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     

Some trace element relationships among liquid and solid phases in the course of the fractional crystallization of magmas

The classical equations relating the trace element concentrations of the liquid and solid phases coexisting in the simple fractional crystallization of a parental magma have been put in a simple graphical form, which allows rapid analysis of the possible genetic relationships in a given rock suite. The effects of an incomplete separation between the two phases are taken into account. The approach does not require the use of otherwise estimated partition coefficients. Trace element data concerning the minerals of cumulates, where available, may provide an independent estimation of the effective mineral-liquid partition coefficients. With reasonable assumptions, this approach may even be applied to plutonic rocks. Interpretation of the published rare earth element data from the Southern California Batholith by this procedure suggests that a tonalitic parental magma could generate a granodioritic liquid by crystallizing 40–50 wt % of a solid residue of gabbroic composition, in agreement with Larsen's (Mem. Geol. Soc. Amer. 29, 1948) calculations. The calculated mineral-liquid partition coefficients for the REE fall in the range of published phenocryst-groundmass values for acidic volcanic rocks.     

Kimberlites and megacrystic suite: Isotope-geochemical studies

Major and rare-earth element data on Cr-poor megacrystic suite from Yakutian kimberlites were generalized. Sr-Nd isotopes were studied in garnet, clinopyroxene, and phlogopite megacrysts as well as in garnet and clinopyroxene from deformed xenoliths. It was shown that Sr-Nd composition of these minerals is similar to that in the least altered diamondiferous kimberlites. The crystallization age of megacrystic minerals was determined by Rb-Sr isochron and Ar-Ar (for phlogopite megacrysts) methods. Obtained data indicate that crystallization of Cr-poor megacrystic suite began at the prekimberlitic stage and continued to the pipe emplacement. It was established that garnets from coarse-porphyric deformed lherzolites and megacrysts are similar in major and rare-earth element compositions and were derived from a common asthenospheric source. However, the distribution of incompatible elements and P-T estimates of crystallization cannot be explained by hypothesis of fractional crystallization of garnet megacrysts. It is suggested that megacrystic assemblage crystallized directly in asthenospheric melt. En route to the surface, this melt caused a metasomatic reworking of lithospheric mantle, on the one hand, and was enriched in Mg and Cr owing to the contamination by lithospheric material, on the other hand.     

Distribution coefficients of major and trace elements; fractional crystallization in the alkali basalt series of Chaîne des Puys (Massif Central,France)

Major and seventeen trace element distribution coefficients between main phenocrysts (olivine, clinopyroxene, amphibole, mica, feldspars and Fe-Ti oxides) and groundmass have been measured in the alkali basalt suite of Chaîne des Puys (Massif Central, France). The suite appears to be a well behaved crystal fractionation series. We pinpoint key elements whose behavior is closely related to the appearance or disappearance of specific crystal phases in the fractionation process. Ta, for instance, clearly indicates the role of hydrous silicates (amphiboles and micas). Distribution coefficients are shown to vary systematically along the differentiation trend. Significantly the hygromagmaphile tendency (Treuilet al., 1979) of U, Th, Ta and La is variable along the series.The mass balance equations,

$\text{D}{}^{\mathrm{i}}\text{=}\text{∑}\text{;}\text{x}{}_{\mathrm{j}}\text{D}{}_{\mathrm{j}}{}^{\mathrm{ii}}$

where Dⁱ and D_jⁱ are the bulk and mineral/liquid distribution coefficients respectively, and x_j the weight fractions of the fractionating phases, are solved by least square resolution of the overdetermined system, taking into account the analytical errors on data. The solution applied to the Chaîne des Puys suite leads to a coherent and quantitative model of the fractional crystallization process. The suite has apparently evolved in three stages. Each stage is characterized by constant bulk distribution coefficients and a specific mineral assemblage. Amphibole fractionation plays an important role in the early stages. Some intensive parameters (T, ? ?_O2, P_H2O) as well as f (weight fraction of residual liquid) are also estimated.     

A 3500 Ma plutonic and volcanic calc-alkaline province in the Archaean East Pilbara Block

Variably foliated, predominantly granodioritic plutonic rocks from the northern part of the Shaw Batholith in the east Pilbara Archaean craton are dated at 3,499±22 Ma (2σ errors) by a whole-rock Pb-Pb isochron. These rocks intrude the surrounding greenstone sequence, and their age is indistinguishable from that sequence. High strain grey gneisses which occupy much of the western and southern Shaw Batholith are chemically and isotopically similar to the North Shaw suite and are inferred to have been derived from this suite by tectonic processes. Felsic volcanics within the greenstones together with a major portion of the granitic batholiths apparently formed in a calc-alkaline volcanic and plutonic province at ～3,500 Ma. This volcanic and plutonic suite is similar to modern calc-alkaline suites on the basis of major element, rare earh element and most other trace element contents. The Archaean suite contrasts with modern equivalents only in having lower concentrations of HREE and higher concentrations of Ni and Cr. The average composition of the North Shaw suite is similar to that of Archaean gneiss belts for most elements and is consistent with the previously formulated hypothesis that the Shaw Batholith is transitional to the upper crustal level of a high-grade gneiss belt. Enrichment of the gneissic crust in the Shaw Batholith in alkali and heat-producing elements is inferred to have taken place by both igneous and hydrothermal processes over a protracted time interval. Late- and post-tectonic adamellite and granite melts intrude the gneissic rocks and there is isotopic evidence consistent with the gneisses being substantially enriched in Rb by pegmatite injection at ～3,000 Ma.     

Petrogenesis of Coarse-grained Intrusives from Tahiti Nui and Raiatea (Society Islands, French Polynesia)

This study is based on a set of coarse-grained igneous rockscollected from two zoned plutons located in the central partof Tahiti Nui and Raiatea. The Ahititera pluton (central depressionof Tahiti Nui) comprises a great diversity of rocks, rangingfrom ultrabasic to felsic in composition. It shows a concentriczonation with nepheline-free rocks in its periphery and nepheline-bearingrocks in its central part. The Faaroa pluton (central depressionof Raiatea) is entirely mafic and includes only gabbros andtheralites. The two plutons have variable Nd–Sr isotopicsignatures, especially the Ahititera rocks, which are subdividedinto three groups based on their mineralogy, geochemistry andisotope composition. The isotopic variability probably reflectslocal heterogeneities in the Society mantle plume. Petrographicand isotopic data have been used to define two magmatic suitesin Ahititera, identifiable from their degree of Si undersaturation.The evolution of the mildly Si-undersaturated suite is controlledby simple fractional crystallization, whereas the strongly Si-undersaturatedsuite requires additional H₂O influx. The third isotopic groupincludes only theralites. The rare earth element (REE) compositionsof the mafic rocks from both plutons do not correlate with theirisotopic signature. The REE patterns of the most Si-undersaturatedrocks are systematically characterized by steeper slopes. Suchfeatures are also observed in lavas from seamounts located withinthe present-day hotspot area. It appears that REE concentrationsin Society lavas and intrusives are probably mainly governedby variable degrees of partial melting of a garnet-free mantlesource and are independent of their isotopic signature. KEY WORDS: cumulates; fractional crystallization; partial melting; French Polynesia; plutonic rocks; Society Islands; Tahiti; Raiatea     

Cumulate gabbros from the Southwest Indian Ridge, 54°S-7° 16′ E: implications for magmatic processes at a slow spreading ridge

A diverse volcanic and plutonic rock suite was recovered from the center of the 80 km long ridge segment of the Southwest Indian Ridge (54°S, 7°16 E) between the Islas Orcadas and Shaka Fracture Zones. The cumulus nature of the gabbroic rocks in the suite is indicated by phase, modal and cryptic layering, igneous lamination, and low incompatible element abundances. We present a mass-balance model for calculating the proportions and compositions of cumulus phases and crystallized intercumulus liquid from bulk-rock major element compositions. The model is based on the ability to define a compositional array of basaltic liquids and on the assumption that cumulus minerals are initially in equilibrium with trapped liquid. Calculated proportions of trapped liquid range from 3%–15%; values that are characteristic of adcumulates to mesocumulates. Models of postcumulus crystallization indicate significant enrichments of incompatible elements and buffering of compatible elements in residual trapped liquids, thus explaining the high TiO₂ contents observed in magnesian clinopyroxenes. Cumulus phase assemblages and compositions suggest solidification in shallow level magma chambers, but disequilibrium plagioclase compositions suggest some crystallization at greater depth. Furthermore, basalt compositions projected onto the olivine-clinopyroxenequartz pseudoternary suggest magma generation over a range of pressures (from less than 10 to greater than 20 kb) as well as polybaric fractional crystallization. We suggest that the Southwest Indian Ridge is characterized by low magma supply with small batches of melt that either ascend directly to the surface having undergone limited polybaric crystallization or are trapped in shallow crustal magma chambers where they evolve and solidify to form cumulate gabbros. The adcumulus nature of the gabbros investigated here suggests slow cooling rates typical of large intrusions implying relatively large, but ephemeral magma chambers below segments of the Southwest Indian Ridge.     

Late Cretaceous coeval acidic and basic magmatism,Karacaali Magmatic Complex,Central Anatolia,Turkey

The Central Anatolia Crystalline Complex (CACC) is characterized by Late Cretaceous high-temperature metamorphic rocks intruded by S-, I-, and A-type granitoids. Coeval basic plutonic and volcanic rocks also crop out in the complex. The NE–SW-trending Karacaali Magmatic Complex (KMC) represents a clear example of synchronous basic and acidic magmatic associations. We present new data on this coeval magmatism. The KMC plutonic rocks mainly consist of monzonite, granite, and gabbro, whereas the associated volcanic rocks are chiefly of basalt and rhyolite. All of the units have been cut by quartz, quartz-tourmaline, and calcite veins and by porphyritic leucogranite, aplitic, and basaltic dikes. The rhyolitic, basaltic, and gabbroic samples yield well-defined ⁴⁰Ar/³⁹Ar plateau ages of 69.1 ± 1.3, 58 ± 10, and 66.4 ± 1 million years, respectively; these data indicate that a younger multiphase basic magma was injected into a partially crystallized monzonitic magma chamber. The basic intrusions added heat to the system and gave rise to the re-fusion of the already crystallized parts of the monzonitic melt, forming the younger leucogranitic magma. The gradational contacts, cross-cutting relationships, trace element contents, trace element patterns, rare-earth element (REE) patterns, and ⁴⁰Ar/³⁹Ar geochronological data of the studied igneous suite clearly demonstrate that the acidic and basic rocks of the KMC were contemporaneous and are produced by partial melting of distinct sources rather than by fractional crystallization of a single source.     

Zonation des éléments en traces au cours de la croissance des cristaux dans les bains silicatés: l'exemple de Rb,Cs, Sr et Ba dans le système Qz-Ab-Or-H2O

An indirect method was used to study Na, K, Rb, Cs, Sr and Ba partition coefficients between crystals and silicate melt. Equilibria between a hydrothermal solution and the melt at 800°C and 2 kb and between a hydrothermal solution and crystals at 750°C and 2 kb were separately achieved.For major element partitioning (Na and K), the results obtained here are in good agreement with those of Tuttle and Bowen (1958) which allow us to follow crystal evolution during a fractional crystallization process where the growth of zoned crystals takes place.For minor elements Rb, Cs, Sr, Ba, melt/aqueous solution partition coefficients depend on Na/K as well as the silica content of the melt. These effects are rather small for Rb and Cs, but are much more important for the alkaline earths. The feldspar/aqueous solution partition coefficients also depend on Na/K.The variations of the partition coefficients feldspar/melt are complex in the part of the Qz-Ab-Or diagram located below the cotectic line.During fractional crystallization following the Rayleigh law (assuming that there are no kinetic phenomena) Sr (D > 10) is almost totally removed from the melt in the early stages whereas Cs (D < 0.1) remains in the melt during the whole process. Rb and Ba have partition coefficients closer to unity. The variation of these coefficients, due to changes in bulk composition of liquid and crystals during fractional crystallization, can lead to complex zoning with possible concentration maxima at some stages. Similar phenomena can be expected in non-ideal natural solid solutions, even if no discontinuities can be detected in the physicochemical evolution of the parent magma.     

Geochemical and thermodynamic modeling of the petrogenesis of A1-type granites and associated intermediate rocks: A case study from the central Fennoscandian Shield

The origin of ferroan A-type granites in anorogenic tectonic settings remains a long-standing petrological puzzle. The proposed models range from extreme fractional crystallization of mantle-derived magmas to partial melting of crustal rocks, or involve combination of both. In this study, we apply whole-rock chemical and Sm-Nd isotopic compositions and thermodynamically constrained modeling (Magma Chamber Simulator, MCS) to decipher the genesis of a suite of A1-type peralkaline to peraluminous granites and associated intermediate rocks (monzodiorite-monzonite, syenite) from the southwestern margin of the Archean Karelia craton, central Finland, Fennoscandian Shield. These plutonic rocks were emplaced at ca. 2.05 Ga during an early stage of the break-up of the Karelia craton along its western margin and show trace element affinities to ocean island basalt-type magmas. The intermediate rocks show positive ε_Nd(2050 Ma) values (+1.3 to +2.6), which are only slightly lower than the estimated contemporaneous depleted mantle value (+3.4), but much higher than average ε_Nd(2050 Ma) of Archean TTGs (–10) in the surrounding bedrock, indicating that these rocks were essentially derived from a mantle source. The ε_Nd(2050 Ma) values of the peralkaline and peraluminous granite samples overlap (–0.9 to +0.6 and –3.2 to +0.9, respectively) and are somewhat lower than those in the intermediate rocks, suggesting that the mafic magmas parental to granite must have assimilated some amount of older Archean continental crust during their fractionation, which is consistent with the continental crust-like trace element signatures of the granite members. The MCS modeling indicates that fractional crystallization of mantle-derived magmas can explain the major element characteristics of the intermediate rocks. The generation of the granites requires further fractional crystallization of these magmas coupled with assimilation of Archean crust. These processes took place in the middle to upper crust (∼2–4 kbar, ∼7–15 km) and involved crystallization of large amounts of clinopyroxene, plagioclase and olivine. Our results highlight the importance of coupled FC-AFC processes in the petrogenesis of A-type magmas and support the general perception that magmas of A-type ferroan granites become more peraluminous by assimilation of crust. They further suggest that variable fractionation paths of the magmas upon the onset of assimilation may explain the broad variety of A-type felsic and intermediate igneous rocks that is often observed emplaced closely in time and space within the same igneous complex.     

Geochemical evolution of Jurassic diorites from the Bristol Lake region,California, USA,and the role of assimilation

Late Jurassic dioritic plutons from the Bristol Lake region of the eastern Mojave Desert share several geochemical attributes with high-alumina basalts, continental hawaiite basalts, and high-K are andesites including: high K₂O concentrations; high Al₂O₃ (16–19 weight %); elevated Zr/TiO₂; LREE (light-rare-earth-element) enrichment (La/Yb_CN=6.3–13.3); and high Nb. Pearce element ratio analysis supported by petrographic relations demonstrates that P, Hf, and Zr were conserved during differentiation. Abundances of conserved elements suggest that dioritic plutons from neighboring ranges were derived from similar parental melts. In the most voluminous suite, correlated variations in elemental concentrations and (⁸⁷Sr/⁸⁶Sr)_i indicate differentiation by fractional crystallization of hornblende and plagioclase combined with assimilation of a component characterized by abundant radiogenic Sr. Levenberg-Marquardt and Monte Carlo techniques were used to obtain optimal solutions to non-linear inverse models for fractional crystallization-assimilation processes. Results show that the assimilated material was chemically analogous to lower crustal mafic granulites and that the mass ratio of contaminant to parental magma was on the order of 0.1. Lack of enrichment in ¹⁸O with differentiation is consistent with the model results. Elemental concentrations and O, Sr, and Nd isotopic data point to a hydrous REE-enriched subcontinental lithospheric source similar to that which produced some Cenozoic continental hawaiites from the southern Cordillera. Isotopic compositions of associated granitoids suggest that partial melting of this subcontinental lithosphere may have been an important process in the development of the Late Jurassic plutonic arc of the eastern Mojave Desert.     

Geochemical evolution of historical lavas from Askja Volcano, Iceland: Implications for mechanisms and timescales of magmatic differentiation

The mechanisms and the timescales of magmatic evolution were investigated for historical lavas from the Askja central volcano in the Dyngjufjöll volcanic massif, Iceland, using major and trace element and Sr, Nd, and Pb isotopic data, as well as ²³⁸U-²³⁰Th-²²⁶Ra systematics. Lavas from the volcano show marked compositional variation from magnesian basalt through ferrobasalt to rhyolite. In the magnesian basalt-ferrobasalt suite (5-10 wt% MgO), consisting of lavas older than 1875 A.D., ⁸⁷Sr/⁸⁶Sr increases systematically with increasing SiO₂ content; this suite is suggested to have evolved in a magma chamber located at ∼600 MPa through assimilation and fractional crystallization. On the other hand, in the ferrobasalt-rhyolite suite (1-5 wt% MgO), including 1875 A.D. basalt and rhyolite and 20th century lavas, ⁸⁷Sr/⁸⁶Sr tends to decrease slightly with increasing SiO₂ content. It is suggested that a relatively large magma chamber occupied by ferrobasalt magma was present at ∼100 MPa beneath the Öskjuvatn caldera, and that icelandite and rhyolite magmas were produced by extraction of the less and more evolved interstitial melt, respectively, from the mushy boundary layer along the margin of the ferrobasalt magma chamber, followed by accumulation of the melt to form separate magma bodies. Ferrobasalt and icelandite lavas in the ferrobasalt-rhyolite suite have a significant radioactive disequilibrium in terms of (²²⁶Ra/²³⁰Th), and its systematic decrease with magmatic evolution is considered to reflect aging, along with assimilation and fractional crystallization processes. Using a mass-balance model in which simultaneous fractional crystallization, crustal assimilation, and radioactive decay are taken into account, the timescale for the generation of icelandite magma from ferrobasalt was constrained to be <∼3 kyr which is largely dependent on Ra crystal-melt partition coefficients we used.     

Petrogenesis of Early Cretaceous bimodal volcanic rocks in the Fanchang Basin,SE China: an energy-constrained assimilation–fractional crystallization model

Volcanic rocks in the Middle–Lower Yangtze River Valley (MLYRV) constitute a bimodal magmatic suite, with a significant compositional gap (between 50% and 63% SiO₂) between the mafic and felsic members. The suite is characterized by a relatively wide spectrum of rock types, including basalts, trachytes, and rhyolites. The basaltic rocks have low-to-moderate SiO₂ contents of 46.00–50.01%, whereas the trachytes and rhyolites possess SiO₂ contents in the range of 63.08–77.61%. Rocks of the bimodal suite show moderate enrichment of LILEs, negative Nb, Ta, and Ti anomalies, and are significantly enriched in LREEs. The basalts were most likely generated by parental mafic magmas derived from enriched lithospheric mantle with minor assimilation of crustal materials involving coeval crystal fractionation during magma evolution. The results of energy-constrained assimilation and fractional crystallization simulations demonstrate that the felsic magma was produced by the mixing of 5–20% lower crustal anatectic melts with an evolved mafic magma (～48% SiO₂) and accompanied by extensive clinopyroxene, plagioclase, biotite, and Fe–Ti oxide fractionation. Our model for the genesis of felsic rocks in bimodal suites is different from the traditional models of crustal melting and fractional crystallization or assimilation–fractional crystallization of basaltic liquids.     

Distribution of REE,LILE, and HFSE between biotite,feldspar, and the melt in the granulite facies migmatite,nimnyr block,Aldan shield

The behavior of trace elements under conditions of partial melting of granitoid rocks has been studied. The element’s partition coefficients between minerals and the melt D_i^min/melt depends, in the first place, on the composition of the primary melt. In biotite the HREE D_i are a little below 1, while those of LREE, especially D_i for Ce, are 1–3 orders of magnitude less. This leads to an efficient differentiation of REEs in anatexic melts especially when biotite is the main mineral phase of restite. On the contrary, there are feldspars, the D_i of which cannot provide such a magnitude of differentiation. Unlike garnets and pyroxenes, whose stability in restite permits enrichment of anatexic melts produced in migmatization zones with Nb, Ti, and Cr, the presence of biotite in restite causes depletion of melts with those elements as well as with Rb. Feldspars, under conditions of their fractional crystallization or during differentiation of an anatexic melt, deplete the latter with Sr, Ba, and Rb, but enrich it with Nb, Ti, Cr, Y, Zr, and V.     

Geochemical Evolution of the Soufriere Hills Volcano, Montserrat, Lesser Antilles Volcanic Arc

The geochemical evolution of Montserrat provides an importantbackground to understanding the current activity of this islandarc volcano. Here we present major and trace element, and U-,Th- and O-isotope data for rocks generated in the last 300 kyrthat provide constraints on the magmatic processes occurringbeneath the volcano. Samples range from low- to medium-K calc-alkalinebasalts to dacites. Three suites can be distinguished on thebasis of major and trace element compositions: the South SoufrièreHills suite; the Soufrière Hills suite, including thelava from the current eruption; and the mafic inclusions. Magmaticdifferentiation of the magma that crystallized to form the maficinclusions appears to have been governed by closed-system processes,modelled by fractional crystallization (F     

Field and petrological evidence for the development of an ensialic marginal basin related to the Hercynian orogeny in the Massif Central,France

Six lithologic units in tectonic contact with each other have been defined during mapping of the Devonian in the Beaujolais area of the northeastern Massif Central. Five main igneous suites have been recognized:

1. A transitional basaltic suite restricted to a single unit.
2. An acid volcanic-plutonic suite the members of which are related by fractional crystallization and magma mixing.
3. Low-TiO₂ volcanic rocks with calc-alkaline affinities.
4. A TiO₂-rich tholeiitic suite related to an ophiolitic complex.
5. A plutonic suite with close resemblances to Alaskantype intrusions.

The transitional metabasalts (1) form the oldest igneous suite and could represent either an intraplate magmatic forerunner of rifting or tectonic slices of weakly metamorphosed rocks representing a pre-Acadian event. The next three suites may be related to a short-lived ensialic marginal basin that developed between the Acadian and Bretonian orogenies. The basin is asymmetric, with the ophiolite of the central part flanked by an acid ridge on one side and a passive continental margin on the other. Quartz-keratophyres (2) and calc-alkalic basic volcanic rocks (3) were intercalated in varying proportions to form a bimodal volcanic pile before the rifting event that led to the formation of the ophiolites (4). The acid ridge (2) may be due to the reactivation of a continental basement. Cumulate rocks with Alaskan-type affinities occur as olistoliths, emplaced before the formation of the rift basin, supporting a comparison of the Hercynian belt with accreted magmatic arc terranes.     

The age of the martian meteorite Northwest Africa 1195 and the differentiation history of the shergottites

Samarium-neodymium isotopic analyses of unleached and acid-leached mineral fractions from the recently identified olivine-bearing shergottite Northwest Africa 1195 yield a crystallization age of 347 ± 13 Ma and an value of +40.1 ± 0.9. Maskelynite fractions do not lie on the Sm-Nd isochron and appear to contain a martian surface component with low ¹⁴⁷Sm/¹⁴⁴Nd and ¹⁴³Nd/¹⁴⁴Nd ratios that was added during shock. The Rb-Sr system is disturbed and does not yield an isochron. Terrestrial Sr appears to have affected all of the mineral fractions, although a maximum initial ⁸⁷Sr/⁸⁶Sr ratio of 0.7016 is estimated by passing a 347 Ma reference line through the maskelynite fraction that is least affected by contamination. The high initial value and the low initial ⁸⁷Sr/⁸⁶Sr ratio, combined with the geologically young crystallization age, indicate that Northwest Africa 1195 is derived from a source region characterized by a long-term incompatible-element depletion.The age and initial Sr and Nd isotopic compositions of Northwest Africa 1195 are very similar to those of Queen Alexandra Range 94201, indicating these samples were derived from source regions with similar Sr-Nd isotopic systematics. These similarities suggest that these two meteorites share a close petrogenetic relationship and might have been erupted from a common volcano. The meteorites Yamato 980459, Dar al Gani 476, Sayh al Uhaymir 005/008, and Dhofar 019 also have relatively old ages between 474 and 575 Ma and trace element and/or isotopic systematics that are indicative of derivation from incompatible-element-depleted sources. This suggests that the oldest group of meteorites is more closely related to one another than they are to the younger meteorites that are derived from less incompatible-element-depleted sources. Closed-system fractional crystallization of this suite of meteorites is modeled with the MELTS algorithm using the bulk composition of Yamato 980459 as a parent. These models reproduce many of the major element and mineralogical variations observed in the suite. In addition, the rare earth element systematics of these meteorites are reproduced by fractional crystallization using the proportions of phases and extents of crystallization that are calculated by MELTS. Other shergottites that demonstrate enrichments in incompatible-elements and have evolved Sr and Nd isotopic systematics have some geochemical systematics that are similar to those observed in the depleted group. Most notably, although they exhibit a very limited range of incompatible trace element and isotopic compositions, they have highly variable major element compositions. This is also consistent with evolution from a common mantle source region by variable amounts of fractional crystallization. If this scenario is correct, it suggests that the combined effects of source composition and fractional crystallization are likely to account for the major element, trace element, and isotopic diversity of all shergottites.     

Trace element distribution patterns and their relationship to the crystallization of granitic melts

The distribution of Ba, Rb and Sr during crystallization of a granitic melt is examined in a number of theoretical models. The modes of crystallization considered are perfect fractional crystallization, perfect equilibrium crystallization, and an intermediate mode, incremental equilibrium crystallization. The effect of the degree of separation of cumulus minerals from melt during crystallization is also considered. Perfect fractional and incremental equilibrium crystallization (with small increments) are broadly similar, but differ in the final stages of crystallization in that the latter mode defines a finite trace element composition for the last solid. The effect of intercumulus melt in both modes of crystallization imparts a ‘liquid’ character to the solids, and suppresses the degree of enrichment of Rb and depletion of Ba and Sr in late solids and melts.Examination of trace element data for the Acid Phase of the Bushveld Igneous Complex in the light of these models suggests that these granites represent a suite of cumulate rocks, containing relatively large amounts of intercumulus melt.     

Platinum-group element systematics in Mid-Oceanic Ridge basaltic glasses from the Pacific, Atlantic, and Indian Oceans

The concentrations of Ir, Ru, Pt and Pd have been determined in 29 Mid-Oceanic Ridge basaltic (MORB) glasses from the Pacific (N = 7), the Atlantic (N = 10) and the Indian (N = 11) oceanic ridges and the Red Sea (N = 1) spreading centers. The effect of sulfide segregation during magmatic differentiation has been discussed with sample suites deriving from parental melts produced by high (16%) and low (6%) degrees of partial melting, respectively. Both sample suites define positive and distinct covariation trends in platinum-group elements (PGE) vs. Ni binary plots. The high-degree melting suite displays, for a given Ni content, systematically higher PGE contents relative to the low-degree melting suite. The mass fraction of sulfide segregated during crystallization (X_sulf), the achievement of equilibrium between sulfide melt and silicate melts (R_eff), and the respective proportions between fractional and batch crystallization processes (S_b) are key parameters for modeling the PGE partitioning behavior during S-saturated MORB differentiation. Regardless of the model chosen, similar sulfide melt/silicate melt partition coefficients for Ir, Ru, Pt and Pd are needed to model the sulfide segregation process, in agreement with experimental data. When corrected for the effect of magmatic differentiation, the PGE data display coherent variations with partial melting degrees. Iridium, Ru and Pt are found to be compatible in nonsulfide minerals whereas the Pd behaves as a purely chalcophile element. The calculated partition coefficients between mantle sulfides and silicate melts (assuming a PGE concentration in the oceanic mantle at ∼0.007 × CI-chondritic abundances) increase from Pd (∼10³) to Ir (∼10⁵). This contrasting behavior of PGE during S-saturated magmatic differentiation and mantle melting processes can be accounted for by assuming that Monosufide Solid Solution (Mss) controls the PGE budget in MORB melting residues whereas MORB differentiation processes involve Cu-Ni-rich sulfide melt segregation.     

Partition coefficients of trace elements: Application to volcanic rocks of St. Vincent,West Indies

Island arc basaltic rocks (basalts and basic andesites with SiO₂ < 56.5%) from the Soufrière volcano. St. Vincent, West Indies (prehistoric lavas and 1902 and 1979 eruptions) underwent extensive fractional crystallization at various levels during the ascent of the magma. Although the precipitation of minerals occurring in coarse-grained cumulate inclusions dominated the derivation of basic andesites from basaltic magma, the distribution of the trace elements is not consistent with a simple fractional crystallization process. The lavas have a partially cumulate character and were probably generated from similar but separate parental magmas. The partition coefficients of transition and large ion lithophile elements are given for clinopyroxene, amphibole. olivine, plagioclase and titanomagnetite in basaltic liquid which crystallized under well-defined P-T conditions. The temperatures obtained from the geothermometers based upon the distribution of the major elements are in good agreement with the data from trace element geothermometers.