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James B. Shanley

Publications and source records attributed to James B. Shanley.

At least 19 recordsLinked to original sources
USGS2026

Multiple lines of evidence reveal rapid, seasonal watershed responses to enhanced weathering

Enhanced weathering accelerates carbon dioxide removal from the atmosphere through the rapid dissolution of land amendments of crushed, cation-rich rocks. The export of enhanced weathering dissolution products to drainage networks has important implications for carbon dioxide removal durability and measurement yet has received little attention. Here we observe rapid and pronounced streamwater chemistry responses within weeks of a crushed basalt application to a temperate headwater catchment: alkalinity exceeded counterfactual estimates by as much as 557 μeq l −1 , accompanied by changes in silica, lithium and major-ion chemistry consistent with basalt weathering. Difference-in-differences analysis identified repeated treatment effects with enhanced weathering accounting for 7–17% of streamwater alkalinity in successive summers and autumns, but less in winter and spring. This seasonal response reflects a combination of temperature controls on basalt dissolution kinetics and hydrologic controls on weathering-product export. Over 2 years, 9.5–11% of theoretical carbon dioxide removal potential was exported as alkalinity (34.7 t CO 2 km −2 yr −1 ).

Vermont↗
USGS2026

Potential warming-induced changes in stream water sources between proglacial and non-glacial streams, south-central Alaska

Snow and ice-melt are essential for global water resources. Rising air temperatures are causing vegetation encroachment and shrubification of previously snow- and ice-covered landscapes, and precipitation regimes are changing. Collectively, these changes will likely affect the hydrology of mountain environments, although the exact ways in which the hydrology will change are poorly understood. Changing source waters (i.e., the proportion of ice-melt, snowmelt, rain and groundwater) affect the timing and magnitude of streamflow and affect stream temperature, sediment, solute and nutrient fluxes. We investigate spatial and seasonal source water contributions across sub-watersheds of the Nellie Juan River watershed on Alaska's Kenai Peninsula, which differ in glacier cover, elevation and land cover, using a space-for-time approach. To do so, we use a three-endmember mixing model to quantify the contribution of rain, snow/ice-melt and deep groundwater. We show that snow/ice-melt peak later in proglacial streams compared to non-glacial streams. Endmember contributions in non-glacial streams generally vary with elevation and season. We also found that groundwater is a major contributor to streamflow across the study area, contributing between 12% and 47% seasonally, and may become increasingly important as snowpack and ice-melt decrease. This research characterises the shift from a glacierised to a deglaciating landscape through the lens of source water contribution. Broadly, these findings could help improve understanding of how water resources in glacierised watersheds are affected by warming air temperatures.

Alaska↗
USGS2025

Seasonal synchronicity and multi-decadal stability of headwater biogeochemistry in the northern temperate zone

Temporal patterns in chemistry of headwater streams reflect responses of water and elemental cycles to perturbations occurring at local to global scales. We evaluated multi-scale temporal patterns in up to 32 y of monthly observations of stream chemistry (ammonium, calcium, dissolved organic carbon, nitrate, total dissolved phosphorus, and sulfate) in 22 reference catchments within the northern temperate zone of North America. Multivariate autoregressive state-space (MARSS) models were applied to quantify patterns at multi-decadal, seasonal, and shorter intervals during a period that encompassed warming climate, seasonal changes in precipitation, and regional declines in atmospheric deposition. Significant long-term trends in solute concentrations within a subset of the catchments were consistent with recovery from atmospheric deposition (e.g., calcium, nitrate, sulfate) and increased precipitation (e.g., dissolved organic carbon). Lack of evidence for multi-decadal trends in most catchments suggests resilience of northern temperate ecosystems or that subtle net effects of simultaneous changes in climate and disturbance regimes do not result in directional trends. Synchronous seasonal oscillations of solute concentrations occurred across many catchments, reflecting shared climate and biotic drivers of seasonality within the northern temperate zone. Despite shared patterns among catchments at a seasonal scale, multi-scale temporal patterns were statistically distinct among even adjacent headwater catchments, implying that local attributes of headwater catchments modify the signals imparted by atmospheric phenomena and regional disturbances. To effectively characterize hydrologic and biogeochemical responses to changing climate and disturbance regimes, catchment monitoring programs could include multiple streams with contributing areas that encompass regional heterogeneity in vegetation, topography, and elevation. Overall, detection of long-term patterns and trends requires monitoring multiple catchments at a frequency that captures periodic variation (e.g., seasonality) and a duration encompassing the perturbations of interest.

Biogeochemistry↗
USGS2025

Assessing and enhancing national water model streamflow predictions for montane catchments in the northeastern United States

This study evaluates National Water Model (NWM) performance in low-order montane catchments across the northeastern United States by comparing retrospective simulations to measured observations. To address deficiencies, we develop a machine learning (ML) correction model for selected sites using LightGBM, a different approach from conventional bias correction methods. Montane, low-order streams play a crucial role in water quality and flood generation but pose challenges for streamflow prediction and are under-represented in the national streamgaging network. NWM provides streamflow forecasts across the United States; yet a focused assessment of its performance in these settings has not been comprehensively undertaken. Results indicate NWM performance varied seasonally, with the best performance during the fall and particularly poor performance during snowmelt, spring runoff, and high flow events, with a tendency towards flow underestimation. The ML correction model markedly improved hourly streamflow prediction accuracy based on continuous time series and runoff event-based metrics. Including antecedent water level measurements as input, even from distant sites, greatly improved model performance, demonstrating the potential to improve predictions by deploying supplemental low-cost water level sensors. We demonstrate that NWM performance can be improved in these complex watersheds using ML tools. This approach could be implemented elsewhere to improve NWM streamflow predictions.

Maine, Massachusetts, New Hampshire, New York, Pen↗
USGS2025

Long‑term monitoring of mercury in Vermont’s forest soils: Trends over 20 years in near–surface horizons

Mercury is a soil pollutant of widespread concern, usually derived from airborne deposition. A long–term forest soil monitoring program began in 2002 at five sites (elevation 590–1140 m) in Vermont, USA. Total mercury (THg) and soil organic carbon (SOC) were assessed in the uppermost humified soil layer, either an Oa or A horizon. Sampling occurred every 5 years from ten subplots at each site. Tree species ranged from deciduous, mixed deciduous/conifer, to all conifer. After five samplings, the site means for THg ranged from 167 to 447 µg kg –1 and increased linearly with elevation ( R 2 = 0.78). One site had a significant temporal increase in THg of 3.9 µg kg –1 yr –1 ( p = 0.02). Overall SOC site means ranged from 133 to 434 g kg –1 . One site showed a significant temporal increase in SOC ( p = 0.01). The mean ratio of THg:SOC was similar at four of the sites (1318–1518 µg kg –1 ) but much lower (648 µg kg –1 ) at the site with the highest SOC and the temporal increase in THg. Within individual subplots, THg increased up to a maximum SOC concentration of ~ 320 g kg –1 and usually decreased above that threshold. Although both wet and dry mercury deposition in the northeast USA have declined, no evidence of declining soil THg concentration was found, likely due to strong retention by SOC. Continued monitoring is essential considering ongoing changes in deposition and future changes in the source–sink balance of mercury.

Vermont↗
USGS2025

Mercury cycling in the Czech GEOMON network catchments recovering from acid deposition and facing climate change

We used the catchment mass balance approach to investigate mercury (Hg) cycling at the 14 forested GEOMON catchments of the Czech Geological Survey. The temperate forest catchments had variable exposure to historic high sulfur (S) and Hg emissions, and span a range of size and elevation. We monitored monthly Hg inputs (bulk precipitation, throughfall, litterfall) and outputs (stream runoff) during 2020–2022. The catchments spanned a large gradient of historic Hg deposition, but current Hg patterns more closely aligned with catchment factors like local climate, as influenced by elevation, dissolved organic carbon (DOC) concentrations, and geology. The dominant pathway of Hg input was litterfall (averaging 44.5 ± 15.7 µg m −2 yr −1 ; > 91% of total input). Two surprising findings were that GEOMON had low Hg concentrations and fluxes in general but had the highest litterfall Hg fluxes in Europe, and these increased even further in forested areas that had bark beetle infestations. Gaseous elemental mercury (GEM), measured using passive samplers, was consistently low (1.25 to 1.66 ng m −3 ) across the 14 catchments. Stream Hg output varied across catchments and averaged 1.5 ± 1.7 µg m −2 yr −1 . The average Hg retention rate at the 14 GEOMON catchments, calculated as the fraction of average Hg inputs (throughfall + litterfall) that remained in the catchment and did not run off in streamwater, was 97%. The high catchment Hg retention combined with its strong association with DOC suggests that with climate change intensification of carbon cycling, these catchments will be a Hg source for decades to come.

Biogeochemistry↗
USGS2025

Nitrate loads and concentrations from forested watersheds and implications for Long Island Sound

Reduction in point sources of nitrogen has led to improvement in water quality of the Long Island Sound (LIS) since 2000, but changes in nonpoint sources are less clear. A significant yet poorly quantified nonpoint nitrogen source is the forested landscape. Because a large proportion of the LIS basin is forested, even small areal inputs from the forested landscape have a large cumulative effect on nitrogen loading to LIS. Atmospheric nitrogen deposition, the primary source of nitrogen to forested landscapes in LIS basin, has been declining for several decades. However, nitrogen export in streams does not necessarily mirror nitrogen deposition. To assess forest nitrogen export to LIS, we estimated annual average concentrations and fluxes of nitrate in 17 forested watersheds in and near the LIS basin. Average flow-normalized nitrate-nitrogen concentrations ranged from less than 0.05–0.43 mg per liter among all sites; annual flow-normalized yields ranged from 0.45 to 4.3 kg per hectare. Flow-normalized annual average concentrations and yields of nitrate between water years 1991–2021 did not monotonically increase or decrease at most watersheds. Where determined, the other major N species generally had comparable magnitude and trends. Based on the watersheds analyzed in this study, forested areas are not responding uniformly to the continued decline of atmospheric nitrogen deposition. The variability among sites may indicate that local-scale factors exert substantial influence over the magnitude and trends in nitrogen exports. One watershed that had increasing development showed an increasing trend in nitrate, but not in dissolved organic nitrogen.

Connecticut, Massachusetts, New Hampshire, New Yor↗
USGS2025

Leveraging high-frequency sensor data and U.S. National Water Model output to forecast turbidity in a drinking water supply basin

As high-frequency sensor networks increasingly enhance data-driven models of water quality, process-based models like the U.S. National Water Model (NWM) are generating accessible forecasts of streamflow at increasingly dense scales. There is now an opportunity to combine these products to construct actionable water quality forecasts. To that end, we couple streamflow forecasts from the NWM to a gradient-boosted decision tree algorithm (LightGBM) trained on 5+ years of high-frequency monitoring data to forecast in-stream turbidity levels in the Catskill Mountains, NY, USA. Results indicate LightGBM models are capable of relatively skillful predictions, which enable robust forecasts for 1–3 days lead times. LightGBM models offer improvements over a simplified linear model across the entire forecast horizon, and more spatially complex models are more resilient to error at shorter lead times (1–3 days). Moreover, interpretation of model features emphasizes high flows as a driver of turbidity in the region. Results suggest that interpretable, flexible, and efficient machine learning algorithms can produce capable water quality forecasts from streamflow forecasts and expand understanding of process dynamics. The use case illustrated here—to our knowledge the first NWM-based water quality forecast—underscores the potential to employ the NWM to expand national water quality forecasting capacity and can overall serve as a guide for similar efforts in basins across the country.

New York↗
USGS2025

Long-term trends of streamwater chemistry in an agricultural watershed: Effects of anthropogenic and climatic factors

The chemistry of headwater streams is a key indicator of the health of riparian zones and surrounding terrestrial ecosystems. This chemistry is shaped by biogeochemical processes, including chemical weathering, and anthropogenic activities that interact with one another and are sensitive to climate. Elucidating trends in streamwater chemistry and the drivers that underpin them is essential for informing land-management decisions and anticipating water-quality issues that may affect downstream waters. In this work, we investigated the effects of anthropogenic and climatic factors on long-term variations in the chemistry of a first-order stream draining an agricultural catchment nested within the Sleepers River Research Watershed in Vermont, USA. We observed statistically significant increases in alkalinity and the concentrations of calcium and magnesium over a 31-year period for which 17 years of measurements were available. Through the application of generalized linear models, we found that the upward trends in alkalinity and calcium were associated with rising air temperatures, while a response to historical acid deposition played a minor role. We hypothesize that increased production of biogenic carbon dioxide and organic acids in soil and groundwater may lead to increases in chemical weathering rates under warmer climate conditions. This study emphasizes the important role of rising temperatures in the long-term increase in streamwater alkaline solutes, potentially overshadowing other influences like acidification recovery and agricultural practices. It also highlights the importance of comprehensive, long-term research to understand climate impacts on chemical weathering and inland water chemistry, which is critical for managing water quality and understanding regional and global carbon cycles.

Vermont↗
USGS2024

Forest cover lessens hurricane impacts on peak streamflow

Cyclonic storms (i.e., hurricanes) are powerful disturbance events that often cause widespread forest damage. Storm-related canopy damage reduces rainfall interception and evapotranspiration, but impacts on streamflow regimes are poorly understood. We quantify streamflow changes in Puerto Rico following Hurricane Maria in September 2017, and evaluate whether forest cover and storm-related canopy damage account for the differences. Streams are particularly vulnerable to flooding in early post-disturbance stages during hurricane season, so we focus on 3 months (Oct–Dec) following the hurricane. To discern changes in rainfall responses, we partitioned streamflow into baseflow and quickflow using a digital filter. We collected 2010–2017 streamflow and rainfall data from 18 watersheds and compared the relative magnitude of post- to pre-hurricane double mass curve slopes of baseflow and quickflow volumes against rainfall. Several watersheds displayed higher post-hurricane quickflow and baseflow, however, the response was variable. The magnitude of quickflow increase was greater in watersheds with high forest damage. Under the same level of relative damage, watersheds with low initial forest cover had greater quickflow increases than highly forested ones. Conversely, baseflow generally increased, but increases were greater in highly forested watersheds and smaller in highly damaged watersheds. These results suggest that post-storm baseflow increases were due to recharge of hurricane-related rainfall, as well as forest transpiration interruption and soil disturbance enhancing recharge of post-hurricane rainfall, while increases to quickflow are related to loss of canopy rainfall interception and higher soil saturation decreasing infiltration. Our research demonstrates that forest damage from disturbance lowers quickflow and elevates baseflow in highly forested watersheds, and elevates quickflow and lowers baseflow in less-forested watersheds. Less-forested watersheds may be closer to the forest cover loss threshold needed to elicit a streamflow response following disturbance, suggesting higher flooding potential downstream, and a lower storm-related forest disturbance threshold than in heavily forested watersheds.

Puerto Rico↗
USGS2024

Illuminating the “invisible”: Substantial deep respiration and lateral export of dissolved carbon from beneath soil

Dissolved organic and inorganic carbon (DOC and DIC) influence water quality, ecosystem health, and carbon cycling. Dissolved carbon species are produced by biogeochemical reactions and laterally exported to streams via distinct shallow and deep subsurface flow paths. These processes are arduous to measure and challenge the quantification of global carbon cycles. Here we ask: when, where, and how much is dissolved carbon produced in and laterally exported from the subsurface to streams? We used a catchment-scale reactive transport model, BioRT-HBV, with hydrometeorology and stream carbon data to illuminate the “invisible” subsurface processes at Sleepers River, a carbonate-based catchment in Vermont, United States. Results depict a conceptual model where DOC is produced mostly in shallow soils (3.7 ± 0.6 g/m 2 /yr) and in summer at peak root and microbial respiration. DOC is flushed from soils to the stream (1.0 ± 0.2 g/m 2 /yr) especially during snowmelt and storms. A large fraction of DOC (2.5 ± 0.2 g/m 2 /yr) percolates to the deeper subsurface, fueling deep respiration to generate DIC. DIC is exported predominantly from the deeper subsurface (7.1 ± 0.4 g/m 2 /yr, compared to 1.3 ± 0.3 g/m 2 /yr from shallow soils). Deep respiration reduces DOC and increases DIC concentrations at depth, leading to commonly observed DOC flushing (increasing concentrations with discharge) and DIC dilution patterns (decreasing concentrations with discharge). Surprisingly, respiration processes generate more DIC than weathering in this carbonate-based catchment. These findings underscore the importance of vertical connectivity between the shallow and deep subsurface, highlighting the overlooked role of deep carbon processing and export.

Vermont↗
USGS2023

Atmospheric mercury and its deposition during the phasing out of an amalgam electrolysis plant: Temporal, seasonal, and spatial patterns

Large amounts of mercury (Hg) were consumed and emitted into the atmosphere during the process of amalgam electrolysis used to produce chlorine and caustic soda since the nineteenth century. In Europe, amalgam electrolysis has been gradually replaced by advanced Hg-free technologies. In this work, we describe changes in atmospheric Hg and bulk Hg wet deposition during the phasing out of an amalgam electrolytic production line of a chlor-alkali plant in Neratovice, Czech Republic, central Europe. Bulk wet deposition Hg near the chlor-alkali plant was low at 3.6 ± 0.8 μg m −2 year −1 due in part to low annual precipitation amounts (486 ± 97 mm) in the period 2015–2021. Nevertheless, Hg deposition was elevated relative to a nearby reference site both before and after decommissioning of the electrolytic line. Switching off the amalgam electrolytic line did not notably affect bulk wet deposition Hg near the chlor-alkali plant. Levels of gaseous elemental Hg (GEM) and particle-bound Hg (PBM) monitored seasonally four times per year over 24-h time periods indicated rapid declines in four nearby settlements set in cardinal directions from the Hg emission source. Mean atmospheric GEM and PBM concentrations decreased rapidly from 9.0 ± 2.1 ng m −3 and 243 ± 255 pg m −3 in the period 2013–2017 when amalgam electrolysis was operating to 3.3 ± 0.4 ng m −3 and 32 ± 6 pg m −3 in the period 2018–2021 after its decommissioning in November 2017. Seasonal changes of GEM coincided with changes in temperature with the highest concentrations in summer, while PBM air levels were lowest in summer due to the highest seasonal precipitation amount. GEM concentrations at the four monitored settlements at Neratovice remained elevated at 2.8 ng m −3 with respect to regional background, but PBM levels decreased to background levels.

Neratovice↗
USGS2023

Disentangling the responses of dissolved organic carbon and nitrogen concentrations to overlapping drivers in a northeastern United States forested watershed

The concurrent reduction in acid deposition and increase in precipitation impact stream solute dynamics in complex ways that make predictions of future water quality difficult. To understand how changes in acid deposition and precipitation have influenced dissolved organic carbon (DOC) and nitrogen (N) loading to streams, we investigated trends from 1991 to 2018 in stream concentrations (DOC, ~3,800 measurements), dissolved organic nitrogen (DON, ~1,160 measurements), and dissolved inorganic N (DIN, ~2,130 measurements) in a forested watershed in Vermont, USA. Our analysis included concentration-discharge (C-Q) relationships and Seasonal Mann-Kendall tests on long-term, flow-adjusted concentrations. To understand whether hydrologic flushing and changes in acid deposition influenced long-term patterns by liberating DOC and dissolved N from watershed soils, we measured their concentrations in the leachate of 108 topsoil cores of 5 cm diameter that we flushed with solutions simulating high and low acid deposition during four different seasons. Our results indicate that DOC and DON often co-varied in both the long-term stream dataset and the soil core experiment. Additionally, leachate from winter soil cores produced especially high concentrations of all three solutes. This seasonal signal was consistent with C-Q relation showing that organic materials (e.g., DOC and DON), which accumulate during winter, are flushed into streams during spring snowmelt. Acid deposition had opposite effects on DOC and DON compared to DIN in the soil core experiment. Low acid deposition solutions, which mimic present day precipitation, produced the highest DOC and DON leachate concentrations. Conversely, high acid deposition solutions generally produced the highest DIN leachate concentrations. These results are consistent with the increasing trend in stream DOC concentrations and generally decreasing trend in stream DIN we observed in the long-term data. These results suggest that the impact of acid deposition on the liberation of soil carbon (C) and N differed for DOC and DON vs. DIN, and these impacts were reflected in long-term stream chemistry patterns. As watersheds continue to recover from acid deposition, stream C:N ratios will likely continue to increase, with important consequences for stream metabolism and biogeochemical processes.

Vermont↗
USGS2022

Optical properties of dissolved organic matter in throughfall and stemflow vary across tree species and season in a temperate headwater forest

Tree-derived dissolved organic matter (DOM) comprises a significant carbon flux within forested watersheds. Few studies have assessed the optical properties of tree-derived DOM. To increase understanding of the factors controlling tree-derived DOM quality, we measured DOM optical properties, dissolved organic carbon (DOC) and calcium concentrations in throughfall and stemflow for 17 individual rain events during summer and fall in a temperate deciduous forest in Vermont, United States. DOC and calcium fluxes in throughfall and stemflow were enriched on average 4 to 70 times incident fluxes in rain. A multiway model was developed using absorbance and fluorescence spectroscopy to further characterize DOM optical properties. Throughfall contained a higher percentage of protein-like DOM fluorescence than stemflow while stemflow was characterized by a higher percentage of humic-like DOM fluorescence. DOM absorbance spectral slopes in yellow birch ( Betula alleghaniensis ) stemflow were significantly higher than in sugar maple ( Acer saccharum ) stemflow. DOM optical metrics were not influenced by rainfall volume, but percent protein-like fluorescence increased in throughfall during autumn when leaves senesced. Given the potential influence of tree-derived DOM fluxes on receiving soils and downstream ecosystems, future modeling of DOM transport and soil biogeochemistry should represent the influence of differing DOM quality in throughfall and stemflow across tree species and seasons.

Vermont↗
USGS2022

Spatial and temporal patterns in atmospheric deposition of dissolved organic carbon

Atmospheric deposition of dissolved organic carbon (DOC) to terrestrial ecosystems is a small, but rarely studied component of the global carbon (C) cycle. Emissions of volatile organic compounds (VOC) and organic particulates are the sources of atmospheric C and deposition represents a major pathway for the removal of organic C from the atmosphere. Here, we evaluate the spatial and temporal patterns of DOC deposition using 70 data sets at least one year in length ranging from 40° south to 66° north latitude. Globally, the median DOC concentration in bulk deposition was 1.7 mg L −1 . The DOC concentrations were significantly higher in tropical (<25°) latitudes compared to temperate (>25°) latitudes. DOC deposition was significantly higher in the tropics because of both higher DOC concentrations and precipitation. Using the global median or latitudinal specific DOC concentrations leads to a calculated global deposition of 202 or 295 Tg C yr −1 respectively. Many sites exhibited seasonal variability in DOC concentration. At temperate sites, DOC concentrations were higher during the growing season; at tropical sites, DOC concentrations were higher during the dry season. Thirteen of the thirty-four long-term (>10 years) data sets showed significant declines in DOC concentration over time with the others showing no significant change. Based on the magnitude and timing of the various sources of organic C to the atmosphere, biogenic VOCs likely explain the latitudinal pattern and the seasonal pattern at temperate latitudes while decreases in anthropogenic emissions are the most likely explanation for the declines in DOC concentration.

Global Biogeochemical Cycles↗
USGS2022

Using dissolved organic matter fluorescence to predict total mercury and methylmercury in forested headwater streams, Sleepers River, Vermont USA

Aqueous transport of mercury (Hg) across the landscape is closely linked to dissolved organic matter (DOM). Both quantity and quality of DOM affect Hg mobility, as well as the formation and transport of toxic methylmercury (MeHg), but only a limited number of field studies have investigated Hg and MeHg with respect to specific DOM components. We investigated these interactions at the 41-ha forested W-9 catchment at Sleepers River, Vermont, which has a long history of mercury and other biogeochemical research. We examined spatial and temporal patterns of filtered Hg fractions and dissolved organic carbon (DOC) concentration, DOM quality, and major solutes at 12 stream sites within W-9 and the downstream W-3 gage (837 ha) over five sampling campaigns including a large (79 mm) fall storm, spring snowmelt, and three seasonally contrasting base flow periods. Filtered total Hg (THg), MeHg, and DOC concentrations increased in order base flow < snowmelt < fall storm, except that MeHg remained at baseflow levels during snowmelt. Ranges of median concentrations across sites for the five campaigns were THg, <0.2–4.1 ng L −1 ; MeHg, <0.03–0.45 ng L −1 ; and DOC, 0.8–14.0 mg L −1 . Humic-like DOM fluorescence components, as determined by parallel factor analysis (PARAFAC), dominated the fluorescence across sites and sampling campaigns. THg correlated strongly ( r > 0.94) with these humic components, but even more strongly with bulk DOC and absorbance at 254 nm (UV 254 ; r > 0.96), and less strongly with protein-like DOM (0.7 < r < 0.9). MeHg correlated in the same order but less strongly with humic- (0.8 < r < 0.9) and protein-like (0.6 < r < 0.8) DOM. MeHg increased in summer, potentially in response to enhanced microbial production in warmer periods. MeHg formation may have been linked to protein-like DOM, but its transport was linked to humic-like DOM.

Vermont↗
USGS2022

Hydrology and biogeochemistry datasets from Sleepers River Research Watershed, Danville, Vermont, USA

The Sleepers River Research Watershed (SRRW) in Danville, Vermont, USA, was established in 1957 by the U.S Department of Agriculture, Agricultural Research Service (ARS). The 111-km 2 area was selected as a representative mixed-land-use upland landscape in the northeastern USA, with the objective to study fundamental hydrological processes. The U.S. Geological Survey (USGS) currently operates SRRW and is the fourth federal agency to lead it. SRRW has hosted historic research on snowmelt modelling and streamflow generation processes, and USGS has augmented this hydrological foundation with biogeochemical cycling research. This data note describes five freely available data releases in stable repositories, extending to the late 2010s, from the indicated start date: aqueous chemistry and isotopes (1991); precipitation, water temperature, and streamflow (1991); groundwater levels (1991); ground frost depth (1983); and snow depth and water equivalent (1960). USGS research at SRRW is expected to continue, and we plan to update these releases every 1–3 years.

Vermont↗