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At least 181 records · Page 10
All sourcesNASA NTRSDOE OSTI
NASA NTRS2022

Calcium Isotope Constraints on Recycled Carbonates in Subduction-related Magmas

Calcium isotope ratios are readily mass-fractionated by low-temperature depositional processes that can be recorded in sedimentary rocks and, therefore, have the potential to track distinct geochemical signatures of recycled materials in mantle-derived igneous rocks. In this study, I report calcium isotopic compositions for well-characterized lavas from the Central American volcanic arc that exhibit a range of trace element and radiogenic isotope signatures that have been used to indicate variable amounts of subducted marine carbonate and hemipelagic sedimentary rocks, fresh carbonatite lavas from Oldoinyo Lengai Volcano, Tanzania, and an intrusive carbonatite clast erupted 12.8 ka from the Laacher See Volcano, Germany. I observed no calcium isotope evidence for recycled sedimentary rocks in the Central American arc magmas or in the Oldoinyo Lengai carbonatite volcanic rocks. They all exhibit isotopic compositions similar to rocks dominated by a primitive, mantle-like, bulk silicate Earth (BSE) composition. The exception in this work is the calcium isotope composition measured in the intrusive Laacher See carbonatite that is resolvable from BSE (δ^44 Ca = 0.0). Although this calcium isotopic signature might be related to ancient carbonate recycling, the magnitude and relatively light calcium isotopic composition (δ^44 Ca = –0.4) of this carbonatite could also reflect an origin that involved partial melting of altered lithospheric mantle, from which isotopically heavy Ca-bearing fluids have been lost. The decoupled signatures between trace elements and their radiogenic isotopes and those recorded by calcium isotope data are important because they likely reflect different sources and processes, and demonstrate that sediment subduction is not a bulk mixing process.

Ca isotopes↗
NASA NTRSDate not supplied

A New Era of H-O-C-S Magma Solubility Modeling: Better, Faster, Stronger

H 2 O, CO 2 , and S are the most abundant volatiles in magmatic systems and are critical to understanding magma storage, phase equilibria, and volcanic eruptions. Models that consider all three of these components, however, may not allow for critical examination and adjustment of assumptions underlying the model, or provide benchmark testing or extensible interfaces. Thus, understanding why models produce different results can be challenging. We have gathered authors of established (D-Compress) and recent (VolFe, EVo, Sulfur_X, MAGEC) H-O-C-S volatile solubility models to work together to understand how and why our models diverge. We present a series of benchmark basalt degassing scenarios revealing that often understated model assumptions such as fO 2 buffer equations, fO 2 -Fe 3+ /ΣFe relationships, and even major element normalization routines have outsized effects on model results. All models consider S 2- and S 6+ melt species but with different approaches to sulfate/sulfide capacities, partition coefficients, and species fugacities, leading to divergence in the evolution of modeled gas compositions, melt S and Fe speciation, and fO 2 , with the extent of divergence depending on melt composition. Such scenarios enable meaningful intercomparison of existing models and lay the groundwork for a user-friendly yet powerful solubility modeling framework. Given our wealth of existing solubility literature, we suggest that the field of magmatic volatiles should focus now on the creation of modern tools and the modular implementation of existing model equations or methods, and that the evaluation of code usability, transparency, and benchmarking should be codified pillars of the peer-review process. As an example of such an endeavor, we present early work coupling these sulfur solubility models with VESIcal, an extensible and rigorously tested python library containing seven existing H 2 O-CO 2 solubility models. VESIcal includes the ability to extract, edit, and even interchange assumptions underlying any model. For example, users may combine or swap separately published H 2 O, CO 2 , and S models, as well as underlying model choices, such as Equations of State and redox models.

volatiles in magmas↗
DOE OSTI2025

Building wet planets through high-pressure magma–hydrogen reactions

Close-in transiting sub-Neptunes are abundant in our Galaxy. Planetary interior models based on their observed radius–mass relationship suggest that sub-Neptunes contain a discernible amount of either hydrogen (dry planets) or water (wet planets) blanketing a core composed of rocks and metal. Water-rich sub-Neptunes have been believed to form farther from the star and then migrate inwards to their present orbits. Here we report experimental evidence of reactions between warm, dense hydrogen fluid and silicate melt that release silicon from the magma to form alloys and hydrides at high pressures. We found that oxygen liberated from the silicate melt reacts with hydrogen, producing an appreciable amount of water up to a few tens of weight per cent, which is much greater than previously predicted based on low-pressure ideal gas extrapolation. Consequently, these reactions can generate a spectrum of water contents in hydrogen-rich planets, with the potential to reach water-rich compositions for some sub-Neptunes, implying an evolutionary relationship between hydrogen-rich and water-rich planets. Therefore, detection of a large amount of water in exoplanet atmospheres may not be the optimal evidence for planet migration in the protoplanetary disk, calling into question the assumed link between composition and planet formation location.

Horn, H. W. [Arizona State University, Tempe, AZ (↗
DOE OSTI2020

Unraveling the Effects of Melt–Mantle Interactions on the Gold Fertility of Magmas

The oxidation state of the Earth’s mantle and its partial melting products exert a key control on the behavior and distribution of sulfur and chalcophile and siderophile elements between the mantle and crust, underpinning models of ore deposit formation. Whether the oxidized nature of magmas is inherited from the asthenospheric mantle source or acquired during ascent and differentiation is vigorously debated, limiting our understanding of the mechanisms of extraction of sulfur and metals from the mantle. Here, we focused on the redox-sensitive behavior of sulfur in apatite crystallized from quenched alkaline basaltic melts preserved within a peridotite xenolith from the El Deseado Massif auriferous province in southern Patagonia. We took advantage of this unique setting to elucidate the redox evolution of melts during their ascent through the subcontinental lithospheric mantle (SCLM) and grasp the inner workings of the Earth’s mantle during gold metallogenesis. Our data reveal that an initially reduced silicate melt (ΔFMQ -2.2 to -1.2) was oxidized to ΔFMQ between 0 and 1.2 during percolation and interaction with the surrounding peridotite wall-rock (ΔFMQ 0 to +0.8). This process triggered changes in sulfur speciation and solubility in the silicate melt, boosting the potential of the melt to scavenge ore metals such as gold. We suggest that large redox gradients resulting from the interaction between ascending melts and the surrounding mantle can potentially modify the oxidation state of primitive melts and enhance their metallogenic fertility. Among other factors including an enriched metal source and favorable geodynamic conditions, redox gradients in the mantle may exert a first-order control on the global-scale localization of crustal provinces endowed with gold deposits.

58 GEOSCIENCES↗
NASA NTRS1973

Oxygen fugacity values of Apollo 12, 14, and 15 lunar samples and reduced state of lunar magmas

The oxygen fugacity values of lunar samples were measured directly with an improved solid-electrolyte oxygen cell between 1000 and 1200 C with an accuracy mostly better than 0.2 log f(02) unit. The bulk rock f(02) values of basaltic igneous rocks 12009, 12053, 15058, and 15595 ranged from 10 to -15.4 power to 10 to the -15.7 power at 1000 C and from 10 to the -12.3 power to 10 to the -12.8 power at 1200 C. Those of microbreccia 14321 also fell in this range, but the change of oxygen fugacity with temperature was irregular in the first heating cycle in comparison to the smooth changes observed with the basaltic igneous rocks. Two different samples of rock 14310 also showed similar f(02) values below 1170 C, but exhibited irreversible sudden rise in f(02) at this temperature for reasons yet to be determined. The data on the phenocryst olivine and the groundmass of basalt 12009 do not conclusively indicate progressive reduction of the lunar magma during cooling.

Sato, M.↗
NASA NTRS1976

Differentiation of an Apollo 12 picrite magma

The Apollo 12 olivine basalt suite shows a strong positive correlation of grain size with normative olivine content. This correlation is interpreted to mean that the suite of samples represents the basal portion of a cooling unit which differentiated by simple olivine settling. The grain size of plagioclase observed in the coarsest samples indicates the cooling unit may have been as much as 30 m thick. The amount of olivine concentration observed in the suite is quantitatively internally consistent with simple olivine settling in a magma body of this size which has the composition of the chill margin.

Walker, D.↗
NASA NTRS1977

Chemistry of Apollo 12 mare basalts - Magma types and fractionation processes

Major and trace element data for a large suite of petrographically diverse Apollo 12 mare basalts are presented, and magma types sampled at the Apollo 12 site are characterized. The data confirm earlier classifications of the basalts into olivine, pigeonite, ilmenite, and feldspathic basalts. The olivine and pigeonite basalts are shown to be comagnetic and related by olivine fractionation. The other types, which differ in trace element and isotopic characteristics, are derived from different sources within the lunar interior. The spatial relations between the main basalt types are discussed in terms of local cratering events, and it is suggested that the younger ilmenite basalts overlie the olivine-pigeonite basalts. The role of olivine-dominated near-surface crystal fractionation in causing chemical variation is examined, and a relation between inferred cooling rate and the position of a sample in the fractionation sequence is determined.

Rhodes, J. M.↗
NASA NTRS1979

Apollo 17 high-Ti mare basalts - New bulk compositional data, magma types, and petrogenesis

Bulk compositional and mineral chemical data for 28 previously unanalyzed samples support the classification of Apollo-17 high-Ti mare basalts into three-types (A, B, and C), defined on the basis of analyses of fine-grained basalts. The most MgO- and TiO2-rich fine-grained basalts of these types appear to be the best choices for representing the compositions of the parent magmas.

Warner, R. D.↗
NASA NTRS1981

Steady-state magma discharge at Etna 1971-81

Throughout the past decade Mount Etna has been in almost continuous activity and even during periods of repose incandescent lava has often been visible in at least one of the summit vents. Using observations by Italian, British and French volcanological teams, the volumes of lava produced by each eruption from 1971 to July 1981 have been estimated. The computed output of magma for this period approximates to a rate of 0.7 cu m/s. This is compared with the output rate estimates for Etna's historic past. The steady-state nature of the output during the past decade has implications for the interpretation of the volcano's internal plumbing and the petrology of its lavas, and the assumption that this state will be maintained allows a discussion of the timing and magnitude of future eruptions.

Wadge, G.↗
NASA NTRS1980

The lunar magma ocean - A transient lunar phenomenon

The time required for the solidification of a lunar magma ocean is considered. In the absence of a thermal boundary crust, heat loss is by radiation and the ocean will solidify in a few decades. However, only a few millimeters of crust would effectively limit radiation. The current investigation has the objective to present estimates of conduction boundary (crust) thickness based on several models of the mechanism of crustal formation. Three different models for estimating conduction boundary layer thickness are discussed. They are based on the formation of a chill margin, a plagioclase flotation layer, and a layer which is continually destroyed by meteorite impacts and regrows by conductive heat loss. Based on these models, the maximum solidification time for a 200 km thick ocean is about 100 million years. A more probable solidification time based on a plagioclase flotation crust model is about 60 million years.

Minear, J. W.↗
NASA NTRS1982

Chemical composition of the Howardite Parent Body deduced from Kapoeta primary 'mafic' magmas

Chemical data are presented for three 'mafic' clasts extracted from the Kapoeta howardite. Bulk compositions and petrologic observations suggest that two of these lithic clasts represent olivine-plagioclase bearing orthopyroxenites. Chondrite-relative refractory large ion lithophile abundances of two of the clasts are inferred to represent primary Mg-rich magmas produced by extensive (greater than about 70%) partial melting of a source composition indistinguishable from the silicate fraction of average CH-CL ordinary chondrites, with the exception of the depletion of the alkalis Na and K by a factor of 13 + or - 1 in the source composition. A metal-free and volatile depleted Kapoeta Parent Body (KPB) is subsequently deduced and is shown to compare very well with other similarly derived Achondrite Parent Body and Howardite Parent Body estimates but not to parent body estimates derived from inferences based on eucrite phase equilibrium studies. Other implications suggest that the KPB is heterogeneous with respect to Fe/Mg ratios.

Smith, M. R.↗
NASA NTRS1984

Geochemical constraints on magma processes in a peralkaline system - The Paisano volcano, west Texas

Petrographic and trace element data from a continuous stratigraphic sequence of flows from the peralkaline Paisano Volcano in west Texas are used to delineate magnetic processes responsible for the chemical evolution of this volcano. It is shown that crystal fractionation of the phenocrystic assemblage explains the main compositional variation, but magma mixing of a less evolved melt composition also affected the chemical evolution of the volcano.

Mcdonough, W. F.↗
NASA NTRS1985

The magma ocean concept and lunar evolution

The model of lunar evolution in which the anorthositic plagioclase-rich oldest crust of the moon is formed over a period of 300 Myr or less by crystallization as it floats on a global ocean of magma tens or hundreds of km thick is examined in a review of petrological and theoretical studies. Consideration is given to the classification of lunar rocks, the evidence for primordial deep global differentiation, constraints on the depth of the molten zone, the effects of pressure on mineral stability relationships, mainly-liquid vs mainly-magmifer ocean models, and the evidence for multiple ancient differentiation episodes. A synthesis of the model of primordial differentiation and its aftereffects is presented, and the generalization of the model to the earth and to Mars, Mercury, Venus, and the asteroids is discussed.

Warren, P. H.↗
NASA NTRS1985

Ultramafic parent magmas for mare basalts?

Solidification products of basaltic magmas (fine grained basalts and ultramafic glasses) at the Apollo 15 site were examined. Consideration of simple MgO-6IO2-Al2O3 systematics plus results of calculations of fractional crystallization was reviewed. Suggestions are presented to account for the lack of correlation between the ultramafic glasses and basalts.

Longhi, J.↗