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Human-induced and natural carbon storage in floodplains of the Central Valley of California

Active floodplains can putatively store large amounts of organic carbon (SOC) in subsoils originating from catchment erosion processes with subsequent floodplain deposition. Our study focussed on the assessment of SOC pools associated with alluvial floodplain soils that are affected by human-induced changes in floodplain deposition and in situ SOC mineralisation due to land use change and drainage. We evaluated depth-dependent SOC contents based on 23 soil cores down to 3 m and 10 drillings down to 7 m in a floodplain area of the lower Cosumnes River. An estimate of 266 Mg C ha −1 or about 59% of the entire SOC stored within the 7 m profiles was found in the upper 2 m. Most profiles (n = 25) contained discrete buried A horizons at depths of approximately 0.8 m. These profiles had up to 130% higher SOC stocks. The mean δ 13 C of all deep soil profiles clearly indicated that arable land use has already altered the stable isotopic signature in the first meter of the profile. Radiocarbon dating showed that the 14 C age in the buried horizon was younger than in overlaying soils indicating a substantial sedimentation phase for the overlaying soils. An additional analysis of total mercury contents in the soil profiles indicated that this sedimentation was associated with upstream hydraulic gold mining after the 1850s. In summary, deep alluvial soils in floodplains store large amounts of SOC not yet accounted for in global carbon models. Historic data give evidence that large amounts of sediment were transported into the floodplains of most rivers of the Central Valley and deposited over organically rich topsoil, which promoted the stabilization of SOC, and needs to be considered to improve our understanding of the human-induced interference with C cycling.

California↗

Natural and anthropogenic influences on benthic cyanobacteria in streams of the northeastern United States

Benthic cyanobacteria are widespread in streams and rivers and have the potential to release toxins. In large numbers, these microorganisms and their toxins present a risk to human health. Cyanobacterial abundance in stream biofilms is typically related to single or a limited set of environmental factors, mainly light availability, water temperature, and nutrient concentrations. However, these factors may act synergistically with watershed characteristics and other stressors, such as anthropogenic pollutants, to affect cyanobacteria. We investigated the influence of multiple regional and local variables on the abundance of benthic cyanobacterial genera in streams using all subsets generalized additive modeling. We examined watershed factors (topography, geology, and climate) alongside in-stream factors (geomorphology, hydrology, pH, specific conductance, nutrients, organic contaminants, and dissolved metals) from 76 sites along an urban gradient in the northeast United States. Each genus responded to a distinct combination of environmental variables, demonstrating strong intergeneric variation in environmental selection of realized niches. Four of the 7 potentially toxigenic genera that we modeled were positively influenced by water temperature or nutrients. Nonetheless, watershed characteristics, streamflow, and/or other water quality pollutants were equally or more influential for the potentially toxigenic genera. Additionally, the relationships between cyanobacterial abundance and environmental factors varied in shape and direction across many genera. In particular, with increasing concentrations of herbicides, polychlorinated biphenyls, or metals, the abundance of roughly half of the affected genera decreased, while the others increased. These results likely demonstrate novel toxic effects of the pollutants on cyanobacterial genera in the environment, while indicating that unmeasured biotic interactions may lead to positive responses for other genera. Our results emphasize the need to consider variables beyond those that are most frequently measured or implicated (e.g., water temperature and nutrients) to more fully understand the environmental conditions that influence the distributions and abundance of potentially harmful cyanobacteria.

Connecticut, Massachusetts, New Hampshire. New Yor↗

Carbon isotopic constraints on the contribution of plant material to the natural precursors of trihalomethanes

The δ 13 C values of individual trihalomethanes (THM) formed on reaction of chlorine with dissolved organic carbon (DOC) leached from maize (corn; Zea maize L. ) and Scirpus acutus (an aquatic bulrush), and with DOC extracted from agricultural drainage waters were determined using purge and trap introduction into a gas chromatograph-combustion-isotope ratio monitoring mass spectrometer. We observed a 16.8‰ difference between the δ 13 C values of THM produced from the maize and Scirpus leachates, similar to the isotopic difference between the whole plant materials. Both maize and Scirpus formed THM 12‰ lower in 13 C than whole plant material. We suggest that the low value of the THM relative to the whole plant material is evidence of distinct pools of THM-forming DOC, representing different biochemical types or chemical structures, and possessing different environmental reactivity.

Organic Geochemistry↗

Evaluation of undiscovered natural gas in the Upper Cretaceous Ferron Coal/Wasatch Plateau Total Petroleum System, Wasatch Plateau and Castle Valley, Utah

The Total Petroleum System approach was used to estimate undiscovered gas potential of the Wasatch Plateau and Castle Valley, central Utah. The Ferron Coal/Wasatch Plateau Total Petroleum System was geologically defined and subdivided into seven assessment units, six of which were formally evaluated. Geologic data considered in defining the assessment unit boundaries included thermal maturity, coal presence and thickness, overburden thickness, and faulting intensity. Historical production data were also used to estimate volumes of gas from undrilled areas. The one conventional assessment unit includes almost the entire area of the petroleum system and is characterized by known accumulations that occur in structural or combination traps in sandstone reservoirs. The estimated undiscovered conventional producible gas that may be added to reserves of this unit ranges from a low (F95) of 14.8 billion cubic feet (BCFG) [419 million cubic meters (Mm3)] of gas to a high (F5) of 82 BCFG [2321 Mm3] and a mean value of 39.9 BCFG [1130 Mm3]. Continuous gas accumulations are those in which the entire assessment unit is considered to be gas-charged. Within these assessment units, there may be wells drilled that are not economic successes but all are expected to contain gas. Coalbed gas is in this continuous category. Mean estimates of undiscovered gas for the five continuous assessment units are: (1) Northern Coal Fairway/Drunkards Wash-752.3 BCFG [21,323 Mm3]; (2) Central Coal Fairway/Buzzard Bench-536.7 BCFG [15,194 Mm3]; (3) Southern Coal Fairway-152.6 BCFG [4320 Mm3]; (4) Deep (6000 feet plus) Coal and Sandstone-59.1 BCFG [1673 Mm3]; (5) Southern Coal Outcrop-10.6 BCFG [300 Mm3]; and Joes Valley and Musinia Grabens-not assessed.The mean estimate of undiscovered gas for the entire TPS is 1551.2 BCFG [43,914 Mm3]. There is a 95% chance that at least 855.7 BCFG [24,225 Mm3] and a 5% chance that at least 2504 BCFG [70,888 Mm3] of undiscovered producible gas remain in the TPS. ?? 2003 Published by Elsevier B.V.

International Journal of Coal Geology↗

Modern marine sediments as a natural analog to the chemically stressed environment of a landfill

Chemical reactions that occur in landfills are analogous to those reactions that occur in marine sediments. Lateral zonation of C, N, S, O, H, Fe and Mn species in landfills is similar to the vertical zonation of these species in marine sediments and results from the following reaction sequence: (1) oxidation of C, N and S species in the presence of dissolved free oxygen to HCO 3 - , NO 3 - and SO 4 2 ; (2) after consumption of molecular oxygen, then NO 3 - is reduced, and Fe and Mn are solubilized; (3) SO 4 2- is reduced to sulfide; and (4) organic compounds become the source of oxygen, and CH 4 and NH 4 + are formed as fermentation products. In a landfill in Delaware the oxidation potential increases down-gradient and the redox zones in the reducing plume are characterized by: CH 4 , NH 4 + ,Fe 2+ . Mn 2+ , HCO 3 - and NO 3 - . Lack of SO 4 2- at that landfill eliminates the sulfide zone. Although it has not been observed at landfills, mineral alteration should result in precipitation of pyrite and/or siderite downgradient. Controls on the pH of leachate are the relative rates of production of HCO 3 - , NH 4 + and CH 4 . Production of methane by fermentation at landfills results in 13 C isotope fractionation and the accumulation of isotopically heavy σ CO 2 (+10 to +18 0 / 00 PDB). Isotope measurements may be useful to determine the extent of CO 2 reduction in landfills and extent of dilution downgradient. The boundaries of reaction zones in stressed aquifers are determined by head distribution and flow velocity. Thus, if the groundwater flow is rapid relative to reaction rates, redox zones will develop downgradient. Where groundwater flow velocities are low the zones will overlap to the extent that they may be indeterminate.

Journal of Hydrology↗

Progression of natural attenuation processes at a crude oil spill site: II. Controls on spatial distribution of microbial populations

A multidisciplinary study of a crude-oil contaminated aquifer shows that the distribution of microbial physiologic types is strongly controlled by the aquifer properties and crude oil location. The microbial populations of four physiologic types were analyzed together with permeability, pore-water chemistry, nonaqueous oil content, and extractable sediment iron. Microbial data from three vertical profiles through the anaerobic portion of the contaminated aquifer clearly show areas that have progressed from iron-reduction to methanogenesis. These locations contain lower numbers of iron reducers, and increased numbers of fermenters with detectable methanogens. Methanogenic conditions exist both in the area contaminated by nonaqueous oil and also below the oil where high hydrocarbon concentrations correspond to local increases in aquifer permeability. The results indicate that high contaminant flux either from local dissolution or by advective transport plays a key role in determining which areas first become methanogenic. Other factors besides flux that are important include the sediment Fe(II) content and proximity to the water table. In locations near a seasonally oscillating water table, methanogenic conditions exist only below the lowest typical water table elevation. During 20 years since the oil spill occurred, a laterally continuous methanogenic zone has developed along a narrow horizon extending from the source area to 50–60 m downgradient. A companion paper [J. Contam. Hydrol. 53, 369–386] documents how the growth of the methanogenic zone results in expansion of the aquifer volume contaminated with the highest concentrations of benzene, toluene, ethylbenzene, and xylenes.

Journal of Contaminant Hydrology↗

The nature of the crust under Cayman Trough from gravity

Considerable crustal thickness variations are inferred along Cayman Trough, a slow-spreading ocean basin in the Caribbean Sea, from modeling of the gravity field. The crust to a distance of 50 km from the spreading center is only 2–3 km thick in agreement with dredge and dive results. Crustal thickness increases to ∼5.5 km at distances between 100 and 430 km west of the spreading center and to 3.5–6 km at distances between 60 and 370 km east of the spreading center. The increase in thickness is interpreted to represent serpentinization of the uppermost mantle lithosphere, rather than a true increase in the volume of accreted ocean crust. Serpentinized peridotite rocks have indeed been dredged from the base of escarpments of oceanic crust rocks in Cayman Trough. Laboratory-measured density and P-wave speed of peridotite with 40–50% serpentine are similar to the observed speed in published refraction results and to the inferred density from the model. Crustal thickness gradually increases to 7–8 km at the far ends of the trough partially in areas where sea floor magnetic anomalies were identified. Basement depth becomes gradually shallower starting 250 km west of the rise and 340 km east of the rise, in contrast to the predicted trend of increasing depth to basement from cooling models of the oceanic lithosphere. The gradual increase in apparent crustal thickness and the shallowing trend of basement depth are interpreted to indicate that the deep distal parts of Cayman Trough are underlain by highly attenuated crust, not by a continuously accreted oceanic crust.

Marine and Petroleum Geology↗

Spatial variability of shelf sediments in the STRATAFORM natural laboratory, Northern California

The "Correlation Length Experiment", an intensive box coring effort on the Eel River shelf (Northern California) in the summer of 1997, endeavored to characterize the lateral variability of near-surface shelf sediments over scales of meters to kilometers. Coring focused on two sites, K60 and S60, separated by ??? 15 km along the 60 m isobath. The sites are near the sand-to-mud transition, although K60 is sandier owing to its proximity to the Eel River mouth. Nearly 140 cores were collected on dip and strike lines with core intervals from < 10m to 1 km. Measurements on each core included bulk density computed from gamma-ray attenuation, porosity converted from resistivity measurements, and surficial grain size. Grain size was also measured over the full depth range within a select subset of cores. X-radiograph images were also examined. Semi-variograms were computed for strike, dip, and down-hole directions at each site. The sand-to-mud transition exerts a strong influence on all measurements: on average, bulk density increases and porosity decreases with regional increases in mean grain size. Analysis of bulk density measurements indicates very strong contrasts in the sediment variability at K60 and S60. No coherent bedding is seen at K60; in the strike direction, horizontal variability is "white" (fully uncorrelated) from the smallest scales examined (a few meters) to the largest (8 km), with a variance equal to that seen within the cores. In contrast, coherent bedding exists at S60 related to the preservation of the 1995 flood deposit. A correlatable structure is found in the strike direction with a decorrelation distance of ??? 800 m, and can be related to long-wavelength undulations in the topography and/or thickness of the flood layer or overburden. We hypothesize that the high degree of bulk density variability at K60 is a result of more intense physical reworking of the seabed in the sandier environment. Without significant averaging, the resistivity-based porosity measurements are only marginally correlated to gamma-ray-bulk density measurements, and are largely independent of mean grain size. Furthermore, porosity displays a high degree of incoherent variability at both sites. Porosity, with a much smaller sample volume than bulk density, may therefore resolve small-scale biogenic variability which is filtered out in the bulk density measurement. ?? 2002 Elsevier Science Ltd. All rights reserved.

Continental Shelf Research↗

Determination of uranium in natural waters

The fluorophotometric determination of uranium was studied to develop a procedure applicable to the routine analysis of waters. Three grams of the high carbonate flux are used in a dilution procedure with spiking. Because of the comparatively high reflectivity of this large disk and the low uranium concentration, a correction for nonquenched light is required. A formula is developed to compensate for the effect, an electrical fusion device is described, and the problem of fixing uranium in waters is discussed.

Analytical Chemistry↗

Concentration method for the spectrochemical determination of seventeen minor elements in natural water

A method for the quantitative spectrochemical determination of microgram amounts of 17 minor elements in water is given. The chelating reagents 8-quinolinol, tannic acid, and thionalide are utilized to concentrate traces (1 to 500 μ g.) of aluminum, cobalt, chromium, copper, iron, gallium, germanium, manganese, nickel, titanium, vanadium, bismuth, lead, molybdenum, cadmium, zinc, and beryllium. Indium is added as a buffer, and palladium is used as an internal standard. The ashed oxides of these 17 metals are subsequently subjected to direct current arcing conditions during spectrum analysis. The method can be used to analyze waters with dissolved solids ranging from less than 100 to more than 100,000 p.p.m. There is no limiting concentration range for the determination of the heavy metals since any volume of sample can be used that will contain a heavy metal concentration within the analytical range of the method. Both the chemical and spectrographic procedures are described, and precision and accuracy data are given.

Analytical Chemistry↗

Transport and natural attenuation of Cu, Zn, As, and Fe in the acid mine drainage of Leviathan and Bryant Creeks

The Leviathan and Bryant Creek (LBC) drainage system, on the border of California and Nevada, flows through overburden and waste from a former open-pit sulfur mine. The drainage contains acid mine waters with high concentrations of several trace elements, including Cu, Zn, and As, derived from oxidative weathering of sulfides in the wastes and altered bedrock. In June and October, 1982, the mainstream and tributary flows of the LBC drainage were measured and the waters sampled and analyzed for major and trace elements. Empirical mass flow and metal attenuation rates were determined, and chemical models were used to examine mechanisms of trace element removal during downstream transport. In June the flow in the mainstream was 2-5 times greater than in October, and with higher contributions from the acid mine effluent. Seasonal variations in the attenuation rates of Cu, Zn, and As were directly related to this increase in acid mine-effluent production, and to the consequent increase in the acidity of the mainstream drainage. Although As concentrations immediately below the mine site were high in June, As was readily removed from solution by adsorption onto an assumed iron(III) oxyhydroxysulfate precipitate, whereas Cu was incompletely adsorbed and Zn remained unaffected by adsorption. In October, the smaller discharge of acidic LBC drainage waters were more readily diluted (and neutralized) by other regional tributaries. Arsenic concentrations remained low, and both Cu and Zn were removed from solution by adsorption onto iron(III) oxyhydroxysulfate in the lower regions of the LBC drainage system.

California, Nevada↗

Organic geochemistry and sources of natural aquatic foams

Aquatic foams and stream-water samples were collected from two pristine sites for humic substances isolation and characterization. Biomarker compounds identified in foam and stream humic substances included phospholipid fatty acids, steroids, and lignin. Results showed that foams had a 10 to 20 fold greater DOC concentration and were enriched in humic substances (90% by weight of DOC) that showed increased hydrophobicity, aliphatic character, and compositional complexity compared to host stream humic substances (55 to 81% by weight of DOC). Foam humic substances also were enriched in humic acid (36 to 83% by weight) compared to host stream humic substances (10 to 14% by weight). Biomarkers, which contributed less than 5% by weight to the DOC pool, indicated higher plants, bacteria, algae, fungi, and diatoms as DOC sources. It is proposed that aquatic foams may be important media for the concentration and transport of organic substances in the aquatic environment.

ACS Symposium Series↗