存在初始“传导盖层”的月球岩浆洋演化与月壳成因

月球早期经历了岩浆洋阶段,岩浆洋的研究对认识月球内部构造有着重要意义。月球岩浆洋演化主导模型认为:岩浆洋结晶到80%左右,斜长石开始结晶,并上浮形成斜长岩月壳。该模型与观察事实存在两点矛盾:1)基于该模型计算结晶的斜长石An牌号比高地样品斜长石An牌号测试结果低;2)该模型散热速率计算指示岩浆洋在几个百万年时间内固化,而同位素体系对月球岩石样品定年结果表明月壳的结晶年龄十分古老,并且结晶区间跨越了270Myr,这与主导模型之间存在矛盾。以解决以上两点矛盾为目的,本文论证岩浆洋在演化之初硕部存在冷却"盖层",并将硅酸盐熔体在温度梯度下的热扩散效应引入岩浆洋演化模型。热扩散效应指均一的物质在温度梯度下发生分异的过程。本文工作模型是:由于月球的重力常数小,不能有效的保持大气,因此月球的岩浆洋表面温度很低。此时岩浆洋自上而下存在一个过渡的瞬态固化"盖层"(淬火层),岩浆洋自上而下存在温度梯度,岩浆洋在该梯度下发生热扩散效应(Soret效应),Soret效应导致上部结晶斜长石的熔体富Ca和贫Na,因此结晶的斜长石An牌号高。     

月球的化学演化

月球是一个发生了化学分异的星球,它由月壳、月幔±一个小的金属月核组成。大量观察事实显示月球曾经有过岩浆洋,岩浆洋的结晶分异主导了月球的化学演化。目前主流观点认为,月球是在太阳系演化的早期,至少45亿年前,一个火星大小的星球,与即将完成原始吸积的地球胚胎发生偏心撞击,造成地球的熔融,形成岩浆洋,飞溅出来的物质迅速吸积形成绕地球运动的月球,并且在月球上形成了全球规模的岩浆洋,进而发生了结晶分异。,由于月球上没有海洋和板块俯冲,岩浆洋分异是其化学演化的主要途径。月球岩浆洋的80％～85％在大撞击后的100Ma内已经固化,这可能是由于月球体积小、表面没有大气包裹所致。月球极贫水,因此在岩浆结晶过程中斜长石首先结晶。斜长石由于密度小于玄武质岩浆而漂浮在岩浆洋的表层,橄榄石等密度大的矿物则堆积在岩浆洋的底部。随着结晶分异的进行,残余岩浆不断富集不相容元素,包括K、U等放射性元素;与此同时,密度较大的钛铁矿开始结晶,造成高钛堆晶岩密度大于其下的橄榄石堆晶岩的不稳定结构,进而发生月幔翻转,引发一系列岩浆活动,进而形成月球上特有的镁质系列、碱质系列等岩石。由于月球氧逸度较低,Eu主要以＋2价形式存在,因此斜长石高度富集Eu,相应地除高地斜长岩外,其他岩石均表现为Eu高度亏损的特点。与此同时,Re在低氧逸度下表现为强亲铁元素的特点,Re／Os在月球岩浆过程中不发生分异。月球的体积远小于地球,因而其演化时间远远短于地球,很多原始的分异被完整地保留下来。因此月球的化学演化是类地行星早期演化过程的“化石”,尽管与现代的地球存在较大差异,但是对于认识地球早期演化具有借鉴意义。     

江西会昌锡矿花岗质喷出——侵入岩建造的岩石特点及其成因

本文通过对会昌岩背火山岩、花岗岩的地质学、岩石学、地球化学特征研究，认为火山岩与花岗岩是同源岩浆结晶分异的产物。花岗岩是由于地幔或下地壳富碱稀薄岩浆上侵，引起上地壳物质同熔，形成中酸性岩浆，经在深部岩浆房充分分异演化，形成酸性岩浆上侵结晶形成的产物。     

热力学计算模拟对初始月幔结构的约束SCIEI北大核心CSCD

月球岩浆洋结晶形成的初始月球内部结构是其后续演化过程的开端,其结晶过程受月球岩浆洋的初始深度和物质组成这两个参数的制约。由于缺少直接来自月球深部的岩石样品,目前关于月球岩浆洋演化过程的探讨主要依赖实验和计算模拟手段。岩浆洋模型中形成的月壳厚度是否与探测结果一致是月球岩浆洋演化模型合理性的重要约束。最新的GRAIL(Gravity Recovery and Interior Laboratory)探测数据推算月壳厚度为34~43km,低于阿波罗时期认为的约70km,这对已有的月球岩浆洋演化模型提出了挑战。本文采用并修正FXMOTR程序包,针对月球岩浆洋在不同的初始深度和物质组成情况下的结晶过程,进行了一系列热力学计算模拟。通过量化月球岩浆洋的初始深度和物质组成对月壳厚度的影响,结合关于月球内部微量元素分配的研究结果,对比了月球岩浆洋结晶后期的残余熔体与原始克里普组分(urKREEP)的成分。本文的模拟结果显示,一个全月幔熔融且初始成分为月球初始上月幔组成(LPUM)的岩浆洋将在其深部结晶2.5%石榴子石,形成的月壳厚度符合GRAIL的约束,并且结晶出了合适的urKREEP成分。在此模型的基础上获取了月球初始的内部成分和密度结构,并对后期月幔翻转(Overturn)的程度进行了探讨。     

南澜沧江结合带火山岩岩浆成因——洋脊洋岛与弧岩浆作用的性质

在对滇西南昌宁—孟连带石炭—二叠纪火山岩和南澜沧江带二叠—三叠纪火山岩的微量元素和稀土元素研究的基础上,划分了岩浆作用类型和岩浆演化系列,探讨了岩浆源区成分特点。昌宁—孟连带玄武质岩浆的演化主要受部分熔融和分离结晶作用控制;这些岩浆可以划分为３个岩浆演化系列：（１）稀土曲线平坦型的洋脊型拉斑玄武岩浆演化系列,其岩浆起源于亏损型地幔;（２）稀土曲线中等富集型的准洋脊型拉斑玄武岩浆演化系列,其岩浆起源于过渡型地幔;（３）稀土曲线强烈富集型的洋岛型碱性玄武岩浆演化系列,其岩浆起源于富集型地幔。南澜沧江带弧火山岩的岩浆成因主要受分离结晶作用控制,也可以划分为３个岩浆演化系列：（１）二叠纪低钾拉斑—中钾钙碱性岩浆演化系列;（２）中南段的晚三叠世低钾拉斑—中钾钙碱性岩浆演化系列;（３）北段的晚三叠世钾玄岩—高钾钙碱性岩浆演化系列     

固体地球系统的复杂性与自组织临界性

（上接第３期第１８２页）３４壳幔核边界的深部过程———固体地球动力学问题之二属于本主题研究的主要课题有：①行星和地球上的岩浆洋;②地幔对流与壳幔相互关系;③洋脊下岩浆的成生与运移;④俯冲带岩浆作用;⑤地壳岩浆房中岩浆的分异与演化;⑥地球电动机（ｇｅ...     

岩浆熔体中的挥发性组分及其岩石学意义

文章论述了挥发性组分在岩浆熔体中的溶解行为及其在岩浆熔体中溶解的限制条件，在此基础上讨论了挥发性组分对岩浆演化及岩石学成因方面的意义：溶解在岩浆中的水可明显地改变矿物从岩浆中结晶出的顺序，改变岩浆熔体的演化轨迹。含水玄武岩浆在其早期结晶出铁的氧化物并与Ｓｉ和富碱质组分分异从而使其成为Ｆｅ亏损的钙－碱性系列的岩浆，而无水玄武岩浆演化的早期不能结晶出磁铁矿，因而演化成富Ｆｅ且具中等Ｓｉ含量的拉斑玄武岩系列。溶解于岩浆中Ｈ２Ｏ的离解将产生高ｆＯ２环境，从而导致Ｆｅ的氧化物在岩浆演化早期沉淀。     

新疆东准噶尔老鸦泉碱性岩及相关锡矿的岩石地球化学特征

老鸦泉富碱花岗岩杂岩体与侵入其中的富碱花岗斑岩岩体及云英岩型锡矿体、石英脉型锡矿体等REE配分曲线类似,均具有强烈的Eu亏损,它们的微量元素蛛网图等岩石地球化学特征也类似,是同源岩浆结晶分异演化的结果。锡矿体是老鸦泉富碱岩浆分异演化及以钠质为主的强烈碱交代自变质作用的最终产物。侵入于老鸦泉岩体内的花岗斑岩为锡矿体的直接围岩,它是岩浆结晶分异更晚期混入了更多地壳组分,并向酸性方向演化的产物,该花岗斑岩经自变质热液蚀变作用造成锡的富集并成矿。因此,碱性岩浆结晶分异晚期混有地壳组分,岩浆向酸性演化可能是碱性花岗岩形成锡矿的重要条件之一。     

荡坪钨矿的岩浆分异与成矿

根据荡坪钨矿岩浆岩的相变规律、岩脉活动特征、岩脉与矿脉间的过渡现象,结合岩浆岩石化学等方面的研究,认为该区矿化是岩浆长期分异演化的产物,分异演化最好的岩浆阶段是该区矿化的最好时期。     

冲绳海槽玄武岩中中酸性残余熔体研究及其岩石学意义

与洋壳有关的酸性岩由于对了解幔源岩浆的演化以及判别古老蛇绿岩套及其构造位置的重要意义而倍受岩石学家和构造地质学家的关注。本对发现于冲绳海槽玄武岩基质中的中酸性到酸性残余熔体进行了详细研究，它们提供了幔源玄武岩浆结晶分异形成酸性岩浆的直接证据。在细小的基质矿物间分布有一种玻璃质的残余熔体，其成分随距冷凝边距离(L)的增加而越来越酸性。在SiO2对Na2O K2O图解上，残余熔体的投影点从玄武岩到英安岩均有分布，反映了一个连续的演化系列。在AFM图解上，残余熔体表现出与Thingmuli火山岩系列类似的拉斑玄武岩系列的演化趋势。我们的研究表明：残余熔体的演化受结晶分异作用控制。在早期结晶阶段，辉石的结晶起主导作用，结果造成残余熔体中SiO2、Al2O3，Na2O的迅速增加，FeO、MgO、CaO迅速降低。在晚期结晶阶段，斜长石成为主导结晶相，导致残余熔体中Al2O3，Na2O的迅速消减。Al2O3、Na2O从增加到降低的转变出现在SiO2=62％左右。在L=27．5mm处，85～90％的基质岩浆已发生了结晶作用，导致残余熔体中SiO2含量达到69～70％，而且此处还新出现了一种富FeTi的氧化物。该玄武岩中残余熔体和基质矿物的成分及演化特征分别与Thingmuli火山岩系列中酸性端元的组成相似，在也佐证了Thingmuli火山岩系列是幔源岩浆结晶分异的产物.     

Effect of crustal porosity on lunar magma ocean solidification

Acta Geochimica - The lunar ferroan anorthosites, formed by plagioclase flotation from the crystallization of the lunar magma ocean, have an age span of over ~ 200 Ma. However,...     

The pattern of Ni and Co abundances in lunar olivines

Near liquidus experiments on peridotite and other olivine normative compositions from 1.7 to 6 GPa confirm the applicability of exchange-based empirical models of Ni and Co partitioning between olivine and silicate liquids with compositions close to the liquidus of peridotite. Given that most estimates of lunar bulk composition are peridotitic, the partitioning models thus lend themselves to calculation of olivine compositions produced during the early stages of magma ocean crystallization. Calculation of olivine compositions produced by fractional crystallization of a model lunar magma ocean, initially 700 km deep, reveals a prominent maximum in Ni concentration versus fraction crystallized or Mg’ (molar MgO/(MgO + FeO)), but a pattern of monotonically increasing Co concentration. These patterns qualitatively match the puzzling patterns of Ni and Co concentrations observed in lunar rocks in which forsteritic olivines in magnesian suite cumulates have lower Ni and Co abundances than do less magnesian olivines from low-Ti mare basalts, and olivines from the ferroan anorthosite suite (FAS) have lower Ni, but similar Co to mare basalt olivines.The Ni and Co abundances in olivines from the magnesian suite cumulates can be reconciled in terms of fractional crystallization of a deep magma ocean which initially produces a basal dunite comprised of the hottest and most magnesian olivine overlain by an olivine-orthopyroxene (harzburgite) layer that is in turn overlain by an upper zone of plagioclase-bearing cumulates. The ultramafic portion of the cumulate pile overturns sending the denser harzburgite layer, which later becomes a portion of the green glass source region, to the bottom of the cumulate pile with Ni- and Co-rich olivine. Meanwhile, the less dense, but hottest, most magnesian olivines with much lower Ni and Co abundances are transported upward to the base of the plagioclase-bearing cumulates where subsequent heat transfer leads to melting of mixtures of primary dunite, norite, and gabbronorite with KREEP (a K-REE-P enriched component widely believed to be derived from the very latest stage magma ocean liquid). These hybrid melts have Al₂O₃, Ni, and Co abundances and Mg’ appropriate for parent magmas of the magnesian suite. Ni and Co abundances in the FAS are consistent with either direct crystallization from the magma ocean or crystallization of melts of primary dunite-norite mixtures without KREEP.     

A Rb-Sr and Sm-Nd isotope geochronology and trace element study of lunar meteorite LaPaz Icefield 02205

Rubidium-strontium and samarium-neodymium isotopes of lunar meteorite LaPaz Icefield (LAP) 02205 are consistent with derivation of the parent magma from a source region similar to that which produced the Apollo 12 low-Ti olivine basalts followed by mixing of the magma with small amounts (1-2 wt%) of trace element-enriched material similar to lunar KREEP-rich sample SaU 169. The crystallization age of LAP 02205 is most precisely dated by an internal Rb-Sr isochron of 2991 ± 14 Ma, with an initial ⁸⁷Sr/⁸⁸Sr at the time of crystallization of 0.699836 ± 0.000010. Leachable REE-rich phosphate phases of LAP 02205 do not plot on a Sm-Nd mineral isochron, indicating contamination or open system behavior of the phosphates. Excluding anomalous phases from the calculation of a Sm-Nd isochron yields a crystallization age of 2992 ± 85 (initial ε¹⁴³Nd = +2.9 ± 0.8) that is within error of the Rb-Sr age, and in agreement with other independent age determinations for LAP 02205 from Ar-Ar and U-Pb methods. The calculated ¹⁴⁷Sm/¹⁴⁴Nd source ratios for LAP 02205, various Apollo 12 and 15 basalts, and samples with strong affinities to KREEP (SaU 169, NWA 773, 15386) are uncorrelated with their crystallization ages. This finding does not support the involvement of a common KREEP component as a heat source for lunar melting events that occurred after crystallization of the lunar magma ocean.     

Evolution of major mineral compositions and trace element abundances during fractional crystallization of a model lunar composition

The evolution of major mineral compositions and trace element abundances during fractional crystallization of a model lunar magma ocean have been calculated. A lunar bulk composition consistent with petrological constraints has been selected. Major mineral compositions have been calculated using published studies of olivine-melt, plagioclase-melt, and pyroxene-olivine equilibria. Trace element abundances have been calculated using experimentally-determined partition coefficients where possible. In the absence of experimental determinations, published partition coefficients obtained by analyzing phase separates from porphyritic volcanic rocks have been used. Trace elements studied are La, Sm, Eu, Lu, Rb, Sr( Eu²⁺), Ni, Co, and Cr.The first mineral to crystallize is olivine, which varies in composition from Fo₉₈ at the liquidus to Fo₉₅ at 50% solidification. Orthopyroxene crystallizes from 50 to 60% solidification with a restricted composition range of En₉₅-En₉₃. Plagioclase and Ca-rich clinopyroxene (X_Wo arbitrarily set equal to 0.5) co-crystallize during the final 40% solidification. Plagioclase changes in composition from An₉₇ to approximately An₉₃, while clinopyroxene evolves from En₄₆ to approximately En₄₀. The concomitant evolution of major element abundances in the melt is also discussed.The concentration of Ni in the melt decreases rapidly because solid-melt partition coefficients are significantly greater than unity at all stages of crystallization. The concentration of Cr in the melt increases slowly during olivine crystallization, then drops precipitously during the crystallization of orthopyroxene and clinopyroxene. The concentration of Co in the melt decreases slowly during olivine and orthopyroxene crystallization, after which it returns slowly to its initial concentration. Rubidium and Sr are not fractionated relative to one another until the onset of plagioclase crystallization. Ratios of Rb/Sr, normalized to their initial concentrations in the magma, do not rise above 10 until 95% of the magma has solidified. The ratios of Eu/Sm and La/Lu, normalized to their initial concentrations in the magma, remain essentially unfractionated until the onset of crystallization of clinopyroxene plus plagioclase, at which point the normalized La/Lu ratio increases to approximately 1.3 at 100% solidification and the normalized Eu/Sm ratio decreases to approximately 0.2 at 100% solidification.The model calculations are used to place approximate constraints on the bulk composition of the primitive Moon. Consideration of the effect on plagioclase composition of the activities of NaO_0.5 and SiO₂ in the melt suggests that the primitive Moon contained less than 0.4 wt % NaO_0.5 and approximately 42–43 wt % SiO₂. Concentrations of the REE in model lunar anorthosites are consistent with the returned samples. Concentrations of the REE in several model ‘highland basalts’ (considered to be representative of the average lunar terrae) are too low when compared with returned samples. Several possible explanations of this discrepancy are considered. The possible role of spinel in a twostage geochemical evolution of mare basalt liquids is discussed.     

Chemical composition of lunar meteorites and the lunar crust

The paper presents the first analyses of major and trace elements in 19 lunar meteorites newly found in Oman. These and literature data were used to assay the composition of highland, mare, and transitional (highland-mare interface) regions of the lunar surface. The databank used in the research comprises data on 44 meteorites weighing 11 kg in total, which likely represent 26 individual falls. Our data demonstrate that the lunar highland crust should be richer in Ca and Al but poorer in mafic and incompatible elements than it was thought based on studying lunar samples and the first orbital data. The Ir concentration in the highland crust and the analysis of lunar crater population suggest that most lunar impactites were formed by a single major impact event, which predetermined the geochemical characteristics of these rocks. Lunar mare regions should be dominated by low-Ti basalts, which are, however, enriched in LREEs compared to those sampled by lunar missions. The typical material of mare-highland interface zones can contain KREEP and magnesian VLT basalts. The composition of the lunar highland crust deduced from the chemistry of lunar meteorites does not contradict the model of the lunar magma ocean, but the average composition of lunar mare meteorites is inconsistent with this concept and suggests assimilation of KREEP material by basaltic magmas. The newly obtained evaluations of the composition of the highland crust confirm that the Moon can be enriched in refractory elements and depleted in volatile and siderophile elements.     

Heat-producing elements in the lunar mantle: Insights from ion microprobe analyses of lunar pyroclastic glasses

We provide new estimates for the abundance of heat-producing elements in the lunar mantle by using SIMS techniques to measure the concentrations of thorium and samarium in lunar pyroclastic glasses. Lunar pyroclastic glasses are utilized in this study because they represent quenched products of near-primary melts from the lunar mantle and as such, they provide compositional information about the mantle itself. Thorium and samarium were measured because: (1) Th is not significantly fractionated from Sm during partial melting of the pyroclastic glass source regions, which are dominated by olivine and pyroxene. Therefore, the Th/Sm ratios that we measure in the pyroclastic glasses reflect the Th/Sm ratio of the pyroclastic glass source regions. (2) Strong correlations between Th, U, and K on the Moon allow us to use measured Th concentrations to estimate the concentrations of U and K in the pyroclastic glasses. (3) Th, Sm, U, and K are radioactive elements and as such, their concentrations can be used to investigate heat production in the lunar mantle.The results from this study show that the lunar mantle is heterogeneous with respect to heat-producing elements and that there is evidence for mixing of a KREEP component into the source regions of some of the pyroclastic glasses. Because the source regions for many of the glasses are deep (?400 km), we propose that a KREEP component was transported to the deep lunar mantle. KREEP enriched sources produce 138% more heat than sources that do not contain KREEP and therefore, could have provided a source of heat for extended periods of nearside basaltic magmatism. Data from this study, in conjunction with models for the fractional crystallization of a lunar magma ocean, are used to show that the average lunar mantle contains 0.15 ppm Th, 0.54 ppm Sm, 0.039 ppm U, and 212 ppm K. This is a greater enrichment in radiogenic elements than some earlier estimates, suggesting a more prolonged impact of radiogenic heat on nearside basaltic volcanism.     

Anorthosite formation by plagioclase flotation in ferrobasalt and implications for the lunar crust

The Sept Iles layered intrusion (Quebec, Canada) is dominated by a basal Layered Series made up of troctolites and gabbros, and by anorthosites occurring (1) at the roof of the magma chamber (100-500 m-thick) and (2) as cm- to m-size blocks in gabbros of the Layered Series. Anorthosite rocks are made up of plagioclase, with minor clinopyroxene, olivine and Fe-Ti oxide minerals. Plagioclase displays a very restricted range of compositions for major elements (An₆₈-An₆₀), trace elements (Sr: 1023-1071 ppm; Ba: 132-172 ppm) and Sr isotopic ratios (⁸⁷Sr/⁸⁶Sr_i: 0.70356-0.70379). This compositional range is identical to that observed in troctolites, the most primitive cumulates of the Layered Series, whereas plagioclase in layered gabbros is more evolved (An₆₀-An₃₈). The origin of Sept Iles anorthosites has been investigated by calculating the density of plagioclase and that of the evolving melts. The density of the FeO-rich tholeiitic basalt parent magma first increased from 2.70 to 2.75 g/cm³ during early fractionation of troctolites and then decreased continuously to 2.16 g/cm³ with fractionation of Fe-Ti oxide-bearing gabbros. Plagioclase (An₆₉-An₆₀) was initially positively buoyant and partly accumulated at the top of the magma chamber to form the roof anorthosite. With further differentiation, plagioclase (<An₆₀) became negatively buoyant and anorthosite stopped forming. Blocks of anorthosite (autoliths) even fell downward to the basal cumulate pile. The presence of positively buoyant plagioclase in basal troctolites is explained by the low efficiency of plagioclase flotation due to crystallization at the floor and/or minor plagioclase nucleation within the main magma body. Dense mafic minerals of the roof anorthosite are shown to have crystallized from the interstitial liquid.The processes related to floating and sinking of plagioclase in a large and shallow layered intrusion serve as a proxy to refine the crystallization model of the lunar magma ocean and explain the vertically stratified structure of the lunar crust, with (gabbro-)noritic rocks at the base and anorthositic rocks at the top. We propose that the lunar crust mainly crystallized bottom-up. This basal crystallization formed a mafic lower crust that might have a geochemical signature similar to the magnesian-suite without KREEP contamination, while flotation of some plagioclase grains produced ferroan anorthosites in the upper crust.     

月球形成演化与月球地质图编研

按照大碰撞假说,月球形成于一次大碰撞事件,抛射出的高能量物质留在绕地轨道上,最后吸积形成月球。月球核幔在早期迅速发生分离,并出现全球性的岩浆熔融,形成了岩浆圈层（岩浆洋）。岩浆洋的结晶分异和固化导致了月壳的形成。随着月壳与月幔发生持续分异,形成了固化的月壳。而在月球后期的演化历史中,撞击作用是最重要的地质作用,形成了多尺度、多期次的撞击盆地和撞击坑,而大型撞击盆地多形成于月球演化的早期。月球地质图是开展月球形成与演化研究的重要手段,从20世纪60年代起,到70年代末止,通过对阿波罗时代探月成果的系统总结,完成了第一轮月球地质图的研制。但尽管从20世纪90年代以来国际月球探测和月球科学的研究进入一个新的高潮,获得了大量有关月球形成和演化的新认识,但还没有正式的新的月球地质图发布,因此开展新一轮月球地质图的编研,系统总结后阿波罗时代的月球探测与研究成果,是非常必要和迫切的。在新一轮月球地质图的编制过程中,需重点关注图件比例尺的选择、月面历史的划分以及月球构造和岩石建造的表达。     

月球岩浆洋演化的实验岩石学研究进展SCIEI北大核心CSCD

由于缺少直接来自月球深部的岩石样品,实验和计算模拟是认识早期月球演化过程的有效方法和手段。20世纪70年代以来,陆续开展了大量的实验岩石学和实验地球化学工作对月球岩浆洋(lunar magma ocean,LMO)演化模型进行验证和修正。但是,学界对LMO模型中的两个关键性参数,即初始物质组成和熔融深度,仍然存在不同的认识。根据月震和重力探测数据推测的平均月壳厚度的差异、月球样品含水量的研究以及新的遥感数据解译发现月表广泛分布富镁铝尖晶石(Cr#<5)等等,直接影响我们对月球初始物质组成和LMO深度以及月球深部高压矿物相的评估。本文通过整理高温高压实验岩石学和实验地球化学在研究LMO演化方面的一系列研究成果,主要聚焦以下几个科学问题:(1)月球初始物质组成中的难熔元素和挥发分含量,以及LMO深度对月壳厚度、结晶矿物的种类及含量有着决定性的影响;(2)高压矿物相石榴子石在月球深部稳定存在的可能性及其对残余岩浆中微量元素的分配行为的制约;(3)特殊类型的月球样品(包括火山玻璃、镁质岩套等)的成因机制对月球深部物质组成具有指示意义;(4)月核的不同物质组成对LMO模型的初始成分含量,特别是微量元素的限定作用。我们以最新的观测数据和月球样品的分析结果为依据,对已有的LMO演化模型进行重新评估,提出月球深部含有石榴子石的LMO演化模型的可能性,并对该方向亟需开展的工作进行探讨。     

Origin of titaniferous lunar basalts

Delineation of low pressure phase equilibria in the composition space relevant to titaniferous lunar basalts demonstrates a significant degree of control by those equilibria on the compositions of the basalts. The existence of two distinct chemical groups of basalts (high and low-K) which cannot be related one to the other by fractional crystallization at any pressure, suggests that melting is responsible for the two groups. Consideration of the pressure shift required to produce the differences between groups constrains magma segregation to have occurred in the outer 150 km of the Moon. It is difficult to relate low-Ti and high-Ti basalts to the same source region. The preferred source region of high-Ti basalts, based on phase equilibrium considerations, is a late ilmenite-rich cumulate produced from the residual liquid of the primordial differentiation of the outer portions of the Moon. This ilmenite-rich layer is sandwiched between the lunar feldspathic crust and a complementary mafic cumulate.