- Evolution of mammals
Further information: Evolutionary history of life
The evolution of mammals within the synapsid lineage (sometimes called "mammal-like reptiles") was a gradual process that took approximately 70 million years, beginning in the mid-Permian. By the mid-Triassic, there were many species that looked like mammals, and the first true mammals appeared in the early Jurassic. The earliest known marsupial, Sinodelphys, appeared 125 million years ago in the early Cretaceous, around the same time as Eomaia, the first known eutherian (member of placentals' "parent" group); and the earliest known monotreme, Teinolophos, appeared two million years later. After the Cretaceous-Tertiary extinction wiped out the non-avian dinosaurs (birds are generally regarded as the surviving dinosaurs) and several other mammalian groups, placental and marsupial mammals diversified into many new forms and ecological niches throughout the Tertiary, by the end of which all modern orders had appeared.
From the point of view of phylogenetic nomenclature, mammals are the only surviving synapsids. The synapsid lineage became distinct from the sauropsid ("reptile") lineage in the late Carboniferous period, between 320 and 315 million years ago, and were the most common and largest land vertebrates of the Permian period. But in the Triassic period a previously obscure group of sauropsids, the archosaurs, became the dominant vertebrates and one archosaur group, the dinosaurs, dominated the rest of the Mesozoic era. These changes forced the Mesozoic mammalaiforms ("nearly mammals") into nocturnal niches, and may have contributed greatly to the development of mammalian traits such as endothermy, hair and a large brain. Later in the Mesozoic mammals spread into other ecological niches, for example aquatic, gliding and even preying on dinosaurs. Non-mammalian synapsids are often called mammal-like reptiles despite diverging very early from the other reptilian lines.
Most of the evidence consists of fossils. For many years fossils of Mesozoic mammals and their immediate ancestors were very rare and fragmentary, but since the mid 1990s there have been many important new finds, especially in China. The relatively new techniques of molecular phylogenetics have also shed light on some aspects of mammalian evolution by estimating the timing of important divergence points for modern species. When used carefully, these techniques often, but not always, agree with the fossil record.
Although mammary glands are a signature feature of modern mammals, little is known about the evolution of lactation, and virtually nothing is known about the evolution of another distinctive feature, the neocortex region of the brain. This is because these soft tissues are not often preserved in the fossil record. Hence, most study of the evolution of mammals centers around the development of the middle ear bones from components of the ancestral amniote jaw joint. Other much-studied aspects include the evolution of erect limb posture, a bony secondary palate, fur and hair, and warm-bloodedness.
Definition of "mammal"
Living mammal species can be identified by the presence of milk-producing mammary glands in females. Other features are required when classifying fossils, since mammary glands and other soft-tissue features are not visible in fossils.
Paleontologists therefore use a distinguishing feature that is shared by all living mammals (including monotremes) but is not present in any of the early Triassic therapsids: Mammals use two bones for hearing that all other amniotes use for eating. The earliest amniotes had a jaw joint composed of the articular (a small bone at the back of the lower jaw) and the quadrate (a small bone at the back of the upper jaw). All non-mammalian amniotes use this system including lizards, crocodilians, dinosaurs (and their descendants the birds), and therapsids. But mammals have a different jaw joint, composed only of the dentary (the lower jaw bone, which carries the teeth) and the squamosal (another small skull bone). In mammals, the quadrate and articular bones have become the incus and malleus bones in the middle ear.
Mammals also have a double occipital condyle; they have two knobs at the base of the skull that fit into the topmost neck vertebra, and other vertebrates have a single occipital condyle. But paleontologists use only the jaw joint and middle ear as criteria for identifying fossil mammals, as it would be confusing if they found a fossil that had one feature but not the other (e.g. a mammalian jaw and ear but a non-mammalian single occipital condyle).
Due to the incremental changes in transitional fossils, it has been said
We may again ask the question, What is a mammal? Where we draw the line between reptile and mammal has no biological significance. It is purely a matter of convenience. There are two obvious choices, both immediately following a period of rapid evolution that make as definite a break as we can hope to find.
The ancestry of mammals
Sauropsids (including dinosaurs)
The first fully terrestrial vertebrates were amniotes — their eggs had internal membranes that allowed the developing embryo to breathe but kept water in. This allowed amniotes to lay eggs on dry land, while amphibians generally need to lay their eggs in water (a few amphibians, such as the Surinam toad, have evolved other ways of getting around this limitation). The first amniotes apparently arose in the late Carboniferous from the ancestral reptiliomorphs.
Within a few million years two important amniote lineages became distinct: mammals' synapsid ancestors and the sauropsids, from which lizards, snakes, crocodilians, dinosaurs and birds are descended. The earliest known fossils of synapsids and sauropsids (such as Archaeothyris and Hylonomus resp.) date from about 320 to 315 million years ago. Unfortunately it is difficult to be sure about when each of them evolved, since vertebrate fossils from the late Carboniferous are very rare, and therefore the actual first occurrences of each of these types of animal might have been considerably earlier.
Synapsid skulls are identified by the distinctive pattern of the holes behind each eye, which served the following purposes:
- made the skull lighter without sacrificing strength.
- saved energy by using less bone.
- probably provided attachment points for jaw muscles. Having attachment points further away from the jaw made it possible for the muscles to be longer and therefore to exert a strong pull over a wide range of jaw movement without being stretched or contracted beyond their optimum range.
Early Permian terrestrial fossils indicate that one synapsid group, the pelycosaurs, were the most common land vertebrates of their time and included the largest land animals of the time.
Therapsids descended from pelycosaurs in the middle Permian and took over their position as the dominant land vertebrates. They differ from pelycosaurs in several features of the skull and jaws, including larger temporal fenestrae and incisors that are equal in size.
The therapsids went through a series of stages, beginning with animals that were very like their pelycosaur ancestors and ending with some that could easily be mistaken for mammals:
- gradual development of a bony secondary palate. Most books and articles interpret this as a prequisite for the evolution of mammals' high metabolic rate, because it enabled these animals to eat and breathe at the same time. But some scientists point out that some modern ectotherms use a fleshy secondary palate to separate the mouth from the airway, and that a bony palate provides a surface on which the tongue can manipulate food, facilitating chewing rather than breathing. The interpretation of the bony secondary palate as an aid to chewing also suggests the development of a faster metabolism, since chewing makes it possible to digest food more quickly. In mammals the palate is formed by two specific bones, but various Permian therapsids had other combinations of bones in the right places to function as a palate.
- the dentary gradually becomes the main bone of the lower jaw.
- progress towards an erect limb posture, which would increase the animals' stamina by avoiding Carrier's constraint. But this process was erratic and very slow — for example: all herbivorous therapsids retained sprawling limbs (some late forms may have had semi-erect hind limbs); Permian carnivorous therapsids had sprawling forelimbs, and some late Permian ones also had semi-sprawling hindlimbs. In fact, modern monotremes still have semi-sprawling limbs.
- in the Triassic, progress towards the mammalian jaw and middle ear.
- there is plausible evidence of hair in Triassic therapsids, but none for Permian therapsids (see below).
- some scientists have argued that some Triassic therapsids show signs of lactation (see below).
Therapsid family tree
(simplified from; only those that are most relevant to the evolution of mammals are described below)
Therapsids Eutherapsida Neotherapsida Anomodonts Theriodontia Eutheriodontia Cynodontia
Only the dicynodonts, therocephalians and cynodonts survived into the Triassic.
The Biarmosuchia were the most primitive and pelycosaur-like of the therapsids.
Dinocephalians ("terrible heads") were large, some as large as a rhinoceros, and included both carnivores and herbivores. Some of the carnivores had semi-erect hindlimbs, but all dinocephalians had sprawling forelimbs. In many ways they were very primitive therapsids, for example they had no secondary palate and their jaws were rather "reptilian".
The anomodonts ("anomalous teeth") were the most successful of the herbivorous therapsids — one sub-group, the dicynodonts, survived almost to the end of the Triassic. But anomodonts were very different from modern herbivorous mammals, as their only teeth were a pair of fangs in the upper jaw and it is generally agreed that they had beaks like those of birds or ceratopsians.
The theriodonts ("beast teeth") and their descendants had jaw joints in which the lower jaw's articular bone tightly gripped the skull's very small quadrate bone. This allowed a much wider gape, and one group, the carnivorous gorgonopsians ("gorgon faces"), took advantage of this to develop "sabre teeth". But the theriodont's jaw hinge had a longer term significance — the much reduced size of the quadrate bone was an important step in the development of the mammalian jaw joint and middle ear.
The gorgonopsians still had some primitive features: no bony secondary palate (but other bones in the right places to perform the same functions); sprawling forelimbs; hindlimbs that could operate in both sprawling and erect postures. But the therocephalians ("beast heads"), which appear to have arisen at about the same time as the gorgonopsians, had additional mammal-like features, e.g. their finger and toe bones had the same number of phalanges (segments) as in early mammals (and the same number that primates have, including humans).
The cynodonts, a theriodont group that also arose in the late Permian, include the ancestors of all mammals — one sub-group, the tritheledonts, is widely regarded as the most likely to contain mammals' ancestor. Cynodonts' mammal-like features include further reduction in the number of bones in the lower jaw, a secondary bony palate, cheek teeth with a complex pattern in the crowns, and a brain which filled the endocranial cavity.
Multi-chambered burrows have been found, containing as many as 20 skeletons of the Early Triassic cynodont Trirachodon; the animals are thought to have been drowned by a flash flood. The extensive shared burrows indicate that these animals were capable of complex social behaviors.
The catastrophic Permian-Triassic mass extinction slightly more than 250 million years ago killed off about 70 percent of terrestrial vertebrate species and the majority of land plants.
As a result, ecosystems and food chains collapsed, and the establishment of new stable ecosystems took about 30 million years. With the disappearance of the gorgonopsians, who were dominant predators in the late Permian, the way was open for the cynodonts to compete with another previously obscure group, the archosaurs, for dominance of the carnivorous niches. The archosaurs include the ancestors of crocodilians, dinosaurs and birds.
The archosaurs quickly became the dominant carnivores, a development often called the "Triassic takeover." Their success may have been due to the fact that the early Triassic was predominantly arid and therefore archosaurs' superior water conservation gave them a decisive advantage. All known archosaurs have glandless skins and eliminate nitrogenous waste in a uric acid paste containing little water, while the cynodonts probably excreted most such waste in a solution of urea, as mammals do today; considerable water is required to keep urea dissolved.
But the Triassic takeover may have been a vital factor in the evolution of the mammals. Two groups stemming from the early cynodonts were successful in niches with minimal competition from the archosaurs: the tritylodonts, who were herbivores, and the mammals, who were small nocturnal insectivores. As a result:
- The therapsid trend towards differentiated teeth with precise occlusion accelerated, because of the need to hold captured arthropods and crush their exoskeletons.
- As the body length of the mammals' ancestors fell below 50 mm (2 inches), advances in thermal insulation and temperature regulation became necessary for nocturnal life.
- Acute senses of hearing and smell became vital.
- This accelerated the development of the mammalian middle ear, and therefore of the mammalian jaw since bones that had been part of the jaw joint became part of the middle ear.
- The increase in the size of the olfactory lobes of the brain increased brain weight as a percentage of total body weight. Brain tissue requires a disproportionate amount of energy. The need for more food to support the enlarged brains increased the pressures for improvements in insulation, temperature regulation and feeding.
- As a side-effect of the nocturnal life, discerning colors became less important (they lost two out of four opsins), and this is reflected in the fact that most mammals have poor color vision, including the "lower primates" such as lemurs.
From cynodonts to true mammals
The Triassic takeover probably accelerated the evolution of mammals. The nearly-mammals are preserved in few good fossils, mainly because they were mostly smaller than rats:
- They were largely restricted to environments that are less likely to provide good fossils. Floodplains as the best terrestrial environments for fossilization provide little fossils of nearly-mammals, because they are dominated by medium to large animals, and the Triassic therapsids and near-mammals could not compete with archosaurs in the medium to large size range.
- Their delicate bones were vulnerable to being destroyed before they could be fossilized — by scavengers (including fungi and bacteria) and by being trodden on.
- Small fossils are harder to spot and more vulnerable to being destroyed by weathering and other natural stresses before they are discovered.
The problem of the lack of good fossils of nearly-mammals is a part of the general problem that Mesozoic mammals were, until recently, known almost exclusively by teeth and jaws. Since the 1980s, the number of Mesozoic fossil mammals has increased decisively, from 116 genera known in 1979 to about 310 in 2007, with an increase in quality such that "at least 18 Mesozoic mammals are represented by nearly complete skeletons".
As a result:
- In many cases it is difficult to assign a Mesozoic mammal or near-mammal fossil to a genus.
- All the available fossils of a genus seldom add up to a complete skeleton, and hence it is difficult to decide which genera are most like each other and therefore most likely to be closely related. In other words, it becomes very difficult to classify them by means of cladistics, which is the most reliable and least subjective method currently available.
So the evolution of mammals in the Mesozoic is full of uncertainties, although there is no room for doubt that true mammals did first appear in the Mesozoic.
Mammals or mammaliaformes?
One result of these uncertainties has been a change in the paleontologists' definition of "mammal". For a long time a fossil was considered a mammal if it met the jaw-ear criterion (the jaw joint consists only of the squamosal and dentary; and the articular and the quadrate bones have become the middle ear's malleus and incus). But more recently some paleontologists have usually defined "mammal" as the crown group mammals, i.e. the last common ancestor of monotremes, marsupials and placentals and all of its descendants. The need to address the animals that are more mammal-like than cynodonts, but less closely related to monotremes, marsupials and placentals, led to erecting the group mammaliaformes to accommodate these primitive forms. Mammaliaformes is a paraphyletic taxon, representing the early radiation of mammals after the jaw-ear criterion. Although this now appears to be the majority approach, some paleontologists have resisted it because it simply moves most of the problems into the new taxon (a paraphyletic one at that) without solving the original problem; the Mammaliaformes includes some animals with "mammalian" jaw joints and some with "reptilian" (articular-to-quadrate) jaw joints; and the newer definition of "mammal" and "mammaliaformes" depends on last common ancestors of both groups, which have not yet been found. Despite these objections, this article follows the majority approach and treats most of the cynodonts' Mesozoic descendants as mammaliaformes.
Family tree — cynodonts to mammals
(based on Mammaliformes - Palaeos)
Cynodontia Epicynodontia Eucynodontia Probainognathia
crown group Mammals
Multituberculates (named for the multiple tubercles on their "molars") are often called the "rodents of the Mesozoic" but this is an example of convergent evolution rather than meaning that they are closely related to the Rodentia. At first sight they look like mammals: their jaw joints consists of only the dentary and squamosal bones, and the quadrate and articular bones are part of the middle ear; their teeth are differentiated, occlude and have mammal-like cusps; they have a zygomatic arch; the structure of the pelvis suggests that they gave birth to tiny helpless young, like modern marsupials. And they lived for over 120 million years (from mid Jurassic, about 160M years ago, to early Oligocene, about 35M years ago), which in terms of clade longevity would make them the most successful mammaliaformes ever. But a closer look shows that they are very different from modern mammals:
- Their "molars" have two parallel rows of tubercles, unlike the tribosphenic (three-peaked) molars of early mammals.
- The chewing action is completely different. Mammals chew with a side-to-side grinding action, which means that usually the molars occlude on only one side at a time. Multituberculates' jaws were incapable of side-to-side movement and chewed by dragging the lower teeth backwards against the upper ones as the jaw closed.
- The anterior (forward) part of the zygomatic arch mostly consists of the maxilla (upper jawbone) rather than the jugal, and the jugal is a small bone in a little slot in the maxillary process (extension).
- The squamosal does not form part of the braincase.
- The rostrum (snout) is unlike that of mammals, in fact it looks more like that of a pelycosaur such as Dimetrodon. The multituberculate rostrum is box-like, with the large flat maxillae forming the sides, the nasal the top, and the tall premaxilla at the front.
The Morganucodontidae first appeared in the late Triassic, about 205M years ago. They are an excellent example of transitional fossils, since they have both the dentary-squamosal and articular-quadrate jaw joints. They were also one of the first discovered and most thoroughly studied of the mammaliaformes, since an unusually large number of morganucodont fossils have been found.
The most notable member of the docodonts is Castorocauda ("beaver tail"), which lived in the mid Jurassic about 164M years ago and was first discovered in 2004 and described in 2006. Castorocauda was not a typical docodont (most were omnivores) and not a true mammal, but it is extremely important in the study of the evolution of mammals because the first find was an almost complete skeleton (a real luxury in paleontology) and it breaks the "small nocturnal insectivore" stereotype:
- It was noticeably larger than most Mesozoic mammal-like fossils — about 17 in (43 cm) from its nose to the tip of its 5-inch (130 mm) tail, and may have weighed 500–800 g (18–28 oz).
- It provides the earliest absolutely certain evidence of hair and fur. Previously the earliest was Eomaia, a true mammal from about 125M years ago.
- It had aquatic adaptations including flattened tail bones and remnants of soft tissue between the toes of the back feet, suggesting that they were webbed. Previously the earliest known semi-aquatic mammal-like animals were from the Eocene, about 110M years later.
- Castorocauda's powerful forelimbs look adapted for digging. This feature and the spurs on its ankles make it resemble the platypus, which also swims and digs.
- Its teeth look adapted for eating fish: the first two molars had cusps in a straight row, which made them more suitable for gripping and slicing than for grinding; and these molars are curved backwards, to help in grasping slippery prey.
The consensus family tree above shows Hadrocodium as an "aunt" of crown mammals, while symmetrodonts and kuehneotheriids are more closely related to true mammals. But fossils of symmetrodonts and kuehneotheriids are so few and fragmentary that they are poorly understood and may be paraphyletic. On the other hand there are good fossils of Hadrocodium (about 195M years ago in the very early Jurassic) and they have some important features: 
- The jaw joint consists only of the squamosal and dentary bones, and the jaw contains no smaller bones to the rear of the dentary, unlike the therapsid design.
- In therapsids and most mammaliaformes the eardrum stretched over a trough at the rear of the lower jaw. But Hadrocodium had no such trough, which suggests its ear was part of the cranium, as it is in mammals — and hence that the former articular and quadrate had migrated to the middle ear and become the malleus and incus. On the other hand the dentary has a "bay" at the rear that mammals lack. This suggests that Hadrocodium's dentary bone retained the same shape that it would have had if the articular and quadrate had remained part of the jaw joint, and therefore that Hadroconium or a very close ancestor may have been the first to have a fully mammalian middle ear.
- Therapsids and earlier mammaliaforms had their jaw joints very far back in the skull, partly because the ear was at the rear end of the jaw but also had to be close to the brain. This arrangement limited the size of the braincase, because it forced the jaw muscles to run round and over it. Hadrocodium's braincase and jaws were no longer bound to each other by the need to support the ear, and its jaw joint was further forward. In its descendants or those of animals with a similar arrangement, the brain case was free to expand without being constrained by the jaw and the jaw was free to change without being constrained by the need to keep the ear near the brain — in other words it now became possible for mammal-like animals both to develop large brains and to adapt their jaws and teeth in ways that were purely specialized for eating.
The earliest crown mammals
The crown group mammals are the extant mammals and their relatives back to their last common ancestor, variously called 'crown mammals' or 'true mammals'. This part of the story introduces new complications, since the crown group are the only group that still has living members, enabling both anatomical and DNA analysis:
- One has to distinguish between extinct groups and those that have living representatives.
- One often feels compelled to try to explain the evolution of features that do not appear in fossils. This endeavor often involves Molecular phylogenetics, a technique that has become popular since the mid-1980s but is still often controversial because of its assumptions, especially about the reliability of the molecular clock.
Family tree of early crown mammals
(based on Mammalia: Overview - Palaeos; X marks extinct groups)
Australosphenida and Ausktribosphenidae
Ausktribosphenidae is a group name that has been given to some rather puzzling finds that:
- appear to have tribosphenic molars, a type of tooth that is otherwise known only in placentals and marsupials.
- come from mid Cretaceous deposits in Australia — but Australia was connected only to Antarctica, and placentals originated in the northern hemisphere and were confined to it until continental drift formed land connections from North America to South America, from Asia to Africa and from Asia to India (the late Cretaceous map at  shows how the southern continents are separated).
- are represented only by teeth and jaw fragments, which is not very helpful.
Australosphenida is a group that has been defined in order to include the Ausktribosphenidae and monotremes. Asfaltomylos (mid- to late Jurassic, from Patagonia) has been interpreted as a basal australosphenid (animal that has features shared with both Ausktribosphenidae and monotremes; lacks features that are peculiar to Ausktribosphenidae or monotremes; also lacks features that are absent in Ausktribosphenidae and monotremes) and as showing that australosphenids were widespread throughout Gondwanaland (the old Southern hemisphere super-continent).
But recent analysis of Teinolophos suggests Teinolophos (about 115M years ago) was a "crown group" (advanced and relatively specialised) monotreme, so the basal (most primitive) monotremes must have appeared considerably earlier; that some alleged Australosphenids were also "crown group" monotremes (e.g. Steropodon); and that other alleged Australosphenids (e.g. Ausktribosphenos, Bishops, Ambondro, Asfaltomylos) are therefore more closely related to and possibly members of the Therian mammals (group that includes marsupials and placentals, see below).
The earliest known monotreme is Teinolophos, which lived about 123M years ago in Australia. Recent (2007, published 2008) analysis suggest that it was not a basal (primitive, ancestral) monotreme but a full-fledged platypus, and therefore that the platypus and echidna lineages diverged considerably earlier and that basal monotremes were even earlier.
A more recent study (2009), however, has suggested that while Teinolophis was a type of platypus, it also was a basal monotreme and predated the radiation of modern monotremes. The semi-aquatic lifestyle of platypuses prevented them from being outcompeted by the marsupials that migrated to Australia millions of years ago, since joeys need to keep attached to their mothers and would drown if their mothers ventured into water. Genetic evidence has determined that echidnas diverged from the platypus lineage as recently as 19-48M when they made their transition from semi-aquatic to terrestrial lifestyle.
Monotremes have some features that may be inherited from the cynodont ancestors:
- they use the same orifice to urinate, defecate and reproduce ("monotreme" means "one hole") — as lizards and birds also do.
- they lay eggs that are leathery and uncalcified, like those of lizards, turtles and crocodilians.
Unlike in other mammals, female monotremes do not have nipples and feed their young by "sweating" milk from patches on their bellies.
Of course these features are not visible in fossils, and the main characteristics from paleontologists' point of view are:
- a slender dentary bone in which the coronoid process is small or non-existent.
- the external opening of the ear lies at the posterior base of the jaw.
- the jugal bone is small or non-existent.
- a primitive pectoral girdle with strong ventral elements: coracoids, clavicles and interclavicle. Note: therian mammals have no interclavicle.
- sprawling or semi-sprawling forelimbs.
Theria ("beasts") is a name applied to the hypothetical group from which both metatheria (which include marsupials) and eutheria (which include placentals) descended. Although no convincing fossils of basal therians have been found (just a few teeth and jaw fragments), metatheria and eutheria share some features that one would expect to have been inherited from a common ancestral group:
- no interclavicle.
- coracoid bones non-existent or fused with the shoulder blades to form coracoid processes.
- a type of crurotarsal ankle joint in which: the main joint is between the tibia and astragalus; the calcaneum has no contact with the tibia but forms a heel to which muscles can attach. (The other well-known type of crurotarsal ankle is seen in crocodilians and works differently — most of the bending at the ankle is between the calcaneum and astragalus).
- tribosphenic molars.
The living Metatheria are all marsupials ("animals with pouches"). A few fossil genera such as the Mongolian late Cretaceous Asiatherium may be marsupials or members of some other metatherian group(s).
The oldest known marsupial is Sinodelphys, found in 125M-year-old early Cretaceous shale in China's northeastern Liaoning Province. The fossil is nearly complete and includes tufts of fur and imprints of soft tissues.
Didelphimorphia (common opossums of the Western Hemisphere) first appeared in the late Cretaceous and still have living representatives, probably because they are mostly semi-arboreal unspecialized omnivores.
The best-known feature of marsupials is their method of reproduction:
- The mother develops a kind of yolk sack in her womb that delivers nutrients to the embryo. Embryos of bandicoots, koalas and wombats additionally form placenta-like organs that connect them to the uterine wall, although the placenta-like organs are smaller than in placental mammals and it is not certain that they transfer nutrients from the mother to the embryo.
- Pregnancy is very short, typically four to five weeks. The embryo is born at a very young age of development, and is usually less than 2 in (5.1 cm) long at birth. It has been suggested that the short pregnancy is necessary to reduce the risk that the mother's immune system will attack the embryo.
- The newborn marsupial uses its forelimbs (with relatively strong hands) to climb to a nipple, which is usually in a pouch on the mother's belly. The mother feeds the baby by contracting muscles over her mammary glands, as the baby is too weak to suck. The newborn marsupial's need to use its forelimbs in climbing to the nipple has prevented the forelimbs from evolving into paddles or wings and has therefore prevented the appearance of aquatic or truly flying marsupials (although there are several marsupial gliders).
Although some marsupials look very like some placentals (the thylacine or "marsupial wolf" is a good example), marsupial skeletons have some features that distinguish them from placentals:
- Some, including the thylacine, have 4 molars. No placentals have more than 3.
- All have a pair of palatal fenestrae, window-like openings on the bottom of the skull (in addition to the smaller nostril openings).
Marsupials also have a pair of marsupial bones (sometimes called "epipubic bones"), which support the pouch in females. But these are not unique to marsupials, since they have been found in fossils of multituberculates, monotremes, and even eutherians — so they are probably a common ancestral feature that disappeared at some point after the ancestry of living placental mammals diverged from that of marsupials. Some researchers think the epipubic bones' original function was to assist locomotion by supporting some of the muscles that pull the thigh forwards.
EutheriaMain article: Eutheria
The living Eutheria ("true beasts") are all placentals. But the earliest known eutherian, Eomaia, found in China and dated to 125M years ago, has some features that are more like those of marsupials (the surviving metatherians):
- Epipubic bones extending forwards from the pelvis, which are not found in any modern placental, but are found in all other mammals — non-placental eutherians, marsupials, monotremes and mammaliaformes — and even in the cynodont therapsids that are closest to mammals. Their function is to stiffen the body during locomotion. This stiffening would be harmful in pregnant placentals, whose abdomens need to expand.
- A narrow pelvic outlet, which indicates that the young were very small at birth and therefore pregnancy was short, as in modern marsupials. This suggests that the placenta was a later development.
- 5 incisors in each side of the upper jaw. This number is typical of metatherians, and the maximum number in modern placentals is 3, except for homodonts such as the armadillo. But Eomaia's molar to premolar ratio (it has more pre-molars than molars) is typical of eutherians, including placentals, and not normal in marsupials.
Eomaia also has a Meckelian groove, a primitive feature of the lower jaw that is not found in modern placental mammals.
These intermediate features are consistent with molecular phylogenetics estimates that the placentals diversified about 110M years ago, 15M years after the date of the Eomaia fossil.
Eomaia also has many features that strongly suggest it was a climber, including several features of the feet and toes; well-developed attachment points for muscles that are used a lot in climbing; and a tail that is twice as long as the rest of the spine.
Placentals' best-known feature is their method of reproduction:
- The embryo attaches itself to the uterus via a large placenta via which the mother supplies food and oxygen and removes waste products.
- Pregnancy is relatively long and the young are fairly well-developed at birth. In some species (especially herbivores living on plains) the young can walk and even run within an hour of birth.
It has been suggested that the evolution of placental reproduction was made possible by retroviruses that:
- make the interface between the placenta and uterus into a syncytium, i.e. a thin layer of cells with a shared external membrane. This allows the passage of oxygen, nutrients and waste products but prevents the passage of blood and other cells, which would cause the mother's immune system to attack the fetus.
- reduce the aggressiveness of the mother's immune system (which is good for the foetus but makes the mother more vulnerable to infections).
From a paleontologist's point of view, eutherians are mainly distinguished by various features of their teeth, ankles and feet.
Expansion of ecological niches in the Mesozoic
There is still some truth in the "small, nocturnal insectivores" stereotype but recent finds, mainly in China, show that some mammaliaforms and true mammals were larger and had a variety of lifestyles. For example:
- Castorocauda, a member of Docodonta which lived in the middle Jurassic about 164 million years, was about 42.5 cm (16.7 in) long, weighed 500–800 g (18–28 oz), had limbs that were adapted for swimming and digging and teeth adapted for eating fish.
- Multituberculates, are allotherians that survived for over 125 million years (from mid Jurassic, about 160M years ago, to early Oligocene, about 35M years ago) are often called the "rodents of the Mesozoic", because they had continuously growing incisors like those of modern rodents.
- Fruitafossor, from the late Jurassic period about 150 million years ago, was about the size of a chipmunk and its teeth, forelimbs and back suggest that it broke open the nest of social insects to prey on them (probably termites, as ants had not yet appeared).
- Volaticotherium, allotherians from the boundary the early Cretaceous about 125M years ago, is the earliest-known gliding mammal and had a gliding membrane that stretched out between its limbs, rather like that of a modern flying squirrel. This also suggests it was active mainly during the day.
- Repenomamus, tricodonts from the early Cretaceous 130 million years ago, was a stocky, badger-like predator that sometimes preyed on young dinosaurs. Two species have been recognized, one more than 1 m (39 in) long and weighing about 12–14 kg (26–31 lb), the other less than 0.5 m (20 in) long and weighing 4–6 kg (8.8–13 lb).
Evolution of major groups of living mammals
There are currently vigorous debates between traditional paleontologists ("fossil-hunters") and molecular phylogeneticists about how and when the modern groups of mammals diversified, especially the placentals. Generally the traditional paelontologists date the appearance of a particular group by the earliest known fossil whose features make it likely to be a member of that group, while the molecular phylogeneticists suggest that each lineage diverged earlier (usually in the Cretaceous) and that the earliest members of each group were anatomically very similar to early members of other groups and differed only in their genetics. These debates extend to the definition of and relationships between the major groups of placentals — the controversy about Afrotheria is a good example.
Fossil-based family tree of placental mammals
Here is a very simplified version of a typical family tree based on fossils, based on Cladogram of Mammalia - Palaeos. It tries to show the nearest thing there is at present to a consensus view, but some paleontologists have very different views, for example:
- The most common view is that placentals originated in the southern hemisphere, but some paleontologists argue that they first appeared in Laurasia (old supercontinent containing modern Asia, N. America and Europe).
- Paleontologists differ about when the first placentals appeared, with estimates ranging from 20M years before the end of the Cretaceous to just after the end of the Cretaceous. And molecular biologists argue for a much earlier origin.
- Most paleontologists suggest that placentals should be divided into Xenarthra and the rest, but a few think these animals diverged later.
For the sake of brevity and simplicity the diagram omits some extinct groups in order to focus on the ancestry of well-known modern groups of placentals — X marks extinct groups. The diagram also shows the following:
- the age of the oldest known fossils in many groups, since one of the major debates between traditional paleontologists and molecular phylogeneticists is about when various groups first became distinct.
- well-known modern members of most groups.
Xenarthra (late cretaceous)
(armadillos, anteaters, sloths)
Pholidota (late cretaceous)
Epitheria (latest Cretaceous)
(some extinct groups) X
Insectivora (latest Cretaceous)
(hedgehogs, shrews, moles, tenrecs)
Zalambdalestidae X (late Cretaceous)
Macroscelidea (late Eocene)
Glires (early Paleocene)
(rabbits, hares, pikas)
Rodentia (late Paleocene)
(mice & rats, squirrels, porcupines)
Scandentia (mid Eocene)
Primates (early Paleocene)
(tarsiers, lemurs, monkeys, apes including humans)
Dermoptera (late Eocene)
Ungulatomorpha (late Cretaceous) Eparctocyona (late Cretaceous)
(some extinct groups) X
Arctostylopida X (late Paleocene)
Mesonychia X (mid Paleocene)
(predators / scavengers, but not closely related to modern carnivores)
Cetacea (early Eocene)
(whales, dolphins, porpoises)
Artiodactyla (early Eocene)
(even-toed ungulates: pigs, hippos, camels, giraffes, cattle, deer)
Perissodactyla (late Paleocene)
(odd-toed ungulates: horses, rhinos, tapirs)
Tubulidentata (early Miocene)
Paenungulata ("not quite ungulates")
Hyracoidea (early Eocene)
Sirenia (early Eocene)
Proboscidea (early Eocene)
This family tree contains some surprises and puzzles. For example:
- The closest living relatives of cetaceans (whales, dolphins, porpoises) are artiodactyls, hoofed animals, which are almost all pure vegetarians.
- Bats are fairly close relatives of primates.
- The closest living relatives of elephants are the aquatic sirenians, while their next relatives are hyraxes, which look more like well-fed guinea pigs.
- There is little correspondence between the structure of the family (what was descended from what) and the dates of the earliest fossils of each group. For example the earliest fossils of perissodactyls (the living members of which are horses, rhinos and tapirs) date from the late Paleocene but the earliest fossils of their "sister group" the Tubulidentata date from the early Miocene, nearly 50M years later. Paleontologists are fairly confident about the family relationships, which are based on cladistic analyses, and believe that fossils of the ancestors of modern aardvarks have simply not been found yet.
Family tree of placental mammals according to molecular phylogenetics
Molecular phylogenetics uses features of organisms' genes to work out family trees in much the same way as paleontologists do with features of fossils — if two organisms' genes are more similar to each other than to those of a third organism, the two organisms are more closely related to each other than to the third.
Molecular phylogeneticists have proposed a family tree that is very different from the one with which paleontologists are familiar. Like paleontologists, molecular phylogeneticists have different ideas about various details, but here is a typical family tree according to molecular phylogenetics: Note that the diagram shown here omits extinct groups, as one cannot extract DNA from fossils.
Eutheria Atlantogenata ("born round the Atlantic ocean")
Xenarthra (armadillos, anteaters, sloths)
Afroinsectiphilia (golden moles, tenrecs, otter shrews)
Macroscelidea (elephant shrews)
Paenungulata ("not quite ungulates")
Sirenia (manatees, dugongs)
Boreoeutheria ("northern true / placental mammals") Laurasiatheria
Erinaceomorpha (hedgehogs, gymnures)
Soricomorpha (moles, shrews, solenodons)
Cetartiodactyla (camels and llamas, pigs and peccaries, ruminants, whales and hippos)
Carnivora (cats, dogs, bears, seals)
Perissodactyla (horses, rhinos, tapirs).
Lagomorpha (rabbits, hares, pikas)
Rodentia (late Paleocene)(mice & rats, squirrels, porcupines)
Scandentia (tree shrews)
Primates (tarsiers, lemurs, monkeys, apes including humans)
Here are the most significant of the many differences between this family tree and the one familiar to paleontologists:
- The top-level division is between Atlantogenata and Boreoeutheria, instead of between Xenarthra and the rest. However, analysis of transposable element insertions supports a 3-way top-level split between Xenarthra, Afrotheria and Boreoeutheria  and the Atlantogenata clade does not receive significant support in recent distance-based molecular phylogenetics.
- Afrotheria contains several groups that are only distantly related according to the paleontologists' version: Afroinsectiphilia ("African insectivores"), Tubulidentata (aardvarks, which paleontologists regard as much closer to odd-toed ungulates than to other members of Afrotheria), Macroscelidea (elephant shrews, usually regarded as close to rabbits and rodents). The only members of Afrotheria that paleontologists would regard as closely related are Hyracoidea (hyraxes), Proboscidea (elephants) and Sirenia (manatees, dugongs).
- Insectivores are split into 3 groups: one is part of Afrotheria and the other two are distinct sub-groups within Boreoeutheria.
- Bats are closer to Carnivora and odd-toed ungulates than to primates and Dermoptera (colugos).
- Perissodactyla (odd-toed ungulates) are closer to Carnivora and bats than to Artiodactyla (even-toed ungulates).
The grouping together of the Afrotheria has some geological justification. All surviving members of the Afrotheria originate from South American or (mainly) African lineages — even the Indian elephant, which diverged from an African lineage about 7.6 million years ago. As Pangaea broke up Africa and South America separated from the other continents less than 150M years ago, and from each other between 100M and 80M years ago. The earliest known eutherian mammal is Eomaia, from about 125M years ago. So it would not be surprising if the earliest eutherian immigrants into Africa and South America were isolated there and radiated into all the available ecological niches.
Nevertheless these proposals have been controversial. Paleontologists naturally insist that fossil evidence must take priority over deductions from samples of the DNA of modern animals. More surprisingly, these new family trees have been criticised by other molecular phylogeneticists, sometimes quite harshly:
- Mitochondrial DNA's mutation rate in mammals varies from region to region — some parts hardly ever change and some change extremely quickly and even show large variations between individuals within the same species.
- Mammalian mitochondrial DNA mutates so fast that it causes a problem called "saturation", where random noise drowns out any information that may be present. If a particular piece of mitochondrial DNA mutates randomly every few million years, it will have changed several times in the 60 to 75M years since the major groups of placental mammals diverged.
Timing of placental evolution
Recent molecular phylogenetic studies suggest that most placental orders diverged about 100M to 85M years ago, but that modern families first appeared in the late Eocene and early Miocene.
Some paleontologists object that no placental fossils have been found from before the end of the Cretaceous — for example Maelestes gobiensis, from about 75M years ago, is a eutherian but not a true placental. Many Cretaceous fossil sites contain well-preserved lizards, salamanders, birds, and mammals, but not the modern forms of mammals. It is likely that they simply did not exist, and that the molecular clock runs fast during major evolutionary radiations. On the other hand there is fossil evidence from 85 million years ago of hoofed animals that may be ancestors of modern ungulates.
Fossils of the earliest members of most modern groups date from the Paleocene, a few date from later and very few from the Cretaceous, before the extinction of the dinosaurs. But some paleontologists, influenced by molecular phylogenetic studies, have used statistical methods to extrapolate backwards from fossils of members of modern groups and concluded that primates arose in the late Cretaceous. However statistical studies of the fossil record confirm that mammals were restricted in size and diversity right to the end of the Cretaceous, and rapidly grew in size and diversity during the Early Paleocene.
Evolution of mammalian features
Jaws and middle ears
See also Evolution of mammalian auditory ossicles
Hadrocodium, whose fossils date from the early Jurassic, provides the first clear evidence of fully mammalian jaw joints and middle ears, in which the jaw joint is formed by the dentary and squamosal bones while the articular and quadrate move to the middle ear, where they are known as the incus and malleus. Traditionally, separate ear bones have been used as the diagnostic cut-off point from mammals, making Hadrocodium the oldest known mammal. It does however fall outside the mammalian crown group of extant species, and is thus classified as a member of the mammaliaformes rather than as a true mammal by the crown group phylogenetic definition.
One analysis of the monotreme Teinolophos suggested that this animal had a pre-mammalian jaw joint formed by the angular and quadrate bones and that the typical mammalian middle ear evolved twice independently, in monotremes and in therian mammals, but this idea has been disputed. In fact 2 of the suggestion's authors co-authored a later paper that reinterpreted the same features as evidence that Teinolophos was a full-fledged platypus, which means it would have had a mammalian jaw joint and middle ear.
Milk production (lactation)Main article: Lactation#Evolution
It has been suggested that lactation's original function was to keep eggs moist. Much of the argument is based on monotremes (egg-laying mammals):
- Monotremes do not have nipples but secrete milk from a hairy patch on their bellies.
- During incubation, monotremes' eggs are covered in a sticky substance whose origin is not known. Before the eggs are laid, their shells have only three layers. Afterwards a fourth layer appears, and its composition is different from that of the original three. The sticky substance and the fourth layer may be produced by the mammary glands.
- If so, that may explain why the patches from which monotremes secrete milk are hairy — it is easier to spread moisture and other substances over the egg from a broad, hairy area than from a small, bare nipple.
Later research demonstrated that caseins already appeared in the common mammalian ancestor approximately 200-310 Millions of years ago.
Hair and furSee also: Evolution of hair
The first clear evidence of hair or fur is in fossils of Castorocauda, from 164M years ago in the mid Jurassic.
From 1955 onwards some scientists have interpreted the foramina (passages) in the maxillae (upper jaws) and premaxillae (small bones in front of the maxillae) of cynodonts as channels that supplied blood vessels and nerves to vibrissae (whiskers), and suggested that this was evidence of hair or fur. But foramina do not necessarily show that an animal had vibrissae — for example the modern lizard Tupinambis has foramina that are almost identical to those found in the non-mammalian cynodont Thrinaxodon.
The evolution of erect limbs in mammals is incomplete — living and fossil monotremes have sprawling limbs. In fact some scientists think that the parasagittal (non-sprawling) limb posture is a synapomorphy (distinguishing characteristic) of the Boreosphenida, a group that contains the Theria and therefore includes the last common ancestor of modern marsupials and placentals — and therefore that all earlier mammals had sprawling limbs.
Sinodelphys (the earliest known marsupial) and Eomaia (the earliest known eutherian) lived about 125M years ago, so erect limbs must have evolved before then.
"Warm-bloodedness" is a complex and rather ambiguous term, because it includes some or all of the following:
- Endothermy, i.e. the ability to generate heat internally rather than via behaviors such as basking or muscular activity.
- Homeothermy, i.e. maintaining a fairly constant body temperature.
- Tachymetabolism, i.e. maintaining a high metabolic rate, particularly when at rest. This requires a fairly high and stable body temperature, since biochemical processes run about half as fast if an animal's temperature drops by 10°C; most enzymes have an optimum operating temperature and their efficiency drops rapidly outside the preferred range.
Since scientists cannot know much about the internal mechanisms of extinct creatures, most discussion focuses on homeothermy and tachymetabolism.
Modern monotremes have a lower body temperature and more variable metabolic rate than marsupials and placentals. So the main question is when a monotreme-like metabolism evolved in mammals. The evidence found so far suggests Triassic cynodonts may have had fairly high metabolic rates, but is not conclusive.
Modern mammals have respiratory turbinates, convoluted structures of thin bone in the nasal cavity. These are lined with mucous membranes that warm and moisten inhaled air and extract heat and moisture from exhaled air. An animal with respiratory turbinates can maintain a high rate of breathing without the danger of drying its lungs out, and therefore may have a fast metabolism. Unfortunately these bones are very delicate and therefore have not yet been found in fossils. But rudimentary ridges like those that support respiratory turbinates have been found in Triassic therapsids such as Thrinaxodon and Diademodon, which suggests that they may have had fairly high metabolic rates.  
Bony secondary palate
Mammals have a secondary bony palate, which separates the respiratory passage from the mouth, allowing them to eat and breathe at the same time. Secondary bony palates have been found in the more advanced cynodonts and have been used as evidence of high metabolic rates. But some cold-blooded vertebrates have secondary bony palates (crocodilians and some lizards), while birds, which are warm-blooded, do not have them.
A muscular diaphragm helps mammals to breathe, especially during strenuous activity. For a diaphragm to work, the ribs must not restrict the abdomen, so that expansion of the chest can be compensated for by reduction in the volume of the abdomen and vice versa. The advanced cynodonts have very mammal-like rib cages, with greatly reduced lumbar ribs. This suggests that these animals had diaphragms, were capable of strenuous activity for fairly long periods and therefore had high metabolic rates. On the other hand these mammal-like rib cages may have evolved to increase agility. The movement of even advanced therapsids was however "like a wheelbarrow", with the hindlimbs providing all the thrust while the forelimbs only steered the animal, in other words advanced therapsids were not as agile as either modern mammals or the early dinosaurs. So the idea that the main function of these mammal-like rib cages was to increase agility is doubtful.
The therapsids had sprawling forelimbs and semi-erect hindlimbs. This suggests that Carrier's constraint would have made it rather difficult for them to move and breathe at the same time, but not as difficult as it is for animals such as lizards, which have completely sprawling limbs. The cynodonts (advanced therapsids) had costal plates that stiffened the rib cage and therefore may have reduced sideways flexing of the trunk while moving, which would have made it a little easier for them to breathe while moving . These facts suggest that advanced therapsids were significantly less active than modern mammals of similar size and therefore may have had slower metabolisms.
Insulation (hair and fur)
Insulation is the "cheapest" way to maintain a fairly constant body temperature, without consuming energy to produce more body heat. Therefore, possession of hair or fur would be good evidence of homeothermy but would not be such strong evidence of a high metabolic rate. 
The first clear evidence of hair or fur is in fossils of Castorocauda, from 164M years ago in the mid Jurassic; arguments that advanced therapsids had hair are unconvincing.
Mammals are noted for their large brain size relative to body size, compared to other animal groups. Recent findings suggest that the first brain area to expand was the brain area involved in smell. Scientists scanned the skulls of early mammal species dating back to 190-200 million years ago and compared the brain case shapes to earlier pre-mammal species and found that the brain area involved in the sense of smell was the first to enlarge. This change may have allowed these early mammals to hunt insects at night when dinosaurs were not active.
- ^ a b "Amniota - Palaeos". http://www.palaeos.org/Amniota.
- ^ a b "Synapsida overview - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit390/000.html.
- ^ a b Mammalia: Overview - Palaeos
- ^ Cowen, R. (2000). History of Life. Oxford: Blackwell Science. pp. 432. ISBN 0726602876.
- ^ K. A. Kermack, Frances Mussett and H. W. RIgney (January 1981). "The skull of Morganucodon". Zoological Journal of the Linnean Society 71 (1): page 148. doi:10.1111/j.1096-3642.1981.tb01127.x.
- ^ "Synapsida: Varanopseidae - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit390/200.html.
- ^ a b "Therapsida - Palaeos". http://www.palaeos.com/Vertebrates/Units/400Therapsida/100.html.
- ^ Kermack, D.M.; Kermack, K.A. (1984). The evolution of mammalian characters. Croom Helm. ISBN 079915349.
- ^ a b c d Bennett, A.F.; Ruben, J.A. (1986). "The metabolic and thermoregulatory status of therapsids". In Hotton III, N; MacLean, P.D.; Roth, J.J. et al.. The ecology and biology of mammal-like reptiles. Washington: Smithsonian Institution Press, Washington. pp. 207–218.
- ^ "Dinocephalia - Palaeos". http://www.palaeos.com/Vertebrates/Units/400Therapsida/300.html.
- ^ "Neotherapsida - Palaeos". http://www.palaeos.com/Vertebrates/Units/400Therapsida/700.html.
- ^ "Theriodontia - Paleos". http://www.palaeos.com/Vertebrates/Units/400Therapsida/400.800.html.
- ^ "Cynodontia Overview - Palaeos". http://www.palaeos.com/Vertebrates/Units/410Cynodontia/410.000.html.
- ^ Groenewald, G.H., Welman, J. and MacEachern, J.A. (April 2001). "Vertebrate Burrow Complexes from the Early Triassic Cynognathus Zone (Driekoppen Formation, Beaufort Group) of the Karoo Basin, South Africa". PALAIOS 16 (2): 148–160. doi:10.1669/0883-1351(2001)016<0148:VBCFTE>2.0.CO;2. ISSN 0883-1351. http://palaios.sepmonline.org/cgi/content/abstract/16/2/148. Retrieved 2008-07-07.
- ^ "Olenekian Age of the Triassic - Palaeos". http://www.palaeos.com/Mesozoic/Triassic/Olenekian.html.
- ^ a b Benton, M.J. (2004), Vertebrate Palaeontology (3rd ed.), Oxford: Blackwell Science, ISBN 978-0-632-05637-8
- ^ Campbell, J.W. (1979). C.L. Prosser. ed. Comparative Animal Physiology (3rd ed.). W. B. Sauders. pp. 279–316.
- ^ Ruben, J.A., and Jones, T.D. (2000). "Selective Factors Associated with the Origin of Fur and Feathers". American Zoologist 40 (4): 585–596. doi:10.1093/icb/40.4.585. http://icb.oxfordjournals.org/cgi/content/full/40/4/585.
- ^ Rowe, T.B.; Macrini, T.E.; Luo, Zhe-Xi (2011). "Fossil evidence on origin of the mammalian brain". Science 332: 955-957.
- ^ Raichle, M.E.; Gusnard, D.A. (August 6, 2002). "Appraising the brain's energy budget". PNAS 99 (16): 10237–10239. Bibcode 2002PNAS...9910237R. doi:10.1073/pnas.172399499. PMC 124895. PMID 12149485. http://www.pnas.org/cgi/content/full/99/16/10237.
- ^ "Brain power". New Scientist. 2006. http://www.newscientist.com/blog/shortsharpscience/2006/09/brain-power.html.
- ^ Travis, J (October 2003). "Visionary research: scientists delve into the evolution of color vision in primates". Science News 164 (15). http://findarticles.com/p/articles/mi_m1200/is_15_164/ai_110266608.
- ^ a b Cifelli, R.L. (November 2001). "Early mammalian radiations". Journal of Paleontology 75 (6): 1214. doi:10.1666/0022-3360(2001)075<1214:EMR>2.0.CO;2. ISSN 0022-3360. http://findarticles.com/p/articles/mi_qa3790/is_200111/ai_n8958762/pg_6.
- ^ Luo, Z.-X. (2007). "Transformation and diversification in early mammal evolution". Nature 450 (7172): 1011–1019. Bibcode 2007Natur.450.1011L. doi:10.1038/nature06277. PMID 18075580.
- ^ a b c "Mammaliformes - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit420/420.100.html.
- ^ "Morganucodontids & Docodonts - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit420/420.200.html.
- ^ a b c Ji, Q.; Luo, Z-X, Yuan, C-X, and Tabrum, A.R. (February 2006). "A Swimming Mammaliaform from the Middle Jurassic and Ecomorphological Diversification of Early Mammals". Science 311 (5764): 1123–7. Bibcode 2006Sci...311.1123J. doi:10.1126/science.1123026. PMID 16497926. http://www.sciencemag.org/cgi/content/abstract/311/5764/1123. See also the news item at "Jurassic "Beaver" Found; Rewrites History of Mammals". http://news.nationalgeographic.com/news/2006/02/0223_060223_beaver.html.
- ^ "Symmetrodonta - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit420/420.300.html.
- ^ Luo, Z-X., Crompton, A.W., and Sun, A-L. (May 2001). "A New Mammaliaform from the Early Jurassic and Evolution of Mammalian Characteristics". Science 292 (5521): 1535–1540. Bibcode 2001Sci...292.1535L. doi:10.1126/science.1058476. PMID 11375489. http://www.sciencemag.org/cgi/content/full/292/5521/1535. Retrieved 2008-09-08.
- ^ a b "Mammalia - Palaeos". http://www.palaeos.com/Vertebrates/Units/430Mammalia/430.100.html.
- ^ a b Jacobs, L.L., Winkler, D.A., and Murry P.A. (July 1, 1989). "Modern Mammal Origins: Evolutionary Grades in the Early Cretaceous of North America". Proceedings of the National Academy of Sciences of the USA 86 (13): 4992–4995. Bibcode 1989PNAS...86.4992J. doi:10.1073/pnas.86.13.4992. ISSN 0027-8424. JSTOR 34031. PMC 297542. PMID 2740336. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=297542.
- ^ Rauhut, O.W.M., Martin, T., Ortiz-Jaureguizar, E. and Puerta, P. (14 March 2002). "A Jurassic mammal from South America". Nature 416 (6877): 165–168. doi:10.1038/416165a. PMID 11894091. http://www.nature.com/nature/journal/v416/n6877/full/416165a.html.
- ^ a b c Rowe, T., Rich, T.H., Vickers-Rich, P., Springer, M., and Woodburne, M.O. (January 2008). "The oldest platypus and its bearing on divergence timing of the platypus and echidna clades". Proceedings of the National Academy of Sciences 105 (4): 1238–1242. Bibcode 2008PNAS..105.1238R. doi:10.1073/pnas.0706385105. PMC 2234122. PMID 18216270. http://www.pnas.org/cgi/content/full/105/4/1238.
- ^ "Molecules, morphology, and ecology indicate a recent, amphibious ancestry for echidnas". http://www.pnas.org/content/106/40/17089.
- ^ a b "Appendicular Skeleton". http://courses.washington.edu/chordate/453lectures/set2/453-appendskel-06.htm.
- ^ "Mammalia: Spalacotheroidea & Cladotheria - Palaeos". http://www.palaeos.com/Vertebrates/Units/430Mammalia/430.500.html.
- ^ "Metatheria - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit440/440.100.html.
- ^ Szalay, F.S.; Trofimov, B.A. (1996). "The Mongolian Late Cretaceous Asiatherium, and the early phylogeny and paleobiogeography of Metatheria" (— Scholar search). Journal of Vertebrate Paleontology 16 (3): 474–509. doi:10.1080/02724634.1996.10011335. http://www.vertpaleo.org/jvp/16-474-509.html. [dead link]
- ^ "Oldest Marsupial Fossil Found in China". National Geographic News. 2003-12-15. http://news.nationalgeographic.com/news/2003/12/1215_031215_oldestmarsupial.html.
- ^ "Didelphimorphia - Palaeos". http://www.palaeos.com/Vertebrates/Units/Unit440/440.100.html#Didelphimorphia.
- ^ "Family Peramelidae (bandicoots and echymiperas)". http://animaldiversity.ummz.umich.edu/site/accounts/information/Peramelidae.html.
- ^ "Species is as species does... Part II". http://lancelet.blogspot.com/2005/12/species-is-as-species-does-part-ii.html.
- ^ "Marsupials". http://paleo.amnh.org/bjburger/fossilmammal/ma3.html.
- ^ Novacek, M.J.; Rougier, G.W.; Wible, J.R.; McKenna, M.C.; Dashzeveg, D; Horovitz, I (1997). "Epipubic bones in eutherian mammals from the late Cretaceous of Mongolia". Nature 389 (6650): 440–441. Bibcode 1997Natur.389..483N. doi:10.1038/39020. PMID 9333234.
- ^ White, T.D. (August 9, 1989). "An analysis of epipubic bone function in mammals using scaling theory". Journal of Theoretical Biology 139 (3): 343–57. doi:10.1016/S0022-5193(89)80213-9. PMID 2615378.
- ^ "Eomaia scansoria: discovery of oldest known placental mammal". http://www.evolutionpages.com/Eomaia%20scansoria.htm.
- ^ Reilly, S.M., and White, T.D. (January 2003). "Hypaxial Motor Patterns and the Function of Epipubic Bones in Primitive Mammals". Science 299 (5605): 400–402. Bibcode 2003Sci...299..400R. doi:10.1126/science.1074905. PMID 12532019. http://www.sciencemag.org/cgi/content/full/299/5605/400. Retrieved 2008-09-24.
- ^ Novacek, M.J., Rougier, G.W, Wible, J.R., McKenna, M.C, Dashzeveg, D., and Horovitz, I. (October 1997). "Epipubic bones in eutherian mammals from the Late Cretaceous of Mongolia". Nature 389 (6650): 483–486. Bibcode 1997Natur.389..483N. doi:10.1038/39020. PMID 9333234. http://www.nature.com/nature/journal/v389/n6650/full/389483a0.html. Retrieved 2008-09-24.
- ^ Fox, D (1999). "Why we don't lay eggs". New Scientist. http://www.newscientist.com/article/mg16221904.800-why-we-dont-lay-eggs.html.
- ^ "Eutheria - Palaeos". http://www.palaeos.com/Vertebrates/Units/450Eutheria/450.100.html#Eutheria.
- ^ Ji, Q., Luo, Z-X., Yuan, C-X.,Wible, J.R., Zhang, J-P., and Georgi, J.A. (April 2002). "The earliest known eutherian mammal". Nature 416 (6883): 816–822. doi:10.1038/416816a. PMID 11976675. http://www.nature.com/nature/journal/v416/n6883/full/416816a.html. Retrieved 2008-09-24.
- ^ Luo, Z.-X., Wible, J.R. (2005). "A Late Jurassic Digging Mammal and Early Mammal Diversification". Science 308 (5718): 103–107.. Bibcode 2005Sci...308..103L. doi:10.1126/science.1108875. PMID 15802602.
- ^ Meng, J., Hu, Y., Wang, Y., Wang, X., Li, C. (December 2006). "A Mesozoic gliding mammal from northeastern China". Nature 444 (7121): 889–893. Bibcode 2006Natur.444..889M. doi:10.1038/nature05234. PMID 17167478. http://www.nature.com/nature/journal/v444/n7121/abs/nature05234.html.
- ^ Li, J., Wang, Y., Wang, Y., Li, C. (2000). "A new family of primitive mammal from the Mesozoic of western Liaoning, China". Chinese Science Bulletin 46 (9): 782–785. doi:10.1007/BF03187223. abstract, in English
- ^ Hu, Y., Meng, J., Wang, Y., Li, C. (2005). "Large Mesozoic mammals fed on young dinosaurs". Nature 433 (7022): 149–152. Bibcode 2005Natur.433..149H. doi:10.1038/nature03102. PMID 15650737. http://bill.srnr.arizona.edu/classes/182/NatureDownloads/LargeMesMamm-Na.pdf.
- ^ Wible, J.R., Rougier, G.W., Novacek, M.J., and Asher, R.J. (2007). "Cretaceous eutherians and Laurasian origin for placental mammals near the K/T boundary". Nature 447 (7147): 1003–1006. Bibcode 2007Natur.447.1003W. doi:10.1038/nature05854. PMID 17581585. http://www.nature.com/nature/journal/v447/n7147/full/nature05854.html.
- ^ Murphy, W.J., Eizirik, E., Springer, M.S et al. (14 December 2001). "Resolution of the Early Placental Mammal Radiation Using Bayesian Phylogenetics". Science 294 (5550): 2348–2351. Bibcode 2001Sci...294.2348M. doi:10.1126/science.1067179. PMID 11743200.
- ^ Kriegs, J.O., Churakov, G., Kiefmann, M., et al. (2006). "Retroposed Elements as Archives for the Evolutionary History of Placental Mammals". PLoS Biol 4 (4): e91. doi:10.1371/journal.pbio.0040091. PMC 1395351. PMID 16515367. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1395351. (pdf version)
- ^ Nishihara, H., Maruyama, S. & Okada, N. 2009. Retroposon analysis and recent geological data suggest near-simultaneous divergence of the three superorders of mammals. PNAS 106: 5235-40.
- ^ Churakov, G., Kriegs, J.O., Baertsch, R., Zemann, A., Brosius, J. & Schmitz, J. 2009. Mosaic retroposon insertion patterns in placental mammals. Genome Research 19: 868-75.
- ^ Robert W. Meredith et al., 2011, Impacts of the Cretaceous Terrestrial Revolution and KPg extinction on mammal diversification., Science 334:521-4.
- ^ "Scientists map elephant evolution". BBC News. 2007-07-24. http://news.bbc.co.uk/2/hi/science/nature/6913934.stm. Retrieved 2008-08-11.
- ^ Historical perspective (the Dynamic Earth, USGS)
- ^ Cretaceous map
- ^ Insectivora Overview - Palaeos
- ^ Springer, M.S.; Douzery, E. (1996). "Secondary Structure and patterns of evolution among mammalian mitochondrial 12S rRNA molecules". J. Mol. Evol. 43 (4): 357–373. doi:10.1007/BF02339010. PMID 8798341.
- ^ Springer, M.S.; Hollar, L.J.; Burk, A. (1995). "Compensatory substitutions and the evolution of the mitochondrial 12S rRNA gene in mammals". Mol. Biol. Evol. 12 (6): 1138–1150. PMID 8524047.
- ^ Li, W-H (1997). Molecular Evolution. Sinauer Associates. ISBN 0878932666.
- ^ Bininda-Emonds, O.R.P.; Cardillo, M.; Jones, K.E.; 'et al.', Ross D. E.; Beck, Robin M. D.; Grenyer, Richard; Price, Samantha A.; Vos, Rutger A. et al. (2007). "The delayed rise of present-day mammals". Nature 446 (7135): 507–511. Bibcode 2007Natur.446..507B. doi:10.1038/nature05634. PMID 17392779. http://scienceblogs.com/pharyngula/2007/03/dont_blame_the_dinosaurs.php.
- ^ Dinosaur Extinction Spurred Rise of Modern Mammals
- ^ Benton, M.J. (December 1999). "Early origins of modern birds and mammals: molecules vs. morphology". BioEssays 21 (12): 1043–1051. doi:10.1002/(SICI)1521-1878(199912)22:1<1043::AID-BIES8>3.0.CO;2-B. PMID 10580989.
- ^ Archibald, J.D. (May 1996). "Fossil Evidence for a Late Cretaceous Origin of "Hoofed" Mammals". Science 272 (5265): 1150–1153. Bibcode 1996Sci...272.1150A. doi:10.1126/science.272.5265.1150. PMID 8662448. http://www.sciencemag.org/cgi/content/abstract/272/5265/1150. Retrieved 2008-09-08.
- ^ Martin, R.D.; Soligo, C.; Tavaré, S. (2007). "Primate Origins: Implications of a Cretaceous Ancestry" (PDF). Folia Primatologica 78 (5-6): 277–296. doi:10.1159/000105145. PMID 17855783. http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=105145&Ausgabe=233328&ProduktNr=223842&filename=105145.pdf. — a similar paper by these authors is free online at New light on the dates of primate origins and divergence
- ^ Alroy J. (March 1999). "The fossil record of North American mammals: evidence for a Paleocene evolutionary radiation". Systematic biology 48 (1): 107–18. doi:10.1080/106351599260472. PMID 12078635.
- ^ Archibald J.D., and Deutschman D.H. (June 2001). "Quantitative Analysis of the Timing of the Origin and Diversification of Extant Placental Orders". Journal of Mammalian Evolution 8 (2): 107–124. doi:10.1023/A:1011317930838. http://www.ingentaconnect.com/content/klu/jomm/2001/00000008/00000002/00342277. Retrieved 2008-09-24.
- ^ Rich, T.H., Hopson, J.A., Musser, A.M., Flannery., T.GF., and Vickers-Rich, P. (11 February 2005). "Independent Origins of Middle Ear Bones in Monotremes and Therians". Science 307 (5711): 910–914. Bibcode 2005Sci...307..910R. doi:10.1126/science.1105717. PMID 15705848. http://www.sciencemag.org/cgi/content/abstract/307/5711/910. For other opinions see "Technical comments" linked from same Web page
- ^ Oftedal, O.T. (2002). "The mammary gland and its origin during synapsid evolution". Journal of Mammary Gland Biology and Neoplasia 7 (3): 225–252. doi:10.1023/A:1022896515287. PMID 12751889.
- ^ Oftedal, O.T. (2002). The origin of lactation as a water source for parchment-shelled eggs=Journal of Mammary Gland Biology and Neoplasia. 7. pp. 253–266.
- ^ Lactating on Eggs
- ^ Borders, R.; Robertson, W. (1993). "Washington's pesticide panel: process and product". Veterinary and human toxicology 35 (3): 258–259. PMID 8351802.
- ^ a b c d Brink, A.S. (1955). "A study on the skeleton of Diademodon". Palaeontologia Africana 3: 3–39.
- ^ a b c d Kemp, T.S. (1982). Mammal-like reptiles and the origin of mammals. London: Academic Press. pp. 363. ISBN 0124041205.
- ^ Estes, R. (1961). "Cranial anatomy of the cynodont reptile Thrinaxodon liorhinus". Bulletin of the Museum of Comparative Zoology (1253): 165–180.
- ^ Kielan−Jaworowska, Z.; Hurum, J.H.. (2006). "Limb posture in early mammals: Sprawling or parasagittal" (PDF). Acta Palaeontologica Polonica 51 (3): 10237–10239. http://www.app.pan.pl/archive/published/app51/app51-393.pdf. Retrieved 2008-09-24.
- ^ Paul, G.S. (1988). Predatory Dinosaurs of the World. New York: Simon and Schuster. pp. 464. ISBN 0671619462.
- ^ Hillenius, W.H. (1992). "The evolution of nasal turbinates and mammalian endothermy". Paleobiology 18 (1): 17–29.
- ^ Ruben, J. (1995). "The evolution of endothermy in mammals and birds: from physiology to fossils". Annual Review of Physiology 57: 69–95. doi:10.1146/annurev.ph.57.030195.000441. PMID 7778882.
- ^ McNab, B.K. (1978). "The evolution of endothermy in the phylogeny of mammals". American Naturalist 112 (983): 1–21. doi:10.1086/283249.
- ^ Ccowen, R. (2000). History of Life. Oxford: Blackwell Science. pp. 432.
- ^ Jenkins, F.A., Jr (1971). "The postcranial skeleton of African cynodonts". Bulletin of the Peabody Museum of Natural History (36): 1–216.
- ^ Pough, F.H; Heiser, J.B.; McFarland, W.N. (1996). Vertebrate Life. New Jersey: Prentice-Hall. pp. 798. ISBN 0023963700.
- ^ Sidor, C.A.; Hopson, J.A. (1998). "Ghost lineages and "mammalness": assessing the temporal pattern of character acquisition in the Synapsida". Paleobiology (24): 254–273.
- ^ Schmidt-Nielsen, K. (1975). Animal physiology: Adaptation and environment. Cambridge: Cambridge University Press. pp. 699. ISBN 0521381967.
- ^ Withers, P.C. (1992). Comparative Animal Physiology. Fort Worth: Saunders College. pp. 949. ISBN 0030128471.
- ^ a b c Victoria Gill (20 May 2011). "Mammals' large brains evolved for smell". BBC News. http://www.bbc.co.uk/nature/13448202. Retrieved 22 May 2011.
- Robert L. Carroll, Vertebrate Paleontology and Evolution, W. H. Freeman and Company, New York, 1988 ISBN 0-716-71822-7. Chapters XVII through XXI
- Nicholas Hotton III, Paul D. MacLean, Jan J. Roth, and E. Carol Roth, editors, The Ecology and Biology of Mammal-like Reptiles, Smithsonian Institution Press, Washington and London, 1986 ISBN 0-87474-524-1
- T. S. Kemp, The Origin and Evolution of Mammals, Oxford University Press, New York, 2005 ISBN 0-19-850760-7
- Zofia Kielan-Jaworowska, Richard L. Cifelli, and Zhe-Xi Luo, Mammals from the Age of Dinosaurs: Origins, Evolution, and Structure, Columbia University Press, New York, 2004 ISBN 0-231-11918-6. Comprehensive coverage from the first mammals up to the time of the K-T mass extinction.
- Zhe-Xi Luo, "Transformation and diversification in early mammal evolution", Nature volume 450 number 7172 (13 December 2007) pages 1011–1019. doi:10.1038/nature06277. A survey article with 98 references to the scientific literature.
- The Cynodontia covers several aspects of the evolution of cynodonts into mammals, with plenty of references.
- Evolution by taxon
- Mammal anatomy
- Prehistoric mammals
Wikimedia Foundation. 2010.