Fine,nickel-poor Fe-Ni grains in the olivine of unequilibrated ordinary chondrites

Fine (?2 μm), Ni-poor (? 10 mg/g) Fe-Ni grains are common inclusions in the olivine in porphyritic chondrules in unequilibrated ordinary chondrites. The olivine grains appear to be relicts that survived chondrule formation without melting. The most common occurrence of this “dusty” metal is in the core of olivine grains having clear Fe-poor rims and surrounded either by small euhedral clear olivine grains zoned with FeO increasing toward the border of the grains or by large elongated Fe-poor orthopyroxenes oriented parallel to the chondrule surface and enclosing small round olivine grains. Various amounts of Ca, Al-rich glass are always present. The dusty metal is occasionally found in the rims of olivine grains either isolated in the matrix or included in chondrules. A rare occurrence is as bands in highly deformed olivines.This dusty metal appears to be the product of in situ reduction of FeO from the host olivine. Among the possible reductants H₂ or carbonaceous matter (CH₂)_n seem the most likely. Hydrogen may have been implanted by solar-wind or solar-flare irradiation, but this requires that dissipation of nebular gas occurred before the end of the chondrule formation process. Carbonaceous matter may have been implanted by shock. Less likely reductants are nebular CO or C dissolved in the olivine lattice. The large relict olivine grains may be nebular condensates or, more likely, fragments broken off earlier generations of chondrules.     

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.     

The compositional classification of chondrites: III. Ungrouped carbonaceous chondrites

Seven carbonaceous chondrites (Allan Hills A77307, Adelaide, Al Rais, Coolidge, Grosnaja, Karoonda and Renazzo) with uncertain classifications were analyzed by instrumental and radiochemical neutron activation analysis for 29 elements: Na, Mg, Al, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, Ga, Ge, As, Se, Br, Ru, Cd, Sb, La, Sm, Eu, Yb, Lu, Os, Ir and Au. Five of these chondrites (A77307, Adelaide, Al Rais, Karoonda and Renazzo) are unique ‘grouplets’, not closely related to other groups or to each other. Only Coolidge (CV4) and Grosnaja (CV3-an) are members of previously established groups. A77307 and Adelaide have refractory lithophile abundances similar to those in the CM-CO clan; A77307 probably is a member of that clan, but Adelaide, which shows CV-like petrographic characteristics, cannot as yet be assigned to a clan. Al Rais and Renazzo have similar refractory lithophile abundances (essentially at CI levels) and probably belong to the same clan, i.e., formed in the same region of the nebula. There are insufficient data to determine whether they formed at the same general region as the CI chondrites, but separates having O-isotope compositions near the terrestrial fractionation line indicate that this is plausible. Karoonda has refractory lithophile abundances ~ 1.21 × CI and appears to belong to a new clan distinct from CM-CO (1.11 × CI) and CV (1.34×).     

Chemical and physical studies of type 3 chondrites—V: The enstatite chondrites

We report instrumental neutron activation analysis determinations of 19 major, minor and trace elements in three enstatite chondrites. Based on these, and literature data on the bulk and mineral composition of enstatite chondrites, we discuss the history of the type 3 or unequilibrated enstatite chondrites, and their relationship with the other enstatite chondrites. The type 3 enstatite chondrites have E chondrite lithophile element abundances and their siderophile element abundances place them with the EH chondrites, well resolved from the EL chondrites. Moderately volatile chalcophile elements are at the low end of the EH range and Cr appears to be intermediate between EH and EL. We suggest that the type 3 enstatite chondrites are EH chondrites which have suffered small depletions of certain chalcophile elements through the loss of shock-produced sulfurous liquids. The oxygen isotope differences between type 3 and other enstatite chondrites is consistent with equilibration with the nebula gas ~30° higher than the others, or with the loss of a plagioclase-rich liquid. The mineral chemistry of the type 3 chondrites is consistent with either low temperature equilibration, or, in some instances, with shock effects.     

The matrices of unequilibrated ordinary chondrites: Implications for the origin and history of chondrites

The matrices of sixteen unequilibrated ordinary chondrites (all witnessed falls) were studied microscopically in transmitted and reflected light and analyzed by electron microprobe. Selected specimens were also studied by scanning electron microscopy. These studies indicate that the fine-grained, opaque, silicate matrix of type 3 unequilibrated chondrites is compositionally, mineralogically and texturally distinct from the chondrules and chondrule fragments and may be the low temperature condensate proposed by Larimer and Anders (1967, 1970). Examination of the matrices of unequilibrated chondrites also shows that each meteorite has been metamorphosed, with the alteration ranging in intensity from quite mild, where the matrix has been only slightly altered, to a more severe metamorphism that has completely recrystallized the opaque matrix. Most of the metamorphic changes in the matrix occurred without significant effects on the compositions or textures of the chondrules. The metamorphic alteration probably resulted from a combination of processes including thermal metamorphism and the passage of shock waves. The present appearance of each unequilibrated chondrite is a result of the particular temperature and pressure conditions under which it and its components formed, plus the subsequent metamorphic alteration it experienced.     

Crystallization of chondrules in ordinary chondrites

The process of crystallization and the origin of chondrules are discussed, in terms of the phase relations of the minerals in chondrules in six ordinary chondrites of the Yamato-74 meteorites, especially the Yamato-74191 (L3).Chondrules are classified into six types. The bulk compositions of chondrules projected onto the MgO-FeO-SiO₂ system show that the compositions of chondrules vary widely. Investigations by means of the MgO-Al₂O₃-SiO₂ system indicate that porphyritic chondrules can be regarded as products of supercooling crystallization. The growth rates of crystals in porphyritic chondrules were fairly small. The difference between types of chondrules is interpreted in terms of the compositions of chondrules and the nucleation temperatures of the supercooled droplets.All these observations and estimations must be taken into account for discussing the origin of chondrules. The impact and dust fusion theories do not appear to be plausible. Molten droplets due to these mechanisms will be glassy spherules, or crystallize at equilibrium. Only a liquid condensation theory can well explain the characteristic features and the process of the crystallization of chondrules.     

Compositions of three low-FeO ordinary chondrites: Indications of a common origin with the H chondrites

Burnwell, EET 96031, and LAP 04575 are ordinary chondrites (OC) that possess lower than typical olivine Fa content than has been established for the H chondrites (<∼17 mol%). Mean low-Ca pyroxene Fs contents are typically lower than mean Fa content, with generally ?16 mol% Fs. We have investigated these three low-FeO chondrites by measuring their trace element abundances, oxygen isotopic compositions, and examining their three-dimensional (3D) petrography with synchrotron X-ray microtomography. We compare our results with those established for more common OC. The low FeO chondrites studied here have bulk trace element abundances that are identical to the H chondrites. From bulk oxygen isotopic analysis, we show that Burnwell, EET 96010, and LAP 04757 sampled oxygen reservoirs identical to the H chondrites. Burnwell, EET 96031, and LAP 04575 possess common 3D opaque mineral structures that could be distinct from the H chondrites, as evidenced by X-ray microtomographic analysis, but our comparison suite of H chondrites is small and unrepresentative. Overall, our data suggest a common origin for the low-FeO chondrites Burnwell, EET 96010, and LAP 04757 and the H chondrites. These three samples are simply extreme members of a redox process where a limiting nebular oxidizing agent, probably ice, reacted with material containing slightly higher amounts of metal than typically seen in the H chondrites.     

Oxygen isotope studies of carbonaceous chondrites

The carbonaceous chondrites display the widest range of oxygen isotopic composition of any meteorite group, as a consequence of the interaction of primordial isotopic reservoirs in the solar nebula. These isotopic variations can be used to identify the reservoirs and to determine conditions and loci of their interactions. We present a comprehensive set of whole-rock analyses of CV, CO, CK, CM, CR, CH, and CI chondrites, as well as selected components of some of these meteorites. A simple model is developed which describes the isotopic behavior during parent-body aqueous alteration processes. The process of thermal dehydration also produces a recognizable effect in the oxygen isotopic composition.     

Trace elements in primitive meteorites—V. Abundance patterns of thirteen trace elements and interelement relationships in enstatite chondrites

Neutron activation analysis was used to determine As, Au, Bi, Cd, Co, Cu, Ga, In, Sb, Se, Te, Tl and Zn in 11 samples representing 9 chondrites of grades E4–6. These chondrites exhibit systematic intra- and inter-grade differences particularly for highly-variable elements, the differences being E4 ? E3 > E6 ? E5. The abundance pattern for these 13 and an additional 16 elements in E3-6 chondrites differs from those of other primitive meteorites—the carbonaceous and unequilibrated ordinary chondrites. A search for statistically-significant interelement relationships among the 13 elements (for grades E4–6) reveal that 40 elementpairs are linearly and/or exponentially correlated. Similar consideration of data for 37 elements in 12 chondrites (grades E3–6) reveals that 191 element-pairs exhibit such relationships, 170 involving linear and/or exponential correlations, the remainder involving anti-correlations. The patterns depicting these relationships—i.e. the correlation profiles—and elemental abundance patterns, factor analysis and two-element correlation diagrams are consistent with all enstatite chondrites representing a single evolutionary sequence. The primary process responsible for the chemical trends of these chondrites involved thermal fractionation accompanied by geochemical fractionation of sulfide-plus-metal from silicate, probably during condensation and accretion of solid material from the solar nebula. Chalcophile elements may have been fractionated during condensation or, after accretion, during thermal metamorphism in the parent body. No genetic model proposed thus far accounts for the detailed chemical trends, although the constrained equilibrium theory and two-component condensation theories qualitatively seem most satisfactory. The correlation profiles of enstatite, carbonaceous and unequilibrated ordinary chondrites are distinctly different, pointing to major differences in the formation conditions of these different sorts of primitive meteorites.     

Siderophile elements in chondrules of CV chondrites

New bulk compositional data for 34 Allende chondrules are presented. Whole chondrules were analyzed by instrumental neutron activation analysis (INAA). The new data set is evaluated together with older INAA data on Allende chondrules and recent INAA data on Mokoia chondrules. The Ni/Co ratios of 200 chondrules are close to the CI- or solar ratio. The chondritic Ni/Co ratios require an unfractionated chondritic metal source and set a limit to the fraction of metal lost from molten chondrules. The bulk chondrule Fe/Ni and Fe/Co ratios are more variable but on average chondritic. Iridium and other refractory metals have extremely variable concentrations in chondrules. High Ir chondrules have chondritic Ir/Sc ratios. They are dominated by CAI (Ca,Al-rich inclusion) components. Low Ir chondrules have approximately chondritic Ir/Ni ratios reflecting mixing with chondritic metal. In low Ir chondrules Ir correlates and in high Ir chondrules Ir does not correlate with Ni or Co. A large fraction of Ir may have entered chondrules in variable amounts as tiny grains of refractory metal alloys.Most Allende chondrules have Ir/Sc ratios below bulk meteorite ratios. Matrix must have a complementary high Ir/Sc ratio, as bulk Allende has approximately chondritic Ir/Sc ratio. Similarly, the high average Ir/Ni ratios of Allende chondrules must be balanced by low Ir/Ni ratios in matrix to obtain the bulk Allende Ir/Ni ratio, which is close to the average solar system ratio.More recent data on single chondrules from Allende by ICP-MS (Inductively Coupled Plasma Mass Spectrometry) and ICP-OES (Inductively Coupled Optical Emission Spectrometry) show the same trends as the INAA data discussed here.     

An Fe isotope study of ordinary chondrites

The Fe isotope composition of ordinary chondrites and their constituent chondrules, metal and sulphide grains have been systematically investigated. Bulk chondrites fall within a restricted isotopic range of <0.2‰ δ⁵⁶Fe, and chondrules define a larger range of >1‰ (−0.84‰ to 0.21‰ relative to the IRMM-14 Fe standard). Fe isotope compositions do not vary systematically with the very large differences in total Fe concentration, or oxidation state, of the H, L, and LL chondrite classes. Similarly, the Fe isotope compositions of chondrules do not appear to be determined by the H, L or LL classification of their host chondrite. This may support an origin of the three ordinary chondrite groups from variable accretion of identical Fe-bearing precursors.A close relationship between isotopic composition and redistribution of Fe during metamorphism on ordinary chondrite parent bodies was identified; the largest variations in chondrule compositions were found in chondrites of the lowest petrologic types. The clear link between element redistribution and isotopic composition has implications for many other non-traditional isotope systems (e.g. Mg, Si, Ca, Cr). Isotopic compositions of chondrules may also be determined by their melting history; porphyritic chondrules exhibit a wide range in isotope compositions whereas barred olivine and radial pyroxene chondrules are generally isotopically heavier than the ordinary chondrite mean. Very large chondrules preserve the greatest heterogeneity of Fe isotopes.The mean Fe isotope composition of bulk ordinary chondrites was found to be −0.06‰ (±0.12‰ 2 SD); this is isotopically lighter than the terrestrial mean composition and all other published non-chondritic meteorite suites e.g. lunar and Martian samples, eucrites, pallasites, and irons. Ordinary chondrites, though the most common meteorites found on Earth today, were not the sole building blocks of the terrestrial planets.     

Progressive aqueous alteration of CM carbonaceous chondrites

CM chondrites are aqueously altered rocks that contain ∼9 wt% H₂O⁺ (i.e., indigenous water) bound in phyllosilicates; also present are clumps of serpentine-tochilinite intergrowths (previously called “poorly characterized phases” or PCP), pentlandite and Ni-bearing pyrrhotite. We studied 11 CM chondrites that span the known range from least altered to most altered. We used various petrologic properties (many previously identified) that provide information regarding the degree of aqueous alteration. There are no known unaltered or slightly altered CM chondrites (e.g., rocks containing numerous chondrules with primary igneous glass). Some CM properties result from processes associated with early and intermediate stages of the alteration sequence (i.e., hydration of matrix, alteration of chondrule glass, and production of large PCP clumps). Other petrologic properties reflect processes active throughout the alteration sequence; these include oxidation of metallic Fe-Ni, alteration of chondrule phenocrysts, changes in PCP composition (reflecting an increase in the phyllosilicate/sulfide ratio), and changes in carbonate mineralogy (reflecting the development of dolomite and complex carbonates at the expense of Ca carbonate).On the basis of these parameters, we propose a numerical alteration sequence for CM chondrites. Because there are no known CM samples that display only incipient alteration, the least altered sample was arbitrarily assigned to subtype 2.6. The most altered CM chondrites, currently classified CM1, are assigned to subtype 2.0. These highly altered rocks have essentially no mafic silicates; they contain chondrule pseudomorphs composed mainly of phyllosilicate. However, their bulk compositions are CM-like, and they are closer in texture to other C2 chondrites than to CI1 chondrites (which lack chondrule pseudomorphs). Using several diagnostic criteria, we assigned petrologic subtypes (±0.1) to every CM chondrite in our study: QUE 97990, CM2.6; Murchison, CM2.5; Kivesvaara, CM2.5; Murray, CM2.4/2.5; Y 791198, CM2.4; QUE 99355, CM2.3; Nogoya, CM2.2; Cold Bokkeveld, CM2.2; QUE 93005, CM2.1; LAP 02277, CM2.0; MET 01070, CM2.0.The proposed CM numerical alteration sequence improves upon the existing scheme of Browning et al. (1996) in that it does not require a complicated algorithm applied to electron-microprobe data to determine the average matrix phyllosilicate composition. The new sequence is more comprehensive and employs petrologic subtypes that are easier to use and remember than mineralogic alteration index values.New neutron-activation analyses of QUE 97990, QUE 93005, MET 01070, Murchison and Crescent, together with literature data, confirm the compositional uniformity of the CM group; different degrees of alteration among CM chondrites do not lead to resolvable bulk compositional differences. This suggests that the textural differences among individual CM chondrites reflect progressive alteration of similar hypothetical CM3.0 starting materials in different regions of the same parent body, with minimal aqueous transport of materials over appreciable (e.g., meters) distances.     

Trace elements in primitive meteorites—VI. Abundance patterns of thirteen trace elements and interelement relationships in unequilibrated ordinary chondrites

Neutron activation analysis was used to determine As, Au, Bi, Cd, Co, Cu, Ga, In, Sb, Se, Te, Tl and Zn in 13 different unequilibrated ordinary chondrites (UOC), i.e. those having chemicallyinhomogeneous silicates. This study together with prior data completes our coverage of this group of 23 primitive chondrites. Four elements are quite variable in UOC (Cd—20 x, In—30 x, Bi—300 x and Tl—1300 x), the others varying by 2–8 x. Three highly-depleted elements—Bi, In and Tl—are richer by 5–35 x in unequilibrated chondrites than in their equilibrated congeners. All 3 elements vary directly in characteristic fashion with disequilibrium parameters for olivine and pyroxene in UOC and generally with petrologic type 3 > 4 > 5 > 6. The data do not provide unambiguous evidence for nebular fractionation of siderophile elements. Examination of statistically-significant interelement relationships among various ordinary chondrite populations involving 34 elements reveals patterns distinct from those of other chondritic groups. These patterns reflect nebular metal-silicate fractionation which preceded or accompanied thermal fractionation. The results point to significant differences in the formation of primitive carbonaceous, enstatite and ordinary chondrites.     

Brecciation and chemical heterogeneities of CI chondrites

Fragments in the size range from 40 μm to several hundred μm in the CI chondrites Orgueil, Ivuna, Alais, and Tonk show a wide range of chemical compositions with variations in major elements such as iron (10.4-42.4 wt% FeO), silicon (12.7-42.2 wt% SiO₂), and sulfur (1.01-15.8 wt% SO₃), but also important minor elements such as phosphorous (up to 5.2 wt% P₂O₅) or calcium (up to 6.6 wt% CaO). These variations are the result of the varying mineralogical compositions of these fragments. The distribution of phyllosilicates, magnetites, and possibly ferrihydrite, in particular, control the abundances of these elements. High REE contents—up to 150 times the solar abundances—were observed in phosphates, while matrix and sulfates are REE-depleted. The studied 113 fragments were subdivided into eight lithologies with similar mineralogical and thus chemical properties. The most common is the CGA lithology, consisting of a groundmass of Mg-rich, coarse-grained phyllosilicates and varying abundances of inclusions such as magnetite. The second most abundant lithology is the FGA lithology, consisting of a groundmass of fine-grained Fe-rich phyllosilicates. A rare, but important lithology consists of fragments with high contents of phosphates and other minerals. The proposed model for the evolution of these lithologies is based on a closed system alteration, where mineralogical differences in the lithologies reflect heterogeneities in the starting material. Comparison of our results with literature data indicates a general similarity of the four CI chondrites analyzed. Further comparison of bulk analyses suggests that the mass ‘threshold’ for chemical heterogeneities in CI chondrite samples is smaller than ∼1-2 g.     

Organic matter and metamorphic history of CO chondrites

The metamorphic grades of a series of eight CO3 chondrites (ALHA77307, Colony, Kainsaz, Felix, Lancé, Ornans, Warrenton and Isna) have been quantified. The method used was based on the structural grade of the organic matter trapped in the matrix, which is irreversibly transformed by thermal metamorphism. The maturation of the organic matter is independent with respect to the mineralogical context and aqueous alteration. This metamorphic tracer is thus valid whatever the chemical class of chondrites. Moreover, it is sensitive to the peak metamorphic temperature.The structural grade of the organic matter was used along with other metamorphic tracers such as petrography of opaque minerals, Fa and Fs silicate composition in type I chondrules, presolar grains and noble gas (P3 component) abundance. The deduced metamorphic hierarchy and the attributed petrographic types are the following: ALHA77307 (3.03) < Colony (3.1) < Kainsaz (3.6) < Felix (3.6 (1)) < Ornans (3.6 (2)) < Lancé (3.6 (3)) < Warrenton (3.7 (1)) < Isna (3.7 (2)).For most metamorphosed objects, the peak metamorphic temperature can be estimated using a geothermometer calibrated with terrestrial metasediments [Beyssac O., Goffe B., Chopin C., and Rouzaud J. N. (2002) Raman spectrum of carbonaceous material in metasediments: a new geothermometer. J. Metamorph. Geol., 20, 859-871]. A value of 330 °C was obtained for Allende (CV chondrite), Warrenton and Isna, consistent with temperatures estimated from Fe diffusion [Weinbruch S., Armstrong J., and Palme H. (1994). Constraints on the thermal history of the Allende parent body as derive from olivine-spinel thermometry and Fe/Mg interdiffusion in olivine. Geochim. Cosmochim. Acta58(2), 1019-1030.], from the Ni content in sulfide-metal assemblages [Zanda B., Bourot-Denise M., and Hewins R. (1995) Condensate sulfide and its metamorphic transformations in primitive chondrites. Meteorit. Planet. Sci.30, A605.] and from the d₀₀₂ interlayer spacing in poorly graphitized carbon [Rietmeijer, F., and MacKinnon, I. (1985) Poorly graphitized carbon as a new cosmothermometer for primitive extraterrestrial materials. Nature, 315, 733-736]. The trapped noble gas and C content appear to be sensitive but not precise metamorphic tracers, indicating that the “Ornans paradox” does not exist. Major problems with the current petrologic types derived from Induced ThermoLuminescence are pointed out.     

Abundance of 17 trace elements in carbonaceous chondrites

Seventeen trace elements (Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Rb, Re, Sb, Se, Te, Tl, U and Zn) were measured by neutron activation analysis in 8 C1 samples (1 Alais, 3 Ivuna, 4 Orgueil) and in 3 C2 samples (one each of Mighei, Murchison, Murray). The results show far less scatter than earlier literature data. The standard deviation of a single measurement from the mean of 8 C1 samples lies between 2 and 14 per cent, except for the following 4 elements: Au ±18 per cent, Ag ±22 per cent, Rb ±19 per cent and Br ±33 per cent. The first two probably reflect contamination and sample heterogeneity, the last two, analytical error. Apparently C1 chondrites have a far more uniform composition than some authors have claimed.The new data suggest significant revisions in cosmic abundance for the following elements (old values in parentheses): Zn 1250 (1500), Cd 1.51 (2.12), Ir 0.72 (0.43) atoms/10⁶ Si atoms. The Br value is also lower, 6.8 vs 20.6, but may be affected by analytical error.Relative to C1 chondrites, the C2 chondrites Mighei, Murchison and Murray are depleted in volatile elements by a factor of 0.508 ± 0.038, much more constant than indicated by oldor data. Ordinary chondrites also show a more uniform depletion relative to the new C1 data. The mean depletion factor of Sb, F, Cu, Ga, Ge, Sn, S, Se, Te and Ag is 0.227 ± 0.027 in H-chondrites. This constancy further strengthens the case for the two-component model of chondrite formation.     

Elemental composition of individual chondrules from ordinary chondrites

Sequential non-destructive neutron activation analysis was used to determine the bulk abundance of Fe, Al, Na, Mn, Or, Sc, Co and Ir in approximately 300 individual chondrules from 16 chondrites representing the H (3–5), L4 and LL(3–6) compositional and petrologic classes. For some of the chondrules, Si, Ni, Ca and V were also determined. The histograms indicate that the most probable abundances for lithophilic elements, except Cr, are enriched in the chondrules, while the siderophilic elements are depleted in the chondrules compared to the whole chondrite. Some of the abundance populations, such as Al and Fe, appear to be multimodal. Systematic variations in the composition of the chondrules with increasing petrologic type were observed; most consistent are an increasing Na-Al and Cr-Al correlation, a decreasing Na-Mn correlation, increasing Na abundance and decreasing Na and Mn dispersions among chondrules. The systematic compositional variations with increasing petrologic type are consistent with an increasing approach to equilibrium between chondrules and matrix.Observed elemental correlations are generally consistent with mineralogical controls expected on the basis of geochemical affinities suggested by the mineral assemblages present in the chondrules. However, a prevalent Al-Ir correlation was observed, and is most pronounced for a group of chondrules belonging to a population high in Al. A Sc-Ir correlation was observed. Also, an anti-correlation between chondrule masses and Al (and Ir for some chondrules) content of the chondrules was observed. These correlations are attributed to a fractionation during condensation or chondrule formation and cannot be attributed to classical geochemical similarities i.e. these correlations result from a cosmochemical fractionation. From the compositional evidence, it is suggested that there may be two mechanisms for chondrule production. Some high Al chondrules which exhibit the Al-Ir correlation are believed to be remelted primitive high-temperature aggregates. The elemental composition of the chondrules from the lower Al abundance population is consistent with a preferential remelting of pre-existing silicates.