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At least 775 records · Page 43Linked to original sources
USGS1996

Uranium-series disequilibrium, sedimentation, diatom frustules, and paleoclimate change in Lake Baikal

The large volume of water, approximately one-fifth of the total surface fresh water on the planet, contained in Lake Baikal in southeastern Siberia is distinguished by having a relatively high concentration of uranium (ca. 2 n M ), and, together with the surface sediments, an unusually high 234 U 238 U alpha activity ratio of 1.95. About 80% of the input of uranium to the lake, with a 234 U 238 U ratio of 2.0, comes from the Selenga River. Profiles of uranium, as well as the extent of isotopic disequilibrium in a 9 m sediment core collected on Academic Ridge, generally show high values during interglacial periods corresponding to high diatom frustule numbers (DiFr) and biogenic silica (BSi) data that have been reported elsewhere. During glacial periods (low DiFr and BSi), uranium progeny ( 234 U and 230 Th) were in secular equilibrium with low concentrations of their parent 238 U. Radionuclide distributions were interpreted in terms of a quantitative model allowing for adsorption of riverine inputs of uranium onto two classes of sedimenting particles with differing 238 U 232 Th ratios and uranium progeny in secular equilibrium. If the 234 U 238 U activity ratio of adsorbed uranium has remained constant, mean sedimentation rates can be independently estimated as 3.6 ± 0.6 and 3.7 ± 0.9 cm · kyr −1 for the decay of 234 U and in-growth of 230 Th, respectively. These rates are consistent with a mean rate of 3.76 cm · kyr −1 , calculated by optimization of the correspondence between adsorbed 238 U and δ 18 O in dated oceanic sediments. The adsorbed uranium apparently tracks variable river flow during interglacials and is drastically reduced during periods of glaciation. Evidently, uranium has not been significantly redistributed within Baikal sediments over at least the past 250 kyr and is a unique, biologically non-essential, tracer for climate-sensitive processes, which provide their own internal geochronometers, potentially useful for ages up to 1 Myr BP.

Earth and Planetary Science Letters↗
USGS1980

Some factors controlling the concentration of uranium in the world ocean

Low-temperature alteration of the oceanic crust is a major sink for the U supplied to the oceans and may account for about 50% of the estimated present-day input of this element. Uranium uptake by organic-rich sediments and coexisting phosphorites on continental margins is also important and may remove in excess of 10% of the total supply. High-temperature alteration of oceanic basalts, metalliferous sediments, carbonate sediments, and sediments in anoxic basins deeper than 200 m play a relatively minor role in the removal of U. Each of these sinks is responsible for the uptake of less than 5% of the overall input.

Geochimica et Cosmochimica Acta↗
USGS1985

Geochemistry of great Salt Lake, Utah II: Pleistocene-Holocene evolution

Sedimentologic and biostratigraphic evidence is used to develop a geochemical model for Great Salt Lake, Utah, extending back some 30,000 yrs. B.P. Hydrologie conditions as defined by the water budget equation are characterized by a lake initially at a low, saline stage, rising by about 17,000 yrs. B.P. to fresh water basin-full conditions (Bonneville level) and then, after about 15,000 yrs. B.P., dropping rapidly to a saline stage again, as exemplified by the present situation. Inflow composition has changed through time in response to the hydrologie history. During fresh-water periods high discharge inflow is dominated by calcium bicarbonate-type river waters; during saline stages, low discharge, NaCl-rich hydrothermal springs are significant solute sources. This evolution in lake composition to NaCl domination is illustrated by the massive mirabilite deposition, free of halite, following the rapid drawdown until about 8,000 years ago, while historic droughts have yielded principally halite. Hydrologic history can be combined with inferred inflow composition to derive concentration curves with time for each major solute in the lake. Calcium concentrations before the drawdown were controlled by calcite solubility, and afterwards by aragonite. Significant amounts of solutes are removed from the lake by diffusion into the sediments. Na+, Cl- and SO42- are also involved in salt precipitation. By including pore fluid data, a surprisingly good fit has been obtained between solute input over the time period considered and the amounts actually found in lake brines, pore fluids, salt beds and sediments. Excess amounts are present for calcium, carbonate and silica, indicating detrital input.

Utah↗
USGS1987

Biogeochemical cycling in an organic-rich coastal marine basin. 7. Sulfur mass balance, oxygen uptake and sulfide retention

Sulfur and oxygen fluxes were quantified in the seasonally varying anoxic marine sedimentary system of Cape Lookout Bight, N.C., U.S.A. Over the three year study period, 1981–1983, the mean annual sulfate reduction rate was determined to be 18.2 ± 1.6 moles · m −2 · y −1 . This value, added to the estimate of the detrital sulfur input of 1.2 ± 4.4 gave a total sulfur input of 19.4 ± 4.7 moles · m −2 · y −1 . The sulfide flux to the sediment-water interface, measured in anaerobic benthic chambers was 4.6 ± 0.5 moles · m −2 · y −1 , and represented 37% of the annual oxygen uptake rate of 25.2 ± 2.8 moles · m −2 · y −1 . The sulfide burial rate, determined to be 15.5 ± 3.1 moles · m −2 · y −1 , was within 5% of the value predicted by summing the fluxes at the sediment-water interface. The C S "> CS weight ratio of sediment below the depth of diagenetic reaction was determined to be 2.75. The sulfide retention rate in these rapidly accumulating sediments (10 cm/yr) was 77 ± 19%. Comparison of this result with previous studies shows that rapid sediment accumulation and the lack of bioturbation control this unusually high degree of sulfide retention.

Geochimica et Cosmochimica Acta↗
USGS1987

Biogeochemical cycling in an organic-rich coastal marine basin. 8. A sulfur isotopic budget balanced by differential diffusion across the sediment-water interface

The sulfur isotopic composition of the sulfur fluxes occurring in the anoxic marine sediments of Cape Lookout Bight, N.C., U.S.A., was determined, and the result of isotopic mass balance was obtained via the differential diffusion model. Seasonal pore water sulfate δ 34 S measurements yielded a calculated sulfate input of 0.6%.. Sulfate transported into the sediments via diffusion appeared to be enriched in the lighter isotope because its concentration gradient was steeper, due to the increase in the measured isotopic composition of sulfate with depth. Similarly, the back diffusion of dissolved sulfide towards the sediment-water interface appeared enriched in the heavier isotope. The isotopic composition of this flux was calculated from measurements of the δ 34 S of dissolved sulfide and was determined to be 15.9%.. The isotopic composition of buried sulfide was determined to be −5.2%. and the detrital sulfur input was estimated to be −6.2%.. An isotope mass balance equation based upon the fluxes at the sediment-water interface successfully predicted the isotopic composition of the buried sulfur flux within 0.5%., thus confirming that isotopes diffuse in response to their individual concentration gradients.

Geochimica et Cosmochimica Acta↗
USGS1989

Organic markers as source discriminants and sediment transport indicators in south San Francisco Bay, California

Sediment samples from nearshore sites in south San Francisco Bay and from streams flowing into that section of the Bay have been characterized in terms of their content of biogenic and anthropogenic molecular marker compounds. The distributions, input sources, and applicability of these compounds in determining sediment movement are discussed. By means of inspection and multivariate analysis, the compounds were grouped according to probable input sources and the sampling stations according to the relative importance of source contributions. A suite of polycyclic aromatic hydrocarbons (PAHs) dominated by pyrene, fluoranthene and phenanthrene, typical of estuarine environments worldwide, and suites of mature sterane and hopane biomarkers were found to be most suitable as background markers for the Bay. A homologous series of long-chain n-aldehydes (C12-C32) with a strong even-over-odd carbon number dominance in the higher molecular weight range and the ubiquitous n-alkanes (n-C24-C34) with a strong odd-over-even carbon number dominance were utilized as terrigenous markers. Several ratios of these terrigenous and Bay markers were calculated for each station. These ratios and the statistical indicators from the multivariate analysis point toward a strong terrigenous signal in the terminus of South Bay and indicate net directional movement of recently introduced sediment where nontidal currents had been considered to be minimal or nonexistent and tidal currents had been assumed to be dominant.

California↗
USGS1982

Natural groundwater recharge in an upland area of central North Dakota, U.S.A.

The magnitude of groundwater recharge to coal aquifers in a 150-km 2 area in west-central North Dakota was determined using three separate approaches: (1) the net water level rise in water-table wells; (2) calculations of the fluid flux between nested piezometers, using the Darcy equation and measured values of hydraulic conductivity and vertical gradients; and (3) evaluation of the inputs to and outputs from the coal aquifer, using a steady-state control volume approach in which the aquifer was divided into semi-rectangular cells bounded by equipotential lines and flow lines. Measurements of potential gradients and hydraulic conductivity permitted indirect determination of all components of flow into and out of the cell except the recharge input, which was determined by difference. All methods yielded consistent results on the order of 0.04-0.01 m yr. −1 These values, which represent 2–9% of the annual precipitation, are consistent with results of other studies on recharge throughout the prairies of North America. Evaluation of site hydrology and stable-isotope data indicates that recharge is restricted in both time and place. Most recharge occurs in late spring and in the fall following heavy rainfall events. During these seasons the ground is not frozen and vegetation is not transpiring large amounts of water. Some recharge may occur during very heavy localized summer storms, but it is not considered volumetrically significant. Major permanent depressions on the site are a source of significant recharge. In addition, the extensive area of ephemeral standing water bodies that result from snowmelt can produce significant amounts of infiltration over the entire site.

central North Dakota↗
USGS1992

Residence times in river basins as determined by analysis of long-term tritium records

The US Geological Survey has maintained a network of stations to collect samples for the measurement of tritium concentrations in precipitation and streamflow since the early 1960s. Tritium data from outflow waters of river basins draining 4500–75000 km 2 are used to determine average residence times of water within the basins. The basins studied are the Colorado River above Cisco, Utah; the Kissimmee River above Lake Okeechobee, Florida; the Mississippi River above Anoka, Minnesota; the Neuse River above Streets Ferry Bridge near Vanceboro, North Carolina; the Potomac River above Point of Rocks, Maryland; the Sacramento River above Sacramento, California; the Susquehanna River above Harrisburg, Pennsylvania. The basins are modeled with the assumption that the outflow in the river comes from two sources—prompt (within-year) runoff from precipitation, and flow from the long-term reservoirs of the basin. Tritium concentration in the outflow water of the basin is dependent on three factors: (1) tritium concentration in runoff from the long-term reservoir, which depends on the residence time for the reservoir and historical tritium concentrations in precipitation; (2) tritium concentrations in precipitation (the within-year runoff component); (3) relative contributions of flow from the long-term and within-year components. Predicted tritium concentrations for the outflow water in the river basins were calculated for different residence times and for different relative contributions from the two reservoirs. A box model was used to calculate tritium concentrations in the long-term reservoir. Calculated values of outflow tritium concentrations for the basin were regressed against the measured data to obtain a slope as close as possible to 1. These regressions assumed an intercept of zero and were carried out for different values of residence time and reservoir contribution to maximize the fit of modeled versus actual data for all the above rivers. The final slopes of the fitted regression lines ranged from 0.95 to 1.01 (correlation coefficient > 0.96) for the basins studied. Values for the residence time of waters within the basins and average relative contributions of the within-year and long-term reservoirs to outflow were obtained. Values for river basin residence times ranged from 2 years for the Kissimmee River basin to 20 years for the Potomac River basin. The residence times indicate the time scale in which the basin responds to anthropogenic inputs. The modeled tritium concentrations for the basins also furnish input data for urban and agricultural settings where these river waters are used.

Journal of Hydrology↗
USGS2017

A reevaluation of the timing and causes of high lake phases in the Lake Michigan basin

Radiocarbon age control on the type Glenwood, Calumet, and Toleston shoreline features and on the abandoned Chicago outlet at the south end of the Lake Michigan basin provides a basis for reevaluating the timing and causes of high lake phases in the basin. Radiocarbon dates suggest that Glenwood-level (195 m) shoreline features formed between 14,100 and 12,700 yr B.P. (Glenwood I and II phases), Calumet-level (189 m) between 12,700 and 11,000 yr B.P. (Calumet I and II phases), and Toleston-level (184.5 m) between 5000 and 4000 yr B.P. (Nipissing phase), and that the Chicago outlet was cut to its present level (180 m) on bedrock while the lake was at the Glenwood level. This new chronology is inconsistent with J H. Bretz' hypothesis ((1951) American Journal of Science249, 401-429) that the progressive lowering of lake level resulted from episodic down-cutting of the outlet. Instead, the changes in lake level appear to relate to changes in the amount of glacial meltwater and precipitation entering the basin. We hypothesize that the Glenwood phases correspond with times when discharge from the Huron and Erie basins also entered the Lake Michigan basin (Lake Border and early Port Huron glacial phases), the Calumet phases with times when drainage was from the Lake Michigan basin alone (late Port Huron and Two Rivers glacial phases), and the Nipissing phase with the postglacial middle Holocene transgression caused by differential uplift in the basin. Estimates of relative net inputs to the basin during the Glenwood, Calumet, and Nipissing lake phases are consistent with estimates of relative outputs (i.e., discharge through the Chicago outlet); the magnitude of relative differences in inputs and outputs between phases is sufficient to explain lake-level changes of 4.5 to 6 m. ?? 1988.

Quaternary Research↗
USGS1990

Temporally intensive study of trace metals in sediments and bivalves from a large river-estuarine system: Suisun Bay/delta in San Francisco Bay

Distributions in time and space of Ag, Cd, Cr, Cu, Pb and Zn were determined in fine-grained sediments and in the filter-feeding bivalve Corbicula sp. of Suisun Bay/delta at the mouth of the Sacramento and San Joaquin Rivers in North San Francisco Bay. Samples were collected from seven stations at near-monthly intervals for 3 years. Aggregated data showed little chronic contamination with Ag, Zn and Pb in the river and estuary. Substantial chronic contamination with Cd, Cu and Cr in Suisun Bay/delta occurred, especially in Corbicula, compared with the lower San Joaquin River. Salinity appeared to have secondary effects, if any, on metal concentrations in sediments and metal bioavailability to bivalves. Space/time distributions of Cr were controlled by releases from a local industry. Analyses of time series suggested substantial inputs of Cu might originate from the Sacramento River during high inflows to the Bay, and Cd contamination had both riverine and local sources. Concentrations of metals in sediments correlated with concentrations in Corbicula only in annually or 3-year aggregated data. Condition index for Corbicula was reduced where metal contamination was most severe. The biological availability of Cu and Cd to benthos was greater in Suisun Bay than in many other estuaries. Thus small inputs into this system could have greater impacts than might occur elsewhere; and organisms were generally more sensitive indicators of enrichment than sediments in this system.

California↗
USGS1993

Factors affecting the geochemistry of a thick, subbituminous coal bed in the Powder River Basin: Volcanic, detrital, and peat-forming processes

The inorganic geochemistry and mineralogy of three cores from the Anderson-Dietz 1 coal bed, a 15.2-m-thick subbituminous coal bed in the Tongue River Member (Paleocene) of the Fort Union Formation, were examined (1) to determine if the cores could be correlated by geochemical composition alone over a total distance of 2 km and (2) to identify the major factors that influenced the geochemistry of the coal bed. Chemical data (46 elements on a coal-ash basis) for 81 coal samples and 4 carbonaceous rock samples, with most samples representing a 0.6-m-thick (2-ft) interval of core, were grouped into compositional clusters by means of cluster analysis. Seven major clusters were produced; two of these clusters can be used to correlate the coal bed throughout the study area. Data from scanning electron and optical microscope analyses indicate that several factors influenced the geochemistry of the Anderson-Dietz 1 coal bed. The majority of mineral grains in the coal bed are interpreted to be detrital (water borne); evidence includes the presence of rounded to subrounded quartz grains having two-phase, aqueous fluid inclusions characteristic of hydrothermal or low-to-moderate grade metamorphic quartz. These quartz grains are found throughout the coal bed but are most abundant in samples from the midpart of the bed, which was influenced by detrital input associated with the deposition of the clastic rocks that form the split between the Anderson and Dietz 1 coal beds 900 m to the east of the study area. In addition to the detrital minerals mentioned above, volcanic ash that was fluvially transported to the sites of peat deposition or possibly deposited as air-fall volcanic ash also affected the geochemistry of the coal bed. For example, crandallite(?), a mineral reported to form as an alteration product of volcanic ash, is found in seven samples from the coal bed. The presence of quartz grains containing silicate-melt inclusions in eight samples from the coal bed.provides further support for a volcanic ash component. Other factors that probably affected the geochemistry of the coal bed include (1) detrital input associated with the deposition of the roof rocks of the coal bed, (2) peat-forming processes and plant material, and (3) epigenetic ground-water flow.

Montana, Wyoming↗
USGS1987

An oxygen isotope model for interpreting carbonate diagenesis in nonmarine rocks (Green River Basin, Wyoming, USA)

A closed-system model is used for predicting the δ 18 O of formation waters in the deep portions of the northern Green River basin, Wyoming. δ 18 O calcite is calculated from this modeled water and compared with the δ 18 O of measured calcites to help interpret diagenesis in the basin. The modification of 18 O water , which may be caused by diagenetic reactions at elevated temperatures, is modeled from two mass-balance equations. Three diagenetic reactions used to modify δ 18 O water include: detrital limestoneå calcite cement; detrital quartz→ quartz cement; and detrital clay å authigenic illite/smectite. A weighted average δ 18 O water and δ 18 O of calcite, quartz and illite/smectite in equilibrium with this water are calculated at 500-m increments. For a closed-system model, calculated variables at one depth are used for input variables at the next depth. An open system can be crudely simulated by adjusting the input variables at each depth. Petrographic and hydrologic data suggest that throughout much of the basin an open hydrochemical system overlies a relatively closed system which is below 3000 m. From the surface to 3000 m deep, δ 18 O calcite measured in sandstone cements deviates from calculated 18 O calcite for the closed-system model. Below 3000 m, δ 18 O calcite of cement and bulk shale converge from opposite directions with increasing depth toward the calculated δ 18 O calcite . Adjusting the calculated δ 18 O calcite to match the measured δ 18 O calcite indicates that the deviation above 3000 m results from mixing of meteoric waters with 18 O-rich formation water.

Chemical Geology↗
USGS1989

Spatial and temporal variability in South San Francisco Bay (USA). I. Horizontal distributions of salinity, suspended sediments, and phytoplankton biomass and productivity

The horizontal pattern of mesoscale (1–4 km) variability in salinity was a poor predictor of mesoscale patterns in chlorophyll a , suspended particulate matter, and daily primary productivity in the South San Francisco Bay estuary during spring 1987. The tidally-averaged salinity distribution varied over weekly time scales, reflecting inputs of freshwater as well as transport processes. Spatial distributions of the other quantities also varied weekly, but not in concert with the salt field. Spatial patterns of phytoplankton biomass (chlorophyll a ) deviated from the salinity patterns, largely reflecting in situ production of phytoplankton biomass during the spring bloom. The tidally-averaged distribution of suspended particulate matter (SPM) was highly dynamic and responded to (1) the riverine input of suspended sediment during a freshet, (2) neap-spring variations in tidally-driven resuspension, and (3) resuspension in shallows following a period of wind mixing. Two-dimensional distributions of primary productivity P ′, derived from maps of biomass and turbidity (SPM), also varied weekly, but the spatial variability of P ′ was only about half that of SPM and chlorophyll. Since the magnitude and patterns of spatial variability differ among nonconservative quantities, at least in part because of local sources and sinks, we conclude that the spatial distributions of nonconservative quantities cannot be predicted from distributions of conservative tracers, such as salinity.

California↗
USGS1990

Radium and radon in Charlotte Harbor Estuary, Florida

Radium-226 and 222 Rn activities are greater in the estuarine waters of northern Charlotte Harbor and the lower tidal Peace and Myakka Rivers, Florida, than in either the freshwater reaches of the rivers or waters of the lower estuary and the Gulf of Mexico. The activity of 226 Ra in the tidal rivers increases with decreasing river inflow, with a maximum value of 548 dpm 1001 −1 measured in the tidal Myakka River. The source of the high activity of 226 Ra and 222 Rn is predominantly ground water inflow. Because of the large ground water input, the contribution of 226 Ra from suspended and bottom sediments is a smaller fraction of the total 226 Ra input than in many other estuaries. Although ground water 226 Ra activity in the area varies widely, we estimate that artesian ground water inflow to the tidal rivers is similar in magnitude to the flow of the rivers above the tidal reach during the dry season.

Florida↗
USGS1991

The interaction between biology and the management of aquatic macrophytes

‘Management’ refers to controlling nuisance aquatic species and to restoring or restructing aquatic plant communities. Producing stable, diverse, aquatic plant communities containing a high percentage of desirable species is a primary management goal. There are a variety of techniques including harvesting, herbicides, water-level fluctuation, sediment alteration, nutrient limitation, light alteration, and biological controls which can be used for managing macrophytes. These techniques are briefly reviewed along with discussions of biological considerations important to the efficacy of the technique and the environmental impacts of the technique. There is a growing interest in restoring and restructing aquatic plant communities. Techniques for community restoration are discussed as are emerging management technologies using growth regulators and bioengineering. New management technologies will probably be limited by costs and environmental impacts. In the near future, better macrophyte management will come through better planning and more effective use of present technology. The challenge is to make current planning and management techniques more effective through increased biological inputs. The potential for biological input ranges from subcellular biology to species biology, to community and ecosystem biology. Some information needs are identified.

Aquatic Botany↗
USGS1990

Estimates of ion sources in deciduous and coniferous throughfall

Estimates of external and internal sources of ions in net througfall deposition were derived for a deciduous and coniferous canopy by use of multiple regression. The external source component appears to be dominated by dry deposition of Ca 2+ , SO 2 and NO 3 − during dormant and growing seasons for the two canopy types. Increases in the leaching rates of K + and Mg 2+ during the growing season reflect the presence of leaves in the deciduous canopy and increased physiological activity in both canopies. Internal leaching rates for SO 4 2− doubled during the growing season presumably caused by increased physiological activity and uptake of SO 2 through stomates. Net deposition of SO 4 2− in throughfall during the growing season appears highly dependent on stomatal uptake of SO 2 . Estimates of SO 2 deposition velocities were 0.06 cm s −1 and 0.13 cm s −1 for the deciduous and coniferous canopies, respectively, during the dormant seasons, and 0.30 cm s −1 and 0.43 cm s −1 for the deciduous and coniferous canopies, respectively, during the growing season. For the ions of major interest with respect to ecosystem effects, namely H + , NO 3 − and SO 4 2− , precipitation inputs generally outweighed estimates of dry deposition input. However, net throughfall deposition of NO 3 − and SO 4 2− accounted for 20–47 and 34–50 per cent, respectively, of total deposition of those ions. Error estimates of ion sources were at least 50–100 per cent and the method is subject to several assumptions and limitations.

Virginia↗
USGS1994

Particulate carbonate matter in snow from selected sites in the south-central Rocky Mountains

Trends in snow acidity reflect the balance between strong acid inputs and reactions with neutralizing materials. Carbonate dust can be an important contributor of buffering capacity to snow however, its concentration in snow is difficult to quantify because it dissolves rapidly in snowmelt. In snow with neutral or acidic pH, most calcite would dissolve during sample melting if snow samples were processed using standard techniques. Here a method is described for separating particulate carbonate matter from snow. Snow samples were melted in solutions close to saturation with calcite, decreasing the dissolution rate by a factor of 100-200 compared with natural melting of snow. Particulate matter larger than 0.45 ??m in diameter was then filtered from solution and analysed for carbonate content. Particulate carbonate matter concentrations are reported for 25 sites in the south-central Rocky Mountains. Results are compared with Ca2+ and H+ concentrations and regional trends are evaluated. In Colorado, mean particulate carbonate in snow was 43 ??g kg-1 at sampling sites in the southern mountains and only 4 ??g kg-1 at sites in the northern mountains. The higher calcite concentrations in the south probably are related to the proximity of sampling sites to major outcrops of limestone. Particulate carbonate at sampling sites in Utah and Wyoming ranged from 3-35 ??g kg-1. The levels of particulate calcite measured in snow samples are sufficient to neutralize an average of 0.4 ??eq H+ kg-1 snow. Strong acid anion concentrations in samples from east of Craig, Colorado, were 30-50% higher than in samples from the Colorado Front Range, but H+ concentrations were 400-600% higher east of Craig. Relatively low Ca2+ concentrations in the samples from east of Craig indicate that the difference in snow acidity was due mostly to lower concentrations of neutralizing materials.Trends in snow acidity reflect the balance between strong acid inputs and reactions with neutralizing materials. Carbonate dust can be an important contributor of buffering capacity to snow; however, its concentration in snow is difficult to quantify because it dissolves rapidly in snowmelt. In snow with neutral or acidic pH, most calcite would dissolve during sample melting if snow samples were processed using standard techniques. Here a method is described for separating particulate carbonate matter from snow. Snow samples were melted in solutions close to saturation with calcite, decreasing the dissolution rate by a factor of 100-200 compared with natural melting of snow. Particulate matter larger than .45 micrometers in diameter was then filtered from solution and analyzed for carbonate content.

Atmospheric Environment↗
USGS1977

Suspended particle transport and circulation in San Francisco Bay - an overview

Differences in the relative magnitude and timing of wind stress and river inflow in the northern and southern reaches of San Francisco Bay create different sedimentary conditions. The northern reach is a partially to well mixed estuary receiving most of the total annual fresh-water input (840 m 3 sec −1 ) and suspended sediment input (4 × 10 6 metric tons) into the bay; more than 80% of the sediment is received during winter. Density-driven nontidal estuarine circulation (~5 cm sec −1 ) maintains a turbidity maximum which changes seasonally in particle concentration (40 to 80 mg litre −1 ). Strong tidal currents (≤225 cm sec −1 ) and wind-generated waves resuspend sediment from the shallow bay floor: some of the riverborne sediment deposited during winter is resuspended during summer and transported landward to the turbidity maximum. Long-term sediment data (extrapolated from bathymetrie charts) indicate that the northern reach is an effective sediment trap. In contrast, long-term sediment data suggest that the southern reach is experiencing net erosion. The southern reach receives little river inflow or riverborne suspended sediment, and the average nontidal circulation is weak (≤2 cm sec −1 ). The principal source of suspended sediment (25 mg litre −1 ) in the southern reach is the shallow bay floor (average depth 6 m).

Book chapter↗