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Gilbert C. Bortleson

Publications and source records attributed to Gilbert C. Bortleson.

10 recordsLinked to original sources
USGS2003

Phosphorus, iron, and manganese distribution in sediment cores of six Wisconsin lakes

Depositional patterns of iron, manganese, and phosphorus in one central and five northern Wisconsin lakes ranging from oligotrophic to eutrophic, primarily from natural causes, have been investigated. One-meter cores from one or more locations within each lake were analyzed. The historical pattern of iron and manganese deposition is closely related to the pattern of phosphorus deposition in most of the cores. Four of the nine cores show a strong positive correlation coefficient between P and Fe and seven between P and Mn. Manganese has more predictive value than iron for determining the concentration of phosphorus in a given core; however, the iron content appears to be the dominant factor in the phosphorus sorptive and retentive capacity of sediments.

Wisconsin↗
USGS1987

Water quality in the lower Puyallup River valley and adjacent uplands, Pierce County, Washington

The quality of most ground and surface water within and adjacent to the lower Puyallup River valley is suitable for most typical uses; however, some degradation of shallow groundwater quality has occurred. High concentrations of iron and manganese were found in groundwater, sampled at depths of < 40 ft, from wells tapping alluvial aquifers and in a few wells tapping deeper aquifers. Volatile and acid- and base/neutral-extractable organic compounds were not detected in either shallow or deep groundwater samples. The quality of shallow groundwater was generally poorer than that of deep water. Deep ground water (wells set below 100 ft) appears suitable as a supplementary water supply for fish-hatchery needs. Some degradation of water quality, was observed downstream from river mile 1.7 where a municipal wastewater-treatment plant discharges into the river. In the Puyallup River, the highest concentrations of most trace elements were found in bed sediments collected downstream from river mile 1.7. Median concentrations of arsenic, lead, and zinc were higher in bed sediments from small streams compared with those from the Puyallup River, possibly because the small stream drainages, which are almost entirely within developed areas, receive more urban runoff as a percentage of total flow. Total-recoverable trace-element concentrations exceeded water-quality criteria for acute toxicity in the Puyallup River and in some of the small streams. In most cases, high concentrations of total-recoverable trace elements occurred when suspended-sediment concentrations were high. Temperatures in all streams except Wapato Creek and Fife Dutch were within limits (18 C) for Washington State class A water. Minimum dissolved oxygen concentrations were relatively low at 5.6 and 2.0 mg/L, respectively, for Wapato Creek and Fife Dutch. The poorest surface-water quality, which can be characterized as generally unsuitable for fish, was in Fife Dutch, a manmade channel and therefore uncharacteristic of other small streams. (Author 's abstract)

Water-Resources Investigations Report↗
USGS1986

Occurrence of dissolved sodium in ground waters in basalts underlying the Columbia Plateau, Washington

Basalt aquifers of the Columbia River Basalt Group are a principal source of water for agricultural, domestic, and municipal use. Concern has been expressed in this agriculture-dependent region about problems associated with the use of groundwaters with a high sodium concentration relative to the calcium and magnesium content (high sodium-adsorption ratio). Continued irrigation with such waters can reduce soil permeability to the degree that water cannot effectively reach plant roots. Groundwaters within a flow path evolved from a calcium magnesium bicarbonate type in shallow and upgradient locations to a sodium potassium bicarbonate type in deeper and downgradient locations. Most of the intermediate and high sodium adsorption ratio values were observed in discharge areas near major streams and in pumping centers within the central part of the plateau. Ninety-six percent of the groundwaters sampled had a low sodium absorption ratio, indicating that, for irrigation purposes, there is probably little danger of harmful levels of exchangeable sodium occurring on soil. However, water from 18 of 418 wells sampled had a sodium absorption ratio grater than 8.0 and were classified as having a medium, high, or very high sodium hazard.

Idaho, Washington↗
USGS1985

Geochemical controls on dissolved sodium in basalt aquifers of the Columbia Plateau, Washington

Miocene basaltic aquifers of the Columbia Plateau are the principal source of water for agricultural, domestic, and municipal use in Washington State. Irrigation with groundwaters with relatively high sodium concentrations has been cause for concern in recent years, because of the tendency of such waters to reduce soil permeability. Chemical reactions involving groundwater and the basalts are the primary mechanisms responsible for the input of sodium to groundwater in the plateau. This conclusion is supported by the sequence of secondary alteration products found and by progressive changes in groundwater chemistry with depth and position along regional flow paths. Upgradient and shallow groundwaters have low sodium concentrations and sodium-adsorption ratios (SAR's), and are predominantly calcium sodium bicarbonate waters. Groundwaters from deeper and downgradient locations have higher sodium concentrations and SAR 's and are predominantly sodium bicarbonate water. Volcanic glass and cryptocrystalline matrix are the major sources of groundwater sodium, and are dissolved by a combination of silicate hydrolysis and dissolution by carbonic acid. Magnesium, iron, and calcium are removed from solution by the formation of an iron magnesium smectite, calcite , and amorphous iron oxyhydroxide. The addition of sodium, silicon, and potassium by dissolution of basalt exceeds their removal by the precipitation of secondary minerals, and their concentrations increase in the initial stages of this process. In later stages, these continued increases produce a water saturated with clinoptilolite and silica phases, and these begin to precipitate. While the timing of these processes is unclear, the mineralogy of secondary alteration and estimated cooling rates of the basalt flows suggest that observed alteration products formed primarily at low temperature, under conditions similar to those existing at the present time. (USGS)

Water-Resources Investigations Report↗
USGS1985

Controls on ground-water chemistry in the Horse Heaven Hills, south-central Washington

Miocene basaltic aquifers are the source of domestic and municipal water, and about 20,000 acre-feet of irrigation water annually, in the Horse Heaven Hills in south-central Washington State. Groundwater chemical variations derive from the hydraulic characteristics is of the geohydrologic system, from groundwater basalt reactions, and from irrigation. Some dissolved species concentrations increase with residence time; others decrease. Recharge area groundwaters are calcium magnesium sodium bicarbonate waters with sodium-adsorption ratios (SAR's) less than 1.0. They evolve to sodium potassium bicarbonate waters with SAR 's as high as 17. Glassy and cryptocrystalline phases of the basalt are the main sources of dissolved sodium. They dissolve by silicate hydrolysis in carbon dioxide charged waters that recharge the aquifer system. Dissolved silicon, iron, and aluminum concentrations are controlled by the solubilities of amorphous secondary alteration products, which order to silica phases, oxyhydroxides, and smectite. Carbonate mineral precipitation is induced by increasing pH from the hydrolysis reaction. Sodium and potassium concentrations increase until clinoptilolite saturation is reached and precipitation begins. Deviations from the general variation patterns are due to localized geologic structures which distort the groundwater flow system, and to the irrigation use of Columbia River water. (USGS)

Water-Resources Investigations Report↗
USGS1975

Recent sedimentary history of Lake Monona, Wisconsin

Chemical analyses from two short cores in Lake Monona show that pronounced changes in chemical stratigraphy have occurred since white man moved into Madison and southern Wisconsin and began modifying the area. Since the mid to late 1800's, there has been an appreciable increase in P, Fe, Mn, Al, and K in the uppermost sediments. Maximum concentrations of P were observed near the turn of the century and in the most recent sediment layers.

Wisconsin↗