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22 records · Page 2Linked to original sources
USGS2012

Geochemistry, mineralogy, and petrogenesis of basalt from the Gorda Ridge

Basalt pillow lava with glassy rims was dredged from 17 sites along the Gorda Ridge between latitudes 43°N and 40.8°N. All samples are low-K 2 O mid-ocean ridge tholeiitic basalt having a narrow compositional range with Mg numbers clustered around 60–62; more primitive and evolved compositions are present but rare. None of the more fractionated samples is as evolved as ferrobasalt from the Juan de Fuca Ridge. Incompatible trace element ratios are typical of normal mid-ocean ridge basalt but show considerable scatter. The 87 Sr/ 86 Sr ratios, ranging from 0.70233 to 0.70267, are near the low end of the range for normal mid-ocean ridge basalt. The phenocrysts present are abundant plagioclase, less abundant olivine ± spinel, and traces of sulfide. Clinopyroxene is absent in the glasses. The mineral chemistry is typical of ocean floor basalt. However, unusually anorthitic plagioclase in some highly plagioclasephyric samples, complex zoning in plagioclase and olivine, and other disequilibrium features indicate complex petrogenetic processes involving magma mixing. Glass inclusions in olivine and plagioclase indicate primitive trapped melts. The chemical diversity of Gorda Ridge lava appears to have been primarily caused by variable degrees of partial melting, but crystal fractionation and magma mixing were also important processes. Compositional variations along the strike of the ridge indicate that lava from the segment south of the offset at latitude 41.6°N was generated by the smallest percentage of partial melting of a source less depleted than that of the two northern segments. Lava from the central and northern segments was generated by variable percentages of partial melting of a uniformly depleted source. Lava from the northern segment shows the greatest diversity with a large range in percentage of melting and both relatively primitive and evolved compositions in spatially and temporally closely associated lava. The diversity of lava from the northern segment may result from thermal perturbations caused by proximity to the Blanco Fracture Zone. Gorda Ridge lava is more similar to that from the Mid-Atlantic Ridge at 22°–25°N than to that from other spreading centers in the Pacific Ocean. Magma chambers under the Gorda Ridge appear to be small, discontinuous in time and space and possibly at greater depth than those beneath other Pacific spreading centers.

Journal of Geophysical Research Solid Earth↗
USGS2017

Lithological influences on contemporary and long-term regolith weathering at the Luquillo Critical Zone Observatory

Lithologic differences give rise to the differential weatherability of the Earth’s surface and globally variable silicate weathering fluxes, which provide an important negative feedback on climate over geologic timescales. To isolate the influence of lithology on weathering rates and mechanisms, we compare two nearby catchments in the Luquillo Critical Zone Observatory in Puerto Rico, which have similar climate history, relief and vegetation, but differ in bedrock lithology. Regolith and pore water samples with depth were collected from two ridgetops and at three sites along a slope transect in the volcaniclastic Bisley catchment and compared to existing data from the granitic Río Icacos catchment. The depth variations of solid-state and pore water chemistry and quantitative mineralogy were used to calculate mass transfer (tau) and weathering solute profiles, which in turn were used to determine weathering mechanisms and to estimate weathering rates. Regolith formed on both lithologies is highly leached of most labile elements, although Mg and K are less depleted in the granitic than in the volcaniclastic profiles, reflecting residual biotite in the granitic regolith not present in the volcaniclastics. Profiles of both lithologies that terminate at bedrock corestones are less weathered at depth, near the rock-regolith interfaces. Mg fluxes in the volcaniclastics derive primarily from dissolution of chlorite near the rock-regolith interface and from dissolution of illite and secondary phases in the upper regolith, whereas in the granitic profile, Mg and K fluxes derive from biotite dissolution. Long-term mineral dissolution rates and weathering fluxes were determined by integrating mass losses over the thickness of solid-state weathering fronts, and are therefore averages over the timescale of regolith development. Resulting long-term dissolution rates for minerals in the volcaniclastic regolith include chlorite: 8.9 × 10 −14 mol m −2 s −1 , illite: 2.1 × 10 −14 mol m −2 s −1 and kaolinite: 4.0 × 10 −14 mol m −2 s −1 . Long-term weathering fluxes are several orders of magnitude lower in the granitic regolith than in the volcaniclastic, despite higher abundances of several elements in the granitic regolith. Contemporary weathering fluxes were determined from net (rain-corrected) solute profiles and thus represent rates over the residence time of water in the regolith. Contemporary weathering fluxes within the granitic regolith are similar to the long-term fluxes. In contrast, the long-term fluxes are faster than the contemporary fluxes in the volcaniclastic regolith. Contemporary fluxes in the granitic regolith are generally also slightly faster than in the volcaniclastic. The differences in weathering fluxes over space and time between these two watersheds indicate significant lithologic control of chemical weathering mechanisms and rates.

Bisley watersheds↗
USGS2023

Summary of the history and research of the U.S. Geological Survey gas hydrate properties laboratory in Menlo Park, California, active from 1993 to 2022

The U.S. Geological Survey (USGS) Clathrate Hydrate Properties Project, active from 1993 to 2022 in Menlo Park, California, stemmed from an earlier project on the properties of planetary ices supported by the National Aeronautics and Space Administration’s (NASA’s) Planetary Geology and Geophysics Program. We took a material science approach in both projects, emphasizing chemical purity of samples, having controlled grain size and grain texture, and having verified crystal structures and phase relations. A foundational contribution from our USGS Gas Hydrate Properties Laboratory (GHPL) was in demonstrating the ability to reproducibly create such pure clathrate hydrate samples for study. Clathrate sample synthesis was achieved by heating sieved and weighed pure granular water ice in the presence of cold clathrate-forming gas or liquid. During heating, the ice melts at the grain scale and reacts with the gas to form clathrate. The resulting material has the desired uniformity and purity, with known intergranular porosity; our subsequent measurements showed that these clathrates exhibited the established clathrate structures and phase relations. This novel synthesis method was successful in creating clathrates of pure methane, ethane, propane, carbon dioxide, and multi-component gases. By mixing sand or silt with granular ice, we were also able to make clathrate-sediment aggregates with controlled grain textures. This simple method, adopted by many others in the community, permitted us to measure the physical and chemical properties of well-characterized and well-crystallized clathrates and clathrate/sediment aggregates. At about the same time, we adapted conventional scanning electron microscopy to cryogenic conditions for analysis of grain-scale characteristics of clathrates made in the GHPL as well as those collected from nature by drill core. The uniformity and reproducibility of our samples also allowed us to investigate how clathrates respond to environmental changes in chemistry, temperature, and pressure: we measured chemical exchange rates with dissolved gas species—such as noble gases and chlorofluorocarbons—as well as rates of clathrate dissolution and decomposition. These advances include the first accurate mapping of the conditions that promote the remarkable process of “anomalous preservation” at room pressure, a metastability that offers potential application for low-cost and safe transportation of natural gas from gas fields far from pipelines. Another advancement stemming from the GHPL was the compaction of as-synthesized porous clathrates to nearly full density by applying external pressure using three different techniques. Compaction allows for high-accuracy measurements of many fundamental physical and chemical properties of these materials, such as elastic wavespeeds and moduli, complete thermal properties, decomposition rates, thermal expansion, and clathrate equations of state. These properties and others, in turn, have helped USGS scientists to interpret geophysical well logs and active geophysical surveys, as well as model the rates of gas production from hydrate deposits in nature. Studying this class of icy minerals that occur in abundance on Earth and in the outer solar system has been a fascinating laboratory journey. Here, we summarize the history and major findings of the USGS GHPL in Menlo Park, including both in-house research as well as findings from the synergistic collaborations with other agencies and institutes that were key to the success of our laboratory. The Menlo Park GHPL was more formally incorporated within the USGS Gas Hydrates Project, a collaboration among multiple USGS Science Centers, in the early 2000s under the leadership of Deborah Hutchinson, and now under the leadership of Carolyn Ruppel and Timothy Collett.

Open-File Report↗
USGS2021

Clustering supported classification of ChemCam data from Gale crater, Mars

The Chemistry and Camera (ChemCam) instrument on board the MSL rover Curiosity has collected a very large and unique dataset of in-situ spectra and images of Mars since landing in August 2012. More than 800,000 single shot LIBS (laser-induced breakdown spectroscopy) spectra measured on more than 2,500 individual targets were returned so far by ChemCam. Such a dataset is ideally suited for the application of statistical methods for the recognition of patterns that are difficult to observe by humans. In this work, we develop an approach relying on the feature extraction method non-negative matrix factorization (NMF) and the repetition of k-means clustering to classify ChemCam spectra. A strong consistency of the clustering results among the repetitions were found, which allowed us to identify six clusters representing the dominant compositions measured by ChemCam in Gale crater so far. By tracking clusters across the rover traverse from landing to sol 2756, we are able to provide a chemostratigraphic overview of Gale crater from the ChemCam perspective. Transitions between major geologic groups (such as the Bradbury and the Mt. Sharp groups) are identifiable demonstrating that they are compositionally distinct, consistent with previous work. Compositional differences between their members also appear in the results. Furthermore, a first approach in which a random forest classifier was trained and validated with the obtained cluster assignments, reveals promising results for predicting cluster memberships of new ChemCam LIBS data acquired after sol 2756.

Earth and Space Science↗