Soil incubation methods lead to large differences in inferred methane production temperature sensitivity

Abstract Quantifying the temperature sensitivity of methane (CH 4 ) production is crucial for predicting how wetland ecosystems will respond to climate warming. Typically, the temperature sensitivity (often quantified as a Q 10 value) is derived from laboratory incubation studies and then used in bi...

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Bibliographic Details
Published in:Environmental Research Letters
Main Authors: Li, Zhen, Grant, Robert F, Chang, Kuang-Yu, Hodgkins, Suzanne B, Tang, Jinyun, Cory, Alexandra, Mekonnen, Zelalem A, Saleska, Scott R, Brodie, Eoin L, Varner, Ruth K, Rich, Virginia I, Wilson, Rachel M, Chanton, Jeff P, Crill, Patrick, Riley, William J
Other Authors: National Science Foundation, Biology Integration Institutes Program, Lawrence Berkeley National Laboratory, Biological and Environmental Research
Format: Article in Journal/Newspaper
Language:unknown
Published: IOP Publishing 2024
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Online Access:http://dx.doi.org/10.1088/1748-9326/ad3565
https://iopscience.iop.org/article/10.1088/1748-9326/ad3565
https://iopscience.iop.org/article/10.1088/1748-9326/ad3565/pdf
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Summary:Abstract Quantifying the temperature sensitivity of methane (CH 4 ) production is crucial for predicting how wetland ecosystems will respond to climate warming. Typically, the temperature sensitivity (often quantified as a Q 10 value) is derived from laboratory incubation studies and then used in biogeochemical models. However, studies report wide variation in incubation-inferred Q 10 values, with a large portion of this variation remaining unexplained. Here we applied observations in a thawing permafrost peatland (Stordalen Mire) and a well-tested process-rich model ( ecosys ) to interpret incubation observations and investigate controls on inferred CH 4 production temperature sensitivity. We developed a field-storage-incubation modeling approach to mimic the full incubation sequence, including field sampling at a particular time in the growing season, refrigerated storage, and laboratory incubation, followed by model evaluation. We found that CH 4 production rates during incubation are regulated by substrate availability and active microbial biomass of key microbial functional groups, which are affected by soil storage duration and temperature. Seasonal variation in substrate availability and active microbial biomass of key microbial functional groups led to strong time-of-sampling impacts on CH 4 production. CH 4 production is higher with less perturbation post-sampling, i.e. shorter storage duration and lower storage temperature. We found a wide range of inferred Q 10 values (1.2–3.5), which we attribute to incubation temperatures, incubation duration, storage duration, and sampling time. We also show that Q 10 values of CH 4 production are controlled by interacting biological, biochemical, and physical processes, which cause the inferred Q 10 values to differ substantially from those of the component processes. Terrestrial ecosystem models that use a constant Q 10 value to represent temperature responses may therefore predict biased soil carbon cycling under future climate scenarios.