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Geology topics

J. H. Feth

Publications and source records attributed to J. H. Feth.

14 recordsLinked to original sources
USGS2014

Discussion of symposium on land erosion “Piping”

The present writers are familiar only with the Picacho and San Pedro areas, among those cited by the authors, and therefore limit discussion to the occurrence of earth cracks in these areas. The existence of piping is not questioned, and the five conditions suggested by the authors are a justified explanation in the San Pedro area, for example. It is thought, however, that some of the phenomena described as piping are earth cracks whose origins are governed by factors other than those outlined. Once formed, certain earth cracks may facilitate the development of piping by providing ready access to downward and lateral movement of water.

Arizona↗
USGS2010

Solute erosion and chloride balance in selected river basins of the western conterminous United States

The estimated average rates of annual solute erosion in 11 important western river basins range from 180 tons per square mile (Willamette basin) to 4.2 tons per square mile (Gila basin). An average rate of 58 tons per square mile is indicated for the entire 545,000‐square‐mile area drained by the 11 rivers. The wide range in tonnage is the result of a complex of causes, among which differences in geology, gross climatic environments, and activities of man are the most important. Rates of solute erosion are highest in areas of abundant precipitation and runoff, in contrast to rates of suspended‐sediment removal, which are characteristically highest in basins subjected to only 10–15 inches of effective annual precipitation. Tonnages of chloride brought into the 11 river basins by rain and snow make up an equivalent of about 1.6 to about 17% of the chloride removed in runoff during an average year. The range of percentages reflects differences in the relative importance of oceanic and continental solute contributions. This paper is not subject to U.S. copyright. Published in 1965 by the American Geophysical Union.

Water Resources Research↗
USGS2010

Nitrogen compounds in natural water—A review

Nitrogen compounds in natural water are significant in public health, agriculture, industry, and geochemistry. The many sources of nitrogen compounds and the deep involvement of nitrogen in the life processes of organisms makes the study of such compounds difficult. The sources include natural aerosols, precipitation, fixation by micro‐organisms in soil and water, decaying organic matter, and animal and industrial wastes, as well as probably undiscovered sources in consolidated and unconsolidated rocks. Nitrogen compounds are both oxidized and reduced by organisms. Some nitrogen compounds are adsorbed on clay. The theoretical end product in water and the compound probably most often determined is NO 3 −1 . The concentration of nitregen compounds ranges from 0.0 to >100 ppm (parts per million) in surface water and from 0.0 to >1000 ppm in groundwater. Seasonal fluctuations occur. Much further research is needed, including improvements in methods of analysis, further investigation of sources, and detailed study of the nitrogen cycle in small drainage basins. (Key words: Geochemistry; quality of water.) This paper is not subject to U.S. copyright. Published in 1966 by the American Geophysical Union.

Water Resources Research↗
USGS2010

Applications of factor analysis in study of chemistry of groundwater quality, Mojave River Valley, California

Factor analysis is applied to results of chemical analyses of 103 water samples from wells in the Upper and Middle Mojave River valley, San Bernardino County, California. Chemical analyses showed that there are three principal chemical types of water, calcium bicarbonate, sodium sulfate, and sodium chloride, as well as many mixtures of the three. Data were studied by factor analysis to learn the relative importance of each principal ion in determining the variations among the samples, and to examine the possibility of chemical equilibrium between aqueous and solid phases in the aquifers. Most of the covariance in the system may be accounted for by variances of Ca +2 , Mg +2 , Na +1 , SO 4 −2 , and Cl −1 . There is almost identical loading on the constituents Na +1 and Cl −1 . The variance in chemical composition of the hydrochemical system is governed largely by sources of sodium chloride. None of the components is controlled by equilibrium between ions in the water and minerals in the aquifers. Concentrations of NO 3 −1 and F −1 vary independently of other constituents. Geographic distribution of statistical loadings of the principal constituents at individual wells does not reveal sources of the constituents, which must be deduced from geologic and hydrologic evidence. Factor analysis, however, furnished the critical information on chemical relationships basic to the deduction.

California↗
USGS2010

Saline groundwater resources of the conterminous United States

Saline water is arbitrarily defined as water containing more than 1000 milligrams per liter of dissolved solids. Saline ground water is known to underlie about two‐thirds of the 48 states. Locally, aquifers yield saline ground water in profuse quantities, some of which is used by industry, particularly for cooling. Generally, however, saline water has been considered a nuisance. In this report it is dealt with as a resource, especially for the future. Forty chemical types of mineralized ground water were recognized, but sodium chloride dominates the occurrences and is almost the only type found where concentrations exceed about 20,000 mg/l. The occurrence and hydrologic properties of saline water aquifers deserve much more study than they have had. Copyright 1970 by the American Geophysical Union.

Water Resources Research↗
USGS2006

Hidden Recharge

“Hidden recharge” is defined as subsurface percolation of water from basin‐margin mountains directly into aquifers of the valley basins. It is an important, and sometimes neglected, item in hydrologic equations. Locally, geologic conditions permit inter‐basin circulation of ground water. The concept that ground‐water basins necessarily terminate at the contact between alluvium and hardrock is not tenable. Copyright © 1964, Wiley Blackwell. All rights reserved

Ground Water↗
USGS1979

Map showing occurrences of spring-deposited travertine in the conterminous Western United States

Extinct travertine terraces occur hundreds of meters above present levels of spring activity and have potentials for interpretation of ancient hydrologic systems, rates of downcutting, or rates of tectonic uplift that remain virtually unexploited. The abundance and size of extinct travertine deposits suggest that in many places, such as pinnacles at the southwest end of the Searles Lake basin, California, spring activity was once more widespread and copious than it is now. Travertine of Eocene age has been reported, and a scattering of later Tertiary occurrences is known. But where age has been inferred, the inferred ages are predominantly Pleistocene or younger. So travertine seems to be a geologically transient phenomenon, subject either to removal by erosion or to burial and disappearance. Many travertine deposits are known to be on or close to faults. Their occurrence in otherwise structurally featureless alluvial valleys may, therefore, suggest the possibility of a hidden fault. From the Front Range to the Pacific, more than 300 travertime deposits have been identified. The map shows that the deposits are widely dispersed. However, there are apparent groupings on the Wasatch Fault and associated tectonic areas trending northward in Utah and southern Idaho, and also near the great fault zone that marks the eastern boundary of the Sierra Nevada, California. (Lantz-PTT)

Water-Resources Investigations Report↗
USGS1961

Aqua de Ney, California, a spring of unique chemical character

The chemistry of water of Aqua de Ney, a cold spring of unusual character located in Siskiyou County, Calif., has been re-examined as part of a study of the relation of water chemistry to rock environment. The water has a pH of 11·6 and a silica content of 4000 parts per million (p.p.m.), the highest values known to occur in natural ground waters. The rocks exposed nearby consist of two volcanic sequences, one predominantly basaltic in composition, the other highly siliceous. Neither these rocks nor the sedimentary and igneous rocks presumed to underlie the area at depth seem to offer explanation of the unusual mineralization which includes 240 p.p.m. of boron, 1000 p.p.m. of sulphide (as H 2 S), and 148 p.p.m. of ammonia nitrogen (as NH 4 ) in a water that is predominantly sodium chloride and sodium carbonate in character. By analogy, it is assumed that water from Aqua de Ney is the product of an initial mixture of connate sea water with a calcium magnesium sulphate water. It is postulated that ion exchange has increased the content of sodium and reduced that of calcium and magnesium, and that sulphate reduction has brought about the high alkalinity, high pH, and high content of sulphide. The large silica value is explained as the result of solution of silica by water having the high pH observed.

California↗
USGS1961

Recent chemical analyses of waters from several closed-basin lakes and their tributaries in the western United States

Some of the classic closed-basin lakes of the western United States have been resampled, and the waters have been analyzed by modern wet-chemical methods. Included are waters from Borax and Little Borax lakes and Mono Lake in California; Big Soda, Pyramid, and Walker Lakes in Nevada; Abert Lake, Oregon; and Great Salt Lake, Utah. Tributary streams and springs have also been sampled and are reported upon. © 1961, The Geological Society of America, Inc.

Geological Society of America Bulletin↗