Experimental investigation of CaMg exchange between olivine,orthopyroxene, and clinopyroxene: potential for geobarometry

The distribution of Ca and Mg among coexisting olivine, clinopyroxene and orthopyroxene has been studied in a piston-cylinder apparatus in the temperature range 1100–1300°C and pressure range 9–41 kbar. Ca in olivine decreases with increasing pressure and decreasing temperature. The pressure effect is the result of Ca going into the higher-coordination M2 site in clinopyroxene as pressure is increased. For the CaMg exchange reaction between olivine and clinopyroxene, ΔV°=0.249J bar^?1 mole^?1; this is sufficient for pressure estimates accurate to ±3kbar if temperatures of equilibration are independently known. CaMg exchange between olivine and orthopyroxene is not sufficiently pressure dependent to be used as a geobarometer.Application of the olivine-clinopyroxene geobarometer to coarse garnet lherzolites from southern Africa gives P-T results consistent with a continental geotherm. For spinel lherzolites from southwestern United States, the geotherm appears to be displaced to higher temperatures indicating oceanic affinities. Application of the geobarometer to natural systems requires assumptions about activity relationships in clinopyroxene which should be checked by experiment.     

Origin and ascent history of unusually crystal-rich alkaline basaltic magmas from the western Pannonian Basin

The last eruptions of the monogenetic Bakony-Balaton Highland Volcanic Field (western Pannonian Basin, Hungary) produced unusually crystal- and xenolith-rich alkaline basalts which are unique among the alkaline basalts of the Carpathian–Pannonian Region. Similar alkaline basalts are only rarely known in other volcanic fields of the world. These special basaltic magmas fed the eruptions of two closely located volcanic centres: the Bondoró-hegy and the Füzes-tó scoria cone. Their uncommon enrichment in diverse crystals produced unique rock textures and modified original magma compositions (13.1–14.2 wt.% MgO, 459–657 ppm Cr, and 455–564 ppm Ni contents). Detailed mineral-scale textural and chemical analyses revealed that the Bondoró-hegy and Füzes-tó alkaline basaltic magmas have a complex ascent history, and that most of their minerals (～30 vol.% of the rocks) represent foreign crystals derived from different levels of the underlying lithosphere. The most abundant xenocrysts, olivine, orthopyroxene, clinopyroxene, and spinel, were incorporated from different regions and rock types of the subcontinental lithospheric mantle. Megacrysts of clinopyroxene and spinel could have originated from pegmatitic veins/sills which probably represent magmas crystallized near the crust–mantle boundary. Green clinopyroxene xenocrysts could have been derived from lower crustal mafic granulites. Minerals that crystallized in situ from the alkaline basaltic melts (olivine with Cr-spinel inclusions, clinopyroxene, plagioclase, and Fe–Ti oxides) are only represented by microphenocrysts and overgrowths on the foreign crystals. The vast amount of peridotitic (most common) and mafic granulitic materials indicates a highly effective interaction between the ascending magmas and wall rocks at lithospheric mantle and lower crustal levels. However, fragments from the middle and upper crust are absent from the studied basalts, suggesting a change in the style (and possibly rate) of magma ascent in the crust. These xenocryst- and xenolith-rich basalts yield divers tools for estimating magma ascent rate that is important for hazard forecasting in monogenetic volcanic fields. According to the estimated ascent rates, the Bondoró-hegy and Füzes-tó alkaline basaltic magmas could have reached the surface within hours to few days, similarly to the estimates for other eruptive centres in the Pannonian Basin which were fed by “normal” (crystal and xenoliths poor) alkaline basalts.     

Petrogenesis of anhydrous clinopyroxenite xenoliths and clinopyroxene megacrysts in alkali basalts from the Ganseong area of South Korea

Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO₂ abundances in spinels and high TiO₂ and Na₂O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.     

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

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

Magnetic stratigraphy and magnetic-petrologic properties of Precambrian Gardar lavas,South Greenland

We present major and trace element data for olivines and rapidly quenched groundmass material separated from eight samples of basaltic rock. From these data apparent olivine/liquid distribution coefficients (D) for the elements Mg, Mn, Ni, Co, Cr, Sc, Na, Sm, and Ca have been calculated. Petrographic and electron microprobe studies indicate that olivines in most of these samples are but slightly zoned and groundmass glasses are essentially uniform in composition; these data suggest that the co-existing olivine-groundmass pairs are in equilibrium. In addition, olivine crystallization temperatures were calculated using experimental calibrations of lnD vs.1/T for the elements Mg, Fe, Mn, Ni, and Co. A high degree of concordancy for the resulting temperatures, based on five different elements for most samples, also suggests that olivine-groundmass equilibrium was obtained. We conclude that the apparent olivine/liquidD's derived from this study are representative of equilibriumD's, but emphasize that variations in temperature, and possibly bulk composition, strongly affect suchD's in natural magmas.     

Chrome spinel in normal MORB‐type greenstones from the Paleozoic–Mesozoic Mino terrane,East Takayama area,central Japan: Crystallization course with a U‐turn

Phenocrystic chrome spinel crystallized in normal MORB‐type greenstones in the East Takayama area. Associated phenocryst minerals show a crystallization sequence that was olivine first, followed by plagioclase, and finally clinopyroxene. Chrome spinel ranges from 0.54 to 0.77 in Mg/(Mg+Fe²⁺) and 0.21 to 0.53 in Cr/(Cr+Al); the Fe³⁺ content varies from 0.07 to 0.22 p.f.u. (O = 4). Significant compositional differences of spinel were observed among the phenocryst mineral assemblages. Chrome spinel in the olivine–spinel assemblage shows a wide range in Cr/(Cr+Al), and is depleted in Fe²⁺ and Fe³⁺. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage is Fe²⁺‐ and Fe³⁺‐rich at relatively high Cr/(Cr+Al) ratios. Basalt with the olivine–plagioclase–spinel assemblage contains both aluminous spinel and Fe²⁺‐ and Fe³⁺‐rich spinel. The assumed olivine–spinel equilibrium suggests that chrome spinel in the olivine–spinel assemblage changed in composition from Cr‐ and Fe²⁺‐rich to Al‐ and Mg‐rich with the progress of fractional crystallization. Chrome spinel in the olivine–plagioclase–clinopyroxene–spinel assemblage, on the other hand, exhibits the reversed variations in Mg/(Mg+Fe²⁺) and in Cr/(Cr+Al) ratios that decrease and increase with the fractional crystallization, respectively. The entire crystallization course of chrome spinel, projected onto the Mg/(Mg+Fe²⁺)–Cr/(Cr+Al) diagram, exhibits a U‐turn, and appears to be set on a double‐lane route. The U‐turn point lies in the compositional field of chrome spinel in the olivine–plagioclase–spinel assemblage, and may be explained by plagioclase fractionation that began during the formation of the olivine–plagioclase–spinel assemblage.     

Rift Valley in the Atlantic Ocean near 36°50′N: petrology and geochemistry of basaltic rocks

Dredged rocks from an area of about 15 km² within the inner floor and on the adjacent walls of the Rift Valley were collected. Based on petrographic and chemical data, four types of basaltic rocks were recognized: (1) picritic basalts with olivine xenocrysts, TiO₂ < 0.6%, K₂O < 0.1%, (2) olivine basalts with olivine megacrysts, TiO₂ = 0.8–1.5%,K₂O = 0.1–0.2%, (3) highly phyric and moderately phyric plagioclase basalts with megacrystic plagioclase, TiO₂ < 1.3%, K₂O < 0.3%, and (4) pyroxene basalts with pyroxene > plagioclase, TiO₂ = 0.8–1%,K₂O = 0.2–0.4%. The Cr and Ni having high partition coefficients show different variation trends for each type of rock and their values decrease continuously as crystallization proceeds within each type of basalt. It is speculated that two different magmas have given rise to the above-mentioned rocks. One has yielded the picritic basalts and subsequently the olivine basalts after a separation of the olivine cumulates; the other gave rise to the plagioclase basalts.     

Petrology of basalts from Loihi Seamount,Hawaii

Loihi Seamount is the southeasternmost active volcano of the Emperor-Hawaii linear volcanic chain. It comprises a spectrum of basalt compositional varieties including basanite, alkali basalt, transitional basalt and tholeiite. Samples from four dredge collections made on Scripps Institution of Oceanography Benthic Expedition in October 1982 are tholeiite. The samples include highly vesicular, olivine-rich basalt and dense glass-rich pillow fragments containing olivine and augite phenocrysts. Both quartz-normative and olivine-normative tholeiites are present. Minor and trace element data indicate relatively high abundances of low partition coefficient elements (e.g., Ti, K, P. Rb, Ba, Zr) and suggest that the samples were derived by relatively small to moderate extent of partial melting, of an undepleted mantle source. Olivine composition, MgO, Cr and Ni abundances, and Mg/(Mg+Fe), are typical of moderately fractionated to relatively unfractionated “primary” magmas. The variations in chemistry between samples cannot be adequately explained by low-pressure fractional crystallization but can be satisfied by minor variations in extent of melting if a homogeneous source is postulated. Alternatively, a heterogeneous source with variable abundances of certain trace elements, or mixing of liquids, may have been involved. Data for ³He/⁴He, presented in a separate paper, implies a mantle plume origin for the helium composition of the Loihi samples. There is little variation in the helium isotope ratio for samples having different compositions and textures. The helium data are not distinctive enough to unequivocally separate the magma sources for the tholeiitic rocks from the other rock types such as Loihi alkalic basalts and the whole source region for Loihi may have a nearly uniform helium compositions even though other element abundances may be variable. Complex petrologic processes including variable melting, fractional crystallization and magma mixing may have blurred original helium isotopic signatures.     

Petrography and geochemistry of basaltic rocks from the Conrad fracture zone on the America-Antarctica Ridge

Intrusive and extrusive basaltic rocks have been dredged from the Conrad fracture zone (transecting the slow-spreading America-Antarctica Ridge). The majority of rocks recovered are holocrystalline with the dominant mineral assemblage being plagioclase plus clinopyroxene with or without minor Fe-Ti oxides (olivine occurs in only three samples) and many of the samples show evidence of extensive alteration. Secondary minerals include chlorite, actinolite, K- and Na-feldspar, analcite and epidote. In terms of bulk chemistry the rocks are characterized by their generally evolved and highly variable compositions (e.g.Mg^*=0.65?0.35;TiO₂=0.7?3.6%;Zr=31?374ppm;Nb=<3?21ppm;Y=17?96ppm;Ni=100?9ppm), but with respect to the immobile incompatible element ratios (e.g. Zr/Nb, Y/Nb, La/Sm) are similar to “normal” or depleted mid-oceanic ridge basalts.Quantitative major and trace element modelling indicate that most of the variation observed can be attributed to low-pressure fractional crystallization of plagioclase plus clinopyroxene in approximately equal proportions with or without minor Fe-Ti oxides. The range in composition can be accounted for by up to 76% fractional crystallization. Although ferrobasalts have not frequently been associated with slow spreading ridges, the extreme differentiation observed in the Conrad fracture zone basalts implies some additional constraint other than spreading rate on the formation of ferrobasalt and reaffirms the importance of extensive crustal differentiation during the production of this basalt type.     

Barren Island Volcano (NE Indian Ocean): Island-arc high-alumina basalts produced by troctolite contamination

Barren Island (BI) is a subduction-related volcanic island lying in the northeastern Indian Ocean, about 750 km north of the northern tip of Sumatra. Rising from a depth of ∼2300 m on the Andaman Sea floor, BI has a submarine volume estimated at ∼400 km³, but the island is just 3 km across, reaches a maximum elevation of 355 m, and has a subaerial volume of only ∼1.3 km³. The first historical eruption began in 1787 when a cinder cone grew in the center of a pre-historical caldera 2-km in diameter and sent lava flows westward to reach the sea; activity continued intermittently until 1832. Two subsequent eruptions modified the central cone and also sent lava flows westward to reach the sea in 1991 and 1994–1995.A suite of 28 lava, scoria, and ash samples were investigated from various stages of the subaerial eruptive history of BI. Most are basalts (including all 10 samples from the 1994–1995 eruption) and basaltic andesites (including 7 of 8 samples from the 1991 eruption), but 2 pre-1787 andesites were also studied. On multi-element spider diagrams the BI suite shows subparallel trends for most elements that reflect an important role for fractional crystallization, along with the characteristic depletions of Nb–Ta and enrichments of K–Rb–Pb found in other subduction-related island-arc suites. The typical relative enrichment of Ba is not present, likely because the subducted sediments in the Andaman arc are not Ba-rich. Wide compositional ranges for Cs, Th, Rb, U, and Pb may trace different degrees of scavenging from the underlying volcanic pile.BI basalts and basaltic andesites have variable abundances of phenocrystic–microphenocrystic olivine plus Cr–Al–Mg spinel inclusions, plagioclase, and clinopyroxene, embedded in a matrix of glass, the same minerals, and titanomagnetite (mostly exsolved). The most remarkable mineralogical feature of certain BI basalts and basaltic andesites is the presence of abundant (to 40 vol.%) and large (to 5 mm) crystals of relatively homogeneous anorthitic plagioclase (to An_95.7). These have inclusions of Mg olivine (to Fo₇₉) and thin (10–150 μm) normally zoned margins that reach to the more sodic compositions of the plagioclase phenocryst and microphenocryst rims. Anorthitic plagioclase crystals are common at many subduction-related volcanoes. At BI, the anorthitic plagioclase and associated olivine crystals are thought to have entered the magmas through disaggregation of troctolitic crystal mushes or plutonic xenoliths. This process affected bulk-rock compositions in many ways, including raising Al₂O₃ contents to values as high as 22.8 wt.% and Eu / Eu* values up to 1.05. Compared to a large petrological and geochemical database for Indonesian volcanic rocks, the BI suite falls at the most depleted end for levels of K and incompatible trace elements, and Sr, Nd, and Pb isotopic ratios. Consequently, the BI suite defines an excellent primitive baseline against which Indonesian volcanic suites can be compared.     

Bimodal tholeiitic and mildly alkalic basalts from Bhir area,central Deccan Volcanic Province,India: Geochemistry and petrogenesis

Bimodal tholeiitic and mildly alkalic basalts occur near Bhir, in the central part of Deccan Volcanic Province (DVP). Major and trace element concentrations show that, of the ten flows, nine are tholeiitic and one is an alkalic basalt. The Bhir basalts have a wide range of chemical composition. Geochemical variations in the stratigraphic section define three distinct phases of evolution (zones 1 to 3). Crystal fractionation of plagioclase, clinopyroxene, olivine and Fe–Ti oxide expanded the compositional range. Low Mg#s (39–55), low concentrations of Ni and Cr and high Zr suggest the evolved nature of the Bhir basalts. Fractionation modeling suggests about 42% fractional crystallization.In spite of the dominant role of fractional crystallization in the evolution of Bhir basalts, some other processes must be sought to explain the chemical variations. Crustal contamination, magma mixing and degree of partial melting are suggested to explain the observed chemical variations. Resorption, reverse zoning and compositional bimodality in plagioclase phenocrysts indicate magma mixing. Samples of flows one and four suspected of being contaminated all have enriched SiO₂ and LILE (K, Rb, and Ba) contents and depletion in Ti and P, believed to be due to ‘granitic’ crustal contamination.As compared to tholeiitic basalts, the alkalic basalts are characterized by low SiO₂ and high TiO₂, Na₂O, K₂O and P₂O₅. Alkalic basalts are richer in LILE (Rb and Ba), HFSE (Nb, Zr, and Y) and REE than the tholeiitic basalts. The alkalic basalt occurrence is important from a petrogenetic point of view and also suggests that the sources of alkalic basalt magmas may be of variable ages under different parts of the DVP. Based on major, trace and rare earth element distributions it is suggested that asthenospheric mantle having affinities with the source of OIB was the source material of the magmas and the range in the composition of tholeiitic and alkalic basalts was probably controlled by different degrees of melting and/or inhomogeneities in the mantle source.     

Chromite in the Paricutin lava flows (1943–1952)

Small euhedral chromite crystals are found in olivine macrophenocrysts (Fo_80–84) from the basaltic andesites (150 ppm Cr) erupted in 1943–1947, and in orthopyroxene macrophenocrysts of the andesites (75 ppm Cr) erupted in 1947–1952. The majority of the chromite octahedra are 5–20 μm in diameter, and some are found in clusters and linear chains of three or more oriented chromite crystals. The composition of the majority of the chromite grains within olivine and orthopyroxene macrophenocrysts is Fe²⁺/(Fe²⁺+Mg)=0.5–0.6, Cr/(Cr+Al)=0.5–0.6 and Fe³⁺/(Fe³⁺+Al+Cr)=0.2–0.3. The chromite crystals in contact with the groundmass are larger, subhedral, and grade in composition from chromite cores to magnetite rims. Comparison of the composition of chromite with those of other volcanic rocks shows that the most primitive Paricutin chromite is richer in total iron and higher in Fe³⁺/(Fe³⁺+Al+Cr) than primary chromite in most lavas. The linear chains of oriented chromite octahedra are found in olivine and orthopyroxene macrophenocrysts, and in the groundmass. These chromite chains are thought to result from diffusion-controlled crystallization because of the very high partition coefficient (1000) of Cr between chromite and melt. We conclude that chromite was a primary phase in the lavas at the time of extrusion and that magnetite only crystallized after extrusion during cooling of the lava flows. The presence of chromite microphenocrysts in andesitic lavas containing as little as 70 ppm Cr can be explained by dissolved H₂O in the melt depressing the liquidus temperature for orthopyroxene such that chromite becomes a liquidus phase. The influence of dissolved H₂O can also explain the lack of plagioclase macrophenocrysts in most of the lavas and the relatively high partition coefficient (20) of Ni between olivine and melt and the high partition coefficient (40) of Cr between orthopyroxene and melt. The liquidus temperature of the basaltic andesite is estimated to have been less than 1140°C, assuming H₂O>1 wt.%, and the log f_O2 to have been above that of the QFM buffer. The chromite and orthopyroxene liquidus temperature of the andesites, assuming H₂O>1 wt.%, is estimated to have been 1100°C or less. The derivation of the later andesites from the earlier basaltic andesites has been explained by a combination of fractional crystallization of olivine, orthopyroxene and plagioclase, and assimilation of xenoliths. The significantly lower Cr, Ni and Mg of the andesites may have been in part due to the separation of olivine macrophenocrysts plus enclosed chromite crystals from the earlier basaltic andesites.     

Olivine basalts at the Karymskii Volcanic Center: Mineralogy, petrogenesis, and magma sources

The olivine basalts of the Karymskii Volcanic Center (KVC) can be traced during the history of the area from the Lower Pleistocene until recently (the 1996 events); they are typical low-and moderate-potassium tholeiite basalts of the geochemical island-arc type. We have investigated the compositions of phenocryst minerals represented by plagioclase, olivine, clinopyroxene, as well as solid-phase inclusions of spinel in olivine, and more rarely in anorthite. The evolutionary trends of the rock-forming minerals provide evidence of the comagmaticity of these basalts, and thus of a long-lived intermediate magma chamber in the interior of the structure. The activity of this chamber is related to periodic transport of high temperature basalt melts to the surface. The geochemistry of the basalts is controlled by their origin at the same depleted magma source close to N-MORB, by successive crystallization of the primary melt, and by restricted mixing with magma components that are crystallizing at different depths. It is hypothesized that the solid-phase inclusions of high alumina spinel (hercynite?) found in olivine (and anorthite) of the basalts in the KVC north sector are of relict origin.     

On the origin of an amphibole-rich vein in a peridotite inclusion from the Lunar Crater Volcanic Field,Nevada, U.S.A.

Late Cenozoic alkali basaltic lavas of the Lunar Crater Volcanic Field (LCVF), located in the center of the Great Basin of the Western U.S.A., contain a diverse suite of nodule samples of the lower crust and upper mantle. This paper documents a composite nodule from the Marcath flow in which an amphibole-bearing wehrlite (59% olivine, 30% clinopyroxene, 6% amphibole) is cut by a 6–9 mm wide vein of andesine-amphibolite (80% kaersutite, 15% andesine, 3% ilmenite). Aside from nodule-basalt reaction at the nodule exterior, there is little chemical variation either within or between individual grains of hydrous and anhydrous phases in the vein and host wehrlite. Furthermore, there is no systematic compositional zoning in the wehrlite relative to vein proximity. The whole-rock major and trace element composition of the vein is similar to a primitive (Mg/(Mg+Fe)=0.692) basaltic liquid and has Al, Fe, Mg, Ca, Mn, Na, K, Zr, Y and Sr contents similar to basalts observed in the LCVF. In contrast to the Sr isotopic equilibrium displayed by vein feldspar and vein amphibole, Sr isotopic disequilibrium is exhibited between the vein (0.70318(4)), wehrlite (0.70322(4)), and host basalt (0.70357(5) n=3). However, the Sr isotopic ratios of older LCVF basalts (0.7030–0.7038; n=14) overlap those of the vein and wehrlite, and the magmatic activity leading to vein and wehrlite formation could be related to this older phase of LCVF volcanism. Petrographic and geochemical evidence is not consistent with a metasomatic origin for the vein and instead supports the view that the vein originated by the intrusion into a wehrlite mass and subsequent crystallization of a relatively primitive alkali basaltic magma in the lower crust or upper mantle. The wehrlite contains olivine of FO₇₁ and probably originated by crystal separation and accumulation from a relatively differentiated basaltic magma in the lower crust or upper mantle.     

Magmatic gases extracted and analysed from ocean floor volcanics

Magmatic gases extracted and analysed from basaltic rocks collected in the FAMOUS area near 36°50′ N in the Atlantic ocean show that the total amount of gas included in the samples varies between about 500 ppm to 1600 ppm. The main gaseous phases included in the various types of basalts consist of CO₂ (270–700 ppm), CO (150–800 ppm), HCl (100–1000 ppm), H₂ (0–50 ppm), SO₂ (up to 175 ppm), N₂ (up to about 213 ppm) and traces of hydrocarbons (up to about 24 ppm). The relative amount of CO, CO₂ and SO₂ varies with both the degree of crystallinity of the rock and with fractional crystallization and/or fractional melting. The glassy margin of pillow lavas have a higher CO/CO₂ ratio than the more crystalline interior. The most fractionated rocks of the series rich in clinopyroxene are depleted in the CO/CO₂ ratio and have a higher SO₂ content than do the most mafic end members rich in olivine. Early-formed olivine was crystallized in a reducing environment rich in CO and H₂ with respect to later formed mineral associations. It is likely that the carbon and sulfur oxidation is taking place at a relatively shallow depth during magmatic ascent or during volcanism. The ocean floor volcanics when compared to subaerial basalts are depleted in SO₂ and have on the average ten times more H₂.     

Petrology of tholeiitic lavas from Tanna Island (New Hebrides): Importance of cumulative processes in Island arc magmatism

Tanna, one of the southernmost islands of the New Hebrides volcanic arc, is made of Late Pliocene to Recent island arc tholeiitic basalts and andesites, with SiO₂ contents ranging from 45 to 57%. These lavas are highly porphyritic (30–50% in volume): phenocrysts of plagioclase are the most abundant, together with olivine and clinopyroxene. The groundmass contain plagioclase, augite, olivine, magnetite and glass; pigeonite, tridymite, sanidine and, rarely, biotite may also occur. The olivines and clinopyroxenes show an iron enrichment from the cores of phenocrysts to their rims and the groundmass crystals, but their compositional variations are not correlated with the Mg/Fe ratio of bulk host rocks, the most Fe-rich compositions being found in Mg-rich lavas. Plagioclase compositions range from An₉₅ to An₆₀ in the basalts and An₆₀ to An₅₀ in the andesites, but, within each group, they are not correlated with SiO₂ or Na₂O contents of host lavas. Consequently, the bulk major element compositions of Tanna volcanic rocks cannot be considered as primarily controlled by crystal separation from successive liquids. The oxyde-SiO₂ variations diagrams, and the modal compositions and mineral chemistry show that crystal accumulation is the predominant mechanism accounting for bulk rock compositions. However, this does not exclude fractional crystallization: the variation of the calculated groundmass mineralogy strongly suggest the occurrence of crystal removal mainly clinopyroxene and magnetite.     

The gabbroic rocks of the Peninsular ranges batholith, Southern California: cumulate rocks associated with calc-alkalic basalts and andesites

Gabbroic rocks occur only in the west, and are the oldest intrusions in the Peninsular Ranges Cordilleran batholith. They comprise an olivine-pyroxene gabbronorite series and an amphibole gabbro series both of which contain abundant plagioclase and amphibole. They formed by crystal accumulation and in situ differentiation, in multiple intrusive complexes, and are not considered to be related by fractionation to the granitoid rocks of the batholith.Pure mineral separates of plagioclase, olivine, clinopyroxene, orthopyroxene, and amphibole were obtained by magnetic and heavy-liquid methods from a representative suite of gabbroic rocks. Their major- and trace-element contents were determined by X-ray fluorescence, and the data used to test hypotheses on the genesis and fractionation of the gabbros.The plagioclases range from An₉₈ to An₆₅ in composition, olivines, Fo₇₉ to Fo₇₀, occur in rocks where An>₃₆. All clinopyroxenes are augite with Mg #'s varying from 81.1 to 64.7. Orthopyroxene occurs where An<₉₂, and is generally inverted pigeonite or bronzite, and has Mg #'s ranging from 77.9 to 52.1. The amphiboles include tschermakite, tschermakitic hornblende, pargasite, pargasitic hornblende, ferroan pargasite, magnesio-hornblende, and magnesio-taramite, Mg #'s range from 80.4 to 62.5. Systematic chemical and mineralogical changes confirm that differentiation, controlled by mineral assemblages of plagioclase, olivine, spinel, and clinopyroxene initially, and orthopyroxene, amphibole, and magnetite later, took place between intrusive episodes and in situ.The highly clacic plagioclase coexisting with olivine and amphibole suggests that the gabbros were formed from hydrous mafic magmas. The modal mineralogy of the gabbros, and the chemistry of the minerals is very similar to that of the cumulate blocks of the Lesser Antillean volcanoes. These features confirm that the gabbros were derived from a hydrous mafic magma, with high Al₂O₃ and low TiO₂ contents, typical of orogenic environments.Cumulate minerals from the gabbros show little or no zoning and are considered to have formed in equilibrium with the evolving melts. Selected trace-element contents and distribution coefficients are used to calculate the compositions of the melts. The calculations show that the melts in equilibrium with the olivine-pyroxene gabbronorite series contain approximately 100–200 ppm Ba, 200–400 ppm Sr, 30-10 ppm Ni, 20-10 ppm Co, and 300-100 ppm V. K/Rb ratios of the melts, derived from post-cumulus and prismatic amphiboles, are generally in the range 550-250. These values are typical of calc-alkalic basalts and andesites, and it is suggested that they may have erupted at the surface to form a coeval calc-alkalic volcanic sequence.     

Occurrence of ten metals in Mytilus edulis L. and Cardium glaucum L. from the Gdańsk Bay

The determination of Fe, Mn, Ni, Pb, Cu, Co, Zn, Cd, Ca and Mg was carried out in the soft tissues and shells of Mytilus edulis and Cardium glaucum from Gdańsk Bay. This paper reports on the influence of size (age) on the metal concentration in molluscs. Both species-dependent variability and regional variations of metal concentrations in molluscs were observed. The correlation coefficients between the concentrations of metal in the soft tissues and shells were determined. The correlation coefficients between hard and soft parts metals were calculated for Mytilus edulis.     

Petrology of clinopyroxene-amphibole inclusions from the roque nublo volcanics,gran canaria,canary islands

Inclusions consisting of clinopyroxene, amphibole, Fe-Ti oxides and apatitc are abundant in the Roque Nublo volcanics, a unit of Late Tertiary age that is widespread on Gran Canaria Island. The unit includes alkalic basalts and breccias. Mafic minerals in several inclusions and in one basalt host have been analysed with the electron microprobe. Although the inclusions vary in size, texture and mineralogy, they show certain common teatures. The pyroxenes analyzed are all salites-augites and their position in the Ca-Fe Mg quadrilateral suggests that they are early formed representatives of the pyroxene crystallization trend characteristic of alkaliolivine basalt. The amphibole is invariably kaersutite. A common variety of inclusion is composed largely of kaersutite and titaniferous clinopyroxene. The kaersutite (TiO₂ 5.27%, K₂O 1.58%) is homogeneous, except for slight iron enrichment in the margins of crystals. The clinopyroxene is an hourglass-zoned, brownish titansalite, Ca 50 Mg 35 Fe 15, TiO₂ 3.08%, with a green core of Ca 49 Mg 38 Fe 13, TiO₂ 2.15%. Compositions of coexisting titanilerous magnetite and ilmenite, Usp 44 Mt 56 and Ilm 85 Hem 15, respectively, indicate they formed at approximately 975°C and pO, 10^?10.5 atm. In another type of inclusion and its host basalt, pyroxene relations are more complex. Inclusion pyroxene is markedly but diffusely zoned. Predominant is a green salite, Ca 47 Mg 38 Fe 15, TiO₂ 1.11%, which has small, patchy core zones of brownish. Ti-rich salite. Ca 48 Mg 35 Fe 17, TiO₂ 1.94%. Cores of crystals in the host basalt are Ca 47 Mg 41 Fe 12, TiO₂ 2.23%; rims are pale green, Cr-rich diopsidic augite, Ca 44 Mg 45 Fe 11, TiO₂ 1.32%, Cr₂O₃ 0.48%. This «reverse» Fe-Mg zoning is attributed to increasing partial pressure of oxygen as crystallization proceeded. Kaersutite similar to that mentioned above occurs in both the inclusion and its host, in which it is highly resorbed. The available field and analytical evidence strongly suggests that the inclusions and the associated basalts are genetically related. Resorption of the kaersutite at depth may have given rise to the alkalic basalts of the Roque Nublo series.     

Partial melting controls on the northwest Kyushu basalts from Saga-Futagoyama

Abstract   The major element and compatible trace element compositions of the northwest Kyushu basalts (NWKBs) collected from Saga-Futagoyama were analyzed to examine the petrogenesis of these basalts. Although nepheline-normative alkaline basalts are not found in the basalts from Saga-Futagoyama, the Saga-Futagoyama basalts almost cover the major element variations of NWKBs. The basalts can be chemically divided into two groups: an Fe-poor group (IPG) and an Fe-rich group (IRG). The compositional variation of IPG basalts is essentially controlled by the partial melting of the source as suggested by the following: (i) bulk rock MgO, FeO and NiO compositions indicate that some IPG samples were equilibrated with mantle olivine; and (ii) correlations between Al₂O₃, CaO and MgO are consistent with those of experimental partial melts of peridotites. The inconsistent behaviors of the elements compatible with clinopyroxene (Cpx), such as V (Sc and Cu), preclude the significant role of the fractional crystallization of Cpx and spinel in IPG variation. IPG basalts have low Al and high Fe concentrations compared to the products of melting experiments involving peridotites and pyroxenites, suggesting that the IPG source would have a lithology and bulk rock composition different from those of typical peridotites and pyroxenites. IRG basalts have negative correlations between Fe₂O₃* and MgO, and between V and Fe₂O₃*/MgO, indicating that IRG basalts would have fractionated Cpx. However, the anomalously Fe-rich feature of IRG basalts compared with NWKBs collected from other areas suggests that the role of Cpx fractionation in NWKBs is minor. Relatively low melting temperatures would have principally caused the large chemical variation of NWKBs.