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At least 703 records · Page 39Linked to original sources
USGS1979

Effects of converting sagebrush cover to grass on the hydrology of small watersheds at Boco Mountain, Colorado

Changes in runoff and sediment yield caused by changing sagebrush cover to grass cover were studied at four small watersheds in western Colorado during a 9-year period, from 1965 to 1978. Measurements of runoff and sediment yield from the four watersheds were made for 8 years, at which time two watersheds were plowed and seeded to beardless bluebunch wheatgrass. The same measurements were then continued for an additional 6 years. Measurements indicated that conversion to grass caused a reduction in runoff from summer rainstorms of about 75 percent. Runoff from spring snowmelt increased about 12 percent, and annual runoff from treated watersheds decreased about 20 percent when compared to control watersheds. Sediment yield from the seeded watersheds was reduced by about 80 percent; most of this reduction is related to the decrease in runoff from summer rainstorms. The size of barren interspaces between plants was reduced on the converted water- sheds to about 30 percent of those on the untreated watersheds. Linear regression analysis indicates that a reduction of 38 percent in the amount of bare soil resulting from planting grass would result in a decrease of 73 percent in sediment concentration.

Colorado↗
USGS1961

Progress report on wells penetrating artesian aquifers in South Dakota

Artesian aquifers underlie most of South Dakota and large areas in adjacent States. About 15,000 wells have been completed since 1881 in these aquifers within South Dakota. Many wells that originally flowed have ceased to flow and have been abandoned, and others have been equipped with pumps. Many thousands, however, continue to flow. This report presents data collected through June 1958 and includes records of 1,045 flowing and nonflowing artesian wells Sufficient information is not available at present (1958) to permit a detailed description of the geologic and hydrologic properties of artesian aquifers or their correlation in South Dakota. The description of the various aquifers given in this report is, therefore, necessarily a general one.

South Dakota↗
USGS1961

Geologic control of mineral composition of stream waters of the eastern slope of the Southern Coast Ranges, California

Chemical analyses of waters of streams that drain the semiarid eastern slope of the southern Coast Ranges in California demonstrate that differences in the anion composition, especially in the ratio of bicarbonate to sulfate, are related chiefly to the lithologic character of the rocks exposed in the tributary drainage area. Where more than hall the drainage area of a typical eastern-slope stream is underlain by clastic marine sedimentary rocks of Jurassic and Cretaceous age, bicarbonate generally predominates over sulfate; the ratio of bicarbonate to sullate, both expressed in equivalents per million, in samples of the streams at low-flow stage ranges from 0.8 to 6. Conversely, where more than hall the drainage area is underlain by marine and continental deposits of Tertiary age and continental deposits of Quaternary age, sulfate predominates over bicarbonate, and the ratio of bicarbonate to sulfate in samples taken during the low-flow stage ranges from 0.02 to 0.7. Organic siliceous marine shale of Tertiary age deposited in a reducing environment is probably the primary source of sullate in the region. Secondary deposits of sulfate minerals, chiefly gypsum, which are abundant in the continental deposits of late Tertiary and Quaternary age, also contribute sullate to the stream waters.

Water Supply Paper↗
USGS1964

Field measurement of alkalinity and pH

The behavior of electrometric pH equipment under field conditions departs from the behavior predicted from Nernst's law. The response is a linear function of pH, and hence measured pH values may be corrected to true pH if the instrument is calibrated with two reference solutions for each measurement. Alkalinity titrations may also be made in terms of true pH. Standard methods, such as colorimetric titrations, were rejected as unreliable or too cumbersome for rapid field use. The true pH of the end point of the alkalinity titration as a function of temperature, ionic strength, and total alkalinity has been calculated. Total alkalinity in potable waters is the most important factor influencing the end point pH, which varies from 5.38 (0 ? C, 5 ppm (parts per million) HC0a-) to 4.32 (300 ppm HC0a-,35 ? C), for the ranges of variables considered. With proper precautions, the pH may be determined to =i:0.02 pH and the alkalinity to =i:0.6 ppm HCO3- for many naturally occurring bodies of fresh water.

Water Supply Paper↗
USGS1967

Annual variations in chemical composition of atmospheric precipitation, eastern North Carolina and southeastern Virginia

A 2-year study of precipitation composition over eastern North Carolina and southeastern Virginia has been completed. Chemical analyses were made of the major ions in monthly rainfall samples from each of 12 sampling locations. Areal and seasonal distributions were determined for chloride, calcium, magnesium, sodium, potassium, sulfate, and nitrate. Annual changes in loads and in geographical distribution of sulfate and of nitrate are small. Yearly rainfall sulfate loads amount to approximately 7 tons per square mile, whereas deposition of nitrate is about 2 tons per square mile per year in the interior of the network and less near the coast. Areal patterns of chloride content are consistent with the assumption that the ocean is the only major source of rainfall chloride in the area. Chloride loads were 2.1 and 1.8 tons per square mile per year; the difference can be attributed to meteorological conditions. Cation concentrations in network precipitation appear to depend on localized sources, probably soil dust. Annual loads of the major cations are approximately 2 tons per square mile of calcium, 1.8 tons per square mile of sodium, 0.5 ton per square mile of magnesium, and 0.3 ton per square mile of potassium; considerable year-to-year differences were noted in these values. Bicarbonate and hydrogen ion in network rainfall are closely related to the relative concentrations of sulfate and calcium. Apparently, reaction of an acidic sulfur-containing aerosol with an alkaline calcium source is one of the principal controls on precipitation alkalinity and pH. Ions in precipitation contribute substantially to the quality of surface water in the network area. Comparisons between precipitation input and stream export of ions for four North Carolina rivers show that rainfall sulfate is equal to sulfate discharged, whereas nitrate in rain slightly exceeds stream nitrate. Contributions of cations to the streams by way of precipitation range from about 20 percent for potassium to almost 50 percent for calcium. Chloride deposited by precipitation amounts to about one-fourth of the stream load. Additions of manufactured salt may account for much of the remainder of the surface-water load.

Water Supply Paper↗
USGS1969

Occurrence and distribution of molybdenum in the surface water of Colorado

Molybdenum was detected in 89 percent of the samples collected from all the principal Colorado streams and their chief tributaries and from a few reservoirs and lakes. Amounts detected ranged from 1 to 3,800 micrograms per liter. The greatest amounts of molybdenum detected were in samples from the Colorado River at and below Kremmling, the Dillon Reservoir, the Blue River below Dillon Dam, the Eagle River, and Tenmile Creek.

Colorado↗
USGS1980

The effect of dissolution of volcanic glass on the water chemistry in a tuffaceous aquifer, Rainier Mesa, Nevada

Geochemistry of ground water associated with the Tertiary tuffs within Rainier Mesa, southern Nevada, was investigated to determine the relative importance of glass dissolution in controlling water chemistry. Water samples were obtained both from interstitial pores in core sections and from free-flowing fractures. Cation com- positions showed that calcium and magnesium decreased as a function of depth in the mesa, as sodium increased. The maximum effect occurs within alteration zones containing clinoptilolite and montmorillonite, suggesting these minerals effectively remove bivalent cations from the system. Comparisons are made between compositions of ground waters found within Rainier Mesa that apparently have not reacted with secondary minerals and compositions of waters produced by experimental dissolution of vitric and crystalline tufts which comprise the principal aquifers in the area. The two tuff phases have the same bulk chemistry but produce aqueous solutions of different chemistry. Rapid parabolic dissolution of sodium and silica from, and the retention of, potassium within the vitric phase verify previous predictions concerning water compositions associated with vitric volcanic rocks. Parabolic dissolution of the crystalline phase results in solutions high in calcium and magnesium and low in silica. Extrapolation of the parabolic dissolution mechanism for the vitric tuff to long times successfully reproduces, at com- parable pH, cation ratios existing in Rainier Mesa ground water. Comparison of mass- transfer rates of the vitric and crystalline tuffs indicates that the apparent higher glass-surface to aqueous-volume ratio associated with the vitric rocks may account for dominance of the glass reaction.

Water Supply Paper↗
USGS1960

Borehole geophysical methods for analyzing specific capacity of multiaquifer wells : ground-water hydraulics

Conventional well-logging techniques, combined with measurements of flow velocity in the borehole, can provide information on the discharge-drawdown characteriBtic8 of the several aquifers penetrated by a well. The information is most conveniently presented in a graph showing aquifer discharges as functions of the water level in the well at a particular time. To determine the discharge-drawdown characteristics, a well is pumped at a steady rate for a certain length of time. While the well is being pumped, measurements are made of drawdown and of the discharge rates of the individual aquifers within the well. Discharge rates and drawdowns ,are usually recorded as functions of time, and their values for any given time during the test are obtained by interpolation. The procedure is repeated for several different rates of total well discharge. The well may be allowed to recover after each step, or discharge may be changed from one rate to another, and changes in discharge and drawdown may be measured by extrapolation. The flow measurements within the well may be made by use of a subsurface flowmeter or by one of several techniques involving the injection of electrolytic or radioactive tracers. The method was tested on a well in Mercer County, Pa., and provided much useful information on aquifer yields, 'thieving,' and hydrostatic heads of the individual zones.

Water Supply Paper↗