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Placental mammals ( Placentalia ) are one of the three extant subdivisions of the class , the other two being and . Placentalia contains the vast majority of extant mammals, which are partly distinguished from monotremes and marsupials in that the fetus is carried in the of its mother to a relatively late stage of development. The name is something of a misnomer, considering that marsupials also nourish their fetuses via a , though for a relatively briefer period, giving birth to less-developed young, which are then nurtured for a period inside the mother's pouch. Placentalia represents the only living group within , which contains all mammals that are more closely related to placentals than they are to marsupials.


Anatomical features
Placental mammals are anatomically distinguished from other mammals by:
  • a sufficiently wide opening at the bottom of the to allow the birth of a large baby relative to the size of the mother.
  • the absence of extending forward from the pelvis, which are found in all other mammals. (Their function in non-placental mammals is to stiffen the body during locomotion, but in placentals they would inhibit the expansion of the abdomen during pregnancy.)
  • the rearmost bones of the foot fit into a socket formed by the ends of the and , forming a complete mortise and tenon upper ankle joint.
  • the presence of a at the bottom of the fibula.
  • instead of a Exceptional adult placentals that retain a cloaca are , , , and some . like monotremes, marsupials and most other , the urogenital ducts exit through the or and the opens as the .
    (1992). 9780226870137, University of Chicago Press. .
  • the presence of a in between the cerebral hemispheres.


Subdivisions
Analysis of molecular data led to rapid changes in assessments of the phylogeny of placental orders at the close of the 20th century. A novel phylogeny and classification of placental orders appeared with Waddell, Hasegawa and Okada in 1999. "Jumping genes"-type presence/absence patterns have provided corroboration of phylogenetic relationships inferred from molecular sequences. It is now widely accepted that there are three major subdivisions or lineages of placental mammals: , , and . All of these diverged from common ancestors.

2022 studies of Bertrand, O. C. and Sarah L. Shelley have identified and as basal placental mammal clades.Sarah L. Shelley (2022.) "The phylogeny of Paleocene mammals and the evolution of Placentalia", in "The Society of Vertebrate Paleontology 82nd annual meeting"

The 19 living orders of Placentalia in the three groups are:

The exact relationships among these three lineages is currently a subject of debate, and four different hypotheses have been proposed with respect to which group is basal or diverged first from other placentals. These hypotheses are (basal Boreoeutheria), (basal Xenarthra), Exafroplacentalia (basal Afrotheria) and a hypothesis supporting a near simultaneous divergence. Estimates for the divergence times among these three placental groups mostly range from 105 to 120 million years ago (MYA), depending on the type of DNA, whether it is translated, and the phylogenetic method (e.g. or mitochondrial), and varying interpretations of data. In addition, a strict molecular clock does not hold, so it is necessary to assume models of how evolutionary rates change along lineages. These assumptions alone can make substantial differences to the relative ages of different mammal groups estimated with genomic data.

and classification based on Amrine-Madsen, H. et al. (2003) and Asher, R. J. et al. (2009) Compare with Waddell, Hasegawa and Okada (1999) and Waddell et al. (2001).


Genomics
, the has been sequenced for at least one species in each extant placental order and in 83% of families (105 of 127 extant placental families).Zoonomia Consortium (2020) A comparative genomics multitool for scientific discovery and conservation. Nature 587, 240–245

See list of sequenced animal genomes.


Evolutionary history
True placental mammals (the including all modern placentals) arose from stem-group members of the clade , which had existed since at least the epoch, about 170 mya. These early eutherians were small, nocturnal insect eaters, with adaptations for life in trees.

True placentals may have originated in the around 90 mya, but the earliest undisputed fossils are dated to the Cretaceous–Paleogene boundary (K-Pg boundary). The genus is sometimes placed as a stem-ungulate, with probably the earliest known species P. coombsi from the strata within the Hell Creek Formation specifically dated to at least 300,000 years before the K-Pg boundary. The genus , sometimes considered a stem-primate, appears no more than 300,000 years after the K-Pg boundary. One study has recovered both genera to be closely related and as stem- outside modern placental mammals, but others have recovered Protungulatum as a based on phylogenetic analysis and inner ear anatomy different from non-placentals. The rapid appearance of placentals after the mass extinction at the end of the suggests that the group had already originated and undergone an initial diversification in the Late Cretaceous, as suggested by . The lineages leading to Xenarthra and Afrotheria probably originated around 90 mya, and Boreoeutheria underwent an initial diversification around 70-80 mya, producing the lineages that eventually would lead to modern primates, rodents, , , and .

However, modern members of the placental orders originated in the around 66 to 23 mya, following the Cretaceous–Paleogene extinction event. The evolution of crown orders such modern primates, rodents, and carnivores appears to be part of an adaptive radiation that took place as mammals quickly evolved to take advantage of ecological that were left open when most dinosaurs and other animals disappeared following the Chicxulub asteroid impact. As they occupied new niches, mammals rapidly increased in body size, and began to take over the large herbivore and large carnivore niches that had been left open by the decimation of the dinosaurs (and perhaps more relevantly competing ). Mammals also exploited niches that the non-avian dinosaurs had never touched: for example, evolved flight and echolocation, allowing them to be highly effective nocturnal, aerial insectivores; and whales first occupied freshwater lakes and rivers and then moved into the oceans. Primates, meanwhile, acquired specialized grasping hands and feet which allowed them to grasp branches, and large eyes with keener vision which allowed them to forage in the dark.

The evolution of land placentals followed different pathways on different continents since they cannot easily cross large bodies of water. An exception is smaller placentals such as rodents and primates, who left and colonized Africa and then South America via .

In Africa, the underwent a major adaptive radiation, which led to elephants, , , , , and . In South America a similar event occurred, with radiation of the Xenarthra, which led to modern , , and , as well as the extinct and . Expansion in Laurasia was dominated by Boreoeutheria, which includes primates and rodents, , carnivores, and . These groups expanded beyond a single continent when land bridges formed linking Africa to Eurasia and South America to North America.

A study on eutherian diversity suggests that placental diversity was constrained during the , while mammals diversified; afterwards, multituberculates decline and placentals explode in diversity.


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