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At least 1,477 records · Page 82Linked to original sources
USGS2022

Estimates of metals contained in abyssal manganese nodules and ferromanganese crusts in the global ocean based on regional variations and genetic types of nodules

Deep-ocean ferromanganese crusts and manganese nodules are important marine repositories for global metals. Interest in these minerals as potential resources has led to detailed sampling in many regions of the global ocean, allowing for updated estimates of their global extent. Here, we present global estimates of total tonnage as well as contained metal concentrations and tonnages for ferromanganese crusts and manganese nodules using the most extensive compilation of geochemical data collected to date, along with updated boundaries of regions of interest for these minerals. We present results from mean composition calculated in two ways: first, a global flat average of regional mean compositions, and second, a regionally weighted average that considers differences in chemistry among genetic types and/or oceanographic and geologic settings for these mineral occurrences. For nodules, we use the three genetic types: (1) hydrogenetic, typified by nodules from the West Pacific Nodule Field and Penrhyn Basin; (2) diagenetic, typified by nodules from the Peru Basin; (3) mixed hydrogenetic-diagenetic, typified by nodules from the Clarion–Clipperton Zone and the Central Indian Ocean Basin, and Atlantic Ocean regional type hydrogenetic nodules. All crusts considered here are of hydrogenetic origin, which we divide into seven regional types that reflect a combination of ocean basin and other source inputs. Crust types include Arctic Ocean, Atlantic Ocean, Indian Ocean, Continental Margin, Prime Crust Zone (PCZ), North Pacific (non PCZ), and South Pacific. Based on our areal estimates, we find that abyssal regions likely to contain hydrogenetic-type nodules are by far the most widespread in the global ocean (47% of total area), Atlantic Ocean (28%) are next, followed by mixed diagenetic-hydrogenetic (22%) and diagenetic (3%) types. For crusts, the Prime Crust Zone is the most extensive global region (27% of total area) followed by South Pacific (20%), Indian Ocean (18%), North Pacific (12%), Continental Margins (11%), Atlantic Ocean (10%), and Arctic Ocean (2%) types. The global total tonnage estimates that we calculated from this method are 21 × 10 10 dry tons for manganese nodules, within the range of previous estimates, and 93 × 10 10 dry tons for ferromanganese crusts, which is 4.5 times higher than the 20 × 10 10 dry tons reported by Hein et al. (2003). This geology and oceanography driven approach to marine mineral quantification contrasts with estimates typically carried out for terrestrial mineral resource deposits. Nevertheless, these estimates and the data that support them demonstrate that marine minerals are an impressive repository for global metals.

Book chapter↗
USGS2023

The composition of Io

Io is unlike any other body in the Solar System making questions about its chemical composition especially interesting and challenging. This chapter examines the many different, but frustratingly indirect, constraints we have on the bulk composition of this restless moon. A detailed consideration of Io’s lavas is used to illustrate how decades of research have bounded, but not pinned down, the chemistry of Io. A self-consistent model for the core, mantle and crust is constructed based on a conventional chondritic composition but exotic alternatives cannot be ruled out. The study of Io’s composition should provide a fertile and exciting realm for future scientists.

Book chapter↗
USGS2025

Geochemical monitoring of volcanic fluids in the twenty-first century

This chapter reviews the state-of-the-art of geochemical volcano monitoring techniques. We cover in-situ monitoring technologies that rely on sampling fluids (direct sampling) and on instrumental analysis of the composition of such fluids in real-time (remote sensing of volcanic fluids is covered elsewhere in this book). We first review key concepts and principles in the field, and then review the results of some selected case studies and applications. We cover the large variety of fluid categories emitted by volcanoes, in both the near-(crater fumaroles and lakes, and plumes) and far-(degassing soils, groundwaters) fields. Our aim is to demonstrate the utility of measuring the chemistry of fluids released by volcanoes, and how these can help characterize volcano unrest, and eventually the increased likelihood of eruption. We conclude with a brief discussion of current challenges and knowledge gaps, and on future directions in geochemical monitoring.

Book chapter↗
USGS2025

Modeling byproduct and coproduct mine production and mineral substitution using multidimensional supply curves: Application to the Cu-Co-Ni system and beyond

Rapid demand growth is expected for many metals used in the energy transition. Many of these metals are byproducts of other commodities. Byproduct production’s price response is tied to host mineral economics, complicating its supply dynamics. Moreover, many of these metals are used in applications where the material properties desired are difficult to substitute; effectively, limiting how quickly demand can adapt to changes in commodity price. Previous work has demonstrated the interconnectivity of jointly produced mineral commodities from the supply side, where the copper–cobalt–nickel system was used and demand was assumed independent across commodities. Studies to understand byproduct-coproduct market interconnectivity on the demand side are limited, while studies on the interconnectivity of supply and demand simultaneously are even more so. We propose a modification to the multicommodity supply curve method to enable inter-commodity effects on demand simultaneous with supply. In batteries, high cobaltprices may push consumers to transition to high-nickel chemistries, causing the nickel demand surface to decrease with nickel price but increase with cobaltprice, creating a two-dimensional demand surface. Below cross-price elasticities of 0.05, inter-commodity effects were found to be negligible, potentially permitting exclusion of these effects for many commodities. This additional demand curve complexity introduces potential computation challenges alongside the capacity to model many interrelated commodity systems such as rare earth elements, ferroalloys, country-oriented subsidies or restrictions, and bifurcated sustainable metals markets. By presenting the work done on multicommodity supply surfaces to date and potential new directions, this work aims to catalyze the next round of innovative approaches to modeling jointly produced commodities.

Conference Paper↗
USGS2016

Soil moisture and biogeochemical factors influence the distribution of annual Bromus species

Abiotic factors have a strong influence on where annual Bromus species are found. At the large regional scale, temperature and precipitation extremes determine the boundaries of Bromus occurrence. At the more local scale, soil characteristics and climate influence distribution, cover, and performance. In hot, dry, summer-rainfall-dominated deserts (Sonoran, Chihuahuan), little or no Bromus is found, likely due to timing or amount of soil moisture relative to Bromus phenology. In hot, winter-rainfall-dominated deserts (parts of the Mojave Desert), Bromus rubens is widespread and correlated with high phosphorus availability. It also responds positively to additions of nitrogen alone or with phosphorus. On the Colorado Plateau, with higher soil moisture availability, factors limiting Bromus tectorum populations vary with life stage: phosphorus and water limit germination, potassium and the potassium/magnesium ratio affect winter performance, and water and potassium/magnesium affect spring performance. Controlling nutrients also change with elevation. In cooler deserts with winter precipitation (Great Basin, Columbia Plateau) and thus even greater soil moisture availability, B. tectorum populations are controlled by nitrogen, phosphorus, or potassium. Experimental nitrogen additions stimulate Bromus performance. The reason for different nutrients limiting in dissimilar climatic regions is not known, but it is likely that site conditions such as soil texture (as it affects water and nutrient availability), organic matter, and/or chemistry interact in a manner that regulates nutrient availability and limitations. Under future drier, hotter conditions, Bromus distribution is likely to change due to changes in the interaction between moisture and nutrient availability.

Book chapter↗
USGS2016

Lake transparency: a window into decadal variations in dissolved organic carbon concentrations in Lakes of Acadia National Park, Maine

A forty year time series of Secchi depth observations from approximately 25 lakes in Acadia National Park, Maine, USA, evidences large variations in transparency between lakes but relatively little seasonal cycle within lakes. However, there are coherent patterns over the time series, suggesting large scale processes are responsible. It has been suggested that variations in colored dissolved organic matter (CDOM) are primarily responsible for the variations in transparency, both between lakes and over time and further that CDOM is a robust optical proxy for dissolved organic carbon (DOC). Here we present a forward model of Secchi depth as a function of DOC based upon first principles and bio-optical relationships. Inverting the model to estimate DOC concentration from Secchi depth observations compared well with the measured DOC concentrations collected since 1995 (RMS error < 1.3 mg C l-1). This inverse model allows the time series of DOC to be extended back to the mid 1970s when only Secchi depth observations were collected, and thus provides a means for investigating lake response to climate forcing, changing atmospheric chemistry and watershed characteristics, including land cover and land use.

Book chapter↗
USGS2013

A geochemical and geophysical assessment of coastal groundwater discharge at select sites in Maui and O’ahu, Hawai’i

This chapter summarizes fieldwork conducted to derive new estimates of coastal groundwater discharge and associated nutrient loadings at select coastal sites in Hawai’i, USA. Locations for this work were typically identified based on pronounced, recent ecosystem degradation that may at least partially be attributable to sustained coastal groundwater discharge. Our suite of tools used to evaluate groundwater discharge included select U/Th series radionuclides, a broad spectrum of geochemical analytes, multi-channel electrical resistivity, and in situ oceanographic observations. Based on the submarine groundwater discharge tracer 222Rn, coastal groundwater discharge rates ranged from about 22–50 cm per day at Kahekili, a site in the Ka’anapali region north of Lahaina in west Maui, while at Black Point in Maunalua Bay along southern O’ahu, coastal groundwater discharge rates ranged up to 700 cm per day, although the mean discharge rate at this site was 60 cm per day. The water chemistry of the discharging groundwater can be dramatically different than ambient seawater at both coastal sites. For example, at Kahekili the average concentrations of dissolved inorganic nitrogen (DIN), dissolved silicate (DSi) and total dissolved phosphorus (TDP) were roughly 188-, 36-, and 106-times higher in the discharging groundwater relative to ambient seawater, respectively. Such data extend our basic understanding of the physical controls on coastal groundwater discharge and provide an estimate of the magnitude and physical forcings of submarine groundwater discharge and associated trace metal and nutrient loads conveyed by this submarine route.

Hawaii↗
USGS2013

Ecosystem services: developing sustainable management paradigms based on wetland functions and processes

In the late nineteenth century and twentieth century, there was considerable interest and activity to develop the United States for agricultural, mining, and many other purposes to improve the quality of human life standards and prosperity. Most of the work to support this development was focused along disciplinary lines with little attention focused on ecosystem service trade-offs or synergisms, especially those that transcended boundaries of scientific disciplines and specific interest groups. Concurrently, human population size has increased substantially and its use of ecosystem services has increased more than five-fold over just the past century. Consequently, the contemporary landscape has been highly modified for human use, leaving behind a fragmented landscape where basic ecosystem functions and processes have been broadly altered. Over this period, climate change also interacted with other anthropogenic effects, resulting in modern environmental problems having a complexity that is without historical precedent. The challenge before the scientific community is to develop new science paradigms that integrate relevant scientific disciplines to properly frame and evaluate modern environmental problems in a systems-type approach to better inform the decision-making process. Wetland science is a relatively new discipline that grew out of the conservation movement of the early twentieth century. In the United States, most of the conservation attention in the earlier days was on wildlife, but a growing human awareness of the importance of the environment led to the passage of the National Environmental Policy Act in 1969. Concurrently, there was a broadening interest in conservation science, and the scientific study of wetlands gradually gained acceptance as a scientific discipline. Pioneering wetland scientists became formally organized when they formed The Society of Wetland Scientists in 1980 and established a publication outlet to share wetland research findings. In comparison to older and more traditional scientific disciplines, the wetland sciences may be better equipped to tackle today’s complex problems. Since its emergence as a scientific discipline, the study of wetlands has frequently required interdisciplinary and integrated approaches. This interdisciplinary/integrated approach is largely the result of the fact that wetlands cannot be studied in isolation of upland areas that contribute surface and subsurface water, solutes, sediments, and nutrients into wetland basins. However, challenges still remain in thoroughly integrating the wetland sciences with scientific disciplines involved in upland studies, especially those involved with agriculture, development, and other land-conversion activities that influence wetland hydrology, chemistry, and sedimentation. One way to facilitate this integration is to develop an understanding of how human activities affect wetland ecosystem services, especially the trade-offs and synergisms that occur when land-use changes are made. Used in this context, an understanding of the real costs of managing for a particular ecosystem service or groups of services can be determined and quantified in terms of reduced delivery of other services and in overall sustainability of the wetland and the landscapes that support them. In this chapter, we discuss some of the more salient aspects of a few common wetland types to give the reader some background on the diversity of functions that wetlands perform and the specific ecosystem services they provide to society. Wetlands are among the most complex ecosystems on the planet, and it is often difficult to communicate to a diverse public all of the positive services wetlands provide to mankind. Our goal is to help the reader develop an understanding that management options can be approached as societal choices where decisions can be made within a spatial and temporal context to identify trade-offs, synergies, and effects on long-term sustainability of wetland ecosystems. This will be especially relevant as we move into alternate climate futures where our portfolio of management options for mitigating damage to ecosystem function or detrimental cascading effects must be diverse and effective.

Book chapter↗
USGS2017

Application of molluscan analyses to the reconstruction of past environmental conditions in estuaries

Molluscs possess a number of attributes that make them an excellent source of past environmental conditions in estuaries: they are common in estuarine environments; they typically have hard shells and are usually well preserved in sediments; they are relatively easy to detect in the environment; they have limited mobility as adults; they grow by incremental addition of layers to their shells; and they are found in all the major environments surrounding estuaries—terrestrial, freshwater, brackish, and marine waters. Analysis of molluscan assemblages can contribute information about past changes in sea level, climate, land use patterns, anthropogenic alterations, salinity, and other parameters of the benthic habitat and water chemistry within the estuary. High-resolution (from less than a day to annual) records of changes in environmental parameters can be obtained by analyzing the incremental growth layers in mollusc shells (sclerochronology). The shell layers retain information on changes in water temperature, salinity, seasonality, climate, river discharge, productivity, pollution and human activity. Isotopic analyses of mollusc shell growth layers can be problematic in estuaries where water temperatures and isotopic ratios can vary simultaneously; however, methods are being developed to overcome these problems. In addition to sclerochronology, molluscs are important to Holocene and Pleistocene estuarine palaeoenvironmental studies because of their use in the development of age models through radiocarbon dating, amino acid racemization, uranium-thorium series dating, and electron spin resonance (ESR) dating.

Book chapter↗
USGS1996

Episodic acidification of a coastal plain stream in Virginia

This study investigates the episodic acidification of Reedy Creek, a wetland-influenced coastal plain stream near Richmond, Virginia. Primary objectives of the study were to quantify the episodic variability of acid- base chemistry in Reedy Creek, to examine the seasonal variability in episodic response and to explain the hydrological and geochemical factors that contribute to episodic acidification. Chemical response was similar in each of the seven storms examined, however, the ranges in concentrations observed were commonly greater in summer/fall storms than in winter/spring storms. An increase in SO4/2- concentration with discharge was observed during all storms and peak concentration occurred at or near peak flow. Small increases in Mg2+, Ca2+, K+ concentrations and dissolved organic carbon (DOC) were observed during most storms. At the same time, ANC, Na+ and Cl- concentrations usually decreased with increasing discharge. In summer/fall storms, the absolute increase in SO4/2- concentration was one-third to 15 times the increase observed in winter/spring storms; the decrease in ANC during summer/fall storms was usually within the range of the decrease observed in winter/spring storms. In contrast, the decrease in Na+ and Cl- concentrations during winter/spring storms was much greater than that observed during summer/fall storms. Data show that while base flow anion deficit was higher in summer/fall than in winter/spring, anion deficit decreased during most summer/fall storms. In contrast, base flow anion deficit was lower in spring and winter, but increased during winter/spring storms. Increased SO4/2- concentration was the main cause of episodic acidification during storms at Reedy Creek, but increased anion deficit indicates organic acids may contribute to episodic acidification during winter/spring storms. Changes in SO4/2- concentration coincident with the hydrograph rise indicate quick routing of water through the watershed. Saturation overland flow appears to be the likely mechanism by which solutes are transported to the stream during storm flow.

Water, Air, & Soil Pollution↗
USGS1989

Late Quaternary paleolimnology of Walker Lake, Nevada

Diatoms, crustaceans, and pollen from sediment cores, in conjunction with dated shoreline tufas provide evidence for lake level and environmental fluctuations of Walker Lake in the late Quaternary. Large and rapid changes of lake chemistry and level apparently resulted from variations in the course and discharge of the Walker River. Paleolimnological evidence suggests that the basin contained a relatively deep and slightly saline to freshwater lake before ca. 30 000 years B.P. During the subsequent drawdown, the Walker River apparently shifted its course and flowed northward into the Carson Sink. As a result, Walker Lake shallowed and became saline. During the full glacial, cooler climates with more effective moisture supported a shallow brine lake in the basin even without the Walker River. As glacial climates waned after 15 000 years ago, Walker Lake became a playa. The Walker River returned to its basin 4700 years ago, filling it with fresh water in a few decades. Thereafter, salinity and depth increased as evaporation concentrated inflowing water, until by 3000 years ago Walker Lake was nearly 90 m deep, according to dated shoreline tufas. Lake levels fluctuated throughout this interval in response to variations in Sierra Nevada precipitation and local evaporation. A drought in the Sierras between 2400 and 2000 years ago reduced Walker Lake to a shallow, brine lake. Climate-controlled refilling of the lake beginning 2000 years ago required about one millennium to bring Walker lake near its historic level. Through time, lake basins in the complex Lake Lahontan system, fill and desiccate in response to climatic, tectonic and geomorphic events. Detailed, multidisciplinary paleolimnologic records from related subbasins are required to separate these processes before lake level history can be reliably used to interpret paleoclimatology. ?? 1989 Kluwer Academic Publishers.

Journal of Paleolimnology↗
USGS1992

Mount St. Helens a decade after the 1980 eruptions: magmatic models, chemical cycles, and a revised hazards assessment

Available geophysical and geologic data provide a simplified model of the current magmatic plumbing system of Mount St. Helens (MSH). This model and new geochemical data are the basis for the revised hazards assessment presented here. The assessment is weighted by the style of eruptions and the chemistry of magmas erupted during the past 500 years, the interval for which the most detailed stratigraphic and geochemical data are available. This interval includes the Kalama (A. D. 1480-1770s?), Goat Rocks (A.D. 1800-1857), and current eruptive periods. In each of these periods, silica content decreased, then increased. The Kalama is a large amplitude chemical cycle (SiO2: 57%-67%), produced by mixing of arc dacite, which is depleted in high field-strength and incompatible elements, with enriched (OIB-like) basalt. The Goat Rocks and current cycles are of small amplitude (SiO2: 61%-64% and 62%-65%) and are related to the fluid dynamics of magma withdrawal from a zoned reservoir. The cyclic behavior is used to forecast future activity. The 1980-1986 chemical cycle, and consequently the current eruptive period, appears to be virtually complete. This inference is supported by the progressively decreasing volumes and volatile contents of magma erupted since 1980, both changes that suggest a decreasing potential for a major explosive eruption in the near future. However, recent changes in seismicity and a series of small gas-release explosions (beginning in late 1989 and accompanied by eruption of a minor fraction of relatively low-silica tephra on 6 January and 5 November 1990) suggest that the current eruptive period may continue to produce small explosions and that a small amount of magma may still be present within the conduit. The gas-release explosions occur without warning and pose a continuing hazard, especially in the crater area. An eruption as large or larger than that of 18 May 1980 (???0.5 km3 dense-rock equivalent) probably will occur only if magma rises from an inferred deep (???7 km), relative large (5-7 km3) reservoir. A conservative approach to hazard assessment is to assume that this deep magma is rich in volatiles and capable of erupting explosively to produce voluminous fall deposits and pyroclastic flows. Warning of such an eruption is expectable, however, because magma ascent would probably be accompanied by shallow seismicity that could be detected by the existing seismic-monitoring system. A future large-volume eruption (???0.1 km3) is virtually certain; the eruptive history of the past 500 years indicates the probability of a large explosive eruption is at least 1% annually. Intervals between large eruptions at Mount St. Helens have varied widely; consequently, we cannot confidently forecast whether the next large eruption will be years decades, or farther in the future. However, we can forecast the types of hazards, and the areas that will be most affected by future large-volume eruptions, as well as hazards associated with the approaching end of the current eruptive period. ?? 1992 Springer-Verlag.

Bulletin of Volcanology↗
USGS1991

Metasomatic oxidation of upper mantle periodotite

Examination of Fe3+ in metasomatized spinel peridotite xenoliths reveals new information about metasomatic redox processes. Composite xenoliths from Dish Hill, California possess remnants of magmatic dikes which were the sources of the silicate fluids responsible for metasomatism of the peridotite part of the same xenoliths. Mo??ssbauer spectra of mineral separates taken at several distances from the dike remnants provide data on Fe3+ contents of minerals in the metasomatized peridotite. Clinopyroxenes contain 33% of total iron (FeT) as Fe3+ (Fe3+/FeT=0.33); orthopyroxenes contain 0.06-0.09 Fe3+/FeT; spinels contain 0.30-0.40 Fe3+/FeT; olivines contain 0.01-0.06 Fe3+/FeT; and metasomatic amphibole in the peridotite contains 0.85-0.90 Fe3+/FeT. In each mineral, Fe3+ and Fe2+ cations per formula unit (p.f.u.) decrease with distance from the dike, but the Fe3+/FeT ratios of each mineral do not vary. Clinopyroxene, spinel, and olivine Fe3+/FeT ratios are significantly higher than in unmetasomatized spinel peridotites. Metasomatic changes in Fe3+/FeT ratios in each mineral are controlled by the oxygen fugacity of the system, but the mechanism by which each phase accommodates this ratio is affected by crystal chemistry, kinetics, rock mode, fluid composition, fluid/rock ratio, and fluid-mineral partition coefficients. Ratio increases in pyroxene and spinel occur by exchange reactions involving diffusion of Fe3+ into existing mineral grains rather than by oxidation of existing Fe2+ in peridotite mineral grains. The very high Fe3+/FeT ratio in the metasomatic amphibole may be a function of the high Fe3+/FeT of the metasomatic fluid, crystal chemical limitations on the amount of Fe3+ that could be accommodated by the pyroxene, spinel, and olivine of the peridotite, and the ability of the amphibole structure to accommodate large amounts of 3 + valence cations. In the samples studied, metasomatic amphibole accounts for half of the bulk-rock Fe2O3. This suggests that patent metasomatism may produce a greater change in the redox state of mantle peridotite than cryptic metasomatism. Comparison of the metasomatized samples with unmetasomatized peridotites reveals that both Fe2+ and Fe3+ cations p.f.u. were increased during metasomatism and 50% or more of iron added was Fe3+. With increasing distance from the dike, the ratio of added Fe3+ to added Fe2+ increases. The high Fe3+/FeT of amphibole and phlogopite in the dikes and in the peridotite, and the high ratios of added Fe3+/added Fe2+ in pyroxenes and spinel suggest that the Fe3+/FeT ratio of the metasomatic silicate fluid was high. As the fluid perolated through and reacted with the peridotite, Fe3+ and C-O-H volatile species were concentrated in the fluid, increasing the fluid Fe3+/FeT. ?? 1991 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1996

Sediment quality triad assessment survey of the Galveston Bay, Texas system

To characterize the quality of sediments at key sites in the Galveston Bay Estuary, sediment samples were collected concurrently for chemical and physical analyses, toxicity testing and an assessment of benthic community structure. Significant toxicity, as determined by the sea urchin ( Arbacia punetulata ) pore water embryological development assay, was observed at 12 of the 24 sites investigated in this study. No toxicity was observed at any of the sites with the amphipod ( Grandidierella japonica ) solid-phase test. There were a number of sites with elevated levels of trace metals and petroleum hydrocarbons. The chemistry, toxicity and benthic data were ranked by station and a scaled rank sum was calculated to facilitate comparisons among the stations. Five sites exhibited strong evidence of contaminant-induced degradation, while 15 stations showed no evidence of contaminant-induced degradation. At eight additional sites the sediment quality triad (SQT) data indicated that unmeasured chemicals or conditions were stressing the system. Contaminant impacts could be reduced or eliminated by alternative regulatory and management practices, including the restriction of produced water discharges into coastal estuaries and the use of dredge material disposal practices that minimize the reintroduction of sediment-associated contaminants to the bays.

Texas↗
USGS1967

Mineral and chemical variations within an ash-flow sheet from Aso caldera, Southwestern Japan

Although products of individual volcanic eruptions, especially voluminous ash-flow eruptions, have been considered among the best available samples of natural magmas, detailed petrographic and chemical study indicates that bulk compositions of unaltered Pleistocene ash-flow tuffs from Aso caldera, Japan, deviate significantly from original magmatic compositions. The last major ash-flow sheet from Aso caldera is as much as 150 meters thick and shows a general vertical compositional change from phenocryst-poor rhyodacite upward into phenocryst-rich trachyandesite; this change apparently reflects in inverse order a compositionally zoned magma chamber in which more silicic magma overlay more mafic magma. Details of these magmatic variations were obscured, however, by: (1) mixing of compositionally distinct batches of magma during upwelling in the vent, as indicated by layering and other heterogeneities within single pumice lumps; (2) mixing of particulate fragments-pumice lumps, ash, and phenocrysts-of varied compositions during emplacement, with the result that separate pumice lenses from a single small outcrop may have a compositional range nearly as great as the bulk-rook variation of the entire sheet; (3) density sorting of phenocrysts and ash during eruption and emplacement, resulting in systematic modal variations with distance from the caldera; (4) addition of xenocrysts, resulting in significant contamination and modification of proportions of crystals in the tuffs; and (5) ground-water leaching of glassy fractions during hydration after cooling. Similar complexities characterize ash-flow tuffs under study in southwestern Nevada and in the San Juan Mountains, Colorado, and probably are widespread in other ash-flow fields as well. Caution and careful planning are required in study of the magmatic chemistry and phenocryst mineralogy of these rocks. ?? 1967 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1976

Serpentinization and alteration in an olivine cumulate from the Stillwater Complex, Southwestern Montana

Some of the olivine cumulates of the Ultramafic zone of the Stillwater Complex, Montana, are progressively altered to serpentine minerals and thompsonite. Lizardite and chrysotile developed in the cumulus olivine and postcumulus pyroxenes; thompsonite developed in postcumulus plagioclase. The detailed mineralogy, petrology, and chemistry indicate that olivine and plagioclase react to form the alteration products, except for H 2 O, without changes in the bulk composition of the rocks.

Montana↗
USGS1981

Stable isotope systematics in mesozoic granites of Central and Northern California and Southwestern Oregon

18O, D, and H2O+ contents were measured for whole-rock specimens of granitoid rocks from 131 localitics in California and southwestern Oregon. With 41 new determinations in the Klamath Mountains and Sierra Nevada, initial strontium isotope ratios are known for 104 of these samples. Large variations in ??18O (5.5 to 12.4), ??D (-130 to -31), water contents (0.14 to 2.23 weight percent) and initial strontium isotope ratios (0.7028 to 0.7095) suggest a variety of source materials and identify rocks modified by secondary processes. Regular patterns of variation in each isotopic ratio exist over large geographical regions, but correlations between the ratios are generally absent except in restricted areas. For example, the regular decrease in ??D values from west to east in the Sierra Nevada batholith is not correlative with a quite complex pattern of ??18O values, implying that different processes were responsible for the isotopic variations in these two elements. In marked contrast to a good correlation between (87Sr/86Sr)o and ??18O observed in the Peninsular Ranges batholith to the south, such correlations are lacking except in a few areas. ??D values, on the other hand, correlate well with rock types, chemistry, and (87Sr/86Sr)o except in the Coast Ranges where few of the isotopic signatures are primary. The uniformly low ??D values of samples from the Mojave Desert indicate that meteoric water contributed much of the hydrogen to the rocks in that area. Even so, the ??18O values and 18O fractionations between quartz and feldspar are normal in these same rocks. This reconnaissance study has identified regularities in geochemical parameters over enormous geographical regions. These patterns are not well understood but merit more detailed examination because they contain information critical to our understanding of the development of granitoid batholiths. ?? 1981 Springer-Verlag.

Contributions to Mineralogy and Petrology↗
USGS1984

Sm-Nd, K-Ar and petrologic study of some kimberlites from eastern United States and their implication for mantle evolution

We provide new data on Sm-Nd systematics, K-Ar dating and the major element chemistry of kimberlites from the eastern United States (mostly from central New York State) and their constituent mineral phases of olivine, clinopyroxene, garnet, phlogopite and perovskite. In addition, we report Nd-isotopes in a few kimberlites from South Africa, Lesotho and from the eastern part of China. The major element compositions of the New York dike rocks and of their constituent minerals including a xenolith of eclogite are comparable with those from the Kimberley area in South Africa. The K-Ar age of emplacement of the New York dikes is further established to be 143 Ma. We have analyzed the Nd-isotopic composition of the following kimberlites and related rocks: Nine kimberlite pipes from South Africa and Lesotho, two from southern India; one from the U.S.S.R., fifteen kimberlite pipes and related dike rocks from eastern and central U.S. and two pipes from the Shandong Province of eastern China. The age of emplacement of these kimberlites ranges from 1300 million years to 90 million years. The initial Nd-isotopic compositions of these kimberlitic rocks expressed as e{open}NdIwith respect to a chondritic bulk-earth growth-curve show a range between 0 and +4, with the majority of the kimberlites being in the range 0 to +2. This range is not matched by any other suite of mantle-derived igneous rocks. This result strengthens our earlier conclusion that kimberlitic liquids are derived from a relatively primeval and unique mantle reservoir with a nearly chondritic Sm/Nd ratio. ?? 1984 Springer-Verlag.

Contributions to Mineralogy and Petrology↗