A mammal () is a vertebrate animal of the class Mammalia (). Mammals are characterized by the presence of milk-producing for feeding their young, a neocortex region of the brain, fur or hair, and three middle ear bones. These characteristics distinguish them from and , from which their ancestors diverged in the Carboniferous Period over 300 million years ago. Around 6,400 extant taxon species of mammals have been described and divided into 29 orders.
The largest orders of mammals, by number of species, are the rodents, bats, and Eulipotyphla (including , moles and ). The next three are the (including , and ), the even-toed ungulates (including , , and ), and the Carnivora (including Felidae, Canidae, and pinniped).
Mammals are the only living members of ; this clade, together with Sauropsida (reptiles and birds), constitutes the larger amniote clade. The early synapsids were Sphenacodontia, a group that included the famous Dimetrodon. The synapsids split into several diverse groups of non-mammalian synapsids—traditionally and incorrectly referred to as mammal-like reptiles or by the term , and now known as stem mammals or protomammals—before giving rise to Therapsida during the beginning of the Guadalupian period. Mammals originated from , an advanced group of therapsids, during the Late Triassic-Early Jurassic. The modern mammalian orders arose in the Paleogene and Neogene periods of the Cenozoic era, after the extinction of non-avian dinosaurs, and have been the dominant terrestrial animal group from 66 million years ago to the present.
The basic mammalian body type is quadruped, and most mammals use their four extremities for terrestrial locomotion; but in some, the extremities are adapted for marine mammal, in the air, in trees, fossorial, or bipedalism. Mammals range in size from the bumblebee bat to the blue whale—possibly the largest animal to have ever lived. Maximum lifespan varies from two years for the shrew to 211 years for the bowhead whale. All modern mammals give birth to live young, except the five species of , which are egg-laying mammals. The most species-rich group of mammals, the cohort called placentals, have a placenta, which enables the feeding of the fetus during gestation.
Most mammals are animal cognition, with some possessing large brains, self-awareness, and tool use. Mammals can communicate and vocalize in several ways, including the production of ultrasound, scent-marking, , singing, echolocation; and, in the case of humans, complex language. Mammals can organize themselves into fission-fusion societies, harems, and hierarchy—but can also be solitary and territorial. Most mammals are polygynous, but some can be monogamous or polyandrous.
Domestication of many types of mammals by humans played a major role in the Neolithic Revolution, and resulted in agriculture replacing hunter-gatherer as the primary source of food for humans. This led to a major restructuring of human societies from nomadic to sedentary, with more co-operation among larger and larger groups, and ultimately the development of the first . Domesticated mammals provided, and continue to provide, power for transport and agriculture, as well as food (meat and ), fur, and leather. Mammals are also hunting and raced for sport, and are used as in science. Mammals have been depicted in art since Paleolithic times, and appear in literature, film, mythology, and religion. Decline in numbers and extinction of many mammals is primarily driven by human poaching and habitat destruction, primarily deforestation.
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Mammal classification has been through several revisions since Carl Linnaeus initially defined the class, and at present, no classification system is universally accepted. McKenna & Bell (1997) and Wilson & Reeder (2005) provide useful recent compendiums.
Most mammals, including the six most species-rich orders, belong to the placental group. The three largest orders in numbers of species are : Mouse, , , , , and other gnawing mammals; Chiroptera: bats; and Soricomorpha: , moles, and . The next three biggest orders, depending on the biological classification scheme used, are the : , , and ; the Cetartiodactyla: and even-toed ungulates; and the Carnivora which includes , , , , Pinniped, and allies. According to Mammal Species of the World, 5,416 species were identified in 2006. These were grouped into 1,229 genus, 153 families and 29 orders. In 2008, the International Union for Conservation of Nature (IUCN) completed a five-year Global Mammal Assessment for its IUCN Red List, which counted 5,488 species. According to research published in the Journal of Mammalogy in 2018, the number of recognized mammal species is 6,495, including 96 recently extinct.
T. S. Kemp has provided a more traditional definition: " that possess a dentary–squamosal bone jaw articulation and occlusion between upper and lower molars with a transverse component to the movement" or, equivalently in Kemp's view, the clade originating with the last common ancestor of Sinoconodon and living mammals. The earliest known synapsid satisfying Kemp's definitions is Tikitherium, dated , so the appearance of mammals in this broader sense can be given this Late Triassic date.
In the following list, extinct groups are labelled with a dagger (†).
Class Mammalia
Estimates for the divergence times between these three placental groups range from 105 to 120 million years ago, depending on the type of DNA used (such as nuclear DNA or mitochondrial) and varying interpretations of paleogeographic data.
The cladogram above is based on Tarver et al.. (2016)
The first amniotes apparently arose in the Pennsylvanian subperiod of the Carboniferous. They descended from earlier Reptiliomorpha amphibious tetrapods, which lived on land that was already inhabited by and other invertebrates as well as , and other plants. Within a few million years, two important amniote lineages became distinct: the , which would later include the common ancestor of the mammals; and the , which now include , , , and (including ). Synapsids have a single hole (temporal fenestra) low on each side of the skull. Primitive synapsids included the largest and fiercest animals of the early Permian such as Dimetrodon. Nonmammalian synapsids were traditionally—and incorrectly—called "mammal-like reptiles" or pelycosaurs; we now know they were neither reptiles nor part of reptile lineage.
, a group of synapsids, evolved in the Guadalupian, about 265 million years ago, and became the dominant land vertebrates. They differ from basal Eupelycosauria in several features of the skull and jaws, including: larger skulls and which are equal in size in therapsids, but not for eupelycosaurs. The therapsid lineage leading to mammals went through a series of stages, beginning with animals that were very similar to their early synapsid ancestors and ending with , some of which could easily be mistaken for mammals. Those stages were characterized by:
The first mammals (in Kemp's sense) appeared in the Late Triassic epoch (about 225 million years ago), 40 million years after the first therapsids. They expanded out of their nocturnal insectivore niche from the mid-Jurassic onwards;
One of the earliest known monotremes was Teinolophos, which lived about 120 million years ago in Australia. Monotremes have some features which may be inherited from the original amniotes such as the same orifice to urinate, defecate and reproduce (cloaca)—as lizards and birds also do—
The earliest clear evidence of hair or fur is in fossils of Castorocauda and Megaconus, from 164 million years ago in the mid-Jurassic. In the 1950s, it was suggested that the foramina (passages) in the and (bones in the front of the upper jaw) of cynodonts were channels which supplied blood vessels and nerves to vibrissae (whiskers) and so were evidence of hair or fur;
When endothermy first appeared in the evolution of mammals is uncertain, though it is generally agreed to have first evolved in non-mammalian therapsids. Modern monotremes have lower body temperatures and more variable metabolic rates than marsupials and placentals, but there is evidence that some of their ancestors, perhaps including ancestors of the therians, may have had body temperatures like those of modern therians. Likewise, some modern therians like afrotheres and xenarthrans have secondarily developed lower body temperatures.
The evolution of erect limbs in mammals is incomplete—living and fossil monotremes have sprawling limbs. The parasagittal (nonsprawling) limb posture appeared sometime in the late Jurassic or early Cretaceous; it is found in the eutherian Eomaia and the metatherian Sinodelphys, both dated to 125 million years ago. Epipubic bones, a feature that strongly influenced the reproduction of most mammal clades, are first found in Tritylodontidae, suggesting that it is a synapomorphy between them and mammaliformes. They are omnipresent in non-placental mammaliformes, though Megazostrodon and Erythrotherium appear to have lacked them.
It has been suggested that the original function of lactation (milk production) was to keep eggs moist. Much of the argument is based on monotremes, the egg-laying mammals.
In human females, mammary glands become fully developed during puberty, regardless of pregnancy.
Molecular phylogenetic studies initially suggested that most placental orders diverged about 100 to 85 million years ago and that modern families appeared in the period from the late Eocene through the Miocene. However, no placental fossils have been found from before the end of the Cretaceous. The earliest undisputed fossils of placentals come from the early Paleocene, after the extinction of the non-avian dinosaurs. (Scientists identified an early Paleocene animal named Protungulatum donnae as one of the first placental mammals, but it has since been reclassified as a non-placental eutherian.) Recalibrations of genetic and morphological diversity rates have suggested a Maastrichtian origin for placentals, and a Paleocene origin for most modern clades.
The earliest known ancestor of primates is Archicebus achilles from around 55 million years ago. This tiny primate weighed 20–30 grams (0.7–1.1 ounce) and could fit within a human palm.
Many traits shared by all living mammals appeared among the earliest members of the group:
For the most part, these characteristics were not present in the Triassic ancestors of the mammals. Nearly all mammaliaforms possess an epipubic bone, the exception being modern placentals.
The stomach of even-toed ungulates (Artiodactyla) is divided into four sections: the rumen, the reticulum, the omasum and the abomasum (only have a rumen). After the plant material is consumed, it is mixed with saliva in the rumen and reticulum and separates into solid and liquid material. The solids lump together to form a bolus (or cud), and is regurgitated. When the bolus enters the mouth, the fluid is squeezed out with the tongue and swallowed again. Ingested food passes to the rumen and reticulum where cellulolytic (bacteria, protozoa and Fungus) produce cellulase, which is needed to break down the cellulose in plants. Perissodactyls, in contrast to the ruminants, store digested food that has left the stomach in an enlarged cecum, where it is fermented by bacteria.
Some mammals have a large larynx and thus a low-pitched voice, namely the hammer-headed bat ( Hypsignathus monstrosus) where the larynx can take up the entirety of the thoracic cavity while pushing the lungs, heart, and trachea into the abdomen. Large vocal pads can also lower the pitch, as in the low-pitched roars of . The production of infrasound is possible in some mammals such as the African elephant ( Loxodonta spp.) and . Small mammals with small larynxes have the ability to produce ultrasound, which can be detected by modifications to the middle ear and cochlea. Ultrasound is inaudible to birds and reptiles, which might have been important during the Mesozoic, when birds and reptiles were the dominant predators. This private channel is used by some rodents in, for example, mother-to-pup communication, and by bats when echolocating. Toothed whales also use echolocation, but, as opposed to the vocal membrane that extends upward from the vocal folds, they have a melon to manipulate sounds. Some mammals, namely the primates, have air sacs attached to the larynx, which may function to lower the resonances or increase the volume of sound.
The vocal production system is controlled by the cranial nerve nuclei in the brain, and supplied by the recurrent laryngeal nerve and the superior laryngeal nerve, branches of the vagus nerve. The vocal tract is supplied by the hypoglossal nerve and . Electrical stimulation of the periaqueductal gray (PEG) region of the mammalian midbrain elicit vocalizations. The ability to learn new vocalizations is only exemplified in humans, seals, cetaceans, elephants and possibly bats; in humans, this is the result of a direct connection between the motor cortex, which controls movement, and the in the spinal cord.
Camouflage is a powerful influence in a large number of mammals, as it helps to conceal individuals from predators or prey. In arctic and subarctic mammals such as the arctic fox ( Alopex lagopus), collared lemming ( Dicrostonyx groenlandicus), stoat ( Mustela erminea), and snowshoe hare ( Lepus americanus), seasonal color change between brown in summer and white in winter is driven largely by camouflage. Some arboreal mammals, notably primates and marsupials, have shades of violet, green, or blue skin on parts of their bodies, indicating some distinct advantage in their largely arboreal habitat due to convergent evolution.
Aposematism, warning off possible predators, is the most likely explanation of the black-and-white pelage of many mammals which are able to defend themselves, such as in the foul-smelling skunk and the powerful and aggressive honey badger. Coat color is sometimes sexually dimorphic, as in many primate species. Differences in female and male coat color may indicate nutrition and hormone levels, important in mate selection. Coat color may influence the ability to retain heat, depending on how much light is reflected. Mammals with a darker colored coat can absorb more heat from solar radiation, and stay warmer, and some smaller mammals, such as , have darker fur in the winter. The white, pigmentless fur of arctic mammals, such as the polar bear, may reflect more solar radiation directly onto the skin. The dazzling black-and-white striping of appear to provide some protection from biting flies.
The ancestral condition for mammal reproduction is the birthing of relatively undeveloped, either through direct vivipary or a short period as soft-shelled eggs. This is likely due to the fact that the torso could not expand due to the presence of epipubic bones. The oldest demonstration of this reproductive style is with Kayentatherium, which produced undeveloped , but at much higher litter sizes than any modern mammal, 38 specimens. Most modern mammals are viviparity, giving birth to live young. However, the five species of monotreme, the platypus and the four species of echidna, lay eggs. The monotremes have a sex-determination system different from that of most other mammals. In particular, the of a platypus are more like those of a chicken than those of a therian mammal.
Viviparous mammals are in the subclass Theria; those living today are in the marsupial and placental infraclasses. Marsupials have a short gestation period, typically shorter than its estrous cycle and generally giving birth to a number of undeveloped newborns that then undergo further development; in many species, this takes place within a pouch-like sac, the marsupium, located in the front of the mother's abdomen. This is the Symplesiomorphy condition among viviparous mammals; the presence of epipubic bones in all non-placental mammals prevents the expansion of the torso needed for full pregnancy.
The of mammals are specialized to produce milk, the primary source of nutrition for newborns. The monotremes branched early from other mammals and do not have the seen in most mammals, but they do have mammary glands. The young lick the milk from a mammary patch on the mother's belly. Compared to placental mammals, the milk of marsupials changes greatly in both production rate and in nutrient composition, due to the underdeveloped young. In addition, the mammary glands have more autonomy allowing them to supply separate milks to young at different development stages.
Animals will use different gaits for different speeds, terrain and situations. For example, horses show four natural gaits, the slowest horse gait is the walk, then there are three faster gaits which, from slowest to fastest, are the trot, the canter and the gallop. Animals may also have unusual gaits that are used occasionally, such as for moving sideways or backwards. For example, the main human gaits are bipedal walking and running, but they employ many other gaits occasionally, including a four-legged crawl in tight spaces. Mammals show a vast range of , the order that they place and lift their appendages in locomotion. Gaits can be grouped into categories according to their patterns of support sequence. For quadrupeds, there are three main categories: walking gaits, running gaits and leaping gaits.
The wings of bats are much thinner and consist of more bones than those of birds, allowing bats to maneuver more accurately and fly with more lift and less drag. By folding the wings inwards towards their body on the upstroke, they use 35% less energy during flight than birds. The membranes are delicate, ripping easily; however, the tissue of the bat's membrane is able to regrow, such that small tears can heal quickly.
Fossorial mammals have a fusiform body, thickest at the shoulders and tapering off at the tail and nose. Unable to see in the dark burrows, most have degenerated eyes, but degeneration varies between species; , for example, are only semi-fossorial and have very small yet functional eyes, in the fully fossorial marsupial mole the eyes are degenerated and useless, talpa moles have vestigial eyes and the cape golden mole has a layer of skin covering the eyes. External ears flaps are also very small or absent. Truly fossorial mammals have short, stout legs as strength is more important than speed to a burrowing mammal, but semi-fossorial mammals have cursorial legs. The front paws are broad and have strong claws to help in loosening dirt while excavating burrows, and the back paws have webbing, as well as claws, which aids in throwing loosened dirt backwards. Most have large incisors to prevent dirt from flying into their mouth.
Many fossorial mammals such as shrews, hedgehogs, and moles were classified under the now obsolete order Insectivora.
Semi-aquatic mammals, like pinnipeds, have two pairs of flippers on the front and back, the fore-flippers and hind-flippers. The elbows and ankles are enclosed within the body.
Mammals signal by a variety of means. Many give visual anti-predator signals, as when deer and gazelle stotting, honest signal their fit condition and their ability to escape,
The size of an animal is also a factor in determining diet type (Allen's rule). Since small mammals have a high ratio of heat-losing surface area to heat-generating volume, they tend to have high energy requirements and a high metabolism. Mammals that weigh less than about are mostly insectivorous because they cannot tolerate the slow, complex digestive process of an herbivore. Larger animals, on the other hand, generate more heat and less of this heat is lost. They can therefore tolerate either a slower collection process (carnivores that feed on larger vertebrates) or a slower digestive process (herbivores). Furthermore, mammals that weigh more than usually cannot collect enough insects during their waking hours to sustain themselves. The only large insectivorous mammals are those that feed on huge colonies of insects ( or ).
Some mammals are omnivores and display varying degrees of carnivory and herbivory, generally leaning in favor of one more than the other. Since plants and meat are digested differently, there is a preference for one over the other, as in bears where some species may be mostly carnivorous and others mostly herbivorous. They are grouped into three categories: mesocarnivore (50–70% meat), hypercarnivore (70% and greater of meat), and hypocarnivore (50% or less of meat). The dentition of hypocarnivores consists of dull, triangular carnassial teeth meant for grinding food. Hypercarnivores, however, have conical teeth and sharp carnassials meant for slashing, and in some cases strong jaws for bone-crushing, as in the case of , allowing them to consume bones; some extinct groups, notably the Machairodontinae, had saber-shaped maxillary canine.
Some physiological carnivores consume plant matter and some physiological herbivores consume meat. From a behavioral aspect, this would make them omnivores, but from the physiological standpoint, this may be due to zoopharmacognosy. Physiologically, animals must be able to obtain both energy and nutrients from plant and animal materials to be considered omnivorous. Thus, such animals are still able to be classified as carnivores and herbivores when they are just obtaining nutrients from materials originating from sources that do not seemingly complement their classification. For example, it is well documented that some ungulates such as giraffes, camels, and cattle, will gnaw on bones to consume particular minerals and nutrients. Also, cats, which are generally regarded as obligate carnivores, occasionally eat grass to regurgitate indigestible material (such as ), aid with hemoglobin production, and as a laxative.
Many mammals, in the absence of sufficient food requirements in an environment, suppress their metabolism and conserve energy in a process known as hibernation. In the period preceding hibernation, larger mammals, such as bears, become polyphagic to increase fat stores, whereas smaller mammals prefer to collect and stash food. The slowing of the metabolism is accompanied by a decreased heart and respiratory rate, as well as a drop in internal temperatures, which can be around ambient temperature in some cases. For example, the internal temperatures of hibernating arctic ground squirrels can drop to , however the head and neck always stay above . A few mammals in hot environments aestivate in times of drought or extreme heat, for example the fat-tailed dwarf lemur ( Cheirogaleus medius).
Tool use by animals may indicate different levels of learning and Animal cognition. The sea otter uses rocks as essential and regular parts of its foraging behaviour (smashing abalone from rocks or breaking open shells), with some populations spending 21% of their time making tools. Other tool use, such as using twigs to "fish" for termites, may be developed by watching others use tools and may even be a true example of animal teaching.
Brain size was previously considered a major indicator of the intelligence of an animal. Since most of the brain is used for maintaining bodily functions, greater ratios of brain to body mass may increase the amount of brain mass available for more complex cognitive tasks. Allometric analysis indicates that mammalian brain size scales at approximately the or exponent of the body mass. Comparison of a particular animal's brain size with the expected brain size based on such allometric analysis provides an encephalisation quotient that can be used as another indication of animal intelligence. have the largest brain mass of any animal on earth, averaging and in mature males.
Self-awareness appears to be a sign of abstract thinking. Self-awareness, although not well-defined, is believed to be a precursor to more advanced processes such as metacognition. The traditional method for measuring this is the mirror test, which determines if an animal possesses the ability of self-recognition. Mammals that have passed the mirror test include Asian elephants (some pass, some do not); chimpanzees; ; ;
Presociality is when animals exhibit more than just sexual interactions with members of the same species, but fall short of qualifying as eusocial. That is, presocial animals can display communal living, cooperative care of young, or primitive division of reproductive labor, but they do not display all of the three essential traits of eusocial animals. Humans and some species of Callitrichidae ( and ) are unique among primates in their degree of cooperative care of young. Harry Harlow set up an experiment with , presocial primates, in 1958; the results from this study showed that social encounters are necessary in order for the young monkeys to develop both mentally and sexually.
A fission-fusion society is a society that changes frequently in its size and composition, making up a permanent social group called the "parent group". Permanent social networks consist of all individual members of a community and often varies to track changes in their environment. In a fission–fusion society, the main parent group can fracture (fission) into smaller stable subgroups or individuals to adapt to environmental or social circumstances. For example, a number of males may break off from the main group in order to hunt or forage for food during the day, but at night they may return to join (fusion) the primary group to share food and partake in other activities. Many mammals exhibit this, such as primates (for example orangutans and ), elephants, , lions, and dolphins.
Solitary animals defend a territory and avoid social interactions with the members of its species, except during breeding season. This is to avoid resource competition, as two individuals of the same species would occupy the same niche, and to prevent depletion of food.
In a hierarchy, individuals are either dominant or submissive. A despotic hierarchy is where one individual is dominant while the others are submissive, as in wolves and lemurs, and a pecking order is a linear ranking of individuals where there is a top individual and a bottom individual. Pecking orders may also be ranked by sex, where the lowest individual of a sex has a higher ranking than the top individual of the other sex, as in hyenas. Dominant individuals, or alphas, have a high chance of reproductive success, especially in harems where one or a few males (resident males) have exclusive breeding rights to females in a group. Non-resident males can also be accepted in harems, but some species, such as the common vampire bat ( Desmodus rotundus), may be more strict.
Some mammals are perfectly monogamous, meaning that they pair bond and take no other partners (even after the original mate's death), as with wolves, , and otters. There are three types of polygamy: either one or multiple dominant males have breeding rights (polygyny), multiple males that females mate with (polyandry), or multiple males have exclusive relations with multiple females (polygynandry). It is much more common for polygynous mating to happen, which, excluding lek mating, are estimated to occur in up to 90% of mammals. Lek mating occurs when males congregate around females and try to attract them with various courtship displays and vocalizations, as in harbor seals.
All (excluding monotremes) share two major adaptations for care of the young: live birth and lactation. These imply a group-wide choice of a degree of parental care. They may build nests and dig burrows to raise their young in, or feed and guard them often for a prolonged period of time. Many mammals are K-selected, and invest more time and energy into their young than do r-selected animals. When two animals mate, they both share an interest in the success of the offspring, though often to different extremes. Mammalian females exhibit some degree of maternal aggression, another example of parental care, which may be targeted against other females of the species or the young of other females; however, some mammals may "aunt" the infants of other females, and care for them. Mammalian males may play a role in child rearing, as with tenrecs, however this varies species to species, even within the same genus. For example, the males of the southern pig-tailed macaque ( Macaca nemestrina) do not participate in child care, whereas the males of the Japanese macaque ( M. fuscata) do.
Domestication mammals form a large part of the livestock raised for meat across the world. They include (2009) around 1.4 billion cattle, 1 billion sheep, 1 billion , and (1985) over 700 million rabbits. Working animal including cattle and horses have been used for work and transport from the origins of agriculture, their numbers declining with the arrival of mechanised transport and agricultural machinery. In 2004 they still provided some 80% of the power for the mainly small farms in the third world, and some 20% of the world's transport, again mainly in rural areas. In mountainous regions unsuitable for wheeled vehicles, continue to transport goods.
Despite the benefits domesticated mammals had for human development, humans have an increasingly detrimental effect on wild mammals across the world. It has been estimated that the mass of all wild mammals has declined to only 4% of all mammals, with 96% of mammals being humans and their livestock now (see figure). In fact, terrestrial wild mammals make up only 2% of all mammals.
Artificial selection, the deliberate selective breeding of domestic animals, is being used to breeding back recently extinct animals in an attempt to achieve an animal breed with a phenotype that resembles that extinct wildtype ancestor. A breeding-back (intraspecific) hybrid may be very similar to the extinct wildtype in appearance, ecological niche and to some extent genetics, but the initial gene pool of that wild type is lost forever with its extinction. As a result, bred-back breeds are at best vague look-alikes of extinct wildtypes, as Heck cattle are of the aurochs.
Purebred wild species evolved to a specific ecology can be threatened with extinction through the process of genetic pollution, the uncontrolled hybridization, introgression genetic swamping which leads to homogenization or out-competition from the heterosis hybrid species. When new populations are imported or selectively bred by people, or when habitat modification brings previously isolated species into contact, extinction in some species, especially rare varieties, is possible. Interbreeding can swamp the rarer gene pool and create hybrids, depleting the purebred gene pool. For example, the endangered wild water buffalo is most threatened with extinction by genetic pollution from the Water buffalo. Such extinctions are not always apparent from a morphological standpoint. Some degree of gene flow is a normal evolutionary process, nevertheless, hybridization threatens the existence of rare species.
Various species are predicted to become extinct in the near future, among them the rhinoceros, giraffes, and species of primates and pangolins. According to the WWF's 2020 Living Planet Report, vertebrate wildlife populations have declined by 68% since 1970 as a result of human activities, particularly overconsumption, population growth and intensive farming, which is evidence that humans have triggered a sixth mass extinction event. Hunting alone threatens hundreds of mammalian species around the world. Scientists claim that the growing demand for meat is contributing to biodiversity loss as this is a significant driver of deforestation and habitat destruction; species-rich habitats, such as significant portions of the Amazon rainforest, are being converted to agricultural land for meat production. Another influence is over-hunting and poaching, which can reduce the overall population of game animals, especially those located near villages,
Attention is being given to endangered species globally, notably through the Convention on Biological Diversity, otherwise known as the Rio Accord, which includes 189 signatory countries that are focused on identifying endangered species and habitats.
Recent extinctions can be directly attributed to human influences. The IUCN characterizes 'recent' extinction as those that have occurred past the cut-off point of 1500, and around 80 mammal species have gone extinct since that time and 2015.
Evolution
Origins
Evolution from older amniotes
First mammals
Earliest appearances of features
Rise of the mammals
Anatomy
Distinguishing features
Sexual dimorphism
Biological systems
Circulatory systems
Respiratory systems
Integumentary systems
Digestive systems
Excretory and genitourinary systems
Sound production
Fur
Thermoregulation
Coloration
Reproductive system
Endothermy
Species lifespan
Locomotion
Terrestrial
Arboreal
Aerial
Fossorial and subterranean
Aquatic
Behavior
Communication and vocalization
Feeding
Intelligence
Social structure
Humans and other mammals
In human culture
Uses and importance
Hybrids
Threats
Notes
See also
External resources
Further reading
External links
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