In terrestrial zoology, megafauna (from Greek μέγας megas "large" and New Latin fauna "animal life") are large or giant animals. The most common thresholds used are weight over 40 kilograms (90 lb) or 44 kilograms (100 lb) (i.e., comparable or larger in mass than a human) or over a metric ton, 1,000 kilograms (2,205 lb) (i.e., comparable or larger in mass than an ox). The first of these include many species not popularly thought of as overly large, such as white-tailed deer and red kangaroo.
In practice, the most common usage encountered in academic and popular writing describes land mammals roughly larger than a human that are not (solely) domesticated. The term is especially associated with the Pleistocene megafauna – the land animals often larger than modern counterparts considered archetypical of the last ice age, such as mammoths, the majority of which in northern Eurasia, the Americas and Australia became extinct within the last forty thousand years. It is also commonly used for the largest extant wild land animals, especially elephants, giraffes, hippopotamuses, rhinoceroses, and large bovines. Megafauna may be subcategorized by their trophic position into megaherbivores (e.g., elk), megacarnivores (e.g., lions), and, more rarely, megaomnivores (e.g., bears).
Other common uses are for giant aquatic species, especially whales, any larger wild or domesticated land animals such as larger antelope and cattle, as well as numerous dinosaurs and other extinct giant reptilians.
The term is also sometimes applied to animals (usually extinct) of great size relative to a more common or surviving type of the animal, for example the 1 m (3 ft) dragonflies of the Carboniferous period.
Megafauna – in the sense of the largest mammals and birds – are generally K-strategists, with high longevity, slow population growth rates, low mortality rates, and (at least for the largest) few or no natural predators capable of killing adults. These characteristics, although not exclusive to such megafauna, make them vulnerable to human overexploitation, in part because of their slow population recovery rates.
Evolution of large body size
One observation that has been made about the evolution of larger body size is that rapid rates of increase that are often seen over relatively short time intervals are not sustainable over much longer time periods. In an examination of mammal body mass changes over time, the maximum increase possible in a given time interval was found to scale with the interval length raised to the 0.25 power. This is thought to reflect the emergence, during a trend of increasing maximum body size, of a series of anatomical, physiological, environmental, genetic and other constraints that must be overcome by evolutionary innovations before further size increases are possible. A strikingly faster rate of change was found for large decreases in body mass, such as may be associated with the phenomenon of insular dwarfism. When normalized to generation length, the maximum rate of body mass decrease was found to be over 30 times greater than the maximum rate of body mass increase for a ten-fold change.
In terrestrial mammals
Subsequent to the Cretaceous–Paleogene extinction event that eliminated the non-avian dinosaurs about 66 Ma (million years) ago, terrestrial mammals underwent a nearly exponential increase in body size as they diversified to occupy the ecological niches left vacant. Starting from just a few kg before the event, maximum size had reached ~50 kg a few million years later, and ~750 kg by the end of the Paleocene. This trend of increasing body mass appears to level off about 40 Ma ago (in the late Eocene), suggesting that physiological or ecological constraints had been reached, after an increase in body mass of over three orders of magnitude. However, when considered from the standpoint of rate of size increase per generation, the exponential increase is found to have continued until the appearance of Indricotherium 30 Ma ago. (Since generation time scales with body mass0.259, increasing generation times with increasing size cause the log mass vs. time plot to curve downward from a linear fit.)
Megaherbivores eventually attained a body mass of over 10,000 kg. The largest of these, indricotheres and proboscids, have been hindgut fermenters, which are believed to have an advantage over foregut fermenters in terms of being able to accelerate gastrointestinal transit in order to accommodate very large food intakes. A similar trend emerges when rates of increase of maximum body mass per generation for different mammalian clades are compared (using rates averaged over macroevolutionary time scales). Among terrestrial mammals, the fastest rates of increase of body mass0.259 vs. time (in Ma) occurred in perissodactyls (a slope of 2.1), followed by rodents (1.2) and proboscids (1.1), all of which are hindgut fermenters. The rate of increase for artiodactyls (0.74) was about a third that of perissodactyls. The rate for carnivorans (0.65) was slightly lower yet, while primates, perhaps constrained by their arboreal habits, had the lowest rate (0.39) among the mammalian groups studied.
Terrestrial mammalian carnivores from several eutherian groups (the mesonychid Andrewsarchus, the creodonts Megistotherium and Sarkastodon, and the carnivorans Amphicyon and Arctodus) all reached a maximum size of about 1000 kg (the carnivoran Arctotherium apparently actually got somewhat larger). The largest known metatherian carnivore, Proborhyaena gigantea, apparently reached 600 kg, also close to this limit. A similar theoretical maximum size for mammalian carnivores has been predicted based on the metabolic rate of mammals, the energetic cost of obtaining prey, and the maximum estimated rate coefficient of prey intake. It has also been suggested that maximum size for mammalian carnivores is constrained by the stress the humerus can withstand at top running speed.
Analysis of the variation of maximum body size over the last 40 Ma suggests that decreasing temperature and increasing continental land area are associated with increasing maximum body size. The former correlation would be consistent with Bergmann's rule, and might be related to the thermoregulatory advantage of large body mass in cool climates, better ability of larger organisms to cope with seasonality in food supply, or other factors; the latter correlation could be explained in terms of range and resource limitations. However, the two parameters are interrelated (due to sea level drops accompanying increased glaciation), making the driver of the trends in maximum size more difficult to identify.
In marine mammals
Since tetrapods (first reptiles, later mammals) returned to the sea in the Late Permian, they have dominated the top end of the marine body size range, due to the more efficient intake of oxygen possible using lungs. The ancestors of cetaceans are believed to have been the semiaquatic pakicetids, no larger than wolves, of about 53 million years (Ma) ago. By 40 Ma ago, cetaceans had attained a length of 20 m or more in Basilosaurus, an elongated, serpentine whale that differed from modern whales in many respects and was not ancestral to them. Following this, the evolution of large body size in cetaceans appears to have come to a temporary halt, and then to have backtracked, although the available fossil records are limited. However, in the period from 31 Ma ago (in the Oligocene) to the present, cetaceans underwent a significantly more rapid sustained increase in body mass (a rate of increase in body mass0.259 of a factor of 3.2 per million years) than achieved by any group of terrestrial mammals. This trend led to the largest animal of all time, the modern blue whale. Several reasons for the more rapid evolution of large body size in cetaceans are possible. Fewer biomechanical constraints on increases in body size may be associated with suspension in water as opposed to standing against the force of gravity, and with swimming movements as opposed to terrestrial locomotion. Also, the greater heat capacity and thermal conductivity of water compared to air may increase the thermoregulatory advantage of large body size in marine endotherms, although diminishing returns apply.
Cetaceans are not the only marine mammals to reach unprecedented size in the modern era. The largest carnivoran of all time is the mostly aquatic modern southern elephant seal.
In flightless birds
Because of the small initial size of all mammals following the extinction of the dinosaurs, nonmammalian vertebrates had a roughly ten-million-year-long window of opportunity (during the Paleocene) for evolution of gigantism without much competition. During this interval, apex predator niches were often occupied by reptiles, such as terrestrial crocodilians (e.g. Pristichampsus), large snakes (e.g. Titanoboa) or varanid lizards, or by flightless birds (e.g. Paleopsilopterus in South America). This is also the period when megafaunal flightless herbivorous gastornithid birds evolved in the Northern Hemisphere, while flightless paleognaths evolved to large size on Gondwanan land masses and Europe. Gastornithids and at least one lineage of flightless paleognath birds originated in Europe, both lineages dominating niches for large herbivores while mammals remained below 45 kg (in contrast with other landmasses like North America and Asia, which saw the earlier evolution of larger mammals) and were the largest European tetrapods in the Paleocene.
Flightless paleognaths, termed ratites, have traditionally been viewed as representing a lineage separate from that of their small flighted relatives, the Neotropic tinamous. However, recent genetic studies have found that tinamous nest well within the ratite tree, and are the sister group of the extinct moa of New Zealand. Similarly, the small kiwi of New Zealand have been found to be the sister group of the extinct elephant birds of Madagascar. These findings indicate that flightlessness and gigantism arose independently multiple times among ratites via parallel evolution.
Predatory megafaunal flightless birds were often able to compete with mammals in the early Cenozoic. Later in the Cenozoic, however, they were displaced by advanced carnivorans and died out. In North America, the bathornithids Paracrax and Bathornis were apex predators but became extinct by the Early Miocene. In South America, the related phorusrhacids shared the dominant predatory niches with metatherian sparassodonts during most of the Cenozoic but declined and ultimately went extinct after eutherian predators arrived from North America (as part of the Great American Interchange) during the Pliocene. In contrast, large herbivorous flightless ratites have survived to the present.
However, none of the largest predatory (Brontornis), possibly omnivorous (Dromornis) or herbivorous (Aepyornis) flightless birds of the Cenozoic ever grew to masses much above 500 kg, and thus never attained the size of the largest mammalian carnivores, let alone that of the largest mammalian herbivores. It has been suggested that the increasing thickness of avian eggshells in proportion to egg mass with increasing egg size places an upper limit on the size of birds.[note 1] The largest species of Dromornis, D. stirtoni, may have gone extinct after it attained the maximum avian body mass and was then outcompeted by marsupial diprotodonts that evolved to sizes several times larger.
In giant turtles
Giant tortoises were very important components of late Cenozoic faunas, occurring in virtually every continent until the arrival of homininans. The largest known terrestrial tortoise was Megalochelys atlas, an animal that probably weighed about 1,000 kg.
Some earlier aquatic Testudines, e.g. the marine Archelon of the Cretaceous and freshwater Stupendemys of the Miocene, were considerably larger, weighing more than 2,000 kg.
Megafaunal mass extinctions
Timing and possible causes
The Holocene extinction (see also Quaternary extinction event), occurred at the end of the last ice age glacial period (a.k.a. the Würm glaciation) when many giant ice age mammals, such as woolly mammoths, went extinct in the Americas and northern Eurasia. An analysis of the extinction event in North America found it to be unique among Cenozoic extinction pulses in its selectivity for large animals.(Fig. 10) Various theories have attributed the wave of extinctions to human hunting, climate change, disease, a putative extraterrestrial impact, or other causes. However, this extinction near the end of the Pleistocene was just one of a series of megafaunal extinction pulses that have occurred during the last 50,000 years over much of the Earth's surface, with Africa and southern Asia (where the local megafauna had a chance to evolve alongside modern humans) being comparatively less affected. The latter areas did suffer a gradual attrition of megafauna, particularly of the slower-moving species (a class of vulnerable megafauna epitomized by giant tortoises), over the last several million years.
Outside the mainland of Afro-Eurasia, these megafaunal extinctions followed a highly distinctive landmass-by-landmass pattern that closely parallels the spread of humans into previously uninhabited regions of the world, and which shows no overall correlation with climatic history (which can be visualized with plots over recent geological time periods of climate markers such as marine oxygen isotopes or atmospheric carbon dioxide levels). Australia and nearby islands (e.g., Flores) were struck first around 46,000 years ago, followed by Tasmania about 41,000 years ago (after formation of a land bridge to Australia about 43,000 years ago), Japan apparently about 30,000 years ago, North America 13,000 years ago,[note 2] South America about 500 years later, Cyprus 10,000 years ago, the Antilles 6,000 years ago, New Caledonia and nearby islands 3,000 years ago, Madagascar 2,000 years ago, New Zealand 700 years ago, the Mascarenes 400 years ago, and the Commander Islands 250 years ago. Nearly all of the world's isolated islands could furnish similar examples of extinctions occurring shortly after the arrival of humans, though most of these islands, such as the Hawaiian Islands, never had terrestrial megafauna, so their extinct fauna were smaller.
An analysis of the timing of Holarctic megafaunal extinctions and extirpations over the last 56,000 years has revealed a tendency for such events to cluster within interstadials, periods of abrupt warming, but only when humans were also present. Humans may have impeded processes of migration and recolonization that would otherwise have allowed the megafaunal species to adapt to the climate shift. In at least some areas, interstadials were periods of expanding human populations.
An analysis of Sporormiella fungal spores (which derive mainly from the dung of megaherbivores) in swamp sediment cores spanning the last 130,000 years from Lynch's Crater in Queensland, Australia, showed that the megafauna of that region virtually disappeared about 41,000 years ago, at a time when climate changes were minimal; the change was accompanied by an increase in charcoal, and was followed by a transition from rainforest to fire-tolerant sclerophyll vegetation. The high-resolution chronology of the changes supports the hypothesis that human hunting alone eliminated the megafauna, and that the subsequent change in flora was most likely a consequence of the elimination of browsers and an increase in fire. The increase in fire lagged the disappearance of megafauna by about a century, and most likely resulted from accumulation of fuel once browsing stopped. Over the next several centuries grass increased; sclerophyll vegetation increased with a lag of another century, and a sclerophyll forest developed after about another thousand years. During two periods of climate change about 120,000 and 75,000 years ago, sclerophyll vegetation had also increased at the site in response to a shift to cooler, drier conditions; neither of these episodes had a significant impact on megafaunal abundance. Similar conclusions regarding the culpability of human hunters in the disappearance of Pleistocene megafauna were derived from high-resolution chronologies obtained via an analysis of a large collection of eggshell fragments of the flightless Australian bird Genyornis newtoni, from analysis of Sporormiella fungal spores from a lake in eastern North America and from study of deposits of Shasta ground sloth dung left in over half a dozen caves in the American southwest.
Continuing human hunting and environmental disturbance has led to additional megafaunal extinctions in the recent past, and has created a serious danger of further extinctions in the near future (see examples below).
A number of other mass extinctions occurred earlier in Earth's geologic history, in which some or all of the megafauna of the time also died out. Famously, in the Cretaceous–Paleogene extinction event the non-avian dinosaurs and most other giant reptilians were eliminated. However, the earlier mass extinctions were more global and not so selective for megafauna; i.e., many species of other types, including plants, marine invertebrates and plankton, went extinct as well. Thus, the earlier events must have been caused by more generalized types of disturbances to the biosphere.
Consequences of depletion of megafauna
Effect on nutrient transport
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.
Effect on methane emissions
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. This hypothesis is relatively new. 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 following are some notable examples of animals often considered as megafauna (in the sense of the "large animal" definition). This list is not intended to be exhaustive:
- Clade Synapsida
- Class Mammalia (phylogenetically, a clade within Therapsida; see below)
- Infraclass Metatheria
- Order Diprotodontia
- The red kangaroo (Macropus rufus) is the largest living Australian mammal and marsupial at a weight of up to 85 kg (187 lb). However, its extinct relative, the giant short-faced kangaroo Procoptodon goliah reached 230 kg (510 lb), while extinct diprotodonts attained the largest size of any marsupial in history, up to an estimated 2,750 kg (6,060 lb). The extinct marsupial lion (Thylacleo carnifex), at up to 160 kg (350 lb) was much larger than any extant carnivorous marsupial.
- Infraclass Eutheria
- Superorder Afrotheria
- Order Proboscidea
- Elephants are the largest living land animals. They and their relatives arose in Africa, but until recently had a nearly worldwide distribution. The African bush elephant (Loxodonta africana) has a shoulder height of up to 4.3 m (14 ft) and weighs up to 13 tons. Among recently extinct proboscideans, mammoths (Mammuthus) were close relatives of elephants, while mastodons (Mammut) were much more distantly related. The steppe mammoth (M. trogontherii) is estimated to have commonly weighed around 10 tonnes, making it possibly the largest proboscid, which would make it the second largest land mammal after indricotherines.
- Order Sirenia
- The largest sirenian at up to 1,500 kg (3,300 lb) is the West Indian manatee (Trichechus manatus). Steller's sea cow (Hydrodamalis gigas) was probably around five times as massive, but was exterminated by humans within 27 years of its discovery off the remote Commander Islands in 1741. In prehistoric times this sea cow also lived along the coasts of northeastern Asia and northwestern North America; it was apparently eliminated from these more accessible locations by aboriginal hunters.
- Superorder Xenarthra
- Superorder Euarchontoglires
- Order Primates
- Order Rodentia
- The extant capybara (Hydrochoerus hydrochaeris) of South America, the largest living rodent, weighs up to 65 kg (143 lb). Several recently extinct North American forms were larger: the capybara Neochoerus pinckneyi (another neotropic migrant) was about 40% heavier; the giant beaver (Castoroides ohioensis) was similar. The extinct blunt-toothed giant hutia (Amblyrhiza inundata) of several Caribbean islands may have been larger still. However, several million years ago South America harbored much more massive rodents. Phoberomys pattersoni, known from a nearly full skeleton, probably reached 700 kg (1,500 lb). Fragmentary remains suggest that Josephoartigasia monesi grew to upwards of 1,000 kg (2,200 lb).
- Superorder Laurasiatheria
- Order Carnivora
- Big cats include the tiger (Panthera tigris) and lion (Panthera leo). According to Bergmann's rule, the Siberian tiger (P. t. tigris) should be the biggest tiger and wild felid, but this is disputable.[note 3] Members of Panthera are distinguished by morphological features which enable them to roar. Larger extinct felids include the American lion (P. leo atrox or P. atrox) and the South American saber-toothed cat (Smilodon populator).
- Bears are large carnivorans of the caniform suborder. The largest living forms are the polar bear (Ursus maritimus), with a body weight of up to 680 kg (1,500 lb), and the similarly sized Kodiak bear (Ursus arctos middendorffi), again consistent with Bergmann's rule. Arctotherium augustans, an extinct short-faced bear from South America, was the largest predatory land mammal ever with an estimated average weight of 1,600 kg (3,500 lb).
- Seals, sea lions, and walruses are amphibious marine carnivorans that evolved from bearlike ancestors. The southern elephant seal (Mirounga leonina) of Antarctic and subantarctic waters is the largest carnivoran of all time, with bull males reaching a maximum length of 6–7 m (20–23 ft) and maximum weight of 5,000 kg (11,000 lb).
- Order Perissodactyla
- Tapirs are browsing animals, with a short prehensile snout and pig-like form that appears to have changed little in 20 million years. They inhabit tropical forests of Southeast Asia and South and Central America, and include the largest surviving land animals of the latter two regions. There are four species.
- Rhinoceroses are odd-toed ungulates with horns made of keratin, the same type of protein composing hair. They are among the second-largest living land mammals at 850-3,800 kg. Three of five extant species are critically endangered. Their extinct central Asian relatives the indricotherines were the largest terrestrial mammals of all time.
- Order Artiodactyla
- Giraffes (Giraffa spp.) are the tallest living land animals, reaching heights of up to nearly 6 m (20 ft). The average weight is 1,192 kg (2,628 lb) for an adult male and 828 kg (1,825 lb) for an adult female with maximum weights of 1,930 kg (4,250 lb) and 1,180 kg (2,600 lb) recorded for males and females, respectively.
- Bovine ungulates include the largest surviving land animals of Europe and North America. The water buffalo (Bubalis arnee), bison (Bison bison and B. bonasus), and gaur (Bos gaurus) can all grow to weights of over 900 kg (2,000 lb).
- The semiaquatic hippopotamus (Hippopotamus amphibius) is the heaviest living even-toed ungulate, mean adult weight is around 1,500 kg (3,300 lb) and 1,300 kg (2,900 lb) for males and females respectively. It and the critically endangered pygmy hippo (Choeropsis liberiensis) are believed to be the closest extant relatives of cetaceans. Hippos are among the megafaunal species most dangerous to humans.
- Infraorder Cetacea
- Order Pelycosauria (traditional; paraphyletic)
- Order Therapsida
- Clade Sauropsida
- Class Aves (phylogenetically, a clade within Coelurosauria, a taxon within the order Saurischia; see below)
- Class Reptilia (traditional; paraphyletic)
- Order Crocodilia
- Alligators and crocodiles are large semiaquatic reptiles, the largest of which, the saltwater crocodile (Crocodylus porosus), can grow to a weight of 1,360 kg (3,000 lb). Crocodilians' distant ancestors and their kin, the pseudosuchians (traditional crurotarsans), dominated the world in the late Triassic, until the Triassic–Jurassic extinction event allowed dinosaurs to overtake them. They remained diverse during the later Mesozoic, when crocodyliforms such as Deinosuchus and Sarcosuchus reached lengths of 12 m. Similarly large crocodilians, such as Mourasuchus and Purussaurus, were present as recently as the Miocene in South America.
- Order Saurischia
- Order Squamata
- While the largest extant lizard, the Komodo dragon (Varanus komodoensis), another island giant, can reach 3 m (10 ft) in length, its extinct Australian relative Megalania may have reached more than twice that size. These monitor lizards' marine relatives, the mosasaurs, were apex predators in late Cretaceous seas.
- The heaviest extant snake is considered to be the green anaconda (Eunectes murinus), while the reticulated python (Python reticulatus), at up to 8.7 m or more, is considered the longest. An extinct Australian Pliocene species of Liasis, the Bluff Downs giant python, reached 10 m, while the Paleocene Titanoboa of South America reached lengths of 12–15 m and an estimated weight of about 1,135 kilograms (2,500 pounds).
- Order Testudines
- Class Amphibia (in the wide, probably paraphyletic, sense)
- Order Temnospondyli (relationship to extant amphibians is unclear)
- The Permian temnospondyl Prionosuchus, the largest amphibian known, reached 9 m in length and was an aquatic predator resembling a crocodilian. After the appearance of real crocodilians, temnospondyls such as Koolasuchus (5 m long) had retreated to the Antarctic region by the Cretaceous, before going extinct.
- Class Actinopterygii
- Class Chondrichthyes
- Order Lamniformes
- The largest living predatory fish, the great white shark (Carcharodon carcharias), reaches weights up to 2,240 kg (4,940 lb). Its extinct relative C. megalodon (the disputed genus being either Carcharodon or Carcharocles) was more than an order of magnitude larger, and is the largest predatory shark or fish of all time (and possibly the largest predator in vertebrate history); it preyed on whales and other marine mammals.
- Order Orectolobiformes
- Order Rajiformes
- The manta ray (Manta birostris) is another filter feeder and the largest ray, growing to up to 2300 kg.
- Class Placodermi
- Class Cephalopoda
- Order Teuthida
- A number of deep ocean creatures exhibit abyssal gigantism. These include the giant squid (Architeuthis) and colossal squid (Mesonychoteuthis hamiltoni); both (although rarely seen) are believed to attain lengths of 12 m (39 ft) or more. The latter is the world's largest invertebrate, and has the largest eyes of any animal. Both are preyed upon by sperm whales.
- Stem-group Arthropoda
- Order Radiodonta
- Order Eurypterida
- Eurypterids (sea scorpions) were a diverse group of aquatic and possibly amphibious predators that included the most massive arthropods to have existed. They survived over 200 million years, but finally died out in the Permian–Triassic extinction event along with trilobites and most other forms of life present at the time, including most of the dominant terrestrial therapsids. The Early Devonian Jaekelopterus reached an estimated length of 2.5 m (8.2 ft), not including its raptorial chelicerae, and is thought to have been a freshwater species.
Indricotheres, the land mammals closest to sauropods in size and lifestyle, were Asian rhinos.
Hippo-sized Diprotodon of Australia, the largest marsupial of all time, became extinct 40,000 years ago.
Megalania, a giant carnivorous goanna of Australia, might have grown to 7 metres long.
The manta, a filter feeder, is the largest ray at up to 7.6 m across, yet can breach clear of the water.
- ^ Nonavian dinosaur size was not similarly constrained because they had a different relationship between body mass and egg size than birds. The 400 kg Aepyornis had larger eggs than nearly all dinosaurs.
- ^ Analysis indicates that 35 genera of North American mammals went extinct more or less simultaneously in this event.
- ^ Siberian tigers do tend to be the largest of tigers in captivity; historically, those in the wild have declined in size, and they are now smaller than Bengal tigers.
- ^ Perspective makes the fish appear larger relative to the man standing behind it (another example of a megafaunal species) than it actually is.
- ^ a b c d Stuart, A. J. (November 1991). "Mammalian extinctions in the Late Pleistocene of northern Eurasia and North America". Biological Reviews. Wiley. 66 (4): 453–562. doi:10.1111/j.1469-185X.1991.tb01149.x. PMID 1801948.
- ^ Martin, P. S. (1984). "Prehistoric overkill: The global model". In Martin, P. S.; Klein, R. G. Quaternary Extinctions: A Prehistoric Revolution. University of Arizona Press. pp. 354–403. ISBN 978-0-8165-1100-6. OCLC 258362030.
- ^ Martin, P. S.; Steadman, D. W. (1999-06-30). "Prehistoric extinctions on islands and continents". In MacPhee, R. D. E. Extinctions in near time: causes, contexts and consequences. Advances in Vertebrate Paleobiology. 2. New York: Kluwer/Plenum. pp. 17–56. ISBN 978-0-306-46092-0. OCLC 41368299. Retrieved 2011-08-23. see page 17
- ^ Richard A. Farina, Sergio F. Vizcaino, Gerry De Iuliis (2013). "The Great American Biotic Interchange". Megafauna: Giant Beasts of Pleistocene South America. Indiana University Press, Bloomington, Indiana. p. 150. ISBN 978-0-253-00230-3.
- ^ Bernhard A. Huber, Bradley J. Sinclair, Karl-Heinz Lampe (2005). "Historical Determinants of Mammal Species in Africa". African Biodiversity: Molecules, Organisms, Ecosystems. Springer. p. 294. ISBN 0387243151.
- ^ Ice Age Animals. Illinois State Museum
- ^ [www.britannica.com]. Britannica. Retrieved 2017-4-2.
- ^ Barnosky, A. D. (2004-10-01). "Assessing the Causes of Late Pleistocene Extinctions on the Continents". Science. 306 (5693): 70–75. doi:10.1126/science.1101476. PMID 15459379.
- ^ Brook, B. W.; Johnson, C. N. (2006). "Selective hunting of juveniles as a cause of the imperceptible overkill of the Australian Pleistocene megafauna". Alcheringa: An Australasian Journal of Palaeontology. 30 (sup1): 39–48. doi:10.1080/03115510609506854.
- ^ a b c d e f g Evans, A. R.; Jones, D.; Boyer, A. G.; Brown, J. H.; Costa, D. P.; Ernest, S. K. M.; Fitzgerald, E. M. G.; Fortelius, M.; Gittleman, J. L.; Hamilton, M. J.; Harding, L. E.; Lintulaakso, K.; Lyons, S. K.; Okie, J. G.; Saarinen, J. J.; Sibly, R. M.; Smith, F. A.; Stephens, P. R.; Theodor, J. M.; Uhen, M. D. (2012-01-30). "The maximum rate of mammal evolution". PNAS. 109 (11): 4187–4190. doi:10.1073/pnas.1120774109. Retrieved 2011-02-11.
- ^ a b c d e f g Smith, F. A.; Boyer, A. G.; Brown, J. H.; Costa, D. P.; Dayan, T.; Ernest, S. K. M.; Evans, A. R.; Fortelius, M.; Gittleman, J. L.; Hamilton, M. J.; Harding, L. E.; Lintulaakso, K.; Lyons, S. K.; McCain, C.; Okie, J. G.; Saarinen, J. J.; Sibly, R. M.; Stephens, P. R.; Theodor, J.; Uhen, M. D. (2010-11-26). "The Evolution of Maximum Body Size of Terrestrial Mammals". Science. 330 (6008): 1216–1219. Bibcode:2010Sci...330.1216S. doi:10.1126/science.1194830. Retrieved 2012-01-07.
- ^ Clauss, M.; Frey, R.; Kiefer, B.; Lechner-Doll, M.; Loehlein, W.; Polster, C.; Roessner, G. E.; Streich, W. J. (2003-04-24). "The maximum attainable body size of herbivorous mammals: morphophysiological constraints on foregut, and adaptations of hindgut fermenters". Oecologia. 136 (1): 14–27. doi:10.1007/s00442-003-1254-z. PMID 12712314. Retrieved 2012-01-08.
- ^ a b Sorkin, B. (2008-04-10). "A biomechanical constraint on body mass in terrestrial mammalian predators". Lethaia. 41 (4): 333–347. doi:10.1111/j.1502-3931.2007.00091.x. Retrieved 2011-08-02.
- ^ Carbone, C.; Teacher, A; Rowcliffe, J. M. (2007-01-16). "The Costs of Carnivory". PLoS Biology. 5 (2, e22): 363–368. doi:10.1371/journal.pbio.0050022. PMC 1769424 . PMID 17227145. Retrieved 2012-01-08.
- ^ a b c Ashton, K. G.; Tracy, M. C.; de Queiroz, A. (October 2000). "Is Bergmann's Rule Valid for Mammals?". The American Naturalist. 156 (4): 390–415. doi:10.1086/303400. JSTOR 10.1086/303400.
- ^ Webb, J. (2015-02-19). "Evolution 'favours bigger sea creatures'". BBC. Retrieved 2015-02-22.
- ^ Heim, N. A.; Knope, M. L.; Schaal, E. K.; Wang, S. C.; Payne, J. L. (2015-02-20). "Cope's rule in the evolution of marine animals". Science. 347 (6224): 867–870. doi:10.1126/science.1260065. PMID 25700517. Retrieved 2015-02-20.
- ^ Thewissen, J. G. M.; Bajpai, S. (1 January 2001). "Whale Origins as a Poster Child for Macroevolution". BioScience. 51 (12): 1037–1049. doi:10.1641/0006-3568(2001)051[1037:WOAAPC]2.0.CO;2. ISSN 0006-3568.
- ^ a b c Mitchell, K. J.; Llamas, B.; Soubrier, J.; Rawlence, N. J.; Worthy, T. H.; Wood, J.; Lee, M. S. Y.; Cooper, A. (2014-05-23). "Ancient DNA reveals elephant birds and kiwi are sister taxa and clarifies ratite bird evolution". Science. 344 (6186): 898–900. doi:10.1126/science.1251981. PMID 24855267.
- ^ Buffetaut, E.; Angst, D. (November 2014). "Stratigraphic distribution of large flightless birds in the Palaeogene of Europe and its palaeobiological and palaeogeographical implications". Earth-Science Reviews. 138: 394–408. doi:10.1016/j.earscirev.2014.07.001.
- ^ Phillips MJ, Gibb GC, Crimp EA, Penny D (January 2010). "Tinamous and moa flock together: mitochondrial genome sequence analysis reveals independent losses of flight among ratites". Systematic Biology. 59 (1): 90–107. doi:10.1093/sysbio/syp079. PMID 20525622.
- ^ Baker, A. J.; Haddrath, O.; McPherson, J. D.; Cloutier, A. (2014). "Genomic Support for a Moa-Tinamou Clade and Adaptive Morphological Convergence in Flightless Ratites". Molecular Biology and Evolution. 31: 1686–1696. doi:10.1093/molbev/msu153. PMID 24825849.
- ^ Murray, Peter F.; Vickers-Rich, Patricia (2004). Magnificent Mihirungs: The Colossal Flightless Birds of the Australian Dreamtime. Indiana University Press. pp. 51, 314. ISBN 978-0-253-34282-9. Retrieved 7 January 2012.
- ^ Ibid. p. 212.
- ^ Kenneth Carpenter (1999). Eggs, Nests, and Baby Dinosaurs: A Look at Dinosaur Reproduction. Indiana University Press. ISBN 978-0-253-33497-8. OCLC 42009424. Retrieved 6 May 2013.
- ^ Jackson, F. D.; Varricchio, D. J.; Jackson, R. A.; Vila, B.; Chiappe, L. M. (2008). "Comparison of water vapor conductance in a titanosaur egg from the Upper Cretaceous of Argentina and a Megaloolithus siruguei egg from Spain". Paleobiology. 34 (2): 229–246. doi:10.1666/0094-8373(2008)034[0229:COWVCI]2.0.CO;2. ISSN 0094-8373.
- ^ Ibid. p. 277.
- ^ a b c Hansen, D. M.; Donlan, C. J.; Griffiths, C. J.; Campbell, K. J. (April 2010). "Ecological history and latent conservation potential: large and giant tortoises as a model for taxon substitutions" (PDF). Ecography. Wiley. 33 (2): 272–284. doi:10.1111/j.1600-0587.2010.06305.x. Archived from the original (PDF) on July 24, 2011. Retrieved 2011-02-26.
- ^ a b Cione, A. L.; Tonni, E. P.; Soibelzon, L. (2003). "The Broken Zig-Zag: Late Cenozoic large mammal and tortoise extinction in South America" (PDF). Rev. Mus. Argentino Cienc. Nat., n.s. 5 (1): 1–19. ISSN 1514-5158. Archived from the original (PDF) on July 6, 2011. Retrieved 2011-02-06.
- ^ Alroy, J. (1999), "Putting North America's End-Pleistocene Megafaunal Extinction in Context: Large-Scale Analyses of Spatial Patterns, Extinction Rates, and Size Distributions", in MacPhee, R. D. E., Extinctions in Near Time: Causes, Contexts, and Consequences, Advances in Vertebrate Paleobiology, 2, New York: Plenum, pp. 105–143, doi:10.1007/978-1-4757-5202-1_6, ISBN 978-1-4757-5202-1, OCLC 41368299
- ^ Corlett, R. T. (2006). "Megafaunal extinctions in tropical Asia" (PDF). Tropinet. 17 (3): 1–3. Retrieved 2010-10-04.
- ^ Edmeades, Baz. "Megafauna — First Victims of the Human-Caused Extinction". (internet-published book with Foreword by Paul S. Martin). Retrieved 2010-10-04.
- ^ a b Martin, P. S. (2005). "Chapter 6. Deadly Syncopation". Twilight of the Mammoths: Ice Age Extinctions and the Rewilding of America. University of California Press. pp. 118–128. ISBN 0-520-23141-4. OCLC 58055404. Retrieved 2014-11-11.
- ^ a b Burney, D. A.; Flannery, T. F. (July 2005). "Fifty millennia of catastrophic extinctions after human contact" (PDF). Trends in Ecology & Evolution. Elsevier. 20 (7): 395–401. doi:10.1016/j.tree.2005.04.022. PMID 16701402. Archived from the original (PDF) on 2010-06-10. Retrieved 2014-11-11.
- ^ Roberts, R. G.; Flannery, T. F.; Ayliffe, L. K.; Yoshida, H.; Olley, J. M.; Prideaux, G. J.; Laslett, G. M.; Baynes, A.; Smith, M. A.; Jones, R.; Smith, B. L. (2001-06-08). "New Ages for the Last Australian Megafauna: Continent-Wide Extinction About 46,000 Years Ago" (PDF). Science. 292 (5523): 1888–1892. Bibcode:2001Sci...292.1888R. doi:10.1126/science.1060264. PMID 11397939. Retrieved 2011-08-26.
- ^ Callaway, E. (2016-09-21). "Human remains found in hobbit cave". Nature. doi:10.1038/nature.2016.20656.
- ^ Diamond, Jared (2008-08-13). "Palaeontology: The last giant kangaroo". Nature. 454 (7206): 835–836. Bibcode:2008Natur.454..835D. doi:10.1038/454835a. PMID 18704074. Retrieved 2011-05-08.
- ^ Turney, C. S. M.; Flannery, T. F.; Roberts, R. G.; Reid, C.; Fifield, L. K.; Higham, T. F. G.; Jacobs, Z.; Kemp, N.; Colhoun, E. A.; Kalin, R. M.; Ogle, N. (2008-08-21). "Late-surviving megafauna in Tasmania, Australia, implicate human involvement in their extinction". PNAS. NAS. 105 (34): 12150–12153. Bibcode:2008PNAS..10512150T. doi:10.1073/pnas.0801360105. PMC 2527880 . PMID 18719103. Retrieved 2011-05-08.
- ^ Roberts, R.; Jacobs, Z. (October 2008). "The Lost Giants of Tasmania" (PDF). Australasian Science. 29 (9): 14–17. Archived from the original (PDF) on 2011-09-27. Retrieved 2011-08-26.
- ^ Norton, C. J.; Kondo, Y.; Ono, A.; Zhang, Y.; Diab, M. C. (2009-05-23). "The nature of megafaunal extinctions during the MIS 3–2 transition in Japan". Quaternary International. 211 (1–2): 113–122. Bibcode:2010QuInt.211..113N. doi:10.1016/j.quaint.2009.05.002. Retrieved 2011-08-30.
- ^ Faith, J. T.; Surovell, T. A. (2009-12-08). "Synchronous extinction of North America's Pleistocene mammals". Proceedings of the National Academy of Sciences. 106 (49): 20641–20645. doi:10.1073/pnas.0908153106. PMC 2791611 . PMID 19934040.
- ^ Haynes, Gary (2009). "Introduction to the Volume". In Haynes, Gary. American Megafaunal Extinctions at the End of the Pleistocene. Springer. pp. 1–20. doi:10.1007/978-1-4020-8793-6_1. ISBN 978-1-4020-8792-9.
- ^ Fiedel, Stuart (2009). "Sudden Deaths: The Chronology of Terminal Pleistocene Megafaunal Extinction". In Haynes, Gary. American Megafaunal Extinctions at the End of the Pleistocene. Springer. pp. 21–37. doi:10.1007/978-1-4020-8793-6_2. ISBN 978-1-4020-8792-9.
- ^ Simmons, A. H. (1999). Faunal extinction in an island society: pygmy hippopotamus hunters of Cyprus. Interdisciplinary Contributions to Archaeology. Kluwer Academic/Plenum Publishers. p. 382. doi:10.1007/b109876. ISBN 978-0-306-46088-3. OCLC 41712246.
- ^ Simmons, A. H.; Mandel, R. D. (December 2007). "Not Such a New Light: A Response to Ammerman and Noller". World Archaeology. 39 (4): 475–482. doi:10.1080/00438240701676169. JSTOR 40026143.
- ^ Steadman, D. W.; Martin, P. S.; MacPhee, R. D. E.; Jull, A. J. T.; McDonald, H. G.; Woods, C. A.; Iturralde-Vinent, M.; Hodgins, G. W. L. (2005-08-16). "Asynchronous extinction of late Quaternary sloths on continents and islands". Proc. Natl. Acad. Sci. USA. National Academy of Sciences. 102 (33): 11763–11768. Bibcode:2005PNAS..10211763S. doi:10.1073/pnas.0502777102. PMC 1187974 . PMID 16085711.
- ^ Cooke, S. B.; Dávalos, L. M.; Mychajliw, A. M.; Turvey, S. T.; Upham, N. S. (2017). "Anthropogenic Extinction Dominates Holocene Declines of West Indian Mammals". Annual Review of Ecology, Evolution, and Systematics. 48 (1): 301–327. doi:10.1146/annurev-ecolsys-110316-022754.
- ^ Anderson, A.; Sand, C.; Petchey, F.; Worthy, T. H. (2010). "Faunal extinction and human habitation in New Caledonia: Initial results and implications of new research at the Pindai Caves". Journal of Pacific Archaeology. 1 (1): 89–109. hdl:10289/5404.
- ^ White, A. W.; Worthy, T. H.; Hawkins, S.; Bedford, S.; Spriggs, M. (2010-08-16). "Megafaunal meiolaniid horned turtles survived until early human settlement in Vanuatu, Southwest Pacific". Proc. Natl. Acad. Sci. USA. 107 (35): 15512–15516. Bibcode:2010PNAS..10715512W. doi:10.1073/pnas.1005780107. PMC 2932593 . PMID 20713711.
- ^ Burney, D. A.; Burney, L. P.; Godfrey, L. R.; Jungers, W. L.; Goodman, S. M.; Wright, H. T.; Jull. A. J. T. (July 2004). "A chronology for late prehistoric Madagascar". Journal of Human Evolution. 47 (1–2): 25–63. doi:10.1016/j.jhevol.2004.05.005. PMID 15288523. Retrieved 2011-08-30.
- ^ Holdaway, R. N.; Jacomb, C. (2000-03-24). "Rapid Extinction of the Moas (Aves: Dinornithiformes): Model, Test, and Implications". Science. 287 (5461): 2250–2254. Bibcode:2000Sci...287.2250H. doi:10.1126/science.287.5461.2250. PMID 10731144. Retrieved 2011-08-30.
- ^ Janoo, A. (April 2005). "Discovery of isolated dodo bones (Raphus cucullatus (L.), Aves, Columbiformes) from Mauritius cave shelters highlights human predation, with a comment on the status of the family Raphidae Wetmore, 1930". Annales de Paléontologie. 91 (2): 167–180. doi:10.1016/j.annpal.2004.12.002. Retrieved 2011-08-30.
- ^ Anderson, P. K. (July 1995). "Competition, Predation, and the Evolution and Extinction of Steller's Sea Cow, Hydrodamalis gigas". Marine Mammal Science. Society for Marine Mammalogy. 11 (3): 391–394. doi:10.1111/j.1748-7692.1995.tb00294.x. Retrieved 2011-08-30.
- ^ Cooper, A.; Turney, C.; Hughen, K. A.; Brook, B. W.; McDonald, H. G.; Bradshaw, C. J. A. (2015-07-23). "Abrupt warming events drove Late Pleistocene Holarctic megafaunal turnover". Science. 349: 602–6. doi:10.1126/science.aac4315. PMID 26250679.
- ^ Müller, U. C.; Pross, J.; Tzedakis, P. C.; Gamble, C.; Kotthoff, U.; Schmiedl, G.; Wulf, S.; Christanis, K. (February 2011). "The role of climate in the spread of modern humans into Europe". Quaternary Science Reviews. 30 (3–4): 273–279. doi:10.1016/j.quascirev.2010.11.016.
- ^ Biello, D. (2012-03-22). "Big Kill, Not Big Chill, Finished Off Giant Kangaroos". Scientific American news. Retrieved 2012-03-25.
- ^ McGlone, M. (2012-03-23). "The Hunters Did It". Science. 335 (6075): 1452–1453. Bibcode:2012Sci...335.1452M. doi:10.1126/science.1220176. Retrieved 2012-03-25.
- ^ a b c Rule, S.; Brook, B. W.; Haberle, S. G.; Turney, C. S. M.; Kershaw, A. P. (2012-03-23). "The Aftermath of Megafaunal Extinction: Ecosystem Transformation in Pleistocene Australia". Science. 335 (6075): 1483–1486. Bibcode:2012Sci...335.1483R. doi:10.1126/science.1214261. PMID 22442481. Retrieved 2012-03-25.
- ^ a b Johnson, C. N.; Alroy, J.; Beeton, N. J.; Bird, M. I.; Brook, B. W.; Cooper, A.; Gillespie, R.; Herrando-Pérez, S.; Jacobs, Z.; Miller, G. H.; Prideaux, G. J.; Roberts, R. G.; Rodríguez-Rey, M.; Saltré, F.; Turney, C. S. M.; Bradshaw, C. J. A. (10 February 2016). "What caused extinction of the Pleistocene megafauna of Sahul?". Proceedings of the Royal Society B: Biological Sciences. 283 (1824): 20152399. doi:10.1098/rspb.2015.2399.
- ^ Miller, G. H.; Magee, J. W.; Johnson, B. J.; Fogel, M. L.; Spooner, N. A.; McCulloch, M. T.; Ayliffe, L. K. (1999-01-08). "Pleistocene Extinction of Genyornis newtoni: Human Impact on Australian Megafauna". Science. 283 (5399): 205–208. doi:10.1126/science.283.5399.205. PMID 9880249.
- ^ Miller, G.; Magee, J.; Smith, M.; Spooner, N.; Baynes, A.; Lehman, S.; Fogel, M.; Johnston, H.; Williams, D.; Clark, P.; Florian, C.; Holst, R.; DeVogel, S. (2016-01-29). "Human predation contributed to the extinction of the Australian megafaunal bird Genyornis newtoni ∼47 ka". Nature Communications. 7: 10496. doi:10.1038/ncomms10496. PMC 4740177 . PMID 26823193.
- ^ Johnson, C. (2009-11-20). "Megafaunal Decline and Fall". Science. 326 (5956): 1072–1073. doi:10.1126/science.1182770. PMID 19965418.
- ^ Gill, J. L.; Williams, J. W.; Jackson, S. T.; Lininger, K. B.; Robinson, G. S. (2009-11-20). "Pleistocene Megafaunal Collapse, Novel Plant Communities, and Enhanced Fire Regimes in North America". Science. 326 (5956): 1100–1103. doi:10.1126/science.1179504. PMID 19965426.
- ^ Fiedal, Stuart (2009). "Sudden Deaths: The Chronology of Terminal Pleistocene Megafaunal Extinction". In Haynes, Gary. American Megafaunal Extinctions at the End of the Pleistocene. Springer. pp. 21–37. doi:10.1007/978-1-4020-8793-6_2. ISBN 978-1-4020-8792-9.
- ^ Martin, P. S. (2005). "Chapter 4. Ground Sloths at Home". Twilight of the Mammoths: Ice Age Extinctions and the Rewilding of America. University of California Press. pp. 78–99. ISBN 0-520-23141-4. OCLC 58055404. Retrieved 2014-11-11.
- ^ Alroy, J. (2008-08-12). "Dynamics of origination and extinction in the marine fossil record". PNAS. 105 Suppl 1 (Supplement_1): 11536–11542. Bibcode:2008PNAS..10511536A. doi:10.1073/pnas.0802597105. PMC 2556405 . PMID 18695240.
- ^ Wolf, A.; Doughty, C. E.; Malhi, Y. (2013). "Lateral Diffusion of Nutrients by Mammalian Herbivores in Terrestrial Ecosystems". PLoS ONE. 8 (8): e71352. doi:10.1371/journal.pone.0071352. PMC 3739793 . PMID 23951141.
- ^ Marshall, M. (2013-08-11). "Ecosystems still feel the pain of ancient extinctions". New Scientist. Retrieved 2013-08-12.
- ^ a b Doughty, C. E.; Wolf, A.; Malhi, Y. (2013-08-11). "The legacy of the Pleistocene megafauna extinctions on nutrient availability in Amazonia". Nature Geoscience. 6: 761–764. doi:10.1038/ngeo1895.
- ^ a b c Wilkinson, D. M.; Nisbet, E. G.; Ruxton, G. D. (2012-05-08). "Could methane produced by sauropod dinosaurs have helped drive Mesozoic climate warmth?". Current Biology. 22 (9): R292–R293. doi:10.1016/j.cub.2012.03.042. Retrieved 2012-05-08.
- ^ "Dinosaur gases 'warmed the Earth'". BBC Nature News. 2012-05-07. Retrieved 2012-05-08.
- ^ a b c Smith, F. A.; Elliot, S. M.; Lyons, S. K. (2010-05-23). "Methane emissions from extinct megafauna". Nature Geoscience. Nature Publishing Group. 3 (6): 374–375. Bibcode:2010NatGe...3..374S. doi:10.1038/ngeo877. Retrieved 2011-02-26.
- ^ Kelliher, F. M.; Clark, H. (2010-03-15). "Methane emissions from bison—An historic herd estimate for the North American Great Plains". Agricultural and Forest Meteorology. 150 (3): 473–577. doi:10.1016/j.agrformet.2009.11.019.
- ^ a b Fariña, Richard A.; Vizcaíno, Sergio F.; De Iuliis, Gerry (22 May 2013). Megafauna: Giant Beasts of Pleistocene South America. Indiana University Press. ISBN 0-253-00719-4. OCLC 779244424.
- ^ Ruff, C. B.; Trinkaus, E.; Holliday, T. W. (1997-05-08). "Body mass and encephalization in Pleistocene Homo". Nature. 387 (6629): 173–176. Bibcode:1997Natur.387..173R. doi:10.1038/387173a0. PMID 9144286. Retrieved 2012-05-25.
- ^ Grine, F. E.; Jumgers, W. L.; Tobias, P. V.; Pearson, O. M. (June 1995). "Fossil Homo femur from Berg Aukas, northern Namibia". American Journal of Physical Anthropology. 97 (2): 151–185. doi:10.1002/ajpa.1330970207. PMID 7653506.
- ^ Smith, Chris; Burger, Lee (November 2007). "Our Story: Human Ancestor Fossils". The Naked Scientists. Retrieved 2011-02-19.
- ^ Kappelman, John (1997-05-08). "They might be giants" (PDF). Nature. 387 (6629): 126–127. Bibcode:1997Natur.387..126K. doi:10.1038/387126a0. PMID 9144276. Retrieved 2011-02-19.
- ^ Kitchener, A.C., Breitenmoser-Würsten, C., Eizirik, E., Gentry, A., Werdelin, L., Wilting, A. and Yamaguchi, N. (2017). "A revised taxonomy of the Felidae: The final report of the Cat Classification Task Force of the IUCN Cat Specialist Group" (PDF). Cat News. Special Issue 11.
- ^ Brakefield, Tom (1993). Big Cats: Kingdom of Might. Voyageur Press. p. 44. ISBN 978-0-89658-329-0.
- ^ Nowell, Kristin; Jackson, Peter (1996). Wild Cats: Status Survey and Conservation Action Plan (PDF). Gland, Switzerland: IUCN/SSC Cat Specialist Group. pp. 1–334. ISBN 2-8317-0045-0.
- ^ Ronald Tilson, Philip J. Nyhus (2010), "Tiger morphology", Tigers of the world, Academic Press, ISBN 9780815515708
- ^ "Tiger Facts". BigCatRescue.org. 2015-03-15. Retrieved 2017-11-28.
- ^ Slaght, J. C., Miquelle, D. G., Nikolaev, I. G., Goodrich, J. M., Smirnov, E. N., Traylor-Holzer, K., Christie, S., Arjanova, T., Smith, J. L. D. and Karanth, K. U. (2005). "Chapter 6. Who's king of the beasts? Historical and contemporary data on the body weight of wild and captive Amur tigers in comparison with other subspecies" (PDF). In D. G. Miquelle; E. N. Smirnov; J.M. Goodrich. Tigers in Sikhote-Alin Zapovednik: Ecology and Conservation. Vladivostok, Russia: PSP. pp. 25–35. (in Russian)
- ^ Soibelzon, L. H.; Schubert, B. W. (January 2011). "The Largest Known Bear, Arctotherium angustidens, from the Early Pleistocene Pampean Region of Argentina: With a Discussion of Size and Diet Trends in Bears". Journal of Paleontology. Paleontological Society. 85 (1): 69–75. doi:10.1666/10-037.1. Retrieved 2011-06-01.
- ^ Swift, E. M. (1997-11-17). "What Big Mouths They Have: Travelers in Africa who run afoul of hippos may not live to tell the tale". Sports Illustrated Vault. Time Inc. Retrieved 2011-11-16.
- ^ ^ J. Calambokidis and G. Steiger (1998). Blue Whales. Voyageur Press. ISBN 0-89658-338-4.
- ^ ^ "Animal Records". Smithsonian National Zoological Park. Retrieved 2007-05-29.
- ^ Anteosaurus. Palaeos.org (2013-04-22)
- ^ Palmer, D. (1 July 2002). The Marshall Illustrated Encyclopedia of Dinosaurs and Prehistoric Animals. New Line Books. ISBN 978-1-57717-293-2. OCLC 183092423. Retrieved 2013-06-10.
- ^ Monster fish crushed opposition with strongest bite ever. The Sydney Morning Herald. November 30, 2006.
- ^ Anderson, P. S.L; Westneat, M. W (2006-11-28). "Feeding mechanics and bite force modelling of the skull of Dunkleosteus terrelli, an ancient apex predator". Biology Letters. 3 (1): 77–80. doi:10.1098/rsbl.2006.0569. ISSN 1744-9561.
- ^ Anderson, P.S.L. (2010-05-04). "Using linkage models to explore skull kinematic diversity and functional convergence in arthrodire placoderms". Journal of Morphology: 990–1005. doi:10.1002/jmor.10850. ISSN 0362-2525.
- ^ Van Roy, P.; Daley, A. C.; Briggs, D. E. G. (11 March 2015). "Anomalocaridid trunk limb homology revealed by a giant filter-feeder with paired flaps". Nature. Nature Publishing Group. 522: 77–80. doi:10.1038/nature14256. PMID 25762145.
- ^ Sample, Ian (19 February 2010). "Great white shark is more endangered than tiger, claims scientist". The Guardian. Retrieved 14 August 2013.