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At least 55 records · Page 3Linked to original sources
USGS2002

Assessment of relative accuracy in the determination of organic matter concentrations in aquatic systems

Accurate determinations of total (TOC), dissolved (DOC) and particulate (POC) organic carbon concentrations are critical for understanding the geochemical, environmental, and ecological roles of aquatic organic matter. Of particular significance for the drinking water industry, TOC measurements are the basis for compliance with US EPA regulations. The results of an interlaboratory comparison designed to identify problems associated with the determination of organic matter concentrations in drinking water supplies are presented. The study involved 31 laboratories and a variety of commercially available analytical instruments. All participating laboratories performed well on samples of potassium hydrogen phthalate (KHP), a compound commonly used as a standard in carbon analysis. However, problems associated with the oxidation of difficult to oxidize compounds, such as dodecylbenzene sulfonic acid and caffeine, were noted. Humic substances posed fewer problems for analysts. Particulate organic matter (POM) in the form of polystyrene beads, freeze-dried bacteria and pulverized leaf material were the most difficult for all analysts, with a wide range of performances reported. The POM results indicate that the methods surveyed in this study are inappropriate for the accurate determination of POC and TOC concentration. Finally, several analysts had difficulty in efficiently separating inorganic carbon from KHP solutions, thereby biasing DOC results.

Journal of Environmental Monitoring↗
USGS1973

Microprobe analyses of sericite, chlorite, and epidote from Jerome, Arizona

Volcanic rocks in the vicinity of the massive sulfide deposits at the United Verde mine, Jerome, Ariz., have been modified in several periods of hydrothermal alteration and greenschist metamorphism. Chlorite, 2M, mica (sericite), and epidote are characteristic alteration products. Microprobe analyses for sericite, chlorite, and epidote are recalculated to structural formulas by the method employing oxygen anion equivalents. The sericite has the general composition of muscovite, but is moderately phengitic, and two samples have 6-12 percent paragonite in solid solution. Most of the chlorite is ripidolite with approximately one-third of the tetrahedral sites filled by aluminum; octahedral aluminum slightly exceeds tetrahedral. Fe:Fe+Mg+Mn ratios range from 0.34 to 0.66; low values are associated with sulfide minerals; higher values occur in a sample peripheral to the massive sulfide deposit. The epidote is a solid solution of 70 percent epidote, 30 percent clinozoisite.

Arizona↗
USGS1977

Derivation of solute-transport equations for a turbulent natural-channel flow

The continuity equation of water and the convection-diffusion equation for a solute are derived by use of an orthogonal curvilinear (natural) coordinate system, which follows the meandering and irregular pattern of natural channel geometry. The solute is assumed to be neutrally buoyant, conservative, and passive. The three-, two-, and one-dimensional equations derived herein represent one of the most satisfactory descriptions of solute transport by turbulent flow in a natural channel.

Journal of Research of the U.S. Geological Survey↗
USGS2014

Reply to: Turner, R.E., 2014. Discussion of: Olea, R.A. and Coleman, J.L., Jr., 2014. A synoptic examination of causes of land loss in southern Louisiana as related to the exploitation of subsurface geologic resources, Journal of Coastal Research, 30(5), 1025–1044; Journal of Coastal Research, 30(6), 1330–1334.

To a large extent, geology is a science of solving inverse problems based on some data and scientific principles. Solutions to these types of problems are not unique, especially when using different data, invoking different principles, or both. It is not surprising that the discussant and we have reached different conclusions on the same specific issue of land loss along the coast of Louisiana because we use different observations and view those observations in a different context. The objective of this reply is to orient the reader, who then can decide which approach is more likely to be the correct analysis.

Journal of Coastal Research↗
USGS2010

Time-dependent seismic tomography

Of methods for measuring temporal changes in seismic-wave speeds in the Earth, seismic tomography is among those that offer the highest spatial resolution. 3-D tomographic methods are commonly applied in this context by inverting seismic wave arrival time data sets from different epochs independently and assuming that differences in the derived structures represent real temporal variations. This assumption is dangerous because the results of independent inversions would differ even if the structure in the Earth did not change, due to observational errors and differences in the seismic ray distributions. The latter effect may be especially severe when data sets include earthquake swarms or aftershock sequences, and may produce the appearance of correlation between structural changes and seismicity when the wave speeds are actually temporally invariant. A better approach, which makes it possible to assess what changes are truly required by the data, is to invert multiple data sets simultaneously, minimizing the difference between models for different epochs as well as the rms arrival-time residuals. This problem leads, in the case of two epochs, to a system of normal equations whose order is twice as great as for a single epoch. The direct solution of this system would require twice as much memory and four times as much computational effort as would independent inversions. We present an algorithm, tomo4d, that takes advantage of the structure and sparseness of the system to obtain the solution with essentially no more effort than independent inversions require. No claim to original US government works Journal compilation ?? 2010 RAS.

Geophysical Journal International↗
USGS2026

Advances and applications of Unoccupied Aerial Systems (UAS) research in landscape ecology

Landscape ecologists have long depended on satellite and aerial remote sensing to address questions about landscape pattern and process, structure, and change (Foody 2023 ). Unoccupied aerial systems/vehicles (UAS/UAV, a.k.a. drones) technology is becoming an increasingly popular research tool in environmental sciences allowing scientists to generate low-cost, high-quality, and high-resolution imagery on demand that can be tailored to specific research questions. While satellite data are of a fixed resolution and temporal interval, UAS offer researchers control and flexibility to design studies and collect data at resolutions and scales that provide ecologically relevant information at finer spatial resolutions (e.g., < 30 cm) than what is currently available from satellite platforms (typically > 3m), thus helping capture objects such as individual plant canopies, micro-topography, and individual animals. Unlike satellites with fixed orbits, UAS can be deployed at more optimal temporal frequencies for ecological monitoring. We organized the special collection “Advances and Applications of Unoccupied Aerial Systems (UAS) Research in Landscape Ecology” to showcase the many ways that UAS tools and technologies are currently applied to advance landscape ecological research. When we announced the collection in 2023, only 11 papers published in the journal Landscape Ecology used UAS data, which was a notably small number compared to many other general ecology, environmental science and remote sensing journals. In an attempt to understand why UAS were not more widely used in landscape ecology and provide possible solutions, we published a review article (Villarreal et al. 2025) that identified the challenges, knowledge gaps, and obstacles for the adoption of UAS technologies in landscape ecology research. The main issues we identified include: (1) an abundance of UAS methods papers in the existing literature, with comparatively few studies demonstrating how UAS can be applied to address ecological questions; (2) a perceived scale mismatch between the geographic extent of UAS data collection (local) compared to larger study areas (landscapes) and a need to design robust scaling approaches to connect fine-scale UAS data with broader ecological patterns; and (3) a need for improved integration of UAS data with other commonly used remote sensing datasets including historical high resolution aerial imagery. Additionally, researchers new to UAS remote sensing may be discouraged or overwhelmed by the general lack of scientific consensus and standardized protocols for typical tasks such as data collection, vegetation classification, and change detection, as well as restrictive and/or confusing policy, regulatory, and legal issues surrounding UAS operations (Villarreal et al. 2025).

Landscape Ecology↗
USGS1988

Experimental studies in stream-aquifer interaction along the Arkansas River in Central Kansas - Field testing and analysis

During the last several years, streamflows of a number of Kansas streams have been reduced as a result of groundwater declines. In order to better understand and quantify stream-aquifer interrelationships, an eight-day comprehensive stream-aquifer pumping test, followed by recovery monitoring, was conducted along the Arkansas River near Great Bend, Kansas. In addition to water level monitoring in numerous observation wells, streamflow data, streambed hydraulic gradients, neutron probe-based water content of dewatered sediments, water chemistry and other data were collected. The alluvial aquifer is shown to be highly transmissive ( T = 1803 m 2 d −1 ) with the pumping stress (9538 m 3 d −1 ) having a radius of influence larger than 1.77 km, impacting both the aquifer levels and the streamflow in the nearby Arkansas River. Drawdown and recharge boundary effects were observed in all observation wells, including those on the opposite side of the river. The alluvial aquifer did not exhibit a water table behavior and responded as a leaky confined aquifer. A semiconfining clay layer less than 3 m thick and an additional recharge source from a nearby stream-alluvial system were the probable causes of the observed phenomena. Actual streamflow depletion is shown to be appreciably less than the computed depletion based on analytical solutions.

Kansas↗
USGS2006

Effects of watershed-scale land use change on stream nitrate concentrations

The Walnut Creek Watershed Monitoring Project was conducted from 1995 through 2005 to evaluate the response of stream nitrate concentrations to changing land use patterns in paired 5000-ha Iowa watersheds. A large portion of the Walnut Creek watershed is being converted from row crop agriculture to native prairie and savanna by the U.S. Fish and Wildlife Service at the Neal Smith National Wildlife Refuge (NSNWR). Before restoration, land use in both Walnut Creek (treatment) and Squaw Creek (control) watersheds consisted of 70% row crops. Between 1990 and 2005, row crop area decreased 25.4% in Walnut Creek due to prairie restoration but increased 9.2% in Squaw Creek due to Conservation Reserve Program (CRP) grassland conversion back to row crop. Nitrate concentrations ranged between <0.5 to 14 mg L-1 at the Walnut Creek outlet and 2.1 to 15 mg L-1 at the downstream Squaw Creek outlet. Nitrate concentrations decreased 1.2 mg L-1 over 10 yr in the Walnut Creek watershed but increased 1.9 mg L-1 over 10 yr in Squaw Creek. Changes in nitrate were easier to detect and more pronounced in monitored subbasins, decreasing 1.2 to 3.4 mg L-1 in three Walnut Creek subbasins, but increasing up to 8.0 and 11.6 mg L-1 in 10 yr in two Squaw Creek subbasins. Converting row crop lands to grass reduced stream nitrate levels over time in Walnut Creek, but stream nitrate rapidly increased in Squaw Creek when CRP grasslands were converted back to row crop. Study results highlight the close association of stream nitrate to land use change and emphasize that grasslands or other perennial vegetation placed in agricultural settings should be part of a long-term solution to water quality problems. ?? ASA, CSSA, SSSA.

Journal of Environmental Quality↗
USGS1976

Classification of organic solutes in water by using macroreticular resins

A series of macroreticular resin adsorbents was evaluated for ability to extract and fractionate organic solutes found in natural waters. Studies with organic solute standards and natural water samples lead to the development of dissolved organic carbon (DOC) fractionation analysis whereby the DOC is concentrated and fractionated by macroreticular resins into acid, base, and neutral hydrophobic organic solute fractions and into acid, base, and neutral hydrophilic organic solute fractions. The hydrophobic solutes were sorbed and fractionated on nonionic, nonpolar macroreticular resins, and the hydrophilic solutes were sorbed and fractionated by macroreticular ion-exchange resins. Organic-inorganic complexes as well as organic solutes were isolated by resin sorption. DOC fractionation analysis was developed to serve as a compound classification that fills the gap in organic solute characterization between the organic solute concentration (DOC) and specific compound identification.

Journal of Research of the U.S. Geological Survey↗
USGS1977

Routing of stormwater flows through storm drains

Storm-drain flow-routing methods based on kinematic-wave routing and storage-routing methods are compared with the MLSR (multiple-linearization storm-drain routing) method for hypothetical circular pipe problems. The MLSR method, based on a diffusion-wave routing concept, is shown to give very good results without incurring the numerical solution or damping problems of other methods.

Journal of Research of the U.S. Geological Survey↗
USGS1976

Bicarbonate content of groundwater in carbonate rock in eastern North America

In carbonate-rock terrane the most effective solution occurs where soil and vegetative cover facilitate biogenic production and storage of CO 2 in the soil until part of it is carried downward in percolating water. Bicarbonate data for groundwater in eastern North America are examined in the light of these conditions, of the CO 2 content of soil gas, and of the timing of groundwater recharge relative to seasonal changes in soil temperature. There appears to be no well-marked relation between latitude and bicarbonate content of groundwater in this region. Interplay of all the factors listed above, and of lithology and soil types, is evidently such that under optimum conditions the amount of solution of carbonate rock is roughly comparable, per unit of groundwater recharge, over the region from Ohio to Florida (and, perhaps, to Puerto Rico and Yucatan). Relatively low HCO 3 concentrations observed in much of the southern United States are attributed to low production and storage of CO 2 in sandy soil that is poor in organic matter. On the other hand, concentrations observed in Ontario, New York and Michigan are markedly higher than is to be expected from interrelations of the factors considered. These high values, apparently anomalous, are attributed in part to solution of granular glacial drift derived largely from carbonate rock.

Journal of Hydrology↗
USGS1991

The effects of overburden stress on the specific storage and hydraulic conductivity of artesian aquifers

A mathematical algorithm is developed to determine the depth-dependent profiles of specific storage and hydraulic conductivity resulting from overburden stress in horizontally isotropic artesian aquifers. Vertical variations in the void ratio of the aquifer matrix brought about by overburden stresses determine the pore-volume compressibility and matrix permeability at specific depths within the aquifers which, in turn, determine the depth-dependent profiles of specific storage and hydraulic conductivity. Time-drawdown curves are obtained for two sands subjected to different overburden stresses. For shallow artesian aquifers with low overburden stress and high aquifer matrix compressibility, noticeable vertical gradients in specific storage occur. These vertical gradients cause deviations from the classical time-drawdown curves defined by the Theis solution. These deviations are negligible for deep artesian aquifers.

Journal of Hydrology↗
USGS1985

Effect of ACTH on plasma corticosterone and cortisol in eagles and condors

The effect of ACTH on plasma corticosterone and cortisol was determined in 12 eagles (Haliaeetus leucocephalus) and in 6 Andean condors (Vultur gryphus). In all raptors, the concentration of plasma corticosterone was substantially greater than that of cortisol. After ACTH administration, the eagles had a marked increase (P less than 0.001) in plasma corticosterone concentrations, but not in plasma cortisol. Administration of saline solution did not induce increased plasma corticosterone concentrations in the eagles. The condors had a smaller increase (P less than 0.002) in plasma corticosterone concentrations after ACTH administration, as compared with that of the eagles. However, administration of saline solution in 2 condors resulted in an increase in corticosterone similar to the increase after ACTH administration. In the condor, a stress-related release of endogenous ACTH may have an effect similar to that induced by exogenously administered ACTH. Plasma cortisol concentrations did not increase significantly after administration of ACTH or saline solution in either raptor species.

Journal of the American Veterinary Medical Associa↗
USGS1975

Whitlockite and apatite of surficial phosphate occurrences on Enderbury Island, Phoenix Islands, Pacific Ocean

Whitlockite and apatite are the principal phosphate minerals in the surficial deposits of Enderbury Island; monetite and brushite are present in small amounts. All are derived from the guano of sea birds. The abundance of whitlockite discovered on Enderbury, and reported in samples from Remire Island in the Indian Ocean, indicates that the mineral is probably of common occurrence in young insular phosphate deposits. The composition of whitlockite from Enderbury Island is roughly (Ca, Mg, Sr, Na) 3 (PO 4 , CO 3 ) 2 , similar to the composition indicated for other insular occurrences by the sparse data available. The variety of apatite found on the island is carbonate fluor-hydroxylapatite, low in fluorine content. Whitlockite appears to have formed directly from guano components in surficial aqueous solutions, possibly accompanied by apatite, but changes with time to apatite.

Enderbury Island, Phoenix Islands↗
USGS2004

Combined interpretation of radar, hydraulic, and tracer data from a fractured-rock aquifer near Mirror Lake, New Hampshire, USA

An integrated interpretation of field experimental cross-hole radar, tracer, and hydraulic data demonstrates the value of combining time-lapse geophysical monitoring with conventional hydrologic measurements for improved characterization of a fractured-rock aquifer. Time-lapse difference-attenuation radar tomography was conducted during saline tracer experiments at the US Geological Survey Fractured Rock Hydrology Research Site near Mirror Lake, Grafton County, New Hampshire, USA. The presence of electrically conductive saline tracer effectively illuminates permeable fractures or pathways for geophysical imaging. The geophysical results guide the construction of three-dimensional numerical models of ground-water flow and solute transport. In an effort to explore alternative explanations for the tracer and tomographic data, a suite of conceptual models involving heterogeneous hydraulic conductivity fields and rate-limited mass transfer are considered. Calibration data include tracer concentrations, the arrival time of peak concentration at the outlet, and steady-state hydraulic head. Results from the coupled inversion procedure suggest that much of the tracer mass migrated outside the three tomographic image planes, and that solute is likely transported by two pathways through the system. This work provides basic and site-specific insights into the control of permeability heterogeneity on ground-water flow and solute transport in fractured rock.

New Hampshire↗
USGS2011

Loss of volatile hydrocarbons from an LNAPL oil source

The light nonaqueous phase liquid (LNAPL) oil pool in an aquifer that resulted from a pipeline spill near Bemidji, Minnesota, was analyzed for volatile hydrocarbons (VHCs) to determine if the composition of the oil remains constant over time. Oil samples were obtained from wells at five locations in the oil pool in an anaerobic part of the glacial outwash aquifer. Samples covering a 21-year period were analyzed for 25 VHCs. Compared to the composition of oil from the pipeline source, VHCs identified in oil from wells sampled in 2008 were 13 to 64% depleted. The magnitude of loss for the VHCs analyzed was toluene ≫ o-xylene, benzene, C 6 and C 10–12 n-alkanes > C 7 –C 9 n-alkanes > m-xylene, cyclohexane, and 1- and 2-methylnaphthalene > 1,2,4-trimethylbenzene and ethylbenzene. Other VHCs including p-xylene, 1,3,5- and 1,2,3-trimethylbenzenes, the tetramethylbenzenes, methyl- and ethyl-cyclohexane, and naphthalene were not depleted during the time of the study. Water–oil and air–water batch equilibration simulations indicate that volatilization and biodegradation is most important for the C 6 –C 9 n-alkanes and cyclohexanes; dissolution and biodegradation is important for most of the other hydrocarbons. Depletion of the hydrocarbons in the oil pool is controlled by: the lack of oxygen and nutrients, differing rates of recharge, and the spatial distribution of oil in the aquifer. The mass loss of these VHCs in the 5 wells is between 1.6 and 7.4% in 29 years or an average annual loss of 0.06–0.26%/year. The present study shows that the composition of LNAPL changes over time and that these changes are spatially variable. This highlights the importance of characterizing the temporal and spatial variabilities of the source term in solute-transport models.

Minnesota↗
USGS1983

High-performance liquid chromatography of quinoidal imminium compounds derived from triphenylmethanes

A series of eleven p -aminotriphenylmethane dyes have been studied by high-performance liquid chromatography (HPLC). The combined use of HPLC and spectrophotometry permits specific detection of these compounds in the visible range around 600 nm. As the high affinity of the imminium cations for the active sites of the hydrocarbonaceous stationary phase has presented difficulties for reversed-phase HPLC with pure solvents, organic electrolytes were added to the mobile phase to facilitate the elution of the components with improved selectivity, sensitivity (minimum detection limit, 0.1 &mu;g/ml), and peak symmetry. The effects of chromatographic variables on the component retentivity were investigated. Retention times of the dye analytes decreased with increasing concentration of the added ionic reagent and with decreasing number of the hydrophobic alkyl substituents on the nitrogen atom. The influence of pH on the retention parameters appears to parallel that observed previously for cationic quaternary ammonium compounds. Among the acidic reagents employed, naphthalenesulfonic acid yielded the most satisfactory results. The use of binary electrolyte systems invariably improved the chromatographic behavior of the imminium solutes analyzed. Results obtained with two different octadecylsilica columns have been compared.

Journal of Chromatography↗