Great Oxidation Event
The Great Oxidation Event (GOE), sometimes also called the Great Oxygenation Event, Oxygen Catastrophe, Oxygen Crisis, Oxygen Holocaust, or Oxygen Revolution, was a time period when the Earth's atmosphere and the shallow ocean first experienced a rise in oxygen, approximately 2.4–2.0 Ga (billion years ago) during the Paleoproterozoic era. Geological, isotopic, and chemical evidence suggest that biologically-produced molecular oxygen (dioxygen, O2) started to accumulate in Earth's atmosphere and changed it from a weakly reducing atmosphere to an oxidizing atmosphere, causing many existing species on Earth to die out. The cyanobacteria producing the oxygen caused the event, which enabled the subsequent development of multicellular life forms.
The early atmosphere
The composition of the Earth's earliest atmosphere is not known with certainty. However, the bulk of the atmosphere was likely dinitrogen, N
2, and carbon dioxide, CO
2, which are also the predominant carbon- and nitrogen-bearing gases that are produced by volcanism today. These are relatively inert gases. The Sun shone at about 70% of its current brightness 4 billion years ago, but there is strong evidence that liquid water existed on Earth at the time. A warm Earth, in spite of a faint Sun, is known as the faint young Sun paradox. Either carbon dioxide levels were much higher at the time, in order to provide enough of a greenhouse effect to warm the Earth, or other greenhouse gases were present. The most likely such gas is methane, CH
4, which is a powerful greenhouse gas and was produced by early forms of life known as methanogens. Scientists continue to research how the Earth was warmed before life arose.
An atmosphere of N
2 and CO
2 with trace amounts of H
4, carbon monoxide (CO), and hydrogen (H
2), is described as a weakly reducing atmosphere. Such an atmosphere contains practically no oxygen. The modern atmosphere contains abundant oxygen, making it an oxidizing atmosphere. The rise in oxygen is attributed to photosynthesis by cyanobacteria, which are thought to have evolved as early as 3.5 billion years ago.
The current scientific understanding of when and how the Earth's atmosphere changed from a weakly reducing atmosphere to a strongly oxidizing atmosphere largely began with the work of the American geologist, Preston Cloud, in the 1970s. Cloud observed that detrital sediments older than about 2 billion years ago contained grains of pyrite, uraninite, and siderite, all minerals containing reduced forms of iron or uranium that are not found in younger sediments because they are rapidly oxidized in an oxidizing atmosphere. He further observed that continental redbeds, which get their color from the oxidized (ferric) mineral hematite, began to appear in the geological record at about this time. Banded iron formation largely disappears from the geological record at 1.85 billion years ago, after peaking at about 2.5 billion years ago. Banded iron formation can form only when abundant dissolved ferrous iron is transported into depositional basins, and an oxygenated ocean blocks such transport by oxidizing the iron to form insoluble ferric iron compounds. The end of the deposition of banded iron formation at 1.85 billion years ago is therefore interpreted as marking the oxygenation of the deep ocean. Heinrich Holland further elaborated these ideas through the 1980s, placing the main time interval of oxygenation between 2.2 and 1.9 billion years ago, and they continue to shape the current scientific understanding.
Evidence for the Great Oxidation Event is provided by a variety of petrological and geochemical markers.
Paleosols, detrital grains, and redbeds are evidence of low-level oxygen. Paleosols (fossil soils) older than 2.4 billion years old have low iron concentrations that suggest anoxic weathering. Detrital grains found in sediments older than 2.4 billion years old contain minerals that are stable only under low oxygen conditions. Redbeds are red-colored sandstones that are coated with hematite, which indicates that there was enough oxygen to oxidize iron to its ferric state.
Banded iron formation (BIF)
Banded iron formations are composed of thin alternating layers of chert (a fine-grained form of silica) and the iron oxides, magnetite and hematite. Extensive deposits of this rock type are found around the world, almost all of which are older than 1.85 billion years old and most of which were deposited around 2.5 billion years ago. The iron in banded iron formation is partially oxidized, with roughly equal amounts of ferrous and ferric iron. Deposition of banded iron formation requires both an anoxic deep ocean capable of transporting iron in soluble ferrous form, and an oxidized shallow ocean where the ferrous iron is oxidized to insoluble ferric iron and precipitates onto the ocean floor. The deposition of banded iron formation before 1.8 billion years ago suggests the ocean was in a persistent ferruginous state, but deposition was episodic and there may have been significant intervals of euxenia.
Black laminated shales, rich in organic matter, are often regarded as a marker for anoxic conditions. However, the deposition of abundant organic matter is not a sure indication of anoxia, and burrowing organisms that destroy lamination had not yet evolved during the time frame of the Great Oxygenation Event. Thus laminated black shale by itself is a poor indicator of oxygen levels. Scientists must look instead for geochemical evidence of anoxic conditions. These include ferruginous anoxia, in which dissolved ferrous iron is abundant, and euxinia, in which hydrogen sulfide is present in the water.
Examples of such indicators of anoxic conditions include the degree of pyritization (DOP), which is the ratio of iron present as pyrite to the total reactive iron. Reactive iron, in turn, is defined as iron found in oxides and oxyhydroxides, carbonates, and reduced sulfur minerals such as pyrites, in contrast with iron tightly bound in silicate minerals. A DOP near zero indicates oxidizing conditions, while a DOP near 1 indicates euxenic conditions. Values of 0.3 to 0.5 are transitional, suggesting anoxic bottom mud under an oxygenated ocean. Studies of the Black Sea, which is considered a modern model for ancient anoxic ocean basins, indicate that high DOP, a high ratio of reactive iron to total iron, and a high ratio of total iron to aluminum are all indicators of transport of iron into a euxinic environment. Ferruginous anoxic conditions can be distinguished from euxenic conditions by a DOP less than about 0.7.
The currently available evidence suggests that the deep ocean remained anoxic and ferruginous as late as 580 million years ago, well after the Great Oxygenation Event, remaining just short of euxenic during much of this interval of time. Deposition of banded iron formation ceased when conditions of local euxenia on continental platforms and shelves began precipitating iron out of upwelling ferruginous water as pyrite.
Some of the most persuasive evidence for the Great Oxidation Event is provided by the mass-independent fractionation (MIF) of sulfur. The chemical signature of the MIF of sulfur is found prior to 2.4–2.3 billion years ago but disappears thereafter. The presence of this signature all but eliminates the possibility of an oxygenated atmosphere.
Different isotopes of a chemical element have slightly different atomic masses. Most of the differences in geochemistry between isotopes of the same element scale with this mass difference. these include small differences in molecular velocities and diffusion rates, which are described as mass-dependent fractionation processes. By contrast, mass-independent fractionation describes processes that are not proportional to the difference in mass between isotopes. The only such process likely to be significant in the geochemistry of sulfur is photodissociation. This is the process in which a molecule containing sulfur is broken up by solar ultraviolet (UV) radiation. The presence of a clear MIF signature for sulfur prior to 2.4 billion years ago shows that UV radiation was penetrating deep into the Earth's atmosphere. This in turn rules out an atmosphere containing more than traces of oxygen, which would have produced an ozone layer that shielded the lower atmosphere from UV radiation. The disappearance of the MIF signature for sulfur indicates the formation of such an ozone shield as oxygen began to accumulate in the atmosphere.
Mass-dependent fractionation also provides clues to the Great Oxygenation Event. For example, oxidation of manganese in surface rocks by atmospheric oxygen leads to further reactions that oxidize chromium. The heavier 53Cr is oxidized preferentially over the lighter 52Cr, and the soluble oxidized chromium carried into the ocean shows this enhancement of the heavier isotope. The chromium isotope ratio in banded iron formation suggests small but significant quantities of oxygen in the atmosphere before the Great Oxidation Event, and a brief return to low oxygen abundance 500 million years after the Great Oxidation Event. However, the chromium data may conflict with the sulfur isotope data, which calls the reliability of the chromium data into question. It is also possible that oxygen was present earlier only in localized "oxygen oases". Since chromium is not easily dissolved, its release from rocks requires the presence of a powerful acid such as sulfuric acid (H2SO4) which may have formed through bacterial oxidation of pyrite. This could provide some of the earliest evidence of oxygen-breathing life on land surfaces.
Other elements whose mass-dependent fractionation may provide clues to the Great Oxidation Event include carbon, nitrogen, transitional metals such as molybdenum and iron, and non-metal elements such as selenium.
Fossils and biomarkers
Structures interpreted as fossils of cyanobacteria exist in rock as old as 3.5 billion years old. These include microfossils of individual cyanobacteria cells, which are best preserved in chert. Such fossils show forms very similar to modern cyanobacteria. Macrofossils include stromatolites, which are interpreted as large colonies of cyanobacteria that formed characteristic layered structures. These strongly resemble living stromatolites found in harsh modern environments, such as Shark Bay in western Australia. Some of these fossils contain biomarkers, also known as molecular fossils, interpreted as breakdown products of photosynthetic pigments. For example, traces of 2α-methylhopanes thought to be from cyanobacteria were found in Pilbara, Western Australia. However, the biomarker data has since been shown to have been contaminated and so results are no longer accepted.
The presence of fossils resembling cyanobacteria in form is not in itself conclusive proof of early oxygen photosynthesis. There is evidence that the earliest ancestors of cyanobacteria were not photosynthetic, and acquired the ability to carry out oxygen photosynthesis only later, from horizontal gene transfer. Thus biomarkers for molecules associated with photosynthetic metabolism are eagerly sought. One such family of molecules are the steranes, which are thought to require oxygen for their synthesis. Mid‐chain branched monomethylalkanes are also a promising candidate for such biomarkers.
Some elements in marine sediments are sensitive to different levels of oxygen in the environment such as transition metals molybdenum and rhenium. Non-metal elements such as selenium and iodine are also indicators of oxygen levels.
The ability to generate oxygen via photosynthesis likely first appeared in the ancestors of cyanobacteria. These organisms evolved at least 2.45–2.32 billion years ago, and probably as early as 2.7 billion years ago or earlier. However, oxygen remained scarce in the atmosphere until around 2.0 billion years ago, and banded iron formation continued to be deposited until around 1.85 billion years ago. Given the rapid multiplication rate of cyanobacteria under ideal conditions, an explanation is needed for the delay of at least 400 million years between the evolution of oxygen-producing photosynthesis and the appearance of significant oxygen in the atmosphere.
Hypotheses to explain this gap must take into consideration the balance between oxygen sources and oxygen sinks. Oxygenic photosynthesis produces organic carbon that must be segregated from oxygen to allow oxygen accumulation in the surface environment, otherwise the oxygen back-reacts with the organic carbon and does not accumulate. The burial of organic carbon, sulfide, and minerals containing ferrous iron (Fe2+) is a primary factor in oxygen accumulation. When organic carbon is buried without being oxidized, the oxygen is left in the atmosphere. In total, the burial of organic carbon and pyrite today creates 15.8±3.3 Tmol (1 Tmol = 1012 moles) of O2 per year. This creates a net O2 flux from the global oxygen sources.
The rate of change of oxygen can be calculated from the difference between global sources and sinks. The oxygen sinks include reduced gases and minerals from volcanoes, metamorphism and weathering. The GOE started after these oxygen-sink fluxes and reduced-gas fluxes were exceeded by the flux of O2 associated with the burial of reductants, such as organic carbon. For the weathering mechanisms, 12.0±3.3 Tmol of O2 per year today goes to the sinks composed of reduced minerals and gases from volcanoes, metamorphism, percolating seawater and heat vents from the seafloor. On the other hand, 5.7±1.2 Tmol of O2 per year today oxidizes reduced gases in the atmosphere through photochemical reaction. On the early Earth, there was visibly very little oxidative weathering of continents (e.g., a lack of redbeds) and so the weathering sink on oxygen would have been negligible compared to that from reduced gases and dissolved iron in oceans.
Dissolved iron in oceans exemplifies O2 sinks. Free oxygen produced during this time was chemically captured by dissolved iron, converting iron Fe and Fe2+ to magnetite (Fe2+Fe3+
4) that is insoluble in water, and sank to the bottom of the shallow seas to create banded iron formations such as the ones found in Minnesota and Pilbara, Western Australia. It took 50 million years or longer to deplete the oxygen sinks. The rate of photosynthesis and associated rate of organic burial also affect the rate of oxygen accumulation. When land plants spread over the continents in the Devonian, more organic carbon was buried and likely allowed higher O2 levels to occur. Today, the average time that an O2 molecule spends in the air before it is consumed by geological sinks is about 2 million years. That residence time is relatively short in geologic time - so in the Phanerozoic there must have been feedback processes that kept the atmospheric O2 level within bounds suitable for animal life.
Evolution by stages
Preston Cloud originally proposed that the first cyanobacteria had evolved the capacity to carry out oxygen-producing photosynthesis, but had not yet evolved enzymes (such as superoxide dismutase) for living in an oxygenated environment. These cyanobacteria would have been protected from their own poisonous oxygen waste through its rapid removal via the high levels of reduced ferrous iron, Fe(II), in the early ocean. Cloud suggested that the oxygen released by photosynthesis oxidized the Fe(II) to ferric iron, Fe(III), which precipitated out of the sea water to form banded iron formation. Cloud interpreted the great peak in deposition of banded iron formation at the end of the Archean as the signature for the evolution of mechanisms for living with oxygen. This ended self-poisoning and produced a population explosion in the cyanobacteria that rapidly oxygenated the ocean and ended banded iron formation deposition. However, improved dating of Precambrian strata showed that the late Archean peak of deposition was spread out over tens of millions of years, rather than taking place in a very short interval of time following the evolution of oxygen-coping mechanisms. This made Cloud's hypothesis untenable.
More recently, families of bacteria have been discovered that show no indication of ever having had photosynthetic capability, but which otherwise closely resemble cyanobacteria. These may be descended from the earliest ancestors of cyanobacteria, which only later acquired photosynthetic ability by lateral gene transfer. Based on molecular clock data, the evolution of oxygen-producing photosynthesis may have occurred much later than previously thought, at around 2.5 billion years ago. This reduces the gap between the evolution of oxygen photosynthesis and the appearance of significant atmospheric oxygen.
A second possibility is that early cyanobacteria were starved for vital nutrients and this checked their growth. However, a lack of the scarcest nutrients, iron, nitrogen, and phosphorus, could have slowed, but not prevented, a cyanobacteria population explosion and rapid oxygenation. The explanation for the delay in the oxygenation of the atmosphere following the evolution of oxygen-producing photosynthesis likely lies in the presence of various oxygen sinks in the young Earth.
Early chemosynthetic organisms likely produced methane, an important trap for molecular oxygen, since methane readily oxidizes to carbon dioxide (CO2) and water in the presence of UV radiation. Modern methanogens require nickel as an enzyme cofactor. As the Earth's crust cooled and the supply of volcanic nickel dwindled, oxygen-producing algae began to out-perform methane producers, and the oxygen percentage of the atmosphere steadily increased. From 2.7 to 2.4 billion years ago, the rate of deposition of nickel declined steadily from a level 400 times today's.
Some people suggest that GOE is caused by the increase of the source of oxygen. One hypothesis argues that GOE was the immediate result of photosynthesis, although the majority of scientists suggest that a long-term increase of oxygen is more likely the case. Several model results show possibilities of long-term increase of carbon burial, but the conclusions are indecisive.
In contrast to the increasing flux hypothesis, there are also several hypotheses that attempt to use decrease of sinks to explain GOE. One theory suggests that composition of the volatiles from volcanic gases was more oxidized. Another theory suggests that the decrease of metamorphic gases and serpentinization is the main key of GOE. Hydrogen and methane released from metamorphic processes are also lost from Earth's atmosphere over time and leave the crust oxidized. Scientists realized that hydrogen would escape into space through a process called methane photolysis, in which methane decomposes under the action of ultraviolet light in the upper atmosphere and releases its hydrogen. The escape of hydrogen from the Earth into space must have oxidized the Earth because the process of hydrogen loss is chemical oxidation. This process of hydrogen escape required the generation of methane by methanogens, so that methanogens actually helped create the conditions necessary for the oxidation of the atmosphere.
One hypothesis suggests that the oxygen increase had to await tectonically driven changes in the Earth, including the appearance of shelf seas, where reduced organic carbon could reach the sediments and be buried. The newly produced oxygen was first consumed in various chemical reactions in the oceans, primarily with iron. Evidence is found in older rocks that contain massive banded iron formations apparently laid down as this iron and oxygen first combined; most present-day iron ore lies in these deposits. It was assumed oxygen released from cyanobacteria resulted in the chemical reactions that created rust, but it appears the iron formations were caused by anoxygenic phototrophic iron-oxidizing bacteria, which does not require oxygen. Evidence suggests oxygen levels spiked each time smaller land masses collided to form a super-continent. Tectonic pressure thrust up mountain chains, which eroded to release nutrients into the ocean to feed photosynthetic cyanobacteria.
Another hypothesis posits a model of the atmosphere that exhibits bistability: two steady states of oxygen concentration. The state of stable low oxygen concentration (0.02%) experiences a high rate of methane oxidation. If some event raises oxygen levels beyond a moderate threshold, the formation of an ozone layer shields UV rays and decreases methane oxidation, raising oxygen further to a stable state of 21% or more. The Great Oxygenation Event can then be understood as a transition from the lower to the upper steady states.
Consequences of oxygenation
Eventually, oxygen started to accumulate in the atmosphere, with two major consequences.
- Oxygen likely oxidized atmospheric methane (a strong greenhouse gas) to carbon dioxide (a weaker one) and water. This weakened the greenhouse effect of the Earth's atmosphere, causing planetary cooling, which has been proposed to have triggered a series of ice ages known as the Huronian glaciation, bracketing an age range of 2.45–2.22 billion years ago.
- The increased oxygen concentrations provided a new opportunity for biological diversification, as well as tremendous changes in the nature of chemical interactions between rocks, sand, clay, and other geological substrates and the Earth's air, oceans, and other surface waters. Despite the natural recycling of organic matter, life had remained energetically limited until the widespread availability of oxygen. This breakthrough in metabolic evolution greatly increased the free energy available to living organisms, with global environmental impacts. For example, mitochondria evolved after the GOE, giving organisms the energy to exploit new, more complex morphology interacting in increasingly complex ecosystems, although these did not appear until the late Proterozoic and Cambrian.
Role in mineral diversification
The Great Oxygenation Event triggered an explosive growth in the diversity of minerals, with many elements occurring in one or more oxidized forms near the Earth's surface. It is estimated that the GOE was directly responsible for more than 2,500 of the total of about 4,500 minerals found on Earth today. Most of these new minerals were formed as hydrated and oxidized forms due to dynamic mantle and crust processes.
Role in cyanobacteria evolution
In field studies done in Lake Fryxell, Antarctica, scientists found that mats of oxygen-producing cyanobacteria produced a thin layer, one to two millimeters thick, of oxygenated water in an otherwise anoxic environment, even under thick ice. By inference, these organisms could have adapted to oxygen even before oxygen accumulated in the atmosphere. The evolution of such oxygen-dependent organisms eventually established an equilibrium in the availability of oxygen, which became a major constituent of the atmosphere.
Origin of eukaryotes
It has been proposed that a local rise in oxygen levels due to cyanobacterial photosynthesis in ancient microenvironments was highly toxic to the surrounding biota, and that this selective pressure drove the evolutionary transformation of an archaeal lineage into the first eukaryotes. Oxidative stress involving production of reactive oxygen species (ROS) might have acted in synergy with other environmental stresses (such as ultraviolet radiation and/or desiccation) to drive selection in an early archaeal lineage towards eukaryosis. This archaeal ancestor may already have had DNA repair mechanisms based on DNA pairing and recombination and possibly some kind of cell fusion mechanism. The detrimental effects of internal ROS (produced by endosymbiont proto-mitochondria) on the archaeal genome could have promoted the evolution of meiotic sex from these humble beginnings. Selective pressure for efficient DNA repair of oxidative DNA damages may have driven the evolution of eukaryotic sex involving such features as cell-cell fusions, cytoskeleton-mediated chromosome movements and emergence of the nuclear membrane. Thus the evolution of eukaryotic sex and eukaryogenesis were likely inseparable processes that evolved in large part to facilitate DNA repair.
The rise in oxygen content was not linear: instead, there was positive excursion in oxygen content followed by a negative excursion during 2.22-2.06 Ga. The positive excursion, or more precisely, the carbon isotopic excursion evidencing it, is called the Lomagundi-Jatuli event (LJE) or Lomagundi event, and the time period has been termed Jatulian. In the Lomagundi-Jatuli event, oxygen content reached as high as modern levels, followed by a fall to very low levels during the following stage where black shales were deposited. The negative excursion is called the Shunga-Francevillian event. Evidence for the Lomagundi-Jatuli event has been found globally: in Fennoscandia and northern Russia, Scotland, Ukraine, China, Wyoming craton in the North America, Brazil, South Africa, India and Australia. Oceans seem to have been oxygenated for some time even after the termination of the isotope excursion itself.
It has been hypothesized that eukaryotes first evolved during the LJE. The Lomagundi-Jatuli event coincides with the appearance, and subsequent disappearance, of curious fossils found in Gabon, termed Francevillian biota, which seem to have been multicellular. This appears to represent a "false start" of multicellular life. The organisms apparently went extinct when the LJE ended, because they are absent in the layers of shale deposited after the LJE.
- Geological history of oxygen – Timeline of the development of free oxygen in the Earth's oceans and atmosphere
- Medea hypothesis
- Pasteur point
- Rare Earth hypothesis – Hypothesis that complex extraterrestrial life is an extremely rare phenomenon
- Stromatolite – Layered sedimentary structures formed by the growth of bacteria or algae
- Holland, Heinrich D. (2006). "The oxygenation of the atmosphere and oceans". Philosophical Transactions of the Royal Society: Biological Sciences. 361 (1470): 903–915. doi:10.1098/rstb.2006.1838. PMC 1578726. PMID 16754606.
- Margulis, Lynn; Sagan, Dorion (1986). "Chapter 6, 'The Oxygen Holocaust'". Microcosmos: Four Billion Years of Microbial Evolution. California: University of California Press. p. 99. ISBN 9780520210646.
- Lyons, Timothy W.; Reinhard, Christopher T.; Planavsky, Noah J. (February 2014). "The rise of oxygen in Earth's early ocean and atmosphere". Nature. 506 (7488): 307–315. Bibcode:2014Natur.506..307L. doi:10.1038/nature13068. ISSN 0028-0836. PMID 24553238. S2CID 4443958.
- Sosa Torres, Martha E.; Saucedo-Vázquez, Juan P.; Kroneck, Peter M.H. (2015). "Chapter 1, Section 2: The rise of dioxygen in the atmosphere". In Kroneck, Peter M.H.; Sosa Torres, Martha E. (eds.). Sustaining Life on Planet Earth: Metalloenzymes Mastering Dioxygen and Other Chewy Gases. Metal Ions in Life Sciences volume 15. 15. Springer. pp. 1–12. doi:10.1007/978-3-319-12415-5_1. ISBN 978-3-319-12414-8. PMID 25707464.
- Hodgskiss, Malcolm S. W.; Crockford, Peter W.; Peng, Yongbo; Wing, Boswell A.; Horner, Tristan J. (27 August 2019). "A productivity collapse to end Earth's Great Oxidation". PNAS. 116 (35): 17207–17212. Bibcode:2019PNAS..11617207H. doi:10.1073/pnas.1900325116. PMC 6717284. PMID 31405980.
- "Great Oxidation Event: More oxygen through multicellularity". ScienceDaily. University of Zurich. 17 January 2013. Retrieved 27 August 2019.
- Kasting, J. (12 February 1993). "Earth's early atmosphere". Science. 259 (5097): 920–926. doi:10.1126/science.11536547.
- Shaw, George H. (August 2008). "Earth's atmosphere – Hadean to early Proterozoic". Geochemistry. 68 (3): 235–264. doi:10.1016/j.chemer.2008.05.001.
- Wiechert, U. H. (20 December 2002). "GEOLOGY: Earth's Early Atmosphere". Science. 298 (5602): 2341–2342. doi:10.1126/science.1079894.
- Baumgartner RJ, et al. (2019). "Nano-porous pyrite and organic matter in 3.5-billion-year-old stromatolites record primordial life" (PDF). Geology. 47 (11): 1039–43. Bibcode:2019Geo....47.1039B. doi:10.1130/G46365.1.
- Kasting 1993, p. 923.
- Trendall, A.F. (2002). "The significance of iron-formation in the Precambrian stratigraphic record". In Altermann, Wladyslaw; Corcoran, Patricia L. (eds.). Precambrian Sedimentary Environments: A Modern Approach to Ancient Depositional Systems. Blackwell Science Ltd. pp. 33–36. ISBN 0-632-06415-3.
- Cox, Grant M.; Halverson, Galen P.; Minarik, William G.; Le Heron, Daniel P.; Macdonald, Francis A.; Bellefroid, Eric J.; Strauss, Justin V. (December 2013). "Neoproterozoic iron formation: An evaluation of its temporal, environmental and tectonic significance". Chemical Geology. 362: 232–249. doi:10.1016/j.chemgeo.2013.08.002.
- Catling, David C.; Kasting, James F. (2017). Atmospheric Evolution on Inhabited and Lifeless Worlds. Cambridge: Cambridge University Press. doi:10.1017/9781139020558. ISBN 9781139020558.
- Utsunomiya, Satoshi; Murakami, Takashi; Nakada, Masami; Kasama, Takeshi (January 2003). "Iron oxidation state of a 2.45 Byr-old paleosol developed on mafic volcanics". Geochimica et Cosmochimica Acta. 67 (2): 213–221. Bibcode:2003GeCoA..67..213U. doi:10.1016/s0016-7037(02)01083-9. ISSN 0016-7037.
- Hofmann, Axel; Bekker, Andrey; Rouxel, Olivier; Rumble, Doug; Master, Sharad (September 2009). "Multiple sulphur and iron isotope composition of detrital pyrite in Archaean sedimentary rocks: A new tool for provenance analysis" (PDF). Earth and Planetary Science Letters. 286 (3–4): 436–445. Bibcode:2009E&PSL.286..436H. doi:10.1016/j.epsl.2009.07.008. hdl:1912/3068. ISSN 0012-821X.
- Eriksson, Patrick G.; Cheney, Eric S. (January 1992). "Evidence for the transition to an oxygen-rich atmosphere during the evolution of red beds in the lower proterozoic sequences of southern Africa". Precambrian Research. 54 (2–4): 257–269. Bibcode:1992PreR...54..257E. doi:10.1016/0301-9268(92)90073-w. ISSN 0301-9268.
- Trendall, A.F.; Blockley, J.G. (2004). "Precambrian iron-formation". In Eriksson, P.G.; Altermann, W.; Nelson, D.R.; Mueller, W.U.; Catuneanu, O. (eds.). Evolution of the Hydrosphere and Atmosphere. Developments in Precambrian Geology. Developments in Precambrian Geology. 12. pp. 359–511. doi:10.1016/S0166-2635(04)80007-0. ISBN 9780444515063.
- Cox et al. 2013.
- Canfield, Donald E.; Poulton, Simon W. (1 April 2011). "Ferruginous Conditions: A Dominant Feature of the Ocean through Earth's History". Elements. 7 (2): 107–112. doi:10.2113/gselements.7.2.107. ISSN 1811-5209.
- Lyons, Timothy W.; Anbar, Ariel D.; Severmann, Silke; Scott, Clint; Gill, Benjamin C. (May 2009). "Tracking Euxinia in the Ancient Ocean: A Multiproxy Perspective and Proterozoic Case Study". Annual Review of Earth and Planetary Sciences. 37 (1): 507–534. Bibcode:2009AREPS..37..507L. doi:10.1146/annurev.earth.36.031207.124233. ISSN 0084-6597.
- Scholz, Florian; Severmann, Silke; McManus, James; Noffke, Anna; Lomnitz, Ulrike; Hensen, Christian (December 2014). "On the isotope composition of reactive iron in marine sediments: Redox shuttle versus early diagenesis". Chemical Geology. 389: 48–59. doi:10.1016/j.chemgeo.2014.09.009.
- Farquhar, J. (4 August 2000). "Atmospheric Influence of Earth's Earliest Sulfur Cycle". Science. 289 (5480): 756–758. Bibcode:2000Sci...289..756F. doi:10.1126/science.289.5480.756. ISSN 0036-8075. PMID 10926533. S2CID 12287304.
- Wiechert 2002.
- Frei, R.; Gaucher, C.; Poulton, S.W.; Canfield, D.E. (2009). "Fluctuations in Precambrian atmospheric oxygenation recorded by chromium isotopes". Nature. 461 (7261): 250–253. Bibcode:2009Natur.461..250F. doi:10.1038/nature08266. PMID 19741707. S2CID 4373201. Lay summary.
- Kerr, R. A. (17 June 2005). "EARTH SCIENCE: The Story of O2". Science. 308 (5729): 1730–1732. doi:10.1126/science.308.5729.1730.
- "Evidence of Earliest Oxygen-Breathing Life on Land Discovered". LiveScience.com. Retrieved 6 April 2016.
- "Cyanobacteria: Fossil Record". Universityh of California Museum of Paleontology. University of California Berkeley. Retrieved 8 March 2021.
- French, Katherine L.; Hallmann, Christian; Hope, Janet M.; Schoon, Petra L.; Zumberge, J. Alex; Hoshino, Yosuke; Peters, Carl A.; George, Simon C.; Love, Gordon D. (27 April 2015). "Reappraisal of hydrocarbon biomarkers in Archean rocks". Proceedings of the National Academy of Sciences. 112 (19): 5915–5920. Bibcode:2015PNAS..112.5915F. doi:10.1073/pnas.1419563112. ISSN 0027-8424. PMC 4434754. PMID 25918387.
- Blankenship, Robert E. (31 March 2017). "How Cyanobacteria went green". Science. 355 (6332): 1372–1373. doi:10.1126/science.aam9365.
- Hamilton, Trinity L.; Bryant, Donald A.; Macalady, Jennifer L. (February 2016). "The role of biology in planetary evolution: cyanobacterial primary production in low-oxygen Proterozoic oceans: Primary production in Proterozoic oceans". Environmental Microbiology. 18 (2): 325–340. doi:10.1111/1462-2920.13118.
- Anbar, Ariel D.; Rouxel, Olivier (May 2007). "Metal Stable Isotopes in Paleoceanography". Annual Review of Earth and Planetary Sciences. 35 (1): 717–746. Bibcode:2007AREPS..35..717A. doi:10.1146/annurev.earth.34.031405.125029. ISSN 0084-6597. S2CID 130960654.
- Stüeken, E.E.; Buick, R.; Bekker, A.; Catling, D.; Foriel, J.; Guy, B.M.; Kah, L.C.; Machel, H.G.; Montañez, I.P. (1 August 2015). "The evolution of the global selenium cycle: Secular trends in Se isotopes and abundances". Geochimica et Cosmochimica Acta. 162: 109–125. Bibcode:2015GeCoA.162..109S. doi:10.1016/j.gca.2015.04.033. ISSN 0016-7037.
- Cardona, T.; Murray, J. W.; Rutherford, A. W. (May 2015). "Origin and Evolution of Water Oxidation before the Last Common Ancestor of the Cyanobacteria". Molecular Biology and Evolution. 32 (5): 1310–1328. doi:10.1093/molbev/msv024. PMC 4408414. PMID 25657330.
- Tomitani, Akiko (April 2006). "The evolutionary diversification of cyanobacteria: Molecular–phylogenetic and paleontological perspectives". PNAS. 103 (14): 5442–5447. Bibcode:2006PNAS..103.5442T. doi:10.1073/pnas.0600999103. PMC 1459374. PMID 16569695.
- "Cyanobacteria: Fossil Record". Ucmp.berkeley.edu. Retrieved 26 August 2010.
- Dutkiewicz, A.; Volk, H.; George, S.C.; Ridley, J.; Buick, R. (2006). "Biomarkers from Huronian oil-bearing fluid inclusions: An uncontaminated record of life before the Great Oxidation Event". Geology. 34 (6): 437. Bibcode:2006Geo....34..437D. doi:10.1130/G22360.1.
- Caredona, Tanai (6 March 2018). "Early Archean origin of heterodimeric Photosystem I". Heliyon. 4 (3): e00548. doi:10.1016/j.heliyon.2018.e00548. PMC 5857716. PMID 29560463.
- Howard, Victoria (7 March 2018). "Photosynthesis originated a billion years earlier than we thought, study shows". Astrobiology Magazine. Retrieved 23 March 2018.
- Holland, Heinrich D. (November 2002). "Volcanic gases, black smokers, and the great oxidation event". Geochimica et Cosmochimica Acta. 66 (21): 3811–3826. Bibcode:2002GeCoA..66.3811H. doi:10.1016/s0016-7037(02)00950-x. ISSN 0016-7037.
- University of Zurich (17 January 2013). "Great Oxidation Event: More oxygen through multicellularity". ScienceDaily.
- Anbar, A.; Duan, Y.; Lyons, T.; Arnold, G.; Kendall, B.; Creaser, R.; Kaufman, A.; Gordon, G.; Scott, C.; Garvin, J.; Buick, R. (2007). "A whiff of oxygen before the great oxidation event?". Science. 317 (5846): 1903–1906. Bibcode:2007Sci...317.1903A. doi:10.1126/science.1140325. PMID 17901330. S2CID 25260892.
- Dahl, T.W.; Hammarlund, E.U.; Anbar, A.D.; Bond, D.P.G.; Gill, B.C.; Gordon, G.W.; Knoll, A.H.; Nielsen, A.T.; Schovsbo, N.H. (30 September 2010). "Devonian rise in atmospheric oxygen correlated to the radiations of terrestrial plants and large predatory fish". Proceedings of the National Academy of Sciences. 107 (42): 17911–17915. Bibcode:2010PNAS..10717911D. doi:10.1073/pnas.1011287107. ISSN 0027-8424. PMC 2964239. PMID 20884852.
- Catling, David C.; Claire, Mark W. (August 2005). "How Earth's atmosphere evolved to an oxic state: A status report". Earth and Planetary Science Letters. 237 (1–2): 1–20. Bibcode:2005E&PSL.237....1C. doi:10.1016/j.epsl.2005.06.013. ISSN 0012-821X.
- Cloud, Preston E. (1968). "Atmospheric and Hydrospheric Evolution on the Primitive Earth". Science. 160 (3829): 729–736. doi:10.1126/science.160.3829.729. JSTOR 1724303. PMID 5646415.
- Cloud, P. (1973). "Paleoecological Significance of the Banded Iron-Formation". Economic Geology. 68 (7): 1135–1143. doi:10.2113/gsecongeo.68.7.1135.
- "Breathing Easy Thanks to the Great Oxidation Event". Scientific American. Retrieved 6 April 2016.
- Konhauser, Kurt O.; et al. (2009). "Oceanic nickel depletion and a methanogen famine before the Great Oxidation Event". Nature. 458 (7239): 750–753. Bibcode:2009Natur.458..750K. doi:10.1038/nature07858. PMID 19360085. S2CID 205216259.
- Kirschvink, Joseph L.; Kopp, Robert E. (27 August 2008). "Palaeoproterozoic ice houses and the evolution of oxygen-mediating enzymes: the case for a late origin of photosystem II". Philosophical Transactions of the Royal Society B: Biological Sciences. 363 (1504): 2755–2765. doi:10.1098/rstb.2008.0024. ISSN 0962-8436. PMC 2606766. PMID 18487128.
- des Marais, David J.; Strauss, Harald; Summons, Roger E.; Hayes, J.M. (October 1992). "Carbon isotope evidence for the stepwise oxidation of the Proterozoic environment". Nature. 359 (6396): 605–609. Bibcode:1992Natur.359..605M. doi:10.1038/359605a0. ISSN 0028-0836. PMID 11536507. S2CID 4334787.
- Krissansen-Totton, J.; Buick, R.; Catling, D.C. (1 April 2015). "A statistical analysis of the carbon isotope record from the Archean to Phanerozoic and implications for the rise of oxygen". American Journal of Science. 315 (4): 275–316. Bibcode:2015AmJS..315..275K. doi:10.2475/04.2015.01. ISSN 0002-9599. S2CID 73687062.
- Catling, D.C. (3 August 2001). "Biogenic Methane, Hydrogen Escape, and the Irreversible Oxidation of Early Earth". Science. 293 (5531): 839–843. Bibcode:2001Sci...293..839C. doi:10.1126/science.1061976. PMID 11486082. S2CID 37386726.
- Lenton, T.M.; Schellnhuber, H.J.; Szathmáry, E. (2004). "Climbing the co-evolution ladder". Nature. 431 (7011): 913. Bibcode:2004Natur.431..913L. doi:10.1038/431913a. PMID 15496901. S2CID 27619682.
- Eguchi, James; Seales, Johnny; Dasgupta, Rajdeep (2019). "Great Oxidation and Lomagundi events linked by deep cycling and enhanced degassing of carbon". Nature Geoscience. 13 (1): 71–76. Bibcode:2019NatGe..13...71E. doi:10.1038/s41561-019-0492-6. PMC 6894402. PMID 31807138.
- "Iron in primeval seas rusted by bacteria". Phys.org. April 2013.
- American, Scientific. "Abundant Oxygen Indirectly Due to Tectonics". Scientific American. Retrieved 6 April 2016.
- Goldblatt, C.; Lenton, T.M.; Watson, A.J. (2006). "Bistability of atmospheric oxygen and the Great Oxidation". Nature. 443: 683–686. doi:10.1038/nature05169.
- Claire, M.W.; Catling, D.C.; Zahnle, K.J. (December 2006). "Biogeochemical modelling of the rise in atmospheric oxygen". Geobiology. 4 (4): 239–269. doi:10.1111/j.1472-4669.2006.00084.x. ISSN 1472-4677.
- Bekker, Andrey (2014). "Huronian Glaciation". In Amils, Ricardo; Gargaud, Muriel; Cernicharo Quintanilla, José; Cleaves, Henderson James (eds.). Encyclopedia of Astrobiology. Springer Berlin Heidelberg. pp. 1–8. doi:10.1007/978-3-642-27833-4_742-4. ISBN 9783642278334.
- Kopp, Robert E.; Kirschvink, Joseph L.; Hilburn, Isaac A.; Nash, Cody Z. (2005). "The Paleoproterozoic snowball Earth: A climate disaster triggered by the evolution of oxygenic photosynthesis". Proceedings of the National Academy of Sciences of the United States of America. 102 (32): 11131–11136. Bibcode:2005PNAS..10211131K. doi:10.1073/pnas.0504878102. PMC 1183582. PMID 16061801.
- Lane, Nick (5 February 2010). "First breath: Earth's billion-year struggle for oxygen". New Scientist. No. 2746.
- Sperling, Erik; Frieder, Christina; Raman, Akkur; Girguis, Peter; Levin, Lisa; Knoll, Andrew (August 2013). "Oxygen, ecology, and the Cambrian radiation of animals". Proceedings of the National Academy of Sciences of the United States of America. 110 (33): 13446–13451. Bibcode:2013PNAS..11013446S. doi:10.1073/pnas.1312778110. PMC 3746845. PMID 23898193.
- Sverjensky, Dimitri A.; Lee, Namhey (1 February 2010). "The Great Oxidation Event and Mineral Diversification". Elements. 6 (1): 31–36. doi:10.2113/gselements.6.1.31. ISSN 1811-5209.
- "Evolution of Minerals". Scientific American. March 2010.
- "Oxygen oasis in Antarctic lake reflects Earth in distant past". ScienceDaily.com. September 2015.
- Doran, Peter T.; Jungblut, Anne D.; Mackey, Tyler J.; Hawes, Ian; Sumner, Dawn Y. (1 October 2015). "Antarctic microbial mats: A modern analog for Archean lacustrine oxygen oases". Geology. 43 (10): 887–890. Bibcode:2015Geo....43..887S. doi:10.1130/G36966.1. hdl:10092/12361. ISSN 0091-7613.
- Gross, J.; Bhattacharya, D. (August 2010). "Uniting sex and eukaryote origins in an emerging oxygenic world". Biol. Direct. 5: 53. doi:10.1186/1745-6150-5-53. PMC 2933680. PMID 20731852.
- Hörandl E, Speijer D (February 2018). "How oxygen gave rise to eukaryotic sex". Proc. Biol. Sci. 285 (1872): 20172706. doi:10.1098/rspb.2017.2706. PMC 5829205. PMID 29436502.
- Bernstein, H.; Bernstein, C. (2017). "Sexual communication in archaea, the precursor to meiosis". In Witzany, Guenther (ed.). Biocommunication of Archaea. Springer International Publishing. pp. 103–117. doi:10.1007/978-3-319-65536-9. ISBN 978-3-319-65535-2. S2CID 26593032.
- Bernstein, Harris; Bernstein, Carol (2013). "Chapter 3 – Evolutionary origin and adaptive function of meiosis". In Bernstein, Carol; Bernstein, Harris (eds.). Meiosis. Intech Publ. pp. 41–75.
- Lane, Nick (5 February 2010). "First breath: Earth's billion-year struggle for oxygen". New Scientist. No. 2746. Archived 2011-01-06 at the Wayback Machine