Lunar monazite: A late-stage (mesostasis) phase in mare basalt

Thorium-poor monazite occurs as an inclusion in a ferrohedenbergite grain within a mesostasis area of the relatively coarse-grained Apollo 11 basalt 10047,68. Only a single grain of monazite (～ 4 × 15 μm) has been observed but it is possible that monazite may exist as a more significant phase at smaller grain sizes. Electron probe analyses indicate chondrite-normalized REE fractionation patterns for both lunar and terrestrial monazites in which the light REE's (La to Sm) are highly enriched relative to the heavy REE's (Gd to Lu). Lunar monazite shows a distinct Eu anomaly which is absent from the terrestrial sample. Crystallization of monazite from late-stage liquids forming during crystallization of lunar igneous rocks could lead to these liquids becoming increasingly depleted in the light REE's relative to the heavy REE's.     

Rare earth element abundances in rocks and minerals from the Fiskenaesset Complex,West Greenland

Rare earth element (REE) abundances determined by activation analysis in rocks, plagioclase and mafic separates from the Fiskenaesset Complex are presented together with data on major and trace elements in the minerals. The REE data for the rocks and plagioclases are distinct from those of many other anorthositic complexes and the abundances are some of the lowest recorded for plagioclase from terrestrial anorthosites. The bulk and trace element compositions of the Fiskenaesset plagioclases show a number of similarities to those of lunar plagioclases. The plagioclases show a positive Eu anomaly of about 10 and a depletion in the heavy REE relative to the light ones. The mafic separates are enriched in the heavy REE relative to the light ones, and show no Eu anomaly except in one sample with a positive anomaly not attributable to plagioclase contamination. It is estimated, from experimental partition coefficient data, that the REE pattern in the magma at an early stage of fractionation was La (17×) to Lu (0.7× chondrites) with a possible positive Eu anomaly. This highly fractionated REE pattern may be attributed to partial melting of a garnet-bearing source.     

Fission-track retention age of the Bondoc mesosiderite

Whitlockites have been extracted from the Bondoc mesosiderite and found to contain ～(0.7–2.7) × 10⁶ cm^?2 of spontaneous-fission tracks. Thermal-neutron irradiation of these crystals along with terrestrial apatite age standards, and measurement of the track densities so induced, lead to the determination of a whitlockite track-retention age of 2.68 (±0.30) Gyr for Bondoc, which is essentially independent of the initial (Pu/U) ratio.This young age is in qualitative, and, within the experimental uncertainties, in quantitative, agreement with the slow cooling rates determined for many mesosiderites [1,2] and specifically for Bondoc [6] from Ni distributions in the metal phase.     

Apatite/liquid partition coefficients for the rare earth elements and strontium

Sixteen sets of apatite/liquid partition coefficients (D^ap/liq) for the rare earth elements (REE; La, Sm, Dy, Lu) and six values for Sr were experimentally determined in natural systems ranging from basanite to granite. The apatite + melt (glass) assemblages were obtained from starting glasses artificially enriched in REE, Sr and fluorapatite components; these were run under dry and hydrous conditions of 7.5–20 kbar and 950–1120°C in a solid-media, piston-cylinder apparatus. An SEM-equipped electron microprobe was used for subsequent measurement of REE and Sr concentrations in coexisting apatites and quenched glasses. The resulting partition coefficient patterns resemble previously determined apatite phenocryst/groundmass concentration ratios in the following respects: (1) the rare earth patterns are uniformly concave downward (i.e., the middle REE are more compatible in apatite than the light and heavy REE); (2) D_REE^ap/liq is much higher for silicic melts than for basic ones; and (3) strontium (and therefore Eu²⁺) is less concentrated by apatite than are the trivalent REE. The effects of both temperature and melt composition on D_REE^ap/liq are systematic and pronounced. At 950°C, for example, a change in melt SiO₂ content from 50 to 68 wt.% causes the average REE partition coefficient to increase from ～7 to ～30. A 130°C increase in temperature, on the other hand, results in a two-fold decrease in D_REE^ap/liq. Partitioning of Sr is insenstitive to changes in melt composition and temperature, and neither the Sr nor the REE partition coefficients appear to be affected by variations in pressure or H₂O content of the melt.The experimentally determined partition coefficients can be used not only in trace element modelling, but also to distinguish apatite phenocrysts from xenocrysts in rocks. Reported apatite megacryst/host basalt REE concentration ratios [12], for example, are considerably higher than the equilibrium partition coefficients, which suggest that in this particular case the apatite is actually xenocrystic.A reversal experiment incorporated in our study yielded diffusion profiles of REE in apatite, from which we extracted a REEαCa interdiffusion coefficient of 2–4×10^?14 cm²/s at 1120°C. Extrapolated downward to crustal temperatures, this low value suggests that complete REE equilibrium between felsic partial melts and residual apatite is rarely established.     

Genesis of the Angra dos Reis and other achondritic meteorites

Major, minor and trace element abundances were determined in seven Angra dos Reis samples including whole rocks, fassaite (clinopyroxene), olivine and whitlockite separates via sequential instrumental neutron activation analysis. The chondritic normalized rare earth element (REE) abundance pattern for the Angra dos Reis clinopyroxene separates shows a concave downward shape with a small negative Eu anomaly. The strong fractionation between the light and the heavy REE in olivine separates could be attributed to the presence of islands of kirschsteinite in the olivines. The large-ion lithophile trace elements were highly enriched in the whitlockite separate as expected (e.g. La ≈ 370 ppm). The lower Hf and Sc abundances in whitlockite compared to that in the equilibrium “magma” could be the result of favorable partitioning of Hf and Sc in baddeleyite, which may have crystallized prior to or with whitlockite in the interstitial liquid. Comparison of whole rock with mineral separate data shows the presence of ～3% olivine, ～2.6% spinel and small amounts of metallic Ni-Fe and troilite in the whole rock.The trace element abundances in the derivative magma from which the Angra dos Reis clinopyroxene crystallized were estimated from the clinopyroxene data and the clinopyroxene mineral-liquid partition coefficients. From the derivative magma, the trace element abundances in the possible parent magmas were calculated by assuming that these parent magmas have undergone different degrees of clinopyroxene fractional crystallization to yield the Angra dos Reis derivative magma. Using the trace element abundances in these possible parent magmas, a two-stage crystal-liquid fractionation model with source material containing olivine, orthopyroxene and clinopyroxene is presented for the genesis of Angra dos Reis. Possible combinations of the degree of equilibrium non-modal partial melting, the source mineral composition and the initial element abundances required to generate possible Angra dos Reis parent magmas are calculated by the multilinear regression analysis method. Favorable solutions for this two-stage crystal-liquid fractionation model could be that Angra dos Reis crystallized at ～70% fractional crystallization of clinopyroxene from magmas generated by reasonable degrees of equilibrium partial melting (～7–10%) of deep-seated primitive source materials (olivine ～54–30%, orthopyroxene ～33–53%, and clinopyroxene ～13–17%) with trace element (Ba, Sr, REE and Sc) abundances ～3.5–4.7 × chondrites. These calculated REE abundances in the Angra dos Reis parent body are very similar to those suggested for the primordial moon (～3–5 × chondrites).Possible genetic relationships between Angra dos Reis and other achondrites, especially cumulate eucrites and nakhlites, are studied. Apparently, the unique Angra dos Reis could not be related to those achondrites by crystal-liquid fractionation of the same parent body.     

Phosphate in Angra dos Reis: Structure and composition of the Ca3(PO4)2 minerals

Extraterrestrial calcium phosphates (“whitlockites”) have the anhydrous β-Ca₃(PO₄)₂ structure, which is different from that of hydrous terrestrial whitlockite. This has been confirmed by X-ray refinement of the structure of a phosphate from the achondrite Angra dos Reis. In the β-Ca₃(PO₄)₂ structure, there is one crystallographic site, Ca(IIA), which is half-occupied by calcium, and which seems to have an energetically unfavorable configuration; natural phosphates with this configuration (including Angra dos Reis) have composition Ca₁₉(Mg,Fe)₂(PO₄)₁₄. Stability of the structure is probably increased by substitution of Na for Ca in Ca(IIA) giving composition Ca₁₈ (Mg,Fe)₂Na₂(PO₄)₁₄, which occurs in chondrites; by vacancy of Ca(IIA), with rare earths and yttrium substituting for calcium in other sites for charge balance, giving composition Ca₁₆(Y,RE)₂(Mg,Fe)₂(PO₄)₁₄, found in lunar rocks; or by replacing Ca with hydrogen, giving composition Ca₁₈(Mg,Fe)₂H₂(PO₄)₁₄, which is terrestrial whitlockite. Lack of the favorable substitutions of Na, (Y, RE) or H in Angra dos Reis phosphate implies that these elements were relatively scarce in its environment of formation.     

The Néel transition and magnetic properties of terrestrial,synthetic, and lunar ilmenites

The magnetic susceptibility of a terrestrial, synthetic and lunar ilmenite specimen has been measured from 4 to 300 K. All specimens had a single Néel temperature transition which ranged from 56 to 57.7 K. In one case the powdered specimen was partially aligned in the magnetic field prior to the susceptibility measurements and the Néel transition was observed to shift to 60 K indicating magnetic anisotropy. A study of several magnetic parameters calculated from the experimental data showed gross impurities in the terrestrial specimen, single-domain to multi-domain metallic iron in the synthetic specimen, and a small amount of superparamagnetic metallic iron in the lunar sample. No multidomain iron was observed in the lunar ilmenite. The results of electron spin resonance measurements were also in general agreement with these findings. Because of the absence of Fe³⁺ compared to most terrestrial samples it is suggested that the anisotropic magnetic parameters be determined on lunar ilmenite when a large enough single crystal becomes available.     

X-ray study and mössbauer spectroscopy on lunar ilmenites (Apollo 11)

A comparison of lunar ilmenites (Apollo 11, 10047, 13) with terrestrial ilmenites by means of electron microprobe analysis, X-ray and Mössbauer spectrometry showed that the lunar samples contained no Fe³⁺ but excess Ti³⁺. This causes an increase of thec-axis as compared with stoichiometric ilmenite.     

A komatiite component in Apollo 16 highland breccias: implications for the nickel-cobalt systematics and bulk composition of the moon

The lunar crust at the Apollo 16 landing site contains substantial amounts of a “primitive component” in which the ferromagnesian group of elements is concentrated. The composition of this component can be retrieved via an analysis of mixing relationships displayed by lunar breccias. It is found to be a komatiite which is compositionally similar to terrestrial komatiites both in major and minor elements. The komatiite component of the lunar crust is believed to have formed by extensive degrees of melting of the lunar interior at depths greater than were involved in the formation of the lunar magma ocean which was parental to the crust. After formation of the anorthositic crust, it was invaded by extensive flows and intrusions of komatiite magma from these deeper source regions. The komatiites became intimately mixed with the anorthosite by intensive meteoroid impacts about 4.5 b.y. ago, thereby accounting for the observed mixing relationships displayed by the crust. The compositional similarity between lunar and terrestrial komatiites strongly implies a corresponding similarity between the compositions of their source regions in the lunar interior and the Earth's upper mantle. The composition of the lunar interior can be modelled more specifically by combining the komatiite composition with its liquidus olivine composition (as determined experimentally) in proportions chosen so as to produce a cosmochemically acceptable range of Mg/Si ratios for the bulk Moon. Except for higher FeO and lower Na₂O, the range of compositions thereby obtained for the bulk moon is very similar to the composition of the Earth's upper mantle.The effects of meteoritic contamination on the abundances of cobalt and nickel in lunar highland breccias were subtracted on the assumption that the contaminating projectiles were chondritic. The cobalt and nickel residuals thereby obtained were found to correlate strongly with the (Mg + Fe) content of the breccias, demonstrating that the Co and Ni are associated with the ferromagnesian component of the breccias and are genuinely indigenous to the Moon. The lunar highland Co and Ni residuals also display striking Ni/Co versus Ni correlations which follow a similar trend to those displayed by terrestrial basalts, picrites and komatiites. The lunar trends provide further decisive evidence of the indigenous nature of the Co and Ni residuals and suggest the operation of extensive fractionation controlled by olivine-liquid equilibria in producing the primitive component of the lunar breccias. Indigenous nickel abundances at the Apollo 14, 15 and 17 sites are much lower than at the Apollo 16 site, although rocks from all sites follow the same Ni/Co versus Ni trends. It is suggested that the primitive component at the Apollo 14, 15 and 17 sites was generally of basaltic composition, in contrast to the komatiitic nature of the Apollo 16 primitive component.     

Chemical fractionation in the silicate vapor atmosphere of the Earth

Despite its importance to questions of lunar origin, the chemical composition of the Moon is not precisely known. In recent years, however, the isotopic composition of lunar samples has been determined to high precision and found to be indistinguishable from the terrestrial mantle despite widespread isotopic heterogeneity in the Solar System. In the context of the giant-impact hypothesis, this level of isotopic homogeneity can evolve if the proto-lunar disk and post-impact Earth undergo turbulent mixing into a single uniform reservoir while the system is extensively molten and partially vaporized. In the absence of liquid–vapor separation, such a model leads to the lunar inheritance of the chemical composition of the terrestrial magma ocean. Hence, the turbulent mixing model raises the question of how chemical differences arose between the silicate Earth and Moon. Here we explore the consequences of liquid–vapor separation in one of the settings relevant to the lunar composition: the silicate vapor atmosphere of the post-giant-impact Earth. We use a model atmosphere to quantify the extent to which rainout can generate chemical differences by enriching the upper atmosphere in the vapor, and show that plausible parameters can generate the postulated enhancement in the FeO/MgO ratio of the silicate Moon relative to the Earth's mantle. Moreover, we show that liquid–vapor separation also generates measurable mass-dependent isotopic offsets between the silicate Earth and Moon and that precise silicon isotope measurements can be used to constrain the degree of chemical fractionation during this earliest period of lunar history. An approach of this kind has the potential to resolve long-standing questions on the lunar chemical composition.     

Petrology and chemistry of two “large” granite clasts from the moon

Pristine granite clasts in Apollo-14 breccias 14321 and 14303 have estimated masses of 1.8 and 0.17 g, respectively. The 14321 clast is ～ 60% K-feldspar and 40% quartz, with traces of extremely Mg-poor mafic silicates and ilmenite. The 14303 clast is roughly 33% plagioclase, 32% K-feldspar, 23% quartz, 11% pyroxene, and 1% ilmenite; pyroxene and ilmenite are moderately Mg-rich; plagioclase and pyroxene are strongly zoned. Both clasts are severely brecciated, but monomict (pristine). Both have abundant graphic intergrowths of K-feldspar with quartz. Unlike the majority of similar Earth rocks, both clasts are devoid of hydrous phases. The bulk composition of the 14321 clast is similar to those of several other lunar granitic samples, but the 14303 clast is unique: it bears as close a resemblance to KREEP as it does to other lunar granites. Silicate liquid immiscibility may explain why the granites are low in REE relative to KREEP.     

Discovery of Cu-Zn,Cu-Sn intermetallic minerals and its significance for genesis of the Mianning-Dechang REE Metallogenic Belt,Sichuan Province,China

The Mianning-Dechang REE metallogenetic belt is among the most important of its kind in China. The typical geologic features and multiple economically- valuable components in this belt have caught attention from more and more geologists. Wide investigations from petrology, petrochemistry to rare earth and trace element geochemistry, have been carried out recently, and a large quantity of geochemical data have already been obtained[1―11]. Maoniuping REE deposit is the largest of this belt,…     

Bearing of rare earth patterns of apatites from igneous and metamorphic rocks

Twelve apatite samples from igneous and metamorphic rocks from the Black Forest and igneous rocks from the Kaiserstuhl were analysed for their REE content. The ΣREE range from 0.116 to 1.69 wt.%; the lowest values were found in the metamorphic rocks. All apatites from the various parent rocks show a general enrichment of the lighter rare earths over the heavier and their chondrite-normalized rare earth patterns exhibit a more or less pronounced negative Ce anomaly. This Ce depletion is accompanied by relatively low La and Pr values. In addition, the apatites from igneous rocks from the Black Forest show a marked negative Eu anomaly. An explanation is offered for the simultaneous occurrence of a negative Ce and a negative Eu anomaly in one investigated rock system. The negative Ce anomaly is attributed to the occurrence of phases enriched in Ce (e.g., monazite, allanite) which crystallized prior to or simultaneously with apatite. The negative Eu anomaly in these magmatic apatites most probably is caused by discrimination of Eu²⁺ from the apatite lattice. The result of this discrimination is a selective Eu enrichment in the later crystallizing feldspars, plagioclase and orthoclase. At least in this case, the positive Eu anomaly in feldspars is not a reliable indicator of low oxygen fugacity during their crystallization; the Eu depletion of the earlier crystallized apatites is preferable for this purpose.     

Sm-Nd age of lherzolite 67667: implications for the processes involved in lunar crustal formation

Pristine samples from the lunar highlands potentially offer important information bearing on the nature of early crustal development on all the terrestrial planets. One apparently unique sample of this group of lunar crustal rocks, the feldspathic lherzolite 67667, was studied utilizing the Sm-Nd radiometric system in an attempt to define its age and the implications of that age for the evolution of the lunar highlands. Data for 67667 precisely define an isochron corresponding to an age of 4.18±0.07 AE. The observed lack of disturbance of the Sm-Nd system of this sample may suggest that this time marks its crystallization at shallow depth in the lunar crust. However, the possibility that this age, as well as those of other highland rocks, indicate the time of their impact-induced excavation from regions deep enough in the lunar crust to allow subsolidus isotopic equilibrium to be produced or maintained between their constituent minerals is also considered. Taken together, bulk rock Sm-Nd data for four “high-Mg” rocks, including 67667, indicate that the chemical characteristics of all their source materials were established 4.33±0.08 AE ago and were intimately associated with the parent materials of KREEP. This finding provides more support for the concept of a large-scale differentiation episode early in lunar history. The possible roles of the crystallization of a global magma ocean, endogenous igneous activity, and of planetesimal impact, in producing the observed geochemical and chronological aspects of lunar highland rocks are discussed.     

Lunar Laser Ranging: Glorious Past And A Bright Future

Lunar Laser Ranging (LLR), a part of the NASA Apollo program, has beenon-going for more than 30 years. It provides the grist for a multi-disciplinarydata analysis mill. Results exist for solid Earth sciences, geodesy and geodynamics,solar system ephemerides, terrestrial and celestial reference frames, lunar physics,general relativity and gravitational theory. Combined with other data, it treatsprecession of the Earth's spin axis, lunar induced nutation, polar motion/Earthrotation, Earth orbit obliquity to the ecliptic, intersection of the celestial equatorwith the ecliptic, luni-solar solid body tides, lunar tidal deceleration, lunar physicaland free librations, structure of the moon and energy dissipation in the lunar interior.LLR provides input to lunar surface cartography and surveying, Earth station and lunar retroreflector location and motion, mass of the Earth-moon system, lunar and terrestrial gravity harmonics and Love numbers, relativistic geodesic precession, and the equivalence principle of general relativity. With the passive nature of the reflectors and steady improvement in observing equipment and data analysis, LLR continues to provide state-of-the-art results. Gains are steady as the data-base expands. After more than 30 years, LLR remains the only active Apollo experiment. It is important to recognize examples of efficient and cost effective progress of research. LLR is just such an example.     

Oxygen isotope constraints on the origin and differentiation of the Moon

We report new high-precision laser fluorination three-isotope oxygen data for lunar materials. Terrestrial silicates with a range of δ¹⁸O values (− 0.5 to 22.9‰) were analyzed to independently determine the slope of the terrestrial fractionation line (TFL; λ = 0.5259 ± 0.0008; 95% confidence level). This new TFL determination allows direct comparison of lunar oxygen isotope systematics with those of Earth. Values of Δ¹⁷O for Apollo 12, 15, and 17 basalts and Luna 24 soil samples average 0.01‰ and are indistinguishable from the TFL. The δ¹⁸O values of high- and low-Ti lunar basalts are distinct. Average whole-rock δ¹⁸O values for low-Ti lunar basalts from the Apollo 12 (5.72 ± 0.06‰) and Apollo 15 landing sites (5.65 ± 0.12‰) are identical within error and are markedly higher than Apollo 17 high-Ti basalts (5.46 ± 0.11‰). Evolved low-Ti LaPaz mare-basalt meteorite δ¹⁸O values (5.67 ± 0.05‰) are in close agreement with more primitive low-Ti Apollo 12 and 15 mare basalts. Modeling of lunar mare-basalt source composition indicates that the high- and low-Ti mare-basalt mantle reservoirs were in oxygen isotope equilibrium and that variations in δ¹⁸O do not result from fractional crystallization. Instead, these differences are consistent with mineralogically heterogeneous mantle sources for mare basalts, and with lunar magma ocean differentiation models that result in a thick feldspathic crust, an olivine–pyroxene-rich mantle, and late-stage ilmenite-rich zones that were convectively mixed into deeper portions of the lunar mantle. Higher average δ¹⁸O (WR) values of low-Ti basalts compared to terrestrial mid ocean ridge basalts (Δ=0.18‰) suggest a possible oxygen isotopic difference between the terrestrial and lunar mantles. However, calculations of the δ¹⁸O of lunar mantle olivine in this study are only 0.05‰ higher than terrestrial mantle olivine. These observations may have important implications for understanding the formation of the Earth–Moon system.     

Terrestrial chondrules,glass spherules and accretionary lapilli from the suevite,Ries Crater,Germany

Until recently, no terrestrial analogues of meteoritic and lunar chondrules were known. Only rare glass spherules from the Lonar Crater, India, and black magnetic spherules from various localities have been recorded. The impact breccia suevite of the No¨rdlinger Ries Crater, Germany, contains both chondrules and glass spherules, and in addition, accretionary lapilli, all of which are found imbedded within the fine-grained matrix of the suevite. The chondrules display many of the textural features characteristic of meteoritic and lunar chondrules. Lithic chondrules and fluid drop chondrules are present, the latter having a composition quite similar to that of glass bombs and glass fragments in the suevite. Fluid drop chondrules developed from glass spherules by slow devitrification in the hot suevite ejecta masses after deposition. On the whole, fluid drop chondrules, lithic chondrules and glass spherules are rare in the suevite, with fluid drop chondrules prevailing. Detection of chondrules from a terrestrial impact crater supports theories of an impact origin for meteoritic and lunar chondrules. Accretionary lapilli also represent material formed as a result of impact.     

地震活动的月相效应

本文利用中国大陆１９１０年以来６．０级以上和首都圈地区１９６６以来１．０级以上大量地震资料，对地震活动的月相效应进行了研究。结果表明，发生在各个月相上的地震频次明显受月相的调制和制约，并且有一定的规律性，月相效应的最大幅度可影响地震活动平均频次的２５％以上，证明了地震活动的月相效应明显存在，其影响不可忽略。结果还表明，月相效应的基本特征是具有半月和全月周期性，此外，对首都圈地区地震活动以及唐山，邢     

Minor elements in perovskite from kimberlites and distribution of the rare earth elements: An electron probe study

We report REE and minor element distributions for perovskites from seven kimberlites (South Africa and U.S.A.). The REE (1.6–6.3 oxides wt.%) are always strongly light REE enriched, often with Ce > La (chondrite-normalized), and show an expected close correlation with whole-rock analyses. Where examined, perovskite contains far more REE than coexisting apatite, by about an order of magnitude. Calculations indicate that iron is mostly present as Fe³⁺ and is low (1.0–2.9 wt.% Fe₂O₃) compared with perovskite from carbonatite complexes such as Oka (4.4 wt.% FeO [3]). In addition to established Nb (0.3–1.7 oxide wt.%), geochemically interesting elements encountered include Zr (up to 1.5 oxide wt.%), Ba and Sr (up to 0.2, 0.4 oxide wt.% respectively). Specific geological applications suggest a possible genetic link between Wesselton pipe and Benfontein Sills kimberlites, and that carbonate-rich dikes in the Premier mine were derived from kimberlites. The overall similarities with incompatible element-rich titanates in veined mantle peridotites suggest a more direct link between kimberlite magmatism and mantle metasomatism.     

The age of ferroan anorthosite 60025: oldest crust on a young Moon?

SmNd isotopic data for mineral separates from the ferroan anorthosite 60025 define a precise isochron of 4.44 ± 0.02Ga age. This age is roughly 110 m.y. younger than the formation of the first large solid objects in the solar nebula, as recorded by the radiometric ages of the differentiated meteorites. In the magma ocean model for early lunar differentiation, ferroan anorthosites are the first crustal rocks to form on the Moon. If the Moon is as old as the oldest meteorites, the relatively young age determined for 60025 implies either that the magma ocean did not form synchronously with lunar formation, or that the magma ocean required over 100 m.y. before reaching the stage of ferroan anorthosite crystallization. Alternatively, we propose that the accumulated body of radiogenic isotope data for lunar rocks permit the Moon to be as young as 4.44–4.51 Ga. If so, isotopic evidence for chemical differentiation on the Earth at about this same time suggests that the formation of the Moon is reflected in the chemical evolution of the Earth. This, in turn, is consistent with the idea that the materials that now make up the Moon were derived from the Earth, perhaps ejected by collision between the Earth and another very large planetesimal during the final stages of accumulation of the terrestrial planets. Terrestrial origin models for the Moon lessen the requirement that the Earth and Moon each have near chondritic relative abundances of the refractory elements and could require that certain chemical and isotopic characteristics of both bodies be considered in the framework of the chemical mass-balance of the combined Earth-Moon system.