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At least 1,657 records · Page 92Linked to original sources

USGS2003

Heavy metals and metalloids in egg contents and eggshells of passerine birds from Arizona

Concentrations of inorganic elements were determined in eggs of passerine birds including the endangered southwestern willow flycatcher ( Empidonax traillii extimus ) from four regions in Arizona. The main aim of the study was to determine the distribution of metals in egg contents and eggshells, with emphasis on the deposition of Sr in eggshells. Seventy eggs of 11 passerine species were collected at four nesting locations during 2000. Aluminum, Ba, Cr, Cu, Mn, Se, Sr, and Zn, were detected primarily in egg contents of all bird species. Arsenic, Ni, Pb, and V were detected primarily in eggshells. A proportion of most inorganic elements accumulated in the eggshell. Concentrations of Ba, Cu, Mn, Se, Sr, and Zn in egg contents and As, Ba, Cu, and V in eggshells of yellow-breasted chats ( Icteria virens ) were similar among locations. However, concentrations of Mn, Ni, Sr, and Zn in eggshells were significant different among locations. Except for Cu, Mn, Se, and Zn, concentrations of inorganic elements were 2–35 times greater in eggshells than in eggs. Most concentrations of metals and metalloids in eggs and eggshells of all the bird species were below levels known to affect reproduction or that have other deleterious effects. However, I found somewhat elevated concentrations of Sr in eggshells (highest mean=1505 μg/g dw, n =3) of yellow-breasted chats and willow flycatchers, and in egg contents of yellow warblers ( Dendroica petechia) and song sparrows ( Melospiza melodia ). Whether current observed concentrations of Sr in eggshells are affecting nesting birds in Arizona remains to be determined. Strontium and other metals could be associated with lower hatching success in some areas. This study shows that a proportion of many inorganic elements accumulates in the eggshell and that the potential effects on the proper structure and functioning of the eggshell should not be ignored.

Environmental Pollution↗

USGS1998

Parallel iterative solution for h and p approximations of the shallow water equations

A p finite element scheme and parallel iterative solver are introduced for a modified form of the shallow water equations. The governing equations are the three-dimensional shallow water equations. After a harmonic decomposition in time and rearrangement, the resulting equations are a complex Helmholz problem for surface elevation, and a complex momentum equation for the horizontal velocity. Both equations are nonlinear and the resulting system is solved using the Picard iteration combined with a preconditioned biconjugate gradient (PBCG) method for the linearized subproblems. A subdomain-based parallel preconditioner is developed which uses incomplete LU factorization with thresholding (ILUT) methods within subdomains, overlapping ILUT factorizations for subdomain boundaries and under-relaxed iteration for the resulting block system. The method builds on techniques successfully applied to linear elements by introducing ordering and condensation techniques to handle uniform p refinement. The combined methods show good performance for a range of p (element order), h (element size), and N (number of processors). Performance and scalability results are presented for a field scale problem where up to 512 processors are used.

Advances in Water Resources↗

USGS1999

Occurrence and transport of total mercury and methyl mercury in the Sacramento River Basin, California

Mercury poses a water-quality problem for California's Sacramento River, a large river with a mean annual discharge of over 650 m3/s. This river discharges into the San Francisco Bay, and numerous fish species of the bay and river contain mercury levels high enough to affect human health if consumed. Two possible sources of mercury are the mercury mines in the Coast Ranges and the gold mines in the Sierra Nevada. Mercury was once mined in the Coast Ranges, west of the Sacramento River, and used to process gold in the Sierra Nevada, east of the river. The mineralogy of the Coast Ranges mercury deposits is mainly cinnabar (HgS), but elemental mercury was used to process gold in the Sierra Nevada. Residual mercury from mineral processing in the Sierra Nevada is mainly in elemental form or in association with oxide particles or organic matter and is biologically available. Recent bed-sediment sampling, at sites below large reservoirs, showed elevated levels of total mercury (median concentration 0.28 ??g/g) in every large river (the Feather, Yuba, Bear, and American rivers) draining the Sierra Nevada gold region. Monthly sampling for mercury in unfiltered water shows relatively low concentrations during the nonrainy season in samples collected throughout the Sacramento River Basin, but significantly higher concentrations following storm-water runoff. Measured concentrations, following storm-water runoff, frequently exceeded the state of California standards for the protection of aquatic life. Results from the first year of a 2-year program of sampling for methyl mercury in unfiltered water showed similar median concentrations (0.1 ng/l) at all sampling locations, but with apparent high seasonal concentrations measured during autumn and winter. Methyl mercury concentrations were not significantly higher in rice field runoff water, even though rice production involves the creation of seasonal wetlands: higher rates of methylation are known to occur in stagnant wetland environments that have high dissolved carbon.Mercury poses a water-quality problem for California's Sacramento River, a large river with a mean annual discharge of over 650 m3/s. This river discharges into the San Francisco Bay, and numerous fish species of the bay and river contain mercury levels high enough to affect human health if consumed. Two possible sources of mercury are the mercury mines in the Coast Ranges and the gold mines in the Sierra Nevada. Mercury was once mined in the Coast Ranges, west of the Sacramento River, and used to process gold in the Sierra Nevada east of the river. The mineralogy of the Coast Ranges mercury deposits is mainly cinnabar (HgS), but elemental mercury was used to process gold in the Sierra Nevada. Residual mercury from mineral processing in the Sierra Nevada is mainly in elemental form or in association with oxide particles or organic matter and is biologically available. Recent bed-sediment sampling, at sites below large reservoirs, showed elevated levels of total mercury (median concentration 0.28 ??g/g) in every large river (the Feather, Yuba, Bear, and American rivers) draining the Sierra Nevada gold region. Monthly sampling for mercury in unfiltered water shows relatively low concentrations during the nonrainy season in samples collected throughout the Sacramento River Basin, but significantly higher concentrations following storm-water runoff. Measured concentrations, following storm-water runoff, frequently exceeded the state of California standards for the protection of aquatic life. Results from the first year of a 2-year program of sampling for methyl mercury in unfiltered water showed similar median concentrations (0.1 ng/l) at all sampling locations, but with apparent high seasonal concentrations measured during autumn and winter. Methyl mercury concentrations were not significantly higher in rice field runoff water, even though rice production involves the creation of seasonal wetlands: higher rates of methylation a

Journal of Geochemical Exploration↗

USGS1997

Arsenic and lead concentrations in the Pond Creek and Fire Clay coal beds, eastern Kentucky coal field

The Middle Pennsylvanian Breathitt Formation (Westphalian B) Pond Creek and Fire Clay coal beds are the 2 largest producing coal beds in eastern Kentucky. Single channel samples from 22 localities in the Pond Creek coal bed were obtained from active coal mines in Pike and Martin Countries, Kentucky, and a total of 18 Fire Clay coal bed channel samples were collected from localities in the central portion of the coal field. The overall objective of this study was to investigate the concentration and distribution of potentially hazardous elements in the Fire Clay and Pond Creek coal beds, with particular emphasis on As and Pb, 2 elements that are included in the 1990 Clean Air Act Amendments as potential air toxics. The 2 coals are discussed individually as the depositional histories are distinct, the Fire Clay coal bed having more sites where relatively high-S lithologies are encountered. In an effort to characterize these coals, 40 whole channel samples, excluding 1-cm partings, were analyzed for major, minor and trace elements by X-ray fluorescence and proton-induced X-ray emission spectroscopy. Previously analyzed samples were added to provide additional geographic coverage and lithotype samples from one site were analyzed in order to provide detail of vertical elemental trends. The As and Pb levels in the Fire Clay coal bed tend to be higher than in the Pond Creek coal bed. One whole channel sample of the Fire Clay coal bed contains 1156 ppm As (ash basis), with a single lithotype containing 4000 ppm As (ash basis). Most of the As and Pb appears to be associated with pyrite, which potentially can be removed in beneficiation (particularly coarser pyrite). Disseminated finer pyrite may not be completely removable by cleaning. In the examination of pyrite conducted in this study, it does not appear that significant concentration of As or Pb occurs in the finer pyrite forms. The biggest potential problem of As- or Pb-enriched pyrite is, therefore, one of refuse disposal.

Applied Geochemistry↗

USGS2019

Laser-induced breakdown spectroscopy

Laser-Induced Breakdown Spectroscopy (LIBS) is the remote elemental analysis technique used by the ChemCam instrument on the Curiosity rover. LIBS involves remotely ablating material from rocks and soils with a focused high-energy laser, which generates an optically excited plasma from which the elements in the rock or soil sample are quantitatively determined. The LIBS technique offers many advantages for remote chemical analysis. LIBS provides very rapid analyses without the need for any sample preparation. LIBS is capable of detecting all elements present above the detection limits independent of the atomic mass. LIBS quantitative analysis continues to evolve and produce accurate compositions with decreasing uncertainties. Furthermore, the matrix effects that tend to complicate most elemental analysis techniques like LIBS are increasingly exploited to extract more sample details. The focus of this chapter is to describe the current state of LIBS chemical analysis for remote planetary science.

Book chapter↗

USGS2012

A new basaltic glass microanalytical reference material for multiple techniques

The U.S. Geological Survey (USGS) has been producing reference materials since the 1950s. Over 50 materials have been developed to cover bulk rock, sediment, and soils for the geological community. These materials are used globally in geochemistry, environmental, and analytical laboratories that perform bulk chemistry and/or microanalysis for instrument calibration and quality assurance testing. To answer the growing demand for higher spatial resolution and sensitivity, there is a need to create a new generation of microanalytical reference materials suitable for a variety of techniques, such as scanning electron microscopy/X-ray spectrometry (SEM/EDS), electron probe microanalysis (EPMA), laser ablation inductively coupled mass spectrometry (LA-ICP-MS), and secondary ion mass spectrometry (SIMS). As such, the microanalytical reference material (MRM) needs to be stable under the beam, be homogeneous at scales of better than 10–25 micrometers for the major to ultra-trace element level, and contain all of the analytes (elements or isotopes) of interest. Previous development of basaltic glasses intended for LA-ICP-MS has resulted in a synthetic basaltic matrix series of glasses (USGS GS-series) and a natural basalt series of glasses (BCR-1G, BHVO-2G, and NKT-1G). These materials have been useful for the LA-ICP-MS community but were not originally intended for use by the electron or ion beam community. A material developed from start to finish with intended use in multiple microanalytical instruments would be useful for inter-laboratory and inter-instrument platform comparisons. This article summarizes the experiments undertaken to produce a basalt glass reference material suitable for distribution as a multiple-technique round robin material. The goal of the analytical work presented here is to demonstrate that the elemental homogeneity of the new glass is acceptable for its use as a reference material. Because the round robin exercise is still underway, only nominal compositional ranges for each element are given in the article.

Microscopy Today↗

USGS2011

Interagency partnering for weed prevention-- Progress on development of a National Early Detection and Rapid Response System for Invasive Plants in the United States

Over the past 50 years, experience has shown that interagency groups provide an effective forum for addressing various invasive species issues and challenges on multiple land units. However, more importantly, they can also provide a coordinated framework for early detection, reporting, identification and vouchering, rapid assessment, and rapid response to new and emerging invasive plants in the United States. Interagency collaboration maximizes the use of available expertise, resources, and authority for promoting early detection and rapid response (EDRR) as the preferred management option for addressing new and emerging invasive plants. Currently, an interagency effort is underway to develop a National EDRR System for Invasive Plants in the United States. The proposed system will include structural and informational elements. Structural elements of the system include a network of interagency partner groups to facilitate early detection and rapid response to new invasive plants, including the Federal Interagency Committee for the Management of Noxious and Exotic Weeds (FICMNEW), State Invasive Species Councils, State Early Detection and Rapid Response Coordinating Committees, State Volunteer Detection and Reporting Networks, Invasive Plant Task Forces, and Cooperative Weed Management Areas. Informational elements and products being developed include Regional Invasive Plant Atlases, and EDRR Guidelines for EDRR Volunteer Network Training, Rapid Assessment and Rapid Response, and Criteria for Selection of EDRR Species. System science and technical support elements which are provided by cooperating state and federal scientists, include EDRR guidelines, training curriculum for EDRR volunteers and agency field personnel, plant identification and vouchering, rapid assessments, as well as predictive modeling and ecological range studies for invasive plant species.

Book chapter↗

USGS2005

Chemical loading into surface water along a hydrological, biogeochemical, and land use gradient: A holistic watershed approach

Identifying the sources and impacts of organic and inorganic contaminants at the watershed scale is a complex challenge because of the multitude of processes occurring in time and space. Investigation of geochemical transformations requires a systematic evaluation of hydrologic, landscape, and anthropogenic factors. The 1160 km 2 Boulder Creek Watershed in the Colorado Front Range encompasses a gradient of geology, ecotypes, climate, and urbanization. Streamflow originates primarily as snowmelt and shows substantial annual variation. Water samples were collected along a 70-km transect during spring-runoff and base-flow conditions, and analyzed for major elements, trace elements, bulk organics, organic wastewater contaminants (OWCs), and pesticides. Major-element and trace-element concentrations were low in the headwaters, increased through the urban corridor, and had a step increase downstream from the first major wastewater treatment plant (WWTP). Boron, gadolinium, and lithium were useful inorganic tracers of anthropogenic inputs. Effluent from the WWTP accounted for as much as 75% of the flow in Boulder Creek and was the largest chemical input. Under both hydrological conditions, OWCs and pesticides were detected in Boulder Creek downstream from the WWTP outfall as well as in the headwater region, and loads of anthropogenic-derived contaminants increased as basin population density increased. This report documents a suite of potential endocrine-disrupting chemicals in a reach of stream with native fish populations showing indication of endocrine disruption.

Environmental Science & Technology↗

USGS2005

Accumulation of contaminants in fish from wastewater treatment wetlands

Increasing demands on water resources in arid environments make reclamation and reuse of municipal wastewater an important component of the water budget. Treatment wetlands can be an integral part of the water-reuse cycle providing both water-quality enhancement and habitat functions. When used for habitat, the bioaccumulation potential of contaminants in the wastewater is a critical consideration. Water and fish samples collected from the Tres Rios Demonstration Constructed Wetlands near Phoenix, Arizona, which uses secondary-treated wastewater to maintain an aquatic ecosystem in a desert environment, were analyzed for hydrophobic organic compounds (HOC) and trace elements. Semipermeable membrane devices (SPMD) were deployed to investigate uptake of HOC. The wetlands effectively removed HOC, and concentrations of herbicides, pesticides, and organic wastewater contaminants decreased 40−99% between inlet and outlet. Analysis of Tilapia mossambica and Gambusia affinis indicated accumulation of HOC, including p,p ‘-DDE and trans -nonachlor. The SPMD accumulated the HOC detected in the fish tissue as well as additional compounds. Trace-element concentrations in whole-fish tissue were highly variable, but were similar between the two species. Concentrations of HOC and trace elements varied in different fish tissue compartments, and concentrations in Tilapia liver tissue were greater than those in the whole organism or filet tissue. Bioconcentration factors for the trace elements ranged from 5 to 58 000 and for the HOC ranged from 530 to 150 000.

Environmental Science & Technology↗

USGS1999

Correlation of soil and sediment organic matter polarity to aqueous sorption of nonionic compounds

Polarities of the soiL/sediment organic matter (SOM) in 19 soil and 9 freshwater sediment sam pies were determined from solid-state 13C-CP/MAS NMR spectra and compared with published partition coefficients (K(oc)) of carbon tetrachloride (CT) from aqueous solution. Nondestructive analysis of whole samples by solid-state NMR permits a direct assessment of the polarity of SOM that is not possible by elemental analysis. The percent of organic carbon associated with polar functional groups was estimated from the combined fraction of carbohydrate and carboxylamide-ester carbons. A plot of the measured partition coefficients (K(oc)) of carbon tetrachloride (CT) vs. percent polar organic carbon (POC) shows distinctly different populations of soils and sediments as well as a roughly inverse trend among the soil/sediment populations. Plots of K(oc) values for CT against other structural group carbon fractions did not yield distinct populations. The results indicate that the polarity of SOM is a significant factor in accounting for differences in K(oc) between the organic matter in soils and sediments. The alternate direct correlation of the sum of aliphatic and aromatic structural carbons with K(oc) illustrates the influence of nonpolar hydrocarbon on solute partition interaction. Additional elemental analysis data of selected samples further substantiate the effect of the organic matter polarity on the partition efficiency of nonpolar solutes. The separation between soil and sediment samples based on percent POC reflects definite differences of the properties of soil and sediment organic matters that are attributable to diagenesis.Polarities of the soil/sediment organic matter (SOM) in 19 soil and 9 freshwater sediment samples were determined from solid-state 13C-CP/MAS NMR spectra and compared with published partition coefficients (Koc) of carbon tetrachloride (CT) from aqueous solution. Nondestructive analysis of whole samples by solid-state NMR permits a direct assessment of the polarity of SOM that is not possible by elemental analysis. The percent of organic carbon associated with polar functional groups was estimated from the combined fraction of carbohydrate and carboxyl-amide-ester carbons. A plot of the measured partition coefficients (Koc) of carbon tetrachloride (CT) vs. percent polar organic carbon (POC) shows distinctly different populations of soils and sediments as well as a roughly inverse trend among the soil/sediment populations. Plots of Koc values for CT against other structural group carbon fractions did not yield distinct populations. The results indicate that the polarity of SOM is a significant factor in accounting for differences in Koc between the organic matter in soils and sediments. The alternate direct correlation of the sum of aliphatic and aromatic structural carbons with Koc illustrates the influence of nonpolar hydrocarbon on solute partition interaction. Additional elemental analysis data of selected samples further substantiate the effect of the organic matter polarity on the partition efficiency of nonpolar solutes. The separation between soil and sediment samples based on percent POC reflects definite differences of the properties of soil and sediment organic matters that are attributable to diagenesis.

Environmental Science & Technology↗

USGS2004

Concentrations of arsenic, cadmium, copper, lead, selenium, and zinc in fish from the Mississippi River Basin, 1995

Fish were collected in late 1995 from 34 National Contaminant Biomonitoring Program (NCBP) stations and 12 National Water Quality Assessment Program (NAWQA) stations in the Mississippi River basin (MRB), and in late 1996 from a reference site in West Virginia. The NCBP sites represented key points (dams, tributaries, etc.) in the largest rivers of the MRB. The NAWQA sites were typically on smaller rivers and were selected to represent dominant land uses in their watersheds. The West Virginia site, which is in an Eastern U.S. watershed adjacent to the MRB, was selected to document elemental concentrations in fish used for other aspects of a larger study and to provide additional contemporaneous data on background elemental concentrations. At each site four samples, each comprising (nominally) 10 adult common carp ( Cyprinus carpio , `carp') or black bass ( Micropterus spp., `bass') of the same sex, were collected. The whole fish were composited by station, species, and gender for analysis of arsenic (As), lead (Pb), and selenium (Se) by atomic absorption spectroscopy and for cadmium (Cd), copper (Cu), and zinc (Zn) by inductively-coupled plasma emission spectroscopy. Concentrations of most of the elements examined were lower in both carpand bass from the reference site, a small impoundment located in a rural area, than from the NCBP and NAWQA sites on rivers and larger impoundments. In contrast, there were few overall differences between NCBP sites NAWQA sites. The 1995 results generally confirmed the continued weathering and re-distribution of these elemental contaminants in the MRB; concentrations declined or were unchanged from 1984–1986 to 1995 at most NCBP sites, thus continuing two-decade trends. Exceptions were Se at Station 77 (Arkansas R. at John Martin Reservoir, CO), where concentrations have been elevated historically and increased slightly (to 3.8–4.7 μg g -1 in bass and carp); and Pb, Cd, and Zn at Station 67 (Allegheny R. at Natrona, PA), where levels of these metals were high in the past and increased from 1986 to 1995.

Environmental Monitoring and Assessment↗

USGS2000

Mineralogic and compositional properties of Martian soil and dust: results from Mars Pathfinder

Mars Pathfinder obtained multispectral, elemental, magnetic, and physical measurements of soil and dust at the Sagan Memorial Station during the course of its 83 sol mission. We describe initial results from these measurements, concentrating on multispectral and elemental data, and use these data, along with previous Viking, SNC meteorite, and telescopic results, to help constrain the origin and evolution of Martian soil and dust. We find that soils and dust can be divided into at least eight distinct spectral units, based on parameterization of Imager for Mars Pathfinder (IMP) 400 to 1000 nm multispectral images. The most distinctive spectral parameters for soils and dust are the reflectivity in the red, the red/blue reflectivity ratio, the near-IR spectral slope, and the strength of the 800 to 1000 nm absorption feature. Most of the Pathfinder spectra are consistent with the presence of poorly crystalline or nanophase ferric oxide(s), sometimes mixed with small but varying degrees of well-crystalline ferric and ferrous phases. Darker soil units appear to be coarser-grained, compacted, and/or mixed with a larger amount of dark ferrous materials relative to bright soils. Nanophase goethite, akaganeite, schwertmannite, and maghemite are leading candidates for the origin of the absorption centered near 900 nm in IMP spectra. The ferrous component in the soil cannot be well-constrained based on IMP data. Alpha proton X-ray spectrometer (APXS) measurements of six soil units show little variability within the landing site and show remarkable overall similarity to the average Viking-derived soil elemental composition. Differences exist between Viking and Pathfinder soils, however, including significantly higher S and Cl abundances and lower Si abundances in Viking soils and the lack of a correlation between Ti and Fe in Pathfinder soils. No significant linear correlations were observed between IMP spectral properties and APXS elemental chemistry. Attempts at constraining the mineralogy of soils and dust using normative calculations involving mixtures of smectites and silicate and oxide minerals did not yield physically acceptable solutions. We attempted to use the Pathfinder results to constrain a number of putative soil and dust formation scenarios, including palagonitization and acid-fog weathering. While the Pathfinder soils cannot be chemically linked to the Pathfinder rocks by palagonitization, this study and McSween et al. [1999] suggest that palagonitic alteration of a Martian basaltic rock, plus mixture with a minor component of locally derived andesitic rock fragments, could be consistent with the observed soil APXS and IMP properties.

Journal of Geophysical Research E: Planets↗

USGS2018

Origin of primitive tholeiitic and calc-alkaline basalts at Newberry Volcano, Oregon

Major and trace element and radiogenic isotopic characteristics of primitive mafic Pleistocene and Holocene lavas from Newberry Volcano, Oregon, define two groups. The first consists of dry tholeiitic high-alumina olivine basalts that are slightly enriched in highly incompatible elements. The second group consists of calc-alkaline basalts that contained 2–4 wt % H 2 O prior to eruption and shows strong enrichment in the light rare earth elements, Ba, and Sr, and deficits in Nb, Ta, Hf, and Zr. The tholeiitic basalts reflect 6–11% anhydrous adiabatic decompression melting of spinel peridotite. The calc-alkaline basalts derived from compositionally distinct sources with strong LIL enrichment and relative depletion in HFSE, but with Sr, Nd, Hf, and Pb isotopic composition only slightly distinct from the sources of the tholeiitic magmas. Radiogenic Os correlates with LREE enrichment in the calc-alkaline magmas, which indicates that their source materials include a contribution from a mafic component that was melted in the garnet stability field. The calc-alkaline magmas were derived by melting of peridotite metasomatized by a fluid/melt that originated by melting of a mixture of the sediment plus MORB basalt/mantle in the underlying subducting oceanic plate. While the trace element characteristics of the calc-alkaline magmas were determined by the subduction component, their isotopic characteristics were modified during transit through the mantle by interaction with the highly magmatically processed mantle wedge beneath Newberry Volcano that, without the slab component, serves as the source of the tholeiitic magmas.

Oregon↗

USGS2022

Overview of the morphology and chemistry of diagenetic features in the clay-rich Glen Torridon Unit of Gale Crater, Mars

The clay-rich Glen Torridon region of Gale crater, Mars, was explored between sols 2300 and 3007. Here, we analyzed the diagenetic features observed by Curiosity , including veins, cements, nodules, and nodular bedrock, using the ChemCam, Mastcam, and Mars Hand Lens Imager instruments. We discovered many diagenetic features in Glen Torridon, including dark-toned iron- and manganese-rich veins, magnesium- and fluorine-rich linear features, Ca-sulfate cemented bedrock, manganese-rich nodules, and iron-rich strata. We have characterized the chemistry and morphology of these features, which are most widespread in the higher stratigraphic members in Glen Torridon, and exhibit a wide range of chemistries. These discoveries are strong evidence for multiple generations of fluids from multiple chemical endmembers that likely underwent redox reactions to form some of these features. In a few cases, we may be able to use mineralogy and chemistry to constrain formation conditions of the diagenetic features. For example, the dark-toned veins likely formed in warmer, highly alkaline, and highly reducing conditions, while manganese-rich nodules likely formed in oxidizing and circumneutral conditions. We also hypothesize that an initial enrichment of soluble elements, including fluorine, occurred during hydrothermal alteration early in Gale crater history to account for elemental enrichment in nodules and veins. The presence of redox-active elements, including Fe and Mn, and elements required for life, including P and S, in these fluids is strong evidence for habitability of Gale crater groundwater. Hydrothermal alteration also has interesting implications for prebiotic chemistry during the earliest stages of the crater’s evolution and early Mars.

JGR - Planets↗

USGS2012

Lunar ferroan anorthosites: mineralogy, compositional variations, and petrogenesis

Detailed petrologic study of a suite of lunar ferroan anorthosites indicates that their mineral compositional variations are generally consistent with derivation of these anorthosites from a common parent magma. There are continuous compositional variations in major elements and smooth trends in minor elements (Mg, Fe in plagioclase; Al, Ti, Cr in pyroxene). Relict textures, zoning, and possible primary trends of mineral compositional variations are preserved in many of the anorthosites. The presence of heterogeneous, bimodal, and/or trimodal pyroxene compositions suggests that some of the anorthosites are polymict rocks; however, they are composed entirely of ferroan-anorthosite-suite lithologies. Some aspects of the mineral composition data suggest that complex processes operated during formation of the ferroan anorthosites. The lack of a well-defined, positive or negative trend of pyroxene Mg/(Mg + Fe) versus plagioclase anorthite content, the homogenization of mineral compositions in some anorthosites, and the varied and apparently enriched Mn contents of pyroxenes in some anorthosites suggest that original igneous compositional characteristics have been altered during and/or after crystallization. Processes operative during anorthosite formation may have included some mixing of different melts, trapping of variable amounts of intercumulus liquid, postcrystallization redistribution of elements, or perturbations both during adcumulus growth and subsequent to crystallization by impact events. FeO and MgO contents of the highly calcic plagioclase typical of these anorthosites suggest that the plagioclase-melt distribution coefficients for these elements need to be reassessed.

Journal of Geophysical Research↗

USGS2010

Comparison of deep structure along three transects of the western North American continental margin

Similarities in geology and potential field data that have in the past been noted among the regions of southern Alaska, southern Vancouver Island, and central California are now seen to be accompanied by similarities in deep crustal structure. A number of tectonic elements have been identified in the deep structure along transects in these three regions, although not all elements are present along each transect. These elements are (A) an actively subducting oceanic plate and (B) an overriding continental plate that consists of (1) a Cenozoic accretionary prism, (2) a Mesozoic accretionary prism, (3) a backstop to the Mesozoic prism, (4) a tectonically underplated body of oceanic rocks, and (5) a crustal root. The Mesozoic prism is in some cases an underthrust body (type 2a) but in other cases forms the principal component of a landward verging tectonic wedge (type 2b). The technically underplated body of oceanic rocks extends landward from the fault contact between the Cenozoic and Mesozoic prisms to a point beneath the backstop. The crustal root lies beneath the backstop and landward of the underplated body. All of these elements are interpreted to be present along the Alaskan and Vancouver Island transects. In Alaska the underplated body is interpreted to be fragments of the Kula plate; the same may be true at Vancouver Island. These two transects appear to differ in that, in Alaska, the Mesozoic prism, in one interpretation, is the principal component of a tectonic wedge (type 2b), whereas at Vancouver Island, it is an underthrust body (type 2a). Along the central California transect, active subduction is no longer taking place, and the San Andreas fault has removed the Cenozoic prism from this region of the North American plate. On the North American plate (i.e., east of the San Andreas fault), the Mesozoic prism, interpreted as the main component of a tectonic wedge (type 2b), and the backstop to the Mesozoic prism are present. There is, however, no clear evidence of tectonically underplated oceanic rocks, and the crust is thin (no root). In both Alaska and Vancouver Island, the Mesozoic prisms above the underplated bodies experienced low-pressure/high-temperature metamorphism at about the time of tectonic underplating; no such metamorphism is currently exposed in California. The metamorphism may have been caused by the underplating of young, hot oceanic crust, or, alternatively, by subduction of an oceanic ridge. The presence of a tectonic wedge (type 2b) in Alaska and California and the absence of such a wedge at Vancouver Island could arise either from the fact that in the former two locations the Mesozoic prisms were more voluminous, owing to either more rapid trench sedimentation or more rapid convergence, or to the possibility that at the latter location the Mesozoic prism was juxtaposed with the backstop primarily by strike-slip faulting.

Alaska, California↗

USGS2012

Origin of Hawaiian tholeiite: A metasomatic model

Two voluminous magma types generated in the mantle underlying the Pacific plate are mid‐ocean ridge tholeiite (MORB) erupted at the East Pacific Rise spreading center and Hawaiian tholeiite (HT) erupted above the Hawaiian hot spot or melting anomaly. MORB has low initial 87 Sr/ 86 Sr ratios and low amounts of all incompatible trace elements including rare earths; chondrite‐normalized patterns are depleted in light rare earths. HT, by contrast, has higher initial 87 Sr/ 86 Sr and higher amounts of incompatible trace elements; chondrite‐nor‐malized patterns are enriched in the middle and light rare earths. HT is generally poorer in CaO and Al 2 O 3 and much richer in total iron and TiO 2 compared with MORB having the same MgO content. Primary magma compositions for the two volcanic systems are calculated in Fe‐Mg equilibrium with residual olivine (Fo 92 ). MORB is generated by partial melting of a trace element depleted Iherzolite source leaving a residual assemblage dominated by olivine and orthopyroxene. The percentage of partial melting for a primary magma containing 15% MgO is calculated to be 35–42% in a source mantle having a heavy rare earth content of 3×chondrite and 33–35% MgO. HT, represented by Kilauea tholeiite, is generated by partial melting of a mixture of unmelted and residual mantle for MORB which has been modified by metasomatic addition of a nephelinitic fluid, amphibole, and minor amounts of apatite and Fe‐bearing phases such as sulfide and magnetite/ilmenite. This model yields a picritic magma in equilbrium with magnesian dunite at high (>40%) degrees of partial melting. The source also has 35% MgO before partial melting. Melting in both systems in polyvariant and not controlled by lower‐temperature invariant equilibria. The low‐velocity zone is considered to be the source of metasomatic fluids that are driven upward into the lowermost lithosphere in response to a thermal plume. Picritic primary magmas are produced by shear melting, localized in the zone of thinned and metasomatized lithosphere beneath Hawaii. Melt extraction is rapid and episodic at intervals of months to decades; magma is not stored in the mantle but passes upward to a plexus of storage reservoirs located 2–6 km beneath the surface of Kilauea. Kilauea primary magmas fractionate olivine during upward transport to reach bulk compositions of 13–14% MgO in storage. Different magma batches erupted to the surface, distinguished by different major and minor element compositons compared at similar MgO content, represent combinations of differing degrees of metasomatic enrichment, differing degrees of partial melting, and some effects of premelting mantle heterogeneity.

Hawaii↗

USGS2012

Petrologic evolution of divergent peralkaline magmas from the Silent Canyon caldera complex, southwestern Nevada volcanic field

The Silent Canyon volcanic center consists of a buried Miocene peralkaline caldera complex and outlying peralkaline lava domes. Its location has been corroborated by geophysical data and more than 50 drill holes. Two widespread ash flow sheets, the Tub Spring and overlying Grouse Canyon members of the Miocene Belted Range Tuff, were erupted from the caldera complex and have volumes of 60–100 km 3 and 200 km 3 , respectively. Eruption of the ash flows was preceded by widespread extrusion of precaldera comendite domes and was followed by extrusion of postcollapse peralkaline lavas and tuffs within and outside the caldera complex. Lava flows and tuffs were also deposited between the two major ash flow sheets. Rocks of the Silent Canyon center vary significantly in silica content and peralkalinity. The most mafic rocks are precollapse and postcollapse trachytes (65–69% SiO 2 ). Low-silica comendites (69–73% SiO 2 ) were erupted as the mafic upper part of the chemically zoned Grouse Canyon Member and as postcollapse lavas. The lower part of the Grouse Canyon Member and the underlying rhyolite of Split Ridge are moderately peralkaline comendite (PI is molar ratio Na + K/Al is 1.17–1.26). These comendites have major element characteristics and trace element enrichments approaching those of pantellerites. The Tub Spring Member, by contrast, is a weakly peralkaline chemically unzoned silicic comendite (75–76% SiO 2 ) ash flow tuff. Weakly peralkaline silicic comendites (PI 1.0–1.1) are the most abundant precaldera lavas. Postcollapse lavas range from trachyte to silicic comendite; some have anomalous light rare earth element (LREE) enrichments. Silent Canyon rocks follow a common petrologic evolution from trachyte to low-silica comendite; above 73% SiO 2 , compositions of the moderately peralkaline comendites diverge from those of the weakly peralkaline silicic comendites. These contrasting differentiation paths are shown in the behavior of Fe and other transition metals, Al, Na, K; the trace elements Ba, Zr, Nb; and probably F and Cl. Weakly peralkaline silicic comendites show a LREE/heavy REE crossover in early erupted/late erupted rocks; moderately peralkaline comendites are enriched in all REE. The development of divergent peralkaline magmas, toward both pantelleritic and weakly peralkaline compositions, is unusual in a single volcanic center.

Journal of Geophysical Research Solid Earth↗