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Roger Fujii

Publications and source records attributed to Roger Fujii.

At least 19 recordsLinked to original sources
USGS2018

Potential for negative emissions of greenhouse gases (CO2, CH4 and N2O) through coastal peatland re-establishment: Novel insights from high frequency flux data at meter and kilometer scales

High productivity temperate wetlands that accrete peat via belowground biomass (peatlands) may be managed for climate mitigation benefits due to their global distribution and notably negative emissions of atmospheric carbon dioxide (CO 2 ) through rapid storage of carbon (C) in anoxic soils. Net emissions of additional greenhouse gases (GHG)—methane (CH 4 ) and nitrous oxide (N 2 O)—are more difficult to predict and monitor due to fine-scale temporal and spatial variability, but can potentially reverse the climate mitigation benefits resulting from CO 2 uptake. To support management decisions and modeling, we collected continuous 96 hour high frequency GHG flux data for CO 2 , CH 4 and N 2 O at multiple scales—static chambers (1 Hz) and eddy covariance (10 Hz)—during peak productivity in a well-studied, impounded coastal peatland in California's Sacramento Delta with high annual rates of C fluxes, sequestering 2065 ± 150 g CO 2 m −2 y −1 and emitting 64.5 ± 2.4 g CH 4 m −2 y −1 . Chambers ( n = 6) showed strong spatial variability along a hydrologic gradient from inlet to interior plots. Daily (24 hour) net CO 2 uptake (NEE) was highest near inlet locations and fell dramatically along the flowpath (−25 to −3.8 to +2.64 g CO 2 m −2 d −1 ). In contrast, daily net CH 4 flux increased along the flowpath (0.39 to 0.62 to 0.88 g CH 4 m −2 d −1 ), such that sites of high daily CO 2 uptake were sites of low CH 4 emission. Distributed, continuous chamber data exposed five novel insights, and at least two important datagaps for wetland GHG management, including: (1) increasing dominance of CH 4 ebullition fluxes (15%–32% of total) along the flowpath and (2) net negative N 2 O flux across all sites as measured during a 4 day period of peak biomass (−1.7 mg N 2 O m −2 d −1 ; 0.51 g CO 2 eq m −2 d −1 ). The net negative emissions of re-established peat-accreting wetlands are notably high, but may be poorly estimated by models that do not consider within-wetland spatial variability due to water flowpaths.

California↗
USGS2016

Variation of energy and carbon fluxes from a restored temperate freshwater wetland and implications for carbon market verification protocols

Temperate freshwater wetlands are among the most productive terrestrial ecosystems, stimulating interest in using restored wetlands as biological carbon sequestration projects for greenhouse gas reduction programs. In this study, we used the eddy covariance technique to measure surface energy carbon fluxes from a constructed, impounded freshwater wetland during two annual periods that were 8 years apart: 2002–2003 and 2010–2011. During 2010–2011, we measured methane (CH 4 ) fluxes to quantify the annual atmospheric carbon mass balance and its concomitant influence on global warming potential (GWP). Peak growing season fluxes of latent heat and carbon dioxide (CO 2 ) were greater in 2002–2003 compared to 2010–2011. In 2002, the daily net ecosystem exchange reached as low as −10.6 g C m −2  d −1 , which was greater than 3 times the magnitude observed in 2010 (−2.9 g C m −2  d −1 ). CH 4 fluxes during 2010–2011 were positive throughout the year and followed a strong seasonal pattern, ranging from 38.1 mg C m −2  d −1 in the winter to 375.9 mg C m −2  d −1 during the summer. The results of this study suggest that the wetland had reduced gross ecosystem productivity in 2010–2011, likely due to the increase in dead plant biomass (standing litter) that inhibited the generation of new vegetation growth. In 2010–2011, there was a net positive GWP (675.3 g C m −2  yr −1 ), and when these values are evaluated as a sustained flux, the wetland will not reach radiative balance even after 500 years.

California↗
USGS2012

Mercury dynamics in a San Francisco estuary tidal wetland: assessing dynamics using in situ measurements

We used high-resolution in situ measurements of turbidity and fluorescent dissolved organic matter (FDOM) to quantitatively estimate the tidally driven exchange of mercury (Hg) between the waters of the San Francisco estuary and Browns Island, a tidal wetland. Turbidity and FDOM—representative of particle-associated and filter-passing Hg, respectively—together predicted 94 % of the observed variability in measured total mercury concentration in unfiltered water samples (UTHg) collected during a single tidal cycle in spring, fall, and winter, 2005–2006. Continuous in situ turbidity and FDOM data spanning at least a full spring-neap period were used to generate UTHg concentration time series using this relationship, and then combined with water discharge measurements to calculate Hg fluxes in each season. Wetlands are generally considered to be sinks for sediment and associated mercury. However, during the three periods of monitoring, Browns Island wetland did not appreciably accumulate Hg. Instead, gradual tidally driven export of UTHg from the wetland offset the large episodic on-island fluxes associated with high wind events. Exports were highest during large spring tides, when ebbing waters relatively enriched in FDOM, dissolved organic carbon (DOC), and filter-passing mercury drained from the marsh into the open waters of the estuary. On-island flux of UTHg, which was largely particle-associated, was highest during strong winds coincident with flood tides. Our results demonstrate that processes driving UTHg fluxes in tidal wetlands encompass both the dissolved and particulate phases and multiple timescales, necessitating longer term monitoring to adequately quantify fluxes.

California↗
USGS2011

Re-establishing marshes can return carbon sink functions to a current carbon source in the Sacramento-San Joaquin Delta of California, USA

The Sacramento-San Joaquin Delta in California was an historic, vast inland freshwater wetland, where organic soils almost 20 meters deep formed over the last several millennia as the land surface elevation of marshes kept pace with sea level rise. A system of levees and pumps were installed in the late 1800s and early 1900s to drain the land for agricultural use. Since then, land surface has subsided more than 7 meters below sea level in some areas as organic soils have been lost to aerobic decomposition. As land surface elevations decrease, costs for levee maintenance and repair increase, as do the risks of flooding. Wetland restoration can be a way to mitigate subsidence by re-creating the environment in which the organic soils developed. A preliminary study of the effect of hydrologic regime on carbon cycling conducted on Twitchell Island during the mid-1990s showed that continuous, shallow flooding allowing for the growth of emergent marsh vegetation re-created a wetland environment where carbon preservation occurred. Under these conditions annual plant biomass carbon inputs were high, and microbial decomposition was reduced. Based on this preliminary study, the U.S. Geological Survey re-established permanently flooded wetlands in fall 1997, with shallow water depths of 25 and 55 centimeters, to investigate the potential to reverse subsidence of delta islands by preserving and accumulating organic substrates over time. Ten years after flooding, elevation gains from organic matter accumulation in areas of emergent marsh vegetation ranged from almost 30 to 60 centimeters, with average annual carbon storage rates approximating 1 kg/m2, while areas without emergent vegetation cover showed no significant change in elevation. Differences in accretion rates within areas of emergent marsh vegetation appeared to result from temporal and spatial variability in hydrologic factors and decomposition rates in the wetlands rather than variability in primary production. Decomposition rates were related to differences in hydrologic conditions, including water temperature, pH, dissolved oxygen concentration, and availability of alternate electron acceptors. The study showed that marsh re-establishment with permanent, low energy, shallow flooding can limit oxidation of organic soils, thus, effectively turning subsiding land from atmospheric carbon sources to carbon sinks, and at the same time reducing flood vulnerability.

California↗
USGS2010

Processes affecting the distribution of selenium in shallow groundwater of agricultural areas, western San Joaquin Valley, California

A study was undertaken to evaluate the processes affecting the chemistry of shallow groundwater associated with agricultural drainage systems in the western San Joaquin Valley, California. The study was prompted by a need for an understanding of selenium mobility in areas having high selenium concentrations in shallow groundwater. Groundwater samples were collected along transects in three artificially drained fields where the age of the drainage system varied (15, 6, and 1.5 years). Selenium concentrations in the drain water also varied (430, 58, and 3700 μg/L, respectively). Isotopic enrichment and chemical composition of the groundwater samples indicate that saline- and selenium-enriched water has evolved as a result of evaporation or transpiration of groundwater. This evaporated, isotopically enriched water is being displaced by more recent, less saline irrigation water percolating through the root zone. This displacement seems to be a process whereby sodium chloride and sodium sulfate water is being replaced by more dilute calcium sulfate and calcium bicarbonate water.

California↗
USGS2010

California's BAY-DELTA: USGS Science Supports Decision Making

U.S. Geological Survey (USGS) scientists are in the forefront of the effort to understand what causes changes in the hydrology, the ecology and the water quality of the Sacramento-San Joaquin River Delta and the San Francisco Bay estuary. Their scientific findings play a crucial role in how agencies manage the Bay-Delta on a daily basis.

Fact Sheet↗
USGS2008

Subsidence reversal in a re-establish wetland in the Sacramento-San Joaquin Delta, California, USA

The stability of levees in the Sacramento-San Joaquin Delta is threatened by continued subsidence of Delta peat islands. Up to 6 meters of land-surface elevation has been lost in the 150 years since Delta marshes were leveed and drained, primarily from oxidation of peat soils. Flooding subsided peat islands halts peat oxidation by creating anoxic soils, but net accumulation of new material in restored wetlands is required to recover land-surface elevations. We investigated the subsidence reversal potential of two 3 hectare, permanently flooded, impounded wetlands re-established on a deeply subsided field on Twitchell Island. The shallower wetland (design water depth 25 cm) was almost completely colonized by dense emergent marsh vegetation within two years; whereas, the deeper wetland (design water depth 55 cm) which developed spatially variable depths as a result of heterogeneous colonization by emergent vegetation, still had some areas remaining as open water after nine years. Changes in land-surface elevation were quantified using repeated sedimentation-erosion table measurements. New material accumulating in the wetlands was sampled by coring. Land-surface elevations increased by an average of 4 cm/yr in both wetlands from 1997 to 2006; however, the rates at different sites in the wetlands ranged from -0.5 to +9.2 cm/yr. Open water areas of the deeper wetland without emergent vegetation had the lowest rates of land-surface elevation gain. The greatest rates occurred in areas of the deeper wetland most isolated from the river water inlets, with dense stands of emergent marsh vegetation (tules and cattails). Vegetated areas of the deeper wetland in the transition zones between open water and mature emergent stands had intermediate rates of land-surface gain, as did the entire shallower wetland. These results suggest that the dominant component contributing to land-surface elevation gain in these wetlands was accumulation of organic matter, rather than mineral sediment, and that accumulation of organic matter in emergent marshes is strongly affected by hydrologic factors. Re-established, non-tidal wetlands with managed hydrology can produce significant increases in land-surface elevations, which can help to improve levee stability and protect subsided islands from future flooding.

California↗
USGS2003

Evaluation of specific ultraviolet absorbance as an indicator of the chemical composition and reactivity of dissolved organic carbon

Specific UV absorbance (SUVA) is defined as the UV absorbance of a water sample at a given wavelength normalized for dissolved organic carbon (DOC) concentration. Our data indicate that SUVA, determined at 254 nm, is strongly correlated with percent aromaticity as determined by 13C NMR for 13 organic matter isolates obtained from a variety of aquatic environments. SUVA, therefore, is shown to be a useful parameter for estimating the dissolved aromatic carbon content in aquatic systems. Experiments involving the reactivity of DOC with chlorine and tetramethylammonium hydroxide (TMAH), however, show a wide range of reactivity for samples with similar SUVA values. These results indicate that, while SUVA measurements are good predictors of general chemical characteristics of DOC, they do not provide information about reactivity of DOC derived from different types of source materials. Sample pH, nitrate, and iron were found to influence SUVA measurements.

Environmental Science & Technology↗
USGS2003

Processes affecting the trihalomethane concentrations associated with the third injection, storage, and recovery rest at Lancaster, Antelope Valley, California, March 1998 through April 1999

The formation and fate of trihalomethanes (THM) during the third injection, storage, and recovery test at Lancaster, Antelope Valley, California, were investigated as part of a program to assess the long-term feasibility of using injection, storage, and recovery as a water-supply method and as a way to reduce water-level declines and land-subsidence in the Antelope Valley. The program was conducted by the U.S. Geological Survey in cooperation with the Los Angeles County Department of Public Works and the Antelope Valley-East Kern Water Agency. The water used for injection, storage, and recovery must be disinfected before injection and thus contains THMs and other disinfection by-products. THMs (chloroform, CHCl3, bromodichloromethane, CHCl2Br, dibromochloromethane, CHClBr2, and bromoform, CHBr3) are formed by reaction between natural dissolved organic carbon that is present in water and chlorine that is added during the disinfection step of the drinking water treatment process. THMs are carcinogenic compounds, and their concentrations in drinking water are regulated by the U.S. Environmental Protection Agency. During previous cycles of the Lancaster program, extracted water still contained measurable concentrations of THMs long after continuous pumping had extracted a greater volume of water than had been injected. This raised concerns about the potential long-term effect of injection, storage, and recovery cycles on ground-water quality in Antelope Valley aquifers. The primary objectives of this investigation were to determine (1) what controlled continued THM formation in the aquifer after injection, (2) what caused of the persistence of THMs in the extracted water, even after long periods of pumping, (3) what controlled the decrease of THM concentrations during the extraction period, and (4) the potential for natural attenuation of THMs in the aquifer. Laboratory experiments on biodegradation of THMs in microcosms of aquifer materials indicate that aquifer bacteria did not degrade CHCl3 or CHBr3 under aerobic conditions, but did degrade CHBr3 under anaerobic conditions. However, the aquifer is naturally aerobic and CHCl3 is the dominant THM species; therefore, biodegradation is not considered an important attenuation mechanism for THMs in this aquifer. The alluvial-fan sediments comprising the aquifer have very low contents of organic matter; therefore, sorption is not considered to be an important attenuation mechanism for THMs in this aquifer. Laboratory experiments on formation of THMs in the injection water indicate that continued THM formation in the injection water after injection into the aquifer was limited by the amount of residual chlorine in the injection water at the time of injection. After accounting for THMs formed by reaction of this residual chlorine, THMs behaved as conservative constituents in the aquifer, and the only process affecting the concentration of THMs was mixing of the injection water and the ground water. The mixing process was quantified using mass balances of injected constituents, the sulfur hexafluoride (SF6) tracer that was added to the injected water, and a simple descriptive mathematical mixing model. Mass balance calculations show that only 67 percent of the injected THMs and chloride were recovered by the time that a volume of water equivalent to 132 percent of the injection water volume was extracted. Pumping 250 percent of the injection water volume only increased recovery of injected THMs to 80 percent. THM and SF6 concentrations in the extracted water decreased concomitantly during the extraction period, and THM concentrations predicted from SF6 concentrations closely matched the measured THM concentrations. Because SF6 is a conservative tracer that was initially only present in the injection water, parallel decreases in SF6 and THM concentrations in the extracted water must be due to dilution of injection water with ground water. The simple descriptive mixing mode

Water-Resources Investigations Report↗
USGS2002

Water-quality monitoring and studies of the formation and fate of trihalomethanes during the third injection, storage and recovery test at Lancaster, Antelope Valley, California, March 1998 through April 1999

The U.S. Geological Survey, in cooperation with the Los Angeles County Department of Public Works and the Antelope Valley-East Kern Water Agency, conducted three cycles of injection, storage, and recovery tests to evaluate the feasibility of artificially recharging ground water in the Lancaster area of Antelope Valley, California. During the third cycle (March 1998 through April 1999), the tests included investigations of the formation and fate of trihalomethanes in the aquifer. Trihalomethanes are disinfection by-products formed by reaction between natural dissolved organic carbon that is present in water and chlorine that is added during the drinking-water-treatment process. This report includes a discussion of the design of the investigation; descriptions of the sampling, analytical, and experimental methods used in the investigation; and a presentation of the data collected. During the third cycle, 60 million gallons of chlorinated water was injected into the aquifer through well 7N/12W-27P2 in the Los Angeles County Department of Public Works well field in Lancaster between April 15 and June 16, 1998. One hundred fifty million gallons of water was extracted from the same well between June 30, 1998, and April 29, 1999. Water-quality samples were collected during the entire cycle from the well and from a nearby set of nested piezometers, and were analyzed for residual chlorine, dissolved organic carbon, trihalomethane, major anion, and dissolved solid concentrations; ultraviolet absorbance spectra; and a number of field water-quality parameters. A statistical analysis was done to evaluate the analytical precision of the residual chlorine, dissolved organic carbon, trihalomethane, and ultraviolet absorbance measurements on these samples. The formation of trihalomethanes in the injection water was examined in laboratory experiments: Trihalomethane concentrations in samples of injection water were monitored during a storage period, and trihalomethane formation potential in the presence of excess chlorine was measured. The role of mixing between injection water and ground water and the conservative or non-conservative behavior of trihalomethanes was studied by adding a conservative tracer, sulfur hexafluoride, to the injection water and monitoring its concentration in the extraction water. The potential for biodegradation of trihalomethanes by aquifer bacteria was assessed in laboratory experiments: Microcosms containing ground water or extraction water and sediment or concentrated bacteria were spiked with trihalomethanes, and the amount of trihalomethanes was monitored during an incubation period. The potential for sorption of trihalomethanes to aquifer sediments was assessed in laboratory experiments: Mixtures of sediment and water were spiked with trihalomethanes, and then the trihalomethane concentrations were measured after an equilibration period.

Open-File Report↗
USGS2000

Hydrologic treatments affect gaseous carbon loss From organic soils, Twitchell Island, California, October 1995–December 1997

Subsidence of organic soils in the Sacramento-San Joaquin Delta, California, has increased the potential for levee failure and flooding in the region. Because oxidation of the peat soils is a primary cause of subsidence, reversion of affected lands to wetlands has been proposed as a mitigation tool. To test this hypothesis, three 10 x 10 meter enclosures were built on Twitchell Island in the Delta and managed as different wetland habitats. Emissions of carbon dioxide and methane were measured in situ from October 1995 through December 1997, from the systems that developed under the different water-management treatments. Treatments included a seasonal control (SC) under current island management conditions; reverse flooding (RF), where the land is intentionally flooded from early dry season until midsummer; permanent shallow flooding (F); and a more deeply flooded, open-water (OW) treatment. Hydrologic treatments affected microbial processes, plant community and temperature dynamics which, in turn, affected carbon cycling. Water-management treatments with a period of flooding significantly decreased gaseous carbon emissions compared to the seasonal control. Permanent flooding treatments showed significantly higher methane fluxes than treatments with some period of aerobic conditions. Shallow flooding treatments created conditions that support cattail [Typha species (spp.)] marshes, while deep flooding precluded emergent vegetation. Carbon inputs to the permanent shallow flooding treatment tended to be greater than the measured losses. This suggests that permanent shallow flooding has the greatest potential for managing subsidence of these soils by generating organic substrate more rapidly than is lost through decomposition. Carbon input estimates of plant biomass compared to measurements of gaseous carbon losses indicate the potential for mitigation of subsidence through hydrologic management of the organic soils in the area.

California↗
USGS1998

Dissolved organic carbon concentrations and compositions, and trihalomethane formation potentials in waters from agricultural peat soils, Sacramento-San Joaquin Delta, California; implications for drinking-water quality

Water exported from the Sacramento-San Joaquin River delta (Delta) is an important drinking-water source for more than 20 million people in California. At times, this water contains elevated concentrations of dissolved organic carbon and bromide, and exceeds the U.S. Environmental Protection Agency's maximum contaminant level for trihalomethanes of 0.100 milligrams per liter if chlorinated for drinking water. About 20 to 50 percent of the trihalomethane precursors to Delta waters originates from drainage water from peat soils on Delta islands. This report elucidates some of the factors and processes controlling and affecting the concentration and quality of dissolved organic carbon released from peat soils and relates the propensity of dissolved organic carbon to form trihalomethanes to its chemical composition. Soil water was sampled from near-surface, oxidized, well-decomposed peat soil (upper soil zone) and deeper, reduced, fibrous peat soil (lower soil zone) from one agricultural field in the west central Delta over 1 year. Concentrations of dissolved organic carbon in the upper soil zone were highly variable, with median concentrations ranging from 46.4 to 83.2 milligrams per liter. Concentrations of dissolved organic carbon in samples from the lower soil zone were much less variable and generally slightly higher than samples from the upper soil zone, with median concentrations ranging from 49.3 to 82.3 milligrams per liter. The dissolved organic carbon from the lower soil zone had significantly higher aromaticity (as measured by specific ultraviolet absorbance) and contained significantly greater amounts of aromatic humic substances (as measured by XAD resin fractionation and carbon-13 nuclear magnetic resonance analysis of XAD isolates) than the dissolved organic carbon from the upper soil zone. These results support the conclusion that more aromatic forms of dissolved organic carbon are produced under anaerobic conditions compared to aerobic conditions. Dissolved organic carbon concentration, trihalomethane formation potential, and ultraviolet absorbance were all highly correlated, showing that trihalomethane precursors increased with increasing dissolved organic carbon and ultraviolet absorbance for whole water samples. Contrary to the generally accepted conceptual model for trihalomethane formation that assumes that aromatic forms of carbon are primary precursors to trihalomethanes, results from this study indicate that dissolved organic carbon aromaticity appears unrelated to trihalomethane formation on a carbon-normalized basis. Thus, dissolved organic carbon aromaticity alone cannot fully explain or predict trihalomethane precursor content, and further investigation of aromatic and nonaromatic forms of carbon will be needed to better identify trihalomethane precursors.

California↗
USGS1995

Areal distribution of selected trace elements, salinity, and major ions in shallow ground water, Tulare Basin, Southern San Joaquin Valley, California

The distribution of salinity and selected trace elements in shallow ground water in the Tulare Basin, California, was assessed to evaluate potential problems related to disposal in evaporation ponds of irrigation drain water containing elevated concentrations of selenium and other trace elements. The constituents of primary concern were selenium, arsenic, and salinity; uranium, boron, and molybdenum also were evaluated. Samples from 117 shallow wells were analyzed, and the results for samples from 110 of the wells were interpreted in relation to surficial geology, sediment depositional environment, soil characteristics, and hydrologic processes to determine the geochemical and hydrologic factors affecting the distribution of these constituents in ground water. In general, shallow ground water in areas where concentrations of salinity and most trace elements are elevated is influenced primarily by sediments derived from marine sedimentary rocks originating in the Coast Range, San Emigdio Mountains, and Tehachapi Mountains, and probably by unusual exposures of similar marine formations in the Sierra Nevada. Ground water in areas where concentrations of salinity and trace elements are significantly lower generally is influenced by igneous and metamorphic rocks exposed in the Sierra Nevada. In addition to sources of sediments, evaporation of shallow ground water, as indicated by isotopic enrichment of oxygen-18 and deuterium, increases salinity and concentrations of conservative trace elements such as selenium (under oxidizing conditions) and boron. Redox conditions affect the oxidation state of all trace elements of concern, except boron, and were found to be a major influence on trace-element solubility. Under oxidized conditions, selenate predominates and behaves conservatively, and arsenate predominates and is affected by sorption reactions that can limit arsenic solubility. Under reduced conditions, selenium is reduced to insoluble elemental selenium and arsenite predominates and generally is more soluble than arsenate. Elevated concentrations of uranium in shallow ground water probably are associated with uranium deposits in Kern County and other parts of the basin where oxidized conditions cause the more soluble uranyl species to predominate. Boron was correlated with salinity and behaved conservatively, whereas adsorption and precipitation of molybdenum minerals probably limited molybdenum solubility. Interrelations among constituents were examined with principal component analysis. The first two principal components explained 50.7 percent of the variance in the data. The first principal component was related to salinity, and the second principal component was related to redox conditions, reflecting two of the major influences on shallow groundwater quality found in this study.

California↗
USGS1994

Water-quality, lithologic, and water-level data for wells in Tulare Basin, Kings, Kern, and Tulare Counties, California, August 1990 to February 1993

Much of the Tulare Basin is characterized by saline shallow ground water containing elevated concen- trations of arsenic, selenium, and other trace elements. A comprehensive investigation of ground-water geochemist, and, to a limited extent, hydrology was initiated in response to concerns related to (1) adverse effects on migratory waterfowl of high concentrations of selenium in agricultural drainwater disposed of in evaporation ponds and (2) adverse effects on human health due to potential downward migration of ground water containing high concentrations of arsenic to regional aquifers used as drinking-water sources. This report presents data collected during the initial phase of this investigation. A total of 20 observation wells were installed at 5 locations in the basin. Four observation wells in a cluster were installed at each location at depths of about 20, 50, 100, and 200 feet. Water samples collected from each site were analyzed for major ions, trace elements (including arsenic and selenium), nutrients, and selected isotopes. Lithologic logs and well-construction information for each site and water-level measurements for each well measured periodically from August 1990 to February 1993 also are reported.

Open-File Report↗
USGS1991

Selenium mobility and distribution in irrigated and nonirrigated alluvial soils

Dissolution and leaching of soil salts by irrigation water is a primary source of Se to shallow groundwater in the western San Joaquin Valley, California. In this study, the mobility and distribution of selenite and selenate in soils with different irrigation and drainage histories was evaluated using sorption experiments and an advection-dispersion model. The sorption studies showed that selenate (15–12400 µg Se L −1 ) is not adsorbed to soil, whereas selenite (10–5000 µg Se L −1 ) is rapidly adsorbed. The time lag between adsorption and desorption of selenite is considerable, indicating a dependence of reaction rate on reaction direction (hysteresis). Selenite adsorption and desorption isotherms were different, and both were described with the Freundlich equation. Model results and chemical analyses of extracts from the soil samples showed that selenite is resistant to leaching and therefore can represent a potential long-term source of Se to groundwater. In contrast, selenate behaves as a conservative constituent under alkaline and oxidized conditions and is easily leached from soil.

Soil Science Society of America Journal↗