Petrogenesis of picritic mare magmas: Constraints on the extent of early lunar differentiation

Calculations of isobaric batch, polybaric batch, and polybaric fractional melting have been carried out on a variety of proposed lunar and terrestrial source region compositions. Results show that magmas with a generally tholeiitic character—plagioclase and high-Ca pyroxene crystallize before low-Ca pyroxene reflecting relatively high Al₂O₃ concentrations (>12 wt%)—are the inevitable consequence of anhydrous partial melting of source regions composed primarily of olivine and two pyroxenes with an aluminous phase on the solidus. Low-Al₂O₃ magmas (<10 wt%), as typified by the green picritic glasses in the lunar maria require deep (700–1000 km), low-Al₂O₃ source regions without an aluminous phase. The difference between primitive and depleted mantle beneath mid-ocean ridges amounts to less than 0.1 wt% Al₂O₃, whereas formation of the green glass source region requires a net loss of between 1.5 and 2.5 wt% Al₂O₃. Basalt extraction cannot account for fractionations of this magnitude. Accumulation of olivine and pyroxene at the base of a crystallizing magma ocean is, however, an effective method for producing the necessary Al₂O₃ depletions. Both olivine-rich and pyroxene-rich source regions can produce the picritic magmas, but mixing calculations show that both types of source region are likely to be hybrids consisting of an early- to intermediate-stage cumulate (olivine plus enstatite) and a later stage cumulate assemblage. Mass balance calculations show that refractory element-enriched bulk Moon compositions contain too much Al₂O₃ to allow for the deep low-Al₂O₃ source regions even after extraction of an Al₂O₃-rich (26–30 wt%) crust between 50 and 70 km thick.     

Average compositions of magmas and mantle sources of mid-ocean ridges and intraplate oceanic and continental settings estimated from the data on melt inclusions and quenched glasses of basalts

Based on the generalization of the compositions of melt inclusions and quenched glasses from basaltic rocks, the average compositions of magmas were estimated for mid-ocean ridges (MOR), intraplate continental environments (CR), and ocean islands and plateaus (OI). These compositions were used to constrain the average contents of trace and volatile elements in mantle sources. A procedure was developed for the estimation of the average contents of incompatible elements, including volatiles (H₂O, Cl, F, and S), in the mantle. A comparison of the obtained average contents for the depleted mantle (DM) with the available published estimates showed that the contents of most incompatible trace elements (H₂O, Cl, F, Be, B, Rb, Sr, Zr, Ba, La, Ce, Nd, Sm, Eu, Hf, Ta, Th, and U) can be reliably estimated from the ratio of K to the desired trace element in the MOR magmas and the average content of K in the DM. For Nb, Ti, P, S, Li, Y, and heavy REE, we used the ratios of their contents to an element with a similar degree of incompatibility in MOR magmas (U for Nb and Dy for the other elements). This approach was used to determine the average contents of incompatible elements in oceanic plume mantle (OPM) and the subcontinental mantle of intraplate settings or continental plume mantle (CPM). It was shown that the average composition of both suboceanic and subcontinental mantle plumes is moderately enriched compared with the DM in the most incompatible elements (K, U, Ba, and La) and volatile components (H₂O, Cl, and F). The extent of volatile component enrichment in the plume mantle (500–1500 ppm H₂O) is insufficient for a significant depression of the mantle solidus. Therefore, mantle plumes must be hotter than the ambient depleted mantle. The average contents of incompatible trace elements in the OPM are similar to those of the primitive mantle, which could be related either to the retention of primitive mantle material in the regions of plume generation or to DM fertilization at the expense of the deep mantle recycling of crustal materials. In the latter case, the negative anomaly of water in the trace-element distribution patterns of the OPM is explained by the participation of dehydrated crust in its formation. Variations in the compositions of magmas and their sources were considered for various geodynamic settings, and it was shown that the sources are heterogeneous with respect to trace and volatile components. The chemical heterogeneity of the magma sources and gradual transitions between them suggest that the mantle reservoirs interact with each other. Chemical variations in continental and oceanic plume magmas can be attributed to the existence of several interacting sources, including one depleted and at least two enriched reservoirs with different contents of volatiles. These variations are in agreement with the zoned structure of mantle plumes, which consist of a hot and relatively dry core, a colder outer shell with high contents of volatile components, and a zone of interaction between the plume and depleted mantle.     

An experimental study of anorthosite dissolution in lunar picritic magmas: Implications for crustal assimilation processes

Experiments characterizing the kinetics of anorthosite dissolution in lunar picritic magmas (very low-Ti, low-Ti, and high-Ti picritic glasses) were conducted at 0.6 GPa and 1250-1400 °C using the dissolution couple method. Reaction between the anorthosite and lunar picritic magmas at 1250-1300 °C produced a spinel + melt layer. Reaction between the anorthosite and an olivine-saturated low-Ti magma at 1250-1300 °C produced a crystal-free region between the spinel + melt layer and the olivine-saturated magma. The anorthosite dissolution experiments conducted at 1400 °C simply dissolved anorthosite and did not result in a crystal-bearing region. The rate of anorthosite dissolution strongly depends on temperature and composition of the reacting melt. Concentration profiles that develop during anorthosite dissolution are nonlinear and extend from the picritic glass compositions to anorthite. These profiles feature a large and continuous variation in melt density and viscosity from the anorthosite-melt interface to the initial picritic magmas. In both the low-Ti and high-Ti magmas the diffusive fluxes of TiO₂, Al₂O₃, and SiO₂ are strongly coupled to the concentration gradients of CaO and FeO. Anorthosite dissolution may play an important role in producing the chemical variability of the lunar picritic magmas, the origin of spinel in the lunar basalts and picritic glasses, and the petrogenesis of the high-Al basalts.     

Parental magmas of the Nain Plutonic Suite anorthosites and mafic cumulates: a trace element modelling approach

Equilibrium melt trace element contents are calculated from Proterozoic Nain Plutonic Suite (NPS) mafic and anorthositic cumulates, and from plagioclase and orthopyroxene megacrysts. Assumed trapped melt fractions (TMF) <20% generally eliminate all minor phases in most mafic cumulate rocks, reducing them to mixtures of feldspar, pyroxene and olivine, which would represent the high-temperature cumulus assemblage. In anorthosites, TMF <15% generally reduce the mode to a feldspar-only assemblage. All model melts have trace element profiles enriched in highly incompatible elements relative to normal mid-ocean ridge basalt (NMORB); commonly with negative Nb and Th anomalies. Most mafic cumulates yield similar profiles with constant incompatible element ratios, and can be linked through fractional crystallization. High K-La subtypes probably represent crust-contaminated facies. Mafic cumulates are inferred to belong to a tholeiitic differentiation series, variably contaminated by upper and lower crustal components, and probably related to coeval tholeiitic basaltic dyke swarms and lavas in Labrador. Model melts from anorthosites and megacrysts have normalized trace element profiles with steeper slopes than those calculated from mafic cumulates, indicating that mafic cumulates and anorthosites did not crystallize from the same melts. Orthopyroxene megacrysts yield model melts that are more enriched than typical anorthositic model melts, precluding an origin from parental melts. Jotunites have lower K-Rb-Ba-Y-Yb and higher La-Ce than model residues from fractionation of anorthositic model melts, suggesting they are not cosanguineous with them, but provide reasonable fits to evolved mafic cumulate model melts. Incompatible element profiles of anorthositic model melts closely resemble those of crustal melts such as tonalites, with steep Y-Yb-Lu segments that suggest residual garnet in the source. Inversion models yield protoliths similar to depleted lower crustal granulite xenoliths with aluminous compositions, suggesting that the incompatible trace element budget of the anorthosites are derived from remobilization of the lower crust. The similarity of the highly incompatible trace elements and LILE between anorthositic and mafic cumulate model melts suggests that the basalts parental to the mafic cumulates locally assimilated considerable quantities of the same crust that yielded the anorthosites. The reaction between underplating basalt and aluminous lower crust would have forced crystallization of abundant plagioclase, and remobilization of these hybrid plagioclase-rich mushes then produced the anorthosite massifs.     

Proterozoic VanDieland in Central Victoria: ages,compositions and source depths for late devonian silicic magmas

The Proterozoic to Cambrian VanDieland microcontinent was accreted to mainland Australia at ca 400?Ma, and its northern tip, the Selwyn Block, forms the basement in central Victoria. Here, mainly Late Devonian, silicic magmas were derived from the Selwyn Block and intruded into the shallow crust. We use the phase petrology of Late Devonian, S-type rhyolitic ignimbrites and a xenolith of pelitic migmatite, together with Nd-model ages for the silicic magmatic rocks to constrain the lithological characteristics of the metasedimentary component of the Selwyn Block, to infer minimum depths and temperature conditions here in the Late Devonian, and the likely ages of the source rocks for the S-type magmas. The most abundant source rocks are inferred to be volcaniclastic metagreywackes, with minor metadacites, meta-andesites and metapelites. The metapelitic xenolith cannot have been the source for any of the silicic magmas but constrains the upper amphibolite-facies part of the Selwyn Block to depths around 17?km, where temperatures reached ～775?°C. The older ignimbrite magma was formed by partial melting at perhaps 770?°C and a depth of at least 33?km, while the younger ignimbrite magma formed at ～23?km and 900?°C. These depths suggest source rocks in the Paleoproterozoic to Mesoproterozoic lower parts of the Selwyn Block. Nd-model ages of the silicic magmatic rocks confirm a dominance of Mesoproterozoic to Paleoproterozoic sources. If the inferred rock types in the Mesoproterozoic formations were as current correlations suggest, the sources for the Late Devonian silicic magmas would have to lie in the undocumented Paleoproterozoic basement of the Selwyn Block. Rock types here must include andesitic to dacitic volcanic components as well as volcaniclastic greywackes and minor pelites, which suggests a continental arc setting. The Late Devonian magmatism in the region may record the progression from amphibolite- to granulite-facies conditions during post-orogenic extension, with heat advected to the crust by mantle-derived mafic magmas. These processes would have resulted in mafitisation of the deep Selwyn Block.     

月球物质的Re-Os同位素组成研究：对月球后期增生历史的指示

Re-Os同位素体系是理解月球强亲铁元素的分布规律和示踪月球的后期增生历史的重要手段。目前人们对月球物质Re-Os同位素成分的了解还是十分有限的,已有的Re-Os同位素数据显示一些能代表月幔成分特征的月海玄武岩具有很低的Re和Os的浓度,以及类似于球粒陨石的187Os／188Os成分特征,而月球火山玻璃和月壤等表现出相对高的Re-Os丰度和相对富放射成因Re-Os同位素成分。一般认为月球月幔的Re、0s和其他强亲铁元素相对球粒陨石是非常亏损的,而地球地幔则具有相对较高的强亲铁元素丰度（0．008倍CI球粒陨石的丰度）。新的Re-Os同位素结果证明月幔确实是亏损的,但是月球和地球在太阳系演化的较晚时期都有外来的球粒陨石物质的大量加入,即后期增生（late accretion）过程,导致了月球和地球上部物质（如月球火山玻璃、月壤等）相对地富集Os同位素和强亲铁元素,这些外来物质的后期增生可能是长期和持续的,增生过程主要发生在3．9～4．4Ga。但目前仍不清楚后期增生的陨石物质是被逐渐加入的,还是在一个相对较短的时期大量加入的,因此尚需对更多的月球物质做进一步的Re-Os同位素和强亲铁元素成分的研究。     

Genetic relations between meteorites and terrestrial and lunar rocks

According to their genesis, meteorites are classified into heliocentric (which originate from the asteroid belt) and planetocentric (which are fragments of the satellites of giant planets, including the Proto-Earth). Heliocentric meteorites (chondrites and primitive meteorites genetically related to them) used in this study as a characteristic of initial phases of the origin of the terrestrial planets. Synthesis of information on planetocentric meteorites (achondrites and iron meteorites) provides the basis for a model for the genesis of the satellites of giant planets and the Moon. The origin and primary layering of the Earth was initially analogously to that of planets of the HH chondritic type, as follows from similarities between the Earth’s primary crust and mantle and the chondrules of Fe-richest chondrites. The development of the Earth’s mantle and crust precluded its explosive breakup during the transition from its protoplanetary to planetary evolutionary stage, whereas chondritic planets underwent explosive breakup into asteroids. Lunar silicate rocks are poorer in Fe than achondrites, and this is explained in the model for the genesis of the Moon by the separation of a small metallic core, which sometime (at 3–4 Ga) induced the planet’s magnetic field. Iron from this core was involved into the generation of lunar depressions (lunar maria) filled with Fe- and Ti-rich rocks. In contrast to the parent planets of achondrites, the Moon has a olivine mantle, and this fact predetermined the isotopically heavier oxygen isotopic composition of lunar rocks. This effect also predetermined the specifics of the Earth’s rocks, whose oxygen became systematically isotopically heavier from the Precambrian to Paleozoic and Mesozoic in the course of olivinization of the peridotite mantle, a processes that formed the so-called roots of continents.     

Possible europium-normal rare-earth abundances estimated from the lunar samples,and the terrestrial analogue

From the mathematical analysis of the rare-earth data on some of the Apollo 12 samples studied by Hubbard et al. (1971), the possible europium-normal primitive rare-earth pattern, in which europium is normal with respect to the adjacent rare-earth elements, has been estimated. A fact that the igneous rocks (Japanese geosynclinal basalts) appearing to reflect the analogous effect occur locally on the earth enhances our interests in the pattern resulting from the above estimation.     

Univariate data analysis system: deciphering mean compositions of island and continental arc magmas,and influence of the underlying crust

Our aim is to determine the mean compositions of modern island and continental arcs, along with dispersion estimates, and use them to evaluate their similarities and differences in such subduction settings. First, following the conventional approach, the statistical parameters of mean, median, and standard deviation were simply calculated from the available combined data from all island or continental arcs. However, it is mandatory to ascertain from significance tests that all island or continental arcs used for these estimates are statistically similar in their compositions before combining the data from different arcs and calculating the mean values and their uncertainties for the chemical parameters of interest. A new computer program, Univariate Data Analysis System (UDASYS), was developed for this purpose because the available programs are not efficient for applying the significance test of analysis of variance (ANOVA) to large numbers of sample groups, as in the present work. Compositional data for 16 island and 12 continental arcs around the world were compiled and processed in UDASYS. The best compositional estimates for all three types of magmas (basic, intermediate, and acid) from island and continental arcs were statistically evaluated to document, for the first time, significant differences for 64–94% of the geochemical parameters under study. These differences in large-ion lithophile elements, light rare earth elements, high-field strength elements, and numerous log-ratios are likely caused by different types of underlying crust beneath island and continental arcs. More specifically, the examination of two nearby arcs, Izu-Bonin (island) arc and Japan (continental) arc, confirmed that about 65–77% of the parameters showed significant differences, which may be related to the different types of crusts beneath these spatially close areas. The differences between the log-ratios of island and continental arc basic magmas further indicate that new multi-dimensional discrimination diagrams can certainly be proposed in future to discriminate such basic magmas from these two very similar tectonic settings, which at present is possible only from diagrams for intermediate and acid magmas.     

Carbon,nitrogen and sulfur in lunar fines 15012 and 15013: abundances,distributions and isotopic compositions

Lunar fines 15012,16 and 15013,3 were analyzed by stepwise pyrolysis and acid hydrolysis as well as complete combustion in oxygen to determine carbon, nitrogen and sulfur. In addition, hydrogen was analysed during pyrolysis as well as during hydrolysis. In the former case, it was released by mineral grains to which it was adsorbed or from cavities within which it had been captured. Hydrogen released during hydrolysis had largely resulted from dissolution of metallic iron.By comparison of the distribution frequencies of C, N, S, H₂ and Fe with ⁴He, considered to have arisen from solar wind contribution, it is concluded that nitrogen and hydrogen have largely a solar origin. Carbon has a significant solar contribution, and metallic iron may have resulted from solar wind interaction with ferrous minerals on the lunar surface. Sulfur probably has a predominantly lunar origin. There is no direct evidence for meteoritic contribution to these samples.Solar wind interaction also has a marked effect on the stable isotope distribution of ¹³C/¹²C, ¹⁵N/¹⁴N, and ³⁴S/³²S. In all cases, the heavy isotope was most enriched in the smallest grain-size fraction. During stepwise pyrolysis, CH₄, CO₂, CO and N₂ were obtained at different temperatures and displayed different isotopic ratios. The carbon fraction most enriched in ¹³C, was CH₄ liberated at 600–800°C with $\text{δ}{}^{13}\text{C = +45.7\%.}$. Between 400 and 600°C, N₂ was liberated with (δ¹⁵N ≈ +119% and at 600–800°C, N₂ was liberated with $\text{δ}{}^{15}\text{N = +75\%.}$ relative to terrestrial atmospheric nitrogen.     

广西柳东地区火山岩锆石U-Pb-Hf同位素特征及其对岩浆源区的限定

【研究目的】柳东地区位于右江盆地东缘,近年来该地区早三叠世石炮组中首次发现一套火山岩夹层,为研究盆地东缘的构造演化特征提供了重要依据。【研究方法】本文以新发现的柳东地区火山岩为研究对象,通过LAICP-MS锆石U-Pb年龄及Hf同位素分析,研究右江盆地东缘火山岩的形成时代及岩浆源区特征。【研究结果】结果表明,火山岩的岩性为凝灰岩-凝灰质熔岩-凝灰质火山角砾岩组合,指示了典型的火山岩特征。其2件凝灰岩样品中锆石LA-ICP-MS U-Pb加权平均年龄分别为（244.0±1.9） Ma和（247.1±0.9） Ma,锆石微量元素（U、Th、Hf、Nb）表现出大陆岩浆弧属性特征。锆石Hf同位素结果显示ε_Hf （t）为-13.2~-1.2,二阶段模式年龄（T_DM^C）为1.35~2.06 Ga,其岩浆源区主要为地壳物质,平均地壳存留年龄为1.7~2.06 Ga。【结论】该火山岩夹层与其所出露的地层时代基本相符,属于早三叠世末期—中三叠世早期火山喷发产物,火山岩形成于火山弧-同碰撞的构造环境,代表了弧后盆地的沉积环境,与印支期古特提斯洋的闭合相关。该成果为古特提斯构造域的演化研究提供了新的基础资料,具有重要意义。创新点：柳东地区火山岩属于早三叠世末期—中三叠世早期火山喷发产物,形成于印支期古特提斯洋的闭合条件下的火山弧-同碰撞构造环境。     

Irradiation records in regolith materials. I: isotopic compositions of solar-wind neon and argon in single lunar mineral grains

We have applied a stepwise pyrolytic extraction technique to eleven individual lunar regolith grains to investigate the compositions of light noble gases embedded in grain surfaces by solar wind irradiation, with emphasis on the rather poorly known isotopic composition of solar-wind argon. Results are intriguing: average ²⁰Ne/²²Ne ratios observed in early pyrolytic releases from ilmenite grains separated from lunar soils 71501, 79035 and 10084 agree very well with both direct measures of the solar wind neon composition in the Apollo foils and with values obtained in first releases from acid-etched ilmenites by the Zürich laboratory, whereas these same pyrolytic and acid-etch fractions carry argon isotopic signatures that significantly disagree—average ³⁶Ar/³⁸Ar ratios near 5.8 for thermal extraction compared to 5.4–5.5 for chemical etching at Zürich. Consideration of the isotopic and elemental data from these grains in the context of first-order diffusive modeling calculations points to gas release at low temperatures, without significant isotopic or elemental fractionation, from isolated grain-surface reservoirs of solar wind composition. The physical nature of these reservoirs is presently unknown. In this interpretation the preferred solar wind ²⁰Ne/²²Ne and ²¹Ne/²²Ne ratios deduced from this study are respectively 13.81 ± 0.08 and 0.0333 ± 0.0003, both within error of the Zürich acid-etch values, and ³⁶Ar/³⁸Ar = 5.77 ± 0.08. It may be possible to reconcile the discrepancy between the acid-etch and pyrolytic estimates for the solar wind ³⁶Ar/³⁸Ar ratio in the context of arguments originally advanced by Benkert et al. (1993) to account for their He and Ne isotopic compositions. At the other, high-temperature end of the release profile from one of these grains there are clear isotopic indications of the presence of a Ne constituent with ²⁰Ne/²²Ne close to the 11.2 ratio found at Zürich and attributed by these workers to a deeply-sited component implanted by solar energetic particles.     

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.     

Classification problems of samples of finite mixtures of compositions

A discriminant technique based on mixture models is presented to be applied when observations are a sample of a mixture of compositions with each component following an additive logistic normal distribution on the d-dimensional simplex. The efficiency of this discriminant technique is compared empirically with the efficiency of the standard discriminant technique based on logcontrast. Simulated compositional data and a real dataset are used to carry out these comparisons.     

High-Mg diorites derived from sanukitic HMA magmas, Kyushu Island, southwest Japan arc: evidence from clinopyroxene and whole rock compositions

High-Mg diorites that have similar whole rock composition to high-Mg andesites (HMAs) should not be simply interpreted as rocks solidified from the HMA magmas, because the high-Mg diorites may be mafic cumulates derived from a different magma from the HMAs.

The HMAs contain unique clinopyroxenes with higher Mg# and Si than those of other sub-alkaline series igneous rocks. The Mg# and Si are controlled by the source magma composition rather than its crystallized conditions such as pressure and temperature. The chemical composition of clinopyroxenes would present important information for the investigation of the source of high-Mg diorites.

We considered the source of Early Cretaceous high-Mg diorites on Kyushu Island, southwest Japan arc, based on their clinopyroxene and whole rock compositions. The clinopyroxenes have similar chemical characteristics to those in HMAs rather than those in other sub-alkaline rocks. Moreover, the whole rock compositions are equivalent to the sanukitic HMA and do not show features of mafic cumulates. This indicates that the high-Mg diorites solidified from sanukitic HMA magmas. It is generally believed that the sanukitic HMA magmas involve the subduction of a young and/or hot oceanic slab was situated in their genesis. Therefore, the occurrence of the high-Mg diorites suggests that Kyushu was situated in the tectonic setting of young and/or hot slab subduction in the Early Cretaceous.     

Contribution of Asian dust to soils in Southeast China estimated with Nd and Pb isotopic compositions

Acta Geochimica - Asian dust has been identified in subtropical soils of China. Neodymium (Nd) and lead (Pb) elemental and isotopic geochemistry of soils in Southeast China were used to assess the...     

Genetic relations among basic lavas and ultramafic nodules: Evidence from oxygen isotope compositions

¹⁸O values of unaltered basic lavas range from 4.9 to 8.3 but different types of basalts are usually restricted to narrow and distinct ranges of isotopic composition. The average ¹⁸O values for Hawaiian tholeiites, mid-ocean ridge tholeiites, and alkali basalts are 5.4, 5.7, and 6.2 permil, respectively. Potassic lavas and andesites tend to be more ¹⁸O rich with ¹⁸O values between 6.0 and 8.0 permil. The differences among the oxygen isotopic compositions of most of these lavas can be attributed to partial melting of isotopically distinct sources. The oxygen isotope compositions of the sources may be a function of prior melting events which produce ¹⁸O-depleted partial melts and ¹⁸O-enriched residues as a consequence of relatively large isotopic fractionations that exist at high temperatures. It is proposed that lavas with relatively low ¹⁸O values are derived from primitive, ¹⁸O-depleted sources whereas ¹⁸O-rich basalts are produced from refractory sources that have already produced partial melts. High temperature fractionations among silicate liquids and coexisting minerals can be used in conjunction with the oxygen isotope compositions of ultramafic nodules to place constraints on the genetic relations between some nodules and different types of basic lavas.