The effects of heating on low-temperature susceptibility and hysteresis properties of basalts

The variation of the low-field susceptibility of basalts down to liquid-nitrogen temperature always falls into one of three types that depend on the composition and grain size of the titanomagnetite grains present. Group 1 basalts contain predominantly unoxidised, multidomain homogeneous titanomagnetites having x 0.3. Group 2 basalts contain predominantly titanomagnetite grains with many exsolved ilmenite lamallae that subdivide the grains so that they act similarly to single domains. Group 3 basalts contain predominantly multidomain magnetite or magnetite-rich titanomagnetite having x 0.15. After repeated heating to 615°C, the group 1 basalts gradually oxidise above 300°C to produce the characteristics of group 2 basalts, owing to the exsolution of ilmenite. On the other hand, both group 2 and 3 basalts are stable to oxidation until at least 500°C. They are therefore the most useful material for palaeointensity studies.     

Characteristic magnetic properties of titanomagnetites in continental igneous rocks

Curie temperatures, hysteresis, alternating field properties and anhysteretic and ordinary susceptibilities have been used to characterize the titanomagnetites in a large collection of continental granites, diorites, syenites, anorthosites, gabbros, diabases and basalts. Low-Curie-point titanomagnetites or titanomaghemites were found only in basalts. In all shallow and deep-seated intrusive rocks, the predominant magnetic phase was nearly-titanium-free titanomagnetite with a Curie point of 520–580°C. Most felsic plutonic rocks owed their magnetic properties to coarse, discrete titanomagnetites with truly multidomain properties. Many mafic plutonic rocks (anorthosites, gabbros, norites) displayed bimodal magnetic properties, strong-field properties being due to the discrete titanomagnetites and weak-field properties being due to fine magnetite inclusions in deuterically altered silicates. The Lowrie-Fuller test and the anhysteretic induction curve were the most diagnostic tests of this bimodal behaviour. Grain-size variation within a single diabase dike or sill had a strong expression in all magnetic properties, except H_R/H_c and the Lowrie-Fuller test. On the other hand, the Lowrie-Fuller test was a sensitive indicator of changes in “effective” grain size in basalts due to the subdivision of grains by ilmenite lamellae.     

Thermal and electric conductivity of three basaltic rocks of the Bohemian Massif under high temperatures

Summary The thermal, temperature and electric conductivities of three alkaline basalts are compared for temperatures ranging from 20 to 900 °C.     

Major element chemistry of Galapagos Rift Zone magmas and their phenocrysts

Basalts dredged from the Galapagos Rift Zone between 85°W and 100°W were analyzed by electron microprobe to determine the chemistry of the glass exteriors and included phenocrysts, microphenocrysts and quench minerals. The basalts come from both “normal” mid-ocean ridge segments and from ridge segments that cross the Galapagos Platform. The basalts fall into two chemical and geographical groups. Group A basalts come from outside the central region of the Galapagos Platform (i.e., outside 89–92.5°W) and are chemically similar to basalts from “normal” ocean ridge segments. Group B basalts come from the center of the Galapagos Platform (89–92.5°W) and are enriched in incompatible elements like “plume-influenced” basalts from the Mid-Atlantic Ridge. The spinel, olivine, plagioclase and clinopyroxene phenocrysts in both groups of basalts are low-pressure, equilibrium phases, but the chemical difference among basalts from within each group indicates high-pressure fractional crystallization is also responsible for the chemical evolution of some of these basalts. Presently, no crystallization or partial melting model can relate the chemistry of the two groups of basalts and the compositional influence of a large-ion-lithophile elements and water-rich mantle beneath the Galapagos Platform is a viable alternate hypothesis. The eruption temperature of magmas from the “normal” ridge segments, as determined by olivine-liquid thermometry is 1217±10°C, suggesting steady-state conditions but on the Galapagos Platform the eruption temperatures are lower and more variable than on the “normal” ridge (1186°C±30°C) suggesting a more complex plumbing system and the absence of a steady-state magma chamber beneath the platform.     

The origin of high-amplitude magnetic anomalies at the intersection of the Juan de Fuca ridge and Blanco fracture zone

The intersection of the Juan de Fuca ridge and Blanco fracture zone is characterized by unusually high amplitude magnetic anomalies (over 1500 nT) which appear to be associated with a body roughly 50 km in length and 20 km in width aligned along the fracture zone. Simple three-dimensional magnetic models indicate that this anomaly is probably caused by a highly magnetized block of material situated in the western end of the Blanco fracture zone near its intersection with the Juan de Fuca ridge. Rock magnetization studies of tholeiitic basalts dredged from this area confirm the presence of highly magnetized basalts near the ridge crest/transform fault intersection. These tholeiitic basalts are enriched in iron and titanium relative to “normal” oceanic tholeiites, apparently the result of extensive shallow fractionation involving olivine, plagioclase, and clinopyroxene. Magnetic model studies indicate that an average thickness of no more than 500 m of these iron-rich basalts is necessary to produce the observed anomaly pattern. Comparison of these basalts with samples previously dredged from the Juan de Fuca ridge crest suggests that these Fe-rich, highly magnetized basalts probably “leaked” out of the southernmost portion of the Juan de Fuca ridge.     

The distribution of titanium on the lunar surface

Titanium concentrations have been derived from measurements with the lunar-orbiting gamma-ray experiment on Apollo 15 and 16 by analyzing a spectral interval in which the titanium signal is relatively enhanced. Landing site soil values provide the reference for a regression curve from which Ti concentrations in 137 regions of adequate counting statistics are calculated. Among the mare regions overflown, the southern portion of Mare Tranquillitatis contains the highest Ti concentration (4.4%), Mare Serenitatis, Mare Fecunditatis, and Mare Smythii have intermediate values corresponding to low-Ti basalts, and Mare Crisium is conspicuously low in Ti (0.9%). Regional values in the western maria range from 1.1% to 4.1%, somewhat higher in the north than in the south, with the highest values seen south and west of Aristarchus. The Aristarchus Plateau appears chemically distinct from the surrounding mare. The younger western basalts mapped by the experiment do not appear to be identical to the Apollo 11 and Apollo 17 high-Ti basalts. Low-Ti basalts predominate in the observed mare regions. Highland Ti concentrations range from undetectable to 1.5% with several exceptions; accuracy is limited by the relatively large uncertainty. Highland results suggest a north-south asymmetry which is not consistent with previously reported results for Fe and Th. Comparisons with telescopic spectral reflectance studies of the maria do not show complete agreement and suggest that effects due to Fe may not have been fully removed from the reflectance data.     

Low temperature magnetic properties of basalts containing near ~TM30 titanomagnetite

The paper is devoted to studying the mineral composition and magnetic properties, mainly at the cryogenic temperatures, of the Middle–Late Devonian basalts from North Timan. The magnetic minerals in these basalts are dominated by intermediate-composition titanomagnetites (TM25–TM30) which demonstrate unusual magnetic properties in a wide temperature range. At room temperature, a low coercive force coexists with relatively high M_rs/M_s ratios. At cryogenic temperatures, the dependences of magnetic susceptibility on the temperature and frequency of the applied field are characteristic of this titanomagnetite composition, whereas the remanent saturation magnetization acquired at 2 K is destroyed at significantly lower temperatures compared to the synthetic analogs. The obtained results again highlight the necessity of studying the low-temperature properties of titanomagnetite samples with a controlled composition and grain size.     

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

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

Fission track annealing and correction procedures for oceanic basalt glasses

Most published and unpublished fission track ages for glasses from oceanic basalts are low relative to age estimates from geologic evidence. Experiments reported here strongly suggest that this results from track annealing at ambient sea-floor temperatures. Four Deep Sea Drilling Project basalts exhibiting this effect were subjected to two independent correction procedures in an attempt to determine their true crystallization times. In all cases larger ages resulted, but dates by the two methods are not generally concordant and do not always agree with the estimated sea-floor age.     

Methods for estimating Curie temperatures of titanomaghemites from experimentalJs-T data

Methods for determining the Curie temperature (T_c) of titanomaghemites from experimental saturation magnetization-temperature (J_s-T) data are reviewed.J_s-T curves for many submarine basalts and synthetic titanomaghemites are irreversible and determining Curie temperatures from these curves is not a straightforward procedure. Subsequently, differences of sometimes over 100°C in the values ofT_c may result just from the method of calculation. Two methods for determiningT_c will be discussed: (1) the graphical method, and (2) the extrapolation method. The graphical method is the most common method employed for determining Curie temperatures of submarine basalts and synthetic titanomaghemites. The extrapolation method based on the quantum mechanical and thermodynamic aspects of the temperature variation of saturation magnetization nearT_c, although not new to solid state physics, has not been used for estimating Curie temperatures of submarine basalts. The extrapolation method is more objective than the graphical method and uses the actual magnetization data in estimatingT_c.     

Trace elements in ocean ridge basalts

A correlary of sea floor spreading is that the production rate of ocean ridge basalts exceeds that of all other volcanic rocks on the earth combined. Basalts of the ocean ridges bring with them a continuous record in space and time of the chemical characteristics of the underlying mantle. The chemical record is once removed, due to chemical fractionation during partial melting. Chemical fractionations can be evaluated by assuming that peridotite melting has proceeded to an olivine-orthopyroxene stage, in which case the ratios of a number of magmaphile elements in the extracted melt closely match the ratios in the mantle. Comparison of ocean ridge basalts and chondritic meteorites reveals systematic patterns of element fractionation, and what is probably a double depletion in some elements. The first depletion is in volatile elements and is due to high accretion temperatures of a large percentage of the earth from the solar nebula. The second depletion is in the largest, most highly charged lithophile elements (“incompatible elements”), probably because the mantle source of the basalts was melted previously, and the melt, enriched in these elements, was removed. Migration of melt relative to solid under ocean ridges and oceanic plates, element fractionation at subduction zones, and fractional melting of amphibolite in the Precambrian are possible mechanisms for depleting the mantle in incompatible elements. Ratios of transition metals in the mantle source of ocean ridge basalts are close to chondritic, and contrast to the extreme depletion of refractory siderophile elements, the reason for which remains uncertain. Variation of ocean ridge basalt chemistry along the length of the ridge has been correlated with ridge elevation. Thus chemically anomalous ridge segments up to 1000 km long appear to broadly coincide with regions of high magma production (plumes, hot spots). Basalt heterogeneity at a single location indicates mantle heterogeneity on a smaller scale. Variation of ocean ridge basalt chemistry with time has not been established, in fact, criteria for recognizing old oceanic crust in ophiolite terrains are currently under debate. The similarity of rare earth element patterns in basalt from ocean ridges, back-arc basins, some young island arcs, and some continental flood basalts illustrates the dangers of tectonic labeling by rare earth element pattern.     

Origin of Icelandic basalts: A review of their petrology and geochemistry

The petrology and geochemistry of Icelandic basalts have been studied for more than a century. The results reveal that the Holocene basalts belong to three magma series: two sub-alkaline series (tholeiitic and transitional alkaline) and an alkali one. The alkali and the transitional basalts, which occupy the off-rift volcanic zones, are enriched in incompatible trace elements compared to the tholeiites, and have more radiogenic Sr, Pb and He isotope compositions. Compared to the tholeiites, they are most likely formed by partial melting of a lithologically heterogeneous mantle with higher proportions of melts derived from recycled oceanic crust in the form of garnet pyroxenites compared to the tholeiites. The tholeiitic basalts characterise the mid-Atlantic rift zone that transects the island, and their most enriched compositions and highest primordial (least radiogenic) He isotope signature are observed close to the centre of the presumed mantle plume. High-MgO basalts are found scattered along the rift zone and probably represent partial melting of refractory mantle already depleted of initial water-rich melts. Higher mantle temperature in the centre of the Iceland mantle plume explains the combination of higher magma productivity and diluted signatures of garnet pyroxenites in basalts from Central Iceland. A crustal component, derived from altered basalts, is evident in evolved tholeiites and indeed in most basalts; however, distinguishing between contamination by the present hydrothermally altered crust, and melting of recycled oceanic crust, remains non-trivial. Constraints from radiogenic isotope ratios suggest the presence of three principal mantle components beneath Iceland: a depleted upper mantle source, enriched mantle plume, and recycled oceanic crust.The study of glass inclusions in primitive phenocrysts is still in its infancy but already shows results unattainable by other methods. Such studies reveal the existence of mantle melts with highly variable compositions, such as calcium-rich melts and a low-¹⁸O mantle component, probably recycled oceanic crust. Future high-resolution seismic studies may help to identify and reveal the relative proportions of different lithologies in the mantle.     

Basalt geochemistry and tectonic discrimination within continental flood basalt provinces

Continental flood basalts are usually regarded as a single tectonomagmatic entity but frequently quoted examples exhibit a variety of tectonic settings. In one well-studied, classic, flood basalt province, the Mesozoic Karoo province of southern Africa, magmatism occurred in the following tectonic settings: (a) continental rifting leading to ocean-floor spreading in the South Atlantic Ocean (Etendeka suite of Namibia); (b) stretched continental lithosphere and rifting not leading directly to ocean-floor formation (Lebombo suite of southeastern Africa); and (c) an a-tectonic, within-plate, continental setting characterized by an absence of faulting or warping (Lesotho highlands and Karoo dolerites of South Africa). By means of spidergrams of the elements Rb, Ba, Th, Nb, K, La, Ce, Sr, Nd, P, Hf, Zr, Sm, Ti, Tb, Y, V, Ni and Cr, uncontaminated tholeiites from (c) above [i.e. the Lesotho-type continental flood basalts (LTCFB)] are compared with mid-ocean ridge basalts (MORB), ocean-island tholeiites (OIT), and tholeiites and calc-alkali basalts from subduction environments. The comparison reveals the LTCFBs are geochemically distinct. The differences are reflected in relative enrichments or depletions of the more incompatible elements (Rb-Ce) to less incompatible elements (Ce-Y), i.e. the overall slope of the spidergrams, and in anomalous enrichments or depletions of one or more of the elements Th, K, Nb, Sr, Ti, Hf, and Zr. The distinctive geochemical character of the Lesotho LTCFBs is interpreted in terms of a lithospheric mantle source for the basalts. This is supported by isotopic data. There are no major geochemical differences between Lesotho CFBs and basalts of the rift-related Etendeka and Lebombo suites, although the latter are somewhat enriched in Rb, Ba and K. However, unlike the Lesotho basalts, the Lebombo and Etendeka basalts are associated with voluminous silicic volcanics or intrusive centres and late-stage dolerites having MORB/OIT (i.e. asthenospheric) geochemical characteristics. The flood basalt/silicic magmatism/late-stage dyke swarm association is characteristic of several rift or thinned lithosphere environments (e.g., Ethiopia, Skye, eastern Greenland) but in many of these the flood basalts have ocean-island basalt (OIT) geochemical characteristics. The Lesotho-type CFB geochemistry is exhibited by the Grande Ronde Basalt of the Columbia River Group (a possible subduction-related flood basalt province) and the basic rocks associated with Mesozoic rifting in the North and South Atlantic. Basalt geochemistry alone is unhelpful in determining the tectonic setting of CFBs although the rift-related environments may be identified by the petrology and geochemistry of the whole igneous suite. A two-source model is proposed for the mantle-derived basic rocks in rift-related CFB provinces. Early enriched basalts are derived from the lithosphere and, following pronounced lithospheric attenuation or rifting, later MORB-like melts are emplaced from the rising asthenosphere. The presence of both Lesotho- and OIT-type geochemical patterns in rift-related CFBs suggests that the lithosphere exhibits different styles of enrichment.     

Oxygen and carbon isotope evidence for seawater-hydrothermal alteration of the Macquarie Island ophiolite

Rocks of the Miocene Macquarie Island ophiolite, south of New Zealand, have oxygen and carbon isotopic compositions comparable to those of seafloor rocks. Basalt glass and weathered basalts have δ¹⁸O values at 5.8–6.0‰ and 7.9–9.5‰, respectively, similar to drilled seafloor rocks including samples from the Leg 29 DSDP holes near Macquarie Island. Compared to the basalt glass, the greenschist to amphibolite facies metaintrusives are depleted in¹⁸O (δ¹⁸O=3.2–5.9‰) similar to dredged seafloor samples, whereas the metabasalts are enriched (δ¹⁸O=7.1–9.7‰). Although the gabbros are only slightly altered in thin-section they have exchanged oxygen with a hydrothermal fluid to a depth of at least 4.5 km. There is an approximate balance between¹⁸O depletion and enrichment in the exposed ophiolite section. The carbon isotopic composition of calcite in the weathered basalts (δ¹³C=1.0–2.0‰) is similar to those of drilled basalts, but the metamorphosed rocks have low δ¹³C values (?14.6 to 0.9‰).These data are compatible with two seawater circulation regimes. In the upper regime, basalts were weathered by cold seawater in a circulation system with high water/rock ratios (?1.0). Based on calcite compositions weathering temperatures were less than 20°C and the carbon was derived from a predominantly inorganic marine source. As previously suggested for the Samail ophiolite, it is postulated that the lower hydrothermal regime consisted of two coupled parts. At the deeper levels, seawater circulating at low water/rock ratios (0.2–0.3) and high temperatures (300–600°C) gave rise to¹⁸O-depleted gabbro and sheeted dikes via open system exchange reactions. During reaction the seawater underwent a shift in oxygen isotopic composition (δ¹⁸O=1.0–5.0‰) and subsequently caused¹⁸O enrichment of the overlying metabasalts. In the shallower part of the hydrothermal regime the metabasalts were altered at relatively high water/rock ratios (1.0–10.0) and temperatures in the range 200–300°C. The relatively low water/rock ratios in the hydrothermal regime are supported by the low δ¹³C values of calcite, interpreted as evidence of juvenile carbon in contrast to the inorganic marine carbon found in the weathered basalts.     

Geothermal exploration in the azores: 0/0 in calcites from volcanic rocks

The oxygen isotope composition of calcite veins and vugs in basalts from a drill site on the island of Sao Miguel show near-equilibration with fresh water at observed temperatures only at a depth of 600–700 m. This is interpreted to mean that the greatest flow of hot water may be occurring in this depth interval.     

The spread of subducted lithospheric material along the mid-mantle boundary

Studies of phase transitions in silicate minerals at high temperatures and pressures suggest that the bulk density of subducted lithosphere at the mid-mantle boundary is intermediate between the densities of the upper and lower mantle. We argue that, if this is the case, then the lithospheric material will intrude along the mid-mantle boundary driven by buoyancy forces resulting from the compositional density differences between the intrusion and its surroundings. The rate of spread of the intrusion is given by a balance between these buoyancy forces and the viscous resistance of the mantle to motion. Using results from our recent studies of the fluid mechanics of such viscous gravity currents, we find that lithospheric material can propagate between one thousand and two thoudand kilometres in a hundred million years and can cover the entire boundary in one to six billion years. This spreading may be reflected in the global distribution of the isotopic characteristics of oceanic basalts.     

The isotopic composition of strontium and oxygen in lavas from St. Helena,South Atlantic

Strontium and oxygen isotope measurements on the alkali basalt-trachyte-phonolite suite of St. Helena show that some of the late-fractionated rocks are enriched in ⁸⁷Sr and depleted in ¹⁸O relative to the older basalts. The data rule out both the formation of the late-fractionated rocks by the partial melting of hydrothermally altered oceanic crust and the contamination of the volcanic rocks by oceanic sediment. It also appears to be incompatible with models based either on the melting of previously fractionated and crystallized liquids in the volcanic pile, or the long-term fractionation of lavas over several millions of years in a sub-volcanic magma chamber.It is concluded that hydrothermal interaction with meteoric water is the most important cause of the ¹⁸O depletion. If the interaction occurred at widely differing temperatures, and involved meteoric and seawaters, it might conceivably have caused both the oxygen and strontium isotope heterogeneities.     

The Karoo igneous province — A problem area for inferring tectonic setting from basalt geochemistry

Tholeiitic basalts and associated intrusives are the major component of the Karoo igneous province. They are of Mesozoic age and constitute one of the world's classic continental flood basalt (CFB) provinces. It has been argued that most Karoo basalts have not undergone significant contamination with continental crust and that their lithospheric mantle source areas were enriched in incompatible minor and trace elements during the Proterozoic. The only exceptions to this are late-stage MORB-like dolerites near the present-day continental margins which are considered to be of asthenospheric origin.When data for the “southern” Karoo basalts are plotted on many of the geochemical discriminant diagrams which have been used to infer tectonic setting, essentially all of them would be classified as calc-alkali basalts (CAB's) or low-K tholeiites. Virtually none of them plot in the compositional fields designated as characteristic of “within-plate” basalts. There is little likelihood that the compositions of the Karoo basalts can be controlled by active subduction at the time of their eruption and no convincing evidence that a “subduction component” has been added to the subcontinental lithospheric mantle under the entire area in which the basalts crop out. It must be concluded that the mantle source areas for CAB's and the southern Karoo basalts have marked similarities.In contrast, the data for “northern” Karoo basalts largely plot in the “within-plate” field on geochemical discriminant diagrams. Available data suggest that the source composition and/or the restite mineralogy and degree of partial melting are different for southern and northern Karoo basalts. There is no evidence for any difference in tectonic setting between the southern and northern Karoo basalts at the time they were erupted. This appears to be clear evidence that specific mantle source characteristics and/or magmatic processes can vary within a single CFB province to an extent that renders at least some geochemical discriminant diagrams most unreliable for classifying tectonic environment with respect to continental volcanic rocks.     

Transitional basalts from the eastern Australian tertiary province

Study of Tertiary volcanic rocks from Mt. Tamborine in S. E. Queensland, Australia, suggests that some basalts from the large Tweed vent are intermediate in character between true tholeiites and well documented alkaline basalts of the Australian Tertiary province. Geochemical evidence and comparison with synthetic systems suggests that the transitional lavas are derived by continuous fractional crystallization during the ascent of a parent magma produced by substantial partial melting of the upper mantle at moderate depths and pressures. Alkaline basalts that underlie the transitional basalts are the result of relatively rapid, intermittent extrusion of magma generated by a smaller degree of partial melting of the upper mantle. This interpretation resolves the difficulties posed by an apparent inversion of the usual stratigraphic relationship of tholeiites capped by alkali basalts, and is in accord with recent seismic studies of the continental margin of eastern Australia.     

Palaeomagnetism and basalts

Among the various types of rocks, basalts are by far most suitable for palaeomagnetic studies. However, the magnetic parameters of basaltic rocks vary over a wide range and so also the magnetic stability. These features have been studied extensively for samples from Deccan and Rajmahal traps. The implications of the results on the palaeomagnetism of these formations in particular and that of basalts in general are discussed.