Terrestrial Kr-Kr ages of Antarctic meteorites

The production rate of ³⁸Ar in meteorites—P(38)—has been determined, as a function of the sample's chemical composition, from ⁸¹Kr-Kr exposure ages of four eucrite falls. The cosmogenic ⁷⁸Kr/⁸³Kr ratio is used to estimate the shielding dependence of P(38).

From the “true” ³⁸Ar exposure ages and the apparent ⁸¹Kr-Kr exposure ages of nine Antarctic eucrite finds, terrestrial ages are calculated. They range from about 3 × 10⁵ a (Pecora Escarpment 82502) to very recent falls (Thiel Mountains 82502). Polymict eucrites from the Allan Hills (A78132, A79017 and A81009) have within the limits of error the same exposure age (15.2 × 10⁶ a) and the same terrestrial age (1.1 × 10⁵ a). This is taken as strong evidence that these meteorites are fragments of the same fall. A similar case are the Elephant Moraine polymict eucrites A79005, A79006 and 82600 with an exposure age of 26 × 10⁶ a and a terrestrial age of 1.8 × 10⁵ a. EETA79004 may be different from this group because its exposure age and terrestrial age are 21 × 10⁶ a and 2.5 × 10⁵ a, respectively.

The distribution of terrestrial ages of Allan Hills meteorites is discussed. Meteorites from this blue ice field have two sources: Directly deposited falls and meteorites transported to the Allan Hills inside the moving Antarctic ice sheet. During the surface residence time meteorites decompose due to weathering processes. The weathering “half-life” is about 1.6 × 10⁵ a. From the different age distributions of Allan Hills and Yamato meteorites, it is concluded that meteorite concentrations of different Antarctic ice fields need different explanations.     

Noble gases and nitrogen in Martian meteorites Dar al Gani 476, Sayh al Uhaymir 005 and Lewis Cliff 88516: EFA and extra neon

Meteorite “finds” from the terrestrial hot deserts have become a major contributor to the inventory of Martian meteorites. In order to understand their nitrogen and noble gas components, we have carried out stepped heating experiments on samples from two Martian meteorites collected from hot deserts. We measured interior and surface bulk samples, glassy and non-glassy portions of Dar al Gani 476 and Sayh al Uhaymir 005. We have also analyzed noble gases released from the Antarctic shergottite Lewis Cliff 88516 by crushing and stepped heating. For the hot desert meteorites significant terrestrial Ar, Kr, Xe contamination is observed, with an elementally fractionated air (EFA) component dominating the low temperature releases. The extremely low Ar/Kr/Xe ratios of EFA may be the result of multiple episodes of trapping/loss during terrestrial alteration involving aqueous fluids. We suggest fractionation processes similar to those in hot deserts to have acted on Mars, with acidic weathering on the latter possibly even more effective in producing elementally fractionated components. Addition from fission xenon is apparent in DaG 476 and SaU 005. The Ar-Kr-Xe patterns for LEW 88516 show trends as typically observed in shergottites - including evidence for a crush-released component similar to that observed in EETA 79001. A trapped Ne component most prominent in the surface sample of DaG 476 may represent air contamination. It is accompanied by little trapped Ar (²⁰Ne/³⁶Ar > 50) and literature data suggest its presence also in some Antarctic finds. Data for LEW 88516 and literature data, on the other hand, suggest the presence of two trapped Ne components of Martian origin characterized by different ²⁰Ne/²²Ne, possibly related to the atmosphere and the interior. Caution is recommended in interpreting nitrogen and noble gas isotopic signatures of Martian meteorites from hot deserts in terms of extraterrestrial sources and processes. Nevertheless our results provide hope that vice-versa, via noble gases and nitrogen in meteorites and other relevant samples from terrestrial deserts, Martian secondary processes can be studied.     

Parentage Identification of Differentiated Achondritic Meteorites by Hand‐held Energy Dispersive X‐Ray Fluorescence Spectrometry

We evaluate the potential of a hand‐held energy dispersive XRF spectrometer for the preliminary classification of non‐chondritic differentiated meteorites. The studied achondrites include nine lunar meteorites, seventeen Martian meteorites, five angrites and eighteen meteorites from asteroid 4 Vesta. Analytical precision and accuracy was tested on thirty‐nine terrestrial igneous rock slabs with a wide range of composition. Replicate analyses, performed on the studied meteorites, show that Fe/Mn values together with Si and Ca/K ratio can be used in the discrimination of different achondrite groups. Fusion crust's Fe/Mn values of meteorites from Vesta and Mars are indistinguishable from those of the interior implying that even measurements on the fusion‐crusted external surface could be sufficient to pigeonhole non‐chondritic meteorites. Hand‐held energy dispersive XRF spectrometer is a non‐destructive but very effective technique for preliminary classification of achondrites in the field and in laboratory and for the identification of mislabelled meteorites in museum collections.     

风化作用对铁陨石矿物学特征影响的探讨

本文对南丹IIICD铁陨石的矿物学特征进行了研究,并与同为铁陨石但化学分类不同的阿根廷IAB铁陨石和西伯利亚IIB铁陨石进行了对比,重点探讨了风化作用对铁陨石矿物学特征的影响.首先用偏光显微镜、静水称重、扫描电镜观察了样品的基本矿物学特征和微形貌特征,然后用振动式样品磁强计、X射线衍射与电子探针能谱半定量测试研究了样品的磁学性质、物相和化学组成.研究结果表明,南丹铁陨石在较强的自然风化作用下,光泽变弱为土状光泽,相对密度降低;风化产生的反铁磁性物质会使陨石的磁性下降;另外,样品表面物相组成也发生较大变化,以针铁矿(FeOOH)和磁铁矿(Fe₃O₄)等铁的次生矿物为主;但风化壳以下的矿物物相及化学成分均未发生明显变化,以Fe、Ni为主的铁纹石、镍纹石物相存在.     

玄武质陨石NWA8545的岩石地球化学特征以及对其母体岩浆过程的启示

NWA 8545 是一块玄武质无球粒陨石,它与碳质陨石(CC)NWA 011 成对.CC 被认为是来自于外太阳系的一类物质,由于同位素异常,它们区别于来自内太阳系的非碳质陨石(NC).NWA 011 及其成对陨石作为CC中稀有的玄武质无球粒陨石,其记录的岩浆过程可以被用来研究外太阳系早期行星母体的岩浆活动.本文利用扫描电镜、电子探针和激光剥蚀电感耦合等离子质谱仪(LA-ICP-MS)对NWA 8545 中的辉石、斜长石和陨磷钙钠石进行岩相学以及原位主微量元素的分析,并根据矿物模式丰度计算全岩稀土元素含量.电子探针结果显示NWA 8545 与 HED族陨石Eucrite(钙长辉长无球粒陨石)具有相似的主量元素特征,同时其岩相学与5 型Eucrite类似.激光微量数据表明辉石、斜长石和陨磷钙钠石的稀土元素配分都表现出略微的Ce异常,但其辉石的Ba、Sr等元素并未出现明显的富集现象,即该陨石受地球风化作用影响不明显.利用辉石和斜长石的稀土元素含量,计算平衡熔体的成分,显示其平衡熔体的成分都与全岩的成分比较接近,可以认为两者是在封闭的体系下接近同时结晶.结合变质过程和母体岩浆的成分,本文认为NWA 8545 是由其母体岩浆在经历分离结晶过程后喷发到母体行星表面冷却形成的.     

The geochemical composition of the terrestrial surface (without soils) and comparison with the upper continental crust

The terrestrial surface, the “skin of the earth”, is an important interface for global (geochemical) material fluxes between major reservoirs of the Earth system: continental and oceanic crust, ocean and atmosphere. Because of a lack in knowledge of the geochemical composition of the terrestrial surface, it is not well understood how the geochemical evolution of the Earth’s crust is impacted by its properties. Therefore, here a first estimate of the geochemical composition of the terrestrial surface is provided, which can be used for further analysis. The geochemical average compositions of distinct lithological classes are calculated based on a literature review and applied to a global lithological map. Comparison with the bulk composition of the upper continental crust shows that the geochemical composition of the terrestrial surface (below the soil horizons) is significantly different from the assumed average of the upper continental crust. Specifically, the elements Ca, S, C, Cl and Mg are enriched at the terrestrial surface, while Na is depleted (and probably K). Analysis of these results provide further evidence that chemical weathering, chemical alteration of minerals in marine settings, biogeochemical processes (e.g. sulphate reduction in sediments and biomineralization) and evaporite deposition are important for the geochemical composition of the terrestrial surface on geological time scales. The movement of significant amounts of carbonate to the terrestrial surface is identified as the major process for observed Ca-differences. Because abrupt and significant changes of the carbonate abundance on the terrestrial surface are likely influencing CO₂-consumption rates by chemical weathering on geological time scales and thus the carbon cycle, refined, spatially resolved analysis is suggested. This should include the recognition of the geochemical composition of the shelf areas, now being below sea level.     

The distribution of total nitrogen in iron meteorites

Total nitrogen abundances in 123 iron meteorites have been determined by inert carrier-gas fusion extraction-gas chromatography. The median value for the iron meteorites was found to be 18 ppm N. The N contents of Sulfide inclusions are greater, in nine cases out of ten, than the corresponding metallic phase. The N content of the iron meteorites is positively correlated with germanium content. The effects of terrestrial weathering and heat treatment by man are discussed in relation to the N contents measured for certain specimens. A correlation between N and cooling rates was found, with lower cooling rates associated with greater N abundances.     

Planetesimal sulfate and aqueous alteration in CM and CI carbonaceous chondrites

Water-soluble sulfate salts extracted from six CM chondrites have oxygen isotope compositions that are consistent with an extraterrestrial origin. The Δ¹⁷O of sulfate are correlated with previously reported whole rock δ¹⁸O and with an index of meteorite alteration, and may display a correlation with the date of the fall. The enrichments and depletions for Δ¹⁷O of water-soluble sulfate from the CM chondrites relative to the terrestrial mass dependent fractionation line are consistent with sulfate formation in a rock dominated asteroidal environment, and from aqueous fluids that had undergone relatively low amounts of oxygen isotope exchange and little reaction with anhydrous components of the meteorites. It is unresolved how the oxidation of sulfide to sulfate can be reconciled with the inferred low oxidation state during the extraterrestrial alteration process. Oxygen isotope data for two CI chondrites, Orgueil and Ivuna, as well as the ungrouped C2 chondrite Essebi are indistinguishable from sulfate of terrestrial origin and may be terrestrial weathering products, consistent with previous assertions. Our oxygen isotope data, however, can not rule out a preterrestrial origin either.     

鄂尔多斯盆地中部气田奥陶系风化壳气藏天然气来源及混源比计算

对鄂尔多斯盆地中部气田天然气碳同位素资料按不同地区、不同层位进行了分析,认为奥陶系风化壳气藏甲烷碳同位素值与石炭-二叠系气藏的接近,在平面上变化趋势相似,而与风化壳之下奥陶系自生自储的油型气相差较大。奥陶系风化壳气藏的来源是以石炭-二叠系煤成气为主,定量计算表明,在中部气田的大部分地区,石炭-二叠系来源气的比例大于70％。     

Mechanisms of weathering of meteorites recovered from hot and cold deserts and the formation of phyllosilicates

Petrographic, mineralogical and chemical analysis of naturally weathered equilibrated ordinary chondrites collected from ‘ hot’ deserts and Antarctica has revealed striking similarities and also pronounced differences in weathering between the two environments. Terrestrial weathering in all meteorites studied is dominated by oxidation and hydration of Fe,Ni metal, producing Fe-oxides and oxyhydroxides that have partially replaced the metal grains and have also occluded primary intergranular pores to form veins. Troilite weathers readily in ‘ hot’ desert environments but undergoes very little alteration under Antarctic conditions. Most of the primary porosity of ordinary chondrites has been occluded by the time that ∼ 15 to 25% of the initial Fe⁰ and Fe²⁺ has been oxidised to Fe³⁺ in both environments. Results from modelling the volume changes upon alteration of primary minerals to a range of weathering products demonstrates that the primary porosity of most meteorites is sufficient to accommodate weathering products. Dilation of primary pores and brecciation, which has been observed in parts of some meteorites, will only occur if the meteorite is especially metal-rich, or has a low primary porosity. These weathering products are absent from recent falls but have formed in a fall after ∼ 100 yr of museum storage.Cl-bearing akaganéite and hibbingite are common weathering products in Antarctic finds but occur in abundance in only one ‘ hot’ desert meteorite, Daraj 014. The majority of Fe-rich weathering products in meteorites from both environments contain low, but variable concentrations of Si, Mg and Ca. In most meteorites a proportion of these elements are inferred to be present as a very finely crystalline mineral with a ∼ 1.0-nm lattice fringe spacing; where seen within intragranular fractures this mineral has a topotactic relationship with olivine and orthopyroxene. In the heavily-weathered Antarctic finds ALHA 78045 and 77002, Si is concentrated in cronstedtite, a Fe-rich phyllosilicate. An unidentified hydrous Si-Fe-Ni-Mg mineral or gel has also partially replaced taenite in ALHA 78045. In addition to Fe-rich weathering products, ‘ hot’ desert meteorites contain sulphates, Ca-carbonate and silica, whereas such minerals are largely absent from Antarctic finds. The abundance of silicate weathering products in Antarctic meteorites is unexpected and indicates that olivine and pyroxene undergo significant chemical weathering in these environments. As preterrestrial cronstedtite is abundant in CM2 carbonaceous chondrites, the Antarctic environment may be a powerful analog for aqueous alteration in the asteroidal parent bodies of primitive meteorites.     

Hydrocarbon components in carbonaceous meteorites

Currently, the presence of free n-alkanes and isoprenoid alkanes in carbonaceous meteorites is usually explained either by microbial contamination during the period between the meteorite fall and collection or by contamination from the environment of analytical laboratories and museums. The goal of this research was to repeat analysis of hydrocarbon components in meteorites and to investigate possible meteorite contamination routes discussed in the literature. Experimental analysis of free organic constituents in five carbonaceous meteorites by infrared spectroscopy (IR) and gas chromatographic (GC) methods confirmed the presence of extractable aliphatic components, n-alkanes in the C₁₅H₃₂-C₂₇H₅₆ range and isoprenoid alkanes (phytane, pristane, and norpristane), in some of these meteorites. The contents of these compounds vary depending on the source. Insoluble organic components of two meteorites (meteorite kerogens) were isolated, and their composition was analyzed by IR and cracking/GC methods. Comparison with the data on several terrestrial contamination sources proposed in the literature shows that the presence of free saturated hydrocarbons in meteorites and the composition of the meteorite kerogen could not be explained either by microbial contamination or by contamination from the laboratory environment. The types of the hydrocarbons in meteorites resemble those typical of ancient terrestrial deposits of organic-rich sediments, except for the absence of lighter hydrocarbons, which apparently slowly evaporated in space, and multi-ring naphthenic compounds of the biologic origin, steranes, terpanes, etc. The prevailing current explanation for the presence of free linear saturated hydrocarbons in carbonaceous meteorites, apart from contamination, is the abiotic route from hydrogen and carbon monoxide. However, the data on the structure of meteorite kerogens require a search for different routes that initially produce complex polymeric structures containing n-alkyl and isoprenoid chains which are attached, via polar links (esters, salts, etc.), to a cross-linked polymer matrix. Later, the polymer slowly decomposes with the liberation of free aliphatic hydrocarbons.     

碰撞作用与类地行星起源探讨

类地行星挥发性元素普遍亏损很可能是由于太阳星云早期剧烈的太阳活动引起的。当气体、尘粒、挥发性元素和水被驱赶出内太阳系时，只有米级到公里级的物质保存下来并堆积成星子，最终吸积星子形成类地行星。我们认为类地行星的初始物质主要是已分异的星子和一些未分异的球粒陨石质星子或不同类型的陨石母体，最靠近太阳形成的星子具有最低的ＦｅＯ／（ＦｅＯ＋ＭｇＯ）值，水星是在靠近太阳的高度还原条件下吸积成分类似ＥＨ球粒陨石的星子形成的。地球的初始物质为分异的铁陨石及Ｈ群球粒陨石。随着距太阳距离增大及温度降低，陨石形成的部位大致为：ＥＨ、ＥＬ－ＩＡＢ－ＳＮＣ（辉玻无球粒陨石、辉橄无球粒陨石、纯橄无球粒陨石）－Ｅｕｃ（钙长辉长无球粒陨石）－Ｈ、Ｌ、ＬＬ－ＣＶ、ＣＭ、ＣＯ－Ｃｌ－彗星。物体之间、星子之间及行星与星子之间的碰撞对太阳系的形成和演化起着重要的作用。     

Origine du matériel altéré et hétérogénéité du matériel originel de la météorite Foum Tatahouine (Tunisie) : éléments traces et isotopes du SrOrigin of altered material and heterogeneity of original material in the Foum Tatahouine meteorite (Tunisia): Trace elements and Sr isotopes

Foum Tatahouine is one of the rare meteorites that allow studying weathering effects since their fall on Earth. The comparison between clasts collected the very day of the fall (1931) and in 1994 showed some chemical modifications. We report data obtained on samples collected in 2000. The purpose of this study is: (1) to define (REE, Sr isotopes) the terrestrial weathering origin that is to be found in soil carbonates, (2) to show (Sr, Rb, REE) that the weathering effects are small on centimetre-sized samples, and (3) to emphasise (HREE) Foum Tatahouine samples heterogeneity. To cite this article: Y. Bentahila et al., C. R. Geoscience 334 (2002) 267–272.     

The Abnormal Condition Analysis used to characterize weathered discard coals

Coal, by its nature, is unstable and weathers when exposed to moisture and oxygen. Weathering can result in a general decline on the commercial value and technological properties of coal. Coals of similar chemical properties have been shown to combust differently, and the differences can be attributed to petrographic composition variations, poor combustion environments, and weathered particles. Stockpiled and dumped discard coals have been targeted for use by a lower power utility, and a novel technique was developed to quantify and qualify the degree of weathering in these coals. The petrographic based Abnormal Condition Analysis (previously referred to as the Weathering Index Analysis) considers features not typically characterized during routine petrographic analyses, but which may have an impact on the technological properties of coals. Discard coals ranging in age from 5 to 40 years where characterized to determine the extent of secondary weathering. Eight secondary weathering features, clearly different from inherent weathering, were qualified and quantified. Margin effect appears to be an early microscopic indicator of weathering, followed by discoloration. Alteration minerals have only been observed in stockpiled and dumped coals and hence could be a useful feature to benchmark when considering whether or not a coal has been stored. Long-term stored coals have microcrack and fissure patterns clearly different from fresh coals. The length of exposure to weathering processes was determined to be proportional to the extent of weathering as determined petrographically. The Abnormal Condition Analysis should be used as a supplement to routine coal petrography as it can assist with the determination of anomalous behavior of coals.     

Noble gas and carbon abundances of the Haverö, Dingo Pup Donga,and North Haig ureilites

Total carbon determinations on the Haverö, Dingo Pup Donga, and North Haig ureilites yield values of 2.07, 3.17, and 5.58 wt.%, respectively. Haverö and Dingo Pup Donga contain relatively large amounts of trapped Ar, Kr and Xe, which like the carbon content varies with grain size for Haverö. These two meteorites also contain dominant cosmic rayproduced He and Ne, and show ³He exposure ages of ~23 m.y. and ~7 m.y., respectively. North Haig contains much smaller amounts of trapped gases and spallogenic gases, which may result from loss due to terrestrial weathering. The isotopic composition of Xe in five grain size analyses of Haverö and a whole rock analysis of Dingo Pup Donga shows the presence of a major solar-like Xe component. The presence of this solar component adds an additional complication to the concept of forming ureilites from carbonaceous chondrites.     

Petrology and origin of the shergottite meteorites

Shergottites contain cumulus pigeonite and augite, probably without cumulus plagioclase and crystallized under relatively oxidizing conditions. Shergotty and Zagami may differ in the relative proportions of cumulus pyroxenes and crystallized intercumulus liquid, but the compositions of pyroxenes and liquid are similar in both meteorites. Absence of olivine in melting experiments suggests that the shergottites crystallized from fractionated derivatives of primary liquids. Low-Ca pyroxene and augite apparently began to crystallize from these primary liquids prior to plagioclase. Shergottites can be readily distinguished from other achondrite groups by their mineralogies, crystallization sequences and inferred source region compositions. However, the source regions of the shergottites may be related to those of other achondrite types by addition or loss of volatile components.The bulk composition of the Earth's upper mantle overlaps that of permissible shergottite source regions. Shergottites and terrestrial basalts display similarities in oxidation state and concentrations of trace and minor elements with a wide range of cosmochemical and geochemical affinities. Accretion of similar materials to produce the terrestrial upper mantle and the shergottite parent body or accretion of the Earth's upper mantle from planetesimals similar to the shergottite parent body may account for many of their similarities. Models of the origin of the Earth's upper mantle which attribute its oxidation state, its siderophile element abundances and its volatile element abundances to uniquely terrestrial processes or conditions, or to factors unique to the origin and differentiation of large bodies, are unattractive in light of the similarities between shergottites and terrestrial basalts.     

The vanadium isotopic composition of L ordinary chondrites

Stable isotopic data of meteorites are critical for understanding the evolution of terrestrial planets. In this study, we report high-precision vanadium (V) isotopic compositions of 11 unequilibrated and equilibrated L chondrites. Our samples show an average δ⁵¹V of ??1.25‰?±?0.38‰ (2SD, n?=?11), which is ~?0.5‰ lighter than that of the bulk silicate Earth constrained by mantle peridotites. Isotopic fractionation in type 3 ordinary chondrites vary from ??1.76‰ to ??1.29‰, whereas the δ⁵¹V of equilibrated chondrites vary from ??1.37‰ to ??1.08‰. δ⁵¹V of L chondrites do not correlate with thermal metamorphism, shock stage, or weathering degree. Future studies are required to explore the reason for V isotope variation in the solar system.     

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     

Silicate inclusions in group IAB irons and a relation to the anomalous stones Winona and Mt Morris (Wis)

Silicates are found in many group IAB irons; in some cases as abundant angular cm-sized inclusions and in other cases as smaller fragments or single grains in troilite or graphite nodules. The mineralogy of the silicates is chondritic—olivine, pyroxene, albitic plagioclase—as is the bulk composition. The degree of oxidation of the olivine and pyroxene is intermediate between E and H chondrites (Fa 1–8, Fs 4–9). IAB inclusions have ages of about 4.5 Gyr, I¹²⁹-Xe¹²⁹ formation intervals in the ranges of chondrites and contain planetary-type rare gases.Samples of San Cristobal, Campo del Cielo, Mundrabilla and Woodbine were examined by microprobe and bulk inclusions from Campo del Cielo, Copiapo, Landes and Woodbine were analyzed by instrumental and radiochemical neutron activation analysis. Nonvolatile lithophilic and siderophih'c elements in Copiapo, Landes and Woodbine have approximately chondritic abundances. The chondritic level of lithophiles indicates the inclusions have not undergone igneous differentiation while the chondritic levels of siderophiles is evidence the metal is native to the inclusions and not matrix metal injected into the silicates. The two Campo del Cielo inclusions analyzed have roughly chondritic abundances of lithophiles but have fractionated rare earth patterns and widely varying amounts and abundances (relative to Ni) of siderophiles. These inclusions appear to have experienced some partial melting. Siderophile ratios for the inclusions have some differences when compared to matrix metal. One Campo del Cielo inclusion contains kamacite (5.5% Ni) with over 1000 μg Ge.Three-isotope O analyses by Clayton and coworkers of parts of the same or neighboring inclusions to those analyzed chemically place the inclusions slightly below the terrestrial fractionation line of clayton et al. (1976) and rule out the possibility of the inclusions being trapped fragments of one of the ordinary chondrite groups.The IAB silicates formed probably in a similar manner as chondrite groups but in a different region of the nebula and they record the O₂ fugacity and O isotopic composition of that location. They later became trapped in the metal-rich matrix probably as the result of collisions producing the breccialike texture. The relationship of the silicates to the kamacite-taenite structure of the metal requires that the metal-silicate mix have been heated to over 1000 K for an extended period.Two anomalous stony meteorites, Winona and Mt. Morris (Wis), are similar to IAB inclusions in mineralogy, bulk composition, $\text{FeO}\text{(FeO + Mg)}$ ratio of the silicates, and chromite composition and are possibly related to the IAB silicates. Winona also has an age of 4.6 Gyr and contains planetary-type rare gases. Microprobe data are reported for the major minerals of these anomalous meteorites. Although attempts to detect IAB levels of Ge in the metal phases were not successful, the weight of the evidence favors a relationship between these meteorites and IAB     

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.