首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 390 毫秒
1.
Abstract— We report on the bulk composition and petrography of four new basaltic meteorites found in Antarctica—LAP (LaPaz Icefield) 02205, LAP 02224, LAP 02226, and LAP 02436—and compare the LAP meteorites to other lunar mare basalts. The LAP meteorites are coarse‐grained (up to 1.5 mm), subophitic low‐Ti basalts composed predominantly of pyroxene and plagioclase, with minor amounts of olivine, ilmenite, and a groundmass dominated by fayalite and cristobalite. All of our observations and results support the hypothesis that the LAP stones are mutually paired with each other. In detail, the geochemistry of LAP is unlike those of any previously studied lunar basalt except lunar meteorite NWA (Northwest Africa) 032. The similarities between LAP and NWA 032 are so strong that the two meteorites are almost certainly source crater paired and could be two different samples of a single basalt flow. Petrogenetic modeling suggests that the parent melt of LAP (and NWA 032) is generally similar to Apollo 15 low‐Ti, yellow picritic glass beads, and that the source region for LAP comes from a similar region of the lunar mantle as previously analyzed lunar basalts.  相似文献   

2.
Abstract— Five basaltic meteorites from the LaPaz ice field are paired on the basis of their mineralogy and texture, and represent a unique basalt type distinct from those in the Apollo or Luna sample collections. LaPaz Icefield (LAP) 02205, LAP 02224, LAP 02226, LAP 02436 and LAP 03632 all contain plagioclase, pyroxene, ilmenite, spinel, olivine, and minor troilite, metal, phosphate, baddeleyite and silica (cristobalite). Brown glassy melt veins are ubiquitous and cross the primary igneous texture. Plagioclase, the major mineral and occurring as laths in a subophitic texture, is of narrow compositional range, from An85–89. Pyroxene, also a major mineral, is strongly zoned, from augite and pigeonite cores to very iron‐rich rims. Ilmenite laths comprise approximately 3–5% of the basalts. Spinels show a large compositional range, comparable to that documented in Apollo 15 basalts, indicating an early chromite‐rich stage followed by an intermediate to late stage with Cr‐rich ulvöspinel. Relatively large, subhedral to skeletal olivine crystals (Fo46–62) are sparse, and are too Forich to be in equilibrium with the bulk rock, indicating that these are xenocrysts rather than phenocrysts. The presence of melt veins with a similar composition to the bulk rock, maskelynitized plagioclase feldspar, and metastable cristobalite indicate that these rocks underwent significant shock, between 30 and 50 GPa. Calculated oxygen fugacity, using spinel‐ilmenite‐iron metal equilibria, is within the range defined by previous studies of lunar materials. The bulk composition (low MgO) and low calculated temperatures, together with modelling calculations, indicate an origin by fractional crystallization of a more primitive low TiO2 parent liquid similar to Apollo 12 olivine basalt.  相似文献   

3.
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   

4.
Abstract— Found during the 2004 U.S. Antarctic Search for Meteorites season, LaPaz Icefield (LAP) 04841 represents an addition to the LaPaz lunar basalts suite and brings the total mass collected to 1.93 kg. The presence of FeNi grains, troilite, and the anorthositic composition of plagioclase are evidence for the lunar origin of this meteorite. Pyroxene and olivine Mn/Fe values plot along the trend set for lunar basalts. Analyses of chromite grains provide a V/(Al + Cr) ratio of 1.33 ± 13, translating to an fO2 one log unit below the IW buffer, in accordance with previous fO2 estimates for lunar basalts. Application of the Zr‐cooling speedometer, for ilmenite and ulvöspinel pairs, gives a cooling rate of 5.2 °C/day, matching previous estimates of cooling rates for the LaPaz lunar meteorites and Apollo mare basalts. Mineral modes and chemistries, as well as trace‐element patterns, provide compelling evidence for pairing of this meteorite to others in the LaPaz lunar basalt suite.  相似文献   

5.
Abstract There are two types of glass-rich chondrules in unequilibrated ordinary chondrites (OC): (1) porphyritic chondrules containing 55–85 vol% glass or microcrystalline mesostasis and (2) nonporphyritic chondrules, containing 90–99 vol% glass. These two types are similar in mineralogy and bulk composition to previously described Al-rich chondrules in OC. In addition to Si-, Al- and Na-rich glass or Ca-Al-rich microcrystalline mesostasis, glass-rich chondrules contain dendritic and skeletal crystals of olivine, Al2O3-rich low-Ca pyroxene and fassaite. Some chondrules contain relict grains of forsterite ± Mg-Al spinel. We suggest that glass-rich chondrules were formed early in nebular history by melting fine-grained precursor materials rich in refractory (Ca, Al, Ti) and moderately volatile (Na, K) components (possibly related to Ca-Al-rich inclusions) admixed with coarse relict forsterite and spinel grains derived from previously disrupted type-I chondrules.  相似文献   

6.
Abstract— We petrologically examined the Miller Range (MIL) 03346 nakhlite. The main‐phase modal abundances are 67.7 vol% augite, 0.8 vol% olivine, and 31.5 vol% mesostasis. Among all known nakhlites, MIL 03346's modal abundance of olivine is the smallest and of mesostasis is the largest. Augite occurs as cumulus phenocrysts having a homogeneous core composition (En36–38Fs24–22Wo40), which is identical with other nakhlites. They accompany thin ferroan rims divided into inner and outer rims with a compositional gap at the boundary between the two rims. Olivine grains have magnesian cores (Fa ≥ 55) and show normal zoning toward ferroan rims (Fa ≤ 84). Mesostasis consists mostly of glass (26.0 vol%) with minor skeletal fayalites, skeletal titanomagnetites, acicular phosphate, massive cristobalite, and sulfides. We conclude that MIL 03346 is the most rapidly cooled nakhlite among all known nakhlites based on the petrography. We obtain the intercumulus melt composition for MIL 03346 from the mass balance calculation using the modal abundances and discuss the crystallization sequence of MIL 03346 in comparison with that of Yamato (Y‐) 000593. Although magnesian olivines of Y‐000593 are phenocrystic, magnesian olivine grains of MIL 03346 seem to have texturally crystallized from the intercumulus melt. After the MIL 03346 magma intruded upward to the Martian surficial zone, the magnesian olivine crystallized, and then the ferroan inner rim formed on phenocrystic core augite. The outer rim of phenocrystic augites formed after the crystallization of skeletal fayalites and skeletal titanomagnetites, resulting in a compositional gap between the inner and outer rims. Finally, glassy mesostasis formed from the residual melt. This crystallization sequence of MIL 03346 is different from those of other nakhlites, including Y‐000593.  相似文献   

7.
Northwest Africa (NWA) 4734 is an unbrecciated basaltic lunar meteorite that is nearly identical in chemical composition to basaltic lunar meteorites NWA 032 and LaPaz Icefield (LAP) 02205. We have conducted a geochemical, petrologic, mineralogic, and Sm‐Nd, Rb‐Sr, and Ar‐Ar isotopic study of these meteorites to constrain their petrologic relationships and the origin of young mare basalts. NWA 4734 is a low‐Ti mare basalt with a low Mg* (36.5) and elevated abundances of incompatible trace elements (e.g., 2.00 ppm Th). The Sm‐Nd isotope system dates NWA 4734 with an isochron age of 3024 ± 27 Ma, an initial εNd of +0.88 ± 0.20, and a source region 147Sm/144Nd of 0.201 ± 0.001. The crystallization age of NWA 4734 is concordant with those of LAP 02205 and NWA 032. NWA 4734 and LAP 02205 have very similar bulk compositions, mineral compositions, textures, and ages. Their source region 147Sm/144Nd values indicate that they are derived from similar, but distinct, source materials. They probably do not sample the same lava flow, but rather are similarly sourced, but isotopically distinct, lavas that probably originate from the same volcanic complex. They may have experienced slightly different assimilation histories in route to eruption, but can be source‐crater paired. NWA 032 remains enigmatic, as its source region 147Sm/144Nd definitively precludes a simple relationship with NWA 4734 and LAP 02205, despite a similar bulk composition. Their high Ti/Sm, low (La/Yb)N, and Cl‐poor apatite compositions rule out the direct involvement of KREEP. Rather, they are consistent with low‐degree partial melting of late‐formed LMO cumulates, and indicate that the geochemical characteristics attributed to urKREEP are not unique to that reservoir. These and other basaltic meteorites indicate that the youngest mare basalts originate from multiple sources, and suggest that KREEP is not a prerequisite for the most recent known melting in the Moon.  相似文献   

8.
Abstract– Northwest Africa (NWA) 2977 is an olivine‐gabbro lunar meteorite that has a distinctly different petrographic texture from other lunar basalts. We studied this rock with a series of in situ analytical methods. NWA 2977 consists mainly of olivine and pyroxene with minor plagioclase. It shows evidence of intense shock metamorphism, locally as high as shock‐stage S6. Olivine adjacent to a melt vein has been partially transformed into ringwoodite and Al,Ti‐rich chromite grains have partially transformed into their high‐pressure polymorph (possibly CaTi2O4‐structure). Olivine in NWA 2977 contains two types of lithic inclusions. One type is present as Si,Al‐rich melt inclusions that are composed of glass and, in most cases, dendritic pyroxene. The other type is mafic and composed of relatively coarse‐grained augite with accessory chromite, RE‐merrillite, and baddeleyite. Two Si,Al‐rich melt inclusions are heavy rare earth elements (REE) enriched, whereas the mafic inclusion has high REE concentrations and a KREEP‐like pattern. The mafic inclusion could be a relict fragment captured during the ascent of the parent magma of NWA 2977, whereas the Si,Al‐rich inclusions may represent the original NWA 2977 melt. The calculated whole‐rock composition has a KREEP‐like REE pattern, suggesting that NWA 2977 has an affinity to KREEP rocks. Baddeleyite has recorded a young crystallization age of 3123 ± 7 Ma (2σ), which is consistent with results from previous whole‐rock and mineral Sm‐Nd and Rb‐Sr studies. The petrography, mineralogy, trace element geochemistry, and young crystallization age of NWA 2977 support the possibility of pairing between NWA 2977 and the olivine‐gabbro portion of NWA 773.  相似文献   

9.
Abstract— We have performed petrologic and geochemical studies of Patuxent Range (PAT) 91501 and Lewis Cliff (LEW) 88663. PAT 91501, originally classified as an L7 chondrite, is rather a unique, near total impact melt from the L‐chondrite parent body. Lewis Cliff 88663 was originally classified as an “achondrite (?)”, but we find that it is a very weakly shocked L7 chondrite. PAT 91501 is an unshocked, homogeneous, igneous‐textured ultramafic rock composed of euhedral to subhedral olivine, low‐Ca pyroxene, augite and chrome‐rich spinels with interstitial albitic plagioclase and minor silica‐alumina‐alkali‐rich glass. Only ~10% relic chondritic material is present. Olivine grains are homogeneous (Fa25.2–26.8). Low‐Ca pyroxene (Wo1.9–7.2En71.9–78.2Fs19.9–20.9) and augite (Wo29.8–39.0En49.2–55.3Fs11.8–14.9) display a strong linear TiO2‐Al2O3 correlation resulting from igneous fractionation. Plagioclase is variable in composition; Or3.0–7.7Ab79.8–84.1An8.2–17.2.‐Chrome‐rich spinels are variable in composition and zoned from Cr‐rich cores to Ti‐Al‐rich rims. Some have evolved compositions with up to 7.9 wt% TiO2. PAT 91501 bulk silicate has an L‐chondrite lithophile element composition except for depletions in Zn and Br. Siderophile and chalcophile elements are highly depleted due to sequestration in centimeter‐size metal‐troilite nodules. The minerals in LEW 88663 are more uniform in composition than those in PAT 91501. Olivine grains have low CaO and Cr2O3 contents similar to those in L5–6 chondrites. Pyroxenes have high TiO2 contents with only a diffuse TiO2‐Al2O3 correlation. Low‐Ca pyroxenes are less calcic (Wo1.6–3.1En76.5–77.0Fs20.4–21.4), while augites (Wo39.5–45.6En46.8–51.1Fs7.6–9.4) and plagioclases (Or2.6–5.7Ab74.1–83.1An11.2–23.3) are more calcic. Spinels are homogeneous and compositionally similar to those in L6 chondrites. LEW 88663 has an L‐chondrite bulk composition for lithophile elements, and only slight depletions in siderophile and chalcophile elements that are plausibly due to weathering and/or sample heterogeneity.  相似文献   

10.
Abstract— We have done a detailed petrologic study of the angrite, D'Orbigny, and geochemical study of it and Sahara 99555. D'Orbigny is an igneous‐textured rock composed of Ca‐rich olivine, Al‐Ti‐diopside‐hedenbergite, subcalcic kirschsteinite, two generations of hercynitic spinel and anorthite, with the mesostasis phases ulvöspinel, Ca‐phosphate, a silico‐phosphate phase and Fe‐sulfide. We report an unknown Fe‐Ca‐Al‐Ti‐silicate phase in the mesostasis not previously found in angrites. One hercynitic spinel is a large, rounded homogeneous grain of a different composition than the euhedral and zoned grains. We believe the former is a xenocryst, the first such described from angrites. The mafic phases are highly zoned; mg# of cores for olivine are ?64, and for clinopyroxene ?58, and both are zoned to Mg‐free rims. The Ca content of olivine increases with decreasing mg#, until olivine with ?20 mol% Ca is overgrown by subcalcic kirschsteinite with about 30–35 mol% Ca. Detailed zoning sequences in olivine‐subcalcic kirschsteinite and clinopyroxene show slight compositional reversals. There is no mineralogic control that can explain these reversals, and we believe they were likely caused by local additions of more primitive melt during crystallization of D'Orbigny. D'Orbigny is the most ferroan angrite with a bulk rock mg# of 32. Compositionally, it is virtually identical to Sahara 99555; they are the first set of compositionally identical angrites. Comparison with the other angrites shows that there is no simple petrogenetic sequence, partial melting with or without fractional crystallization, that can explain the angrite suite. Angra dos Reis remains an anomalous angrite. Angrites show no evidence for the brecciation, shock, impact metamorphism, or thermal metamorphism that affected the howardite, eucrite, diogenite (HED) suite and ordinary chondrites. This suggests that the angrite parent body may have followed a fundamentally different evolutionary path than did these other parent bodies.  相似文献   

11.
Abstract– The nakhlites contain small proportions of Cu‐Fe‐Ni sulfide minerals; we have studied these sulfides in Northwest Africa (NWA) 998, Nakhla, Governador Valadares, and NWA 817 with optical microscopy, scanning electron microscope, and electron microprobe. Modal abundances of magmatic sulfides, as estimated by image analysis on thin section, are uniformly low (0.02 to 0.05 ± 0.03 vol%), i.e., a factor 5 lower than in shergottites. Sulfides occur within the glassy mesostasis, as composite two‐phase Fe‐Ti oxide‐sulfide grains, intimately associated with interstitial grains or locally enclosed in postcumulus melt inclusions (e.g., Governador Valadares) in olivine. They exhibit a uniform low‐Ni monoclinic pyrrhotite composition ± chalcopyrite. There is a gradation of sulfide grain sizes and textures across the nakhlites flow(s): droplets in NWA 817; resorbed blebs in Governador Valadares; more massive, true intercumulus blebs in Nakhla and NWA 998. These nakhlites also show evidence for sulfide weathering. Hot desert finds (e.g., NWA 998 and NWA 817) show a few percent fracture‐filling iron (oxy) hydroxides of likely terrestrial origin. Original sulfides are 50% altered in our NWA 998 section, with iron (oxy) hydroxides at grain boundaries and as complete pseudomorphs. The compositions of unaltered pyrrhotites are homogeneous, close to that of the monoclinic endmember Fe7S8, and are too sulfur‐rich to have been in chemical equilibrium with the late magmatic redox state fixed by the fayalite‐magnetite‐quartz buffer. Therefore, the compositions of the pyrrhotites must have been altered during the later stages of magmatic crystallization, by assimilation of S‐rich regolith and hydrothermal circulation.  相似文献   

12.
Abstract— We report on the discovery of a new shergottite from South Morocco. This single stone weighing 320 g is referenced as Northwest Africa (NWA) 856 with Djel Ibone as a synonymous name. It is a fresh, fine‐grained basaltic rock consisting mainly of two pyroxenes (total ?68 vol%: 45% pigeonite, En61‐16Wo9–22Fs26–68; 23% augite, En46‐26Wo34‐29Fs21–43) and plagioclase converted to maskelynite (?23 vol%, Ab43–57Or1–5An54‐36). Accessory minerals include merrillite, Cl‐apatite, pyrrhotite, ilmenite, ulvöspinel, silica (stishovite and glass), amorphous K‐feldspar and baddeleyite. Amorphous mixtures of maskelynite and silica occur most commonly as median layers inside maskelynite laths. In addition, melt pockets (?2 vol%) were recognized with relics of maskelynite, pyroxene and both dense silica glass and stishovite occurring as both grains and submicrometer needles. The compositions of the melt pockets are consistent with mixtures of maskelynite and pyroxenes with an average of ?50 vol% maskelynite. The meteorite is highly fractured at all scales. The bulk composition of NWA 856 has been measured for 44 elements. It is an Al‐poor ferroan basaltic rock which strongly resembles Shergotty and Zagami in its major and trace element composition. The nearly flat rare earth element (REE) pattern (La/Lu)n = 0.9, is similar to that of Shergotty or Zagami and differs significantly from NWA 480, another Moroccan shergottite recently described. According to the U, Ba and Sr abundances, NWA 856 is not significantly weathered. The oxygen isotopes (δ18O = +5.03%, δ17O = +3.09%, and Δ17O = +0.47%) are in agreement with the martian origin of this meteorite. On the basis of grain size, pyroxene zoning and composition, abundance of silica inclusions associated with maskelynite, trace element abundances, REE pattern and oxygen isotopes, pairing with NWA 480 is excluded. The similarity with Shergotty and Zagami is striking. The only significant differences are a larger grain size, a greater abundance of silica and melt pockets, a slightly more restricted range of pyroxene compositions and the absence of significant mesostasis.  相似文献   

13.
Remotely sensed observations from recent missions (e.g., GRAIL, Kaguya, Chandrayaan‐1) have been interpreted as indicating that the deep crust and upper mantle are close to or at the lunar surface in many large impact basins (e.g., Crisium, Apollo, Moscoviense). If this is correct, the capability of either impact or volcanic processes to transport mantle lithologies to the lunar surface should be enhanced in these regions. Somewhat problematic to these observations and interpretations is that examples of mantle lithologies in the lunar sample collection (Apollo Program, Luna Program, lunar meteorites) are at best ambiguous. Dunite xenoliths in high‐Ti mare basalt 74275 are one of these ambiguous examples. In this high‐Ti mare basalt, olivine occurs in three generations: olivine associated with dunite xenoliths, olivine megacrysts, and olivine microphenocrysts. The dunite xenoliths are anhedral in shape and are generally greater than 800 μm in diameter. The interior of the xenoliths are fairly homogeneous with regard to many divalent cations. For example, the Mg# (Mg/Mg + Fe × 100) ranges from 82 to 83 in their interiors and decreases from 82 to 68 over the 10–30 μm wide outer rim. Titanium and phosphorus X‐ray maps of the xenolith illustrate that these slow diffusing elements preserve primary cumulate zoning textures. These textures indicate that the xenoliths consist of many individual olivine grains approximately 150–200 μm in diameter with low Ti, Al, and P cores. These highly incompatible elements are enriched in the outer Fe‐rich rims of the xenoliths and slightly enriched in the rims of the individual olivine grains. Highly compatible elements in olivine such as Ni exhibit a decrease in the rim surrounding the xenolith, an increase in the incompatible element depleted cores of the individual olivine grains, and a slight decrease in the “interior rims” of the individual olivine grains. Inferred melt composition, liquid lines of descent, and zoning profiles enable the reconstruction of the petrogenesis of the dunite xenoliths. Preservation of primary magmatic zoning (Ti, P, Al) and lack of textures similar to high‐pressure mineral assemblages exhibited by the Mg‐suite (Shearer et al. 2015) indicate that these xenoliths do not represent deep crustal or shallow mantle lithologies. Further, they are chemically and mineralogically distinct from Mg‐suite dunites identified from the Apollo 17 site. More likely, they represent olivine cumulates that crystallized from a low‐Ti mare basalt at intermediate to shallow crustal levels. The parent basalt to the dunite xenolith lithology was more primitive than low‐Ti basalts thus far returned from the Moon. Furthermore, this parental magma and its more evolved daughter magmas are not represented in the basalt sample suite returned from the Taurus‐Littrow Valley by the Apollo 17 mission. The dunite xenolith records several episodes of crystallization and re‐equilibration. During the last episode of re‐equilibration, the dunite cumulate was sampled by the 74275 high‐Ti basalt and transported over a period of 30–70 days to the lunar surface.  相似文献   

14.
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   

15.
The valences of Ti, V, and Cr in olivine and pyroxene, important indicators of the fO2 of the source region of their host rocks, can be readily measured nondestructively by XANES (X‐ray absorption near edge structure) spectroscopy, but little such work has been done on lunar rocks, and there is some uncertainty regarding the presence of Ti3+ in lunar silicates and the redox state of the lunar mantle. This is the first study involving direct XANES measurement of valences of multivalent cations in lunar rocks. Because high alumina activity facilitates substitution of Ti cations into octahedral rather than tetrahedral sites in pyroxene and Ti3+ only enters octahedral sites, two aluminous basalts from Apollo 14, 14053 and 14072, were studied. Most pyroxene contains little or no detectable Ti3+, but in both samples relatively early, magnesian pyroxene was found that has Ti valences that are not within error of 4; in 14053, this component has an average Ti valence of 3.81 ± 0.06 (i.e., Ti3+/[Ti3+ + Ti4+ = 0.19]). This pyroxene has relatively low atomic Ti/Al ratios (<0.4) due to crystallization before plagioclase, contrary to the long‐held belief that lunar pyroxene with Ti/Al > 0.5 contains Ti3+ and pyroxene with lower ratios does not. Later pyroxene, with lower Mg/Fe and higher Ti/Al ratios, has higher proportions of Ti (all Ti4+) in tetrahedral sites. All pyroxene analyzed contains divalent Cr, ranging from 15 to 30% of the Cr present, and all but one analysis spot contains divalent V, accounting for 0 to 40% (typically 20–30%) of the V present. Three analyses of olivine in 14053 do not show any Ti3+, but Ti valences in 14072 olivine range from 4 down to 3.70 ± 0.10. In 14053 olivine, ~50% of the Cr and 60% of the V are divalent. In 14072 olivine, the divalent percentages are ~20% for Cr and 20–60% for V. These results indicate significant proportions of divalent Cr and V and limited amounts of trivalent Ti in the parental melts, especially when crystal/liquid partitioning preferences are taken into account. These features are consistent with an fO2 closer to IW ? 2 than to IW ? 1. Apollo 15 basalt 15555, analyzed for comparison with A‐14 materials, has olivine with strongly reduced Cr (Cr2+/(Cr2+ + Cr3+) ~0.9). Basalts from different sites may record redox differences between source regions.  相似文献   

16.
Abstract— Miller Range (MIL) 05035 is a low‐Ti mare basalt that consists predominantly of pyroxene (62.3 vol%) and plagioclase (26.4 vol%). Pyroxenes are strongly shocked and complexly zoned from augite (Wo33) and pigeonite (Wo17) cores with Mg# = 50–54 to hedenbergite rims. Coexisting pyroxene core compositions reflect crystallization temperatures of 1000 to 1100 °C. Plagioclase has been completely converted to maskelynite with signs of recrystallization. Maskelynite is relatively uniform in composition (An94Ab6–An91Ab9), except at contacts with late‐stage mesostasis areas (elevated K contents, An82Ab15Or3). Symplectites (intergrowth of Fe‐augite, fayalite, and silica) of different textures and bulk compositions in MIL 05035 suggest formation by decomposition of ferro‐pyroxene during shock‐induced heating, which is supported by the total maskelynitization of plagioclase, melt pockets, and the presence of a relict pyroxferroite grain. Petrography and mineral chemistry imply that crystallization of MIL 05035 occurred in the sequence of Fe‐poor pyroxenes (Mg# = 50–54), followed by plagioclase and Fe‐rich pyroxenes (Mg# = 20–50), and finally hedenbergite, Fe‐Ti oxides, and minor late‐stage phases. Petrography, bulk chemistry, mineral compositions, and the age of MIL 05035 suggest it is possibly source crater‐paired with Asuka (A‐) 881757 and Yamato (Y‐) 793169, and may also be launch‐paired with Meteorite Hills (MET) 01210. MIL 05035 represents an old (?3.8–3.9 Ga), incompatible element‐depleted low‐Ti basalt that was not sampled during the Apollo or Luna missions. The light‐REE depleted nature and lack of Eu anomalies for this meteorite are consistent with an origin distant from the Procellarum KREEP Terrane, and genesis from an early cumulate mantle‐source region generated by extensive differentiation of the Moon.  相似文献   

17.
Abstract– The feldspathic lunar meteorites contain rare fragments of crystalline basalts. We analyzed 16 basalt fragments from four feldspathic lunar meteorites (Allan Hills [ALHA] 81005, MacAlpine Hills [MAC] 88104/88105, Queen Alexandra Range [QUE] 93069, Miller Range [MIL] 07006) and utilized literature data for another (Dhofar [Dho] 1180). We compositionally classify basalt fragments according to their magma’s estimated TiO2 contents, which we derive for crystalline basalts from pyroxene TiO2 and the mineral‐melt Ti distribution coefficient. Overall, most of the basalt fragments are low‐Ti basalts (1–6% TiO2), with a significant proportion of very‐low‐Ti basalts (<1% TiO2). Only a few basalt clasts were high‐Ti or intermediate Ti types (>10% TiO2 and 6–10% TiO2, respectively). This distribution of basalt TiO2 abundances is nearly identical to that obtained from orbital remote sensing of the moon (both UV‐Vis from Clementine, and gamma ray from Lunar Prospector). However, the distribution of TiO2 abundances is unlike those of the Apollo and Luna returned samples: we observe a paucity of high‐Ti basalts. The compositional types of basalt differs from meteorite to meteorite, which implies that all basalt subtypes are not randomly distributed on the Moon, i.e., the basalt fragments in each meteorite probably represent basalts in the neighborhood of the meteorite launch site. These differences in basalt chemistry and classifications may be useful in identifying the source regions of some feldspathic meteorites. Some of the basalt fragments probably originate from ancient cryptomaria, and so may hold clues to the petrogenesis of the Moon’s oldest volcanism.  相似文献   

18.
Lunar breccias preserve the records of geologic processes on the Moon. In this study, we report the occurrence, petrography, mineralogy, and geologic significance of the observed secondary olivine veinlets in lunar feldspathic breccia meteorite Northwest Africa (NWA) 11273. Bulk‐rock composition measurements show that this meteorite is geochemically similar to other lunar highland meteorites. In NWA 11273, five clasts are observed to host veinlets that are dominated by interconnecting olivine mineral grains. The host clasts are mainly composed of mafic minerals (i.e., pyroxene and olivine) and probably sourced from a basaltic lithology. The studied olivine veinlets (~5 to 30 μm in width) are distributed within the mafic mineral host, but do not extend into the adjacent plagioclase. Chemically, these olivine veinlets are Fe‐richer (Fo41.4–51.9), compared with other olivine grains (Fo54.3–83.1) in lithic clasts and matrix of NWA 11273. By analogy with the secondary olivine veinlets observed in meteorites from asteroid Vesta (howardite–eucrite–diogenite group samples) and lunar mare samples, our study suggests that the newly observed olivine veinlets in NWA 11273 are likely formed by secondary deposition from a lunar fluid, rather than by crystallization from a high‐temperature silicate melt. Such fluid could be sulfur‐ and phosphorous‐poor and likely had an endogenic origin on the Moon. The new occurrence of secondary olivine veinlets in breccia NWA 11273 reveals that the fluid mobility and deposition could be a previously underappreciated geological process on the Moon.  相似文献   

19.
Abstract— Evidence in favor of the model fusion of the finest fraction (F3) for the origin of lunar agglutinitic glass has been accruing. They include (1) theoretical expectations that shock pulses should engulf and melt smaller grains more efficiently than larger grains, (2) experimental results of impact shock, albeit at lower than presumed hypervelocity impacts of micrometeorites on the lunar regolith, and (3) new analyses confirming previous results that average compositions of agglutinitic glass are biased towards that of the finest fraction of lunar soils from which they had formed. We add another reason in support of the F3 model. Finer grains of lunar soils are also much more abundant. Hence, electrostatic forces associated with the rotating terminator region bring the finest grains that are obviously much lighter than courser grains to the surface of the Moon. This further contributes to the preferential melting of the finest fraction upon micrometeoritic impacts. New backscattered electron imaging shows that agglutinitic glass is inhomogeneous at submicron scale. Composition ranges of agglutinitic glass are extreme and deviate from that of the finest fraction, even by more than an order of magnitude for some components. Additionally, we show how an ilmenite grain upon impact would produce TiO2‐rich agglutinitic glass in complete disregard to the requirements of fusion of the finest fraction. We propose an addition to the F3 model to accommodate these observations (i.e., that micrometeorite impacts indiscriminately melt the immediate target regardless of grain size or grain composition). We, therefore, suggest that (1) agglutinitic glass is the sum of (a) the melt produced by the fusion of the finest fraction of lunar soils and (b) the microvolume of the indiscriminate target, which melts at high‐shock pressures from micrometeoritic impacts, and that (2) because of the small volume of the melt and incorporating cold soil grains, the melt quenched so rapidly that it did not mix and homogenize to represent any preferential composition, for example, that of the finest fraction.  相似文献   

20.
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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号