At 8:30 P.M. local time in Renazzo, Italy, a bright light was seen and three detonations heard by residents as several stones fell. Three individual stones were recovered having a combined weight of 10 kg, the largest weighing ~5 kg. Renazzo is a brecciated meteorite with a shock stage ranging from S1 to S3. This meteorite is a preserved fall with a unique volatile element and N-isotopic composition that distinguishes it from the other carbonaceous chondrite groups. It serves as the type specimen of the Renazzo-type chondrites, which are considered to be among the least thermally altered of the known meteorite groups.
While Renazzo ranks among the most primitive meteorites under study, new Cr2O3 abundance data obtained by Schrader et al. (2015) indicates that EET 96259 might represent the least thermally altered, most pristine sample of the CR parent body presently known (subtype 3.00; see diagram below). Other pristine CR chondrites with very low thermal alteration include MIL 090657 (2.7, based on bulk isotopic composition, presolar grain abundance, and Cr content of ferroan olivine; Davidson et al., 2015), QUE 99177 [2.8], MET 00426 [2.8], and LAP 02342 [2.8]. Details of a new petrographic-based aqueous alteration scale for CR chondrites proposed by Harju et al. (2015) are presented farther down the page.
Diagram adapted from Schrader et al. (and references therein), MAPS, vol. 50, #1, p. 37 (2015)
'The formation and alteration of the Renazzo-like carbonaceous chondrites III: Toward understanding the genesis of ferromagnesian chondrules'
The matrix component in Renazzo, which includes igneous fragments, isolated mineral grains, CAIs, AOAs, dark inclusions, and metal grains, accounts for ~3540 vol% of the bulk composition (Bayron et al., 2014). The abundance of chondrules and chondrule fragments in Renazzo is ~5060 vol%. Multilayered, FeO-poor (type-I) chondrules (mostly porphyritic attesting to partially melting) constitute the vast majority of the chondrules, with the remainder consisting of sulfide-rich, FeO-rich (type-II) chondrules and chondrule fragments. Rare relict type-I grains (and/or compositionally similar precursor material) have been identified within some type-II chondrules (Schrader et al., 2015). Al-rich chondrules have also been identified in minor abundances. The chondrules, metal, and matrix formed under variable conditions from a common nebula reservoir. This is attested by the complimentary chemical composition of these components, as well as by the enrichment and depletion in metal and silicate (respectively) of the same presolar s-process carrier phase (observed as a correlation in nucleosynthetic Mo and W isotope anomalies) (Budde et al., 2018). All of these components ultimately agglomerated in the outer solar system (beyond Jupiter) at approximately the same heliocentric distance as the CI chondrites.
Based on the initial 26Al/27Al ratios calculated for chondrules from unequilibrated ordinary chondrites and CO3.0 chondrites, they are considered to have formed 12 m.y. after CV CAIs (age = ~4.567 b.y.). By contrast, the lower initial 26Al/27Al ratios inferred for chondrules in CR chondrites are consistent with a relatively late formation of ~2.5 m.y. after CAIs (Scott et al., 2007; Nagashima et al., 2008). A similar age of 2.5 (±0.9) m.y. after CAIs was determined by Amelin et al. (2002) utilizing the PbPb dating method, which was translated by Connelly et al. (2012) to 3.66 (±0.63) m.y. after CAIs by employing a corrected 238U/235U ratio. The PbPb chronometer was also applied to the CR chondrite NWA 6043, and it revealed a wide range of agesfrom the oldest known chondrule at 4.5673 (±0.0010) b.y., to chondrules as much as 3.64 m.y. younger (Bollard et al., 2014). They reasoned that the latest formation of chondrules 4.56366 (±0.00091) b.y. ago establishes a benchmark for the time of dissipation of the solar accretion disk. In a comprehensive study of CR chondrules by Schrader et al. (2016) that included AlMg systematics, they recognized three distinct populations of chondrules dated at 2.2 (+0.1/0.2), 2.9 (+0.2/0.2), and 4.4 (+0.7/0.4) m.y. after CV CAIs; the latter oldest age represents the largest population in the study. They concluded that accretion of the CR parent body continued for at least ~4.0 m.y. after formation of the earliest solids in the solar nebula as represented by CAIs in CV chondrites. Moreover, their study indicates that 26Al was uniformly distributed in the CR chondrite formation region. From a weighted mean of 21 CR chondrules, Schrader et al. (2017) obtained a preferred AlMg age of 3.75 (±0.24) m.y. after CAIs. A high-precision HfW isotopic analysis of Renazzo and three other CR chondrites was conducted by Budde et al. (2018) in order to constrain the timing of chondrule formation, accretion, and metalsilicate segregation for the CR parent body. They determined a HfW age of 3.6 (±0.6) m.y., which is in agreement with that determined by the PbPb and AlMg chronometers. In addition, they ascertained a weighted mean age based on all three chronometers of 3.73 (±0.21) m.y. after CAIs.
Utilizing MnCr systematics, Trinquier et al. (2008) calculated an equilibrium age for CR2 chondrites of between 1.1 and 6.2 m.y. after CAIs. Because the CR chondrules were accreted into the developing parent body after most of the radiogenic 26Al had decayed, the degree of thermal metamorphism was limited. Among other petrographic features, the high abundance of Cr2O3 that remains in the metal phase attests to this low degree of thermal metamorphism (Wasson and Rubin, 2010; Schrader et al., 2015 [see diagram above]). Jilly-Rehak et al. (2016) conducted new 53Mn53Cr analyses of secondary carbonatescalcite in the matrices of Renazzo and GRO 95577 and of dolomite in a Renazzo dark inclusion. They determined aqueous alteration ages anchored to the D'Orbigny angrite of 4.5634 (+0.0028/0.0074) b.y. for Renazzo calcite, and 4.5554 (+0.0014/0.0021) b.y. for GRO 95577 calcite; these ages correspond to 4.6 (+7.4/2.8) m.y. and 12.6 (+2.1/1.4) m.y. after CV CAIs (4.56794 [±0.00031] b.y.; Bouvier et al., 2011), respectively. The prolonged period of aqueous alteration revealed by this study indicates that impact shock was necessarily a significant heating mechanism on the CR parent body following the cessation of radiogenic heating from 26Al decay.
A basic scenario for the early petrogenesis of Renazzo has been described. Initially, Ti-bearing perovskite condensates facilitated the condensation of forsterite. Lower temperatures and more highly reducing conditions prevailed as small low-Ni, FeNi-metal grains and fine-grained pyroxene dust combined to form aggregates. Thereafter, these precursor coarse-grained aggregates were melted by a solar heat pulse and then cooled from peak temperatures at rates of 0.996.7 K/hour. These conditions are more consistent with nebula shock wave-induced heating rather than through lightning or the x-wind (Chaumard et al., 2015). These melted aggregates ultimately coalesced to form the Ti-enriched, FeO-poor, porphyritic type-I chondrules composing Renazzo. Nebular-condensed C was dissolved in the metal and later exsolved in the newly formed chondrules (Kong et al., 1999). Contemporaneously, mineral assemblages comprising FeNi-metal, sulfides (pentlandite and pyrrhotite), and phosphate were formed in the aftermath of high-temperature gassolid sulfidation processes in the solar nebula (Schrader et al., 2008, 2015).
Igneous rims composed of silica-rich pyroxene are present on most CR type-I chondrules (although not evident in Renazzo or Al Rais due to their higher degree of aqueous alteration). These rims are presumed to have formed by direct condensation of silica onto chondrule surfaces from a cooling, fractionated nebular gas (Krot et al., 2003, 2004). FeNi-metal occurs along the rims of a significant portion (~40%) of type-I chondrules in CR chondrites, and also occurs both in chondrule interiors and as isolated grains in interchondrule matrix material. The amoeboid-shaped metal grains on chondrule rims were once considered to have formed by migration of FeNi-metal grains from chondrule interiors through centrifugal forces associated with rapid spinning of these chondrules (Grossman and Wasson, 1985; Kong and Palme, 1999); however, the distribution of the metal bears more resemblence to a discontinuous shell than a ring. Noting the minor effects centrifugal forces may have, it was argued by Wasson and Rubin (2009) that under high temperature conditions, with the molten metal having lower surface tension with respect to the vacuum of space than to the molten silicates, metal was induced to form along the outer surface. Upon cooling, the interface tension became more influential than the surface tension, causing the metal to take the form of small globules. The formation of metal in CR chondrites was examined in-depth by Jacquet et al. (2013, 2014), who assessed the likelihood of the four competing theories: 1) direct condensation from the nebula, 2) silicate reduction processes, 3) evaporation/recondensation, and 4) desulfurization of FeS. A brief synopsis of their scenario is presented below (∗). A fifth mechanism has been proposed by Chaumard et al. (2014) to describe the formation of an isolated, igneously-zoned, mm-sized matrix metal grain in Renazzofractional crystallization of a molten droplet with subsequent recondensation of volatile siderophile elements on the exterior margin which diffused inwards during cooling.
Utilizing 3-D microtomographic imaging of Renazzo chondrules, Ebel et al. (2009) and Ebel and Downen (2011) discovered that some chondrules exhibit multiple discrete, concentric, metallic layers alternating with silicate layers, suggesting sequential accretion of independent metal and silicate components. These represent sequential generations of chondrule formation attributable to multiple local heating events within the same unique nebular source region. These accretionary periods were followed by intervals of rapid annealing, which occurred in a cooling disk environment under reducing conditions. During this period, impacts produced a petrofabric in the form of chondrule flattening in this matrix-rich (31 vol%) meteorite, resulting in a chondrule axial ratio of ~1.3 (Kallemeyn et al., 1994).
The finer-grained matrix material was also formed in this same Ti-depleted nebular region, but only after substantial cooling had occurred. During this time, abundant water ices that had accreted along with the matrix material promoted the formation of phyllosilicates. All of these various components constituting the CR parent body agglomerated in a geological instant, at a time ~2.5 m.y. after CAI formation. It was demonstrated that if the bulk chemical compositions of both the highly variable population of Renazzo chondrules and the matrix materials are calculated together, they preserve the solar elemental abundance ratios. This complementarity indicates that the accretion process of CR chondrites probably occurred as a closed system within a unique chondritic region of the protoplanetary disk (Ebel et al., 2009).
The much rarer FeO-rich (type-II) chondrules present in CR chondrites lack accretionary rims, exhibit mostly broken surfaces, and some contain relict grains with Fa values and O-isotopic ratios indicative of recycling from an earlier generation of type-I chondrules (Connolly et al., 2003, 2008). They exhibit a wide range of bulk FeO and O-isotopic compositions and have a heavier O-isotopic signature than that of type-I chondrules. It is considered that the gas may have evolved from reducing to highly oxidizing during the interval between type-I and type-II chondrule formation. In addition, the O-isotopic signature evolved from 16O-rich to 16O-poor; this enrichment of heavy oxygen isotopes was due to the evaporation of water ice, which also created a more highly oxidizing environment (Connolly and Huss, 2010). The O-isotopic composition of type-II chondrules overlaps that of ordinary chondrites, suggesting a complex formation history in an oxidizing and sulfidizing environment. After an episode of fragmentation, which was possibly associated with the accretion of the CR parent body, the type-II chondrules were subjected to impact heating and aqueous alteration from previously accreted water ices. Consistent with its content of magnetite, Renazzo reflects a greater degree of aqueous alteration than many CR group members. Aside from its brecciated structure, the extent of aqueous alteration is responsible for a porosity that ranges from 3.7% to 18.2% (Macke et al., 2011).
Results of trace-element studies have identified primitive glass inclusions within olivines that sample the liquidvapor barrier that lead to olivine formation. These inclusion glasses formed contemporaneously with the host olivine in a dust- and oxygen-enriched region of the condensing nebula. These primary glass inclusions are found to be either Al-rich and derived from unfractionated nebular condensates, Al-poor and derived through fractionation and removal of refractory components from the nebula vapor, or Na-rich and derived from Al-rich parental glass after a metasomatic (solidvapor) exchange of Ca for Na in the nebula (Varela et al., 2001). Presolar grains containing anomalous Xe isotopes (Xe-HL) have been identified in Renazzo. Rare presolar silicate grains representing ~18 ppm, plus rare presolar silicon carbide grains representing ~55 ppm, have been identified in fine-grained accretionary chondrule rims (Leitner et al., 2012).
Refractory inclusions in Renazzo are small (generally <1 mm and most <0.5 mm) and scarce, just as in other CR chondrites. They include pristine 16O-rich CAIs that were formed over a period of ~100,000 to 400,000 years in a similar nebular reservoir as those in CV chondrites (Makide et al., 2009). CAIs constitute <1 vol% of CR chondrites and have primarily melilite-rich compositions, while others are grossite- or hibonite-rich, or more rarely, anorthite-rich. Fine-grained aggregates of nebular gas-solid condensation, known as amoeboid olivine aggregates (AOAs), are minor constituents in Renazzo. These AOAs preserve some of the most primitive relicts of early nebular condensation similar to those present in CAIs, including refractory minerals such as perovskite and spinel, and Mn-rich forsterite; primary FeNi-metal blebs also occur in some (Weisberg et al., 2008). Evidence indicates that AOAs formed during a period intermediate between the final stages of Wark-Lovering rim formation on type-A CAIs and the onset of chondrule formation. The occurrence of CAIchondrule compound objects attests to subsequent remelting of some CAIs with chondrules in an evolved, 16O-depleted solar nebula. Both AOAs and CAIs have similar 26Mg excesses derived from initial 26Al values, and they share an 16O-rich composition likely derived from the same nebular gas reservoir (Weisberg et al., 2004; 2007). Following their formation, AOAs did not experience further equilibration with the cooling nebular vapor.
The small component of Al-rich (>10 wt% Al2O3) chondrules are thought to have formed by melting of spinelanorthitepyroxene CAI precursor material that was mixed with type-I precursor material (Krot et al., 2006). In contrast to the 16O-poor type-I and -II ferromagnesian chondrules, a significant percentage of Al-rich chondrules exhibit O-isotopic heterogeneity due to inclusion of 16O-rich relict CAI material, and to isotopic exchange processes with an evolving nebular gas.
The CR group contains unusually high abundances of FeNi-metal in the form of taenite and kamacite (59 vol%), and the metal-bearing sulfides pyrrhotite and pentlandite (14 vol%) contribute to this high metal content. FeNi-metal occurs in Renazzo in chondrule interiors, on chondrule rims, and as separate finer grains in the matrix. It has been suggested (Connolly et al., 2001; Zanda et al., 2002) that during the heating event(s) in which chondrules were forming, FeO and other volatiles present in the precursor condensates were evaporated and then recondensed onto the chondrule rims, later diffusing inward. The chondrules that were melted to the highest degree, corresponding to those with the most circular shapes, developed the highest abundance of metal grains on their rims. Because of the evaporation and migration of Fe to the rim metalthe most stable arrangement (factoring in properties such as surface tension and temperature)and then its incomplete rediffusion back into the interior metal, the metal in the chondrule interiors became enriched in Ni, P, and other siderophile components. Trace element data and NiCo correlations support this scenario, although they indicate that certain components of chondrule metal, especially the core grains, did originate through direct, high temperature nebular condensation processes (Schönbeck and Palme, 2003; Ebel et al., 2009). The subsequent introduction of the chondrules to an oxidizing environment may also be responsible for the removal of Fe from the core.
In contrast to the argument of Wood (1963) and others for a direct condensation model, Wasson and Rubin (2010) proposed that a nebular fractional crystallization process, occurring at ~1750K and proceeded by a slow cooling rate, was responsible for producing the observed Ni gradients (core to rim decrease) and granoblastic textures of chondrules. They found that this nebular process, rather than either reduction of FeO or evaporation/recondensation, was more consistent with creating the positive correlation between Co and Ni in surface metal, as well as the negative correlation between olivine Fa content and Ni. The subsequent evaporation of S from the surficial FeS component of the chondrule rim would then increase the interface tension, ultimately leading to surface energy forces influencing the formation of coarse metal globules rather than a potential homogeneous metal film.
Still, other components of CR metal are consistent with an origin through high-temperature silicate reduction and metalsilicate equilibrium processes, as evidenced through results of Fe-isotopic mass fractionation studies. Experimental results by Cohen et al. (2006) demonstrate that type-I chondrule metal is consistent with formation by such a reduction process, and constrains the associated chondrule formation time to ~1 hour. Based on the results of evaporation experiments in a low-pressure furnace, Cohen and Hewins (2004) advanced a model in which the FeNi-metal found in Renazzo and other chondrites was a product of desulfurization of sulfides through volatilation, possibly as FeS liquid was condensing from the solar nebula at high temperature (~1565°C) and high pressure (~1 atm); the heat for this process may have been generated by the passage of a shock wave. They also argued that the FeNi-metal inclusions present within olivine grains, commonly known as "dusty olivine", are best modeled as having been formed through the reduction of FeO in the presence of carbon (kerogen).
∗ In an effort to establish a definitive history of the FeNi-metal in CR chondrites, Jacquet et al. (2013) conducted trace element analyses of numerous metal grains from nine CR chondrites. These metal grains were present in three configurationsas chondrule "interior grains", as chondrule surface, rim, or "margin grains", and as chondrite matrix or "isolated grains". After examining the geochemical relationships among these different metal grains, a formation scenario for CR type-I chondrules was developed which is consistent with the totality of their findingssome aspects of their scenario are contrary to portions of previous propositions outlined above:
Precursor grains were produced under conditions of incomplete condensation, inheriting a depleted volatile element abundance, and began to aggregate into chondrules.
As small interior metal grains were heated and melted, they coalesced to form rounded grains.
An extended period (>1 day) of high temperatures resulted in equilibration between the interior metal grains and olivine, accompanied by evaporative loss of some Fe from those chondrules which were completely melted (leaving them Ni-enriched); an open-system redox processing is favored by the evidence.
Continued accretion and heating of fine-grained material onto these early-formed chondrules produced the igneous rims; this period reflects either a single prolonged accretional/heating event, or possibly involves multiple heating events.
As the cooling rate began to increase, a layer of pyroxene formed at the chondrule periphery, possibly by interaction with a Si-enriched gas, and these newly accreted margin grains coalesced and experienced a lower-degree of melting to form zoned amoeboid-shaped grains.
Continued accretion of some fine-grained material onto chondrules proceeded.
If a single localized heating episode was involved, whereas these stages occurred concurrently, then this may be indicative of these chondrules forming in a high-temperature region with a high dust density, followed by a sudden onset of cooling upon exiting this region; the temperature curve fitting this scenario is inferred to be inconsistent with that of the often cited shock wave model of chondrule formation.
Sketch of the formation scenario for CR type-I chondrules
Image credit: Jacquet et al., MAPS, vol. 48, #10, p. 1995 (2013)
'Trace element geochemistry of CR chondrite metal' (http://dx.doi.org/10.1111/maps.12212)
In their studies of primitive chondrites, Kimura et al. (2008) found that the FeNi-metal phases serve as one of the most sensitive indicators of the onset of thermal metamorphism. Their work reveals that primary martensite decomposes to fine-grained plessite during low degrees of metamorphism as observed in the LL chondrite Semarkona, but that this has not occurred in the more pristine ungrouped (probably CO-related; Simon and Grossman, 2015) carbonaceous chondrite Acfer 094. Furthermore, they found that metal in and around Semarkona chondrules does not show a solar ratio of Co/Ni like that in Acfer 094, and that low temperature aqueous alteration has occurred in Semarkona as well. In addition, Kimura et al. (2008) included the carbonaceous chondrites of groups CR, CH, CB, and CM as probable 3.00 subtype specimens, notwithstanding the fact that some are currently designated as subtype 2 due to aqueous alteration features. In light of this petrologic typing paradox, they proposed that a separate scale be adopted to describe aqueous alteration which is distinct from the scale currently used for thermal metamorphism.
A preliminary aqueous alteration scale analogous to that employed for CM chondrites has been constructed for CR chondrites by Harju et al. (2011, 2014, 2015). This scale has a range from petrologic type 2.0, which is equivalent to highly altered type 1, to petrologic type 3.0, representing virtually no alteration; it was found that ~70% of CR chondrites are type 2.8. As alteration increases petrologic changes occur:
chondrule igneous rim material (and later, mesostasis) is altered to phyllosilicates
FeNi-metal grains undergo conversion to magnetite, along with increasing abundances of oxide phases and Fe-carbonate
Δ17O values tend to increase from ~ 2.6 in type 2.8 to ~ 0.4 in type 2.0, likely due to exchange with 16O-poor fluids
abundances of amino acids and O-anomalous presolar grains tend to decrease
According to this scale, Renazzo has been designated petrologic subtype 2.4. Hydrothermal alteration phases are abundant in Renazzo, including serpentine, smectite, and certain chlorite group minerals, which suggest an alteration temperature no higher than ~50150°C; other CR chondrites have compositions more consistent with alteration temperatures as high as ~300°C. This isotopically heavy fluid (D-enrichment higher than that found in comets) has transformed the composition of certain CR samples to a greater degree than othersthe CR2.3 chondrite Al Rais represents an isotopically heavy endmember, while the CR2.8 QUE 99177 represents an isotopically light endmember. The variability of D-enrichment within samples has been attributed to parent body processes rather than to accretion of an ice mixture (Bonal et al., 2013). Studies by Abreu and Stanek (2012) demonstrate that the CR chondrites which experienced the highest degrees of aqueous alteration now have the lowest Fe and the highest S content, while those that experienced the highest shock stages accompanied by volatile loss now have the highest Fe and the lowest S contents. The water/rock ratio on the CR parent body was calculated to be as high as 1.157 (Schrader et al., 2010).
Abundant xenolithic dark clasts are present in CR chondrites (~8 vol%), but oxygen isotopic data indicate their precursor is different from the CR parent body; they were likely accreted by the CR parent body during its early formative stage. Oxygen isotopic compositions and mineralogical characteristics of these dark clasts show similarities to type 3 carbonaceous chondrites that were aqueously altered prior to their incorporation into the CR host. Important similarities exist between the CR group and the CI group, suggesting that they both formed in a similar nebular region, but with the CR chondrites undergoing reduction during metamorphism and hydrothermal alteration.
Interstellar-sourced organic compounds enriched in deuterium (D) and heavy nitrogen (15N) are present in Renazzo and other CR chondrites, which is considered to reflect accretion within the cold outer region of the protoplanetary disk (Budde et al., 2006 and references therein). These isotopes are associated with carbon (C) contents of between 1.2 and 2.7 wt%. These organic macromolecules are composed of mostly 14 ring (up to 15 rings have been identified) aromatic C compounds comprising both oxidized (hydrous alteration) and reduced (anhydrous alteration) species. Minimal aqueous processing in Renazzo and other CR carbonaceous chondrites is indicated by the low degree of hydroxylation of toluene to phenols, and by the failure to liberate 15N-rich organic species, as well as by the presence in the insoluble organic material of an inclusion with the largest known alkyl component (Cody and Alexander, 2005). In addition, the organic material maturity parameter, PAI 1, indicates only mild aqueous alteration was involved (Pearson et al., 2006). The low degree of sulfur-based thiophenes is indicative of a low degree of thermal metamorphism. In addition, through organic material maturity parameters (such as MNR), it is demonstrated that Renazzo has experienced the least thermal processing among the CR chondrite members.
Floss and Stadermann (2009) identified high abundances of both nanocrystalline and amorphous, O-anomalous, ferromagnesian presolar silicate grains in the mostly unaltered CR2.8 chondrites QUE 99177 and MET 00426 (hydrated to serpentine in the latter; Le Guillou et al., 2013). These presolar grains are thought to have originated in oxygen-rich, low-mass red giant and asymptotic giant branch (AGB) stars. The silicate/oxide ratios of these presolar grains are higher than those found in the most primitive meteorites analyzed (Acfer 094 and ALHA77307), and are similar to those found in interplanetary dust particles (IDPs); this attests to the pristine nature of these CR chondrites, and may indicate the actual protosolar cloud abundances of presolar silicate and oxide grains. These presolar grains also contain primitive C of interstellar origin and have a high amino acid content. It appears likely that the high degree of aqueous alteration experienced by other CR chondrites is the reason they lack similar presolar silicate grains. In the CR2.8 GRV 021710, an abundance of 174 (±30) ppm O-anomalous grains, 203 (±36) ppm C-anomalous grains, 165 (±29) ppm presolar silicate grains, 9 (±6) ppm presolar oxide grains, 135 (±35) ppm SiC grains, and 50 (±12) ppm carbonaceous grains were calculated to be present (Zhao et al., 2011).
It was discovered that some Antarctic CR chondrites contain the highest amino acid abundances measured in any meteorite group. These are extraterrestrial amino acids as evidenced by their enrichment of 13C, and they have C-isotope values similar to those present in CM2 chondrites, possibly indicating a common presolar precursor. It is thought that final synthesis of certain amino acids, such as the α-amino acids alanine, glycine, isovaline, and α-aminoisobutyric acid, took place on the parent asteroid through aqueous alteration of existing presolar carbonyl precursors (Martins et al., 2007). Renazzo has a relatively low abundance of amino acids, probably due to degradation through higher degrees of aqueous alteration.
Using Raman spectroscopy, researchers have demonstrated that the degree of structural order of the organic matter in Renazzo and other unequilibrated ordinary chondrites is correlated with their petrologic type (Quirico et al., 2003). They also found that the abundances of D and 15N were also correlated. From these data they determined that Renazzo contains the most pristine organic matter among all chondrites, and that LL3.01 Semarkona, which was identified as being slightly less primitive than Renazzo, is by far the most pristine among the ordinary chondrite groups. In addition, a study of FeNi-metal and sulfide composition and texture by Kimura et al. (2006) has revealed that the anomalous carbonaceous chondrite Acfer 094 experienced even less metamorphism than Semarkona, and is consistent with the lowest petrologic type assignment of 3.00.
One CR chondrite with a very high degree of hydration, GRO 95577, was classified by Weisberg and Huber (2007) as the first CR1 chondrite (CR2.0 after Harju et al., 2011). Although the chondrules have been completely replaced by phyllosilicate layers, magnetite, and various sulfides, their textural integrity has been preserved and they are still discernible as type-I. Similarly, all of the metal has been replaced by magnetite, and there is a prevalence of sulfides and carbonates where matrix and dark inclusions had previously been located. Alteration processes involving hydrothermal fluids probably occurred at temperatures of ~300°C.
Also of note is a meteorite previously classified as C3-ungrouped, Sah 00182, which shares many similarities with the CR chondrite group (Weisberg, 2001). In addition to having similar chondrule textures, most chondrules in both Sah 00182 and other CR members are Mg-rich type-I. Metal within chondrules has a similar Ni content (4.76.6 wt%) and Co/Ni ratio. Although Sah 00182 lacks hydrous phyllosilicates consistent with a petrologic grade of 3, it is nevertheless petrographically similar to the CR chondrites given their degree of aqueous alteration. However, the O-isotopic ratios of Sah 00182 plot within the field of the CV chondrites, and therefore Sah 00182 remains an ungrouped carbonaceous chondrite which has retained a pristine nebular signature within its components (chondrules, FeNi-metal, CAIs, AOAs), and it has experienced very little thermal metamorphism. In addition, a few meteorites have alteration histories that may be consistent with a CR3 classification, including Acfer 324 (Sipiera and Cole, 2004).
Although recognizing the existence of significant petrological differences among them, Weisberg et al. (1995) proposed to include the CB, CH, and CR chondrite groups within a clan hierarchy based on similarities in mineralogical, bulk chemical, and O- and N-isotopic characteristics. In a contrary opinion, Makide et al. (2009) argue that the CR chondrite group should not be included with the CB and CH groups because of its dissimilarities in chondrule texture, metal abundance, matrix abundance, CAI composition and isotopic systematics, and component history (pristine nebula vs. impact vapor plume).
The ungrouped C3 chondrite LEW 85332 is considered to be the closest match to the likely precursor material of the CR-clan with regard to its isotopic and chemical properties (Clayton and Mayeda, 1999). From comparisons made between the reflectance spectrum of asteroid 2 Pallas and that of the carbonaceous chondrite groups, it was shown that a close similarity exists to Renazzo. Compared to all other meteorite groups, both CR chondrites and IIC irons have significant δ183W excesses, have elevated δ15N, and share similar Mo isotope systematics, and therefore a genetic link is inferred (Kruijer et al. (2017; Budde et al., 2018).
The brecciated nature of Renazzo is also manifest as heterogeneity in its porosity, which ranges from 3.7% to 18.2% (Macke et al., 2011). The specimen of Renazzo pictured above is a 1.1 g partial end section with the fresh fusion-crusted side shown beneath.