Distribution of Olivine and Pyroxene Derived from Clementine Data in Crater Copernicus

In order to derive the distribution of olivine and pyroxene in Crater Copernicus,we compute two band ratios(950/750 and 2 000/1 500 nm) ,percent content of elements(Al%,Ca%,Mg%,FeO%) and maturity(Is/FeO) based on Clementine UVVIS and NIR image data.The central peaks of Copernicus,which are known to be olivine-rich or pyroxene-rich,are chosen as ground truth and ROIs used to derive the distribution of olivine and pyroxene with a decision tree and spectral angle mapper(SAM) .Additionally,we compared previous ...     

Lunar surface geochemistry: Global concentrations of Th, K, and FeO as derived from lunar prospector and Clementine data

Accurate estimates of global concentrations of Th, K, and FeO have an important bearing on understanding the bulk chemistry and geologic evolution of the Moon. We present empirical ground-truth calibrations (transformations) for Lunar Prospector gamma-ray spectrometer data (K and Th) and a modified algorithm for deriving FeO concentrations from Clementine spectral reflectance data that incorporates an adjustment for TiO₂ content. The average composition of soil samples for individual landing sites is used as ground-truth for remotely sensed data. Among the Apollo and Luna sites, Apollo 12 and 14 provide controls for the incompatible-element-rich compositions, Apollo 16 and Luna 20 provide controls for the feldspathic and incompatible-element-poor compositions, and Apollo 11, 15, and 17, and Luna 16 and 24 provide controls for Fe-rich compositions. In addition to these Apollo and Luna sample data we include the composition of the feldspathic lunar meteorites as a proxy for the northern farside highlands to extend the range of the calibration points, thus providing an additional anorthositic end-member composition. These empirical ground-truth calibrations for Lunar Prospector Th and K provide self consistency between the existing derived data and lunar-sample data. Clementine spectral-reflectance data are used to construct a TiO₂-sensitive FeO calibration that yields higher FeO concentrations in areas of high-Fe, low-Ti, mare-basalt-rich surfaces than previous FeO algorithms. The data set so derived is consistent with known sample compositions and regolith mixing relationships.     

Refinement of a lunar FeO mapping method

Clementine UVVIS and NIR data from the lunar sampling sites (totaling 46 sampling sites) were processed and used to refine the iron determination method of Le Mouéic et al. (2000, 2002). We found that about 21 sampling sites are unsuitable to Le Mouéic et al's spectral parameters ("slope" and "depth l") because their 1500 nm filter could not be used as spectral parameters' right shoulders and to evaluate the depth of the 1-μm absorption feature accurately. We used the rest 25 sampling sites to refine the method developed by Le Mouéic et al. (2000, 2002 ) and obtained our own equation of FeO content determination. We tested our own equation, and the results are satifactory. In our work we also acquired some useful experiences in scientific applications of our own dataset of the Chang'E-1 mission.     

The production of iron oxide during peridotite serpentinization: Influence of pyroxene

Serpentinization produces molecular hydrogen(H2)that can support communities of microorganisms in hydrothermal fields;H2 results from the oxidation of ferrous iron in olivine and pyroxene into ferric iron,and consequently iron oxide(magnetite or hematite)forms.However,the mechanisms that control H2 and iron oxide formation are poorly constrained.In this study,we performed serpentinization experiments at 311℃ and 3.0 kbar on olivine(with 5% pyroxene),orthopyroxene,and peridotite.The results show that serpentine and iron oxide formed when olivine and orthopyroxene individually reacted with a saline starting solution.Olivine-derived serpentine had a significantly lower FeO content(6.57±1.30 wt.%)than primary olivine(9.86 wt.%),whereas orthopyroxene-derived serpentine had a comparable FeO content(6.26±0.58 wt.%)to that of primary orthopyroxene(6.24 wt.%).In experiments on peridotite,olivine was replaced by serpentine and iron oxide.However,pyroxene transformed solely to serpentine.After 20 days,olivine-derived serpentine had a FeO content of 8.18±1.56 wt.%,which was significantly higher than that of serpentine produced in olivine-only experiments.By contrast,serpentine after orthopyroxene had a slightly higher FeO content(6.53±1.01 wt.%)than primary orthopyroxene.Clinopyroxene-derived serpentine contained a significantly higher FeO content than its parent mineral.After 120 days,the FeO content of olivine-derived serpentine decreased significantly(5.71±0.35 wt.%),whereas the FeO content of orthopyroxene-derived serpentine increased(6.85±0.63 wt.%)over the same period.This suggests that iron oxide preferentially formed after olivine serpentinization.Pyroxene in peridotite gained some Fe from olivine during the serpentinization process,which may have led to a decrease in iron oxide production.The correlation between FeO content and SiO_2 or AI_2 O_3 content in olivine-and orthopyroxene-derived serpentine indicates that aluminum and silica greatly control the production of iron oxide.Based on our results and data from natural serpentinites reported by other workers,we propose that aluminum may be more influential at the early stages of peridotite serpentinization when the production of iron oxide is very low,whereas silica may have a greater control on iron oxide production during the late stages instead.     

Fine,nickel-poor Fe-Ni grains in the olivine of unequilibrated ordinary chondrites

Fine (?2 μm), Ni-poor (? 10 mg/g) Fe-Ni grains are common inclusions in the olivine in porphyritic chondrules in unequilibrated ordinary chondrites. The olivine grains appear to be relicts that survived chondrule formation without melting. The most common occurrence of this “dusty” metal is in the core of olivine grains having clear Fe-poor rims and surrounded either by small euhedral clear olivine grains zoned with FeO increasing toward the border of the grains or by large elongated Fe-poor orthopyroxenes oriented parallel to the chondrule surface and enclosing small round olivine grains. Various amounts of Ca, Al-rich glass are always present. The dusty metal is occasionally found in the rims of olivine grains either isolated in the matrix or included in chondrules. A rare occurrence is as bands in highly deformed olivines.This dusty metal appears to be the product of in situ reduction of FeO from the host olivine. Among the possible reductants H₂ or carbonaceous matter (CH₂)_n seem the most likely. Hydrogen may have been implanted by solar-wind or solar-flare irradiation, but this requires that dissipation of nebular gas occurred before the end of the chondrule formation process. Carbonaceous matter may have been implanted by shock. Less likely reductants are nebular CO or C dissolved in the olivine lattice. The large relict olivine grains may be nebular condensates or, more likely, fragments broken off earlier generations of chondrules.     

新疆北山地区坡北镁铁-超镁铁岩体单斜辉石的矿物学特征及其地质意义

单斜辉石是坡北镁铁-超镁铁杂岩体的主要造岩矿物之一,在各岩相中普遍存在。本文对岩体各岩相中单斜辉石的矿物化学组成进行了电子探针和LA-ICPMS分析,以探明岩体性质、形成的构造背景及演化过程。分析表明,单斜辉石主要氧化物含量为:SiO21.05%~54.00%、MgO 13.95%~17.64%、CaO 19.87%~23.56%、FeO3.44%~6.58%、TiO20.13%~1.36%、Al2O32.17%~4.21%、Na2O 0.17%~0.50%、Cr2O30.01%~1.27%。岩石判别图解表明寄主岩浆为亚碱性拉斑玄武岩,形成于岛弧环境。单斜辉石的结晶温度范围介于1 141~1 221℃。∑REE和(Ce/Yb)N值表明从(异剥)橄榄岩和橄榄单辉辉石岩到橄榄辉长岩和角闪辉长岩,岩浆结晶作用增强。与岩浆正常结晶演化相比,(异剥)橄榄岩和橄榄单辉辉石岩中单斜辉石的SiO2、Na2O含量有所增大,角闪辉长岩和橄榄辉长岩中单斜辉石的CaO含量略有富集,结合前人研究成果和围岩性质,初步认为成岩过程中,可能发生过地壳同化混染作用,其中大理岩为角闪辉长岩和橄榄辉长岩提供了部分Ca元素,而黑云母石英片岩则为(异剥)橄榄岩和橄榄单辉辉石岩贡献了Si、Na等。(异剥)橄榄岩和橄榄单辉辉石岩具较低的FeO含量,此外黑云母石英片岩混入其中,这可能是引起硫化物熔离的重要因素。     

On the nature and origin of isolated olivine grains in carbonaceous chondrites

Many carbonaceous chondrites contain discrete olivine fragments that have been considered to be primitive material, i.e. direct condensates from the solar nebula or pre-solar system material. Olivine occurring in chondrules and as isolated grains in C3(0) chondrites has been characterized chemically and petrographically. Type I chondrules contain homogeneous forsterite grains that exhibit a negative correlation between FeO and CaO. Type II chondrules contain zoned fayalite olivines in which FeO is positively correlated with CaO and MnO. The isolated olivines in C3(0) chondrites form two compositional populations identical to olivines in the two types of porphyritic olivine chondrules in the same meteorites. Isolated olivines contain trapped melt inclusions similar in composition to glassy mesostasis between olivines in chondrules. Such glasses can be produced by fractional crystallization of olivine and minor spinel in the parent chondrule melts if plagioclase does not nucleate. The isolated olivine grains are apparently clastic fragments of chondrules. Some similarities between olivines in C3(0), C2, and Cl chondrites may suggest that olivine grains in all these meteorites crystallized from chondrule melts.     

The effects of FeO on the system CMAS at low pressure and implications for basalt crystallization processes

The common occurrence of olivine, clinopyroxene and plagioclase in natural basalts may suggest that crystallization of these phases exerts important controls on the evolution of natural basalts at low pressure. In order to understand the effects of such an assemblage on the evolution of basalt, an experimental study of the divariant assemblage 1+an+cpx+ol in the system CMAS + FeO was undertaken at 1 bar and under very reducing conditions. Experiments have been performed along three isothernal sections. Detailed electron microprobe data have been collected on all the coexisting phases. Combining these data with available data in the system CMAS, the compositions of all the coexisting phases have been described as functions of temperature and CaO content in the melt by applying a multiple linear regression method. This allows a quantitative characterization of the divariant assemblage 1+an+epx+ol in the system CMAS + FeO, from 1275°C to 1160°C, with liquid compositions ranging from mg#=1 to mg#=0.28. Knowing the composition-temperature relationships, the basic T-X configuration of the assemblage 1+an+cpx+ol has been analysed, and mass balance calculations have been performed to examine the FeO effect on different crystallization processes. Addition of FeO to the system CMAS transforms the thermal divide in the assemblage 1+an+cpx+ol to a thermal ridge, and shifts the spine of the thermal ridge towards SiO₂-poor compositions with decreasing temperature. This indicates that tholeiitic basalts can be relatively silica-poor, and evolve towards slightly more silica-poor compositions. With increasing FeO content, pigeonite replaces ortheonstatite as a crystallizing phase along the silica-rich boundary of the assemblage 1+an+cpx+ol. In some iron, and silica rich composition, olivine possibly terminates its crystallization or even starts resorption prior to pigeonite precipitation; this suppresses silica enrichment in the melt. Crystallization paths of the assemblage 1+an+cpx+ol are determined by the detailed T-X relations of the thermal ridge with the melt evolving away from the spine. The liquid evolution trend depends strongly on the initial compositions. A tholeiitic liquid can follow a moderate silica enrichment path at the same very reducing condition of there is a high modal proportion of olivine. ‘A Fenner mechanism therefore is at work at the same place as a Bowen mechanism’.     

Aleutian tholeiitic and calc-alkaline magma series I: The mafic phenocrysts

Diagnostic mafic silicate assemblages in a continuous spectrum of Aleutian volcanic rocks provide evidence for contrasts in magmatic processes in the Aleutian arc crust. Tectonic segmentation of the arc exerts a primary control on the variable mixing, fractional crystallization and possible assimilation undergone by the magmas. End members of the continuum are termed calc-alkaline (CA) and tholeiitic (TH). CA volcanic rocks (e.g., Buldir and Moffett volcanoes) have low FeO/MgO ratios and contain compositionally diverse phenocryst populations, indicating magma mixing. Their Ni and Cr-rich magnesian olivine and clinopyroxene come from mantle-derived mafic olivine basalts that have mixed with more fractionated magmas at mid-to lower-crustal levels immediately preceding eruption. High-Al amphibole is associated with the mafic end member. In contrast, TH lavas (e.g., Okmok and Westdahl volcanoes) have high FeO/MgO ratios and contain little evidence for mixing. Evolved lavas represent advanced stages of low pressure crystallization from a basaltic magma. These lavas contain groundmass olivine (FO 40–50) and lack Ca-poor pyroxene. Aleutian volcanic rocks with intermediate FeO/MgO ratios are termed transitional tholeiitic (TTH) and calc-alkaline (TCA). TCA magmas are common (e.g., Moffett, Adagdak, Great Sitkin, and Kasatochi volcanoes) and have resulted from mixing of high-Al basalt with more evolved magmas. They contain amphibole (high and low-Al) or orthopyroxene or both and are similar to the Japanese hypersthene-series. TTH magmas (e.g., Okmok and Westdahl) contain orthopyroxene or pigeonite or both, and show some indication of upper crustal mixing. They are mineralogically similar to the Japanese pigeonite-series. High-Al basalt lacks Mg-rich mafic phases and is a derivative magma produced by high pressure fractionation of an olivine tholeiite. The low pressure mineral assemblage of high-Al basalt results from crystallization at higher crustal levels.     

嫦娥一号干涉成像光谱仪数据再校正与全月铁钛元素反演

月球表面的元素和物质成分分布是理解月球成岩与地质演化历史的重要线索。嫦娥一号干涉成像光谱仪(IIM)是我国首台月球探测成像光谱仪器,其获得的大量月球高光谱数据已成为我国未来探测月球成分与地质演化研究的宝贵基础数据。本文利用探月工程地面应用系统发布的IIM B版本2C级数据,开发出一套数据再定标流程,获得了较为可靠的月表相对反射率数据。我们在新校正数据的基础上开展月球表面FeO、TiO_2的反演建模,获得了全月FeO和TiO_2分布图,这些图件是进行月球地质填图的基础。校正数据反演的FeO和TiO_2分布与前人对Clementine UVVIS数据的反演结果相近,表明干涉成像光谱仪数据具有较大的应用潜力。高地的低铁岩石成分(一般小于8%)佐证了月球月壳形成的过程中的岩浆洋分异假说,而月海玄武岩的TiO_2成分变化范围较大(0~13%)则表明月海玄武岩来源于不同的月幔源区。根据嫦娥一号干涉成像光谱仪全月FeO分布图,可将月球表面物质类型总体划分为高地斜长岩和月海玄武岩,而根据TiO_2分布可以进一步将月海玄武岩划分为5种不同钛含量的玄武岩岩石类型。FeO和TiO_2在全月范围内的分布表明Apollo和Luna返回的月球样品不能够代表全月范围内的矿物成分多样性,月球岩浆演化历史比前人认为的要复杂。未来月球样品返回任务(如嫦娥五号)如能赴这些特殊地区进行取样,将很有可能返回重要的月球科学研究发现和成果。     

Massive chromite in the Brenham pallasite and the fractionation of Cr during the crystallization of asteroidal cores

Large (≥2 mm) chromite grains are present in IIIAB iron meteorites and in the main-group pallasites (pmg), closely related to high-Au IIIAB irons. Pallasites seem to have formed by the intrusion of a highly evolved metallic magma from a IIIAB-like core into fragmented olivine of the overlying dunite mantle. High Cr contents are commonly encountered during the analyses of metallic samples of high-Au IIIAB irons and main-group pallasites, an indication that Cr contents were high in the intruding liquid and that Cr behaved as an incompatible element during the crystallization of the IIIAB magma, contrary to expectations based on the negative IIIAB Cr-Ni and Cr-Au trends among low-Au IIIAB irons.In a region about 10 cm across in the Brenham main-group pallasite massive chromite fills the interstices between olivine grains, the site normally occupied by metal in Brenham and other pallasites. The massive chromite may have formed as a late cumulus phase; because Fe-Ni was also crystallizing, its absence in the chromite-rich region suggests a separation associated with differences in liquid buoyancy. The coexisting chromite and olivine are zoned; in the olivine FeO is highest in pallasitic (olivine-metal) regions, lowest in rims adjacent to chromite, and intermediate in the cores of these olivines. Chromite shows the opposite zoning, with the highest FeO contents at grain edges adjacent to olivine. The observed gradients are those expected to form by Fe-Mg exchange between olivine and chromite during slow cooling at subsolidus temperatures. Compared to normal Brenham, contents of phosphoran olivine and phosphates are higher in the chromitic pallasitic region. We also report data for large-to-massive chromites present in pmg Molong and in high-Au IIIAB Bear Creek that, like Brenham, formed from a highly evolved magma. The Bear Creek chromite has a much lower Mg content than that in the pallasites, implying that, in the pmg, the Mg was extracted from the olivine during high-temperature reaction with the precipitating chromite. There are other circumstantial arguments indicating that Cr was incompatible in the metal during the crystallization of the IIIAB magma, with the concentration in the residual magma rising from an initial value of about 300 μg/g to a value around 700 μg/g when Bear Creek and Brenham were formed. We consider possible explanations for these negative Cr-Au and Cr-Ni trends and find the most probable one to be that they reflect sampling artefacts resulting from analysts avoiding visible chromite (and the commonly associated phase FeS) when choosing metal samples.     

Picritic primary magma and its source mantle for Oshima-Ōshima and back-arc side volcanoes,Northeast Japan arc

Oshima-shima volcano is an endmember of a geochemical variation which is characterized by a low FeO content toward the back-arc side across the NE Japan arc. Analyses of the basalts show primitive characteristics. Variation trends of the chemical compositions indicate initial olivine control then olivine+clinopyroxene control from a picritic to a differentiated basalt. The more magnesian basalts have the more magnesian olivine phenocrysts. The most magnesian (MgO 15%) of all rock samples, contains olivine phenocrysts with a composition of Fo 93.7 as a liquidus phase and is considered a product of a mantle-derived magma. The possible range in FeO and MgO content of source mantle for the Oshima-shima magma can be demonstrated. Ichinomegata lherzolite inclusions, also from the back-arc side of NE Japan, is unlikely to be a candidate for the source mantle for high FeO. The upper mantle beneath the back-arc side is considered to be compositionally zoned; a Fe-rich mantle (Ichinomegata lherzolite) at shallower place and a Fe-poor mantle (the source mantle for back-arc side volcanoes).     

The origin of basaltic rocks in Niutoushan area— high pressure differentiation

The Niutoushan basaltic cone, consisting of subalkali (quartz-tholeiite and olivine-tholeiite) and alkali basalts, is Late Tertiary in age. Its major characteristics are generalized as follows:

1. Both early subalkali and late alkali bali basalts are formed under the same geological environment.
2. The continuity in chemical composition from subalkali to alkali and the low FeO/MgO in alkali basalts show that they are the products of cognate magmatic differentiation.
3. The change from low REE abundance and weak enrichment of LREE in subalkali to high REE abundance and strong enrichment of LREE in alkali basalts indicates obvious REE enrichment and fractionation during magmatic differentiation. Weak positive Eu anomalies in the REE patterns are indicative of their formation under low oxygen fugacity conditions.
4. According to the calculated values, 70–75% of the primary olivine tholeiitic magma had been separated as subalkaline basaltic magma, the rest residual magma became alkaline basaltic magma. This result is consistent to the field observation that the outcrop area of subalkali basalts is four times as much as that of alkali basalts.
5. The basaltic rocks of Niutoushan show an S-type distribution straddling the thermal barrier on Ol′-Ne′-Qu′ diagram and an evolution tendency for Ne to increase with increasing FeO/MgO. This is in agreement with the melting experimental data on olivine basalts at 10–20 kb.
6. Mantle-derived inclusions (spinel lherzolite) in this area occur in both alkali olivine basalts and olivine tholeiites. The latter is of extremely rare occurrence. The formation temperature and pressure of the inclusions in alkalibasalts and olivine tholeiites have been calculated. The results show that the alkaline basaltic magma was separated from the subalkaline basaltic magma at about 20 kb.

Basaltic rocks in Niutoushan were formed through the so-called “high pressure differentiation”, that is, at about 20 kb the crystallization of clinopyroxene and orthpyroxene resulted in the separation of subalkaline basaltic magma from the primary olivine tholeiitic magma, and then the residue gradually became alkaline olivine basaltic magma.     

Basalt evolution at low pressure: implications from an experimental study in the system CaO-FeO-MgO-Al2O3-SiO2

New experiments have been performed in the system CaO+MgO+Al₂O₃+SiO₂ (CMAS)+FeO at atmospheric pressure. Most of the experiments were conducted on Fe-rich compositions, in the low-temperature field of the assemblage liq(liquid)+an(anorthite) +aug(augite)+ol(olivine), and mostly along five isotherms. Others were located on, or nearby the assemblage boundaries. These experiments, together with the previously reported high temperature experiments (Shi and Libourel 1991; Libourel et al. 1989), permit contouring the complete liq+an+aug+ol divariant field, and tracing out some of its boundaries. The boundary of the assemplage liq+an+aug+ol consists of six segments, with the appearance of one of the following phases, orthopyroxene, pigeonite, tridymite, bustamite, kirschsteinite, and spinel, as an additional phase. Within the stability field of the assemblage liq+an+aug+ol, the compositions of all the coexisting phases have been described as functions of temperature and silica content in the melt by applying a multiple linear regression method. This allows a quantitative characterization of the divariant assemblage liq+an+aug+ol in the system CMAS+FeO, from 1273°C to 1055°C, with olivine compositions ranging from Mg^*[Mg/(Mg+Fe)]=1 to 0.08. Knowing the composition-temperature relationships, the basic T-X configuration of the assemblage liq+an +aug+ol has been analysed, and mass-balance calculations have been performed to examine the FeO effect on different crystallization processes. Addition of FeO to the system CMAS transforms the thermal divide in the assemblage liq+an+di(diopside)+fo(forsterite) into a thermal ridge. With decreasing temperature, the spine of the thermal ridge moves towards Si-poor compositions at Mg-rich end but towards Si-rich compositions at the Fe-rich end. This indicates that late-stage tholeiitic liquids can follow a trend of silica enrichment without the crystallization of an oxide phase. Crystallization paths of the assemblage liq+an+aug+ol are determined by the detailed T-X relations of the thermal ridge with the melt evolving away from the spine. The boundary reactions with decreasing temperature have also been characterized numerically.     

Crystallization conditions of leucite-bearing magmas and their implications on the magmatological evolution of ultrapotassic magmas: the Vico Volcano, Central Italy

Summary Mineral compositions in leucite-bearing and leucite-free rocks from Vico volcano are reported. FeO/MgO partitioning (Kd_ol/liq) between olivine and latite (0.14–0.22), and between olivine and trachyte (0.06–0.10) indicates a lack of equilibrium between mineral and host rock. This suggests that mingling and/or mixing between magmas was a leading process during magmatic differentiation. In addition, a phono-tephrite olivine population with high (0.84) and equilibrium (0.23–0.29) Kd_ol/liq values has been produced by the interaction of differently evolved magmas. Zoning in clinopyroxene and plagioclase from these rocks recorded the same processes. In addition, resorbed quartz xenocrysts with coronas of clinopyroxene microlites indicate that digestion of crustal rocks occurred during the residence of magma in a shallow level reservoir. Increasing Fe coupled with decreasing Ca in diopside crystals from some phonolites, together with the petrographic and trace element data, indicate that polybaric fractional crystallisation also may be involved in the genesis of magmas of the second period of Vico activity. Leucite-free trachybasalts erupted in a late stage contain highly forsteritic olivine phenocrysts (forsterite 84–88 mol.%) in-equilibrium (Kd_ol/liq = 0.24–0.35) with the host rock, which indicate that they did not suffer chemical modification at low pressure. Received November 28, 2000; revised version accepted September 27, 2001     

Spinel-anthophyllite rocks of the Kokchetav massif (northern Kazakhstan)

Spinel-anthophyllite rocks that may be classified as ultrabasic low-Ca spinel amphibolites have been first discovered in the Kokchetav collision zone (northern Kazakhstan). They outcrop 2 km west of Enbek-Berlyk Village among schists and quartzites and are closely associated with spinel harzburgites and garnet pyroxenites. The main hosted minerals are spinel (hercynite) and anthophyllite. The rocks bear magnetite-hornblende-spinel-anthophyllite pseudomorphs with rounded and polygonal sections, which might have been resulted from the replacement of garnet grains. The prismatic anthophyllite crystals and scarce olivine relics contain elongate parallel spinel inclusions resembling spinel-olivine syntactic intergrowths in the Enbek-Berlyk spinel harzburgites. The spinel-anthophyllite rocks are similar to the associated spinel harzburgites in CaO, MnO, SiO₂, and Al₂O₃ contents but are richer in FeO and poorer in MgO (F = FeO/(FeO + MgO) = 57% against 35% in the harzburgites). Geological, mineralogical, and geochemical data suggest that the spinel-anthophyllite rocks formed during the isochemical contact metamorphism of garnet-bearing spinel harzburgites, which contained more FeO and less MgO than garnet-free harzburgites of the same area. Variations in FeO and MgO contents in both types of harzburgites seem to be due to different chemical compositions of the chlorite protoliths of these rocks.     

Partitioning of iron and magnesium between crystals and partial melts in peridotite upper mantle

The iron-magnesium distribution coefficient, $$K'_D = (X_{\Sigma {\text{FeO}}} /X_{{\text{MgO}}} )^{{\text{olivine}}} (X_{{\text{MgO}}} /X_{\Sigma {\text{FeO}}} )^{{\text{liquid}}} ,$$ has frequently been used as a means of testing whether experimental and natural silicate liquids could have been in equilibrium with olivine of mantle composition. It is shown here that this K′ _D decreases with increasing oxygen fugacity (xxx) for a hydrous partial melt in equilibrium with a natural spinel peridotite assemblage under pressure and temperature conditions corresponding to those of the upper mantle (from 0.52 at the xxx of the iron-wüstite buffer to 0.04 at the xxx of the magnetite-hematite buffer). K′ _D also increases with increasing pressure, with decreasing temperature, and probably with increasing Mg/(Mg+∑ Fe) of the parental peridotite, suggesting that $$K_D = (X_{{\text{FeO}}} /X_{{\text{MgO}}} )^{{\text{olivine}}} (X_{{\text{MgO}}} /X_{{\text{FeO}}} )^{{\text{liquid}}}$$ also increases with increasing pressure and decreasing temperature. Thus, unless these four variables (P, T, xxx, silicate composition) are known for a natural magma, K′ _D and probably K _D are variables, and the Mg/(Mg+∑ Fe) of such a magma cannot be correlated to that of the parent. The K _D determined at 1 atm pressure by Roeder and Emslie has frequently been used to test whether the Mg/(Mg+∑ Fe) ratios of experimentally formed liquids at high pressure in equilibrium with olivine of known Fo content represent the equilibrium Mg/(Mg+Fe²⁺) of this liquid, assuming that ∑Fe=Fe²⁺ and that K′ _D does not vary with P, T, and composition of the system. Published data demonstrate that the oxygen fugacities of the experimental designs employed by different laboratories vary between those of the magnetite-hematite and magnetite-wüstite buffers (6 orders of magnitude), resulting in K′ _D between 0.04 and 0.31 at 1050° C and 15 kbar, for example. Thus, published arguments as to whether the quenched liquids represent equilibrium compositions based on iron-magnesium partitioning are inadequate. The effects of P, T, xxx, and the composition of the starting material must also be considered.     

Thermodynamic data for phases in the FeO-MgO-SiO2 system and phase relations in the mantle transition zone

Based on the available experimental data on phase equilibria in the FeO -MgO -SiO₂ system the mixing properties of the solid solutions (olivine, β- and γ-spinel, pyroxene, majorite, ilmenite and perovskite and magnesiowustite), the enthalpies of FeO and fictive FeSiO₃ phases with ilmenite and majorite structures have been assessed. The entropies, temperature dependance of heat capacities for fictive FeSiO₃ end-members were estimated from structural analogies. The calculated phase diagrams for Mg₂SiO₄-Fe₂SiO₄ and MgSiO₃ — FeSiO₃ systems at pressures up to 30 GPa and temperatures between 1000 and 2100 K are quite consistent with the available experimental determinations except for the fine features of the phase diagram at 2073 K.     

月表澄海—静海区遥感地质分析

月海盆地作为月球表面重要的地貌单元,分析其玄武岩喷发历史和构造作用,对于了解月球演化有着重要的意义。文中以澄海和静海两个相连通盆地为研究区,通过对LRO的DEM数据进行处理,获得两个月海的地形特征。基于Clementine多光谱数据处理,提取TiO2、FeO含量和成熟度分布图。经过对嫦娥一号CCD影像数据并结合LRO和LO全色波段影像的解译,提取了研究区126条月岭和114条月溪,并对比Cle-mentine提取的重力分布图,对其展布形式进行研究。综合分析结果表明,两个盆地虽然相邻连通,但岩性和构造分布有着明显的差别,玄武岩喷发不同期次界限明显,且澄海玄武岩年龄普遍晚于静海,相通处玄武岩与静海北部玄武岩同源。澄海中的线状构造展布形式与静海中的明显不同,呈现出一定规律,与质量瘤的有无及重力展布形式有关。     

月球风暴洋火山口暗物质矿物反演及地质意义

月表主要矿物的空间分布是研究月球起源及演化等科学问题的重要信息之一.以风暴洋地区为例, 根据不同矿物光谱在可见光-近红外波段的吸收特征, 使用印度M3(moon mineralogy mapper)数据, 应用波谱特征拟合法(SFF)反演了火山口附近暗物质区域的单斜辉石、斜方辉石、橄榄石和尖晶石等铁镁质矿物的分布, 反演结果显示: 风暴洋地区提取的铁镁质矿物分布较集中, 其中辉石含量较多, 橄榄石和尖晶石含量相对较少.另外着重分析了橄榄石、尖晶石与周围矿物的关系及其地质意义.将提取结果与Lucey用于Clementine影像的光学模型填图结果进行对比显示, 提取的橄榄石分布集中, 但不存在大尺度的分布, 这与本文的研究区域面积有关; 就位置而言, 二者具有较好的一致性.