Geochemical and mineralogical evidence for the occurrence of at least three distinct magma types in the ‘famous’ region

Bulk rock major and trace element variations in selected basalts from the Famous area, in conjunction with a detailed study of the chemical compositions of phenocryst minerals and associated melt inclusions are used to place constraints on the genetic relationship among the various lava types. The distribution of NiO in olivine and Cr-spinel phenocrysts distinguishes the picritic basalts, plagioclase phyric basalts and plagioclase-pyroxene basalts from the olivine basalts. For a given Mg/Mg+Fe²⁺ atomic ratio of the mineral, the NiO content of these phenocrysts in the former three basalt types is low relative to that in the phenocrysts in the olivine basalts. The Zr/Nb ratio of the lavas similarly distinguishes the olivine basalts from the plagioclase phyric and plagioclase pyroxene basalts and, in addition, distinguishes the picritic basalts from the other basalt types. These differences indicate that the different magma groups could not have been processed through the same magma chamber, and preclude any direct inter-relationship via open or closed system fractional crystallization.The Fe-Mg partitioning between olivine and host rock suggests that the picritic basalts represent olivine (±Cr-spinel) enriched magmas, derived from a less MgO rich parental magma. The partitioning of Fe and Mg between olivine, Cr-spinel and coexisting liquid is used to predict a primary magma composition parental to the picritic basalts. This magma is characterized by relatively high MgO (12.3%) and CaO (12.6%) and low FeO^* (7.96%) and TiO₂ (0.63%).Least squares calculations indicate that the plagioclase phyric basalts are related to the plagioclase-pyroxene basalts by plagioclase and minor clinopyroxene and olivine accumulation. The compositional variations within the olivine basalts can be accounted for by fractionation of plagioclase, clinopyroxene and olivine in an open system, steady state, magma chamber in the average proportions 453223. It is suggested that the most primitive olivine basalts can be derived from a pristine mantle composition by approximately 17% equilibrium partial melting. Although distinguished by its higher Zr/Nb ratio and lower NiO content of phenocryst phases, the magma parental to the picritic basalts can be derived from a similar source composition by approximately 27% equilibrium partial melting. It is suggested that the parental magma to the plagioclase-pyroxene and plagioclase phyric basalts might have been derived from greater depth resulting in the fractionation of the Zr/Nb ratio by equilibration with residual garnet.C.O.B. Contribution No. 722     

An experimental investigation of Iceland and Reykjanes Ridge tholeiites: I. Phase relations

Tholeiite basalts from 60° N to 65° N on the Mid-Atlantic Ridge were melted and recrystallized at atmospheric pressure in a CO₂-H₂ gas mixture. Seven basalts are from the Langjokull-Thingvellir volcanic zone and the Reykjanes Peninsula of Iceland and nine are from the Reykjanes Ridge. The crystallization sequence in both Iceland and Reykjanes Ridge basalts with (Total Fe as FeO)/(Total Fe as FeO+ MgO) [F/F + M] less than 0.6 is olivine, plagioclase, clinopyroxene. Chromian spinel crystallizes before plagioclase in one Iceland and one Reykjanes Ridge basalt with F/F+M less than 0.57. Chemical differences of the two groups of basalts (lower SiO₂ and higher alkalis in Iceland basalts) can not simply be a result of low pressure fractional crystallization. Liquidus temperatures of the seven Iceland basalts decreases from 1,230° C to 1,170° C as the F/F+M of the rock increases from 0.52 to 0.70. The liquidus temperatures of the Reykjanes Ridge basalts are about 10° C lower than those of the Iceland basalts for the same F/F+M value. The profile of measured liquidus temperatures from 65° N on Iceland to 60° N on the Reykjanes Ridge has a minimum value at 63.2° N on the Reykjanes Ridge just south of Iceland. Model calculations of the pressure of phenocryst crystallization indicate that olivine and plagioclase in Langjokull basalts could have equilibrated between 2.0 and 6.2 kb (200 to 620 MPa). Phenocryst assemblages in Reykjanes Ridge basalts at 60° N could have crystallized together at greater than 2 kb (200 MPa) and probably less than 8 kb (800 MPa). A minimum in the equilibrium pressure of phenocryst crystallization occurs between 62.9° and 64° N and coincides with the minimum in the experimentally determined liquidus temperatures. The more extensive fractionation at low pressure in this area could be related to the shift of the Mid-Atlantic Ridge axis along the leaky transform fault from the Reykjanes Ridge to the Thingvellir volcanic zone.     

Experimental petrology of normal MORB near the Kane Fracture Zone: 22°–25° N,mid-Atlantic ridge

Melting experiments carried out at 1-atm and at 2 kbar on mid-ocean ridge basalts dredged from the mid-Atlantic ridge near the Kane Fracture Zone (KFZ, 22° to 25° N. latitude) provide a basis for evaluating the role of crystal fractionation in generating compositional variability observed in normal mid-ocean ridge basalt. The 1-atm olivine-plagioclase-clinopyroxene saturation boundary for KFZ lavas defines a path in mineral projection schemes and in oxide-oxide diagrams that is displaced from the same experimentally determined boundaries in FAMOUS (Grove and Bryan 1983) and Oceanographer Fracture Zone (Walker et al. 1979) basalts. The glass margins of sparsely phyric KFZ lavas record small amounts of near surface, low pressure fractional crystallization, and their glass and bulk rock compositions are similar. An important signature of low pressure differentiation is recorded in the quenched glass margins of moderately phyric KFZ lavas compared to their bulk rock compositions, and the glass has evolved along low-pressure fractionation paths that are similar to those produced in the 1-atm experiments. Many of the lavas have retained phenocrysts in equilibrium proportions, so that their bulk rock compositions represent liquid compositions. When the effects of near-surface differentiation and crystal accumulation are removed from the Kane data set, and only liquid compositions are considered, a suite of basalt magmas can be identified that forms a trend in mineral component projection schemes parallel to the 1-atm oliv-plag-cpx multiple saturation boundary, but displaced from it toward olivine. These basalts have only olivine and plagioclase as phenocrysts, and are well removed from clinopyroxene saturation at low pressure. The compositional variation can not be generated by mixing any primary liquid composition with a low pressure liquid that has evolved along the oliv-plag-cpx multiple saturation boundary. Major and trace element models of this trend using olivine, plagioclase and clinopyroxene as fractionating phases match the compositional variability. This compositional trend is generated by fractionation at pressures greater than 2 kbar, but within the plagioclase stability field. A review of the data for other normal MORB suites from this part of the mid-Atlantic ridge reveals a similar elevated pressure fractionation signature which persists when the effects of low pressure magma mixing are removed from the data set.     

Magma fractionation systems beneath the mid-Atlantic ridge at 36–37 ° N

Variation of major and trace elements in drilled basalts from the Mid-Atlantic Ridge (DSDP Leg 37) reflects distinct cycles of low pressure fractionation operating independently within a complex network of magma storage reservoirs beneath the crustal spreading axis. Low pressure phase relations are determined by parental magma composition, which varies from An-rich (An/Di > ca. 1.4) to Di-rich (An/Di < ca. 1.4). High An/Di magmas probably formed under slightly hydrous conditions in the mantle. They have low LIL element contents, low P/Y and high Mg/(Mg + Fe) ratios. Zr, P and Y abundance and inter-element ratios are highly diagnostic of primary magma type, and are used to quantify fractional crystallization models.Low pressure fractionation hypotheses were tested by least-squares modelling of whole-rock and phenocryst chemistry, which indicated removal or addition of phenocryst assemblages: ol; pl; ol + pl; ol + pl + cpx; pl + cpx, (± sp). Accumulation of plagioclase or olivine is an important mechanism for generating highly porphyritic rocks. A rare 3-phase (ol + pl + cpx) cumulate resulted from cotectic fractionation of a low An/Di magma type. Olivine and plagioclase cumulates appear to be related to high An/Di magmas. Olivine accumulation has been monitored by comparison of olivine/bulk rock partitioning of Fe and Mg to experimental measurements of the equilibrium K_D value. A single extensive sub-axial magma chamber could not account for the observed chemical variation and would probably be dynamically unstable.     

Residual glasses and melt inclusions in basalts from DSDP Legs 45 and 46: Evidence for magma mixing

Compositional relations among natural glasses in basalts recovered by Legs 45 and 46 (DSDP) provide powerful constraints on their differentiation histories. Residual glass compositions in the moderately evolved aphyric and abundantly phyric basalts within each site demonstrate that none of the units is mutually related to any other or to a common parent by simple fractional crystallization. At Site 396, where clinopyroxene phenocrysts are absent, progressively more evolved liquids (lower Mg/ (Mg+Fe) and higher TiO₂) are characterized by lower calcium-aluminum ratios, which can only be generated by clinopyroxene fractionation. This paradox is amplified by some melt inclusions in olivine phenocrysts that have higher CaO/Al₂O₃ and lower TiO₂ than any residual glasses. The occurrences of these distinctive compositions are correlated with the highly magnesian character of the host olivines (Fo_90–89), and the melts are interpreted as trapped primitive liquids, parental to the more fractionated derivatives.Melt inclusions intermediate in composition between the residual glasses and the most primitive olivine melt inclusions are present in the cores of some plagioclase phenocrysts that have had a history of resorption. On the basis of a petrographic and microprobe analysis of the zoning relations in these phenocrysts, the inclusions are inferred to be melts entrapped at the time of extensive corrosion of the host crystals.Interpreted in conjunction with other mineral and geochemical data, the compositional trends in the glasses indicate that magma mixing has played a major role in the genesis of the Leg 45 and 46 basalts. The reality of mixing is demonstrated by extensive disequilibrium textures in the plagioclase phenocrysts and the presence in evolved lavas of refractory plagioclase and olivine phenocrysts bearing primitive melt inclusions. The chemical imprint of clinopyroxene fractionation despite the absence of clinopyroxene phenocrysts is believed to be accomplished by plating of gabbro on to the upper walls of the subvolcanic magma chamber as it evolves between mixing events. Repeated influxes of primitive magma batches will move the resultant hybrids alway from clinopyroxene saturation and generate olivine-plagioclase cotectic magmas. This model provides a physical buffering mechanism that accounts for the volumetric dominance of moderately evolved basalts among ocean floor tholeiites. Major and trace element models based on the combination of mixing and fractional crystallization also explain heretofore enigmatic geochemical characteristics of MORB.Lunar and Planetary Institute Contribution no. 326After August 1, 1978: Department of Geological Sciences, Southern Methodist University, Dallas, TX 75275, USAThe Lunar and Planetary Institute is operated by the Universities Space Research Association under Contract No. NSR 09-051-001 with the National Aeronautics and Space Administration     

Geochemistry, Mineralogy and Magmatic Evolution of the Basaltic and Trachytic Lavas from Gough Island, South Atlantic

The Gough Island lavas range from picrite basalt through tosodalite-bearing aegirine-augite trachyte. The basaltic lavasare predominantly nepheline normative alkali basalts, althougha group of hypersthene normative tholeiitic basalts does occur.The oldest lavas on the island, represented by the Lower Basaltseries, are approximately 1?0 m.y. old and the youngest arethe Upper Basalts with an age of {small tilde} 0?13 m.y. Relatively coherent variations are described by the basalticand trachytic lavas with respect to both bulk rock major andtrace element geochemistry and mineral chemistry, and quantitativepetrogenetic modelling suggests that most of the variation canbe attributed to crystal fractionation/accumulation processesacting on a number of geochemically distinct parental magmas.The Upper Basalts and Lower Basalts have (within the limitsof sampling) a relatively restricted composition compared tothe Middle Basalt series lavas, with the latter ranging frompicrite basalt through to trachyandesite. The picrite basaltsand coarsely pyroxene-olivine phyric basalts represent partialcumulates with varying proportions (up to 40 wt. per cent) ofaccumulated olivine and clinopyroxene. In contrast, the moderatelyphyric and aphyric/finely porphyritic lavas represent the productsof crystal fractionation with the most evolved lavas havingexperienced at least 40 per cent fractional crystallizationof clinopyroxene, olivine, plagioclase and minor Fe-Ti oxidesand apatite. The detailed abundance variations in these lavasindicate that a number of parental magma compositions have fractionatedto produce the overall variations in basalt geochemistry, andsome of the magmas have interacted through mixing processes. The trachytic lavas show a large range in trace element abundance,but have only a limited major element variation. Most of thisvariation can be attributed to extensive (up to 70 per cent)fractional crystallization of predominantly alkali feldsparwith minor clinopyroxene, olivine, biotite, titano-magnetiteand apatite. A number of genetically distinct trachytes canbe recognized which are probably not related to each other byany simple fractional crystallization process. The compositionof the least evolved trachytes can be adequately accounted forby relatively extensive (up to 60 per cent) fractionation ofthe more evolved Middle Basalt series lavas. The trace element and isotopic characteristics of primitiveGough Island basalts support the concept that the source region(s)giving rise to these lavas is extremely enriched in highly incompatibleelements relative to primordial or ‘undepleted’mantle of bulk earth composition. It is unlikely that the lavashave sampled undepleted mantle as might be suggested by thesimilarity of the Sr and Nd isotopic ratios to ‘bulk earth’values. Rather, a model is favoured whereby the lavas are derivedfrom previously enriched sub-oceanic mantle which was subsequentlyinvaded and further enriched, at some time prior to partialmelting, by melts or fluids highly enriched in incompatibleelements. The enrichment could have occurred as veining by smalldegree partial melts or by infiltration of metasomatic fluids.     

Petrography and mineral chemistry of neovolcanics occurring between Pacific and Nazca Plate boundaries

Mid-Oceanic Ridge Basalt (MORB) samples collected from southern East Pacific Rise (SEPR) have been investigated. These highly phyric plagioclase basalts (HPPB) and moderately phyric plagioclase basalts (MOPB) show rare cumulate and vitrophyric textures with plagioclase (>10% as phenocryst) and abundant glass (>72%). Electron Probe Micro Analysis (EPMA) showed large compositional variations in the megacrysts as well as microcrysts of plagioclase (An₆₂ to An₈₂), olivine (Fo₇₈ to Fo₈₇), pyroxene (ferroaugite to augite) and iron oxides, mostly titaniferous magnetite. Olivine grains show high Mg# (>80%) and distinctly low in NiO (0.01–0.2%). Ferroan trevorite (NiO =16.22 and FeO_(t) =83.06) a characteristic meteoritic mineral has been identified from the olivine megacrysts of MORB, possibly attributed to Ni-enrichment, resulted from heterogeneity of the lower mantle. Wide range of An composition in plagioclase is indicative of large pressure range of crystal nucleation under decompression at a depth of ∼70 km (An₈₂) up to the ocean spreading centre. Absence of zoning observed in all the minerals present in the MORB samples, possibly attributed to unmixing and dominant fractionation process.     

Plagioclase zonation styles in hornblende gabbro inclusions from Little Glass Mountain,Medicine Lake volcano,California: implications for fractionation mechanisms and the formation of composition gaps

The rhyolite of Little Glass Mountain (73–74% SiO₂) is a single eruptive unit that contains inclusions of quenched andesite liquid (54–61% SiO₂) and partially crystalline cumulate hornblende gabbro (53–55% SiO₂). Based on previous studies, the quenched andesite inclusions and host rhyolite lava are related to one another through fractional crystallization and represent an example of a fractionation-generated composition gap. The hornblende gabbros represent the cumulate residue associated with the rhyolite-producing and composition gap-forming fractionation event. This study combines textural (Nomarski Differential Interference Contrast, NDIC, imaging), major element (An content) and trace element (Mg, Fe, Sr, K, Ti, Ba) data on the style of zonation of plagioclase crystals from representative andesite and gabbro inclusions, to assess the physical environment in which the fractionation event and composition gap formation took place. The andesite inclusions (54–61% SiO₂) are sparsely phyric with phenocrysts of plagioclase, augite and Fe-oxide±olivine, +/–orthopyroxene, +/–hornblende set within a glassy to crystalline matrix. The gabbro cumulates (53–55% SiO₂) consist of an interconnected framework of plagioclase, augite, olivine, orthopyroxene, hornblende and Fe-oxide along with highly vesicular interstitial glass (70–74% SiO₂). The gabbros record a two-stage crystallization history of plagioclase+olivine+augite (Stage I) followed by plagioclase+orthopyroxene+ hornblende+Fe-oxide (Stage II). Texturally, the plagioclase crystals in the andesite inclusions are characterized by complex, fine-scale oscillatory zonation and abundant dissolution surfaces. Compositionally (An content) the crystals are essentially unzoned from core-to-rim. These features indicate growth within a dynamic (convecting?), reservoir of andesite magma. In contrast, the plagioclase crystals in the gabbros are texturally smooth and featureless with strong normal zonation from An₇₄ at the core to around An₃₀. K, and Ba abundances increase and Mg abundances decrease steadily towards the rim. Ti, Fe, and Sr abundances increase and then decrease towards the rim. The trace element variations are fully consistent with the two-stage crystallization sequence inferred from the gabbro mineralogy. These results indicate progressive closed-system in situ crystallization in a quiescent magmatic boundary layer environment located along the margins of the andesite magma body. The fractional crystallization that generated the host rhyolite lava is one of inward solidification of a crystallizing boundary layer followed by melt extraction and accumulation of highly evolved interstitial liquid. This mechanism explains the formation of the composition gap between parental andesite and rhyolite magma compositions.     

The time scales of magma mixing and mingling involving primitive melts and melt–mush interaction at mid-ocean ridges

We have studied the chemical zoning of plagioclase phenocrysts from the slow-spreading Mid-Atlantic Ridge and the intermediate-spreading rate Costa Rica Rift to obtain the time scales of magmatic processes beneath these ridges. The anorthite content, Mg, and Sr in plagioclase phenocrysts from the Mid-Atlantic Ridge can be interpreted as recording initial crystallisation from a primitive magma (~11 wt% MgO) in an open system. This was followed by crystal accumulation in a mush zone and later entrainment of crystals into the erupted magma. The initial magma crystallised plagioclase more anorthitic than those in equilibrium with any erupted basalt. Evidence that the crystals accumulated in a mush zone comes from both: (1) plagioclase rims that were in equilibrium with a Sr-poor melt requiring extreme differentiation; and (2) different crystals found in the same thin section having different histories. Diffusion modelling shows that crystal residence times in the mush were <140 years, whereas the interval between mush disaggregation and eruption was ≤1.5 years. Zoning of anorthite content and Mg in plagioclase phenocrysts from the Costa Rica Rift show that they partially or completely equilibrated with a MgO-rich melt (>11 wt%). Partial equilibration in some crystals can be modelled as starting <1 year prior to eruption but for others longer times are required for complete equilibration. This variety of times is most readily explained if the mixing occurred in a mush zone. None of the plagioclase phenocrysts from the Costa Rica Rift that we studied have Mg contents in equilibrium with their host basalt even at their rims, requiring mixing into a much more evolved magma within days of eruption. In combination these observations suggest that at both intermediate- and slow-spreading ridges: (1) the chemical environment to which crystals are exposed changes on annual to decadal time scales; (2) plagioclase crystals record the existence of melts unlike those erupted; and (3) disaggregation of crystal mush zones appears to precede eruption, providing an efficient mechanism by which evolved interstitial melt can be mixed into erupted basalts.     

Petrology of middle proterozoic diabases and picrites from Lake Nipigon,Canada

Mafic rocks at Lake Nipigon provide a record of rift-related continental basaltic magmatism during the Keweenawan event at 1109 Ma. The mafic rocks consist of an early, volumetrically minor suite of picritic intrusions varying in composition from olivine gabbro to peridotite and a later suite of tholeiitic diabase dikes, sheets and sills. The diabase occurs primarily as two 150 to 200 m thick sills with a textural stratigraphy indicating that the sills represent single cooling units. Compositional variation in the sills indicates that they crystallized from several magma pulses.The diabases are similar in chemistry to olivine tholeiite flood basalts of the adjacent Keweenawan rift, particularly with respect to low TiO₂, K₂O and P₂O₅. The picrites have higher TiO₂, K₂O and P₂O₅ than the diabases and are similar to, but more primitive than, high Fe-Ti basalts which erupted early in the Keweenawan volcanic sequence.All of the rocks crystallized from fractionated liquids. The picrites are cumulate rocks derived at shallow crustal depths from a magma controlled predominantly by olivine fractionation. Picritic chills are in equilibrium with olivine phenocrysts of composition Fo₈₀ and are interpreted to represent the least evolved liquids observed. The parental magma of the picrites was probably Fe rich relative to the parental magma of the diabase. The diabase sills crystallized from an evolved basaltic liquid controlled by cotectic crystallization of plagioclase and lesser olivine and pyroxene.The emplacement of dense olivine phyric picritic magmas early in the sequence, followed by later voluminous compositionally evolved magmas of lower density suggests the development of a crustal density filter effect as the igneous event reached a peak. Delamination of the crust-mantle interface may have resulted in the transition from olivine controlled primitive magma to fractionated magma through the development of crustal underplating.     

Abyssal tholeiites from the Oceanographer Fracture Zone

Fresh basalts from the Oceanographer Fracture Zone are petrographically and chemically similar to typical abyssal tholeiites, but are somewhat enriched in large ion lithophile elements, with consistent differences among separate dredge hauls. Olivine compositions are in equilibrium with host basalt for reasonable K _D values, but some plagioclases are anomalously calcic (e.g., a rock highly differentiated in Mg/Mg+Fe bears some plagioclase of An₈₆). Ti/Al in clinopyroxene is approximately constant at 1/6, but Ti+Al abundance decreases in the sequence basalt groundmass cpx, basalt phenocryst+microphenocryst cpx, gabbro cpx (samples from adjacent dredges), an effect that may be related to decrease in cooling rate. Least-squares calculations indicate that 45% of magma with the composition of the more primitive sample must be removed as plagioclase, clinopyroxene and olivine (in the ratio 4.42.71, respectively) to obtain the composition of the more differentiated sample. Both samples have excess plagioclase on the liquidus, however, which should not be the case for the differentiated composition if it is produced by fractionation of all three phases. The excess of plagioclase and the anomalous plagioclase compositions indicate that the samples cannot be related solely by fractional crystallization. Additional processes such as magma mixing or plagioclase accumulation (or both) must have effected these differences.     

The Macquarie Island ophiolite complex: Mid-Tertiary oceanic lithosphere from a major ocean basin

The rocks of Macquarie Island are part of the mid-Tertiary oceanic lithosphere from a major ocean basin. They were probably created at the Indian—Australian—Pacific spreading ridge.The basalts and dolerites are usually porphyritic, carry plagioclase (An_87-80) as a dominant phenocryst phase with less abundant olivine (Fo_89-85), chrome spinel and rare clinopyroxene (Ca₄₅Mg₅₀Fe₅|Ca₃₈Mg₅₀Fe₁₂) phenocrysts. Normatively the rocks range from ne- to Q-bearing, with most falling near the critical plane of normative silica undersaturation. Dykes tend to be more Fe-rich than lavas, and to include the more di-poor rocks. The rocks also range compositionally from typical ocean floor basalts through to varieties relatively enriched in some incompatible trace elements, particularly Nb (20–60 ppm), that otherwise retain ocean-floor basalt phenocryst assemblages, major-element compositions and Ti, Ni, Cr and Zr contents. This enrichment, also characteristic of ocean-floor basalts from the “abnormal” ridge segments near 45° N and 36° N (FAMOUS area) on the Mid-Atlantic Ridge, causes the rocks to plot away from the ocean-floor basalt fields on popular trace-element diagrams intended to identify tectonic affinities of basalts.The upper parts of the Macquarie Island oceanic lithosphere section can be thought of as a vertical slice through a magma column, differentiating at shallow levels. The layered and massive gabbros that underlie the basalts and dolerites are composed essentially of olivine, plagioclase and clinopyroxene. Olivine and plagioclase are cumulate phases in the layered rocks, clinopyroxene is postcumulus. Mineral compositions of the gabbros, particularly those of the layered rocks, are closely resembled by phenocryst compositions in the basalts and dolerites. Plagiogranites and trondheimites are unknown from the island, and norites very rare. Thus, Macquarie Island basalts, dolerites and gabbros form a distinctive igneous association that ought to make Macquarie Island-type ophiolite complexes from major ocean basins an easily recognized ophiolite type in continental orogenic terranes, even when dismembered.     

Chemistry and distribution pattern of recent basaltic rocks in Iceland

A survey of Recent basaltic rocks in Iceland is presented. The basalts are classified into three groups: tholeiites, transitional alkali basalts and alkali olivine basalts. The basalts can be divided into petrological regions where the composition of lavas seem to have been fairly constant throughout postglacial and possibly late-Pleistocene time. The tholeiites delineate the crest region of the Mid-Atlantic Ridge as it transects Iceland, and the mildly alkali olivine basalts and the transitional alkali basalts characterize the flank volcanic zones. Tholeiitic and alkalic diffrentiated rocks appear to have a distribution in accordance with the basalt distribution pattern. There is some correlation between the chemistry of the zones and the crustal structure of Iceland. Areal discharge of volcanic rocks varies consistently between the petrological regions being highest in the tholeiite regions. The total output of volcanic rocks along the Mid-Atlantic Ridge in the Iceland area reaches maximum in middle Iceland.     

Crustal contamination of Late Neogene basalts in the Dien Bien Phu Basin,NW Vietnam: Some insights from petrological and geochronological studies

Early Pliocene (Zanclean) basalts in the Dien Bien Phu pull-apart basin in NW Vietnam, associated with the presently sinistral Dien Bien Phu Fault Zone, have been dated by the K–Ar method at 4.4–4.9 and 5.4–5.2 Ma. Rapid migration of basaltic magma to the surface in the Dien Bien Phu Fault Zone may be due to Pliocene transtension of the crust in this region, resulting from asthenospheric upwelling induced by lateral displacement of the mantle. The basalts are moderately phyric ( < 10%) and consist of olivine (hyalosiderite), plagioclase (bytownite–labradorite) and orthopyroxene (bytownite–labradorite) phenocrysts, and a fine-grained crystalline matrix (olivine–hortonolite, plagioclase–labradorite, clinopyroxene–pigeonite and augite, K-feldspar). The presence of Fe-rich olivine and orthopyroxene phenocrysts indicates that the basalts are SiO₂-saturated/oversaturated olivine tholeiites which formed under water-undersaturated conditions. The Dien Bien Phu basalts contain both mantle-derived (pyroxenites, dunites, gabbros) and crustal (sillimanite/mullite + Mg–Fe spinel), wallrock xenoliths, indicative of crustal contamination during the ascent of the basaltic magma. The basalts show selective enrichment in some mobile elements (K, Rb, Sr and Th), a feature considered to be a result of metasomatism. These rocks, classified on the basis of their normative composition as quartz tholeiites, could represent primary olivine tholeiites/basalts, in which the geochemical signatures were modified by the processes of contamination.     

Volcanic rocks and processes of the Mid-Atlantic Ridge rift valley near 36 ° 49′ N

Eighty samples of submarine basaltic lava were sampled from an 8 km segment of the floor and walls of the inner rift valley of the Mid-Atlantic Ridge during the French American Mid-Ocean Undersea Study (project Famous). The samples were collected from outcrops and talus slopes by the three submersibles: Alvin, Archimede, and Cyana at water depths of about 2600 meters.The early formed mineral content of the pillow lavas' glassy margins enables classification of the rocks into 5 types: (1) olivine basalt, (2) picritic basalt, (3) plagioclase-olivine-pyroxene basalt, (4) aphyric basalt, and (5) plagioclase-rich basalt. Chemical and mineralogical study indicates that at least 4 types are directly interrelated and that types (1) and (2) are higher-temperature, primitive lavas, and types (3) and (4) are lower-temperature, differentiated lavas derived from the primitive ones by crystal-liquid differentiation. The plagioclase-rich basalts also have a chemical composition of their glass comparable to that of the most differentiated basalts (types 3 and 4) but they differ in their greater amount of early formed plagioclase (12–35%).In general, the mineralogical variation across the rift valley shows an assymetrical distribution of the major basalt types. Despite the mineralogical diversity of the early formed crystals, the chemistry of the basalt glasses indicates a symmetrical and a gradual compositional change across the rift valley. Based primarily on their chemistry, the rock types 1 and 2 occupy an axial zone 1.1 km wide and make up the central volcanic hills. Differentiated lavas (types 3, 4) occupy the margins and walls of the inner rift valley and also occur near the center of the rift valley between the central hills.FeO/MgO ratios of olivine and coexisting melt indicate that the average temperature of eruption was 40 ° C higher for the primitive melts (types 1 and 2). Aside from major elements trends, the higher temperature character of the primitive basalts is shown by their common content of chrome spinel.The thickness of manganese oxide and palagonite on glassy lava provide an estimate of age. In a general fashion the relative age of the various volcanic events follow the compositional zoning observed in the explored area. Most of the youngest samples are olivine basalt of the axial hills. Most older samples occur in the margins of the rift valley (West and N.E. part of explored area) but are significantly younger than the spreading age of the crust on which they are erupted. Intermediate lava types occur mainly east of the rift valley axis and in other areas where plagioclase—olivine—pyroxene basalt and aphyric basalt are present.The above relations indicate that the diverse lava types were erupted from a shallow, zoned magma chamber from fissures distributed over the width of the inner rift valley and elongate parallel to it. Differentiation was accomplished by cooling and crystallization of plagioclase, olivine, and clinopyroxene toward the margins of the chamber. The centrally located hills were built by the piling up of frequent eruption of mainly primitive lavas which also are the youngest flows. In contrast smaller and less frequent eruptions of more differentiated lavas were exposed on both sides of the rift valley axis.Contribution n ° 480 du Départment Scientifique, Centre Océanologique de Bretagne     

The influence of primary magma composition,H2O and pressure on mid-ocean ridge basalt differentiation

MORB suites display variations in their chemical differentiation trends which are closely related to the incompatible element enrichment of the basalts. We examine suites of primitive to evolved basalts from the Pacific-Nazca Ridge at 28° S (mostly depleted); from the Juan Fernandez microplate region (depleted) and from the Explorer Ridge, northeast Pacific (mostly enriched). Trends for incompatible element enriched MORBs consistently show less depletion of Al₂O₃ and less enrichment of FeO when plotted on MgO variation diagrams.Least squares modeling indicates that enriched basalts have undergone less plagioclase crystallization than depleted basalts especially in the early stages of differentiation. Using thermodynamic modelling, we show that variations between MORB differentiation trends result largely from differences in the major element chemistry and H₂O content of primary magmas. Our chosen enriched and depleted near-primary magmas are similar in major element chemistry but the enriched near-primary magma has higher H₂O and lower Al₂O₃ than the depleted near-primary magma. The MORB crystallization sequence is: olivineolivine+plagioclase olivine+plagioclase+high-Ca pyroxene; and the separate and combined effects of lower Al₂O₃ and higher H₂O are to cause plagioclase to crystallize later (lower temperature), and to make the interval of olivine+plagioclase crystallization shorter. As a result, enriched differentiates have higher Al₂O₃ and lower FeO than depleted MORBs at a given MgO content, even though their parents' Al₂O₃ is lower. Crystallization of enriched basalts at higher pressure than depleted basalts is not able to account for differences between the differentiation trends because the proportion of plagioclase is higher during three-phase crystallization at high pressure.The variations in trends do not depend on geographic location and thus are superimposed on any regional variations in MORB chemistry or mantle source. Nor are they related to spreading rate. Depleted basalts from the fast-spreading 28° S and Juan Fernandez ridges have differentiation trends similar to depleted basalts from the medium-spreading Galapagos Spreading Center, whereas differentiation trends for enriched basalts from the medium-spreading Explorer Ridge are quite different. Fe³⁺/Fe_total is similar (and quite low) for enriched and depleted basalts, indicating that neither oxidation state nor early magnetite crystallization are important.     

Petrogenesis of Cenozoic Basaltic Rocks from Jiangsu Province,China:Evidence from Geochemical Constraints

Cenozoic（Miocene to Pleistocene） basaltic rocks in Jiangsu province of eastern China include olivine tholeiite and alkali basalt.We present major,trace element and Sr-Nd isotopic data as well as Ar-Ar dating of these basalts to discuss the petrogenesis of the basalts and identify the geological processes beneath the study area.On the basis of chemical compisitions and Ar-Ar dating of Cenonoic basaltic rocks from Jiangsu province,we suggest that these basalts may belong to the same magmatic system.The alkali basalts found in Jiangsu province have higherΣFeO,MgO,CaO,Na₂O, TiO₂ and P₂O₅ and incompatible elements,but lower Al₂O₃ and compatible elements contents than olivine tholeiite which may be caused by fractional crystallization of olivine,pyroxene and minor plagioclase.In Jiangsu basaltic rocks the incompatible elements increase with decreasing MgO/ΣFeO ratios.The primitive mantle-normalized incompatible elements and chondrite-normalized REE patterns of basaltic rocks found in Jiangsu province are similar to those of OIB.Partial loss of the mantle lithosphere accompanied by rising of asthenospheric mantle may accelerate the generation of the basaltic magma.The ¹⁴³Nd/¹⁴⁴Nd vs.⁸⁷Sr/⁸⁶Sr plot indicates a mixing of a depleted asthenospheric mantle source and an EMI component in the study area.According to Shaw’s equation,the basalts from Jiangsu province may be formed by l%-5%partial melting of a depleted asthenospheric mantle source.On the basis of Ar-Ar ages of this study and the fractional crystallization model proposed by Brooks and Nielsen（1982）,we suggest that basalts from Jiangsu province may belong to a magmatic system with JF-2 as the primitive magma which has undergone fractional crystallization and evolved progressively to produce other types of basalts.     

The importance of fractional crystallization and magma mixing in controlling chemical differentiation at Süphan stratovolcano,eastern Anatolia,Turkey

Süphan is a 4,050 m high Pleistocene-age stratovolcano in eastern Anatolia, Turkey, with eruptive products consisting of transitional calc-alkaline to mildly alkaline basalts through trachyandesites and trachytes to rhyolites. We investigate the relative contributions of fractional crystallization and magma mixing to compositional diversity at Süphan using a combination of petrology, geothermometry, and melt inclusion analysis. Although major element chemistry shows near-continuous variation from basalt to rhyolite, mineral chemistry and textures indicate that magma mixing played an important role. Intermediate magmas show a wide range of pyroxene, olivine, and plagioclase compositions that are intermediate between those of basalts and rhyolites. Mineral thermometry of the same rocks yields a range of temperatures bracketed by rhyolite (~750°C) and basalt (~1,100°C). The linear chemical trends shown for most major and trace elements are attributed to mixing processes, rather than to liquid lines of descent from a basaltic parent. In contrast, glassy melt inclusions, hosted by a wide range of phenocryst types, display curved trends for most major elements, suggestive of fractional crystallization. Comparison of these trends to experimental data from basalts and trachyandesites of similar composition to those at Süphan indicates that melt inclusions approximate true liquid lines of descent from a common hydrous parent at pressures of ~500 MPa. Thus, the erupted magmas are cogenetic, but were generated at depths below the shallow, pre-eruptive magma storage region. We infer that chemical differentiation of a mantle-derived basalt occurred in the mid- to lower crust beneath Süphan. A variety of more and less evolved melts with ≥55 wt% SiO₂ then ascended to shallow level where they interacted. The presence of glomerocrysts in many lavas suggests that cogenetic plutonic rocks were implicated in the interaction process. Blending of diverse, but cogenetic, minerals, and melts served to obscure the true liquid lines of descent in bulk rocks. The fact that chemical variation in melt inclusions preserves deep-seated chemical differentiation indicates that inclusions were trapped in phenocrysts prior to shallow-level blending. Groundmass glasses evolved after mixing and display trends that are distinct from those of melt inclusions.     

Textural and compositional evidence for magma mixing and its mechanism,Abu volcano group,southwestern Japan

Quaternary basalts, andesites and dacites from the Abu monogenetic volcano group, SW Japan, (composed of more than 40 monogenetic volcanoes) show two distinct chemical trends especially on the FeO^*/MgO vs SiO₂ diagram. One trend is characterized by FeO^*/MgO-enrichment with a slight increase in SiO₂ content (Fe-type trend), whereas the other shows a marked SiO₂-enrichment with relatively constant FeO^*/MgO ratios (Si-type trend). The Fe-type trend is explained by fractional crystallization with subtraction of olivine and augite from a primitive alkali basalt magma. Rocks of the Si-type trend are characterized by partially melted or resorbed quartz and sodic plagioclase phenocrysts and/or fine-grained basaltic inclusions. They are most likely products of mixing of a primitive alkali basalt magma containing olivine phenocrysts with a dacite magma containing quartz, sodic plagioclase and hornblende phenocrysts. Petrographic variation as well as chemical variation from basalt to dacite of the Si-type trend is accounted for by various mixing ratios of basalt and dacite magmas. Pargasitic hornblende and clinopyroxene phenocrysts in andesite and dacite may have crystallized from basaltic magma during magma mixing. Olivine and spinel, and quartz, sodic plagioclase and common hornblende had crystallized in basaltic and dacitic magmas, respectively, before the mixing. Within a lava flow, the abundance of basaltic inclusions decreases from the area near the eruptive vent towards the perimeter of the flow, and the number of resorbed phenocrysts varies inversely, suggesting zonation in the magma chamber.The mode of mixing changes depending on the mixing ratio. In the mafic mixture, basalt and dacite magmas can mix in the liquid state (liquid-liquid mixing). In the silicic mixture, on the other hand, the basalt magma was quenched and formed inclusions (liquid-solid mixing). During mixing, the disaggregated basalt magma and the host dacite magma soon reached thermal equilibrium. Compositional homogenization of the mixed magma can occur only when the equilibrium temperature is sufficiently above the solidus of the basalt magma. The Si-type trend is chemically and petrographically similar to the calc-alkalic trend. Therefore, a calc-alkalic trend which is distinguished from a fractional crystallization trend (e.g. Fe-type trend) may be a product of magma mixing.     

Systematics of modal phenocryst assemblages in submarine basalts: Petrologic implications

Phenocryst assemblages in ocean-ridge basalts generally show an increasing proportion of plagioclase as the total amount of phenocrysts increases. The variations in phase assemblages, as well as most crystal-liquid K_d's, are similar to variations (equimodal trends) predicted by low-pressure laboratory experiments, suggesting that many of these basalts have experienced varying degrees of low-pressure cyrstallization prior to quenching, with little sorting of crystals and liquid. Important exceptions include moderately to highly phyric basalts enriched either in plagioclase or olivine which lie well off the experimental trends. In these basalts, megacrysts and xenocrysts usually cited as evidence for magma mixing commonly represent a small proportion of the total crystalline phase assemblage. However, phase proportions for many of these basalts lie well outside the range that could be produced by simple mixing; selective gravitative sorting either prior or subsequent to mixing appears to be the likely explanation for these phyric basalts. A relation between spreading rate and phase proportions is neither supported nor refuted by the data, which as yet do not adequately represent fast-spreading ridges. Pyroxene-phyric varieties are especially common among LIL-element enriched (Group 2) basalts, and these basalts also show the greatest abundance of olivine-enriched (picritic) samples. Selective enrichment in plagioclase is more common among LIL-element depleted (Group 1) basalts, and pyroxene appears in Group 1 basalts only at relatively high degrees of crystallinity. These differences are consistent with expected compositional effects (including volatiles) on phase boundaries, as well as likely differences in depth (pressure) of mantle melting and magma fractionation. Sparsely to moderately phyric basalts tend to contain only olivine (±spinel) as phenocrysts, and lie in the olivine field in the projection from plagioclase in the CMAS tetrahedron. This is consistent with the concept that these magmas approach low-pressure equilibrium by olivine fractionation from a more picritic parent. The origin of these basalts, and relationships between them, remains an important fundamental problem. Phenocryst phase assemblages are consistent with the low-pressure phase saturation indicated by the projected positions of the associated glasses in CMAS. It is suggested that, in contrast to the classical practice of classifying basalts according to phase proportions, a classification based on presence and/or first appearance of each crystalline phase is both practical and petrogenetically significant for water-quenched submarine basalts.