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1.
Abstract— t‐Impact‐generated glasses from fallout suevite deposits at the Ries impact structure have been investigated using analytical scanning electron microscopy. Approximately 320 analyses of glass clasts were obtained. Four glass types are distinguished on the basis of composition and microtextures. Type 1 glasses correspond to the aerodynamically shaped glass bombs studied previously by many workers. Major oxide concentrations indicate the involvement of granitic rocks, amphibolites, and minor Al‐rich gneisses during melting. Type 2 glasses are chemically heterogeneous, even within individual clasts, with variations of several wt% in most of the major oxides (e.g., 57–70 wt% SiO2). This suggests incomplete mixing of: 1) mineral‐derived melts or 2) whole rock melts from a wide range of lithologies. Aluminium‐rich clinopyroxene and Fe‐Mg‐rich plagioclase quench crystals are present in type 1 and 2 glasses, respectively. Type 3 glasses contain substantial amounts of H2O (?12–17 wt%), low SiO2 (50–53 wt%), high Al2O3 (17–21 wt%), and high CaO (5–7 wt%) contents. This suggests an origin due to shock melting of part of the sedimentary cover. Type 4 glasses form a ubiquitous component of the suevites. Based on their high SiO2 content (?85–100 wt%), the only possible protolith are sandstones in the lowermost part of the sedimentary succession. Calcite forms globules within type 1 glasses, with which it develops microtextures indicative of liquid immiscibility. Unequivocal evidence also exists for liquid immiscibility between what are now montmorillonite globules and type 1, 2, and 4 glasses, indicating that montmorillonite was originally an impact melt glass. Clearly, the melt zone at the Ries must have incorporated a substantial fraction of the sedimentary cover, as well as the underlying crystalline basement rocks. Impact melts were derived from different target lithologies and these separate disaggregated melts did not substantially mix in most cases (type 2, 3, and 4 glasses and carbonate melts).  相似文献   

2.
Shock-induced recovery experiments were performed to investigate melt formation in porous sandstones in the low shock pressure regime between 2.5 and 17.5 GPa. The sandstone shocked at 2.5 and 5 GPa is characterized by pore closure, fracturing of quartz (Qtz), and compression and deformation of phyllosilicates; no melting was observed. At higher pressures, five different types of melts were generated around pores and alongside fractures in the sandstone. Melting of kaolinite (Kln), illite (Ill), and muscovite (Ms) starts at 7.5, 12, and 15 GPa, respectively. The larger the amount of water in these minerals (Kln ~14 wt%, Ill ~6–10 wt%, and Ms ~4 wt% H2O), the higher the shock compressibility and the lower the shock pressure required to induce melting. Vesicles in the almost dry silicate glasses attest to the loss of structural water during the short shock duration of the experiment. The compositions of the phyllosilicate-based glasses are identical to the composition of the parental minerals or their mixtures. Thus, this study has demonstrated that phyllosilicates in shocked sandstone undergo congruent melting during shock loading. In experiments at 10 GPa and higher, iron melt from the driver plate was injected into the phyllosilicate melts. During this process, Fe is partitioned from the metal droplets into the surrounding silicate melts, which induced unmixing of silicate melts with different chemical properties (liquid immiscibility). At pressures between 7.5 and 15 GPa, a pure SiO2 glass was formed, which is located as short and thin bands within Qtz grains. These bands were shown to contain tiny crystals of experimentally generated stishovite.  相似文献   

3.
Abstract— To test whether aubrites can be formed by melting of enstatite chondrites and to understand igneous processes at very low O fugacities, we have conducted partial melting experiments on the Indarch (EH4) chondrite at 1000–1500 °C. Silicate melting begins at 1000 °C, and Indarch is completely melted by 1500 °C. The metal-sulfide component melts completely at 1000 °C. Substantial melt migration occurs at 1300–1400 °C, and metal migrates out of the silicate charge at 1450 °C and ～50% silicate partial melting. As a group, our experiments contain three immiscible metallic melts (Si-, P-, and C-rich), two immiscible sulfide melts (Fe- and FeMgMnCa-rich), and silicate melt. Our partial melting experiments on the Indarch (EH4) enstatite chondrite suggest that igneous processes at low fO2 exhibit several unique features. The complete melting of sulfides at 1000 °C suggests that aubritic sulfides are not relics. Aubritic oldhamite may have crystallized from Ca and S complexed in the silicate melt. Significant metal-sulfide melt migration might occur at relatively low degrees of silicate partial melting. Substantial elemental exchange occurred between different melts (e.g., S between sulfide and silicate, Si between silicate and metal), a feature not observed during experiments at higher fO2. This exchange may help explain the formation of aubrites from known enstatite chondrites.  相似文献   

4.
Abstract— The 24 km diameter Ries impact crater in southern Germany is one of the most studied impact structures on Earth. The Ries impactor struck a Triassic to Upper Jurassic sedimentary sequence overlying Hercynian crystalline basement. At the time of impact (14.87 × 0.36 Ma; Storzer et al., 1995), the 350 m thick Malm limestone was present only to the south and east of the impact site. To the north and west, the Malm had been eroded away, exposing the underlying Dogger and Lias. The largest proportion of shocked target material is in the impact-melt-bearing breccia suevite. The suevite had been believed to be derived entirely from the crystalline basement. Calcite in the suevite has been interpreted as a postimpact hydrothermal deposit. From optical inspection of 540 thin sections of suevite from 32 sites, I find that calcite in the suevite shows textural evidence of liquid immiscibility with the silicate impact melt. Textural evidence of liquid immiscibility between silicate and carbonate melt in the Ries suevite includes carbonate globules within silicate glass, silicate globules embedded in carbonate, deformable and coalescing carbonate spheres within silicate glass, sharp menisci or cusps and budding between silicate and carbonate melt, fluidal textures and gas vesicles in carbonate schlieren, a quench crystallization sequence of the carbonate, spinifex textured quenched carbonate, separate carbonate spherules in the suevite mineral-fragment matrix, and inclusions of mineral fragments suspended in carbonate blebs. Given this evidence of liquid immiscibility, the carbonate in the suevite therefore has—like the silicate melt—a primary origin by impact-shock melting. Evidence of carbonate-silicate liquid immiscibility is abundant in the suevites from the southwest to east of the Ries crater. The rarer suevites to the west to northeast of the crater are nearly devoid of carbonate melts. This correspondence between the occurrence of outcropping limestones at the target surface and the formation of carbonate melt indicates that the Malm limestones are the source rocks of the carbonate impact melt. This correspondence shows that the suevites preserve a compositional memory of their source rocks. From the regional distribution of suevites with or without immiscible carbonate melts, it is inferred that the Ries impactor hit the steep Albtrauf escarpment at its toe, in an oblique impact from the north.  相似文献   

5.
We simulated entrainment of carbonates (calcite, dolomite) in silicate impact melts by 1-bar laser melting of silicate–carbonate composite targets, using sandstone, basalt, calcite marble, limestone, dolomite marble, and iron meteorite as starting materials. We demonstrate that carbonate assimilation by silicate melts of variable composition is extremely fast (seconds to minutes), resulting in contamination of silicate melts with carbonate-derived CaO and MgO and release of CO2 at the silicate melt–carbonate interface. We identify several processes, i.e., (1) decomposition of carbonates releases CO2 and produces residual oxides (CaO, MgO); (2) incorporation of residual oxides from proximally dissociating carbonates into silicate melts; (3) rapid back-reactions between residual CaO and CO2 produce idiomorphic calcite crystallites and porous carbonate quench products; (4) high-temperature reactions between Ca-contaminated silicate melts and carbonates yield typical skarn minerals and residual oxide melts; (5) mixing and mingling between Ca- or Ca,Mg-contaminated and Ca- or Ca,Mg-normal silicate melts; (6) precipitation of Ca- or Ca,Mg-rich silicates from contaminated silicate melts upon quenching. Our experiments reproduce many textural and compositional features of typical impact melts originating from silicate–carbonate targets. They reinforce hypotheses that thermal decomposition of carbonates, rapid back-reactions between decomposition products, and incorporation of residual oxides into silicate impact melts are prevailing processes during impact melting of mixed silicate–carbonate targets. However, by comparing our results with previous studies and thermodynamic considerations on the phase diagrams of calcite and quartz, we envisage that carbonate impact melts are readily produced during adiabatic decompression from high shock pressure, but subsequently decompose due to heat influx from coexisting silicate impact melts or hot breccia components. Under certain circumstances, postshock conditions may favor production and conservation of carbonate impact melts. We conclude that the response of mixed carbonate–silicate targets to impact might involve melting and decomposition of carbonates, the dominant response being governed by a complex variety of factors.  相似文献   

6.
Recent studies geared toward understanding the volatile abundances of the lunar interior have focused on the volatile‐bearing accessory mineral apatite. Translating measurements of volatile abundances in lunar apatite into the volatile inventory of the silicate melts from which they crystallized, and ultimately of the mantle source regions of lunar magmas, however, has proved more difficult than initially thought. In this contribution, we report a detailed characterization of mesostasis regions in four Apollo mare basalts (10044, 12064, 15058, and 70035) in order to ascertain the compositions of the melts from which apatite crystallized. The texture, modal mineralogy, and reconstructed bulk composition of these mesostasis regions vary greatly within and between samples. There is no clear relationship between bulk‐rock basaltic composition and that of bulk‐mesostasis regions, indicating that bulk‐rock composition may have little influence on mesostasis compositions. The development of individual melt pockets, combined with the occurrence of silicate liquid immiscibility, exerts greater control on the composition and texture of mesostasis regions. In general, the reconstructed late‐stage lunar melts have roughly andesitic to dacitic compositions with low alkali contents, displaying much higher SiO2 abundances than the bulk compositions of their host magmatic rocks. Relevant partition coefficients for apatite‐melt volatile partitioning under lunar conditions should, therefore, be derived from experiments conducted using intermediate compositions instead of compositions representing mare basalts.  相似文献   

7.
Abstract— The Asuka 881931 meteorite is an unbrecciated ferroan ureilite and consists mainly of equi—granular olivine and pigeonite grains, a metal—sulfide network, interstitial silicates, and glass. Peripheral portions of equigranular olivine grains are often replaced by fine-grained forsterite—metal aggregates and sometimes by fine-grained enstatite—metal aggregates. These aggregates may have been produced from the equigranular olivine by reduction. Peripheral portions of equigranular pigeonite grains also are sometimes replaced by fine-grained orthopyroxene aggregates with tiny patches of Si-rich glass and may have been produced from the pigeonite by reduction reaction with silicate melt. Interstitial silicates are mainly orthopyroxene, magnesian pigeonite, high-Ca pyroxene (diopside/fassaite), and CaO-poor enstatite; and they crystallized from interstitial silicate melt. Interstitial glass is classified into two types—-Si-poor and Si-rich. The Si-poor glass is always in contact with equigranular olivine, but the Si-rich glass never contacts equigranular olivine and is in contact with pyroxene and the metal—sulfide network. Both types of glass were produced from an original interstitial silicate melt, but the Si-poor glass formed mainly by fractional crystallization of pyroxenes, and the Si-rich glass may have formed by addition of Si mainly from nearby metal—sulfide melt, as well as crystallization of pyroxenes. The Si-poor and Si-rich melts were finally quenched as interstitial glasses under rapid cooling conditions.  相似文献   

8.
Abstract— We investigated the ballistically dispersed melts from Meteor Crater, Arizona, USA to determine the stratigraphic extent of its melt zone from the compositional relationship of melts and target rocks. Most melt particles are crystallized, hydrated, and oxidized; pristine glasses are rare. Hydration and oxidation occurred at ambient temperatures long after the impact. The preserved glasses are generally clear and texturally homogeneous, but unlike typical impact melts, they have unusually heterogeneous compositions, both within individual particles and from sample to sample. For example, the average SiO2 for individual particles ranges from 43 to 65%. The projectile content is unusually high and it is distributed bimodally, with specific samples containing either 5–10% or 20–30% FeO. These compositional heterogeneities most likely reflect the high carbonate content of the target rocks and the release of copious CO2 that dispersed the melts, thereby terminating melt flow and mixing. The high projectile content and the CO2 depleted residue of purely sedimentary rocks produced mafic melts that crystallized fine‐grained olivine and pyroxene. The melts fall into three compositional groups reflecting variable proportions of the major target formations, Moenkopi, Kaibab, and Coconino. Least‐square mixing calculations revealed one group to contain 55% Moenkopi, 40% quartz‐rich, upper Kaibab, and 5% meteorite, suggesting a source depth of <30 m from the pre‐impact surface. The other two melt groups have higher contents of meteorite (15–20%) and Kaibab (50–70%) and contain more SiO2 than average Kaibab. The additional quartz may have been derived from Coconino or the upper Kaibab, implying melt depths >90 m or <30 m, respectively. Additional studies, especially hydrocode calculations, are needed to better understand the source depth of these melts and their exceptionally high projectile content.  相似文献   

9.
Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo1–4Fs25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.  相似文献   

10.
Al Haggounia 001 and paired specimens (including Northwest Africa [NWA] 2828 and 7401) are part of a vesicular, incompletely melted, EL chondrite impact melt rock with a mass of ~3 metric tons. The meteorite exhibits numerous shock effects including (1) development of undulose to weak mosaic extinction in low‐Ca pyroxene; (2) dispersion of metal‐sulfide blebs within silicates causing “darkening”; (3) incomplete impact melting wherein some relict chondrules survived; (4) vaporization of troilite, resulting in S2 bubbles that infused the melt; (5) formation of immiscible silicate and metal‐sulfide melts; (6) shock‐induced transportation of the metal‐sulfide melt to distances >10 cm; (7) partial resorption of relict chondrules and coarse silicate grains by the surrounding silicate melt; (8) crystallization of enstatite in the matrix and as overgrowths on relict silicate grains and relict chondrules; (9) crystallization of plagioclase from the melt; and (10) quenching of the vesicular silicate melt. The vesicular samples lost almost all of their metal during the shock event and were less susceptible to terrestrial weathering; in contrast, the samples in which the metal melt accumulated became severely weathered. Literature data indicate the meteorite fell ~23,000 yr ago; numerous secondary phases formed during weathering. Both impact melting and weathering altered the meteorite's bulk chemical composition: e.g., impact melting and loss of a metal‐sulfide melt from NWA 2828 is responsible for bulk depletions in common siderophile elements and in Mn (from alabandite); weathering of oldhamite caused depletions in many rare earth elements; the growth of secondary phases caused enrichments in alkalis, Ga, As, Se, and Au.  相似文献   

11.
Abstract— The impact melt breccias from the Tenoumer crater (consisting of a fine‐grained intergrowth of plagioclase laths, pyroxene crystals, oxides, and glass) display a wide range of porosity and contain a large amount of target rock clasts. Analyses of major elements in impact melt rocks show lower contents of SiO2, Al2O3, and Na2O, and higher contents of MgO, Fe2O3, and CaO, than the felsic rocks (i.e., granites and gneisses) of the basement. In comparison with the bulk analyses of the impact melt, the glass is strongly enriched in Si‐Al, whereas it is depleted both in Mg and Fe; moreover, the impact melt rocks are variably enriched or depleted in some REE with respect to the felsic and mafic bedrock types. Gold is slightly enriched in the impact melt, and Co, Cr, and Ni abundances are possibly due to a contribution from mafic bedrock. Evidences of silicate‐carbonate liquid immiscibility, mainly as spherules and globules of calcite within the silicate glass, have been highlighted. HMX mixing calculation confirm that the impact melt rocks are derived from a mixing of at least six different target lithologies outcropping in the area of the crater. A large contribution is derived from granitoids (50%) and mica schist (17–19%), although amphibolites (?15%), cherty limestones (?10%), and ultrabasites (?6%) components are also present. The very low abundances of PGE in the melt rock seem to come mainly from some ultrabasic target rocks; therefore, the contamination from the meteoritic projectile appears to have been negligible.  相似文献   

12.
Abstract— The enstatite chondrite reckling peak (rkp) a80259 contains feldspathic glass, kamacite, troilite, and unusual sets of parallel fine‐grained enstatite prisms that formed by rapid cooling of shock melts. Metallic Fe,Ni and troilite occur as spherical inclusions in feldspathic glass, reflecting the immiscible Fe‐Ni‐S and feldspathic melts generated during the impact. The Fe‐Ni‐S and feldspathic liquids were injected into fractures in coarse‐grained enstatite and cooled rapidly, resulting in thin (≤ 10 μm) semicontinuous to discontinuous veins and inclusion trails in host enstatite. Whole‐rock melt veins characteristic of heavily shocked ordinary chondrites are conspicuously absent. Raman spectroscopy shows that the feldspathic material is a glass. Elevated MgO and SiO2 contents of the glass indicate that some enstatite and silica were incorporated in the feldspathic melt. Metallic Fe,Ni globules are enclosed by sulfide and exhibit Nienrichment along their margins characteristic of rapid crystallization from a Fe‐Ni‐S liquid. Metal enclosed by sulfide is higher in Si and P than metal in feldspathic glass and enstatite, possibly indicating lower O fugacities in metal/sulfide than in silicate domains. Fine‐grained, elongate enstatite prisms in troilite or feldspathic glass crystallized from local pyroxene melts that formed along precursor grain boundaries, but most of the enstatite in the target rock remained solid during the impact and occurs as deformed, coarsegrained crystals with lower CaO, Al2O3, and FeO than the fine‐grained enstatite. Reckling Peak A80259 represents an intermediate stage of shock melting between unmelted E chondrites and whole‐rock shock melts and melt breccias documented by previous workers. The shock petrogenesis of RKPA80259 reflects the extensive impact processing of the enstatite chondrite parent bodies relative to those of other chondrite types.  相似文献   

13.
We have analyzed glasses in eight howardites with the aim of distinguishing their origins as impact melts or pyroclasts. Although theoretical calculations predict that pyroclastic eruptions could have taken place on Vesta, the occurrence of pyroclastic glasses in HED meteorites has not been documented. This study involved petrographic examination of textures, electron microprobe analysis of major and minor elements, and LA‐ICP‐MS analysis for selected trace elements. Previously documented textural and compositional differences between lunar impact‐melt and pyroclastic glasses partly guided this study. This work yielded no positive identification of pyroclastic glasses. The most likely explanation is that pyroclastic glasses never formed, either because Vesta contains insufficient volatiles to have powered explosive eruptions, or because eruptive conditions produced optically dense fire‐fountains that allowed melt drops to collect as lava ponds. The impact‐melt glasses were grouped (low‐alkali, Ca‐rich, and K‐rich) based on compositions. We suggest that these glasses are the result of impacts onto known HED lithologies. The low‐alkali glasses are impact melts of bulk HED lithologies. We hypothesize that the Ca‐rich and K‐rich glasses result from oversampling of plagioclase and of mesostasis that experienced liquid immiscibility, respectively, during micrometeorite impacts into eucrite targets.  相似文献   

14.
We present results of petrographic, mineralogical, and chemical investigations of three Chelyabinsk meteorite fragments. Three distinct lithologies were identified: light S3 LL5, dark S4–S5 LL5 material, and opaque fine-grained former impact melt. Olivine–spinel thermometry revealed an equilibration temperature of 703 ± 23 °C for the light lithology. All plagioclase seems to be secondary, showing neither shock-induced fractures nor sulfide-metal veinlets. Feldspathic glass can be observed showing features of extensive melting and, in the dark lithology, as maskelynite, lacking melt features and retaining grain boundaries of former plagioclase. Olivine of the dark lithology shows planar deformation features. Impact melt is dominated by Mg-rich olivine and resembles whole-rock melt. Melt veins (<2 mm) are connected to narrower veinlets. Melt vein textures are similar to pegmatite textures showing chilled margins, a zone of inward-grown elongated crystals and central vugs, suggesting crystallization from supercooled melt. Sulfide-metal droplets indicate liquid immiscibility of both silicate and sulfide as well as sulfide and metal melts. Impact melting may have been an important factor for differentiation of primitive planetary bodies. Graphite associated with micrometer-sized melt inclusions in primary olivine was detected by Raman mapping. Carbon isotopic studies of graphite could be applied to test a possible presolar origin.  相似文献   

15.
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16.
Abstract— A series of 59 impacts in the laboratory reduced a coherent 460 g piece of the L6 ordinary chondrite ALH 85017 to a coarse‐grained “regolith.” We then subjected the 125–250 μm fines from this sample to reverberation shock stresses of 14.5–67 GPa in order to delineate the melting behavior of porous, unconsolidated, chondritic asteroid surfaces during meteorite impact. The initial pore space (40–50%) was completely closed at 14.5 GPa and a dense aggregate of interlocking grains resulted. Grain‐boundary melting commenced at <27 GPa and ?50% of the total charge was molten at 67 GPa; this stress corresponds to typical asteroid impacts at ?5 km/sec. Melting of the entire sample most likely mandates >80 GPa, which is associated with impact velocities >8 km/sec. The Fe‐Ni and troilite clasts of the original meteorite melted with particular ease, forming immiscible melts that are finely disseminated throughout the silicate glass. These metal droplets are highly variable in size, extending to <100 nm and most likely to superparamagnetic domains; such opaques are also observed in the natural melt veins of ordinary chondrites. It follows that melting and dissemination of pre‐existing, Fe‐rich phases may substantially affect the optical properties of asteroidal surfaces. It seems unnecessary to invoke reduction of Fe2+ (or Fe3+) by sputtering or impact‐processes—in analogy to the lunar surface—to produce “space weathering” effects on S‐type asteroids. We note that HED meteorites contain ample FeO (comparable to that in lunar basalts) for reduction processes to take place, yet their probable parent object(s), Vesta and its collisional fragments, display substantially unweathered surfaces. Howardites, eucrites, and diogenites (HEDs), however, contain little native metal (typically <0.5%), in contrast to ordinary chondrites (commonly 10–15%) and their S‐type parent objects. These considerations suggest that the modal content of native metal and sulfides is more important for space weathering on asteroids than total FeO.  相似文献   

17.
Abstract— The Chicxulub Scientific Drilling Project (CSDP), Mexico, produced a continuous core of material from depths of 404 to 1511 m in the Yaxcopoil‐1 (Yax‐1) borehole, revealing (top to bottom) Tertiary marine sediments, polymict breccias, an impact melt unit, and one or more blocks of Cretaceous target sediments that are crosscut with impact‐generated dikes, in a region that lies between the peak ring and final crater rim. The impact melt and breccias in the Yax‐1 borehole are 100 m thick, which is approximately 1/5 the thickness of breccias and melts exposed in the Yucatán‐6 exploration hole, which is also thought to be located between the peak ring and final rim of the Chicxulub crater. The sequence and composition of impact melts and breccias are grossly similar to those in the Yucatán‐6 hole. Compared to breccias in other impact craters, the Chicxulub breccias are incredibly rich in silicate melt fragments (up to 84% versus 30 to 50%, for example, in the Ries). The melt in the Yax‐1 hole was produced largely from the silicate basement lithologies that lie beneath a 3 km‐ thick carbonate platform in the target area. Small amounts of immiscible molten carbonate were ejected with the silicate melt, and clastic carbonate often forms the matrix of the polymict breccias. The melt unit appears to have been deposited while molten but brecciated after solidification. The melt fragments in the polymict breccias appear to have solidified in flight, before deposition, and fractured during transport and deposition.  相似文献   

18.
Abstract— We present here ion microprobe analyses of rare earth and other selected trace and minor elements in pyroxenes of shergottite Queen Alexandra Range 94201 and lunar basalt 15555. Pyroxene zonation patterns record the crystallization histories of these two basaltic samples from Mars and the Moon, respectively, and allow a comparison of mafic melt evolution on these two planetary bodies. Elemental abundances and trends in pyroxenes of these two rocks indicate that their minerals formed by continuous, closed system fractional crystallization of their respective parent melts. This further supports the idea that QUE 94201 closely represents the composition of a true Martian basaltic melt (McSween et al., 1996). The main differences in pyroxene elemental zonation patterns in these two objects are attributed to earlier crystallization of whitlockite in QUE 94201 (i.e., before the Fe-rich pyroxenes) than in 15555 (after the Fe-rich pyroxenes). The size of Eu anomalies in pyroxenes of QUE 94201 is intermediate between that in pyroxenes of 15555 and the other shergottites and may imply that fO2 conditions during crystallization of this Martian basalt were significantly more reducing than for other shergottites, although not quite as reducing as for lunar basalts. Cerium anomalies appear to be less prevalent in pyroxenes of QUE 94201 than other Antarctic shergottites and could be indicative of lesser degree of weathering in the Antarctic.  相似文献   

19.
We shocked calcite in an unconfined environment by launching small marble cylinders at 0.8–5.5 km s?1 into aluminum or copper plates, producing shock stresses between 5 and 79 GPa. The resulting 5–20 mm craters contained intimately mixed clastic and molten projectile residues over the entire pressure range, with melting commencing already at 5 GPa. Stoichiometrically pure calcite melts were not observed as all melts contained target metal. Some of these residues were distinctly depleted in CO2 and some contained even tiny CaO crystals, thus illustrating partial to complete loss of CO2. We interpret a thin seam of finely crystalline calcite to be the product of back reactions between CaO and CO2. The amount of carbonate residue in these craters, especially those at low velocities (<2 km s?1), is dramatically less than that of silicate impactors in similar cratering experiments, and we suggest that this is due to substantial outgassing of CO2. Similarly, the volume of carbonate melts relative to the volume of limestone or dolomite in many terrestrial crater structures seems insignificant as well, as is the volume of carbonate melt compared to the volume of impact melts derived from silicates. These volume considerations suggest that volatilization of CO2 is the dominant process in carbonate‐containing targets. Because we have difficulties in explaining naturally occurring calcite melts by shock processes in dolomite‐dominated targets, we speculate—essentially via process of elimination—that such carbonate melt blebs might be condensation products from an impact‐produced vapor cloud.  相似文献   

20.
The Lonar crater is a ~0.57‐Myr‐old impact structure located in the Deccan Traps of the Indian peninsula. It probably represents the best‐preserved impact structure hosted in continental flood basalts, providing unique opportunities to study processes of impact cratering in basaltic targets. Here we present highly siderophile element (HSE) abundances and Sr‐Nd and Os isotope data for target basalts and impactites (impact glasses and impact melt rocks) from the Lonar area. These tools may enable us to better constrain the interplay of a variety of impact‐related processes such as mixing, volatilization, and contamination. Strontium and Nd isotopic compositions of impactites confirm and extend earlier suggestions about the incorporation of ancient basement rocks in Lonar impactites. In the Re‐Os isochron plot, target basalts exhibit considerable scatter around a 65.6 Myr Re‐Os reference isochron, most likely reflecting weathering and/or magma replenishment processes. Most impactites plot at distinctly lower 187Re/188Os and 187Os/188Os ratios compared to the target rocks and exhibit up to two orders of magnitude higher abundances of Ir, Os, and Ru. Moreover, the impactites show near‐chondritic interelement ratios of HSE. We interpret our results in terms of an addition of up to 0.03% of a chondritc component to most impact glasses and impact melt rocks. The magnitude of the admixture is significantly lower than the earlier reported 12–20 wt% of extraterrestrial component for Lonar impact spherules, reflecting the typical difference in the distribution of projectile component between impact glass spherules and bulk impactites.  相似文献   

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