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CHROMIUM ISOTOPE SYSTEMATICS OF ACHONDRITES: CHRONOLOGY AND ISOTOPIC HETEROGENEITY OF THE INNER SOLAR SYSTEM BODIES

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Published 2010 August 6 © 2010. The American Astronomical Society. All rights reserved.
, , Citation Akane Yamakawa et al 2010 ApJ 720 150 DOI 10.1088/0004-637X/720/1/150

0004-637X/720/1/150

ABSTRACT

The standard planetary formation models assume that primitive materials, such as carbonaceous chondrites, are the precursor materials of evolved planetesimals. Past chronological studies have revealed that planetesimals of several hundred kilometers in size, such as the Howardite–Eucrite–Diogenite (HED) parent body (Vesta) and angrite parent body, began their differentiation as early as ∼3 million years of the solar system formation, and continued for at least several million years. However, the timescale of planetesimal formation in distinct regions of the inner solar system, as well as the isotopic characteristics of the reservoirs from which they evolved, remains unclear. Here we present the first report for the precise 53Mn–53Cr ages of monomict ureilites. Chemically separated phases from one monomict ureilite (NWA 766) yielded the Mn–Cr age of 4564.60 ± 0.67 Ma, identical within error to the oldest age preserved in other achondrites, such as angrites and eucrites. The 54Cr isotopic data for this and seven additional bulk ureilites show homogeneous ε54Cr of ∼−0.9, a value distinct from other achondrites and chondrites. Using the ε54Cr signatures of Earth, Mars, and Vesta (HED), we noticed a linear decrease in the ε54Cr value with the heliocentric distance in the inner region of the solar system. If this trend can be extrapolated into the outer asteroid belt, the ε54Cr signatures of monomict ureilites will place the position of the ureilite parent body at ∼2.8 AU. These observations imply that the differentiation of achondrite parent bodies began nearly simultaneously at ∼4565 Ma in different regions of the inner solar system. The distinct ε54Cr value between ureilite and carbonaceous chondrite also implies that a genetic link commonly proposed between the two is unlikely.

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1. INTRODUCTION

The timescale for the formation of meteorite parent bodies and their spatial distributions within the inner solar system are important physical parameters that need to be addressed in order to understand the mechanism of the solar system evolution. Extensive work has been carried out to constrain the timescale of achondrite formation, and has revealed that melting/differentiation of some achondrite parent bodies began within 3 million years of the origin of the solar system (e.g., Lugmair & Shukolyukov 1998). However, high-precision chronological information of other achondrites such as ureilite is still poorly constrained. Since ureilite is the second most abundant achondrite that uniquely preserves both primitive and igneous signatures (e.g., Goodrich 1992; Mittlefehldt et al. 1998), unraveling the age of its parent body, as well as the chemical characteristics of its precursor, may provide important constraints on the dynamics of planetary formation and isotopic structure of the solar system. Precise age determination of ureilites using conventional chronometers, however, is often hampered by their depletion in incompatible lithophile elements, such as U, Th, Rb, and REE, commonly used for radiometric dating. For this reason, extinct chronometers such as the Al–Mg and Mn–Cr chronometers were applied to plagioclase-bearing polymict ureilites, plausible missing basalts complementary to monomict ureilites. The obtained Al–Mg and Mn–Cr ages were nearly identical, ∼4562 Ma, when translated to an absolute timescale (Goodrich et al. 2002; Kita et al. 2003, 2007). However, polymict ureilites are characterized by clasts of different origins (e.g., Jaques & Fitzerald 1982), so the correlation line on the ε53Cr versus 55Mn/52Cr evolution diagram might be a mixing line with no chronological implication. For this reason, it is critical to extract high-resolution time information from monomict ureilites instead of polymict ureilites. In this study, we have applied the 53Mn–53Cr chronometer (half-life (t1/2): 3.7 ± 0.4 Ma (Honda & Imamura 1971)) to eight monomict ureilites (Table 1). The main obstacle in the Mn–Cr age determination of monomict ureilite lies in its limited spread in the Mn/Cr ratio of its main constituent mineral phases, which, in turn, leads to limited variation in the 53Cr/52Cr ratio. In order to overcome this problem, a high-precision Cr isotopic measurement technique recently developed by Yamakawa et al. (2009) was applied to the analyses of monomict ureilites.

Table 1. 55Mn/52Cr Ratios and ε54Cr Ratios in Ureilites

Sample Description Mn (ppm) Cr (ppm) Fe (%) 55Mn/52Cr ε53Cr ε54Cr
NWA 766 LE 1       3.32 0.30 ± 0.06 −0.94 ± 0.13
  LE 2       1.41 0.32 ± 0.04 −0.85 ± 0.08
  LE 3       1.37 0.29 ± 0.04 −0.85 ± 0.09
  LE 4       1.19 0.31 ± 0.03 −0.87 ± 0.06
  LE 5       0.496 0.06 ± 0.05 −0.94 ± 0.07
  LE 6       0.172 0.04 ± 0.05 −0.96 ± 0.07
  Cr-rich Spinel       0.011 −0.05 ± 0.04 −1.00 ± 0.09
  Silicates       0.915 0.22 ± 0.03 −0.89 ± 0.08
  WR 3032 4993 16.1 0.686 0.17 ± 0.05 −0.92 ± 0.08
NWA 1241 LE 1       1.51 0.16 ± 0.07 −0.90 ± 0.20
  LE 2       0.699 0.13 ± 0.08 −0.95 ± 0.15
  LE 3       0.327 0.06 ± 0.06 −0.92 ± 0.07
  LE 4       0.367 0.13 ± 0.05 −0.92 ± 0.08
  LE 5       0.992 0.11 ± 0.05 −0.85 ± 0.08
  LE 6       0.235 0.11 ± 0.03 −1.02 ± 0.09
  WR 2151 4922 13.6 0.494 0.09 ± 0.04 −0.98 ± 0.08
El Gouanem WR 2150 3765 12.4 0.645 0.17 ± 0.06 −0.93 ± 0.09
Dhofar 132 WR 2897 4792 10.7 0.683 0.09 ± 0.04 −0.97 ± 0.09
Dhofar 836 WR 2179 3375 12.3 0.729 0.19 ± 0.06 −0.89 ± 0.07
NWA 2376 WR 2413 3658 14.1 0.745 0.16 ± 0.04 −0.84 ± 0.07
DaG 340 WR 2868 5237 13.4 0.619 0.12 ± 0.04 −0.98 ± 0.10
DaG 868 WR 2832 4324 14.6 0.740 0.18 ± 0.04 −0.88 ± 0.10
            Mean −0.92 ± 0.02

Notes. The Cr isotopic composition is expressed in ε-units, where εiCr = [(iCr/52Cr)sample/(iCr/52Cr)terrestrial standard −1] × 104. The error for 55Mn/52Cr is better than 2%. WR and LE stand for whole rock and leachate, respectively.

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2. SAMPLES AND EXPERIMENTS

The whole rock powders for eight monomict ureilites (NWA766, NWA1241, El Gouanem, Dhofar 132, Dhofar 836, NWA 2376, DaG 340, and DaG 868) were dissolved in Teflon bomb using HF and HNO3. Along with the whole-rock analyses, we have performed stepwise dissolutions for two of these samples (NWA766 and NWA1241) to obtain data from phases with various Mn/Cr ratios (cf. Rotaru et al. 1992). The first two steps of the leaching experiment (LE 1 and LE 2; 30 minutes using 0.5M-acetic acid and 0.2M-HNO3, respectively) were designed to dissolve materials in the vein such as carbonate. In the third step, the Fe metal in the reduction rim (i.e., Fe metal on the rims of olivine grains where they are in contact with the vein) was attacked using 1M-HCl (LE 3; 1 hr dissolution). More acid-resistant phases, such as olivine and pyroxene, were subsequently dissolved using 6M-HCl (LE 4; 48 hr), and a mixture of concentrated HNO3 and HF (LE 5; 24 hr), respectively. All procedures (LE 1 to LE 5) were carried out using ultrasonic bath under room temperature. Finally, a small amount of the remaining silicates and refractory phases were completely dissolved under high temperature/pressure in Teflon bomb using a mixture of concentrated HNO3 and HF (190°C, >60 hr). For NWA 766, a unique monomict ureilite known to contain Cr-rich spinel (Sikirdji & Warren 2001), an additional experiment was performed, where everything except the refractory phase was dissolved using concentrated HF–HNO3 mixture (labeled "silicates" in Table 1) and the remaining refractory phase (labeled "Cr-rich spinel") was dissolved in a Teflon bomb. The Cr isotope and Mn/Cr ratios were measured using the Thermo-Finnigan TRITON TI thermal-ionization mass spectrometer and Thermo-Electron Neptune MC-ICP-MS, respectively, at the Pheasant Memorial Laboratory, Institute for Study of the Earth's Interior, Okayama University. Details of the Cr isotope analyses are described in Yamakawa et al. (2009). Procedure for the Mn/Cr ratio measurements is given in Makishima et al. (2010).

3. RESULTS AND DISCUSSIONS

3.1. Age of the Ureilite Parent Body (UPB)

All absolute ages reported here are calculated relative to the angritic achondrite D'Orbigny, which has a Pb–Pb age of 4564.42 ± 0.12 Ma (Amelin 2008), and an initial 53Mn/55Mn ratio of (3.24 ± 0.04) × 10−6 (Glavin et al. 2004). If we calculate the absolute age using the LEW 86010 angrite instead of D'Orbigny, the ages will be ∼0.8 Ma younger (Table 2). All data from NWA 766, excluding the first leachate (LE 1), define a linear correlation on an isochron plot (Figure 1(a)). However, since the materials in the reduction rim and vein are likely a product of a later process that occurred in the ureilite parent body (UPB; Walker & Grove 1993), the calculation for the age was made by eliminating the data points from LE 1 to LE 3. While the NWA 766 silicates and whole rock contain materials from the reduction rim and vein, their influence on the Cr isotope is small, as estimated from mass balance, and thus they were included in the calculation of the isochron (See Table 3). The slope of the obtained isochron translates to an absolute age of 4564.60 ± 0.67 Ma (Figure 1(b)), which we consider the best estimate for the differentiation age of NWA 766. The data for the whole rock samples are also scattered along the isochron (Figure 1(c)), suggesting that ureilites are derived from an isotopically uniform reservoir. The NWA 1241, on the other hand, exhibits a uniform ε53Cr value of ∼+0.12. This implies that both the differentiation and the reduction of NWA 1241 took place close to or after the extinction of 53Mn. The regression through all the data points shows a nearly flat slope with a corresponding age of <4561 Ma (Figure 1(b)). These age constraints indicate that the UPB forming process started by 4564.60 ± 0.67 Ma and continued for at least 3.6 Ma. It is important to note that the age of NWA 766 is similar to the age of oldest eucrite and whole rock angrites using the same age anchor (4565.57 ± 0.39 Ma for eucrite Asuka 881394 (Wadhwa et al. 2005) and 4564.68 ± 0.26 Ma for whole rock angrites (Shukolyukov & Lugmair 2007); Table 2). This indicates that the differentiation of achondrite asteroids of several hundred kilometers in size began at about the same time of ∼4565 Ma in the inner solar system.

Figure 1.

Figure 1. 53Mn–53Cr isochron for the whole rock samples, and the leachates and residues of NWA 766 (solid circles) and NWA 1241 (open squares). (a) All data points obtained from whole rock measurements, and acid leaching experiments. (b) An enlargement figure of the squared area in Figure 1(a). Sample names are labeled for NWA 766 (bold) and NWA 1241 (squared italic). Data of LE 1–3 are removed from the calculation of Mn–Cr age of NWA 766 (see the text for details). Absolute ages reported here are calculated relative to D'Orbigny, which has a Pb–Pb age of 4564.42 ± 0.12 Ma (Amelin 2008), and an initial 53Mn/55Mn ratio of (3.24 ± 0.04) × 10−6 (Glavin et al. 2004). NWA 766: (53Mn/55Mn) = (3.35 ± 0.41) × 10−6 and ε53Cr (i) = −0.05 ± 0.03. NWA 1241: (53Mn/55Mn) = (3.5 ± 5.5) × 10−7 and ε53Cr (i) = 0.09 ± 0.03. (c) Whole rock Mn–Cr isotopic data. Shown together as a reference is the isochron for NWA 766.

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Table 2. 53Mn–53Cr Ages of Two Monomict Ureilites NWA766 and NWA 1241 Compared with the Ages of Oldest Eucrite and Angrite

Meteorite Sample 53Mn/55Mn (×10−6) D'Orbigny Age (Ma) LEW 86010 Age (Ma)
Ueilites NWA 766 without LE1 to LE3 3.35 ± 0.41 4564.60 ± 0.67 4563.81 ± 0.90
  NWA 1241 0.35 ± 0.55 <4561 <4560
Eucrites Asuka 881394 4.02 ± 0.26 (Ref. 1) 4565.57 ± 0.39 4564.79 ± 0.78
Angrites Whole rock angrite 3.40 ± 0.14 (Ref. 2) 4564.68 ± 0.26 4563.89 ± 0.66

References. (1) Wadhwa et al. 2005; (2) Shukolyukov & Lugmair 2007.

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Table 3. Proportion of Mn and Cr Leached During Each Leaching Step

Step NWA 766 NWA 1241
  Mn(%) Cr(%) Mn(%) Cr(%)
LE 1 2 <1 2 <1
LE 2 5 3 1 <1
LE 3 6 3 5 8
LE 4 68 41 36 46
LE 5 9 13 44 21
LE 6 10 40 12 24

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3.2. 54Cr Isotopic Heterogeneities Preserved in the Inner Solar System Materials

The additional advantage of investigating the Cr isotopic signature of meteorites is the presence of distinct 54Cr isotopic signature in various meteorite classes. Since each meteoritic group possesses its own ε54Cr value (Shukolyukov & Lugmair 2006a; Trinquier et al. 2007; Qin et al. 2010), our data may provide an insight into a genetic relationship between ureilites and other meteoritic groups. The obtained ε54Cr values from the whole rock samples and the leachates and residues of NWA 766 and NWA 1241 all possess identical ε54Cr with a mean value of −0.92 ± 0.02 (Table 1), the lowest deficit found for meteoritic samples (cf. Shukolyukov & Lugmair 2006b; Ueda et al. 2006). Previous studies have proposed a genetic link between ureilites and carbonaceous chondrites based on petrography, oxygen isotopes, planetary-type noble gases within carbon and metal with high abundances of siderophile trace elements (e.g., Goodrich 1992; Mittlefehldt et al. 1998). It has been suggested that ureilites may be a cumulate crystallized from a melt derived from the partial melting of a chondritic source, or a residue after such a partial melting event(s). However, our ε54Cr isotopic data are distinct from those of bulk carbonaceous chondrites (Shukolyukov & Lugmair 2006a; Trinquier et al. 2007; Yin et al. 2009). Although the bulk carbonaceous chondrites are characterized by positive ε54Cr values, they are mixtures of phases with both positive and negative ε54Cr values when investigated in mineralogical scale (Rotaru et al. 1992; Trinquier et al. 2007, 2008). Therefore, it may be possible to produce melt with ε54Cr of −0.9 by preferentially melting phases with negative ε54Cr (low temperature phases such as carbonates, sulfides, sulfates, and metals, plus some silicates), leaving high ε54Cr phases (silicates and refractory phases such as spinel) as a residue. Using the data of Rotaru et al. (1992) and Trinquier et al. (2008), simple mass balance calculation will imply an equilibration of Cr, which resides in all the low temperature phases, plus 45%–100% of silicate (and in some cases, additional contribution from the equilibration of refractory phases is also required) to produce melt with ε54Cr of −0.9 if the ureilite precursor material was a CI-CM-CV chondrite-like material. However, such a high degree of processing will likely eliminate the oxygen isotope heterogeneity of the precursor material but this is not the case for ureilites (Clayton & Mayeda 1988). The residue after such a melting event, on the other hand, will be characterized by ε54Cr value greater than that of the initial carbonaceous chondrite. This is at odds with the Cr isotopic signature of ureilites. Therefore, our data suggest that a genetic link between the carbonaceous chondrite and ureilite is unlikely.

When the ε54Cr isotope data from the Earth, Mars, and Vesta (HED parent body) are used as anchors, we noted that the ε54Cr value of the inner solar system bodies decreases linearly with heliocentric distance in the terrestrial planet region (Figure 2(a)). If this linear trend extends outward into the exterior of the asteroid belt, the ε54Cr isotopic signature of ureilites will place the location of UPB at around 2.8 AU. This is consistent with the findings of Jenniskens et al. (2009), who suggested that the F-type asteroids, located in the region between 2.5 and 3.5 AU (Gradie & Tedesco 1982), are possible candidates of the UPB. If we accept the location of the UPB to be around 2.8 AU, a very similar linear trend is observed for 50Ti (Figure 2(b)), an isotope that is produced in Type 1a supernovae along with 54Cr and 48Ca (Clayton 2003; Hartman et al. 1985). Because Cr and Ti with negative ε54Cr and ε50Ti values do not always reside in the same mineral phase within the primitive meteorites (Trinquier et al. 2008, 2009), the observed 54Cr and 50Ti correlation with heliocentric distance is unlikely to be explained by preferential addition or removal of selected mineral phases into or from the chondritic precursor prior to the accumulation of these parent bodies. Rather, it is more likely to represent the heterogeneous distribution of these isotopes in the region of the inner solar system where these parent bodies evolved. Since the mixing timescale of injected nuclides is believed to be very short, ranging from 1000 years up to 1 million years (Ouellette et al. 2009), the presence of 54Cr–50Ti heterogeneity in the inner solar system hints toward the possible injection of isotopes from Type 1a supernovae shortly before the accumulation of inner solar system materials (i.e., 103–106 years before the formation of the inner solar system bodies).

Figure 2.

Figure 2. 54Cr and 50Ti anomalies in the inner solar system materials vs. their heliocentric distance. (a) ε54Cr data for the shergottite, nakhlite, and chassigny (SNC) and Howardites, Eucrites, and Diogenites (HED) are from Trinquier et al. (2007) and (b) ε50Ti data are from Trinquier et al. (2009). Bars on the data points represent the range of data reported in the literatures.

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The Cr isotopic signature of carbonaceous chondrites that have reflective spectra similar to C-type asteroids located in the outer region of the asteroid belt beyond ∼2.7 AU (Pang et al. 1978), on the other hand, clearly deviates from this linear trend. The reason for this is not clear at this stage, and may imply that the linear decrease in the ε54Cr (as well as ε50Ti) value is valid only for differentiated bodies. However, recent numerical calculation has demonstrated that a migration of primordial trans-Neptunian objects into the outer asteroid belt was plausible as a result of dynamical evolution of the giant-planet orbit (Levison et al. 2009). If this is the case, the current position of the carbonaceous chondrite parent body (C-type and possibly some D/P-type asteroids) may not represent the location of their original formation. This issue clearly deserves further investigation.

4. CONCLUSIONS

In summary, the high-precision Cr isotopic signatures of ureilites and other achondrites indicate that the initiation of achondrite parent body differentiation in different regions of the inner solar system began nearly simultaneously at around 2–3 Ma after the CAI formation (Jacobsen et al. 2008) and continued for at least several million years. The precursor materials of these parent bodies may have been contaminated in neutron-rich isotopes such as 54Cr and 50Ti from Type 1a supernovae just before their accumulation, as shown by their heterogeneous ε54Cr and ε50Ti values. However, the injection of 54Cr was decoupled from the incorporation of other Cr isotopes into the solar system on a scale of the meteorite parent body, as inferred from nucleosynthetic models (Clayton 2003), as well as the generally homogeneous nature of 53Cr in the early solar system as opposed to the heterogeneous distribution of 54Cr on the planetary scale (Trinquier et al. 2007, 2008). Furthermore, distinct 54Cr (as well as 50Ti) isotopic signatures between most differentiated meteorites and chondrites indicate that chondrites as we see today may not be the only building blocks of the inner solar system materials. A missing reservoir or primitive precursor(s) with negative ε54Cr and ε50Ti is necessary to explain the low isotopic signatures of achondrites. A comprehensive study of Cr–Ti isotopic analysis, possibly combined with leaching experiment, for both primitive and differentiated meteorites may help us further explore this issue.

We thank Drs. Seiji Maruyama, Naotaka Tomioka, and the members of the Pheasant Memorial Laboratory for fruitful discussion and laboratory support. Comments from Dr. Q.Z. Yin (U.C. Davis) have significantly improved the quality of the manuscript. Appreciation is also extended to Dr. Noboru Nakamura, Dr. Noriko Kita, Kaori Sakuragi, Midori Yajima, Yasuko Nagata, and Tetsuhiko Ueda for their support during the early stage of this work, and to the reviewer for constructive comments. This research was supported by Grants-in-aid from Japan Society for the Promotion of Science (JSPS), and the program of the "Center of Excellence for the 21th Century in Japan" from the Ministry of Education, Culture, Sports, Science and Technology (MEXT).

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10.1088/0004-637X/720/1/150