对南极类C1陨石成因和星云水化作用范围的几点看法

南极陨石的研究发现，有几个碳质球粒陨石富含与ＣＩ陨石类似的含水层状硅酸盐集合体及其角砾，其氧同位素比值也与ＣＩ接近，因而称之为类Ｃ１陨石。类Ｃ１陨石与Ｃ１陨石的区别是：类Ｃ１陨石中的含水层状硅酸盐既以基质的形式产出，也出现在球粒中；类Ｃ１陨石中含有球粒及有关组分，如球粒碎块、矿物集合体等。每个陨石中所含这些组分的数量不同，其矿物的成分也差别很大，从而说明它们形成的星云环境不同。因此笔者认为类Ｃ１陨     

太阳星云凝聚过程的岩石学模型：（Ⅱ）非球陨石、C1陨石及类C1陨石的凝聚成因和小行星区星云凝聚作用

综述了非球陨石（铁陨石，石铁陨石和无球粒陨石）在成分结构方面的非分异成因证据，推断其成因是：星云盘中心层中的星云发生气－液凝聚作用形成的熔滴，在较高温度下彼此合并形成了较大熔体，熔体固化后形成该类陨石母体。根据Ｃ１陨石不含球粒和其它成分特征，推断它们是星云只发生气－固凝聚作用的产物。对近年来新发现的一些特殊成分的碳质球粒陨石进行了综合分析，暂定名为类Ｃ１陨石。通过类Ｃ１陨石与其它球粒陨石及Ｃ１陨石成分结构特征的对比，推断它们是星云盘边缘层星云发生气－液－固和气－固联合凝聚作用，同时发生水化作用的产物。最后，在对所有陨石凝聚成因进行解释的基础上，建立了小行星区星云凝聚模型。     

肇东和亳县陨石中的黑包体及其成因意义

肇东、毫县陨石中的黑包体在总体成分、形状、大小上与陨石球粒相似,但两者的内部结构以及矿物组合不同。黑包体中矿物呈密堆状,主要由细粒橄榄石以及其它硅酸盐微晶组成,不含火成玻璃等特点表明黑包体未经历过熔融,它们可能是形成球粒的毛坯。因此认为球粒的形成有三个阶段:星云凝聚形成尘粒—尘粒吸积形成黑包体—黑包体熔融形成球粒。     

太阳星云凝集过程的岩石学模型：（Ⅲ）类地行星区星云凝集作用和地球…

在建立了小行星星云凝聚模型的基础上，对类地行星区中土物质（硅酸盐、氧化物、金属、硫化物等）的凝聚作用，以及凝聚物的水化作用进行了讨论。进而建立了包括小行星区在内的整个类地行星区的星云凝聚模式。根据地球核幔质量比和关于地球初期演化的研究结果：使用顽光辉石球粒陨石和Ｃ１陨石的化学成分分别做为地球形成区中类顽光辉石球粒陨石质星子和类Ｃ１陨石质星子和类Ｃ１陨石质星子的成分数据，假定类顽光辉石无球粒陨石质昨     

山东省鄄城陨石中的金属矿物及组构特征

1997年降落在山东省鄄城县的陨石雨,是橄榄石-古铜辉石球粒陨石。该陨石中的金属矿物主要为铁纹石和陨硫铁,其次为镍纹石,金属矿物呈填隙状分布于以橄榄石和古铜辉石为主的硅酸盐矿物粒间及球粒周围。陨石中可见由铁纹石和镍纹石组成的显微蠕虫状连晶,是陨石中金属矿物在降温冷却过程中发生固溶体分离作用而成。陨石中金属矿物的分布特征表明,金属Fe-Ni和硫化物（FeS）应该是星云凝聚不同阶段的产物。陨石中金属矿物的成分和组构特征及陨石中出现的球粒结构、橄榄石的炉条结构等特征表明,该球粒陨石是星云物质快速冷却的产物。     

太阳星云凝集过程的岩石学模式：（Ⅱ）非球陨石,C1陨石及类C1陨石的凝…

综述了非球陨石（铁陨石、石铁陨石和无球粒陨石）在成分结构方面的非分异成因证据，推断其成因是：星云盘中心层中的星云发生气－液凝聚作用形成的熔滴，在较高温度下彼此合并形成了较大熔体，熔体固化后形成该类陨石母体。根据Ｃ１陨石不含球粒和其它成分特征。推断它们是星云只发生气－固凝集作用的产物。     

太阳星云凝聚过程的岩石学模型：（Ⅲ）类地行星区星云凝聚作用和地球原始成分的估算

在建立了小行星区星云凝聚模型的基础上，对类地行星区中上物质（硅酸盐、氧化物、金属、硫化物等）的凝聚作用，以及凝聚物的水化作用进行了讨论，进而建立了包括小行星区在内的整个类地行星区的星云凝聚模式。根据地球核慢质量比和关于地球初期演化的研究结果；使用顽火辉石球粒陨石和Ｃ１陨石的化学成分分别做为地球形成区中类顽火辉石球粒陨石质星子和类Ｃ１陨石质星子的成分数据；假定类顽火辉石无球粒陨石质星子的成分与类顽火辉石球粒陨石质星子的硅酸盐部分成分相同，计算出原始地球可能由１．５８％的类铁陨石质星子、１３．９％的类顽火辉石无球粒陨石质星子、８２．５２％类顽火辉石球粒陨石质星子、２％的类Ｃ１陨石质星子组成。     

陨石含水矿物成因评述和地球水来源的探讨

简要介绍了球粒陨石中含水矿物的种类和主要特点，根据陨石中含水矿物与无水矿物，有机质的关系，太阳星云凝聚模型中有关水蒸汽与无水矿物反应的理论，以及有关的同位素资料的综合分析，推断形成含水矿物的水化作用是太阳星云凝聚作用的一个阶段，通过不同类型球粒陨石氧同位素组成和含水矿物数量的比较，论证了太阳星云盘中发生水作用的范围，从而对地球水的来源进行了讨论。     

普通球粒陨石NWA15004岩石矿物学特征及球粒类型研究

普通球粒陨石是目前发现数量最多的陨石,对认识早期太阳星云演化和太阳系物质成分具有重要的意义。Northwest Africa (NWA) 15004是一块非洲西北部新发现的普通球粒陨石。本次研究使用光学显微镜、电子探针以及扫描电镜等分析仪器对该陨石进行详细的岩石学、矿物学及球粒特征研究。结果表明该陨石球粒轮廓较为模糊,基质重结晶明显,橄榄石平均Fa值为25.4 mol%(PMD为2.65%),低钙辉石的平均Fs值21.3 mol%(PMD为3.95%),硅酸盐矿物化学成分较为均一,根据岩相学及矿物学特征将其划分为L5型普通球粒陨石。橄榄石和辉石颗粒发育波状消光和面状破裂,且观察到有熔融囊的出现,表明该陨石受到S3以上的冲击变质作用。球粒的成因和形成的星云环境需要准确的球粒类型划分,球粒按结构类型分类较多,但其化学成分均一,该陨石所有球粒的橄榄石辉石的Mg^#约为74.5,均为Ⅱ型富铁球粒,结合“CIPW标准”计算基质化学成分均为A5型球粒。利用共生单斜辉石和斜方辉石矿物对成分特征计算得到NWA 15004陨石热变质平衡温度为814℃,说明该陨石母体经历了较高程度热变...     

清镇顽辉石球粒陨石（EH3）不透明相的岩石,矿物学研究

通过对最新鲜、最原始的ＥＨ３型损石－清镇员石不透明矿物的岩石学、矿物学研究，揭示了不透明矿物化学组成与产状的成因关系，提出了星云冷凝，金属与星去气相组分的硫化反应，矿物出熔及矿物分解等四种形成机制。对不透明物的各种环带结构及闪锌矿、矿镁矿等矿物温度计的研究，揭示了该陨石在星云阶段和母体中的热历史，与Ｙａｍａｔｏ－６９１（ＥＨ３）的对比表明，清镇陨石不透明矿物形成于更加还原的星云条件。     

Matrix phyllosilicates and associated minerals in C2M carbonaceous chondrites

TEM, HRTEM, HVEM and SEM methods, coupled with energy dispersive X-ray analysis, have been used to study the microstructure and the phases comprising the matrix of carbonaceous chondrites Murchison, Cold Bokkeveld, Nawapali and Cochabamba. A wide variety of phyllosilicate morphologies occurs in each. Very small crystals and clasts of olivine, pyroxene and other unhydrated minerals are mixed intimately with the phyllosilicates. Intergrowths of carbonates and Sulfides within the phyllosilicates also occur, as well as a ubiquitous spongey material which is difficult to characterize, but contains elementary phyllosilicate units and embryo crystals. The identifiable large crystalline phyllosilicates are principally Fe-rich serpentine-group minerals and intermediate more Mg-rich chrysotilelike group members, with characteristic ~ 7.0–7.4 Å basal layer spacings. Complex interlayered and intergrown hydrous minerals also occur associated with the spongey material, and other poorly crystalline silicates and finely divided Fe-Ni sulphides. Fe/Si and Mg/Si ratios vary on a sub-micron scale, and the morphologies of the larger phyllosilicate crystals correlate broadly with these variations. Small crystals of sodium chloride and potassium chloride have been identified, occluded within a predominantly organic mass.The matrix minerals have a multistage history of formation in which the effects of aqueous alteration are dominant. Few, if any, of matrix minerals can be unmodified nebular condensates, although some clasts and inclusions have escaped alteration and predate the alteration process.     

The Confirmation of a New Type of Chondrites and Their Cosmochemical Significance

The data available show that some Antarctic carbonaceous chondrites are similar to Cl meteorites.Tehy contain a lot of phyllosilicate aggregates and the oxygen isotopic composition of the whole-rock samples is approximate to that of C1 chondrites,so they are named after quasi-C1(Q-C1)chondrites Unlike Cl metcorites,the Q-Cl chondites possess chondrule structrue,and the compositions of hih temperature condensates(chondrule fragments,mineral grains or aggregates)show that the oxygen fugacity varied within a wide range in the surroundings where they were formed,similar to the variation range from E.H.L,LL to C group chondrites.It is inferred that the Q-C1 chondrites could be formed at the edges far from the equator in the whole asteroid region of the solar nebular disk.where the nebula was lower in density and the condensates were lower in accretion velocity,so that the hydration of chon drules and matrix occurred during the late stage of nebular condensation.The discovery of the Q-Cl chondrites and the fact that the earth and other terrestrial planets contain water indicate that at the edges far from the equator in the terrestrial reigion of the solar nebular disk,a large amount of water was incorporated into the lattice of minerals in the condensates as a result of hydration during nebular condensation,and then found its way into the interior parts of the Earth and other terrestrial planets due to accretion.     

Cumberland Falls chondritic inclusions—II. Trace element contents of forsterite chondrites and meteorites of similar redox state

Mineralogic study of black inclusions in the Cumberland Falls enstatite achondrite revealed that they constitute a highly unequilibrated chondritic suite distinct from other chondrite groups. This highly shocked suite, the forsterite (F) chondrites, exhibits mineralogic trends apparently produced during primary nebular condensation and accretion over a broad redox range. We analyzed these samples and possibly related meteorites for Ag, As, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Sb, Se, Te, Tl, U and Zn, trace elements known to yield important genetic information. The results demonstrate the compositional coherence and distinctiveness of the F chondrite suite relative to other chondrites. The Antarctic aubrite, ALH A78113, may include more F chondrite material. Trace element contents do not vary with mineral compositions hence do not reflect redox variations during formation of F chondrite parental matter. Trace element mobilization—during secondary heating episodes in the F chondrite parent or during its disruptive collision with the enstatite meteorite parent body—is not detectable. Chemical trends in F chondrites apparently reflect primary nebular processes. Cosmochemical fractionation of lithophiles from siderophiles and chalcophiles occurred at moderately high temperatures, certainly higher than those existing during formation of primitive carbonaceous, enstatite and ordinary chondrites of petrologic type ≤3.     

Hydrous mineralogy of CM and CI chondrites from infrared spectroscopy and their relationship with low albedo asteroids

IR spectroscopy is one of the few techniques that can directly probe water molecules in rocks. This method has been used to characterize the mineralogy of hydrated/hydrous carbonaceous chondrites, and to link known meteorite families with spectroscopic observations of low albedo asteroids. In this paper, we present measurements of the infrared transmission spectra of matrix chunks from 3 CI and 9 CM chondrites. Spectra were measured at ambient conditions and then at different temperatures along a dehydration path toward high-T (∼300 °C) under primary vacuum. At ambient conditions, the 3-μm spectral range is always dominated by adsorbed atmospheric water molecules. Upon moderate (∼100 °C) and high (∼300 °C) heating under low pressure (P < 10⁻⁴ mbar), adsorbed water and then phyllosilicates interlayer water are removed, revealing a residual absorption band around 3 μm. This band is a characteristic IR feature of the phyllosilicate phases which dominate the mineralogical assemblage of hydrated carbonaceous chondrites. Among the CM chondrites, the high-T spectra reveal a strong variability that appears correlated with the alteration classification scheme of Rubin et al. (2007) and Howard et al. (2009a). The 3-μm band continuously evolves from a broad feature peaking at 3550-3600 cm⁻¹ for the weakly altered CMs (Murchison-type) to a sharp asymmetric peak at ∼3675 cm⁻¹ for the more extensively altered samples (Cold Bokkeveld-type). We attribute this spectral evolution to variations in the chemistry of the phyllosilicate phases from Fe-rich to Mg-rich. On the other hand, the 10-μm spectral region shows a single broad peak which does not compare with known terrestrial serpentine spectra, probably due to high structural disorder of the chondrite phyllosilicate phases. The present work clearly shows that previously published reflectance spectra of chondrites are biased by the presence of adsorbed terrestrial water molecules. Laboratory data collected under dry conditions are needed to reinterpret the chondrite-asteroid connection from the comparison of their 3-μm absorption features.     

Indicators of parent-body processes: Hydrated chondrules and fine-grained rims in the Mokoia CV3 carbonaceous chondrite

A petrographic and electron microscopic study of the Mokoia CV3 carbonaceous chondrite shows that all of the chondrules and inclusions (>400 μm in diameter) and most of their fine-grained rims studied (referred to as chondrules/rims) contain various amounts of hydrous phyllosilicates (mostly saponite) formed by aqueous alteration of anhydrous silicates. The rims mainly consist of fine-grained olivine and saponite in varying proportions and contain crosscutting veins of Fe-rich olivine. The boundaries between the chondrules and their rims are irregular and show abundant evidence of aqueous alteration interactions between them. In contrast, the host matrix contains very minor amounts of saponite and shows no evidence of such extensive aqueous alteration. The boundaries between the chondrules/rims and the matrix are sharp and show no traces of the matrix having been involved in the alteration of the chondrules/rims. These observations indicate that the aqueous alteration in the chondrules/rims did not occur in the present setting.We suggest that the chondrules/rims are actually clasts transported from a location on the meteorite parent body different from where the Mokoia meteorite was from. The aqueous alteration of the chondrules/rims probably occurred there. The veins in the rims were originally fractures produced in an interchondrule matrix by impacts; these were later filled by Fe-rich olivine during aqueous activity. This location was then involved in impact brecciation, and individual chondrules were ejected as clasts with remnants of the matrix surrounding them. During the continuing brecciation, those chondrule/rim clasts were transported, mixed with anhydrous matrix grains, and finally lithified to the present meteorite. Therefore, the rims are fragmented remnants of a former matrix.Textures characterized by fine-grained rims surrounding chondrules in chondrites have been widely thought to have formed in the solar nebula before they accreted into their parent bodies. However, our results suggest that some textures may not be explained by such an accretionary model; instead, the multi-stage parent-body process modeled for the Mokoia rim formation may be a more plausible explanation.     

The mineral chemistry and origin of inclusion matrix and meteorite matrix in the Allende CV3 chondrite

The two textural varieties of olivine-rich Allende inclusions (rimmed and unrimmed olivine aggregates) consist primarily of a porous, fine-grained mafic constituent (inclusion matrix) that differs from the opaque meteorite matrix of CV3 chondrites by being relatively depleted in sulfides, metal grains, and (perhaps) carbonaceous material. Olivine is the most abundant mineral in Allende inclusion matrix; clinopyroxene, nepheline, sodalite, and Ti-Al-pyroxene occur in lesser amounts. Olivine in unrimmed olivine aggregates (Type 1A inclusions) is ferrous and has a narrow compositional range (Fo_50–65). Olivine in rimmed olivine aggregates (Type 1B inclusions) is, on average, more magnesian, with a wider compositional range (Fo_53–96). Olivine grains in the granular rims of Type 1B inclusions are zoned, with magnesian cores (Fo_>80) and ferrous rinds (Fo_<70). Ferrous olivines (Fo_<65) in both varieties of inclusions commonly contain significant amounts of Al₂O₃ (as much as ~0.7 wt%), CaO (as much as ~0.4 wt%), and TiO₂ (as much as ~0.2 wt%), refractory elements that probably occur in submicroscopic inclusions of Ca,Al,Ti-rich glass (rather than in the olivine crystal structure). Defocussed beam analyses of Allende matrix materials demonstrate that: (1) inclusion matrix in Type 1A inclusions is more enriched in olivine and FeO than inclusion matrix in the cores of Type 1B inclusions; (2) opaque matrix materials are depleted in feldspathoids and enriched in sulfides and metal grains relative to inclusion matrix; (3) the bulk compositions of Type 1A and Type 1B inclusions overlap; and (4) excluding sulfides and metal, the bulk compositions of Allende matrix materials cluster in a complementary pattern around the bulk composition of C1 chondrites.Inclusion matrix and meteorite matrix in Allende and other CV3 chondrites are probably relatively primitive nebular material, but a careful evaluation of the equilibrium condensation model suggests that these matrix materials do not consist of crystalline phases that formed under equilibrium conditions in a relatively cool gas of solar composition. Allende inclusion matrix is interpreted as an aggregate of condensates that formed under relatively oxidizing, non-equilibrium conditions from supercooled, supersaturated vapors produced during the vaporization of interstellar dust by aerodynamic drag heating in the solar nebula; CV3 meteorite matrix contains, in addition, a proportion of interstellar material that was heated (but not vaporized) in the nebula. Granular olivine in rimmed olivine aggregates may have formed during the recrystallization and incipient melting of aggregates of inclusion matrix in the nebula. The mineral chemistry of matrix olivine in Allende seems to have been established by three different processes: non-equilibrium vapor → solid condensation; recrystallization and partial melting in the nebula; and $\text{Fe}\text{Mg}$ equilibration (without textural homogenization) in the meteorite parent body.