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1.
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   

2.
Abstract— We report Sr-Nd isotope parameters, rare earth element (REE), and major element data for isolated findings of tektite-like objects from western Siberia (urengoites, South-Ural glass), as well as for two indochinites. The latter were recovered in Vietnam and their overall geochemical characteristics equal those of other tektites from the indochinite subgroup of the Australasian strewn field. The three urengoites (～24 Ma) are extremely silica-rich (89 to 96 wt% SiC2), and their REE abundances vary between 45 and 76 ppm. With LaN/YbN ranging from 7.6 to 10.4 and EuN/EU* between 0.69 and 0.75, their REE distribution patterns match that of average upper crust. The urengoites have present-day ?Sr of +155 to +174 and ?Nd ranging from ?18 to ?23. Their model ages in million years are: TSruR = 1200 up to 4060 and TNdcHUR = 1570 up to 2070. Data points for the urengoites plot colinearly in the Rb-Sr evolution diagram. The age corresponding to the slope is 183 ± 30 Ma (2s?), which is indistinguishable from the intercept age of 211 Ma in the TSrUR vs. l/fRb diagram. Rubidium-strontium and Sm-Nd systematics of the urengoites indicate a heterogeneous precursor material, derived from Paleoproterozoic continental crust, which underwent Rb/Sr fractionation and partial Sr isotope homogenization in Jurassic times. Any relation between the urengoites and the Haughton impact crater, having within 2s? errors an identical age, can be excluded on the basis of isotope relationships and geochemical data. The only known South-Ural glass (～6.2 Ma) is characterized by intermediate SiO2 (65 wt%), high Al2O3 (14 wt%) and CaO (12 wt%), and low FeOTOT (0.4 wt%) contents. This unique tektite-like object contains 110 ppm REE displaying a steeply negative C1 normalized distribution with LaN/YbN of 17, and EuN/Eu1 of 0.71. The Rb abundance (10 ppm) and Rb/Sr ratio are low, and combined with a “crustal” 87Sr/86Sr ratio of 0.722, yielding an unrealistic TSruR age of 2.5 Ga. The Rb-Sr systematics imply a rather recent parent/daughter element decoupling. The TNdCHUR age of the South-Ural glass is ～1690 Ma. Geochemical data suggest that urengoites and the South-Ural glass belong to two discrete groups of tektites, whose source craters remain to be discovered.  相似文献   

3.
The unique occurrence of abundant (~1 vol%) near‐pure‐Fe metal in the Camel Donga eucrite is more complicated than previously believed. In addition to that component of groundmass metal, scattered within the meteorite are discrete nodules of much higher kamacite abundance. We have studied the petrology and composition of two of these nodules in the form of samples we call CD2 and CD3. The nodules are ovoids 11 (CD2) to 15 (CD3) mm across, with metal, or inferred preweathering metal, abundances of 12–17 vol% (CD2 is unfortunately quite weathered). The CD3 nodule also includes at its center a 5 mm ovoid clumping (6 vol%) of F‐apatite. Both nodules are fine‐grained, so the high Fe metal and apatite contents are clearly not flukes of inadequate sampling. The metals within the nodules are distinctly Ni‐rich (0.3–0.6 wt%) compared to the pure‐Fe (Ni generally 0.01 wt%) groundmass metals. Bulk analyses of three pieces of the CD2 nodule show that trace siderophile elements Ir, Os, and Co are commensurately enriched; Au is enriched to a lesser degree. The siderophile evidence shows the nodules did not form by in situ reduction of pyroxene FeO. Moreover, the nodules do not show features such as silica‐phase enrichment or pyroxene with reduced FeO (as constrained by FeO/MgO and especially FeO/MnO) predicted by the in situ reduction model. The oxide minerals, even in groundmass samples well away from the nodules, also show little evidence of reduction. Although the nodule boundaries are generally sharp, groundmass‐metal Ni content is anti‐correlated with distance from the CD3 nodule. We infer that the nodules represent materials that originated within impactors into the Camel Donga portion of the eucrite crust, but probably were profoundly altered during later metamorphism/metasomatism. Origin of the pure‐Fe groundmass metal remains enigmatic. In situ reduction probably played an important role, and association in the same meteorite of the Fe‐nodules is probably significant. But the fluid during alteration was probably not (as previously modeled) purely S and O, of simple heat‐driven internal derivation. We conjecture a two‐stage metasomatism, as fluids passed through Camel Donga after impact heating of volatile‐rich chondritic masses (survivors of gentle accretionary impacts) within the nearby crust. First, reduction to form troilite may have been triggered by fluids rich in S2 and CO (derived from the protonodules?), and then in a distinct later stage, fluids were (comparatively) H2O‐rich, and thus reacted with troilite to form pure‐Fe metal along with H2S and SO2. The early eucrite crust was in places a dynamic fluid‐bearing environment that hosted complex chemical processes, including some that engendered significant diversity among metal+sulfide alterations.  相似文献   

4.
Abstract— We report here the petrography, mineralogy, and geochemistry of lunar meteorite Sayh al Uhaymir 300 (SaU 300). SaU 300 is dominated by a fine‐grained crystalline matrix surrounding mineral fragments (plagioclase, pyroxene, olivine, and ilmenite) and lithic clasts (mainly feldspathic to noritic). Mare basalt and KREEPy rocks are absent. Glass melt veins and impact melts are present, indicating that the rock has been subjected to a second impact event. FeNi metal and troilite grains were observed in the matrix. Major element concentrations of SaU 300 (Al2O3 21.6 wt% and FeO 8.16 wt%) are very similar to those of two basalt‐bearing feldspathic regolith breccias: Calcalong Creek and Yamato (Y‐) 983885. However, the rare earth element (REE) abundances and pattern of SaU 300 resemble the patterns of feldspathic highlands meteorites (e.g., Queen Alexandra Range (QUE) 93069 and Dar al Gani (DaG) 400), and the average lunar highlands crust. It has a relatively LREE‐enriched (7 to 10 x CI) pattern with a positive Eu anomaly (?11 x CI). Values of Fe/Mn ratios of olivine, pyroxene, and the bulk sample are essentially consistent with a lunar origin. SaU 300 also contains high siderophile abundances with a chondritic Ni/Ir ratio. SaU 300 has experienced moderate terrestrial weathering as its bulk Sr concentration is elevated compared to other lunar meteorites and Apollo and Luna samples. Mineral chemistry and trace element abundances of SaU 300 fall within the ranges of lunar feldspathic meteorites and FAN rocks. SaU 300 is a feldspathic impact‐melt breccia predominantly composed of feldspathic highlands rocks with a small amount of mafic component. With a bulk Mg# of 0.67, it is the most mafic of the feldspathic meteorites and represents a lunar surface composition distinct from any other known lunar meteorites. On the basis of its low Th concentration (0.46 ppm) and its lack of KREEPy and mare basaltic components, the source region of SaU 300 could have been within a highland terrain, a great distance from the Imbrium impact basin, probably on the far side of the Moon.  相似文献   

5.
Abstract— We report on the major and trace element abundances of 18 diogenites, and O‐isotopes for 3 of them. Our analyses extend significantly the diogenite compositional range, both in respect of Mg‐rich (e.g., Meteorite Hills [MET] 00425, MgO = 31.5 wt%) and Mg‐poor varieties (e.g., Dhofar 700, MgO = 23 wt%). The wide ranges of siderophile and chalcophile element abundances are well explained by the presence of inhomogeneously distributed sulfide or metal grains within the analyzed chips. The behavior of incompatible elements in diogenites is more complex, as exemplified by the diversity of their REE patterns. Apart from a few diogenite samples that contain minute amounts of phosphate, and whose incompatible element abundances are unlike the orthopyroxene ones, the range of incompatible element abundances, and particularly the range of Dy/Yb ratios in diogenites is best explained by the diversity of their parental melts. We estimate that the FeO/MgO ratios of the diogenite parental melts range from about 1.4 to 3.5 and therefore largely overlap the values obtained for non‐cumulate eucrites. Our results rule out the often accepted view that all the diogenites formed from parental melts more primitive than eucrites during the crystallization of a magma ocean. Instead, they point to a more complex history, and suggest that diogenites were derived from liquids produced by the remelting of cumulates formed from the magma ocean.  相似文献   

6.
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   

7.
Abstract– Impact events are a significant surface‐modifying process on solar system objects lacking frequent resurfacing by atmospheric or igneous processes. To better explore the effects of impacts on surface materials, we measured the water and trace element compositions of tektites from Da Lat, Vietnam. Fourier transform infrared spectroscopy was used for water measurements and laser ablation inductively coupled plasma mass spectrometry was used for trace element measurements. Consistent with previous investigations of tektites, we found that the samples are depleted in volatile metals (e.g., Zn, Pb) as well as in water compared with the average continental crust, although water contents are still extremely high for rocks melted at atmospheric pressure. While Zn and Pb concentrations are linearly correlated with each other, there is no correlation between H2O and Zn or Pb contents. Combined with water contents of other tektites in the Australasian strewn field, our results demonstrate that the source impact occurred at a wet site in or off the coast of the Indochina peninsula.  相似文献   

8.
We present a study of the petrology and geochemistry of basaltic shergottite Northwest Africa 2975 (NWA 2975). NWA 2975 is a medium‐grained basalt with subophitic to granular texture. Electron microprobe (EMP) analyses show two distinct pyroxene compositional trends and patchy compositional zoning patterns distinct from those observed in other meteorites such as Shergotty or QUE 94201. As no bulk sample was available to us for whole rock measurements, we characterized the fusion crust and its variability by secondary ion mass spectrometer (SIMS) measurements and laser ablation inductively coupled plasma spectroscopy (LA‐ICP‐MS) analyses as a best‐available proxy for the bulk rock composition. The fusion crust major element composition is comparable to the bulk composition of other enriched basaltic shergottites, placing NWA 2975 within that sample group. The CI‐normalized REE (rare earth element) patterns are flat and also parallel to those of other enriched basaltic shergottites. Merrillite is the major REE carrier and has a flat REE pattern with slight depletion of Eu, parallel to REE patterns of merrillites from other basaltic shergottites. The oxidation state of NWA 2975 calculated from Fe‐Ti oxide pairs is NNO‐1.86, close to the QFM buffer. NWA 2975 represents a sample from the oxidized and enriched shergottite group, and our measurements and constraints on its origin are consistent with the hypothesis of two distinct Martian mantle reservoirs: a reduced, LREE‐depleted reservoir and an oxidized, LREE‐enriched reservoir. Stishovite, possibly seifertite, and dense SiO2 glass were also identified in the meteorite, allowing us to infer that NWA 2975 experienced a realistic shock pressure of ~30 GPa.  相似文献   

9.
Abstract– Fragments of magnesian anorthositic granulite are found in the lunar highlands meteorites Allan Hills (ALH) A81005 and Dhofar (Dho) 309. Five analyzed clasts of meteoritic magnesian anorthositic granulite have Mg′ [molar Mg/(Mg + Fe)] = 81–87; FeO ≈ 5% wt; Al2O3 ≈ 22% wt; rare earth elements abundances ≈ 0.5–2 × CI (except Eu ≈ 10 × CI); and low Ni and Co in a non‐chondritic ratio. The clasts have nearly identical chemical compositions, even though their host meteorites formed at different places on the Moon. These magnesian anorthositic granulites are distinct from other highlands materials in their unique combination of mineral proportions, Mg′, REE abundances and patterns, Ti/Sm ratio, and Sc/Sm ratio. Their Mg′ is too high for a close relationship to ferroan anorthosites, or to have formed as flotation cumulates from the lunar magma ocean. Compositions of these magnesian anorthositic granulites cannot be modeled as mixtures of, or fractionates from, known lunar rocks. However, compositions of lunar highlands meteorites can be represented as mixtures of magnesian anorthositic granulite, ferroan anorthosite, mare basalt, and KREEP. Meteoritic magnesian anorthositic granulite is a good candidate for the magnesian highlands component inferred from Apollo highland impactites: magnesian, feldspathic, and REE‐poor. Bulk compositions of meteorite magnesian anorthositic granulites are comparable to those inferred for parts of the lunar farside (the Feldspathic Highlands Terrane): ～4.5 wt% FeO; ～28 wt% Al2O3; and Th <1 ppm. Thus, magnesian anorthositic granulite may be a widespread and abundant component of the lunar highlands.  相似文献   

10.
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   

11.
Abstract— All groups of chondritic meteorites contain discrete grains of forsteritic olivine with FeO contents below 1 wt% and high concentrations of refractory elements such as Ca, Al, and Ti. Ten such grains (52 to 754 μg) with minor amounts of adhering matrix were separated from the Allende meteorite. After bulk chemical analysis by instrumental neutron activation analysis (INAA), some samples were analyzed with an electron microprobe and some with an ion microprobe. Matrix that accreted to the forsterite grains has a well‐defined unique composition, different from average Allende matrix in having higher Cr and lower Ni and Co contents, which implies limited mixing of Allende matrix. All samples have approximately chondritic relative abundances of refractory elements Ca, Al, Sc, and rare‐earth elements (REE), although some of these elements, such as Al, do not quantitatively reside in forsterite; whereas others (e.g., Ca) are intrinsic to forsterite. The chondritic refractory element ratios in bulk samples, the generally high abundance level of refractory elements, and the presence of Ca‐Al‐Ti‐rich glass inclusions suggest a genetic relationship of refractory condensates with forsteritic olivine. The Ca‐Al‐Ti‐rich glasses may have acted as nuclei for forsterite condensation. Arguments are presented that exclude an origin of refractory forsterite by crystallization from melts with compositions characteristic of Allende chondrules: (a) All forsterite grains have CaO contents between 0.5 and 0.7 wt% with no apparent zoning, requiring voluminous parental melts with 18 to 20 wt% CaO, far above the average CaO content of Allende chondrules. Similar arguments apply to Al contents. (b) The low FeO content of refractory forsterite of 0.2‐0.4 wt% imposes an upper limit of ～1 wt% of FeO on the parental melt, too low for ordinary and carbonaceous chondrule melts, (c) The Mn contents of refractory forsterites are between 30 to 40 ppm. This is at least one order of magnitude below the Mn content of chondrule olivines in all classes of meteorites. The observed Mn contents of refractory forsterite are much too low for equilibrium between olivine and melts of chondrule composition, (d) As shown earlier, refractory forsterites have O‐isotopic compositions different from chondrules (Weinbruch et al., 1993a). Refractory olivines in carbonaceous chondrites are found in matrix and in chondrules. The compositional similarity of both types was taken to indicate that all refractory forsterites formed inside chondrules (e.g., Jones, 1992). As refractory forsterite cannot have formed by crystallization from chondrule melts, we conclude that refractory forsterite from chondrules are relic grains that survived chondrule melting and probably formed in the same way as refractory forsterite enclosed in matrix. We favor an origin of refractory forsterite by condensation from an oxidized nebular gas.  相似文献   

12.
Abstract— An experimental investigation of the Shergotty meteorite was performed at 0.1 MPa under anhydrous conditions at the quartz‐fayalite‐magnetite buffer and at 100 and 200 MPa under H2O‐saturated conditions at the nickel‐nickel oxide buffer. The results of these experiments are used to infer magmatic conditions recorded by co‐crystallization of augite and pigeonite phenocrysts found in Shergotty and to investigate the effect of H2O on fractional crystallization paths followed by shergottite magmas. The phase relations and compositions of the homogeneous magnesian pyroxene cores in Shergotty are most closely approximated by crystallization under H2O‐saturated conditions at 1120 °C (± 10 °C) and 56 MPa (± 18 MPa), corresponding to dissolved H2O contents of 1.8 wt% (± 0.6 wt%) and a depth of 5 km (± 1.5 km) in the martian crust (uncertainties are 2s? values). The Shergotty magma then lost this water during ascent and eruption. Fractional crystallization of the Shergotty magma under anhydrous conditions produces liquids that follow a strong Fe‐enrichment trend at nearly constant SiO2. Crystallization under H2O‐saturated conditions generates derivative liquids, depleted in FeO and Al2O3 and enriched in SiO2, that are compositionally similar to the Mars Pathfinder andesite rock composition. The presence of ～1.8 wt% water in Shergotty parental magmas could result from assimilation of hydrated crustal materials or from dehydration of hydrous phases in the mantle source region.  相似文献   

13.
Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO2 phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr2O3) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na2O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.  相似文献   

14.
Abstract— We have studied the CB carbonaceous chondrites Queen Alexandra Range (QUE) 94411, Hammadah al Hamra (HH) 237, and Bencubbin with an emphasis on the petrographical and mineralogical effects of the shock processing that these meteorite assemblages have undergone. Iron‐nickel metal and chondrule silicates are the main components in these meteorites. These high‐temperature components are held together by shock melts consisting of droplets of dendritically intergrown Fe,Ni‐metal/sulfide embedded in silicate glass, which is substantially more FeO‐rich (30–40 wt%) than the chondrule silicates (FeO <5 wt%). Fine‐grained matrix material, which is a major component in most other chondrite classes, is extremely scarce in QUE 94411 and HH 237, and has not been observed in Bencubbin. This material occurs as rare, hydrated matrix lumps with major and minor element abundances roughly similar to the ferrous silicate shock melts (and CI). We infer that hydrated, fine‐grained material, compositionally similar to these matrix lumps, was originally present between the Fe,Ni‐metal grains and chondrules, but was preferentially shock melted. Other shock‐related features in QUE 94411, HH 237, and Bencubbin include an alignment and occasionally strong plastic deformation of metal and chondrule fragments. The existence of chemically zoned and metastable Fe,Ni‐metal condensates in direct contact with shock melts indicates that the shock did not substantially increase the average temperature of the rock. Because porphyritic olivine‐pyroxene chondrules are absent in QUE 94411, HH 237, and Bencubbin, it is difficult to determine the precise shock stage of these meteorites, but the shock was probably relatively light (S2–S3), consistent with a bulk temperature increase of the assemblages of less than ?300 °C. The apparently similar shock processing of Bencubbin, Weatherford, Gujba (CBa) and QUE 94411/HH 237 (CBb) supports the idea of a common asteroidal parent body for these meteorites.  相似文献   

15.
Two irghizites, three zhamanshinites and one sample each of lechatelierite, vein-quartz, Palaeogene silty clay and Palaeogene quartzite were analyzed using neutron activation analysis. A silicate analysis of the Palaeogene silty clay has also been performed, as well as an incomplete analysis of the Palaeogene quartzite from the Zhamanshin impact crater. The REE abundances of irghizites resemble those of sedimentary rocks. On the Köhler and Raaz diagram all projection points of irghizites lie inside the field of tektites, and indicate that they were derived from terrestrial sedimentary rocks. The Zhamanshin impact glasses may be divided into three types: (a) silica-rich zhamanshinites (x?SiO2 = 73.89%), (b) zhamanshinites (x?SiO2 = 54.34%), and (c) silica-poor zhamanshinites (x?SiO2 = 39.64%). These are also characterized by varying proportions of alkalis and Al. Mn and Ca contents. Irghizites and silica-rich zhamanshinites display a depletion of Eu. Zhamanshinites do not show this Eu depletion. Partial melting is assumed to be an important process in the origin of zhamanshinites.  相似文献   

16.
Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al2O3, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An96.9Ab3.0Or0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm2 exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO2 than any mare basalt. It also has higher FeO and lower Al2O3 than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.  相似文献   

17.
The lunar interior is comprised of two major petrological provinces: (1) an outer zone several hundred km thick which experienced partial melting and crystallization differentiation 4.4–4.6 b.y. ago to form the lunar crust together with an underlying complementary zone of ultramafic cumulates and residua, and (2) the primordial deep interior which was the source region for mare basalts (3.2–3.8 b.y.) and had previously been contaminated to varying degrees with highly fractionated material derived from the 4.4–4.6 b.y. differentiation event. In both major petrologic provinces, basaltic magmas have been produced by partial melting. The chemical characteristics and high-pressure phase relationships of these magmas can be used to constrain the bulk compositions of their respective source regions.Primitive low-Ti mare basalts (e.g., 12009, 12002, 15555 and Green Glass) possessing high normative olivine and high Mg and Cr contents, provide the most direct evidence upon the composition of the primordial deep lunar interior. This composition, as estimated on the basis of high pressure equilibria displayed by the above basalts, combined with other geochemical criteria, is found to consist of orthopyroxene + clinopyroxene + olivine with total pyroxenes > olivine, 100 MgO/(MgO + FeO) = 75–80, about 4% of CaO and Al2O3 and 2× chondritic abundances of REE, U and Th. This composition is similar to that of the earth's mantle except for a higher pyroxene/olivine ratio and lower 100 MgO/(MgO + FeO).The lunar crust is believed to have formed by plagioclase elutriation within a vast ocean of parental basaltic magma. The composition of the latter is found experimentally by removing liquidus plagioclase from the observed mean upper crust (gabbroic anorthosite) composition, until the resulting composition becomes multiply saturated with plagioclase and a ferromagnesian phase (olivine). This parental basaltic composition is almost identical with terrestrial oceanic tholeiites, except for partial depletion in the two most volatile components, Na2 and SiO2. Similarity between these two most abundant classes of lunar and terrestrial basaltic magmas strongly implies corresponding similarities between their source regions. The bulk composition of the outer 400 km of the Moon as constrained by the 4.6-4.4 b.y. parental basaltic magma is found to be peridotitic, with olivine > pyroxene, 100 MgO/ (MgO + FeO) 86, and about 2× chondritic abundances of Ca, Al and REE. The Moon thus appears to have a zoned structure, with the deep interior (below 400 km) possessing somewhat higher contents of FeO and SiO2 than the outer 400 km. This zoned model, derived exclusively on petrological grounds, provides a quantitative explanation of the Moon's mean density, moment of inertia and seismic velocity profile.The bulk composition of the entire Moon, thus obtained, is very similar to the pyrolite model composition for the Earth's mantle, except that the Moon is depleted in Na (and other volatile elements) and somewhat enriched in iron. The similarity in major element composition extends also to the abundances of REE, U and Th. These compositional similarities, combined with the identity in oxygen isotope ratios between the Moon and the Earth's mantle, are strongly suggestive of a common genetic relationship.  相似文献   

18.
Abstract– We studied three large (2–4 mm diameter) igneous‐textured inclusions in the Buzzard Coulee (H4) chondrite using microanalytical techniques (OLM, SEM, EMPA, SIMS) to better elucidate the origins of igneous inclusions in ordinary chondrites. The inclusions are clasts that come in two varieties (1) white inclusions Bz‐1 and Bz‐2 represent a nearly holocrystalline assemblage of low‐Ca and high‐Ca pyroxene (63–66 area%) and cristobalite (33–36%) and (2) tan inclusion Bz‐3 is glass‐rich (approximately 60%) with low‐Ca and high‐Ca pyroxene phenocrysts. The bulk compositions of the inclusions determined by modal reconstruction are all SiO2‐rich (approximately 67 wt% for Bz‐1 and Bz‐2, approximately 62% for Bz‐3), but Bz‐3 is enriched in incompatible elements (e.g., REE approximately 4–5 × CI abundances), whereas Bz‐2 and Bz‐1 are depleted in those elements that are most incompatible in pyroxene (e.g., La‐Ho approximately 0.15–0.4 × CI abundances). These bulk compositions do not resemble what one would expect for partial or complete shock melting of a chondritic precursor, and show no evidence for overall volatility control. We infer that the inclusions originated through igneous differentiation and FeO reduction, with Bz‐3 forming as an “andesitic” partial melt (approximately 30–40% partial melting of an H chondrite precursor), and Bz‐1 and Bz‐2 forming as pyroxene‐cristobalite cumulates from an Si‐rich melt. We suggest that both types of melts experienced a period of transit through a cold, low‐pressure space environment in which cooling, FeO reduction, and interaction with a vapor occurred. Melts may have been lofted into space by excavation or splashing during collisions, or by pyroclastic volcanism. Our results indicate intriguing similarities between the inclusions in Buzzard Coulee and the silicates in some iron (IIE‐type) and stony iron (IVA‐type) meteorites, suggesting a genetic relationship.  相似文献   

19.
Dar al Gani (DaG) 400, Meteorite Hills (MET) 01210, Pecora Escarpment (PCA) 02007, and MacAlpine Hills (MAC) 88104/88105 are lunar regolith breccia meteorites that provide sampling of the lunar surface from regions of the Moon that were not visited by the US Apollo or Soviet Luna sample return missions. They contain a heterogeneous clast population from a range of typical lunar lithologies. DaG 400, PCA 02007, and MAC 88104/88105 are primarily feldspathic in nature, and MET 01210 is composed of mare basalt material mixed with a lesser amount of feldspathic material. Here we present a compositional study of the impact melt and impact melt breccia clast population (i.e., clasts that were generated in impact cratering melting processes) within these meteorites using in situ electron microprobe and LA‐ICP‐MS techniques. Results show that all of the meteorites are dominated by impact lithologies that are relatively ferroan (Mg#<70), have high Sc/Sm ratios (typically >10), and have low incompatible trace element (ITE) concentrations (i.e., typically <3.2 ppm Sm, <1.5 ppm Th). Feldspathic impact melt in DaG 400, PCA 02007, and MAC 88104/05 are similar in composition to that estimated composition for upper feldspathic lunar crust ( Korotev et al. 2003 ). However, these melt types are more mafic (i.e., less Eu, less Sr, more Sc) than feldspathic impact melts returned by the Apollo 16 mission (e.g., the group 3 and 4 varieties). Mafic impact melt clasts are common in MET 01210 and less common in PCA 02007 and MAC 88104/05. We show that unlike the Apollo mafic impact melt groups ( Jolliff 1998 ), these meteorite impact melts were not formed from melting large amounts of KREEP‐rich (typically >10 ppm Sm), High Magnesium Suite (typically >70 Mg#) or High Alkali Suite (high ITEs, Sc/Sm ratios <2) target rocks. Instead the meteorite mafic melts are more ferroan, KREEP‐poor and Sc‐rich, and represent mixing between feldspathic lithologies and low‐Ti or very low‐Ti (VLT) basalts. As PCA 02007 and MAC 88104/05 were likely sourced from the Outer‐Feldspathic Highlands Terrane our findings suggest that these predominantly feldspathic regions commonly contain a VLT to low‐Ti basalt contribution.  相似文献   

20.
A significant opaque component in Mercury’s crust is inferred based on albedo and spectral observations. Previous workers have favored iron-titanium bearing oxide minerals as the spectrally neutral opaque. A consequence of this hypothesis is that Mercury’s surface would have a high FeO content. An array of remote sensing techniques have not provided definitive constraints on the FeO content of Mercury’s surface. However, spectral observations have not detected a diagnostic 1 μm absorption band and have thus limited the FeO in coexisting silicates to <2 wt.% FeO. In this paper, we assess equilibrium among oxide and silicate minerals to constrain the distribution of iron between opaque oxides and silicates under a variety of environmental conditions. Equilibrium modeling is favored here because the geologic process that produced Mercury’s low-albedo intermediate terrain must have occurred globally, which favors a common widespread igneous process. Based on our modeling, we find that iron-rich ilmenite cannot occur with silicates that do not display a 1 μm absorption feature unless plagioclase abundances are high. However, such high plagioclase abundances are precluded by Mercury’s low albedo. Incorporating equilibrium crystallization modeling with spectral and albedo constraints we find the iron abundance of Mercury’s intermediate terrain is ?10 wt.% FeO. This intermediate iron composition matches constraints provided by visible albedo and total neutron absorption observed by MESSENGER. In fact, the total neutron absorption of mixtures of oxide, plagioclase, olivine and pyroxene for the oxide abundances estimated for Mercury, favor Mg-rich members of the ilmenite-geikielite solid-solution series. This work offers compositional constraints for Fe, Ti, and Mg that will be testable by various MESSENGER instrument data sets after it begins its orbital mission.  相似文献   

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