Articles | Volume 22, issue 18
https://doi.org/10.5194/bg-22-4885-2025
© Author(s) 2025. This work is distributed under
the Creative Commons Attribution 4.0 License.A niche for diverse cable bacteria in continental margin sediments overlain by oxygen-deficient waters
Download
- Final revised paper (published on 24 Sep 2025)
- Supplement to the final revised paper
- Preprint (discussion started on 14 Mar 2025)
- Supplement to the preprint
Interactive discussion
Status: closed
Comment types: AC – author | RC – referee | CC – community | EC – editor | CEC – chief editor
| : Report abuse
-
RC1: 'Comment on egusphere-2025-817', Maxime Daviray, 15 Apr 2025
- AC1: 'Reply on RC1', Caroline P. Slomp, 14 May 2025
-
RC2: 'Comment on egusphere-2025-817', Anonymous Referee #2, 18 Apr 2025
- AC2: 'Reply on RC2', Caroline P. Slomp, 14 May 2025
Peer review completion
AR: Author's response | RR: Referee report | ED: Editor decision | EF: Editorial file upload
ED: Reconsider after major revisions (30 May 2025) by Edouard Metzger

AR by Caroline P. Slomp on behalf of the Authors (16 Jun 2025)
Author's response
Author's tracked changes
Manuscript
ED: Referee Nomination & Report Request started (20 Jun 2025) by Edouard Metzger
RR by Maxime Daviray (30 Jun 2025)

RR by Anonymous Referee #2 (04 Jul 2025)

ED: Publish as is (11 Jul 2025) by Edouard Metzger
AR by Caroline P. Slomp on behalf of the Authors (15 Jul 2025)
General comments:
In this manuscript, Slomp et al. initially described the continental margin sediments (>100 m deep) of hypo- to anoxic nitrogenous basins as a niche for the development of cable bacteria (CB). Then, they estimated the abundance and diversity within the Cadidatus Electrothrix lineage to provide an overview of the recently described diversity of this group, and to suggest a new genus adapted to these environmental conditions. The manuscript is fairly well structured, and its objectives are clear. The methodological approaches are comprehensive and aim to characterise the geochemical conditions of the bottom waters, the sedimentary compartment (pore-water and solid phases) and the microbial community concerned. The data sets are freely accessible on Zenodo. Despite the wide range and quality of the data, it is a snapshot in time, which limits the scope of the discussion on the factors controlling the CB dynamics in this potential niche. Overall, I think this is a robust and very interesting research paper which corresponds to the scope of Biogeosciences.
Specific comments:
Line 104: you present bibliographical data on Thioploca in the Soledad basin, but nothing on the other groups presented in the introduction (Beggiatoaceae and Thiomargarita). Is there any information available on this subject in these basins? Similarly, in line 108, you present (admittedly old) data on the meiofauna and macrofauna of this same basin, but you say nothing about the other basins? Have no data been published?
Lines 133-135: only one O2 profile was done in San Clemente? How were the pH and H2S measurements set up to achieve complete microprofiling to a depth of over 3 cm in less than 15 minutes? I assume that the waiting and measurement times are particularly short. Is this relevant for this type of measurement?
Line 160: one point I don't understand about the analysis of dissolved metals: why didn't you use the pore water Mn data from Bruggmann et al. (2023), as you did for Fe, in order to have the same vertical resolution for both? The vertical resolution in Bruggmann et al. (2023) is low and I find it relevant that you have carried out higher resolution analyses for Mn. But in that case, why didn't you do the same for Fe to get geochemistry within the same core?
Section 4.1: the densities observed in these hypo-anoxic basins are like those observed in situ on estuarine intertidal mudflats (oxygenated environment + sulphides) where CB could be particularly active (Daviray et al., 2024), or in the rhizosphere of aquatic plants (Scholz et al., 2019, 2021).
The presence of CB (DNA data) but the absence of activity also raises a hypothesis that is not discussed here: could it be the result of CB-enriched sediment transport into the basins? Do you have any information on the marine currents affecting these locations? In this case, it could be better to talk about a ‘potential’ niche.
Section 4.2: The discussion of the sources of H2S and its temporal dynamics is stimulating. However, it remains hypothetical and suffers from a lack of (temporal) data, in my opinion. Have you tested correlations between the various parameters (i.e., Corg, total S, Fe sulphides, etc.) to perhaps highlight this dynamic and support a periodic (seasonal?) increase in sulphate reduction?
Lines 434-447: in my opinion, this paragraph lacks any link with the biogeochemical data to explain the diversity observed.
Line 441: what electron acceptor do the Bacteroidota use?
Line 453: it's a shame that we don't have this data, as it would have helped to underpin the discussion on interspecific competition.
Line 461: any suggestions on these factors (bioturbation or others generating sediment heterogeneity, Fe curtain, etc.)?
Lines 475-476: out of curiosity, do you have any idea what these benefits might be? The same for the selective pressures mentioned line 489. The section 4.4 is very interesting and frustrating: we want to know more!
Section 4.5: this section could perhaps be further summarised and incorporated into the second paragraph of the conclusion.
Figures:
Figure 1: the blue colour contrast is poor. Would it be possible to improve it like in Bruggmann et al., 2023?
Figure 2: you write that triplicates were achieved for pH and H2S µprofiles. Is the absence of standard deviation on these profiles justified by their high reproducibility? I suppose so for H2S (because there isn't any), but what about pH?
Figures 2, 3 and 4: please, put the unit of the vertical axis in cm.