Category Archives: Geobiology, palaeontology, and evolution

Something large moved 2 billion years ago

More than 50 years ago a group of schoolchildren discovered a fronded fossil (Charnia) in the Precambrian rocks of Charnwood Forest in the English Midlands. Since then it has been clear that multicellular life originated before the Cambrian Period, when the first tangible life had previously been considered to have emerged. Discovery of the rich Ediacaran fauna of quilted, baglike and disc-like animals in 635 Ma old Neoproterozoic sediments in South Australia, and many other occurrences re-established the start of the ‘carnival of animals’ in the Ediacaran Period (635 to 541 Ma). It happened to follow the climatic and environmental turmoil of at least two Snowball Earth episodes during the preceding Cryogenian Period (850 to 635 Ma), which has led to a flurry of suggestions for the transition from protozoan to metazoan life. Yet, applying a ‘molecular-clock’ approach to the genetic differences between living metazoan organisms seems to suggest a considerable earlier evolutionary event that started ‘life as we know it’. That may have been confirmed by a discovery in much older sediments in Gabon, West Africa.

A sequence of shallow-marine sediments in the Francevillian Series in Gabon was laid down at a time of fluctuating sea level around 2100 Ma ago, when the upper oceans had become oxygenated. In them are black shales that preserve an abundance of intricate sedimentary features. Among them are curious stringy structures rich in crystalline pyrite (Fe2S). They are infilled wiggly tubes that lie in the shale bedding. CT scans reveal that the bedding has been flattened around the tubules as it became lithified. So the tubes formed while the sediment was wet and soft (El Albani, A. and 22 others 2019. Organism motility in an oxygenated shallow-marine environment 2.1 billion years ago. Proceedings of the National Academy of Sciences, online preprint; DOI: 10.1073/pnas.1815721116). They look very like burrows. Up to 5 mm across, they can be considered large by comparison with almost all organisms known from that time. The exception comes from the same stratigraphic Series in Gabon. In 2010, El Albani and colleagues published an account of fossils preserved by pyrite that look like fried eggs, 1 to 2 cm across, with scalloped edges. Internal structures revealed by CT scanning include radial slits in the ‘whites’ and folding within the central ‘yolk’. That paper reported the geochemical presence in the host shales of steranes, which are breakdown products of steroids that are unique to eukaryotes. Could these organisms and the wiggly tube-like trace fossils indicate the presence of the earliest metazoans in the Francevillian Series?


Palaeoproterozoic fossils from the Francevillian Series in Gabon. Top: greytone photographs of burrow-like trace fossils (Credit: El Albani et al. 2019; Fig.1). Bottom: colour photograph and 3 CT scans of discoidal fossil (Credit: El Albani et al. 2010; Fig. 4).

Until the discoveries in Gabon, the oldest organic structure that had been suggested to be a metazoan was the rare Grypania, a spiral, strap-like fossil found in a variety of strata ranging in age from 1870 to 650 Ma. Being made of a structureless ribbon of graphite, Grypania seems most likely to have been made by colonial bacteria. The two Gabon life forms cannot be disposed of quite so easily. The discoids have organised structures rivalling those in Ediacaran animals, while the wiggly tubes clearly seem to indicate something capable of movement. In both cases preservation is by iron sulfide, which suggests the presence at some stage of chemo-autotrophic bacteria that reduce sulfate ions to sulfide. Could these not have formed mats taking up irregular discs and plates? The burrows may have been formed by unicellular eukaryotes, one type of which – the slime moulds – is capable of aggregating together to form multi-celled reproductive structures as well as living freely as single amoeba. Some form slug-like masses that are capable of movement; not metazoans, but perhaps their precursors.

A unifying idea for the origin of life

The nickel in stainless steel, the platinum in catalytic converters and the gold in jewellery, electronic circuits and Fort Knox should all be much harder to find in the Earth’s crust. Had the early Earth formed only by accretion and then the massive chemical resetting mechanism of the collision that produced the Moon all three would lie far beyond reach. Both formation events would have led to an extremely hot young Earth; indeed the second is believed to have left the outer Earth and Moon completely molten. All three are siderophile metals and have such a strong affinity for metallic iron that they would mostly have been dragged down to each body’s core as it formed in the early few hundred million years of the Earth-Moon system, leaving very much less in the mantle than rock analyses show. This emerged as a central theme at the Origin of Life Conference held in Atlanta GA, USA in October 2018. The idea stemmed from two papers published in 2015 that reported excessive amounts in basaltic material from both Earth and Moon of a tungsten isotope (182W) that forms when a radioactive isotope of hafnium (182Hf), another strongly siderophile metal, decays. Hafnium too must have been strongly depleted in the outer parts of both bodies when their cores formed. The excesses are explained by substantial accretion of material rich in metallic iron to their outer layers shortly after Moon-formation, some being in large metallic asteroids able to penetrate to hundreds of kilometres. Hot iron is capable of removing oxygen from water vapour and other gases containing oxygen, thereby being oxidised. The counterpart would have been the release of massive amounts of hydrogen, carbon and other elements that form gases when combined with oxygen. The Earth’s atmosphere would have become highly reducing.

Had the atmosphere started out as an oxidising environment, as thought for many decades, it would have posed considerable difficulties for the generation at the surface of hydrocarbon compounds that are the sine qua non for the origin of life. That is why theories about abiogenesis (life formed from inorganic matter) hitherto have focussed on highly reducing environments such as deep-sea hydrothermal vents where hydrogen is produced by alteration of mantle minerals. The new idea revitalises Darwin’s original idea of life having originated in ‘a warm little pond’. How it has changed the game as regards the first step in life, the so-called ‘RNA World’ can be found in a detailed summary of the seemingly almost frenzied Origin of Life Conference (Service, R.F. 2019. Seeing the dawn. Science, v. 363, p. 116-119; DOI: 10.1126/science.363.6423.116).

Isotope geochemistry has also entered the mix in other regards, particularly that gleaned from tiny grains of the mineral zircon that survived intact from as little as 70 Ma after the Moon-forming and late-accretion events to end up (3 billion years ago) in the now famous Mount Narryer Quartzite of Western Australia. The oldest of these zircons (4.4 Ga) suggest that granitic rocks had formed the earliest vestiges of continental crust far back in the Hadean Eon: Only silica-rich magmas contain enough zirconium for zircon (ZrSiO4) to crystallise. Oxygen isotope studies of them suggest that at that very early date they had come into contact with liquid water, presumably at the Earth’s surface. That suggests that perhaps there were isolated islands of early continental materials; now vanished from the geological record. A 4.1 Ga zircon population revealed something more surprising: graphite flakes with carbon isotopes enriched in 12C that suggests the zircons may have incorporated carbon from living organisms.


A possible timeline for the origin of life during the Hadean Eon (Credit: Service, R.F. 2019, Science)

Such a suite of evidence has given organic chemists more environmental leeway to suggest a wealth of complex reactions at the Hadean surface that may have generated the early organic compounds needed as building blocks for RNA, such as aldehydes and sugars (specifically ribose that is part of both RNA and DNA), and the amino acids forming the A-C-G-U ‘letters’ of RNA, some catalysed by the now abundant siderophile metal nickel. One author seems gleefully to have resurrected Darwin’s ‘warm little pond’ by suggesting periodic exposure above sea level of abiogenic precursors to volcanic sulfur dioxide that could hasten some key reactions and create large masses of such precursors which rain would have channelled into ‘puddles and lakes’. The upshot is that the RNA World precursor to the self-replication conferred on subsequent life by DNA is speculated to have been around 4.35 Ga, 50 Ma after the Earth had cooled sufficiently to have surface water dotted with specks of continental material.

There are caveats in Robert Services summary, but the Atlanta conferences seems set to form a turning point in experimental palaeobiology studies.

Pterosaurs had feathers and fur

Pterosaurs, which include the pterodactyls and pteranodons, were the first vertebrates to achieve proper, flapping flight. In the popular imagination they are regarded as ‘flying dinosaurs’, whereas the anatomy of the two groups is significantly different. The first of them appeared in the Upper Triassic around 235 Ma ago, at roughly the same time as the earliest known dinosaurs. The anatomical differences make it difficult to decide on a common ancestry for the two. But detailed analysis of pterosaur anatomy suggests that they share enough features with dinosaurs, crocodiles and birds for all four groups to have descended from ancestral archosaurs that were living in the early Triassic, and they survived the mass extinction at the end of that Period. Birds, on the other hand, first appear in the fossil record during the Upper Jurassic 70 Ma later than pterosaurs. They are now widely regarded as descendants of early theropod dinosaurs, which are known commonly to have had fur and feathers.

Pterosaurs leapt into the public imagination in the final chapter of Sir Arthur Conan Doyle’s Lost World with a clatter of ‘dry, leathery wings’ as Professor George Challenger’s captive pterodactyl from northern Brazil’s isolated Roraima tepui plateau made its successful bid for escape from a Zoological Institute meeting in Queens Hall. Yet, far from being leathery, pterosaurs turned out, in the late 1990’s, to have carried filamentous pycnofibres akin to mammalian hair. Widespread reports in the world press during the week before Christmas in 2018 hailed a further development that may have rescued pterosaurs from Conan Doyle’s 1912 description before it sprang from its perch:

It was malicious, horrible, with two small red eyes as bright as points of burning coal. Its long, savage mouth, which it held half-open, was full of a double row of sharp-like teeth. Its shoulders were humped, and round them was draped what appeared to be a faded grey shawl. It was the devil of our childhood in person.

Two specimens from the Middle to Upper Jurassic Yanliiao lagerstätte in China show far more (Yang, Z. and 8 others 2018. Pterosaur integumentary structures with complex feather-like branching. Nature Ecology & Evolution, v. 3, p. 24-30; DOI: 10.1038/s41559-018-0728-7). Their pycnofibres show branching tufts, similar to those found in some theropods dinosaurs, including tyrannosaurs. They also resemble mammalian underfur fibres, whose air-trapping properties provide efficient thermal insulation. Both body and wings of these pterosaurs are furry, which the authors suggest may also have helped reduce drag during flight, while those around the mouth may have had a sensory function similar to those carried by some living birds. Moreover, some of the filaments contain black and red pigments.


Artist’s impression of a Jurassic anurognathid pterosaur from China (Credit: Yang et al 2018; Fig. 4)

Pterosaurs may have independently developed fur and feathers; a case of parallel evolution in response to similar evolutionary pressures facing dinosaurs, birds and mammals. Alternatively, they may have had a deep evolutionary origin in the common ancestors of all these animal groups as far back as the Upper Carboniferous and Lower Permian.

Related articles: Nature Editorial 2018. Fur and fossils. Nature, v. 564, p. 301-302; DOI: 10.1038/d41586-018-07800-4; King, A. 2018. Pterosaurs sported feathers, claim scientists (The Scientist); Conniff, R. 2018. Pterosaurs just keep getting weirder (Scientific American); New discovery pushes origin of feathers back by 70 million years (Science Daily)

Oceanic hydrothermal vents and the origin of life

A range of indirect evidence has been used to suggest that life originated deep in the oceans around hydrothermal vents, such as signs of early organic matter in association with Archaean pillow lavas. One particularly persuasive observation is that a number of proteins and other cell chemicals are constructed around metal sulfide groups. Such sulfides are common around hydrothermal ‘smokers’ associated with oceanic rift systems. Moreover, Fischer-Tropsch reactions between carbon monoxide and hydrogen produce quite complex hydrocarbon molecules under laboratory conditions. Such hydrogenation of a carbon-bearing gas requires a catalyst, a commonly used one being chromium oxide (see Abiotic formation of hydrocarbons by oceanic hydrothermal circulation May 2004). It also turns out that fluids emitted by sea-floor hydrothermal systems are sometimes rich in free hydrogen, formed by the breakdown of olivine in ultramafic rocks to form hydroxylated minerals such as serpentine and talc. The fact that chromium is abundant in ultramafic rocks, in the form of its oxide chromite, elevates the possibility that Fischer-Tropsch reactions may have been a crucial part of the life-forming process on the early Earth. What is needed is evidence that such reactions do occur in natural settings.


A white carbonate mound forming at the Lost City hydrothermal vent field on the Mid-Atlantic Ridge (Credit: Baross 2018)

One site on the mid-Atlantic ridge spreading centre, the Lost City vent field, operates because of serpentinisation of peridotites exposed on the ocean floor, to form carbonate-rich plumes and rocky towers; ‘white smokers’. So that is an obvious place to test the abiotic theory for the origin of life. Past analyses of the vents have yielded a whole range of organic molecules, including alkanes, formates, acetates and pyruvates, that are possible precursors for such a natural process. Revisiting Lost City with advanced analytical techniques has taken the quest a major step forward (Ménez, B. et al. 2018. Abiotic synthesis of amino acids in the recesses of the oceanic lithosphere. Nature, advance online publication; DOI: 10.1038/s41586-018-0684-z). The researchers from France and Kazakhstan focused on rock drilled from 170 m below the vent system, probably beyond the influence of surface contamination from living organisms. Using several methods they detected the nitrogen-containing amino acid tryptophan, and that alone. Had they detected other amino acids their exciting result would have been severely tempered by the possibility of surface organic contamination. The formation of tryptophan implies that its abiotic formation had to involve the reduction of elemental nitrogen (N2) to ammonia (NH3). Bénédicte Ménez and colleagues suggest that the iron-rich clay saponite, which is a common product of serpentine alteration at low temperatures, may have catalysed such reduction and amino-acid synthesis through Friedel–Crafts reactions. Fascinating as this discovery may be, it is just a step towards confirming life’s abiogenesis. It also permits speculation that similar evidence may be found elsewhere in the Solar System on rocky bodies, such as the moons Enceladus and Europa that orbit Saturn and Jupiter respectively. That is, if the rock base of hydrothermal systems thought to occur there can be reached.

Related article: Baross, J.A. 2018. The rocky road to biomolecules. Nature, v. 564, p. 42-43; DOI: 10.1038/d41586-018-07262-8.

Neanderthal Mum meets Denisovan Dad

Two bone fragments from the Denisova Cave – the former abode of an 18th century Russian hermit called Denis – in the Altai region of Siberia yielded ancient  DNA. One matches that from previously analysed Neanderthal remains and the other a genome that could only be ascribed to a hitherto unknown ancient-human population, now known as the Denisovans. Since their discovery further analysis of both modern and ancient DNA has shown that modern humans living outside of Africa contain a few percent of DNA from both ancient-human groups. Soon after leaving Africa some of their ancestors interbred with both; indeed a 40 ka-old modern-human jaw from Romania revealed genetic evidence that the individual had a Neanderthal great-great grandparent. Their descendants spread far and wide to populate Eurasia, Australasia and the Americas. Using the ancient DNA to peer back in time suggests that Neanderthals and Denisovans diverged from a common ancestor between 470 and 380 ka, itself having split from modern-human ancestry between 770 to 550 ka. Denisovan DNA also contains evidence that its ancestry included segments that could only have come from a totally unknown hominin species. Interestingly, DNA from the Neanderthal bone fragment found at Denisova contains fragments from an anatomically modern-human.

Tourists at the entrance to Denisova Cave, Rus...

Tourists at the entrance to Denisova Cave, Russia (credit: Wikipedia)

With such riches from tiny fragments of human bones unearthed from the Denisova Cave, it is no surprise that the team led by Svante Pääbo at the Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany, has subsequently analysed others that showed signs of human proteins. The latest ‘takes the biscuit’. A fragment of limb bone from someone who was at least 13 years old yielded DNA commensurate with their having been the child of a Neanderthal mother and a Denisovan father (Slon, V. and 18 others 2018. The genome of the offspring of a Neanderthal mother and a Denisovan father. Nature, v. 560, published on-line; doi: 10.1038/s41586-018-0455-x). Their child was a girl, who has been nicknamed ‘Denny’ by the team, though ‘Denise’ might seem more appropriate. The only clues to what her father, or any Denisovan, might have looked like stem from a few teeth and a skull fragment from the cave that have yielded Denisovan DNA. The teeth are much larger and the skull fragment is thicker than those of Neanderthals, suggesting that Denisovans were distinctly bigger and more robust than even the sturdy Neanderthals.

The father came from a population related to a later Denisovan found in the cave – the first to be sequenced. This suggests long-term occupancy of the area by Denisovans. But his genome also carries traces of Neanderthal ancestry. Surprisingly, the mother is more closely related to Croatian Neanderthals, rather than to an earlier Neanderthal found in the cave. Neanderthals were clearly capable of migrating between Europe and eastern Eurasia; more than 5000 km in this case. Even though very few archaic humans have been genetically sequenced it is beginning to look as if genetic mixing between diverse hominin groups in the last half million years was common, when they actually met. A custom of marrying outside a closely related group (exogamy) has been popular throughout recorded history; indeed it makes sound genetic sense. With the tiny human population density during the Late Pleistocene, it may then have been cause for mutual celebration.  As documented in Chapters 2 and 3 of David Reich’s Who We Are and How We Got Here (Oxford University Press, 2018) human origins since about 470 ka until the present chart a history of episodic migrations and genetic mixing that certainly makes nonsense of earlier ideas of ‘racial purity’ and casts doubt even on the term ‘species’ as regards members of the genus Homo.

If we are ever to discover who the Denisovans were and what they looked like, the evidence is likely to come from East Asia at latitudes where climate favours preservation of DNA. Advanced sequencing equipment and techniques are now operational in China, where suspected Denisovan remains have been found

See also: Warren, M. 2018. First ancient-human hybrid. Nature, v. 560, p. 417-418; doi: 10.1038/d41586-018-06004-0); Sample, I. 2018. Offspring of Neanderthal and Denisovan identified for first time. The Guardian (22 August 2918).

A revised and updated edition of Steve Drury’s book Stepping Stones: The Making of Our Home World can now be downloaded as a free eBook

A hint of life on Mars

We can be certain that life was around on Planet Earth around 3.5 billion years ago, if not before, because unmetamorphosed sedimentary rocks of that age from Western Australia in which stromatolites occur contain a black to brownish, structureless material known as kerogen. The material is a hodgepodge of organic compounds that form during the breakdown of proteins and carbohydrates in living matter. It is the source material for petroleum compounds when kerogen-rich rocks are heated during burial. The vast bulk of organic compounds preserved on Earth are in the form of ancient kerogen, whose mass exceeds that of the living biosphere by about 10 thousand times. A good sign that it does represent ancient life lies in sedimentary kerogen’s depletion in ‘heavy’ 13C compared with 12C (negative values of δ13C), because in metabolising carbon dioxide living cells preferentially use the lighter of these two isotopes. Conceivably, 13C can be removed from inorganic carbon by metamorphic processes, so low values of δ13C in metasediments from West Greenland might be organically derived or, equally, they might not.

At the time of writing, geoscientists specialising in Martian matters had become excited by some results from the geochemical system aboard the surviving functional NASA rover. Curiosity has slowly been making its way up Mount Sharp at the centre of Gale Crater near to Mars’s equator. Analysis of high-resolution images taken from orbit suggest that the rocks forming the mountain are sediments. the lowest and oldest strata are suspected to have been deposited in a crater lake when conditions were warmer and wetter on Mars, about 3 billion years ago. Curiosity was equipped with a drill to penetrate and sample sediment unaffected by ultraviolet radiation that long ago would have destroyed any hydrocarbons exposed at the surface. In late 2016, before the rover had reached the lake sediments, the drill’s controller broke down. Since then, Curiosity had moved on to younger, less promising sediments. More than a year later mission engineers fixed the problem and the rover backtracked to try again. Heating the resulting samples to almost 900°C yields any volatile components as a gas to a mass spectrometer, results from which give clues to the molecules released.

‘Selfie’ of Curiosity rover en route to Mount Sharp. (Credit: NASA)

The Sample Analysis at Mars (SAM) team report a range of thiophenic, aromatic and aliphatic molecules of compounds of carbon, hydrogen and sulfur (Eigenbrode, J.L and 21 others 2018. Organic matter preserved in 3-billion-year-old mudtsones at Gale crater, Mars. Science, v. 360, p. 1096-1101; doi:10.1126/science.aas9185). The blend of pyrolysis products closely resembles those which form from heated terrestrial kerogens and coals, but also from pyrolysis of carbonaceous chondrite meteorites. So, the presence of Martian kerogen is not proven. But the results are so promisingly rich in hydrocarbons that another weapon in SAM’s armoury will be deployed, dissolving organic compounds directly from the drill cuttings. This may provide more convincing evidence of collagen. Yet only when samples are returned to labs on Earth will there be a chance to say one way or the other that there was once life on Mars. The results reported in Science’s 8 June issue will surely add weight to the clamour for the Mars 2020 sample-return mission to be funded. Whether or not there is life on Mars demands a great deal more investment still…

A fully revised edition of Steve Drury’s book Stepping Stones: The Making of Our Home World can now be downloaded as a free eBook

The great Cambrian unconformity

My first field trip from the Geology Department at the University of Birmingham in autumn 1964 was located within hooter distance of the giant British Leyland car plant at Longbridge. It involved a rubbish-filled linear quarry behind a row of shops on the main road through south Birmingham. Not very prepossessing but it clearly exposed a white quartzite, which we were told was a beach deposit laid down by a massive marine transgression at the start of the Cambrian. An hour later we were shown an equally grim exposure of weathered volcanic rocks in the Lickey Hills; they were a sort of purple brown, and said to be Precambrian in age. Not an excellent beginning to a career, but from time to time other Cambrian quartzites sitting unconformably on Precambrian rocks entered our field curriculum: in the West Midlands, Welsh Borders and much further afield in NW Scotland, as it transpired on what had been two separate continental masses of Avalonia and Laurentia. This had possibly been a global marine transgression.

In North America, then the Laurentian continent, what John Wesley Powell dubbed the Great Unconformity in the Grand Canyon has as its counterpart to the Lickey Quartzite the thrillingly named Tonto Group of the Lower Cambrian resting on the Vishnu Schists that are more than a billion years older. Part of the Sauk Sequence, the Tonto Group is, sadly, not accompanied by the Lone Ranger Group, but the Cambrian marine transgression crops out across the continent. In fact it was a phenomenon common to all the modern continents. Global sea level rose relative to the freeboard of the continents then existing. A recent study has established the timing for the Great Unconformity in the Grand Canyon by dating detrital zircons above and below the unconformity (Karlstrom, K, et al. 2018. Cambrian Sauk transgression in the Grand Canyon region redefined by detrital zircons. Nature Geoscience, v. 11, p. 438-443; doi:10.1038/s41561-018-0131-7). Rather than starting at the outset of the Cambria at 542 Ma, the marine transgression was a protracted affair that began around 527 Ma with flooding reaching a maximum at the end of the Cambrian.

Extensive flooding of the continents at the end of the Cambrian (credit: Ron Blakey , Colorado Plateau Geosystems)

It seems most likely that the associated global rise in sea level relative to the continents was a response to the break-up of the Rodinia supercontinent by considerable sea-floor spreading. The young ocean floor, having yet to cool to an equilibrium temperature, would have had reduced density so that the average depth of the ocean basins decreased, thereby flooding the continents. The creation of vast shallow seas across the continents has been suggested to have been a major factor in the explosive evolution of Cambrian shelly faunas, partly by expanding the range of ecological niches and partly due to increased release of calcium ions to to seawater as a result of chemical weathering.

A fully revised edition of Steve Drury’s book Stepping Stones: The Making of Our Home World can now be downloaded as a free eBook

Humans and mass extinction

It is often said that the biosphere is currently undergoing species losses that may rival those of the ‘Big Five’ mass extinction, with the rate of new extinctions being estimated at about 100 times the background rate during geological time. Scientifically, this is probably a dodgy assumption for palaeobiologists simply do not have the evidence to suggest what such a ‘normal’ rate might be. The fossil record is notoriously incomplete for a whole variety of reasons largely to do with both preservation and fossil collection strategies. For instance, as today, some genera may have been very common and widespread in past times, whereas others rare and restricted to small ecological niches. The record of life is prone to huge errors so that only huge, global shifts in diversity, such as mass extinctions, can be viewed with statistical rigour; and then only with caveats. For sure, the rapid demise of species today is cause for alarm and dismay, and more taxa – mainly of smaller and more restricted groups – probably have escaped identification, and will continue to do so. In the context of growing human impacts on ecosystems across the globe extinction is an increasingly emotive topic, as witness the clamour among some geoscientists for adding a new Anthropocene Epoch to the to the Stratigraphic Column. Does that require renaming the Holocene, beginning 11,700 years ago at the end of the last Ice Age, during which agriculture began? Should its start be assigned to some event during recorded history, such as the European invasion of the Americas after 1493, the beginning of the Industrial Revolution or the explosion of the first thermonuclear weapons in the 1940s and 50s? Or did humans begin significantly to affect the biosphere once their spread from Africa started after about 130 ka ago, i.e. in the late Pleistocene? That argument may well run and run: it is foremost a scientific issue, to which rules apply. A cogent example is that of the fate of megafaunas on the major continents except Antarctica as humans migrated far and wide.

The demise of the large flightless birds of Madagascar and New Zealand form a well known case as they almost certainly followed first colonisation by humans around 200 BC and 1300 CE respectively. The megafaunas of the much larger continents of Australia and the Americas have been deemed to have been more than decimated in the same way after about 65 ka and 15 ka respectively. There are no longer giant armadillos and ground sloths in South America, mammoths ceased to roam North America, and giant wombats, marsupial predators and kangaroos only remain as bones, to name but a few. It has been argued that their extinctions stemmed from the first human migrants literally eating their way through vast terrains. Yet the vast herds of Africa seem not to have been affected in the same way, until much more recently as population grew and modern projectile weapons became widely available. That has been suggested to have resulted from co-evolution of humans and megafauna over two million years, together with instinctive caution among large African beasts, whereas the ‘naivety’ of their counterparts in the Americas and Australia doomed them to extinction. Of course, it is likely that things were a great deal more complicated in every case, as argued in a review of Late Pleistocene megafaunal extinctions by Gilbert Price of the University of Queensland, and colleagues from Australia, the US and Denmark (Price, G.J. et al. 2018. Big data little help in megafauna mysteries. Nature, v. 558, p. 23-25;  doi:10.1038/d41586-018-05330-7).

The gist of Price and colleagues’ critique of meta-analyses of data – 32 since 1997 – concerning allegedly human-induced extinctions is that much of the pertinent data is either low quality or poorly understood. For starters, much of the dating is questionable, either using inaccurate and outdated methods or based on inference. For instance, fossils of some alleged victim, e.g.  Australian land crocodiles (Quinkana) and giant wombats (Ramsayia), have never been dated. Moreover, dates of the last known fossils are used when they may have remained extant until more recently: wooly Eurasian mammoths were long supposed not to have survived the last glacial maximum, yet recently mammoth bones from Wrangel island were found to be as young as the second millennium BCE. In 2010 spores of the fungus Sporormiella, in sediment cores, which grows only on digested plant matter in herbivore dung, was used as a proxy for the former presence or absence of large herbivore herds. Its decline in sediments after 13 ka in North America happened to coincide roughly with the start of the North American Clovis hunter culture, which was used to show that extinctions of large herbivores were linked to human predation. Yet such fungi also live on excrement of many animals both large and small, and its preservation is affected by changes in climate and water flow. To properly link declines and extinctions in human prey animals requires concrete evidence of predation, such as cut marks on identifiable bones within middens associated with human habitation, such as hearths.

When emotion, ambition and bandwagon tendencies become associated with science, objectivity sometimes gets compromised.

A fully revised edition of Steve Drury’s book Stepping Stones: The Making of Our Home World can now be downloaded as a free eBook

Mystery of upside-down dinosaurs resolved

Remains of ankylosaurs, a popular family of heavily armoured dinosaurs, occur in sedimentary sequences that range in age from early Jurassic to the close of the Cretaceous. Their defences seem almost impregnable, being constructed of thick, fused scales, often bearing formidable spines, which covered them completely. They bore a crude resemblance to modern armadillos apart from the fact that they were unable to roll-up defensively. In some species the rigid tail bears a large, knob of scale tissue. At up to 3 m long, were the tail to be swung it would have packed bone-cracking momentum. Interestingly, to a poorly sighted predator the club may have been mistaken for the animal’s head at the end of a long neck, so perhaps it lured a potential assailant within range of its devastating power. The largest ankylosaur, from the Cretaceous of western Canada, was the size of a small bus, up to 8m long, 1.5 m wide, standing 1.7 m high and weighing in at around 5 to 8 t. Such dimensions would have made it almost impossible to be bitten, even by the largest predatory dinosaurs, and difficult to turn over. Their teeth show that ankylosaurs were herbivorous, and their somewhat bulbous bodies almost certainly contained a massive digestion system.

Polski: JuraPark Bałtów - Park Dinozaurów - An...

Recfonstruction of Ankylosaurus at the JuraPark Bałtówin Poland (credit: Wikipedia)

The mystery lies in the fact that most ankylosaur fossils are found lying on their backs. Early dinosaur aficionados suggested a tendency for the lumbering beasts to tumble down slopes and become stranded on their backs, so to die miserably. Such clumsiness is hardly a positive characteristic of evolutionary fitness for such a long-lived group, and, besides, the sedimentary formations in which they are found indicate very gentle slopes. So, were they flipped by dextrous predators, as imagined in some early films purporting to look to the distant past? Probably not, for most well preserved fossils show no sign of bites or gnawing. From a study of 36 late-Cretaceous ankylosaurs from Alberta four Canadian and US palaeontologists (Mallon, J.C. et al. 2018. A “bloat-and-float” taphonomic model best explains the upside-down preservation of ankylosaurs. Palaeogeography, Palaeoclimatology, Palaeoecology, v. 497, p. 117-127; doi:10.1016/j.palaeo.2018.02.010 support the idea of their carcases or even living animals having been picked up by flood waters when their high centre of gravity would have flipped them upside down. Bloating through decay might then allow them to be transported large distances. Unsurprisingly, their conclusions rest on model simulations.

When dinosaurs roamed the Western Isles

Cuillin Hills, Isle of Skye, Scotland, UK

Cuillin Hills, Isle of Skye, Scotland, UK (credit: Wikipedia)

The Isle of Skye off the northwest coast of Scotland  is known largely as a prime tourist destination, such as Dunvegan Castle with a real clan chief (The MacLeod of MacLeod) and its Faerie Flag; Britain’s only truly challenging mountains of the Black Cuillin; and, of course, the romantic connection with the Young Pretender, Charles Edward Stuart and his escape, in drag, from the clutches of the Duke ‘Butcher’ Cumberland, hence the Skye Boat Song. Geologists know it best for its flood basalts with classic stepped topography and the exhumed guts of a massive central volcano (the Cuillin), relics of the Palaeocene-Eocene (62 to 54 Ma) North Atlantic Large Igneous Province. The spectacular Loch Coruisk, a glacial corrie drowned by the sea, exposes the deepest part of the main magma chamber. It is also the lair of Scotland’s lesser known Monster, the dread Each Uisge (Water Horse). Yet evidence is emerging for the former presence in the Hebrides of other, more tangible monsters.

Skye’s great volcanic edifice rests on Mesozoic sedimentary rocks including shallow-water muddy limestones of the Great Estuarine Group of Middle Jurassic (Bathonian, 174–164 Ma) age. For dinosaur specialists this is of the time when meat-eating theropods and herbivorous sauropods began growing to colossal sizes. Yet the Bathonian is notable for its global paucity in well exposed terrestrial and near-shore sedimentary sequences. Easily accessible, the Skye Bathonian sequence is much visited and has yielded a rich, though generally fragmentary fauna. A group of recent visiting palaeontologists from the University of Edinburgh, the Chinese Academy of Sciences and Skye’s Staffin Museum have discovered an extensive tract of wave-cut platform on the east shore of the Trotternish Peninsula where lagoonal carbonate muds were trampled by several dinosaurs that left around 50 tracks (dePolo, P.E. et al. 2018. A sauropod-dominated tracksite from Rubha nam Brathairean (Brothers’ Point), Isle of Skye, Scotland. Scottish Journal of Geology, online; doi:10.1144/sjg2017-016).

Dinosaur foot prints from Skye. Left example of a sauropod rear-foot print; right theropod. (credit dePolo, P.E. et al. 2018, modified from Figs 8 and 9a)

Some are of medium-sized sauropods (either Parabrontopodus or Breviparopus – both names for footprints rather than any genus of dinosaur) whose crudely elephant-like footprints are up to 0.5 m across (the largest, from Western Australia, are about 1.7 m across). Although there are fragmentary dinosaur bones from the same strata, assigning the footprint to a known species is not possible. However, foot size can be used to estimate how high the creatures’ hips stood (2 to 2.5 m): hefty beasts but not the true giants of later times A variety of three-toed, clawed, somewhat bird-like, footprints also occur. They are assigned to probably bipedal carnivores or theropods. Variation in foot size suggests a range of hip-height from about 0.9 to 2 metres, so these carnivores would have been pretty formidable.

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