Abstract
Subsurface environments host most of the fresh water on Earth as well as diverse microorganisms that may constitute a significant part of the biosphere. However, the dynamics and spatial distribution of subsurface microorganisms and their response to hydrological processes are poorly understood. Here we used chemical and metagenomic analyses of groundwater in a fractured rock aquifer in western France to determine the role of fractures in the formation of deep microbial hotspots in the subsurface. The majority of fractures, sampled in a 130-m-deep borehole, were anoxic, but a fracture carrying oxic groundwater was detected at 54-m depth, associated with a fivefold increase in the abundance of iron-oxidizing bacteria. We developed a mechanistic model of fluid flow and mixing in fractures and found that such microbial hotspots are sustained by the mixing of fluids with contrasting redox chemistries at intersections of fractures. The model predicts that metre-scale changes in near-surface water table levels cause intermittent oxygen delivery through deep fractures, which can extend the depth of the habitable zone for iron-oxidizing bacteria hundreds of metres into the subsurface. Given that fractures are ubiquitous at multiple scales in the subsurface, such deep microbial hotspots may substantially influence microbial communities and their effect on Earth’s biogeochemical cycles.
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Data availability
The data that support the findings of this study were measured at the Ploemeur fractured rock observatory, belonging to the French network of hydrogeological sites H+ (hplus.ore.fr). They are available from the H+ database: http://hplus.ore.fr/bochet-et-al-2019-data.
Code availability
The Matlab code developed to simulate the depth of the habitable zone for FeOB (Fig. 4) is available at http://hplus.ore.fr/bochet-et-al-2019-data.
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Acknowledgements
Funding was provided by the ERC project ReactiveFronts (648377), the ANR projects CRITEX (ANR-11-EQPX-0011), Subsurface mixing and reactions (ANR-14-CE04-0003) and Stock-en-Socle (ANR-13-SEED-0009), ADEME and Région Bretagne. We thank the Ploemeur observatory (H+ network hplus.ore.fr and OZCAR Network of Critical Zone Observatories) for providing data and field support for this study. We thank L. Longuevergne and O. Bour, respectively principal investigators of the Ploemeur site and of the H+ network, for providing access to the site and to the data, and support for the organization of field campaigns. We thank M. Bouhnik-Le-Coz and P. Petitjean for chemical analysis, CMEBA for SEM imaging, CONDATE EAU for dissolved gas analysis, M. Chorin for light and fluorescence microscopy, A. Quaiser, S. Michon-Coudouel and M. Biget for metagenome sequencing and S. Gu for the Chinese translation of the abstract. We finally thank Y. Duclos, S. Ben Maamar, T. Babey, G. Baby and P. Davy for their help and stimulating scientific discussions.
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O.B. led the field campaigns, batch tests, data interpretation, model development and results formatting. L.B. carried out metagenome production and draft genome assembly. A.D. supervised metagenomic data analysis and interpretation. J.F. managed bacteria sampling and characterization in field campaigns and batch experiments, and performed hydrochemical borehole logging. M.P. performed chemical and SEM analysis of fluids and microbial mat sampled in field campaigns and batch experiments. T.L. and E.C. managed measurements of dissolved gases and CFC in field campaigns. N.L. developed the packer system and managed borehole flow and pressure measurements. C.P. handled logistics related to field campaigns. B.W.A. contributed to formalize biogeochemical implications of results, manuscript editing and proofreading. L.A. supervised geochemical and metagenomic data interpretation. T.L.B. designed the research and supervised data interpretation, modelling and manuscript writing.
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Extended data
Extended Data Fig. 1 Distribution of oxygen and flow patterns at the study site.
a. Map of borehole locations and oxygen distribution at 20 meters depth interpolated from borehole oxygen profiles (Extended Data Fig. 2b). b. Conceptual model of oxic and anoxic flow in the subsurface. Oxic boreholes (PZ15, PZ21, PSR1 and PSR2) are located on high topographic areas, where the near surface piezometric level is higher than the deep piezometric level (recharges areas). This induces downward flow of oxygen in permeable fractures. Anoxic boreholes (PZ2, PZ19, PZ22, PZ23, PZ24, PZ25, PZ26, PSR5) are located in low topographic areas, where the deep piezometric levels are higher than near surface piezometric levels (discharge areas). This induces upward flow of reduced water up to the surface. As these fluxes occur through a complex fracture network, this leads to mixing of oxic and anoxic fluids at fracture intersections (yellow dots).
Extended Data Fig. 2 Piezometric levels and oxygen profiles.
a. Evolution of piezometric levels over time for two boreholes located respectively in recharge (PZ15) and discharge (PZ23) areas. b. Oxygen concentration profiles with depth in the 12 boreholes. The boreholes representative of recharge areas are represented in shades of blue colors, while those representative of discharge areas are represented in shades of red colors. A model of average oxygen concentration decay by biogeochemical activity (equation (4)) is fitted from the oxygen evolution with depth observed in the deepest boreholes representative of recharge areas, PSR1 and PSR2 (dashed black line).
Extended Data Fig. 3 Intermittent oxygen delivery in the subsurface in response to water table change during a hydrological year.
a. Evolution of the piezometric levels during the hydrological year 2016/2017 in boreholes representative respectively of the recharge areas (PZ15, blue line) and of the deep fractured zone (PZ23, orange line) in response to the cumulative rainfall (grey histogram). b. Temperature (left) and oxygen (right) profiles at two different times, representative of the recharge period (13/04/2017, blue lines) and of the dry period (20/10/2017, red lines).
Extended Data Fig. 4 Optical logs and video images of borehole PZ26.
a. Snapshots of \(36{0}^{\circ }\) optical logs showing the main permeable fractures. The dark regions correspond to open fractures. Small fractures composing F37 and F59 are highlighted in red. The vertical and horizontal scales are indicated at the bottom left. b. Location and relative transmissivity of the main permeable fractures. c. Snapshots of borehole video showing an example location where the microbial mat is clogging the borehole (30 m), the oxic fracture F54 (53.6 m), an example of non fractured zone (68.6 m) and a deep reduced fracture (73.6 m), see also Supplementary Video.
Extended Data Fig. 5 Sampling of fracture fluid in borehole PZ26.
a. Natural discharge from the deep fractures towards the surface in the PZ26 artesian borehole. All fractures are under pressure and constantly produce flow towards the top of the borehole. Therefore, dissolved oxygen cannot diffuse from the surface through the borehole and any oxygen molecule contributing to iron oxidation has to be transported through the fracture network. b. Field sampling of pristine fracture fluid in borehole PZ26 with a packer. c. Sketch of the packer sampling method. In this example, the targeted fracture is F37. The large pump at the top of the well draws water from all fractures above the packer. Hence the small pump in front of F37 only pumps water from F37. The packer prevents any flow from fractures located below it.
Extended Data Fig. 6 Batch experiments for monitoring the kinetics of iron oxidation and oxygen consumption during mat formation.
a. Formation of the microbial mat in the sampling bottles. b. Evolution of dissolved oxygen (blue) and iron (orange) concentration, pH (green), and redox potential (purple) as a function of time.
Extended Data Fig. 7 Estimated depths, hydraulic properties, apertures and sampling radii of the permeable fractures in borehole PZ26.
The depth of permeable fracture is estimated from the flow and optical logs (Fig. 2). Relative and absolute fractures transmissivities are estimated from equation (1) with \({T}_{tot}=5.1{0}^{-3}\,{\rm{m}}^{2}\,.{\rm{s}}^{-1}\). The fracture aperture is estimated by inverting equation (2) with \(\rho =1{0}^{3}\,{\rm{kg}}/{\rm{m}}^{3}\), \(g = 9.81\,{\rm{m}}/{\rm{s}}^{2}\) and \(\mu = 1.1410^{-3}\,{\rm{kg}}/{\rm{m}}/{\rm{s}}\). The sampling radius is estimated from equation (3).
Extended Data Fig. 8
Iron speciation in each sampled zone.
Supplementary information
Supplementary Information
Details of the model derivation and metagenomic analysis, Figs. 1–5 and Tables 1–3.
Supplementary Video 1
A borehole video (.avi format) showing the distribution of the FeOB microbial mat in borehole PZ26. The video shows selected sections of the borehole up to 84-m depth.
Supplementary Video 2
The same as Video 1 in .mov format.
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Bochet, O., Bethencourt, L., Dufresne, A. et al. Iron-oxidizer hotspots formed by intermittent oxic–anoxic fluid mixing in fractured rocks. Nat. Geosci. 13, 149–155 (2020). https://doi.org/10.1038/s41561-019-0509-1
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DOI: https://doi.org/10.1038/s41561-019-0509-1
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