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Possible nitrogen fertilization of the early Earth Ocean by microbial continental ecosystems



While significant efforts have been invested in reconstructing the early evolution of the Earth’s atmosphere–ocean–biosphere biogeochemical nitrogen cycle, the potential role of an early continental contribution by a terrestrial, microbial phototrophic biosphere has been largely overlooked. By transposing to the Archean nitrogen fluxes of modern topsoil communities known as biological soil crusts (terrestrial analogs of microbial mats), whose ancestors might have existed as far back as 3.2 Ga ago, we show that they could have impacted the evolution of the nitrogen cycle early on. We calculate that the net output of inorganic nitrogen reaching the Precambrian hydrogeological system could have been of the same order of magnitude as that of modern continents for a range of inhabited area as small as a few percent of that of present day continents. This contradicts the assumption that before the Great Oxidation Event, marine and continental biogeochemical nitrogen cycles were disconnected.


In the last decade significant progress has been made in reconstructing the evolution of the nitrogen (N) biogeochemical cycle through Earth’s history, with an increasing focus on the Archean period, from 4.0 to 2.5 Ga1,2,3,4. A general time frame (Fig. 1) emerged from these recent contributions that proposes the following sequence of events: from 3.6 to 3.2 Ga during the Paleoarchean, microbial diazotrophy evolved and supported the nitrogen demand of the earliest ecosystems3,5, between 2.7 and 2.6 Ga an oxic pathway of the nitrogen cycle emerged even before full atmospheric oxygenation at 2.45 Ga during the Great Oxidation Event6,7,8 (GOE), at 2.3 Ga nitrate became more widely available due to ocean oxygenation9, from 1.9 Ga onwards, during the mid-Proterozoic, aerobic and anaerobic nitrogen cycling were spatially separated between surface and deep waters1,10,11,12, and eventually, around 750 Ma (but possibly back to 1 Ga) during the Neoproterozoic, there arose a modern nitrogen cycle featuring widespread aerobic activity13,14. This sequential evolution of the N cycle involving changes in the balance of N source and sink fluxes has been tentatively linked to important atmospheric pressure fluctuations observed during the Precambrian15. The main drivers of these changes are biological evolution16 along with redox variations in Earth’s surface environments, primarily due to the oxygenation of the atmosphere–ocean system1,2.

Fig. 1

Secular variation of the sedimentary δ15N record through geological time. The stepwise evolution of the biogeochemical nitrogen cycling is shown as blue shaded areas. The Great Oxidation Event (GOE) and first evidence of terrestrial biological soil crusts (BSCs) are shown in red and yellow, respectively (δ15N data compilation after refs. 1,9,74)

This scenario is largely based on the interpretation of secular variation of the nitrogen isotopes from the sedimentary rock record1,2,9. Physical, chemical, and biological processes differentially incorporate the two stable N isotopes (15N and 14N), leading to measurable differences in the 15N/14N ratio of sedimentary nitrogen. Nitrogen isotopes can provide a record of specific biosignatures and are sensitive to environmental redox changes17, making them a good proxy to track the evolution of N reservoirs and fluxes throughout Earth history. However, their use is challenging due to a number of technical pitfalls, including the fact that nitrogen is found and preserved in measurable quantities in relatively few phases, primarily organic matter, phyllosilicates, feldspars, magnetite, and fluid inclusions (a compilation of Precambrian δ15N data is in ref. 1). Another limitation arises from the scarcity of the Archean sedimentological record (compared to that of the Phanerozoic) and the even poorer archive of continental paleosols. Altogether, this led to the use of geochemical box models to reconstruct the Precambrian balance of N source and sink fluxes without taking into account the possible role of an evolving continental biosphere reservoir15,18.

During the Archean, the lack of an ozone layer resulted in higher short-wavelength irradiance than today despite the fact that the sun was 30% dimmer19. Because of this peculiar environmental condition Berkner & Marshall20 first postulated that the colonization of the landmasses was not possible before the formation of an ozone shield. However, recent findings demonstrate that in the primitive anoxic atmosphere sulfur vapor composed of sulfur molecules and hydrocarbon smog may have strongly attenuated ultraviolet radiation21. Also, a high concentration of ferrous ion (Fe II) may have been present in anoxic waters to significantly screen UV radiation22. Moreover, Cockell & Raven23 show that under a worst-case UV flux (no environmental UV screen) on the Archean Earth, the landmasses could have been colonized by early photosynthetizers. Therefore, despite a “faint young sun” and the absence of a UV-protective ozone layer in the Archean24,25 a terrestrial phototrophic biosphere composed of systems similar to modern biological soil crusts (BSCs) may have existed early, before the GOE26, and could have colonized the exposed land surfaces27.

Modern BSCs are arguably the most extensive biofilm on the planet covering up to 12% of Earth’s continental area28, and while they are composed of a wide diversity of microorganisms they are primarily built by cyanobacteria performing oxygenic photosynthesis29. With fresh volcanic material to act as fertile soil, in the absence of plant root systems and grazers, one could entertain the idea that BSCs should have had the potential to rapidly develop and thrive during Archean time due to lack of competition, even beyond their restricted modern habitat, which is circumscribed to areas devoid of extensive plant cover. The oldest direct evidence for fossil BSCs comes from the 1.2 Ga mid-Proterozoic Apache Supergroup in the Dripping Springs Formation of Arizona, including sedimentological evidence for microbially induced sedimentary structures (MISS) and cyanobacteria-like organic microfossils30. But, indirect evidence of BSCs developing on Archean coastal plain paleosols date them back to 3.0 Ga31. Tufted microbial mats inhabiting coastal habitats have also been described within the Moodies Group (South Africa) at 3.2 Ga32. Chemical pieces of evidence based on element mobility patterns in several paleosols also suggest the presence of an ancient terrestrial biosphere where organic ligands chelated metals during weathering33,34. Modern BSC do indeed produce such chelators35, and are known to mobilize metals36. The evidence timeline for BSC development is consistent with results of molecular clock estimates, that place the colonization of land at the latest between 3.05 and 2.78 Ga based on shared properties of pigment synthesis and resistance to desiccation exhibited by typically terrestrial extant bacterial phyla37,38. The impact of a pre-GOE BSCs colonization of the continents has already been explored in the framework of atmospheric oxygen concentration evolution. Pre-GOE BSC-driven photosynthetic oxygen flux to the atmosphere and ensuing oxidative weathering efficiency was proposed as a scenario to explain the existence of transient episodes of mild environmental oxygenation (so called “whiffs of oxygen”) and oxidative continental weathering26,39,40. This scenario echoes theoretical predictions of a long lasting, mass-independent sulfur isotopic signal due to long-term sedimentary recycling of rare sulfur isotope anomalies41.

Here, we address at a theoretical level the impact of early colonization of Archean continental landmasses by BSCs in terms of N species source fluxes to the ocean. We show that the colonization of a minor fraction of Archean landmasses by BSCs should have sufficed to attain the modern equivalent land-to-ocean N export flux of ammonium and nitrate. We suggest that the ocean could have acted as a net sink for ammonium and nitrate during the Archean before oceanic nitrate concentration reached a steady state at around 2.3 Ga.


Nitrogen export capacity of modern BSCs

Modern BSCs play a significant role in the N cycle within arid and semiarid ecosystems, as they contribute to major N inputs via biological fixation42, harbor intense internal N transformation processes, and direct N losses via dissolved, gaseous, and erosional processes (Fig. 2). Since denitrification rates within BSCs are extremely low and because of limited respiration and ammonia oxidation, BSCs function as net exporters of ammonium, nitrate, and organic N to the soils they cover, in approximately stoichiometrically equal proportions43. Importantly, N cycling by BSCs likely regulates short-term soil N availability, as well as long-term N accumulation and maintenance of soil fertility43. Whereas multiple studies have examined a single compartment of the modern BSCs N budgets, the lack of studies that simultaneously address N inputs, losses, and soil pools, preclude the construction of definitive N balances (see a review of estimate fluxes of these processes in ref. 44). Nonetheless, Walvoord et al. 45 reported on the existence of a large reservoir of nitrate beneath desert soils, that clearly indicates long-term net export of N from topsoil to arid land subsoils. Some studies give direct estimates of this export flux of N and leachates from BSCs colonizing beach dunes at the Indiana Dunes National Lakeshore along southern Lake Michigan in Indiana, USA46 and at the Colorado Plateau, USA43. Both studies simulate rain events and measured resulting net N outputs from crusts to subsurface soil. The N outputs from crusts of the Colorado Plateau ranged from 0.98 to 5.02 g NH4+  N m2 yr1 and 1.10 to 3.8 g NO3  N m2 yr1, commensurate with rates of N-fixation at the study site, although this was a measurement carried out at a maximal depth of only 20 cm below the crusts. At Indiana Dunes National Lakeshore, the net N outputs from crusts to subsurface soil were measured after a long-term greenhouse experiment in which intact soil cores composed of a population of mixed cyanobacteria, algae, and bryophytes forming BSCs were subjected to artificial rainfall over a full growth season46. Fluxes there ranged from 0.01 to 0.19 g NH4+  N m2 yr1 and 0.01 to 0.61 g NO3  N m2 yr1. Accordingly, in this system the total inorganic N inputs to Lake Michigan sand dune ecosystem from BSCs ranged from 0.02 g N m2 yr1 to 0.8 g N m2 yr1. These two studies give congruent estimates of N export (slightly larger for the Colorado Plateau BSCs) and indicate the presence of net production zones of nitrate in all crusts. However, because incubations used by Johnson et al.43 were performed on short timescale (20 days) the authors acknowledge that their outputs fluxes might be slightly overestimated due to non steady-state situation with respect to production, consumption and diffusion of N species. In the experiment designed by Thiet et al.46, N was measured after it had leached beyond a depth of 7 cm and for some 75 days. For these reasons the measurements of N production and leachates of BSCs given by Thiet et al.46 probably represent a more realistic appraisal. Estimates of N outputs from BSCs to subsurface soil can also be evaluated indirectly using the rule of thumb that 19–28% of the nitrogen fixed by soil crusts ends up in the underlying topsoil47,48. Biological soil crusts in cold deserts are estimated to fix 1–10 g N m2 yr1 49,50, while estimates for the Sonoran desert and Australia range from 0.7–1.8 g N m2 yr1 and 0.13 g  N m2 yr1, respectively51,52. The full range of indirect estimates is indeed quite large, ranging from 0.07 to 10 g N m2 yr1 53,54,55,56,57,58,59,60. Quantification of N fixation by biocrusts in a global survey yielded a geometric mean value of 0.76 g N m2 yr1 42. Using these range of estimates and a minimum export rate of 19%, we could scale indirect estimates of N crust output to subsurface soil from 0.013 to 1.9 g N m2 yr1 with a mean of 0.144 g  N m2 yr1 (Table 1).

Fig. 2

Biological soil crusts and associated nitrogen cycling. Modern biological soil crusts (a), and a scheme of its internal structure showing close association between filamentous cyanobacteria and mineral grains. Schematic illustration of nitrogen cycling transformations in modern biological soil crusts (b), reprinted/adapted by permission from ref. 44

Table 1 Compilation N outputs estimates from biocrusts to subsurface soil from various location worldwide and the respective percentage of Archean land crust cover needed to reach the modern N land-to-ocean export flux

Parameters driving the fate of nitrogen: past and present

Additionally and importantly for our tentative deep-time transposition, Thiet et al.46 demonstrated that the proportional cover of cyanobacteria and mosses did not significantly affect these fluxes. An increase in light intensity directly increased the N throughput, while its decrease when combined with an increase in rainfall intensity indirectly increased the N output fluxes by maximizing the leachate volume. Moreover, while it had been postulated that the export range might also depend on the BSCs ecosystem structure and especially the proportion of N-fixing organisms and their N-fixation rates61 compared with the proportion and activity of denitrifiers, recent direct evidence shows that these factors are unimportant62. Using modern desert BSCs obtained across biogeographic regions in the Southwestern United States from the Colorado Plateau and the Mojave, Sonoran and Chihuahuan Deserts, Strauss et al.62 showed that the measured rates of major biogeochemical N-transformations (N-fixation, aerobic ammonia oxidation, anammox, and denitrification) despite the demonstrable differences in microbial community composition and soil material displayed a remarkably consistent pattern of internal N cycling. Dinitrogen fixation and aerobic ammonia oxidation were prominent transformations at all sites, while anaerobic ammonia oxidation (anammox) rates were below the detection limit in all cases, and heterotrophic denitrification was also of little consequence for the flow of N, with rates at least an order of magnitude smaller than those of N-fixation. These modern examples of BSCs from sandy soils are good analogs of the environment available for the development of BSCs on Archean continents given the aggressive weathering regime postulated for the early Earth63 when sedimentation was largely dominated by siliciclastic inputs64, and with aeolian sand systems reported as early as 3.2 Ga (Lower Moodies Group of the Swaziland Supergroup in South Africa32). Environmental parameters may therefore primarily control the export rate in BSCs over a wide range of microbial community composition and soil material, and the main N escape routes are likely to depend more on hydrology than on biology. While the fate of these exports remains to be assessed, it is likely that soil bacterial populations, depending on available oxidants, will rapidly use organic N and ammonium. But, nitrate exports are probably of longer range, because the molecule is environmentally mobile and biologically less desirable than ammonium.

Quantitative modeling

On the geological timescale of interest here, a hypothetical contribution of BSCs in transferring atmospheric fixed N2 to the ocean in the form of organic nitrogen, ammonium and nitrate (Fig. 2) may have had consequences for the evolution of the global N cycle, which would have eventually been recorded in the δ15N secular variation. This prompted us to evaluate the pertinence of this hypothesis quantitatively by modeling the fluxes of N that may have been exported to the underlying soil and hydrogeological system by BSCs using the fluxes obtained in modern studies. For the sake of clarity, we express those as a function of a percent of colonized modern continental area or Archean equivalent landmasses (assuming a total emerged surface of about 90 Mkm2 at around 2.45 Ga, i.e., 60% of the present day value65). We hypothesized that N outputs from BSCs to subsurface soil and hydrogeological system were delivered to the oceanic basin after weathering, without further remobilization. This first-order hypothesis probably tends to overestimate N transport to the ocean but is consistent with Archean BSCs developing in coastal habitats close to oceanic basins31,32 and with a reduced soil biological demand. The results are presented in Table 1 and Fig. 3 as the N transport of inorganic N for a variety of net N throughput scenarios based on the direct and indirect results from modern BSCs studies. We calculate that the total inorganic N transport is likely to have been quite substantial, reaching the proposed value for the Phanerozoic land-to-ocean N flux (around 0.15 ± 0.03 Tmol yr−1 based on N/C data from shales and continental organics15) when Precambrian areas colonized by BSCs attained anywhere from <1% to more than 113% of the modern continental area if one includes the full range of modern net N outputs (from 0.0133 to 8.820 g N m2 yr1, Supplementary Table 1). Table 1 summarizes the literature estimates that were used for our calculations. It shows that published estimates vary by more than two orders of magnitude. Based on the available data, however, all but three reported values support the idea that the colonization of a minor fraction of Archean landmasses by BSCs (<18%) would suffice to attain the modern equivalent N export flux. More precisely, the geometric mean value computed by Elbert et al., which is the most robust global estimate available to date, suggests that 16% of land colonization by biocrust would be enough to recapitulate the modern N export. Overall, in both modern and Archean configurations, a high to moderate range of net N outputs from BSCs to subsurface soil of 0.8 to 0.1 g N m2 yr1 (with a mean indirect estimate of 0.144 g N m2 yr1 42) implies a total inorganic N transport comparable to Phanerozoic land-to-ocean N fluxes at a rather small continental cover (≈3 to 25% based on Thiet et al.46 direct estimates and 16% based on Elbert et al.42 indirect estimate) (Fig. 3). Given that current cover by crusts, even when their current potential habitat is restricted to lands with sparse higher plant vegetation, is some 12% of the continents28, those levels of Precambrian cover seem plausible.

Fig. 3

Modeling results of the land-to-ocean N export fluxes from biological soil crusts as a function of the percentage of modern continental area colonized, for a variety of net N transport fluxes. a Modeled export fluxes (Tmol yr1) from biological soil crusts (BSCs) as a function of the percentage of modern continental area colonized (from 0 to 100%) for a variety of net N transport fluxes to underlying soil within the range of estimates for modern BSCs. b Close in from 0 to 20% continental cover. c Close in from 0 to 10% continental cover. The upper X-axis shows the percentage of modern continental area, the size of France and Europe are included as an intuitive benchmark. The lower X-axis shows the corresponding percentage of Archean continental area. The Phanerozoic N flux from land into the ocean (0.15 ± 0.03 Tmol yr−1) is denoted by the horizontal black bold line. Asterisks denote data from direct measurements of N export fluxes, all other values are indirectly obtained from nitrogen import fluxes (see Methods)


These results are based on the assumption that modern analogs are fair proxies to ancient systems and thus may suffer from some pitfalls, especially when considering the high uncertainty in the exact nature of the Archean paleoenvironment, including aspects such as the range of air pressure156667 or temperature68. Based on 2.73 Ga fossil raindrop imprint67, Archean Earth air pressure estimates range from 0.52 to 1.1 bar; nitrogen and argon isotopic studies suggest a pN2 upper limit of 0.5–1.2 bar at around 3.0 to 3.5 Ga66; pressure calculated from subaerial lava flows a lower sea-level air pressure at 2.74 Ga at 0.23 ± 0.23 bar15. However, even with significant atmospheric pN2 swings on the early Earth, it is unlikely that nitrogen could become a limiting factor to nitrogen fixation-based microbial primary productivity3,5. Future works are nevertheless needed to better-characterized variations in the kinetic rate of N-fixation with changing pressure temperature.

Moreover, the fate of Archean N outputs in the form of nitrate may have also differed from those in the present day surface environment due to different redox conditions. Indeed, it is well established that before 2.4 Ga the early Earth was anoxic with atmospheric pO2 below 10−5-fold the present atmospheric level69. The existence of oxygen oases in restricted ecosystems (e.g., lake, water bound) is nonetheless often argued to account for the occurrence of redox cycling of elements (including nitrogen but also, sulfur, carbon, and metallic elements26). In any case, while we could speculate that the Archean low O2 concentration might have favored the removal of nitrate from the hydrological system to the atmosphere by denitrification (early on, close to the production site, or later and more distally in the ocean), even today43,62 denitrification is not highly relevant to modern BSCs. Therefore, we suggest here that accumulation and transfer of nitrate and ammonium in the Archean continental system is a plausible hypothesis worthy of attention and further investigation.

Ultimately, the proposed transfer of N from the continent to the ocean might not have had long-term consequences for the atmospheric N2 reservoir size because BSCs and the biosphere in general is a minute, transient reservoir, and the only forms of N that can accumulate over geologic timescales are N2 in the atmosphere and reduced N in rocks. It has been shown that carbon residence time in BSCs is very short in geological scales42. However, the flux of fixed N from BSCs would be significantly larger than that from abiotic sources70 and it could have helped overcome the limitation of early biosphere to fixed N using diazotrophy71 and fuel primary productivity with newly available nitrogen species.

The delivery of nitrate and ammonium to the hydrogeological reservoir would also have provided a new evolutionary driver and an opportunity to trigger diversification of prokaryotes and eukaryotic phytoplankton able to use fixed nitrogen as a source of nutrient before nitrate concentrations stabilized in the ocean at around 2.3 Ga. As a corollary, BSCs may have enabled the return of nitrogen to the atmosphere via nitrate released to the ocean well before the GOE. Given the potential importance of this transfer compared to estimates of the Phanerozoic oxidative weathering N flux, an early Archean development of BSCs should be taken into account when modeling Archean surface atmospheric pressure15 and pN2 secular variation2,18.

Finally, a complex redox inorganic nitrogen cycle involving ammonium, nitrite, and nitrate may have arisen in Archean paleosols. Here, we calculate that this niche potentially delivered significant quantities of ammonium and nitrate to the ocean before the GOE. Secular variation of sedimentary δ15N in fact is consistent with these hypotheses, as lines of evidence exist for the presence of aerobic, nitrate-based nitrogen cycling in Meso to Neo-archean sediments from 2.7 to 2.5 Ga6,7,8,72 (Fig. 1). There is also evidence for late mesoarchean methanotrophs using nitrate in ephemeral ponds and shallow water environments33,73. While better quantification needs to be achieved and the potential feedback of such changes on the early Earth system is yet to be thoroughly evaluated, our results speak for a renewed relevance of future research on the Archean record of BSCs, bringing together the community working on the biogeochemistry of modern BSCs with deep-time biogeochemists.


Flux calculations

The N export fluxes from BSCs (Fs; Tmol yr−1) was calculated using the full range of direct and indirect (compilation of nitrogen input times 19% of export) estimates of N transport fluxes (F) to underlying soil (between 0.0133 and 8.820 g N m2 yr1, see Table 1) and integrated over the surface of colonized continental (S; m2) using the following equation: \({{FS}} = \frac{{F \times 10^{ - 12} \times S}}{M}\), where M is the molar mass of nitrogen species. Calculated surface was subsequently scaled as percentages of either the modern or Archean landmasses.

Data availability

The authors declare that the data supporting the findings of this study are available within the paper and its Supplementary Information files.


  1. 1.

    Ader, M. et al. Interpretation of the nitrogen isotopic composition of Precambrian sedimentary rocks: assumptions and perspectives. Chem. Geol. 429, 93–110 (2016).

    ADS  Article  CAS  Google Scholar 

  2. 2.

    Stüeken, E. E. et al. Modeling pN2 through geological time: implications for planetary climates and atmospheric biosignatures. Astrobiology 16, 949–963 (2016).

    ADS  Article  PubMed  CAS  Google Scholar 

  3. 3.

    Weiss, M. C. et al. The physiology and habitat of the last universal common ancestor. Nat. Microbiol. 1, 16116 (2016).

    Article  PubMed  CAS  Google Scholar 

  4. 4.

    Johnson, B. W. & Goldblatt, C. A secular increase in continental crust nitrogen during the Precambrian. Geochem. Persp. Let. 4, 24–28 (2017).

    Article  Google Scholar 

  5. 5.

    Stüeken, E. E., Buick, R., Guy, B. M. & Koehler, M. C. Isotopic evidence for biological nitrogen fixation by molybdenum-nitrogenase from 3.2 Gyr. Nature 520, 666–669 (2015).

    ADS  Article  PubMed  CAS  Google Scholar 

  6. 6.

    Garvin, J., Buick, R., Anbar, A. D., Arnold, G. L. & Kaufman, A. J. Isotopic evidence for an aerobic nitrogen cycle in the latest Archean. Science 323, 1045–1048 (2009).

    ADS  Article  PubMed  CAS  Google Scholar 

  7. 7.

    Godfrey, L. V. & Falkowski, P. G. The cycling and redox state of nitrogen in the Archaean ocean. Nat. Geosci. 2, 725–729 (2009).

    ADS  Article  CAS  Google Scholar 

  8. 8.

    Thomazo, C., Ader, M. & Philippot, P. Extreme 15N enrichments in 2.72 Gyr old sediments: evidence for a turning point in the nitrogen cycle. Geobiology 9, 107–120 (2011).

    Article  PubMed  CAS  Google Scholar 

  9. 9.

    Zerkle, A. L. et al. Onset of the aerobic nitrogen cycle during the Great Oxidation Event. Nature 542, 465–467 (2017).

    ADS  Article  PubMed  CAS  Google Scholar 

  10. 10.

    Papineau, D. & Fogel, M. L. High primary productivity and nitrogen cycling after the Paleoproterozoic phosphogenic event in the Aravalli Supergroup, India. Precambr. Res. 171, 37–56 (2009).

    ADS  Article  CAS  Google Scholar 

  11. 11.

    Stüeken, E. E. A test of the nitrogen-limitation hypothesis for retarded eukaryote radiation: nitrogen isotopes across a Mesoproterozoic basinal profile. Geochim. Cosmochim. Acta 120, 121–139 (2013).

    ADS  Article  CAS  Google Scholar 

  12. 12.

    Koehler, M. C., Stüeken, E. E., Kipp, M. A., Buick, R. & Knoll, A. H. Spatial and temporal trends in Precambrian nitrogen cycling: a Mesoproterozoic offshore nitrate minimum. Geochim. Cosmochim. Acta 198, 315–337 (2017).

    ADS  Article  CAS  Google Scholar 

  13. 13.

    Thomazo, C. & Papineau, D. Biogeochemical cycling of nitrogen on the early Earth. Elements 9, 345–351 (2013).

    Article  CAS  Google Scholar 

  14. 14.

    Ader, M. et al. Ocean redox structure across the late Neoproterozoic oxygenation event: a nitrogen isotope perspective. Earth Planet. Sci. Lett. 396, 1–13 (2014).

    ADS  Article  CAS  Google Scholar 

  15. 15.

    Som, S. M. et al. Earth’s air pressure 2.7 billion years ago constrained to less than half of modern levels. Nat. Geosci. 9, 448–451 (2016).

    ADS  Article  CAS  Google Scholar 

  16. 16.

    Klotz, M. G. & Stein, L. Y. Nitrifier genomics and evolution of the nitrogen cycle. FEMS Microbiol. Lett. 278, 146–156 (2008).

    Article  PubMed  CAS  Google Scholar 

  17. 17.

    Thomazo, C. et al. Biological activity and the Earth’s surface evolution: insights from carbon, sulfur, nitrogen and iron stable isotopes in the rock record. Comptes Rendus Palevol 8, 665–678 (2009).

    Article  Google Scholar 

  18. 18.

    Zerkle, A. L. & Mikhail, S. The geobiological nitrogen cycle: from microbes to the mantle. Geobiology 15, 343–352 (2017).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  19. 19.

    Castenholz, R. W., & Garcia-Pichel, F. in The Ecology of Cyanobacteria (eds Whitton, B. A. & Potts, M.) 591–611 (Kluwer Academic Publishers, Dordrecht, 2000).

  20. 20.

    Berkner, L. V. & Marshall, L. C. History of major atmospheric components. Proc. Natl Acad. Sci. USA  53, 1215–1225 (1965).

    ADS  Article  PubMed Central  CAS  Google Scholar 

  21. 21.

    Kasting, J. F., Zahnle, K. J., Pinto, J. P. & Young, A. T. Sulfur, ultraviolet radiation and the early evolution of life. Orig. Life Evol. Biosph. 19, 95–108 (1989).

    ADS  Article  PubMed  CAS  Google Scholar 

  22. 22.

    Pierson, B. K. in Early Life on Earth (eds Bengtson, S., Bergström, J., Vidal, G. & Knoll, A.)161–180 (Columbia University Press, New York, NY, 1994).

  23. 23.

    Cockell, C. S. & Raven, J. A. Ozone and life on the early Earth. Philos. Transact. A Math. Phys. Eng. Sci. 365, 1889–1901 (2007).

    Article  CAS  Google Scholar 

  24. 24.

    Kasting, J. F. Earth’s early atmosphere. Science 259, 920–926 (1993).

    ADS  Article  PubMed  CAS  Google Scholar 

  25. 25.

    Garcia-Pichel, F. Solar Ultraviolet and the evolutionary history of cyanobacteria. Orig. Life Evol. Biosphere 28, 321–347 (1998).

    ADS  Article  CAS  Google Scholar 

  26. 26.

    Lalonde, S. V. & Konhauser, K. O. Benthic perspective on Earth’s oldest evidence for oxygenic photosynthesis. Proc. Natl. Acad. Sci. 112, 995–1000 (2015).

    ADS  Article  PubMed  PubMed Central  CAS  Google Scholar 

  27. 27.

    Simpson, E. L. et al. Evidence for 2.0 Ga continental microbial mats in a paleodesert setting. Precambr. Res. 237, 36–50 (2013).

    ADS  Article  CAS  Google Scholar 

  28. 28.

    Rodriguez-Caballero, E. et al. Dryland photoautotrophic soil surface communities endangered by global change. Nat. Geosci. 11, 185–189 (2018).

    ADS  Article  CAS  Google Scholar 

  29. 29.

    Garcia-Pichel, F. in Encyclopedia of Environmental Microbiology (ed Bitton, G.) 1019–1023 (John Wiley, New York, NY, 2002).

  30. 30.

    Beraldi-Campesi, H., Farmer, J. & Garcia-Pichel, F. Modern terrestrial sedimentary biostructures and their fossil analogs in Mesoproterozoic subaerial deposits. PALAIOS 29, 45–54 (2014).

    ADS  Article  Google Scholar 

  31. 31.

    Retallack, G. J., Krinsley, D. H., Fischer, R., Razink, J. J. & Langworthy, K. A. Archean coastal-plain paleosols and life on land. Gondwana Res. 40, 1–20 (2016).

    ADS  Article  CAS  Google Scholar 

  32. 32.

    Homann, M., Heubeck, C., Airo, A. & Tice, M. M. Morphological adaptations of 3.22 Ga-old tufted microbial mats to Archean coastal habitats (Moodies Group, Barberton Greenstone Belt, South Africa). Precambr. Res. 266, 47–64 (2015).

    ADS  Article  CAS  Google Scholar 

  33. 33.

    Rye, R. & Holland, H. D. Life associated with a 2.76 Ga ephemeral pond?: evidence from Mount Roe #2 paleosol. Geology 28, 483–486 (2000).

    ADS  Article  PubMed  CAS  Google Scholar 

  34. 34.

    Driese, S. G. et al. Neoarchean paleoweathering of tonalite and metabasalt: Implications for reconstructions of 2.69 Ga early terrestrial ecosystems and paleoatmospheric chemistry. Precambr. Res. 189, 1–17 (2011).

    ADS  Article  CAS  Google Scholar 

  35. 35.

    Noonan, K. A. Element Use and Acquisition Strategies in Biological Soil Crusts. PhD thesis, Arizona State Univ. (2012).

  36. 36.

    Beraldi-Campesi, H., Hartnett, H., Anbar, A., Gordon, G. & Garcia-Pichel, F. Effects of biological soil crusts on soil elemental concentrations; implications for biogeochemistry and as traceable biosignatures of ancient life on land. Geobiology 7, 348–359 (2009).

    Article  PubMed  CAS  Google Scholar 

  37. 37.

    Battistuzzi, F. U., Feijao, A. & Hedges, S. B. A genomic timescale of prokaryote evolution: Insights into the origin of methanogenesis, phototrophy, and the colonization of land. BMC Evol. Biol. 4, 44 (2004).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  38. 38.

    Blank, C. E. & Sanchez-Baracaldo, P. Timing of morphological and ecological innovations in the cyanobacteria–a key to understanding the rise in atmospheric oxygen. Geobiology 8, 1–23 (2010).

    Article  PubMed  CAS  Google Scholar 

  39. 39.

    Kendall, B., Creaser, R. A., Reinhard, C. T., Lyons, T. W. & Anbar, A. D. Transient episodes of mild environmental oxygenation and oxidative continental weathering during the late Archean. Sci. Adv. 1, e1500777 (2015).

    ADS  Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Stüeken, E. E., Catling, D. C. & Buick, R. Contributions to late Archaean sulphur cycling by life on land. Nat. Geosci. 5, 722–725 (2012).

    ADS  Article  CAS  Google Scholar 

  41. 41.

    Reinhard, C. T., Planavsky, N. J. & Lyons, T. W. Long-term sedimentary recycling of rare sulphur isotope anomalies. Nature 497, 100–103 (2013).

    ADS  Article  PubMed  CAS  Google Scholar 

  42. 42.

    Elbert, W. et al. Contribution of cryptogamic covers to the global cycles of carbon and nitrogen. Nat. Geosci. 5, 459–462 (2012).

    ADS  Article  CAS  Google Scholar 

  43. 43.

    Johnson, S. L., Neuer, S. & Garcia-Pichel, F. Export of nitrogenous compounds due to incomplete cycling within biological soil crusts of arid lands. Environ. Microbiol. 9, 680 (2007).

    Article  PubMed  CAS  Google Scholar 

  44. 44.

    Barger, N. N., Weber, B., Garcia-Pichel, F., Zaady, E. & Belnap, J. in Biological Soil Crusts: An Organizing Principle in Drylands (eds Weber, B., Büdel, B. & Belnap, J.) 257–285 (Springer International Publishing, 2016).

  45. 45.

    Walvoord, M. A. et al. A reservoir of nitrate beneath desert soils. Science 302, 1021–1024 (2003).

    ADS  Article  PubMed  CAS  Google Scholar 

  46. 46.

    Thiet, R. K., Boerner, R. E., Nagy, M. & Jardine, R. The effect of biological soil crusts on throughput of rainwater and N into Lake Michigan sand dune soils. Plant Soil 278, 235–251 (2005).

    Article  CAS  Google Scholar 

  47. 47.

    Guo, Y., Zhao, H., Zuo, X., Drake, S. & Zhao, X. Biological soil crust development and its topsoil properties in the process of dune stabilization, Inner Mongolia, China. Environ. Geol. 54, 653–662 (2008).

    ADS  Article  CAS  Google Scholar 

  48. 48.

    Kershaw, K. A. Physiological Ecology of Lichens (Cambridge University Press, London, 1985).

    Google Scholar 

  49. 49.

    Rychert, R. C. & Skujins, J. Nitrogen fixation by blue-green algae-lichen crusts in the Great Basin Desert. Soil Sci. Soc. Am. Proc. 38, 768–771 (1974).

    ADS  Article  CAS  Google Scholar 

  50. 50.

    West, N. E. & Skujins, J. The nitrogen cycle in North American cold-winter semi-desert ecosystems. Oecologia 12, 45–53 (1977).

    CAS  Google Scholar 

  51. 51.

    Rychert, R. C., Skukins, J., Sorensen, D. & Porcella, D. in Nitrogen in Desert Ecosystems Dowden (eds West, N. E. & Skujins, J. J.) 20–30 (Hutchinson and Ross, Inc, Stroudsburg, 1978).

  52. 52.

    Evans, R. D. & Johansen, J. R. Microbiotic crusts and ecosystem processes. Crit. Rev. Plant Sci. 18, 183–225 (1999).

    Article  Google Scholar 

  53. 53.

    Evans, R. D. & Lange, O. L. in Biological Soil Crusts: Structure, Function, and Management, Ecological Studies, Vol. 150 (eds Belnap, J. & Lange, O. L.) 264–279 (Springer-Verlag, Berlin, 2001).

  54. 54.

    Belnap, J. Nitrogen fixation in biological soil crusts from southeast Utah, USA. Biol. Fertil. Soils 35, 128–135 (2002).

    Article  CAS  Google Scholar 

  55. 55.

    Belnap, J. Impacts of off road vehicles on nitrogen cycles in biological soil crusts: resistance in different US deserts. J. Arid Environ. 52, 155–165 (2002).

    ADS  Article  Google Scholar 

  56. 56.

    Russow, R., Veste, M. & Böhme, F. A natural 15N approach to determine the biological fixation of atmospheric nitrogen by biological soil crusts of the Negev Desert. Rapid Commun. Mass Spectrom. 19, 3451–3456 (2005).

    Article  PubMed  ADS  CAS  Google Scholar 

  57. 57.

    Stewart, K. J., Coxson, D. & Grogan, P. Nitrogen inputs by associative cyanobacteria across a low arctic tundra landscape. Arct. Antarct. Alp. Res. 43, 267–278 (2011).

    Article  Google Scholar 

  58. 58.

    Stewart, K. J., Coxson, D. & Siciliano, S. D. Small-scale spatial patterns in N2-fixation and nutrient availability in an arctic hummock–hollow ecosystem. Soil Biol. Biochem. 43, 133–140 (2011).

    Article  CAS  Google Scholar 

  59. 59.

    Stewart, K. J., Lamb, E. G., Coxson, D. S. & Siciliano, S. D. Bryophyte-cyanobacterial associations as a key factor in N2-fixation across the Canadian Arctic. Plant Soil 344, 335–346 (2011).

    Article  CAS  Google Scholar 

  60. 60.

    Caputa, K., Coxson, D. & Sanborn, P. Seasonal patterns of nitrogen fixation in biological soil crusts from British Columbias Chilcotin grasslands. Botany 641, 631–641 (2013).

    Article  CAS  Google Scholar 

  61. 61.

    Silvester, W. B., Parsons, R. & Watt, P. W. Direct measurement of release and assimilation of ammonia in the Gunnera-Nostoc symbiosis. New Phytol. 132, 617–625 (1996).

    Article  CAS  Google Scholar 

  62. 62.

    Strauss, S. L., Day, T. A. & Garcia-pichel, F. Nitrogen cycling in desert biological soil crusts across biogeographic regions in the Southwestern United States. Biogeochemistry 108, 171–182 (2012).

    Article  Google Scholar 

  63. 63.

    Corcoran, P. L. & Mueller, W. U. in The Precambrian Earth: Tempos and Events (eds Eriksson, P. G., Altermann, W., Nelson, D. R., Mueller, W. U. & Catuneanu, O.) 613–625 (Elsevier, Amsterdam, 2004).

  64. 64.

    Bose, P. K. et al. Sedimentation patterns during the Precambrian: a unique record? Mar. Pet. Geol. 33, 34–68 (2012).

    Article  Google Scholar 

  65. 65.

    Teitler, Y., Le Hir, G., Fluteau, F., Philippot, P. & Donnadieu, Y. Investigating the Paleoproterozoic glaciations with 3-D climate modeling. Earth Planet. Sci. Lett.  395, 71–80 (2014).

    ADS  Article  CAS  Google Scholar 

  66. 66.

    Marty, B., Zimmermann, L., Pujol, M., Burgess, R. & Philippot, P. Nitrogen isotopic composition and density of the Archean atmosphere. Science 342, 101–104 (2013).

    ADS  Article  PubMed  CAS  Google Scholar 

  67. 67.

    Som, S. M., Catling, D. C., Harnmeijer, J. P., Polivka, P. M. & Buick, R. Air density 2.7 billion years ago limited to less than twice modern levels by fossil raindrop imprints. Nature 484, 359–362 (2012).

    ADS  Article  PubMed  CAS  Google Scholar 

  68. 68.

    Jaffres, J. B. D., Shields, G. A. & Wallmann, K. The oxygen isotope evolution of seawater: a critical review of a long-standing controversy and an improved geological water cycle model for the past 3.4 billion years. Earth Sci. Rev. 83, 83–122 (2007).

    ADS  Article  Google Scholar 

  69. 69.

    Pavlov, A. A. & Kasting, J. F. Mass-independent fractionation of sulfur isotopes in Archean sediments: strong evidence for an anoxic Archean atmosphere. Astrobiology 2, 27–41 (2002).

    ADS  Article  PubMed  CAS  Google Scholar 

  70. 70.

    Stüeken, E. E., Kipp, M. A., Koehler, M. C. & Buick, R. The evolution of Earth’s biogeochemical nitrogen cycle. Earth Sci. Rev.  160, 220–239 (2016).

    Article  CAS  Google Scholar 

  71. 71.

    Navarro-González, R., McKay, C. P. & Mvondo, D. N. A possible nitrogen crisis for Archaean life due to reduced nitrogen fixation by lightning. Nature 412, 61–64 (2001).

    ADS  Article  PubMed  Google Scholar 

  72. 72.

    Busigny, V., Lebeau, O., Ader, M., Krapež, B., & Bekker, A. Nitrogen cycle in the Late Archean ferruginous ocean. Chem. Geol. 362, 115–130 (2013).

    ADS  Article  CAS  Google Scholar 

  73. 73.

    Thomazo, C., Ader, M., Farquhar, J. & Philippot, P. Methanotrophs regulated atmospheric sulfur isotope anomalies during the Mesoarchean (Tumbiana Formation, Western Australia). Earth Planet. Sci. Lett. 279, 65–75 (2009).

    ADS  Article  CAS  Google Scholar 

  74. 74.

    Algeo, T. J., Meyers, P. A., Robinson, R. S., Rowe, H. & Jiang, G. Q. Icehouse-greenhouse variations in marine denitrification. Biogeosciences 11, 1273–1295 (2014).

    ADS  Article  CAS  Google Scholar 

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This project was funded by the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement no 328530. We thank Arnaud Brayard and the members of the GPI for fruitful discussions.

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C.T., E.C. and F.G.-P. designed the project, participated to the data analysis, contributed to the biogeochemical N cycle interpretations, and wrote the manuscript.

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Correspondence to Christophe Thomazo.

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Thomazo, C., Couradeau, E. & Garcia-Pichel, F. Possible nitrogen fertilization of the early Earth Ocean by microbial continental ecosystems. Nat Commun 9, 2530 (2018).

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