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K. Futa

Publications and source records attributed to K. Futa.

11 recordsLinked to original sources

Polybaric evolution of phonolite, trachyte, and rhyolite volcanoes in eastern Marie Byrd Land, Antarctica: Controls on peralkalinity and silica saturation

In the Marie Byrd Land volcanic province, peralkaline and metaluminous trachytes, phonolites, and rhyolites occur in 18 large shield volcanoes that are closely associated in time and space. They are arrayed radially across an 800 km wide structural dome, with the oldest at the crest and the youngest around the flanks. Several lines of evidence suggest that these rocks evolved via opensystem, polybaric fractionation. We have used mass balance modeling of major elements together with trace-element data and mineral chemistry to help explain the evolution of this diverse suite of felsic rocks, which appear to have been generated coevally in isolated magma chambers, and erupted close to each other in patterns related to tectonic uplift and extension within the West Antarctic rift system. Isotopic and trace-element data indicate that this occurred with only minimal crustal contamination. We focus on volcanoes of the Executive Committee Range and Mount Murphy, where we find good representation of basalts and felsic rocks within a small area. Our results suggest that the felsic rocks were derived from basaltic magmas that differentiated at multiple levels during their passage to the surface: first to ferrogabbroic compositions near the base of the lithosphere, then to intermediate compositions near the base of the crust, and finally to felsic compositions in mid- to upper crustal reservoirs. The high-pressure history has been largely masked by low-pressure processes. The best indications of a high-pressure history are the mineral phases in cumulate nodules and their correlation with modeling results, with REE anomalies, and with the composition of an unusual gabbroic intrusion. Silica saturation characteristics are believed to have originated in magma chambers near the base of the crust, via fractionation of variable proportions of kaersutite and plagioclase. Development of peralkalinity in felsic rocks took place in upper crustal reservoirs by fractionating a high ratio of plagioclase to clinopyroxene under conditions of low pH 2 O. With increasing pH 2 O, the ratio plagioclase/clinopyroxene in the fractionated assemblage decreases and metaluminous liquids resulted. Crustal contamination seems to have had a role in suppressing peralkalinity , and was probably a factor in the origin of high- silica metaluminous rhyolite , but metaluminous rocks are uncommon. The volume and diversity of felsic rocks were probably enhanced by the structure of the lithosphere, the persistence of plume activity, and the immobility of the Antarctic plate. Mechanical boundaries at the base of the lithosphere and crust, and within the crust, appear to have acted as filters, trapping magmas at multiple levels, and prolonging the fractionation process. Final volumes would have been further enhanced by repeated refluxing of the same magma chambers, controlled by plume activity and plate immobility.

International Geology Review

Evidence for ground-water stratification near Yucca Mountain, Nevada

Major- and trace-element concentrations and strontium isotope ratios (strontium-87/strontium-86) in samples of ground water potentially can be useful in delineating flow paths in the complex ground-water system in the vicinity of Yucca Mountain, Nevada. Water samples were collected from boreholes to characterize the lateral and vertical variability in the composition of water in the saturated zone. Discrete sampling of water-producing intervals in the saturated zone includes isolating borehole sections with packers and extracting pore water from core obtained by sonic drilling. Chemical and isotopic stratification was identified in the saturated zone beneath southern Fortymile Wash.

Conference Paper

Ancient maize from Chacoan great houses: Where was it grown?

In this article, we compare chemical ( 87 Sr/ 86 Sr and elemental) analyses of archaeological maize from dated contexts within Pueblo Bonito, Chaco Canyon, New Mexico, to potential agricultural sites on the periphery of the San Juan Basin. The oldest maize analyzed from Pueblo Bonito probably was grown in an area located 80 km to the west at the base of the Chuska Mountains. The youngest maize came from the San Juan or Animas river floodplains 90 km to the north. This article demonstrates that maize, a dietary staple of southwestern Native Americans, was transported over considerable distances in pre-Columbian times, a finding fundamental to understanding the organization of pre-Columbian southwestern societies. In addition, this article provides support for the hypothesis that major construction events in Chaco Canyon were made possible because maize was brought in to support extra-local labor forces.

Proceedings of the National Academy of Sciences of

Isotopic tracers of gold deposition in Paleozoic limestones, southern Nevada

Strontium isotopic analyses of barren and mineralized Paleozoic carbonate rocks show that hydrothermal fluids added radiogenic strontium (87Sr) to the mineralized zones. At Bare Mountain, samples collected from mineralized areas have ??87Srt values (per mil deviation from primary marine values) ranging from +3.0 to +23.0 (mean of this log-normal distribution is +7.0), whereas unmineralized carbonate rocks have ??87Srt values of -0.6 to +2.9 (mean of +1.07??1.03). In other ranges (Striped Hills, Spring Mountains, and ranges in the vicinity of Indian Springs Valley), ??87Srt values of the unmineralized carbonate rocks are even lower and virtually indistinguishable from primary marine values. This correlation of elevated ??87Srt values with mineralized zones provided a useful technique for assessing the mineral potential of the Paleozoic basement beneath Yucca Mountain, and may find broader use in mineral exploration in the Basin and Range province as a whole.

Conference Paper

A comparison of Sr-Nd-Pb isotopes in young and old continental lithospheric mantle: Patagonia and eastern China

It is commonly accepted that beneath the continental crust lies a keel of lithospheric mantle, which extends 50–200 kilometres downward to a transition zone into the asthenosphere. The chemical and physical properties of this reservoir are best known through studies of the basalts and xenoliths that provide samples of the subcrustal mantle. Although sharing many characteristics with oceanic island basalts, some continental basalts become increasingly distinct isotopically as crustal age increases, strongly supporting a permanent association between crust and mantle. Consequently, the distinctive trace element and isotope composition of the lithospheric mantle is able to give important clues to its origin and evolution. The mantle under newly‐created crust is typified by a radiogenic isotope variability that emphasizes the materials from which the continental lithosphere is assembled. Old lithospheric mantle, on the other hand, exhibits more evolved isotopic patterns that attest to the existence of long‐lived, chemically complex systems. A comparison of the Pb, Sr and Nd isotopes in alkalic to sub‐alkalic basalt derived from Phanerozoic (Patagonia) and Middle Archaean to Early Proterozoic (eastern China) subcrustal mantle is useful for identifying ‘end‐member’ components of the lithosphere. One component, having an isotopic composition close to PREMA, either continues to evolve virtually unchanged after incorporation into the lithosphere or is, itself, a relatively new addition even to old lithosphere. Another component, beginning with the isotopic composition of BSE, undergoes significant reduction in U/Pb and Sm/Nd (but not Rb/Sr) upon incorporation into the lithosphere and, with time, shows an increasingly retarded evolution of 206 Pb/ 204 Pb and negative ε Nd‐values approaching the isotopic composition of EMI. Five models are discussed that relate the isotopic composition of the continental lithospheric mantle to that of other parts of the terrestrial system, which may be involved in its origin and evolution. The potential locations of the contributing components and the mechanisms and timing of their assembly into lithosphere are considered. Current knowledge, however, does not allow us to distinguish unequivocally among the various scenarios for the creation and evolution of this reservoir.

Australian Journal of Earth Sciences

Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc to back-arc volcanism in southern South America. The "cratonic" basalts do not contain the slab-derived components that impart the higher Ba/La, Ba/Nb, La/Nb, Cs/Rb, 87Sr/86Sr at a given 143Nd/144Nd, 207Pb/204Pb at a given 208Pb/204Pb, and ??18O to Andean orogenic arc basalts. Instead, these basalts are formed by relatively low degrees of partial melting of heterogeneous lower continental lithosphere and/or asthenosphere, probably due to thermal and mechanical pertubation of the mantle in response to subduction of oceanic lithosphere below the western margin of the continent. The "transitional" basalts do contain components added to their source region by either (1) active input of slab-derived components in amounts smaller than the contribution to the mantle below the arc and/or with lower Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios than below the arc due to progressive downdip dehydration of the subducted slab; or (2) subarc source region contamination processes which affected the mantle source of the "transitional" basalts earlier in the Cenozoic. ?? 1990 Springer-Verlag.

Contributions to Mineralogy and Petrology

Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the Southern Andes

Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33–46°S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49–54°S) range for 87 Sr/ 86 Sr from 0.70280 to 0.70591 and for 143 Nd/ 144 Nd from 0.51314 to 0.51255. The ranges are significantly greater than previously reported from the southern Andes but are different from the isotopic compositions of volcanoes in the central and northern Andes. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have 87 Sr/ 86 Sr , 143 Nd/ 144 Nd , La/Yb , Ba/La , and Hf/Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35°S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33° and 34°S, basaltic andesites and andesites have higher 87 Sr/ 86 Sr , Rb/Cs , and Hf/Lu , and lower 143 Nd/ 144 Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54°S) has Sr and Nd isotopic compositions and KR/b and Ba/La similar to MORB. The high La/Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO 2 , K 2 O, Rb, Ba, Ba/La , and 87 Sr/ 86 Sr/ and decrease in MgO, Sr, KR/b , Rb/Cs , and 143 Nd/ 144 Nd , suggesting increasingly greater degrees of fractional crystallization and associated intra-crustal contamination.

Earth and Planetary Science Letters

Pb-, Sr- and Nd-Isotopic systematics and chemical characteristics of cenozoic basalts, Eastern China

Forty-eight Paleogene, Neogene and Quaternary basaltic rocks from northeastern and east-central China have been analyzed for major-element composition, selected trace-element contents, and Pb, Sr and Nd isotopic systematics. The study area lies entirely within the marginal Pacific tectonic domain. Proceeding east to west from the continental margin to the interior, the basalts reveal an isotopic transition in mantle source material and/or degree of crustal interaction. In the east, many of the rocks are found to merge both chemically and isotopically with those previously reported from the Japanese and Taiwan island-arc terrains. In the west, clear evidence exists for component(s) of Late Archean continental lithosphere to be present in some samples. A major crustal structure, the Tan-Lu fault, marks the approximate boundary between continental margin and interior isotopic behaviors. Although the isotopic signature of the western basalts has characteristics of lower-crustal contamination, a subcrustal lithosphere, i.e. an attached mantle keel, is probably more likely to be the major contributor of their continental “flavor”. The transition from continental margin to interior is very pronounced for Pb isotopes, although Sr and Nd isotopes also combine to yield correlated patterns that deviate strikingly from the mid-ocean ridge basalt (MORB) and oceanic-island trends. The most distinctive chemical attribute of this continental lithosphere component is its diminished U/Pb as reflected in the Pb isotopic composition when compared to sources of MORB, oceanic-island and island-arc volcanic rocks. Somewhat diminished Sm/Nd and elevated Rb/Sr, especially in comparison to the depleted asthenospheric mantle, are also apparent from the Nd- and Sr-isotopic ratios.

Chemical Geology

A reconnaissance Rb-Sr, Sm-Nd, U-Pb, and K-Ar study of some host rocks and ore minerals in the West Shasta Cu- Zn district, California

The Copley Greenstone, Balaklala Rhyolite, and Mule Mountain stock in the West Shasta Cu-Zn district, California, have Rb-Sr, Sm-Nd, U-Pb, and K-Ar systematics that indicate they are a cogenetic suite of ensimatic island-arc rocks about 400 m.y. Pervasive alteration and mineralization of these rocks, for the most part, was syngenetic and the major component of the mineralizing fluid was Devonian seawater. K-Ar ages of quartz-sericite concentrates from ore horizons and Rb-Sr systematics of a few rock and ore specimens record a later thermal and mineralizing event in the district of about 260 m.y. Contamination of some rocks with pelagic sediments is indicated by the Sm-Nd data.

Economic Geology

Sm-Nd systematics of a tonalitic augen gneiss and its constituent minerals from northern Michigan

The Sm-Nd isotopic system of a tonalitic augen gneiss and its constituent minerals from northern Michigan was disturbed during metamorphism. Sm-Nd zircon ages are lower than the wholerock Sm-Nd model age. However, closely associated pairs of minerals (for example, sphene and biotite or apatite and plagioclase) retain their apparent metamorphic ages. The Sm-Nd model age for the tonalitic augen gneiss of 3919 ± 30 myr , appears to reflect open system behavior during metamorphism. A mineralogically different gneiss from the same location has a Sm-Nd model age of 3520 ± 70 myr . The two whole rocks differ in their Sm-Nd and Rb-Sr systematics and in their chondrite-normalized rare earth element (REE) patterns. The whole-rock-normalized mineral REE patterns show the contribution of the major and trace minerals to the REE content of the whole rock. The trace minerals contain a significant amount of the total REE.

Geochimica et Cosmochimica Acta

Trace element and strontium isotope characteristics of volcanic rocks from Isla Tortuga: A young seamount in the Gulf of California

Isla Tortuga is a small isolated central volcano which is located near an actively spreading trough in the Gulf of California. The basalt lavas from Tortuga which have the highest Mg/Fe and Ni contents have trace element abundances and ratios and 87 Sr/ 86 Sr which are similar to those of mid-ocean ridge tholeiite. The major element, rare earth element and Sr abundances of fractionated tholeiite (low Mg/Fe) and tholeiitic andesite of Tortuga are consistent with an origin by closed-system fractional crystallization. This hypothesis is not supported by K, Na, Rb and Ba abundances in the lavas nor by their variable 87 Sr/ 86 Sr (0.7024–0.7035). It is proposed that the apparent decoupling of light rare earth elements, other incompatible trace elements and 87 Sr/ 86 Sr is due to contamination of some Tortuga magmas while they are fractionated in a high-level crustal magma chamber. The mantle source of least-contaminated, high Mg/Fe basalt lavas of Tortuga is similar, although not identical to the source of normal mid-ocean ridge tholeiite; significant differences exist. The reasons for these differences are not yet known.

Earth and Planetary Science Letters