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Kate Wilkins

Publications and source records attributed to Kate Wilkins.

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Tracking the sources of metals to the San Juan River, Four Corners Region, USA: An introduction to the thematic issue

Surface water quantity and quality is important for arid and semi-arid regions where many people, including underserved and Indigenous communities, rely on a scarce resource for drinking water, irrigation, livestock and ceremonial uses. The southwestern United States, and specifically the Four Corners Region (Colorado, Arizona, New Mexico and Utah), is an example of this situation. Elevated concentrations of metals including aluminium, arsenic and lead were identified in previous studies and this study in the San Juan River from below the Navajo Dam, through the Navajo Nation to Mexican Hat, Utah. An interdisciplinary team applied approaches and principles of geology, geochemistry, geomorphology, hydrology and statistics to gain a better understanding of the tributaries supplying the source(s) of metals to the San Juan River. This introductory paper provides an overview of the ‘Metal geochemical fingerprinting to identify sub-watershed source contributions to surface water at a regional arid watershed scale, Four Corners Region, USA’ thematic collection . An overview of sampling sites, techniques and potential sources of metals is provided. Approaches used in this study could be applied to investigations in similar systems globally.

Four Corners region

Assessment of per- and polyfluoroalkyl substances in water resources of New Mexico, 2020–21

Per- and polyfluoroalkyl substances (PFAS) have been detected in public and private drinking-water wells, springs, and surface waters in New Mexico; however, the presence and distribution of PFAS in water resources across the State are not well characterized. From August 2020 to October 2021, the U.S. Geological Survey, in cooperation with the New Mexico Environment Department, collected water-quality samples from groundwater and surface-water sites throughout New Mexico. One hundred and seventeen groundwater wells were sampled from unconfined water-table aquifers for PFAS and a geochemical suite including major ions, trace elements, nutrients, dissolved organic carbon (DOC), stable isotopes of oxygen and hydrogen, tritium, and carbon-14 to provide context for groundwater age and geochemical evolution. Eighteen surface-water samples were analyzed for PFAS, and select samples were analyzed for wastewater tracers, major ions, trace elements, and DOC. Blanks and replicates indicated low bias and variability for PFAS, wastewater tracers, and geochemical compounds. Twenty-seven of the 117 groundwater sites had PFAS concentrations reported above the detection level, and there were no exceedances of the 2016 U.S. Environmental Protection Agency health advisory of 70 nanograms per liter (ng/L) perfluorooctanoic acid plus perfluorooctane sulfonic acid. Twenty-two sites were resampled and showed similar signatures, excluding some springs. Total PFAS concentrations ranged from 0.91 to 80.3 ng/L. The most frequently detected PFAS at groundwater sites were perfluorobutanesulfonic acid (PFBS; 11 sites), perfluoropentanoic acid (10 sites), and perfluorohexanoic acid (9 sites). Correlations were found between certain PFAS compounds that suggest similar sources. PFAS were also correlated with tritium, DOC, and nitrate, which indicated that a presence of anthropogenic compounds could in turn indicate a likelihood of PFAS occurrence. In addition, a cluster analysis showed that varying geochemical processes and sources of anthropogenic compounds likely contribute to the PFAS signature of each groundwater sample. Surface-water samples showed variable total PFAS concentrations ranging from 1.0 to 155.4 ng/L. Sites downstream from urban areas showed numerous PFAS detections. Some undeveloped areas where minimal PFAS detections would be expected had PFAS detections. Correlations between PFAS were found that suggested similar sources. Perfluoropentanoic acid and PFBS were the most frequently detected PFAS, and PFBS had the highest single concentration of 93 ng/L. Results of the study provide an overview of PFAS occurrences in the water resources of New Mexico along with geochemical context and are used to identify areas for further scientific investigations that could further characterize PFAS occurrences in New Mexico.

New Mexico

Assessing Escherichia coli and microbial source tracking markers in the Rio Grande in the South Valley, Albuquerque, New Mexico, 2020–21

The Rio Grande, in southern Albuquerque, New Mexico, is a Clean Water Act Section 303(d) Category 5 impaired reach for Escherichia coli ( E. coli ). The reach is 5 miles in length, extending from Tijeras Arroyo south to the Isleta Pueblo boundary. An evaluation of E. coli and microbial source tracking markers (human-, canine-, and waterfowl-specific sources) was conducted by the U.S. Geological Survey to determine the extent and source of fecal bacteria within the impaired reach of the Rio Grande, primarily during the dry season (November through June) in 2020 and 2021. Samples were collected in the river cross section at three locations within each site and collected during both the dry season and the wet season, thereby providing data over a range of flow conditions to better understand the extent and source of fecal bacteria. Because fecal microorganisms may readily attach to sediments, riverbed material samples were also collected. During the dry season, E. coli concentrations in water were primarily detected below the New Mexico Surface Water Quality Standard of 410 colony forming units per 100 milliliters and mostly human and canine sources were detected. However, approximately 40 percent of the water samples exceeded the Isleta Pueblo water quality standard of 88 colony forming units per 100 milliliters. E. coli concentrations in bed material were detected at low concentrations, and the bed material was a sandy substrate, with little fine-grained material, a suitable habitat that would allow for bacterial growth during the dry season. Significant spatial and temporal differences, where p-values were less than 0.05, were found in water-quality samples for E. coli (seasonal) and the human tracker concentrations (between sites and within a cross section of a site). Given the lack of correlation between discharge and E. coli concentration and the human marker being most prevalent in the study area, the sources of E. coli in the dry season are likely nonpoint sources. The results from this study will help decision makers determine the efficacy of their best management practices and guide new practices to improve water quality in the reach.

New Mexico

Comparison of passive and pumped sampling methods for analysis of groundwater quality, Kirtland Air Force Base, Albuquerque, New Mexico, 2019

A plume of ethylene dibromide (EDB) dissolved in groundwater extends northeast from the Bulk Fuels Facility on Kirtland Air Force Base, New Mexico. The leading edge of the EDB plume is upgradient from several water-supply wells. In 2013, the U.S. Geological Survey (USGS), in cooperation with the Albuquerque Bernalillo County Water Utility Authority and the U.S. Air Force, installed four sentinel well nests and two aquifer-test pumping wells between the EDB plume and the water-supply wells to serve as an early warning if the plume travels toward the water-supply wells. Since 2015, the USGS has used submersible pumps to sample the sentinel wells quarterly. In February 2017, the USGS began using dual-membrane passive diffusion bag samplers for quarterly sampling in the wells. To ensure that the passive samplers are obtaining representative samples of the groundwater contaminants, the USGS, in cooperation with the U.S. Air Force, initiated a study in 2019 to compare results from pump sampling and passive samplers and to use vertical profiling to determine the optimal depth for passive sampler placement in the screened interval to better inform long-term monitoring of the site. Vertical profiling included deploying passive samplers throughout the submerged screened interval of four shallow sentinel wells. After retrieval of the passive samplers, pump samples were collected. The results of analyses of both types of samples were compared. Volatile organic compound results for this study were all below the raised reporting levels, which is a level five times the maximum concentration detected in a blank and determined by an in-depth quality assessment; therefore, this study focused on inorganic constituent results, including major ions, trace elements, and stable isotopes of water, to calculate the relative percent difference (RPD) between the pump and passive sampling method results as a way to determine where passive samplers would be best placed in each of the wells. Several analytes had an RPD of more than plus or minus 50 percent, and several analytes were not within the estimated variability for each sampling method. Additionally, the variability within each sampling method was quantified and compared. Factors that likely contributed to the lack of comparison between each sampling method included temporal variability, flow regime, volume of sample integrated through different aquifer intervals, and reduction/oxidation processes. RPD and method variability were used to determine the intervals within each well with the greatest agreement between sampling methods. Optimal sampling depths for each well were then correlated to the intervals where quarterly sampling has been occurring.

New Mexico