Search USGSSearch

Geology topics

B.F. Jones

Publications and source records attributed to B.F. Jones.

28 records · Page 2Linked to original sources

Mineralogy of fine-grained alluvium from borehole U11g, expl. 1, northern Frenchman Flat area, Nevada Test Site

The mineralogy of matrix fines in alluvium from borehole Ullg, expl. 1, north of Frenchman Flat, Nevada Test Site, has been examined for evidence of past variations in water table elevation. Although greater abundance of zeolite and slightly more expanded basal spacings in smectite clays suggest effects of increased hydration of material up to 50 m above the present water table, these differences might also be related to provenance of environment of deposition. The relative uniformity of clay hydration properties in the 50 meters above the current water table suggest long-term stability near the present level. (USGS)

Open-File Report

Geochemical evolution of brines in the Salar of Uyuni, Bolivia.

Recent analyses of brines from the Salars of Uyuni and Coipasa have been compared with published data for Lakes Titicaca and Poopo to evaluate solute compositional trends in these remnants of two large Pleistocene lakes once connected by overflow from the N to the S of the Bolivian Altiplano. From Titicaca to Poopo the water shows an increase in Cl and N somewhat greater than the total solutes. Ca and SO4 increase to a lesser extent than total dissolved solids, and carbonate species are relatively constant. Between Poopo and Coipasa proportions of Ca, SO4 and CO3 continue to decrease. At Coipasa and Uyuni, the great salars frequently evaporate to halite saturation. Halite crystallization is accompanied by an increased K, Mg and SO4 in residual brines. - from Authors

Chemical Geology

Ion association in natural brines

Natural brines, both surface and subsurface, are highly associated aqueous solutions. Ion complexes in brines may be ion pairs in which the cation remains fully hydrated and the bond between the ions is essentially electrostatic, or coordination complexes in which one or more of the hydration water molecules are replaced by covalent bonds to the anion. Except for Cl − , the major simple ions in natural brines form ion pairs; trace and minor metals in brines form mainly coordination complexes. Limitations of the Debye-Hückel relations for activity coefficients and lack of data on definition and stability of all associated species in concentrated solutions tend to produce underestimates of the degree of ion association, except where the brines contain a very high proportion of Cl − . Data and calculations on closed basin brines of highly varied composition have been coupled with electrode measurements of single-ion activities in an attempt to quantify the degree of ion association. Such data emphasize the role of magnesium complexes. Trace metal contents of closed basin brines are related to complexes formed with major anions. Alkaline sulfo- or chlorocarbonate brines (western Great Basin) carry significant trace metal contents apparently as hydroxides or hydroxy polyions. Neutral high chloride brines (Bonneville Basin) are generally deficient in trace metals. With a knowledge of the thermodynamic properties of a natural water, many possible reactions with other phases (solids, gases, other liquids) may be predicted. A knowledge of these reactions is particularly important in the study of natural brines which may be saturated with many solid phases (silicates, carbonates, sulfates, etc.), which may have a high pH and bring about dissolution of other phases (silica, amphoteric hydroxides, CO 2 , etc.), and which because of their high density may form relatively stable interfaces with dilute waters.

Chemical Geology

Interstitial brines in playa sediments

Study of several closed drainages in the Great Basin has shown that the interstitial solutions of shallow, fine-grained playa deposits store a large quantity of dissolved solids and are often more concentrated than associated lakes and ponds, except in peripheral zones of stream or ground-water inflow. These interstitial fluids, when compared with local runoff, impoundments, or spring waters, commonly have a distinctive ionic composition which sometimes cannot be explained by either simple mixing of surface and subsurface inflow or by evaporative concentration. At Abert Lake, Oregon, the interstitial solute concentrations increased with depth to values as much as five times greater than the lake, except where springs indicate significant ground-water input. Where Na + , Cl, and CO 2 species constitute more than 90% of the solutes, Na + Cl − "> Na+Cl− ratios in the lake water are lower than in interstitial solutions of bottom cores and higher than in playa fluids. At the same time, Na + K + "> Na+K+ ratios are highest in the fluids of lake bottom muds and lowest in playa interstitials. In deeper playa profiles, interstitial Na + Cl − "> Na+Cl− tended to decrease with depth (5 ft. maximum). In the Abert Lake area, as in other parts of the western Great Basin, Na + Cl − "> Na+Cl− ratios are indicative of total CO 2 in solution and the effects of organic decay in surficial sediments. These ratios, coupled with data on silica and bulk density, show that higher P CO2 accompanying decay promotes silicate dissolution and hydrogen ion exchange, stripping alkalis from sediment which had preferentially adsorbed K + when entering the lake. On subsequent loss of pore fluid in the playa regime, silica initially released to solution in the lake environment is readsorbed on dissolution products.

Oregon

Isotope studies of dolomite formation under sedimentary conditions

Measurements of stable isotope abundances of the carbonate portion of the sediment in Deep Springs Lake, California, indicate the presence of at least three phases: a magnesian calcite, a primary sedimentary dolomite, and a detrital dolomite. The former two have isotopic compositions consistent with precipitation at isotopic equilibrium from waters of the lake area. The measured isotopic fractionation factor between sedimentary dolomite and its interstitial water is 1.0351, which is outside the range possible for calcite-water. This indicates that the dolomite has formed by direct crystallization from solution and not from a caloite precursor without further isotope exchange. Isotopic and X-ray evidence does not support the contention of Peterson et al . (1966) that Deep Springs Lake dolomite crystals grow by means of a calcite-like surface layer.

Geochimica et Cosmochimica Acta

Gels composed of sodium-aluminum silicate, Lake Magadi, Kenya

Sodium-aluminum silicate gels are found in surficial deposits as thick as 5 centimeters in the Magadi area of Kenya. Chemical data indicate they are formed by the interaction of hot alkaline springwaters (67° to 82°C; p H, about 9) with alkali trachyte flows and their detritus, rather than by direct precipitation. In the process, Na 2 O is added from and silica is released to the saline waters of the springs. Algal mats protect the gels from erosion and act as thermal insulators. The gels are probably yearly accumulates that are washed into the lakes during floods. Crystallization of these gels in the laboratory yields analcite; this fact suggests that some analcite beds in lacustrine deposits may have formed from gels. Textural evidence indicates that cherts of rocks of the Pleistocene chert series in the Magadi area may have formed from soft sodium silicate gels. Similar gels may have acted as substrates for the accumulation and preservation of prebiological organic matter during the Precambrian.

Lake Magadi

Silica in alkaline brines

Analysis of sodium carbonate-bicarbonate brines from closed basins in volcanic terranes of Oregon and Kenya reveals silica contents of up to 2700 parts per million at p H's higher than 10. These high concentrations of SiO 2 can be attributed to reaction of waters with silicates, and subsequent evaporative concentration accompanied by a rise in p H. Supersaturation with respect to amorphous silica may occur and persist for brines that are out of contact with silicate muds and undersaturated with respect to trona; correlation of SiO 2 with concentration of Na and total CO 2 support this interpretation. Addition of more-dilute waters to alkaline brines may lower the p H and cause inorganic precipitation of substantial amounts of silica.

Science

Calcium and bromide contents of natural waters

The linear relation observed in a log Ca ++ versus log Br - plot for subsurface Cl - waters is attributed to ultrafiltration by shale of sea water and fresh water that have passed through sedimentary rocks since their formation. Reactions between these solutions and sedimentary minerals, particularly dolomitization, must have contributed additional Ca ++ to solution.

Science

Glass electrode determination of sodium in closed basin waters

Because of its direct relation to total dissolved solids content, sodium concentration is the most useful single hydrochemical parameter of closed basin waters in the western United States. Therefore, it is advantageous to have a rapid method for sodium determination which could be readily adapted to field use. Accordingly, thirty waters of highly variable concentration and anionic composition from the western Great Basin have been analyzed with a sodium-sensitive glass electrode. Na + values ranged from 10 to 130,000 ppm in waters containing from 102 to 401,000 ppm total dissolved solids. The electrode values were compared with conventional sodium determinations; results differed by as much as 11 per cent, although over two-thirds were within 5 per cent. No significant relation was found between the glass electrode and conventional method differences and the total dissolved solids or sodium concentration. The comparative accuracy of electrode and conventional procedures was checked, employing solutions of known sodium concentration. It was concluded that for the analysis of sodium in natural waters the glass electrode method offers results comparable in accuracy to those obtained by conventional methods, but with increased simplicity, and therefore the possibility of rapid, accurate field measurements.

Geochimica et Cosmochimica Acta

Chemical quality of surface waters and sedimentation in the Saline River basin, Kansas

This report gives the results of an investigation of the sediment and dissolved minerals that are transported by the Saline River and its tributaries. The Saline River basin is in western and central Kansas; it is long and narrow and covers 3,420 square miles of rolling plains, which is broken in some places by escarpments and small areas of badlands. In the western part the uppermost bedrock consists predominantly of calcareous elastic sedimentary rocks of continental origin of Pliocene age and in most places is covered by eolian deposits of Pleistocene and Recent age. In the central part the ex posed bedrock consists predominantly of calcareous marine sedimentary rocks of Late Cretaceous age. In the eastern part the exposed bedrock consists mainly of noncalcareous continental and littoral elastic sedimentary rocks of Early Cretaceous and Permian age. Fluvial deposits are in the valleys, and eolian materials are present over much of the uplands. Average precipitation increases rather uniformly from about 18 inches per year in the west to almost 28 inches per year in the east. Runoff is not affected by irrigation nor regulated by large structures, but it is closely related to precipitation. Average runoff increases from less than 0.2 inch per year in the west to more than 1.5 inches per year in the east. Aquifers of the flood-plain and terrace deposits and of the Cretaceous Dakota Sandstone are the major sources of ground-water accretion to the streams. In the upper reaches of the Saline River, the water is only slightly mineralized; during the period of record the specific conductance near Wakeeney never exceeded 750 micromhos per centimeter. In the lower reaches, however, the water is slightly mineralized during periods of high flow and is highly mineralized during periods of low flow; the specific conductance near Russell exceeded 1,500 micromhos per centimeter more than 80 percent of the time. Near Russell, near Wilson, and at Tescott the water is of the calcium bicarbonate type when the specific conductance is less than about 1,000 micromhos per centimeter, but it is of the sodium chloride type when the specific conductance is more than about 1,500 micromhos per centimeter. The water is off the calcium bicarbonate, sodium bicarbonate, or sodium chloride type when the conductance is between 1,000 and 1,500 micromhos per centimeter. Most of the increase in mineralization of the water is caused by inflow of highly mineralized ground water. The ground-water inflow was estimated to be 22 percent of the total streamflow at Tescott in 1948 and 60 percent in 1952. Mineralization increases and water quality deteriorates progressively downstream along nearly the entire Saline River, especially in the part of the area directly underlain by the Dakota Sandstone between the vicinities of Fairport and Wilson: sodium and chloride are the principal constituents of water contributed by the Dakota. The total percentage of the salt in the Saline River that comes from oil-field brines is considered to be small. The water in the upper Saline River is of good quality for domestic use except that it is hard; the water in the lower Saline River is of poor quality for domestic use because most of the time it is highly mineralized, is hard, and contains high concentrations of chloride and sulfate. In the upper reaches of the river, the water is of good quality for irrigation. In the lower reaches, if the water were impounded in a reservoir, it would be of good quality for irrigation during years of high flow and of very poor quality during years of low flow. The water in the lower reaches is of poor quality for industrial use because it is highly mineralized most of the tinge. Relations of suspended-sediment discharge to water discharge were used with the long-term streamflow duration curves to compute the long-term aver age suspended-sediment discharges and concentrations at five indications. Sediment discharge is closely related to runoff. S

Water Supply Paper