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1.
Abstract— We have analyzed fluorine and boron in nine tektites from all four strewn fields, and in a suite of impact glasses and target rocks from the Zhamanshin and Darwin impact craters, as well as Libyan Desert Glass and Aouelloul impact glass samples. Fluorine and boron are useful indicators for the volatilization and temperature history of tektites and impact glasses. Tektites from different strewn fields show a limited range of F and B contents and have F/B ratios near unity. Most splash-form tektites have lower average F and B contents than Muong Nong type tektites, which is similar to the relation between irghizites and zhamanshinites. The F and B contents in target rocks from the Zhamanshin and Darwin impact craters are similar to normal terrestrial sediments. Fluorine in impact glasses and tektites is more depleted compared to their (known or inferred) target rocks than is boron, which is caused by the higher volatility of F. The F/B ratios therefore decrease with increasing temperature of formation (suggesting that irghizites were formed at a higher temperature than zhamanshinites, and Muong Nong type tektites at a lower temperature than splash-form tektites). Mixing of local country rocks together with partial loss of the volatiles F and B can reproduce the F and B contents of impact glasses.  相似文献   

2.
Fluorine (by combined distillation-spectrophotometry) and chlorine (by X-ray fluorescence spectrometry) contents were determined in normal and Muong Nong-type tektites. Contents of F (78–285 ppm) and Cl (3–44 ppm) in normal tektites are about 4 and 10 times lower, respectively, than in the Earth's continental crust and this is attributed to selective volatilization during impact melting. Muong Nong-type tektites are characterised by similar F (124–312 ppm) but higher Cl (65–205 ppm) contents and may have resulted from a lower temperature event.  相似文献   

3.
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.  相似文献   

4.
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   

5.
Spherical translucent green glasses found in New Guinea for many years have the external appearance of stream abraded tektites, but are chemically distinct from known tektite groups. Their chemical composition is most similar to artificial glasses. If these objects are the source of reports of tektites occurring in New Guinea, the existence of New Guinea tektites must now be discounted.  相似文献   

6.
Abstract— Depth-profiles of F, Cl, Br and I concentrations were determined in four different Antarctic H5 chondrites from the Allan Hills and in the two chondrites Allende (C3) and Holbrook (L6). Pieces of the meteorites were studied by analysis of stepwise removed layers of 0.5–1.0 mm thickness up to a depth of 9 mm. Neutron activation analysis and ion-selective potentiometry were used for the determination of Cl, Br, I and for F, respectively. The Antarctic meteorites show higher concentrations of the halogens at the surface compared to the interior. The highest enrichment factors are found for I and Cl and the lowest for Br. In contrast, F shows the steepest concentration gradient and is only enriched in the first 2.5 mm below the surface. The other halogens have penetrated deeper into the meteorites. The measured enrichments at the surfaces are not correlated to the visible degree of weathering. The analysed non-Antarctic meteorites, which were recovered shortly after their observed fall, demonstrate similar halogen concentrations at the surface, including the fusion crust, as in the interior. Based on these results we present a model to estimate the degree of contamination and the relation to the duration of exposure at the surface of the Antarctic ice.  相似文献   

7.
Abstract— Heavy noble gas concentrations in tektites (splash-form type) are considerably lower than those in impact glasses. This can not be explained only by high formation temperatures for tektites, as might be expected from low concentrations of water and most volatile elements in tektites, and indicates that tektites solidified in an atmosphere with an ambient pressure of much less than 1 atm. The heavy noble gas concentrations may be an indicator of the height to which tektites were carried by the impact before they solidified.  相似文献   

8.
Abstract— The distribution and petrography of surficial suevite breccias of the Ries impact crater in Southern Germany are reviewed, and the morphology, petrography and chemical composition of impact glasses in suevite breccias and their postdepositional devitrification is synthesized. Origin and thermal history of suevite breccia and suevite glasses are inferred from these data and from recent results of cooling and crystallization experiments with suevite glass melts under controlled conditions. In a montmorillonitic groundmass, the suevite breccia contains pieces of glass, up to some decimeters in size, and crystalline rock clasts of all stages of shock metamorphism. The glass particles originated in impact melt of basement gneisses and cooled by adiabatic pressure release from ～80 GPa to atmospheric pressure during ejection from the crater. They were deposited on the ground together with the other suevite components at a temperature of ～750 °C. Fractured glass pieces in the breccia show that during deposition of the suevite the temperature was below the temperature at which undercooled melt transforms to rigid glass. The suevite cooled after deposition mainly by convection of heat by emanating gases and vapors. In chilled layers at the base and at the top of suevite deposits, the glasses are preserved in vitreous state. Between these zones, the glasses were devitrified, yet crystallization of pyroxene, plagioclase and magnetite took place below the glass-transformation temperature. Annealing experiments show that this unusual devitrification below the transformation temperature can be explained by the impact origin of suevite glasses. Due to rapid adiabatic cooling on decompression, the glasses were oversaturated with water and internally strained. Under these conditions, devitrification, especially the formation of plagioclase, was possible at temperatures below the transformation range. The origin from adiabatically cooled impact melt of deep-seated rocks distinguishes water-bearing suevite glasses from the Ries-derived, water-free moldavite tektites, which are interpreted as condensates of vaporized, surficial sediments (Engelhardt et al., 1987).  相似文献   

9.
Abstract— The origin of tektites has been obscure because of the following dilemma. The application of physical principles to the data available on tektites points strongly to origin from one or more lunar volcanoes; but few glasses of tektite composition have hitherto been reported from the lunar samples. Instead, the lunar silicic glasses consist chiefly of a material very rich in K2O and poor in MgO. The ratio of K2O/MgO is higher in these glasses than in any tektites reported. The solution of the dilemma seems to come from the study of some recently discovered terrestrial deposits of tektite glass with high values of K2O/MgO at the Cretaceous-Tertiary boundary. These glasses are found to be very vulnerable to crystallization into sandine or to alteration to smectite. These end products are known and are more abundant than any terrestrial deposits of tektite glass. It seems possible that, in fact, the moon produces tektite glass, mostly of the high K2O-low MgO type; but on Earth these deposits are destroyed. The much less abundant deposits with lower K and higher Mg are observed because they survive. Other objections to the lunar origin hypothesis appear to be answerable.  相似文献   

10.
Abstract— The El'gygytgyn impact structure is about 18 km in diameter and is located in the central part of Chukotka, arctic Russia. The crater was formed in volcanic rock strata of Cretaceous age, which include lava and tuffs of rhyolites, dacites, and andesites. A mid‐Pliocene age of the crater was previously determined by fission track (3.45 ± 0.15 Ma) and 40Ar/39Ar dating (3.58 ± 0.04 Ma). The ejecta layer around the crater is completely eroded. Shock‐metamorphosed volcanic rocks, impact melt rocks, and bomb‐shaped impact glasses occur in lacustrine terraces but have been redeposited after the impact event. Clasts of volcanic rocks, which range in composition from rhyolite to dacite, represent all stages of shock metamorphism, including selective melting and formation of homogeneous impact melt. Four stages of shocked volcanic rocks were identified: stage I (≤35 GPa; lava and tuff contain weakly to strongly shocked quartz and feldspar clasts with abundant PFs and PDFs; coesite and stishovite occur as well), stage II (35–45 GPa; quartz and feldspar are converted to diaplectic glass; coesite but no stishovite), stage III (45–55 GPa; partly melted volcanic rocks; common diaplectic quartz glass; feldspar is melted), and stage IV (>55 GPa; melt rocks and glasses). Two main types of impact melt rocks occur in the crater: 1) impact melt rocks and impact melt breccias (containing abundant fragments of shocked volcanic rocks) that were probably derived from (now eroded) impact melt flows on the crater walls, and 2) aerodynamically shaped impact melt glass “bombs” composed of homogeneous glass. The composition of the glasses is almost identical to that of rhyolites from the uppermost part of the target. Cobalt, Ni, and Ir abundances in the impact glasses and melt rocks are not or only slightly enriched compared to the volcanic target rocks; only the Cr abundances show a distinct enrichment, which points toward an achondritic projectile. However, the present data do not allow one to unambiguously identify a meteoritic component in the El'gygytgyn impact melt rocks.  相似文献   

11.
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.  相似文献   

12.
Abstract— Five indochinites from Hainan Island and the Leizhou Peninsula, China were analyzed for noble gas abundances and isotopic ratios. These splash‐form tektites show vesiculation ranging from 0.4 vol% to 8 vol%, as determined by digital image analysis (software SXM®) on thin section photographs. To study the distribution of noble gases in vesicles and in glass, the gases were extracted by heating and by crushing, respectively, on 2 aliquots of the same sample. The results show that 5 to 53% of the total measured 20Ne resides in vesicles. The calculated concentration of neon dissolved in the glass is higher (0.7‐1 times 10?7 cm3STP/g) than that expected from solubility equilibrium (1 times 10?8 cm3STP/g), assuming solubility data from MORB glasses. The neon concentration of splash‐form tektites, those analyzed in this work and those from other strewn‐fields worldwide, is correlated with the SiO2 content of glass and with the nonbridging oxygen per tetrahedral cation in the melt (hereafter NBO/T ratio), the latter being an index of the free‐volume in the silica network where neon could be dissolved. These correlations suggest that the glass structure of tektite has a larger free‐volume available for dissolving noble gases than MORB glasses.  相似文献   

13.
Abstract— Fifty-odd years of tektite research are reviewed, proceeding from the discovery of the first North American tektites in 1936. This included the early recognition that tektites were terrestrial objects rather than meteorites and that the glassy particles in tektites were fused quartz (lechatelierite). Later, during National Science Foundation-supported research, it was found that some tektites appeared to have formed as puddles of melt, that the content and character of bubbles in lechatelierite can be used as a relative temperature scale, that rayed bubbles in tektites formed from hydrous minerals, that bubbles in tektites formed chiefly from water which was absorbed into the walls of the bubbles leaving vacuums, and that “fingers” in the surficial part of some tektites may have formed by differential volatilization. Some unpublished observations and adventures are briefly reported.  相似文献   

14.
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.  相似文献   

15.
Drill core UNAM‐7, obtained 126 km from the center of the Chicxulub impact structure, outside the crater rim, contains a sequence of 126.2 m suevitic, silicate melt‐rich breccia on top of a silicate melt‐poor breccia with anhydrite megablocks. Total reflection X‐ray fluorescence analysis of altered silicate melt particles of the suevitic breccia shows high concentrations of Br, Sr, Cl, and Cu, which may indicate hydrothermal reaction with sea water. Scanning electron microscopy and energy‐dispersive spectrometry reveal recrystallization of silicate components during annealing by superheated impact melt. At anhydrite clasts, recrystallization is represented by a sequence of comparatively large columnar, euhedral to subhedral anhydrite grains and smaller, polygonal to interlobate grains that progressively annealed deformation features. The presence of voids in anhydrite grains indicates SOx gas release during anhydrite decomposition. The silicate melt‐poor breccia contains carbonate and sulfate particles cemented in a microcrystalline matrix. The matrix is dominated by anhydrite, dolomite, and calcite, with minor celestine and feldspars. Calcite‐dominated inclusions in silicate melt with flow textures between recrystallized anhydrite and silicate melt suggest a former liquid state of these components. Vesicular and spherulitic calcite particles may indicate quenching of carbonate melts in the atmosphere at high cooling rates, and partial decomposition during decompression at postshock conditions. Dolomite particles with a recrystallization sequence of interlobate, polygonal, subhedral to euhedral microstructures may have been formed at a low cooling rate. We conclude that UNAM‐7 provides evidence for solid‐state recrystallization or melting and dissociation of sulfates during the Chicxulub impact event. The lack of anhydrite in the K‐Pg ejecta deposits and rare presence of anhydrite in crater suevites may indicate that sulfates were completely dissociated at high temperature (T > 1465 °C)—whereas ejecta deposited near the outer crater rim experienced postshock conditions that were less effective at dissociation.  相似文献   

16.
Detailed statistical examination of Cl, Br, and S distributions, in martian soil profiles at Gusev Crater and Meridiani Planum, indicates decreasing Br abundance and weakening Br–S association towards the surface. All three elements decrease towards the surface in the order Cl < S < Br. Furthermore, Br variability decouples from potential cations such as Mg at the surface relative to the subsurface. These observations support a relative loss of surficial Br compared to S and Cl, all highly mobile elements in aqueous environments. We propose that Br may have converted preferentially to gas phases (e.g., BrO), driven either by UV photolysis or by chemical oxidants. Such volatilization pathways may in turn impart a global signature on Mars by acting as controls on oxidants such as ozone and perchlorates. S/Cl mass ratios vary with depth (∼4–5 in the subsurface; 1.8–3.6 on the surface) as well, with a strong correlation of S and Cl near the surface but more variable at depth, consistent with differential vertical mobility, but not volatilization of Cl. Elevated S/Cl in subsurface soil also suggests that the ratio may be higher in bulk soil – a key repository of martian geologic and climatic records – than previously thought.  相似文献   

17.
The Australasian tektites are quench melt glass ejecta particles distributed over the Asian, Australian, and Antarctic regions, the source crater of which is currently elusive. New 40Ar/39Ar age data from four tektites: one each from Thailand, China, Vietnam, and Australia measured using three different instruments from two different laboratories and combined with published 40Ar/39Ar data yield a weighted mean age of 788.1 ± 2.8 ka (±3.0 ka, including all sources of uncertainties) (P = 0.54). This age is five times more precise compared to previous results thanks, in part, to the multicollection capabilities of the ARGUS VI noble gas mass spectrometer, which allows an improvement of almost fourfold on a single plateau age measurement. Diffusion experiments on tektites combined with synthetic age spectra and Monte Carlo diffusion models suggest that the minimum temperature of formation of the Thai tektite is between 2350 °C and 3950 °C, hence a strict minimum value of 2350 °C.  相似文献   

18.
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.  相似文献   

19.
It is shown that the enhanced abundance of siderophile elements and chromium in tektite-like glasses from the two impact craters of Zhamanshin and Aouelloul cannot be explained as a result of contamination of the country rock by meteorites nor, probably, comets. The pattern is, however, like that found in certain Australasian tektites, and in Ivory Coast tektites. It is concluded, in agreement with earlier suggestions by Campbell-Smith and Hey, that these craters were formed by the impact of large masses of tektite-like glass, of which the glasses which were studied are fragments. It follows that it is necessary, in considering an impact crater, to bear in mind that the projectile may have been a glass.  相似文献   

20.
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.  相似文献   

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