4.6 Article

Permafrost Carbon and CO2 Pathways Differ at Contrasting Coastal Erosion Sites in the Canadian Arctic

期刊

FRONTIERS IN EARTH SCIENCE
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/feart.2021.630493

关键词

Arctic; coastal erosion; carbon cycling; biogeochemistry; greenhouse gases; carbon dioxide; biomarkers

资金

  1. H2020 project NUNATARYUK [773421]
  2. ERC StG project THAWSOME [676982]
  3. Changing Arctic Ocean program (NERC-BMBF project CACOON) [03F0806A]
  4. German research foundation DFG [BE 6485/1-1]
  5. Helmholtz young investigators group TEAM [VH-NG-821]
  6. European Research Council (ERC) [676982] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Warming temperatures and sea-level rise in the Arctic have led to increased erosion of permafrost coasts, affecting organic matter pathways and potentially leading to the release of greenhouse gases. Research on two erosion scenarios on Qikiqtaruk - Herschel Island in Canada demonstrates varying levels of CO2 release based on erosion types and residence time onshore, highlighting the importance of understanding organic carbon degradation during coastal erosion for improving carbon models.
Warming air and sea temperatures, longer open-water seasons and sea-level rise collectively promote the erosion of permafrost coasts in the Arctic, which profoundly impacts organic matter pathways. Although estimates on organic carbon (OC) fluxes from erosion exist for some parts of the Arctic, little is known about how much OC is transformed into greenhouse gases (GHGs). In this study we investigated two different coastal erosion scenarios on Qikiqtaruk - Herschel Island (Canada) and estimate the potential for GHG formation. We distinguished between a delayed release represented by mud debris draining a coastal thermoerosional feature and a direct release represented by cliff debris at a low collapsing bluff. Carbon dioxide (CO2) production was measured during incubations at 4 degrees C under aerobic conditions for two months and were modeled for four months and a full year. Our incubation results show that mud debris and cliff debris lost a considerable amount of OC as CO2 (2.5 +/- 0.2 and 1.6 +/- 0.3% of OC, respectively). Although relative OC losses were highest in mineral mud debris, higher initial OC content and fresh organic matter in cliff debris resulted in a similar to three times higher cumulative CO2 release (4.0 +/- 0.9 compared to 1.4 +/- 0.1 mg CO2 gdw(-1)), which was further increased by the addition of seawater. After four months, modeled OC losses were 4.9 +/- 0.1 and 3.2 +/- 0.3% in set-ups without seawater and 14.3 +/- 0.1 and 7.3 +/- 0.8% in set-ups with seawater. The results indicate that a delayed release may support substantial cycling of OC at relatively low CO2 production rates during long transit times onshore during the Arctic warm season. By contrast, direct erosion may result in a single CO2 pulse and less substantial OC cycling onshore as transfer times are short. Once eroded sediments are deposited in the nearshore, highest OC losses can be expected. We conclude that the release of CO2 from eroding permafrost coasts varies considerably between erosion types and residence time onshore. We emphasize the importance of a more comprehensive understanding of OC degradation during the coastal erosion process to improve thawed carbon trajectories and models.

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