Crystal fractionation of the basalt comendite series of the mount Edziza volcanic complex, British Columbia: Major and trace elements

The Mount Edziza Volcanic Complex in north-central British Columbia includes a group of overlapping basaltic shields, salic composite volcanoes, domes and small calderas that range in age from 7.5 Ma to less than 2000 years B.P. The volcanic assemblage is chemically bimodal, comprising voluminous alkali olivine basalt and hawaiite, a salic suite of mainly peralkaline trachyte and comendite, plus a relatively small volume of intermediate rocks (trachybasalt, tristanite, mugearite, benmoreite). The complex is the product of five cycles of magmatic activity, each of which began with alkali olivine basalt and culminated with the eruption of salic magma. The regular chemical variation shown by almost 100 major- and trace-element analyses suggests a genetic lineage between the basic and salic members of each cycle. Least-squares mathematical modelling, indicates that the salic rocks (trachyte and comendite) have formed by fractionation of observed phenocryst and cumulate nodule mineral phases from a common alkali olivine basalt parent magma.Hawaiite is thought to be a cumulate rock, formed by partial fractionation and feldspar accumulation within rising columns of primary alkali olivine basalt. Fractionation leading from alkali olivine basalt through trachybasalt and trachyte to comendite is believed to have taken place where primary basalt became trapped in large crustal reservoirs. The early removal of olivine, clinopyroxene and plagioclase, leading to a trachytic residuum, and subsequent fractionation of mainly alkali feldspar, leading to the peralkaline end members, is consistent with major- and trace-element variation and with isotopic and REE data.The chemical diversity of the complex is attributed to its location over a zone of crustal extension where mantle-derived basalt, trapped in large high-level reservoirs, underwent prolonged fractionation.     

Inversion of titanomaghemite in oceanic basalt during heating

We studied the change of magnetic behaviour upon laboratory heating of altered mid-ocean ridge basalt (MORB) samples in the age range of 16-35 Ma to determine the influence of titanomaghemite inversion on the thermal demagnetisation of natural remanent magnetisation (NRM) of these basalts. MORB samples were heated to successively higher temperatures and at the same time the temperature dependence of either saturation magnetisation or NRM was monitored continuously. After each heating step, hysteresis loops and remanent magnetisation curves between 10 K and room temperature were measured. With this procedure, it is shown that the dominant magnetic remanence carrier in our MORB samples is cation deficient titanomaghemite. Moreover, it is demonstrated that the titanomaghemite is gradually changing to a Ti-poor titanomagnetite as the final inversion product. During inversion, both the Curie temperature as well as the maximum unblocking temperature of the NRM are gradually increasing. We show that the paradox of unblocking temperatures above the Curie temperatures often observed for altered MORBs is an artefact of this gradual, heating induced inversion process.     

Analysis of the natural remanent magnetization of rocks by measuring the efficiency ratio through alternating field demagnetization spectra

The REM(AF) method is a new tool for the analysis of the origin and alternating field demagnetization coercivity spectra of the remanent magnetization. We applied this method on precambrian Gila diabase sheets from Arizona in order to identify the high coercivity magnetic carrier, and on artificially shocked Rowley Regis basalt from UK in order to analyze the effect of the shock on the natural remanent magnetization. In the Gila diabase the high coercivity magnetic component was identified to be most likely represented by the acicular magnetite (increase in the efficiency ratio in the high coercivity region). In the Rowley Regis basalt, the REM(AF) analysis revealed that comparing to NRM, the shock produced a different distribution of the AF demagnetization coercivity spectra due to the occurrence of the Shock Remanent Magnetization.     

A 3.5 Ga record of water-limited, acidic weathering conditions on Mars

The secondary mineral budget on Earth is dominated by clay minerals, Al-hydroxides, and Fe-oxides, which are formed under the moderate pH, high water-to-rock ratio conditions typical of Earth's near-surface environment. In contrast, geochemical analyses of rocks and soils from landed missions to Mars indicate that secondary mineralogy is dominated by Mg (± Fe, Ca)-sulfates and Fe-oxides. This discrepancy can be explained as resulting from differences in the chemical weathering environment of Earth and Mars. We suggest that chemical weathering processes on Mars are dominated by: (1) a low-pH, sulfuric acid-rich environment in which the stoichiometric dissolution of labile mineral phases such as olivine and apatite (± Fe–Ti oxides) is promoted; and (2) relatively low water-to-rock ratio, such that other silicate phases with slower dissolution rates (e.g., plagioclase, pyroxene) do not contribute substantially to the secondary mineral budget at the Martian surface. Under these conditions, Al-mobilization is limited, and the formation of significant Al-bearing secondary phases (e.g., clays, Al-hydroxides, Al-sulfates) is inhibited. The antiquity of rock samples analyzed in-situ on Mars suggest that water-limited acidic weathering conditions have more than likely been the defining characteristic of the Martian aqueous environment for billions of years.     

Magnetic parameters and variations in the composition of igneous rocks of the Franz Josef Land archipelago

A combined study of magnetic parameters of basalt and andesite samples is performed in the framework of geological investigations of the Franz Josef Land at the paleomagnetic laboratory of Munich University. The study included the determination of the coercivity, saturation magnetization, Curie points, natural remanent magnetization (NRM), and magnetic susceptibility and the examination of ferromagnetic minerals with a microscope. Data on the chemical composition of rocks are obtained for all samples, and radiological ages are determined for the majority of rocks.Thermomagnetic curves of samples are subdivided into four types depending on the composition of ferromagnetic NRM carriers.The data obtained point to multiple changes in the predominant composition of igneous rocks. Each stage of magmatism is characterized by a specific type of the ferromagnetic component in the rocks and, therefore, magnetomineralogical investigations can be used for differentiation and correlation of the igneous rocks.     

High-pressure inclusions in tholeiitic basalt and the range of lherzolite-bearing magmas in the Tasmanian volcanic province

Spinel-lherzolite xenoliths have been found in olivine tholeiite near Andover in the Tasmanian Tertiary volcanic province. They show a high-pressure mineralogy of predominant olivine (Mg₉₀), with aluminous enstatite (Mg₉₀) and lesser aluminous diopside and chrome-bearing spinel, and resemble lherzolite xenoliths commonly found in undersaturated lavas. Such xenoliths are unusual in tholeiitic basalts and the occurrence directly attests to a mantle origin for at least some tholeiitic magmas.The lherzolites are accompanied by doleritic and pyroxenitic xenoliths and by olivine, orthopyroxene, clinopyroxene and plagioclase xenocrysts. If near-liquidus phases are represented amongst the xenocrysts, then the magnesian number of the host basalt and its xenocryst assemblage provisionally suggest a magma derived by more than 15–20% partial melting of mantle peridotite, before commencing xenocryst crystallisation at pressures between 8–13 kbar.With this new record, lherzolite-bearing lavas in Tasmania now cover an extremely wide compositional range, extending from highly undersaturated olivine melilitite to olivine tholeiite. They also include a considerable number of fractionated alkaline rocks that are only sparsely reported in the literature as lherzolite hosts. This latter group contains representatives of a previously suggested but unestablished alkaline fractionation series based on olivine nephelinite, viz. calcic olivine nephelinite → sodic olivine nephelinite → potassi-sodic olivine nephelinite → mafic nepheline benmoreite → mafic phonolite.Lherzolite and megacryst-bearing lavas are relatively more abundant in peripheral parts to the main basalt sequences in Tasmania. This suggests that they developed in fringing zones of less intense mantle melting which enhanced stagnation and fractionation of magmas within the mantle before eruption. Calculated crustal thicknesses under these areas suggest that the magmas were generated at pressures exceeding 6–11 kbar, with the Andover tholeiitic magma exceeding 9 kbar.     

Magnetic anomalies and rock magnetism of basalts from Reykjanes (SW-Iceland)

This study presents rock magnetic properties along with magnetic field measurements of different stratigraphic and lithologic basalt units from Reykjanes, the southwestern promontory of the Reykjanes peninsula, where the submarine Reykjanes Ridge passes over into the rift zone of southwestern Iceland. The basaltic fissure eruptions and shield lava of tholeiitic composition (less than 11500 a old) show a high natural remanent magnetization (NRM, J_r) up to 33.6 A/m and high Koenigsberger ratio (Q) up to 52.2 indicating a clear dominance of the NRM compared to the induced part of the magnetization. Pillow basalts and picritic shield lava show distinctly lower J_r values below 10 A/m. Magnetic susceptibility (κ) ranges for all lithologies from 2.5 to 26×10⁻³ SI.     

Complete and partial self-reversal of natural remanent magnetization of basaltic rocks from Lower Silesia,Poland

Summary Experiments of heating-cooling cycles in zero magnetic field were performed in order to study self-reversal of NRM in basaltic rocks from Lower Silesia. Complete self-reversal occurred in one sample containing titanomagnetite withT _c of 170°C and a small amount of a phase with higher Curie point. During consecutive heat treatments the phenomenon became less conspicuous. In three samples of higher oxidation level, containing several magnetic phases, only partial self-reversal of NRM occurred. For the most oxidized sample no changes of direction of NRM were observed. We suggest that the investigated phenomenon of self-reversal of NRM is due to a negative magnetic interaction between primary titanomagnetite and products of its oxidation. It seems that complete self-reversal can take place in a restricted state of oxidation.     

Lateral variation of basalt magma type across continental margins and Island Arcs

Quaternary basalt magmas in the Circum-Pacific belt and island arcs and also in Indonesia change continuously from less alkalic and more siliceous type (tholeiite) on the oceanic side to more alkalic and less siliceous type (alkali olivine basalt) on the continental side. In the northeastern part of the Japanese Islands and in Kamchatka, zones of tholeiite, high-alumina basalt, and alkali olivine basalt are arranged parallel to the Pacific coast in the order just named, whereas in the southwestern part of the Japanese Islands, the Aleutian Islands, northwestern United States, New Zealand, and Indonesia, zones of high-alumina basalt and alkali olivine basalt are arranged parallel to the coast. In the Izu-Mariana, Kurile, South Sandwich and Tonga Islands, where deep oceans are present on both sides of the island arcs, only a zone of tholeiite is represented. Thus the lateral variation of magma type is characteristic of the transitional zone between the oceanic and continental structures. Because the variation is continuous, the physico-chemical process attending basalt magma production should also change continuously from the oceanic to continental mantle. Suggested explanations for the lateral variation assuming a homogeneous mantle are: 1) Close correspondence between the variations of depth of earthquake foci in the mantle and of basalt magma type in the Japanese Islands indicates that different magmas are produced at different depths where the earthquakes are generated by stress release: tholeiite at depths around 100 km, high-alumina basalt at depths around 200 km, and alkali olivine basalt at depths greater than 250 km. 2) Primary olivine tholeiite magma is produced at a uniform level of the mantle (100–150 km), and on the oceanic side of the continental margin, it leaves the source region immediately after its production and forms magma reservoirs at shallow depths, perhaps in the crust, where it undergoes fractionation to produce SiO₂-oversaturated tholeiite magma, whereas on the continental side, the primary magma forms reservoirs near the source region and stays there long enough to be fractionated to produce alkali olivine basalt magma, and in the intermediate zone, the primary magma forms reservoirs at intermediate depths where it is fractionated to produce high-alumina basalt magma.     

Relationship between the chemistry and axial dimensions of some shallow water pillow lavas of alkaline olivine basalt-and olivine tholeiitic composition

The axial ratio of basalt pillows in some shallow water pillow lava sequences from Azores and Iceland, is defined as V/H, where V and H represent the vertical and horizontal axes in cross section perpendicular to the elongate direction of undisturbed pillows. The axial ratios show a great spread of overlapping values for pillows from different sequences. However, alkaline olivine basaltic pillows tend to be more flattened than the olivine tholeiitic pillows. Another, and probably more discriminative feature between the two, is the difference in the maximum size of V and H of a pillow body. The limit for V and H for alkaline olivine basalt pillows is significantly lower than that of the olivine tholeiite pillows. A lower viscosity for alkaline olivine basalt than for olivine tholeiite probably accounts for the differences.     

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.     

Geobarometry of ultramafic xenoliths from Loihi Seamount,Hawaii, on the basis of CO2 inclusions in olivine

Abundant fluid inclusions in olivine of dunite xenoliths (～1–3 cm) in basalt dredged from the young Loihi Seamount, 30 km southeast of Hawaii, are evidence for three coexisting immiscible fluid phases—silicate melt (now glass), sulfide melt (now solid), and dense supercritical CO₂ (now liquid + gas)—during growth and later fracturing of some of these olivine crystals. Some olivine xenocrysts, probably from disaggregation of xenoliths, contain similar inclusions.Most of the inclusions (2–10 μm) are on secondary planes, trapped during healing of fractures after the original crystal growth. Some such planes end abruptly within single crystals and are termed pseudosecondary, because they formed during the growth of the host olivine crystals. The “vapor” bubble in a few large (20–60 μm), isolated, and hence primary, silicate melt inclusions is too large to be the result of simple differential shrinkage. Under correct viewing conditions, these bubbles are seen to consist of CO₂ liquid and gas, with an aggregate ? = ～ 0.5–0.75 g cm^?3, and represent trapped globules of dense supercritical CO₂ (i.e., incipient “vesiculation” at depth). Some spinel crystals enclosed within olivine have attached CO₂ blebs. Spherical sulfide blebs having widely variable volume ratios to CO₂ and silicate glass are found in both primary and pseudosecondary inclusions, demonstrating that an immiscible sulfide melt was also present.Assuming olivine growth at ～ 1200°C and hydrostatic pressure from a liquid lava column, extrapolation of CO₂P-V-T data indicates that the primary inclusions were trapped at ～ 220–470 MPa (2200–4700 bars), or ～ 8–17 km depth in basalt magma of ? = 2.7 g cm^?3. Because the temperature cannot change much during the rise to eruption, the range of CO₂ densities reveals the change in pressure from that during original olivine growth to later deformation and rise to eruption on the sea floor. The presence of numerous decrepitated inclusions indicates that the inclusion sample studied is biased by the loss of higher-density inclusions and suggests that some part of these olivine xenoliths formed at greater depths.     

Emplacement processes of proto-arc basalt in the Izu–Bonin–Mariana arc system

Ascertaining the emplacement mechanism of oceanic basaltic lavas is important in understanding how ocean floor topography is produced and oceanic plates evolve, particularly during the early stages of crustal development of a supra-subduction zone. A detailed study of the volcanic stratigraphy at International Ocean Discovery Program (IODP) Site U1438 in the Amami Sankaku Basin, west of the Kyushu–Palau Ridge, has revealed the development of lava accretion and ridge topography on the Philippine Sea plate at about 49 Ma. Igneous basement rocks penetrated at Site U1438 are the uppermost 150 m of ~6 km-thick oceanic crust, and comprise, in a downhole direction, sheet flows (12.6 m), lobate sheet flows (61.3 m), pillow lavas (50.7 m), and thin sheet flows (25.3 m). The lowermost sheet flows are intercalated with layers of limestone and epiclastic tuff. Lithofacies analysis reveals that the lowermost sheet flows, limestone, and tuff formed on an axial rise, the pillow lavas were emplaced on a ridge slope, and the lobate sheet flows formed off ridge on an abyssal plain. The lithofacies of the basement basalt corresponds to the upper portions of fast-spreading oceanic crust, suggesting that subduction initiation was associated with intermediate to fast rates of seafloor spreading. The surface sheet flows are olivine–clinopyroxene-phyric basalt and differ from the lower basalt flows that contain phenocrysts of olivine and plagioclase, with or without clinopyroxene. The depleted chrome-spinel composition and olivine–clinopyroxene phenocryst assemblage in the surface sheet flows suggests a slight contribution of water for magma generation not present for the lower basalt flows. Considering the lithological difference between the backarc and forearc oceanic crust in the Izu–Bonin–Mariana arc, with sheet flow dominant in the former, seafloor spreading occurred faster in the later stage of subduction initiation.     

Petrogenesis of basalts from the project FAMOUS area: experimental study from 0 to 15 kbars

Tholeiitic basalt glasses from the FAMOUS area of the Mid-Atlantic Ridge are among the most primitive basaltic liquids reported from the ocean basins. One of the more primitive of these[Mg/(Mg+Fe²⁺) = 0.68;Ni= 232ppm;TiO₂ = 0.61] glasses (572-1-1) was selected for an experimental investigation. This study found olivine to be the liquidus phase from 1 atm to 10.5 kbar where it is replaced by clinopyroxene. The sequence of appearance of phases at 1 atm pressure is olivine (1268°C), plagioclase (1235°C) and clinopyroxene (1135°C). The sample is multiply saturated at 10.5 kbar with olivine (Fo₈₈), clinopyroxene (Wo₃₂En₆₀Fs₉), and orthopyroxene (Wo₅En₈₃Fs₁₂). From the 1-atm data we have measured (FeO/MgO) olivine/(FeO*/MgO) liquid (K′_D) for olivine-melt pairs equilibrated at 12 temperatures in the range 1268–1205°C.K′_D varies from 0.30 at 1205°C to 0.27 at 1268°C. Analysis of high-pressure olivine melt pairs indicates a systematic increase inK′_D with pressure.Evaluation of the 1-atm experiments reveals that fractionation of olivine followed by olivine + plagioclase can generate much of the variation in major element chemistry observed in the FAMOUS basalt glasses. However, it cannot account for the entire spectrum of glass compositions — particularly with respect to TiO₂ and Na₂O. The variations in these components are such as to require different primary liquids.Comparison of clinopyroxene microphenocrysts/xenocrysts found in oceanic tholeiites with experimental clinopyroxenes reveal that the majority of those in the tholeiites may have crystallized from the magma at pressures greater than ～ 10 kbar and are not accidental xenocrysts. Clinopyroxene fractionation at high pressures may be a viable mechanism for fractionating basaltic magmas.The major and minor element mineral/meltK′_d's from our experiments have been used to model the source region residual mineralogy for given percentages of partial melting. These data suggest that ～20% partial melting of a lherzolite source containing 0–10% clinopyroxene can generate the major and minor element concentrations in the parental magmas of the Project FAMOUS basalt glasses.     

Origin of the magnetization of Permo-Carboniferous sediments of Spitsbergen, Svalbard Archipelago

Rock magnetic investigations of Permo-Carboniferous carbonate sediments from two areas on Spitsbergen are described, conducted to identify the carriers of the NRM in these rocks. Since microscopic and magnetic separation techniques could not profitably be applied, the nature of magnetic minerals was investigated by thermal demagnetization of the NRM and decay of saturation isothermal remanence (I_rs) during heating to 600°C, as well as by the distribution of the median destructive fields of the NRM and observation of magnetic susceptibility after subsequent heatings. The results show that the NRM of these limestones resides mainly in magnetite, but creation of magnetic pyrrhotite and of fresh magnetite is observed during heating to 600°C. Presence of sulphides indicates that magnetite is an oxidation product of pyrite or of non-magnetic pyrrhotite. Examination of rock magnetic properties of limestones leads to the conclusion that most of the magnetite in the rocks of the Bellsund area is of detrital origin, whereas the rocks at Festningen contain magnetite derived from pyrite probably during an early stage of the diagenetic process.     

Magnetic properties of the Olivenza meteorite—possible implications for its evolution and an early solar system magnetic field

The magnetic properties of samples of the Olivenza chondrite (LL5) obtained from four collections have been investigated. The natural remanent magnetization (NRM) consists of a very stable primary component, which is randomly scattered in direction on a scale of 1 mm³ or less within the samples, and a secondary magnetization widely varying in intensity, and probably also in direction. The origin of the secondary NRM is not clear, and may be of terrestrial origin. It is concluded that the NRM is carried by the ordered nickel-iron mineral, tetrataenite. The origin of the primary NRM could be a magnetic field associated with the solar nebula, out of which the metal grains condensed and acquired a thermo-remanent magnetization (TRM), or Olivenza could be a fine-grained breccia, the constituent fragments possessing randomly directed magnetization. The implications for the origin and evolution of Olivenza and its parent body if the former magnetizing process has occurred are discussed.     

Origin of high-magnesian andesites in the Setouchi volcanic belt,southwest Japan,II. Melting phase relations at high pressures

Melting phase relations of an augite-olivine high-magnesian andesite and an augite-olivine basalt from the Miocene Setouchi volcanic belt in southwest Japan have been studied under water-saturated, water-undersaturated and under anhydrous conditions. Both the andesite and the basalt are characterized by low FeO*/MgO ratios (0.86 and 0.76 in weight, respectively) and qualify as primary magmas derived from the upper mantle.The andesite melt coexists with olivine, orthopyroxene and clinopyroxene at 15 kbar and 1030°C under water-saturated conditions, and at 10 kbar and 1070°C under water-undersaturated conditions (7 wt.% H₂O in the melt). The basalt-melt also coexists with the above three phases at 11 kbar and 1305°C under anhydrous conditions, and at 15 kbar and 1205°C in the presence of 4 wt.% water.Present studies indicate that high-magnesian andesite magmas may be produced even under water-undersaturated conditions by partial melting of mantle peridotite. It is suggested that two types of high-magnesian andesites in the Setouchi volcanic belt (augite-olivine and bronzite-olivine andesites) were produced by different degrees of partial melting; augite-olivine andesite magmas, whose mantle residual is lherzolite, were formed by lower degrees of partial melting than bronzite-olivine andesite magmas, which coexist with harzburgite. The basalt magmas, which were often extruded in close proximity to the high-magnesian andesite magmas, are not partial melting products of a mantle peridotite which had previously melted to yield high-magnesian andesite magmas.     

Apollo 17 KREEPy basalt: A rock type intermediate between mare and KREEP basalts

The Apollo 17 KREEPy basalt is a unique lunar volcanic rock, observed only as clasts in the light friable breccia matrix (72275) of Boulder 1, Station 2 at Taurus-Littrow. Its status as a volcanic rock is confirmed by the absence of any meteoritic contamination, a lack of cognate inclusions or xenocrystal material, and low Ni contents in metal grains.The basalt was extruded 4.01 ± 0.04 b.y. ago, approximately contemporaneously with the high-alumina mare basalts at Fra Mauro; shortly afterwards it was disrupted, probably by the Serenitatis impact, and its fragments emplaced in the South Massif. The basalt, which is quartz-normative and aluminous, is chemically and mineralogically intermediate between the Apollo 15 KREEP basalts and the high-alumina mare basalts in most respects. It consists mainly of plagioclase and pigeonitic pyroxene in approximately equal amounts, and 10–30% of mesostatis. Minor phases outside of the mesostatis are chromite, a silica mineral, Fe-metal, and rare olivine; the mesostatis consists primarily of ilmenite, Fe-metal, troilite, and ferroaugite, set in a glassy or microcrystalline Si-rich base.Chemical and isotopic data indicate that an origin by partial melting of a distinct source region is more probable than hybridization or contamination of magmas, and is responsible for the transitional composition of the basalt. The moon did not produce two completely distinct volcanic groups, the KREEP basalts and the mare/mare-like basalts; some intermediate rock types were generated as well. A corresponding spectrum of source regions must exist in the interior of the moon.