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James W. McClelland

Publications and source records attributed to James W. McClelland.

8 recordsLinked to original sources

Wind-modulated groundwater discharge along a microtidal Arctic coastline

Groundwater discharge transports dissolved constituents to the ocean, affecting coastal carbon budgets and water quality. However, the magnitude and mechanisms of groundwater exchange along rapidly transitioning Arctic coastlines are largely unknown due to limited observations. Here, using first-of-its-kind coastal Arctic groundwater timeseries data, we evaluate the magnitude and drivers of groundwater discharge to Alaska's Beaufort Sea coast. Darcy flux calculations reveal temporally variable groundwater fluxes, ranging from −6.5 cm d −1 (recharge) to 14.1 cm d −1 (discharge), with fluctuations in groundwater discharge or aquifer recharge over diurnal and multiday timescales during the open-water season. The average flux during the monitoring period of 4.9 cm d −1 is in line with previous estimates, but the maximum discharge exceeds previous estimates by over an order-of-magnitude. While the diurnal fluctuations are small due to the microtidal conditions, multiday variability is large and drives sustained periods of aquifer recharge and groundwater discharge. Results show that wind-driven lagoon water level changes are the dominant mechanism of fluctuations in land–sea hydraulic head gradients and, in turn, groundwater discharge. Given the microtidal conditions, low topographic relief, and limited rainfall along the Beaufort Sea coast, we identify wind as an important forcing mechanism of coastal groundwater discharge and aquifer recharge with implications for nearshore biogeochemistry. This study provides insights into groundwater flux dynamics along this coastline over time and highlights an oft overlooked discharge and circulation mechanism with implications towards refining solute export estimates to coastal Arctic waters.

Alaska

Long-term trends in Arctic riverine chemistry signal multi-faceted northern change

Rivers integrate processes occurring throughout their watersheds and are therefore sentinels of change across broad spatial scales. River chemistry also regulates ecosystem function across Earth’s land–ocean continuum, exerting control from the micro- (for example, local food web) to the macro- (for example, global carbon cycle) scale. In the rapidly warming Arctic, a wide range of processes—from permafrost thaw to biological uptake and transformation—might reasonably alter river water chemistry. Here we use data from major rivers that collectively drain two-thirds of the Arctic Ocean watershed to assess widespread change in biogeochemical function within the pan-Arctic basin from 2003 to 2019. While the oceanward flux of alkalinity and associated ions increased markedly over this time frame, nitrate and other inorganic nutrient fluxes declined. Fluxes of dissolved organic carbon showed no overall trend. This divergence in response indicates the perturbation of multiple processes on land, with implications for biogeochemical cycling in the coastal ocean. We anticipate that these findings will facilitate refinement of conceptual and numerical models of current and future functioning of Arctic coastal ecosystems and spur research on scale-dependent change across the river-integrated Arctic domain.

Arctic

Geochemistry of coastal permafrost and erosion-driven organic matter fluxes to the Beaufort Sea near Drew Point, Alaska

Accelerating erosion of the Alaska Beaufort Sea coast is increasing inputs of organic matter from land to the Arctic Ocean, and improved estimates of organic matter stocks in eroding coastal permafrost are needed to assess their mobilization rates under contemporary conditions. We collected three permafrost cores (4.5–7.5 m long) along a geomorphic gradient near Drew Point, Alaska, where recent erosion rates average 17.2 m year −1 . Down-core patterns indicate that organic-rich soils and lacustrine sediments (12–45% total organic carbon; TOC) in the active layer and upper permafrost accumulated during the Holocene. Deeper permafrost (below 3 m elevation) mainly consists of Late Pleistocene marine sediments with lower organic matter content (∼1% TOC), lower C:N ratios, and higher δ 13 C values. Radiocarbon-based estimates of organic carbon accumulation rates were 11.3 ± 3.6 g TOC m −2 year −1 during the Holocene and 0.5 ± 0.1 g TOC m −2 year −1 during the Late Pleistocene (12–38 kyr BP). Within relict marine sediments, porewater salinities increased with depth. Elevated salinity near sea level (∼20–37 in thawed samples) inhibited freezing despite year-round temperatures below 0°C. We used organic matter stock estimates from the cores in combination with remote sensing time-series data to estimate carbon fluxes for a 9 km stretch of coastline near Drew Point. Erosional fluxes of TOC averaged 1,369 kg C m −1 year −1 during the 21st century (2002–2018), nearly doubling the average flux of the previous half-century (1955–2002). Our estimate of the 21st century erosional TOC flux year −1 from this 9 km coastline (12,318 metric tons C year −1 ) is similar to the annual TOC flux from the Kuparuk River, which drains a 8,107 km 2 area east of Drew Point and ranks as the third largest river on the North Slope of Alaska. Total nitrogen fluxes via coastal erosion at Drew Point were also quantified, and were similar to those from the Kuparuk River. This study emphasizes that coastal erosion represents a significant pathway for carbon and nitrogen trapped in permafrost to enter modern biogeochemical cycles, where it may fuel food webs and greenhouse gas emissions in the marine environment.

Alaska

Landscape matters: Predicting the biogeochemical effects of permafrost thaw on aquatic networks with a state factor approach

Permafrost thaw has been widely observed to alter the biogeochemistry of recipient aquatic ecosystems. However, research from various regions has shown considerable variation in effect. In this paper, we propose a state factor approach to predict the release and transport of materials from permafrost through aquatic networks. Inspired by Hans Jenny's seminal description of soil‐forming factors, and based on the growing body of research on the subject, we propose that a series of state factors—including relief, ice content, permafrost extent, and parent material—will constrain and direct the biogeochemical effect of thaw over time. We explore state‐factor‐driven variation in thaw response using a series of case studies from diverse regions of the permafrost‐affected north, and also describe unique scaling considerations related to the mobile and integrative nature of aquatic networks. While our cross‐system review found coherent responses to thaw for some biogeochemical constituents, such as nutrients, others, such as dissolved organics and particles, were much more variable in their response. We suggest that targeted, hypothesis‐driven investigation of the effects of state factor variation will bolster our ability to predict the biogeochemical effects of thaw across diverse and rapidly changing northern landscapes.

Permafrost and Periglacial Processes

Mercury export from Arctic great rivers

Land–ocean linkages are strong across the circumpolar north, where the Arctic Ocean accounts for 1% of the global ocean volume and receives more than 10% of the global river discharge. Yet estimates of Arctic riverine mercury (Hg) export constrained from direct Hg measurements remain sparse. Here, we report results from a coordinated, year-round sampling program that focused on the six major Arctic rivers to establish a contemporary (2012–2017) benchmark of riverine Hg export. We determine that the six major Arctic rivers exported an average of 20 000 kg y –1 of total Hg (THg, all forms of Hg). Upscaled to the pan-Arctic, we estimate THg flux of 37 000 kg y –1 . More than 90% of THg flux occurred during peak river discharge in spring and summer. Normalizing fluxes to watershed area (yield) reveals higher THg yields in regions where greater denudation likely enhances Hg mobilization. River discharge, suspended sediment, and dissolved organic carbon predicted THg concentration with moderate fidelity, while suspended sediment and water yields predicted THg yield with high fidelity. These findings establish a benchmark in the face of rapid Arctic warming and an intensifying hydrologic cycle, which will likely accelerate Hg cycling in tandem with changing inputs from thawing permafrost and industrial activity.

Environmental Science & Technology

Multi-decadal increases in dissolved organic carbon and alkalinity flux from the Mackenzie drainage basin to the Arctic Ocean

Riverine exports of organic and inorganic carbon (OC, IC) to oceans are intricately linked to processes occurring on land. Across high latitudes, thawing permafrost, alteration of hydrologic flow paths, and changes in vegetation may all affect this flux, with subsequent implications for regional and global carbon (C) budgets. Using a unique, multi-decadal dataset of continuous discharge coupled with water chemistry measurements for the Mackenzie River, we show major increases in dissolved OC (DOC) and IC (as alkalinity) fluxes since the early 1970s, for a watershed that covers 1.8 M km 2 of northwestern Canada, and provides substantial inputs of freshwater and biogeochemical constituents to the Arctic Ocean. Over a 39-year period of record, DOC flux at the Mackenzie mouth increased by 39.3% (44.5 ± 22.6 Gmol), while alkalinity flux increased by 12.5% (61.5 ± 60.1 Gmol). Isotopic analyses and substantial increases in sulfate flux indicate that increases in alkalinity are driven by accelerating sulfide oxidation, a process that liberates IC from rock and soils in the absence of CO 2 consumption. Seasonal and sub-catchment trends suggest that permafrost thaw plays an important role in the observed increases in DOC and alkalinity: sub-catchment increases for all constituents are confined to northern, permafrost-affected regions, while observed increases in autumn to winter are consistent with documented landscape-scale changes that have resulted from changing thaw dynamics. This increase in DOC and sulfide-derived alkalinity represents a substantial intensification of land-to-ocean C mobilization, at a level that is significant within the regional C budget. The change we observe, for example, is similar to current and projected future rates of CO 2 consumption by weathering in the Mackenzie basin.

Environmental Research Letters

Insights and issues with simulating terrestrial DOC loading of Arctic river networks

Terrestrial carbon dynamics influence the contribution of dissolved organic carbon (DOC) to river networks in addition to hydrology. In this study, we use a biogeochemical process model to simulate the lateral transfer of DOC from land to the Arctic Ocean via riverine transport. We estimate that, over the 20th century, the pan-Arctic watershed has contributed, on average, 32 Tg C/yr of DOC to river networks emptying into the Arctic Ocean with most of the DOC coming from the extensive area of boreal deciduous needle-leaved forests and forested wetlands in Eurasian watersheds. We also estimate that the rate of terrestrial DOC loading has been increasing by 0.037 Tg C/yr2 over the 20th century primarily as a result of climate-induced increases in water yield. These increases have been offset by decreases in terrestrial DOC loading caused by wildfires. Other environmental factors (CO2 fertilization, ozone pollution, atmospheric nitrogen deposition, timber harvest, agriculture) are estimated to have relatively small effects on terrestrial DOC loading to Arctic rivers. The effects of the various environmental factors on terrestrial carbon dynamics have both offset and enhanced concurrent effects on hydrology to influence terrestrial DOC loading and may be changing the relative importance of terrestrial carbon dynamics on this carbon flux. Improvements in simulating terrestrial DOC loading to pan-Arctic rivers in the future will require better information on the production and consumption of DOC within the soil profile, the transfer of DOC from land to headwater streams, the spatial distribution of precipitation and its temporal trends, carbon dynamics of larch-dominated ecosystems in eastern Siberia, and the role of industrial organic effluents on carbon budgets of rivers in western Russia.

Ecological Applications

Landscape-level controls on dissolved carbon flux from diverse catchments of the circumboreal

While much of the dissolved organic carbon (DOC) within rivers is destined for mineralization to CO 2 , a substantial fraction of riverine bicarbonate (HCO 3 - ) flux represents a CO 2 sink, as a result of weathering processes that sequester CO 2 as HCO 3 - . We explored landscape-level controls on DOC and HCO 3 - flux in subcatchments of the boreal, with a specific focus on the effect of permafrost on riverine dissolved C flux. To do this, we undertook a multivariate analysis that partitioned the variance attributable to known, key regulators of dissolved C flux (runoff, lithology, and vegetation) prior to examining the effect of permafrost, using riverine biogeochemistry data from a suite of subcatchments drawn from the Mackenzie, Yukon, East, and West Siberian regions of the circumboreal. Across the diverse catchments that we study, controls on HCO 3 - flux were near-universal: runoff and an increased carbonate rock contribution to weathering (assessed as riverwater Ca:Na) increased HCO 3 - yields, while increasing permafrost extent was associated with decreases in HCO 3 - . In contrast, permafrost had contrasting and region-specific effects on DOC yield, even after the variation caused by other key drivers of its flux had been accounted for. We used ionic ratios and SO 4 yields to calculate the potential range of CO 2 sequestered via weathering across these boreal subcatchments, and show that decreasing permafrost extent is associated with increases in weathering-mediated CO 2 fixation across broad spatial scales, an effect that could counterbalance some of the organic C mineralization that is predicted with declining permafrost.

Global Biogeochemical Cycles