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At least 739 records · Page 41Linked to original sources

USGS2012

Using hydrogeology to identify the source of groundwater to Montezuma Well, a natural spring in central Arizona: part 1

Montezuma Well is a natural spring located within a “sinkhole” in the desert environment of the Verde Valley in Central Arizona. It is managed by the National Park Service as part of Montezuma Castle National Monument. Because of increasing development of groundwater in the area, this research was undertaken to better understand the sources of groundwater to Montezuma Well. The use of well logs and geophysics provides details on the geology in the area around Montezuma Well. This includes characterizing the extent and position of a basalt dike that intruded a deep fracture zone. This low permeability barrier forces groundwater to the surface at the Montezuma Well “pool” with sufficient velocity to entrain sand-sized particles from underlying bedrock. Permeable fractures along and above the basalt dike provide conduits that carry deep sourced carbon dioxide to the surface, which can dissolve carbonate minerals along the transport path in response to the added carbon dioxide. At the ground surface, CO 2 degasses, depositing travertine. Geologic cross sections, rock geochemistry, and semi-quantitative groundwater flow modeling provide a hydrogeologic framework that indicates groundwater flow through a karstic limestone at depth (Redwall Limestone) as the most significant source of groundwater to Montezuma Well. Additional groundwater flow from the overlying formations (Verde Formation and Permian Sandstones) is a possibility, but significant flow from these units is not indicated.

Arizona↗

USGS1989

Sedimentary framework of the southern Maine inner continental shelf: Influence of glaciation and sea-level change

Although the tidally influenced shoreline of Maine is longer than that of virtually any other state, almost no research on its geology has been published. In order to go some way towards remedying this, 1500 km of high-resolution seismic reflection data and 800 km of sidescan sonar imagery have been collected. On the basis of these data and observations made during ten submersible dives, more than 800 bottom samples were collected and evaluated for texture and composition. The understanding of the sedimentary framework of the southern Maine shelf and the processes that maintain it are summarized, and future research directions to evaluate the strategic mineral potential are indicated. In the past 14,000 years, the Maine shelf has experienced a deglaciation and two marine transgressions separated by a regression. The deglaciation was accompanied by the first transgression and deposited till interbedded with up to 40 m of glaciomarine sediment (the Presumpscot Formation) across the shelf. The first transgression culminated about 12,500 yrs B.P., and its landward limit is marked by large glaciomarine deltas 50-100 km landward of the present-day coast. Sea level fell until about 9500 yrs B.P., when shorelines were cut at about the 65 m depth and some large "lowstand deltas" were deposited. Sea level has risen since then and in the general absence of modern river sediment input marine processes have reworked the older sediment. Five shelf environments have been defined in terms of their surficial sediment and stratigraphy. Nearshore ramps are sandy regions extending to about 30 m deep offshore of sandy beaches. These may be reworked lowstand deltas, and possess the thickest bodies of sand in the region. Nearshore basins are mud-filled troughs seaward of coastal areas lacking significant river input. Slumping glaciomarine deposits provide most of the Holocene mud that floors these basins. Rocky zones are extensive areas of exposed rock most common in the 30-50 m depth range. These are areas of high carbonate productivity and provide shell fragments to adjacent areas. The outer basins are muddy regions that begin at the 65 m shoreline and extend beyond the 100 m isobath to the deep Gulf of Maine. Finally, shelf valleys are former stream courses that connect nearshore ramps and basins to the outer basins. These bedrock-framed valleys are filled with sand and mud and are apparently still active conduits for the offshore movement of sediment. The mineralogy of the shelf sediment is complex, and it is not yet clear whether glacial homogenization has obliterated distinctions between river drainage basins and the adjacent shelf. Studies are continuing into northern Maine and analysis of the heavy mineralogy of the shelf sediment utilizing a 2 m Humphrey Spiral to process large grab samples and cores has begun. ?? 1989.

Marine Geology↗

USGS2006

Coastal groundwater/surface-water interactions: a Great Lakes case study

Key similarities exist between marine and Great Lakes coastal environments. Water and nutrient fluxes across lakebeds in the Great Lakes are influenced by seiche and wind set-up and set-down, analogous to tidal influence in marine settings. Groundwater/surface-water interactions also commonly involve a saline-fresh water interface, although in the Great-Lakes cases, it is groundwater that is commonly saline and surface water that is fresh. Evapotranspiration also affects nearshore hydrology in both settings. Interactions between groundwater and surface water have recently been identified as an important component of ecological processes in the Great Lakes. Water withdrawals and the reversal of the groundwater/surface water seepage gradient are also common to many coastal areas around the Great Lakes. As compared to surface water, regional groundwater that discharges to western Lake Erie from Michigan is highly mineralized. Studies conducted by the U.S. Geological Survey at Erie State Game Area in southeastern Michigan, describe groundwater flow dynamics and chemistry, shallow lake-water chemistry, and fish and invertebrate communities. Results presented here provide an overview of recent progress of ongoing interdisciplinary studies of Great Lakes nearshore systems and describe a conceptual model that identifies relations among geologic, hydrologic, chemical, and biological processes in the coastal habitats of Lake Erie. This conceptual model is based on analysis of hydraulic head in piezometers at the study site and chemical analysis of deep and shallow coastal groundwater.

Book chapter↗

USGS2013

First evidence of grass carp recruitment in the Great Lakes Basin

We use aging techniques, ploidy analysis, and otolith microchemistry to assess whether four grass carp Ctenopharyngodon idella captured from the Sandusky River, Ohio were the result of natural reproduction within the Lake Erie Basin. All four fish were of age 1 +. Multiple lines of evidence indicate that these fish were not aquaculture-reared and that they were most likely the result of successful reproduction in the Sandusky River. First, at least two of the fish were diploid; diploid grass carp cannot legally be released in the Great Lakes Basin. Second, strontium:calcium (Sr:Ca) ratios were elevated in all four grass carp from the Sandusky River, with elevated Sr:Ca ratios throughout the otolith transect, compared to grass carp from Missouri and Arkansas ponds. This reflects the high Sr:Ca ratio of the Sandusky River, and indicates that these fish lived in a high-strontium environment throughout their entire lives. Third, Sandusky River fish were higher in Sr:Ca ratio variability than fish from ponds, reflecting the high but spatially and temporally variable strontium concentrations of southwestern Lake Erie tributaries, and not the stable environment of pond aquaculture. Fourth, Sr:Ca ratios in the grass carp from the Sandusky River were lower in their 2011 growth increment (a high water year) than the 2012 growth increment (a low water year), reflecting the observed inverse relationship between discharge and strontium concentration in these rivers. We conclude that these four grass carp captured from the Sandusky River are most likely the result of natural reproduction within the Lake Erie Basin.

Ohio↗

USGS1988

Lacustrine varve formation through time

Studies using sediment traps in lakes reveal that the seasonal flux of sediment regulates both the composition and timing of deposition of materials that reach the bottoms of lakes. If the bottom waters of a lake are partly or totally anoxic, the seasonally deposited materials are preserved as annual groupings of laminae (varves). Common components that form individual laminae consist of allochthonous clastic material derived from the drainage basin, precipitated carbonate minerals, diatom frustules, iron-rich and manganese-rich flocs, autochthonous organic detritus, and autochthonous and allochthonous materials resuspended from the bottom. The "style" of varving has changed over geologic time, reflecting changes in biologic evolution and types of materials available. Precipitated iron-rich laminations were common in the middle Precambrian. Graded sets of clastic organic laminations persisted through the Precambrian, prior to the evolution of bioturbating benthic organisms. Glaciolacustrine varves appear to have retained their distinctive character through time. Carbonate-rich varves occurred sporadically in the Precambrian and Phanerozoic. With the exception of diatoms, major components of modern lacustrine varves were present through the Paleozoic and Mesozoic, and yet varves are rare in strata of these ages, and may have accumulated in marine to brackish-water environments. Diatoms were introduced into lacustrine systems in Early Tertiary time and are common components of varves from then on. Diatom laminae, combined with a greater chance for geologic preservation of younger lake deposits, have increased the number of geologically young occurrences of varved sediments. However, seasonal associations of modern varve components, and the processes they represent, are present in ancient deposits and provide clues to the interpretation of ancient environments.

Palaeogeography, Palaeoclimatology, Palaeoecology↗

USGS2009

Sulfur- and oxygen-isotopes in sediment-hosted stratiform barite deposits

Sulfur- and oxygen-isotope analyses have been obtained for sediment-hosted stratiform barite deposits in Alaska, Nevada, Mexico, and China to examine the environment of formation of this deposit type. The barite is contained in sedimentary sequences as old as Late Neoproterozoic and as young as Mississippian. If previously published data for other localities are considered, sulfur- and oxygen-isotope data are now available for deposits spanning a host-rock age range of Late Neoproterozoic to Triassic. On a ??34S versus ??18O diagram, many deposits show linear or concave-upward trends that project down toward the isotopic composition of seawater sulfate. The trends suggest that barite formed from seawater sulfate that had been isotopically modified to varying degrees. The ??34S versus ??18O patterns resemble patterns that have been observed in the modern oceans in pore water sulfate and water column sulfate in some anoxic basins. However, the closest isotopic analog is barite mineralization that occurs at fluid seeps on modern continental margins. Thus the data favor genetic models for the deposits in which barium was delivered by seafloor seeps over models in which barium was delivered by sedimentation of pelagic organisms. The isotopic variations within the deposits appear to reflect bacterial sulfate reduction operating at different rates and possibly with different electron donors, oxygen isotope exchange between reduction intermediates and H2O, and sulfate availability. Because they are isotopically heterogeneous, sediment-hosted stratiform barite deposits are of limited value in reconstructing the isotopic composition of ancient seawater sulfate.

Geochimica et Cosmochimica Acta↗

USGS2006

Perspectives on basaltic magma crystallization and differentiation: Lava-lake blocks erupted at Mauna Loa volcano summit, Hawaii

Explosive eruptions at Mauna Loa summit ejected coarse-grained blocks (free of lava coatings) from Moku'aweoweo caldera. Most are gabbronorites and gabbros that have 0–26 vol.% olivine and 1–29 vol.% oikocrystic orthopyroxene. Some blocks are ferrogabbros and diorites with micrographic matrices, and diorite veins (≤2 cm) cross-cut some gabbronorites and gabbros. One block is an open-textured dunite. The MgO of the gabbronorites and gabbros ranges ∼ 7–21 wt.%. Those with MgO >10 wt.% have some incompatible-element abundances (Zr, Y, REE; positive Eu anomalies) lower than those in Mauna Loa lavas of comparable MgO; gabbros (MgO <10 wt.%) generally overlap lava compositions. Olivines range Fo 83–58 , clinopyroxenes have Mg#s ∼83–62, and orthopyroxene Mg#s are 84–63 — all evolved beyond the mineral-Mg#s of Mauna Loa lavas. Plagioclase is An 75–50 . Ferrogabbro and diorite blocks have ∼ 3–5 wt.% MgO (TiO 2 3.2–5.4%; K 2 O 0.8–1.3%; La 16–27 ppm), and a diorite vein is the most evolved (SiO 2 59%, K 2 O 1.5%, La 38 ppm). They have clinopyroxene Mg#s 67–46, and plagioclase An 57–40 . The open-textured dunite has olivine ∼ Fo 83.5 . Seven isotope ratios are 87 Sr/ 86 Sr 0.70394–0.70374 and 143 Nd/ 144 Nd 0.51293–0.51286, and identify the suite as belonging to the Mauna Loa system. Gabbronorites and gabbros originated in solidification zones of Moku'aweoweo lava lakes where they acquired orthocumulate textures and incompatible-element depletions. These features suggest deeper and slower cooling lakes than the lava lake paradigm, Kilauea Iki, which is basalt and picrite. Clinopyroxene geobarometry suggests crystallization at <1 kbar P. Highly evolved mineral Mg#s, <75, are largely explained by cumulus phases exposed to evolving intercumulus liquids causing compositional ‘shifts.’ Ferrogabbro and diorite represent segregation veins from differentiated intercumulus liquids filter pressed into rigid zones of cooling lakes. Clinopyroxene geobarometry suggests <300 bar P. Open-textured dunite represents olivine-melt mush, precursor to vertical olivine-rich bodies (as in Kilauea Iki). Its Fo 83.5 identifies the most primitive lake magma as ∼8.3 wt.% MgO. Mass balancing and MELTS show that such a magma could have yielded both ferrogabbro and diorite by ≥50% fractional crystallization, but under different fO 2 : < FMQ (250 bar) led to diorite, and FMQ (250 bar) yielded ferrogabbro. These segregation veins, documented as similar to those of Kilauea, testify to appreciable volumes of ‘rhyolitic’ liquid forming in oceanic environments. Namely, SiO 2 -rich veins are intrinsic to all shields that reached caldera stage to accommodate various-sized cooling, differentiating lava lakes.

Hawaii↗

USGS2008

Inverse geochemical modeling of groundwater evolution with emphasis on arsenic in the Mississippi River Valley alluvial aquifer, Arkansas (USA)

Inverse geochemical modeling (PHREEQC) was used to identify the evolution of groundwater with emphasis on arsenic (As) release under reducing conditions in the shallow (25-30 m) Mississippi River Valley Alluvial aquifer, Arkansas, USA. The modeling was based on flow paths defined by high-precision (??2 cm) water level contour map; X-ray diffraction (XRD), scanning electron microscopic (SEM), and chemical analysis of boring-sediments for minerals; and detailed chemical analysis of groundwater along the flow paths. Potential phases were constrained using general trends in chemical analyses data of groundwater and sediments, and saturation indices data (MINTEQA2) of minerals in groundwater. Modeling results show that calcite, halite, fluorite, Fe oxyhydroxide, organic matter, H2S (gas) were dissolving with mole transfers of 1.40E - 03, 2.13E - 04, 4.15E - 06, 1.25E + 01, 3.11, and 9.34, respectively along the dominant flow line. Along the same flow line, FeS, siderite, and vivianite were precipitating with mole transfers of 9.34, 3.11, and 2.64E - 07, respectively. Cation exchange reactions of Ca2+ (4.93E - 04 mol) for Na+ (2.51E - 04 mol) on exchange sites occurred along the dominant flow line. Gypsum dissolution reactions were dominant over calcite dissolution in some of the flow lines due to the common ion effect. The concentration of As in groundwater ranged from <0.5 to 77 ??g/L. Twenty percent total As was complexed with Fe and Mn oxyhydroxides. The redox environment, chemical data of sediments and groundwater, and the results of inverse geochemical modeling indicate that reductive dissolution of Fe oxyhydroxide is the dominant process of As release in the groundwater. The relative rate of reduction of Fe oxyhydroxide over SO42 - with co-precipitation of As into sulfide is the limiting factor controlling dissolved As in groundwater. ?? 2007 Elsevier B.V. All rights reserved.

Journal of Hydrology↗

USGS2014

Inhalable desert dust, urban emissions, and potentially biotoxic metals in urban Saharan-Sahelian air

Saharan dust incursions and particulates emitted from human activities degrade air quality throughout West Africa, especially in the rapidly expanding urban centers in the region. Particulate matter (PM) that can be inhaled is strongly associated with increased incidence of and mortality from cardiovascular and respiratory diseases and cancer. Air samples collected in the capital of a Saharan–Sahelian country (Bamako, Mali) between September 2012 and July 2013 were found to contain inhalable PM concentrations that exceeded World Health Organization (WHO) and US Environmental Protection Agency (USEPA) PM 2.5 and PM 10 24-h limits 58 – 98% of days and European Union (EU) PM 10 24-h limit 98% of days. Mean concentrations were 1.2-to-4.5 fold greater than existing limits. Inhalable PM was enriched in transition metals, known to produce reactive oxygen species and initiate the inflammatory response, and other potentially bioactive and biotoxic metals/metalloids. Eroded mineral dust composed the bulk of inhalable PM, whereas most enriched metals/metalloids were likely emitted from oil combustion, biomass burning, refuse incineration, vehicle traffic, and mining activities. Human exposure to inhalable PM and associated metals/metalloids over 24-h was estimated. The findings indicate that inhalable PM in the Sahara–Sahel region may present a threat to human health, especially in urban areas with greater inhalable PM and transition metal exposure.

Bamako↗

USGS1999

Mapping the glacial geology of the Central Great Lakes region in three dimensions: A model for state-federal cooperation

Planners need to evaluate complex and competing public-policy options for managing water, land, and biological resources; they must ensure economic growth, meet the needs of an increasing population, assess hazards, and manage the environment in a sustainable manner. The State Geological Surveys of Illinois, Indiana, Michigan, and Ohio and the U.S. Geological Survey (USGS) receive many requests from local, State, and Federal planners and officials for geologic information. Thick and complex layers of glacial and related sediments blanket the bedrock of these States: a three-dimensional understanding of these deposits is critical to making informed resource-management and other planning decisions. At two recent forums (in Indianapolis, March 1997, and Columbus, Ohio, February 1999), more than 200 attendees from more than 60 local, State, and Federal agencies provided a clear message. They need three-dimensional geologic information to use in making decisions on the following issues: • Quality, quantity, distribution, and accessibility of surface and ground water • Aggregate sources and land-use conflicts • Energy and mineral resource management • Environmental management and mitigation of land and water contamination • Acceleration of the permitting processes of regulatory agencies • Industrial, commercial, residential, and infrastructure siting and construction • Agricultural land loss, erosion, sedimentation, and agrichemical use • Waste-disposal planning and mitigation • Habitat alteration and biodiversity • Coastal erosion, landslides, radon, floods, and earthquakes

Illinois, Indiana, Michigan, Ohio↗

USGS2017

Sediment deposition and sources into a Mississippi River floodplain lake; Catahoula Lake, Louisiana

Floodplain lakes are important wetlands on many lowland floodplains of the world but depressional floodplain lakes are rare in the Mississippi River Alluvial Valley. One of the largest is Catahoula Lake, which has existed with seasonally fluctuating water levels for several thousand years but is now in an increasingly hydrologically altered floodplain. Woody vegetation has been encroaching into the lake bed and the rate of this expansion has increased since major human hydrologic modifications, such as channelization, levee construction, and dredging for improvement of navigation, but it remains unknown what role those modifications may have played in altering lake sedimentation processes. Profiles of thirteen 137 Cs sediment cores indicate sedimentation has been about 0.26 cm y − 1 over the past 60 years and has been near this rate since land use changes began about 200 years ago ( 210 Pb, and 14 C in Tedford, 2009). Carbon sequestration was low (10.4 g m − 2 y − 1 ), likely because annual drying promotes mineralization and export. Elemental composition (high Zr and Ti and low Ca and K) and low pH of recent (<~60 y) or surface sediments suggest Gulf Coastal Plain origin, but below the recent sediment deposits, 51% of sediment profiles showed influence of Mississippi River alluvium, rich in base cations such as K + , Ca 2 + , and Mg 2 + . The recent shift to dominance of Coastal Plain sediments on the lake-bed surface suggests hydrologic modification has disconnected the lake from sediment-bearing flows from the Mississippi River. Compared to its condition prior to hydrologic alterations that intensified in the 1930s, Catahoula Lake is about 15 cm shallower and surficial sediments are more acidic. Although these results are not sufficient to attribute ecological changes directly to sedimentological changes, it is likely the altered sedimentary and hydrologic environment is contributing to the increased dominance of woody vegetation.

Louisiana↗

USGS2022

Geochemical insights into formation of enigmatic ironstones from Rio Grande rise, South Atlantic Ocean

Rio Grande Rise (RGR) is an intraplate oceanic elevation in the South Atlantic Ocean that formed at a hotspot on the Mid-Atlantic Ridge during the Cretaceous. In spreading center and hotspot environments, ironstones form mainly by biomineralization of reduced Fe from hydrothermal fluids or oxidation of sulfide deposits. However, RGR has been considered aseismic and volcanically inactive for the past 46 Ma. Here, we investigate the origin of ironstones collected from the summit of RGR using multiple techniques: petrographic observations, X-ray diffraction, U-Th/He geochronology, and chemical composition. The ironstones from RGR consist of finely laminated goethite containing igneous rock fragments, carbonate fluorapatite, and calcite. Our results suggest that Fe oxyhydroxides were precipitated by Fe-oxidizing bacteria forming bacterial mats. The bacterial Fe mats underwent compaction, dewatering, goethite crystallization, and cementation that created the ironstone deposits. U-Th/He geochronology reveals protracted goethite minimum ages extending from the late Miocene to the Quaternary, probably due to multiple generations of mats, slow mineralization rates, and Fe-oxide dissolution-reprecipitation cycles. Flame-like goethite structures underneath FeMn crusts and a chimney-shaped goethite sample with a central channel indicate that the dewatering fluid flowed upward through the deposits, or a thermal fluid source may have been introduced from below the ironstone deposits. High Fe/Mn ratios, low trace metals contents (Ni + Co + Cu), and very low Fe/REY ratios suggest ironstone precipitation from a hydrothermal fluid; however, REY SN plots and bivariate Ce SN /Ce SN ⁎ versus Y SN /Ho SN and Ce SN /Ce SN ⁎ versus Nd plots are inconclusive, and a proximal source of magma was unlikely during the period of mat formation. Given this evidence, we hypothesize that a geothermal circulation system may have facilitated ironstone mineralization at RGR.

Marine Geology↗

USGS2022

A model of the spatiotemporal dynamics of soil carbon following coastal wetland loss applied to a Louisiana salt marsh in the Mississippi River Deltaic Plain

The potential for carbon sequestration in coastal wetlands is high due to protection of carbon (C) in flooded soils. However, excessive flooding can result in the conversion of the vegetated wetland to open water. This transition results in the loss of wetland habitat in addition to the potential loss of soil carbon. Thus, in areas experiencing rapid wetland submergence, such as the Mississippi River Delta, coastal wetlands could become a significant source of carbon emissions if land loss is not mitigated. To accurately assess the capacity of wetlands to store (or emit) carbon in dynamic environments, it is critical to understand the fate of soil carbon following the transition from vegetated wetland to open water. We developed a simple soil carbon model representing soil depths to 1 m using the data collected from a Louisiana coastal salt marsh in the Mississippi River Deltaic Plain to predict soil carbon density and stock following the transition from a vegetated salt marsh to an open water pond. While immediate effects of ponding on the distribution of carbon within the 1-m soil profile were apparent, there were no effects of ponding on the overall, integrated, carbon stocks 14 years, following wetland submergence. Rather, the model predicts that soil carbon losses in the first meter will be realized over long periods of time (∼200 years) due to changes in the source of carbon (biomass vs. mineral sediment) with minimal losses through mineralization.

Louisiana↗

USGS2015

A pan-Arctic synthesis of CH 4 and CO 2 production from anoxic soil incubations

Permafrost thaw can alter the soil environment through changes in soil moisture, frequently resulting in soil saturation, a shift to anaerobic decomposition, and changes in the plant community. These changes, along with thawing of previously frozen organic material, can alter the form and magnitude of greenhouse gas production from permafrost ecosystems. We synthesized existing methane (CH 4 ) and carbon dioxide (CO 2 ) production measurements from anaerobic incubations of boreal and tundra soils from the geographic permafrost region to evaluate large-scale controls of anaerobic CO 2 and CH 4 production and compare the relative importance of landscape-level factors (e.g., vegetation type and landscape position), soil properties (e.g., pH, depth, and soil type), and soil environmental conditions (e.g., temperature and relative water table position). We found fivefold higher maximum CH 4 production per gram soil carbon from organic soils than mineral soils. Maximum CH 4 production from soils in the active layer (ground that thaws and refreezes annually) was nearly four times that of permafrost per gram soil carbon, and CH 4 production per gram soil carbon was two times greater from sites without permafrost than sites with permafrost. Maximum CH 4 and median anaerobic CO 2 production decreased with depth, while CO 2 :CH 4 production increased with depth. Maximum CH 4 production was highest in soils with herbaceous vegetation and soils that were either consistently or periodically inundated. This synthesis identifies the need to consider biome, landscape position, and vascular/moss vegetation types when modeling CH 4 production in permafrost ecosystems and suggests the need for longer-term anaerobic incubations to fully capture CH 4 dynamics. Our results demonstrate that as climate warms in arctic and boreal regions, rates of anaerobic CO 2 and CH 4 production will increase, not only as a result of increased temperature, but also from shifts in vegetation and increased ground saturation that will accompany permafrost thaw.

Global Change Biology↗

USGS2015

Soil geochemical survey of abandoned mining sites in the Eastern-Central Peloritani Mountains, Sicily, Italy

This investigation focused on topsoils ( n = 122) and vertical profiles ( n = 6) distributed over an area of 250 km 2 in the eastern-central Peloritani Mountains, northeastern Sicily. Georeferenced concentration of 53 elements (including potentially harmful ones), determined by ICP-MS after an aqua regia leach, were used to produce geochemical maps by means of a GIS-aided spatial interpolation process. Results show that there are two distinct areas: the larger, located between the Fiumendinisi, Budali and Ali villages, and the other between C. Postlioni and Femmina Morta, which contain anomalous As (up to 727 mg/kg), Sb (up to 60 mg/kg), Ag (up to 1 mg/kg) and Au (up to 0.1 mg/kg) concentrations. Most of the investigated areas have high contamination levels for As, Zn, Sb, and Pb that exceed the threshold values (As = 20 mg/kg, Zn = 150 mg/kg, Sb = 10 mg/kg and Pb = 100 mg/kg) established for soils by the Italian Environmental Law ( Decreto Legislativo 2006 , number 152). The isotopic ratios of 206 Pb/ 207 Pb and 208 Pb/ 207 Pb have been measured in selected soils on both leaches [using 1M HNO 3 –1.75M HCl (50:50)] and residues thereof. Soil leach reflects possible anthropogenic contamination, whereas soil residues indicate geogenic contributions. Results suggest that most of contamination in the soils is related to the presence of sulphide and sulphosalt rock-forming minerals in the surveyed area. The soil fraction contains a Pb value >1600 mg/kg and has ratios of 1.1695 for 206 Pb/ 207 Pb and 2.4606 for 208 Pb/ 207 Pb. Only one soil leach isotopic composition could reflect possible anthropogenic contamination. The correlation among As, Zn, Pb contents v. Pb isotopic signatures of 206 Pb/ 207 Pb indicates that surface and deep soils collected from profiles are dominated by geogenic compositions.

Peloritani Mountains, Sicily↗

USGS2008

Potential for 4- n -nonylphenol biodegradation in stream sediments

The potential for in situ biodegradation of 4-nonylphenol (4-NP) was investigated in three hydrologically distinct streams impacted by wastewater treatment plants (WWTPs) in the United States. Microcosms were prepared with sediments from each site and amended with [U-ring- 14 C]4- n -nonylphenol (4- n -NP) as a model test substrate. Microcosms prepared with sediment collected upstream of the WWTP outfalls and incubated under oxic conditions showed rapid and complete mineralization of [U-ring- 14 C]4- n -NP to 14 CO 2 in all three systems. In contrast, no mineralization of [U-ring- 14 C]4- n -NP was observed in these sediments under anoxic (methanogenic) conditions. The initial linear rate of [U-ring-14C]4-n-NP mineralization in sediments from upstream and downstream of the respective WWTP outfalls was inversely correlated with the biochemical oxygen demand (BOD) of the streambed sediments. These results suggest that the net supply of dissolved oxygen to streambed sediments is a key determinant of the rate and extent of 4-NP biodegradation in stream systems. In the stream systems considered by the present study, dissolved oxygen concentrations in the overlying water column (8–10 mg/L) and in the bed sediment pore water (1–3 mg/L at a depth of 10 cm below the sediment–water interface) were consistent with active in situ 4-NP biodegradation. These results suggest WWTP procedures that maximize the delivery of dissolved oxygen while minimizing the release of BOD to stream receptors favor efficient biodegradation of 4-NP contaminants in wastewater-impacted stream environments.

Colorado, Iowa↗

USGS1983

Selective concentration of cesium in analcime during hydrothermal alteration, Yellowstone National Park, Wyoming

Chemical and mineralogical studies of fresh and hydrothermally altered rhyolitic material in Upper and Lower Geyser Basins, Yellowstone National Park, show that all the altered rocks are enriched in Cs and that Cs is selectively concentrated in analcime. The Cs content of unaltered rhyolite lava flows, including those from which the altered sediments are derived, ranges from 2.5 to 7.6 ppm. The Cs content of analcime-bearing altered sedimentary rocks is as high as 3000 ppm, and in clinoptilolite-bearing altered sedimentary rocks Cs content is as high as 180 ppm. Altered rhyolite lava flows which were initially vitrophyres, now contain up to 250 ppm Cs, and those which were crystallized prior to hydrothermal alteration contain up to 14 ppm. Mineral concentrates of analcime contain as much as 4700 ppm Cs. The Cs must have been incorporated into the analcime structure during crystallization, rather than by later cation substitution, because analcime does not readily exchange Cs. The Cs Cl "> CsCl of the fluids circulating through the hydrothermal system varies, suggesting that Cs is not always a conservative ion and that Cs is lost from upflowing thermal waters due to water-rock interaction resulting in crystallization of Cs-bearing analcime. The source of Cs for Cs enrichment of the altered rocks is from leaching of rhyolitic rocks underlying the geyser basins, and from the top of the silicic magma chamber that underlies the area. Analcime is an important natural Cs sink, and the high Cs concentrations reported here may prove to be an important indicator of the environment of analcime crystallization.

Geochimica et Cosmochimica Acta↗

USGS2015

Uranium in the Islamic Republic of Mauritania (phase V, deliverable 81)

Mauritania has 80 known uranium mineral occurrences and is the current focus of active exploration for uranium by a number of private companies. Seventeen occurrences have had resource estimates published and can be considered as mineral deposits. Fourteen of these are calcrete-type deposits with a total resource of 138.3 million tonnes at an average grade of 331 ppm U3O8. The three bedrock-hosted deposits are granite hosted vein/shear zone type deposits with a total resource of 46.5 million tonnes at a grade of 248 ppm U3O8. All of the deposits and the majority of the other uranium occurrences are found in the Paleoproterozoic Rgueïbat Shield in areas underlain by the Cortege de Yetti, the Complexe de Tmeïmichatt Ghallamane and the Complexe d'Adam Esseder. This area is also visible in the PRISM airborne radiometric data as an extensive >4 ppm equivalent uranium anomaly. Uranium occurrences are also reported in the Tasiast-Tijirit Terrane of the Archean Rgueïbat Shield, the Mauritanide Belt, and the Coastal Basin. Geologic environments permissive for eight types of uranium deposits are recognized in Mauritania. These deposit types include: calcrete, granite-hosted vein/shear, alkaline intrusive, unconformity-associated, quartz pebble conglomerate, phosphate, sandstone, and red bed-type uranium deposits.

Open-File Report↗