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Paul J. Lamothe

Publications and source records attributed to Paul J. Lamothe.

28 records · Page 2Linked to original sources

Multi-decadal impacts of grazing on soil physical and biogeochemical properties in southeast Utah

Many soils in southeastern Utah are protected from surface disturbance by biological soil crusts that stabilize soils and reduce erosion by wind and water. When these crusts are disturbed by land use, soils become susceptible to erosion. In this study, we compare a never-grazed grassland in Canyonlands National Park with two historically grazed sites with similar geologic, geomorphic, and geochemical characteristics that were grazed from the late 1800s until 1974. We show that, despite almost 30 years without livestock grazing, surface soils in the historically grazed sites have 38–43% less silt, as well as 14– 51% less total elemental soil Mg, Na, P, and Mn content relative to soils never exposed to livestock disturbances. Using magnetic measurement of soil magnetite content (a proxy for the stabilization of far-traveled eolian dust) we suggest that the differences in Mg, Na, P, and Mn are related to wind erosion of soil fine particles after the historical disturbance by livestock grazing. Historical grazing may also lead to changes in soil organic matter content including declines of 60–70% in surface soil C and N relative to the never-grazed sites. Collectively, the differences in soil C and N content and the evidence for substantial rock-derived nutrient loss to wind erosion implies that livestock grazing could have long-lasting effects on the soil fertility of native grasslands in this part of southeastern Utah. This study suggests that nutrient loss due to wind erosion of soils should be a consideration for management decisions related to the long-term sustainability of grazing operations in arid environments.

Utah

Selenium loading through the Blackfoot River watershed--linking sources to ecosystem

The upper Blackfoot River watershed in southeast Idaho receives drainage from 11 of 16 phosphate mines that have extracted ore from the Phosphoria Formation, three of which are presently active. Toxic effects from selenium (Se), including death of livestock and deformity in aquatic birds, were documented locally in areas where phosphatic shales are exposed ( Piper et al., 2000 ; Presser et al., Chapter 11). Current drainage conditions are leading to Se bioaccumulation at concentrations that pose a risk to fish in the Blackfoot River and its tributaries (Hamilton et al., Chapter 18). A gaging station on the Blackfoot River was re-activated in April 2001 to assess hydrologic conditions and concentration, load, and speciation for Se discharges on a watershed scale. The gaging-station data are considered to represent regional drainage conditions in the upper Blackfoot River water- shed because of its location near the outlet of the watershed and directly upstream of the Blackfoot Reservoir. Watershed discharges for 2001 and 2002 were below minimum hydrologic conditions for the gage as documented by the historical record. Drought emergencies were declared in the area in both 2001 and 2002. Unmonitored diversions for irrigation that routinely take place during the snowmelt season also affected conditions downstream. Annual cycles in Se concentration, load, and selenate (Se 6+ ) reached maxima in the spring during the period of maximum flow at the gaging station. Thirty-seven to 44% of annual flow occurred dur- ing the three-month high-flow season (April through June) in 2001 and 56% of annual flow occurred during that time period in 2002. Extrapolation from historical hydrographs for average and wet years and a limited data set of regional Se concentrations for 2001 and 2002 indicated potential for a 3.6- to 7.4-fold increase in Se loading because of increased seasonal flows in the Blackfoot River watershed. Supplementation data indicate that: (a) the difference between total Se and dissolved Se, as a measure of the contribution of particulate Se, was < 10% except at the peak of con- centration when total Se was 18% more than dissolved Se; (b) selenite (Se 4+ ) represented less than 10% of the dissolved species during all months of 2001; and (c) dissolved Se was approximately a 50:50 mixture of selenate and organic selenide (operationally defined Se 2- ) during summer 2001 (June through August). Ecological risk based on regional Se drainage occurred during both the high- and low-flow seasons. Seventy to 83% of the Se load occurred during the high-flow season. During early May of both years, dissolved-Se concentrations exceeded the criterion for the protection of aquatic life and the ecological threshold of 5 gL 1 Se at which sub- stantive risk occurs. During the majority of the three-month high-flow season, dissolved- Se concentrations exceeded the 2 gL 1 Se concern level for aquatic biota. The Se concentration in suspended material during high flow in 2002 was within the range of marginal risk to aquatic life (2-4 gg 1 Se, dry weight). Selenate was the major species during peak flows, with both selenate and organic selenide being major species during relatively low-flow periods in summer. A change in speciation to reduced Se may indicate elevated biotic productivity during summer months and could result in enhanced Se uptake in food webs. In addition to the magnitude of regional Se release in the Blackfoot River watershed, Se concentrations in individual source drains and waste-rock seeps, and those predicted by experimental column leaching of proposed mining overburden materials, also indicate that drainage options that currently meet existing demands for phosphate mining cause eco- logical risk thresholds to be exceeded. At times, the drinking-water Se standard (50 g L 1 Se) and the criterion for hazardous Se waste (1000 L -1 Se) ( US Department of the Interior, 1998 ; US Environmental Protection Agency, 1987 ) are also exceeded. For water-years 2001 and 2002, seasonal increased input of water in the mining area resulted in increased Se transport, suggesting a mechanism of contamination that involves a significant Se reservoir. Hence, recognition and monitoring of Se loading to the envi- ronment on a mass balance basis (i.e. inputs, fluxes and storage within environmental media, and outputs) are essential to evaluating how to control Se concentrations within environmentally protective ranges ( Presser and Piper, 1998 ). In areas where release of Se to aquatic systems is anticipated as a product of future expansion of phosphate mining, continuous monitoring of flow and development of seasonal Se loading patterns would help to model watersheds in terms of sources, flow periods, and environmental-Se con- centrations that most influence bioavailability. These data, in turn, could be linked to Se- bioaccumulation models specific to food webs and vulnerable species of the impacted areas to accurately project ecological effects. Gaging at this site on the Blackfoot River is planned to continue in order to establish a long-term (>10 year) record of hydrologic conditions.

Idaho

Use of an intact core and stable-metal isotopes to examine leaching characteristics of a fluvial tailings deposit

The upper Arkansas River south of Leadville, Colorado, USA, contains deposits of fluvial tailings from historical mining operations in the Leadville area. These deposits are possible non-point sources of acid and metal contamination to surface- and ground-water systems. We used stable-metal isotopes to help ascertain metal retention and release mechanisms that influence metal transport from the deposits to shallow ground-water systems. To accomplish this, we excavated an intact core from a small fluvial tailings deposit and performed laboratory column experiments to examine the amount of metals leaching through the core. Deionised water was continuously applied to the top of the core, and effluent was collected from the bottom of the core for a period of about two months. Three saturation conditions were used, including unsaturated, partially saturated, and fully saturated. Reducing conditions developed upon partial and complete saturation of the core. During the unsaturated leaching phase, core effluents were acidic (pH 2.8 - 3.5) and contained elevated metal concentrations. During a portion of the unsaturated leaching phase, stable-metal isotope spikes and conservative tracers were simultaneously applied to the top of the core. The isotopes provide a means to delineate metal behaviour within the core. During the unsaturated leaching phase, the isotope spikes did not exhibit breakthrough with simultaneously added conservative tracers. However, some of the stable-metal isotope spikes did break through when reducing conditions occurred in the core (during the partial- and completesaturation conditions). In this paper, we use Cd as an example of the utility of stable-metal isotopes in geochemical studies. In the case of Cd, after the core was partially saturated, the 111 Cd spike was released as evidenced by a change in the Cd isotope ratios in the effluent. This release continued during the fully saturated leaching phase, however, the total Cd concentration did not increase. These results suggest that the 111 Cd spike was retained inside the core during the unsaturated leaching phase, and only partially released as reducing conditions developed. Results from this core-leaching experiment indicate there is a large reservoir of water-soluble material within the fluvial tailings deposit, which yields elevated metal concentrations and high acidity, and which may degrade adjacent ground- and surface-water quality. Use of stable metal isotopes in this study facilitated the determination of different metal-retention processes, metal-release processes, and metal sources in the fluvial tailings deposit in response to changing geochemical conditions.

Conference Paper

Variations in suspended sediment and associated trace element concentrations in selected riverine cross sections

Detailed sampling and subsequent analyses of riverine suspended sediment obtained from six rivers in the United States indicate substantial differences in suspended sediment concentrations and possibly in some associated trace elements, depending on whether depth- and width-integrated, point, or pumping samples are used. In addition, the data from time-series, depth-integrated sampling indicate that there can be substantial short-term (on the order of 20-30 min) spatial and/or temporal variations in suspended-sediment concentrations. Despite this, major element concentrations are remarkably stable both spatially and temporally. Trace element concentrations are generally stable; however, some spatial and temporal variations may occur.

Environmental Science and Technology

Update and revisions for Open-File Report 98-624, synthetic precipitation leaching procedure (SPLP) leachate chemistry data for solid mine-waste composite samples from the Silverton and Leadville districts in Colorado

This report supersedes, revises, and updates information and data previously released in Open-File Report 98-624 (Montour and others, 1998). Data for this report were derived from leaching of mine-waste composite samples using a modification of E.P. A. Method 1312, Synthetic Precipitation Leaching Procedure (SPLP). In 1997, members of the U.S. Geological Survey Mine Waste Characterization Project collected four mine-waste composite samples from mining districts near Silverton, Colorado (MAY and YUK), and near Leadville, Colorado (VEN and SUN). This report presents analytical results from these sites.

Open-File Report

Synthetic Precipitation Leaching Procedure (SPLP) leachate chemistry data for solid mine-waste composite samples from southwestern New Mexico, and Leadville, Colorado

This report details chemistry data derived from leaching of mine-waste composite samples using a modification of E.P.A. Method 1312, Synthetic Precipitation Leaching Procedure (SPLP). In 1998, members of the U.S. Geological Survey Mine Waste Characterization Project collected four mine-waste composite samples from mining districts in southwestern New Mexico (CAR and PET) and near Leadville, Colorado (TUC and MII). Resulting leachate pH values for the four composites ranged from 5.45 to 8.84 and ranked in the following order: CAR < TUC < MII < PET. Specific conductivity values ranged from 85 uS/cm to 847 uS/cm in the following order: PET < MII < CAR < TUC. Geochemical data generated from this investigation reveal that leachate from the CAR composite contains the highest concentrations of Pb, Zn, Ni, Mn, Cu, Cd, and Al

Open-File Report