Geology topics

Megan B. Young

Publications and source records attributed to Megan B. Young.

11 recordsLinked to original sources

USGS2022

Over a third of groundwater in USA public-supply aquifers is Anthropocene-age and susceptible to surface contamination

The distribution of groundwater age is useful for evaluating the susceptibility and sustainability of groundwater resources. Here, we compute the aquifer-scale cumulative distribution function to characterize the age distribution for 21 Principal Aquifers that account for ~80% of public-supply pumping in the United States. The aquifer-scale cumulative distribution function for each Principal Aquifer was derived from an ensemble of modeled age distributions (~60 samples per aquifer) based on multiple tracers: tritium, tritiogenic helium-3, sulfur hexafluoride, chlorofluorocarbons, carbon-14, and radiogenic helium-4. Nationally, the groundwater is 38% Anthropocene (since 1953), 34% Holocene (75 – 11,800 years ago), and 28% Pleistocene (>11,800 years ago). The Anthropocene fraction ranges from <5 to 100%, indicating a wide range in susceptibility to land-surface contamination. The Pleistocene fraction of groundwater exceeds 50% in 7 eastern aquifers that are predominately confined. The Holocene fraction of groundwater exceeds 50% in 5 western aquifers that are predominately unconfined. The sustainability of pumping from these Principal Aquifers depends on rates of recharge and release of groundwater stored in fine-grained layers.

Nature Communications Earth & Environment↗

USGS2022

Ocean connectivity drives trophic support for consumers in an intermittently closed coastal lagoon

Estuarine food webs are complex, as marine, freshwater, and terrestrial inputs combine and contribute variable amounts of organic material. Seasonal fluctuations in precipitation amplify the dynamism inherent to estuarine food webs, particularly in lagoonal estuaries, which can be seasonally closed and disconnected from the ocean in low-runoff periods (bar-built lagoons). Despite their abundance along coastlines in Mediterranean climates, the organic matter sources fueling bar-built lagoon food webs are poorly understood, particularly with respect to seasonal hydrologic variability, episodic marine connections, and internal nutrient cycling. In this study, we evaluate the food web of a bar-built lagoon with respect to seasonal differences in lagoon water quality, the sources of organic matter which support consumers, and the trophic ecology of resident fishes. Observed water quality conditions reflected biogeochemical processes associated with salinity-driven stratification and high lagoon residence times and were associated with strong seasonal differences in the contribution of different organic matter sources to lagoon consumers. A variety of organic matter sources supported consumers; marine inputs were important to lagoon food webs in spring when the lagoon was open, while summer food webs were largely driven by phytoplankton which was likely fueled by internal nutrient cycling. Fish diets were largely comprised of crustaceans and fish eggs, with clearly defined trophic niches in spring but high overlap in summer. This study demonstrates that the seasonal changes in bar-built lagoon food webs are largely dependent on ocean connectivity and internal cycling within the lagoon, rather than watershed processes as is typical for many estuaries.

California↗

USGS2022

Stable isotopes provide insight into sources and cycling of N compounds in the Sacramento-San Joaquin Delta, California, USA

River deltas and their diverse array of aquatic environments are increasingly impacted by anthropogenic inputs of nitrogen (N). These inputs can alter the N biogeochemistry of these systems and promote undesirable phenomena including harmful algae blooms and invasive aquatic macrophytes. To examine N sources and biogeochemical processes in the Sacramento-San Joaquin Delta, a river delta located in central California, USA, that is fed primarily by the Sacramento River, we utilized a multi-tracer approach that measured N species concentrations and stable isotope values monthly from April 2011 to November 2012 in samples collected from the channelized mainstem of the Sacramento River, two channelized distributaries of the Sacramento River, and the Cache Slough Complex, a network of Sacramento River tributaries and shallow water wetland habitat. We found that the Sacramento River and its channelized distributaries received N primarily in the form of NH 4 + from treated wastewater effluent and that NH 4 + was lost rapidly while NO 3 − was gained more slowly during subsequent downstream transit, driven by an array of biogeochemical processes whose identities could be constrained via examination of stable isotope values. The Cache Slough Complex, which was characterized by lower net flows and higher water residence times than the Sacramento River and its distributaries, received variable inputs of low conductivity water elevated in NH 4 + from the Sacramento River and higher conductivity water elevated in NO 3 − from landward tributaries. Deviations from expected conservative mixing of these sources were spatially variable but broadly indicative of local inputs of treated wastewater effluent NO 3 − , conversion of Sacramento River NH 4 + to NO 3 − via nitrification, uptake of NH 4 + and NO 3 − by phytoplankton, and remineralization of organic N. These findings highlight both the diversity in N dynamics in anthropogenically impacted river delta environments and the utility of a multi-tracer approach in constraining these processes in such complex systems.

California↗

USGS2020

Lateral carbon exports from drained peatlands: An understudied carbon pathway in the Sacramento-San Joaquin Delta, California

Degradation of peatlands via drainage is increasing globally and destabilizing peat carbon (C) stores. The effects of drainage on the timing and magnitude of lateral C losses from degraded peatlands remains understudied. We measured spatial and temporal variability in lateral C exports from three drained peat islands in the Sacramento‐San Joaquin Delta in California across the 2017 and 2018 water years using measurements of dissolved inorganic C (DIC), dissolved organic C (DOC), and suspended particulate organic C (POC) concentration combined with discharge. These measurements were supplemented with stable isotope data (δ 13 C‐DIC, δ 13 C‐POC, δ 15 N‐PON, and δ 2 H‐H 2 O values) to provide insight into hydrological and biogeochemical controls on lateral C exports from drained peatlands. Drainage DOC and DIC concentrations were seasonally variable with the highest values in the winter rainy season, when discharge was also elevated. Seasonal differences in the mobilization of dissolved C appeared to result from changing water sources and water table levels. Peat island drainage C contributions to surrounding waterways were also greatest during the winter. Although temporal variability in C cycling processes and trends were generally similar across islands, baseline drainage DIC, DOC, and POC concentrations were spatially variable, likely a result of sub‐island‐scale differences in soil organic matter content and hydrology. This spatial variability complicates system‐wide assessments of C budgets. Net lateral C exports were water year dependent and comparable to previously published vertical C emission rates for this system. This work highlights the importance of including lateral C exports from drained peatlands in local and regional C budgets.

California↗

USGS2018

Tritium deposition in precipitation in the United States, 1953–2012

Tritium is a radioactive isotope of hydrogen (half-life is equal to 12.32 years). Since it is part of the water molecule, tritium can be used to track and date groundwater and surface water when the history of tritium in precipitation and recharge is known. To facilitate that effort, tritium concentrations in precipitation were reconstructed from measurements and correlations for 10 precipitation stations in the continental United States. Using these data, and other data sets and correlations, estimates of tritium concentrations in precipitation from 1953 through 2012 and total tritium deposition from 1953 through 1983 were derived for 2 degrees latitude by 5 degrees longitude quadrangles of the continental United States. For August 1953 through December 1987 correlations were derived from the data of the Ottawa, Canada, station; for estimates after 1987, the Vienna, Austria, station was used. For quadrangles where no precipitation station records are available from measurements or correlations, concentrations were interpolated. The International Atomic Energy Agency has proposed that a correlation with the Vienna, Austria, station, which has been in operation since 1960, be used instead of the Ottawa, Canada, station for the period after 1987. Linear correlations calculated for all stations with the Vienna data are reported. Correlations also have been calculated for each latitude-longitude quadrangle using the estimated concentrations and the measured Vienna data for 1960–87. Because the Vienna, Austria, station is on a different continent, and not subject to the same seasonal weather patterns that affect North American stations, a correlation was obtained for each month individually. This reflects the fact that the North American stations were strongly affected by the input of low-tritium moisture from the south during the summer. The correlated station values were then used with measured Vienna data to obtain estimates of tritium concentrations in precipitation for the period 1988–2012 at each precipitation station and latitude-longitude quadrangles. This approach has two major advantages: (1) it blends the Ottawa correlation with the Vienna correlation to cover the period 1953 to present, and (2) it yields correlation coefficients for each quadrangle that can be used in future years when more data become available from the Vienna, Austria, station. The data, the estimated tritium concentrations derived from the correlations, and the correlation coefficients are provided as spreadsheets and associated comma delimited files in a data release that accompanies this report.

Scientific Investigations Report↗

USGS2018

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↗

USGS2017

Methane fluxes from tropical coastal lagoons surrounded bymangroves, Yucatán, Mexico

Methane concentrations in the water column and emissions to the atmosphere were determined for three tropical coastal lagoons surrounded by mangrove forests on the Yucatán Peninsula, Mexico. Surface water dissolved methane was sampled at different seasons over a period of 2 years in areas representing a wide range of salinities and anthropogenic impacts. The highest surface water methane concentrations (up to 8378 nM) were measured in a polluted canal associated with Terminos Lagoon. In Chelem Lagoon, methane concentrations were typically lower, except in the polluted harbor area (1796 nM). In the relatively pristine Celestún Lagoon, surface water methane concentrations ranged from 41 to 2551 nM. Methane concentrations were negatively correlated with salinity in Celestún, while in Chelem and Terminos high methane concentrations were associated with areas of known pollution inputs, irrespective of salinity. The diffusive methane flux from surface lagoon water to the atmosphere ranged from 0.0023 to 15 mmol CH 4 m −2 d −1 . Flux chamber measurements revealed that direct methane release as ebullition was up to 3 orders of magnitude greater than measured diffusive flux. Coastal mangrove lagoons may therefore be an important natural source of methane to the atmosphere despite their relatively high salinity. Pollution inputs are likely to substantially enhance this flux. Additional statistically rigorous data collected globally are needed to better consider methane fluxes from mangrove-surrounded coastal areas in response to sea level changes and anthropogenic pollution in order to refine projections of future atmospheric methane budgets.

Yucatam↗

USGS2016

Bayesian nitrate source apportionment to individual groundwater wells in the Central Valley by use of elemental and isotopic tracers

Groundwater quality is a concern in alluvial aquifers that underlie agricultural areas, such as in the San Joaquin Valley of California. Shallow domestic wells (less than 150 m deep) in agricultural areas are often contaminated by nitrate. Agricultural and rural nitrate sources include dairy manure, synthetic fertilizers, and septic waste. Knowledge of the relative proportion that each of these sources contributes to nitrate concentration in individual wells can aid future regulatory and land management decisions. We show that nitrogen and oxygen isotopes of nitrate, boron isotopes, and iodine concentrations are a useful, novel combination of groundwater tracers to differentiate between manure, fertilizers, septic waste, and natural sources of nitrate. Furthermore, in this work, we develop a new Bayesian mixing model in which these isotopic and elemental tracers were used to estimate the probability distribution of the fractional contributions of manure, fertilizers, septic waste, and natural sources to the nitrate concentration found in an individual well. The approach was applied to 56 nitrate-impacted private domestic wells located in the San Joaquin Valley. Model analysis found that some domestic wells were clearly dominated by the manure source and suggests evidence for majority contributions from either the septic or fertilizer source for other wells. But, predictions of fractional contributions for septic and fertilizer sources were often of similar magnitude, perhaps because modeled uncertainty about the fraction of each was large. For validation of the Bayesian model, fractional estimates were compared to surrounding land use and estimated source contributions were broadly consistent with nearby land use types.

California↗

USGS2016

Methane and sulfate dynamics in sediments from mangrove-dominated tropical coastal lagoons, Yucatan, Mexico

Porewater profiles in sediment cores from mangrove-dominated coastal lagoons (Celestún and Chelem) on the Yucatán Peninsula, Mexico, reveal the widespread coexistence of dissolved methane and sulfate. This observation is interesting since dissolved methane in porewaters is typically oxidized anaerobically by sulfate. To explain the observations we used a numerical transport-reaction model that was constrained by the field observations. The model suggests that methane in the upper sediments is produced in the sulfate reduction zone at rates ranging between 0.012 and 31 mmol m −2 d − 1 , concurrent with sulfate reduction rates between 1.1 and 24 mmol SO 4 2− m −2 d −1 . These processes are supported by high organic matter content in the sediment and the use of non-competitive substrates by methanogenic microorganisms. Indeed sediment slurry incubation experiments show that non-competitive substrates such as trimethylamine (TMA) and methanol can be utilized for microbial methanogenesis at the study sites. The model also indicates that a significant fraction of methane is transported to the sulfate reduction zone from deeper zones within the sedimentary column by rising bubbles and gas dissolution. The shallow depths of methane production and the fast rising methane gas bubbles reduce the likelihood for oxidation, thereby allowing a large fraction of the methane formed in the sediments to escape to the overlying water column.

Yucatan↗

USGS2014

Use of stable isotopes of nitrogen and water to identify sources of nitrogen in three urban creeks of Durham, North Carolina, 2011-12

A preliminary assessment of nitrate sources was conducted in three creeks that feed nutrient impaired Falls and Jordan Lakes in the vicinity of Durham County, North Carolina, from July 2011 to June 2012. Cabin Branch, Ellerbe Creek, and Third Fork Creek were sampled monthly to determine if sources of nitrate in surface water could be identified on the basis of their stable isotopic compositions. Land use differs in the drainage basins of the investigated creeks—the predominant land use in Cabin Branch Basin is forest, and the Ellerbe and Third Fork Creek Basins are predominantly developed urban areas. Total nutrient concentrations were below 1 milligram per liter (mg/L). All measured nitrate plus nitrite concentrations were below the North Carolina standard of 10 mg/L as nitrogen with the highest concentration of 0.363 mg/L measured in Third Fork Creek. Concentrations of ammonia were generally less than 0.1 mg/L as nitrogen in all creek samples. More than 50 percent of the total nitrogen measured in the creeks was in the form of organic nitrogen. Total phosphorus and orthophosphate concentrations in all samples were generally less than 0.2 mg/L as phosphorus. The isotopic composition of surface water (δ 2 H H20 and δ 18 O H2O ) is similar to that of modern-day precipitation. During July and August 2011 and May and June 2012, surface-water samples displayed a seasonal difference in isotopic composition, indicating fractionation of isotopes as a result of evaporation and, potentially, mixing with local and regional groundwater. The dominant source of nitrate to Cabin Branch, Ellerbe Creek, and Third Fork Creek was the nitrification of soil nitrogen. Two stormflow samples in Ellerbe Creek and Third Fork Creek had nitrate sources that were a mixture of the nitrification of soil nitrogen and an atmospheric source that had bypassed some soil contact through impermeable surfaces within the drainage basin. No influence of a septic or wastewater source was found in Cabin Branch. Results from this study suggest that it is possible to distinguish sources of nitrogen and biogeochemical processes on nitrate using stable isotopes of nitrogen and oxygen in small creeks of Durham County, North Carolina.

North Carolina↗

USGS2009

Applications of stable isotopes for regional to national-scale water quality and environmental monitoring programs

Isotopes are a potentially powerful component of monitoring and assessment programs aimed at quantifying and mitigating alterations to environments from human activities. In particular, isotopic techniques have proved useful for tracing sources and sinks of various pollutants in large river basins, wetlands, and airsheds. Many of these studies have been conducted at the regional to national scale by building on existing large-scale water, air, and ecological monitoring programs managed by federal and state agencies, and demonstrate the usefulness of isotopes as a complement to standard chemical and hydrological mass balance methods. This chapter presents an overview of how nitrate, particulate organic matter, and water isotopes can be used to interpret spatial patterns and temporal changes in pollution sources, biogeochemical processes, and ecosystem function in watersheds, at the regional to national scale. Examples from several recent and ongoing studies are presented. From the insights developed using varied sampling strategies and isoscapes, we suggest guidelines for future studies in biologically active and human-impacted rivers.

Book chapter↗