Trace element and isotopic variations in a zoned pluton and associated volcanic rocks,Unalaska Island,Alaska: A model for fractionation in the Aleutian calcalkaline suite

Trace elements, including rare earth elements (REE), exhibit systematic variations in plutonic rocks from the Captains Bay pluton which is zoned from a narrow gabbroic rim to a core of quartz monzodiorite and granodiorite. The chemical variations parallel those in the associated Aleutian calcalkaline volcanic suite. Concentrations of Rb, Y, Zr and Ba increase as Sr and Ti decrease with progressive differentiation. Intermediate plutonic rocks are slightly enriched in light REE (La/Yb=3.45–9.22), and show increasing light REE fractionation and negative Eu anomalies (Eu/Eu^*=1.03–0.584). Two border-zone gabbros have similar REE patterns but are relatively depleted in total REE and have positive Eu anomalies; indicative of their cumulate nature. Initial ⁸⁷Sr/⁸⁶Sr ratios in 8 samples (0.70299 to 0.70377) are comparable to those of volcanic rocks throughout the arc and suggest a mantle source for the magmas. Oxygen isotopic ratios indicate that many of the intermediate plutonic rocks have undergone oxygen isotopic exchange with large volumes of meteoric water during the late stages of crystallization; however no trace element or Sr isotopic alteration is evident.Major and trace element variations are consistent with a model of inward fractional crystallization of a parental high-alumina basaltic magma at low pressures (6 kb). Least-squares approximations and trace element fractionation calculations suggest that differentiation in the plutonic suite was initially controlled by the removal of calcic plagioclase, lesser pyroxene, olivine and Fe-Ti oxides but that with increasing differentiation and water fugacity the removal of sub-equal amounts of sodic plagioclase and hornblende with lesser Fe-Ti oxides effectively drove residual liquids toward dacitic compositions. Major and trace element compositions of aplites which intrude the pluton are not adequately explained by fractional crystallization. They may represent partial melts derived from the island arc crust. Similarities in Sr isotopes, chemical compositions and differentiation trends between the plutonic series and some Aleutian volcanic suites indicates that shallow-level fractional crystallization is a viable mechanism for generating the Aleutian calcalkaline rock series.LDGO Contribution no. 2964     

Mafic forearc cumulates and associated rocks in the central high-pressure belt of the Acatlán Complex of southern México: geochemical constraints

The high-pressure (HP) Piaxtla Suite at Tehuitzingo contains peridotites, gabbros, and serpentinized peridotites, as well as granitoids and metasedimentary rocks. The HP mafic rocks are characterized by low SiO₂ (38–52 wt.%) and high Mg# (～48–70), Ni (100–470 ppm), and Cr (180–1750 ppm), typical of cumulate compositions. Trace elements and rare earth element (REE) primitive mantle-normalized patterns display generally flat profiles, indicative of derivation from a primitive mantle with two distinct patterns: (1) gabbroic patterns are characterized by a positive Eu anomaly, low REE abundances, and slightly depleted high REE (HREE) relative to low REE (LREE), typical of cumulus olivine, pyroxene, and plagioclase; and (2) mafic-intermediate gabbroic patterns exhibit very flat profiles characteristic of olivine and clinopyroxene as cumulus minerals. Their Nb/Y and Zr/TiO₂ ratios suggest a subalkaline character, whereas low Ti/V ratios indicate that the Tehuitzingo cumulates are island arc tholeiitic basalts that resemble modern, immature oceanic, forearc magmas. These cumulates have high values of ? _Nd(t) = 5.3–8.5 and ¹⁴⁷Sm/¹⁴⁴Nd = 0.18–0.23, which renders calculations of model ages meaningless. Our data are consistent with the Tehuitzingo arc rocks being part of a tectonically extruded Devonian–early Carboniferous arc developed along the west margin of Gondwana.     

A parameterized model for REE distribution between low-Ca pyroxene and basaltic melts with applications to REE partitioning in low-Ca pyroxene along a mantle adiabat and during pyroxenite-derived melt and peridotite interaction

Low-Ca pyroxenes play an important role in mantle melting, melt-rock reaction, and magma differentiation processes. In order to better understand REE fractionation during adiabatic mantle melting and pyroxenite-derived melt and peridotite interaction, we developed a parameterized model for REE partitioning between low-Ca pyroxene and basaltic melts. Our parameterization is based on the lattice strain model and a compilation of published experimental data, supplemented by a new set of trace element partitioning experiments for low-Ca pyroxenes produced by pyroxenite-derived melt and peridotite interaction. To test the validity of the assumptions and simplifications used in the model development, we compared model-derived partition coefficients with measured partition coefficients for REE between orthopyroxene and clinopyroxene in well-equilibrated peridotite xenoliths. REE partition coefficients in low-Ca pyroxene correlate negatively with temperature and positively with both calcium content on the M2 site and aluminum content on the tetrahedral site of pyroxene. The strong competing effect between temperature and major element compositions of low-Ca pyroxene results in very small variations in REE partition coefficients in orthopyroxene during adiabatic mantle melting when diopside is in the residue. REE partition coefficients in orthopyroxene can be treated as constants at a given mantle potential temperature during decompression melting of lherzolite and diopside-bearing harzburgite. In the absence of diopside, partition coefficients of light REE in orthopyroxene vary significantly, and such variations should be taken into consideration in geochemical modeling of REE fractionation in clinopyroxene-free harzburgite. Application of the parameterized model to low-Ca pyroxenes produced by reaction between pyroxenite-derived melt and peridotite revealed large variations in the calculated REE partition coefficients in the low-Ca pyroxenes. Temperature and composition of starting pyroxenite must be considered when selecting REE partition coefficients for pyroxenite-derived melt and peridotite interaction.     

Geochemistry of peridotites from the Yap Trench,Western Pacific: implications for subduction zone mantle evolution

ABSTRACT

This study examines the major and trace elements of peridotites from the Yap Trench in the western Pacific to investigate mantle evolution beneath a subduction zone. Major element results show that the peridotites are low in Al₂O₃ (0.31–0.65 wt.%) and CaO (0.04–0.07 wt.%) contents and high in Mg# (Mg/(Mg+Fe)) (0.91–0.92) and have spinels with Cr# (Cr/(Cr+Al)) higher than 0.6 (0.61–0.73). Trace element results show that the peridotites have extremely low heavy rare earth element (HREE) contents compared with abyssal peridotites but have U-shaped chondrite-normalized rare earth element (REE) patterns. The degree of mantle melting estimated based on the major elements, HREEs, and spinel Cr# range from 19% to 25%, indicating that the Yap Trench peridotites may be residues of melting associated with the presence of water in the mantle source. In addition to light rare earth element (LREE) enrichment, the peridotites are characterized by high contents of highly incompatible elements, positive U and Sr anomalies, negative Ti anomalies, and high Zr/Hf ratios. The correlations between these elements and both the degree of serpentinization and high field strength element (HFSE) contents suggest that fluid alteration alone cannot account for the enrichment of the peridotites and that at least the enrichment of LREEs was likely caused by melt–mantle interaction. Comparison between the peridotites and the depletion trend defined by the primitive mantle (PM) and the depleted mantle (DM) suggests that the Yap Trench mantle was modified by subduction-related melt characterized by high contents of incompatible elements, high Zr/Hf ratios, and low HFSE contents. Hydrous melting may have been enhanced by tectonic erosion of the subducting Caroline Plate with complex tectonic morphostructures at the earliest stages of subduction initiation.     

Rare earth element geochemistry and petrogenesis of miles (IIE) silicate inclusions

An ion probe study of rare earth element (REE) geochemistry of silicate inclusions in the Miles IIE iron meteorite was carried out. Individual mineral phases among inclusions have distinct REE patterns and abundances. Most silicate grains have homogeneous REE abundances but show considerable intergrain variations between inclusions. A few pyroxene grains display normal igneous REE zoning. Phosphates (whitlockite and apatite) are highly enriched in REEs (50 to 2000 × CI) with a relatively light rare earth element (LREE)-enriched REE pattern. They usually occurred near the interfaces between inclusions and Fe host. In Miles, albitic glasses exhibit two distinctive REE patterns: a highly fractionated LREE-enriched (CI normalized La/Sm ∼15) pattern with a large positive Eu anomaly and a relatively heavy rare earth element (HREE)-enriched pattern (CI-normalized Lu/Gd ∼4) with a positive Eu anomaly and a negative Yb anomaly. The glass is generally depleted in REEs relative to CI chondrites.The bulk REE abundances for each inclusion, calculated from modal abundances, vary widely, from relatively depleted in REEs (0.1 to 3 × CI) with a fractionated HREE-enriched pattern to highly enriched in REEs (10 to 100 × CI) with a relatively LREE-enriched pattern. The estimated whole rock REE abundances for Miles are at ∼ 10 × CI with a relatively LREE-enriched pattern. This implies that Miles silicates could represent the product of a low degree (∼10%) partial melting of a chondritic source. Phenocrysts of pyroxene in pyroxene-glassy inclusions were not in equilibrium with coexisting albitic glass and they could have crystallized from a parental melt with REEs of ∼ 10 × CI. Albitic glass appears to have formed by remelting of preexisting feldspar + pyroxene + tridymite assemblage. Yb anomaly played an important role in differentiation processes of Miles silicate inclusions; however, its origin remains unsolved.The REE data from this study suggest that Miles, like Colomera and Weekeroo Station, formed when a molten Fe ball collided on a differentiated silicate regolith near the surface of an asteroid. Silicate fragments were mixed with molten Fe by the impact. Heat from molten Fe caused localized melting of feldspar + pyroxene + tridymite assemblage. The inclusions remained isolated from one another during subsequent rapid cooling.     

四川牦牛坪轻稀土矿床地幔流体特征——铅锶钕和氦氩同位素及稀土元素证据

四川牦牛坪稀土矿床是中国第二大轻稀土矿床。笔者对该矿床进行了较系统的Pb—Sr—Nd同位素、稀有气体同位素地球化学以及稀土元素地球化学研究。稀土元素地球化学特征研究显示,矿区萤石、方解石、氟碳铈矿稀土元素分布模式与区内英碱正长岩相似,表明牦牛坪稀土矿床成矿与英碱正长岩岩浆活动有关以及石英包裹体流体REE曲线平直,Eu与Ce无明显异常,曲线规律性较强,可以认为牦牛坪轻稀土矿床成矿流体稀土元素是深源的。Pb—Sr—Nd同位素组成表明成矿物质来自富集地幔,具深源甚至幔源特征。稀有气体同位素地球化学研究也在一定程度上揭示了牦牛坪轻稀土矿化与地幔过程之间存在着成因关系。     

Trace element distribution between orthopyroxene and clinopyroxene in peridotites from the Gakkel Ridge: a SIMS and NanoSIMS study

Clinopyroxenes (cpx) in abyssal and ophiolitic peridotites are commonly analyzed for lithophile trace element abundances in order to estimate degrees of melting and porosity conditions during melt extraction, assuming that these data reflect near-solidus conditions. During cooling, however, cpxs always exsolve into parallel lamellae of low-Ca enstatite and high-Ca diopside. This may potentially lead to redistribution of the initial trace element budget. Since orthopyroxene (opx) cannot significantly host most incompatible trace elements, exsolution will lead to an enrichment in the cpx lamellae. In order to address a possibly exsolution-controlled partitioning between cpx and opx, we have obtained major and trace element mineral compositions on 14 plagioclase-free ocean floor mantle rocks. They cover the entire abyssal peridotite compositional spectrum from very fertile to highly depleted compositions. The mean volume proportion of opx lamellae in cpx porphyroclasts lies around 15% of the original cpx. For the light to middle rare earth elements, the enrichment in the measured cpx exsolution is exclusively controlled by these phase proportions. Relative to these highly incompatible trace elements, solely Ti and Yb partition significantly into opx. Lamellar interpyroxene partition coefficients, estimated from NanoSIMS analyses, are around three times as high as the ones for near-solidus bulk pyroxene. The equilibration temperatures for the exsolution lamella are slightly higher than 800°C. The bulk cpx can be reconstructed using the lamellar proportions and their relative partitioning. The implication of such a reconstruction is that the cpx rare earth element patterns shift almost in parallel to lower values. These shifts, however, do not affect mantle melting models proposed thus far for mid-ocean ridges. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Experimental constraints on crystallization differentiation in a deep magma ocean

Major and trace element mineral/melt partition coefficients are presented for phases on the liquidus of fertile peridotite at 23-23.5 GPa and 2300 °C. Partitioning models, based on lattice-strain theory, are developed for cations in the ‘8-fold’ sites of majorite and Mg-perovskite. Composition-dependant partitioning models are made for cations in the 12-fold site of Ca-perovskite based on previously published data. D^min/melt is extremely variable for many elements in Ca-perovskite and highly correlated with certain melt compositional parameters (e.g. CaO and Al₂O₃ contents). The 8-fold sites in Mg-perovskite and majorite generally have ideal site radii between 0.8 and 0.9 Å for trivalent cations, such that among rare-earth-elements (REE) D^min/melt is maximum for Lu. Lighter REE become increasingly incompatible with increasing ionic radii. The 12-fold site in Ca-perovskite is larger and has an ideal trivalent site radius of ∼1.05 Å, such that the middle REE has the maximum D^min/melt. Trivalent cations are generally compatible to highly compatible in Ca-perovskite giving it considerable leverage in crystallization models. Geochemical models based on these phase relations and partitioning results are used to test for evidence in mantle peridotite of preserved signals of crystal differentiation in a deep, Hadean magma ocean.Model compositions for bulk silicate Earth and convecting mantle are constructed and evaluated. The model compositions for primitive convecting mantle yield superchondritic Mg/Si and Ca/Al ratios, although many refractory lithophile element ratios are near chondritic. Major element mass balance calculations effectively preclude a CI-chondritic bulk silicate Earth composition, and the super-chondritic Mg/Si ratio of the mantle is apparently a primary feature. Mass balance calculations indicate that 10-15% crystal fractionation of an assemblage dominated by Mg-perovskite, but with minor amounts of Ca-perovskite and ferropericlase, from a magma ocean with model peridotite-based bulk silicate Earth composition produces a residual magma that resembles closely the convecting mantle.Partition coefficient based crystal fractionation models are developed that track changes in refractory lithophile major and trace element ratios in the residual magma (e.g. convecting mantle). Monomineralic crystallization of majorite or Mg-perovskite is limited to less than 5% before certain ratios fractionate beyond convecting mantle values. Only trace amounts of Ca-perovskite can be tolerated in isolation due to its remarkable ability to fractionate lithophile elements. Indeed, Ca-perovskite is limited to only a few percent in a deep mantle crystal assemblage. Removal from a magma ocean of approximately 13% of a deep mantle assemblage comprised of Mg-perovskite, Ca-perovskite and ferropericlase in the proportions 93:3:4 produces a residual magma with a superchondritic Ca/Al ratio matching that of the model convecting mantle. This amount of crystal separation generates fractionations in other refractory lithophile elements ratios that generally mimic those observed in the convecting mantle. Further, the residual magma is expected to have subchondritic Sm/Nd and Lu/Hf ratios. Modeling shows that up to 15% crystal separation of the deep mantle assemblage from an early magma ocean could have yielded a convecting mantle reservoir with ¹⁴³Nd/¹⁴⁴Nd and ¹⁷⁶Hf/¹⁷⁷Hf isotopic compositions that remain internal to the array observed for modern oceanic volcanic rocks. If kept in isolation, the residual magma and deep crystal piles would grow model isotopic compositions that are akin to enriched mantle 1 (EM1) and HIMU reservoirs, respectively, in Nd-Hf isotopic space.     

Geochemical constraints on the genesis of the volcanic rocks in the southeast of Isfahan area, Iran

Late Miocene–Pliocene to Quaternary calc-alkaline lava flows and domes are exposed in southeast of Isfahan in the Urumieh Dokhtar magmatic belt in the Central Iran structural zone. These volcanic rocks have compositions ranging from basaltic andesites, andesites to dacites. Geochemical studies show these rocks are a medium to high K calc-alkaline suite and meta-aluminous. Major element variations are typical for calc-alkaline rocks. The volcanic rocks have SiO₂ contents ranging between 53.8% and 65.3%. Harker diagrams clearly show that the dacitic rocks did not form from the basaltic andesites by normal differentiation processes. They show large ion lithophile elements- and light rare earth elements (LREE)-enriched normalized multielement patterns and negative Nb, Ti, Ta, and P. Condrite-normalized REE patterns display a steep decrease from LREE to light rare earth elements without any Eu anomaly. These characteristics are consistent with ratios obtained from subduction-related volcanic rocks and in collision setting. The melting of a heterogeneous source is possible mechanism for their magma genesis, which was enriched in incompatible elements situated at the upper continental lithospheric mantle or lower crust. The geochemical characteristics of these volcanic rocks suggested that these volcanic rocks evolved by contamination of a parental magma derived from metasomatized upper lithospheric mantle and crustal melts.     

Trace element abundances in megacrysts and their host basalts: Constraints on partition coefficients and megacryst genesis

In an effort to obtain information about mineral/melt trace element partitioning during the high pressure petrogenesis of basic rocks, we determined rare earth and other trace element abundances in megacrysts of clinopyroxene, orthopyroxene, amphibole, mica, anorthoclase, apatite and zircon, and in their host basalts. In general, the ranges of mineral/melt partition coefficients established from experimental partitioning studies and phenocryst/matrix measurements overlap with the ranges of megacryst/host abundance ratios. Our data for Hf, Sc, Ta and Th partitioning represent some of the only estimates available. Consideration of phase equilibria, major element partitioning and isotopic ratios indicate that most of the pyroxene and amphibole megacrysts may have been in equilibrium with their host magmas at high pressures (mostly 10–25 kb). In contrast, it is unlikely that mica, anorthoclase, apatite and zircon megacrysts formed in equilibrium with their host basalts; instead, we conclude that they were precipitated from more evolved magmas and have been mixed into their present host magmas. Consequently, the trace element abundance ratios for megacryst/host should not be interpreted as partition coefficients, but only as guides for understanding trace element partitioning during high pressure petrogenesis. With this caveat, we conclude that the megacryst/ host trace element abundance data indicate that mineral/melt partition coefficients in basaltic systems during high pressure fractionation are not drastically different from partition coefficients valid for low pressure fractionation.     

Geochemical tracers of source rocks in a Cretaceous to Quaternary sedimentary sequence (Eastern Sierras Pampeanas,Argentina)

Metamorphic rocks, granitic rocks, and sediments from the Eastern Sierras Pampanas, Argentina, were analyzed for major and trace element concentrations, including rare earth elements (REE). Parental rocks exhibit distinctive REE normalized diagram patterns and elemental ratios, and some elemental ratios reveal significant differences between rock sources. For example, ratios such as Th/Sc, Cr/Th, and La/Cr have a mean value of 0.7, 8.4 and 0.4 in metamorphic rocks, whereas granitic rocks exhibit means of 1.4, 0.7 and 4.9, respectively. These ratios are also useful in linking detrital materials with the corresponding parental rocks. Metamorphic sources yield sediments with lower Th/Sc and La/Cr, and higher Cr/Th ratios than sediments derived from granitic sources. REE and other elements are enriched in the silt-size fraction, whereas they are diluted by quartz in the sand-size fraction.The size of the Eu/Eu* anomaly can be used as a stratigraphical correlation tool in the sedimentary record: Cretaceous rocks show a mean value of 0.9±0.1, whereas Tertiary rocks have a mean value of 2.9±0.3. The Eu anomaly in Quaternary and modern sediments ranges from 0.5 to 0.8.     

Petrology and trace element geochemistry of Robert Massif 04261 and 04262 meteorites, the first examples of geochemically enriched lherzolitic shergottites

Shergottites sampled two distinct geochemical reservoirs on Mars. Basaltic and olivine-phyric shergottites individually sampled both geochemically enriched and depleted reservoirs, whereas lherzolitic shergottites are previously known only to exhibit a relatively limited intermediate geochemical signature that may have resulted from the mixing of the two geochemical end-member reservoirs. Here we show that recently discovered shergottites Robert Massif (RBT) 04261 and RBT 04262 are the first examples of lherzolitic shergottites originating from the enriched reservoir.RBT 04261 and RBT 04262, initially identified as olivine-phyric shergottites, are actually lherzolitic shergottites. Both meteorites exhibit nearly identical textures and mineral compositions, suggesting that they should be paired. Each consists of two distinct textures: poikilitic and non-poikilitic. The poikilitic areas are composed of pyroxene oikocrysts enclosing olivine grains; all pyroxene oikocrysts have pigeonite cores mantled by augite. The non-poikilitic areas are composed of olivine, pyroxene, maskelynite and minor amounts of merrillite, chromite and ilmenite. Olivine and pyroxene show the lowest Mg-number, and maskelynite has the lowest anorthite component among the lherzolitic shergottites. Moreover, the modal abundances of maskelynite in these two meteorites are distinctly higher than the other lherzolitic shergottites.The rare earth element (REE) budgets of RBT 04261 and RBT 04262 are dominated by merrillite. The slightly light rare earth element (LREE)-enriched pattern of this mineral is similar to that of merrillite in the geochemically enriched basaltic shergottites Shergotty and Zagami, and unlike the LREE-depleted pattern of merrillite in the other lherzolitic shergottites. The REE patterns of both high- and low-Ca pyroxenes are also similar to those in Shergotty and Zagami. The REE pattern of a melt calculated to be in equilibrium with the core of a pyroxene oikocryst is parallel to that of the RBT 04262 whole-rock as well as whole-rock compositions of other geochemically enriched basaltic shergottites. These observations imply that RBT 04262 sampled an enriched and oxidized reservoir similar to that sampled by some of the basaltic shergottites and are consistent with an oxidizing condition for the formation of RBT 04262 (log fO₂ = QFM-1.6).The petrographic and geochemical observations presented here suggest that RBT 04261 and RBT 04262 represent the most evolved magma among the lherzolitic shergottites and that this magma originated from a geochemically enriched reservoir on Mars. Based on an evaluation of the relationship between petrographic, geochemical and chronological signatures for shergottites including RBT 04261 and RBT 04262, we propose that both geochemically enriched and depleted shergottites were ejected from the same launch site on Mars.     

The Rare Earth Elements and Uranium in Garnets from the Beinn an Dubhaich Aureole, Skye, Scotland, UK: Constraints on Processes in a Dynamic Hydrothermal System

Garnets from skarns in the Beinn an Dubhaich granite aureole,Isle of Skye, Scotland, have a large range of concentrationsof uranium (0·2–358 ppm) and the rare earth elements(REE) (23–4724 ppm). Variations in these concentrationscorrelate with major element zonation within the garnets, andwith changes in the shape of REE patterns. Typical patternsin most garnets display light REE (LREE) enrichment, flat heavyREE (HREE) distribution and a negative Eu anomaly. These patternsare interpreted to represent equilibrium trace element exchangebetween pre-existing pyroxene, hydrothermal fluid and calcicgarnets. Iron-rich zones are characterized by positive Eu anomaliesand an increase in the abundance of the LREE relative to theHREE. These patterns are interpreted as resulting from changesin REE speciation related to the introduction of externallybuffered fluid to the skarn system. Relatively Fe-poor zonesshow strongly HREE-enriched patterns with negative Eu anomaliesand in some instances depletions in Y relative to Ho and Dy,which are interpreted as resulting from surface sorption ofthe REE during rapid, disequilibrium garnet growth. Strong correlationsbetween U abundance and the REE patterns indicate that the sameprocesses have affected U distribution. Both types of patterncan be modified by the effects of closed-system crystallizationon REE abundance in the fluid, and changes in fluid major elementchemistry. KEY WORDS: fractionation; garnet; hydrothermal; rare earth elements; skarn     

Geochemistry and mineralogy of two spinel peridotite suites from Dreiser Weiher,West Germany

Among the spinel peridotite nodules from Dreiser Weiher. West Germany which represent fragments of the earth's upper mantle two series may be distinguished. One group (Ib) is anhydrous while the second one (Ia) is characterized by the presence of amphibole and/or breakdown-products of amphibole. Both suites display a wide range in modal composition. Pyroxene geothermometry yields equilibration temperatures of ~ 1150°C for group Ib and ~950°C for group Ia.Rare earth element (REE) patterns reveal marked differences between both groups: nearly unfractionated, light REE depleted or slightly light REE enriched chondrite normalized patterns in nodules from group Ib, but a high relative light REE enrichment in the amphibole containing suite Ia. An inverse correlation between the clinopyroxene content (or CaO) and relative light REE enrichment is observed in group Ia only. Two sources of light REE enrichment of the nodules can be distinguished: The first is a contaminant on mineral surfaces and can be removed by acid leaching. The second is an integral part of the constituent minerals of the nodules. Trace element abundances and modelling show that nodules of group Ib cannot be derived from upper mantle pyrolite by a one-stage partial melting process. Nodules of type Ia are interpreted as being the result of a reaction between Ib-type mantle and a fluid or liquid which provides H₂O and incompatible elements. At Dreiser Weiher this ‘open system’ upper mantle metasomatism may be related to the young uplift of the Rhenish Shield in a similar way as previously proposed by Lloyd and Bailey (1975).A model for the lithospheric mantle below the Westeifel is different from the San Carlos model proposed by Frey and Prinz (1978) and more complex.     

Large-scale silicate liquid immiscibility: a possible example from northeastern Brazil

Ultrapotassic, peralkalic silica-saturated plutons (580 Ma) are widespread in the Cachoeirinha-Salgueiro foldbelt, northeastern Brazil. They consist of alkali-feldspar syenites with pyroxenite as co-magmatic inclusions and syn-plutonic or late-stage dikes. Pyroxenite and syenite have the same mineral phases (aegirine-augite, microcline, sphene, apatite, blue amphibole, magnetite), but only in different proportions. Rare inclusions of a “mixed” rock (about 60% syenite+40% pyroxenite in an emulsion-like texture) are also present. Pyroxenes in the three units are all only slightly zoned, silica-saturated and extremely low in Al₂O₃ (0.2–1.4%). Amphiboles are mostly K-rich richterite, characterized by high SiO₂, low Al₂O₃ and TiO₂ contents and low Mg#.

The three rock types have similar REE chondrite-normalized patterns, with negative slopes and lack of Eu anomaly, with the total REE in the pyroxenite greater than that of the syenite. Trace element patterns for the mixed rock are intermediate between those for the pyroxenite and syenite. Major element partitioning between pyroxenite and syenite has the same sense as that one observed between immiscible liquids in volcanic lavas and trace element partitioning is similar to the experimentally determined partition of immiscible liquid pairs.

The rocks have similar high δ¹⁸O values (avg. w.r.+ 8‰_SMOW, corrected from pyroxene), high initial ⁸⁷Sr/⁸⁶Sr ratios (about 0.710), and low ¹⁴³Nd/¹⁴⁴Nd (avg. 0.51104).

Field and geochemical characteristics indicate chemical equilibrium among the three rock types and suggest liquid immiscibility between syenite and pyroxenite, the mixed rock representing the original magma composition.     

西太平洋海山富钴结壳的稀土和铂族元素特征及其意义

为了探讨富钴结壳的稀土和铂族元素是否有相似的形成机制,对西太平洋海山富钴结壳稀土和铂族元素进行了类比研究.结果表明:富钴结壳的∑REY范围为1 433.7×10-6~2 888.0×10-6,其中Ce占到近50%,北美页岩标准化后显示较平坦的稀土模式和显著的Ce正异常特征.根据稀土配分模式及已有的Nd同位素结果,富钴结壳具有亲陆壳属性.富钴结壳具有极高的Pt (115.5×10-9~1 132.0×10-9)、(Pt/Pd)_N和 (Pt/Os)_N值,Ir与Pt及Rh与Pt显示良好相关性.经球粒陨石标准化后显示较一致PGE (platinum-group elements) 配分模式,从Os到Pt逐渐富集,Pd元素强烈亏损.已有的Os同位素研究结果显示物源在地质历史时期从幔源属性向陆源属性变化,但富钴结壳PGE元素内部相对含量仍在一定程度上保持稳定.研究认为:富钴结壳对海水中的稀土清扫具有选择性,Ce的正异常恰恰是结壳对海水稀土中Ce的优先选择造成的,从而导致海水亏损Ce.然而海水中Ce的亏损并未改变新形成富钴结壳的稀土模式,原因是在海洋中存在适量的具有亏损Ce特征的磷酸盐等组分,理论上只需要氧化物类稀土与磷酸盐类稀土消耗的稀土与海水中的补给平衡即可.只是在相关过程中,海洋中氧化物类对稀土的选择更具有主动性,而磷酸盐类表现更多的继承关系.尽管Os同位素显示物源供给发生变化,然而富钴结壳PGE模式相对稳定.因此富钴结壳PGE模式同样可以用富钴结壳对PGE的选择性吸收解释,因富钴结壳优先选择Pt与Ir以及相对排斥Pd和Os,形成了现有独特的PGE模式.      

Rare earth element partitioning between minerals from anhydrous spinel peridotite xenoliths

REE abundances in minerals from spinel peridotite xenoliths from West Germany, the south-western U.S. and Mongolia decrease in the order clinopyroxene > orthopyroxene > olivine > spinel. While clinopyroxenes are similar in absolute chondrite-normalized concentrations to those known from other studies, orthopyroxenes and olivines are significantly lower in LREE although comparable in HREE. Spinels are much lower in all REE than any previously reported values and are completely negligible for the REE budget of peridotites.Partition coefficients for most orthopyroxene/clinopyroxene pairs increase systematically from La to Lu. Olivine/clinopyroxene and spinel/clinopyroxene partition coefficients increase from the intermediate rare earth elements to Lu and normally are higher for La compared to Sm.The application of Nagasawa's (1966) elastic lattice model suggests that all heavy but only minor amounts of the light REE substitute into structural positions of orthopyroxene and olivine.Significant differences between orthopyroxene/clinopyroxene partition coefficients for various xenoliths may be assigned to dependences upon equilibration temperature and bulk chemistry.Apart from grain surface contaminations, fluid inclusions which are practically always present in mantle minerals, can highly concentrate light rare earth elements and thus may be responsible for unexpectedly high concentrations of incompatible elements frequently reported for mantle olivines or orthopyroxenes.     

Geochemical comparison of woodlawn and mount painter acid volcanics,Southeastern Australia

Major‐ and trace‐element chemistry (including rare‐earth elements), total‐rock Rb‐Sr and U‐Pb and zircon U‐Pb data are used in an attempt to distinguish between two essentially coeval, felsic volcanic suites: the predominantly submarine Woodlawn suite which is associated with massive Cu‐Pb‐Zn sulphide mineralization and the terrestrial Mt Painter suite, with minor vein‐type mineralization. The Woodlawn samples are the unmineralized equivalents of the volcanics in the immediate ore environment.

Alteration perturbs some of the major‐ and trace‐element chemistry, particularly Ca and alkalis, thereby precluding their usefulness. REE patterns exhibit a significant light to heavy rare‐earth enrichment with an average La/Yb of 12 in the Mt Painter volcanics compared with 5.6 in the Woodlawn volcanics. Both suites have a marked negative Eu anomaly, with that of the Woodlawn samples more pronounced (‐45.5) than in the Mt Painter volcanics (‐29.2). A hydrothermally‐altered sample from Woodlawn has apparently lost about 50% of its light rare‐earth elements.

Initial ⁸⁷Sr/⁸⁶Sr ratios at about 0.711 are the same for rocks from both suites and differences in initial lead‐isotopic ratios appear negligible.

Zircons from both suites are a mixture of clear euhedral crystals and rounded discrete crystals or rounded cores overgrown by clear zircon. The U‐Pb data substantiate the morphological features in that the zircon suites both contain older inherited Pb but the Mt Painter zircons contain a greater proportion.

Cs concentrations and Cs/Rb and Ti/Zr ratios can be used to distinguish between the Woodlawn suite and the Mt Painter suite.     

Experimental study of polybaric REE partitioning between olivine, pyroxene and melt of the Yamato 980459 composition: Insights into the petrogenesis of depleted shergottites

A synthetic composition representing the Yamato 980459 martian basalt (shergottite) has been used to carry out phase relation, and rare earth element (REE) olivine and pyroxene partitioning experiments. Yamato 980459 is a sample of primitive basalt derived from a reduced end-member among martian mantle sources. Experiments carried out between 1-2 GPa and 1350-1650 °C simulate the estimated pressure-temperature conditions of basaltic melt generation in the martian mantle. Olivine-melt and orthopyroxene-melt partition coefficients for La, Nd, Sm, Eu, Gd and Yb (D_REE values) were determined by LA-ICPMS, and are similar to the published values for terrestrial basaltic systems. We have not detected significant variation in D-values with pressure over the range investigated, and by comparison with previous studies carried out at lower pressure.We apply the experimentally obtained olivine-melt and orthopyroxene-melt D_REE values to fractional crystallization and partial melting models to develop a three-stage geochemical model for the evolution of martian meteorites. In our model we propose two ancient (∼4.535 Ga) sources: the Nakhlite Source, located in the shallow mantle, and the Deep Mantle Source, located close to the martian core-mantle boundary. These two sources evolved distinctly on the ε¹⁴³Nd evolution curve due to their different Sm/Nd ratios. By partially melting the Nakhlite Source at ∼1.3 Ga, we are able to produce a slightly depleted residue (Nakhlite Residue). The Nakhlite Residue is left undisturbed until ∼500 Ma, at which point the depleted Deep Mantle Source is brought up by a plume mechanism carrying with it high heat flow, melts and isotopic signatures of the deep mantle (e.g., ε¹⁸²W, ε¹⁴²Nd, etc.). The plume-derived Deep Mantle Source combines with the Nakhlite Residue producing a mixture that becomes a mantle source (herein referred to as “the Y98 source”) for Yamato 980459 and the other depleted shergottites with the characteristic range of Sm/Nd ratios of these meteorites. The same hot plume provides a heat source for the formation of enriched and intermediate shergottites. Our model reproduces the REE patterns of nakhlites and depleted shergottites and can explain high ε¹⁴³Nd in depleted shergottites. Furthermore, the model results can be used to interpret whole rock Rb-Sr and Sm-Nd ages of shergottites.     

云南个旧碱性杂岩体的岩石成因及稀土元素富集机制

云南个旧碱性杂岩体由边缘相碱长正长岩和中心相霞石正长岩组成.全岩地球化学分析表明,该碱性杂岩体具有高碱、富钾、富铁、低镁、高分异的碱性-过碱性岩石特征,晚期更富集碱金属元素;LREE/HREE值为20～59,(La/Sm)N = 8～50,(Sm/Yb)N = 1.2～5.0,富集轻稀土元素,轻稀土元素较重稀土元素分馏...