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At least 1,207 records · Page 67Linked to original sources

USGS2017

Exudation rates and δ13C signatures of tree root soluble organic carbon in a riparian forest

Tree root exudation (TRE) of water soluble organic carbon (WSOC) is an important but under-assessed component of net primary production, and is thought to strongly influence rhizosphere biogeochemistry. Riparian systems in particular are often viewed as biogeochemical hot spots fueled partially by root exudate WSOC. However, TRE rates have not been previously reported for these systems. The δ 13 C signatures of exudates may provide important insights into plant physiology and inform isotope-based methods to identify sources of soil CO 2 fluxes, but this information is also generally lacking. In the present study, root exudate WSOC was collected in situ to assess both net exudation rates and exudate δ 13 C values in a temperate riparian forest. Net TRE rates were found to be most strongly related to a combination of tree species, root characteristics and net ecosystem exchange (Adj. R 2 = 0.73; p < 0.001). In contrast, exudate δ 13 C values were correlated to time-lagged vapor pressure deficit (Adj. R 2 = 0.21; p < 0.05) and air temperature (Adj. R 2 = 0.43; p < 0.05), suggesting a rapid transfer of photosynthate from the canopy to the rhizosphere. Extrapolation of mean net TRE rates (13 µmol C g root −1 day −1 ) from a root mass basis to the entire sampling area suggests that TRE may account for as much as 3% of net annual C uptake and represents an important input of organic matter to riparian soils. Our findings of predictable TRE rates and exudate δ 13 C values in the present study suggest that future studies examining δ 13 C values of different plant components, soil organic matter and respired soil CO 2 would benefit by accounting for the impact of root exudates.

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↗

USGS2021

A combined microbial and ecosystem metric of carbon retention efficiency explains land cover-dependent soil microbial biodiversity–ecosystem function relationships

While soil organic carbon (C) is the foundation of productive and healthy ecosystems, the impact of the ecology of microorganisms on C-cycling remains unknown. We manipulated the diversity, applied here as species richness, of the microbial community present in similar soils on two contrasting land-covers—an adjacent pasture and forest—and observed the transformations of plant detritus and soil organic matter (SOM) using stable isotope ( 13 C) tracing coupled with a novel nuclear magnetic resonance (NMR) experiment. The amount of detritus-C degraded was not affected by the microbial diversity (p > 0.05), however the fate of detritus- and SOM-C across the diversity gradient was complex and land cover-dependent. For example, in the pasture soil, higher diversity led to lower CO 2 production (p = 0.001), a trend driven solely by SOM-C mineralization. There was no relationship between diversity and detritus-C mineralization or production of new mineral-associations after one year (p > 0.05). In contrast, in the forest soil higher diversity resulted in increased detritus-C (p = 0.01) and SOM-C (p = 0.0008) mineralization and decreased mineral-associated organic matter formation (p = 0.02). In both land cover types, retention efficiency—a measure that integrates both microbial physiology and the ability of the ecosystem to retain C—explained C loss and transformation trends. Overall, this demonstrates that the trajectory of C gained and lost is altered by land management-induced changes to microbial communities, soil structure, and chemical characteristics underlying SOM persistence.

Biogeochemistry Letters↗

USGS2013

Expert assessment of vulnerability of permafrost carbon to climate change

Approximately 1700 Pg of soil carbon (C) are stored in the northern circumpolar permafrost zone, more than twice as much C than in the atmosphere. The overall amount, rate, and form of C released to the atmosphere in a warmer world will influence the strength of the permafrost C feedback to climate change. We used a survey to quantify variability in the perception of the vulnerability of permafrost C to climate change. Experts were asked to provide quantitative estimates of permafrost change in response to four scenarios of warming. For the highest warming scenario (RCP 8.5), experts hypothesized that C release from permafrost zone soils could be 19–45 Pg C by 2040, 162–288 Pg C by 2100, and 381–616 Pg C by 2300 in CO 2 equivalent using 100-year CH 4 global warming potential (GWP). These values become 50 % larger using 20-year CH 4 GWP, with a third to a half of expected climate forcing coming from CH 4 even though CH 4 was only 2.3 % of the expected C release. Experts projected that two-thirds of this release could be avoided under the lowest warming scenario (RCP 2.6). These results highlight the potential risk from permafrost thaw and serve to frame a hypothesis about the magnitude of this feedback to climate change. However, the level of emissions proposed here are unlikely to overshadow the impact of fossil fuel burning, which will continue to be the main source of C emissions and climate forcing.

Climatic Change↗

USGS2024

Evaluation of a carbon dioxide fish barrier through numerical modelling

The Chicago Area Waterway System (CAWS) is a potential route for the migration of aquatic invasive species from the Mississippi River Basin into the Great Lakes. Electric dispersal barriers were installed in the Chicago Sanitary Ship Canal, within CAWS, to prevent invasive fish from reaching the Great Lakes. Despite the high efficiency of these barriers, occasional maintenance events create a vulnerability that fish can exploit to access the Great Lakes. This study aimed to assess the feasibility of a carbon dioxide (CO 2 ) infusion system to deter fish during the maintenance of the electric barriers. An algebraic slip mixture model was implemented in the OpenFOAM solver to represent the underwater CO 2 bubble plume and predict the concentration of dissolved CO 2 in the canal. Simulations under three canal flowrates and two sparger systems were conducted assuming a constant gas flowrate. Numerical results indicate that, for all simulated conditions, the CO 2 concentration is not fully mixed creating passageways that invasive fish could potentially use to migrate upstream. Injecting 4-mm bubbles induces two large-scale recirculations that are expected to synergistically improve fish avoidance. On the other hand, injection of 20 μ "> μ m bubbles results on almost immediate dissolution with minimal effect on the flow pattern. To improve effectiveness, a gas pulse system was proposed and numerically evaluated. Based on the simulations, this system not only extends the operation of the CO 2 barrier but also increases efficiency creating CO 2 gradients that can promote a more responsive behaviour from fish. Moreover, the pulse concept mitigates potential effect of elevated CO 2 downstream from the treated area.

Illinois↗

USGS2023

Reconnaissance survey for potential energy storage and carbon dioxide storage resources of petroleum reservoirs in western Europe

Energy producers and utilities use oil and gas reservoirs for gas storage to meet peak seasonal demand or to supplement intermittent energy production. These reservoirs are also suitable for the long-term storage of carbon dioxide (CO 2 ), a greenhouse gas. This study reports on a reconnaissance analysis of the potential magnitude of storage resources in 9424 known oil and gas reservoirs from 24 countries within highly industrialized western Europe. To standardize the storage resources of the oil and gas reservoirs, their volumetric capacity is expressed in terms of metric tons (mass) of CO 2 . Estimates of recoverable oil and gas at the surface are converted to subsurface volumes and then converted to the equivalent mass of CO 2 at reservoir conditions. The results indicate 36.7 gigatons of CO 2 could be stored, with oil reservoirs accounting for 32% of that total and natural gas reservoirs comprising the remaining 68%. About four-fifths of the reservoir storage resource is offshore, with about three-fourths of that offshore resource at water depths of 200 m or less. Most countries do not have the reservoir storage resources to store 15 years of CO 2 at 2017 emission levels. With few exceptions the bulk of the storage is offshore for countries that do have at least 15 years of storage. The expansion of natural gas storage for strategic purposes in abandoned onshore gas reservoirs is not expected to seriously impact CO 2 storage. The contribution of this analysis is the description of the spatial distribution of potential storage and physical accessibility.

Natural Resources Research↗

USGS2009

Relations between sinkhole density and anthropogenic contaminants in selected carbonate aquifers in the eastern United States

The relation between sinkhole density and water quality was investigated in seven selected carbonate aquifers in the eastern United States. Sinkhole density for these aquifers was grouped into high (>25 sinkholes/100 km 2 ), medium (1–25 sinkholes/100 km 2 ), or low (<1 sinkhole/100 km 2 ) categories using a geographical information system that included four independent databases covering parts of Alabama, Florida, Missouri, Pennsylvania, and Tennessee. Field measurements and concentrations of major ions, nitrate, and selected pesticides in samples from 451 wells and 70 springs were included in the water-quality database. Data were collected as a part of the US Geological Survey (USGS) National Water-Quality Assessment (NAWQA) Program. Areas with high and medium sinkhole density had the greatest well depths and depths to water, the lowest concentrations of total dissolved solids and bicarbonate, the highest concentrations of dissolved oxygen, and the lowest partial pressure of CO 2 compared to areas with low sinkhole density. These chemical indicators are consistent conceptually with a conduit-flow-dominated system in areas with a high density of sinkholes and a diffuse-flow-dominated system in areas with a low density of sinkholes. Higher cave density and spring discharge in Pennsylvania also support the concept that the high sinkhole density areas are dominated by conduit-flow systems. Concentrations of nitrate-N were significantly higher ( p < 0.05) in areas with high and medium sinkhole density than in low sinkhole-density areas; when accounting for the variations in land use near the sampling sites, the high sinkhole-density area still had higher concentrations of nitrate-N than the low sinkhole-density area. Detection frequencies of atrazine, simazine, metolachlor, prometon, and the atrazine degradate deethylatrazine indicated a pattern similar to nitrate; highest pesticide detections were associated with high sinkhole-density areas. These patterns generally persisted when analyzing the detection frequency by land-use groups, particularly for agricultural land-use areas where pesticide use would be expected to be higher and more uniform areally compared to urban and forested areas. Although areas with agricultural land use and a high sinkhole density were most vulnerable (median nitrate-N concentration was 3.7 mg/L, 11% of samples exceeded 10 mg/L, and had the highest frequencies of pesticide detection), areas with agricultural land use and low sinkhole density still were vulnerable to contamination (median nitrate-N concentration was 1.5 mg/L, 8% of samples exceeded 10 mg/L, and had some of the highest frequencies of detections of pesticides). This may be due in part to incomplete or missing data regarding karst features (such as buried sinkholes, low-permeability material in bottom of sinkholes) that do not show up at the scales used for regional mapping and to inconsistent methods among states in karst feature delineation.

Missouri↗

USGS1973

Thermal conductivity of carbonate rocks

The thermal conductivities of several well-defined carbonate rocks were determined near 40°C. Values range from 1.2 W m −1 C −1 for a highly porous chalk to 5.1 W m −1 C −1 for a dolomite. The thermal conductivity of magnesite (5.0) is at the high end of the range, and that for Iceland Spar Calcite (3.2) is near the middle. The values for limestones decrease linearly with increasing porosity. Dolomites of comparable porosity have greater thermal conductivities than limestones. Water-sorbed samples have expected greater thermal conductivities than air-saturated (dry) samples of the same rock. An anomalously large increase in the thermal conductivity of a water-sorbed clayey dolomite over that of the same sample when dry is attributed to the clay fraction, which swells during water inhibition, causing more solid-to-solid contacts within the dolomite framework. Measurements were made with a Colora Thermoconductometer. Chemical and mineralogical analyses were made and tabulated. Porosity of the rocks was determined by mercury porosimetry and also from density measurements. The Iceland Spar Calcite and magnesite were included for reference.

Engineering Geology↗

USGS1971

C13 and O18 compositions in some fresh-water carbonates associated with ultramafic rocks and serpentinites: Western United States

All carbonates associated with the ultramafic rocks and serpentinites of the western United States are shown by their stable isotope ratios to be of near-surface, low-temperature origin. These include vein materials that have been previously classified as hydrothermal. New laboratory and natural data were obtained on the equilibrium isotope relations between hydromagnesite and water. The origins of travertines in the ultramafic area are easily distinguished on the basis of their stable isotope ratios. The extremely heavy isotope ratios of nesquehonites suggest an intricate evaporating-film mechanism of formation.

Geochimica et Cosmochimica Acta↗

USGS1976

Carbon, hydrogen, and oxygen isotope studies of the regional metamorphic complex at Naxos, Greece

At Naxos, Greece, a migmatite dome is surrounded by schists and marbles of decreasing metamorphic grade. Sillimanite, kyanite, biotite, chlorite, and glaucophane zones are recognized at successively greater distances from the migmatite dome. Quartz-muscovite and quartz-biotite oxygen isotope and mineralogie temperatures range from 350 to 700°C. The metamorphic complex can be divided into multiple schist-rich (including migmatites) and marblerich zones. The δ 18 O values of silicate minerals in migmatite and schist units and quartz segregations in the schist-rich zones decrease with increase in metamorphic grades. The calculated δ 18 O H2O values of the metamorphic fluids in the schist-rich zones decrease from about 15‰ in the lower grades to an average of about 8.5‰ in the migmatite. The δD values of OH-minerals (muscovite, biotite, chlorite, and glaucophane) in the schist-rich zones also decrease with increase in grade. The calculated δD H2O values for the metamorphic fluid decrease from −5‰ in the glaucophane zone to an average of about −70‰ in the migmatite. The δD values of water in fluid inclusions in quartz segregations in the higher grade rocks are consistent with this trend. Theδ 18 O values of silicate minerals and quartz segregations in marble-rich zones are usually very large and were controlled by exchange with the adjacent marbles. The δD values of the OH minerals in some marble-rich zones may reflect the value of water contained in the rocks prior to metamorphism. Detailed data on 20 marble units show systematic variations of δ 18 O values which depend upon metamorphic grade. Below the 540°C isograd very steep δ 18 O gradients at the margins and large δ 18 O values in the interior of the marbles indicate that oxygen isotope exchange with the adjacent schist units was usually limited to the margins of the marbles with more exchange occurring in the stratigraphic bottom than in the top margins. Above the 540°C isograd lower δ 18 O values occur in the interior of the marble units reflecting a greater degree of recrystallization and the occurrence of Ca-Mg-silicates. Almost all the δ 13 C values of the marbles are in the range of unaltered marine limestones. Nevertheless, the δ 13 C values of most marble units show a general correlation with δ 18 O values. The CO 2 H 2 O "> CO 2 H 2 O mole ratio of fluid inclusions in quartz segregations range from 0.01 to 2. Theδ 13 C values of the CO 2 range from −8.0 to 3.6‰ and indicate that at some localities CO 2 in the metamorphic fluid was not in carbon isotopic equilibrium with the marbles.

Geochimica et Cosmochimica Acta↗

USGS1994

Variations in the chemical and stable isotope composition of carbon and sulfur species during organic-rich sediment alteration: An experimental and theoretical study of hydrothermal activity at Guaymas Basin, Gulf of California

Organic-rich diatomaceous ooze was reacted with seawater and a Na-Ca-K-Cl fluid of seawater chlorinity at 325–400°C, 400–500 bars, and fluid/sediment mass ratios of 1.56–2.35 to constrain factors regulating the abundance and stable isotope composition of C and S species during hydrothermal alteration of sediment from Guaymas Basin, Gulf of California. Alteration of inorganic and organic sedimentary components resulted in extensive exchange reactions, the release of abundant H 2 S, CO 2 , CH 4 , and C organic , to solution, and recrystallization of the sediment to an assemblage containing albitic plagioclase, quartz, pyrrhotite, and calcite. The δ 34 S cdt "> δ 34 S cdt values of dissolved H 2 S varied from −10.9 to +4.3‰ during seawater-sediment interaction at 325 and 400°C and from −16.5 to −9.0‰ during Na-Ca-K-Cl fluid-sediment interaction at 325 and 375°C. In the absence of seawater SO 4 , H 2 S is derived from both the transformation of pyrite to pyrrhotite and S released during the degradation of organic matter. In the presence of seawater SO 4 , reduction of SO 4 contributes directly to H 2 S production. Sedimentary organic matter acts as the reducing agent during pyrite and SO 4 reduction. Requisite acidity for the reduction of SO 4 is provided by Mg fixation during early-stage sediment alteration and by albite and calcite formation in Mg-free solutions. Organically derived CH 4 was characterized by δ 13 C pdb "> δ13Cpdb values ranging between −20.8 and −23.1‰, whereas δ 13 C pdb "> δ 13 C pdb values for dissolved C organic ranged between −14.8 and −17.7%. Mass balance calculations indicate that δ 13 C values for organically derived CO 2 were ≥ − 14.8%. Residual solid sedimentary organic C showed small (≤ 0.7‰) depletions in 13 C relative to the starting sediment. The experimental results are consistent with the isotopic and chemical composition of natural hydrothermal fluids and minerals at Guaymas Basin and permit us to better constrain sources and sinks for C and S species in subseafloor hydrothermal systems at sediment-covered spreading centers. Our data show that the sulfur isotope composition of hydrothermal Sulfide minerals in Guaymas Basin can be explained by derivation of S from diagenetic sulfide and seawater sulfate. Basaltic S may also contribute to hydrothermal sulfide precipitates but is not required to explain their isotopic composition. Estimates of seawater/ sediment mass ratios based on sulfur isotopic composition of sulfide minerals and the abundance of dissolved NH 3 in vent fluids range from 3–29 during hydrothermal circulation. Sources of C in Guaymas Basin hydrothermal fluids include thermal degradation of organic matter, bacteriogenic methane production, and dissolution of diagenetic carbonate.

Baja California Sur↗

USGS1992

Morphology and genesis of carbonate soils on the Kyle Canyon fan, Nevada, U.S.A.

The physical and chemical properties of soils formed in an arid climate on calcareous alluvium of the Kyle Canyon alluvial fan, southern Nevada, were studied in order to infer the rates and relative importance of various soil-forming processes. These studies included field and microscopic observations and analyses of thin sections, major oxides, extractable iron, and clay minerals. The results are interpreted to reflect five major pedogenic processes: (1) The calcic horizons and calcretes of Kyle Canyon soils form by precipitation of CaCO 3 , derived from eolian dust and alluvium, as clast coats, matrix cement, and massive layers. (2) The A and uppermost B horizons are essentially dust-derived, for they contain large amounts of detrital material not present in the alluvial parent material, and their major-oxide content is similar to that of modern dust. (3) Clay particles are translocated from A into B horizons. (4) Iron-bearing minerals in the near-surface B horizons are slowly oxidized. (5) Carbonate and aluminosilicate grains are both displaced and replaced by pedogenic CaCO 3 ; the silica released by replacement of aluminosilicates may be locally precipitated as amorphous or opaline silica and (or) incorporated into newly formed palygorskite and sepiolite. Rates of soil development at Kyle Canyon are approximate due to uncertainties in age estimates. Some soil field properties change at rates that are similar to rates for soils formed in rhyolitic parent material near Mercury, Nevada. The rate of accumulation of CaCO 3 (3–5 g m −2 yr −1 ) at Kyle Canyon is an order of magnitude faster than that near Mercury, but is comparable to rates calculated for soils in southern New Mexico and Utah.

Nevada↗

USGS1970

Comparison of chemical hydrogeology of the carbonate peninsulas of Florida and Yucatan

Aquifers of the peninsulas of Florida and northern Yucatan are Tertiary marine carbonate formations showing many lithologic and faunal similarities. In addition, the tropical to subtropical climates of the two areas are similar, each having annual rainfall of about 1000 to 1500 mm. Despite similarities in these fundamental controls, contrasts in the hydrologic and geochemical systems are numerous and striking. For example, Florida has many rivers; Yucatan has none. Maximum thickness of fresh ground water in Florida is about 700 meters; in the Yucatan it is less than 70 meters. In Florida the gradient of the potentiometric surface averages about 1 meter per kilometer; in the Yucatan it is exceedingly low, averaging about 0.02 meter per kilometer. In Florida the chemical character of water changes systematically downgradient, owing to solution of minerals of the aquifer and corresponding increases in total dissolved solids, sulfate, calcium, and Mg-Ca ratio; in the Yucatan no downgradient change exists, and dominant processes controlling the chemical character of the water are solution of minerals and simple mixing of the fresh water and the body of salt water that underlies the peninsula at shallow depth. Hydrologic and chemical differences are caused in part by the lower altitude of the Yucatan plain. More important, however, these differences are due to the lack of an upper confining bed in Yucatan that is hydrologically equivalent to the Hawthorn Formation of Florida. The Hawthorn cover prevents recharge and confines the artesian water except where it is punctured by sinkholes, but sands and other unconsolidated sediments fill sinkholes and cavities and impede circulation. In the Yucatan the permeability of the entire section is so enormous that rainfall immediately infiltrates to the water table and then moves laterally to discharge areas along the coasts.

Florida Peninsula, Yucatan Peninsula↗

USGS1971

Effects of karst features on circulation of water in carbonate rocks in coastal areas

The normal balance between fresh water in coastal aquifers and sea water applies also to carbonate-rock aquifers that have been karstified, but there are local modifications in the balance that need to be considered. Uneven distribution of permeability, expressed by a network of solution channels bounded by relatively impermeabler rock, causes an uneven distribution of head of the environmental water along the seacoast. Where sinkholes and (or) vertical solution shafts below sea level penetrate the aquifer, the fresh ground water may discharge through these karst features if the fresh-water head is greater than that of the salt water. However, under some conditions the salt-water head may exceed that of the fresh water, and the direction of movement is reversed as sea water flows into the aquifer. This sea-water flow into the aquifer occurs (1) where sinkholes, acting as “cased wells,” penetrate less permeable rock before reaching a lateral solution channel and (2) where (or when) the fresh-water head is less than that required to balance the salt water. On Andros Island, Bahamas, the range in tide (as much as 5 feet) from low tide to high tide is sufficient to cause such a reversal locally. During low tide the salt-water head becomes sufficiently low that the ground-water head exceeds that of the sea water, and the ground water flows through the sinkholes to the ocean floor; during high tide sea water flows in the sinkholes. In the Adriatic Sea along the coast of Yugoslavia, apparently the fresh-water head is sufficient to produce perennial springs in some localities, but in other areas, as in the Bay of Kastela near Split, the fresh-water head becomes low enough during some seasons that the flow is reversed and salt water enters the aquifer through the karst features. The development of sinkholes and other karst features near the present coast and extending below sea level occurred generally during a low stand of the Pleistocene sea when the top of the saturated zone stood lower than the bottom of the deepest sinkholes or natural wells. Integrated evaluations of (1) the distribution of permeability in coastal karst regions and (2) the principles relating to the dynamic balance between fresh aquifer water and sea water are leading to better knowledge of methods that may salvage much karst water which is lost to the sea.

Split↗

USGS1993

Use of principal-component, correlation, and stepwise multiple-regression analyses to investigate selected physical and hydraulic properties of carbonate-rock aquifers

Correlation analysis in conjunction with principal-component and multiple-regression analyses were applied to laboratory chemical and petrographic data to assess the usefulness of these techniques in evaluating selected physical and hydraulic properties of carbonate-rock aquifers in central Pennsylvania. Correlation and principal-component analyses were used to establish relations and associations among variables, to determine dimensions of property variation of samples, and to filter the variables containing similar information. Principal-component and correlation analyses showed that porosity is related to other measured variables and that permeability is most related to porosity and grain size. Four principal components are found to be significant in explaining the variance of data. Stepwise multiple-regression analysis was used to see how well the measured variables could predict porosity and (or) permeability for this suite of rocks. The variation in permeability and porosity is not totally predicted by the other variables, but the regression is significant at the 5% significance level.

Journal of Hydrology↗

USGS1987

Kinetics and mechanisms of iron sulfide reductions in hydrogen and in carbon monoxide

The reduction of iron sulfides by hydrogen and by carbon monoxide has been studied using plug flow and thermogravimetric methods. The reactions were studied in the 523–723°K temperature range and were found to be first-order processes. Plug flow studies were used to correlate reaction rates between pyrite and the gases as a function of the surface area of the pyrite. The rate of H 2 S formation increases with the surface area of the pyrite sample. The results of thermogravimetric experiments indicate that the reactions consist of several steps. Rate constants for the pyrite reduction by H 2 and by CO were obtained. The activation energies increased with degree of reduction. Values of E a were 113.2 (step I) and 122.5 kJ/mole (step II) for pyrite reduction with CO and 99.4 (step I), 122.4 (step II), 125.2 (step III), and 142.6 kJ/mole (step IV) for pyrite reduction with hydrogen.

Journal of Solid State Chemistry↗

USGS1996

Overview of a simple model describing variation of dissolved organic carbon in an upland catchment

Hydrological mechanisms controlling the variation of dissolved organic carbon (DOC) were investigated in the Deer Creek catchment located near Montezuma, CO. Patterns of DOC in streamflow suggested that increased flows through the upper soil horizon during snowmelt are responsible for flushing this DOC-enriched interstitial water to the streams. We examined possible hydrological mechanisms to explain the observed variability of DOC in Deer Creek by first simulating the hydrological response of the catchment using TOPMODEL and then routing the predicted flows through a simple model that accounted for temporal changes in DOC. Conceptually the DOC model can be taken to represent a terrestrial (soil) reservoir in which DOC builds up during low flow periods and is flushed out when infiltrating meltwaters cause the water table to rise into this “reservoir”. Concentrations of DOC measured in the upper soil and in streamflow were compared to model simulations. The simulated DOC response provides a reasonable reproduction of the observed dynamics of DOC in the stream at Deer Creek.

Ecological Modelling↗

USGS1977

Techniques for the conversion to carbon dioxide of oxygen from dissolved sulfate in thermal waters

The fractionation of oxygen isotopes between dissolved sulfate ions and water provides a useful geothermometer for geothermal waters. The oxygen isotope composition of dissolved sulfate may also be used to indicate the source of the sulfate and processes of formation. The methods described here for separation, purification and reduction of sulfate to prepare carbon dioxide for mass spectrometric analysis are modifications of methods by Rafter (1967), Mizutani (1971), Sakai and Krouse (1971), and Mizutani and Rafter (1969). ?? 1976.

Geothermics↗