Articles | Volume 23, issue 18
https://doi.org/10.5194/bg-23-6639-2026
© Author(s) 2026. This work is distributed under the Creative Commons Attribution 4.0 License.
Plant belowground traits indicate increased plant-mediated methane transport along a peatland permafrost thaw gradient
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- Final revised paper (published on 21 Sep 2026)
- Preprint (discussion started on 29 Jan 2026)
Interactive discussion
Status: closed
Comment types: AC – author | RC – referee | CC – community | EC – editor | CEC – chief editor
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RC1: 'Comment on egusphere-2026-467', Tim Moore, 25 Feb 2026
- AC1: 'Reply on RC1', Tiia Määttä, 29 Apr 2026
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RC2: 'Comment on egusphere-2026-467', Anonymous Referee #2, 30 Mar 2026
- AC2: 'Reply on RC2', Tiia Määttä, 29 Apr 2026
Peer review completion
AR – Author's response | RR – Referee report | ED – Editor decision | EF – Editorial file upload
ED: Reconsider after major revisions (13 May 2026) by Jack Middelburg
AR by Tiia Määttä on behalf of the Authors (17 Jun 2026)
Author's response
Author's tracked changes
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ED: Publish subject to technical corrections (30 Jun 2026) by Jack Middelburg
AR by Tiia Määttä on behalf of the Authors (01 Jul 2026)
Author's response
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Post-review adjustments
AA – Author's adjustment | EA – Editor approval
AA by Tiia Määttä on behalf of the Authors (03 Sep 2026)
Author's adjustment
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EA: Adjustments approved (07 Sep 2026) by Jack Middelburg
Controls (or drivers) of the exchange of methane between the atmosphere and the surface of various wetlands have always been complicated, because of the nature of the processes and pathways and the large spatial variability across short distances, combined with temporal variability. Initially, simple variables such as temperature, water table and plant functional type were useful in ‘explaining’ patterns of methane exchange across landscapes. Since then, attention has been given to a variety of properties and processes which have led to a better ‘explanation’ and perhaps ‘prediction’ of the methane exchange. For belowground activities, important processes are provision of carbon for methanogenesis and the ability of plants to transport methane directly (avoiding methanotrophy in the profile) as well allowing oxygen to create a potential zone of methanotrophy in the rhizosphere. Thus, linking belowground root/rhizome traits and methane emission can be ‘complicated’ but a necessary advance.
This manuscript is an example of the latter, focusing on the role of root and rhizome traits in the exchange (emission) of methane, based along a gradient created by the thawing of permafrost palsa in northern Sweden. Three ‘thaw stages’ have been recognized at this site, with changes in thermal regime, hydrology and vegetation characteristics creating a very large variation in methane emission rates. The research focuses on determining root and rhizome traits across triplicates of each thaw phase, though this is not done in the automatic flux chambers, but from sites located nearby with similar properties. As noted by the authors, there is not complete species similarity in mean coverage between the triplicate chamber and core data but when combined into herbaceous and shrub categories there is general agreement (Table 1). Daily median flux of methane was calculated, to avoid the usual ‘burp’ of methane occurring occasionally which would be unlikely to be derived from root processes, and chamber carbon dioxide flux was used to define seasonal patterns. Root and rhizome data were collected carefully from depth increments and biogeochemical data were used to provide evidence for some of the processes leading to methane production, and how they might be related to root activity.
The manuscript is well structured and written and provides valuable evidence for the role of belowground plant activities in controlling methane emissions. It is ‘digestible’ in that the information in the manuscript is restricted to two Tables and five Figures, with voluminous supporting data in Appendices. The strong Introduction ends with several expectations/hypotheses based on previous studies, but in this case applied to the specific Stordalen site, in which palsa are thawing and thus perhaps similar to features elsewhere in the Arctic. Based on methane fluxes from the nine chambers and root characteristics from the ‘similar’ sites, the study presents strong evidence for correlations between methane emission rate and the herbaceous and shrub root and rhizome properties, and whether patterns changed with the season, based on carbon dioxide exchange. In general, it appears that correlations were stronger for root properties compared to rhizomes, though there are mixed relationships shown in Figures 3 and 4. The reasons for positive, negative or no correlations were examined in the Discussion and the relevance of these relationships may vary with the specific features of Stordalen, which are somewhat unusual. The relationships between the traits and methane emission were examined in terms of processes related to changes from shrubs to herbaceous plants and the root trait structure (e.g. density, specific length and diameter), and drew upon results presented elsewhere which could be applicable at Stordalen. The overall conclusion was that belowground root/rhizome activities were an important component of methane emission, that change from shrubs to herbaceous would lead to increased emissions, but there is a bit of ‘ying-yang’: shrubs may supply more carbon substrates, whereas herbaceous plants may be important conduits of methane to the atmosphere. Such is life in the real world of Nature and ‘teams’ like these authors are needed to see at least part of the whole.
The study is ‘well referenced’, with 145 in the References, perhaps too many?
Specific comments:
In Table 1, it seems that mosses formed a significant plant cover in the chambers (e.g. Sphagnum balticum, capillifolium and riparium in the three thaw stages). Would methane emission rates be affected by this coverage and some differences between chambers and cores and different wetness? This is addressed in 4.2 line 486 onwards …..
A tremendous amount of work went into this study, particularly in the measurements of root and rhizome properties collected from the cores. If I understand correctly, a 12 cm diameter peat core was dived into 10 cm depth increments and these were then divided into four vertical quarters, which was used for trait measurements, resulting in subsampling of the core sections (and subsampling of that in some cases). This are measurements based on an initial volume of 1130 cm3, and it must take considerable time and patience to extract roots and rhizomes, weighing in some cases to 0.00001 g. pH in 0.01M Cacl2 is much easier and quicker …….
While I accept that the belowground contribution is important to processes such as methane emission, are there any ways of making it ‘easier’ to define and measure these properties over a wider range of sites? If so the properties could be included and tested within models which are grappling with the high spatial and temporal variability of methane emission rates.
Technical issues:
I found few. I thought that the first two sentences of 2.6 (lines 214-215) could be combined into one: they are repetitive. Minor typos in places.
Fig. B13. I was confused the right hand diagram. I think the dashed lines have circles whereas the solid lines have triangles …… not what is written in the legend?
I did find that the total root length of shrubs in the intact sites was about 180 km per square meter (to 30 cm depth). Jeez, as it is 10 km from Stordalen to Abisko, it means that one square meter of intact permafrost has enough shrub root to go back and forth 18 times or perhaps all the way to Norway or the Norwegian Sea? Might get the attention of readers that permafrost is not ‘dead’ but rich in roots and though root length decreases in thawed sites, the impact of roots and rhizomes and change from shrub to herbaceous plants allows for larger methane emission rates.