Establishing the link between the Chesapeake Bay impact structure and the North American tektite strewn field: The Sr‐Nd isotopic evidence

Abstract— The Chesapeake Bay impact structure, which is about 35 Ma old, has previously been proposed as the possible source crater of the North American tektites (NAT). Here we report major and trace element data as well as the first Sr‐Nd isotope data for drill core and outcrop samples of target lithologies, crater fill breccias, and post‐impact sediments of the Chesapeake Bay impact structure. The unconsolidated sediments, Cretaceous to middle Eocene in age, have ?_Sr^{t = 35.7 Ma} of +54 to +272, and ?_Nd^{t = 35.7 Ma} ranging from ?6.5 to ?10.8; one sample from the granitic basement with a T^Nd_CHUR model age of 1.36 Ga yielded an ?_Sr^{t = 35.7 Ma} of +188 and an ?_Nd^{t = 35.7 Ma} of ?5.7. The Exmore breccia (crater fill) can be explained as a mix of the measured target sediments and the granite, plus an as‐yet undetermined component. The post‐impact sediments of the Chickahominy formation have slightly higher T^Nd_CHUR model ages of about 1.55 Ga, indicating a contribution of some older materials. Newly analyzed bediasites have the following isotope parameters: +104 to +119 (?_Sr^{t = 35.7 Ma}), ?5.7 (?_Nd^{t = 35.7 Ma}), 0.47 Ga (T^Sr_UR), and 1.15 Ga (T^Nd_CHUR), which is in excellent agreement with previously published data for samples of the NAT strewn field. Target rocks with highly radiogenic Sr isotopic composition, as required for explaining the isotopic characteristics of Deep Sea Drilling Project (DSDP) site 612 tektites, were not among the analyzed sample suite. Based on the new isotope data, we exclude any relation between the NA tektites and the Popigai impact crater, although they have identical ages within 2s? errors. The Chesapeake Bay structure, however, is now clearly constrained as the source crater for the North American tektites, although the present data set obviously does not include all target lithologies that have contributed to the composition of the tektites.     

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.     

Chicxulub impactites: Geochemical clues to the precursor rocks

Abstract— The 65 Ma Chicxulub impact structure, Mexico, with a diameter of ～180 km is the focus of geoscientific research because of its link to the mass extinction event at the Cretaceous‐Tertiary (K/T) boundary. Chicxulub, now buried beneath thick post‐impact sediments, is probably one of the best‐preserved terrestrial impact structures known. Because of its inaccessibility, only limited samples on the impact lithologies from a few drill cores are available. We report major element and Sr‐, Nd‐, O‐, and C‐isotopic data for Chicxulub impact‐melt lithologies and basement clasts in impact breccias of drill cores C‐1 and Y‐6, and for melt particles in the Chicxulub ejecta horizon at the K/T boundary in Beloc, Haiti. The melt lithologies with SiO₂ ranging from 58 to ～63 wt% show significant variations in the content of Al, Ca, and the alkalies. In the melt matrix samples, δ¹³C of the calcite is about ?3%o. The δ¹⁸O values for the siliceous melt matrices of Y‐6 samples range from 9.9 to 12.4%o. Melt lithologies and the black Haitian glass have rather uniform ⁸⁷Sr/⁸⁶Sr ratios (0.7079 to 0.7094); only one lithic fragment displays ⁸⁷Sr/⁸⁶Sr of 0.7141. The Sr model ages T^SrUR for most lithologies range from 830 to 1833 Ma; unrealistic negative model ages point to an open Rb‐Sr system with loss of Rb in a hydrothermal process. The ¹⁴³Nd/¹⁴⁴Nd ratios for all samples, except one basement clast with ¹⁴³Nd/¹⁴⁴Nd of 0.5121, cluster at 0.5123 to 0.5124. In an ?_Nd‐?_Sr diagram, impactites plot in a field delimited by ?_Nd of ?2 to ?6, and ?_Sr of 55 to 69. This field is not defined by the basement lithologies described to occur as lithic clasts in impact breccias and Cretaceous sediments. At least one additional intermediate to mafic precursor component is required to explain the data.     

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.     

Neodymium,strontium and chromium isotopic studies of the LEW86010 and Angra dos Reis meteorites and the chronology of the angrite parent body

Abstract— Neodymium, strontium, and chromium isotopic studies of the LEW86010 angrite established its absolute age and the formation interval between its crystallization and condensation of Allende CAIs from the solar nebula. Pyroxene and phosphate were found to contain ～98% of its Sm and Nd inventory. A conventional ¹⁴⁷Sm-¹⁴³Nd isochron yielded an age of 4.53 ± 0.04 Ga (2 σ) and ?¹⁴³ _Nd = 0.45 ± 1.1. An ¹⁴⁶Sm-¹⁴²Nd isochron gives initial ¹⁴⁶Sm/¹⁴⁴Sm = 0.0076 ± 0.0009 and ?¹⁴³ _Nd = ?2.5 ± 0.4. The Rb-Sr analyses give initial ⁸⁷Sr/⁸⁶Sr (I⁸⁷_Sr) = 0.698972 ± 8 and 0.698970 ± 18 for LEW and ADOR, respectively, relative to ⁸⁷Sr/⁸⁶Sr = 0.71025 for NBS987. The difference, ΔI⁸⁷_Sr, between I⁸⁷_Sr for the angrites and literature values for Allende CAIs, corresponds to ～9 Ma of growth in a solar nebula with a CI chondrite value of ⁸⁷Rb/⁸⁶Sr = 0.91, or ～5 Ma in a nebula with solar photospheric ⁸⁷Rb/⁸⁶Sr = 1.51. Excess ⁵³Cr from extinct ⁵³Mn (t1/2 = 3.7 Ma) in LEW86010 corresponds to initial ⁵³Mn/⁵⁵Mn = 1.44 ± 0.07 × 10^?6 and closure to Cr isotopic homogenization 18.2 ± 1.7 Ma after formation of Allende inclusions, assuming initial ⁵³Mn/⁵⁵Mn = 4.4 ± 1.0 × 10^?5 for the inclusions as previously reported by the Paris group (Birck and Allegre, 1988). The ¹⁴⁶Sm/¹⁴⁴Sm value found for LEW86010 corresponds to solar system initial (¹⁴⁶Sm/¹⁴⁴Sm)_o = 0.0080 ± 0.0009 for crystallization 8 Ma after Allende, the difference between Pb-Pb ages of angrites and Allende, or 0.0086 ± 0.0009 for crystallization 18 Ma after Allende, using the Mn-Cr formation interval. The isotopic data are discussed in the context of a model in which an undifferentiated “chondritic” parent body formed from the solar nebula ～2 Ma after Allende CAIs and subsequently underwent differentiation accompanied by loss of volatiles. Parent bodies with Rb/Sr similar to that of CI, CM, or CO chondrites could satisfy the Cr and Sr isotopic systematics. If the angrite parent body had Rb/Sr similar to that of CV meteorites, it would have to form slightly later, ～2.6 Ma after the CAIs, to satisfy the Sr and Cr isotopic systematics.     

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.     

Rb‐Sr and Sm‐Nd isotopic systematics of the lherzolitic shergottite GRV 99027

Abstract– Rb‐Sr and Sm‐Nd isotopic analyses of the lherzolitic shergottite Grove Mountains (GRV) 99027 are reported. GRV 99027 yields a Rb‐Sr mineral isochron age of 177 ± 5 (2σ) Ma and an initial ⁸⁷Sr/⁸⁶Sr ratio (I_Sr) of 0.710364 ± 11 (2σ). Due to larger uncertainties of the Sm‐Nd isotopic data, no Sm‐Nd isochron age was obtained for GRV 99027. The ε¹⁴³Nd value is estimated approximately +12.2, assuming an age of 177 Ma. The I_Sr of GRV 99027 is distinguishable from other lherzolitic shergottites, confirming our previous conclusion that it is not paired with them ( Lin et al. 2005 ). The new data of GRV 99027 support the same age of approximately 180 Ma for most lherzolitic shergottites, and fill the small gap of I_Sr between Allan Hills A77005 and Lewis Cliff 88516 ( Borg et al. 2002 ). All available data are consistent with a single igneous source for the intermediate subgroup of lherzolitic shergottites.     

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.     

Geochemistry of Darwin glass and target rocks from Darwin crater,Tasmania, Australia

Abstract— Darwin glass formed about 800,000 years ago in western Tasmania, Australia. Target rocks at Darwin crater are quartzites and slates (Siluro‐Devonian, Eldon Group). Analyses show 2 groups of glass, Average group 1 is composed of: SiO₂ (85%), Al₂O₃ (7.3%), TiO₂ (0.05%), FeO (2.2%), MgO (0.9%), and K₂O (1.8%). Group 2 has lower average SiO₂ (81.1%) and higher average Al₂O₃ (8.2%). Group 2 is enriched in FeO (+1.5%), MgO (+1.3%) and Ni, Co, and Cr. Average Ni (416 ppm), Co (31 ppm), and Cr (162 ppm) in group 2 are beyond the range of sedimentary rocks. Glass and target rocks have concordant REE patterns (La/Lu = 5.9–10; Eu/Eu* = 0.55–0.65) and overlapping trace element abundances. 87Sr/⁸⁶Sr ratios for the glasses (0.80778–0.81605) fall in the range (0.76481–1.1212) defined by the rock samples. ε‐Nd results range from –13.57 to –15.86. Nd model ages range from 1.2–1.9 Ga (CHUR) and the glasses (1.2–1.5 Ga) fall within the range defined by the target samples. The ⁸⁷Sr/⁸⁶Sr versus 8⁷Rb/⁸6Sr regression age (411 ± 42 Ma) and initial ratio (0.725 ± 0.016), and the initial ⁴³Nd/144Nd ratio (0.51153 ± 000011) and regression age (451 ± 140 Ma) indicate that the glasses have an inherited isotopic signal from the target rocks at Darwin crater. Mixing models using target rock compositions successfully model the glass for all elementsexcept FeO, MgO, Ni, Co, and Cr in group 2. Mixing models using terrestrial ultramafic rocks fail to match the glass compositions and these enrichments may be related to the projectile.     

Strontium and neodymium isotopic study of Libyan Desert Glass: Inherited Pan‐African age signatures and new evidence for target material

Abstract— Libyan Desert Glass (LDG) is an impact‐related, natural glass of still unknown target material. We have determined Rb‐Sr and Sm‐Nd isotopic ratios from seven LDG samples and five associated sandstones from the LDG strewn field in the Great Sand Sea, western Egypt. Planar deformation features were recently detected in quartz from these sandstones. ⁸⁷Sr/⁸⁶Sr ratios and ?‐Nd values for LDG range between 0.71219 and 0.71344, and between –16.6 and –17.8, respectively, and hence are distinct from the less radiogenic ⁸⁷Sr/⁸⁶Sr ratios of 0.70910–0.71053 and ?‐Nd values from –6.9 to –9.6 for the local sandstones from the LDG strewn field. Previously published isotopic ratios from the Libyan BP and Oasis crater sandstones are generally incompatible with our LDG values. LDG formation undoubtedly occurred at 29 Ma, but neither the Rb‐Sr nor the Sm‐Nd isotopic system were rehomogenised during the impact event, as we can deduce from Pan‐African ages of ?540 Ma determined from the regression lines from a total of 14 LDG samples from this work and the literature. Together with similar Sr and Nd isotopic values for LDG and granitoid rocks from northeast Africa west of the Nile, these findings point to a sandy matrix target material for the LDG derived from a Precambrian crystalline basement, ruling out the Cretaceous sandstones of the former “Nubian Group” as possible precursors for LDG.     

Partitioning of Rare Earth Elements Between Hibonite and Melt and Implications for Nebular Condensation of the Rare Earth Elements

Abstract— The partitioning of the rare earth elements (REE) between hibonite and silicate melt has been investigated at 1470 °C in the system calcium tschermak's molecule-diopside. Oxygen fugacity was varied between air and the iron-wustite buffer using conventional gas mixing, and to “infinitely reducing” using Sr²⁺ as a surrogate for Eu²⁺. The partition coefficient (D) pattern is light REE enriched with D(La) = 7.15 and D(Yb) = 0.1. D(Eu) varied from about 2 in air to about 0.55 in an “infinitely reducing” atmosphere. Experiments were reversed for Eu and, by implication, a close approach to equilibrium was achieved for other elements. Absolute activity coefficients for REE in hibonite were estimated, yielding γ_La = 330, γ_Eu3+ = 1200, and γ_Yb = 24 000. These results suggest that unless the principal phase(s) into which a trace element is dissolving and the activity—composition relationships for that trace element in that phase(s) are known, condensation temperatures based on assumed ideal solution behavior will generally be in error.     

Potassium isotope abundances in Australasian tektites and microtektites

Abstract— We report electron microprobe determinations of the elemental compositions of 11 Australasian layered tektites and 28 Australasian microtektites; and ion microprobe determinations of the ⁴¹K/³⁹K ratios of all 11 tektites and 13 of the microtektites. The elemental compositions agree well with literature values, although the average potassium concentrations measured here for microtektites, 1.1‐1.6 wt%, are lower than published average values, 1.9‐2.9 wt%. The potassium isotope abundances of the Australasian layered tektites vary little. The average value of ^δ41K, 0.02 ± 0.12%₀ (1 s? mean), is indistinguishable from the terrestrial value (= 0 by definition) as represented by our standard, thereby confirming four earlier tektite analyses of Humayun and Koeberl (2004). In agreement with those authors, we conclude that evaporation has significantly altered neither the isotopic nor the elemental composition of Australasian layered tektites for elements less volatile than potassium. Although the average ⁴¹K/³⁹K ratio of the microtektites, 1.1 ± 1.7%₀ (1 s? mean), is also statistically indistinguishable from the value for the standard, the individual ratios vary over a very large range, from ?10.6 ± 1.4%₀ to +13.8 ± 1.5%₀ and at least three of them are significantly different from zero. We interpret these larger variations in terms of the evaporation of isotopically light potassium; condensation of potassium in the vapor plume; partial or complete stirring and quenching of the melts; and the possible uptake of potassium from seawater. That the average ⁴¹K/³⁹K ratio of the microtektites equals the terrestrial value suggests that the microtektite‐forming system was compositionally closed with respect to potassium and less volatile elements. The possibility remains open that ⁴¹K/³⁹K ratios of microtektites vary systematically with location in the strewn field.     

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.     

Coeval argon‐40/argon‐39 ages of moldavites from the Bohemian and Lusatian strewn fields

Abstract— ⁴⁰Ar/³⁹Ar ages of four tektites (moldavites) from southern Bohemia (near ?eské Budějovice, Czech Republic) and a tektite from Lusatia (near Dresden, Germany) have been determined by 11 step‐degassing experiments. The purpose of the study was to enlarge the ⁴⁰Ar/³⁹Ar data base of moldavites and to check the age relations of the Bohemian and Lusatian samples. The mean plateau‐age of the Bohemian samples, which range from 14.42 to 14.70 Ma, is 14.50 ± 0.16 (0.42) (2σ) Ma (errors in parentheses include age error and uncertainty of standard monitor age). The plateau age of the Lusatian sample of 14.38 ± 0.26 (0.44) (2σ) Ma confirms the previously published ⁴⁰Ar/³⁹Ar age of 14.52 ± 0.08 (0.40) (2σ) Ma, and demonstrates that the fall of Lusatian and Bohemian tektites were contemporaneous. Because of their geochemistry and their ages there is no doubt that the Lusatian tektites are moldavites. Accepting that moldavites are ejecta from the Nördlinger Ries impact, the new ages also date the impact event. This age is slightly younger (about 0.2–0.3 Ma) than the age suggested by earlier K‐Ar determinations.     

Earliest high-Ti volcanism on the Moon: 40Ar-39Ar,Sm-Nd,and Rb-Sr isotopic studies of Group D basalts from the Apollo 11 landing site

Abstract High-Ti basalts from the Apollo collections span a range in age from 3.87 Ga to 3.55 Ga. The oldest of these are the common Apollo 11 Group B2 basalts which yield evidence of some of the earliest melting of the lunar mantle beneath Mare Tranquillitatis. Rare Group D high-Ti basalts from Mare Tranquillitatis have been studied in an attempt to confirm a postulated link with Group B2 basalts (Jerde et al., 1994). The initial Sr isotopic ratio of a known Group D basalt (0.69916 ± 3 at 3.85 Ga) lies at the lower end of the tight range for Group B2 basalts (⁸⁷Sr/⁸⁶Sr = 0.69920 to 0.69921). One known Group D basalt and a second postulated Group D basalt yield indistinguishable initial ?_Nd (1.2 ± 0.6 and 1.2 ± 0.3) and again lie at the lower end of the range for the Group B2 basalts from Apollo 11 (+2.0 ± 0.4 to +3.9 ± 0.6, at 3.85 Ga). A third sample has isotopic (⁸⁷Sr/⁸⁶Sr = 0.69932 ± 2; ?_Nd = 2.5 ± 0.4; at 3.59 Ga; as per Snyder et al., 1994b) and elemental characteristics similar to the Group A high-Ti basalts returned from the Apollo 11 landing site. Ages of ⁴⁰Ar-³⁹Ar have been determined for one known Group D basalt and a second postulated Group D basalt using step-heating with a continuous-wave laser. Suspected Group D basalt, 10002, 1006, yielded disturbed age spectra on two separate runs, which was probably due to ³⁹Ar recoil effects. Using the “reduced plateau age” method of Turner et al. (1978), the ages derived from this sample were 3898 ± 19 and 3894 ± 19 Ma. Three separate runs of known Group D basalt 10002, 116 yielded ⁴⁰Ar/³⁹Ar plateau ages of 3798 ± 9 Ma, 3781 ± 8 Ma, and 3805 ± 7 Ma (all errors 2σ). Furthermore, this sample has apparently suffered significant ⁴⁰Ar loss either due to solar heating or due to meteorite impact. The loss of a significant proportion of ⁴⁰Ar at such a time means that the plateau ages underestimate the “true” crystallization age of the sample. Modelling of this Ar loss yields older, “true” ages of 3837 ± 18, 3826 ± 16, and 3836 ± 14 Ma. These ages overlap the ages of Group B2 high-Ti basalts (weighted average age = 3850 ± 20 Ma; range in ages = 3.80 to 3.90 Ga). The combined evidence indicates that the Group D and B2 high-Ti basalts could be coeval and may be genetically related, possibly through increasing degrees of melting of a similar source region in the upper mantle of the Moon that formed >4.2 Ga ago. The Group D basalts were melted from the source first and contained 3–5×more trapped KREEP-like liquid than the later (by possibly only a few million years) Group B2 basalts. Furthermore, the relatively LREE- and Rb-enriched nature of these early magmas may lend credence to the idea that the decay of heat-producing elements enriched in the KREEP-like trapped liquid of upper mantle cumulates, such as K, U, and Th, could have initiated widespread lunar volcanism.     

Chondrite chronology by initial 87Sr/86Sr in phosphates?

Abstract— We report Rb-Sr analyses of phosphates from nine ordinary chondrites, more than doubling the number of meteorites for which such data are available. Ordinary chondrite phosphates characteristically have Rb/Sr ratios sufficiently low to permit accurate identification of initial ⁸⁷Sr/⁸⁶Sr, which is generally (but not in all cases) found to be significantly higher than the more primitive initial ⁸⁷Sr/⁸⁶Sr ratios inferred for carbonaceous chondrite refractory inclusions (ALL), basaltic achondrites (BABI), or bulk ordinary chondrites (in the ALL-BABI range). Such elevation of initial ⁸⁷Sr/⁸⁶Sr is generally considered to reflect isotopic redistribution during metamorphism, and with a model for Rb/Sr in this environment can lead to an inferred metamorphic timescale. For whole rock Rb/Sr the inferred formation intervals are typically tens of Ma (range nil to > 100 Ma). There is no evident relation between initial Sr elevation and metamorphic grade. There is not a clear difference in initial Sr effects between H and L chondrites; LL chondrites show much less (if any) elevation of initial Sr, but data are available for only two meteorites. For the first time it is possible to make a detailed comparison of initial Sr and I-Xe chronologies for several meteorites: these two potential metamorphic chronometers conspicuously fail to agree, in terms of both age and sequence of ages. A comparably definitive assessment of the comparison between initial Sr and Pb-Pb chronologies is not yet possible, but presently available data suggest that these two approaches to chondrite chronology also fail to agree. Without a correlation with metamorphic grade, or detailed agreement with an independent chronometer, it remains unclear whether initial ⁸⁷Sr/⁸⁶Sr in phosphates can be translated into a reliable chronometer for ordinary chondrite metamorphism, at least within simple interpretational frameworks.     

Fragmentation and hydration of tektites and microtektites

Abstract— An examination of data collected over the last 30 years indicates that the percent of glass fragments vs. whole splash forms in the Cenozoic microtektite strewn fields increases towards the source crater (or source region). We propose that this is due to thermal stress produced when tektites and larger microtektites fall into water near the source crater while still relatively hot (>1150 °C). We also find evidence (low major oxide totals, frothing when melted) for hydration of most of the North American tektite fragments and microtektites found in marine sediments. High-temperature mass spectrometry indicates that these tektite fragments and microtektites contain up to 3.8 wt% H₂O. The H₂O-release behavior during the high-temperature mass-spectrometric analysis, plus high CI abundances (0.05 wt%), indicate that the North American tektite fragments and microtektites were hydrated in the marine environment (i.e., the H₂O was not trapped solely on quenching from a melt). The younger Ivory Coast and Australasian microtektites do not exhibit much evidence of hydration (at least not in excess of 0.5 wt% H₂O); this suggests that the degree of hydration increases with age. In addition, we find that some glass spherules (with <65 wt% SiO₂) from the upper Eocene clinopyroxene-bearing spherule layer in the Indian Ocean have palagonitized rims. These spherules appear to have been altered in a similar fashion to the splash form K/T boundary spherules. Thus, our data indicate that tektites and microtektites that generally contain >65 wt% SiO₂ can undergo simple hydration in the marine environment, while impact glasses (with <65 wt% SiO₂) can also undergo palagonitization.     

87Rb-87Sr DATING OF L CHONDRITES: EFFECTS OF SHOCK AND BRECCIATION

We have analysed whole rock L chondrites and separate minerals from the L3 chondrite Mezö Madaras for ⁸⁷Rb-⁸⁷Sr dating. Contrary to other groups of chondrites, whole rocks do not define a straight line in the (⁸⁷Rb/⁸⁶Sr, ⁸⁷Sr/⁸⁶Sr) diagram. Whereas unshocked meteorites of old K-Ar age plot on the isochron defined by the other chondrites, shocked objects, with younger K-Ar ages, plot above it. Exceptions to this correlation are Bjürbole for the first type and Homestead and Peace River for the second type. Our preferred interpretation is that this displacement in the (⁸⁷Rb/⁸⁶Sr, ⁸⁷Sr/⁸⁶Sr) diagram corresponds to Rb volatilization induced by reheating. Hand-picked and heavy liquid separates from Mezö Madaras scatter in the same diagram. In addition to possible Rb loss from feldspar, evidences are found for migration of Rb and Sr between olivine and feldspar, glass or clinopyroxene. We interpret this as the consequence of a short though important heating at the time of brecciation.     

A review of volatile compounds in tektites,and carbon content and isotopic composition of moldavite glass

Abstract– Tektites, natural silica‐rich glasses produced during impact events, commonly contain bubbles. The paper reviews published data on pressure and composition of a gas phase contained in the tektite bubbles and data on other volatile compounds which can be released from tektites by either high‐temperature melting or by crushing or milling under vacuum. Gas extraction from tektites using high‐temperature melting generally produced higher gas yield and different gas composition than the low‐temperature extraction using crushing or milling under vacuum. The high‐temperature extraction obviously releases volatiles not only from the bubbles, but also volatile compounds contained directly in the glass. Moreover, the gas composition can be modified by reactions between the released gases and the glass melt. Published data indicate that besides CO₂ and/or CO in the bubbles, another carbon reservoir is present directly in the tektite glass. To clarify the problem of carbon content and carbon isotopic composition of the tektite glass, three samples from the Central European tektite strewn field—moldavites—were analyzed. The samples contained only 35–41 ppm C with δ¹³C values in the range from ?28.5 to ?29.9‰ VPDB. This indicates that terrestrial organic matter was a dominant carbon source during moldavite formation.     

Geochemical variability of the Yucatàn basement: Constraints from crystalline clasts in Chicxulub impactites

Abstract— The 65 Ma old Chicxulub impact structure with a diameter of about 180 km is again in the focus of the geosciences because of the recently commenced drilling of the scientific well Yaxcopoil‐ 1. Chicxulub is buried beneath thick post‐impact sediments, yet samples of basement lithologies in the drill cores provide a unique insight into age and composition of the crust beneath Yucatàn. This study presents major element, Sr, and Nd isotope data for Chicxulub impact melt lithologies and clasts of basement lithologies in impact breccias from the PEMEX drill cores C‐1 and Y‐6, as well as data for ejecta material from the K/T boundaries at La Lajilla, Mexico, and Furlo, Italy. The impact melt lithologies have an andesitic composition with significantly varying contents of Al, Ca, and alkali elements. Their present day ⁸⁷Sr/⁸⁶Sr ratios cluster at about 0.7085, and ¹⁴³Nd/¹⁴⁴Nd ratios range from 0.5123 to 0.5125. Compared to the melt lithologies that stayed inside the crater, data for ejecta material show larger variations. The ⁸⁷Sr/⁸⁶Sr ratios range from 0.7081 for chloritized spherules from La Lajilla to 0.7151 for sanidine spherules from Furlo. The ¹⁴³Nd/¹⁴⁴Nd ratio is 0.5126 for La Lajilla and 0.5120 for the Furlo spherules. In an ε^t_CHUR(Nd)‐ε^t_UR(Sr) diagram, the melt lithologies plot in a field delimited by Cretaceous platform sediments, various felsic lithic clasts and a newly found mafic fragment from a suevite. Granite, gneiss, and amphibolite have been identified among the fragments from crystalline basement gneiss. Their ⁸⁷Sr/⁸⁶Sr ratios range from 0.7084 to 0.7141, and their ¹⁴³Nd/¹⁴⁴Nd ratios range from 0.5121 to 0.5126. The T^Nd_DM model ages vary from 0.7 to 1.4 Ga, pointing to different source terranes for these rocks. This leads us to believe that the geological evolution and the lithological composition of the Yucatàn basement is probably more complex than generally assumed, and Gondwanan as well as Laurentian crust may be present in the Yucatàn basement.