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1.
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 ?Srt = 35.7 Ma of +54 to +272, and ?Ndt = 35.7 Ma ranging from ?6.5 to ?10.8; one sample from the granitic basement with a TNdCHUR model age of 1.36 Ga yielded an ?Srt = 35.7 Ma of +188 and an ?Ndt = 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 TNdCHUR 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 (?Srt = 35.7 Ma), ?5.7 (?Ndt = 35.7 Ma), 0.47 Ga (TSrUR), and 1.15 Ga (TNdCHUR), 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.  相似文献   

2.
Abstract— Upper Eocene impact ejecta has been discovered all over the world. The number of upper Eocene impact layers and the geographic distribution of each layer, based on major chemical composition and biostratigraphic data, are not agreed upon. We have performed four Sr‐Nd isotopic analyses of clinopyroxene‐bearing spherules (cpx spherules) and three Sr‐Nd analyses of microtektites from five Deep Sea Drilling Project/Ocean Drilling Program (DSDP/ODP) sites in the South Atlantic and Indian Oceans. Our data support the hypothesis that there is only one cpx spherule layer in upper Eocene sediments. We also find that the microtektites associated with the cpx spherule layer in the South Atlantic and Indian Oceans are not part of the North American tektite strewn field, but belong to the same event that produced the cpx spherules. The microtektites, together with cpx spherules, are more heterogeneous than microtektites/tektites from other strewn fields. No direct link has been established between the microtektites from this study and possible target rock at the Popigai crater.  相似文献   

3.
Abstract— A layer of tektite glass and shock-metamorphosed grains found in an upper Eocene section of core 21 from DSDP Site 612 taken on the continental slope off New Jersey may belong to the North American tektite strewn field. However, the Site 612 glasses generally have higher K2O and lower Na2O contents for a given SiO2 content and different Sr and Nd isotopic compositions. In order to better define the layer, a series of samples was taken continuously through the layer at 1 cm intervals. Tektite fragments are in an 8 cm thick layer; microtektites are concentrated in the upper 4 cm, while spherules with “crystalline” textures (microkrystites) are concentrated in the lower half of the layer. Millimeter-size splash forms are mostly in the lower part of the tektite-bearing layer. Rock and mineral grains showing evidence of shock metamorphism are abundant in the upper half of the tektite-bearing layer. Coesite is abundant, and stishovite was found in one rock fragment. The size and abundance of the tektite glass and the abundance of shocked debris indicate that Site 612 is relatively close to the source crater, which may be to the north of Site 612 on the coastal plain or adjacent continental shelf.  相似文献   

4.
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 (TDM) 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 (TCHUR = 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.  相似文献   

5.
The Fe oxidation state and coordination number of 29 impact glass spherules recently recovered from the Transantarctic Mountains (Antarctica) have been determined by X‐ray absorption near edge structure (XANES) spectroscopy. Based on geochemical, isotopic, and fission track data, these spherules are considered as microtektites from the Australasian tektite/microtektite strewn field. Their find location is the farthest so far discovered from the possible source crater region, and their alkali content is the lowest compared with other published data on Australasian microtektite glasses. The Fe3+/(Fe2++Fe3+) ratio, determined from the analysis of the pre‐edge peak energy position and integrated intensity, is below 0.1 (±0.04) for all the samples, and is comparable to that of most tektites and microtektites from the Australasian strewn field. Also, the pre‐edge peak integrated intensity, which is sensitive to the average Fe coordination geometry, is comparable to that of other Australasian microtektites reported in the literature. The agreement of the Fe oxidation state and coordination number, between the Transantarctic Mountain microtektites (TAM) and the Australasian tektites and microtektites, further confirms the impact origin of these glass spherules and provides an independent suggestion that they represent a major extension southeastward of the Australasian strewn field. The fact that similar redox conditions are observed in tektites and microtektites within the Australasian strewn field regardless of the distance from the source crater area (up to approximately 11000 km) could be an important constraint for better understanding the different processes affecting microtektite formation and transport. The fact that the Fe oxidation state of microtektites does not increase with distance, as in the case of North American microtektites, means that thermal and redox histories of Australasian and TAM microtektites could differ significantly from those of North American microtektites.  相似文献   

6.
Abstract— Late Eocene microtektites and microkrystites recovered from Ocean Drilling Project Hole 689B at Maud Rise (Southern Ocean) are stratigraphically and geochemically compared to spherules from the North American and Pacific strewn fields, and to devitrified spherules from the Eocene-Oligocene global stratotype section and point section in Massignano, Italy. The ODP 689B microkrystites compare well to the Pacific strewn field microkrystites, which suggests that the geographic extent of the Pacific strewn field was much larger than previously documented. The elemental composition of microtektites of ODP Hole 689B is comparable to tektites of the North American strewn field. Their 87Sr/86Sr ratio, however, is different. We tentatively interpret this to reflect geochemical heterogeneity within the North American strewn field but can not exclude the option that the chemical discrepancies result from the existence of a third late Eocene impact site.  相似文献   

7.
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.  相似文献   

8.
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.  相似文献   

9.
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.  相似文献   

10.
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.  相似文献   

11.
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 (ISr) 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 ISr 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 ISr 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.  相似文献   

12.
The recent witnessed fall of the meteorite Tissint represents the delivery of a pristine new sample from the surface of Mars. This meteorite provides an unprecedented opportunity to study a variety of aspects about the planet's evolution. Using the Rb–Sr and Sm–Nd isotopic systems, we determined that Tissint, a depleted shergottite, has a crystallization age of 574 ± 20 Ma, an initial ε143Nd = +42.2 ± 0.5, and an initial 87Sr/86Sr = 0.700760 ± 11. These initial Nd and Sr isotopic compositions suggest that Tissint originated from a mantle source on Mars that is distinct from the source reservoirs of the other Martian meteorites. The known crystallization ages, geochemical characteristics, ejection ages, and ejection dynamics of Tissint and other similarly grouped Martian meteorites suggest that they are likely derived from a source crater up to approximately 90 km in diameter with an age of approximately 1 Ma that is located on terrain that is approximately 600 million years old.  相似文献   

13.
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.  相似文献   

14.
Abstract— The petrology, major and trace element geochemistry, and Nd‐Ar‐Sr isotopic compositions of a ferroan noritic anorthosite clast from lunar breccia 67215 have been studied in order to improve our understanding of the composition, age, structure, and impact history of the lunar crust. The clast (designated 67215c) has an unusually well preserved igneous texture. Mineral compositions are consistent with classification of 67215c as a member of the ferroan anorthositic suite of lunar highlands rocks, but the texture and mineralogy show that it cooled more rapidly and at shallower depths than did more typical ferroan anorthosites (FANs). Incompatible trace element concentrations are enriched in 67215c relative to typical FANs, but diagnostic signatures such as Ti/Sm, Sc/Sm, plagiophile element ratios, and the lack of Zr/Hf and Nb/Ta fractionation show that this cannot be due to the addition of KREEP. Alternatively, 67215c may contain a greater fraction of trapped liquid than is commonly present in lunar FANs. 147Sm‐143Nd isotopic compositions of mineral separates from 67215c define an isochron age of 4.40 ± 0.11 Gyr with a near‐chondritic initial ε143Nd of +0.85 ± 0.53. The 40Ar‐39Ar composition of plagioclase from this clast records a post‐crystallization thermal event at 3.93 ± 0.08 Gyr, with the greatest contribution to the uncertainty in this age deriving from a poorly constrained correction for lunar atmosphere 40Ar. Rb‐Sr isotopic compositions are disturbed, probably by the same event recorded by the Ar isotopic compositions. Trace element compositions of FANs are consistent with crystallization from a moderately evolved magma ocean and do not support a highly depleted source composition such as that implied by the positive initial ε143Nd of the ferroan noritic anorthosite 62236. Alternatively, the Nd isotopic systematics of lunar FANs may have been subject to variable degrees of modification by impact metamorphism, with the plagioclase fraction being more strongly affected than the mafic phases. 147Sm‐143Nd isotopic compositions of mafic fractions from the 4 ferroan noritic anorthosites for which isotopic data exist (60025, 62236, 67016c, 67215c) define an age of 4.46 ± 0.04 Gyr, which may provide a robust estimate for the crystallization age of lunar ferroan anorthosites.  相似文献   

15.
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.  相似文献   

16.
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.  相似文献   

17.
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 (I87Sr) = 0.698972 ± 8 and 0.698970 ± 18 for LEW and ADOR, respectively, relative to 87Sr/86Sr = 0.71025 for NBS987. The difference, ΔI87Sr, between I87Sr 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.  相似文献   

18.
Recent discoveries of microtektite and related crystal bearing microspherule layers in deep-sea sediments of the west equatorial Pacific DSDP Sites 292, 315A and 462, off-shore New Jersey in Site 612 and in southern Spain have confirmed the presence of at least three microspherule layers in Late Eocene sediments. Moreover, these discoveries have extended the North American strewn field from the Caribbean and Gulf of Mexico region to the northwest Atlantic, and have established a third strewn field in western equatorial Pacific and Indian Ocean which may extend to the Mediterranean. Stratigraphically the oldest microspherule layer occurs in the planktonic foraminifer Globigerapsis semiinvoluta Zone about 0.5 m.y. prior to the closely spaced crystal bearing microspherule layer and North American microtektite layer in the Globorotalia cerroazulensis Zone. Major element composition of the G. semiinvoluta Zone layer and the crystal bearing microspherule layer overlap, but there is a clear trend towards higher Al2O3 and FeO values in SiO2 equivalent microspherules of the latter layer. The G. semiinvoluta Zone microspherules also contain a higher percentage of non-crystalline spherules (microtektites) than the crystal bearing microspherule layer, but lower than the North American microtektite layer. Excess iridium due to an abrupt increase in supply is associated with the middle crystal bearing microspherule layer and to a lesser extent with the other two layers. But, Ir excess due to concentration as a result of carbonate loss was also observed at two sites (462, 612). The three late Eocene microspherule layers do not precisely coincide with planktonic foraminiferal species extinctions, but a major faunal assemblage change is associated with the G. semiinvoluta Zone layer. Abundant pyrite is present in the North American microtektite layer of DSDP Site 612 suggesting reducing conditions possibly due to a sudden influx of biologic matter (dead bodies) to the ocean floor, and the crystal bearing microspherule layer coincides with five radiolarian extinctions. All three microspherule layers are associated with decreased carbonate possibly due to sudden productivity changes, increased dissolution as a result of sea-level and climate fluctuations, or the impact events.  相似文献   

19.
Abstract— Australasian microtektites were discovered in Ocean Drilling Program (ODP) Hole 1143A in the central part of the South China Sea. Unmelted ejecta were found associated with the microtektites at this site and with Australasian microtektites in Core SO95–17957–2 and ODP Hole 1144A from the central and northern part of the South China Sea, respectively. A few opaque, irregular, rounded, partly melted particles containing highly fractured mineral inclusions (generally quartz and some K feldspar) and some partially melted mineral grains, in a glassy matrix were also found in the microtektite layer. The unmelted ejecta at all three sites include abundant white, opaque grains consisting of mixtures of quartz, coesite, and stishovite, and abundant rock fragments which also contain coesite and, rarely, stishovite. This is the first time that shock‐metamorphosed rock fragments have been found in the Australasian microtektite layer. The rock fragments have major and trace element contents similar to the Australasian microtektites and tektites, except for higher volatile element contents. Assuming that the Australasian tektites and microtektites were formed from the same target material as the rock fragments, the parent material for the Australasian tektites and microtektites appears to have been a fine‐grained sedimentary deposit. Hole 1144A has the highest abundance of microtektites (number/cm2) of any known Australasian microtektite‐bearing site and may be closer to the source crater than any previously identified Australasian microtektite‐bearing site. A source crater in the vicinity of 22° N and 104° E seems to explain geographic variations in abundance of both the microtektites and the unmelted ejecta the best; however, a region extending NW into southern China and SE into the Gulf of Tonkin explains the geographic variation in abundance of microtektites and unmelted ejecta almost as well. The size of the source crater is estimated to be 43 ± 9 km based on estimated thickness of the ejecta layer at each site and distance from the proposed source. A volcanic ash layer occurs just above the Australasian microtektite layer, which some authors suggest is from a supereruption of the Toba caldera complex. We estimate that deposition of the ash occurred ?800 ka ago and that it is spread over an area of at least 3.7 times 107 km2.  相似文献   

20.
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.  相似文献   

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