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USGS2016

POLARIS: A 30-meter probabilistic soil series map of the contiguous United States

A new complete map of soil series probabilities has been produced for the contiguous United States at a 30 m spatial resolution. This innovative database, named POLARIS, is constructed using available high-resolution geospatial environmental data and a state-of-the-art machine learning algorithm (DSMART-HPC) to remap the Soil Survey Geographic (SSURGO) database. This 9 billion grid cell database is possible using available high performance computing resources. POLARIS provides a spatially continuous, internally consistent, quantitative prediction of soil series. It offers potential solutions to the primary weaknesses in SSURGO: 1) unmapped areas are gap-filled using survey data from the surrounding regions, 2) the artificial discontinuities at political boundaries are removed, and 3) the use of high resolution environmental covariate data leads to a spatial disaggregation of the coarse polygons. The geospatial environmental covariates that have the largest role in assembling POLARIS over the contiguous United States (CONUS) are fine-scale (30 m) elevation data and coarse-scale (~ 2 km) estimates of the geographic distribution of uranium, thorium, and potassium. A preliminary validation of POLARIS using the NRCS National Soil Information System (NASIS) database shows variable performance over CONUS. In general, the best performance is obtained at grid cells where DSMART-HPC is most able to reduce the chance of misclassification. The important role of environmental covariates in limiting prediction uncertainty suggests including additional covariates is pivotal to improving POLARIS' accuracy. This database has the potential to improve the modeling of biogeochemical, water, and energy cycles in environmental models; enhance availability of data for precision agriculture; and assist hydrologic monitoring and forecasting to ensure food and water security.

Geoderma↗

USGS2011

Hillslope chemical weathering across Paraná, Brazil: a data mining-GIS hybrid approach

Self-organizing map (SOM) and geographic information system (GIS) models were used to investigate the nonlinear relationships associated with geochemical weathering processes at local (~100 km 2 ) and regional (~50,000 km 2 ) scales. The data set consisted of 1) 22 B-horizon soil variables: P, C, pH, Al, total acidity, Ca, Mg, K, total cation exchange capacity, sum of exchangeable bases, base saturation, Cu, Zn, Fe, B, S, Mn, gammaspectrometry (total count, potassium, thorium, and uranium) and magnetic susceptibility measures; and 2) six topographic variables: elevation, slope, aspect, hydrological accumulated flux, horizontal curvature and vertical curvature. It is characterized at 304 locations from a quasi-regular grid spaced about 24 km across the state of Paraná. This data base was split into two subsets: one for analysis and modeling (274 samples) and the other for validation (30 samples) purposes. The self-organizing map and clustering methods were used to identify and classify the relations among solid-phase chemical element concentrations and GIS derived topographic models. The correlation between elevation and k-means clusters related the relative position inside hydrologic macro basins, which was interpreted as an expression of the weathering process reaching a steady-state condition at the regional scale. Locally, the chemical element concentrations were related to the vertical curvature representing concave–convex hillslope features, where concave hillslopes with convergent flux tends to be a reducing environment and convex hillslopes with divergent flux, oxidizing environments. Stochastic cross validation demonstrated that the SOM produced unbiased classifications and quantified the relative amount of uncertainty in predictions. This work strengthens the hypothesis that, at B-horizon steady-state conditions, the terrain morphometry were linked with the soil geochemical weathering in a two-way dependent process: the topographic relief was a factor on environmental geochemistry while chemical weathering was for terrain feature delineation.

Parana↗

USGS2026

Revisiting the geochronology of late Quaternary marine terraces and uplift rates in coastal Santa Barbara County, California, USA

In several early studies, central California marine terraces between Santa Barbara and Point Conception were interpreted to record sea-level high stands of the last interglacial complex, ∼80 ka to ∼120 ka (marine isotope stage [MIS] 5). These ages and their elevations (∼20 m to ∼45 m) indicate modest rates of tectonic uplift, similar to those from other localities in southern and central California. A recent study, using a combination of luminescence and radiocarbon dating, has challenged the older age interpretations, implying much younger terrace ages, between ∼40 ka and ∼55 ka (MIS 3). From these new ages and a considerably lower sea level during MIS 3, much higher rates of tectonic uplift are inferred. In the present study, new uranium-series ages of terrace corals and amino acid age estimates of terrace mollusks were determined to test these competing interpretations. With the exception of a low-elevation terrace in Isla Vista (near Santa Barbara) that dates to MIS 3, terraces farther west are interpreted to date to MIS 5 and imply tectonic uplift rates of 0.20–0.34 m/kyr. A compilation of data for the region yields a decreasing rate of late Quaternary uplift from east, near Ventura, to west, near Point Conception. This trend is interpreted to reflect a decreasing influence of the processes of compression and crustal shortening south of the Big Bend in the San Andreas fault.

California↗

USGS2016

The distribution and composition of REE-bearing minerals in placers of the Atlantic and Gulf coastal plains, USA

Rare earth element (REE) resources are currently of great interest because of their importance as raw materials for high-technology manufacturing. The REE-phosphates monazite (light REE enriched) and xenotime (heavy REE enriched) resist weathering and can accumulate in placer deposits as part of the heavy mineral assemblage. The Atlantic and Gulf coastal plains of the southeastern United States are known to host heavy mineral deposits with economic concentrations of zircon, ilmenite and rutile. This study provides a perspective on the distribution and composition of REE phosphate minerals in the region. The elemental chemistry and mineralogy of sands and associated heavy-mineral assemblages from new and archived sediment samples across the coastal plains are examined, along with phase-specific compositions of monazite, xenotime and zircon. Both monazite and xenotime are present across the coastal plains. The phase-specific compositions allow monazite content to be estimated using La as a geochemical proxy. Similarly, both Y and Yb are geochemical proxies for xenotime, but their additional presence in zircon and monazite require a correction to prevent overestimation of xenotime content. Applying this correction, maps of monazite and xenotime content across the coastal plains were generated using sample coverage from the National Geochemical Database (NGS) and National Uranium Resource Evaluation (NURE). The NGS and NURE approach of sampling stream sediments in small watersheds links samples to nearby lithologies. The results show an approximately 40 km-wide band of primarily Cretaceous, marine sediments bordering the Piedmont province from North Carolina to Alabama in which monazite and xenotime content are relatively high (up to 4.4 wt. % in < 150 μm bulk sediment). Strong correlations between concentrations of the two phases were found, with estimated monazite:xenotime ratios ranging approximately 6:1 to 12:1 depending upon the dataset analyzed. From a resource perspective, xenotime correlation with monazite indicates a heavy REE potential in coastal plain placers, and exploration may be warranted within the identified coastal plain band along the boundary of the Piedmont region.

Journal of Geochemical Exploration↗

USGS2013

History and evaluation of national-scale geochemical data sets for the United States

Six national-scale, or near national-scale, geochemical data sets for soils or stream sediments exist for the United States. The earliest of these, here termed the ‘Shacklette’ data set, was generated by a U.S. Geological Survey (USGS) project conducted from 1961 to 1975. This project used soil collected from a depth of about 20 cm as the sampling medium at 1323 sites throughout the conterminous U.S. The National Uranium Resource Evaluation Hydrogeochemical and Stream Sediment Reconnaissance (NURE-HSSR) Program of the U.S. Department of Energy was conducted from 1975 to 1984 and collected either stream sediments, lake sediments, or soils at more than 378,000 sites in both the conterminous U.S. and Alaska. The sampled area represented about 65% of the nation. The Natural Resources Conservation Service (NRCS), from 1978 to 1982, collected samples from multiple soil horizons at sites within the major crop-growing regions of the conterminous U.S. This data set contains analyses of more than 3000 samples. The National Geochemical Survey, a USGS project conducted from 1997 to 2009, used a subset of the NURE-HSSR archival samples as its starting point and then collected primarily stream sediments, with occasional soils, in the parts of the U.S. not covered by the NURE-HSSR Program. This data set contains chemical analyses for more than 70,000 samples. The USGS, in collaboration with the Mexican Geological Survey and the Geological Survey of Canada, initiated soil sampling for the North American Soil Geochemical Landscapes Project in 2007. Sampling of three horizons or depths at more than 4800 sites in the U.S. was completed in 2010, and chemical analyses are currently ongoing. The NRCS initiated a project in the 1990s to analyze the various soil horizons from selected pedons throughout the U.S. This data set currently contains data from more than 1400 sites. This paper (1) discusses each data set in terms of its purpose, sample collection protocols, and analytical methods; and (2) evaluates each data set in terms of its appropriateness as a national-scale geochemical database and its usefulness for national-scale geochemical mapping.

Conterminous United States↗

USGS2020

Effects of John Martin Reservoir on water quality and quantity: Assessment by chemical, isotopic, and mass-balance methods

Water quality and quantity can be influenced by transit through and storage in reservoirs. Assessing such effects can be challenging, however, because of mixing and residence times, and inter-annual net storage and release from both the reservoir itself and surrounding porosity. Here, different methodologies were used to assess the effect of John Martin Reservoir (JMR), located on the Arkansas River, on water volumes and the problematic constituents salinity (total dissolved solids, TDS), selenium (Se), and uranium (U). Methodologies addressed short-term (16 months) and long-term (31 years) effects depending upon data availability. Evaporation was assessed by using isotopes of water to determine 12% short-term evaporation, and by pan evaporation and changes in storage to determine 11% long-term evaporation. Salinity, Se, and U mass balance were assessed by using chloride (Cl−) as an index by which to measure short-term gains or losses between inflows and outflows in the short term. Chloride gain from ungaged inflows skewed those results to overestimate retention. Continuous monitoring of discharge and specific conductance for inflows and outflows, along with discrete sampling for dissolved constituents were used to compute long-term, load-based mass balance. Mild gains of TDS (34,000 ± 15,000 Mg/yr) and U (0.1 ± 0.5 Mg/yr) in JMR were detected. Although the additions are small relative to uncertainty, they indicate little to no retention of TDS and U and likely additions from ungaged inflows. In contrast, an average of 0.6 ± 0.2 Mg/yr or 23% of gaged inflow Se was removed in JMR. The study illustrates the benefit of long-term records for assessing the influence of reservoirs for which net storage and release keep them from approaching steady-state conditions.

Colorado↗

USGS2026

Lunar analog study using portable gamma-ray neutron detector: Radiochemical mapping of silicic-to-basaltic volcanic terrains in the San Francisco Volcanic Field, Arizona

Studying lunar silicic volcanism provides key insights into the Moon’s crustal evolution, magmatic processes, and volcanic history. The Lunar-VISE (Lunar Vulkan Imaging and Spectroscopy Explorer) mission will investigate the Gruithuisen domes, a unique lunar region hypothesized to have formed through silicic volcanism. Using instruments on a Firefly Aerospace lander and a Honeybee Robotics rover, Lunar-VISE will analyze mineralogy, geochemistry, and surface properties to determine the origin and evolution of the domes, with a gamma-ray and neutron spectrometer (LV-GRNS) among its payload instruments. In preparation for this mission, we conducted preliminary fieldwork using a handheld gamma-ray neutron detector with NaI(Tl) and Cs LiYCl :Ce (CLYC) scintillators. This study focuses on various rhyolitic and basaltic volcanic centers in the San Francisco Volcanic Field (SFVF) near Flagstaff, Arizona—specifically Sugarloaf Peak, Bonito Lava Flow, and Robinson Mountain, a region containing several well-characterized lunar analog sites. The SFVF was selected for this study due to its broad compositional diversity spanning basaltic to rhyolitic compositions, its well-preserved volcanic morphologies, and its extensive use in previous NASA field campaigns and astronaut training exercises, making it an ideal terrestrial laboratory for testing planetary exploration techniques. We measured natural radioactivity, specifically from potassium (K), thorium (Th), and uranium (U) and other elements in their decay chains, which serve as diagnostic tracers of magmatic differentiation and crustal evolution processes, to assess geochemical variability across compositionally diverse terrains. The detector’s sensitivity was assessed across varying concentration levels. Regionally averaged concentrations of radioisotopes were determined by gamma-ray spectroscopy at selected sites. Our measurements reveal significant compositional variations between sites, with Sugarloaf Peak (rhyolitic, silicic dome) exhibiting the highest average radioisotope concentrations (K: 3.29 ± 0.24 wt%, U: 14.35 ± 1.81 ppm, Th: 27.14 ± 2.43 ppm), while Bonito Lava Flow (K: 1.13 ± 0.08 wt%, U: 3.86 ± 0.52 ppm, Th: 7.52 ± 1.02 ppm), and Robinson Mountain (K: 1.46 ± 0.16 wt%, U: 5.59 ± 1.06 ppm, Th: 11.75 ± 1.98 ppm) show lower concentrations aligned with basaltic compositions. Gamma-ray fluxes were elevated by a factor of approximately three to four at Sugarloaf Peak relative to nearby basaltic terrains, consistent with expected geochemical differentiation patterns. Furthermore, at meter scales, proximity to geological features significantly affects measurements. Th concentrations adjacent to a cliff face at Sugarloaf’s base were 28% higher than values measured 3-5 meters away from the same feature, demonstrating localized compositional heterogeneity. Analysis of station-by-station measurements reveals that K, U, and Th concentrations show an elevation trend at Robinson Mountain and generally higher concentrations near Sugarloaf Peak’s summit, suggesting progressive magmatic differentiation and/or the presence of more evolved lithologies at higher elevations. By mapping these elements on Earth using GRNS, we aim to optimize measurement techniques for Lunar-VISE and similar rover-borne missions by demonstrating the applicability of portable GRNS instruments for planetary surface exploration in an analog environment.

Arizona↗

USGS2011

Inversion of multi-frequency electromagnetic induction data for 3D characterization of hydraulic conductivity

Electromagnetic induction (EMI) instruments provide rapid, noninvasive, and spatially dense data for characterization of soil and groundwater properties. Data from multi-frequency EMI tools can be inverted to provide quantitative electrical conductivity estimates as a function of depth. In this study, multi-frequency EMI data collected across an abandoned uranium mill site near Naturita, Colorado, USA, are inverted to produce vertical distribution of electrical conductivity ( EC ) across the site. The relation between measured apparent electrical conductivity ( EC a ) and hydraulic conductivity ( K ) is weak (correlation coefficient of 0.20), whereas the correlation between the depth dependent EC obtained from the inversions, and K is sufficiently strong to be used for hydrologic estimation (correlation coefficient of − 0.62). Depth-specific EC values were correlated with co-located K measurements to develop a site-specific ln( EC )–ln( K ) relation. This petrophysical relation was applied to produce a spatially detailed map of K across the study area. A synthetic example based on EC a values at the site was used to assess model resolution and correlation loss given variations in depth and/or measurement error. Results from synthetic modeling indicate that optimum correlation with K occurs at ~ 0.5 m followed by a gradual correlation loss of 90% at 2.3 m. These results are consistent with an analysis of depth of investigation (DOI) given the range of frequencies, transmitter–receiver separation, and measurement errors for the field data. DOIs were estimated at 2.0 ± 0.5 m depending on the soil conductivities. A 4-layer model, with varying thicknesses, was used to invert the EC a to maximize available information within the aquifer region for improved correlations with K . Results show improved correlation between K and the corresponding inverted EC at similar depths, underscoring the importance of inversion in using multi-frequency EMI data for hydrologic estimation.

Journal of Applied Geophysics↗

USGS2012

Effects of sulfate ligand on uranyl carbonato surface species on ferrihydrite surfaces

Understanding uranium (U) sorption processes in permeable reactive barriers (PRB) are critical in modeling reactive transport for evaluating PRB performance at the Fry Canyon demonstration site in Utah, USA. To gain insight into the U sequestration mechanism in the amorphous ferric oxyhydroxide (AFO)-coated gravel PRB, U(VI) sorption processes on ferrihydrite surfaces were studied in 0.01 M Na 2 SO 4 solutions to simulate the major chemical composition of U-contaminatedgroundwater (i.e., [SO 4 2- ]~13 mM L -1 ) at the site. Uranyl sorption was greater at pH 7.5 than that at pH 4 in both air- and 2% pCO 2 -equilibrated systems. While there were negligible effects of sulfate ligands on the pH-dependent U(VI) sorption (<24 h) in both systems, X-ray absorption spectroscopy (XAS) analysis showed sulfate ligand associated U(VI) surface species at the ferrihydrite–water interface. In air-equilibrated systems, binary and mono-sulfate U(VI) ternary surface species co-existed at pH 5.43. At pH 6.55–7.83, a mixture of mono-sulfate and bis-carbonato U(VI) ternary surface species became more important. At 2% pCO 2 , there was no contribution of sulfate ligands on the U(VI) ternary surface species. Instead, a mixture of bis-carbonato inner-sphere (38%) and tris-carbonato outer-sphere U(VI) ternary surface species (62%) was found at pH 7.62. The study suggests that the competitive ligand (bicarbonate and sulfate) coordination on U(VI) surface species might be important in evaluating the U solid-state speciation in the AFO PRB at the study site where pCO 2 fluctuates between 1 and 2 pCO 2 %.

Journal of Colloid and Interface Science↗

USGS2004

Tectonics and metallogenesis of Proterozoic rocks of the Reading Prong

Detailed geologic mapping, petrography, and major and trace-element analyses of Proterozoic rocks from the Greenwood Lake Quadrangle, New York are compared with chemical analyses and stratigraphic information compiled for the entire Reading Prong. A persistent regional stratigraphy is evident in the mapped area whose geochemistry indicates protoliths consistent with a back-arc marginal basin sequence. The proposed marginal basin may have been floored by an older sialic basement and overlain by a basin-fill sequence consisting of a basal tholeiitic basalt, basic to intermediate volcanic or volcaniclastic rocks and carbonate sediments, a bimodal calc-alkaline volcanic sequence, and finally volcaniclastic, marine, and continental sediments. The presence of high-chlorine biotite and scapolite may indicate circulation of brine fluids or the presence of evaporite layers in the sequence. Abundant, stratabound magnetite deposits with a geologic setting very unlike that of cratonic, Proterozoic banded-iron formations are found throughout the proposed basin sequence. Associated with many of the magnetite deposits is unusual uranium and rare-earth element mineralization. It is proposed here that these deposits formed in an exhalative, volcanogenic, depositional environment within an extensional back-arc marginal basin. Such a tectonic setting is consistent with interpretations of protoliths in other portions of the Reading Prong, the Central Metasedimentary Belt of the Canadian Grenville Province, and recent interpretation of the origin of the Franklin lead-zinc deposits, suggesting a more cohesive evolving arc/back-arc tectonic model for the entire Proterozoic margin of the north-eastern portion of the North American craton. Published by Elsevier Ltd.

Journal of Geodynamics↗

USGS2009

A lacustrine record from Lop Nur, Xinjiang, China: Implications for paleoclimate change during Late Pleistocene

Climate variability during the Late Pleistocene is studied from the proxies in core CK-2 drilled from the Luobei Depression (91??03???E, 40??47???N), Lop Nur in the eastern Tarim Basin, Xinjiang, China. Geophysical and geochemical properties, including magnetic susceptibility, granularity, chroma, carbonate content, loss on ignition and trace elements, have been determined to reconstruct the environmental evolution of the area during 32-9 ka BP. The chronology is established by uranium-thorium disequilibrium dating techniques. Our data suggest four paleoclimate stages, indicating glacial variations between cold-humid and warm-arid environments. A period of extreme humidity occurred during 31,900-19,200 yr BP is attributed the last glacial maximum (LGM). The period was followed by a warm-arid episode during 19,200-13,500 yr BP. Then a cold-humid interval during 13,500-12,700 yr BP may correspond to another cooling phases at high latitudes of the Northern Hemisphere. The last stage from 12,700 to 9000 yr BP has a trend that the climate turned warm and arid. The Lop Nur region is characterized by particularly humid stadials and arid interstadials. The climate variability in Lop Nur was constrained by global climate change because it is correlated with Dansgaard-Oeschger and Heinrich events, which were observed at the northern high latitudes. The synchroneity of the palaeoclimatic events suggested that cold air activity at the northern high latitudes was the most important factor that influenced the climate evolution in the Lop Nur region. A probable mechanism that involves the migration of westerly winds is proposed to interpret this synchroneity. ?? 2008 Elsevier Ltd.

Journal of Asian Earth Sciences↗

USGS2020

Dating silica sinter (geyserite): A cautionary tale

We describe a new effort to date hydrothermal silica sinter deposits (geyserite) from the Upper Geyser Basin of Yellowstone National Park using 14C of co-deposited organic matter, U-series and cosmogenic 10Be methods. A majority of the samples were collected from stratigraphic sections, mainly at Riverside, Giant, and Castle Geysers. Ages obtained from 41 14C analyses range from modern to 12.1 cal ka BP. Nearly all the 14C ages show inconsistencies with their stratigraphic positions, and several replicate 14C analyses from the same sample result in significantly different ages. The δ13C values of the organic material in the sinter range from -26.6‰ to -12.7‰. The more enriched values are attributed to microbial fixation of dissolved inorganic carbon (DIC), which has heavier δ13C values and is 14C-depleted relative to atmospheric CO2, leading to apparent older ages. U-series analyses on 4 samples yielded ages between 2.2 and 7.4 ka. Large 230Th/U age uncertainties in the sinter, due to low uranium concentrations along with elevated 232Th and associated initial 230Th, make these ages imprecise for use on Holocene deposits. A single cosmogenic 10Be exposure age of 596±18 ka is considerably older than the age of underlying rhyolite and is thus unreliable. This apparent old age results from contamination by meteoric 10Be trapped in the opal that overprints the very small amount of cosmogenic 10Be. By presenting the problems we encountered and discussing their probable cause, this paper highlights the difficulty in obtaining reliable, high-precision geochronological data necessary to use sinter deposits as paleoenvironmental and paleo-hydrothermal archives.

Wyoming↗

USGS2021

Zircon geochronology and geochemistry of Quaternary rhyolite domes of the Coso volcanic field, Inyo County, California

The Quaternary Coso volcanic field (CVF) is a compositionally bimodal volcanic field located within a releasing bend along the eastern range-front Sierra Nevada fault zone in California's southern Owens Valley. The erupted products of CVF silicic magmatism since ~1 Ma comprise 38 high-silica rhyolite domes, with the volumetric majority (~99%) of rhyolite emplaced within the past ~300 ka. The CVF hosts an economically important geothermal field driven by heat associated with a shallow (~5 km) igneous intrusion. The CVF is potentially an immature analog to the nearby Long Valley system, which culminated in generation and eruption of the voluminous and widespread Bishop Tuff. As such, the CVF represents a considerable volcanic hazard, making a detailed understanding of the eruptive history and pre-eruptive conditions of the system critically important. We present uranium-series isochron dates from zircon ± allanite crystal surfaces and zircon trace element geochemical data on the youngest 17 rhyolite domes at Coso, which represent ~60% (by volume) of the silicic magma erupted by the system. These data suggest: (1) a shorter emplacement duration than previously recognized for these domes, with a duration of 20 ± 5 ka; (2) 4 shorter-duration eruption pulses within this interval, all of which occur during the marine isotope stage (MIS) 5 interglacial period; (3) an uptick in the volume of CVF magma erupted between ~200 ka and ~ 78 ka relative to that emplaced over the lifetime of the system; (4) near-coeval eruption of geochemically distinct magma in close geographic proximity, either sourced from different portions of the same magma system at depth or from discrete, uncommunicating bodies; (5) ambiguity with respect to whether or not CVF magmatism is time-predictable, as previously suggested, or erupted as a series of punctuated episodes; (6) no rhyolite volcanism in the past ~78 kyr.

California↗

USGS2025

Applying U-Th disequilbrium for dating siliceous sinters

Continental hydrothermal systems are critical avenues for the crustal transport of heat and mass captured for geothermal energy and mineral exploration. Thus, understanding their temporal evolution and longevity is important for resource characterization. Deposits of microlaminated siliceous sinter, common surface expressions of high temperature reservoirs (> 170 °C), have the potential to trace hydrothermal histories. Geothermal reservoirs are often located within uranium-bearing silicic volcanic rock where subsurface fluid-rock interactions extract U into hydrothermal fluids. U incorporated in the surface sinter deposit has the potential to provide a U— Th disequilibrium dating option. We focus on samples from El Tatio geyser field in the Altiplano of northern Chile, the largest geothermal system in the Andes. Our resulting 230 Th/U ages, along with the water and deposit elemental compositions, suggest concentrations of U and Th vary predictably along the sinter apron. While distal facies containing the highest U concentrations (> 50 μg/g) are least affected by detrital Th corrections, they can display suspected open-system behavior. In contrast, more medial facies, where bacterial mats and other porous textures are co mmonly concentrated, have only trace amounts of U (< 0.1 μg/g), which leads to unreliable or geologically improbable dates. Proximal facies tend to date most consistently. By comparing existing 14 C ages with 230 Th/U results, 230 Th/U ages tend to be younger than the 14 C ages, supporting the presence of a 14 C-dead carbon influence. New data confirm that the onset of geothermal activity at El Tatio goes back to the late Pleistocene.

Altiplano, El Tatio geyser field↗

USGS2006

Biogeochemical transport in the Loxahatchee River estuary, Florida: The role of submarine groundwater discharge

The distributions of dissolved organic carbon (DOC), Ba, U, and a suite of naturally occurring radionuclides in the U/Th decay series (222Rn, 223,224,226,228Ra) were studied during high- and low-discharge conditions in the Loxahatchee River estuary, Florida to examine the role of submarine groundwater discharge in estuarine transport. The fresh water endmember of this still relatively pristine estuary may reflect not only river-borne constituents, but also those advected during active groundwater/surface water (hyporheic) exchange. During both discharge conditions, Ba concentrations indicated slight non-conservative mixing. Such Ba excesses could be attributed either to submarine groundwater discharge or particle desorption processes. Estuarine dissolved organic carbon concentrations were highest at salinities closest to zero. Uranium distributions were lowest in the fresh water sites and mixed mostly conservatively with an increase in salinity. Suspended particulate matter (SPM) concentrations were generally lowest (< 5??mg L- 1) close to zero salinity and increased several-fold (??? 18??mg L- 1; low discharge) toward the seaward endmember, which may be attributed to dynamic resuspension of bottom sediments within Jupiter Inlet. Surface water-column 222Rn activities were most elevated (> 28??dpm L- 1) at the freshwater endmember of the estuary and appear to identify regions of the river most influenced by the discharge of fresh groundwater. Activities of four naturally occurring isotopes of Ra (223,224,226,228Ra) in this estuary and select adjacent shallow groundwater wells yield mean estuarine water-mass transit times of less than 1 day; these values are in close agreement to those calculated by tidal prism and tidal frequency. Submarine groundwater discharge rates to the Loxahatchee River estuary were calculated using a tidal prism approach, an excess 226Ra mass balance, and an electromagnetic seepage meter. Average SGD rates ranged from 1.0 to 3.8 ?? 105??m3 d- 1 (20-74??L m- 2 d- 1), depending on river-discharge stage. Such calculated SGD estimates, which must include both a recirculated as well as fresh water component, are in close agreement with results obtained from a first-order watershed mass balance. Average submarine groundwater discharge rates yield NH4+ and PO4- 3 flux estimates to the Loxahatchee River estuary that range from 62.7 to 1063.1 and 69.2 to 378.5????mol m- 2 d- 1, respectively, depending on river stage. SGD-derived nutrient flux rates are compared to yearly computed riverine total N and total P load estimates. ?? 2006 Elsevier B.V. All rights reserved.

Marine Chemistry↗

USGS2008

The release of dissolved actinium to the ocean: A global comparison of different end-members

The measurement of short-lived 223Ra often involves a second measurement for supported activities, which represents 227Ac in the sample. Here we exploit this fact, presenting a set of 284 values on the oceanic distribution of 227Ac, which was collected when analyzing water samples for short-lived radium isotopes by the radium delayed coincidence counting system. The present work compiles 227Ac data from coastal regions all over the northern hemisphere, including values from ground water, from estuaries and lagoons, and from marine end-members. Deep-sea samples from a continental slope off Puerto Rico and from an active vent site near Hawaii complete the overview of 227Ac near its potential sources. The average 227Ac activities of nearshore marine end-members range from 0.4??dpm m- 3 at the Gulf of Mexico to 3.0??dpm m- 3 in the coastal waters of the Korean Strait. In analogy to 228Ra, we find the extension of adjacent shelf regions to play a substantial role for 227Ac activities, although less pronounced than for radium, due to its weaker shelf source. Based on previously published values, we calculate an open ocean 227Ac inventory of 1.35 * 1018??dpm 227Acex in the ocean, which corresponds to 37??moles, or 8.4??kg. This implies a flux of 127??dpm m-2 y- 1 from the deep-sea floor. For the shelf regions, we obtain a global inventory of 227Ac of 4.5 * 1015??dpm, which cannot be converted directly into a flux value, as the regional loss term of 227Ac to the open ocean would have to be included. Ac has so far been considered to behave similarly to Ra in the marine environment, with the exception of a strong Ac source in the deep-sea due to 231Paex. Here, we present evidence of geochemical differences between Ac, which is retained in a warm vent system, and Ra, which is readily released [Moore, W.S., Ussler, W. and Paull, C.K., 2008-this issue. Short-lived radium isotopes in the Hawaiian margin: Evidence for large fluid fluxes through the Puna Ridge. Marine Chemistry]. Another potential mechanism of producing deviations in 227Ac/228Ra and daughter isotope ratios from the expected production value of lithogenic material is observed at reducing environments, where enrichment in uranium may occur. The presented data here may serve as a reference for including 227Ac in circulation models, and the overview provides values for some end-members that contribute to the global Ac distribution. ?? 2007 Elsevier B.V. All rights reserved.

Marine Chemistry↗

USGS2012

Holocene seasonal variability inferred from multiple proxy records from Crevice Lake, Yellowstone National Park, USA

A 9400-yr-old record from Crevice Lake, a semi-closed alkaline lake in northern Yellowstone National Park, was analyzed for pollen, charcoal, geochemistry, mineralogy, diatoms, and stable isotopes to develop a nuanced understanding of Holocene environmental history in a region of northern Rocky Mountains that receives both summer and winter precipitation. The limited surface area, conical bathymetry, and deep water (> 31 m) of Crevice Lake create oxygen-deficient conditions in the hypolimnion and preserve annually laminated sediment (varves) for much of the record. Pollen data indicate that the watershed supported a closed Pinus -dominated forest and low fire frequency prior to 8200 cal yr BP, followed by open parkland until 2600 cal yr BP, and open mixed-conifer forest thereafter. Fire activity shifted from infrequent stand-replacing fires initially to frequent surface fires in the middle Holocene and stand-replacing events in recent centuries. Low values of δ 18 O suggest high winter precipitation in the early Holocene, followed by steadily drier conditions after 8500 cal yr BP. Carbonate-rich sediments before 5000 cal yr BP imply warmer summer conditions than after 5000 cal yr BP. High values of molybdenum (Mo), uranium (U), and sulfur (S) indicate anoxic bottom-waters before 8000 cal yr BP, between 4400 and 3900 cal yr BP, and after 2400 cal yr BP. The diatom record indicates extensive water-column mixing in spring and early summer through much of the Holocene, but a period between 2200 and 800 cal yr BP had strong summer stratification, phosphate limitation, and oxygen-deficient bottom waters. Together, the proxy data suggest wet winters, protracted springs, and warm effectively wet summers in the early Holocene and less snowpack, cool springs, warm dry summers in the middle Holocene. In the late Holocene, the region and lake experienced extreme changes in winter, spring, and summer conditions, with particularly short springs and dry summers and winters during the Roman Warm Period (~ 2000 cal yr BP) and Medieval Climate Anomaly (1200–800 cal yr BP). Long springs and mild summers occurred during the Little Ice Age, and these conditions persist to the present. Although the proxy data indicate effectively wet summer conditions in the early Holocene and drier conditions in the middle and late Holocene, none point specifically to changes in summer precipitation as the cause. Instead, summer conditions were governed by multi-seasonal controls on effective moisture that operated over multiple time scales.

Montana↗

USGS2005

Isotopic dating of Meso- and Neoproterozoic mafic magmatism in the southern Tobacco Root Mountains, Southwestern Montana

New isotopic dating of mafic dikes in the southern Tobacco Root Mountains of southwestern Montana provides evidence for two distinct episodes of subparallel Proterozoic mafic magmatism separated by about 700 m.y. Previously published geochemical data from dikes in the southern Tobacco Root Mountains had identified three geochemical groups (termed groups A, B, and C) with apparent Rb–Sr ages of 1455 Ma (group A) and 1100–1120 Ma (groups B and C). Sm–Nd dating of a geochemical group A dike yields an age of 1448 ± 49 Ma that is interpreted to represent the emplacement age of the dikes. This age is similar to published U–Pb dates from mafic sills that intrude the nearby Mesoproterozoic Belt Supergroup and Laramide basement-cored uplifts of the Archean Wyoming Province. Paleomagnetic results from groups A and B dikes are similar, suggesting that the were emplaced at about the same time. We suggest that the mafic magmatism recorded by the southern Tobacco Root Mountains group A/C dikes at about 1450 Ma probably corresponds to continental extension that accompanied development of the Mesoproterozoic Belt Basin. U–Pb dating of baddeleyite from the group B dikes provides evidence for a younger magmatic event with an age of 782.4 ± 4.9 Ma (95% confidence; ±7.1 Ma incorporating uranium decay constant errors). This date is similar to isotopic dates from Neoproterozoic mafic dikes and sills exposed elsewhere in uplifts of the Rocky Mountain foreland and that intrude the Mesoproterozoic strata of the Belt Supergroup. Geochronologic data from elsewhere in the northern Cordillera and Canadian Shield indicate that the group B dikes in the southern Tobacco Root Mountains are part of a regional 780 Ma magmatic event that extended for more than 2400 km along the western margin of Laurentia. The origin of the magmatic event is not clear, but may be related to a mantle plume and crustal extension accompanying initial breakup of the supercontinent Rodinia and development of the proto-Pacific Ocean. No evidence of ca. 1100 Ma mafic magmatism in this part of the northern Cordillera was found.

Montana↗