Abstract

Mounting evidence suggests that biogeochemical processing of permafrost substrate will amplify dissolved inorganic carbon (DIC=E[CO2,HCO3–,CO32–]) production within Arctic freshwaters. The effects of permafrost thaw on DIC may be particularly strong where terrain subsidence following thaw (thermokarst) releases large amounts of sediment into fluvial networks. The mineral composition and chemical weathering of these sediments has critical yet untested implications for the degree to which streams represent a source of CO2 to the atmosphere versus a source of bicarbonate to downstream environments. Here, we experimentally determine the effects of mineral weathering on fluvial CO2 by incubating sediments collected from three retrogressive thaw slump features on the Peel Plateau (NWT, Canada). Prehistoric warming and contemporary thermokarst have exposed sediments on the Peel Plateau to varying degrees of thaw and chemical weathering, allowing us to test the role of permafrost and substrate mineral composition on CO2:HCO3– balance. We found that recently-thawed sediments (within years to decades) and previously un-thawed diamicton from deeper permafrost generated significant solutes and DIC. These solutes and the mineralogy of sediments suggested that carbonate weathering coupled with sulfide oxidation was a net source of abiotic CO2. Yet, on average, 30% of this CO2 was converted to bicarbonate via carbonate buffering reactions. In contrast, the mineralogy and geochemical trends associated with sediments from the modern and paleo-active layer, which were exposed to thaw over longer timescales, more strongly reflected silicate weathering. In treatments with sediment from the modern and paleo-active layer, minor carbonate and sulfide weathering resulted in some DIC and net CO2 production. This CO2 was not measurably diminished by carbonate buffering. Together, these trends suggest that prior exposure to thaw and weathering on the Peel Plateau reduced carbonate and sulfide in upper soil layers. We conclude that thermokarst unearthing deeper tills on the Peel Plateau will amplify regional inorganic carbon cycling for decades to centuries. However, previously-undocumented CO2 consumption via carbonate buffering may partly counterbalance CO2 production and release to the atmosphere. Regional variability in the mineral composition of permafrost, thaw history, and thermokarst intensity are among the primary controls on mineral weathering within permafrost carbon-climate feedbacks.

Highlights

  • Rapid climate warming and intensifying hydrologic cycles at northern latitudes (Serreze and Barry, 2011) are activating immense stores of organic carbon from perennially frozen permafrost soils into modern biogeochemical cycles (Biskaborn et al, 2019; Vonk et al, 2019)

  • Our results indicate that fluvial inorganic carbon cycling on the Peel Plateau is amplified by more intense thermokarst, which thaws deeper sediments containing a greater proportion of carbonate and sulfide

  • We enabled weathering to proceed under closed system conditions by flushing headspace in bottles with N2 gas, enabling dissolved CO2 and O2 to contribute to carbonate weathering and sulfide oxidation

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Summary

Introduction

Rapid climate warming and intensifying hydrologic cycles at northern latitudes (Serreze and Barry, 2011) are activating immense stores of organic carbon from perennially frozen permafrost soils into modern biogeochemical cycles (Biskaborn et al, 2019; Vonk et al, 2019). Carbonate and silicate weathering by carbonic acid [H2CO3∗, including dissolved CO2(g)] transforms atmospheric CO2(g) and biotic CO2 produced by plant root respiration and microbial oxidation of soil organic matter into bicarbonate (HCO−3 ; Equations 1–3) (Berner, 1999), rendering it less susceptible to exchange with the atmosphere: H2O + CO2(g) ⇋ H2CO3∗ ⇋ H+ + HCO−3 ⇋ 2H+

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