Petrological feature of spinel lherzolite xenolith from Oki-Dogo Island: An implication for variety of the upper mantle peridotite beneath southwestern Japan

Abstract   Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo₈₆) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism.     

Garnet clinopyroxenite xenolith from Dish Hill,California

A single garnet clinopyroxenite xenolith found at the Dish Hill basanite cone near Ludlow, California, has well developed unmixing and reaction textures like those found in garnet pyroxenite inclusions in Hawaiian, African and Australian basalts and like those of pyroxenites in some European alpine peridotites. Reconstructed pyroxene compositions suggest that before unmixing the rock consisted of clinopyroxene and about 10% garnet plus spinel, but all of the garnet may have been dissolved in clinopyroxene. Most or all of the garnet formed by exsolution from clinopyroxene and by reaction between clinopyroxene and spinel in an open system. Following exsolution, the rock was deformed and partly recrystallized in the solid state. Similarity of compositions of exsolved and recrystallized minerals suggests recrystallization at P-T conditions similar to those of exsolution.The rock is not the chemical equivalent of the host basanite and cannot represent magma of basanitic composition crystallized in the mantle. Its history of deformation and recrystallization, like that of accompanying spinel lherzolite inclusions, supports the idea that the garnet clinopyroxenite is an accidental inclusion derived from the upper mantle.     

Origins of the mafic and ultramafic rocks in the Ronda peridotite

The Ronda peridotite massif in southern Spain originated from the upper mantle, evidently as a rapidly rising diapir. Major and trace element abundance trends of the peridotites reflect their origin as residues from partial melting of garnet lherzolite. About 5% of the massif consists of mafic rocks, mainly pyroxenites and gabbros. They occur as concordant layers amidst the peridotites, and these layers do not cross-cut each other. However, major and trace element data show that the mafic layers do not have the geochemical characteristics of primary melts. We conclude that crystal/liquid fractionation occurred at high pressures ( > 19 kbar) as melts migrated through magma conduits towards the cooler exterior portion of the diapir. This process generated a sequence of “cumulates” (mainly clinopyroxene + orthopyroxene + spinel and clinopyroxene + garnet) along the walls of the conduits which are now represented by the mafic layers.     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

Complete mantle section of a slow-spreading ridge-derived ophiolite: An example from the Isabela ophiolite in the Philippines

Abstract   The Isabela ophiolite shows a complete ophiolite sequence exposed along the eastern coast of northern Luzon, the Philippines. It forms the Cretaceous basement complex for the northeastern Luzon block. This ophiolite is located at the northern end of a trail of ophiolites and ophiolitic bodies along the eastern margin of the Philippine Mobile Belt. This paper presents new findings regarding the nature and characteristics of the Isabela ophiolite. Peridotites from the Isabela ophiolite are relatively fresh and are composed of spinel lherzolites, clinopyroxene-rich harzburgites, depleted harzburgites and dunites. The modal composition, especially the pyroxene content, defines a northward depletion trend from fertile lherzolite to clinopyroxene-rich harzburgites and more refractory harzburgites. Variation in modal composition is accompanied by petrographic textural variations. The chromium number of spinel, an indicator of the degree of partial melting, concurs with petrographic observations. Furthermore, the Isabela ophiolite peridotites are similar in spinel and olivine major-element geochemistry and clinopyroxene rare earth-element composition to abyssal peridotites from modern mid-oceanic ridges. Petrological and mineral compositions suggest that the Isabela ophiolite is a transitional ophiolite subtype, with the fertile lherzolites representing lower sections of the mantle column that are usually absent in most ophiolitic massifs. The occurrence of the fertile peridotite presents a rare opportunity to document the lower sections of the ophiolitic mantle. The variability in composition of the peridotites in one continuous mantle section may also represent a good analogy of the melting column in the present-day mid-oceanic ridges.     

Subduction of mantle wedge peridotites: Evidence from the Higashi-akaishi ultramafic body in the Sanbagawa metamorphic belt

The Higashi-akaishi garnet-bearing ultramafic body in the Sanbagawa metamorphic belt, Southwest Japan, represents a rare example of oceanic-type ultrahigh-pressure metamorphism. The body of 2 km × 5 km is composed mostly of anhydrous dunite with volumetrically minor lenses of clinopyroxene-rich rocks. Dunite samples contain high Ir-type platinum group elements (PGE) and Cr in bulk rocks, high Mg and Ni in olivine, and high Cr in spinel. On the other hand, clinopyroxene-rich rocks contain low concentrations of Ir-type PGE and Cr, high concentrations of fluid-mobile elements in bulk rocks, and low Ni and Mg in olivine. Clinopyroxene is diopsidic with low Al₂O₃. The compositions of bulk rocks and mineral chemistry of spinel, olivine, and clinopyroxene suggest that the olivine-dominated rocks are residual mantle peridotites after high degrees of influx partial melting, and that the clinopyroxene-rich rocks are cumulates of subduction-related melts. Thus, the Higashi-akaishi ultramafic body originated from the interior of the mantle wedge, most likely the forearc upper mantle. It was then incorporated into the Sanbagawa subduction channel by a mantle flow, and underwent high pressure metamorphism to a depth greater than 100 km. Such a strong active flow in the mantle wedge is likely facilitated by the lack of serpentinites along the interface between the slab and the overlying mantle, as it was too hot for serpentine. These unusually hot conditions and strong active mantle flow may reflect conditions in the earliest stage of development of subduction, and may have been maintained by massive upwelling and subsequent eastward flow of asthenospheric mantle in the northeastern Asian continent in Cretaceous time when the Sanbagawa belt began to form.     

Silicate‐oxide mineral chemistry of mafic–ultramafic rocks as an indicator of the roots of an island arc: The Chilas Complex,Kohistan (Pakistan)

The Chilas Complex is a major lower crustal component of the Cretaceous Kohistan island arc and one of the largest exposed slices of arc magma chamber in the world. Covering more than 8000 km², it reaches a current tectonic width of around 40 km. It was emplaced at 85 Ma during rifting of the arc soon after the collision of the arc with the Karakoram plate. Over 85% of the Complex comprises homogeneous, olivine‐free gabbronorite and subordinate orthopyroxene–quartz diorite association (MGNA), which contains bodies of up to 30 km² of ultramafic–mafic–anorthositic association (UMAA) rocks. Primary cumulate textures, igneous layering, and sedimentary structures are well preserved in layered parts of the UMAA in spite of pervasive granulite facies metamorphism. Mineral analyses show that the UMAA is characterized by more magnesian and more aluminous pyroxene and more calcic plagioclase than those in the MGNA. High modal abundances of orthopyroxene, magnetite and ilmenite (in MGNA), general Mg–Fe–Al spatial variations, and an MFA plot of whole‐rock analyses suggest a calc‐alkaline origin for the Complex. Projection of the pyroxene compositions on the Wo–En–Fs face is akin to those of pyroxenes from island arcs gabbros. The presence of highly calcic plagioclase and hornblende in UMAA is indicative of hydrous parental arc magma. The complex may be a product of two‐stage partial melting of a rising mantle diaper. The MGNA rocks represent the earlier phase melting, whereas the UMAA magma resulted from the melting of the same source depleted by the extraction of the earlier melt phase. Some of the massive peridotites in the UMAA may either be cumulates or represent metasomatized and remobilized upper mantle. The Chilas Complex shows similarities with many other (supra)subduction‐related mafic–ultramafic complexes worldwide.     

Chromian spinel lamellae in olivine from the Iwanai-dake peridotite mass,Hokkaido, Japan

Lamellar inclusions of chromian spinel (Cr/Cr + Al> 0.7), clinopyroxene and chromian spinel-clinopyroxene symplectite occur in olivines from alpine-type peridotites which have equilibrated at relatively low temperature (<700°C). They occur most commonly in dunite with very magnesian olivine (Fo₉₃ to Fo₉₅) and discrete grains of Cr-rich spinel. Olivine which initially equilibrated with magnesian and Cr-rich liquid had contained small amounts of calcium and trivalent chromium in the octahedral site, and lamellar chromian spinel and diopsidic clinopyroxene exsolved during the annealing process. The ordinary depletion of chromium or absence of chromian spinel lamellae in olivines in igneous rocks may be partly due to the effective exclusion of chromium from olivine upon cooling.     

Rare earth element geochemistry of garnet lherzolite and megacrystalline nodules from minette of the Colorado plateau province

Mineral and whole-rock REE abundances in garnet lherzolite and megacrystalline nodules from The Thumb display broad correlations with major element compositions. Lherzolites with > 12 modal % clinopyroxene plus garnet (“high-CaAl lherzolites”) have relatively flat chondrite-normalized whole-rock REE patterns. Lherzolites poor in clinopyroxene and garnet (“low-CaAl lherzolites”) have lower HREE in clinopyroxenes and garnets and higher whole-rock LREE/HREE. It is concluded that the low-CaAl lherzolites may have undergone LREE metasomatism after depletion of the major element compositions by partial melting and that much of the garnet now present was originally dissolved in aluminous orthopyroxene. The high-CaAl lherzolites may be interpreted either as primordial mantle samples or as products of equilibration with very LREE-enriched liquids. The “megacrystalline” nodules are medium- to ultracoarse-grained intergrowths and megacrysts with mineral compositions similar to discrete nodule suites in kimberlites. The REE abundances of the megacrystalline minerals are consistent with an origin as cumulates from magma with extremely fractionated REE, similar to minette or kimberlite.The patterns of correlation of REE and major elements in this inclusion suite are similar to the patterns observed in the garnet lherzolite and discrete nodule suites of southern African kimberlites. Both of the subcontinental mantle provinces represented by these suites contain three distinct petrogenetic components: refractory garnet lherzolite enriched in LREE and depleted in HREE, fertile garnet lherzolite with generally chondritic REE abundances, and a suite of ultracoarse minerals precipitated from magma with extremely fractionated REE generally similar to the host magmas.     

Geochemistry and petrogenesis of ultramafic and mafic plutonic rocks of the Dras ophiolitic melange, Indus suture (northwest Himalaya)

Geochemical data are presented for a suite of ultramafic and related rocks from the Dras ophiolitic melange of the Indus suture zone in the western Himalaya. Harzburgites from the suite have highly refractory chemistry. Lherzolites from the suite represent modified mantle material and are comparable to potential source rocks for MORB and to the lherzolites of the Bay of Islands ophiolites. Cumulus dunite, pyroxenite and gabbro units contain olivine, chromite, clinopyroxene and plagioclase as the major cumulus phases. Orthopyroxene is absent as a cumulus phase and in this respect the Dras ophiolite differs from the Marum, Betts Cove and Troodos ophiolites. However, the Dras cumulates are similar to the Vourinos and Bay of Islands cumulate sequence and are consistent with accumulation of low-pressure liquidus phases of mid-oceanic ridge-type magmas. Magmas parental to the Dras cumulate rocks contained high 100 Mg/(Mg + Fe²⁺) ratios of 77–79, high Ni, Cr and possibly Ca, low Ti and depleted LREE. Parent magmas were probably similar to those of normal MORB formed by two-stage (or dynamic) melting processes in the mantle. Peridotite fabrics suggest high-temperature plastic (mantle) deformation. Disruption, serpentinisation and melange formation were probably produced during emplacement in the Indus suture zone.     

Mare basalt petrogenesis in a dynamic moon

Previous hypotheses for mare basalt petrogenesis involving either the remelting or assimilation of 4.6-4.4-b.y. cumulates cannot satisfactorily account for certain key geochemical similarities between high-Ti and low-Ti primitive basalts, e.g. Mg/(Mg + Fe) ratios, Cr₂O₃ contents, eruption temperatures, and high-pressure liquidus phase relations. In addition, many thermal problems remain unanswered. A new petrogenetic hypothesis which appears to satisfy these constraints, is outlined below.The 4.6-4.4-b.y. melting event affected only the outer few hundred kilometers of the moon, leaving the undifferentiated primordial interior with its full complement of radiogenic elements. The differentiated lithosphere consisted of the crust and an underlying sequence of Mg-rich olivine + pyroxene cumulates and refractory residua. The late-stage differentiates were sandwiched between the crust and the cumulate sequence in large (perhaps 5–20 km diameter) segregations. The plagioclase-depleted late-stage residual system itself differentiated to form dense, Fe, Ti-rich, pyroxene + ilmenite±olivine cumulates, overlain by a complementary, solidified, residual liquid component, rich in incompatible elements. The dynamical consequence of this gravitationally unstable situation was the sinking of the dense (about 3.8 g/cm³) ilmenite-bearing cumulate pods into the lunar interior (density about 3.35 g/cm³). Mean-while the primordial mantle was approaching solidus temperatures due to radiogenic heating. The arrival of the sinking Fe, Ti-rich pods into this region initiated partial melting and complex assimilative interactions. High-Ti hybrid liquids were produced under equilibrium conditions, with olivine-pyroxenite remaining as the refractory residuum. Incompatible elements including Ti, U, and REE (depleted in Eu) derived from the sinking cumulates were strongly partitioned into the liquid, thereby accounting for the high TiO₂ contents, rare earth element characteristics, and two-stage isotopic record displayed by high-Ti mare basalts. Equilibrium between high-Ti hybrid liquids and the olivine-pyroxenite residuum was also responsible for controlling and buffering Mg/(Mg + Fe) and Cr distributions, thereby producing the relatively high Mg and Cr contents of primitive high-Ti magmas.By about 3.3 b.y., the primordial mantle immediately beneath the differentiated lithosphere had experienced partial melting due to radiogenic heating. Smaller and less-efficiently differentiated pods of 4.6-4.4-b.y. late-stage assemblages, sinking more slowly, contaminated the partially molten region and produced low-Ti hybrid liquids in equilibrium with residual olivine-pyroxenite. These hybrid magmas, although predominantly primordial in character, acquired incompatible-element characteristics from the sinking cumulates, and thereby obtained the Eu anomaly in their REE patterns, and their two-stage isotope record.The above model, invoking hybridization at depth accompanied by equilibrium between the hybrid liquids and the local olivine-pyroxenite residuum, accounts for the similar Mg/(Mg + Fe) ratios and Cr₂O₃ contents observed in primitive high-Ti and low-Ti basalts.     

Melting relations of a magnesian abyssal tholeiite and the origin of MORBs

Melting relations of a glassy magnesian olivine tholeiite from the FAMOUS area have been studied within the pressure range 1 atm to 15 kbar. From 1 atm to 10 kbar, olivine is the liquidus phase, followed by plagioclase and Ca-rich clinopyroxene. Above 10 kbar, Ca-rich clinopyroxene appears on the liquidus, followed by orthopyroxene and spinel. Near 10 kbar, olivine, orthopyroxene, clinopyroxene, spinel and plagioclase crystallize within 10°C of the liquidus. This indicates that a liquid of this magnesian olivine tholeiite composition could coexist with mantle peridotite at about 10 kbar. This result is in agreement with the geochemistry of Ni; the Ni concentration of the studied sample corresponds to the theoretical concentration in a primary magma [14,15].These data suggest that at least some magnesian mid-oceanic ridge basalts (MORBs) could be primary melts segregated from the mantle at depths near the transition zone between plagioclase lherzolite and spinel lherzolite (about 10 kbar). Based on this model, the residual mantle after extraction of MORBs should be lherzolite, not harzburgite.High-pressure (7–10 kbar) fractionation models involving olivine, plagioclase and clinopyroxene, which have been proposed by several workers (e.g. [36]) to explain the varieties of MORBs, were re-emphasized based on this melting study. The rare occurrence of clinopyroxene as a phenocryst phase in MORBs is explained by precipitation in a magma chamber at high pressure, or by dissolution of clinopyroxene formed earlier at high pressure.     

F-phlogopites in the Alban Hills Volcanic District (Central Italy): indications regarding the role of volatiles in magmatic crystallisation

A systematic analysis of micas contained in effusive, pyroclastic and hypabyssal rocks of the Alban Hills Volcanic District (AHVD) (Central Italy) was made in order to characterise minerals of pyroclastic units for tephrostratigraphy and to obtain as much information as possible on the activity of volatiles in this magmatic system. The phlogopite shows a large range of F contents (between 0.50 and 7.50 wt%) that make it possible to discriminate different AHVD lithologies; in particular, micas of lava groundmass are characterised by extremely high F (up to 7.50 wt%) and Ba (up to 9.70 wt%) contents, seldom or never found in other magmatic ultrapotassic rocks. Moreover, the micas of pyroclastics, ultramafic cumulates and holocrystalline inclusions made up of leucite, clinopyroxene and phlogopite (hereafter italites) show Mg/(Mg+Fe) values between 0.65 and 0.90 that are not correlated with F contents. The variations in F contents observed in the AHVD micas do not appear to be due to a “temperature” effect or pressure changes, but they may be due to variations in the H₂O and CO₂ activities in the magma chamber. They make it possible to differentiate three crystallisation environments in the AHVD magmatic system. The first one had elevated CO₂ activity and formed the italites near the carbonate contact; these rocks represent, at least those enriched in clinopyroxene without skarn-minerals, the hypabyssal crystallisation of the AHVD magmas at the periphery of magma chamber. The second one, characterised by a higher water activity, is represented by the micas of the ultramafic cumulates and pyroclastic scorias, and is located in the inner part of magma chamber. The third environment, the groundmass of the lavas, it is not related with the previous ones and is characterised by the absence of water and by a high F activity. In general, our results suggest that the compositional variations observed in the micas (Al, Si, Ti, Ba) reflect different H₂O activities (inversely correlated with F activity) in the magma chamber.     

Melt–wall rock interaction in the mantle shown by silicate melt inclusions in peridotite xenoliths from the central Pannonian Basin (western Hungary)

In this paper we present a detailed textural and geochemical study of two equigranular textured amphibole-bearing spinel lherzolite xenoliths from Szigliget, Bakony–Balaton Highland Volcanic Field (BBHVF, western Hungary) containing abundant primary silicate melt inclusions (SMIs) in clinopyroxene rims and secondary SMIs in orthopyroxene (and rarely spinel) along healed fractures. The SMIs are dominantly composed of silicate glass and CO₂-rich bubbles. Clinopyroxene and orthopyroxene are zoned in both studied xenoliths, especially with respect to Fe, Mg, Na, and Al contents. Cores of clinopyroxenes in both xenoliths show trace element distribution close to primitive mantle. Rims of clinopyroxenes are enriched in Th, U, light rare earth elements (LREEs) and medium REEs (MREEs). Amphiboles in the Szg08 xenolith exhibit elevated Rb, Ba, Nb, Ta, LREE, and MREE contents. The composition of silicate glass in the SMIs covers a wide range from the basaltic trachyandesite and andesite to phonolitic compositions. The glasses are particularly rich in P₂O₅. Both primary and secondary SMIs are strongly enriched in incompatible trace elements (mostly U, Th, La, Zr) and display a slight negative Hf anomaly. The development of zoned pyroxenes, as well as the entrapment of primary SMIs in the clinopyroxene rims, happened after partial melting and subsequent crystallization of clinopyroxenes, most probably due to an interaction between hot volatile-bearing evolved melt and mantle wall-rocks. This silicate melt filled microfractures in orthopyroxenes (and rarely spinels) resulting in secondary SMIs.     

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.     

Low- and high-Ti ophiolites in Northern Pindos: Petrological and geological constraints

Ophiolites with different magmatic characteristics are closely associated in space with one another in northern Pindos. Some have affinities with ocean-floor magmas (Group I), and others represent melts which are frequently strongly depleted in «incompatible» elements (Group II). Group I is composed of cumulates, dolerites and lavas, whereas Group II occurs mainly as pillows and dykes, and postdates Group I. The two groups have different geochemical, mineralogical and petrographic features. They exhibit different Ti, Cr, Ni, Y, Zr, P, Si and Mg contents, and clinopyroxenes and spinels of Group I have higher Ti/Al and Ti/Mn ratios, and lower Cr/(Cr + Al) values respectively than those of Group II. Many rocks of Group II are chemically similar to boninites and associated rocks as well as to low-Ti basalts from other areas and ophiolitic complexes. It is concluded that geochemical and mineralogical data alone do not allow a definitive answer about the original tectonic setting of the investigated rocks, although a genesis above a subduction zone seems to be plausible hypothesis.     

Rare earth abundances in hornblende and clinopyroxene of a hornblende lherzolite xenolith: Implications for upper mantle fractionation processes

Hornblende and clinopyroxene of one of a suite of hornblende lherzolite xenoliths probably derived from the upper mantle are rich in light rare earths compared with clinopyroxenes from spinel lherzolite xenoliths. Partial melting of this hornblende lherzolite assemblage could yield a liquid with the rare earths, uranium and potassium abundances of a nephelinite.     

Petrology of ultramafic and mafic xenoliths in picrite of Kahoolawe Island,Hawaii

A picrite lava (22 wt% MgO; 35 vol.% ol) along the western shore of the1.3–1.4 Ma Kahoolawe tholeiitic shield, Hawaii, contains small xenoliths of harzburgite, lherzolite, norite, and wehrlite. The various rock types have textures where either orthopyroxene, clinopyroxene, or plagioclase is in a poikilitic relationship with olivine. The Mg#s of the olivine, orthopyroxene, and clinopyroxene in this xenolith suite range between 86 and 82; spinel Mg#s range from 60 to 49, and plagioclase is An_75–80. A ⁸⁷Sr/⁸⁶Sr ratio for one ol-norite xenolith is 0.70444. In comparison, the host picrite has olivine phenocrysts with an average Mg# of 86.2 (range 87.5–84.5), and a whole-rock ⁸⁷Sr/⁸⁶Sr ratio of 0.70426. Textural and isotopic information together with mineral compositions indicate that the xenoliths are related to Kahoolawe tholeiitic magmatism, but are not crystallization products of the magma represented by their host picrite. Rather, the xenoliths are crystalline products of earlier primitive liquids (FeO/MgO ranging 1 to 1.3) at 5–9 kbar in the cumulate environment of a magma reservoir or conduit system. The presence of ultramafic xenoliths in picrite but not in typical Kahoolawe tholeiitic lava (6–9 wt% MgO) is consistent with replenishment of reservoirs by dense Mg-rich magma emplaced beneath resident, less dense tholeiitic magma. Mg-rich magmas have proximity to reservoir cumulate zones and are therefore more likely than fractionated residual liquids to entrain fragments of cumulate rock.     

On the Magma Chambers beneath Klyuchevskoi Volcano,Kamchatka

Numerous summit and parasitic eruptions of moderate potassium magnesian and high-alumina basalts and basaltic andesites, their mineralogic and geochemical features, and the composition of in situ chilled melt inclusions in the olivine of cinder lapilli discharged by Klyuchevskoi Volcano all provide evidence of the presence of magma chambers beneath the volcano. This is also supported by a dualism in the variation of CaO and Al₂O₃ concentrations in olivine and clinopyroxene during crystallization. The mineralogic features in the high-alumina basalts that were discharged by all parasitic eruptions of Klyuchevskoi provide evidence of magnesian magma being emplaced from a deeper chamber into a shallow high-alumina chamber. The distribution of incoherent elements in the volcano’s magnesian and aluminiferous rocks shows that they came from a single mantle source. The geochemical and mineralogic data are in good agreement with the results of geophysical surveys that concern the structure and properties of the lithosphere beneath Klyuchevskoi.     

A combined rock magnetic and geochemical investigation of Upper Cretaceous volcanic rocks in the Pontides,Turkey

Upper Cretaceous volcanic rocks were collected at 24 sites along the Pontides, N-NE Turkey, for rock magnetic and geochemical studies. Rock magnetic and petrographic methods showed that the lavas are characterized predominantly by titanomagnetites with a mixture of pseudo-single and multi-domain grains, whereas in tephrite single domain titanohematite was dominant. Measurements of magnetic susceptibility and the geochemical properties on different volcanic rock types provide important knowledge about the magnetic stability of the rocks. The magnetic properties are interpreted in terms of the composition, concentration, magma generation. Tephrite and phonotephrites with the highest intensities (5200 mA/m) and high magnetic susceptibility values (2585 × 10⁻⁵), largest grain sizes and Fe/Ti values, showing minor or no alteration are the most magnetic stable samples in contrast to dacites with the lowest intensity-magnetic susceptibility (520 mA/m − 573 × 10⁻⁵) and high alteration degree. The basanite samples show very low NRM (48–165 mA/m) but very high magnetic susceptibility (2906–3100 × 10⁻⁵) values suggesting the alteration of Fe-Ti minerals. It is shown that the magnetic properties of the basic to acidic rocks show a systematic variation with magma differentiation and could be related to fractional crystallization. Major and trace elements revealed that the lavas are compatible with complex magma evolution, with mineral phases of olivine+magnetite+clinopyroxene in basic series, amphibole+ +clinopyroxene in intermediate rocks and plagioclase+clinopyroxene+biotite in acidic series.