Coelom

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Coelom
Annelid redone w white background.svg
Cross-section of an oligochaete worm. The worm's body cavity surrounds the central typhlosole.
Details
Pronunciation( /ˈsləm/ SEE-ləm, plural coeloms or coelomata /sˈlmətə/ see-LOH-mə-tə)
Identifiers
Greek koilōma
Anatomical terminology

The coelom (or celom) [1] is the main body cavity in many animals [2] and is positioned inside the body to surround and contain the digestive tract and other organs. In some animals, it is lined with mesothelium. In other animals, such as molluscs, it remains undifferentiated. In the past, and for practical purposes, coelom characteristics have been used to classify bilaterian animal phyla into informal groups.

Contents

Etymology

The term coelom derives from the Ancient Greek word κοιλία (koilía) 'cavity'. [3] [4] [5]

Structure

Development

The coelom is the mesodermally lined cavity between the gut and the outer body wall.

During the development of the embryo, coelom formation begins in the gastrulation stage. The developing digestive tube of an embryo forms as a blind pouch called the archenteron.

In protostomes, the coelom forms by a process known as schizocoely. [6] The archenteron initially forms, and the mesoderm splits into two layers: the first attaches to the body wall or ectoderm, forming the parietal layer and the second surrounds the endoderm or alimentary canal forming the visceral layer. The space between the parietal layer and the visceral layer is known as the coelom or body cavity.

In deuterostomes, the coelom forms by enterocoely. [6] The archenteron wall produces buds of mesoderm, and these mesodermal diverticula hollow to become the coelomic cavities. Deuterostomes are therefore known as enterocoelomates. Examples of deuterostome coelomates belong to three major clades: chordates (vertebrates, tunicates, and lancelets), echinoderms (starfish, sea urchins, sea cucumbers), and hemichordates (acorn worms and graptolites).

Origins

The evolutionary origin of the coelom is uncertain. The oldest known animal to have had a body cavity was the Vernanimalcula . Current hypothesis include:[ citation needed ] [7]

Functions

A coelom can absorb shock or provide a hydrostatic skeleton. It can also support an immune system in the form of coelomocytes that may either be attached to the wall of the coelom or may float about in it freely. The coelom allows muscles to grow independently of the body wall — this feature can be seen in the digestive tract of tardigrades (water bears) which is suspended within the body in the mesentery derived from a mesoderm-lined coelom.

Coelomic fluid

The fluid inside the coelom is known as coelomic fluid. This is circulated by mesothelial cilia or by contraction of muscles in the body wall.[ clarification needed ] [9] The coelomic fluid serves several functions: it acts as a hydroskeleton; it allows free movement and growth of internal organs; it serves for transport of gases, nutrients and waste products around the body; it allows storage of sperm and eggs during maturation; and it acts as a reservoir for waste. [10]

Classification in zoology

In the past, some zoologists grouped bilaterian animal phyla based on characteristics related to the coelom for practical purposes, knowing, and explicitly stating, that these groups were not phylogenetically related. Animals were classified in three informal groups according to the type of body cavity they possess, in a non-taxonomic, utilitarian way, as the Acoelomata, Pseudocoelomata, and Coelomata. These groups were never intended to represent related animals, or a sequence of evolutionary traits.

However, although this scheme was followed by a number of college textbooks and some general classifications, it is now almost totally abandoned as a formal classification. Indeed, as late as 2010, one author of a molecular phylogeny study mistakenly called this classification scheme the "traditional, morphology-based phylogeny". [11]

Classification of tripoblasts based on body cavities Figure 27 02 05.jpg
Classification of tripoblasts based on body cavities

Coelomate animals or Coelomata (also known as eucoelomates – "true coelom") have a body cavity called a coelom with a complete lining called peritoneum derived from mesoderm (one of the three primary tissue layers). The complete mesoderm lining allows organs to be attached to each other so that they can be suspended in a particular order while still being able to move freely within the cavity. Most bilateral animals, including all the vertebrates, are coelomates.

Pseudocoelomate animals have a pseudocoelom (literally "false cavity"), which is a fluid filled body cavity. Tissue derived from mesoderm partly lines the fluid filled body cavity of these animals. Thus, although organs are held in place loosely, they are not as well organized as in a coelomate. All pseudocoelomates are protostomes; however, not all protostomes are pseudocoelomates. An example of a Pseudocoelomate is the roundworm. Pseudocoelomate animals are also referred to as Blastocoelomate.

Acoelomate animals, like flatworms, have no body cavity at all. Semi-solid mesodermal tissues between the gut and body wall hold their organs in place.

Coelomates

Coeloms developed in triploblasts but were subsequently lost in several lineages. The lack of a coelom is correlated with a reduction in body size. Coelom is sometimes incorrectly used to refer to any developed digestive tract. Some organisms may not possess a coelom or may have a false coelom (pseudocoelom). Animals having coeloms are called coelomates, and those without are called acoelomates. There are also subtypes of coelom:[ citation needed ]

Coelomate phyla

According to Brusca and Brusca, [12] the following bilaterian phyla possess a coelom:

Pseudocoelomates

In some protostomes, the embryonic blastocoele persists as a body cavity. These protostomes have a fluid filled main body cavity unlined or partially lined with tissue derived from mesoderm.

This fluid-filled space surrounding the internal organs serves several functions like distribution of nutrients and removal of waste or supporting the body as a hydrostatic skeleton.

A pseudocoelomate or blastocoelomate is any invertebrate animal with a three-layered body and a pseudocoel. The coelom was apparently lost or reduced as a result of mutations in certain types of genes that affected early development. Thus, pseudocoelomates evolved from coelomates. [15] "Pseudocoelomate" is no longer considered a valid taxonomic group, since it is not monophyletic. However, it is still used as a descriptive term.

Important characteristics:

Pseudocoelomate phyla

Bilaterian pseudocoelomate phyla according to Brusca and Brusca, [12] :

Acoelomates

Acoelomates lack a fluid-filled body cavity between the body wall and digestive tract. This can cause some serious disadvantages. Fluid compression is negligible, while the tissue surrounding the organs of these animals will compress. Therefore, acoelomate organs are not protected from crushing forces applied to the animal’s outer surface. The coelom can be used for diffusion of gases and metabolites etc. These creatures do not have this need, as the surface area to volume ratio is large enough to allow absorption of nutrients and gas exchange by diffusion alone, due to dorso-ventral flattening.

A body cavity is also absent in placozoans, cnidarians (jellyfish and allies) and the ctenophores (comb jellies), but these animals are neither bilaterians or triploblastic.

See also

Related Research Articles

<span class="mw-page-title-main">Anus</span> Digestive tract waste expulsion opening

In mammals, invertebrates and most fish, the anus is the external body orifice at the exit end of the digestive tract (bowel), i.e. the opposite end from the mouth. Its function is to facilitate the expulsion of wastes that remain after digestion.

<span class="mw-page-title-main">Bryozoa</span> Phylum of colonial aquatic invertebrates called moss animals

Bryozoa are a phylum of simple, aquatic invertebrate animals, nearly all living in sedentary colonies. Typically about 0.5 millimetres long, they have a special feeding structure called a lophophore, a "crown" of tentacles used for filter feeding. Most marine bryozoans live in tropical waters, but a few are found in oceanic trenches and polar waters. The bryozoans are classified as the marine bryozoans (Stenolaemata), freshwater bryozoans (Phylactolaemata), and mostly-marine bryozoans (Gymnolaemata), a few members of which prefer brackish water. 5,869 living species are known. At least two genera are solitary ; the rest are colonial.

<span class="mw-page-title-main">Flatworm</span> Phylum of soft-bodied invertebrates

The flatworms, flat worms, Platyhelminthes, or platyhelminths are a phylum of relatively simple bilaterian, unsegmented, soft-bodied invertebrates. Unlike other bilaterians, they are acoelomates, and have no specialised circulatory and respiratory organs, which restricts them to having flattened shapes that allow oxygen and nutrients to pass through their bodies by diffusion. The digestive cavity has only one opening for both ingestion and egestion ; as a result, the food cannot be processed continuously.

<span class="mw-page-title-main">Nemertea</span> Phylum of invertebrates, ribbon worms

Nemertea is a phylum of animals also known as ribbon worms or proboscis worms, consisting of 1300 known species. Most ribbon worms are very slim, usually only a few millimeters wide, although a few have relatively short but wide bodies. Many have patterns of yellow, orange, red and green coloration. The foregut, stomach and intestine run a little below the midline of the body, the anus is at the tip of the tail, and the mouth is under the front. A little above the gut is the rhynchocoel, a cavity which mostly runs above the midline and ends a little short of the rear of the body. All species have a proboscis which lies in the rhynchocoel when inactive but everts to emerge just above the mouth to capture the animal's prey with venom. A highly extensible muscle in the back of the rhynchocoel pulls the proboscis in when an attack ends. A few species with stubby bodies filter feed and have suckers at the front and back ends, with which they attach to a host.

<span class="mw-page-title-main">Bilateria</span> Animals with embryonic bilateral symmetry

Bilateria is a large clade or infrakingdom of animals called bilaterians, characterized by bilateral symmetry during embryonic development. This means their body plans are laid around a longitudinal axis with a front and a rear end, as well as a left–right–symmetrical belly (ventral) and back (dorsal) surface. Nearly all bilaterians maintain a bilaterally symmetrical body as adults; the most notable exception is the echinoderms, which achieve secondary pentaradial symmetry as adults, but are bilaterally symmetrical as an embryo. Cephalization is also a characteristic feature among most bilaterians, where the special sense organs and central nerve ganglia become concentrated at the front/rostral end.

<span class="mw-page-title-main">Body cavity</span> Internal space within a multicellular organism

A body cavity is any space or compartment, or potential space, in an animal body. Cavities accommodate organs and other structures; cavities as potential spaces contain fluid.

A germ layer is a primary layer of cells that forms during embryonic development. The three germ layers in vertebrates are particularly pronounced; however, all eumetazoans produce two or three primary germ layers. Some animals, like cnidarians, produce two germ layers making them diploblastic. Other animals such as bilaterians produce a third layer between these two layers, making them triploblastic. Germ layers eventually give rise to all of an animal's tissues and organs through the process of organogenesis.

The archenteron, also called the gastrocoel, the primitive digestive tube or the primitive gut, is the internal cavity of the primitive gastrointestinal tract that forms during gastrulation in a developing animal embryo. It develops into the endoderm and mesoderm of the animal.

<span class="mw-page-title-main">Serous membrane</span> Smooth coating lining contents and inner walls of body cavities

The serous membrane is a smooth tissue membrane of mesothelium lining the contents and inner walls of body cavities, which secrete serous fluid to allow lubricated sliding movements between opposing surfaces. The serous membrane that covers internal organs is called visceral, while the one that covers the cavity wall is called parietal. For instance the parietal peritoneum is attached to the abdominal wall and the pelvic walls. The visceral peritoneum is wrapped around the visceral organs. For the heart, the layers of the serous membrane are called parietal and visceral pericardium. For the lungs they are called parietal and visceral pleura. The visceral serosa of the uterus is called the perimetrium. The potential space between two opposing serosal surfaces is mostly empty except for the small amount of serous fluid.

Schizocoely is a process by which some animal embryos develop. The schizocoely mechanism occurs when secondary body cavities (coeloms) are formed by splitting a solid mass of mesodermal embryonic tissue. All schizocoelomates are protostomians and they show holoblastic, spiral, determinate cleavage.

Histogenesis is the formation of different tissues from undifferentiated cells. These cells are constituents of three primary germ layers, the endoderm, mesoderm, and ectoderm. The science of the microscopic structures of the tissues formed within histogenesis is termed histology.

<span class="mw-page-title-main">Enterocoely</span> Development process of some animals

Enterocoelom describes both the process by which some animal embryos develop and the origin of the cells involved. In enterocoely, a mesoderm is formed in a developing embryo, in which the coelom appears from pouches growing and separating from the digestive tract. As the incipient coelomic epithelium originates from archenteral diverticula, the endoderm therefore gives rise to the mesodermal cells.

<span class="mw-page-title-main">Animal</span> Kingdom of living things

Animals are multicellular, eukaryotic organisms in the biological kingdom Animalia. With few exceptions, animals consume organic material, breathe oxygen, have myocytes and are able to move, can reproduce sexually, and grow from a hollow sphere of cells, the blastula, during embryonic development. Animals form a single clade.

The urbilaterian is the hypothetical last common ancestor of the bilaterian clade, i.e., all animals having a bilateral symmetry.

<span class="mw-page-title-main">Deuterostome</span> Superphylum of bilateral animals

Deuterostomes are bilaterian animals of the superphylum Deuterostomia, typically characterized by their anus forming before the mouth during embryonic development. Deuterostomia is further divided into 4 phyla: Chordata, Echinodermata, Hemichordata, and the extinct Vetulicolia known from Cambrian fossils. The extinct clade Cambroernida is also thought to be a member of Deuterostomia.

<span class="mw-page-title-main">Phoronid</span> Phylum of marine animals, horseshoe worms

Phoronids are a small phylum of marine animals that filter-feed with a lophophore, and build upright tubes of chitin to support and protect their soft bodies. They live in most of the oceans and seas, including the Arctic Ocean but excluding the Antarctic Ocean, and between the intertidal zone and about 400 meters down. Most adult phoronids are 2 cm long and about 1.5 mm wide, although the largest are 50 cm long.

<span class="mw-page-title-main">Protostome</span> Clade of animals whose mouth develops before the anus

Protostomia is the clade of animals once thought to be characterized by the formation of the organism's mouth before its anus during embryonic development. This nature has since been discovered to be extremely variable among Protostomia's members, although the reverse is typically true of its sister clade, Deuterostomia. Well known examples of protostomes are arthropods, molluscs, annelids, flatworms and nematodes. They are also called schizocoelomates since schizocoely typically occurs in them.

<span class="mw-page-title-main">Brachiopod</span> Phylum of marine animals also known as lamp shells

Brachiopods, phylum Brachiopoda, are a phylum of trochozoan animals that have hard "valves" (shells) on the upper and lower surfaces, unlike the left and right arrangement in bivalve molluscs. Brachiopod valves are hinged at the rear end, while the front can be opened for feeding or closed for protection. Two major categories are traditionally recognized, articulate and inarticulate brachiopods. The word "articulate" is used to describe the tooth-and-groove structures of the valve-hinge which is present in the articulate group, and absent from the inarticulate group. This is the leading diagnostic skeletal feature, by which the two main groups can be readily distinguished as fossils. Articulate brachiopods have toothed hinges and simple, vertically oriented opening and closing muscles. Conversely, inarticulate brachiopods have weak, untoothed hinges and a more complex system of vertical and oblique (diagonal) muscles used to keep the two valves aligned. In many brachiopods, a stalk-like pedicle projects from an opening near the hinge of one of the valves, known as the pedicle or ventral valve. The pedicle, when present, keeps the animal anchored to the seabed but clear of sediment which would obstruct the opening.

<span class="mw-page-title-main">Embryological origins of the mouth and anus</span>

The embryological origin of the mouth and anus is an important characteristic, and forms the morphological basis for separating bilaterian animals into two natural groupings: the protostomes and deuterostomes.

<span class="mw-page-title-main">Xenacoelomorpha</span> A deep-branching bilaterian clade of animals with a simple body plan

Xenacoelomorpha is a small phylum of bilaterian invertebrate animals, consisting of two sister groups: xenoturbellids and acoelomorphs. This new phylum was named in February 2011 and suggested based on morphological synapomorphies, which was then confirmed by phylogenomic analyses of molecular data.

References

  1. "celom". Merriam-Webster.com Dictionary .
  2. "coelom" via The Free Dictionary.
  3. Bailly, Anatole (1981-01-01). Abrégé du dictionnaire grec français. Paris: Hachette. ISBN   2010035283. OCLC   461974285.
  4. Bailly, Anatole. "Greek-french dictionary online". www.tabularium.be. Retrieved 2018-01-14.
  5. Chisholm, Hugh, ed. (1911). "Coelom and Serous Membranes"  . Encyclopædia Britannica . Vol. 6 (11th ed.). Cambridge University Press. p. 642.
  6. 1 2 Lüter, Carsten (2000-06-01). "The origin of the coelom in Brachiopoda and its phylogenetic significance". Zoomorphology. 120 (1): 15–28. doi:10.1007/s004359900019. ISSN   1432-234X. S2CID   24929317.
  7. "Origins and Evolution of Animals". Archived from the original on 2018-11-12.
  8. "McGraw-Hill Dictionary of Scientific and Technical Terms". Answers.com . Archived from the original on 2014-12-20.
  9. Ruppert, Edward E.; Fox, Richard, S.; Barnes, Robert D. (2004). Invertebrate Zoology, 7th edition. Cengage Learning. p. 205. ISBN   978-81-315-0104-7.{{cite book}}: CS1 maint: multiple names: authors list (link)
  10. Dorit, R. L.; Walker, W. F.; Barnes, R. D. (1991). Zoology . Saunders College Publishing. p.  190. ISBN   978-0-03-030504-7.
  11. Nielsen, C. (2010). "The 'new phylogeny'. What is new about it?" Palaeodiversity 3, 149–150.
  12. 1 2 R. C. Brusca, G. J. Brusca. Invertebrates. Sunderland, Massachusetts: Sinauer Associates, 2003 (2nd ed.), p. 47, ISBN   0-87893-097-3.
  13. Nemertea
  14. Coelom development in the priapulid worm Priapulus caudatus
  15. Evers, Christine A., Lisa Starr. Biology:Concepts and Applications. 6th ed. United States:Thomson, 2006. ISBN   0-534-46224-3.
  16. Phylogeny of Syndermata (syn. Rotifera): Mitochondrial gene order verifies epizoic Seisonidea as sister to endoparasitic Acanthocephala within monophyletic Hemirotifera
  17. Study of Rotifers of Safari Zoo Lake Lahore in Relation to Physico-chemical Parameters
  18. Biology of Non-chordates
  19. Comparative genomic studies on Dicyema japonicum: the phylogenetic position of dicyemids and the genomic adaptations to parasitic lifestyle
  20. Xenoturbella bocki exhibits direct development with similarities to Acoelomorpha
  21. Xenacoelomorph-Specific Hox Peptides: Insights into the Phylogeny of Acoels, Nemertodermatids, and Xenoturbellids
  22. R.C.Brusca, G.J.Brusca 2003, p. 379.

Further reading