skip to main content


This content will become publicly available on July 1, 2025

Title: Eroding Permafrost Coastlines Release Biodegradable Dissolved Organic Carbon to the Arctic Ocean
Coastal erosion mobilizes large quantities of organic matter (OM) to the Arctic Ocean where it may fuel greenhouse gas emissions and marine production. While the biodegradability of permafrost‐derived dissolved organic carbon (DOC) has been extensively studied in inland soils and freshwaters, few studies have examined dissolved OM (DOM) leached from eroding coastal permafrost in seawater. To address this knowledge gap, we sampled three horizons from bluff exposures near Drew Point, Alaska: seasonally thawed active layer soils, permafrost containing Holocene terrestrial and/or lacustrine OM, and permafrost containing late‐Pleistocene marine‐derived OM. Samples were leached in seawater to compare DOC yields, DOM composition (chromophoric DOM, Fourier transform ion cyclotron resonance mass spectrometry), and biodegradable DOC (BDOC). Holocene terrestrial permafrost leached the most DOC compared to active layer soils and Pleistocene marine permafrost. However, DOC from Pleistocene marine permafrost was the most biodegradable (33 ± 6% over 90 days), followed by DOC from active layer soils (23 ± 5%) and Holocene terrestrial permafrost (14 ± 3%). Permafrost leachates contained relatively more aliphatic and peptide‐like formulae, whereas active layer leachates contained relatively more aromatic formulae. BDOC was positively correlated with nitrogen‐containing and aliphatic formulae, and negatively correlated with polyphenolic and condensed aromatic formulae. Using estimates of eroding OM, we scale our results to estimate DOC and BDOC inputs to the Alaska Beaufort Sea. While DOC inputs from coastal erosion are relatively small compared to rivers, our results suggest that erosion may be an important source of BDOC to the Beaufort Sea when river inputs are low.  more » « less
Award ID(s):
2336164 1927553 2322664
PAR ID:
10527168
Author(s) / Creator(s):
; ; ; ; ; ;
Publisher / Repository:
JGR Biogeosciences
Date Published:
Journal Name:
Journal of Geophysical Research: Biogeosciences
Volume:
129
Issue:
7
ISSN:
2169-8953
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract

    Dissolved organic matter (DOM) in glacier runoff is aliphatic‐rich, yet studies have proposed that DOM originates mainly from allochthonous, aromatic, and often aged material. Allochthonous organic matter (OM) is exposed to ultraviolet radiation both in atmospheric transport and post‐deposition on the glacier surface. Thus, we evaluate photochemistry as a mechanism to account for the compositional disconnect between allochthonous OM sources and glacier runoff DOM composition. Six endmember OM sources (including soils and diesel particulate matter) were leached and photo‐irradiated for 28 days in a solar simulator, until >90% of initial chromophoric DOM was removed. Ultrahigh‐resolution mass spectrometry was used to compare the molecular composition of endmember leachates pre‐ and post‐irradiation to DOM in supraglacial and bulk runoff from the Greenland Ice Sheet and Juneau Icefield (Alaska), respectively. Photo‐irradiation drove molecular level convergence between the initially aromatic‐rich leachates and aromatic‐poor glacial samples, selectively removing aromatic compounds (−80 ± 19% relative abundance) and producing aliphatics (+75 ± 35% relative abundance). Molecular level glacier runoff DOM composition was statistically indistinguishable to post‐irradiation leachates. Bray‐Curtis analysis showed substantial similarity in the molecular formulae present between glacier samples and post‐irradiation leachates. Post‐irradiation leachates contained 84 ± 7.4% of the molecular formulae, including 72 ± 17% of the aliphatic formulae, detected in glacier samples. Our findings suggest that photodegradation, either in transit to or on glacier surfaces, could provide a mechanistic pathway to account for the disconnect between proposed aromatic, aged sources of OM and the aliphatic‐rich fingerprint of glacial DOM.

     
    more » « less
  2. Abstract

    River organic matter transformations impact the cycling of energy, carbon, and nutrients. The delivery of distinct dissolved organic matter (DOM) sources can alter aquatic DOM cycling and associated biogeochemical processes. Yet DOM source and reactivity are not well‐defined for many river systems, including in western Canada. Here, we explore DOM cycling in the mainstem of the Oldman River (stream order 6–7), a heavily regulated river network in southern Alberta (Canada). We compared seasonal river DOM content, composition, and bioavailability with nine endmember leachates from the river valley using optical properties and incubations to estimate biodegradable dissolved organic carbon (BDOC). River DOM composition was most similar to terrestrial soil leachates, followed by autochthonous DOM leachates. River DOM bioavailability was low (BDOC = 0%–16.6%, mean of 7.1%). Endmember leachate bioavailability increased from soils (BDOC = 23.9%–53.7%), to autochthonous sources (fish excretion, macrophytes, biofilm; BDOC = 49.9%–80.0%), to terrestrial vegetation (leaves, shrubs, grass; BDOC >  80%), scaling positively with protein‐like DOM content and amount of leachable dissolved organic carbon (DOC), and negatively with aromaticity. Seasonally, DOC concentrations changed little despite >15‐fold increases in discharge during spring. River DOM composition shifted modestly toward soil‐like endmembers in spring and more bioavailable autochthonous end members in autumn and winter. Low DOM bioavailability in the river mainstem and low DOC yields shown in previous work point to limited internal processing of DOM and limited bioavailable DOM delivery to downstream habitats, possibly due to upstream flow regulation. Our observations provide important insights into the functioning of western Canadian aquatic networks.

     
    more » « less
  3. Abstract

    Tidal wetlands are a significant source of dissolved organic matter (DOM) to coastal ecosystems, which impacts nutrient cycling, light exposure, carbon dynamics, phytoplankton activity, microbial growth, and ecosystem productivity. There is a wide variety of research on the properties and sources of DOM; however, little is known about the characteristics and degradation of DOM specifically sourced from tidal wetland plants. By conducting microbial and combined UV exposure and microbial incubation experiments of leachates from fresh and senescent plants in Chesapeake Bay wetlands, it was demonstrated that senescent material leached more dissolved organic carbon (DOC) than fresh material (77.9 ± 54.3 vs 21.6 ± 11.8 mg DOC L−1, respectively). Degradation followed an exponential decay pattern, and the senescent material averaged 50.5 ± 9.45% biodegradable DOC (%BDOC), or the loss of DOC due to microbial degradation. In comparison, the fresh material averaged a greater %BDOC (72.6 ± 19.2%). Percent remaining of absorbance (83.3 ± 26.7% for fresh, 90.1 ± 10.8% for senescent) was greater than percent remaining DOC, indicating that colored DOM is less bioavailable than non-colored material. Concentrations of DOC leached, %BDOC, and SUVA280 varied between species, indicating that the species composition of the marsh likely impacts the quantity and quality of exported DOC. Comparing the UV + microbial to the microbial only incubations did not reveal any clear effects on %BDOC but UV exposure enhanced loss of absorbance during subsequent dark incubation. These results demonstrate the impacts of senescence on the quality and concentration of DOM leached from tidal wetland plants, and that microbes combined with UV impact the degradation of this DOM differently from microbes alone.

     
    more » « less
  4. null (Ed.)
    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. 
    more » « less
  5. Jones, Benjamin (Ed.)
    Permafrost sediments contain one of the largest reservoirs of organic carbon on Earth that is relatively stable when it remains frozen. As air temperatures increase, the shallow permafrost thaws which allows this organic matter to be converted into potent greenhouse gases such as methane (CH4) and carbon dioxide (CO2) through microbial processes. Along the Beaufort Sea coast in the vicinity of the Tuktoyaktuk Peninsula, Northwest Territories, Canada, warming air temperatures are causing the active layer above permafrost to deepen, and a number of active periglacial processes are causing rapid erosion of previously frozen permafrost. In this paper, we consider the biogeochemical consequences of these processes on the permafrost sediments found at Tuktoyaktuk Island. Our goals were to document the in situ carbon characteristics which can support microbial activity, and then consider rates of such activity if the permafrost material were to warm even further. Samples were collected from a 12mpermafrost core positioned on the top of the island adjacent to an eroding coastal bluff. Downcore CH4, total organic carbon and dissolved organic carbon (DOC) concentrations and stable carbon isotopes revealed variable in situ CH4 concentrations down core with a sub-surface peak just below the current active layer. The highest DOC concentrations were observed in the active layer. Controlled incubations of sediment from various depths were carried out from several depths anaerobically under thawed (5°C and 15°C) and under frozen (−20°C and −5°C) conditions. These incubations resulted in gross production rates of CH4 and CO2 that increased upon thawing, as expected, but also showed appreciable production rates under frozen conditions. This dataset presents the potential for sediments below the active layer to produce potent greenhouse gases, even under frozen conditions, which could be an important atmospheric source in the actively eroding coastal zone even prior to thawing. 
    more » « less