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Bilateria () is a large of characterised by bilateral symmetry during embryonic development. This means their are laid around a longitudinal axis with a front (or "head") and a rear (or "tail") end, as well as a left–right–symmetrical belly () and back (dorsal) surface. Nearly all bilaterians maintain a bilaterally symmetrical body as adults; the most notable exception is the , which have pentaradial symmetry as adults, but bilateral symmetry as . With few exceptions, bilaterian embryos are , having three : , and , and have complete with a separate and . Some bilaterians lack , while others have a derived from the , or a secondary cavity, the . is a characteristic feature among most bilaterians, where the organs and central nerve become concentrated at the front end of the animal.

Bilaterians constitute one of the five main lineages of animals, the other four being (sponges), (, , and ), (comb jellies) and . They rapidly diversified in the late and the , and are now by far the most successful animal lineage, with over 98% of known animal species. Bilaterians are traditionally classified as either or , based on whether the becomes the anus or mouth. The phylum , once thought to be , was erected in 2011, and has provided an extra challenge to bilaterian taxonomy, as they likely do not belong to either group.


Body plan
Animals with a bilaterally symmetric that mainly move in one direction have a head end (anterior) and a tail (posterior) end as well as a back (dorsal) and a belly (ventral); therefore they also have a left side and a right side.
(2025). 9781605353753, Sinauer Associates.
Having a front end means that this part of the body encounters stimuli, such as food, favouring , the development of a head with and a mouth. Most bilaterians () have a gut that extends through the body from mouth to anus (sometimes called a "through gut"), and sometimes a wormlike body plan with a hydrostatic skeleton. , on the other hand, have a bag gut with one opening. Many bilaterian phyla have primary which swim with and have an apical organ containing sensory cells.
(2025). 9780198566205, Oxford University Press. .

Some bilaterians have only weakly condensed nerve nets (similar to those in ), while others have either a ventral nerve cord, a dorsal nerve cord, or both (e.g. in ).


Evolution

Common ancestor
The hypothetical most recent common ancestor of all Bilateria is termed the ''. The nature of this first bilaterian is a matter of debate. One side suggests that acoelomates gave rise to the other groups (planuloid–aceloid hypothesis by Ludwig von Graff, , , or ). This means that the urbilaterian had a solid body, and all body cavities therefore secondarily arose later in different groups. The other side poses that the urbilaterian had a coelom, meaning that the main acoelomate phyla ( and ) have secondarily lost their body cavities. This is the Archicoelomata hypothesis first proposed by A. T. Masterman in 1899. Variations of the Archicoelomata hypothesis are the by in 1872 or Adam Sedgwick, and more recently the Bilaterogastrea by , and the Trochaea by Claus Nielsen.

One proposal, by Johanna Taylor Cannon and colleagues, is that the original bilaterian was a bottom dwelling worm with a single body opening, similar to . An alternative proposal, by Jaume Baguñà and colleagues, is that it may have resembled the larvae of some , which unlike the radially-symmetric adults have some bilateral symmetry. However, Lewis I. Held presents evidence that it was segmented, as the mechanism for creating segments is shared between vertebrates () and arthropods ().

(2025). 9781107621398, Cambridge University Press.

Bilaterians, presumably including the urbilaterian, share many more controlling the development of their more complex bodies, including , than do the Cnidaria and the Acoelomorpha.


Fossil record
The first evidence of Bilateria in the fossil record comes from trace fossils in sediments, and the first bona fide bilaterian fossil is , dating to . Earlier fossils are controversial; the fossil may be the earliest known bilaterian, but may also represent an infilled bubble. are known from around the time of Vernanimalcula (), but none of these have bilaterian affinities. Burrows believed to have been created by bilaterian life forms have been found in the Tacuarí Formation of Uruguay, and were believed to be at least 585 million years old. However, more recent evidence shows these fossils are actually late Paleozoic, not Ediacaran.


Phylogeny
The Bilateria are now by far the most successful animal lineage, with over 98% of known animal species. The group has traditionally been divided into two main lineages or . The deuterostomes traditionally include the , , , and the extinct . The protostomes include most of the rest, such as , , , and flatworms. There are several differences, most notably in how the develops. In particular, the first opening of the embryo becomes the mouth in protostomes, and the anus in deuterostomes. Many taxonomists now recognise at least two more superphyla among the protostomes, and . The arrow worms () have proven difficult to classify. Studies published in 2004 and 2017, place them in the Gnathifera.

The traditional division of Bilateria into Deuterostomia and Protostomia was challenged when new morphological and molecular evidence supported a sister relationship between the acoelomate taxa, and (together called ), and the remaining bilaterians. The latter clade was called Nephrozoa by Jondelius et al. (2002) and by Baguña and Riutort (2004). The acoelomorph taxa had previously been considered flatworms with secondarily lost characteristics, but the new relationship suggested that the simple acoelomate worm form was the original bilaterian body plan and that the coelom, the digestive tract, excretory organs, and nerve cords developed in the Nephrozoa. Subsequently, the acoelomorphs were placed in phylum Xenacoelomorpha, together with the , and the sister relationship between Xenacoelomorpha and Nephrozoa supported in phylogenomic analyses.

A for Bilateria under the Nephrozoa hypothesis from a 2014 review by Casey Dunn and colleagues, is shown below. The cladogram indicates approximately when some clades radiated into newer clades, in millions of years ago (Mya).

A different hypothesis is that Ambulacraria is sister to Xenacoelomorpha, together forming . Xenambulacraria may be sister to Chordata or to (corresponding to Nephrozoa without Ambulacraria, or, as shown here, to Chordata + Protostomia). A 2019 study by Hervé Philippe and colleagues presents the tree, cautioning that "the support values are very low, meaning there is no solid evidence to refute the traditional protostome and deuterostome dichotomy". As of 2024, the issue of which hypothesis is correct remains unresolved.

Cladogram showing Xenambulacraria hypothesis with a Deuterostomia:

Cladogram showing hypothesis of Xenambulacraria within a monophyletic Deuterostomia:


Taxonomic history
The Bilateria were named by the Austrian embryologist Berthold Hatschek in 1888. In his classification, the group included the Zygoneura, Ambulacraria, and Chordonii (the Chordata). In 1910, the Austrian zoologist renamed the Zygoneura to Protostomia, and created the Deuterostomia to encompass the Ambulacraria and Chordonii.


See also
  • Embryological origins of the mouth and anus


Notes

External links

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