Articles | Volume 22, issue 21
https://doi.org/10.5194/bg-22-6343-2025
© Author(s) 2025. This work is distributed under the Creative Commons Attribution 4.0 License.
Plant community composition explains spatial variation in year-round methane fluxes in a boreal rich fen
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- Final revised paper (published on 05 Nov 2025)
- Preprint (discussion started on 05 Feb 2025)
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-2025-217', Anonymous Referee #1, 11 Mar 2025
- AC1: 'Reply on RC1', Eeva Järvi-Laturi, 10 Apr 2025
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RC2: 'Comment on egusphere-2025-217', Anonymous Referee #2, 12 Mar 2025
- AC2: 'Reply on RC2', Eeva Järvi-Laturi, 10 Apr 2025
Peer review completion
AR: Author's response | RR: Referee report | ED: Editor decision | EF: Editorial file upload
ED: Reconsider after major revisions (16 Apr 2025) by Erika Buscardo
AR by Eeva Järvi-Laturi on behalf of the Authors (13 May 2025)
Author's response
Author's tracked changes
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ED: Referee Nomination & Report Request started (21 May 2025) by Erika Buscardo
RR by Anonymous Referee #1 (31 May 2025)
RR by Anonymous Referee #2 (19 Jun 2025)
RR by Anonymous Referee #3 (02 Jul 2025)
RR by Philip Wookey (12 Jul 2025)
ED: Publish subject to technical corrections (28 Jul 2025) by Erika Buscardo
AR by Eeva Järvi-Laturi on behalf of the Authors (04 Aug 2025)
Author's response
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General comments:
This manuscript by Järvi-Laturi et al, looks into fine-scale spatial variation in methane flux in a boreal peatland over a full year. By measuring species-specific vascular plant and moss biomass together with chamber-based methane flux measurements, the authors found that increasing sedge biomass, in particular that of Carex rostrata, seem to increase methane emissions significantly especially in the snow-free season and full-year scales. Based on their analyses, vegetation composition and biomass seemed to be a stronger driver of methane fluxes than abiotic environmental variables at this site. The authors attributed these results to both enhanced provision of carbon substrates for methanogens and methane transport from soil to the atmosphere.
This is a study that provides the much-needed data and overview of both wintertime and full-year methane fluxes in a peatland, data that still to this day are quite scarce and thus valuable. As the authors mention in the manuscript, regional and global wetland methane budgets contain large uncertainties, some of which are related to the spatial variation in methane fluxes and vegetation composition. Therefore, this study, which looks at small scale (between-plot) methane flux variation, has potential in adding to our understanding of plant-mediated methane emissions in carbon-rich peatland ecosystems. While I see a lot of value and potential in this work, I recommend a list of improvements (major or minor, depending on how biomass measurements were conducted):
Specific comments:
a) It is unclear how you scaled the vascular plant biomass measurements to the collars. You mention that you counted the number of shoots per species within the collar, but did you use this shoot number to scale the mean biomass of 10 samples to the actual collar (or did you actually take average of 20 sample plants if you ignored the fertile/sterile division? See comment 1 c)? If you did not scale these measurements to the collar, you cannot reliably estimate the collar species biomass, and so I recommend to do this and re-analyze your data and fix the results in 3.2, 3.3, 3.4, 3.5 with appropriately scaled biomass values. If you did do this, please explain this clearly and in more detail in the methods section.
b) It is also unclear how you took the moss biomass samples and scaled them to the collar. How did you determine which species were “most common” and which were not? What was the percentage cover limit (if there was one)? What was the spatial scale that you used for estimating the “most common” species- was it across the whole study site or within individual collar? If it was across the whole study site, I don’t quite understand the logic of taking a biomass sample equaling to 5 % of the collar area (i.e. 33.025 cm2) especially if the collar had an actual percentage cover <5%, in which case you may have overestimated the species biomass in the collar. Or did all of these “most common” species have >5% coverage in all collars?
If you looked at this at the scale of individual collars, did you take a sample that was equal to 5 % of the collar area per species for the five most common species within each collar and for the rest of the species found within the collar, you took a sample over an area equal to 1% area of the collar (i.e. 6.605 cm2)? What did you do if there were less than five species within the collar? Did every collar really have 10 species within them (now the text kind of makes it sound like there were but it doesn’t seem likely to me)? Please specify this in the methods.
And, most importantly, how did you scale the moss biomass samples to the percentage coverage within the individual collars? As with the vascular plant biomass, if no scaling was done, the moss biomass measurements do not represent the actual collar moss biomass and the data should be re-analyzed with appropriate scaling. Please specify this clearly in the methods.
c) How did you determine the locations for vascular plant and moss biomass sampling? Were the soil conditions (e.g. pH, soil moisture) similar to the collar? Did you look at and compare the general species composition in the collar vs the plots where you collected the biomass samples (between-species competition could affect some of the plant trait expression and thus biomass), for example by determining percentage cover? How did you decide which plants and moss patches to pick?
For mosses, did you look at e.g. moss stem density in some way to try to estimate the moss biomass in the collar and in the sampling points more reliably than just percentage coverage (the same percentage coverage can represent very different moss biomasses in different collars due to variation in moss stem density and other structural properties)? If not, the moss biomass estimates may be very uncertain and I would recommend discussing these uncertainties explicitly and in much more detail in the manuscript. Given these uncertainties, I would also recommend not to emphasize the ratio between vascular plants and bryophytes as an important methane flux predictor as much as you have so far in this manuscript, or at least combine it with adequate discussion about its uncertainties.
If you did not estimate the similarity (in terms of abiotic/biotic variables) between the collar and the plot where you collected the representative biomass samples, I would be careful making strong conclusions about collar-specific plant species biomass variation.
d) What do you mean by the “fertile” and “sterile” categories for the plant biomass? In my understanding fertile vs sterile categories are used in the context of evolutionary plant biology and plant reproduction (i.e. fertile vs sterile flowers). Or did you use it to somehow determine whether the species had vegetative culms (e.g. for Carex) from previous year? It is unclear to me how this classification is relevant to the topic of methane flux spatial variability, especially because you do not talk about these classes afterwards. If you used some kind of scaling for the collar biomass (see comment 1 a), did you take use of these fertile/sterile classes in that as well? Please add a clarification for this separation, what the rationale is behind it, and what you mean by the terms.
It is now also unclear whether the species-specific plant biomass is calculated as the mean of n=20 biomass samples (fertile + sterile) per species per plot, or are the species-specific plant biomasses actually still divided into the fertile (mean of n=10 biomass samples) and sterile (mean of n=10 biomass samples) classes. Based on your results, it seems that you took the mean of 20 samples by combining the fertile and sterile samples? Please add a clarification to your methods.
Also, the plot numbers themselves do not really give any valuable information for the reader. If you want to show all the plot fluxes separately here, the plot numbers could be replaced with something simpler, such as 1-36, to improve the readability of this figure (the current numbering adds more complexity for the reader who is not familiar with your study site).
On the other hand, if you want to keep the coloring, could you do it based on e.g. vegetation composition grouping (for example based on your vegetation clusters)? If you do this, I would also recommend changing the red color of the soil temperature to black, because the red and green are difficult to separate visually for some readers with color-blindness.
The axis texts are also a bit small so please increase the font size.
a) The correlation between peat depth and plant biomass makes sense in the biological sense that, when there is more peat, there is also more space for roots especially for more deeply-rooting vascular plants. Since you did not find significant correlations between peat depth and methane fluxes, I would be careful drawing strong conclusions about the influence of peat depth on methane fluxes via vegetation (but see my next point).
b) On the other hand, it is also possible that in the presence of deeply-rooted aerenchymatous vegetation, such as C. rostrata, the roots may provide labile carbon substrates in deep peat where methanogenesis increases despite the dominance of recalcitrant peat (i.e. indirect influences of peat depth on methane fluxes). The release of labile carbon compounds via root exudation could also trigger microbial carbon priming (see e.g. Waldo et al 2019: https://doi.org/10.1007/s10533-019-00600-6). However, be careful about your interpretations about the wintertime vegetation influences based on your data (see previous comment about wintertime fluxes), and keep in mind that the direct relationship between peat depth and methane flux was still nonsignificant.
Technical comments: