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Late Pleistocene extinctions

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(Redirected from New World Pleistocene extinctions) Extinctions of large mammals in the Late Pleistocene For extinctions that occurred during the Holocene, see Holocene extinction.

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Late Pleistocene in northern Spain, by Mauricio Antón. Left to right: wild horse; woolly mammoth; reindeer; cave lion; woolly rhinoceros
Mural of the La Brea Tar Pits by Charles R. Knight, including sabertooth cats (Smilodon fatalis, left) ground sloths (Paramylodon harlani, right) and Columbian mammoths (Mammuthus columbi, background)

The Late Pleistocene to the beginning of the Holocene saw the extinction of the majority of the world's megafauna (typically defined as animal species having body masses over 44 kilograms (97 lb)), which resulted in a collapse in faunal density and diversity across the globe. The extinctions during the Late Pleistocene are differentiated from previous extinctions by its extreme size bias towards large animals (with small animals being largely unaffected), and widespread absence of ecological succession to replace these extinct megafaunal species, and the regime shift of previously established faunal relationships and habitats as a consequence. The timing and severity of the extinctions varied by region and are thought to have been driven by varying combinations of human and climatic factors. Human impact on megafauna populations is thought to have been driven by hunting ("overkill"), as well as possibly environmental alteration. The relative importance of human vs climatic factors in the extinctions has been the subject of long-running controversy.

Major extinctions occurred in Australia-New Guinea (Sahul) beginning approximately 50,000 years ago and in the Americas about 13,000 years ago, coinciding in time with the early human migrations into these regions. Extinctions in northern Eurasia were staggered over tens of thousands of years between 50,000 and 10,000 years ago, while extinctions in the Americas were virtually simultaneous, spanning only 3000 years at most. Overall, during the Late Pleistocene about 65% of all megafaunal species worldwide became extinct, rising to 72% in North America, 83% in South America and 88% in Australia, with all mammals over 1,000 kilograms (2,200 lb) becoming extinct in Australia and the Americas, and around 80% globally. Africa, South Asia and Southeast Asia experienced more moderate extinctions than other regions.

Extinctions by biogeographic realm

Summary

Extinctions range of the continental large and medium-sized mammals from 40,000 to 4,000 years BP in different biogeographic realms
Biogeographic realm Giants
(over 1,000 kg) 		Very large
(400–1,000 kg) 		Large
(150–400 kg) 		Moderately large
(50–150 kg) 		Medium
(10–50 kg) 		Total Regions included
Start Loss % Start Loss % Start Loss % Start Loss % Start Loss % Start Loss %
Afrotropic 6 −1 16.6% 4 −1 25% 25 −3 12% 32 0 0% 69 −2 2.9% 136 -7 5.1% Trans-Saharan Africa and Arabia
Indomalaya 5 −2 40% 6 −1 16.7% 10 −1 10% 20 −3 15% 56 −1 1.8% 97 -8 8.2% Indian subcontinent, Southeast Asia, and southern China
Palearctic 8 −8 100% 10 −5 50% 14 −5 35.7% 23 −3 15% 41 −1 2.4% 96 -22 22.9% Eurasia and North Africa
Nearctic 5 −5 100% 10 −8 80% 26 −22 84.6% 20 −13 65% 25 −9 36% 86 -57 66% North America
Neotropic 9 −9 100% 12 −12 100% 17 −14 82% 20 −11 55% 35 −5 14.3% 93 -51 54% South America, Central America, South Florida, and the Caribbean
Australasia 4 −4 100% 5 −5 100% 6 −6 100% 16 −13 81.2% 25 −10 40% 56 -38 67% Australia, New Guinea, New Zealand, and neighbouring islands.
Global 33 −26 78.8% 46 −31 67.4% 86 −47 54.7% 113 −41 36.3% 215 −23 10.1% 493 -168 34%

Introduction

The proportion of extinct large mammal species (more than or equal to 10 kg (22 lb)) in each country during the last 132,000 years, only counting extinctions earlier than 1000 years BP

The Late Pleistocene saw the extinction of many mammals weighing more than 40 kilograms (88 lb), including around 80% of mammals over 1 tonne. The proportion of megafauna extinctions is progressively larger the further the human migratory distance from Africa, with the highest extinction rates in Australia, and North and South America.

The increased extent of extinction mirrors the migration pattern of modern humans: the further away from Africa, the more recently humans inhabited the area, the less time those environments (including its megafauna) had to become accustomed to humans (and vice versa).

There are two main hypotheses to explain this extinction:

  • Climate change associated with the advance and retreat of major ice caps or ice sheets causing reduction in favorable habitat.
  • Human hunting causing attrition of megafauna populations, commonly known as "overkill".

There are some inconsistencies between the current available data and the prehistoric overkill hypothesis. For instance, there are ambiguities around the timing of Australian megafauna extinctions. Evidence supporting the prehistoric overkill hypothesis includes the persistence of megafauna on some islands for millennia past the disappearance of their continental cousins. For instance, ground sloths survived on the Antilles long after North and South American ground sloths were extinct, woolly mammoths died out on remote Wrangel Island 6,000 years after their extinction on the mainland, while Steller's sea cows persisted off the isolated and uninhabited Commander Islands for thousands of years after they had vanished from the continental shores of the north Pacific. The later disappearance of these island species correlates with the later colonization of these islands by humans.

Still, there are some arguments that species responded differently to environmental changes, and no one factor by itself explains the large variety of extinctions. The causes may involve the interplay of climate change, competition between species, unstable population dynamics, and hunting as well as competition by humans.

The original debates as to whether human arrival times or climate change constituted the primary cause of megafaunal extinctions necessarily were based on paleontological evidence coupled with geological dating techniques. Recently, genetic analyses of surviving megafaunal populations have contributed new evidence, leading to the conclusion: "The inability of climate to predict the observed population decline of megafauna, especially during the past 75,000 years, implies that human impact became the main driver of megafauna dynamics around this date."

Africa

Although Africa was one of the least affected regions, the region still suffered extinctions, particularly around the Late Pleistocene-Holocene transition. These extinctions were likely predominantly climatically driven by changes to grassland habitats.

South Asia and Southeast Asia

Giant tapir (Tapirus augustus) restoration
Life-sized models of Stegodon
Palaeoloxodon namadicus
Fossil jaw (Xiahe mandible) of a denisovan

The timing of extinctions on the Indian subcontinent is uncertain due to a lack of reliable dating. Similar issues have been reported for Chinese sites, though there is no evidence for any of the megafaunal taxa having survived into the Holocene in that region. Extinctions in Southeast Asia and South China have been proposed to be the result of environmental shift from open to closed forested habitats.

Europe, Northern and East Asia

Saiga antelope (Saiga spp.) inhabited a range from England and France to Yukon in the Late Pleistocene, diversifying into two species. S. borealis is now extinct and the near-threatened S. tatarica is now limited to the steppe in Kazakhstan and Mongolia
Hippopotamus (Hippopotamus amphibius) formerly inhabited Europe as far north as Great Britain at the beginning of the Late Pleistocene, becoming extinct in Europe around 30,000 years ago
Reconstruction of the five phenotypes of Pleistocene wild horse. The coat colours and dimensions are based on genetic evidence and historic descriptions
Elasmotherium sibiricum reconstruction
Cave paintings of the woolly rhinoceros (Coelodonta antiquitatis) in Chauvet-Pont-d'Arc Cave, France
The 'Gallery of Lions', representations of the Eurasian cave lion in Chauvet-Pont-d'Arc Cave, France
The leopard (Panthera pardus) inhabited the entire expanse of Afro-Eurasia below the 54th parallel north, from modern day Spain and the UK in the west, to South Africa in the south, and Siberia, Japan and Sundaland in the east during the Late Pleistocene
Cave bear (Ursus spelaeus) reconstruction
Cave hyena (Crocuta crocuta spelaea) reconstruction
The woolly mammoth became extinct around 10,000 BCE – except for diminutive relict populations on St. Paul Island and Wrangel Island, which humans did not colonise until 3,600 BCE and 2,000 BCE respectively
Model of the European straight-tusked elephant (Paleoloxodon antiquus)

The Palearctic realm spans the entirety of the European continent and stretches into northern Asia, through the Caucasus and central Asia to northern China, Siberia and Beringia. Extinctions were more severe in Northern Eurasia than in Africa or South and Southeast Asia. These extinctions were staggered over tens of thousands of years, spanning from around 50,000 years Before Present (BP) to around 10,000 years BP, with temperate adapted species like the straight-tusked elephant and the narrow-nosed rhinoceros generally going extinct earlier than cold adapted species like the woolly mammoth and woolly rhinoceros. Climate change has been considered a probable major factor in the extinctions, possibly in combination with human hunting.

See also: List of extinct animals of Europe

North America

See also: List of North American animals extinct in the Holocene

Extinctions in North America were concentrated at the end of the Late Pleistocene, around 13,800–11,400 years Before Present, which were coincident with the onset of the Younger Dryas cooling period, as well as the emergence of the hunter-gatherer Clovis culture. The relative importance of human and climactic factors in the North American extinctions has been the subject of significant controversy. Extinctions totalled around 35 genera. The radiocarbon record for North America south of the Alaska-Yukon region has been described as "inadequate" to construct a reliable chronology.

Long-horned/Giant bison (Bos latifrons), fossil bison skeleton (public display, Cincinnati Museum of Natural History & Science, Cincinnati, Ohio, United States)
Mounted skeleton of a shrub-ox (Euceratherium collinum)
Life restoration of Cervalces scotti
Tetrameryx shuleri restoration
A Chacoan peccary (Catagonus wagneri), believed to be the closest surviving relative of the extinct Platygonus
Western camel (Camelops hesternus) reconstruction
Life restoration of the Yukon horse (Equus lambei)
Reconstruction of Mixotoxodon larenis, a toxodontid notoungulate
Saber-toothed cat (Smilodon fatalis) reconstruction
Scimitar cat (Homotherium serum) reconstruction
American lion (Panthera atrox) reconstruction
The dhole (Cuon alpinus), now restricted to the southern portions of Asia, was present from Iberia to Mexico during the Late Pleistocene
Giant short-faced bear (Arctodus simus) reconstruction
American mastodon (Mammut americanum) reconstruction
Columbian mammoth (Mammuthus columbi) reconstruction
Giant beaver (Castoroides ohioensis) skeleton displayed at the Field Museum of Natural History, Chicago, Illinois, United States
Skull of Paralouatta marianae, one of the two Cuban members of the extinct Antilles monkeys (Xenotrichini)
Eremotherium laurillardi skeleton displayed at the Houston Museum of Natural Science
Life restoration of Nothrotheriops texanus
Glyptotherium reconstruction
Californian turkey (Meleagris californica) and megafaunal Californian condor (Gymnogyps amplus) fossil displays at La Brea Tar Pits
Teratornis merriami skeleton from the La Brea Tar Pits in flight pose
Reconstruction of the Cuban giant owl (Ornimegalonyx oteroi), of Pleistocene Cuba, with the carcass of a large solenodon

North American extinctions (noted as herbivores (H) or carnivores (C)) included:

The survivors are in some ways as significant as the losses: bison (H), grey wolf (C), lynx (C), grizzly bear (C), American black bear (C), deer (e.g. caribou, moose, wapiti (elk), Odocoileus spp.) (H), pronghorn (H), white-lipped peccary (H), muskox (H), bighorn sheep (H), and mountain goat (H); the list of survivors also include species which were extirpated during the Quaternary extinction event, but recolonised at least part of their ranges during the mid-Holocene from South American relict populations, such as the cougar (C), jaguar (C), giant anteater (C), collared peccary (H), ocelot (C) and jaguarundi (C). All save the pronghorns and giant anteaters were descended from Asian ancestors that had evolved with human predators. Pronghorns are the second-fastest land mammal (after the cheetah), which may have helped them elude hunters. More difficult to explain in the context of overkill is the survival of bison, since these animals first appeared in North America less than 240,000 years ago and so were geographically removed from human predators for a sizeable period of time. Because ancient bison evolved into living bison, there was no continent-wide extinction of bison at the end of the Pleistocene (although the genus was regionally extirpated in many areas). The survival of bison into the Holocene and recent times is therefore inconsistent with the overkill scenario. By the end of the Pleistocene, when humans first entered North America, these large animals had been geographically separated from intensive human hunting for more than 200,000 years. Given this enormous span of geologic time, bison would almost certainly have been very nearly as naive as native North American large mammals.

The culture that has been connected with the wave of extinctions in North America is the paleo-American culture associated with the Clovis people (q.v.), who were thought to use spear throwers to kill large animals. The chief criticism of the "prehistoric overkill hypothesis" has been that the human population at the time was too small and/or not sufficiently widespread geographically to have been capable of such ecologically significant impacts. This criticism does not mean that climate change scenarios explaining the extinction are automatically to be preferred by default, however, any more than weaknesses in climate change arguments can be taken as supporting overkill. Some form of a combination of both factors could be plausible, and overkill would be a lot easier to achieve large-scale extinction with an already stressed population due to climate change.

South America

Fossil of Hippidion, a genus of horse native to South America.
Reconstruction of Macrauchenia, a member of the extinct order Litopterna
Skeleton of Toxodon, a member of the extinct order Notoungulata
Reconstruction of the Dire wolf (Aenocyon dirus)
Life restoration of Arctotherium bonariense
Reconstruction of the gomphothere Cuvieronius
Skeleton of the giant ground sloth Megatherium
Reconstruction of the glyptodont Doedicurus clavicaudatus, distributed in the temperate savannah and woodland of South America
Fossil reconstruction of Panochthus frenzelianus with metal model
Fossil of Smilodon populator
See also: List of South American animals extinct in the Holocene

South America suffered among the worst losses of the continents, with around 83% of its megafauna going extinct. These extinctions postdate the arrival of modern humans in South America around 15,000 years ago. Both human and climatic factors have been attributed as factors in the extinctions by various authors. Although some megafauna has been historically suggested to have survived into the early Holocene based on radiocarbon dates this may be the result of dating errors due to contamination. The extinctions are coincident with the end of the Antarctic Cold Reversal (a cooling period earlier and less severe than the Northern Hemisphere Younger Dryas) and the emergence of Fishtail projectile points, which became widespread across South America. Fishtail projectile points are thought to have been used in big game hunting, though direct evidence of exploitation of extinct megafauna by humans is rare, though megafauna exploitation has been documented at a number of sites. Fishtail points rapidly disappeared after the extinction of the megafauna, and were replaced by other styles more suited to hunting smaller prey. Some authors have proposed the "Broken Zig-Zag" model, where human hunting and climate change causing a reduction in open habitats preferred by megafauna were synergistic factors in megafauna extinction in South America.

Sahul (Australia-New Guinea) and the Pacific

See also: List of Australia-New Guinea species extinct in the Holocene, List of New Zealand species extinct in the Holocene, and List of Oceanian animals extinct in the Holocene
Reconstruction of a hippopotamus-sized Diprotodon
Reconstruction of Zygomaturus
Reconstruction of the giant echidna Murrayglossus
Reconstruction of Genyornis newtoni

A scarcity of reliably dated megafaunal bone deposits has made it difficult to construct timelines for megafaunal extinctions in certain areas, leading to a divide among researches about when and how megafaunal species went extinct.

There are at least three hypotheses regarding the extinction of the Australian megafauna:

  1. that they went extinct with the arrival of the Aboriginal Australians on the continent,
  2. that they went extinct due to natural climate change.
Life restoration of Thylacoleo carnifex (also known as the marsupial lion)

This theory is based on evidence of megafauna surviving until 40,000 years ago, a full 30,000 years after homo sapiens first landed in Australia, and thus that the two groups coexisted for a long time. Evidence of these animals existing at that time come from fossil records and ocean sediment. To begin with, sediment core drilled in the Indian Ocean off the SW coast of Australia indicate the existence of a fungus called Sporormiella, which survived off the dung of plant-eating mammals. The abundance of these spores in the sediment prior to 45,000 years ago indicates that many large mammals existed in the southwest Australian landscape until that point. The sediment data also indicates that the megafauna population collapsed within a few thousand years, around the 45,000 years ago, suggesting a rapid extinction event. In addition, fossils found at South Walker Creek, which is the youngest megafauna site in northern Australia, indicate that at least 16 species of megafauna survived there until 40,000 years ago. Furthermore, there is no firm evidence of homo sapiens living at South Walker Creek 40,000 years ago, therefore no human cause can be attributed to the extinction of these megafauna. However, there is evidence of major environmental deterioration of South Water Creek 40,000 years ago, which may have caused the extinct event. These changes include increased fire, reduction in grasslands, and the loss of fresh water. The same environmental deterioration is seen across Australia at the time, further strengthening the climate change argument. Australia's climate at the time could best be described as an overall drying of the landscape due to lower precipitation, resulting in less fresh water availability and more drought conditions. Overall, this led to changes in vegetation, increased fires, overall reduction in grasslands, and a greater competition for already scarce fresh water. These environmental changes proved to be too much for the Australian megafauna to cope with, causing the extinction of 90% of megafauna species.

  1. The third hypothesis shared by some scientists is that human impacts and natural climate changes led to the extinction of Australian megafauna. About 75% of Australia is semi-arid or arid, so it makes sense that megafauna species used the same fresh water resources as humans. This competition could have led to more hunting of megafauna. Furthermore, Homo sapiens used fire agriculture to burn impassable land. This further diminished the already disappearing grassland which contained plants that were a key dietary component of herbivorous megafauna. While there is no scientific consensus on this, it is plausible that homo sapiens and natural climate change had a combined impact. Overall, there is a great deal of evidence for humans being the culprit, but by ruling out climate change completely as a cause of the Australian megafauna extinction we are not getting the whole picture. The climate change in Australia 45,000 years ago destabilized the ecosystem, making it particularly vulnerable to hunting and fire agriculture by humans; this is probably what led to the extinction of the Australian megafauna.

Several studies provide evidence that climate change caused megafaunal extinction during the Pleistocene in Australia. One group of researchers analyzed fossilized teeth found at Cuddie Springs in southeastern Australia. By analyzing oxygen isotopes, they measured aridity, and by analyzing carbon isotopes and dental microwear texture analysis, they assessed megafaunal diets and vegetation. During the middle Pleistocene, southeastern Australia was dominated by browsers, including fauna that consumed C4 plants. By the late Pleistocene, the C4 plant dietary component had decreased considerably. This shift may have been caused by increasingly arid conditions, which may have caused dietary restrictions. Other isotopic analyses of eggshells and wombat teeth also point to a decline of C4 vegetation after 45 Ka. This decline in C4 vegetation is coincident with increasing aridity. Increasingly arid conditions in southeastern Australia during the late Pleistocene may have stressed megafauna, and contributed to their decline.

Procoptodon goliath reconstruction
Xenorhynchopsis tibialis (life reconstruction) was one of four species of flamingo present in Australia in the Quaternary, all of which are now either extinct or extirpated
Megalania skeleton, Melbourne Museum

In Sahul (a former continent composed of Australia and New Guinea), the sudden and extensive spate of extinctions occurred earlier than in the rest of the world. Most evidence points to a 20,000 year period after human arrival circa 63,000 BCE, but scientific argument continues as to the exact date range. In the rest of the Pacific (other Australasian islands such as New Caledonia, and Oceania) although in some respects far later, endemic fauna also usually perished quickly upon the arrival of humans in the late Pleistocene and early Holocene.

Causes

History of research

The megafaunal extinctions were already recognized as a distinct phenomenon by some scientists in the 19th century:

It is impossible to reflect without the deepest astonishment, on the changed state of . Formerly it must have swarmed with great monsters, like the southern parts of Africa, but now we find only the tapir, guanaco, armadillo, capybara; mere pigmies compared to antecedents races... Since their loss, no very great physical changes can have taken place in the nature of the Country. What then has exterminated so many living creatures?

— Charles Darwin, The Voyage of the Beagle (1834)

It is clear, therefore, that we are now in an altogether exceptional period of the earth's history. We live in a zoologically impoverished world, from which all the hugest, and fiercest, and strangest forms have recently disappeared; and it is, no doubt, a much better world for us now they have gone. Yet it is surely a marvellous fact, and one that has hardly been sufficiently dwelt upon, this sudden dying out of so many large mammalia, not in one place only but over half the land surface of the globe. We cannot but believe that there must have been some physical cause for this great change; and it must have been a cause capable of acting almost simultaneously over large portions of the earth's surface, and one which, as far as the Tertiary period at least is concerned, was of an exceptional character.

— Alfred Russel Wallace, The geographical distribution of animals; with a study of the relations of living and extinct faunas as elucidating the past changes of the Earth's surface (1876)

Several decades later in his 1911 book The World of Life (published 2 years before his death), Wallace revisited the issue of the Pleistocene megafauna extinctions, concluding that the extinctons were at least in part the result of human agency in combination with other factors. Discussion of the topic became more widespread during the 20th century, particularly following the proposal of the "overkill hypothesis" by Paul Schultz Martin during the 1960s. By the end of the 20th century, two "camps" of researchers had emerged on the topic, one supporting climate change, the other supporting human hunting as the primary cause of the extinctions.

Hunting

The hunting hypothesis suggests that humans hunted megaherbivores to extinction, which in turn caused the extinction of carnivores and scavengers which had preyed upon those animals. This hypothesis holds Pleistocene humans responsible for the megafaunal extinction. One variant, known as blitzkrieg, portrays this process as relatively quick. Some of the direct evidence for this includes: fossils of some megafauna found in conjunction with human remains, embedded arrows and tool cut marks found in megafaunal bones, and European cave paintings that depict such hunting. Biogeographical evidence is also suggestive: the areas of the world where humans evolved currently have more of their Pleistocene megafaunal diversity (the elephants and rhinos of Asia and Africa) compared to other areas such as Australia, the Americas, Madagascar and New Zealand without the earliest humans. The overkill hypothesis, a variant of the hunting hypothesis, was proposed in 1966 by Paul S. Martin, Professor of Geosciences Emeritus at the Desert Laboratory of the University of Arizona.

Despeciation within the genus Homo.

Circumstantially, the close correlation in time between the appearance of humans in an area and extinction there provides weight for this scenario. Radiocarbon dating has supported the plausibility of this correlation being reflective of causation. The megafaunal extinctions covered a vast period of time and highly variable climatic situations. The earliest extinctions in Australia were complete approximately 50,000 BP, well before the Last Glacial Maximum and before rises in temperature. The most recent extinction in New Zealand was complete no earlier than 500 BP and during a period of cooling. In between these extremes megafaunal extinctions have occurred progressively in such places as North America, South America and Madagascar with no climatic commonality. The only common factor that can be ascertained is the arrival of humans. This phenomenon appears even within regions. The mammal extinction wave in Australia about 50,000 years ago coincides not with known climatic changes, but with the arrival of humans. In addition, large mammal species like the giant kangaroo Protemnodon appear to have succumbed sooner on the Australian mainland than on Tasmania, which was colonised by humans a few thousand years later. A study published in 2015 supported the hypothesis further by running several thousand scenarios that correlated the time windows in which each species is known to have become extinct with the arrival of humans on different continents or islands. This was compared against climate reconstructions for the last 90,000 years. The researchers found correlations of human spread and species extinction indicating that the human impact was the main cause of the extinction, while climate change exacerbated the frequency of extinctions. The study, however, found an apparently low extinction rate in the fossil record of mainland Asia. A 2020 study published in Science Advances found that human population size and/or specific human activities, not climate change, caused rapidly rising global mammal extinction rates during the past 126,000 years. Around 96% of all mammalian extinctions over this time period are attributable to human impacts. According to Tobias Andermann, lead author of the study, "these extinctions did not happen continuously and at constant pace. Instead, bursts of extinctions are detected across different continents at times when humans first reached them. More recently, the magnitude of human driven extinctions has picked up the pace again, this time on a global scale." On a related note, the population declines of still extant megafauna during the Pleistocene have also been shown to correlate with human expansion rather than climate change.

The extinction's extreme bias towards larger animals further supports a relationship with human activity rather than climate change. There is evidence that the average size of mammalian fauna declined over the course of the Quaternary, a phenomenon that was likely linked to disproportionate hunting of large animals by humans.

Extinction through human hunting has been supported by archaeological finds of mammoths with projectile points embedded in their skeletons, by observations of modern naive animals allowing hunters to approach easily and by computer models by Mosimann and Martin, and Whittington and Dyke, and most recently by Alroy.

The timing of extinctions follows the "March of Man"

In 2024 a paper was published in Science Advances that added additional support to the overkill hypothesis in North America when the skull of an 18 month old child, dated to 12,800 years ago, was analyzed for chemical signatures attributable to both maternal milk and solid food. Specific isotopes of carbon and nitrogen most closely matched those that would have been found in the mammoth genus and secondarily elk or bison.

A number of objections have been raised regarding the hunting hypothesis. Notable among them is the sparsity of evidence of human hunting of megafauna. There is no archeological evidence that in North America megafauna other than mammoths, mastodons, gomphotheres and bison were hunted, despite the fact that, for example, camels and horses are very frequently reported in fossil history. Overkill proponents, however, say this is due to the fast extinction process in North America and the low probability of animals with signs of butchery to be preserved. The majority of North American taxa have too sparse a fossil record to accurately assess the frequency of human hunting of them. A study by Surovell and Grund concluded "archaeological sites dating to the time of the coexistence of humans and extinct fauna are rare. Those that preserve bone are considerably more rare, and of those, only a very few show unambiguous evidence of human hunting of any type of prey whatsoever." Eugene S. Hunn suggests that the birthrate in hunter-gatherer societies is generally too low, that too much effort is involved in the bringing down of a large animal by a hunting party, and that in order for hunter-gatherers to have brought about the extinction of megafauna simply by hunting them to death, an extraordinary amount of meat would have had to have been wasted. Proponents of hunting as a cause of the extinctions argue that statistical modelling validates that relatively low-level hunting can have significant effect on megafauna populations due to their slow life cycles, and that hunting can cause top-down forcing trophic cascade events that destabilize ecosystems.

Second-order predation

Combination Hypotheses: Climate Change, Overkill + Climate Change, Second-Order Predation + Climate Change
Overkill Hypothesis and Second-Order Predation

The Second-Order Predation Hypothesis says that as humans entered the New World they continued their policy of killing predators, which had been successful in the Old World but because they were more efficient and because the fauna, both herbivores and carnivores, were more naive, they killed off enough carnivores to upset the ecological balance of the continent, causing overpopulation, environmental exhaustion, and environmental collapse. The hypothesis accounts for changes in animal, plant, and human populations.

The scenario is as follows:

  • After the arrival of H. sapiens in the New World, existing predators must share the prey populations with this new predator. Because of this competition, populations of original, or first-order, predators cannot find enough food; they are in direct competition with humans.
  • Second-order predation begins as humans begin to kill predators.
  • Prey populations are no longer well controlled by predation. Killing of nonhuman predators by H. sapiens reduces their numbers to a point where these predators no longer regulate the size of the prey populations.
  • Lack of regulation by first-order predators triggers boom-and-bust cycles in prey populations. Prey populations expand and consequently overgraze and over-browse the land. Soon the environment is no longer able to support them. As a result, many herbivores starve. Species that rely on the slowest recruiting food become extinct, followed by species that cannot extract the maximum benefit from every bit of their food.
  • Boom-bust cycles in herbivore populations change the nature of the vegetative environment, with consequent climatic impacts on relative humidity and continentality. Through overgrazing and overbrowsing, mixed parkland becomes grassland, and climatic continentality increases.

The second-order predation hypothesis has been supported by a computer model, the Pleistocene extinction model (PEM), which, using the same assumptions and values for all variables (herbivore population, herbivore recruitment rates, food needed per human, herbivore hunting rates, etc.) other than those for hunting of predators. It compares the overkill hypothesis (predator hunting = 0) with second-order predation (predator hunting varied between 0.01 and 0.05 for different runs). The findings are that second-order predation is more consistent with extinction than is overkill (results graph at left). The Pleistocene extinction model is the only test of multiple hypotheses and is the only model to specifically test combination hypotheses by artificially introducing sufficient climate change to cause extinction. When overkill and climate change are combined they balance each other out. Climate change reduces the number of plants, overkill removes animals, therefore fewer plants are eaten. Second-order predation combined with climate change exacerbates the effect of climate change. (results graph at right). The second-order predation hypothesis is further supported by the observation above that there was a massive increase in bison populations.

However, this hypothesis has been criticised on the grounds that the multispecies model produces a mass extinction through indirect competition between herbivore species: small species with high reproductive rates subsidize predation on large species with low reproductive rates. All prey species are lumped in the Pleistocene extinction model. Also, the control of population sizes by predators is not fully supported by observations of modern ecosystems. The hypothesis further assumes decreases in vegetation due to climate change, but deglaciation doubled the habitable area of North America. Any vegetational changes that did occur failed to cause almost any extinctions of small vertebrates, and they are more narrowly distributed on average, which detractors cite as evidence against the hypothesis.

Competition for water

In southeastern Australia, the scarcity of water during the interval in which humans arrived in Australia suggests that human competition with megafauna for precious water sources may have played a role in the extinction of the latter.

Landscape alteration

One consequence of the colonisation by humans of lands previously uninhabited by them may have been the introduction of new fire regimes because of extensive fire use by humans. There is evidence that anthropogenic fire use had major impacts on the local environments in both Australia and North America.

Climate change

At the end of the 19th and beginning of the 20th centuries, when scientists first realized that there had been glacial and interglacial ages, and that they were somehow associated with the prevalence or disappearance of certain animals, they surmised that the termination of the Pleistocene ice age might be an explanation for the extinctions.

The most obvious change associated with the termination of an ice age is the increase in temperature. Between 15,000 BP and 10,000 BP, a 6 °C increase in global mean annual temperatures occurred. This was generally thought to be the cause of the extinctions. According to this hypothesis, a temperature increase sufficient to melt the Wisconsin ice sheet could have placed enough thermal stress on cold-adapted mammals to cause them to die. Their heavy fur, which helps conserve body heat in the glacial cold, might have prevented the dumping of excess heat, causing the mammals to die of heat exhaustion. Large mammals, with their reduced surface area-to-volume ratio, would have fared worse than small mammals. A study covering the past 56,000 years indicates that rapid warming events with temperature changes of up to 16 °C (29 °F) had an important impact on the extinction of megafauna. Ancient DNA and radiocarbon data indicates that local genetic populations were replaced by others within the same species or by others within the same genus. Survival of populations was dependent on the existence of refugia and long distance dispersals, which may have been disrupted by human hunters.

Other scientists have proposed that increasingly extreme weather—hotter summers and colder winters—referred to as "continentality", or related changes in rainfall caused the extinctions. It has been shown that vegetation changed from mixed woodland-parkland to separate prairie and woodland. This may have affected the kinds of food available. Shorter growing seasons may have caused the extinction of large herbivores and the dwarfing of many others. In this case, as observed, bison and other large ruminants would have fared better than horses, elephants and other monogastrics, because ruminants are able to extract more nutrition from limited quantities of high-fiber food and better able to deal with anti-herbivory toxins. So, in general, when vegetation becomes more specialized, herbivores with less diet flexibility may be less able to find the mix of vegetation they need to sustain life and reproduce, within a given area. Increased continentality resulted in reduced and less predictable rainfall limiting the availability of plants necessary for energy and nutrition. It has been suggested that this change in rainfall restricted the amount of time favorable for reproduction. This could disproportionately harm large animals, since they have longer, more inflexible mating periods, and so may have produced young at unfavorable seasons (i.e., when sufficient food, water, or shelter was unavailable because of shifts in the growing season). In contrast, small mammals, with their shorter life cycles, shorter reproductive cycles, and shorter gestation periods, could have adjusted to the increased unpredictability of the climate, both as individuals and as species which allowed them to synchronize their reproductive efforts with conditions favorable for offspring survival. If so, smaller mammals would have lost fewer offspring and would have been better able to repeat the reproductive effort when circumstances once more favored offspring survival. A study looking at the environmental conditions across Europe, Siberia and the Americas from 25,000 to 10,000 YBP found that prolonged warming events leading to deglaciation and maximum rainfall occurred just prior to the transformation of the rangelands that supported megaherbivores into widespread wetlands that supported herbivore-resistant plants. The study proposes that moisture-driven environmental change led to the megafaunal extinctions and that Africa's trans-equatorial position allowed rangeland to continue to exist between the deserts and the central forests, therefore fewer megafauna species became extinct there.

Evidence in Southeast Asia, in contrast to Europe, Australia, and the Americas, suggests that climate change and an increasing sea level were significant factors in the extinction of several herbivorous species. Alterations in vegetation growth and new access routes for early humans and mammals to previously isolated, localized ecosystems were detrimental to select groups of fauna.

Some evidence from Europe also suggests climatic changes were responsible for extinctions there, as the individuals extinctions tended to occur during times of environmental change and did not correlate particularly well with human migrations.

In Australia, some studies have suggested that extinctions of megafauna began before the peopling of the continent, favouring climate change as the driver.

In Beringia, megafauna may have gone extinct because of particularly intense paludification and because the land connection between Eurasia and North America flooded before the Cordilleran Ice Sheet retreated far enough to reopen the corridor between Beringia and the remainder of North America. Woolly mammoths became extirpated from Beringia because of climatic factors, although human activity also played a synergistic role in their decline. In North America, a Radiocarbon-dated Event-Count (REC) modelling study found that megafaunal declines in North America correlated with climatic changes instead of human population expansion.

In the North American Great Lakes region, the population declines of mastodons and mammoths have been found to correlate with climatic fluctuations during the Younger Dryas rather than human activity.

In the Argentine Pampas, the flooding of vast swathes of the once much larger Pampas grasslands may have played a role in the extinctions of its megafaunal assemblages.

Critics object that since there were multiple glacial advances and withdrawals in the evolutionary history of many of the megafauna, it is rather implausible that only after the last glacial maximum would there be such extinctions. Proponents of climate change as the extinction event's cause like David J. Meltzer suggest that the last deglaciation may have been markedly different from previous ones. Also, one study suggests that the Pleistocene megafaunal composition may have differed markedly from that of earlier interglacials, making the Pleistocene populations particularly vulnerable to changes in their environment.

Studies propose that the annual mean temperature of the current interglacial that we have seen for the last 10,000 years is no higher than that of previous interglacials, yet most of the same large mammals survived similar temperature increases. In addition, numerous species such as mammoths on Wrangel Island and St. Paul Island survived in human-free refugia despite changes in climate. This would not be expected if climate change were responsible (unless their maritime climates offered some protection against climate change not afforded to coastal populations on the mainland). Under normal ecological assumptions island populations should be more vulnerable to extinction due to climate change because of small populations and an inability to migrate to more favorable climes.

Critics have also identified a number of problems with the continentality hypotheses. Megaherbivores have prospered at other times of continental climate. For example, megaherbivores thrived in Pleistocene Siberia, which had and has a more continental climate than Pleistocene or modern (post-Pleistocene, interglacial) North America. The animals that became extinct actually should have prospered during the shift from mixed woodland-parkland to prairie, because their primary food source, grass, was increasing rather than decreasing. Although the vegetation did become more spatially specialized, the amount of prairie and grass available increased, which would have been good for horses and for mammoths, and yet they became extinct. This criticism ignores the increased abundance and broad geographic extent of Pleistocene bison at the end of the Pleistocene, which would have increased competition for these resources in a manner not seen in any earlier interglacials. Although horses became extinct in the New World, they were successfully reintroduced by the Spanish in the 16th century—into a modern post-Pleistocene, interglacial climate. Today there are feral horses still living in those same environments. They find a sufficient mix of food to avoid toxins, they extract enough nutrition from forage to reproduce effectively and the timing of their gestation is not an issue. Of course, this criticism ignores the obvious fact that present-day horses are not competing for resources with ground sloths, mammoths, mastodons, camels, llamas, and bison. Similarly, mammoths survived the Pleistocene Holocene transition on isolated, uninhabited islands in the Mediterranean Sea until 4,000 to 7,000 years ago, as well as on Wrangel Island in the Siberian Arctic. Additionally, large mammals should have been able to migrate, permanently or seasonally, if they found the temperature too extreme, the breeding season too short, or the rainfall too sparse or unpredictable. Seasons vary geographically. By migrating away from the equator, herbivores could have found areas with growing seasons more favorable for finding food and breeding successfully. Modern-day African elephants migrate during periods of drought to places where there is apt to be water. Large animals also store more fat in their bodies than do medium-sized animals and this should have allowed them to compensate for extreme seasonal fluctuations in food availability.

Some evidence weighs against climate change as a valid hypothesis as applied to Australia. It has been shown that the prevailing climate at the time of extinction (40,000–50,000 BP) was similar to that of today, and that the extinct animals were strongly adapted to an arid climate. The evidence indicates that all of the extinctions took place in the same short time period, which was the time when humans entered the landscape. The main mechanism for extinction was probably fire (started by humans) in a then much less fire-adapted landscape. Isotopic evidence shows sudden changes in the diet of surviving species, which could correspond to the stress they experienced before extinction.

Some evidence obtained from analysis of the tusks of mastodons from the American Great Lakes region appears inconsistent with the climate change hypothesis. Over a span of several thousand years prior to their extinction in the area, the mastodons show a trend of declining age at maturation. This is the opposite of what one would expect if they were experiencing stresses from deteriorating environmental conditions, but is consistent with a reduction in intraspecific competition that would result from a population being reduced by human hunting.

It may be observed that neither the overkill nor the climate change hypotheses can fully explain events: browsers, mixed feeders and non-ruminant grazer species suffered most, while relatively more ruminant grazers survived. However, a broader variation of the overkill hypothesis may predict this, because changes in vegetation wrought by either Second Order Predation (see below) or anthropogenic fire preferentially selects against browse species.

Disease

The hyperdisease hypothesis, as advanced by Ross D. E. MacFee and Preston A. Marx, attributes the extinction of large mammals during the late Pleistocene to indirect effects of the newly arrived aboriginal humans. In more recent times, disease has driven many vulnerable species to extinction; the introduction of avian malaria and avipoxvirus, for example, has greatly decreased the populations of the endemic birds of Hawaii, with some going extinct. The hyperdisease hypothesis proposes that humans or animals traveling with them (e.g., chickens or domestic dogs) introduced one or more highly virulent diseases into vulnerable populations of native mammals, eventually causing extinctions. The extinction was biased toward larger-sized species because smaller species have greater resilience because of their life history traits (e.g., shorter gestation time, greater population sizes, etc.). Humans are thought to be the cause because other earlier immigrations of mammals into North America from Eurasia did not cause extinctions. A similar suggestion is that pathogens were transmitted by the expanding humans via the domesticated dogs they brought with them. A related theory proposes that a highly contagious prion disease similar to chronic wasting disease or scrapie that was capable of infecting a large number of species was the culprit. Animals weakened by this "superprion" would also have easily become reservoirs of viral and bacterial diseases as they succumbed to neurological degeneration from the prion, causing a cascade of different diseases to spread among various mammal species. This theory could potentially explain the prevalence of heterozygosity at codon 129 of the prion protein gene in humans, which has been speculated to be the result of natural selection against homozygous genotypes that were more susceptible to prion disease and thus potentially a tell-tale of a major prion pandemic that affected humans of or younger than reproductive age far in the past and disproportionately killed before they could reproduce those with homozygous genotypes at codon 129.

If a disease was indeed responsible for the end-Pleistocene extinctions, then there are several criteria it must satisfy (see Table 7.3 in MacPhee & Marx 1997). First, the pathogen must have a stable carrier state in a reservoir species. That is, it must be able to sustain itself in the environment when there are no susceptible hosts available to infect. Second, the pathogen must have a high infection rate, such that it is able to infect virtually all individuals of all ages and sexes encountered. Third, it must be extremely lethal, with a mortality rate of c. 50–75%. Finally, it must have the ability to infect multiple host species without posing a serious threat to humans. Humans may be infected, but the disease must not be highly lethal or able to cause an epidemic.

As with other hypotheses, a number of counterarguments to the hyperdisease hypothesis have been put forth. Generally speaking, disease has to be very virulent to kill off all the individuals in a genus or species. Even such a virulent disease as West Nile fever is unlikely to have caused extinction. The disease would need to be implausibly selective while being simultaneously implausibly broad. Such a disease needs to be capable of killing off wolves such as Canis dirus or goats such as Oreamnos harringtoni while leaving other very similar species (Canis lupus and Oreamnos americanus, respectively) unaffected. It would need to be capable of killing off flightless birds while leaving closely related flighted species unaffected. Yet while remaining sufficiently selective to afflict only individual species within genera it must be capable of fatally infecting across such clades as birds, marsupials, placentals, testudines, and crocodilians. No disease with such a broad scope of fatal infectivity is known, much less one that remains simultaneously incapable of infecting numerous closely related species within those disparate clades. On the other hand, this objection does not account for the possibility of a variety of different diseases being introduced around the same era. Numerous species including wolves, mammoths, camelids, and horses had emigrated continually between Asia and North America over the past 100,000 years. For the disease hypothesis to be applicable there it would require that the population remain immunologically naive despite this constant transmission of genetic and pathogenic material. The dog-specific hypothesis in particular cannot account for several major extinction events, notably the Americas (for reasons already covered) and Australia. Dogs did not arrive in Australia until approximately 35,000 years after the first humans arrived there, and approximately 30,000 years after the Australian megafaunal extinction was complete.

Extraterrestrial impact

Main article: Younger Dryas impact hypothesis

An extraterrestrial impact, which has occasionally been proposed as a cause of the Younger Dryas, has been suggested by some authors as a potential cause of the extinction of North America's megafauna due to the temporal proximity between a proposed date for such an impact and the following megafaunal extinctions. However, the Younger Dryas impact hypothesis lacks widespread support among scholars due to various inconsistencies in the hypothesis, and another group of researchers has published a review contesting the arguments for it point by point.

Geomagnetic field weakening

Around 41,500 years ago, the Earth's magnetic field weakened in an event known as the Laschamp event. This weakening may have caused increased flux of UV-B radiation and has been suggested by a few authors as a cause of megafaunal extinctions in the Late Quaternary. The full effects of such events on the biosphere are poorly understood, however these explanations have been criticized as they do not account for the population bottlenecks seen in many megafaunal species and nor is there evidence for extreme radio-isotopic changes during the event. Considering these factors, causation is unlikely.

Effects

The extinction of the megafauna has been argued by some authors to be disappearance of the mammoth steppe rather than the other way around. Alaska now has low nutrient soil unable to support bison, mammoths, and horses. R. Dale Guthrie has claimed this as a cause of the extinction of the megafauna there; however, he may be interpreting it backwards. The loss of large herbivores to break up the permafrost allows the cold soils that are unable to support large herbivores today. Today, in the arctic, where trucks have broken the permafrost grasses and diverse flora and fauna can be supported. In addition, Chapin (Chapin 1980) showed that simply adding fertilizer to the soil in Alaska could make grasses grow again like they did in the era of the mammoth steppe. Possibly, the extinction of the megafauna and the corresponding loss of dung is what led to low nutrient levels in modern-day soil and therefore is why the landscape can no longer support megafauna.

However, more recent authors have viewed it as more likely that the collapse of the mammoth steppe was driven by climatic warming, which in turn impacted the megafauna, rather than the other way around.

Megafauna play a significant role in the lateral transport of mineral nutrients in an ecosystem, tending to translocate them from areas of high to those of lower abundance. They do so by their movement between the time they consume the nutrient and the time they release it through elimination (or, to a much lesser extent, through decomposition after death). In South America's Amazon Basin, it is estimated that such lateral diffusion was reduced over 98% following the megafaunal extinctions that occurred roughly 12,500 years ago. Given that phosphorus availability is thought to limit productivity in much of the region, the decrease in its transport from the western part of the basin and from floodplains (both of which derive their supply from the uplift of the Andes) to other areas is thought to have significantly impacted the region's ecology, and the effects may not yet have reached their limits. The extinction of the mammoths allowed grasslands they had maintained through grazing habits to become birch forests. The new forest and the resulting forest fires may have induced climate change. Such disappearances might be the result of the proliferation of modern humans.

Large populations of megaherbivores have the potential to contribute greatly to the atmospheric concentration of methane, which is an important greenhouse gas. Modern ruminant herbivores produce methane as a byproduct of foregut fermentation in digestion, and release it through belching or flatulence. Today, around 20% of annual methane emissions come from livestock methane release. In the Mesozoic, it has been estimated that sauropods could have emitted 520 million tons of methane to the atmosphere annually, contributing to the warmer climate of the time (up to 10 °C warmer than at present). This large emission follows from the enormous estimated biomass of sauropods, and because methane production of individual herbivores is believed to be almost proportional to their mass.

Recent studies have indicated that the extinction of megafaunal herbivores may have caused a reduction in atmospheric methane. One study examined the methane emissions from the bison that occupied the Great Plains of North America before contact with European settlers. The study estimated that the removal of the bison caused a decrease of as much as 2.2 million tons per year. Another study examined the change in the methane concentration in the atmosphere at the end of the Pleistocene epoch after the extinction of megafauna in the Americas. After early humans migrated to the Americas about 13,000 BP, their hunting and other associated ecological impacts led to the extinction of many megafaunal species there. Calculations suggest that this extinction decreased methane production by about 9.6 million tons per year. This suggests that the absence of megafaunal methane emissions may have contributed to the abrupt climatic cooling at the onset of the Younger Dryas. The decrease in atmospheric methane that occurred at that time, as recorded in ice cores, was 2–4 times more rapid than any other decrease in the last half million years, suggesting that an unusual mechanism was at work.

The extermination of megafauna left many niches vacant, which has been cited as an explanation for the vulnerability and fragility of many ecosystems to destruction in the later Holocene extinction. The comparative lack of megafauna in modern ecosystems has reduced high-order interactions among surviving species, reducing ecological complexity. This depauperate, post-megafaunal ecological state has been associated with diminished ecological resilience to stressors. Many extant species of plants have adaptations that were advantageous in the presence of megafauna but are now useless in their absence. The demise of megafaunal ecosystem engineers in the Arctic that maintained open grassland environments has been highly detrimental to shorebirds of the genus Numenius.

Relationship to later extinctions

Main article: Holocene extinction See also: Timeline of extinctions in the Holocene

There is no general agreement on where the Quaternary extinction event ends, and the Holocene, or anthropogenic, extinction begins, or if they should be considered separate events at all. Some authors have argued that the activities of earlier archaic humans have also resulted in extinctions, though the evidence for this is equivocal.

This hypothesis is supported by rapid megafaunal extinction following recent human colonisation in Australia, New Zealand and Madagascar, in a similar way that any large, adaptable predator moving into a new ecosystem would. In many cases, it is suggested even minimal hunting pressure was enough to wipe out large fauna, particularly on geographically isolated islands. Only during the most recent parts of the extinction have plants also suffered large losses.

See also

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Quaternary Period
Pleistocene EpochHolocene Epoch
Geological history of Earth
Cenozoic Era
(present–66.0 Ma)
Quaternary (present–2.58 Ma)
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Cretaceous (66.0–145 Ma)
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Neoproterozoic (539 Ma–1 Ga)
Mesoproterozoic (1–1.6 Ga)
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Extinction
Phenomena The species Bufo periglenes (Golden Toad) was last reported in 1989
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