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USGS1995

Preliminary analysis of down-core biotic assemblages Bob Allen Keys, Everglades National Park, Florida Bay

Introduction A series of short piston cores (< 2m) were taken from eleven stations in Florida Bay in May, 1994 by researchers from the U.S. Geological Survey (St. Petersburg, FL., Woods Hole, MA., and Denver CO.) in cooperation with South Florida Water Management District, and the Everglades National Park, and the National Oceanic and Atmospheric Administration (NOAA). Core 6A from Bob Allen Keys (25° 1.391” N, 80°39.41” W) penetrated 172 cm of Holocene sediments in 0.6 m of water on a grass covered mud bank, approximately 1.75 miles (2.82 km) east of the water monitoring station on the southern end of the Bob Allen Keys. Core 6A was sampled for particle size, insoluble residue, water content, loss on ignition, Pb 210 , Rasup>222, and paleontologic analyses. Here we present the results of the preliminary paleontologic analyses of the biotic components from core #6A. The Everglades/Florida Bay ecosystem has formed over the last 5000 years at the southern tip of peninsular Florida. Here it has been influenced by Atlantic, Caribbean and Gulf of Mexico waters, and by tropical and subtropical climatic regimes. This location ensures that over time the ecosystem has undergone climatic changes on both a seasonal and long term basis, and that it has been subjected to many major storms. Additionally, in the last century, the hydrologic regime of the region has been altered profoundly through construction of a canal system to control flooding in southern Florida. This system regulates the timing and amount of freshwater flow into Florida Bay. Recently, algal blooms, seagrass, and sponge die-offs, and declining numbers of shellfish, have been reported in Florida Bay; although it has been assumed that these changes have resulted from human alteration of freshwater flow into the bay, this assumption has not been rigorously tested. The research described here is part of a project designed to examine the history of the Everglades/Florida Bay ecosystem over the last 150 years and to test assumptions of cause and effect. The purpose of the project is two-fold; first, to determine the characteristics of the ecosystem prior to significant human-induced alteration, including the natural range of variation in the ecosystem. This information will establish a baseline for restoration of the system. Second, the project aims to establish the extent, range, and timing of changes to the ecosystem over the last 150 years, and to determine whether these changes correlate with human alteration of the environment, or meteorological patterns, such as precipitation and major storms, or a combination of factors.

Florida↗

USGS2024

Investigating the chemical space coverage of multiple chromatographic and ionization methods using non-targeted analysis on surface and drinking water collected using passive sampling

Multiple non-targeted analysis tools were used to look for a broad range of possible chemical contaminants present in surface and drinking water using liquid chromatography separation and high-resolution mass spectrometry detection, including both quadrupole time of flight (Q-ToF) and Orbitrap instruments. Two chromatographic techniques were evaluated on an LC-Q-ToF with electrospray ionization in both positive and negative modes: (1) the traditionally used reverse phase C18 and (2) the hydrophilic interaction liquid chromatography (HILIC) aimed to capture more polar contaminants that may be present in water. Multiple ionization modes were evaluated with an LC-Orbitrap, including electrospray (ESI) and atmospheric pressure chemical ionization (APCI), also in both positive and negative modes. A suspect screening library of over 1300 possible environmental contaminants, including pesticides, pharmaceuticals, personal care products, illicit drugs/drugs of abuse, and various anthropogenic markers was made with experimentally collected data with the LC-Q-ToF with both column types, with 227 chemicals being retained by the HILIC column. The non-targeted methods using multiple chromatographic and ionization modes were applied to environmental water samples collected with polar organic chemical integrative samplers (POCIS), including surface water upstream and downstream from wastewater effluent discharge, and the downstream drinking water intake and treated drinking water for three distinct sampling events. For the LC-Q-ToF, 442 chemical features were detected on the C18 column and 91 with the HILIC column in the POCIS extracts, while 556 features were found on the Orbitrap workflow by ESI and 131 features detected by APCI. Over 100 chemicals were tentatively identified by suspect screening and database searching. The comprehensive and systematic evaluation of these methods serve as a step in characterizing the chemical space covered when utilizing different chromatography and ionization methods, or different instrument workflows on complex environmental mixtures.

Science of the Total Environment↗

USGS2023

Evaluating drivers of hydrology, water quality, and benthic macroinvertebrates in streams of Fairfax County, Virginia, 2007–18

In 2007, the U.S. Geological Survey partnered with Fairfax County, Virginia, to establish a long-term water-resources monitoring program to evaluate the hydrology, water quality, and ecology of Fairfax County streams and the watershed-scale effects of management practices. Fairfax County uses a variety of management practices, policies, and programs to protect and restore its water resources, but the effects of such strategies are not well understood. This report used streamflow, water-quality, and ecological monitoring data collected from 20 Fairfax County watersheds from 2007 through 2018 to assess the effects of management practices, landscape factors, and climatic conditions on observed nutrient, sediment, salinity, and benthic-macroinvertebrate community responses. Urbanization, climatic variability, and an increase in management practices occurred within Fairfax County during the study period. Impervious cover, housing units, wastewater infrastructure, and (or) stormwater infrastructure increased in most study watersheds. Climatic conditions varied among study years; countywide estimates of average-annual air temperature differed by about 3 degrees Celsius, and total precipitation ranged from about 34 to 63 inches per year. The effects of the management practices, implemented to reduce nitrogen, phosphorus, and (or) sediment loads, are considered in this study. These management practices primarily consist of stormwater retrofits and stream restorations; however, stream restorations account for most of the financial investment and expected load reductions. Management practices were implemented in half of the study watersheds, and most practices were installed and reductions credited late in the study period. Changes in hydrologic response during storm events were evaluated over the study period because many management practices that were implemented were designed to achieve nutrient and sediment reductions by slowing or intercepting runoff. The average number and length of storm events was mostly unchanged throughout the monitoring network. Four watersheds with 10 years of streamflow data showed a mixture of trends in stormflow peak, volume, and rate-of-change. Event-mean nutrient and sediment concentrations from these watersheds were evaluated during storm events and generally showed increases in total phosphorus (TP) and suspended sediment and reductions or no changes in total nitrogen (TN). Landscape inputs of nitrogen and phosphorus and the percentage of inputs delivered to streams were estimated for the study watersheds. Estimated phosphorus from fertilizer and nitrogen from atmospheric deposition represented large nutrient inputs in most watersheds; amounts of other nonpoint sources varied based on land use. Estimated nitrogen inputs declined throughout Fairfax County and in most study watersheds from 2008 through 2018; in comparison, phosphorus input changes were relatively small. Most nonpoint-nutrient inputs were retained on the landscape and did not reach streams, with slightly more nitrogen retention than phosphorus, on average. Retention rates were lower for years with more precipitation and streamflow. After adjusting for streamflow, TN and TP loads were generally higher for years with more nutrient inputs. Calculated as a function of flow-adjusted loads, TP retention declined at most stations from 2009 through 2018, in comparison, TN retention was relatively unchanged. Landscape and climatic conditions affected spatial differences and changes in Fairfax County stream conditions from 2009 through 2018. TN concentrations were higher and increases over time were larger in watersheds with elevated septic-system density. TP concentrations were higher in watersheds with more turfgrass; concentrations were lower, but had larger increases over time, in watersheds with deeper soils. Suspended-sediment concentrations were higher in watersheds with greater stream densities. Specific conductance was higher in watersheds with more developed land use and shallower soils. Benthic-macroinvertebrate index of biotic integrity (IBI) scores were lower in watersheds with high road density and had larger increases over time in bigger, more developed watersheds. Annual variability in TN and TP concentrations and benthic-macroinvertebrate IBI scores was affected by precipitation; annual variability in suspended sediment concentrations and specific conductance was affected by air temperature. After accounting for influences from landscape and climatic conditions, expected management-practice effects were not consistently observed in monitored stream responses. These effects were assessed by comparing expected management-practice load reductions with the timing, direction, and magnitude of changes in storm-event hydrology, nutrient and sediment loads, median-annual water-quality conditions, and benthic-macroinvertebrate IBI scores. An important consideration for future investigations of management-practice effects is how to control for water-quality and ecological variability caused by geologic properties, the urban environment, precipitation, and (or) air temperature. The interpretation of management-practice effects in this report was likely influenced by a combination of factors, including (1) the amount, timing, and location of management-practice implementation; (2) unmeasured landscape and climatic factors; (3) uncertain management-practice expectations; (4) hydrologic variability; and (5) analytical assumptions. Through continued data-collection efforts, particularly after management practices have been completed, many of these factors may become less influential in the future.

Virginia↗

USGS2005

Determination of total mercury in biological and geological samples

The analytical chemist is faced with several challenges when determining mercury in biological and geological materials. These challenges include widespread mercury contamination, both in the laboratory and the environment, possible losses of mercury during sample preparation and digestion, the wide range of mercury values commonly observed, ranging from the low nanogram per gram or per liter for background areas to hundreds of milligrams per kilogram in contaminated or ore-bearing areas, great matrix diversity, and sample heterogeneity1. These factors can be naturally occurring or anthropogenic, but must be addressed to provide a precise and accurate analysis. Although there are many instrumental methods available for the successful determination of mercury, no one technique will address all problems or all samples all of the time. The approach for the determination of mercury used at the U.S. Geological Survey, Crustal Imaging and Characterization Team, Denver Laboratories, utilizes a suite of complementary instrumental methods when approaching a study requiring mercury analyses. Typically, a study could require the analysis of waters, leachates or selective digestions of solids, vegetation, and biological materials such as tissue, bone, or shell, soils, rocks, sediments, coals, sludges, and(or) ashes. No one digestion or sample preparation method will be suitable for all of these matrices. The digestions typically employed at our laboratories include: (i) a closed-vessel microwave method using nitric acid and hydrogen peroxide, followed by digestion/dilution with a nitric acid/sodium dichromate solution, (ii) a robotic open test-tube digestion with nitric acid and sodium dichromate, (iii) a sealed Teflon? vessel with nitric acid and sodium dichromate, (iv) a sealed glass bottle with nitric acid and sodium dichromate, or (v) open test tube digestion with nitric and sulfuric acids and vanadium pentoxide. The common factor in all these digestions is that they are very oxidative to ensure the conversion of all mercury forms into Hg (II). Each method of digestion has its advantages and limitations. The method of detection used in our laboratories involves a combination of an in-house, custom, classic continuous-flow cold-vapor atomic absorption spectrometry (CVAAS), a commercially available, automated, flow-injection and a continuous flow cold-vapor atomic fluorescence spectrometry (CV-AFS) systems, and a relatively new, automated and integrated approach where solid or liquid samples are thermally decomposed under an oxygen atmosphere (a nitrogen atmosphere is used for coals) and the released mercury vapor trapped onto a gold gauze and then thermally released into an AAS system. Other less frequently used instrumental methods available for the determination of mercury include inductively coupled plasma ? optical emission spectrometry (ICP-OES), inductively couple plasma ? mass spectrometry (ICP-MS) (both solution nebulization and laser ablation), and instrumental neutron activation analysis (INAA). Results from two case studies involving the determination of mercury in the challenging matrices of biological materials will be presented. These will include fillet, liver and stomach-content samples from grayling for a baseline/background study in Alaska, and samples of meat tissue and shell material from Tanner crabs from Glacier Bay, Alaska. These studies show that the method of digestion is more important than a very sensitive detection limit for mercury.

Open-File Report↗

USGS2001

Relation of Mercury to Other Chemical Constituents in Ground Water in the Kirkwood-Cohansey Aquifer System, New Jersey Coastal Plain, and Mechanisms for Mobilization of Mercury from Sediments to Ground Water

Water from 265 domestic wells that tap the unconfined Kirkwood-Cohansey aquifer system in the Coastal Plain of New Jersey contained concentrations of mercury that are equal to or exceed the U.S. Environmental Protection Agency maximum contaminant level (MCL) of 2 ug/L (micrograms per liter). The wells range in depth from 50 to 200 feet, and are located in 32 discrete, mostly residential, areas that were developed primarily on former agricultural land during the 1950?s through the 1970?s. Concentrations in two other areas exceeded 1 ug/L. Naturally occurring mercury concentrations in ground water from the Kirkwood-Cohansey aquifer system typically are less than 0.01 ug/L, but concentrations in water from some wells were as much as 42 ug/L. No evidence currently exists that conclusively links known point sources such as landfills, industrial operations, or commercial enterprises to most of the elevated concentrations of mercury in ground water in the residential areas. Possible sources of the mercury include pesticides and atmospheric deposition. Analysis of water from wells in 6 of the 34 areas for other constituents indicates that nitrate concentrations also commonly are elevated above background levels (which typically are undetectable at 0.01 milligrams per liter), and exceed the MCL of 10 milligrams per liter in some samples. Several volatile organic compounds (VOCs), including chloroform, also have been measured in water from wells at many of the 34 sites. Analytical results for water samples collected at several depths from boreholes at 2 of the 34 sites indicate elevated concentrations of calcium, magnesium, barium, strontium, nitrate, and chloride, which may be related to both agricultural chemical applications and septic-system effluent. Determinations of tritium and helium concentrations indicate that water containing elevated concentrations of mercury recharged the aquifer between 9.4 and 79 years ago, which includes the period during which many of the 34 sites were undergoing a change from agricultural or undeveloped to residential land use. Batch equilibrium experiments were used to measure adsorption of dissolved mercury, mercuric chloride, and phenylmercuric acetate by aquifer sediments at pH 3.5-4.0, 4.5-5.0, and 5.5-6.0. In nearly all cases, 55 to 95 percent of the mercury added to the sediments was adsorbed. Mercury mobilization from aquifer sediments inoculated with mercury was investigated by leaching the sediments with two concentrations of nitric acid (a component of acid rain), a sodium chloride solution (simulating road salt), and three fertilizer solutions. A solution of 20-20-20 (nitrogenphosphorous-potassium) fertilizer removed virtually all of the mercury with which the sediments had been inoculated. The sodium chloride solution was moderately effective in removing applied mercury from the sediments, as was a solution of nitric acid. A more dilute nitric acid solution and two sodium nitrate fertilizer solutions were less effective. Results of these experiments indicate that mercury adsorbs to aquifer sediments, but that varying amounts can be removed by infiltrating solutions, some of which can be related to specific land uses. Land-use history at the 34 sites generally indicates a change from agricultural or undeveloped settings to residential settings. Whatever the source of mercury to these sites, a change in the geochemical environment of the soil and aquifer brought about by land-use change probably provides mechanisms for mobilizing the mercury from soils and sediments to ground water.

Water-Resources Investigations Report↗

USGS2004

Accuracy of a pulse-coherent acoustic Doppler profiler in a wave-dominated flow

The accuracy of velocities measured by a pulse-coherent acoustic Doppler profiler (PCADP) in the bottom boundary layer of a wave-dominated inner-shelf environment is evaluated. The downward-looking PCADP measured velocities in eight 10-cm cells at 1 Hz. Velocities measured by the PCADP are compared to those measured by an acoustic Doppler velocimeter for wave orbital velocities up to 95 cm s-1 and currents up to 40 cm s-1. An algorithm for correcting ambiguity errors using the resolution velocities was developed. Instrument bias, measured as the average error in burst mean speed, is -0.4 cm s-1 (standard deviation = 0.8). The accuracy (root-mean-square error) of instantaneous velocities has a mean of 8.6 cm s-1 (standard deviation = 6.5) for eastward velocities (the predominant direction of waves), 6.5 cm s-1 (standard deviation = 4.4) for northward velocities, and 2.4 cm s-1 (standard deviation = 1.6) for vertical velocities. Both burst mean and root-mean-square errors are greater for bursts with ub ??? 50 cm s-1. Profiles of burst mean speeds from the bottom five cells were fit to logarithmic curves: 92% of bursts with mean speed ??? 5 cm s-1 have a correlation coefficient R2 > 0.96. In cells close to the transducer, instantaneous velocities are noisy, burst mean velocities are biased low, and bottom orbital velocities are biased high. With adequate blanking distances for both the profile and resolution velocities, the PCADP provides sufficient accuracy to measure velocities in the bottom boundary layer under moderately energetic inner-shelf conditions.

Journal of Atmospheric and Oceanic Technology↗

USGS2020

The response of stream ecosystems in the Adirondack region of New York to historical and future changes in atmospheric deposition of sulfur and nitrogen

The present-day acid-base chemistry of surface waters can be directly linked to contemporary observations of acid deposition; however, pre-industrial conditions are key to predicting the potential future recovery of stream ecosystems under decreasing loads of atmospheric sulfur (S) and nitrogen (N) deposition. The integrated biogeochemical model PnET-BGC was applied to 25 forest watersheds that represent a range of acid sensitivity in the Adirondack region of New York, USA to simulate the response of streams to past and future changes in atmospheric S and N deposition, and calculate the target loads of acidity for protecting and restoring stream water quality and ecosystem health. Using measured data, the model was calibrated and applied to simulate soil and stream chemistry at all study sites. Model hindcasts indicate that historically stream water chemistry in the Adirondacks was variable, but inherently sensitive to acid deposition. The median model-simulated acid neutralizing capacity (ANC) of the streams was projected to be 55 μeq L −1 before the advent of anthropogenic acid deposition (~1850), decreasing to minimum values of 10 μeq L −1 around the year 2000. The median simulated ANC increased to 13 μeq L −1 by 2015 in response to decreases in acid deposition that have occurred over recent decades. Model projections suggest that simultaneous decreases in sulfate, nitrate and ammonium deposition are more effective in restoring stream ANC than individual decreases in sulfur or nitrogen deposition. However, the increases in stream ANC per unit equivalent decrease in S deposition is greater compared to decreases in N deposition. Using empirical algorithms, fish community density and biomass are projected to increase under several deposition-control scenarios that coincide with increases in stream ANC. Model projections suggest that even under the most aggressive deposition-reduction scenarios, stream chemistry and fisheries will not fully recover from historical acidification by 2200.

New York↗

USGS2026

VegET evapotranspiration for Africa: Continental-scale simulation, multi-product evaluation, and drought assessment

Study region Continental Africa, encompassing diverse climatic zones—tropical, arid, and temperate—and spanning major transboundary river basins such as the Nile, Niger, Congo, Volta, and Zambezi River Basins. The region exhibits pronounced hydroclimatic gradients and heterogeneous land use systems ranging from rainfed croplands and rangelands to dense tropical forests and irrigated schemes. Study focus Actual evapotranspiration (ETa) is a central component of the terrestrial water balance, governing the redistribution of water and energy between the land surface and the atmosphere. Accurate estimation of ETa at continental scale is critical for hydrological monitoring, water resource management, and climate adaptation, as well as for quantifying water, energy, and carbon fluxes that underpin sustainable development. In this study, we applied the agro-hydrologic VegET v2 model to simulate a new, high-resolution, continental-scale ETa dataset for Africa (2000–2021). The model results were benchmarked against four widely used remote sensing-based products—MODIS16 v6.1, SSEBop v6.1, WaPOR v3, and GLEAM v4.1a—across major climate zones, land use types, and River Basins, providing a comprehensive multi-product evaluation of evapotranspiration dynamics across the continent. New hydrological insights for the region Validation against eddy covariance flux tower observations at eight representative sites confirmed that VegET v2 accurately reproduces the seasonal dynamics of observed ETa, achieving a correlation (r) of 0.8 and an RMSE of 25 mm month⁻¹ —accuracy that is comparable to or higher than accuracies of satellite-based products MODIS16, SSEBop, and GLEAM. This study represents one of the first Africa-wide hydrological simulations of ETa, extending the VegET model beyond basin-scale applications. Intercomparisons reveal that VegET aligns closely with MODIS16, SSEBop, and GLEAM in humid and tropical regions (r = 0.80–0.90; RMSE < 20 mm month⁻¹), while greater discrepancies appear in arid and semi-arid zones, where WaPOR tends to overestimate ETa (RMSE ≥ 28 mm month⁻¹). Despite these differences, VegET effectively captures spatial and temporal ETa variability across rainfed croplands, forests, and savannas, supporting its utility in regional water balance assessments, water accounting, and drought monitoring. A key application of VegET v2 is the Evapotranspiration Deficit Index (ETDI), derived by integrating VegET-based ETa with potential evapotranspiration (PET) to quantify water stress. ETDI successfully captured major drought episodes across Africa, including persistent Sahelian and southern African dry spells, the 2020–2021 winter drought in the Maghreb, and the 2018–2019 austral summer drought in southern Africa, while identifying positive anomalies over central Africa indicative of recurrent wetness. These results underscore VegET’s capability as a hydrologically consistent, operational tool for continental ETa monitoring and drought assessment, offering support for basin-scale water balance studies, food security planning, and climate resilience across Africa’s diverse hydrological environments.

Journal of Hydrology: Regional Studies↗

USGS2019

Quantifying the eroded and deposited mass of mercury-contaminated sediment by using terrestrial laser scanning at the confluence of Humbug Creek and the South Yuba River, Nevada County, California, 2011–13

High-resolution, terrestrial laser scanning, also known as ground-based lidar (light detection and ranging), was used to quantify the volume of mercury-contaminated sediment eroded from an outcrop of historical placer-mining debris at the confluence of Humbug Creek and the South Yuba River in the Sierra Nevada foothills, about 17 kilometers northeast of Grass Valley, California, and delivered to a zone below an observed flood stage of the South Yuba River. Substantial quantities of mercury were used and lost to the environment from historical placer gold mining activities on the western slope of the Sierra Nevada, California, and recent studies have documented continued persistence of mercury and methylmercury concentrations in water, sediment, fish, and predatory invertebrates in the Yuba River drainage basin in relation to suspected mercury sources. To identify areas that have high levels of mercury contamination as possible remediation targets in the Yuba River drainage basin and other areas in the Sierra Nevada, the U.S. Geological Survey worked in cooperation with the Bureau of Land Management on this and other detailed studies. Malakoff Diggings, one of the largest hydraulic gold mines in the Sierra Nevada, is 3.5 kilometers north of the study site in the Humbug Creek subbasin. Terrestrial laser scanning was used to produce centimeter-scale, three-dimensional maps of the complex outcrop surface, which was composed of an upper erosional area (cliff and over-steepened slope) and a lower depositional area (colluvial slope). The outcrop could not be mapped non-destructively or in sufficient detail by traditional surveying techniques. The study site, which was approximately 70 meters long, 30 meters wide and 20 meters high, was surveyed four times in 2 years (December 15, 2011; October 25, 2012; January 4, 2013; and November 22, 2013) to determine volumetric differences in the upper erosional and lower depositional areas between surveys. Measured changes in volume for the upper erosional area and lower depositional area were multiplied by the corresponding sediment density so that a mass-balance relationship, between the eroded and deposited sediment during each period, could be used to estimate the amount of mercury-contaminated sediment that was transported to below the base of the colluvial slope, where it could be mobilized by the South Yuba River during a flood having a 5-to-10-year recurrence interval. On December 2, 2012, a flood of this estimated magnitude reached the base of the colluvial slope. Between the first and second surveys (December 15, 2011–October 25, 2012), an estimated mass of 18±9.2 kilograms of sediment was transported from steeper slopes to the gently sloping river bank below the base of the colluvial slope. Between the second and third surveys (October 25, 2012–January 4, 2013), an atmospheric river caused heavy precipitation at the study site during late November and early December 2012. This short-duration, high-intensity rain resulted in a large amount of erosion and deposition at the study site and also caused high streamflow (flood stage) in the South Yuba River. From October 2012 to January 2013, 51±31 kilograms of sediment was transported to below the base of the colluvial slope, that is, below the high-water mark of December 2, 2012. Between the third and fourth surveys (January 4, 2013–November 22, 2013), an additional 10±26 kilograms of sediment was transported to below the base of the colluvial slope. During the 24 months of the study, the total mass of sediment delivered below the base of the colluvial slope and the high-water mark of December 2, 2012, was 79±66 kilograms. In any given year there is a 10–20-percent chance (5-to-10-year recurrence interval) of a flood equal to or greater than that of the December 2, 2012, flood, which could transport mercury-contaminated sediment at the study site into the South Yuba River. Hydraulically modeled estimates of the South Yuba River stage during floods having a 50- and 100-year recurrence interval (2- and 1-percent annual exceedance probability, respectively) indicated that resulting river stages could be 2.2–3.0 meters above the base of the colluvial slope, or 2.2–3.0 meters above the high-water mark of December 2, 2012. Such high river stages would be likely to inundate the lower half of the colluvial slope and mobilize a substantial volume of mercury-contaminated sediment to downstream areas.

California↗

USGS2016

Mercury transformation and release differs with depth and time in a contaminated riparian soil during simulated flooding

Riparian soils are an important environment in the transport of mercury in rivers and wetlands, but the biogeochemical factors controlling mercury dynamics under transient redox conditions in these soils are not well understood. Mercury release and transformations in the Oa and underlying A horizons of a contaminated riparian soil were characterized in microcosms and an intact soil core under saturation conditions. Pore water dynamics of total mercury (HgT), methylmercury (MeHg), and dissolved gaseous mercury (Hg0(aq)) along with selected anions, major elements, and trace metals were characterized across redox transitions during 36 d of flooding in microcosms. Next, HgT dynamics were characterized over successive flooding (17 d), drying (28 d), and flooding (36 d) periods in the intact core. The observed mercury dynamics exhibit depth and temporal variability. At the onset of flooding in microcosms (1–3 d), mercury in the Oa horizon soil, present as a combination of ionic mercury (Hg(II)) bound to thiol groups in the soil organic matter (SOM) and nanoparticulate metacinnabar (b-HgS), was mobilized with organic matter of high molecular weight. Subsequently, under anoxic conditions, pore water HgT declined coincident with sulfate (3–11 d) and the proportion of nanoparticulate b-HgS in the Oa horizon soil increased slightly. Redox oscillations in the intact Oa horizon soil exhausted the mobile mercury pool associated with organic matter. In contrast, mercury in the A horizon soil, present predominantly as nanoparticulate b-HgS, was mobilized primarily as Hg0(aq) under strongly reducing conditions (5–18 d). The concentration of Hg0(aq) under dark reducing conditions correlated positively with byproducts of dissimilatory metal reduction (P(Fe,Mn)). Mercury dynamics in intact A horizon soil were consistent over two periods of flooding, indicating that nanoparticulate b-HgS was an accessible pool of mobile mercury over recurrent reducing conditions. The concentration of MeHg increased with flooding time in both the Oa and A horizon pore waters. Temporal changes in pore water constituents (iron, manganese, sulfate, inorganic carbon, headspace methane) all implicate microbial control of redox transitions. The mobilization of mercury in multiple forms, including HgT associated with organic matter, MeHg, and Hg0(aq), to pore waters during periodic soil flooding may contribute to mercury releases to adjacent surface waters and the recycling of the legacy mercury to the atmosphere.

Tennessee↗

USGS2011

Mountain Glaciers and Ice Caps

In addition to the Greenland Ice Sheet, the Arctic contains a diverse array of smaller glaciers ranging from small cirque glaciers to large ice caps with areas up to 20 000 km 2 . Together, these glaciers cover an area of more than 400 000 km 2 , over half the global area of mountain glaciers and ice caps. Their total volume is sufficient to raise global sea level by an average of about 0.41 m if they were to melt completely. These glaciers exist in a range of different climatic regimes, from the maritime environments of southern Alaska, Iceland, western Scandinavia, and Svalbard, to the polar desert of the Canadian Arctic. Glaciers in all regions of the Arctic have decreased in area and mass as a result of the warming that has occurred since the 1920s (in two pulses – from the 1920s to the 1940s and since the mid-1980s). A new phase of accelerated mass loss began in the mid-1990s, and has been most marked in Alaska, the Canadian Arctic, and probably Greenland. Current rates of mass loss are estimated to be in the range 150 to 300 Gt/y; comparable to current mass loss rates from the Greenland Ice Sheet. This implies that the Arctic is now the largest regional source of glacier contributions to global sea-level rise. Most of the current mass loss is probably attributable to a change in surface mass balance (the balance between annual mass addition, primarily by snowfall, and annual mass loss by surface melting and meltwater runoff). Iceberg calving is also a significant source of mass loss in areas such as coastal Alaska, Arctic Canada, Svalbard, and the Russian Arctic. However, neither the current rate of calving loss nor its temporal variability have been well quantified in many regions, so this is a significant source of uncertainty in estimates of the total rate of mass loss. It is, however, clear that the larger Arctic ice caps have similar variability in ice dynamics to that of the Greenland Ice Sheet. That is to say, areas of relatively slow glacier flow (which terminate mainly on land) are separated by faster-flowing outlet glaciers (which terminate mainly in the ocean). Several of these outlet glaciers exhibit surge-type behavior, while others have exhibited substantial velocity changes on seasonal and longer timescales. It is very likely that these changes in ice dynamics affect the rate of mass loss by calving both from individual glaciers and the total ice cover. Projections of future rates of mass loss from mountain glaciers and ice caps in the Arctic focus primarily on projections of changes in the surface mass balance. Current models are not yet capable of making realistic forecasts of changes in losses by calving. Surface mass balance models are forced with downscaled output from climate models driven by forcing scenarios that make assumptions about the future rate of growth of atmospheric greenhouse gas concentrations. Thus, mass loss projections vary considerably, depending on the forcing scenario used and the climate model from which climate projections are derived. A new study in which a surface mass balance model is driven by output from ten general circulation models (GCMs) forced by the IPCC (Intergovernmental Panel on Climate Change) A1B emissions scenario yields estimates of total mass loss of between 51 and 136 mm sea-level equivalent (SLE) (or 13% to 36% of current glacier volume) by 2100. This implies that there will still be substantial glacier mass in the Arctic in 2100 and that Arctic mountain glaciers and ice caps will continue to influence global sea-level change well into the 22nd century.

Book chapter↗

USGS2022

Soil carbon consequences of historic hydrologic impairment and recent restoration in coastal wetlands

Coastal wetlands provide key ecosystem services, including substantial long-term storage of atmospheric CO2 in soil organic carbon pools. This accumulation of soil organic matter is a vital component of elevation gain in coastal wetlands responding to sea-level rise. Anthropogenic activities that alter coastal wetland function through disruption of tidal exchange and wetland water levels are ubiquitous. This study assesses soil vertical accretion and organic carbon accretion across five coastal wetlands that experienced over a century of impounded hydrology, followed by restoration of tidal exchange 5 to 14 years prior to sampling. Nearby marshes that never experienced tidal impoundment served as controls with natural hydrology to assess the impact of impoundment and restoration. Dated soil cores indicate that elevation gain and carbon storage were suppressed 30–70 % during impoundment, accounting for the majority of elevation deficit between impacted and natural sites. Only one site had substantial subsidence, likely due to oxidation of soil organic matter. Vertical and carbon accretion gains were achieved at all restored sites, with carbon burial increasing from 96 ± 33 to 197 ± 64 g C m −2 y −1 . The site with subsidence was able to accrete at double the rate (13 ± 5.6 mm y −1 ) of the natural complement, due predominantly to organic matter accumulation rather than mineral deposition, indicating these ecosystems are capable of large dynamic responses to restoration when conditions are optimized for vegetation growth. Hydrologic restoration enhanced elevation resilience and climate benefits of these coastal wetlands.

Massachusetts↗

USGS2000

Detection of crystalline hematite mineralization on Mars by the Thermal Emission Spectrometer: evidence for near-surface water

The Thermal Emission Spectrometer (TES) instrument on the Mars Global Surveyor (MGS) mission has discovered a remarkable accumulation of crystalline hematite (α-Fe 2 O 3 ) that covers an area with very sharp boundaries approximately 350 by 350–750 km in size centered near 2°S latitude between 0° and 5°W longitude (Sinus Meridiani). Crystalline hematite is uniquely identified by the presence of fundamental vibrational absorption features centered near 300, 450, and >525 cm −1 and by the absence of silicate fundamentals in the 1000 cm −1 region. Spectral features resulting from atmospheric CO 2 , dust, and water ice were removed using a radiative transfer model. The spectral properties unique to Sinus Meridiani were emphasized by removing the average spectrum of the surrounding region. The depth and shape of the hematite fundamental bands show that the hematite is crystalline and relatively coarse grained (>5–10 μm). Diameters up to and greater than hundreds of micrometers are permitted within the instrumental noise and natural variability of hematite spectra. Hematite particles <5–10 μm in diameter (as either unpacked or hard-packed powders) fail to match the TES spectra. The spectrally derived areal abundance of hematite varies with particle size from ∼10% (>30 μm diameter) to 40–60% (10 μm diameter). The hematite in Sinus Meridiani is thus distinct from the fine-grained (diameter <5–10 μm), red, crystalline hematite considered, on the basis of visible, near-IR data, to be a minor spectral component in Martian bright regions like Olympus-Amazonis. Sinus Meridiani hematite is closely associated with a smooth, layered, friable surface that is interpreted to be sedimentary in origin. This material may be the uppermost surface in the region, indicating that it might be a late stage sedimentary unit or a layered portion of the heavily cratered plains units. We consider five possible mechanisms for the formation of coarse-grained, crystalline hematite. These processes fall into two classes depending on whether they require a significant amount of near-surface water: the first is chemical precipitation that includes origin by (1) precipitation from standing, oxygenated, Fe-rich water (oxide iron formations), (2) precipitation from Fe-rich hydrothermal fluids, (3) low-temperature dissolution and precipitation through mobile ground water leaching, and (4) formation of surface coatings, and the second is thermal oxidation of magnetite-rich lavas. Weathering and alteration processes, which produce nanophase and red hematite, are not consistent with the coarse, crystalline hematite observed in Sinus Meridiani. We prefer chemical precipitation models and favor precipitation from Fe-rich water on the basis of the probable association with sedimentary materials, large geographic size, distance from a regional heat source, and lack of evidence for extensive groundwater processes elsewhere on Mars. The TES results thus provide mineralogic evidence for probable large-scale water interactions. The Sinus Meridiani region may be an ideal candidate for future landed missions searching for biotic and prebiotic environments, and the physical characteristics of this site satisfy all of the engineering requirements for the missions currently planned.

Journal of Geophysical Research E: Planets↗

USGS2025

River-to-lake transitional areas contribute disproportionately to in-lake nutrient loading

River-to-lake transitional areas are biogeochemically active sections of the aquatic continuum that are often understudied compared to their adjoining environments. Internal nutrient loading from river-to-lake transitional areas may be a considerable source of nutrients to lakes and if overlooked disconnect upstream management initiatives from in-lake improvements. To contextualize internal nutrient loading by river-to-lake sediments, we conducted sediment core incubations and nutrient assays at 3 time points over a field season from a major contributing tributary of Lake Erie. Using statistical and spatial interpolation models, we upscaled internal nitrogen and phosphorus loading rates across the highly impaired mouth of the Maumee River, which drains into the western basin of Lake Erie. We found that internal nutrient dynamics in this river-to-lake transitional area were regulated by spatial differences in the physical composition and nutrient and organic matter contents of sediments. The Maumee river-to-lake transitional area was largely a source of phosphorus and ammonium nitrogen and a sink of nitrate nitrogen through high denitrification rates. Yet, we observed substantial temporal variation whereby internal nutrient loading was greatest in late summer coinciding with near-zero denitrification. Sediments at this time could contribute an additional ~17% more soluble reactive phosphorus and ~3% more total kjeldahl nitrogen in the bioavailable ammonium nitrogen fraction relative to the daily external nutrient load. High internal nutrient loading rates compared to more offshore areas in western Lake Erie suggest that this degraded river-to-lake transitional area has a disproportional biogeochemical significance and a high potential to contribute to nearshore water quality issues.

Ohio↗

USGS2024

Monitoring marine eruptions

Introduction Submarine volcanoes produce much of the same seismicity and eruptive activity as subaerial volcanoes and can pose hazards to society. Although they can be monitored with similar techniques and methods as described in other chapters of this volume, their submerged location brings unique challenges. This chapter addresses these challenges and provides recommendations for monitoring volcanoes fully or partly in marine environments to meet the capabilities described in other chapters of this volume. The United States and its territories host dozens of submarine volcanoes with most (around 60) in the Commonwealth of the Northern Mariana Islands. Approximately 20 of the Northern Mariana Islands submarine volcanoes are known to be hydrothermally active, and 10 have confirmed eruptions since the 1950s (for example, Baker and others, 2008; Tepp and others, 2019a). Nine of those volcanoes were considered by the National Volcanic Threat Assessment (Ewert and others, 2018) to have a combination of eruptive type and summit depth that poses a higher risk of hazardous eruptions, although only one was listed as a moderate (level 3) threat. Other notable submarine volcanoes of interest to the United States that have historically erupted are Axial Seamount off the Washington State coast, Kamaʻehuakanaloa in Hawaiʻi, and Vailuluʻu seamount in American Samoa. All of these, however, have a low risk of hazards because of their depth (greater than 600 meters below sea level) and eruptive type and so are not included in the National Volcanic Threat Assessment. In addition to submarine volcanoes, the submerged flanks of island volcanoes can also be a source of hazardous submarine eruptions—for example, the 1877 eruption of Mauna Loa, Hawai‘i, in Kealakekua Bay (Wanless and others, 2006). The most notable submarine eruption in recent times was the 2022 eruption of Hunga Tonga–Hunga Haʻapai in Tonga, which was one of the largest eruptions on Earth in the past 100 years. It created a massive volcanic plume, unprecedented shock waves, and far-reaching tsunami (Lynett and others, 2022). Other recent submarine eruptions in the Pacific Ocean Basin have produced subaerial plumes that reached aircraft heights (Carey and others, 2014) and large pumice rafts that can affect marine traffic and harbors (for example, Jutzeler and others, 2014; Kornei, 2019). These examples illustrate the potential hazards of major submarine eruptions. Yet, submarine volcanoes are largely unmonitored, and many eruptions occur that are unnoticed or only identified hours or days afterward. Within U.S. territory, submarine volcanoes in the Northern Mariana Islands have been known to produce eruptive activity that can affect society. Reports from fishermen and other marine vessels in the Northern Mariana Islands have noted underwater explosions, sea-surface discoloration, and bubbling water, all of which are known to be signs of submarine volcanic activity. South Sarigan seamount, located about 160 kilometers (km) north of Saipan, erupted in 2010 from greater than 150 meters below the sea surface, resulting in a gas and ash plume that reached more than 11.9 km into the atmosphere (for example, Searcy, 2013; Embley and others, 2014), high enough to affect international air traffic. Precursory and co-eruptive seismicity was detected on the regional Northern Mariana Islands seismic network (Searcy, 2013) and on global monitoring instruments (Green and others, 2013). Monitoring of submarine volcanoes is best accomplished with marine-based instrumentation, which is also useful for monitoring small island volcanoes that may not have the land area necessary for comprehensive subaerial monitoring. The primary marine-based instrumentation used for submarine volcanoes includes ocean-bottom pressure sensors to assess sea-floor deformation, ocean-bottom seismometers (OBSs) to detect seismicity, and both moored and ocean-bottom hydrophones to detect submarine explosions. Other sensors offer important monitoring data, such as turbidity, temperature, and chemistry of hydrothermal emissions. Marine-based instruments are typically deployed in campaign-style networks with no real-time telemetry owing to cost considerations and technical limitations. However, when necessary, marine instruments can be operated in real time using cables to transmit data to land-based facilities; other technologies for this purpose are in use or in development, such as acoustic transmission from the instrument to a moored buoy (Matsumoto and others, 2016) and a winch-based system with a satellite antenna that is part of the instrument mooring (Matsumoto and others, 2019). Emerging technologies for marine-based monitoring may be considered as part of a future monitoring plan. These technologies include ocean gliders and floats with on-board hydrophones that have been used to record earthquakes and submarine eruptions (for example, Matsumoto and others, 2013; Sukhovich and others, 2015) and fiber-optic cables that have been used as strainmeters to detect earthquakes (for example, Marra and others, 2018; Lindsey and others, 2019). Land-based instruments and satellites can also provide some capability for monitoring submarine volcanoes, but they provide more limited observations than marine-based instrumentation.

Scientific Investigations Report↗

USGS2025

Insights and strategic opportunities from the USGS 2024 Per- and Polyfluoroalkyl Substances (PFAS) Interagency Workshop

Introduction In 2021, the U.S. Geological Survey (USGS) published Circular 1490 titled, “Integrated Science for the Study of Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS) in the Environment: A Strategic Science Vision for the U.S. Geological Survey” (Tokranov and others, 2021). Circular 1490 was created to be a resource for USGS scientists prioritizing and planning research related to per- and polyfluoroalkyl substances (PFAS) and to be a guide for developing partnerships with other scientists, State and Federal agencies, and stakeholders engaged in PFAS research and management and mitigation of the environmental and human-health effects of PFAS. This USGS PFAS Strategic Science Vision document was intended to be the foundation for a “living strategic vision,” periodically providing updates on the state of USGS PFAS research, emerging PFAS data gaps and needs, and progress on interagency and stakeholder PFAS partnerships and priorities. To meet this objective, the USGS planned to host an Interagency and Stakeholder PFAS Workshop every 2–3 years. During September 10–12, 2024, the USGS hosted the first Interagency and Stakeholder PFAS Workshop in Reston, Virginia. The Workshop brought together experts from other Federal agencies (U.S. Environmental Protection Agency, National Institute of Environmental Health Sciences, Food and Drug Administration, Department of Defense [Air Force, Army]), State agencies (Washington Fish and Wildlife, Virginia Department of Transportation), and academia (Harvard University, University of Maryland) to address key challenges relating to the measurement and modeling of PFAS and the implications for environmental health. Participants engaged in in-depth discussions centered around six pivotal topics related to PFAS: (1) sampling protocols, methods and interpretation; (2) environmental sources, source apportionment, and occurrence; (3) environmental fate and transport; (4) human and wildlife exposure routes and risk; (5) bioconcentration, bioaccumulation, and biomagnification; and (6) ecotoxicology and effects. Each topic had three breakout sessions. A recurrent theme of workshop discussions was how data on a nationwide scale for PFAS occurrence in various environmental matrices, including air, water, food crops, biota, soil, and streambed sediment could help to advance scientific understanding. Participants noted significant geospatial data gaps, particularly in the midwestern and southern United States and the Pacific Northwest. PFAS data collection tends to be more robust along the eastern seaboard and in California. Participants stressed how enhancing the integration of large and small datasets across various agencies could help to support national scale understanding of PFAS. To address these gaps, attendees suggested leveraging datasets from Federal entities like the USGS and the U.S. Department of Defense, State agencies, and municipal utility services to develop predictive contaminant detection and transport models. Improved coordination between water quality programs and USGS research could help to facilitate access to valuable data, leading to comprehensive databases that inform PFAS point (wastewater treatment plants and landfills) and nonpoint (runoff from land, atmospheric deposition, food packaging) sources, environmental transport mechanisms, environmental detection and concentrations, potential exposure routes, and health effects on different biota, including humans. A specific request was made to develop a map demarking the depth of modern (1953 or later) groundwater, which is susceptible to surface-derived anthropogenic (that is, human-made) contamination, based on tritium-age dating. Emphasis was placed on incorporation of hydrology, groundwater flow paths, groundwater–surface water interactions, and landscape factors in predictive statistical models as a step to improve contaminant source identification and tracking. Molecular fingerprinting approaches garnered attention as techniques to link specific PFAS mixtures detected in a sample to environmental sources and levels in biota (Dávila-Santiago and others, 2022). Integrating data from abiotic (that is, water, soil, and air) and biotic (that is, living organisms) systems identified as a research opportunity. For example, understanding the composition of soils and sediments, which include a mixture of mineral, plant, and animal components, could advance understanding of exposure pathways. The discussions highlighted opportunities to explore and understand the potential redistribution and biotic exposures of PFAS from biosolid and wastewater treatment plant effluent land application practices, in addition to atmospheric releases and discharges from landfill and wastewater treatment plants. Participants identified research gaps surrounding how these sources may contribute to contamination and may affect surrounding ecosystems, including a better definition of anthropogenic background concentrations. Moving forward, the collection of co-occurrence data was noted as a means to improve understanding of complex mixtures and to leverage companion modeling efforts focused on areas with high and low contamination levels to identify areas of concern and unaffected resources. Participants emphasized how centralized USGS databases and the establishment of sample-metadata archives can help to ensure that samples are preserved and accessible for future research. In conclusion, the workshop participants identified opportunities to bridge data gaps and improve measurement techniques, modeling frameworks, databases, and communication, to enhance the understanding of PFAS and their effects on environmental and human health. Upon completion of the workshop, participants indicated an interest in developing strategic data collection, modeling, and analytical approaches to address these challenges.

Open-File Report↗

USGS2016

Mercury risk to avian piscivores across western United States and Canada

The widespread distribution of mercury (Hg) threatens wildlife health, particularly piscivorous birds. Western North America is a diverse region that provides critical habitat to many piscivorous bird species, and also has a well-documented history of mercury contamination from legacy mining and atmospheric deposition. The diversity of landscapes in the west limits the distribution of avian piscivore species, complicating broad comparisons across the region. Mercury risk to avian piscivores was evaluated across the western United States and Canada using a suite of avian piscivore species representing a variety of foraging strategies that together occur broadly across the region. Prey fish Hg concentrations were size-adjusted to the preferred size class of the diet for each avian piscivore (Bald Eagle = 36 cm, Osprey = 30 cm, Common and Yellow-billed Loon = 15 cm, Western and Clark's Grebe = 6 cm, and Belted Kingfisher = 5 cm) across each species breeding range. Using a combination of field and lab-based studies on Hg effect in a variety of species, wet weight blood estimates were grouped into five relative risk categories including: background (< 0.5 μg/g), low (0.5–1 μg/g), moderate (1–2 μg/g), high (2–3 μg/g), and extra high (> 3 μg/g). These risk categories were used to estimate potential mercury risk to avian piscivores across the west at a 1 degree-by-1 degree grid cell resolution. Avian piscivores foraging on larger-sized fish generally were at a higher relative risk to Hg. Habitats with a relatively high risk included wetland complexes (e.g., prairie pothole in Saskatchewan), river deltas (e.g., San Francisco Bay, Puget Sound, Columbia River), and arid lands (Great Basin and central Arizona). These results indicate that more intensive avian piscivore sampling is needed across Western North America to generate a more robust assessment of exposure risk.

Science of the Total Environment↗

USGS2016

Estimating mercury emissions resulting from wildfire in forests of the Western United States

Understanding the emissions of mercury (Hg) from wildfires is important for quantifying the global atmospheric Hg sources. Emissions of Hg from soils resulting from wildfires in the Western United States was estimated for the 2000 to 2013 period, and the potential emission of Hg from forest soils was assessed as a function of forest type and soil-heating. Wildfire released an annual average of 3100 ± 1900 kg-Hg y − 1 for the years spanning 2000–2013 in the 11 states within the study area. This estimate is nearly 5-fold lower than previous estimates for the study region. Lower emission estimates are attributed to an inclusion of fire severity within burn perimeters. Within reported wildfire perimeters, the average distribution of low, moderate, and high severity burns was 52, 29, and 19% of the total area, respectively. Review of literature data suggests that that low severity burning does not result in soil heating, moderate severity fire results in shallow soil heating, and high severity fire results in relatively deep soil heating (< 5 cm). Using this approach, emission factors for high severity burns ranged from 58 to 640 μg-Hg kg-fuel − 1 . In contrast, low severity burns have emission factors that are estimated to be only 18–34 μg-Hg kg-fuel − 1 . In this estimate, wildfire is predicted to release 1–30 g Hg ha − 1 from Western United States forest soils while above ground fuels are projected to contribute an additional 0.9 to 7.8 g Hg ha − 1 . Land cover types with low biomass (desert scrub) are projected to release less than 1 g Hg ha − 1 . Following soil sources, fuel source contributions to total Hg emissions generally followed the order of duff > wood > foliage > litter > branches.

Science of Total Environment↗