The composition and origin of large microporphyritic chondrules in the Manych (L-3) chondrite

The majority (26/37) of the largest chondrules (d ≥ 1400 μm) exposed in a thin section of the Manych chondrite are more or less rounded fragments of microporphyry, most of which contain from 50 to 80 vol.% olivine. Modal and phase analyses were used to calculate the approximate bulk compositions of nine such chondrules. Six vary modestly around the mean composition of L-group chondrites less most of their metal and troilite and are thought to have formed by bulk melting of L-group material with loss of an immiscible Fe-Ni-S liquid. Two other chondrules, which are olivine-rich and Na- and Si-poor, formed in the same way but with some loss of volatile constituents to a vapor phase. The ninth chondrule, an olivine-poor microporphyry, may be a non-representative sample of a coarser microporphyritic rock.Comparison of these microporphyritic chondrules with the products of controlled cooling experiments and with chemically similar olivine microporphyry in the St. Mesmin chondrite (LL-breccia) suggests that the microporphyritic chondrules are fragments of magmatic rocks which crystallized from masses of liquid no less than 10 cm across.     

Elemental abundances in chondrules from unequilibrated chondrites: Evidence for chondrule origin by melting of pre-existing materials

Bulk abundances of Na, Mg, Al, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, La, Sm, Eu, Yb, Lu, Ir, and Au were determined by neutron activation analysis of chondrules separated from unequilibrated H-, L-, and LL-chondrites (Tieschitz, Hallingeberg, Chainpur, Semarkona) and correlated with chondrule petrographic properties. Despite wellknown compositional differences among the whole-rock chondrites, the geometric mean compositions of their respective chondrule suites are nearly indistinguishable from each other for many elements. Relative to the condensible bulk solar system (approximated by the Cl chondrite Orgueil), chondrules are enriched in lithophile and depleted in siderophile elements in a pattern consistent with chondrule formation by melting of pre-existing materials, preceded or attended by silicate/metal fractionation. Relative to nonporphyritic chondrules, porphyritic chondrules are enriched in refractory and siderophile elements, suggesting that these two chondrule groups may have formed from different precursor materials.     

A combined chemical-petrological study of separated chondrules from the Richardton meteorite

Individual chondrules have been separated from the H5 chondrite Richardton and subjected to a detailed chemical-petrological study. A portion of each chondrule has been examined petrographically and phase chemistry determined by electron microprobe analysis. Of the remaining portion an aliquot was taken for measurement of major element abundances by microprobe using a microfusion technique. Rb, Sr,⁸⁷Sr/⁸⁶Sr and REE were determined by mass spectrometric isotope dilution.The chondrules define a Rb-Sr isochron age of 4.39 ± 0.03Ga(λ = 1.42 × 10^?11 a^?1) and an initial ratio of 0.7003 ± 7. The age is interpreted as a metamorphic age and indicates that Sr isotope equilibration occurred in the Richardton parent body for some 100 Ma or more after condensation of the solar system. Metamorphism had little effect on chondrule textures but effected Fe/Mg exchange to produce highly uniform olivine and pyroxene compositions, and may have caused some redistribution of REE.The major element compositions of Richardton chondrules are mostly constant and close to reported averages for Tieschitz, Bishunpur and Chainpur. They contain high-temperature condensate elements in close to cosmic proportions, but are deficient in Fe. Theories of chondrule origin are briefly reviewed, and while it is difficult to distinguish between direct condensation and dust fusion by impacting, it is postulated that iron was fractionated from silicate prior to or during chondrule formation.     

A new kind of primitive chondrite, Allan Hills 85085

Allan Hills 85085 is a chemically and mineralogically unique chondrite whose components have suffered little metamorphism or alteration. This chondrite is unique because it has fewer and smaller chondrules (4 wt. %; mean diameter 16 μm) than any other chondrite, more metallic Fe,Ni (36%) and lithic and mineral silicate fragments (56%), and a lower abundance of troilite (2%) and volatiles. Most chondrules are cryptocrystalline or glassy and are depleted in volatiles, some small chondrules are also very depleted in refractory lithophiles. Matrix lumps (4%) partly resemble CI and CM matrices and may be foreign to the parental asteroid. Despite these differences, the components of ALH 85085 have some features common to most type 2 and the least metamorphosed type 3 chondrites: metallic Fe,Ni grains that contain 0.1–1 wt.% Cr, Si and P; Fe/(Fe + Mg) values of olivines, pyroxenes and chondrules are concentrated in the range 1–6 at.% with a few percent in the range 7–30%; porphyritic chondrules are chondritic in composition (except for their low volatile abundances). Thus the components of ALH 85085 probably have similar origins to those of components in other chondrites, and their properties largely reflect nebular, not asteroidal, processes.The bulk composition of ALH 85085 fits none of the nine groups of chondrites: it is richer in Fe (1.4 × CI levels when normalized to Si) and poorer in Na and S (0.1–0.2 × CI) than other chondrites. Low volatile concentrations are due to a low matrix abundance and loss of volatiles during or prior to chondrule formation, not to volatile loss during metamorphism. Chondrule textures imply extensive heating of chondrule melts above the liquidus, consistent with loss of volatiles from small volumes of melt during chondrule formation. The small size of chondrules is partly due to extensive fragmentation by impacts, which may have occurred on the parent asteroid or in the solar nebula. Collisions between chondrule precursor aggregates in the nebula could also be responsible for the small sizes of chondrules.Assuming that ALH 85085 is a representative sample of an asteroid, its properties lend support to models for the origins of the Earth, eucrite parent body and volatile-poor iron meteorites that invoke chondritic planetesimals depleted in volatiles. The existence of ALH 85085 and Kakangari suggests that the nine chondrite groups may provide a remarkably poor sample of the primitive chondritic material from which the asteroids formed. Certain similarities between ALH 85085 and Bencubbin and Weatherford suggest that the latter two primitive meteorites may actually be chondrites with even higher metal abundances (50–60 wt.%) and very large, partly fragmented chondrules.     

87Rb87Sr dating of LL chondrites

⁸⁷Rb⁸⁷Sr analyses of LL chondrites have been made in 10 whole rock meteorites, chondrules from Chainpur (LL3) and Soko Banja (LL4), density separates and chondrules from Guidder (LL5) and density separates from Jelica (LL6) and Ensisheim (LL6). Whole rocks define an isochron of age 4.486±0.020 Ga (λ⁸⁷Rb=1.42×10^?11a^?1) and initial ratio (⁸⁷Sr/⁸⁶Sr)_I=0.69887±0.00012. This is in agreement with the results for H- and E-type chondrites. Analyses for chondrules from Soko Banja yield a very good isochron of age 4.452±0.020 Ga and strontium initial ratio 0.69954±0.00024, and give an interval for metamorphism of (37±10)×10⁶ a. A more poorly defined isochron is obtained for Jelica; the age is 4.423±0.041 Ga and the strontium initial ratio 0.69959±0.00029, indicating an interval for metamorphism of (70±60)×10⁶ a. No isochron could be obtained for Chainpur. This could be due to terrestrial alteration or to a late isotopic disturbance of the meteorite. The⁸⁷Rb-⁸⁷Sr system is also disturbed in Guidder and Ensisheim, probably as a consequence of shock. These results are discussed in comparison with our former studies, and in relation with thermal metamorphism in the LL chondrite parent body(ies).     

Evidence for relict grains in chondrules of Qingzhen,an E3 type enstatite chondrite

Petrographic and chemical studies of the Qingzhen chondrite strongly suggest that it is the most highly unequilibrated (type 3) enstatite chondrite recognized so far. Qingzhen contains abundant, well-defined chondrules, some of which were incompletely molten during the chondrule formation process. The relict olivine grains within these chondrules contain dusty inclusions of almost pure metallic Fe, which appear to be the in-situ reduction product of the fayalitic component of the olivine. The reduction process presumably took place at the time of chondrule formation and the chondrule precursor material must have been more oxidized than average enstatite chondrite material. We believe that this oxidized material may have formed at the enstatite chondrite formation location in the solar nebula, provided fluctuations in the degree of oxidation of the nebular gas existed at such locations. Reheating of this material under more reducing conditions would lead to the observed reduction of the olivine. Igneous olivines within chondrules always contain detectable amounts of CaO, while relict olivines are essentially CaO-free. This seems to suggest that the relict olivines did not originate during a previous igneous process of chondrule formation and might represent condensation products from the early solar nebula.     

Petrogenesis of opaque assemblages in the Ningqiang carbonaceous chondrite

Numerous round to oblate opaque assemblages (OAs) are found in chondrules and matrix of the Ningqiang carbonaceous chondrite. They are mainly composed of Ni-rich metal,magnetite,Fe,Ni-sulfides,with minor amounts of phosphate,phosphoran-olivine,pyroxene and trace amounts of nano-sized platinum-group metal alloys. The mineralogy of Ningqiang OAs is very similar to that of OAs previously reported in Ca,Al-rich inclusions of CV chondrites. Being a rare mineral phase in nature,phosphoran-olivine is thought to form by nonequilibrium reactions between P-bearing molten metal and olivine crystals during rapid cooling. Its occurrence in Ningqiang OAs indicates that the precursor of OAs was locally produced during chondrule formation,rather than directly condensed from the solar nebula as previously thought. The petrographic and mineralogical characteristics of Ningqiang OAs reveal that OAs formed by low temperature alterations of pre-existing homogeneous alloys within chondrules on a planetary body.     

New kind of type 3 chondrite with a graphite-magnetite matrix

We have discovered four clasts in three ordinary-chondrite regolith breccias which are a new kind of type 3 chondrite. Like ordinary and carbonaceous type 3 chondrites, they have distinct chondrules, some of which contain glass, highly heterogeneous olivines and pyroxenes, and predominantly monoclinic low-Ca pyroxenes. But instead of the usual fine-grained, Fe-rich silicate matrix, the clasts have a matrix composed largely of aggregates of micron- and submicron-sized graphite and magnetite. The bulk compositions of the clasts as well as the types of chondrules (largely porphyritic) are typical of type 3 ordinary chondrites, although chondrules in the clasts are somewhat smaller (0.1–0.5 mm). A close relationship with ordinary chondrites is also indicated by the presence of similar graphite-magnetite aggregates in seven type 3 ordinary chondrites. This new kind of chondrite is probably the source of the abundant graphite-magnetite inclusions in ordinary-chondrite regolith breccias, and may be more common than indicated by the absence of whole meteorites made of chondrules and graphite-magnetite.     

Oxygen isotopic constraints on the origin of Mg-rich olivines from chondritic meteorites

Chondrules are the major high temperature components of chondritic meteorites which accreted a few millions years after the oldest solids of the solar system, the calcium–aluminum-rich inclusions, were condensed from the nebula gas. Chondrules formed during brief heating events by incomplete melting of solid dust precursors in the protoplanetary disk. Petrographic, compositional and isotopic arguments allowed the identification of metal-bearing Mg-rich olivine aggregates among the precursors of magnesian type I chondrules. Two very different settings can be considered for the formation of these Mg-rich olivines: either a nebular setting corresponding mostly to condensation–evaporation processes in the nebular gas or a planetary setting corresponding mostly to differentiation processes in a planetesimal. An ion microprobe survey of Mg-rich olivines of a set of type I chondrules and isolated olivines from unequilibrated ordinary chondrites and carbonaceous chondrites revealed the existence of several modes in the distribution of the ?¹⁷O values and the presence of a large range of mass fractionation (several ‰) within each mode. The chemistry and the oxygen isotopic compositions indicate that Mg-rich olivines are unlikely to be of nebular origin (i.e., solar nebula condensates) but are more likely debris of broken differentiated planetesimals (each of them being characterized by a given ?¹⁷O). Mg-rich olivines could have crystallized from magma ocean-like environments on partially molten planetesimals undergoing metal–silicate differentiation processes. Considering the very old age of chondrules, Mg-rich olivine grains or aggregates might be considered as millimeter-sized fragments from disrupted first-generation differentiated planetesimals. Finally, the finding of only a small number of discrete ?¹⁷O modes for Mg-rich olivines grains or aggregates in a given chondrite suggests that these shattered fragments have not been efficiently mixed in the disk and/or that chondrite formation occurred in the first vicinity of the breakup of these planetary bodies.     

Cristobalite-pyroxene in an L6 chondrite: implications for metamorphism

CRISPY is a cristobalite-pyroxene assemblage in the L6 chondrite ALHA 76003. It was formed by reaction of a very siliceous inclusion with the surrounding olivine-rich rock. Oxygen isotopes show that the inclusion was derived from a source with non-chondritic isotopic composition. The isotopes also show that the oxygen of the pyroxene reaction product was derived by simple mixing of oxygen from the inclusion and its immediately adjacent surroundings, with exchange with the bulk meteorite limited to a distance of about a millimeter. The persistence of cristobalite in close proximity to olivine, and the lack of isotopic equilibration, show that the metamorphic processes that form petrographic grade 6 chondrites involve transport of major elements over distances only on the order of millimeters.     

Origin of magnetite in oxidized CV chondrites: in situ measurement of oxygen isotope compositions of Allende magnetite and olivine

Magnetite in the oxidized CV chondrite Allende mainly occurs as spherical nodules in porphyritic-olivine (PO) chondrules, where it is associated with Ni-rich metal and/or sulfides. To help constrain the origin of the magnetite, we measured oxygen isotopic compositions of magnetite and coexisting olivine grains in PO chondrules of Allende by an in situ ion microprobe technique. Five magnetite nodules form a relatively tight cluster in oxygen isotopic composition with delta 18O values from -4.8 to -7.1% and delta 17O values from -2.9 to -6.3%. Seven coexisting olivine grains have oxygen isotopic compositions from -0.9 to -6.3% in delta 18O and from -4.6 to -7.9% in delta 17O. The delta 17O values of the magnetite and coexisting olivine do not overlap; they range from -0.4 to -2.6%, and from -4.0 to -5.7%, respectively. Thus, the magnetite is not in isotopic equilibrium with the olivine in PO chondrules, implying that it formed after the chondrule formation. The delta 17O of the magnetite is somewhat more negative than estimates for the ambient solar nebula gas. We infer that the magnetite formed on the parent asteroid by oxidation of metal by H2O which had previously experienced minor O isotope exchange with fine-grained silicates.     

High temperature rims around chondrules in primitive chondrites: evidence for fluctuating conditions in the solar nebula

Rims or rim sequences surrouding chondrules have been identified in carbonaceous and unequilibrated ordinary chondrites. These chondrule rims include three chemical subtypes: Fe,Ca-rich and Fe,Ni-metal-rich rims, which occur predominantly in Kainsaz (CO3), and ferromagnesian rims which occur in Kainsaz (CO3), Allende (CV3), Renazzo (CR2), Chainpur (LL3), Semarkona (LL3), Krymaka (L3), and Tieschitz (H3). The compositions of minerals in these rims are often drastically different from those in the underlying chondrule cores, indicating that the solar nebula was chemically heterogeneous. In many cases the compositions of the rims require an environment that was much more oxidizing than a solar composition gas. Particularly interesting is that some of the Fe,Ca-rich chondrule rims are remarkably similar to some of the rims around refractory inclusions, suggesting that chondrules and refractory inclusions experienced late, coeval processing. The textures of the chondrule rims suggest they formed at high temperatures and that they accreted onto chondrules that had already solidified. The lengthscale of the thermal heterogeneities necessary to make available hot material that could accrete to cold chondrules has been calculated to be less than 10 km, implying there were localized heat sources in the solar nebula.     

Experimental reproduction of textures of chondrules

The textures of chondrules have been reproduced by crystallizing melts of three different compositions at 1 atm with cooling rates ranging from 400 to 20°C/min under 10^?9 to 10^?12 atmP_O2. A porphyritic olivine texture has been formed from a melt of olivine-rich composition (SiO₂ = 45 wt.%), a barred-olivine texture from melt of intermediate composition (SiO₂ = 47 wt.%), and radial-olivine texture from melt of pyroxene-rich composition (SiO₂ = 57 wt.%). The cooling rate for producing barred olivine is most restricted; the rate ranges from 120 to 50°C/min. Other textures can be formed with wider ranges of cooling rate. The results of the experiments indicate that some of the major types of textures of chondrules can be formed with cooling rate of about 100°C/min. With this cooling rate, the texture varies depending on the composition of melt.     

Nitrogen abundances and isotopic compositions in stony meteorites

Nitrogen contents range from a few parts per million in ordinary chondrites and achondrites to several hundred parts per million in enstatite chondrites and carbonaceous chondrites. Four major isotopic groups are recognized: (1) C1 and C2 carbonaceous chondrites have δ¹⁵N of+30to+50%.; (2) enstatite chondrites have δ¹⁵N of?30to?40‰; (3) C3 chondrites have low δ¹⁵N with large internal variations; (4) ordinary chondrites have δ¹⁵N of?10to+20‰. The major variations are primary, representing isotopic abundances established at the time of condensation and accretion. Secondary processes, such as spallation reactions, solar wind implantation and metamorphic loss may cause small but observable isotopic variations in particular cases. The large isotopic difference between enstatite chondrites and carbonaceous chondrites cannot be accounted for by equilibrium condensation from a homogeneous nebular gas, and requires either unusually large kinetic effects, or a temporal or spatial variation of isotopic composition of the nebula. Nitrogen isotopic heterogeneity in the nebula due to nuclear processes has not been firmly established, but may be required to account for the large variations found within the Allende and Leoville meteorites. The unique carbonaceous chondrite, Renazzo, has δ¹⁵N of+170%., which is well beyond the range of all other data, and also requires a special source. It is not yet possible, from the meteoritic data, to establish the mode of accretion of nitrogen onto the primitive Earth.     

Zirconium isotope evidence for incomplete admixing of r-process components in the solar nebula

Isotopic anomalies in Mo and Zr have recently been reported for bulk chondrites and iron meteorites and have been interpreted in terms of a primordial nucleosynthetic heterogeneity in the solar nebula. We report precise Zr isotopic measurements of carbonaceous, ordinary and enstatite chondrites, eucrites, mesosiderites and lunar rocks. All bulk rock samples yield isotopic compositions that are identical to the terrestrial standard within the analytical uncertainty. No anomalies in ⁹²Zr are found in any samples including high Nb/Zr eucrites and high and low Nb/Zr calcium-aluminum-rich inclusions (CAIs). These data are consistent with the most recent estimates of <10⁻⁴ for the initial ⁹²Nb/⁹³Nb of the solar system. There exists a trace of isotopic heterogeneity in the form of a small excess of r-process ⁹⁶Zr in some refractory CAIs and some metal-rich phases of Renazzo. A more striking enrichment in ⁹⁶Zr is found in acetic acid leachates of the Allende CV carbonaceous chondrite. These data indicate that the r- and s-process Zr components found in presolar grains were well mixed on a large scale prior to planetary accretion. However, some CAIs formed before mixing was complete, such that they were able to sample a population of r-process-enriched material. The maximum amount of additional r-process component that was added to the otherwise well-mixed Zr in the molecular cloud or disk corresponds to ∼0.01%.     

ALH85085: a unique volatile-poor carbonaceous chondrite with possible implications for nebular fractionation processes

Allan Hills 85085 is a unique chondrite with affinities to the Al Rais-Renazzo clan of carbonaceous chondrites. Its constituents are less than 50 μm in mean size. Chondrules and microchondrules of all textures are present; nonporphyritic chondrules are unusually abundant. The mean compositions of porphyritic, nonporphyritic and barred olivine chondrules resemble those in ordinary chondrites except that they are depleted in volatile elements. Ca-, Al-rich inclusions are abundant and largely free of nebular alteration; they comprise types similar to those in CM and CO chondrites, as well as unique types. Calcium dialuminate occurs in several inclusions. Metal, silicate and sulfide compositions are close to those in CM-CO chondrites and Al Rais and Renazzo. C1-chondrite clasts and metal-rich “reduced” clasts are present, but opaque matrix is absent. Siderophile abundances in ALH85085 are extremely high (e.g., Fe/Si= 1.7 × solar), and volatiles are depleted (e.g., Na/Si= 0.25 × solar, S/Si= 0.03 × solar). Nonvolatile lithophile abundances are similar to those in Al Rais, Renazzo, and CM and CO chondrites.ALH85085 agglomerated when temperatures in the nebula were near 1000 K, in the same region where Renazzo, Al Rais and the CI chondrites formed. Agglomeration of high-temperature material may thus be a mechanism by which the fractionation of refractory lithophiles occurred in the nebula. Chondrule formation must have occurred at high temperatures when clumps of precursors were small. After agglomeration, ALH85085 was annealed and lightly shocked. C1 and other clasts were subsequently incorporated during late-stage brecciation.     

Fine-grained aggregates in L3 chondrites

The textures and chemical compositions of the constituent minerals of the fine-grained aggregates (FGA's) of L3 chondrites were studied by the backscattered electron image technique, electron probe microanalysis, and transmission electron microscopy. Plagioclase and glass in the interstices between fine grains of olivine and pyroxene indicate that the FGA's once partly melted. Compositional zoning and decomposition texture of pyroxenes are similar to those observed in chondrules, indicating a common cooling history of the FGA's and chondrules. Therefore, the mechanism that caused melting of the FGA's is considered to be the same as for chondrules. Bulk compositions of the FGA's are within the range of those of chondrules, so some chondrules probably were produced by complete melting of the same precursor materials as those of the FGA's. The precursor materials must have included fine olivine and other grains that probably are condensates.     

Reply to Edward Anders: A discussion of alternative models for explaining the distribution of moderately volatile elements in ordinary chondrites

The high observed abundances of Na and Cu in chondrules indicate that the amount of loss during chondrule formation was minor and possibly negligible, consistent with the view that loss was controlled by diffusion kinetics rather than equilibrium volatility, and that the surface of the chondrule quickly cooled to temperatures at which diffusional transport was negligible. Ordinary chondrite/CI abundance ratios appear to be randomly distributed in the range 0.9-0.1. Very few values are observed in the 0.36–0.70 range, but this is not statistically significant, nor is it predicted by the two-component (chondrule-matrix) model.If CI chondrite abundances are representative of mean solar-system material, the very low chondrule content in CM chondrites (<5% of high-temperature materials) indicates that the observed volatile distribution resulted from incomplete accretion of volatile carriers (perhaps a fine aerosol). At the ordinary chondrite formation location the fraction of an element sited in unaccreted carriers increased with decreasing condensation temperature. At the CM location a similar trend is observed for elements less volatile than S, but the unaccreted fraction of more volatile elements was nearly constant.     

Cooling history of pyroxene chondrules in the Yamato-74191 chondrite (L3)—an electron microscopic study

Fine textures of clinopyroxene in an excentroradial pyroxene chondrule (EPC) and a comb-like pyroxene chondrule (CPC) in the Yamato-74191 chondrite (L3) have been studied by analytical electron microscopy. Both pyroxenes consist of three regions different in composition and texture; core, mantle and marginal regions, though the pyroxenes of the CPC are more Fe-rich than those of the EPC. The core region is the most Mg-rich with no Ca component and commonly shows polysynthetic (100) twins. The mantle region is slightly calcic, and the marginal region shows a rapid increase of Ca outward.The polysynthetic twins, cracks and subgrain boundaries in the core in the EPC and CPC must have formed during the transition from proto-type to clino-type pyroxenes. The exsolution textures in the mantle and marginal regions indicate initial crystallization of pigeonite-C followed by decomposition into pigeonite-P and augite. The decomposition must have taken place by nucleation growth in the mantle region and by spinodal decomposition in the marginal region. The periodicity of 15–20 nm in the spinodal decomposition textures indicates that the cooling rate of the pyroxenes, when passing through about 1000°C, was of the order of a few tens to several degrees centigrade per hour. The cooling history of the chondrules has been explained by a monotonous cooling controlled by the cooling rate of the surrounding medium.     

Magnesium isotopes constraints on the origin of Mg-rich olivines from the Allende chondrite: Nebular versus planetary?

High precision Mg isotope measurements by multi-collector ion microprobe show that refractory olivines from the Allende chondrite, either olivines isolated in the matrix (2 samples studied) or olivines in type I chondrules (6 samples studied), have variable δ²⁶Mg* enrichments and deficits (calculated in permil as the ²⁶Mg deviation from the instrumental mass fractionation line) relative to the Earth. Most average δ²⁶Mg* (noted δ²⁶Mg*_av) values (between 10 and 20 analyses per chondrule) are negative but the total range is from ?0.029 (± 0.010) ‰ (2 sigma errors) to + 0.011 (± 0.011) ‰ with an exception of one olivine at + 0.043 (± 0.023) ‰. These variations in δ²⁶Mg*_av reflect the formation of the olivines from reservoirs enriched in various amounts of ²⁶Mg by the decay of short-lived ²⁶Al (T_1/2 = 0.73 Ma). Similarly, 30 analyses of olivines from the Eagle Station pallasite show a δ²⁶Mg*_av value of ?0.033 ± 0.008‰, as negative as some olivines from Allende chondrules and the Solar system initial δ²⁶Mg* value of ?0.038 ± 0.004‰ (defined at the time of formation of type B Ca–Al-rich inclusions – CAIs – when ²⁶Al/²⁷Al = 5.23 × 10^?5, Jacobsen et al., 2008).Because olivines are Al-poor and because their Mg isotopic compositions are not reset during the chondrule forming events, their δ²⁶Mg*_av can be used to calculate model crystallization ages relative to various theoretical Mg isotope growth curves. The two end-member scenarios considered are (i) a “nebular” growth in which the Al/Mg ratio remains chondritic and (ii) a “planetary” growth in which a significant increase of the Al/Mg ratio can be due to, for instance, olivine magmatic fractionation. The low δ²⁶Mg*_av value of olivines from the Eagle Station pallasite demonstrate that metal-silicate differentiation occurred as early as ~ 0. 15_- 0. 23^+ 0. 29 Ma after CAIs in either of the growth scenarios. Similarly the variable δ²⁶Mg*_av values of refractory olivines can be understood if they were formed in planetesimals which started to differentiate as early as the Eagle Station parent body. Accretion of these planetesimals must have been coeval to the formation of CAIs and their disruption could explain why their fragments (Mg-rich olivines) were distributed in the chondrule forming regions of the disk.