USGS Science⌕ Search

Geology topics

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↗
USGS2006

Factors controlling the major ion chemistry of streams in the Blue Ridge and Valley and Ridge physiographic provinces of Virginia and Maryland

The factors controlling the chemistry of 69 low-order streams in the Blue Ridge and Valley and Ridge physiographic provinces of Virginia and Maryland were studied over a 13-month period. Principal component analysis was used to examine regional patterns in stream chemistry and to examine the degree to which the chemistry of low-order streams is controlled by the bedrock upon which they flow. Streams clustered into regionally isolated groups, strongly related to bedrock type, with SO 2− 4 and HCO − 3 the chemical variables of most importance. Sulphate concentrations appear to be strongly controlled by climate and hydrology, and sorption in the soils within the watershed. Much of the atmospherically derived SO 2− 4 accumulates in watersheds during the growing season and is later flushed out. Weathering reactions were found to be particularly important in the production of HCO − 3 , accounting for 91 per cent on an annual basis, and export of divalent cations from these watersheds, accounting for 48–50 per cent on an annual basis. About half of non-anthropogenic Na + was derived from weathering of silicates, whereas nearly all K + was identified with leaching by SO 2− 4 . Water chemistry was strongly related to the rock type in the watershed and the weatherability of the component minerals. Rock type is not a randomly distributed function; instead, it is controlled by geologic factors that result in clusters of similar rock types in a given region. When planning large synoptic studies, it is extremely important to consider that a sampling scheme based on random sampling of a non-randomly distributed function May, not provide the most accurate representation of the variables of interest. Instead, a hierarchical sampling scheme May, be indicated. Our results also suggest that, although one sample in time May, be sufficient to characterize the primary geochemical factors controlling stream chemistry throughout the year, it May, not be sufficient to detect subtle, flow-related alterations in chemistry.

Hydrological Processes↗
USGS2005

The distribution of phosphorus in Popes Creek, VA, and in the Pocomoke River, MD: Two watersheds with different land management practices in the Chesapeake Bay Basin

This paper compares phosphorus (P) concentrations in sediments from two watersheds, one with, and one without, intensive animal agriculture. The watersheds are in the coastal plain of the Chesapeake Bay and have similar physiographic characteristics. Agriculture in the Pocomoke River, MD, watershed supplied 2.7 percent of all broiler chickens produced in the USA in 1997. Poultry litter is an abundant, local source of manure for crops. Broiler chickens are not produced in the Popes Creek, VA, watershed and poultry manure is, therefore, not a major source of fertilizer. The largest concentrations of P in sediment samples are found in floodplain and main-stem bottom sediment in both watersheds. Concentrations of total P and P extracted with 1N HCl are significantly larger in main-stem bottom sediments from the Pocomoke River than in main-stem bottom sediments from Popes Creek. Larger concentrations of P are associated with what are potentially redox sensitive iron oxyhydroxides in sediment samples from the Pocomoke River watershed than are associated with what are potentially redox sensitive iron oxyhydroxides in sediment samples from the Popes Creek watershed. Data for P and iron (Fe) concentrations in sediments from the Popes Creek watershed provide a numerical framework (baseline) with which to compare P and Fe concentrations in sediment from the Pocomoke River watershed. ?? Springer 2005.

Water, Air, & Soil Pollution↗
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↗
USGS1992

Acid rain and its effects on streamwater quality on Catoctin Mountain, Maryland

The U.S. Geological Survey (USGS) is the Nation's largest water-science and water-information agency. The mission of the Water Resources Division of the USGS is to provide the hydrologic information and understanding needed for the best management of the Nation's water resources. To fulfill this mission, the USGS conducts water-quality and other types of investigations of the Nation's surface- and ground-water resources.

Maryland↗
USGS1992

Acid-rain induced changes in streamwater quality during storms on Catoctin Mountain, Maryland

Catoctin Mountain receives some of the most acidic (lowest pH) rain in the United States. In 1990, the U.S. Geological Survey (USGS), in cooperation with the Maryland Department of the Environment (MDE) and the Maryland Department of Natural Resources (DNR), began a study of the effects of acid rain on the quality of streamwater on the part of Catoctin Mountain within Cunningham Falls State Park, Maryland (fig. 1). Samples of precipitation collected on the mountain by the USGS since 1982 have been analyzed for acidity and concentration of chemical constituents. During 1982-91, the volume-weighted average pH of precipitation was 4.2. (Volume weighting corrects for the effect of acids being washed out of the atmosphere at the beginning of rainfall). The pH value is measured on a logarithmic scale, which means that for each whole number change, the acidity changes by a factor of 10. Thus rain with a pH of 4.2 is more than 10 times as acidic as uncontaminated rain, which has a pH of about 5.6. The acidity of rain during several rainstorms on Catoctin Mountain was more than 100 times more acidic than uncontaminated rain.

Maryland↗
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↗