elements were almost all partitioned into silicates and/or sulfides during thermal metamorphism. The similar deficit of Cr, Mn, Ag and Zn was also found in iron meteorites. Our analyses demonstrate similar behaviors of W and Mo as refractory siderophile elements during condensation of the solar nebula, except for slight depletion of Mo in the L3 and H5 chondrites. The Mo-depletion of metallic Fe-Ni from GRV 9919 (L3) relative to GRV 021603 (H3) could be due to a more oxidizing condition of the former than the latter in the solar nebula. In contrast, the Mo-depletion of the metallic Fe-Ni from the H5 chondrites may reflect partition of Mo from metal to silicates and/or sulfides during thermal metamorphism in the asteroidal body.     

Ca-, Al-rich Inclusions in Three New Carbonaceous Chondrites from the Grove Mountains, Antarctica: New Evidence for a Similar Origin of the Objects in Various Groups of Chondrites

Three new carbonaceous chondrites (GRV 020025,021579 and 022459) collected from the Grove Mountains (GRV), Antarctica, have been classified as the CM2, CO3 and CV3 chondrites, respectively. A total of 27 Ca- and Al-rich inclusions have been found in the three meteorites, which are the earliest assemblages formed in the solar nebula. Most of the inclusions are intensively altered, with abundant phyllosilicates in the inclusions from GRV 020025 and FeO enrichment of spinel in those from GRV 022459. Except for one spinel-spherule in each of GRV 020025 and     

The Varre-Sai chondrite,a Brazilian fall: petrology and geochemistry

The Varre-Sai meteorite fell along the border of the states of Espirito Santo and Rio de Janeiro, Brazil; on 19 June 2010 at 5:40 pm. Petrography and X-ray powder diffraction (XRD) indicate that the rock is an L5 S4 chondrite, with blastoporphyritic texture that has not been previously described. Geochemical data based on major and rare-earth elements (REEs) show that Varre-Sai is highly similar to the other L chondrites. In Harker diagrams, Varre-Sai, L, and LL chondrites form a single group, suggesting no significant chemical differences between them and contributing to the long-standing debate of whether LL chondrites form a distinct group or whether they are a subset of the L group. Harker diagrams also define a trend from E to H and L/LL chondrites, similar to the cosmochemical trends suggested by other authors. The behaviour of Fe₂O_3t and NiO indicates a relationship with Fe-Ni alloys, and their trend in the diagram suggests some chemical differentiation in the ordinary chondrite parental bodies. The REE content in Varre-Sai, normalized to C chondrites, falls in the field of L chondrites and others, but with slight REE enrichment. The chemical differences in chondrites, mainly in REEs, Fe₂O_3t and NiO could be alternatively interpreted as variations in the inherited agglutinated materials as chondrules, Ca–Al-rich inclusions and Fe–Ni nodules.     

Composition of the metal phases in ordinary chondrites: implications regarding classification and metamorphism

EMP determinations of Fe, Co and Ni in the metal phases of ordinary chondrites confirm the report of Sears and Axon that kamacite Co contents show restricted, nonoverlapping ranges in the three groups; ranges are 3.3–4.8 mg/g in H, 6.7–8.2 mg/g in L and 15–110 mg/g in LL. Experimental data by Widge and Goldstein show that the Ni concentration of the $\text{α}\text{(α + γ)}$ boundary increases with increasing Co concentration: unexpectedly, we find lower kamacite Ni concentrations in unequilibrated LL chondrites (44–55 mg/g) than in H and L chondrites (57–69 mg/g). We infer that, at temperatures below 550° C increasing Co causes a decrease in the equilibrium kamacite Ni concentration of an α-γ system. Although some evidence indicates that the equilibrated L chondrites Barratta, Knyahinya and Shaw have siderophile concentrations lower than the normal L-group range, they have kamacite and taenite Co concentrations in the L-group range.Metal-phase studies of petrologic type-3 ordinary chondrites having highly unequilibrated silicates showed a wide range in the degree of matrix kamacite equilibration ranging from nearly equilibrated in Mezö-Madaras to highly unequilibrated in Bishunpur, Ngawi and Semarkona. Kamacite in chondrule interiors is highly unequilibrated in all 9 chondrites, and in each setting taenite data are consistent with the expectation that it should be less equilibrated than kamacite. Our kamacite Co data confirm that Sharps is H and Hallingeberg. Khohar and Mezö-Madaras are L chondrites. Chainpur and Parnallee have kamacite Co concentrations between the L and LL ranges: we present evidence indicating that they are truly intermediate, i.e. neither L nor LL. Highly unequilibrated Ngawi is either LL or, less likely, still more oxidized. Bishunpur and Semarkona have mean kamacite Co concentrations in the H range but too unequilibrated to be used for classification. The highly heterogeneous compositions of the metal in Bishunpur, Ngawi and Semarkona indicate that their metal partially preserves properties established during nebular processes. Most of the taenite in these chondrites has high Ni contents (>470 mg/g) and is essentially unzoned; much of the kamacite is polycrystalline with crystals ?5μm across. Metamorphism causes tiny grains to disappear, increases the grain size of both kamacite and taenite, tends to equilibrate metallic minerals and, during cooling, can produce zoned taenite.A petrologic type-5 clast in the Ngawi LL3 chondrite has 3 coexisting metal phases, clear taenite (540 mg/g Ni, 21 mg/g Co), kamacite (30 mg/g Ni, 120 mg/g Co) and a phase tentatively identified as ordered FeCo (8.5 mg/g Ni, 370 mg/g Co).     

南极普通球粒陨石风化等级的重新厘定

在南极格罗夫山普通球粒陨石的风化等级划分中出现了和Wlotzka(1993)标准矛盾的现象。部分普通球粒陨石的金属和陨硫铁氧化不足20%,然而硅酸盐却发生了蚀变。如果考虑金属的氧化量,这种风化程度应为W1,如果考虑硅酸盐的蚀变,这种风化程度应为W5。对于存在如此大的差异本文给出了折衷的解决办法——对金属和硅酸盐同时进行风化等级划分。金属的风化等级划分为W_m0-W_m4五个,硅酸盐风化等级划分为W_s0-W_s3四个。依据新方案,GRV 021588、021636、021772和021957等4块无法用Wlotzka(1993)标准来确定风化等级的陨石的风化等级均为W_m1-W_s1。而陨石GRV 023312的风化等级为W_m3-W_s0,其相当于Wlotzka(1993)标准中的W3。     

我国南极陨石研究与展望

继1998～2000年我国第15、16次南极科考队在南极格罗夫山发现32块陨石之后，2002～2003年第19次科考队成立了以回收陨石为中心任务的格罗夫山综合考察分队，在同一地区成功回收4448块陨石。我国的南极陨石回收工作不但实现了零的突破，而且成为继日本和美国之后拥有南极陨石数量最多的国家之一。通过对第15、16次队回收的32块陨石以及第19次队4448块陨石中的38块代表性样品的化学一岩石类型划分工作,除平衡型普通球粒陨石外，发现了2块火星陨石、2块橄辉无球粒陨石、6块非平衡L3型陨石、4块碳质球粒陨石和1块非平衡型顽辉石球粒陨石等特殊类型陨石。本文主要介绍了南极陨石的回收和研究进展，以及我国在南极格罗夫山回收陨石的情况和已取得的初步研究成果。同时对我国今后的陨石回收与研究工作提出初步设想。     

New data on the abundance of palladium in meteorites

The concentration of Pd in 7 carbonaceous chondrites, 18 ordinary chondrites, 3 achondrites, 29 iron meteorites and other samples has been determined by stable isotope dilution using solid source mass spectrometry. The Cl chondrite Orgueil gives a ‘cosmic’ abundance for Pd of 1.5 (Si = 10⁶ atoms), in good agreement with the currently accepted value.The concentration of Pd shows little variation among the carbonaceous chondrites, but in ordinary chondrites decreases from the H to L to LL groups. Pd in achondrites is approx 100 times lower than in chondrites. Data for iron meteorites plot around the ‘cosmic’ $\text{Pd}\text{Ni}$ ratio; however the Pd data falls into distinct groups, corresponding to the chemical group classification. These results support the hypothesis that at least two fractionation processes have occurred during the formation of iron meteorites.     

Abundance patterns of thirteen trace elements in primitive carbonaceous and unequilibrated ordinary chondrites

A neutron activation analysis technique was used to determine Au, Re, Co, Mo, As, Sb, Ga, Se, Te, Hg, Zn, Bi and Tl in 11 carbonaceous chondrites, 12 unequilibrated ordinary chondrites (UOC), and 4 equilibrated ordinary chondrites. The first 6 elements are ‘undepleted’, the next 3 ‘normally-depleted’ and the last 4 ‘strongly-depleted’. Except for Hg, ‘depleted-element’ abundances in carbonaceous chondrites lead to mean relative ratios of C1:C2:C3 = 1.00:0.53:0.29, i.e. those predicted by a two-component (mixing of high-temperature and low-temperature fractions) model. The last 4 nominally ‘undepleted’ elements are somewhat depleted in ordinary chondrites, As and Sb showing partial depletion in C3 and the latter in C2 chondrites as well. This requires a modification of the two-component model to indicate that deposition of elements during condensation of high temperature material was not an all-or-nothing process.Apart from Bi and Tl, the elements studied have similar abundances in unequilibrated and equilibrated ordinary chondrites and only the former are unquestionably correlated with the degree of disequilibrium in silicate minerals. Only some ‘strongly-depleted’ elements exhibit at least one of the following—proportional depletion in UOC, progressive depletion in petrographic grades 3–6 ordinary chondrites and enrichment in the gas-containing dark portion of gas-rich, light-dark meteorites—indicating that such depletion does not ensure that an element will exhibit these trends. Partly or completely siderophile As, Au, Co, Ga, Mo, Re and Sb vary with chemical type in the same manner in both unequilibrated and equilibrated ordinary chondrites and doubtless reflect a process involving fractionation of metallic iron.     

Petrographic and oxygen-isotopic study of refractory forsterites from R-chondrite Dar al Gani 013 (R3.5-6), unequilibrated ordinary and carbonaceous chondrites

We have conducted petrographic, chemical and in-situ oxygen isotopic studies of refractory forsterites from unequilibrated ordinary and carbonaceous chondrites as well as an unequilibrated R-chondrite. Refractory forsterites occur in all types of unequilibrated chondrites and all have very similar chemical composition with low FeO and high refractory lithophile element (RLE) contents. Refractory forsterites are typically enriched in ¹⁶O relative to ‘normal’ olivine independent of the bulk O-isotope ratios of the parent meteorites. Analyses of refractory forsterites spread along a Δ¹⁷O mixing line with Δ¹⁷O ranging from +2 to −10‰. Due to similarities in oxygen isotopes and chemical compositions, we conclude that refractory forsterites of various types of chondrites come from a single common reservoir. Implications of this hypothesis for the chemical and O-isotope evolution of silicates in the early solar nebular are discussed.