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O.P. Bricker

Publications and source records attributed to O.P. Bricker.

At least 19 recordsLinked to original sources
USGS2012

Geochemistry of water

The quadrennium 1967–1970 has been a productive period in the field of water geochemistry. Field studies, laboratory investigations, and theoretical considerations have led to significant advances in our knowledge of the chemical behavior of natural waters and of the solid earth materials that contain them. A symposium on trace inorganics in water, sponsored by the American Chemical Society, was held in Miami, Florida, in 1967. The proceedings of this conference were published in 1968 in the Advances in Chemistry Series 73. This volume deals with the occurrence, behavior, and analysis of inorganic constituents in natural waters.

Eos, Transactions, American Geophysical Union↗
USGS2004

Bog iron formation in the Nassawango Creek watershed, Maryland, USA

The Nassawango bog ores in the modern environment for surficial geochemical processes were studied. The formation of Nassawango bog ores was suggested to be due to inorganic oxidation when groundwater rich in ferrous iron emerges into the oxic, surficial environment. It was suggested that the process, providing a phosphorus sink, may be an unrecognized benefit for mitigating nutrient loading from agricultural lands. It is found that without the effect of iron fixing bacteria, bog deposites could not form at significant rates.

Conference Paper↗
USGS1996

Trends in the chemistry of precipitation and surface water in a national network of small watersheds

Trends in precipitation and surface water chemistry at a network of 15 small watersheds ( < 10 km2) in the USA were evaluated using a statistical test for monotonic trends (the seasonal Kendall test) and a graphical smoothing technique for the visual identification of trends. Composite precipitation samples were collected weekly and surface water samples were collected at least monthly. Concentrations were adjusted before trend analysis, by volume for precipitation samples and by flow for surface water samples. A relation between precipitation and surface water trends was not evident either for individual inorganic solutes or for solute combinations, such as ionic strength, at most sites. The only exception was chloride, for which there was a similar trend at 60% of the sites. The smoothing technique indicated that short-term patterns in precipitation chemistry were not reflected in surface waters. The magnitude of the short-term variations in surface water concentration was generally larger than the overall long-term trend, possibly because flow adjustment did not adequately correct for climatic variability. Detecting the relation between precipitation and surface water chemistry trends may be improved by using a more powerful sampling strategy and by developing better methods of concentration adjustment to remove the effects of natural variation in surface waters.

Hydrological Processes↗
USGS1993

Hydrologic, chemical, and isotopic characterization of two small watersheds on Catoctin Mountain, north-central Maryland, U.S.A.

Two small (100 ha) watersheds located on Catoctin Mountain in north-central Maryland were intensively instrumented in 1990 and have been hydrologically, chemically, and isotopically monitored for 3 years. Dissolved concentrations of major ions (Ca 2+ , Mg 2+ , Na + , K + , total AI, CI - , NO 3 - , SO 4 2- , HCO 3 - , and SiO 2 ) and stable isotopic (D and 18 O) values have been analyzed for most types of water (precipitation, throughfall, two depths of soil water, shallow groundwater, and streamwater) that enter, travel through, and exit each watershed. The major objectives of the study were to characterize the chemical and isotopic signatures of all aqueous components of the watersheds and to interpret the causes of the changes in chemical and isotopic compositions of streamwater during storm runoff. This paper describes selected results of the study.

Maryland↗
USGS1992

The influence of pH on biotite dissolution and alteration kinetics at low temperature

Biotite dissolution rates in acidic solutions were determined in fluidized-bed reactors and flowthrough columns. Biotite dissolution rates increased inversely as a linear function of pH in the pH range 3–7, where the rate order n = −0.34. Biotite dissolved incongruently over this pH range, with preferential release of magnesium and iron from the octahedral layer. Release of tetrahedral silicon was much greater at pH 3 than at higher pH. Iron release was significantly enhanced by low pH conditions. Solution compositions from a continuous exposure flow-through column of biotite indicated biotite dissolves incongruently at pH 4, consistent with alteration to a vermiculite-type product. Solution compositions from a second intermittent-flow column exhibited elevated cation release rates upon the initiation of each exposure to solution. The presence of strong oxidizing agents, the mineral surface area, and sample preparation methodology also influenced the dissolution or alteration kinetics of biotite.

Geochimica et Cosmochimica Acta↗
USGS1989

Particle-borne radionuclides as tracers for sediment in the Susquehanna River and Chesapeake Bay

The Chesapeake Bay receives nearly 1 000 000 tonnes of sediment annually from its major tributary, the Susquehanna River. The pattern of deposition of this sediment affects the lifetime of the estuarine resource and the fate of any sediment-borne contaminants. Previous estimates of the extent to which Susquehanna River sediment is transported down the Chesapeake have differed considerably. By use of reactor-generated radionuclides adsorbed on the river sediment, a sediment budget has been compiled for the upper Chesapeake Bay and the reservoirs on the lower Susquehanna. Reservoirs impound nearly 1 400 000 tonnes of sediment annually behind the power dams on the lower Susquehanna River. Without the dams, sediment delivery to the upper bay would more than double. The uppermost Chesapeake Bay, within and above the turbidity maximum, retains virtually all of the fluvial sediment delivered to it. The result is an annual sedimentation rate of approximately 3 mm yr −1 in the upper bay, an infilling rate that is nearly equal to the regional rate of sea level rise.

Chesapeake Bay, Susquehanna River↗
USGS1985

Experimental chemical weathering of various bedrock types at different pH-values. 1. Sandstone and granite

Experimental chemical weathering of the so-called Old Rag Granite and Massanutten Sandstone, Virginia, U.S.A., has produced a comparison with the natural environment, and prediction of the effect of acid precipitation. The experimental results of the release of elements, dissolution of minerals, total rock weathered and the degree of weathering as function of volume of leachate were plotted. These data were compared with the natural environment. The use of the plots to predict the effect of high levels of rain acidity on weathering of these rocks is demonstrated. A nonexpandable 14-Å clay was developed from the alteration of biotite during the experimental chemical weathering of the granite at pH 4. This interstratified Al(OH)—mica clay resembles those of the soil developed on the granite and sandstone. Hydroxy-Al may be precipitating between the mica interlayers and producing a 14-Å spacing. Development of this clay by chemical alteration of biotite may change the current hypotheses about its origin in the soils of northeastern U.S.A. While Al-hydroxide seems to regulate Al concentrations in stream waters at the present level of rain acidity, it was found that at lower pH and in the presence of high sulfate concentrations, Al solubility may be controlled by Al-sulfate phase(s).

Virginia↗
USGS1985

Geochemical mass-balance relationships for selected ions in precipitation and stream water, Catoctin Mountains, Maryland

Results of a study of input/output mass balances for major ions based on the chemical composition of precipitation and stream-water, geochemical reactions with different loading rates of hydrogen ion, and watershed processes influencing the chemical character of stream-waters in two small watershed areas are reported with a view to predicting the effect of additions of acidic rain to the watershed systems. Geochemical weathering processes account for the observed changes in the chemistry of stream flow. Although present in bedrock in extremely small quantities, calcite plays an important role in neutralization of the total hydrogen-ion input.

Maryland↗
USGS1981

Reactor-released radionuclides in Susquehanna River sediments

Three Mile Island (TMI) and Peach Bottom (PB) reactors have introduced 137Cs, 134Cs, 60Co, 58Co and several other anthropogenic radionuclides into the lower Susquehanna River. Here we present the release history for these nuclides (Table 1) and radionuclide concentration data (Table 2) for sediment samples collected in the river and upper portions of the Chesapeake Bay (Fig. 1) within a few months after the 28 March 1979 loss-of-coolant-water problem at TMI. Although we found no evidence for nuclides characteristic of a ruptured fuel element, we did find nuclides characteristic of routine operations. Despite the TMI incident, more than 95% of the total 134Cs input to the Susquehanna has been a result of controlled low-level releases from the PB site. 134Cs activity released into the river is effectively trapped by sediments with the major zones of reactor-nuclide accumulation behind Conowingo Dam and in the upper portions of Chesapeake Bay. The reported distributions document the fate of reactor-released radionuclides and their extent of environmental contamination in the Susquehanna-Upper Chesapeake Bay System. ?? 1981 Nature Publishing Group.

Nature↗
USGS1978

A pollution history of Chesapeake Bay

Present day anthropogenic fluxes of some heavy metals to central Chesapeake Bay appear to be intermediate to those of the southern California coastal region and those of Narragansett Bay. The natural fluxes, however, are in general higher. On the bases of Pb-210 and Pu-239 + 240 geochronologies and of the time changes in interstitial water compositions, there is a mixing of the upper 30 or so centimeters of the sediments in the mid-Chesapeake Bay area through bioturbation by burrowing mollusks and polychaetes. Coal, coke and charcoal levels reach one percent or more by dry weight in the deposits, primarily as a consequence of coal mining operations. ?? 1978.

Geochimica et Cosmochimica Acta↗
USGS1976

Hydrogeochemistry of Bermuda: A case history of ground-water diagenesis of biocalcarenites

Bermuda is composed of relatively young skeletal limestones currently undergoing diagenesis by the ground water passing through them. The saturated zone consists of separate fresh-water bodies laterally surrounded and underlain by extensive brackish aureoles, in which the meteoric water is mixed with sea water. The meteoric water enters the aquifer after passing through the soil or through marshes (outcrops of the ground-water bodies), in each case causing an influx of CO 2 to the saturated zone. Examination of the ground-water chemistry enables mapping of (a) the extent of mixing of meteoric ground water and sea water; (b) P CO2 ; (c) the extent of saturation with calcite and aragonite; (d) concentration of Sr; and (e) the amount of calcium and magnesium derived from the limestones. It is concluded that three processes control the chemistry of Bermudian ground water: (a) generation of elevated CO 2 partial pressures in soils and marshes; (b) dissolution of metastable carbonate minerals (principally aragonite); and (c) mixing with sea water. Bermuda ground water apparently approaches a steady state of aragonite dissolution (at slight subsaturation) and concurrent precipitation of calcite cement. Large Sr/Ca ratios in the ground water indicate that the dissolution of aragonite is incongruent. Dissolution is most pronounced near the marshes where CO 2 content is highest. Mixing with sea water is not significant in controlling calcite saturation. Only small amounts of magnesium enter the ground water by incongruent dissolution of magnesium calcite, an apparently slow process on the time scale of passage of the ground water through the saturated zone. All of the waters are well undersaturated with respect to dolomite. It is estimated that the present rate of recrystallization of aragonite to calcite is about 0.32 cm 3 of aragonite to calcite per m 3 of the saturated zone per year. At the present rate of chemical weathering, 360 m 3 of the saturated zone is lost each year through solution and transported to the sea by ground water.

Geological Society of America Bulletin↗
USGS1975

Rates of dissolution of aluminosilicates in seawater

Dissolution of eight clay minerals, four zeolites, and quartz in seawater has been monitored for 8 1 2 years. For most of the minerals, dissolution can be described as a first-order reaction in which dissolved silica approaches from undersaturation steady concentration values with time. Characteristic reaction rate constants (k 1 ) are of the order of 10 -7 sec -1 . One of the zeolites, clinoptilolite, shows a different dissolution behavior: SiO 2 concentration in solution reaches a high value within one year, followed by a decline to a lower value, suggestive of precipitation of another silicate phase (possibly sepiolite). A mathematical solution is given for a kinetic equation combining the parabolic-rate and first-order rate processes. It is shown that in a wide range of silicate dissolution reactions taking place over long periods of time, the presence of the parabolic-rate dissolution processes cannot be detected, thereby making its inclusion in the kinetic equations unnecessary. The experimental rates of dissolution are comparable to the SiO 2 - dissolution rates in oceanic sediments near the sediment/water interface. But deeper in the sediment, the calculated dissolution rates are significantly lower than the near-interface and experimental values. © 1975.

Earth and Planetary Science Letters↗
USGS1974

Oxidation effect on the analysis of iron in the interstitial water of recent anoxic sediments

Recent studies on the changes in composition of interstitial water during its separation from sediments 1-3 prompted us to evaluate the effect of squeezing on the concentration of ferrous iron within the interstitial water. Sediment samples were taken in northern Chesapeake Bay (38°56′ N and 76°25′ W) with a Benthos gravity corer. Layers of sediment were immediately extruded from the plastic coring tube and loaded into nylon squeezer barrels. The interstitial water was squeezed from the sediment through a 0.22 μm Millipore filter by the pressure of nitrogen acting against a rubber diaphragm 4 . The water drained directly into a calibrated test tube containing a solution of o-phenanthroline, buffered at pH 3.6, and the iron content was determined colorimetrically 5 . © 1974 Nature Publishing Group.

Chesapeake Bay↗
USGS1974

Chemical weathering of serpentinite in the eastern Piedmont of Maryland

Weathering processes in a small watershed (Soldiers Delight) underlain by Serpentinite in the Piedmont of Maryland were studied by means of a mass balance technique and were compared with the processes operative in a watershed uncertain by schist. The two terranes are downwasting at a rate of 2.4 m per m.y., but chemical weathering much more strongly affects the Serpentinite (2.2 m per m.y.) than the schist (1.2 m per m.y.). The serpentinite lacks a saprolite cover because resistate minerals are absent and alumina in the bedrock is scarce. In contrast, the schist contains both quartz and a source of alumina in the alumino-silicate minerals and, as a result, has a thick saprolite mantle. Relatively small amounts of secondary quartz, chalcedony, and 14Å clay minerals are synthesized in the serpentinite watershed, but relatively large amounts of gibbsite and clay minerals (kaolinite and vermiculite) are formed during the weathering of the schist. The hydrologic consequences in the serpentinite terrane compared with the schist watershed are increased flood-flow discharge, greater fluctuation in seasonal, instantaneous base-flow discharge, and pronounced seasonal fluctuations in total discharge. The serpentinite stream water averaged 205 ppm of total dissolved solids in the base flow compared to 25 ppm in the schist. Stream water from the serpentinite is of the magnesium bicarbonate type; that from the schist is sodium-calcium bicarbonate type. On the serpentinite, substantial land-surface reduction (denudation) is effected by chemical weathering; mechanical weathering is secondary. On the schist terrane, mechanical weathering is the primary agent that lowers the land surface, even though chemical weathering has reduced the rock mass ay almost one-half. © 1974 Geological Society of America.

Geological Society of America Bulletin↗
USGS1973

Phosphate in interstitial waters of anoxic sediments: Oxidation effects during sampling procedure

Oxidation during sampling procedures significantly decreases the inorganic phosphate concentrations of interstitial water rich in iron (II). All sampling and analytical procedures must be carried out in an inert atmosphere. Orthophosphate in the interstitial water of Cheaspeake Bay sediments, in equilibrium with vivianite, is a potential nutrient source for the overlying water.

Chesapeake Bay↗