Detrital zircon grains extracted from sandstones deposited ~3 billion year (Ga) ago in Western Australia yield the ages at which these grains crystallised. The oldest formed at about 4.4 Ga; only 150 Ma after the origin of the Earth (4.55 Ga). Various lines of evidence suggest that they originally crystallized from magmas with roughly andesitic compositions, which some geochemists suggest to have formed the first continental crust (see:Zircons and early continents no longer to be sneezed at; February 2006). So far, no actual rocks of that age and composition have come to light. The oldest of these zircon grains also contain anomalously high levels of 18O, a sign that water played a role in the formation of these silicic magmas. Modern andesitic magmas – ultimately the source of most continental crust – typically form above steeply-dipping subduction zones where fluids expelled from descending oceanic crust encourage partial melting of the overriding lithospheric mantle. Higher radiogenic heat production in the Hadean and the early Archaean would probably have ensured that the increased density of later oceanic lithosphere needed for steep subduction could not have been achieved. If subduction occurred at all, it would have been at a shallow angle and unable to exert the slab-pull force that perpetuated plate tectonics in later times (see: Formation of continents without subduction, March, 2017).
Landsat image mosaic of the Palaeoarchaean granite-greenstone terrain of the Pilbara Craton, Western Australia. Granite bodies show as pale blobs, the volcanic and sedimentary greenstone belts in shades of grey.
Geoscientists have been trying to resolve this paradox for quite a while. Now a group from Australia, Germany and Austria have made what seems to be an important advance (Hartnady, M. I. H and 8 others 2025. Incipient continent formation by shallow melting of an altered mafic protocrust. Nature Communications, v. 16, article 4557; DOI: 10.1038/s41467-025-59075-9). It emerged from their geochemical studies of rocks in the Pilbara Craton of Western Australia that are about a billion years younger than the aforementioned ancient zircon grains. These are high-grade Palaeoarchaean metamorphic rocks known as migmatites that lie beneath lower-grade ‘granite-greenstone’ terrains that dominate the Craton, which Proterozoic deformation has forced to the surface. Their bulk composition is that of basalt which has been converted to amphibolite by high temperature, low pressure metamorphism (680 to 730°C at a depth of about 30 km). These metabasic rocks are laced with irregular streaks and patches of pale coloured rock made up mainly of sodium-rich feldspar and quartz, some of which cut across the foliation of the amphibolites. The authors interpret these as products of partial melting during metamorphism, and they show signs of having crystallised from a water-rich magma; i.e. their parental basaltic crust had been hydrothermally altered, probably by seawater soon after it formed. The composition of the melt rocks is that of trondhjemite, one of the most common types of granite found in Archaean continental crust. Interestingly, small amounts of trondhjemite are found in modern oceanic crust and ophiolites.
A typical migmatite from Antarctica showing dark amphibolites laced with quartzofeldspathic products of partial melting. Credit: Lunar and Planetary Laboratory, University of Arizona
The authors radiometrically dated zircon and titanite (CaTiSiO₅) – otherwise known as sphene – in the trondhjemites, to give an age of 3565 Ma. The metamorphism and partial melting took place around 30 Ma before the overlying granite-greenstone assemblages formed. They regard the amphibolites as the Palaeoarchaean equivalent of basaltic oceanic crust. Under the higher heat production of the time such primary crust would probably have approached the thickness of that at modern oceanic plateaux, such as Iceland and Ontong-Java, that formed above large mantle plumes. Michael Hartnady and colleagues surmise that this intracrustal partial melting formed a nucleus on which the Pilbara granite-greenstone terrain formed as the oldest substantial component of the Australian continent. The same nucleation may have occurred during the formation of similar early Archaean terrains that form the cores of most cratons that occur in all modern continents.
Judging by the coverage in the media, there is huge excitement about a possible sign of life on a very distant planet. It emerged from a Letter to The Astrophysical Journal posted by a British-US team of astronomers led by Nikku Madhusudhan that was publicised by the Cambridge University Press Office (Madhusudhan, N.et al. 2025. New Constraints on DMS and DMDS in the Atmosphere of K2-18 b from JWST MIRI. The Astrophysical Journal, v. 983, article adc1c8; DOI: 10.3847/2041-8213/adc1c8). K2-18 b is a planet a bit smaller than Neptune that orbits a red dwarf star (K2-18) about 124 light years away. The planet was discovered by NASA’s now-defunct Kepler space telescope tasked with the search for planets orbiting other stars. An infrared spectrometer on the Hubble Space Telescope revealed in 2019 that the atmosphere of K2-18 b contained water vapour, making the planet a target for further study as it may possess oceans. The more sophisticated James Webb Space Telescope IR spectrometer was trained on it a year later to reveal methane and CO2: yet more reason to investigate more deeply, for water and carbon compounds imply both habitability and the potential for life forms being there.
The latest results suggest that that the atmosphere of K2-18 b may contain simple carbon-sulfur gases: dimethyl sulfide ((CH3)2S) and dimethyl disulfide (CH3SSCH3). Bingo! for exobiologists, because on Earth both DMS and DMDS are only produced by algae and bacteria. Indeed they are responsible for the odour of the seaside. They became prominent in 1987 when biogeochemist James Lovelock fitted them into his Gaia Hypothesis. He recognised that they encourage cloud formation and thus increase Earth’s reflectivity (albedo) and also yield sulfuric acid aerosols in the stratosphere when they oxidise: that too increases albedo. DMS generates a cooling feedback loop to counter the warming feedback of greenhouse emissions. That is an idea of planetary self-regulation not much mentioned nowadays. Such gases were proposed by Carl Sagan as unique molecular indicators that could be used to search for extraterrestrial life.
The coma of Comet Churyumov-Gerasimenko yielded both dimethyl sulfide and amino acids to the mass spectrometer carried by ESA’s Rosetta. Credit: ESA.
The discovery of possible DMS and DMDS in K2-18 b’s atmosphere is, of course, currently under intense scientific scrutiny. For a start, the statistics inherent in Madhusudhan et al.’s methodology (3σ or 99.7% probability) fall short of the ‘gold standard’ for discoveries in physics (5σ or 99.99999% probability). Moreover, there’s also a chance that exotic, inorganic chemical processes could also create the gases, such as lightning in an atmosphere containing C, H and S. But this is not the first time that DMS has been discovered in an extraterrestrial body. Comets, having formed in the infancy of the Solar System much further from the Sun than any planets, are unlikely to be ‘teeming with life’. The European Space Agency’s Rosetta spacecraft chased comet 67P/Churyumov-Gerasimenko for 2 years, directly sampling dust and gas that it shed while moving closer to the Sun. A single day’s data from Rosetta’s mass spectrometer showed up DMS, and also amino acids. Both could have formed in comets or interstellar dust clouds by chemistry driven by radiation, possibly to contaminate planetary atmospheres. Almost certainly, further remote sensing of K2-18 b will end up with five-sigma precision and some will say, ‘Yes, there is life beyond Earth!’ and celebrate wildly. But that does not constitute proof, even by the ‘weight of evidence’ criterion of some judiciaries. To me such a conclusion would be unseemly romanticism. Yet such is the vastness of the material universe and the sheer abundance of the elements C H O N and P that make up most living matter that life elsewhere, indeed everywhere, (but not life as we know it) is a near certainty. The issue of intelligent lifeforms ‘out there’ is, however, somewhat less likely to be resolved . . .
Debates around the origin of Earth’s life and what the first organism was like resemble the mythical search for the Holy Grail. Chivalric romanticists of the late 12th and early 13th centuries were pretty clear about the Grail – some kind of receptacle connected either with the Last Supper or Christ’s crucifixion – but never found it. Two big quests that engage modern science centre on how the chemical building blocks of the earliest cells arose and the last universal common ancestor (LUCA) of all living things. Like the Grail’s location, neither is likely to be fully resolved because they can only be sought in a very roundabout way: both verge on the imaginary. The fossil record is limited to organisms that left skeletal remains, traces of their former presence, and a few degraded organic molecules. The further back in geological time the more sedimentary rock has either been removed by erosion or fundamentally changed at high temperatures and pressures. Both great conundrums can only be addressed by trying to reconstruct processes and organisms that occurred or existed more than 4 billion years ago.
Artistic impression of the early Earth dominated by oceans (Credit: Sci-news.com)
In the 1950s Harold Urey of the University of Chicago and his student Stanley Miller mixed water, methane, ammonia and hydrogen sulfide in lab glassware, heated it up and passed electrical discharges through it. They believed the simple set-up crudely mimicked Hadean conditions at the Earth surface. They were successful in generating more complex organic chemicals than their starting materials, though the early atmosphere and oceans are now considered to have been chemically quite different. Such a ‘Frankenstein’ approach has been repeated since with more success (see Earth-logs April 2024), creating 10 of the 20 amino acids plus the peptide bonds that link them up to make all known proteins, and even amphiphiles, the likely founders of cell walls. The latest attempt has been made by Spanish scientists at the Andalusian Earth Sciences Institute, the Universities of Valladolid and Cadiz, and the International Physics Centre in San Sebastian (Jenewein, C. et al 2024. Concomitant formation of protocells and prebiotic compounds under a plausible early Earth atmosphere. Proceedings of the National Academy of Sciences, v. 122, article 413816122; DOI: 10.1073/pnas.241381612).
Biomorphs formed by polymerisation of HCN (Credit: Jenewein, C. et al 2024, Figure 2)
Jenewein and colleagues claim to have created cell-like structures, or ‘biomorphs’ at nanometre- and micrometre scale – spheres and polyp-like bodies – from a more plausible atmosphere of CO2 , H2O, and N2. These ‘protocells’ seem to have formed from minutely thin (150 to 3000 nanometres) polymer films built from hydrogen cyanide that grew on the surface of the reaction chamber as electric discharges and UV light generated HCN and more complex ‘prebiotic’ chemicals. Apparently, these films were catalysed by SiO2 (silica) molecules from the glass reactor. Note: In the Hadean breakdown of olivine to serpentinite as sea water reacted with ultramafic lavas would have released abundant silica. Serpentinisation also generates hydrogen. Intimate release of gas formed bubbles to create the spherical and polyp-like ‘protocells’. The authors imagine the Hadean global ocean permanently teeming with such microscopic receptacles. Such a veritable ‘primordial soup’ would be able to isolate other small molecules, such as amino acids, oligopeptides, nucleobases, and fatty acids, to generate more complex organic molecules in micro-reactors en route to the kind of complex, self-sustaining systems we know as life.
So, is it possible to make a reasonable stab at what that first kind of life may have been? It was without doubt single celled. To reproduce it must have carried a genetic code enshrined in DNA, which is unique not only to all species, but to individuals. The key to tracking down LUCA is that it represents the point at which the evolutionary trees of the fundamental domains of modern life life – eukarya (including animals, plants and fungi), bacteria, and archaea – converge to a single evolutionary stem. There is little point in using fossils to resolve this issue because only multicelled life leaves tangible traces, and the first of those was found in 2,100 Ma old sediments in Gabon (see: The earliest multicelled life; July 2010). The key is using AI to compare the genetic sequences of the hugely diverse modern biosphere. Modern molecular phylogenetics and computing power can discern from their similarities and differences the relative order in which various species and broader groups split from others. It can also trace the origins of specific genes that provides clues about earlier genetic associations. Given a rate of mutation the modern differences provide estimates of when each branching occurred. The most recent genetic delving has been achieved by a consortium based at various institutions in Britain, the Netherlands, Hungary and Japan (Moody, E.R.R. and 18 others 2024. The nature of the last universal common ancestor and its impact on the early Earth system. Nature Ecology & Evolution, v.8, pages 1654–1666; DOI: 10.1038/s41559-024-02461-1).
Moody et al have pushed back the estimated age of LUCA to halfway through the Hadean, between 4.09 to 4.33 billion years (Ga), well beyond the geologically known age of the earliest traces of life (3.5 Ga). That age for LUCA in itself is quite astonishing: it could have been only a couple of hundred million years after the Moon-forming interplanetary collision. Moreover, they have estimated that Darwin’s Ur-organism had a genome of around 2 million base pairs that encoded about 2600 proteins: roughly comparable to living species of bacteria and archaea, and thus probably quite advanced in evolutionary terms. The gene types probably carried by LUCA suggest that it may have been an anaerobic acetogen; i.e. an organism whose metabolism generated acetate (CH3COO−) ions. Acetogens may produce their own food as autotrophs, or metabolise other organisms (heterotrophs). If LUCA was a heterotroph, then it must have subsisted in an ecosystem together with autotrophs which it consumed, possibly by fermentation. To function it also required hydrogen that can be supplied by the breakdown of ultramafic rocks to serpentinites, which tallies with the likely ocean-world with ultramafic igneous crust of the Hadean (see the earlier paragraphs about protocells). If an autotroph, LUCA would have had an abundance of CO2 and H2 to sustain it, and may have provided food for heterotrophs in the early ecosystem. The most remarkable possibility discerned by Moody et al is that LUCA may have had a kind of immune system to stave off viral infection.
The carbon cycle on the Hadean Earth (Credit: Moody et al. 2024; Figure 3e)
The Hadean environment was vastly different to that of modern times: a waterworld seething with volcanism; no continents; a target for errant asteroids and comets; more rapidly spinning with a 12 hour day; a much closer Moon and thus far bigger tides. The genetic template for the biosphere of the following four billion years was laid down then. LUCA and its companions may well have been unique to the Earth, as are their descendants. It is hard to believe that other worlds with the potential for life, even those in the solar system, could have followed a similar biogeochemical course. They may have life, but probably not as we know it . . .
The surface of Venus from the USSR Venera 14 lander
It is often said that Earth has a twin: Venus, the second planet from the Sun. That isn’t true, despite the fact that both have similar size and density. Venus, in fact, is even more inhospitable that either Mars or the Moon, having surface temperatures (~465°C) that are high enough to melt lead or, more graphically, those in a pizza oven. The only vehicles successfully to have landed on Venus (the Russian Venera series) survived for a mere 2 hours, but some did did send back data and images. That near incandescence is masked by the Venusian atmosphere that comprises 96.5% carbon dioxide, 3.5% nitrogen and 0.05 % sulfur dioxide, with mere traces of other gases including extremely low amounts of water vapour (0.002%) and virtually no oxygen. The dense atmosphere imposes a pressure at Venus’s surface tht is 92 times that on Earth: so dense that CO2 and N2 are, strictly speaking, not gases but supercritical fluids at the surface. At present Venus is definitely inimical to any known type of life. It is the victim of an extreme, runaway greenhouse effect.
As it stands, Venus’s geology is also very different from that of the Earth. Because its upper atmosphere contains clouds of highly reflective sulfuric acid aerosols only radar is capable of penetrating to the surface and returning to have been monitored by a couple of orbital vehicles: Magellan (NASA 1990 to 1994) and Venus Express (European Space Agency 2006 to 2014). The latter also carried means of mapping Venus’s surface gravitational field. The radar imagery shows that 80% of the Venusian surface comprises somewhat wrinkled plains that suggests a purely volcanic origin. Indeed more that 85,000 volcanoes have been mapped, 167 of which are over 100 km across. Much of the surface appears to have been broken into polygonal blocks or ‘campuses’ (campus is Latin for field) that give the impression of ‘crazy paving’. A peculiar kind of local-scale tectonics has operated there, but nothing like the plate tectonics on Earth in either shape or scale.
Polygonal blocks or ‘campuses’ on the lowland surface of Venus. Note the zones of ridges that roughly parallel ‘campus’ margins. Credit: Paul K. Byrne, North Carolina State University and Sean C. Solomon, Lamont-Doherty Earth Observatory
Many of the rocky bodies of the solar system are pocked by impact craters – the Earth has few, simply because erosion and sedimentary burial on the continents, and subduction of ocean floors have removed them from view. The Venusian surface has so few that it can, in its entirety, be surmised to have formed by magmatic ‘repaving’ since about 500 Ma ago at least. Earlier geological process can only be guessed at, or modelled in some way. A recent paper postulates that ‘there are several lines of evidence that suggest that Venus once did have a mobile lithosphere perhaps not dissimilar to Earth …’ (Weller, M.B. & Kiefer, W.S. 2025. The punctuated evolution of the Venusian atmosphere from a transition in mantle convective style and volcanic outgassing. Science Advances, v. 11, article eadn986; DOI: 10.1126/sciadv.adn986). One large, but subtle feature may have formed by convergence similar to that of collision tectonics. There are also gravitational features that hint at active subduction at depth, although the surface no longer shows connected features such as trenches and island arcs. Local extension has been inferred from other data.
Weller and Kiefer suspect that Venus in the past may have shifted between a form of mobile plate tectonics and stagnant ‘lid’ tectonics, the vast volcanic plains having formed by processes akin to flood volcanism on a planetary scale. Venus’s similar density to that of Earth suggests that it is made of similar rocky material surrounding a metallic core. However, that planet has a far weaker magnetic field suggesting that the core is unable to convect and behave like a dynamo to generate a magnetic field. That may explain why the atmosphere of Venus is almost completely dry. With no magnetic field to deflect it the solar wind of charged particles directly impacts the upper atmosphere, in contrast to the Earth where only a very small proportion descends at the poles. Together with the action of UV solar radiation that splits water vapour into its constituent hydrogen and oxygen ions, the solar wind adds energy to them so that they escape to space. This atmospheric ‘erosion’ has steadily stripped the atmosphere of Venus – and thus its solid surface – of all but a minute trace of water, leaving behind higher mass molecules, particularly carbon dioxide, emitted by its volcanism. Of course, this process has vastly amplified the greenhouse effect that makes Venus so hot. Early on the planet may have had oceans and even primitive life, which on Earth extract CO2 by precipitating carbonates and by photosynthesis, respectively. But they no longer exist.
The high surface temperature on Venus has made its internal geothermal gradient very different from Earth’s; i.e. increasing from 465°C with depth, instead of from about 15°C on Earth. As a result, everywhere beneath the surface of Venus its mantle has been more able to melt and generate magma. Earlier in its history it may have behaved more like Earth, but eventually flipped to continual magmatic ‘repaving’. To investigate how this evolution may have occurred Weller and Kiefer created 3-D spherical models of geological activity, beginning with Earth-like tectonics – a reasonable starting point because of the probable Earth-like geochemistry of Venus. My simplified impression of what they found is that the periodic blurting of magma well-known from Earth history to have created flood-basalt events without disturbing plate tectonics proceeded on Venus with progressively greater violence. Such events here emitted massive amounts of CO2 into the atmosphere over short (~1 Ma) time scales and resulted in climate change, but Earth’s surface processes have always returned to ‘normal’. Flood-basalt episodes here have had a rough periodicity of around 35 Ma. Weller and Kiefer’s modelling seems to suggest that such events on Venus may have been larger. Repetition of such events, which emitted CO2 that surface processes could not erase before the next event, would progressively ramp up surface temperatures and the geothermal gradient. Eventually climatic heating would drive water from the surface into the atmosphere, to be lost forever through interaction with the solar wind. Without rainfall made acid by dissolved CO2, rock weathering that tempers the greenhouse effect on Earth would cease on Venus. The increased geothermal gradient would change any earlier rigid, Earth-like lithosphere to more ductile material, thereby shutting down the formation of plates, the essence of tectonics on Earth. It may have been something along those lines that made Venus inimical to life, and some may fear that anthropogenic global warming here might similarly doom the Earth to become an incandescent and sterile crucible orbiting the Sun. But as Mark Twain observed in 1897 after reading The New York Herald’s account that he was ill and possibly dying in London, ‘The report of my death was an exaggeration’. It would suit my narrative better had he said ‘… was premature’!
The Earth has a very large Moon because of a stupendous collision with a Mars-sized planet shortly after it accreted. That fundamentally reset Earth’s bulk geochemistry: a sort of Year Zero event. It endowed both bodies with magma oceans from which several tectonic scenarios developed on Earth from Eon to Eon. There is no evidence that Venus had such a catastrophic beginning. By at least 3.7 billion years ago Earth had a strong magnetic field. Protected by that thereafter from the solar wind, it has never lost its huge endowment of water; solid, liquid or gaseous. It seems that it did go through a stagnant lid style of tectonics early on, that transitioned to plate tectonics around the end of the Hadean Eon (~4.0 Ga), with a few hiccups during the Archaean Eon. And it did develop life as an integral part of the rock cycle. Venus, fascinating as it is, shows no sign of either, and that’s hardly surprising. Those factors and its being much closer to the Sun may have condemned it from the outset.
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At the start of the Cambrian Period animal life began to diversify from that of the Ediacaran world. For the first time sediments on the seafloor were explored for sustenance, leading to a variety of burrows that disrupted fine depositional layers. The basal Cambrian sandstones found in Britain and elsewhere are pervasively bioturbated: good evidence for the start of a ‘Worm world’ that marks the Precambrian-Phanerozoic boundary. That is probably a misnomer for the shallow seabed of that time, as fossils of burrowers with a variety of hard parts turn up in the oldest Cambrian sequences. Also appearing for the first time are tooth-like microfossils that took on such a range of bizarre shapes that they have long been used for correlating sedimentary strata in the absence of larger creatures. Some of these conodonts have been attributed to early vertebrates akin to modern lampreys and hag fish, but others may have been the grasping mouth-spines of a group of predatory worms which also survive to the present: chaetognaths. Apart from these oral spines chaetognaths lack hard parts, so anatomical details of ancient ones are only found in sites of exquisite preservation or lagerstätten. In such rare, tranquil places soft tissues such as muscles may be preserved by phosphatisation during decay.
Reconstruction of Timorebestia koprii showing its musculature, nerve system and mouthparts, It probably propelled itself by fluttering its outer and rear flaps, much like a modern flatfish. Credit: Park et al., Fig 4
One of the earliest Phanerozoic lagerstätten (Sirius Passet) occurs in northern Greenland. It is curiously named after the Sirius Dog Sled Patrol, an elite pair of naval troops with a sledge and 12 dogs that enforces Danish sovereignty over the Greenlandic shore of the Arctic Ocean. The Sirius Passet fauna includes a monstrous chaetognath over 30 cm long (Park, T.-Y. S. and 12 others 2024. A giant stem-group chaetognath. Science Advances, v. 10 article eadi6678; DOI: 10.1126/sciadv.adi6678). It is called Timorebestia koprii (Timorebestia is Latin for ‘terror beast’) and was related to the living, but tiny, arrow worms that prey on zooplankton in modern oceans. This description and moniker may seem to be somewhat hyperbolic, but Timorobestia outranks in size any Early Cambrian predatory arthropods. It was probably high in the Early Cambrian trophic pyramid, but was soon relegated by the later Cambrian rise of trilobites and then of cephalopods and eventually jawed vertebrate fishes in the Silurian. One specimen contained shells of a swimming arthropod whose protective spines did not deter the ‘terrible’ chaetognath from swimming them down.
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