Did the Meteor Crater impact in Arizona dam the Grand Canyon 56 thousand years ago?

Meteor Crater, Arizona, USA. Credit: Travel in USA

Meteor Crater, 60 km east of Flagstaff in Arizona, USA, is probably the most visited site of an impact by an extraterrestrial object. At 1.3 km across it isn’t especially big, but it is exceptionally well preserved, having formed a mere 55.6 ka ago. Apart from its shape its impact origin is proved by its rim, which shows overturning and inversion of strata that it penetrated. The 40 metre  diameter nickel-iron object that did the damage arrived at a speed around 13 km s-1 and delivered kinetic energy equivalent to an explosion of 10 million tons of TNT. This was sufficient to vaporise the body, except for a few fragments. Impressive as that is, the impact was tiny compared with others known on Earth, such as the Chicxulub impact that ended the Mesozoic Era 60 Ma ago. Nevertheless, the surface blast would have sterilised an area up to 1000 km2 around the impact, i.e. up to 17 km in all directions. Yet, most of the impact energy would have affected the surrounding crust. It’s a place worth visiting.

The other must-see site in northern Arizona is the Grand Canyon, some 100 km north of Flagstaff by train, and about 320 km by road. Unlike Meteor Crater, whose origins were well established  more than 50 years ago, the Grand Canyon still draws research teams to study the geology of the rock formations through which it cuts and the geomorphological processes that formed it. Several expeditions have examined caves high above the level of the Colorado River that has cut the Canyon since the start of the Pliocene Epoch, some 5 Ma ago. One objective of this research has been to document past flooding, due to the massive landslides and rock falls that must have occurred as cliffs became unstable during canyon formation. One cave – Stanton’s Cave – is 45 m above the present level of the Colorado: about the height of a 16 storey block of flats. The cave floor is made of well-bedded sand that contains driftwood logs, as do other caves along the canyon. Dating the logs from cave to cave should give at least an idea of the history of flooding and thus cliff collapses. In the case of Stanton’s Cave early radiocarbon dating yielded results close to the maximum that the rapid decay of 14C makes possible. Such dating at the limit of the technique is imprecise. The oldest existing radiocarbon age in this case is 43.5 ± 1.5 ka from a 1984 study. Since then, this dating technique has advanced considerably.

Fig Remnants of a landslide, subsequently breached, in the Grand Canyon downstream of Stanton’s Cave. Credit: Richard Hereford

Karl Karlstrom – whose father was also entranced by cave deposits in the Grand Canyon in the 1960s – together with colleagues from the US managed to persuade radiocarbon specialists from Australia and New Zealand to improve the sediment dating (Karlstrom, K.E and 11 others 2025. Grand Canyon landslide-dam and paleolake triggered by the Meteor Crater impact at 56 ka. Geology, v. 53, online article; DOI: 10.1130/G53571.1). The new 14Cage of the logs is  55.25 ± 2.44 ka, confirmed by infrared stimulated luminescence (IRSL) dating of feldspar grains in the cave sand at  56.00 ± 6.39 ka  Combined with a new cosmogenic nuclide exposure age of 56.00 ± 2.40 ka  for the Meteor Crater ejecta the results are exciting. It looks as if the cliff fall that dammed the Colorado River to fill the cave with sediment coincided with the impact. Crater formation is estimated to have resulted in a seismic event of magnitude 5.4. In such a teetering terrain as the Grand Canyon cliffs, the impact-induced earthquake about 100 km away, even if attenuated to an effective magnitude estimated at 3.5  may have been sufficient to topple part of the cliffs. With cliffs that average 1.6 km high, such a collapse would have displaced sufficient debris to create a substantial barrier to flow of the Colorado River, which is tightly constrained between cliffs. The chaotic debris at the suggested dam site is now partly covered by round river cobbles, suggesting that it was soon overtopped, probably within a thousand years of the cliff collapse.

Because all the dates have substantial imprecision, it is not possible to claim that the authors have proved conclusively a direct connection between impact and cliff collapse. But neither do the age data disprove what is a plausible causal connection.

See also: UNM study finds link between Grand Canyon landslide and Meteor Crater impact. University of New Mexico News 15 July 2025

Evolution of pigmentation in anatomically modern humans of Europe: a new paradigm?

The colours of human skin, eyes and hair in living people across the world are determined by variants of genes (alleles) found at the same place on a chromosome. Since chromosomes are inherited from both mother and father, an individual may have the same two alleles (homozygous), or one of each (heterozygous). A dominant allele is always expressed, even if a single copy is present. A recessive allele is only expressed if the individual inherits two copies of it. Most characteristics of individuals result from the interaction of multiple genes, rather than a single gene. A commonly cited example is the coloration of eyes. If we had a single gene for eye colour – that of the iris – that had alleles just for blue (recessive or ‘b’) and one for brown (dominant or ‘B) pigmentation, brown-eyed individuals would have one or two ‘B’ alleles (bB or BB), whereas those with blue eyes would have to have two ‘blue’ alleles (bb). But inheritance is more complicated than that: there are people with green, hazel or grey eyes and even left- and right eyes of different colour. Such examples suggest that there are more than two genes affecting human eye colour, and each must have evolved as a result of mutations. Much the same goes for hair and skin coloration.

A group of scientists from the University of Ferrara in Italy have analysed highly detailed ancient DNA in anatomically modern human remains from Russia (Palaeolithic), Sweden (Mesolithic) and Croatia (Neolithic) to tease out the complexities of pigmentation inheritance. Then they applied a statistical approach learned from that study to predict the likely skin-, eye- and hair pigmentation in 348 less detailed genomes of ancient individuals whose remains date back to 45 Ma ( Silvia Perretti et al, 2025. Inference of human pigmentation from ancient DNA by genotype likelihood. Proceedings of the National Academy of Science, v. 122, article e2502158122; DOI: 10.1073/pnas.2502158122).

An artist’s impression of a Mesolithic woman from southern Denmark (credit: Tom Bjorklund)

All the hunter-gatherer Palaeolithic individuals (12 samples between 45 and 13 ka old) bar one, showed clear signs of dark pigmentation in skin, eyes and hair – the outlier from Russia was probably lighter. Those from the Mesolithic (14 to 4 ka) showed that 11 out of 35 had a light eye colour (Northern Europe, France, and Serbia), but most retained the dark skin and hair expected in descendants of migrants from Africa. Only one 12 ka hunter-gatherer from Sweden had inferred blue eyes, blonde hair, and light skin.  The retention of dark pigmentation by European hunter-gatherers who migrated there from Africa has been noted before, using DNA from Mesolithic human remains and in one case from birch resin chewed by a Mesolithic woman. This called into question the hypothesis that high levels of melatonin in skin, which protects indigenous people in Africa from cancers, would result in their producing insufficient vitamin D for good health. That notion supposed that out-of-Africa migrants would quickly evolve paler skin coloration at higher latitudes. It is now known that diets rich in meat, nuts and fungi – staple for hunter-gatherers – provide sufficient vitamin-D for health at high latitudes. A more recent hypothesis is that pale skins may have evolved only after the widespread Neolithic adoption of farming when people came to rely on a diet dominated by cereals that are a poor source of vitamin-D.

However, 132 Neolithic farmers (10 to 4 ka ago) individuals studied by Perretti et al. showed increased diversity in pigmentation, with more frequent light skin tones, yet dark individuals persisted, particularly in southern and eastern Europe. Hair and eye colour showed considerable variability, the earliest sign of red hair showing up in Turkey. Even Copper- and Bronze Age samples ( 113 from 7 to 3 ka) and those from Iron Age Europeans (25 from 3 to 1.7 ka ago) still indicate common retention of dark skin, eyes and hair, although the proportion of lighter pigmentation increased in some regions of Europe. Other analyses of ancient DNA have shown that the Palaeo- and Mesolithic populations of Europe were quickly outnumbered by influx of early farmers, probably from the Anatolian region of modern Turkey, during the Neolithic. The farming lifestyle seems likely to have allowed the numbers of those who practised it to rise beyond the natural environment’s ‘carrying capacity’ for hunter-gatherers. The former inhabitants of Europe may simply have been genetically absorbed within the growing population of farmers. Much the same absorption of earlier groups seems to have happened with the westward migration from the Ukrainian and Russia steppes of the Yamnaya people and culture, culminating in the start of the European Bronze Age that reached western Europe around 2.1 ka, The Yamnaya introduced metal culture, horse-drawn wheeled vehicles and possibly Indo-European language.

So the novel probabilistic approach to ancient DNA by Perretti et al. also casts doubt on the diet-based evolution of light pigmentation at high latitudes. Instead, pulses of large population movements and thus changes in European population genetics probably account for the persistence of abundant evidence for dark pigmentation throughout Europe until historic times. The ‘lightening’ of Europeans’ physiognomy seems to have been vastly more complex than previously believed. Early Europe seems to have been almost bewilderingly diverse, which make a complete mockery of modern chauvinism and racism. The present European genetic ‘melting pot’ is surprisingly similar to that of Europe’s ancient past.

The end-Triassic mass extinction and ocean acidification

Triassic reef limestones in the Dolomites of northern Italy. Credit: © Matteo Volpone

Four out of six mass extinctions that ravaged life on Earth during the last 300 Ma coincided with large igneous events marked by basaltic flood volcanism. But not all such bursts of igneous activity match significant mass extinctions. Moreover, some rapid rises in the rate of extinction are not clearly linked to peaks in igneous activity. Another issue in this context is that ‘kill mechanisms’ are generally speculative rather than based on hard data. Large igneous events inevitably emit very large amounts of gases and dust-sized particulates into the atmosphere. Carbon dioxide, being a greenhouse gas, tends to heat up the global climate, but also dissolves in seawater to lower its pH. Both global warming and more acidic oceans are possible ‘kill mechanisms’. Volcanic emission of sulfur dioxide results in acid rain and thus a decrease in the pH of seawater. But if it is blasted into the stratosphere it combines with oxygen and water vapour to form minute droplets of sulfuric acid. These form long-lived haze, which reflects solar energy beck into space. Such an increased albedo therefore tends to cool the planet and create a so-called ‘volcanic winter’. Dust that reaches the stratosphere reduces penetration of visible light to the surface, again resulting in cooling. But since photosynthetic organisms rely on blue and red light to power their conversion of CO­2­ and water vapour to carbohydrates and oxygen, these primary producers at the base of the marine and terrestrial food webs decline. That presents a fourth kill mechanism that may trigger mass extinction on land and in the oceans: starvation.

Palaeontologists have steadily built up a powerful case for occasional mass extinctions since fossils first appear in the stratigraphic record of the Phanerozoic Eon. Their data are simply the numbers of species, genera and families of organisms preserved as fossils in packages of sedimentary strata that represent roughly equal ‘parcels’ of time (~10 Ma). Mass extinctions are now unchallengeable parts of life’s history and evolution. Yet, assigning specific kill mechanisms involved in the damage that they create remains very difficult. There are hypotheses for the cause of each mass extinction, but a dearth of data that can test why they happened. The only global die-off near hard scientific resolution is that at the end of the Cretaceous. The K-Pg (formerly K-T) event has been extensively covered in Earth-logs since 2000. It involved a mixture of global ecological stress from the Deccan large igneous event spread over a few million years of the Late Cretaceous, with the near-instantaneous catastrophe induced by the Chicxulub impact, with a few remaining dots and ticks needed on ‘i’s and ‘t’s. Other possibilities have been raised: gamma-ray bursts from distant supernovae; belches of methane from the sea floor; emissions of hydrogen sulfide gas from seawater itself during ocean anoxia events; sea-level changes etc.

The mass extinction that ended the Triassic (~201 Ma) coincides with evidence for intense volcanism in South and North America, Africa and southern Europe, then at the core of the Pangaea supercontinent. Flood basalts and large igneous intrusions – the Central Atlantic Magmatic Province (CAMP) – began the final break-up of Pangaea. The end-Triassic extinction deleted 34% of marine genera. Marine sediments aged around 201 Ma reveal a massive shift in sulfur and carbon isotopes in the ocean that has been interpreted as a sign of acute anoxia in the world’s oceans, which may have resulted in massive burial of oxygen-starved marine animal life. However, there is no sign of Triassic, carbon-rich deep-water sediments that characterise ocean anoxia events in later times. But it is possible that bacteria that use the reduction of sulfate (SO42-) to sulfide (S2-) ions as an energy source for them to decay dead organisms, could have produced the sulfur isotope ‘excursion’. That would also have produced massive amounts of highly toxic hydrogen sulfide gas, which would have overwhelmed terrestrial animal life at continental margins. The solution ofH2S in water would also have acidified the world’s oceans.

Molly Trudgill of the University of St Andrews, Scotland and colleagues from the UK, France, the Netherlands, the US, Norway, Sweden and Ireland set out to test the hypothesis of end-Triassic oceanic acidification (Trudgill, M. and 24 others 2025. Pulses of ocean acidification at the Triassic–Jurassic boundary. Nature Communications, v. 16, article 6471; DOI: 10.1038/s41467-025-61344-6). The team used Triassic fossil oysters from before the extinction time interval. Boron-isotope data from the shells are a means of estimating variations in the pH of seawater. Before the extinction event the average pH in Triassic seawater was about the same as today, at 8.2 or slightly alkaline. By 201 Ma the pH had shifted towards acidic conditions by at least 0.3: the biggest detected in the Phanerozoic record. One of the most dramatic changes in Triassic marine fauna was the disappearance of reef limestones made by the recently evolved modern corals on a vast scale in the earlier Triassic; a so-called ‘reef gap’ in the geological record. That suggests a possible analogue to the waning of today’s coral reefs that is thought to be a result of increased dissolution of CO2 in seawater and acidification, related to global greenhouse warming. Using the fossil oysters, Trudgill et al. also sought a carbon-isotope ‘fingerprint’ for the source of elevated CO2, finding that it mainly derived from the mantle, and was probably emitted by CAMP volcanism. So their discussion centres mainly on end-Triassic ocean acidification as an analogy for current climate change driven by CO2 largely emitted by anthropogenic burning of fossil fuels. Nowhere in their paper do they mention any role for acidification by hydrogen sulfide emitted by massive anoxia on the Triassic ocean floor, which hit the scientific headlines in 2020 (see earlier link).

Sagduction of greenstone belts and formation of Archaean continental crust

Simplified geological map of the Archaean Yilgarn Craton in Western Australia. Credit: Geological Survey of Western Australia

Every ancient craton seen from space shows patterns that are unique to Archaean continental crust: elongated, ‘canoe-shaped’ greenstone belts enveloped by granitic gneisses, both of which are punctured by domes of younger, less deformed granites. The Yilgarn Craton of Western Australia is a typical granite-greenstone terrain. Greenstone belts contain lavas of ultramafic, basaltic and andesitic compositions, which in undeformed settings show the typical pillow structures formed by submarine volcanic extrusion. There are also layered mafic to ultramafic complexes, formed by fractional crystallisation, minor sedimentary sequences and occasionally more felsic lavas and ashes. The enveloping grey gneisses are dominantly highly deformed tonalite-trondhjemite-granodiorite (TTG) composition that suggest that they formed from large volumes of sodium-rich, silicic magmas, probably generated at depth by partial melting of hydrated basaltic rocks.

The heat producing radioactive isotopes of potassium, uranium and thorium in both the Archaean mantle and crust would have been more abundant before 2.5 Ga ago, because they decay over time. Consequently the Earth’s interior would have then generated more heat than now, gradually to escape by thermal conduction towards the cooler surface. The presence of pillow lavas and detrital sediments in greenstone belts indicate that surface temperatures during the Archaean Eon were below the boiling point of water; in fact probably much the same as in the tropics at present. Indeed there is evidence that Earth was then a water world. It may even have been so during the Hadean, as revealed by the oxygen-isotope data in 4.4 Ga zircon grains. The broad conclusion from such findings is that the Archaean geothermal gradient was much steeper; there would have been a greater temperature increase with depth than now and new crust would have cooled more slowly. Subduction of cool lithosphere would have been less likely than in later times, especially as higher mantle heat production would have generated new crust more quickly. Another likely possibility is that far more heat would have been moved by convection: there would have been more mantle-penetrating plumes and they would have been larger. Large mantle plumes of the Phanerozoic have generated vast ocean floor plateaus, such as the Kerguelen and Ontong Java Plateau.

A group of geoscience researchers at The University of Hong Kong and international colleagues recently completed a geological and geochemical study of the North China Craton, analysing their data in the light of recently emerging views on Archaean processes (Dingyi Zhao et al, A two-stage mantle plume-sagduction origin of Archean continental crust revealed by water and oxygen isotopes of TTGs, Science Advances, v. 11, article eadr9513  ; DOI: 10.1126/sciadv.adr9513).They found compelling evidence that ~2.5 Ga-old Neoarchaean TTG gneisses in the North China granite-greenstone terrain formed by partial melting of an earlier mafic-ultramafic greenstone crust with high water content. They consider this to support a two-stage model for the generation of the North China Craton’s crust above a vast mantle plume. The first stage at around 2.7 Ga was the arrival of the plume at the base of the lithosphere, which partially melted as a result of the decompression of the rising ultramafic plume. The resulting mafic magma created an oceanic plateau partly by underplating the older lithosphere, intruding it and erupting onto the older ocean floor. This created the precursors of the craton’s greenstones, the upper part of which interacted directly with seawater to become hydrothermally altered. They underwent minor partial melting to produce small TTG intrusions. A second plume arriving at ~2.5 Ga resulted in sinking of the greenstones under their own weight to mix or ‘hybridise’ with the re-heated lower crust. This caused the greenstones substantially to partially melt and so generate voluminous TTG magmas that rose as the greenstones subsided. . It seems likely that this dynamic, hot environment deformed the TTGs as they rose to create the grey gneisses so typical of Archaean granite-greenstone terranes. [Note: The key evidence for Dingyi Zhao et al.’s conclusions is that the two TTG pulses yielded the 2.7 and 2.5 Ga ages, and show significantly different oxygen isotope data (δ18O)].

Two stages of TTG gneiss formation in the North China Craton and the sinking (sagduction) of greenstone belts in the second phase. Credit: Dingyi Zhao et al., Fig 4)

Such a petrogenetic scenario, termed sagduction by Dingyi Zhao and colleagues, also helps explain the unique keel-like nature of greenstone belts, and abundant evidence of vertical tectonics in many Archaean terrains (see: Vertical tectonics and formation of Archaean crust; January 2002), Their model is not entirely new, but is better supported by data than earlier, more speculative ideas. That such processes have been recognised in the Neoarchaean – the North China Craton is one of the youngest granite-greenstone terrains – may well apply to far older Archaean continental crust generation. It is perhaps the last of a series of such events that began in the Hadean, as summarised in the previous Earth-logs post.