Date created
2021-09-28
Authors/Contributors
Abstract
Lake-rich Arctic deltas differ biogeochemically from tundra lakes, and their role as sources and sinks of greenhouse gases remains poorly understood. Under-ice and open-water changes in methane (CH4) storage (43 lakes, 2014), floating chamber measurements of total and diffusive CH4 evasion to the atmosphere (6 lakes, 2014-2015), and water-column CH4 oxidation (MOX) (6 lakes, 2014-2015) permitted evaluation of how CH4 emissions vary among lakes with differing river-to-lake connection times within the Mackenzie Delta. CH4 emissions during ice-out were considerable, followed by substantial declines as open-water progressed. Water-column MOX rates were highest after ice-out, and declined throughout open-water. After accounting for a strong effect of CH4 substrate levels, MOX rates were inversely related to pH, which can increase to high levels during open-water because of high macrophyte production. Comparisons of water-column CH4 storage versus open-water fluxes (6 lakes) showed that diffusive evasion plus MOX removed most CH4 in the water columns every 1-2 days with only modest changes in storage, suggesting that counter-balancing water-column replenishment is substantial. Lakes with short river-connection times (i.e. most strongly autotrophic and strongly CO2- absorbing in this delta) and thermokarst lakes contribute disproportionately to CH4 flux, relative to lakes with long river-connection times. Thus, this great Arctic delta represents an important system of greenhouse-gas emitting lakes despite prior work showing their net absorption of CO2 during open-water, and having a low landscape area of CO2-saturated thermokarst lakes. Autotrophically absorbed CO2 becomes labile carbon substrate, and is microbially shunted back to the atmosphere as the more potent greenhouse gas CH4.
Description
This manuscript will not be available until October 2022 due to the embargo periods of the journal Biogeochemistry. If you require access sooner please email summit@sfu.ca.
Scholarly level
Peer reviewed?
Yes
Language
English
Member of collection