Tag: Great Oxidation event

The ‘boring billion’ years of the Mesoproterozoic: plate tectonics and the eukaryotes

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The emergence of the eukaryotes – of which we are a late-entry member – has been debated for quite a while. In 2023 Earth-logs reportedthat a study of ‘biomarker’ organic chemicals in Proterozoic sediments suggests that eukaryotes cannot be traced back further than about 900 Ma ago using such an approach. At about the same time another biomarker study showed signs of a eukaryote presence at around 1050 Ma. Both outcomes seriously contradicted a ‘molecular-clock’ approach based on the DNA of modern members of the Eukarya and estimates of the rate of genetic mutation. That method sought to deduce the time in the past when the last eukaryotic common ancestor (LECA) appeared. It pointed to about 2 Ga ago, i.e. a few hundred million years after the Great Oxygenation Event got underway. Since eukaryote metabolism depends on oxygen, the molecular-clock result seems reasonable. The biomarker evidence does not. But were the Palaeo- and Mesoproterozoic Eras truly ‘boring’? A recent paper by Dietmar Müller and colleagues from the Universities of Sydney and Adelaide, Australia definitely shows that geologically they were far from that (Müller, R.D. et al. 2025. Mid-Proterozoic expansion of passive margins and reduction in volcanic outgassing supported marine oxygenation and eukaryogenesis. Earth and Planetary Science Letters, v. 672; DOI: 10.1016/j.epsl.2025.119683).

Carbon influx (million tons per year) into tectonic plates and into the ocean-atmosphere system from 1800 Ma to present. The colour bands represent: total carbon influx into the atmosphere (mauve); sequestered in tectonic plates (green); net atmospheric influx i.e. total minus carbon sequestered into plates (orange). The widths of the bands show the uncertainties of the calculated masses shown as darker coloured lines.

From 1800 to 800 Ma two supercontinents– Nuna-Columbia and Rodinia – aggregated nearly all existing continental masses, and then broke apart. Continents had collided and then split asunder to drift. So plate tectonics was very active and encompassed the entire planet, as Müller et al’s palaeogeographic animation reveals dramatically. Tectonics behaved in much the same fashion through the succeeding Neoproterozoic and Phanerozoic to build-up then fragment the more familiar supercontinent of Pangaea. Such dynamic events emit magma to form new oceanic lithosphere at oceanic rift systems and arc volcanoes above subduction zones, interspersed with plume-related large igneous provinces and they wax and wane. Inevitably, such partial melting delivered carbon dioxide to the atmosphere. Reaction on land and in the rubbly flanks of spreading ridges between new lithosphere and dissolved CO2 drew down and sequestered some of that gas in the form of solid carbonate minerals. Continental collisions raised the land surface and the pace of weathering, which also acted as a carbon sink. But they also involved metamorphism that released carbon dioxide from limestones involved in the crustal transformation. This protracted and changing tectonic evolution is completely bound up through the rock cycle with geochemical change in the carbon cycle.

From the latest knowledge of the tectonic and other factors behind the accretion and break-up of Nuna and Rodinia, Müller et al. were able to model the changes in the carbon cycle during the ‘boring billion’ and their effects on climate and the chemistry of the oceans. For instance, about 1.46 Ga ago, the total length of continental margins doubled while Nuna broke apart. That would have hugely increased the area of shallow shelf seas where living processes would have been concentrated, including the photosynthetic emission of oxygen. In an evolutionary sense this increased, diversified and separated the ecological niches in which evolution could prosper. It also increased the sequestration of greenhouse gas through reactions on the flanks of a multiplicity of oceanic rift systems, thereby cooling the planet. Translating this into a geochemical model of the changing carbon cycle (see figure) suggests that the rate of carbon addition to the atmosphere (outgassing) halved during the Mesoproterozoic. The carbon cycle and probable global cooling bound up with Nuna’s breakup ended with the start of Rodinia’s aggregation about 1000 Ma ago and the time that biomarkers first indicate the presence of eukaryotes.

Simplified structures of (a) a prokaryote cell; (b) a simple eukaryote animal cell. Plants also contain organelles called chloroplasts

So, did tectonics play a major role in the rise of the Eukarya? Well, of course it did, as much as it was subsequently the changing background to the appearance of the Ediacaran animals and the evolutionary carnival of the Phanerozoic. But did it affect the billion-year delay of ‘eukaryogenesis’ during prolonged availability of the oxygen that such a biological revolution demanded? Possibly not. Lyn Margulis’s hypothesis of the origin of the basic eukaryote cell by a process of ‘endosymbiosis’ is still the best candidate 50 years on. She suggested that such cells were built from various forms of bacteria and archaea successively being engulfed within a cell wall to function together through symbiosis. Compared with prokaryote cells those of the eukaryotes are enormously complex. At each stage the symbionts had to be or become compatible to survive. It is highly unlikely that all components entered the relationship together. Each possible kind of cell assembly was also subject to evolutionary pressures. This clearly was a slow evolutionary process, probably only surviving from stage to stage because of the global presence of a little oxygen. But the eukaryote cell may also have been forced to restart again and again until a stable form emerged.

See also: New Clues Show Earth’s “Boring Billion” Sparked the Rise of Life. SciTechDaily, 3  November 2025

Arsenic: an agent of evolutionary change?

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The molecules that make up all living matter are almost entirely (~98 %) made from the elements Carbon, Hydrogen, Oxygen, Nitrogen and Phosphorus (CHONP) in order of their biological importance. All have low atomic numbers, respectively 6th, 1st, 8th, 7th and 15th in the Periodic Table. Of the 98 elements found in nature, about 7 occur only because they form in the decay schemes of radioactive isotopes. Only the first 83 (up to Bismuth) are likely to be around ‘for ever’; the fifteen heavier than that are made up exclusively of unstable isotopes that will eventually disappear, albeit billions of years from now. There are other oddities that mean that the 92 widely accepted  to be naturally occurring is not strictly correct. That CHONP are so biologically important stems partly from their abundances in the inorganic world and also because of the ease with which they chemically combine together. But they are not the only ones that are essential.

About 20 to 25% of the other elements are also literally vital, even though many are rare. Most of the rest are inessential except in vanishingly small amounts that do no damage, and may or may not be beneficial. However some are highly toxic. Any element can produce negative biological outcomes if above certain levels. Likewise, deficiencies can result in ill thrift and event death. For the majority of elements, biologists have established concentrations that define deficiency and toxic excess. The World Health Organisation has charted the maximum safe levels of elements in drinking water in milligrams per litre. In this regard, the lowest safe level is for thallium (Tl) and mercury (Hg) at 0.002 mg l-1.Other highly toxic elements are cadmium (Cd) (0.003 mg l-1), then arsenic (As) and lead (Pb) (0.01 mg l-1) that ‘everyone knows’ are elements to avoid like the plague. In nature lead is very rarely at levels that are unsafe because it is insoluble, but arsenic is soluble under reducing conditions and is currently responsible for a pandemic of related ailments, especially in the Gangetic plains of India and Bangladesh and similar environments worldwide.

Biological evolution has been influenced since life appeared by the availability, generally in water, of both essential and toxic elements. In 2020 Earth-logs summarised a paper about modern oxygen-free springs in Chile in which photosynthetic purple sulfur bacteria form thick microbial mats. The springs contain levels of arsenic that vary from high in winter to low in summer. This phenomenon can only be explained by some process that removes arsenic from solution in summer but not in winter. The purple-bacteria’s photosynthesis uses electrons donated by sulfur, iron-2 and hydrogen – the spring water is highly reducing so they thrive in it. In such a simple environment this suggested a reasonable explanation: the bacteria use arsenic too. In fact they contain a gene (aio) that encodes for such an eventuality. The authors suggested that purple sulfur bacteria may well have evolved before the Great Oxygenation Event (GOE). They reasoned that in an oxygen-free world arsenic, as well as Fe2+ would be readily available in water that was in a reducing state, whereas oxidising conditions after the GOE would suppress both: iron-2 would be precipitated as insoluble iron-3 oxides that in turn efficiently absorb arsenic (see: Arsenic hazard on a global scale, May 2020).

Colour photograph and CT scans of Palaeoproterozoic discoidal fossils from the Francevillian Series in Gabon. (Credit: El Albani et al. 2010; Fig. 4).

A group of geoscientists from France, the UK, Switzerland and Austria have investigated the paradox of probably high arsenic levels before the GOE and the origin and evolution of life during the Archaean  (El Khoury et al. 2025. A battle against arsenic toxicity by Earth’s earliest complex life forms. Nature Communications, v. 16, article 4388; DOI: 10.1038/s41467-025-59760-9). Note that the main, direct evidence for Archaean life are fossilized microbial mats known as stromatolites, some palaeobiologists reckoning they were formed by oxygenic photosynthesising cyanobacteria others favouring the purple sulfur bacteria (above). The purple sulfur bacteria in Chile and other living prokaryotes that tolerate and even use arsenic in their metabolism clearly evolved that potential plus necessary chemical defence mechanisms, probably when arsenic was more available in the anoxic period before the GOE. Anna El Khoury and her colleagues sought to establish whether or not eukaryotes evolved similar defences by investigating the earliest-known examples; the 2.1 Ma old Francevillian biota of Gabon that post-dates the GOE. They are found in black shales, look like tiny fried eggs and are associated with clear signs of burrowing. The shales contain steranes that are breakdown products of steroids, which are unique to eukaryotes.

The fossils have been preserved by precipitation of pyrite (Fe2S) granules under highly reducing conditions. Curiously, the cores of the pyrite granules in the fossils are rich in arsenic, yet pyrite grains in the host sediments have much lower As concentrations. The latter suggest that seawater 2.1 Ma ago held little dissolved arsenic as a result of its containing oxygen. The authors interpret the apparently biogenic pyrite’s arsenic cores as evidence of the organism having sequestered As into specialized compartments in their bodies: their ancestors must have evolved this efficient means of coping with significant arsenic stress before the GOE. It served them well in the highly reducing conditions of black shale sedimentation. Seemingly, some modern eukaryotes retain an analogue of a prokaryote As detoxification gene.

Tectonic history and the Drake Equation

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In 1961 ten scientists interested in a search for extra-terrestrial intelligence met at Green Bank, West Virginia, USA, none of whom were geologists or palaeontologists. The participants called themselves “The Order of the Dolphin”, inspired by the thorny challenge of discovering how small cetaceans communicated: still something of a mystery. To set the ball rolling, Frank Drake an American astrophysicist and astrobiologist, proposed an algorithm aimed at forecasting the number of planets elsewhere in our galaxy on which ‘active, communicative civilisations’ (ACCs) might live. The Drake Equation is formulated as:

ACCs = R* · fp · ne · fl · fi · fc · L

where R* = number of new stars formed per year, fp = the fraction of stars with planetary systems, ne = the average number of planets that could support life (habitable planets) per planetary system, fl = the fraction of habitable  planets that develop primitive life, fi = the fraction of planets with life that evolve intelligent life and civilizations, fc = the fraction of civilizations that become ACCs, L = the length of time that ACCs broadcast radio into space. A team of then renowned scientists from several disciplines discussed what numbers to attach to these parameters. Their ‘educated guesses’ were: R* – one star per year; fp – one fifth to one half of all stars will have planets; ne – 1 to 5 planets per planetary system will be habitable; of which 100% will develop life (fl) and 100% (fi) will eventually develop intelligent life and civilisations; of those civilisations 10 to 20 % (fc) will eventually develop radio communications; which will survive for between a thousand years and 100 Ma (L). Acknowledging the great uncertainties in all the parameters, Drake inferred that between 103 and 108 ACCs exist today in the Milky Way, which is ~100 light years across and contains 1 to 4 x 1011 stars).

Today the values attached to the parameters and the outcomes seem absurdly optimistic to most people, simply because, despite 4 decades of searching by SETI there have been no signs of intelligible radio broadcasts from anywhere other than Earth and space probes launched from here. This is humorously referred to as the Fermi Paradox. There are however many scientists who still believe that we are not alone in the galaxy, and several have suggested reasons why nothing has yet been heard from ACCs. Robert Stern of the University of Texas (Dallas), USA and Taras Gerya of ETH-Zurich, Switzerland have sought clues from the history of life on Earth and that of the inorganic systems from which it arose and in which it has evolved that bear on the lack of any corrigible signals in the 63 years since the Drake Equation (Stern, R.J & Gerya, T.V. 2024. The importance of continents, oceans and plate tectonics for the evolution of complex life: implications for finding extraterrestrial civilizations. Nature (Scientific Reports), v. 14, article 8552; DOI: 10.1038/s41598-024-54700-x – definitely worth reading). Of course, Stern and Gerya too are fascinated by the scientific question as to whether or not there are ‘active, communicative civilisations’ elsewhere in the cosmos. Their starting point is that the Drake Equation is either missing some salient parameters, or that those it includes are assigned grossly optimistic magnitudes.

Life seems to have been present on Earth 3.8 Ga ago but multicelled animals probably arose only in the Late Neoproterozoic since 1.0 Ga ago. So here it has taken a billion years for their evolution to achieve terrestrial ACC-hood. Stern and Gerya address what processes favour life and its rapid evolution. Primarily, life depends on abundant liquid water: i.e. on a planet within the ‘Goldilocks Zone’ around a star. The authors assume a high supply of bioactive compounds – organic carbon, ammonium, ferrous iron and phosphate to watery environments. Phosphorus is critical to their scenario building. It is most readily supplied by weathering of exposed continental crust, but demands continual exposure of fresh rock by erosion and river transport to maintain a steady supply to the oceans. Along with favourable climatic conditions, that can only be achieved by an oxidising environment that followed the Great Oxidation Event (2.4 to 2.1 Ga) and continual topographic rejuvenation by plate tectonics.

A variety of Earth-logs posts have discussed various kinds of evidence for the likely onset of plate tectonics, largely focussing on the Hadean and Archaean. Stern and Gerya prefer the Proterozoic Eon that preserves more strands of relevant evidence, from which sea-floor spreading, subduction and repeated collision orogenies can confidently be inferred. All three occur overwhelmingly in Neoproterozoic and Phanerozoic times. Geologists often refer to the whole of the Mesoproterozoic and back to about 2.0 Ga in the Palaeoproterozoic as the ‘Boring Billion’ during which carbon isotope data suggest very little change in the status of living processes: they were present but nothing dramatic happened after the Great Oxidation Event. ‘Hard-rock’ geology also reveals far less passive extensional events that indicate continental break-up and drift than occur after 1.0 Ga and to the present. It also includes a unique form of magmatism that formed rocks dominated by sodium-rich feldspar (anorthosites) and granites that crystallised from water-poor magmas. They are thought to represent build-ups of heat in the mantle unrelieved by plate-tectonic circulation. Before the ‘Boring Billion’ such evidence as there is does point to some kind of plate motions, if not in the modern style.

How different styles of tectonics influence living processes differently: a single stagnant ‘lid’ versus plate tectonics. (Credit: Stern and Gerya, Fig 2)

Stern and Gerya conclude that the ‘Boring Billion’ was dominated by relative stagnation in the form of lid tectonics.  They compare the influence of stagnant ‘lid’ tectonics on life and evolution with that of plate tectonics in terms of: bioactive element supply; oxygenation; climate control; habitat formation; environmental pressure (see figure). In each case single lid tectonics is likely to retard life and evolution, whereas plate tectonics stimulates them as it has done from the time of Snowball Earth and throughout the Phanerozoic. Only one out of 8 planets that orbit the sun displays plate tectonics and has both oceans and continents. Could habitable planets be a great deal rarer than Drake and his pals assumed? [look at exoplanets in Wikipedia] Whatever, Stern and Gerya suggest that the seemingly thwarted enthusiasm surrounding the Drake Equation needs to be tempered by the addition of two new terms: the fraction of habitable exoplanets with significant continents and oceans (foc)and the fraction of them that have experienced plate tectonics for at least half a billion years (fpt). They estimate foc to be on the order of 0.0002 to 0.01, and suggest a value for fpt of less than 0.17. Multiplied together yields value between less than 0.00003 and 0.002. Their incorporation in the Drake Equation drastically reduces the potential number of ACCs to between <0.006 and <100,000, i.e. to effectively none in the Milky Way galaxy rising to a still substantial number

There are several other reasons to reject such ‘ball-parking’ cum ‘back-of-the-envelope’ musings. For me the killer is that biological evolution can never be predicted in advance. What happened on our home world is that the origin and evolution of life have been bound up with the unique inorganic evolution of the Solar System and the Earth itself over more than 4.5 billion years. That ranges in magnitude from the early collision with another, Mars-sized world that reset the proto-Earth’s geochemistry and created a large moon whose gravity has cycled the oceans through tides and changed the length of the day continually for almost the whole of geological history. At least once, at the end of the Cretaceous Period, a moderately sized asteroid in unstable orbit almost wiped out life at an advanced stage in its evolution. During the last quarter billion years internally generated geological forcing mechanisms have repeatedly and seriously stressed the biosphere in roughly 36 Ma cycles (Boulila, S. et al. 2023. Earth’s interior dynamics drive marine fossil diversity cycles of tens of millions of years. Proceedings of the National Academy of Sciences, v. 120 article e2221149120; DOI: 10.1073/pnas.2221149120). Two outcomes were near catastrophic mass extinctions, at the ends of the Permian and Triassic Periods, from which life struggled to continue. As well as extinctions, such ‘own goals’ reset global ecosystems repeatedly to trigger evolutionary diversification based on the body plans of surviving organisms.

Such unique events have been going on for four billion years, including whatever triggered the Snowball Earth episodes that accompanied the Great Oxygenation Event around 2.4 Ga and returned to coincide with the rise of multicelled animals during the Cryogenian and Ediacaran Periods of the Late Neoproterozoic. For most of the Phanerozoic a background fibrillation of gravitational fields in the Solar System has occasionally resulted in profound cycling between climatic extremes and their attendant stresses on ecosystems and their occupants. The last of these coincided with the evolution of humanity: the only creator of an active, communicative civilisation of which we know anything. But it took four billion years of a host of diverse vagaries, both physical and biological to make such a highly unlikely event possible. That known history puts the Drake Equation firmly in its place as the creature of a bunch of self-publicising and regarding, ambitious academics who in 1961 basically knew ‘sweet FA’. I could go on … but the wealth of information in Stern and  Gerya’s work is surely fodder for a more pessimistic view of other civilisations in the cosmos.

Someone – I forget who – provided another, very practical reason underlying the lack of messages from afar. It is not a good idea to become known to all and sundry in the galaxy, for fear that others might come to exploit, enslave and/or harvest. Earth is still in a kind of  imperialist phase from which lessons could be drawn!

Geochemical evidence for the origin of eukaryotes

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Along with algae, jellyfish, oak trees, sharks and nearly every organism that can be seen with the naked eye, we are eukaryotes. The cells of every member of the Eukarya, one of the three great domains of life, all contain a nucleus – the main location of genetic material – and a variety of other small bodies known as organelles, such as the mitochondria of animals and the chloroplasts of plant cells. The vast bulk of organisms that we can’t see unaided are prokaryotes, divided into the domains of Bacteria and Archaea. Their genetic material floats around in their cells’ fluid. The DNA of eukaryotes shares some stretches with prokaryotes, but no prokaryotes contain any eukaryote genetic material. This suggests that the Eukarya arose after the Bacteria and Archaea, and also that they are a product of evolution from prokaryotes, probably by several combining in symbiotic relationships inside a shared cell membrane. Earth-logs has followed developments surrounding this major issue since 2002, as reflected in some of the posts linked to what follows. 

While prokaryotes can live in every conceivable environment at the Earth’s surface and even in a few kilometres of crust beneath, the vast majority of eukaryotes depend on free oxygen for their metabolism. Logically, the earliest of the Eukarya could only have emerged when oxygen began to appear in the oceans following the Great Oxidation Event around 2.4 billion years ago. That is more than a billion years after the first prokaryotes had left their geological signature in the form of curiously bulbous, layered carbonate structures (stromatolites), probably formed by bacterial mats. The oldest occur in the Archaean rocks of Western Australia as far back as 3.5 Ga, and disputed examples have been found in the 3.7 Ga Isua sediments of West Greenland. The oldest of them are thought to have been produced through the anoxygenic photosynthesis of purple bacteria (See: Molecular ‘fossils’ and the emergence of photosynthesis; September 2000), suggested by organic molecules found in kerogen from early Archaean sediments. Later stromatolites (<3.0 Ga) have provided similar evidence for oxygen-producing cyanobacteria.

Acritarchs are microfossils of single-celled organisms made of kerogen that have been found in sediments up to 1.8 billion years old. Features protruding from their cell walls distinguish them from prokaryote cells, which are more or less ‘smooth’: acritarchs have been considered as possible early eukaryotes. Yet the oldest undisputed eukaryote microfossils – red and green algae – are much younger (about 1.0 Ga). A means of estimating an age for the crown group from which every later eukaryote organism evolved – last eukaryotic common ancestor (LECA) – is to use an assumed rate of mutation in DNA to deduce the time when differences in genetics between living eukaryotes began to diverge: i.e. a ‘molecular clock’. This gives a time around 2 Ga ago, but the method is fraught with uncertainties, not the least being the high possibility of mutation rates changing through time. So, when the Eukarya arose is blurred within the so-called ‘boring billion’ of the early Proterozoic Eon. A way of resolving this uncertainty to some extent is to look for ‘biomarker’ chemicals in the geological record that provide a ‘signature’ for eukaryotes.

A new study has been undertaken by a group of Australian, German and French scientists to analyse sediments ranging in age from 635 to 1640 Ma from Australia, China, Asia, Africa, North and South America (Brocks, J.J and 9 others 2023. Lost world of complex life and the late rise of the eukaryotic crown. Nature, v. 618, p. 767–773; DOI: 10.1038/s41586-023-06170-w; contact for PDF). Their chosen biomarkers are sterols (steroids) that regulate eukaryote cell membranes. Some prokaryotes also synthesise steroids but all of them produce hopanepolyols (hopanoids), which eukaryotes do not. The key measures for the presence/absence of eukaryote remains in ancient sea-floor sediments is thus the relative proportions of preserved steroids and hopanoids, together with those for the breakdown products of both – steranes and hopanesthat are, crudely speaking, carbon ‘skeletons’ of the original chemicals.

Proportions of biomarkers in sediments from present to 1.64 Ga. Cholesteroids – reds; ergosteroids – blues; stigmasteroids – greens; protosteroids magentas, hopanoids – yellows; unsampled – grey. Snowball glaciations are shown in pale blue. (Credit: Simplified from Figure 3 in Brocks et al.)

Interpretation of the results by Jochen Brocks and colleagues is complicated, and what follows is a summary based partly on an accompanying Nature News & Views article(Kenig, F. 2023. The long infancy of sterol biosynthesis. Nature, v. 618, p. 678-680; DOI: 10.1038/d41586-023-01816-1). The conclusions of Brocks et al. are surprising. First, the break-down products of steroids (saturated steranes) that can be attributed to crown eukaryotes (left on the figure above) are only present in sediments going back to about 200 Ma before the first Snowball Earth event (~900 Ma). Before that only hopanes formed by hopanoid degradation are present: a suggestion that LECA only appeared around that time – the authors suggest sometime between 1 and 1.2 Ga. That is far later than the time when eukaryotes could have emerged: i.e. once there was available oxygen after the Great Oxidation Event (~2.4 to 2.2 Ga). So what was going on before this? The authors broke new ground in analysis of biomarkers by being able to detect signs of the presence of actual hopanoids and steroids of several different kinds. Steroids were present as far back as 1.6 Ga in the oldest sediments that were analysed.

Steroids of crown eukaryotes are represented by cholesteroids, ergosteroids and stigmasteroids. All three are present throughout the Phanerozoic Eon and into the time of the Ediacaran Fauna that began 630 Ma ago. In that time span they generally outweigh hopanoids, thus reflecting the dominance of eukaryotes over prokaryotes. Back to about 900 Ma, only cholesteroids are present, together with archaic forms that are not found in living Eukarya, termed protosteroids.  Before that, only protosteroids are found. Moreover, these archaic steroids are not present in sediments that follow the Snowball Earth episodes (the Cryogenian Period).

Thus, it is possible that crown group eukaryotes – and their descendants, including us – evolved from and completely replaced an earlier primitive form (acritarchs?) at around the time of the greatest climatic changes that the Earth had experienced in the previous billion years or more. Moreover, the Cryogenian and Ediacaran Periods seem to show a rapid emergence of stigmasteroid- and ergosteroid production relative to cholesteroid: perhaps a result of explosive evolution of the Eukarya at that time. The organisms that produced protosteroids were present in variable amounts throughout the Mesoproteroic. Clearly there need to be similar analyses of sediments going back to the Great Oxygenation Event and the preceding Archaean to see if the protosteroid producers arose along with increasing levels of molecular oxygen. The ‘boring billion’ (2.0 to 1.0 Ga) may well be more interesting than previously thought.

Banded iron formations (BIFs) reviewed

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During most of the last hundred years every car body, rebar rod in concrete, ship, bridge and skyscraper frame had its origins in vividly striped red rocks from vast open-pit mines. Comprising mainly iron oxides with some silica, these banded iron formations, or BIFs for short, occur in profitable tonnages on every continent.

This image shows a 2.1 billion years old rock ...
2.1 billion years old boulder of banded ironstone. (credit: Wikipedia)

This article can now be read in full at Earth-logs in the Sedimentology and stratigraphy archive for 2017

Earth’s first major glacial epochs

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The global glaciations of the Neoproterozoic that reached low latitudes – the so-called ‘Snowball Earth’ events have dominated accounts of ancient glaciations since the start of the 21st century. Yet they are not the oldest examples of large-scale effects of continental ice sheets. Distinctive tillites or diamictites that contain large clasts of diverse, exotic rocks occur in sedimentary sequences of Archaean and Palaeoproterozoic age.

Diamictite from the Palaoproterozoic Gowganda Formation in Ontario Canada (credit: Candian Sedimentology Research Group)
Diamictite from the Palaeoproterozoic Gowganda Formation in Ontario Canada (credit: Canadian Sedimentology Research Group)

This item can be read in full at Earth-logs in the Palaeoclimatology archive for 2013