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USGS1986

An interpretation of induced electric currents in long pipelines caused by natural geomagnetic sources of the upper atmosphere

Electric currents in long pipelines can contribute to corrosion effects that limit the pipe's lifetime. One cause of such electric currents is the geomagnetic field variations that have sources in the Earth's upper atmosphere. Knowledge of the general behavior of the sources allows a prediction of the occurrence times, favorable locations for the pipeline effects, and long-term projections of corrosion contributions. The source spectral characteristics, the Earth's conductivity profile, and a corrosion-frequency dependence limit the period range of the natural field changes that affect the pipe. The corrosion contribution by induced currents from geomagnetic sources should be evaluated for pipelines that are located at high and at equatorial latitudes. At midlatitude locations, the times of these natural current maxima should be avoided for the necessary accurate monitoring of the pipe-to-soil potential. ?? 1986 D. Reidel Publishing Company.

Surveys in Geophysics↗

USGS1987

Hydrogeologic controls of surface-water chemistry in the Adirondack region of New York State

Relationships between surface-water discharge, water chemistry, and watershed geology were investigated to evaluate factors affecting the sensitivity of drainage waters in the Adirondack region of New York to acidification by atmospheric deposition. Instantaneous discharge per unit area was derived from relationships between flow and staff-gage readings at 10 drainage basins throughout the region. The average chemical composition of the waters was assessed from monthly samples collected from July 1982 through July 1984. The ratio of flow at the 50-percent exceedence level to the flow at the 95-percent exceedence level of flow duration was negatively correlated with mean values of alkalinity or acid-neutralizing capacity (ANC), sum of basic cations (SBC), and dissolved silica, for basins containing predominantly aluminosilicate minerals and little or no carbonate-bearing minerals. Low ratios are indicative of systems in which flow is predominately derived from surface- and ground-water storage, whereas high ratios are characteristic of watersheds with variable flow that is largely derived from surface runoff. In an evaluation of two representative surface-water sites, concentrations of ANC, SBC, and dissolved silica, derived primarily from soil mineral weathering reactions. decreased with increasing flow. Furthermore, the ANC was highest at low flow when the percentage of streamflow derived from ground water was maximum. As flow increased, the ANC decreased because the contribution of dilute surface runoff and lateral flow through the shallow acidic soil horizons to total flow increased. Basins having relatively high ground-water contributions to total flow, in general, have large deposits of thick till or stratified drift. A major factor controlling the sensitivity of these streams and lakes to acidification is the relative contribution of ground water to total discharge. ?? 1987 Martinus Nijhoff/Dr W. Junk Publishers.

Biogeochemistry↗

USGS1994

Aquatic invertebrate production in southeastern USA wetlands during winter and spring

We measured aquatic invertebrate abundance, standing stock biomass, and community production in three types of wetlands on Noxubee National Wildlife Refuge from December 1987 through April 1988. Together, Orthocyclops modestus and Daphnia pulex were the most abundant organisms collected in all habitats during both winter and spring, but each contributed little to total standing stock biomass or production. Caecidotea communis and Pristina osborni made up ≥47% of the total standing stock biomass at each site during both winter (December–February) and spring (March–May). Crangonyx gracilis, Chironomus spp., Chaoborus punctipennis , and Eclipidrilus spp. each contributed ≥5% of the total biomass at one or more wetland habitats. Estimates of aquatic invertebrate community production ranged from 930 to 1,578 mg dry weight/m 2 among wetland types during winter and from 3,306 to 5,421 mg dry weight/m 2 among wetland types during spring. Caecidotea communis and Pristina osborni contributed most to community production during both seasons, but particularly in beaver ponds during spring. Other taxa made up substantial portions of the community production in one or two wetland habitats.

Mississippi↗

USGS2004

Sediment quality in freshwater impoundments at Savannah National Wildlife Refuge

Freshwater impoundments at Savannah National Wildlife Refuge (NWR), South Carolina, provide an important habitat for wildlife species, but degraded sediment quality in the Savannah River downstream of the discharge from two impoundments have caused concern about potential contaminant problems within the impoundments. The quality of sediments from five impoundments (impoundments no. 1, 2, 6, 7, and 17) on the NWR was evaluated using physical and chemical characterization, contaminant concentrations (metals, organochlorine pesticides, polychlorinated biphenyls, and polycyclic aromatic hydrocarbons), and toxicity testing. Survival of Hyalella azteca (freshwater amphipod) exposed for 28 days to solid-phase sediments was not significantly different from controls, but growth was significantly decreased at several sites. Survival in 96-hour exposures to sediment pore water was significantly decreased at most sites. Factors contributing to the toxic responses were low pH (3.7 to 4.1), ammonia (20 mg/L), and increased concentrations of cations in the pore water. The excess of simultaneously extracted metals over the acid volatile sulfides in the sediments was also typical of sites displaying decreased sediment quality. Elemental concentrations in pore water were negatively correlated with pH, and the highest concentrations were observed in impoundment no. 7. The acidic nature of the sediment in this impoundment was exacerbated by recent draining, burning, and disking, which allowed oxidation of the previously anoxic wetland sediment. Sediment disturbance and mixing of vegetation into the sediments by disking may also have contributed to the formation of ammonia caused by microbial decomposition of the fragmented organic matter. Contaminants were not detected in sediments from the impoundments, but releases of acidic water with increased levels of sediment cations from the impoundments may have contributed to the degraded sediment conditions previously observed in the river. The practice of dewatering sediments for vegetation control may exacerbate the acidification of vulnerable sediments within impoundments of this NWR.

Georgia↗

USGS2023

Assessing community assembly controls over community-scale nutrient resorption responses to nitrogen deposition

Nutrient resorption is a fundamental physiological process in plants, with important ecological controls over numerous ecosystem functions. However, the role of community assembly in driving responses of nutrient resorption to perturbation remains largely unknown. Following the Price equation framework and the Community Assembly and Ecosystem Function framework, we quantified the contribution of species loss, species gain, and shared species to the reduction of community-level nutrient resorption efficiency in response to multi-level nitrogen (N) addition in a temperate steppe, after continuous N addition for seven years. Reductions of both N and phosphorus (P) resorption efficiency (NRE and PRE, respectively) were positively correlated with N addition levels. The dissimilarities in species composition between N-enriched and control communities increased with N addition levels, and N-enriched plots showed substantial species losses and gains. Interestingly, the reduction of community-scale NRE and PRE mostly resulted from N-induced decreases in resorption efficiency for the shared species in the control and N-enriched communities. There were negative correlations between the contributions of species richness effect and species identity effect and between the number and identity of species gained for the changes in both NRE and PRE following N enrichment. By simultaneously considering N-induced changes in species composition and in species-level resorption, our work presents a more complete picture of how different community assembly processes contribute to N-induced changes in community-level resorption.

Oecologia↗

USGS2019

Permafrost hydrology drives the assimilation of old carbon by stream food webs in the Arctic

Permafrost thaw in the Arctic is mobilizing old carbon (C) from soils to aquatic ecosystems and the atmosphere. Little is known, however, about the assimilation of old C by aquatic food webs in Arctic watersheds. Here, we used C isotopes (δ 13 C, Δ 14 C) to quantify C assimilation by biota across 12 streams in arctic Alaska. Streams spanned watersheds with varying permafrost hydrology, from ice-poor bedrock to ice-rich loess (that is, yedoma). We measured isotopic content of (1) C sources including dissolved organic C (DOC), dissolved inorganic C (DIC), and soil C, and (2) stream biota, including benthic biofilm and macroinvertebrates, and resident fish species (Arctic Grayling ( Thymallus arcticus ) and Dolly Varden ( Salvelinus malma )). Findings document the assimilation of old C by stream biota, with depleted Δ 14 C values observed at multiple trophic levels, including benthic biofilm ( 14 C ages = 5255 to 265 years before present (y BP)), macroinvertebrates (4490 y BP to modern), and fish (3195 y BP to modern). Mixing model results indicate that DOC and DIC contribute to benthic biofilm composition, with relative contributions differing across streams draining ice-poor and ice-rich terrain. DOC originates primarily from old terrestrial C sources, including deep peat horizons (39–47%; 530 y BP) and near-surface permafrost (12–19%; 5490 y BP). DOC also accounts for approximately half of fish isotopic composition. Analyses suggest that as the contribution of old C to fish increases, fish growth and nutritional status decline. We anticipate increases in old DOC delivery to streams under projected warming, which may further alter food web function in Arctic watersheds.

Alaska↗

USGS2023

To remediate or not? Source identification in an acid mine drainage stream, Warden Gulch, Colorado

A synoptic water quality study was implemented in Warden Gulch, a headwater stream affected by metals that are contributed by both natural and mining-impacted sources. Warden Gulch is a tributary to Peru Creek (Colorado, USA), where emplacement of a mine tunnel bulkhead and other remedial actions have improved water quality upstream of Warden Gulch. The goal of this study was to identify individual source contributions to Warden Gulch and determine if additional remedial actions were warranted. To this end, trace metal loading was quantified from various sources including an actively draining mine. Although highly concentrated waste streams from mining-impacted sites degrade water quality, natural contributions from unmined areas within the Warden Gulch watershed are the dominant sources of metal loading. Further, some mining-impacted sources are associated with diffuse groundwater inflows that may not be amenable to clean up, due to the diffuse nature of the sources and the associated cost. Mining-impacted sources that are amenable to clean up may therefore represent a small portion of the overall metal loading to Warden Gulch. Remedial measures directed at these sources may not substantially improve the water quality of Peru Creek and the larger Snake River watershed.

Colorado↗

USGS2006

Solute sources in stream water during consecutive fall storms in a northern hardwood forest watershed: A combined hydrological, chemical and isotopic approach

Understanding the effects of climate change including precipitation patterns has important implications for evaluating the biogeochemical responses of watersheds. We focused on four storms in late summer and early fall that occurred after an exceptionally dry period in 2002. We analyzed not only the influence of these storms on episodic chemistry and the role of different water sources in affecting surface water chemistry, but also the relative contributions of these storms to annual biogeochemical mass balances. The study site was a well studied 135-ha watershed in the Adirondack Park of New York State (USA). Our analyses integrated measurements on hydrology, solute chemistry and the isotopic composition of NO 3 − (δ 15 N and δ 18 O) and SO 4 2− (δ 34 S and δ 18 O) to evaluate how these storms affected surface water chemistry. Precipitation amounts varied among the storms (Storm 1: Sept. 14–18, 18.5 mm; Storm 2: Sept. 21–24, 33 mm; Storm 3: Sept. 27–29, 42.9 mm; Storm 4: Oct. 16–21, 67.6 mm). Among the four storms, there was an increase in water yields from 2 to 14%. These water yields were much less than in studies of storms in previous years at this same watershed when antecedent moisture conditions were higher. In the current study, early storms resulted in relatively small changes in water chemistry. With progressive storms the changes in water chemistry became more marked with particularly major changes in C b (sum of base cations), Si, NO 3 − , and SO 4 2− , DOC and pH. Analyses of the relationships between Si, DOC, discharge and water table height clearly indicated that there was a decrease in ground water contributions (i.e., lower Si concentrations and higher DOC concentrations) as the watershed wetness increased with storm succession. The marked changes in chemistry were also reflected in changes in the isotopic composition of SO 4 2− and NO 3 − . There was a strong inverse relationship between SO 4 2− concentrations and δ 34 S values suggesting the importance of S biogeochemical redox processes in contributing to SO 4 2− export. The isotopic composition of NO 3 − in stream water indicated that this N had been microbially processed. Linkages between SO 4 2− and DOC concentrations suggest that wetlands were major sources of these solutes to drainage waters while the chemical and isotopic response of NO 3 − suggested that upland sources were more important. Although these late summer and fall storms did not play a major role in the overall annual mass balances of solutes for this watershed, these events had distinctive chemistry including depressed pH and therefore have important consequences to watershed processes such as episodic acidification, and the linkage of these processes to climate change.

Biogeochemistry↗

USGS2020

Phosphorus, nitrogen and dissolved organic carbon fluxes from sediments in freshwater rivermouths entering Green Bay (Lake Michigan; USA)

Transitional areas between ecosystem types are often active biogeochemically due to resource limitation changes. Lotic-to-lentic transitions in freshwaters appear active biogeochemically, but few studies have directly measured nutrient processing rates to assess whether processing within the rivermouth is important for load estimates or the local communities. We measured oxic fluxes of inorganic nitrogen and phosphorus and dissolved organic carbon (DOC) from sediments in two rivermouths of Green Bay (Lake Michigan, USA). Soluble reactive phosphorus (SRP) flux was positive in most cases (overall mean 1.74 mg SRP m − 2 day − 1 ), as was ammonium (NH 4 ) flux (40.6 mg NH 4 m − 2 day − 1 ). Partial least square regression (PLSR) indicated a latent variable associated with both sediment [loosely bound phosphorus (P), iron bound P, organic content] and water column properties [temperature, DOC:dissolved inorganic nitrogen (DIN) and DOC:SRP ratios (negatively)] that was moderately associated with variation in SRP flux. PLSR analysis also indicated several sediment characteristics were moderately related to NH 4 flux, especially organic content, density (negative), and porosity. Flux of nitrates/nitrites (NO X ) and DOC were positively associated with the water column concentrations of NO X and DOC and qualitative estimates of the labile, non-humic types of DOC. In early summer, water column NO X and DOC concentrations were high and labile DOC may have fueled denitrification, resulting in net flux into sediments of both NO X and DOC. By late summer, water column NO X and DOC were very low and both these constituents were fluxing out of sediments into the water column. Based on our estimates for the entire period from April through September, rivermouth sediments were a net source of SRP and DIN, with a DIN:SRP ratio of ~ 44 and a NH 4 :NO X > 1. We estimated that the sediments in the Fox rivermouth probably contributed a small proportion of the total Fox River load during the growing season 2016 (< 5%), but at times may have contributed as much as 14% of the daily load. Despite the small size of the Fox rivermouth (< 0.5% of the watershed area), these results indicate that at times sediments can contribute substantially to the overall delivery of nitrogen and phosphorus to the nearshore zone.

Wisconsin↗

USGS2017

Piscivore diet response to a collapse in pelagic prey populations

Pelagic fish populations in the upper San Francisco Estuary have experienced significant declines since the turn of the century; a pattern known as the pelagic organism decline (POD). This study investigated food habits of piscivorous fishes over two consecutive fall seasons following the decline of pelagic fish prey. Specifically, this study addressed the contribution of pelagic versus benthic prey to piscivorous fish diets, including the frequency of predation on special-status pelagic species, and the spatial variability in prey consumption. The piscivore community was dominated by Striped Bass and also included small numbers of Sacramento Pikeminnow and Largemouth Bass. Overall, pelagic prey items contributed less than 10% of the diet by weight in both years, whereas pre-POD studies gleaned from the literature found contributions of 39–100%, suggesting a major switch from pelagic to benthic prey resources. Between-year variation in piscivore diets reflected differences in environmental conditions associated with variation in freshwater outflow. No special status fish species were detected in any of the piscivore stomachs examined. The consequences of this pelagic to benthic diet shift warrants further investigation to understand its ecological relevance.

California↗

USGS2005

Combined use of rapid bioassessment protocols and sediment quality triad to assess stream quality

Physical, chemical and biological conditions at five stations on a small southeastern stream were evaluated using the Rapid Bioassessment Protocols (RBP) and the Sediment Quality Triad (SQT) to assess potential biological impacts of a municipal wastewater treatment facility (WWTF) on downstream resources. Physical habitat, benthic macroinvertebrates and fish assemblages were impaired at Stations 1 and 2 (upstream of the WWTF), suggesting that the degraded physical habitat was adversely impacting the fish and benthic populations. The SQT also demonstrated that Stations 1 and 2 were degraded, but the factors responsible for the impaired conditions were attributed to the elevated concentrations of polycylclic aromatic hydrocarbons (PAHs) and metals (Mn, Pb) in the sediments. The source of contaminants to the upper reaches of the stream appears to be storm-water runoff from the city center. Increased discharge and stabilized base flow contributed by the WWTF appeared to benefit the physically-altered stream system. Although the two assessment procedures demonstrated biological impairment at the upstream stations, the environmental factors identified as being responsible for the impairment were different: the RBP provided insight into contributions associated with the physical habitat and the SQT contributed information on contaminants and sediment quality. Both procedures are important in the identification of physical and chemical factors responsible for environmental impairment and together they provide information critical to the development of appropriate management options for mitigation.

Environmental Monitoring and Assessment↗

USGS2012

Reconstruction of past methane availability in an Arctic Alaska wetland indicates climate influenced methane release during the past ~12,000 years

Atmospheric contributions of methane from Arctic wetlands during the Holocene are dynamic and linked to climate oscillations. However, long-term records linking climate variability to methane availability in Arctic wetlands are lacking. We present a multi-proxy ~12,000 year paleoecological reconstruction of intermittent methane availability from a radiocarbon-dated sediment core (LQ-West) taken from a shallow tundra lake (Qalluuraq Lake) in Arctic Alaska. Specifically, stable carbon isotopic values of photosynthetic biomarkers and methane are utilized to estimate the proportional contribution of methane-derived carbon to lake-sediment-preserved benthic (chironomids) and pelagic (cladocerans) components over the last ~12,000 years. These results were compared to temperature, hydrologic, and habitat reconstructions from the same site using chironomid assemblage data, oxygen isotopes of chironomid head capsules, and radiocarbon ages of plant macrofossils. Cladoceran ephippia from ~4,000 cal year BP sediments have δ13C values that range from ~−39 to −31‰, suggesting peak methane carbon assimilation at that time. These low δ13C values coincide with an apparent decrease in effective moisture and development of a wetland that included Sphagnum subsecundum. Incorporation of methane-derived carbon by chironomids and cladocerans decreased from ~2,500 to 1,500 cal year BP, coinciding with a temperature decrease. Live-collected chironomids with a radiocarbon age of 1,640 cal year BP, and fossil chironomids from 1,500 cal year BP in the core illustrate that ‘old’ carbon has also contributed to the development of the aquatic ecosystem since ~1,500 cal year BP. The relatively low δ13C values of aquatic invertebrates (as low as −40.5‰) provide evidence of methane incorporation by lake invertebrates, and suggest intermittent climate-linked methane release from the lake throughout the Holocene.

Alaska↗

USGS2018

Fire changes the spatial distribution and sources of soil organic carbon in a grassland-shrubland transition zone

Aims In many mixed grass-shrub ecosystems, increased shrub biomass tends to promote overall carbon storage, but the distribution of carbon pools may be complicated by disturbances such as wildfires. We investigated the spatial distribution of surface soil organic carbon (SOC) and its relative contribution from grasses and shrubs after fires in a grass-shrub transition zone in the northern Chihuahuan Desert, USA. Methods We used a prescribed fire to create a burned treatment, then collected soil and plant samples. The biogeochemical approaches, geostatistical analyses, and carbon partitioning analyses were used to quantify the SOC and soil δ 13 C spatial patterns. Results Before the prescribed fire, up to 98% of the spatial dependence of SOC was autocorrelated at a distance of 1.91 m, corresponding to the approximate average shrub canopy diameter, but the spatial dependence dropped to 81% at a larger autocorrelation distance (3.74 m) two windy seasons after the fire. C 4 grasses and C 3 shrubs contributed approximately equal amounts of carbon to the surface SOC pool before the prescribed fire. However, C 4 grasses became the dominant source of SOC two windy seasons following the fire. For individual microsites, a substantially increased proportion of SOC was derived from C 4 grasses at the shrub microsites following the fire. Conclusions The higher proportion of C 4 grasses-derived SOC at the shrub microsites post-fire suggests that SOC may have preferred pathways to move among different microsites following fire disturbance. The distinct spatial distribution patterns of δ 13 C, and the increased contribution of SOC from grasses may be explained by the rapid recovery of grasses following the fire. Overall, our results provide insights into how fire might be used as a management tool to alter soil carbon pools in the context of shrub encroachment.

Plant and Soil↗

USGS2008

A mass balance mercury budget for a mine-dominated lake: Clear Lake, California

The Sulphur Bank Mercury Mine (SBMM), active intermittently from 1873–1957 and now a USEPA Superfund site, was previously estimated to have contributed at least 100 metric tons (10 5 kg) of mercury (Hg) into the Clear Lake aquatic ecosystem. We have confirmed this minimum estimate. To better quantify the contribution of the mine in relation to other sources of Hg loading into Clear Lake and provide data that might help reduce that loading, we analyzed Inputs and Outputs of Hg to Clear Lake and Storage of Hg in lakebed sediments using a mass balance approach. We evaluated Inputs from (1) wet and dry atmospheric deposition from both global/regional and local sources, (2) watershed tributaries, (3) groundwater inflows, (4) lakebed springs and (5) the mine. Outputs were quantified from (1) efflux (volatilization) of Hg from the lake surface to the atmosphere, (2) municipal and agricultural water diversions, (3) losses from out-flowing drainage of Cache Creek that feeds into the California Central Valley and (4) biotic Hg removal by humans and wildlife. Storage estimates include (1) sediment burial from historic and prehistoric periods (over the past 150–3,000 years) from sediment cores to ca. 2.5m depth dated using dichloro diphenyl dichloroethane (DDD), 210 Pb and 14 C and (2) recent Hg deposition in surficial sediments. Surficial sediments collected in October 2003 (11 years after mine site remediation) indicate no reduction (but a possible increase) in sediment Hg concentrations over that time and suggest that remediation has not significantly reduced overall Hg loading to the lake. Currently, the mine is believed to contribute ca. 322–331 kg of Hg annually to Clear Lake, which represents ca. 86–99% of the total Hg loading to the lake. We estimate that natural sedimentation would cover the existing contaminated sediments within ca. 150–300 years.

Water, Air, & Soil Pollution↗

USGS2016

From "Duck Factory" to "Fish Factory": Climate induced changes in vertebrate communities of prairie pothole wetlands and small lakes

The Prairie Pothole Region’s myriad wetlands and small lakes contribute to its stature as the “duck factory” of North America. The fishless nature of the region’s aquatic habitats, a result of frequent drying, freezing, and high salinity, influences its importance to waterfowl. Recent precipitation increases have resulted in higher water levels and wetland/lake freshening. In 2012–13, we sampled chemical characteristics and vertebrates (fish and salamanders) of 162 Prairie Pothole wetlands and small lakes. We used non-metric multidimensional scaling, principal component analysis, and bootstrapping techniques to reveal relationships. We found fish present in a majority of sites (84 %). Fish responses to water chemistry varied by species. Fathead minnows ( Pimephales promelas ) and brook sticklebacks ( Culaea inconstans ) occurred across the broadest range of conditions. Yellow perch ( Perca flavescens ) occurred in a smaller, chemically defined, subset. Iowa darters ( Etheostoma exile ) were restricted to the narrowest range of conditions. Tiger salamanders ( Ambystoma mavortium ) rarely occurred in lakes with fish. We also compared our chemical data to similar data collected in 1966–1976 to explore factors contributing to the expansion of fish into previously fishless sites. Our work contributes to a better understanding of relationships between aquatic biota and climate-induced changes in this ecologically important area.

North Dakota↗

USGS1962

The solubility of quartz in water in the temperature interval from 25° to 300° C

The solubility of quartz in water was investigated by three sets of experiments at 1000 atm P H 2 O and temperatures ranging from 45° to 300°C at water pressures appropriate for the coexistence of three phases, gaseous water, liquid, and quartz, at temperatures ranging from 69° to 240°C a long term study of the dissolution of quartz grains which were continuously tumbled in water at room temperature. Saturated silica solutions in equilibrium with quartz were obtained in a few days at temperatures above 100°C. Equilibrium is shown by reproducible results for runs of different durations and by the precipitation of quartz from initially supersaturated solutions. The differential heat of solution derived from the data obtained at 1000 atm pressure is 5.38 kcal/mole. At room temperature and pressure, highly supersaturated silica solutions were obtained by continuously rotating quartz grains and water in plastic bottles at 75 rev/min. In one run the amount of silica in solution increased to a maximum value of 395 p.p.m. after 370 days. Another run reached 80 p.p.m. silica after 386 days and then dropped to 6 p.p.m. silica. It is concluded that quartz was precipitated at room temperature from this supersaturated solution and that 6 p.p.m. is essentially the true solubility of quartz at 25°C. In contrast to the runs rotated at 75 rev/min, quartz grains, and also silica glass grains, continuously rotated in water at rev/min, each contributed less than 1 p.p.m. colorimetric silica into solution after 1 year. Thus, vigorous agitation of the liquid is necessary to remove dissolved silica from the vicinity of surfaces of both quartz and glass. Two significant factors that may have contributed to the formation of supersaturated silica solutions in the runs rotated at 75 rev/min at room temperature are stresses and structural irregularities at the surfaces of the crushed quartz grains, which contributed silica into solution more readily than well crystallized quartz the very slow rate at which dissolved silica polymerizes to species appropriate to act as nuclei for quartz growth. At the termination of the runs rotated at 75 rev/min, spikelike projections were present on many of the quartz grains. These are interpreted as indicating that abrasion was not the dominant cause for the great supersaturations which were obtained.

Geochimica et Cosmochimica Acta↗

USGS1964

Minor-element composition and organic carbon content of marine and nonmarine shales of Late Cretaceous age in the western interior of the United States

The composition of nonmarine shales of Cretaceous age that contain less than 1 per cent organic carbon is assumed to represent the inherited minor-element composition of clayey sediments delivered to the Cretaceous sea that occupied the western interior region of North America. Differences in minor-element content between these samples and samples of 1. (a) nonmarine carbonaceous shales (1 to 17 per cent organic carbon), 2. (b) nearshore marine shales (less than 1 per cent organic carbon), and 3. (c) offshore marine shales (as much as 8 per cent organic carbon), all of the same age, reveal certain aspects of the role played by clay minerals and organic materials in affecting the minor-element composition of the rocks. The organic carbon in the nonmarine rocks occurs in disseminated coaly plant remains. The organic carbon in the marine rocks occurs predominantly in humic material derived from terrestrial plants. The close similarity in composition between the organic isolates from the marine samples and low-rank coal suggests that the amount of marine organic material in these rocks is small. The minor-element content of the two kinds of nonmarine shales is the same despite the relatively large amount of organic carbon in the carbonaceous shales. The nearshore marine shales, however, contain larger median amounts of arsenic, boron, chromium, vanadium and zinc than do the nonmarine rocks; and the offshore marine shales contain even larger amounts of these elements. Cobalt, molybdenum, lead and zirconium show insignificant differences in median content between the nonmarine and marine rocks, although as much as 25 ppm molybdenum is present in some offshore marine samples. The gallium content is lower in the marine than in the nonmarine samples. Copper and selenium contents of the two kinds of nonmarine rocks and the nearshore marine samples are the same, but those of the offshore samples are larger. In general, arsenic, chromium, copper, molybdenum, selenium, vanadium and zinc are concentrated in those offshore marine samples having the largest amounts of organic carbon, but samples with equal amounts of vanadium, for instance, may differ by a factor of 3 in their amount of organic carbon. Arsenic and molybdenum occur in some samples chiefly in syngenetic pyrite but also are present in relatively large amounts in samples that contain little pyrite. The data on nonmarine carbonaceous shales indicate that organic matter of terrestrial origin in marine shales contributes little to the minor-element content of such rocks. It is possible that marine organic matter, even though seemingly small in amount in marine shales, contributes to the minor-element composition of the shales. In addition to any such contribution, however, the great effectiveness in sorption processes of humic materials in conjunction with clay minerals suggests that such processes must have played an important role as these materials moved from the relatively dilute solutions of the nonmarine environment to the relatively concentrated solution of sea water. The volumes of sea water sufficient to supply for sorption the amounts of most minor elements in the offshore marine samples are insignificant compared to the volumes of water with which the clay and organic matter were in contact during their transportation and sedimentation. Consequently, the chemical characteristics of the environment in which the clay minerals and organic matter accumulated and underwent diagenesis probably were the most important factors in controlling the degree to which sorption processes and the formation of syngenetic minerals affected the final composition of the rocks.

Geochimica et Cosmochimica Acta↗

USGS1992

The dynamic relationship between ground water and the Columbia River: Using deuterium and oxygen-18 as tracers

Deuterium and oxygen-18 were used as natural tracers to investigate the hydraulic relationship between the Columbia River and the Blue Lake gravel aquifer near Portland, Oregon. A time series of stable-isotope data collected from surface and ground waters during a March 1990 aquifer test confirms that the river and aquifer are hydraulically connected. Calculations based on simple mixing show that the river contributed 40–50% of the yield of three wells after 5–6 days of pumping. Data collected during August 1990, show that the river contributed 65–80% of the yield of one well after 22 days of pumping and indicate that the contribution of the river was still increasing.

Journal of Hydrology↗