Potassium isotopic composition of Australasian tektites

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

Triple oxygen isotope composition of Australasian tektites

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

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.     

Source of Australasian tektites: Investigating possible impact sites in Laos

Abstract— The site of an impact event that spread ejecta in the form of tektites and microtektites over ～5 × 10⁷ km² of the southern Pacific and Indian Ocean area has not yet been discovered. A number of lines of evidence point toward a source in eastern Indochina. From an examination of a digital topographic data set and Landsat imagery, we identified four candidate structures in southern Laos, and we visited these sites in 1995 February. No evidence of impact origin of these structures could be found; flat-lying, undisturbed Mesozoic sedimentary rocks similar to those on Thailand's Khorat Plateau were found over the region. Small layered tektite fragments are relatively common in a lateritic horizon that is characterized by the presence of quartz pebbles. This scene is identical to the situation found several hundred kilometers to the southeast in Thailand. New tektite sites identified on this trip support a previous suggestion that there is a large region in southern NE Thailand and Laos that is rich in Muong Nong-type (layered) tektites but seemingly devoid of the splash-form type tektites.     

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.     

Mechanism of Muong Nong-type tektite formation and speculation on the source of Australasian tektites

Abstract The source crater of the youngest and largest of the tektite strewnfields, the Australasian strewnfield, has not been located. A number of lines of evidence indicate that the Muong Nong-type tektites, primarily found in Indochina, are more primitive than the much more abundant and widespread splash-form tektites, and are proximal to the source. In this study the spatial distribution of Muong Nong-type tektite sites and chemical character have been used to indicate the approximate location of the source. The variation of Muong Nong-type tektite chemical composition appears to be caused by mixing of two silicate rock end-members and a small amount of limestone, and not by vapor fractionation. The variation in composition is not random, and does not support in-situ melting or multiple impact theories. The distribution of both Muong Nong and splash-form tektite sites suggest the source is in a limited area near the southern part of the Thailand-Laos border.     

Ultraprecise age and formation temperature of the Australasian tektites constrained by 40Ar/39Ar analyses

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.     

The chemical variation of moldavite tektites: Simple mixing of terrestrial sediments

Abstract— To test different hypotheses of moldavite formation, a major and trace-element study of 25 moldavite tektites and Sm-Nd isotope measurement of three moldavite tektites was completed. The samples were selected from the classical substrewnfields and the newly described locations in Lusatia (Saxony, Germany). Samples with unusual bulk composition were also included. The results confirm earlier studies that the variation in the chemical composition can be explained by single impact and through incomplete mixing of at least three lithographical components dominated by one of the three minerals or mineral groups: dolomite, clay minerals and quartz. An additional endmember, possibly a rare Earth's mantle component, containing high Co, Cr and Ni concentrations is also needed to explain the observed variations in compatible elements of some tektites. Volatile element abundances are low but not necessarily the result of selective volatilization.     

Origin of tektites

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.     

Constraints on the formation of layered tektites from the excavation and analysis of layered tektites from northeast Thailand

Abstract— The size, shape, composition, and vesicle content of 6 kg of layered tektite fragments, excavated near the town of Huai Sai, Thailand, place some constraints on the formation of layered tektites. The mass, shape, and distribution of the fragments are not consistent with an origin as a “puddle” of impact melt but suggest that they were derived from a single equant block. The presence of vesicles up to 7 mm in mean diameter within the tektite fragments suggests that the material was too viscous to allow for significant gravity-driven flow. These results suggest that layered tektites may be analogous to lava bombs, which may have been stretched and deformed in flight but underwent little flow after landing. Rather than being a product of “unusual circumstances,” such as multiple impacts, layered tektites may differ from splash-form tektites only in initial temperature of formation, speed of ejection, and small differences in initial composition.     

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.     

Lechatelierite inclusions in indochinites and the origin of tektites

Abstract— The grain size distribution and shapes of lechatelierite inclusions (silica glass inclusions) have been determined from 20 splash-form tektites from the Khorat Plateau, northeastern Thailand. The chemical and petrographic properties are reviewed, and the absence of any type of inclusion other than bubbles is confirmed. These data suggest that the parent material for the lechatelierite inclusions is not the conventional detrital quartz. One possible precursor is silica of plant origin in the form of biogenic opal-CT. According to this model, the lechatelierite inclusions are formed by shock melting of opal phytoliths in plants. These opal phytolith melts were included in the shock-melted soil and bedrock, jetted from the impact site. The expansion of the vapor plume ejected the melt droplets in ballistic trajectories. This model is extended to all tektite groups, because of the similarity between lechatelierite inclusions in them.     

A laboratory model of splash‐form tektites

Abstract— Splash‐form tektites are generally acknowledged to have the form of bodies of revolution. However, no detailed fluid dynamical investigation of their form and stability has yet been undertaken. Here, we review the dynamics and stability of spinning, translating fluid drops with a view to making inferences concerning the dynamic history of tektites. We conclude that, unless the differential speed between the molten tektite and ambient is substantially less than the terminal velocity, molten tektites can exist as equilibrium bodies of revolution only up to sizes of 3 mm. Larger tektites are necessarily non‐equilibrium forms and so indicate the importance of cooling and solidification during flight. An examination of the shapes of rotating, translating drops indicates that rotating silicate drops in air will assume the shapes of bodies of rotation if their rotational speed is 1% or more of their translational speed. This requirement of only a very small rotational component explains why most splash‐form tektites correspond to bodies of revolution. A laboratory model that consists of rolling or tumbling molten metallic drops reproduces all of the known forms of splashform tektites, including spheres, oblate ellipsoids, dumbbells, teardrops, and tori. The laboratory also highlights important differences between rolling drops and tumbling drops in flight. For example, toroidal drops are much more stable in the former than in the latter situation.     

Origin of tektites: Constraints from heavy noble gas concentrations

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.     

Micro‐Raman spectroscopic study of fine‐grained,shock‐metamorphosed rock fragments from the Australasian microtektite layer

Abstract— –Shock‐metamorphosed rock fragments have been found in the Australasian microtektite layer from the South China Sea. Previous X‐ray diffraction (XRD) studies indicate that the most abundant crystalline phases in the rock fragments are coesite, quartz, and a 10 Å phase (mica/clay?). In addition, the presence of numerous other phases was suggested by scanning electron microscopy (SEM) and energy‐dispersive X‐ray (EDX) analysis. In the present research, ten of the rock fragments, which had previously been studied using SEM/EDX, were studied by micro‐Raman spectroscopy. The presence of K‐feldspar, plagioclase, rutile, ilmenite, titanite, magnetite, calcite, and dolomite were confirmed. In addition, the high‐pressure TiO₂ polymorph with an α‐PbO₂ structure (i.e., TiO₂II) was found in several rock fragments. Two grains previously thought to have been zircon, based on their compositions, were found to have Raman spectra that do not match the Raman spectra of zircon, reidite, or any of the possible decomposition products of zircon or their high‐pressure polymorphs. We speculate that the ZrSiO₄ phase might be a previously unknown high‐pressure polymorph of zircon or one of its decomposition products (i.e., ZrO₂ or SiO₂). The presence of coesite and TiO₂ II, and partial melting and vesiculation suggest that the rock fragments containing the unknown ZrSiO₄ phase must have experienced shock pressures between 45 and 60 GPa. We conclude that micro‐Raman spectroscopy, in combination with XRD and SEM/EDX, is a powerful tool for the study of small, fine‐grained impact ejecta.     

Report of centimeter-sized tektites in Pima County,Arizona, cannot be verified

Abstract— Glassy objects reportedly found in Pima County, Arizona, have been identified as tektites. A field survey of the area where they were said to occur, however, did not produce any other tektites, nor did it reveal any other geologic features that might indicate a nearby impact crater. The major-, minor-, and trace-element composition of one specimen is similar to those measured in indochinites, which suggests the objects reportedly from Pima County were instead transported to southern Arizona from Indochina by people.     

Layered tektites of southeast Asia: Field studies in central Laos and Vietnam

Abstract— We have recovered 18 kg of layered tektites from 10 tektite-bearing localities in Laos and central Vietnam, including 5 localities around the town of Muong Nong (Laos). Several of these deposits originally contained several hundred kilograms of layered tektite fragments, and one fragmented mass may have been as large as 1000 kg. This is the largest single deposit of tektites yet reported. In this region, layered tektite fragments are found in isolated clusters usually associated with a pebbly laterite horizon that is 0–1 m below the surface. Near Khe Sanh, Vietnam, we estimate the abundance of layered tektite fragments to be ～100 g/m². This is greater than five times the abundance estimated for northeast Thailand (Fiske et al., 1996). In a region that extends from northeast Thailand, through central Laos, and into central Vietnam, we found only layered tektites, which confirmed the existence of a large (>50 000 km²) subfield of the Australasian strewn field with only layered tektites. The east-west extent of the “layered-only” subfield is well constrained, but little field data exist to constrain its north-south extent.     

Fluorine and boron geochemistry of tektites,impact glasses,and target rocks

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.     

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

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

Discovery of the most distal Ries tektites found in Lower Silesia,southwestern Poland

We report the first occurrence of moldavites in Poland. This discovery confirms the hypothesis that moldavites could have been distributed up to 500 km from the Ries crater in Germany. The tektites were reworked from Middle Miocene sediments and redeposited in Late Miocene (Pannonian) fluvial deposits of the Gozdnicka Formation in Lower Silesia. The Polish moldavites are represented by nine (<8 mm) fragments with a total of 0.471 g. The lack of the autochthonous tektites indicates that tektites investigated here had to be redeposited in a fluvial environment, probably from the Lusatian area. The chemical composition of the Polish moldavites plots in the same area with those from other localities.