Variation of chemical composition in Australasian tektites from different localities in Vietnam

Abstract— One hundred and thirteen Australasian tektites from Vietnam (Hanoi, Vinh, Dalat, and Saigon areas) were analyzed for their major and trace element contents. The tektites are either of splash form or Muong Nong‐type. The splash‐form tektites have SiO₂ contents ranging from 69.7 to 76.8 wt%, whereas Muong Nong‐type tektites, which are considerably larger than splash‐form tektites and have a blocky and chunky appearance, have slightly higher silica contents in the range of 74–81 wt%. Major‐element relationships, such as FeO versus major oxides, Na₂O versus K₂O, and oxide ratio plots, were used to distinguish the different groups of the tektites. In addition, correlation coefficients have been calculated for each tektite group of this study. Many chemical similarities are noted between Hanoi and Vinh tektites from the north of Vietnam, except that the Hanoi tektites contain higher contents of CaO than Vinh; the higher content of CaO might be due to some carbonate parent material. Both Dalat and Saigon tektites have nearly similar composition, whereas the bulk chemistries of the tektites from Hanoi and Vinh appear different from those of Saigon and Dalat. There are differences, especially in the lower CaO and Na₂O and higher MgO, FeO, for the tektites of Dalat and Saigon in comparison to that of Hanoi tektites. Furthermore, the Dalat and Saigon tektites show enrichments by factors of 3 and 2 for the Ni and Cr contents, respectively, compared to those of Hanoi and Vinh. The difference in chemistry between the North Vietnam tektites (Hanoi, Vinh) to that of South Vietnam tektites (Saigon, Dalat) of this study indicate that the parent material was heterogeneous and possibly mixing between different source rocks took place. Muong Nong‐type tektites are enriched in the volatile elements such as Br, Zn, As, and Sb compared to the average splash‐form tektites of this study. The chemical compositions of the average splash‐form and Muong Nong‐type tektites of this study closely resemble published data for average splash‐form and Muong Nong‐type indochinites, indicating that they have the same source. The trace element ratios Ba/Rb (2.7), Th/U (5.2), Th/Sc (1.3), Th/Sm (2.2), and the rare earth element (REE) abundances of this study show close similarities to those of average upper continental crust.     

Isotopic signatures of black tektites from the K-T boundary on Haiti: Implications for the age and type of source material

Abstract— U-Th-Pb, Rb-Sr, and Sm-Nd isotopic signatures of corroded, but unaltered, black glassy tektites from Cretaceous-Tertiary (K-T) boundary rock on Haiti are not consistent with their derivation from an impact on MOR-derived oceanic crust or continental regions involving middle Proterozoic or older crustal material. Two single-grain and two batches of these tektites yielded present-day ?_Nd = ?3.0 to ?3.4, ?_Sr = +55 to 56, ²⁰⁶Pb/²⁰⁴Pb = 18.97; ²⁰⁷Pb/²⁰⁴Pb = 15.74; ²⁰⁸Pb/²⁰⁴Pb = 38.91 values, and Pb, Rb, Sr, Sm, and Nd concentrations of ～6, ～45, ～535, ～4.7, and ～22 ppm, respectively. Initial ?_Nd and ?_Sr values for the tektites are different from time-integrated Nd-Sr isotopic signatures for almost all oceanic crustal types. Age-corrected Pb isotopic values are similar to those for pelagic sediments with distinctly higher ²⁰⁷Pb/²⁰⁴Pb values compared to MORB. However, these results do not exclude the possibility of an oceanic impact site, if the tektites were derived from fine-grained sediments that typically overlie such regions, although other mineralogic and chemical evidence from K-T boundary debris suggests otherwise. Moreover, the Nd average crustal residence age of ～ 1080 Ma (T_DM) for the black tektites eliminates impact sites on continental crustal regions involving middle Proterozoic or older rocks, or sedimentary rocks largely derived from them. Previously reported major and trace element data from the black tektites suggest that the source material was possibly sedimentary with a composition similar to average shale or graywacke. If this is the case, then the Nd isotopic data suggest that the source rocks were not older than Silurian (T_CHUR = 400 Ma) in age, and were composed largely of young (< 1080 Ma) crustal material. Of the suspected K-T boundary impact sites, both the Manson (Iowa) and Chicxulub (Yucatan) structures occur in suitable lithologies to yield the Haitian black tektites, although neither structure has as yet proven to be the tektite source.     

Trace element study of high- and low-refractive index Muong Nong-type tektites from Indochina

Abstract— Previous work indicates that Muong Nong-type tektites from Indochina with low refractive indices and high silica contents contain relict mineral grains while those with high refractive indices and low silica contents do not. Instrumental Neutron Activation Analysis (INAA) was used to determine selected trace element concentrations for four Muong Nong-type tektites with high refractive indices and no relict mineral inclusions and one with low refractive index and relict inclusions, to determine if there are any systematic differences in trace element compositions between the two groups. The data also were compared with published trace element data for sixteen Muong Nong-type tektites which have low refractive indices and, therefore, should contain relict inclusions. Except for Ta which had lower concentrations in the high refractive index group, there is no consistent difference in trace element compositions between the two groups. We interpret these results to indicate a single, slightly heterogeneous source for the Muong Nong-type tektites, rather than different source regions.     

Combined noble gas and trace element measurements on individual stratospheric interplanetary dust particles

Abstract— The trace element compositions and noble gas contents of 32 individual interplanetary dust particles (IDPs) collected in the Earth's stratosphere were measured. Trace element compositions are generally similar to CI meteorites, with occasional depletions in Zn/Fe with respect to CI. Noble gases were detected in all but one of the IDPs. Noble gas elemental compositions are consistent with the presence of fractionated solar wind. A rough correlation between surface‐normalized He abundances and Zn/Fe ratios is observed; Zn‐poor particles generally have lower He contents than the other IDPs. This suggests that both elements were lost by frictional heating during atmospheric entry and confirms the view that Zn can serve as an entry‐heating indicator in IDPs.     

Chemical variation within fragments of Australasian tektites

Abstract— In previous studies, intersample variation between compositions of different tektites from one particular group were studied and, in a few cases, major element variations within single tektites. No data for intra‐sample trace element variations existed. Thus, we sectioned a Muong Nong‐type tektite fragment from Vietnam and a splash‐form tektite fragment from the Philippines into eleven and six pieces, respectively, and analyzed the individual fragments for major and trace element contents. The compositions obtained agree well with those found in previous studies, supporting argument that tektites have been derived from terrestrial upper crustal sediments. Chemical variations within the tektite fragments are present, but do not show any systematic trends, probably reflecting incomplete mixing of parent rocks. The intra‐sample heterogeneity of the Muong Nong‐type tektite is more pronounced than that in the philippinite. For the Muong Nong‐type tektite, the intra‐sample variation in the trace element contents is higher than that for the major elements, again reflecting target rock properties. For the philippinite the intra‐sample variations mostly do not exceed the limits imposed by the precision of the analytical data, confirming that the splash form tektites are indeed well homogenized.     

Major and trace element compositions of georgiaites: Clues to the source of North American tektites

Abstract— Electron microprobe and laser ablation, inductively‐coupled plasma mass spectrometer analyses of 24 georgiaites show that these tektites are all Si‐rich (79–83 wt% SiO₂) glasses with variable major and trace element abundances (e.g., FeO varies from 2.1 to 3.7 wt%). Glass compositions are similar to but not identical with average upper continental crust. For example, georgiaites are light rare earth element enriched with small negative Eu anomalies (Eu/Eu*=0.73‐0.86) and La‐Th‐Sc systematics are intermediate between that of Archean and post‐Archean continental crust. When the georgiaite data are placed in the context of data for all North American tektites, triangular arrays appear on some oxide‐oxide plots (e.g., FeO‐MgO). Large variations in refractory element abundances and ratios compared to the variation in SiO₂ favors mixing over volatilization as a cause of the compositional variation. If all the tektites formed as a result of a single impact, then triangular arrays in oxide‐oxide variation diagrams require at least three source components. These components include a Si‐rich material, probably a quartz‐rich sand that was predominant in the formation of georgiaites. Two relatively silica‐poor and Fe‐rich components have compositional characteristics similar to shales and greywackes. The La‐Th‐Sc systematics of the georgiaites and most other North American tektites are distinctive and could potentially be used to link the tektites to Eocene sediments at the Chesapeake Bay impact structure.     

Upper Eocene tektite and impact ejecta layer on the continental slope off New Jersey

Abstract— During Leg 150 of the Ocean Drilling Project (ODP), two sites (903C and 904A) were cored that have sediments of the same biostratigraphic age as the upper Eocene tektite-bearing ejecta layer at Deep Sea Drilling Project (DSDP) Site 612. Core 45X from ODP Site 904A (～4 km north of Site 612) contains a 5 cm thick tektite-bearing ejecta layer, and Core 56 from Site 903C (～8 km north-northwest of Site 904) contains a 2 cm thick layer of impact ejecta without any tektite or impact glass. Shocked quartz and feldspar grains, with multiple sets of planar deformation features (PDFs), and abundant coesite-bearing grains are present at both sites. The major oxide contents, trace element compositions, and rare earth element (REE) patterns of the Site 904 tektites are similar to those of the Site 612 tektites and to North American tektites (especially bediasites). The ?_Sr and ?_Nd values for one composite tektite sample from Site 904 fall within the range previously obtained for the Site 612 tektites, which defines a linear trend that, if extrapolated, would intersect the values obtained for North American tektites. The water contents of eight tektite fragments from Site 904 range from 0.017 to 0.098 wt%, and, thus, are somewhat higher than is typical for tektites. The heavy mineral assemblages of the 63–125 μm size fractions from the ejecta layers at Sites 612, 903, and 904 are all similar. Therefore, we conclude that the ejecta layer at all three sites is from the same impact event and that the tektites at Sites 904 and 612 belong to the North American tektite strewn field. Clinopyroxene-bearing (cpx) spherules occur below, or in the lower part of, the main ejecta layer at all three sites. At all three sites, the cpx spherules have been partly or completely replaced with pyrite that preserved the original crystalline textures. Site 612, 903, and 904 cpx spherules are similar to those found in the Caribbean Sea, Gulf of Mexico, central equatorial Pacific, western equatorial Pacific, and eastern Indian Ocean. The cpx event appears to have preceded the North American tektite event by 10–15 ka or less. The fining-upward sequence at all three sites and concentration of the denser, unmelted impact ejecta at the top of the tektite layer at Sites 612 and 904 suggest that the tektite-bearing ejecta layers are not the result of downslope redeposition and that the unmelted ejecta landed after the glass. Geographic variations in thickness of the tektite-bearing ejecta layer, the lack of carbonate clasts in the ejecta layer, and the low CaO content of the tektite glass suggest that the ejecta (including the tektite glass) were derived from the Chesapeake Bay structure rather than from the Toms Canyon structure. A sharp decline in microfossil abundances suggests that local environmental changes caused by the impact may have had adverse effects on benthic foraminifera, radiolaria, sponges, and fish as well as the planktic foraminifera.     

Triple oxygen isotope composition of Australasian tektites

Major and trace element analyses and triple oxygen isotope measurements were performed on 11 individual specimens of Australasian tektites (AAT) with exactly known field positions from Laos. The sample set was dominated by Muong Nong‐type tektites (MNAAT), including separated layers of glass of different appearance and chemistry from four samples. This first larger set of oxygen isotope data of MNAAT revealed the δ¹⁸O range 8.7 ≤ δ¹⁸O ≤ 11.6‰ on VSMOW2 scale (12 analyses), only slightly wider than the previously reported range for splash‐form AAT. The Δ’¹⁷O values of MNAAT (?0.098 ≤ Δ’¹⁷O ≤ ?0.069‰; 12 analyses) and splash‐form AAT (?0.080 ≤ Δ’¹⁷O ≤ ?0.068‰; three analyses) are all in the range of data typical for terrestrial crustal rocks, with no mass‐independent oxygen isotope fractionation (from impactor or from exchange with atmospheric O₂) being observed.     

Water in tektites and impact glasses by fourier-transformed infrared spectrometry

Abstract— To improve the scarce data base of H₂O content in tektites and impact glasses, we analyzed 26 tektites from all four strewn fields and 25 impact glass samples for their H₂O content. We used the fourier-transformed infrared (FTIR) spectrometry method, which permits measurement of areas of ～40 μm in diameter. Our results show that the tektites have H₂O contents ranging from 0.002 to 0.030 wt% (average 0.014 ± 0.008 wt%). Ivory Coast tektites have the lowest H₂O abundances (0.002–0.003 wt%), and Muong Nong-type indochinites and some North American tektites having the highest contents (up to ～0.03 wt%). Impact glass samples (from the Zhamanshin, Aouelloul, and Rio Cuarto craters) yielded H₂O contents of 0.008 to 0.13 wt% H₂O. Typical impact glasses from the Aouelloul and Zhamanshin craters have low H₂O contents (0.008 to 0.063 wt%). Libyan Desert Glasses and Rio Cuarto glasses have higher H₂O contents (～0.11 wt%). We also analyzed glasses of unknown origin (e.g., urengoites; glass fragments from Tikal), which showed very low H₂O contents, in agreement with an origin by impact. Our data confirm that all tektites found on land have very low H₂O contents (<0.03 wt% H₂O), while impact glasses have slightly higher H₂O contents. Both glass types are very dry compared to volcanic glasses. This study confirms that the low H₂O contents (<0.05 wt%) of such glasses can be considered good evidence for an origin by impact.     

Bosumtwi impact structure,Ghana: Geochemistry of impactites and target rocks,and search for a meteoritic component

Abstract— Major and trace element data, including platinum group element abundances, of representative impactites and target rocks from the crater rim and environs of the Bosumtwi impact structure, Ghana, have been investigated for the possible presence of a meteoritic component in impact‐related rocks. A comparison of chemical data for Bosumtwi target rocks and impactites with those for Ivory Coast tektites and microtektites supports the interpretation that the Bosumtwi structure and Ivory Coast tektites formed during the same impact event. High siderophile element contents (compared to average upper crustal abundances) were determined for target rocks as well as for impactites. Chondrite‐normalized (and iron meteorite‐normalized) abundances for target rocks and impactites are similar. They do not, however, allow the unambiguous detection of the presence, or identification of the type, of a meteoritic component in the impactites. The indigenous siderophile element contents are high and possibly related to regional gold mineralization, although mineralized samples from the general region show somewhat different platinum‐group element abundance patterns compared to the rocks at Bosumtwi. The present data underline the necessity of extensive target rock analyses at Bosumtwi, and at impact structures in general, before making any conclusions regarding the presence of a meteoritic component in impactites.     

Nd and Sr isotopic evidence for the origin of tektite material from DSDP site 612 off the New Jersey coast

Abstract— Late Eocene tektite material from DSDP site 612 is composed of angular to spherical tektites and microtektites containing abundant vesicles and a few unmelted to partially melted mineral inclusions. The major element compositions of the 612-tektites are generally comparable to those of North American tektites, but the physical features suggest that the DSDP-612 tektites were formed by less severe shock melting. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd compositions of 612-tektites: a) show much wider ranges than the tightly constrained group of North American tektites and microtektites, and b) are significantly different from those of other groups of tektites. The existence of large isotopic variations in tektites from DSDP site 612 requires that they were formed from a chemically and isotopically heterogeneous material in a regime that is distinctive from that of other groups of tektites. T^ND_CHUR and T^Sr_UR model ages of the 612-tektites indicate that they were formed from a crustal source of late Precambrian mean age (800–1000 Ma) which in middle Palaeozoic time (?400 Ma) was further enriched in Rb/Sr during sedimentary processes. These source characteristics suggest that the impact which produced the 612-tektites occurred in rocks of the Appalachian orogeny or sediments derived from this orogenic belt. Potential source materials for both 612-tektites and North American tektites are present on the eastern and southeastern part of the North American continent and its adjacent shelf. The distinct isotopic differences between 612-tektites and North American tektites indicate that the two groups of tektites were either formed by the impact of more than one bolide in the same general area, or by a single impact event that sampled different layers.     

Potassium isotopic composition of Australasian tektites

Abstract— We have analyzed the potassium isotopic composition of four tektites from the Australasian strewn field, spanning a wide diversity of thermal histories, inferred from textures and volatile element contents. Our results indicate no isotopic differences between tektites and terrestrial crustal rocks, placing stringent limits of ≤2% loss of potassium during the brief duration of high temperature heating experienced by these samples. This confirms that the chemical composition of tektites is entirely a reflection of source rock composition and has not been modified by the tektiteforming process for elements less volatile than potassium. Losses of more volatile components, e.g., the halogens and water, are not precluded by the present data. Coupling a radiative cooling temperature‐time path with potassium vapor pressure data indicates that tektite melt drops are not likely to develop bulk elemental fractionation during the brief heating episodes of tektites for peak temperatures <2273 K. The extent of K isotopic fractionation is independent of droplet size but dependent on peak heating temperature. The exact peak temperature depends on the choice of vapor pressure data used for K, which need to be better constrained.     

The Cuban Tektite Revisited

Abstract— A tektite, probably found in Cuba, was previously classified as belonging to the North American tektite strewn field on the basis of chemistry, age, isotopic, and petrographic characteristics. New major element analyses and trace element analyses show that the sample falls within the range of other North American tektites, and is close to the bediasite compositions. There are, however, some differences to normal georgiaites and bediasites. In a Na₂O/K₂O diagram the sample plots between the two distinct fields formed by georgiaites and bediasites. The rare earth elements and some lithophile trace elements are slightly enriched compared to bediasites, and much higher than in georgiaites. The discovery of tektite fragments from locations at Barbados and a DSDP site off the coast of New Jersey makes it likely that the North American strewn field is larger than previously thought, in agreement with microtektite distributions. Thus it is possible that the “Cuban” tektite really originated from Cuba.     

ON MOBILE ELEMENT TRANSPORT IN HEATED ABEE

Seven trace elements (Ag, Co, Cs, Ga, In, Te, Tl) are either completely retained or are lost to the same extent in Abee samples heated at 700 °C for one week at 10^?5-10^?3 atm Ne or in 10^?5 atm H₂. Bi and Se are lost significantly more easily and Zn is better retained in samples heated in Ne than in H₂. Zn retention varies inversely with ambient Ne pressure. Mobile element transport seems unaffected by physical interactions in the gas phase but may reflect solid-state surface effects. During week-long heating at low pressures (initially ～ 10^?5 atm H₂) S is mobilized only at 1000 °C while C contents decrease progressively from 600–1000 °C. Apparent activation energies for C are 60 kcal/mole below 700 °C and 16 kcal/mole above this temperature suggesting diffusive loss from different hosts and/or processes over different temperature intervals. In E4–6 chondrites C and S contents largely reflect nebular fractionation and condensation processes.     

Noble gases in Muong Nong‐type tektites and their implications

Abstract— We have the elemental abundances and isotopic compositions of noble gases in Muong Nong‐type tektites from the Australasian strewn field by crushing and by total fusion of the samples. We found that the abundances of the heavy noble gases are significantly enriched in Muong Nong‐type tektites compared to those in normal splash‐form tektites from the same strewn field. Neon enrichments were also observed in the Muong Nong‐type tektites, but the Ne/Ar ratios were lower than those in splash‐form tektites because of the higher Ar contents in the former. The absolute concentrations of the heavy noble gases in Muong Nong‐type tektites are similar to those in impact glasses. The isotopic ratios of the noble gases in Muong Nong‐type tektites are mostly identical to those in air, except for the presence of radiogenic ⁴⁰Ar. The obtained K‐Ar ages for Muong Nong‐type tektites were about 0.7 Myr, similar to ages of other Australasian tektites. The crushing experiments suggest that the noble gases in the Muong Nong‐type tektites reside mostly in vesicles, although Xe was largely affected by adsorbed atmosphere after crushing. We used the partial pressure of the heavy noble gases in vesicles to estimate the barometric pressure in the vesicles of the Muong Nong‐type tektites. Likely, Muong Nong‐type tektites solidified at the altitude (between the surface and a maximum height of 8–30 km) lower than that for splash‐form tektites.     

Effects of impacts on the atmospheric evolution: Comparison between Mars, Earth, and Venus

Classified as a terrestrial planet, Venus, Mars, and Earth are similar in several aspects such as bulk composition and density. Their atmospheres on the other hand have significant differences. Venus has the densest atmosphere, composed of CO₂ mainly, with atmospheric pressure at the planet's surface 92 times that of the Earth, while Mars has the thinnest atmosphere, composed also essentially of CO₂, with only several millibars of atmospheric surface pressure. In the past, both Mars and Venus could have possessed Earth-like climate permitting the presence of surface liquid water reservoirs. Impacts by asteroids and comets could have played a significant role in the evolution of the early atmospheres of the Earth, Mars, and Venus, not only by causing atmospheric erosion but also by delivering material and volatiles to the planets. Here we investigate the atmospheric loss and the delivery of volatiles for the three terrestrial planets using a parameterized model that takes into account the impact simulation results and the flux of impactors given in the literature. We show that the dimensions of the planets, the initial atmospheric surface pressures and the volatiles contents of the impactors are of high importance for the impact delivery and erosion, and that they might be responsible for the differences in the atmospheric evolution of Mars, Earth and Venus.     

Moldavites from Austria

Abstract— Several moldavites have been discovered in the northern part of Lower Austria. Tektites from two new locations (Altenburg and Radessen) have been analyzed. These new finds lend credibility to old reports about tektites from Lower Austria, some of which are associated with artefacts of prehistoric cultures. The new locations are situated between the Bohemian and Moravian parts of the moldavite strewn field, which is thus shown to extend further south than previously known. Most of the samples show clear indications of surface alterations by water and/or humic substances, and one sample shows signs of fluviatile transport. The geological setting of the moldavite-bearing sediments is similar to the Czechoslovakian occurrences but is probably less disturbed. Chemically the samples show considerable variations even within one location. No unambiguous association with either the Bohemian or the Moravian group is evident either for the major or trace element abundances.     

Experimental constraints on the volatility of germanium,zinc, and lithium in Martian basalts and the role of degassing in alteration of surface minerals

The surface of Mars is enriched in Cl and S which is linked to volcanic activity and degassing. Similarly, elevated Ge and Zn levels in Gale crater sedimentary bedrock indicate a magmatic source for these elements. To constrain the relative effects of Cl and S on the outgassing of these trace metals and chemical characteristics of primary magmatic vapor deposits incorporated to Martian surface, we conducted a set of degassing and fumarolic alteration experiments. Ge is found to be more volatile than Zn in all experiments. In S-bearing runs, the loss of Ge and Zn was less than any other experiments. In Cl-only runs, degassing of Zn was more than twice that of Ge within the first 10 min and percent loss increased for both elements with increasing time. In Cl + S runs, S-induced reduction of GeO₂ and ZnO to metallic Ge and Zn switches the preference of chloride formation from Zn to Ge. Up to 90% of Ge and Zn loss in the 1-h no volatile-added (NVA) experiments might be due to the small amounts of Cl contamination in NVA mixes via other oxides used for synthesis. Alteration experiments show different phases between 1-h and 24-/72-h runs. In 1-h runs, anhydrite and langbeinite dominate while in 24-/72-h runs halite and sylvite dominate the condensate assemblages. S-bearing phases form as the intermediate products of fumarolic deposition, while chlorides are common when the system is allowed to cool gradually. One-hour exposure was sufficient to form alteration phases and vapor deposits such as NaCl, KCl, CaSO₄, and langbeinites on the Martian analog minerals. These salts were identified in Martian meteorites and in situ measurements. Our results provide evidence that volcanic degassing along with fumarolic alteration could be a potential source for the enrichment and varying abundances of Cl, S, Fe, Zn, Ge in Martian surface, as well as a cause for Ge depletion in shergottites.     

Krypton and xenon fractionation in North American tektites

Abstract— Elemental and isotopic compositions of the noble gases have been determined in six North American tektites (4 bediasites and 2 georgiaites) and one Ivory Coast tektite. Radiogenically produced ⁴He may explain the large ⁴He/³⁶Ar ratios measured relative to air, despite significant diffusive losses. The Ne isotopic composition is enriched in ²⁰Ne consistent with a single stage mass fractionation process. The enormous ²⁰Ne/³⁶Ar enrichments observed in all tektite samples, similar to those reported from other tektites and impact glasses, are attributed to atmospheric diffusion into the samples following solidification. The North American tektites show a systematic increase in ⁸⁴Kr/³⁶Ar and ¹³²Xe/³⁶Ar relative to air, with enrichments greater than those determined for any other tektite group or terrestrial samples other than shales. These enrichments are inconsistent with existing models of dissolving Kr and Xe in tektite glass without elemental fractionation at atmospheric pressures equivalent to ∼40 km altitude. The Kr and Xe isotopic compositions are indistinguishable from atmospheric within experimental uncertainty.     

Volatile element chemistry during metamorphism of ordinary chondritic material and some of its implications for the composition of asteroids

We used chemical equilibrium calculations to model thermal metamorphism of ordinary chondritic material as a function of temperature, pressure, and trace element abundance and use our results to discuss volatile mobilization during thermal metamorphism of ordinary chondrite parent bodies. We compiled trace element abundances in H-, L-, and LL-chondrites for the elements Ag, As, Au, Bi, Br, Cd, Cs, Cu, Ga, Ge, I, In, Pb, Rb, Sb, Se, Sn, Te, Tl, and Zn, and identified abundance trends as a function of petrographic type within each class. We calculated volatility sequences for the trace elements in ordinary chondritic material, which differ significantly from the solar nebula volatility sequence. Our results are consistent with open-system thermal metamorphism. Abundance patterns of Ag and Zn remain difficult to explain.