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Tamara E. C. Kraus

Publications and source records attributed to Tamara E. C. Kraus.

33 records · Page 2Linked to original sources

Trihalomethane precursors: Land use hot spots, persistence during transport, and management options

To meet drinking water regulations, rather than investing in costly treatment plant operations, managers can look for ways to improve source water quality; this requires understanding watershed sources and fates of constituents of concern. Trihalomethanes (THMs) are one of the major classes of regulated disinfection byproducts, formed when a specific fraction of the organic carbon pool—referred to as THM precursors—reacts with chorine and/or bromine during treatment. Understanding the source, fate, timing and duration of the organic compounds that react to form THMs will allow identification of targeted and effective management actions. In this study we evaluated THM precursor contributions from multiple land use categories and hydrologic contexts, including novel data for urban land uses that demonstrate strong potential to release water with high THM formation potential (THMFP; median 618 μg L −1 ): greater than storm runoff integrated across a mixed-use (1/3 natural, 2/3 agricultural) watershed (median 460 μg L −1 ), irrigation runoff from agricultural systems (357 μg L −1 ), or runoff from a natural forested (median 123 μg L −1 ) and shrubland/grassland (median 259 μg L −1 ) watersheds. While individual storm events released high THM precursor concentrations over short periods, dry season agricultural irrigation as well as urban landscapes have the potential to release water high in THM precursors for several months. Experimental bioassays and sampling along 333 miles of the California Aqueduct confirmed bioavailability and photooxidation potential of less than 10% for THM precursors, suggesting that rivers with residence times of days to weeks may act as THM precursor conduits, shuttling THM precursors from hundreds of miles away to drinking water intakes with minimal degradation. This finding has considerable implications for water managers, who may therefore consider THM precursor management strategies that target even sources located far upstream.

California↗

Changing nitrogen inputs to the northern San Francisco Estuary: Potential ecosystem responses and opportunities for investigation

Anthropogenic activities have resulted in elevated ambient nitrogen (N) and phosphorus (P) concentrations in many regions of the Sacramento-San Joaquin Delta and Suisun Bay (northern San Francisco Estuary, (nSFE). The Sacramento Regional wastewater treatment plant (SRWTP WWTP) currently acts as the largest N point source to the system, discharging 13,000-15,000 kg/d of ammonium-N (NH4) near the nSFE’s northeastern boundary. By end of 2021, SRWTP will complete major upgrades that will reduce its effluent dissolved inorganic nitrogen (DIN) loads by >65% and release the remaining DIN as predominantly nitrate (NO3). This major change in nitrogen inputs provides a unique opportunity to study ecosystem-scale responses to an altered nutrient regime. While, in general, the nSFE has not experienced some classic symptoms of nutrient over-enrichment typical in other estuaries—e.g., large phytoplankton blooms and hypoxia—other concerning nutrient- related impacts have been hypothesized, including: occurrence of harmful algal blooms (HABs) and the production of cyanotoxins; excessive growth of invasive aquatic vegetation; and declines in the abundance and nutritional quality of phytoplankton. These impacts have repercussions for the system’s food web, habitat quality, and the way we manage for transportation, recreation, water conveyance, and drinking water quality. This report develops and applies a framework for i) identifying and examining ecosystem response scenarios to the forthcoming decreased N loads; and ii) identifying opportunities, and constraints or considerations, for investigating those responses, including key data needs or knowledge gaps. Through applying this framework, we identify a set of plausible response scenarios, and evaluate the feasibility of studying or observing those responses along with key study considerations and data and knowledge gaps.

California↗

Chemically enhanced treatment wetland to improve water quality and mitigate land subsidence in the Sacramento-San Joaquin Delta: Cost and design considerations

Water quality impairment and land surface subsidence threaten the viability of the Sacramento-San Joaquin Delta (Delta), a critical component of California’s water conveyance system. Current day irrigation drainage through Delta island peat soils impacts drinking water treatment and is linked to mercury transport, potentially posing both ecological and public health concerns. Hybrid coagulation-treatment wetland systems, termed Chemically Enhanced Treatment Wetlands (CETWs), were studied as a means to cost-effectively treat agricultural drainage water from subsided Delta islands to reduce the export of drinking water quality constituents of concern and mitigate land subsidence through accretion. We provide cost estimates and design recommendations to aid broader implementation of this technology. Over a 20-year horizon using a Total Annualized Cost analysis, we estimate treatment costs of $602 – $747 per acre-foot (ac-ft) water treated and $36 – $70 per kg dissolved organic carbon (DOC) removed depending upon source water DOC concentrations for a small 3-acre CETW system. For larger CETW systems scaled for island sizes of 3,500 – 14,000 acres, costs decrease to $108 – $239 per ac-ft water treated and $11 – $14 per kg DOC removed. The footprints of CETW systems were estimated to be approximately 3% of the area being treated for 4-day hydraulic retention time systems but would decrease to less than 1% for 1-day hydraulic retention time systems. CETWs ultimately address several of the Delta’s key internal issues while keeping water treatment costs competitive with other currently available treatment technologies at similar scales on a per carbon removed basis. CETWs offer a reliable system to reduce out-going DOC and mercury loads and they provide the additional benefit of sediment accretion. System costs and treatment efficacy are highly dependent on inflow source water conditions, land availability and other practical matters. To keep costs low and removal efficacy high, wetland design features will need site-specific evaluation.

California↗

Aluminum- and iron-based coagulation for in-situ removal of dissolved organic carbon, disinfection byproducts, mercury and other constituents from agricultural drain water

Agricultural production on wetland soils can be significant sources of dissolved organic carbon (DOC), disinfection byproduct precursors, mercury and nutrients to downstream water bodies and accelerate land subsidence. Presented as a potential solution for in-situ water quality improvement and land subsidence mitigation, chemically enhanced treatment wetlands (CETWs) were used to leverage both coagulation and wetland processes. In this study, we evaluated the performance of coagulants ferric sulfate (Fe dosing) and polyaluminum chloride (Al dosing) to remove pollutants from agricultural drain water using the coagulation system designed for CETWs. Both coagulation treatments removed over 70% DOC from source waters, resulting in removal efficiencies (mg-DOC removed per mg-metal dosed) of 1 under Al dosing and 0.5 under Fe dosing. Coagulation by both treatments preferentially removed UV254 active compounds compared to the bulk DOC concentration, suggesting coagulation targeted aromatics more effectively. Phosphates and haloacetic acids were also removed more readily, whereas trihalomethanes, dissolved organic nitrogen and filtered mercury species were removed at similar or lower rates than DOC. Dissolved inorganic nitrogen was not amenable to coagulation and removal was not observed. Freundlich, Langmuir and Monod models explained 33% of the variance for Al dosing and 78 – 89% of the variance for Fe dosing. All three models indicated Al dosing had higher removal efficiency and affinity for DOC than Fe dosing under study conditions, but when used to predict maximum removal efficiency there was no cohesiveness between the three models due to different model assumptions. Consideration of fluorescence dissolved organic matter and UV254 as surrogates for DOC concentration showed both were equally suitable before coagulant application, but as surrogates after coagulant application, neither could be deemed more fit as a surrogate since both were shown suitable for different treatment scenarios.

Ecological Engineering↗

Effects of ferric sulfate and polyaluminum chloride coagulation enhanced treatment wetlands on Typha growth, soil and water chemistry

Land surface subsidence is a concern in many deltas worldwide as it contributes to water quality degradation, loss of fertile land and increased potential for levee failure. As a possible solution to these concerns, on-site coagulation enhanced treatment wetlands(CETWs), coagulation water treatment followed by wetland passage serving as a settling basin, were implemented in a field-scale study located on a subsided island of the Sacramento-San Joaquin Delta in northern California under three treatments; coagulation with polyaluminum chloride (PAC), coagulation with ferric sulfate and an untreated control. Because CETWs offer a relatively novel solution for water quality improvement and subsidence reversal due to its low-infrastructure requirements and in-situ nature, effects from these systems remain uncharted and they may have adverse effects on plant biomass production that also contribute to sediment accretion. This study focuses on the effect CETWs had on the growth of Typha spp .; the dominant vegetation in the wetlands. Plant growth parameters and nutrient content were measured in conjunction with soil, pore waterand surface water chemistry. Soil analysis indicated there was no intermixing of newly formed flocs and original soil material. Where there was significant deposition of floc, PAC treatment reduced phosphate concentrations and ferric sulfate treatment increased total Fe concentrations in surrounding water compared to the control. Results indicated coagulation treatments had no negative effects on Typha leaf nutrient content, Typha growth or allometric parameters. Additionally, no signs of plant toxicity such as necrosis, wilting or chlorosis were observed in any of the treatments. Overall, this study suggests that CETWs are viable treatment option for water quality improvement and sediment accretion while having no negative impact on the growth of Typha plants.

Science of the Total Environment↗

Sequestration and transformation in chemically enhanced treatment wetlands: DOC, DBPPs and Nutrients

We examined the effectiveness of chemically enhanced treatment wetlands (CETWs), wetlands that received water treated with coagulants, to remove dissolved organic carbon (DOC), disinfection byproduct precursors (DBPPs), nutrients and metals from agricultural drain water. Wetlands consisted of controls with no coagulant addition, ferric sulfate dosed and polyaluminum chloride dosed treatments. CETWs were more effective in removal of DOC, DBPPs, phosphate, dissolved organic nitrogen and metals than control wetlands. Coagulation treated wetlands removed 245 – 349 g/m2yr DOC, whereas control wetlands produced 51 g/m2yr. Wetland passage released DOC in the controls and treatments; this release was directly correlated to temperature and suggested thermally dependent mechanism(s) were partly responsible. A first-order plug flow reactor kinetic model that considered hydraulic retention time (HRT), temperature and concentration was tested for wetland DOC processing. Models indicate that operating CETWs at high coagulant dosing and low temperature can result in lowest DOC release with additional release suppression. Operating at the lowest HRT to meet discharge targets help overcome wetland processes that increase DOC release and provide the smallest footprint needed for treatment.

Journal of Environmental Engineering↗

Procedures for using the Horiba Scientific Aqualog ® fluorometer to measure absorbance and fluorescence from dissolved organic matter

Advances in spectroscopic techniques have led to an increase in the use of optical measurements (absorbance and fluorescence) to assess dissolved organic matter composition and infer sources and processing. Although optical measurements are easy to make, they can be affected by many variables rendering them less comparable, including by inconsistencies in sample collection (for example, filter pore size, preservation), the application of corrections for interferences (for example, inner-filtering corrections), differences in holding times, and instrument drift (for example, lamp intensity). A documented, standardized procedure to address these variables ensures that the optical (absorbance and fluorescence) measurements collected by U.S. Geological Survey researchers are useful and widely comparable. Rigorous and quantifiable quality assurance and quality control are essential for making these data comparable, particularly because there is no published guideline for the measurement of dissolved organic matter absorbance and fluorescence, and especially because there is no National Institute of Standards and Technology standard for dissolved organic matter. Validation and quality-control samples are analyzed on a monthly basis to determine laboratory and instrument precision and daily (that is, each day samples are run) to ensure repeatability. Data are not considered acceptable unless they meet laboratory criteria: All standards should be within 10 percent of the target value, laboratory replicates should be within 5 percent relative percent difference, and laboratory blanks (that is, laboratory reagent-grade water) should be less than one-tenth of the long-term method detection limit. Finally, for data to be useful, they must be accessible to users in a format that can be easily analyzed and interpreted. The Organic Matter Research Laboratory staff has developed a processing routine that extracts a subset of the data, which is made available to the public through the USGS National Water Quality Information System ( http://nwis.waterdata.usgs.gov/usa/nwis/qwdata ), and organizes the full datasets (that is, complete absorbance spectra and fluorescence excitation-emission matrices) in different forms that allow for these data to be analyzed using multi-parameter and multi-way statistical approaches.

Open-File Report↗

Use of flow cytometry and stable isotope analysis to determine phytoplankton uptake of wastewater derived ammonium in a nutrient-rich river

Anthropogenic alteration of the form and concentration of nitrogen (N) in aquatic ecosystems is widespread. Understanding availability and uptake of different N sources at the base of aquatic food webs is critical to establishment of effective nutrient management programs. Stable isotopes of N ( 14 N, 15 N) are often used to trace the sources of N fueling aquatic primary production, but effective use of this approach requires obtaining a reliable isotopic ratio for phytoplankton. In this study, we tested the use of flow cytometry to isolate phytoplankton from bulk particulate organic matter (POM) in a portion of the Sacramento River, California, during river-scale nutrient manipulation experiments that involved halting wastewater discharges high in ammonium (NH 4 + ). Field samples were collected using a Lagrangian approach, allowing us to measure changes in phytoplankton N source in the presence and absence of wastewater-derived NH 4 + . Comparison of δ 15 N-POM and δ 15 N-phytoplankton ( δ 15 N-PHY) revealed that their δ 15 N values followed broadly similar trends. However, after 3 days of downstream travel in the presence of wastewater treatment plant (WWTP) effluent, δ 15 N-POM and δ 15 N-PHY in the Sacramento River differed by as much as 7 ‰. Using a stable isotope mixing model approach, we estimated that in the presence of effluent between 40 and 90 % of phytoplankton N was derived from NH 4 + after 3 days of downstream transport. An apparent gradual increase over time in the proportion of NH 4 + in the phytoplankton N pool suggests that either very low phytoplankton growth rates resulted in an N turnover time that exceeded the travel time sampled during this study, or a portion of the phytoplankton community continued to access nitrate even in the presence of elevated NH 4 + concentrations.

California↗

Sediment accretion and carbon storage in constructed wetlands receiving water treated with metal-based coagulants

In many regions of the world, subsidence of organic rich soils threatens levee stability and freshwater supply, and continued oxidative loss of organic matter contributes to greenhouse gas production. To counter subsidence in the Sacramento-San Joaquin Delta of northern California, we examined the feasibility of using constructed wetlands receiving drainage water treated with metal-based coagulants to accrete mineral material along with wetland biomass, while also sequestering carbon in wetland sediment. Nine field-scale wetlands were constructed which received local drainage water that was either untreated (control), or treated with polyaluminum chloride (PAC) or iron sulfate (FeSO4) coagulants. After 23 months of flooding and coagulant treatment, sediment samples were collected near the inlet, middle, and outlet of each wetland to determine vertical accretion rates, bulk density, sediment composition, and carbon sequestration rates. Wetlands treated with PAC had the highest and most spatially consistent vertical accretion rates (~6 cm year-1), while the FeSO4 wetlands had similarly high accretion rates near the inlet but rates similar to the untreated wetland (~1.5 cm year-1) at the middle and outlet sites. The composition of the newly accreted sediment in the PAC and FeSO4 treatments was high in the added metal (aluminum and iron, respectively), but the percent metal by weight was similar to native soils of California. As has been observed in other constructed wetlands, the newly accreted sediment material had lower bulk densities than the native soil material (0.04-0.10 g cm-3 versus 0.2-0.3 g cm-3), suggesting these materials will consolidate over time. Finally, this technology accelerated carbon burial, with rates in PAC treated wetland (0.63 kg C m-2 yr-1) over 2-fold greater than the untreated control (0.28 kg C m-2 yr-1). This study demonstrates the feasibility of using constructed wetlands treated with coagulants to reverse subsidence by accreting the resulting organo-metal flocculent and storing carbon at rates exceeding untreated wetlands. Management and design questions remain for how to best integrate this technology into heavily subsided land to lower the risks and consequences associated with levee failure, improve water quality, and ultimately restore these lands to tidal wetlands.

California↗

Wetlands receiving water treated with coagulants improve water quality by removing dissolved organic carbon and disinfection byproduct precursors

Constructed wetlands are used worldwide to improve water quality while also providing critical wetland habitat. However, wetlands have the potential to negatively impact drinking water quality by exporting dissolved organic carbon (DOC) that upon disinfection can form disinfection byproducts (DBPs) like trihalomethanes (THMs) and haloacetic acids (HAAs). We used a replicated field-scale study located on organic rich soils in California's Sacramento-San Joaquin Delta to test whether constructed flow-through wetlands which receive water high in DOC that is treated with either iron- or aluminum-based coagulants can improve water quality with respect to DBP formation. Coagulation alone removed DOC (66–77%) and THM (67–70%) precursors, and was even more effective at removing HAA precursors (77–90%). Passage of water through the wetlands increased DOC concentrations (1.5–7.5 mg L − 1 ), particularly during the warmer summer months, thereby reversing some of the benefits from coagulant addition. Despite this addition, water exiting the wetlands treated with coagulants had lower DOC and DBP precursor concentrations relative to untreated source water. Benefits of the coagulation-wetland systems were greatest during the winter months (approx. 50–70% reduction in DOC and DBP precursor concentrations) when inflow water DOC concentrations were higher and wetland DOC production was lower. Optical properties suggest DOC in this system is predominantly comprised of high molecular weight, aromatic compounds, likely derived from degraded peat soils.

Science of the Total Environment↗

Using paired in situ high frequency nitrate measurements to better understand controls on nitrate concentrations and estimate nitrification rates in a wastewater-impacted river

We used paired continuous nitrate ( ) measurements along a tidally affected river receiving wastewater discharge rich in ammonium ( ) to quantify rates of change in concentration ( ) and estimate nitrification rates. sensors were deployed 30 km apart in the Sacramento River, California (USA), with the upstream station located immediately above the regional wastewater treatment plant (WWTP). We used a travel time model to track water transit between the stations and estimated every 15 min (October 2013 to September 2014). Changes in concentration were strongly related to water temperature. In the presence of wastewater, was generally positive, ranging from about 7 µ M d −1 in the summer to near zero in the winter. Numerous periods when the WWTP halted discharge allowed the to be estimated under no-effluent conditions and revealed that in the absence of effluent, net gains in were substantially lower but still positive in the summer and negative (net sink) in the winter. Nitrification rates of effluent-derived NH 4 ( ) were estimated from the difference between measured in the presence versus absence of effluent and ranged from 1.5 to 3.4 µ M d −1 , which is within literature values but tenfold greater than recently reported for this region. was generally lower in winter (∼2 µ M d −1 ) than summer (∼3 µ M d −1 ). This in situ, high frequency approach provides advantages over traditional discrete sampling, incubation, and tracer methods and allows measurements to be made over broad areas for extended periods of time. Incorporating this approach into environmental monitoring programs can facilitate our ability to protect and manage aquatic systems.

California↗

A river-scale Lagrangian experiment examining controls on phytoplankton dynamics in the presence and absence of treated wastewater effluent high in ammonium

Phytoplankton are critical component of the food web in most large rivers and estuaries, and thus identifying dominant controls on phytoplankton abundance and species composition is important to scientists, managers, and policymakers. Recent studies from a variety of systems indicate that ammonium ( NH + 4 ) in treated wastewater effluent decreases primary production and alters phytoplankton species composition. However, these findings are based mainly on laboratory and enclosure studies, which may not adequately represent natural systems. To test effects of effluent high in ammonium on phytoplankton at the ecosystem scale, we conducted whole-river–scale experiments by halting discharges to the Sacramento River from the regional wastewater treatment plant (WWTP), and used a Lagrangian approach to compare changes in phytoplankton abundance and species composition in the presence (+EFF) and absence (−EFF) of effluent. Over 5 d of downstream travel from 20 km above to 50 km below the WWTP, chlorophyll concentrations declined from 15–25 to ∼2.5 μg L −1 , irrespective of effluent addition. Benthic diatoms were dominant in most samples. We found no significant difference in phytoplankton abundance or species composition between +EFF and −EFF conditions. Moreover, greatest declines in chlorophyll occurred upstream of the WWTP where NH + 4 concentrations were low. Grazing by clams and zooplankton could not account for observed losses, suggesting other factors such as hydrodynamics and light limitation were responsible for phytoplankton declines. These results highlight the advantages of conducting ecosystem-scale, Lagrangian-based experiments to understand the dynamic and complex interplay between physical, chemical, and biological factors that control phytoplankton populations.

California↗

Using continuous underway isotope measurements to map water residence time in hydrodynamically complex tidal environments

Stable isotopes present in water (δ 2 H, δ 18 O) have been used extensively to evaluate hydrological processes on the basis of parameters such as evaporation, precipitation, mixing, and residence time. In estuarine aquatic habitats, residence time (τ) is a major driver of biogeochemical processes, affecting trophic subsidies and conditions in fish-spawning habitats. But τ is highly variable in estuaries, owing to constant changes in river inflows, tides, wind, and water height, all of which combine to affect τ in unpredictable ways. It recently became feasible to measure δ 2 H and δ 18 O continuously, at a high sampling frequency (1 Hz), using diffusion sample introduction into a cavity ring-down spectrometer. To better understand the relationship of τ to biogeochemical processes in a dynamic estuarine system, we continuously measured δ 2 H and δ 18 O, nitrate and water quality parameters, on board a small, high-speed boat (5 to >10 m s –1 ) fitted with a hull-mounted underwater intake. We then calculated τ as is classically done using the isotopic signals of evaporation. The result was high-resolution (∼10 m) maps of residence time, nitrate, and other parameters that showed strong spatial gradients corresponding to geomorphic attributes of the different channels in the area. The mean measured value of τ was 30.5 d, with a range of 0–50 d. We used the measured spatial gradients in both τ and nitrate to calculate whole-ecosystem uptake rates, and the values ranged from 0.006 to 0.039 d –1 . The capability to measure residence time over single tidal cycles in estuaries will be useful for evaluating and further understanding drivers of phytoplankton abundance, resolving differences attributable to mixing and water sources, explicitly calculating biogeochemical rates, and exploring the complex linkages among time-dependent biogeochemical processes in hydrodynamically complex environments such as estuaries.

California↗

Optical properties of dissolved organic matter (DOM): Effects of biological and photolytic degradation

Advances in spectroscopic techniques have led to an increase in the use of optical properties (absorbance and fluorescence) to assess dissolved organic matter (DOM) composition and infer sources and processing. However, little information is available to assess the impact of biological and photolytic processing on the optical properties of original DOM source materials. We measured changes in commonly used optical properties and indices in DOM leached from peat soil, plants, and algae following biological and photochemical degradation to determine whether they provide unique signatures that can be linked to original DOM source. Changes in individual optical parameters varied by source material and process, with biodegradation and photodegradation often causing values to shift in opposite directions. Although values for different source materials overlapped at the end of the 111-day lab experiment, multivariate statistical analyses showed that unique optical signatures could be linked to original DOM source material even after degradation, with 17 optical properties determined by discriminant analysis to be significant (p<0.05) in distinguishing between DOM source and environmental processing. These results demonstrate that inferring the source material from optical properties is possible when parameters are evaluated in combination even after extensive biological and photochemical alteration.

Limnology and Oceanography↗

Investigating the temporal effects of metal-based coagulants to remove mercury from solution in the presence of dissolved organic matter

The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69&ndash;79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81&ndash;95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed.

Environmental Management↗