Plot of extinction intensity (percentage of marine genera that are present in each interval of time but do not exist in the following interval) vs time in the past.
Geological periods are annotated (by abbreviation and colour) above.
The Permian–Triassic extinction event is the most significant event for
marine genera, with just over 50% (according to this source) perishing.
There is evidence for one to three distinct pulses, or phases, of extinction. Suggested mechanisms for the latter include one or more large meteor impact events, massive volcanism such as that of the Siberian Traps, and the ensuing coal or gas fires and explosions, and a runaway greenhouse effect triggered by sudden release of methane from the sea floor due to methane clathrate dissociation according to the clathrate gun hypothesis or methane-producing microbes known as methanogens. Possible contributing gradual changes include sea-level change, increasing anoxia, increasing aridity, and a shift in ocean circulation driven by climate change.
Dating the extinction
Permian–Triassic extinction
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Until 2000, it was thought that rock sequences spanning the
Permian–Triassic boundary were too few and contained too many gaps for
scientists to reliably determine its details. However, it is now possible to date the extinction with millennial precision. U–Pb zircon dates from five volcanic ash beds from the Global Stratotype Section and Point for the Permian–Triassic boundary at Meishan, China,
establish a high-resolution age model for the extinction – allowing
exploration of the links between global environmental perturbation, carbon cycle
disruption, mass extinction, and recovery at millennial timescales. The
extinction occurred between 251.941 ± 0.037 and 251.880 ± 0.031 Ma ago,
a duration of 60 ± 48 ka. A large (approximately 0.9%), abrupt global decrease in the ratio of the stable isotope 13C to that of 12C, coincides with this extinction, and is sometimes used to identify the Permian–Triassic boundary in rocks that are unsuitable for radiometric dating. Further evidence for environmental change around the P–Tr boundary suggests an 8 °C (14 °F) rise in temperature, and an increase in CO
2 levels by 2000 ppm (for comparison, the concentration immediately before the industrial revolution was 280 ppm, and the amount today is about 410 ppm). There is also evidence of increased ultraviolet radiation reaching the earth, causing the mutation of plant spores.
2 levels by 2000 ppm (for comparison, the concentration immediately before the industrial revolution was 280 ppm, and the amount today is about 410 ppm). There is also evidence of increased ultraviolet radiation reaching the earth, causing the mutation of plant spores.
It has been suggested that the Permian–Triassic boundary is
associated with a sharp increase in the abundance of marine and
terrestrial fungi, caused by the sharp increase in the amount of dead plants and animals fed upon by the fungi. For a while this "fungal spike" was used by some paleontologists to identify the Permian–Triassic boundary in rocks that are unsuitable for radiometric dating or lack suitable index fossils,
but even the proposers of the fungal spike hypothesis pointed out that
"fungal spikes" may have been a repeating phenomenon created by the
post-extinction ecosystem in the earliest Triassic. The very idea of a fungal spike has been criticized on several grounds, including: Reduviasporonites, the most common supposed fungal spore, may be a fossilized alga; the spike did not appear worldwide; and in many places it did not fall on the Permian–Triassic boundary.
The reduviasporonites may even represent a transition to a
lake-dominated Triassic world rather than an earliest Triassic zone of
death and decay in some terrestrial fossil beds. Newer chemical evidence agrees better with a fungal origin for Reduviasporonites, diluting these critiques.
Uncertainty exists regarding the duration of the overall
extinction and about the timing and duration of various groups'
extinctions within the greater process. Some evidence suggests that
there were multiple extinction pulses or that the extinction was spread out over a few million years, with a sharp peak in the last million years of the Permian. Statistical analyses of some highly fossiliferous strata in Meishan, Zhejiang Province in southeastern China, suggest that the main extinction was clustered around one peak.
Recent research shows that different groups became extinct at different
times; for example, while difficult to date absolutely, ostracod and brachiopod extinctions were separated by 670,000 to 1.17 million years. In a well-preserved sequence in east Greenland,
the decline of animals is concentrated in a period 10,000 to 60,000
years long, with plants taking an additional several hundred thousand
years to show the full impact of the event. An older theory, still supported in some recent papers,
is that there were two major extinction pulses 9.4 million years apart,
separated by a period of extinctions well above the background level,
and that the final extinction killed off only about 80% of marine
species alive at that time while the other losses occurred during the
first pulse or the interval between pulses. According to this theory one
of these extinction pulses occurred at the end of the Guadalupian epoch of the Permian.
For example, all but one of the surviving dinocephalian genera died out at the end of the Guadalupian, as did the Verbeekinidae, a family of large-size fusuline foraminifera.
The impact of the end-Guadalupian extinction on marine organisms appears to have varied between locations and between taxonomic groups — brachiopods and corals had severe losses.
Extinction patterns
| Marine extinctions | Genera extinct | Notes | ||
|---|---|---|---|---|
| Arthropoda | ||||
| Eurypterids | 100% | May have become extinct shortly before the P–Tr boundary | ||
| Ostracods | 59% | |||
| Trilobites | 100% | In decline since the Devonian; only 2 genera living before the extinction | ||
| Brachiopoda | ||||
| Brachiopods | 96% | Orthids and productids died out | ||
| Bryozoa | ||||
| Bryozoans | 79% | Fenestrates, trepostomes, and cryptostomes died out | ||
| Chordata | ||||
| Acanthodians | 100% | In decline since the Devonian, with only one living family | ||
| Cnidaria | ||||
| Anthozoans | 96% | Tabulate and rugose corals died out | ||
| Echinodermata | ||||
| Blastoids | 100% | May have become extinct shortly before the P–Tr boundary | ||
| Crinoids | 98% | Inadunates and camerates died out | ||
| Mollusca | ||||
| Ammonites | 97% | |||
| Bivalves | 59% | |||
| Gastropods | 98% | |||
| Retaria | ||||
| Foraminiferans | 97% | Fusulinids died out, but were almost extinct before the catastrophe | ||
| Radiolarians | 99% |
| ||
Marine organisms
Marine invertebrates
suffered the greatest losses during the P–Tr extinction. Evidence of
this was found in samples from south China sections at the P–Tr
boundary. Here, 286 out of 329 marine invertebrate genera disappear
within the final two sedimentary zones containing conodonts from the Permian. The decrease in diversity was probably caused by a sharp increase in extinctions, rather than a decrease in speciation.
The extinction primarily affected organisms with calcium carbonate skeletons, especially those reliant on stable CO2 levels to produce their skeletons. These organisms were susceptible to the effects of the ocean acidification that resulted from increased atmospheric CO2.
Among benthic organisms the extinction event multiplied background extinction rates, and therefore caused maximum species loss to taxa that had a high background extinction rate (by implication, taxa with a high turnover). The extinction rate of marine organisms was catastrophic.
Surviving marine invertebrate groups include: articulate brachiopods (those with a hinge), which have undergone a slow decline in numbers since the P–Tr extinction; the Ceratitida order of ammonites; and crinoids ("sea lilies"), which very nearly became extinct but later became abundant and diverse.
The groups with the highest survival rates generally had active control of circulation,
elaborate gas exchange mechanisms, and light calcification; more
heavily calcified organisms with simpler breathing apparatuses suffered
the greatest loss of species diversity. In the case of the brachiopods, at least, surviving taxa were generally small, rare members of a formerly diverse community.
The ammonoids, which had been in a long-term decline for the 30 million years since the Roadian (middle Permian), suffered a selective extinction pulse 10 million years before the main event, at the end of the Capitanian stage. In this preliminary extinction, which greatly reduced disparity,
or the range of different ecological guilds, environmental factors
were apparently responsible. Diversity and disparity fell further until
the P–Tr boundary; the extinction here (P–Tr) was non-selective,
consistent with a catastrophic initiator. During the Triassic, diversity
rose rapidly, but disparity remained low.
The range of morphospace occupied by the ammonoids, that is,
their range of possible forms, shapes or structures, became more
restricted as the Permian progressed. A few million years into the
Triassic, the original range of ammonoid structures was once again
reoccupied, but the parameters were now shared differently among clades.
Terrestrial invertebrates
The
Permian had great diversity in insect and other invertebrate species,
including the largest insects ever to have existed. The end-Permian is
the largest known mass extinction of insects; according to some sources, it is the only insect mass extinction. Eight or nine insect orders became extinct and ten more were greatly reduced in diversity. Palaeodictyopteroids
(insects with piercing and sucking mouthparts) began to decline during
the mid-Permian; these extinctions have been linked to a change in
flora. The greatest decline occurred in the Late Permian and was
probably not directly caused by weather-related floral transitions.
Most fossil insect groups found after the Permian–Triassic
boundary differ significantly from those before: Of Paleozoic insect
groups, only the Glosselytrodea, Miomoptera, and Protorthoptera have been discovered in deposits from after the extinction. The caloneurodeans, monurans, paleodictyopteroids, protelytropterans, and protodonates
became extinct by the end of the Permian. In well-documented Late
Triassic deposits, fossils overwhelmingly consist of modern fossil
insect groups.
Terrestrial plants
Plant ecosystem response
The geological record of terrestrial plants is sparse and based mostly on pollen and spore
studies. Plants are relatively immune to mass extinction, with the
impact of all the major mass extinctions "insignificant" at a family
level. Even the reduction observed in species diversity (of 50%) may be mostly due to taphonomic processes.
However, a massive rearrangement of ecosystems does occur, with plant
abundances and distributions changing profoundly and all the forests
virtually disappearing; the Palaeozoic flora scarcely survived this extinction.
At the P–Tr boundary, the dominant floral groups changed, with many groups of land plants entering abrupt decline, such as Cordaites (gymnosperms) and Glossopteris (seed ferns). Dominant gymnosperm genera were replaced post-boundary by lycophytes—extant lycophytes are recolonizers of disturbed areas.
Palynological or pollen studies from East Greenland of sedimentary rock strata laid down during the extinction period indicate dense gymnosperm woodlands before the event. At the same time that marine invertebrate macrofauna declined, these large woodlands died out and were followed by a rise in diversity of smaller herbaceous plants including Lycopodiophyta, both Selaginellales and Isoetales. Later, other groups of gymnosperms
again become dominant but again suffered major die offs. These cyclical
flora shifts occurred a few times over the course of the extinction
period and afterwards. These fluctuations of the dominant flora between
woody and herbaceous
taxa indicate chronic environmental stress resulting in a loss of most
large woodland plant species. The successions and extinctions of plant
communities do not coincide with the shift in δ13C values, but occurred many years after. The recovery of gymnosperm forests took 4–5 million years.
Coal gap
No coal deposits are known from the Early Triassic, and those in the Middle Triassic are thin and low-grade.
This "coal gap" has been explained in many ways. It has been suggested
that new, more aggressive fungi, insects and vertebrates evolved, and
killed vast numbers of trees. These decomposers themselves suffered heavy losses of species during the extinction, and are not considered a likely cause of the coal gap.
It could simply be that all coal-forming plants were rendered extinct
by the P–Tr extinction, and that it took 10 million years for a new
suite of plants to adapt to the moist, acid conditions of peat bogs. Abiotic factors (factors not caused by organisms), such as decreased rainfall or increased input of clastic sediments, may also be to blame.
On the other hand, the lack of coal may simply reflect the scarcity of all known sediments from the Early Triassic. Coal-producing ecosystems, rather than disappearing, may have moved to areas where we have no sedimentary record for the Early Triassic. For example, in eastern Australia a cold climate had been the norm for a long period, with a peat mire ecosystem adapted to these conditions. Approximately 95% of these peat-producing plants went locally extinct at the P–Tr boundary; Coal deposits in Australia and Antarctica disappear significantly before the P–Tr boundary.
Terrestrial vertebrates
There is enough evidence to indicate that over two-thirds of terrestrial labyrinthodont amphibians, sauropsid ("reptile") and therapsid ("proto-mammal") families became extinct. Large herbivores suffered the heaviest losses.
All Permian anapsid reptiles died out except the procolophonids (although testudines have morphologically anapsid skulls, they are now thought to have separately evolved from diapsid ancestors). Pelycosaurs
died out before the end of the Permian. Too few Permian diapsid fossils
have been found to support any conclusion about the effect of the
Permian extinction on diapsids (the "reptile" group from which lizards, snakes, crocodilians, and dinosaurs (including birds) evolved).
The groups that survived suffered extremely heavy losses of
species, and some terrestrial vertebrate groups very nearly became
extinct at the end-Permian. Some of the surviving groups did not persist
for long past this period, while others that barely survived went on to
produce diverse and long-lasting lineages. Yet it took 30 million years for the terrestrial vertebrate fauna to fully recover both numerically and ecologically.
Possible explanations of these patterns
An analysis of marine fossils from the Permian's final Changhsingian stage found that marine organisms with low tolerance for hypercapnia (high concentration of carbon dioxide) had high extinction rates, while the most tolerant organisms had very slight losses.
The most vulnerable marine organisms were those that produced calcareous hard parts (i.e., from calcium carbonate) and had low metabolic rates and weak respiratory systems—notably calcareous sponges, rugose and tabulate corals, calcite-depositing brachiopods, bryozoans, and echinoderms; about 81% of such genera became extinct. Close relatives without calcareous hard parts suffered only minor losses, for example sea anemones,
from which modern corals evolved. Animals with high metabolic rates,
well-developed respiratory systems, and non-calcareous hard parts had
negligible losses—except for conodonts, in which 33% of genera died out.
This pattern is consistent with what is known about the effects of hypoxia, a shortage but not a total absence of oxygen. However, hypoxia cannot have been the only killing mechanism for marine organisms. Nearly all of the continental shelf waters would have had to become severely hypoxic
to account for the magnitude of the extinction, but such a catastrophe
would make it difficult to explain the very selective pattern of the
extinction. Models
of the Late Permian and Early Triassic atmospheres show a significant
but protracted decline in atmospheric oxygen levels, with no
acceleration near the P–Tr boundary. Minimum atmospheric oxygen levels
in the Early Triassic are never less than present day levels—the decline
in oxygen levels does not match the temporal pattern of the extinction.
Marine organisms are more sensitive to changes in CO
2 (carbon dioxide) levels than are terrestrial organisms for a variety of reasons. CO
2 is 28 times more soluble in water than is oxygen. Marine animals normally function with lower concentrations of CO
2 in their bodies than land animals, as the removal of CO
2 in air-breathing animals is impeded by the need for the gas to pass through the respiratory system's membranes (lungs' alveolus, tracheae, and the like), even when CO
2 diffuses more easily than oxygen. In marine organisms, relatively modest but sustained increases in CO
2 concentrations hamper the synthesis of proteins, reduce fertilization rates, and produce deformities in calcareous hard parts. In addition, an increase in CO
2 concentration is inevitably linked to ocean acidification, consistent with the preferential extinction of heavily calcified taxa and other signals in the rock record that suggest a more acidic ocean. The decrease in ocean pH is calculated to be up to 0.7 units.
2 (carbon dioxide) levels than are terrestrial organisms for a variety of reasons. CO
2 is 28 times more soluble in water than is oxygen. Marine animals normally function with lower concentrations of CO
2 in their bodies than land animals, as the removal of CO
2 in air-breathing animals is impeded by the need for the gas to pass through the respiratory system's membranes (lungs' alveolus, tracheae, and the like), even when CO
2 diffuses more easily than oxygen. In marine organisms, relatively modest but sustained increases in CO
2 concentrations hamper the synthesis of proteins, reduce fertilization rates, and produce deformities in calcareous hard parts. In addition, an increase in CO
2 concentration is inevitably linked to ocean acidification, consistent with the preferential extinction of heavily calcified taxa and other signals in the rock record that suggest a more acidic ocean. The decrease in ocean pH is calculated to be up to 0.7 units.
It is difficult to analyze extinction and survival rates of land
organisms in detail, because few terrestrial fossil beds span the
Permian–Triassic boundary. Triassic insects are very different from
those of the Permian, but a gap in the insect fossil record spans
approximately 15 million years from the late Permian to early Triassic.
The best-known record of vertebrate changes across the Permian–Triassic boundary occurs in the Karoo Supergroup of South Africa, but statistical analyses have so far not produced clear conclusions. However, analysis of the fossil river deposits of the floodplains indicate a shift from meandering to braided river patterns, indicating an abrupt drying of the climate. The climate change may have taken as little as 100,000 years, prompting the extinction of the unique Glossopteris flora and its herbivores, followed by the carnivorous guild. End-Permian extinctions did not occur at an instantaneous time horizon; particularly, floral extinction was delayed in time.
Biotic recovery
Earlier
analyses indicated that life on Earth recovered quickly after the
Permian extinctions, but this was mostly in the form of disaster taxa, opportunist organisms such as the hardy Lystrosaurus.
Research published in 2006 indicates that the specialized animals that
formed complex ecosystems, with high biodiversity, complex food webs and a variety of niches,
took much longer to recover. It is thought that this long recovery was
due to the successive waves of extinction, which inhibited recovery, and
prolonged environmental stress to organisms, which continued into the
Early Triassic. Research indicates that recovery did not begin until the
start of the mid-Triassic, 4 to 6 million years after the extinction; and some writers estimate that the recovery was not complete until 30 Ma after the P–Tr extinction, i.e. in the late Triassic.
A study published in the journal Science
found that during the Great Extinction, ocean surface temperatures
reached 40 °C (104 °F) in some places. This explains why recovery took
so long: it was too hot for life to survive. Anoxic waters may have also delayed the recovery.
A braided river, the Waimakariri River on the South Island of New Zealand
During the early Triassic (4 to 6 million years after the P–Tr extinction), the plant biomass was insufficient to form coal deposits, which implies a limited food mass for herbivores. River patterns in the Karoo changed from meandering to braided, indicating that vegetation there was very sparse for a long time.
Each major segment of the early Triassic ecosystem—plant and animal, marine and terrestrial—was dominated by a small number of genera, which appeared virtually worldwide, for example: the herbivorous therapsid Lystrosaurus (which accounted for about 90% of early Triassic land vertebrates) and the bivalves Claraia, Eumorphotis, Unionites and Promylina. A healthy ecosystem has a much larger number of genera, each living in a few preferred types of habitat.
Disaster taxa took advantage of the devastated ecosystems and enjoyed a temporary population boom and increase in their territory. Microconchids are the dominant component of otherwise impoverished Early Triassic encrusting assemblages. For example: Lingula (a brachiopod); stromatolites, which had been confined to marginal environments since the Ordovician; Pleuromeia (a small, weedy plant); Dicroidium (a seed fern).
Changes in marine ecosystems
Sessile filter feeders like this Carboniferous crinoid, the mushroom crinoid (Agaricocrinus americanus), were significantly less abundant after the P–Tr extinction.
Prior to the extinction, about two-thirds of marine animals were sessile
and attached to the sea floor. During the Mesozoic, only about half of
the marine animals were sessile while the rest were free-living.
Analysis of marine fossils from the period indicated a decrease in the
abundance of sessile epifaunal suspension feeders such as brachiopods and sea lilies and an increase in more complex mobile species such as snails, sea urchins and crabs.
Before the Permian mass extinction event, both complex and simple
marine ecosystems were equally common; after the recovery from the mass
extinction, the complex communities outnumbered the simple communities
by nearly three to one, and the increase in predation pressure led to the Mesozoic Marine Revolution.
Bivalves were fairly rare before the P–Tr extinction but became numerous and diverse in the Triassic, and one group, the rudist clams, became the Mesozoic's
main reef-builders. Some researchers think much of this change happened
in the 5 million years between the two major extinction pulses.
Crinoids ("sea lilies") suffered a selective extinction, resulting in a decrease in the variety of their forms. Their ensuing adaptive radiation was brisk, and resulted in forms possessing flexible arms becoming widespread; motility, predominantly a response to predation pressure, also became far more prevalent.
Land vertebrates
Lystrosaurus was by far the most abundant early Triassic land vertebrate.
Lystrosaurus, a pig-sized herbivorous dicynodont therapsid, constituted as much as 90% of some earliest Triassic land vertebrate fauna. Smaller carnivorous cynodont therapsids also survived, including the ancestors of mammals. In the Karoo region of southern Africa, the therocephalians Tetracynodon, Moschorhinus and Ictidosuchoides survived, but do not appear to have been abundant in the Triassic.
Archosaurs (which included the ancestors of dinosaurs and crocodilians) were initially rarer than therapsids, but they began to displace therapsids in the mid-Triassic. In the mid to late Triassic, the dinosaurs evolved from one group of archosaurs, and went on to dominate terrestrial ecosystems during the Jurassic and Cretaceous. This "Triassic Takeover" may have contributed to the evolution of mammals by forcing the surviving therapsids and their mammaliform successors to live as small, mainly nocturnal insectivores; nocturnal life probably forced at least the mammaliforms to develop fur and higher metabolic rates, while losing part of the differential color-sensitive retinal receptors reptilians and birds preserved.
Some temnospondyl amphibians made a relatively quick recovery, in spite of nearly becoming extinct. Mastodonsaurus and trematosaurians were the main aquatic and semiaquatic predators during most of the Triassic, some preying on tetrapods and others on fish.
Land vertebrates took an unusually long time to recover from the P–Tr extinction; Palaeontologist Michael Benton estimated the recovery was not complete until 30 million years after the extinction, i.e. not until the Late Triassic, in which dinosaurs, pterosaurs, crocodiles, archosaurs, amphibians, and mammaliforms were abundant and diverse.
Theories about cause
Pinpointing
the exact cause or causes of the Permian–Triassic extinction event is
difficult, mostly because the catastrophe occurred over 250 million
years ago, and since then much of the evidence that would have pointed
to the cause has been destroyed or is concealed deep within the Earth
under many layers of rock. The sea floor is also completely recycled every 200 million years by the ongoing process of plate tectonics and seafloor spreading, leaving no useful indications beneath the ocean.
Scientists have accumulated a fairly significant amount of
evidence for causes, and several mechanisms have been proposed for the
extinction event. The proposals include both catastrophic and gradual
processes (similar to those theorized for the Cretaceous–Paleogene extinction event).
- The catastrophic group includes one or more large bolide impact events, increased volcanism, and sudden release of methane from the sea floor, either due to dissociation of methane hydrate deposits or metabolism of organic carbon deposits by methanogenic microbes.
- The gradual group includes sea level change, increasing anoxia, and increasing aridity.
Any hypothesis about the cause must explain the selectivity of the event, which affected organisms with calcium carbonate
skeletons most severely; the long period (4 to 6 million years) before
recovery started, and the minimal extent of biological mineralization
(despite inorganic carbonates being deposited) once the recovery began.
Impact event
Artist's impression of a major impact event: A collision between Earth and an asteroid a few kilometres in diameter would release as much energy as several million nuclear weapons detonating.
Evidence that an impact event may have caused the Cretaceous–Paleogene extinction event
(Cretaceous–Tertiary) has led to speculation that similar impacts may
have been the cause of other extinction events, including the P–Tr
extinction, and thus to a search for evidence of impacts at the times of
other extinctions and for large impact craters of the appropriate age.
Reported evidence for an impact event from the P–Tr boundary level includes rare grains of shocked quartz in Australia and Antarctica; fullerenes trapping extraterrestrial noble gases; meteorite fragments in Antarctica; and grains rich in iron, nickel and silicon, which may have been created by an impact. However, the accuracy of most of these claims has been challenged. For example, quartz from Graphite Peak
in Antarctica, once considered "shocked", has been re-examined by
optical and transmission electron microscopy. The observed features were
concluded to be due not to shock, but rather to plastic deformation, consistent with formation in a tectonic environment such as volcanism.
An impact crater on the sea floor would be evidence of a possible
cause of the P–Tr extinction, but such a crater would by now have
disappeared. As 70% of the Earth's surface is currently sea, an asteroid or comet
fragment is now perhaps more than twice as likely to hit ocean as it is
to hit land. However, Earth's oldest ocean-floor crust is 200 million
years old because it is continually destroyed and renewed by spreading
and subduction. Thus, craters produced by very large impacts may be masked by extensive flood basalting from below after the crust is punctured or weakened.
Yet, subduction should not be entirely accepted as an explanation of
why no firm evidence can be found: as with the K-T event, an ejecta
blanket stratum rich in siderophilic elements (such as iridium) would be expected to be seen in formations from the time.
A large impact might have triggered other mechanisms of extinction described below, such as the Siberian Traps eruptions at either an impact site or the antipode of an impact site. The abruptness of an impact also explains why more species did not rapidly evolve to survive, as would be expected if the Permian-Triassic event had been slower and less global than a meteorite impact.
Possible impact sites
Several
possible impact craters have been proposed as the site of an impact
causing the P–Tr extinction, including the 250 km (160 mi) Bedout structure off the northwest coast of Australia and the hypothesized 480 km (300 mi) Wilkes Land crater of East Antarctica.
In each case, the idea that an impact was responsible has not been
proven and has been widely criticized. In the case of Wilkes Land, the
age of this sub-ice geophysical feature is very uncertain – it may be
later than the Permian–Triassic extinction.
The 40 km (25 mi) Araguainha crater
in Brazil has been most recently dated to 254.7 ± 2.5 million years
ago, overlapping with estimates for the Permo-Triassic boundary. Much of the local rock was oil shale.
The estimated energy released by the Araguainha impact is insufficient
to be a direct cause of the global mass extinction, but the colossal
local earth tremors would have released huge amounts of oil and gas from
the shattered rock. The resulting sudden global warming might have precipitated the Permian–Triassic extinction event.
In May 1992, Michael R. Rampino published an abstract for the American Geophysical Union noting the discovery of a circular gravity anomaly near the Falkland Islands. He suggested this structure might correspond to an impact crater with a diameter of 250 km (160 mi). In August 2017, Rampino, Maximilliano Rocca and Jaime Baez Presser followed up with a paper
providing further seismic and magnetic evidence that the structure is
an impact crater. Estimates for the age of the structure range up to 250
millions years old. If, in fact, this is an impact crater, it would be
substantially larger than the well-known 180 km (110 mi) Chicxulub impact crater
associated with a later extinction event. However, Dave McCarthy and
colleagues from the British Geological Survey not only illustrated that
the gravity anomaly is not circular, but that the seismic data presented
by Rocca, Rampino and Baez Presser did not cross the proposed crater,
nor did it provide any evidence for an impact crater.
Volcanism
The final stages of the Permian had two flood basalt events. A small one, the Emeishan Traps in China, occurred at the same time as the end-Guadalupian extinction pulse, in an area close to the equator at the time. The flood basalt eruptions that produced the Siberian Traps
constituted one of the largest known volcanic events on Earth and
covered over 2,000,000 square kilometres (770,000 sq mi) with lava. The date of the Siberian Traps eruptions and the extinction event are in good agreement.
The Emeishan and Siberian Traps eruptions may have caused dust clouds and acid aerosols, which would have blocked out sunlight and thus disrupted photosynthesis both on land and in the photic zone
of the ocean, causing food chains to collapse. The eruptions may also
have caused acid rain when the aerosols washed out of the atmosphere.
That may have killed land plants and molluscs and planktonic organisms which had calcium carbonate shells. The eruptions would also have emitted carbon dioxide, causing global warming.
When all of the dust clouds and aerosols washed out of the atmosphere,
the excess carbon dioxide would have remained and the warming would have
proceeded without any mitigating effects.
The Siberian Traps had unusual features that made them even more
dangerous. Pure flood basalts produce fluid, low-viscosity lava and do
not hurl debris into the atmosphere. It appears, however, that 20% of
the output of the Siberian Traps eruptions was pyroclastic (consisted of ash and other debris thrown high into the atmosphere), increasing the short-term cooling effect. The basalt lava erupted or intruded into carbonate
rocks and into sediments that were in the process of forming large coal
beds, both of which would have emitted large amounts of carbon dioxide,
leading to stronger global warming after the dust and aerosols settled.
In January 2011, a team, led by Stephen Grasby of the Geological
Survey of Canada—Calgary, reported evidence that volcanism caused
massive coal beds to ignite, possibly releasing more than 3 trillion
tons of carbon. The team found ash deposits in deep rock layers near
what is now Buchanan Lake.
According to their article, "coal ash dispersed by the explosive
Siberian Trap eruption would be expected to have an associated release
of toxic elements in impacted water bodies where fly ash slurries
developed.... Mafic megascale eruptions are long-lived events that would
allow significant build-up of global ash clouds."
In a statement, Grasby said, "In addition to these volcanoes causing
fires through coal, the ash it spewed was highly toxic and was released
in the land and water, potentially contributing to the worst extinction
event in earth history." In 2013, a team led by Q.Y. Yang reported the total amounts of important volatiles emitted from the Siberian Traps are 8.5 × 107 Tg CO2, 4.4 × 106 Tg CO, 7.0 × 106 Tg H2S and 6.8 × 107 Tg SO2,
the data support a popular notion that the end-Permian mass extinction
on the Earth was caused by the emission of enormous amounts of volatiles
from the Siberian Traps into the atmosphere.
In 2015, evidence and a timeline indicated the extinction was caused by events in the Large igneous province of the Siberian Traps.
Methane hydrate gasification
Scientists have found worldwide evidence of a swift decrease of about 1% in the 13C/12C isotope ratio in carbonate rocks from the end-Permian. This is the first, largest, and most rapid of a series of negative and positive excursions (decreases and increases in 13C/12C ratio) that continues until the isotope ratio
abruptly stabilised in the middle Triassic, followed soon afterwards by
the recovery of calcifying life forms (organisms that use calcium carbonate to build hard parts such as shells).
A variety of factors may have contributed to this drop in the 13C/12C ratio, but most turn out to be insufficient to account fully for the observed amount:
- Gases from volcanic eruptions have a 13C/12C ratio about 0.5 to 0.8% below standard (δ13C about −0.5 to −0.8%), but an assessment made in 1995 concluded that the amount required to produce a reduction of about 1.0% worldwide requires eruptions greater by orders of magnitude than any for which evidence has been found. (However, this analysis addressed only CO2 produced by the magma itself, not from interactions with carbon bearing sediments, as later proposed.)
- A reduction in organic activity would extract 12C more slowly from the environment and leave more of it to be incorporated into sediments, thus reducing the 13C/12C ratio. Biochemical processes preferentially use the lighter isotopes since chemical reactions are ultimately driven by electromagnetic forces between atoms and lighter isotopes respond more quickly to these forces, but a study of a smaller drop of 0.3 to 0.4% in 13C/12C (δ13C −3 to −4 ‰) at the Paleocene-Eocene Thermal Maximum (PETM) concluded that even transferring all the organic carbon (in organisms, soils, and dissolved in the ocean) into sediments would be insufficient: even such a large burial of material rich in 12C would not have produced the 'smaller' drop in the 13C/12C ratio of the rocks around the PETM.
- Buried sedimentary organic matter has a 13C/12C ratio 2.0 to 2.5% below normal (δ13C −2.0 to −2.5%). Theoretically, if the sea level fell sharply, shallow marine sediments would be exposed to oxidization. But 6500–8400 gigatons (1 gigaton = 109 metric tons) of organic carbon would have to be oxidized and returned to the ocean-atmosphere system within less than a few hundred thousand years to reduce the 13C/12C ratio by 1.0%, which is not thought to be a realistic possibility. Moreover, sea levels were rising rather than falling at the time of the extinction.
- Rather than a sudden decline in sea level, intermittent periods of ocean-bottom hyperoxia and anoxia (high-oxygen and low- or zero-oxygen conditions) may have caused the 13C/12C ratio fluctuations in the Early Triassic; and global anoxia may have been responsible for the end-Permian blip. The continents of the end-Permian and early Triassic were more clustered in the tropics than they are now, and large tropical rivers would have dumped sediment into smaller, partially enclosed ocean basins at low latitudes. Such conditions favor oxic and anoxic episodes; oxic/anoxic conditions would result in a rapid release/burial, respectively, of large amounts of organic carbon, which has a low 13C/12C ratio because biochemical processes use the lighter isotopes more. That or another organic-based reason may have been responsible for both that and a late Proterozoic/Cambrian pattern of fluctuating 13C/12C ratios.
Other hypotheses include mass oceanic poisoning releasing vast amounts of CO
2 and a long-term reorganisation of the global carbon cycle.
2 and a long-term reorganisation of the global carbon cycle.
Prior to consideration of the inclusion of roasting carbonate
sediments by volcanism, the only proposed mechanism sufficient to cause a
global 1% reduction in the 13C/12C ratio was the release of methane from methane clathrates. Carbon-cycle models confirm that it would have had enough effect to produce the observed reduction. Methane clathrates, also known as methane hydrates, consist of methane molecules trapped in cages of water molecules. The methane, produced by methanogens (microscopic single-celled organisms), has a 13C/12C ratio about 6.0% below normal (δ13C −6.0%). At the right combination of pressure and temperature, it gets trapped in clathrates fairly close to the surface of permafrost and in much larger quantities at continental margins (continental shelves
and the deeper seabed close to them). Oceanic methane hydrates are
usually found buried in sediments where the seawater is at least 300 m
(980 ft) deep. They can be found up to about 2,000 m (6,600 ft) below
the sea floor, but usually only about 1,100 m (3,600 ft) below the sea
floor.
The area covered by lava from the Siberian Traps eruptions is
about twice as large as was originally thought, and most of the
additional area was shallow sea at the time. The seabed probably
contained methane hydrate deposits, and the lava caused the deposits to dissociate, releasing vast quantities of methane.
A vast release of methane might cause significant global warming since methane is a very powerful greenhouse gas.
Strong evidence suggests the global temperatures increased by about
6 °C (10.8 °F) near the equator and therefore by more at higher
latitudes: a sharp decrease in oxygen isotope ratios (18O/16O); the extinction of Glossopteris flora (Glossopteris and plants that grew in the same areas), which needed a cold climate, with its replacement by floras typical of lower paleolatitudes.
However, the pattern of isotope shifts expected to result from a
massive release of methane does not match the patterns seen throughout
the early Triassic. Not only would such a cause require the release of
five times as much methane as postulated for the PETM, but would it also have to be reburied at an unrealistically high rate to account for the rapid increases in the 13C/12C ratio (episodes of high positive δ13C) throughout the early Triassic before it was released again several times.
Anoxia
Evidence for widespread ocean anoxia (severe deficiency of oxygen) and euxinia (presence of hydrogen sulfide) is found from the Late Permian to the Early Triassic. Throughout most of the Tethys and Panthalassic Oceans, evidence for anoxia, including fine laminations in sediments, small pyrite framboids, high uranium/thorium ratios, and biomarkers for green sulfur bacteria, appear at the extinction event.
However, in some sites, including Meishan, China, and eastern Greenland, evidence for anoxia precedes the extinction.
Biomarkers for green sulfur bacteria, such as isorenieratane, the diagenetic product of isorenieratene, are widely used as indicators of photic zone euxinia because green sulfur bacteria
require both sunlight and hydrogen sulfide to survive. Their abundance
in sediments from the P-T boundary indicates hydrogen sulfide was
present even in shallow waters.
This spread of toxic, oxygen-depleted water would have been
devastating for marine life, producing widespread die-offs. Models of
ocean chemistry show that anoxia and euxinia would have been closely
associated with hypercapnia (high levels of carbon dioxide).
This suggests that poisoning from hydrogen sulfide,
anoxia, and hypercapnia acted together as a killing mechanism.
Hypercapnia best explains the selectivity of the extinction, but anoxia
and euxinia probably contributed to the high mortality of the event. The
persistence of anoxia through the Early Triassic may explain the slow
recovery of marine life after the extinction. Models also show that
anoxic events can cause catastrophic hydrogen sulfide emissions into the
atmosphere (see below).
The sequence of events leading to anoxic oceans may have been triggered by carbon dioxide emissions from the eruption of the Siberian Traps.
In that scenario, warming from the enhanced greenhouse effect would
reduce the solubility of oxygen in seawater, causing the concentration
of oxygen to decline. Increased weathering of the continents due to
warming and the acceleration of the water cycle would increase the riverine flux of phosphate
to the ocean. The phosphate would have supported greater primary
productivity in the surface oceans. The increase in organic matter
production would have caused more organic matter to sink into the deep
ocean, where its respiration would further decrease oxygen
concentrations. Once anoxia became established, it would have been
sustained by a positive feedback loop because deep water anoxia tends to increase the recycling efficiency of phosphate, leading to even higher productivity.
Hydrogen sulfide emissions
A severe anoxic event at the end of the Permian would have allowed sulfate-reducing bacteria
to thrive, causing the production of large amounts of hydrogen sulfide
in the anoxic ocean. Upwelling of this water may have released massive hydrogen sulfide emissions into the atmosphere and would poison terrestrial plants and animals and severely weaken the ozone layer, exposing much of the life that remained to fatal levels of UV radiation.
Indeed, biomarker evidence for anaerobic photosynthesis by Chlorobiaceae
(green sulfur bacteria) from the Late-Permian into the Early Triassic
indicates that hydrogen sulfide did upwell into shallow waters because
these bacteria are restricted to the photic zone and use sulfide as an electron donor.
The hypothesis has the advantage of explaining the mass
extinction of plants, which would have added to the methane levels and
should otherwise have thrived in an atmosphere with a high level of
carbon dioxide. Fossil spores from the end-Permian further support the
theory: many show deformities that could have been caused by ultraviolet radiation, which would have been more intense after hydrogen sulfide emissions weakened the ozone layer.
The supercontinent Pangaea
Map of Pangaea showing where today's continents were at the Permian–Triassic boundary
In the mid-Permian (during the Kungurian age of the Permian's Cisuralian epoch), the earth's major continental plates were joined, forming a supercontinent called Pangaea, which was surrounded by the superocean, Panthalassa.
Oceanic circulation and atmospheric weather patterns during the mid-Permian produced seasonal monsoons near the coasts and an arid climate in the vast continental interior of Pangaea.
The extent of biologically diverse and ecologically productive
coastal areas shrank as the supercontinent formed. The elimination of
shallow aquatic environments exposed formerly protected organisms of the
rich continental shelves to increased environmental volatility.
After the formation of Pangaea (see the diagram "Marine genus
biodiversity" at the top of this article), the rate of marine life
depletion approached catastrophic levels; however, marine life
extinction never reached the rate of the "Big Five" mass extinctions.
Pangaea's effect on extinctions on land is thought to have been less significant. In fact, the advance of the therapsids and increase in their diversity is attributed to the late Permian, when Pangaea's global effect was thought to have peaked.
While Pangaea's formation is known to have initiated a long
period of marine life extinction, the significance of its impact on the
"Great Dying" and the end of the Permian is uncertain.
Encounter with spiral arm
John Gribbin argues that the Solar System last passed through a spiral arm of the Milky Way
around 250 million years ago and that the resultant dusty gas clouds
may have caused a dimming of the Sun which combined with the effect of
Pangea to produce an ice age.
Microbes
A hypothesis published in 2014 posits that a genus of anaerobic methanogenic archaea known as Methanosarcina was responsible for the event. Three lines of evidence suggest that these microbes acquired a new metabolic pathway via gene transfer
at about that time, enabling them to efficiently metabolize acetate
into methane. That would have led to their exponential reproduction,
allowing them to rapidly consume vast deposits of organic carbon that
had accumulated in the marine sediment. The result would have been a
sharp buildup of methane and carbon dioxide in the Earth's oceans and
atmosphere, in a manner that may be consistent with the 13C/12C
isotopic record. Massive volcanism facilitated this process by
releasing large amounts of nickel, a scarce metal which is a cofactor
for enzymes involved in producing methane. On the other hand, in the canonical Meishan sections, the nickel concentration increases somewhat after the δ13C concentrations have begun to fall.
Combination of causes
Possible
causes supported by strong evidence appear to describe a sequence of
catastrophes, each worse than the last: the Siberian Traps eruptions
were bad enough alone, but because they occurred near coal beds and the
continental shelf, they also triggered very large releases of carbon
dioxide and methane.
The resultant global warming may have caused perhaps the most severe
anoxic event in the oceans' history: according to this theory, the
oceans became so anoxic, anaerobic sulfur-reducing organisms dominated
the chemistry of the oceans and caused massive emissions of toxic
hydrogen sulfide.
However, there may be some weak links in this chain of events: the changes in the 13C/12C ratio expected to result from a massive release of methane do not match the patterns seen throughout the early Triassic; and the types of oceanic thermohaline circulation that may have existed at the end of the Permian are not likely to have supported deep-sea anoxia.
