Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies

In ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent‐body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4–6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all three OC groups. Apatite in L chondrites is Cl‐rich, similar to H chondrites, whereas apatite in LL chondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend to LL chondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4–6. Alkali‐ and halogen‐rich and likely hydrous metasomatic fluids acted during prograde metamorphism on OC parent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl‐rich composition after the asteroid began to cool. Differences in secondary minerals between H and L, LL chondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology‐dependent apatite compositions. Bulk Cl/F ratios for OCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios in OCs are similar to CI.     

Primary feldspar in the Semarkona LL3.00 chondrite: Constraints on chondrule formation and secondary alteration

Feldspar in ordinary chondrites (OCs) is often associated with thermal metamorphism, as a secondary mineral that forms from the crystallization of matrix and chondrule mesostasis. However, studies of feldspar in equilibrated OCs show that there is a range of plagioclase compositions within chondrules, some of which may be primary products of chondrule crystallization. It is important to recognize primary feldspar within chondrules because it can be used to help understand the secondary effects of thermal metamorphism and aqueous alteration. The presence of primary feldspar also provides important petrologic constraints on chondrule formation time scales. We undertook a careful study of Semarkona (LL3.00) and observed feldspar in 18% of chondrules. The feldspar is plagioclase covering a wide range of compositions (An₂–An₉₉) with little K‐feldspar component (<Or₃). We show that plagioclase is a primary igneous phase, based on grain morphology and compositions consistent with growth from a melt having the bulk compositions of the host chondrules. Based on experimental studies, the presence of plagioclase suggests chondrules cooled slowly at temperatures close to the solidus. We also observed several secondary features consistent with the aqueous alteration. These features include zoning of Na and Ca in plagioclase, heterogeneity in plagioclase compositions in altered chondrules, development of porosity from the dissolution of chondrule glass, and alteration of glass to phyllosilicates. Alteration of major Al‐bearing phases, like plagioclase and glass, has important implications for interpretations of ages derived from Al‐Mg dating of chondrules, if they have been affected by secondary processes.     

The onset of metamorphism in ordinary and carbonaceous chondrites

Abstract— Ordinary and carbonaceous chondrites of the lowest petrologic types were surveyed by X‐ray mapping techniques. A variety of metamorphic effects were noted and subjected to detailed analysis using electron microprobe, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and cathodoluminescence (CL) methods. The distribution of Cr in FeO‐rich olivine systematically changes as metamorphism increases between type 3.0 and type 3.2. Igneous zoning patterns are replaced by complex ones and Cr‐rich coatings develop on all grains. Cr distributions in olivine are controlled by the exsolution of a Cr‐rich phase, probably chromite. Cr in olivine may have been partly present as tetrahedrally coordinated Cr³⁺. Separation of chromite is nearly complete by petrologic type 3.2. The abundance of chondrules showing an inhomogeneous distribution of alkalis in mesostasis also increases with petrologic type. TEM shows this to be the result of crystallization of albite. Residual glass compositions systematically change during metamorphism, becoming increasingly rich in K. Glass in type I chondrules also gains alkalis during metamorphism. Both types of chondrules were open to an exchange of alkalis with opaque matrix and other chondrules. The matrix in the least metamorphosed chondrites is rich in S and Na. The S is lost from the matrix at the earliest stages of metamorphism due to coalescence of minute grains. Progressive heating also results in the loss of sulfides from chondrule rims and increases sulfide abundances in coarse matrix assemblages as well as inside chondrules. Alkalis initially leave the matrix and enter chondrules during early metamorphism. Feldspar subsequently nucleates in the matrix and Na re‐enters from chondrules. These metamorphic trends can be used to refine classification schemes for chondrites. Cr distributions in olivine are a highly effective tool for assigning petrologic types to the most primitive meteorites and can be used to subdivide types 3.0 and 3.1 into types 3.00 through 3.15. On this basis, the most primitive ordinary chondrite known is Semarkona, although even this meteorite has experienced a small amount of metamorphism. Allan Hills (ALH) A77307 is the least metamorphosed CO chondrite and shares many properties with the ungrouped carbonaceous chondrite Acfer 094. Analytical problems are significant for glasses in type II chondrules, as Na is easily lost during microprobe analysis. As a result, existing schemes for chondrule classification that are based on the alkali content of glasses need to be revised.     

Mineral chemistry of MUSES‐C Regio inferred from analysis of dust particles collected from the first‐ and second‐touchdown sites on asteroid Itokawa

The mineralogy and mineral chemistry of Itokawa dust particles captured during the first and second touchdowns on the MUSES‐C Regio were characterized by synchrotron‐radiation X‐ray diffraction and field‐emission electron microprobe analysis. Olivine and low‐ and high‐Ca pyroxene, plagioclase, and merrillite compositions of the first‐touchdown particles are similar to those of the second‐touchdown particles. The two touchdown sites are separated by approximately 100 meters and therefore the similarity suggests that MUSES‐C Regio is covered with dust particles of uniform mineral chemistry of LL chondrites. Quantitative compositional properties of 48 dust particles, including both first‐ and second‐touchdown samples, indicate that dust particles of MUSES‐C Regio have experienced prolonged thermal metamorphism, but they are not fully equilibrated in terms of chemical composition. This suggests that MUSES‐C particles were heated in a single asteroid at different temperatures. During slow cooling from a peak temperature of approximately 800 °C, chemical compositions of plagioclase and K‐feldspar seem to have been modified: Ab and Or contents changed during cooling, but An did not. This compositional modification is reproduced by a numerical simulation that modeled the cooling process of a 50 km sized Itokawa parent asteroid. After cooling, some particles have been heavily impacted and heated, which resulted in heterogeneous distributions of Na and K within plagioclase crystals. Impact‐induced chemical modification of plagioclase was verified by a comparison to a shock vein in the Kilabo LL6 ordinary chondrite where Na‐K distributions of plagioclase have been disturbed.     

Chemical and physical studies of type 3 chondrites XII: The metamorphic history of CV chondrites and their components

Abstract— The induced thermoluminescence (TL) properties of 16 CV and CV-related chondrites, four CK chondrites and Renazzo (CR2) have been measured in order to investigate their metamorphic history. The petrographic, mineralogical and bulk compositional differences among the CV chondrites indicate that the TL sensitivity of the ～130 °C TL peak is reflecting the abundance of ordered feldspar, especially in chondrule mesostasis, which in turn reflects parent-body metamorphism. The TL properties of 18 samples of homogenized Allende powder heated at a variety of times and temperatures, and cathodoluminescence mosaics of Axtell and Coolidge, showed results consistent with this conclusion. Five refractory inclusions from Allende, and separates from those inclusions, were also examined and yielded trends reflecting variations in mineralogy indicative of high peak temperatures (either metamorphic or igneous) and fairly rapid cooling. The CK chondrites are unique among metamorphosed chondrites in showing no detectable induced TL, which is consistent with literature data that suggests very unusual feldspar in these meteorites. Using TL sensitivity and several mineral systems and allowing for the differences in the oxidized and reduced subgroups, the CV and CV-related meteorites can be divided into petrologic types analogous to those of the ordinary and CO type 3 chondrites. Axtell, Kaba, Leoville, Bali, Arch and ALHA81003 are type 3.0–3.1, while ALH84018, Efremovka, Grosnaja, Allende and Vigarano are type 3.2–3.3 and Coolidge and Loongana 001 are type 3.8. Mokoia is probably a breccia with regions ranging in petrologic type from 3.0 to 3.2. Renazzo often plots at the end of the reduced and oxidized CV chondrite trends, even when those trends diverge, suggesting that in many respects it resembles the unmetamorphosed precursors of the CV chondrites. The low-petrographic types and low-TL peak temperatures of all samples, including the CV3.8 chondrites, indicates metamorphism in the stability field of low feldspar (i.e., <800 °C) and a metamorphic history similar to that of the CO chondrites but unlike that of the ordinary chondrites.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

Fe‐Ni metal in primitive chondrites: Indicators of classification and metamorphic conditions for ordinary and CO chondrites

Abstract— We report the results of our petrological and mineralogical study of Fe‐Ni metal in type 3 ordinary and CO chondrites, and the ungrouped carbonaceous chondrite Acfer 094. Fe‐Ni metal in ordinary and CO chondrites occurs in chondrule interiors, on chondrule surfaces, and as isolated grains in the matrix. Isolated Ni‐rich metal in chondrites of petrologic type lower than type 3.10 is enriched in Co relative to the kamacite in chondrules. However, Ni‐rich metal in type 3.15–3.9 chondrites always contains less Co than does kamacite. Fe‐Ni metal grains in chondrules in Semarkona typically show plessitic intergrowths consisting of submicrometer kamacite and Ni‐rich regions. Metal in other type 3 chondrites is composed of fine‐ to coarse‐grained aggregates of kamacite and Ni‐rich metal, resulting from metamorphism in the parent body. We found that the number density of Ni‐rich grains in metal (number of Ni‐rich grains per unit area of metal) in chondrules systematically decreases with increasing petrologic type. Thus, Fe‐Ni metal is a highly sensitive recorder of metamorphism in ordinary and carbonaceous chondrites, and can be used to distinguish petrologic type and identify the least thermally metamorphosed chondrites. Among the known ordinary and CO chondrites, Semarkona is the most primitive. The range of metamorphic temperatures were similar for type 3 ordinary and CO chondrites, despite them having different parent bodies. Most Fe‐Ni metal in Acfer 094 is martensite, and it preserves primary features. The degree of metamorphism is lower in Acfer 094, a true type 3.00 chondrite, than in Semarkona, which should be reclassified as type 3.01.     

The oxygen isotopic properties of olivines in the Semarkona ordinary chondrite

Abstract— In order to explore the origin of chondrules and the chondrites, the O isotopic compositions of nine olivine grains in seven chondrules from the primitive Semarkona LL3.0 chondrite have been determined by ion microprobe. The data plot in the same general region of the three-isotope plot as whole-chondrule samples from ordinary chondrites previously measured by other techniques. There are no significant differences between the O isotopic properties of olivine in the various chondrule groups in the present study, but there is a slight indication that the data plot at the ¹⁶O-rich end of the ordinary chondrite field. This might suggest that the mesostasis contains isotopically heavy O. The olivines in the present study have O isotopic compositions unlike the ¹⁶O-rich olivine grains from the Julesburg ordinary chondrite. Even though olivines in group A chondrules have several properties in common with them, the ¹⁶O-rich Julesburg olivines previously reported are not simply olivines from group A chondrules.     

Bo Xian (LL3.9): Oxygen‐isotopic and mineralogical characterisation of separated chondrules

Abstract— We report the results of a mineralogical and O‐isotopic study of 362 chondrules disaggregated from the Bo Xian chondrite. The range of mineral compositions (Fa = 0.8–31.2%, mean = 23.5%, mode = 27–28%) are consistent with a reclassification of this meteorite from LL4 to LL3.9. Chondrule diameters range from 0.20 to 3.40 mm (mean = 0.74 mm) in the disaggregated population. A lower mean diameter (0.64 mm) calculated from thin‐section measurements partly reflects the high proportion of chondrule fragments. The chondrule size distribution, which is approximately log‐normal, is consistent with size‐sorting mechanisms. This sorting could be linked to the fragmentation of many chondrules on the parent body. However, in detail, the variation in diameter of different chondrule types and a hiatus in the size distribution at 0.6 mm indicate that there may have been complex controls perhaps partly being determined by the chondrule formation mechanism. Seven percent of the sectioned chondrules (102) contain chemically fractionated mineral assemblages: cristobalite‐bearing and Al‐rich. This significant degree of chemical heterogeneity probably resulted from both igneous and volatility controls. Oxygen‐isotopic compositions were determined on mineral separates and 16 of the sectioned chondrules. Three separate isotopic exchange events have been identified. The dominant one is a low‐temperature hydrous gas‐solid exchange event between ¹⁶O‐rich solid and ¹⁶O‐poor gas reservoirs that lay along a slope 1.0 line on three‐isotope plots. Partial equilibration with the gas by feldspar and cristobalite, which exchanged more rapidly than olivine or pyroxene, led to formation of a slope 0.77 mixing line for Bo Xian and other LL chondrites. Mineralogy is the dominant control on the extent of this exchange; no relationship between isotopic composition and chondrule texture or size was identified. The feldspar separate and cristobalite‐rich chondrules have the most ¹⁶O‐poor compositions. Subsequently, thermal metamorphism in the parent body led to partial isotopic equilibration between the different mineral phases. A third exchange event, predating the other two events, is probably shown by one of the Al‐rich chondrules. This has an ¹⁶O‐rich composition, lying below the terrestrial fractionation line. Another Al‐rich chondrule has a normal ordinary chondrite isotopic composition. It is not clear whether the isotopic fractionation recorded in some Al‐rich chondrules can be achieved by the dominant gas‐solid exchange. Instead, the precursor O to the mineral phases may have become ¹⁶O‐rich during an earlier phase of mass‐independent fractionation.     

Peak metamorphic temperatures in type 6 ordinary chondrites: An evaluation of pyroxene and plagioclase geothermometry

Abstract— Quantifying the peak temperatures achieved during metamorphism is critical for understanding the thermal histories of ordinary chondrite parent bodies. Various geothermometers have been used to estimate equilibration temperatures for chondrites of the highest metamorphic grade (type 6), but results are inconsistent and span hundreds of degrees. Because different geothermometers and calibration models were used with different meteorites, it is unclear whether variations in peak temperatures represent actual ranges of metamorphic conditions within type 6 chondrites or differences in model calibrations. We addressed this problem by performing twopyroxene geothermometry, using QUILF95, on the same type 6 chondrites for which peak temperatures were estimated using the plagioclase geothermometer (Nakamuta and Motomura 1999). We also calculated temperatures for published pyroxene analyses from other type 6 H, L, and LL chondrites to determine the most representative peak metamorphic temperatures for ordinary chondrites. Pyroxenes record a narrow, overlapping range of temperatures in H6 (865–926 °C), L6 (812–934 °C), and LL6 (874–945 °C) chondrites. Plagioclase temperature estimates are 96–179 °C lower than pyroxenes in the same type 6 meteorites. Plagioclase estimates may not reflect peak metamorphic temperatures because chondrule glass probably recrystallized to plagioclase prior to reaching the metamorphic peak. The average temperature for H, L, and LL chondrites (～900 °C), which agrees with previously published oxygen isotope geothermometry, is at least 50 °C lower than the peak temperatures used in current asteroid thermal evolution models. This difference may require minor adjustments to thermal model calculations.     

Size‐frequency distributions of chondrules and chondrule fragments in LL3 chondrites: Implications for parent‐body fragmentation of chondrules

Abstract— We measured the sizes and textural types of 719 intact chondrules and 1322 chondrule fragments in thin sections of Semarkona (LL3.0), Bishunpur (LL3.1), Krymka (LL3.1), Piancaldoli (LL3.4) and Lewis Cliff 88175 (LL3.8). The mean apparent diameter of chondrules in these LL3 chondrites is 0.80 φ units or 570 μm, much smaller than the previous rough estimate of ～900 μm. Chondrule fragments in the five LL3 chondrites have a mean apparent cross‐section of 1.60 φ units or 330 μm. The smallest fragments are isolated olivine and pyroxene grains; these are probably phenocrysts liberated from disrupted porphyritic chondrules. All five LL3 chondrites have fragment/ chondrule number ratios exceeding unity, suggesting that substantial numbers of the chondrules in these rocks were shattered. Most fragmentation probably occurred on the parent asteroid. Porphyritic chondrules (porphyritic olivine + porphyritic pyroxene + porphyritic olivine‐pyroxene) are more readily broken than droplet chondrules (barred olivine + radial pyroxene + cryptocrystalline). The porphyritic fragment/chondrule number ratio (2.0) appreciably exceeds that of droplet‐textured objects (0.9). Intact droplet chondrules have a larger mean size than intact porphyritic chondrules, implying that large porphyritic chondrules are fragmented preferentially. This is consistent with the relatively low percentage of porphyritic chondrules within the set of the largest chondrules (57%) compared to that within the set of the smallest chondrules (81%). Differences in mean size among chondrule textural types may be due mainly to parent‐body chondrule‐fragmentation events and not to chondrule‐formation processes in the solar nebula.     

Correlations and zoning patterns of phosphorus and chromium in olivine from H chondrites and the LL chondrite Semarkona

Phosphorus zoning is observed in olivines in high‐FeO (type IIA) chondrules in H chondrites over the entire range of petrologic grades: H3.1–H6. Features in P concentrations such as oscillatory and sector zoning, and high P cores are present in olivines that are otherwise unzoned in the divalent cations. Aluminum concentrations are low and not significantly associated with P zoning in chondrule olivines. In highly unequilibrated H chondrites, phosphorus zoning is generally positively correlated with Cr. Atomic Cr:P in olivine is roughly 1:1 (3:1 for one zone in one olivine in RC 075), consistent with Cr³⁺ charge‐balancing P⁵⁺ substituting for Si⁴⁺. Normal igneous zonation involving the dominant chrome species Cr²⁺ was observed only in the LL3.0 chondrite Semarkona. In more equilibrated chondrites (H3.5–H3.8), Cr spatially correlated with P is occasionally observed but it is diffuse relative to the P zones. In H4–H6 chondrites, P‐correlated Cr is absent. One signature of higher metamorphic grades (≥H3.8) is the presence of near matrix olivines that are devoid of P oscillatory zoning. The restriction to relatively high metamorphic grade and to grains near the chondrule–matrix interface suggests that this is a response to metasomatic processes. We also observed P‐enriched halos near the chondrule–matrix interface in H3.3–H3.8 chondrites, likely reflecting the loss of P and Ca from mesostasis and precipitation of Ca phosphate near the chondrule surface. These halos are absent in equilibrated chondrites due to coarsening of the phosphate and in unequilibrated chondrites due to low degrees of metasomatism. Olivines in type IA chondrules show none of the P‐zoning ubiquitous in type IIA chondrules or terrestrial igneous olivines, likely reflecting sequestration of P in reduced form within metallic alloys and sulfides during melting of type IA chondrules.     

In situ analysis of platinum group elements in equilibrated ordinary chondrite kamacite and taenite

Platinum group element (PGE) concentrations have been determined in situ in ordinary chondrite kamacite and taenite grains via laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS). Results demonstrate that PGE concentrations in ordinary chondrite metal (kamacite and taenite) are similar among the three ordinary chondrite groups, in contrast to previous bulk metal studies in which PGE concentrations vary in the order H < L < LL. PGE concentrations are higher in taenite than kamacite, consistent with preferential PGE partitioning into taenite. PGE concentrations vary between and within metal grains, although average concentrations in kamacite broadly agree with results from bulk studies. The variability of PGE concentrations in metal decreases with increasing petrologic type; however, variability is still evident in most type six ordinary chondrites, suggesting that equilibration of PGEs does not occur between metal grains, but rather within individual metal grains via self‐diffusion during metamorphism. The constant average PGE concentrations within metal grains across different ordinary chondrite groups are consistent with the formation of metal via nebular condensation prior to the accretion of ordinary chondrite parent bodies. Post‐condensation effects, including heating during chondrule‐formation events, may have affected some element ratios, but have not significantly affected average metal PGE concentrations.     

Alkali elemental and potassium isotopic compositions of Semarkona chondrules

Abstract— We report measurements of K isotope ratios in 28 Semarkona chondrules with a wide range of petrologic types and bulk compositions as well as the compositions of CPX‐mesostasis pairs in 17 type I Semarkona chondrules, including two chondrules with radial alkali zonation and 19 type II chondrules. Despite the wide range in K/Al ratios, no systematic variations in K isotopic compositions were found. Semarkona chondrules do not record a simple history of Rayleigh‐type loss of K. Experimentally determined evaporation rates suggest that considerable alkali evaporation would have occurred during chondrule formation. Nevertheless, based on Na CPX‐mesostasis distribution coefficients, the alkali contents of the cores of most chondrules in Semarkona were probably established at the time of final crystallization. However, Na CPX‐mesostasis distribution coefficients also show that alkali zonation in type I Semarkona chondrules was produced by entry of alkalis after solidification, probably during parent body alteration. This alkali metasomatism may have gone to completion in some chondrules. Our preferred explanation for the lack of systematic isotopic enrichments, even in alkali depleted type I chondrule cores, is that they exchanged with the ambient gas as they cooled.     

Bleached chondrules: Evidence for widespread aqueous processes on the parent asteroids of ordinary chondrites

Abstract— We present the first detailed study of a population of texturally distinct chondrules previously described by Kurat (1969), Christophe Michel‐Lévy (1976), and Skinner et al. (1989) that are sharply depleted in alkalis and Al in their outer portions. These “bleached” chondrules, which are exclusively radial pyroxene and cryptocrystalline in texture, have porous outer zones where mesostasis has been lost. Bleached chondrules are present in all type 3 ordinary chondrites and are present in lower abundances in types 4–6. They are most abundant in the L and LL groups, apparently less common in H chondrites, and absent in enstatite chondrites. We used x‐ray mapping and traditional electron microprobe techniques to characterize bleached chondrules in a cross section of ordinary chondrites. We studied bleached chondrules from Semarkona by ion microprobe for trace elements and H isotopes, and by transmission electron microscopy. Chondrule bleaching was the result of low‐temperature alteration by aqueous fluids flowing through finegrained chondrite matrix prior to thermal metamorphism. During aqueous alteration, interstitial glass dissolved and was partially replaced by phyllosilicates, troilite was altered to pentlandite, but pyroxene was completely unaffected. Calcium‐rich zones formed at the inner margins of the bleached zones, either as the result of the early stages of metamorphism or because of fluid‐chondrule reaction. The mineralogy of bleached chondrules is extremely sensitive to thermal metamorphism in type 3 ordinary chondrites, and bleached zones provide a favorable location for the growth of metamorphic minerals in higher petrologic types. The ubiquitous presence of bleached chondrules in ordinary chondrites implies that they all experienced aqueous alteration early in their asteroidal histories, but there is no relationship between the degree of alteration and metamorphic grade. A correlation between the oxidation state of chondrite groups and their degree of aqueous alteration is consistent with the source of water being either accreted ices or water released during oxidation of organic matter. Ordinary chondrites were probably open systems after accretion, and aqueous fluids may have carried volatile elements with them during dehydration. Individual radial pyroxene and cryptocrystalline chondrules were certainly open systems in all chondrites that experienced aqueous alteration leading to bleaching.     

Shock stage distribution of 2280 ordinary chondrites—Can bulk chondrites with a shock stage of S6 exist as individual rocks?

The brecciation and shock classification of 2280 ordinary chondrites of the meteorite thin section collection at the Institut für Planetologie (Münster) has been determined. The shock degree of S3 is the most abundant shock stage for the H and LL chondrites (44% and 41%, respectively), while the L chondrites are on average more heavily shocked having more than 40% of rocks of shock stage S4. Among the H and LL chondrites, 40–50% are “unshocked” or “very weakly shocked.” Considering the petrologic types, in general, the shock degree is increasing with petrologic type. This is the case for all meteorite groups. The main criteria to define a rock as an S6 chondrite are the solid‐state recrystallization and staining of olivine and the melting of plagioclase often accompanied by the formation of high‐pressure phases like ringwoodite. These characteristics are typically restricted to local regions of a bulk chondrite in or near melt zones. In the past, the identification of high‐pressure minerals (e.g., ringwoodite) was often taken as an automatic and practical criterion for a S6 classification during chondrite bulk rock studies. The shock stage classification of many significantly shocked chondrites (>S3) revealed that most ringwoodite‐bearing rocks still contain more than 25% plagioclase (74%). Thus, these bulk chondrites do not even fulfill the S5 criterion (e.g., 75% of plagioclase has to be transformed into maskelynite) and have to be classified as S4. Studying chondrites on typically large thin sections (several cm²) and/or using samples from different areas of the meteorites, bulk chondrites of shock stage S6 should be extremely rare. In this respect, the paper will discuss the probability of the existence of bulk rocks of S6.     

TWO NEW CHONDRITE-FALLS IN JAPAN

In the summer of 1984, two meteorites fell in the northern part of Honshu, Japan; Aomori, at 1:50 p.m. on June 30, and Tomiya, at 1:35 p.m. on August 22. Coordinates of the falls of the Aomori and the Tomiya are at 140°47.1'E., 40°48.6'N., and 140°51.9'E., 38°22.0'N., respectively. Results of chemical analyses of major elements, ratios of Fe_total/SiO₂ (0.546 and 0.803) and Fe_metal/Fe_total (0.332 and 0.581), and molar compositions of olivines (Fa₂₅ and Fa₁₉) indicate that the Aomori and the Tomiya are typical L- and H-group ordinary chondrites, respectively. In the Aomori, chondrules are present as relicts in the well-recrystallized matrix. Olivine and pyroxene are homogeneous in composition, and coarse clear feldspar, up to 100 micrometers in size, is well developed in the chondrules and matrix. Though the Aomori is a petrologic type 6 based on its texture and mineralogy, it includes a few grains of multiple twinned clinobronzite which is rarely observed in highly equilibrated ordinary chondrites. In the Tomiya, chondrules possess a fine-grained mesostasis, and both orthopyroxene and clinobronzite are noticeable in thin sections. Plagioclase is mostly microcrystalline, but is also sparsely present as tiny, visible grains. Thus, the Tomiya was classified to be petrologic type between 4 and 5. The deformation texture of olivine, pyroxene and plagioclase indicates that both meteorites were shocked by 0.2-0.25 Mb. In conjunction with the discussion of the frequency of meteorite-falls, all observed falls of meteorites in Japan are tabulated in this paper.     

The crystalline lunar spherules: Their formation and implications for the origin of meteoritic chondrules

Abstract— Crystalline lunar spherules (CLS) from three thin sections of Apollo 14 regolith breccias (14318,6; 14318,48 and 14315,20) have been examined. The objects have been classified and their abundances, size distributions, bulk compositions, and (where possible) plagioclase compositions determined. By number, 64% consist predominantly of very fine-grained equant plagioclase grains but can also contain larger (～50 μm) feldspar crystals (type X), while 22% contain plagioclase lathes in a fine-grained mafic mesostasis (type Y). Plagioclase in both spherule types displays bright yellow cathodoluminescence that is conspicuous among the blue CL of the normal feldspar of the breccias. Type Z spherules (5%) contain feldspar with blue CL and minor amounts of olivine and pyroxene. Type Q spherules (4%) contain feldspar with yellow CL but in a luminescent mesostasis (of quartz or feldspar?). A few spherules are mixtures of type Y and type X textures. Most type X spherules, and a few type Y spherules, have fine-grained opaque rims. Compound objects were also found and consist of two or more CLS that appear to have collided while still plastic or molten. The CLS are thought to be impact spherules that crystallized in free flight, their coarse textures suggesting fairly slow cooling rates (～ <1 °C/s). The abundance of the CLS resembles that of chondrules in the CM chondrite Murchison, and their cumulative size-frequency distributions are very similar to those of the chondrules in several meteorite classes. The bulk compositions of the CLS do not resemble regoliths at any of the Apollo sites, including Apollo 14, or any of the common impact glasses, but they do resemble the bulk compositions of several lunar meteorites and the impact glasses they contain. The Apollo 14 site is located on a region containing Imbrium ejecta, and we suggest that the CLS derive from the Imbrium impact. Ballistic calculations indicate that only impact events of this size on the Moon are capable of producing melt spherules with the required free flight times and slow cooling rates. Smaller impacts produce glassy spherules and agglutinates. As has been pointed out many times, the CLS have many properties in common with meteoritic chondrules. While much remains unclear, difficulties with a nebular origin and new developments in chondrule chronology, studies of asteroid surfaces and impact ejecta behavior, and the present observations indicate that meteoritic chondrules could have formed by impact.     

Sodic plagioclase thermometry of type 6 ordinary chondrites: Implications for the thermal histories of parent bodies

Abstract— The structural states of sodic plagioclase crystals of ～50 μm in size from three H6, two L6, and one LL6 chondritic meteorites have been determined by measuring the Δ131 parameter with a Gandolfi camera after analyzing chemical compositions. The temperature for each sodic plagioclase crystal has been determined by plotting the Δ131 parameter, corrected for the influence of K, on the relation diagram between the Δ131 parameter and the temperature of synthesis of sodic plagioclase by Smith (1972). The temperature obtained is assigned to the crystallization temperature of sodic plagioclase, and the maximum plagioclase temperature for each meteorite can be assumed to correspond to the maximum temperature attained by each meteorite during metamorphism. The maximum metamorphic temperatures estimated are 725–742 °C for the H6 chondrites, 808–820 °C for the L6 chondrites, and 800 °C for the LL6 chondrite. These temperatures are lower than those based on Ca contents of clinopyroxenes (Dodd, 1981; McSween et al., 1988) but are consistent with those based on Ca contents of orthopyroxenes (McSween and Patchen, 1989; Langenhorst et al., 1995; Jones, 1997). The K content of sodic plagioclase correlates with the temperature obtained from the structural state. This positive correlation suggests that sodic plagioclase has formed in the course of equilibration processes of alkali elements in prograde metamorphism (i.e., during heating processes). The results of this study (i.e., the maximum metamorphic temperature of the H6 chondrites is lower than that of the L6 chondrites by ～80 °C, and meteorites of the same chemical group show very similar maximum metamorphic temperatures) are in accordance with the predictions of calculations based on the ²⁶Al heat source and the onion-shell structure model of the parent bodies.     

A critical evaluation of oxidation versus reduction during metamorphism of L and LL group chondrites,and implications for asteroid spectroscopy

Abstract— Modal mineralogies of individual, equilibrated (petrologic type 4–6 L and LL chondrites have been measured using an electron microprobe mapping technique, and the chemical compositions of coexisting silicate minerals have been analyzed. Progressive changes in the relative abundances and in the molar Fe/Mn and Fe/Mg ratios of olivine, low‐Ca pyroxene, and diopside occur with increasing metamorphic grade. Variations in olivine/low‐Ca pyroxene ratios (Ol/Px) and in metal abundances and compositions with petrologic type support the hypothesis that oxidation of metallic iron accompanied thermal metamorphism in ordinary chondrites. Modal Ol/Px ratios are systematically lower than normative Ol/Px ratios for the same meteorites, suggesting that the commonly used C.I.P.W. norm calculation procedure may not adequately estimate silicate mineral abundances in reduced chondrites. Ol/Px ratios calculated from visible and near‐infrared (VISNIR) reflectance spectra of the same meteorites are not in agreement with other Ol/Px determinations, possibly because of spectral complexities arising from other minerals in chondrites. Characteristic features in VISNIR spectra are sensitive to the proportions and compositions of olivine and pyroxenes, the minerals most affected by oxidative metamorphism. This work may allow spectral calibration for the determination of mineralogy and petrologic type, and thus may be useful for spectroscopic studies of asteroids.