Cnidaria

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Cnidaria
Temporal range: 580–0  Ma
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Ediacaran–Recent
Cnidaria.png
Four examples of cnidaria :
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Subkingdom: Eumetazoa
Clade: ParaHoxozoa
Phylum: Cnidaria
Hatschek, 1888
Type species
Nematostella vectensis [1]
Subphyla and classes [2]
Pacific sea nettles, Chrysaora fuscescens Sea nettles.jpg
Pacific sea nettles, Chrysaora fuscescens

Cnidaria ( /nɪˈdɛəriə,n-/ ) [5] is a phylum under kingdom Animalia containing over 11,000 species [6] of aquatic animals found both in freshwater and marine environments, predominantly the latter.

Contents

Their distinguishing feature is cnidocytes, specialized cells that they use mainly for capturing prey. Their bodies consist of mesoglea, a non-living jelly-like substance, sandwiched between two layers of epithelium that are mostly one cell thick.

Cnidarians mostly have two basic body forms: swimming medusae and sessile polyps, both of which are radially symmetrical with mouths surrounded by tentacles that bear cnidocytes. Both forms have a single orifice and body cavity that are used for digestion and respiration. Many cnidarian species produce colonies that are single organisms composed of medusa-like or polyp-like zooids, or both (hence they are trimorphic). Cnidarians' activities are coordinated by a decentralized nerve net and simple receptors. Several free-swimming species of Cubozoa and Scyphozoa possess balance-sensing statocysts, and some have simple eyes. Not all cnidarians reproduce sexually, with many species having complex life cycles of asexual polyp stages and sexual medusae. Some, however, omit either the polyp or the medusa stage, and the parasitic classes evolved to have neither form.

Cnidarians were formerly grouped with ctenophores in the phylum Coelenterata, but increasing awareness of their differences caused them to be placed in separate phyla. [7] Cnidarians are classified into four main groups: the almost wholly sessile Anthozoa (sea anemones, corals, sea pens); swimming Scyphozoa (jellyfish); Cubozoa (box jellies); and Hydrozoa (a diverse group that includes all the freshwater cnidarians as well as many marine forms, and has both sessile members, such as Hydra , and colonial swimmers, such as the Portuguese Man o' War). Staurozoa have recently been recognised as a class in their own right rather than a sub-group of Scyphozoa, and the highly derived parasitic Myxozoa and Polypodiozoa were firmly recognized as cnidarians in 2007. [8]

Most cnidarians prey on organisms ranging in size from plankton to animals several times larger than themselves, but many obtain much of their nutrition from dinoflagellates, and a few are parasites. Many are preyed on by other animals including starfish, sea slugs, fish, turtles, and even other cnidarians. Many scleractinian corals—which form the structural foundation for coral reefs—possess polyps that are filled with symbiotic photo-synthetic zooxanthellae. While reef-forming corals are almost entirely restricted to warm and shallow marine waters, other cnidarians can be found at great depths, in polar regions, and in freshwater.

Recent phylogenetic analyses support monophyly of cnidarians, as well as the position of cnidarians as the sister group of bilaterians. [9] Fossil cnidarians have been found in rocks formed about 580  million years ago, and other fossils show that corals may have been present shortly before 490  million years ago and diversified a few million years later. However, molecular clock analysis of mitochondrial genes suggests a much older age for the crown group of cnidarians, estimated around 741  million years ago, almost 200 million years before the Cambrian period as well as any fossils. [10]

Distinguishing features

Cnidarians form a phylum of animals that are more complex than sponges, about as complex as ctenophores (comb jellies), and less complex than bilaterians, which include almost all other animals. Both cnidarians and ctenophores are more complex than sponges as they have: cells bound by inter-cell connections and carpet-like basement membranes; muscles; nervous systems; and some have sensory organs. Cnidarians are distinguished from all other animals by having cnidocytes that fire harpoon like structures and are usually used mainly to capture prey. In some species, cnidocytes can also be used as anchors. [11] Cnidarians are also distinguished by the fact that they have only one opening in their body for ingestion and excretion i.e. they don't have a separate mouth and anus.

Like sponges and ctenophores, cnidarians have two main layers of cells that sandwich a middle layer of jelly-like material, which is called the mesoglea in cnidarians; more complex animals have three main cell layers and no intermediate jelly-like layer. Hence, cnidarians and ctenophores have traditionally been labelled diploblastic, along with sponges. [11] [12] However, both cnidarians and ctenophores have a type of muscle that, in more complex animals, arises from the middle cell layer. [13] As a result, some recent text books classify ctenophores as triploblastic, [14] and it has been suggested that cnidarians evolved from triploblastic ancestors. [13]

  Sponges [15] [16] !!Cnidarians [11] [12] !!Ctenophores [11] [14] !!Bilateria [11]
Cnidocytes NoYesNo
Colloblasts NoYesNo
Digestive and circulatory organs NoYes
Number of main cell layersTwo, with jelly-like layer between themTwoTwoThree
Cells in each layer bound togethercell-adhesion molecules, but no basement membranes except Homoscleromorpha. [17] inter-cell connections; basement membranes
Sensory organsNoYes
Number of cells in middle "jelly" layerManyFew(Not applicable)
Cells in outer layers can move inwards and change functionsYesNo(Not applicable)
Nervous systemNoYes, simpleSimple to complex
Muscles NoneMostly epitheliomuscularMostly myoepithelialMostly myocytes

Description

Basic body forms

Cnidaria medusa n polyp.png
Aboral end
Oral end
Mouth
Oral end
Aboral end
  Exoderm
  Gastroderm (Endoderm)
  Mesoglea
  Digestive cavity
Cnidaria medusa n polyp.png
Medusa (left) and polyp (right) [12]
Oral end of actinodiscus polyp Actinodiscus macro.JPG
Oral end of actinodiscus polyp

Most adult cnidarians appear as either free-swimming medusae or sessile polyps, and many hydrozoans species are known to alternate between the two forms.

Both are radially symmetrical, like a wheel and a tube respectively. Since these animals have no heads, their ends are described as "oral" (nearest the mouth) and "aboral" (furthest from the mouth).

Most have fringes of tentacles equipped with cnidocytes around their edges, and medusae generally have an inner ring of tentacles around the mouth. Some hydroids may consist of colonies of zooids that serve different purposes, such as defense, reproduction and catching prey. The mesoglea of polyps is usually thin and often soft, but that of medusae is usually thick and springy, so that it returns to its original shape after muscles around the edge have contracted to squeeze water out, enabling medusae to swim by a sort of jet propulsion. [12]

Skeletons

In medusae the only supporting structure is the mesoglea. Hydra and most sea anemones close their mouths when they are not feeding, and the water in the digestive cavity then acts as a hydrostatic skeleton, rather like a water-filled balloon. Other polyps such as Tubularia use columns of water-filled cells for support. Sea pens stiffen the mesoglea with calcium carbonate spicules and tough fibrous proteins, rather like sponges. [12]

In some colonial polyps, a chitinous periderm gives support and some protection to the connecting sections and to the lower parts of individual polyps. Stony corals secrete massive calcium carbonate exoskeletons. A few polyps collect materials such as sand grains and shell fragments, which they attach to their outsides. Some colonial sea anemones stiffen the mesoglea with sediment particles. [12]

Main cell layers

Cnidaria are diploblastic animals; in other words, they have two main cell layers, while more complex animals are triploblasts having three main layers. The two main cell layers of cnidarians form epithelia that are mostly one cell thick, and are attached to a fibrous basement membrane, which they secrete. They also secrete the jelly-like mesoglea that separates the layers. The layer that faces outwards, known as the ectoderm ("outside skin"), generally contains the following types of cells: [11]

In addition to epitheliomuscular, nerve and interstitial cells, the inward-facing gastroderm ("stomach skin") contains gland cells that secrete digestive enzymes. In some species it also contains low concentrations of cnidocytes, which are used to subdue prey that is still struggling. [11] [12]

The mesoglea contains small numbers of amoeba-like cells, [12] and muscle cells in some species. [11] However, the number of middle-layer cells and types are much lower than in sponges. [12]

Polymorphism

Polymorphism refers to the occurrence of structurally and functionally more than two different types of individuals within the same organism. It is a characteristic feature of Cnidarians, particularly the polyp and medusa forms, or of zooids within colonial organisms like those in Hydrozoa. [19] In Hydrozoans, colonial individuals arising from individuals zooids will take on separate tasks. [20] For example, in Obelia there are feeding individuals, the gastrozooids; the individuals capable of asexual reproduction only, the gonozooids, blastostyles and free-living or sexually reproducing individuals, the medusae.

Cnidocytes

These "nettle cells" function as harpoons, since their payloads remain connected to the bodies of the cells by threads. Three types of cnidocytes are known: [11] [12]

Firing sequence of the cnida in a hydra's nematocyst

Operculum (lid)

"Finger" that turns inside out
/ / / Barbs

Venom

Victim's skin

Victim's tissues Hydra nematocyst firing 01.png
Firing sequence of the cnida in a hydra's nematocyst
  Operculum (lid)
  "Finger" that turns inside out
/ / / Barbs
  Venom
  Victim's skin
  Victim's tissues

The main components of a cnidocyte are: [11] [12]

A hydra's nematocyst, before firing.

"trigger" cilium Hydra nematocyst 01.png
A hydra's nematocyst, before firing.
  "trigger" cilium

It is difficult to study the firing mechanisms of cnidocytes as these structures are small but very complex. At least four hypotheses have been proposed: [11]

Cnidocytes can only fire once, and about 25% of a hydra's nematocysts are lost from its tentacles when capturing a brine shrimp. Used cnidocytes have to be replaced, which takes about 48 hours. To minimise wasteful firing, two types of stimulus are generally required to trigger cnidocytes: nearby sensory cells detect chemicals in the water, and their cilia respond to contact. This combination prevents them from firing at distant or non-living objects. Groups of cnidocytes are usually connected by nerves and, if one fires, the rest of the group requires a weaker minimum stimulus than the cells that fire first. [11] [12]

Locomotion

A swimming sea nettle known as the purple-striped jelly ( Chrysaora colorata )

Medusae swim by a form of jet propulsion: muscles, especially inside the rim of the bell, squeeze water out of the cavity inside the bell, and the springiness of the mesoglea powers the recovery stroke. Since the tissue layers are very thin, they provide too little power to swim against currents and just enough to control movement within currents. [12]

Hydras and some sea anemones can move slowly over rocks and sea or stream beds by various means: creeping like snails, crawling like inchworms, or by somersaulting. A few can swim clumsily by waggling their bases. [12]

Nervous system and senses

Cnidarians are generally thought to have no brains or even central nervous systems. However, they do have integrative areas of neural tissue that could be considered some form of centralization. Most of their bodies are innervated by decentralized nerve nets that control their swimming musculature and connect with sensory structures, though each clade has slightly different structures. [22] These sensory structures, usually called rhopalia, can generate signals in response to various types of stimuli such as light, pressure, and much more. Medusa usually have several of them around the margin of the bell that work together to control the motor nerve net, that directly innervates the swimming muscles. Most Cnidarians also have a parallel system. In scyphozoans, this takes the form of a diffuse nerve net, which has modulatory effects on the nervous system. [23] As well as forming the "signal cables" between sensory neurons and motoneurons, intermediate neurons in the nerve net can also form ganglia that act as local coordination centers. Communication between nerve cells can occur by chemical synapses or gap junctions in hydrozoans, though gap junctions are not present in all groups. Cnidarians have many of the same neurotransmitters as many animals, including chemicals such as glutamate, GABA, and acetylcholine. [24]

This structure ensures that the musculature is excited rapidly and simultaneously, and can be directly stimulated from any point on the body, and it also is better able to recover after injury. [22] [23]

Medusae and complex swimming colonies such as siphonophores and chondrophores sense tilt and acceleration by means of statocysts, chambers lined with hairs which detect the movements of internal mineral grains called statoliths. If the body tilts in the wrong direction, the animal rights itself by increasing the strength of the swimming movements on the side that is too low. Most species have ocelli ("simple eyes"), which can detect sources of light. However, the agile box jellyfish are unique among Medusae because they possess four kinds of true eyes that have retinas, corneas and lenses. [25] Although the eyes probably do not form images, Cubozoa can clearly distinguish the direction from which light is coming as well as negotiate around solid-colored objects. [11] [25]

Feeding and excretion

Cnidarians feed in several ways: predation, absorbing dissolved organic chemicals, filtering food particles out of the water, obtaining nutrients from symbiotic algae within their cells, and parasitism. Most obtain the majority of their food from predation but some, including the corals Hetroxenia and Leptogorgia , depend almost completely on their endosymbionts and on absorbing dissolved nutrients. [11] Cnidaria give their symbiotic algae carbon dioxide, some nutrients, a place in the sun and protection against predators. [12]

Predatory species use their cnidocytes to poison or entangle prey, and those with venomous nematocysts may start digestion by injecting digestive enzymes. The "smell" of fluids from wounded prey makes the tentacles fold inwards and wipe the prey off into the mouth. In medusae the tentacles round the edge of the bell are often short and most of the prey capture is done by "oral arms", which are extensions of the edge of the mouth and are often frilled and sometimes branched to increase their surface area. Medusae often trap prey or suspended food particles by swimming upwards, spreading their tentacles and oral arms and then sinking. In species for which suspended food particles are important, the tentacles and oral arms often have rows of cilia whose beating creates currents that flow towards the mouth, and some produce nets of mucus to trap particles. [11] Their digestion is both intra and extracellular.

Once the food is in the digestive cavity, gland cells in the gastroderm release enzymes that reduce the prey to slurry, usually within a few hours. This circulates through the digestive cavity and, in colonial cnidarians, through the connecting tunnels, so that gastroderm cells can absorb the nutrients. Absorption may take a few hours, and digestion within the cells may take a few days. The circulation of nutrients is driven by water currents produced by cilia in the gastroderm or by muscular movements or both, so that nutrients reach all parts of the digestive cavity. [12] Nutrients reach the outer cell layer by diffusion or, for animals or zooids such as medusae which have thick mesogleas, are transported by mobile cells in the mesoglea. [11]

Indigestible remains of prey are expelled through the mouth. The main waste product of cells' internal processes is ammonia, which is removed by the external and internal water currents. [12]

Respiration

There are no respiratory organs, and both cell layers absorb oxygen from and expel carbon dioxide into the surrounding water. When the water in the digestive cavity becomes stale it must be replaced, and nutrients that have not been absorbed will be expelled with it. Some Anthozoa have ciliated grooves on their tentacles, allowing them to pump water out of and into the digestive cavity without opening the mouth. This improves respiration after feeding and allows these animals, which use the cavity as a hydrostatic skeleton, to control the water pressure in the cavity without expelling undigested food. [11]

Cnidaria that carry photosynthetic symbionts may have the opposite problem, an excess of oxygen, which may prove toxic. The animals produce large quantities of antioxidants to neutralize the excess oxygen. [11]

Regeneration

All cnidarians can regenerate, allowing them to recover from injury and to reproduce asexually. Medusae have limited ability to regenerate, but polyps can do so from small pieces or even collections of separated cells. This enables corals to recover even after apparently being destroyed by predators. [11]

Reproduction

Schleiden-meduse-2.jpg
 1 
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 11 
 12 
 13 
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Schleiden-meduse-2.jpg
Life cycle of a jellyfish: [11] [12]
1–3 Larva searches for site
4–8 Polyp grows
9–11 Polyp strobilates
12–14 Medusa grows

Sexual

Cnidarian sexual reproduction often involves a complex life cycle with both polyp and medusa stages. For example, in Scyphozoa (jellyfish) and Cubozoa (box jellies) a larva swims until it finds a good site, and then becomes a polyp. This grows normally but then absorbs its tentacles and splits horizontally into a series of disks that become juvenile medusae, a process called strobilation. The juveniles swim off and slowly grow to maturity, while the polyp re-grows and may continue strobilating periodically. The adults have gonads in the gastroderm, and these release ova and sperm into the water in the breeding season. [11] [12]

This phenomenon of succession of differently organized generations (one asexually reproducing, sessile polyp, followed by a free-swimming medusa or a sessile polyp that reproduces sexually) [26] is sometimes called "alternation of asexual and sexual phases" or "metagenesis", but should not be confused with the alternation of generations as found in plants.

Shortened forms of this life cycle are common, for example some oceanic scyphozoans omit the polyp stage completely, and cubozoan polyps produce only one medusa. Hydrozoa have a variety of life cycles. Some have no polyp stages and some (e.g. hydra ) have no medusae. In some species, the medusae remain attached to the polyp and are responsible for sexual reproduction; in extreme cases these reproductive zooids may not look much like medusae. Meanwhile, life cycle reversal, in which polyps are formed directly from medusae without the involvement of sexual reproduction process, was observed in both Hydrozoa (Turritopsis dohrnii [27] and Laodicea undulata [28] ) and Scyphozoa (Aurelia sp.1 [29] ). Anthozoa have no medusa stage at all and the polyps are responsible for sexual reproduction. [11]

Spawning is generally driven by environmental factors such as changes in the water temperature, and their release is triggered by lighting conditions such as sunrise, sunset or the phase of the moon. Many species of Cnidaria may spawn simultaneously in the same location, so that there are too many ova and sperm for predators to eat more than a tiny percentage — one famous example is the Great Barrier Reef, where at least 110 corals and a few non-cnidarian invertebrates produce enough gametes to turn the water cloudy. These mass spawnings may produce hybrids, some of which can settle and form polyps, but it is not known how long these can survive. In some species the ova release chemicals that attract sperm of the same species. [11]

The fertilized eggs develop into larvae by dividing until there are enough cells to form a hollow sphere (blastula) and then a depression forms at one end (gastrulation) and eventually becomes the digestive cavity. However, in cnidarians the depression forms at the end further from the yolk (at the animal pole), while in bilaterians it forms at the other end (vegetal pole). [12] The larvae, called planulae, swim or crawl by means of cilia. [11] They are cigar-shaped but slightly broader at the "front" end, which is the aboral, vegetal-pole end and eventually attaches to a substrate if the species has a polyp stage. [12]

Anthozoan larvae either have large yolks or are capable of feeding on plankton, and some already have endosymbiotic algae that help to feed them. Since the parents are immobile, these feeding capabilities extend the larvae's range and avoid overcrowding of sites. Scyphozoan and hydrozoan larvae have little yolk and most lack endosymbiotic algae, and therefore have to settle quickly and metamorphose into polyps. Instead, these species rely on their medusae to extend their ranges. [12]

Asexual

All known cnidaria can reproduce asexually by various means, in addition to regenerating after being fragmented. Hydrozoan polyps only bud, while the medusae of some hydrozoans can divide down the middle. Scyphozoan polyps can both bud and split down the middle. In addition to both of these methods, Anthozoa can split horizontally just above the base. Asexual reproduction makes the daughter cnidarian a clone of the adult. [11] [12]

Classification

Cnidarians were for a long time grouped with Ctenophores in the phylum Coelenterata, but increasing awareness of their differences caused them to be placed in separate phyla. Modern cnidarians are generally classified into four main classes: [11] sessile Anthozoa (sea anemones, corals, sea pens); swimming Scyphozoa (jellyfish) and Cubozoa (box jellies); and Hydrozoa, a diverse group that includes all the freshwater cnidarians as well as many marine forms, and has both sessile members such as Hydra and colonial swimmers such as the Portuguese Man o' War. Staurozoa have recently been recognised as a class in their own right rather than a sub-group of Scyphozoa, and the parasitic Myxozoa and Polypodiozoa are now recognized as highly derived cnidarians rather than more closely related to the bilaterians. [8] [30]

Hydrozoa Scyphozoa Cubozoa Anthozoa Myxozoa
Number of species [31] 3,600228426,1001300
Examples Hydra , siphonophores Jellyfish Box jellies Sea anemones, corals, sea pens Myxobolus cerebralis
Cells found in mesoglea NoYesYesYes
Nematocysts in exodermis NoYesYesYes
Medusa phase in life cycleIn some speciesYesYesNo
Number of medusae produced per polypManyManyOne(not applicable)

Stauromedusae, small sessile cnidarians with stalks and no medusa stage, have traditionally been classified as members of the Scyphozoa, but recent research suggests they should be regarded as a separate class, Staurozoa. [32]

The Myxozoa, microscopic parasites, were first classified as protozoans. [33] Research then found that Polypodium hydriforme , a non-Myxozoan parasite within the egg cells of sturgeon, is closely related to the Myxozoa and suggested that both Polypodium and the Myxozoa were intermediate between cnidarians and bilaterian animals. [34] More recent research demonstrates that the previous identification of bilaterian genes reflected contamination of the Myxozoan samples by material from their host organism, and they are now firmly identified as heavily derived cnidarians, and more closely related to Hydrozoa and Scyphozoa than to Anthozoa. [8] [30] [35] [36]

Some researchers classify the extinct conulariids as cnidarians, while others propose that they form a completely separate phylum. [37]


Current classification according to the World Register of Marine Species:


Ecology

Many cnidarians are limited to shallow waters because they depend on endosymbiotic algae for much of their nutrients. The life cycles of most have polyp stages, which are limited to locations that offer stable substrates. Nevertheless, major cnidarian groups contain species that have escaped these limitations. Hydrozoans have a worldwide range: some, such as Hydra , live in freshwater; Obelia appears in the coastal waters of all the oceans; and Liriope can form large shoals near the surface in mid-ocean. Among anthozoans, a few scleractinian corals, sea pens and sea fans live in deep, cold waters, and some sea anemones inhabit polar seabeds while others live near hydrothermal vents over 10 km (33,000 ft) below sea-level. Reef-building corals are limited to tropical seas between 30°N and 30°S with a maximum depth of 46 m (151 ft), temperatures between 20 and 28 °C (68 and 82 °F), high salinity, and low carbon dioxide levels. Stauromedusae, although usually classified as jellyfish, are stalked, sessile animals that live in cool to Arctic waters. [38] Cnidarians range in size from a mere handful of cells for the parasitic myxozoans [30] through Hydra's length of 5–20 mm (1434 in), [39] to the Lion's mane jellyfish, which may exceed 2 m (6 ft 7 in) in diameter and 75 m (246 ft) in length. [40]

Prey of cnidarians ranges from plankton to animals several times larger than themselves. [38] [41] Some cnidarians are parasites, mainly on jellyfish but a few are major pests of fish. [38] Others obtain most of their nourishment from endosymbiotic algae or dissolved nutrients. [11] Predators of cnidarians include: sea slugs, which can incorporate nematocysts into their own bodies for self-defense; [42] starfish, notably the crown of thorns starfish, which can devastate corals; [38] butterfly fish and parrot fish, which eat corals; [43] and marine turtles, which eat jellyfish. [40] Some sea anemones and jellyfish have a symbiotic relationship with some fish; for example clown fish live among the tentacles of sea anemones, and each partner protects the other against predators. [38]

Coral reefs form some of the world's most productive ecosystems. Common coral reef cnidarians include both Anthozoans (hard corals, octocorals, anemones) and Hydrozoans (fire corals, lace corals). The endosymbiotic algae of many cnidarian species are very effective primary producers, in other words converters of inorganic chemicals into organic ones that other organisms can use, and their coral hosts use these organic chemicals very efficiently. In addition, reefs provide complex and varied habitats that support a wide range of other organisms. [44] Fringing reefs just below low-tide level also have a mutually beneficial relationship with mangrove forests at high-tide level and seagrass meadows in between: the reefs protect the mangroves and seagrass from strong currents and waves that would damage them or erode the sediments in which they are rooted, while the mangroves and seagrass protect the coral from large influxes of silt, fresh water and pollutants. This additional level of variety in the environment is beneficial to many types of coral reef animals, which for example may feed in the sea grass and use the reefs for protection or breeding. [45]

Evolutionary history

Stranded scyphozoans on a Cambrian tidal flat in Blackberry Hill, Wisconsin. Stranded Cambrian scyphozoans.jpg
Stranded scyphozoans on a Cambrian tidal flat in Blackberry Hill, Wisconsin.
The fossil coral Cladocora from Pliocene rocks in Cyprus Cladocora.jpg
The fossil coral Cladocora from Pliocene rocks in Cyprus

Fossil record

The earliest widely accepted animal fossils are rather modern-looking cnidarians, possibly from around 580  million years ago, although fossils from the Doushantuo Formation can only be dated approximately. [46] The identification of some of these as embryos of animals has been contested, but other fossils from these rocks strongly resemble tubes and other mineralized structures made by corals. [47] Their presence implies that the cnidarian and bilaterian lineages had already diverged. [48] Although the Ediacaran fossil Charnia used to be classified as a jellyfish or sea pen, [49] more recent study of growth patterns in Charnia and modern cnidarians has cast doubt on this hypothesis, [50] [51] leaving only the Canadian polyp, Haootia , as the only bona-fide cnidarian body fossil from the Ediacaran. Few fossils of cnidarians without mineralized skeletons are known from more recent rocks, except in lagerstätten that preserved soft-bodied animals. [52]

A few mineralized fossils that resemble corals have been found in rocks from the Cambrian period, and corals diversified in the Early Ordovician. [52] These corals, which were wiped out in the Permian–Triassic extinction event about 252  million years ago, [52] did not dominate reef construction since sponges and algae also played a major part. [53] During the Mesozoic era rudist bivalves were the main reef-builders, but they were wiped out in the Cretaceous–Paleogene extinction event 66  million years ago, [54] and since then the main reef-builders have been scleractinian corals. [52]

Family tree

It is difficult to reconstruct the early stages in the evolutionary "family tree" of animals using only morphology (their shapes and structures), because the large differences between Porifera (sponges), Cnidaria plus Ctenophora (comb jellies), Placozoa and Bilateria (all the more complex animals) make comparisons difficult. Hence reconstructions now rely largely or entirely on molecular phylogenetics, which groups organisms according to similarities and differences in their biochemistry, usually in their DNA or RNA. [55]

Illustrated tree of cnidarians and their closest relatives Radiata diversity.jpg
Illustrated tree of cnidarians and their closest relatives

It is now generally thought that the Calcarea (sponges with calcium carbonate spicules) are more closely related to Cnidaria, Ctenophora (comb jellies) and Bilateria (all the more complex animals) than they are to the other groups of sponges. [56] [57] [58] In 1866 it was proposed that Cnidaria and Ctenophora were more closely related to each other than to Bilateria and formed a group called Coelenterata ("hollow guts"), because Cnidaria and Ctenophora both rely on the flow of water in and out of a single cavity for feeding, excretion and respiration. In 1881, it was proposed that Ctenophora and Bilateria were more closely related to each other, since they shared features that Cnidaria lack, for example muscles in the middle layer (mesoglea in Ctenophora, mesoderm in Bilateria). However more recent analyses indicate that these similarities are rather vague, and the current view, based on molecular phylogenetics, is that Cnidaria and Bilateria are more closely related to each other than either is to Ctenophora. This grouping of Cnidaria and Bilateria has been labelled "Planulozoa" because it suggests that the earliest Bilateria were similar to the planula larvae of Cnidaria. [4] [59]

Within the Cnidaria, the Anthozoa (sea anemones and corals) are regarded as the sister-group of the rest, which suggests that the earliest cnidarians were sessile polyps with no medusa stage. However, it is unclear how the other groups acquired the medusa stage, since Hydrozoa form medusae by budding from the side of the polyp while the other Medusozoa do so by splitting them off from the tip of the polyp. The traditional grouping of Scyphozoa included the Staurozoa, but morphology and molecular phylogenetics indicate that Staurozoa are more closely related to Cubozoa (box jellies) than to other "Scyphozoa". Similarities in the double body walls of Staurozoa and the extinct Conulariida suggest that they are closely related. [4] [60]

However, in 2005 Katja Seipel and Volker Schmid suggested that cnidarians and ctenophores are simplified descendants of triploblastic animals, since ctenophores and the medusa stage of some cnidarians have striated muscle, which in bilaterians arises from the mesoderm. They did not commit themselves on whether bilaterians evolved from early cnidarians or from the hypothesized triploblastic ancestors of cnidarians. [13]

In molecular phylogenetics analyses from 2005 onwards, important groups of developmental genes show the same variety in cnidarians as in chordates. [61] In fact cnidarians, and especially anthozoans (sea anemones and corals), retain some genes that are present in bacteria, protists, plants and fungi but not in bilaterians. [62]

The mitochondrial genome in the medusozoan cnidarians, unlike those in other animals, is linear with fragmented genes. [63] The reason for this difference is unknown.

Interaction with humans

The dangerous Carukia barnesi, one of the known species of box jellyfish which can cause Irukandji syndrome. Cubozoas.JPG
The dangerous Carukia barnesi , one of the known species of box jellyfish which can cause Irukandji syndrome.

Jellyfish stings killed about 1,500 people in the 20th century, [64] and cubozoans are particularly dangerous. On the other hand, some large jellyfish are considered a delicacy in East and Southeast Asia. Coral reefs have long been economically important as providers of fishing grounds, protectors of shore buildings against currents and tides, and more recently as centers of tourism. However, they are vulnerable to over-fishing, mining for construction materials, pollution, and damage caused by tourism.

Avispa marina.jpg
Avispa marina.jpg
The dangerous "sea wasp" Chironex fleckeri

Beaches protected from tides and storms by coral reefs are often the best places for housing in tropical countries. Reefs are an important food source for low-technology fishing, both on the reefs themselves and in the adjacent seas. [65] However, despite their great productivity, reefs are vulnerable to over-fishing, because much of the organic carbon they produce is exhaled as carbon dioxide by organisms at the middle levels of the food chain and never reaches the larger species that are of interest to fishermen. [44] Tourism centered on reefs provides much of the income of some tropical islands, attracting photographers, divers and sports fishermen. However, human activities damage reefs in several ways: mining for construction materials; pollution, including large influxes of fresh water from storm drains; commercial fishing, including the use of dynamite to stun fish and the capture of young fish for aquariums; and tourist damage caused by boat anchors and the cumulative effect of walking on the reefs. [65] Coral, mainly from the Pacific Ocean has long been used in jewellery, and demand rose sharply in the 1980s. [66]

Some large jellyfish species of the Rhizostomae order are commonly consumed in Japan, Korea and Southeast Asia. [67] [68] [69] In parts of the range, fishing industry is restricted to daylight hours and calm conditions in two short seasons, from March to May and August to November. [69] The commercial value of jellyfish food products depends on the skill with which they are prepared, and "Jellyfish Masters" guard their trade secrets carefully. Jellyfish is very low in cholesterol and sugars, but cheap preparation can introduce undesirable amounts of heavy metals. [70]

The "sea wasp" Chironex fleckeri has been described as the world's most venomous jellyfish and is held responsible for 67 deaths, although it is difficult to identify the animal as it is almost transparent. Most stingings by C. fleckeri cause only mild symptoms. [71] Seven other box jellies can cause a set of symptoms called Irukandji syndrome, [72] which takes about 30 minutes to develop, [73] and from a few hours to two weeks to disappear. [74] Hospital treatment is usually required, and there have been a few deaths. [72]

A number of the parasitic Myxozoans are commercially important pathogens in salmonid aquaculture.

Notes

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Further reading

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Polyp (zoology) One of two forms found in the phylum Cnidaria (zoology)

A polyp in zoology is one of two forms found in the phylum Cnidaria, the other being the medusa. Polyps are roughly cylindrical in shape and elongated at the axis of the vase-shaped body. In solitary polyps, the aboral end is attached to the substrate by means of a disc-like holdfast called a pedal disc, while in colonies of polyps it is connected to other polyps, either directly or indirectly. The oral end contains the mouth, and is surrounded by a circlet of tentacles.

Jellyfish Soft-bodied, aquatic invertebrates

Jellyfish and sea jellies are the informal common names given to the medusa-phase of certain gelatinous members of the subphylum Medusozoa, a major part of the phylum Cnidaria. Jellyfish are mainly free-swimming marine animals with umbrella-shaped bells and trailing tentacles, although a few are anchored to the seabed by stalks rather than being mobile. The bell can pulsate to provide propulsion for highly efficient locomotion. The tentacles are armed with stinging cells and may be used to capture prey and defend against predators. Jellyfish have a complex life cycle; the medusa is normally the sexual phase, which produces planula larva that disperse widely and enter a sedentary polyp phase before reaching sexual maturity.

Scyphozoa Class of marine cnidarians, true jellyfish

The Scyphozoa are an exclusively marine class of the phylum Cnidaria, referred to as the true jellyfish. It may include the extinct fossil group the Conulariida, whose affinities are uncertain and widely debated.

Cnidocyte Explosive cell containing one giant secretory organelle (cnida)

A cnidocyte is an explosive cell containing one giant secretory organelle called a cnidocyst that can deliver a sting to other organisms. The presence of this cell defines the phylum Cnidaria. Cnidae are used to capture prey and as a defense against predators. A cnidocyte fires a structure that contains a toxin within the cnidocyst; this is responsible for the stings delivered by a cnidarian.

Ctenophora Phylum of gelatinous marine animals

Ctenophora comprise a phylum of marine invertebrates, commonly known as comb jellies, that inhabit sea waters worldwide. They are notable for the groups of cilia they use for swimming, and they are the largest animals to swim with the help of cilia.

<i>Aurelia aurita</i> Species of jellyfish

Aurelia aurita is a widely studied species of the genus Aurelia. All species in the genus are very similar, and it is difficult to identify Aurelia medusae without genetic sampling; most of what follows applies equally to all species of the genus. The most common method used to identify the species consists of selecting a jellyfish from a harbour using a device, usually a drinking glass and then photographing the subject. This means that they can be released in to the harbour shortly afterwards and return to their natural habitat.

Anthozoa Class of cnidarians without a medusa stage

Anthozoa is a class of marine invertebrates which includes the sea anemones, stony corals and soft corals. Adult anthozoans are almost all attached to the seabed, while their larvae can disperse as part of the plankton. The basic unit of the adult is the polyp; this consists of a cylindrical column topped by a disc with a central mouth surrounded by tentacles. Sea anemones are mostly solitary, but the majority of corals are colonial, being formed by the budding of new polyps from an original, founding individual. Colonies are strengthened by calcium carbonate and other materials and take various massive, plate-like, bushy or leafy forms.

Tentacle

In zoology, a tentacle is a flexible, mobile, elongated organ present in some species of animals, most of them invertebrates. In animal anatomy, tentacles usually occur in one or more pairs. Anatomically, the tentacles of animals work mainly like muscular hydrostats. Most forms of tentacles are used for grasping and feeding. Many are sensory organs, variously receptive to touch, vision, or to the smell or taste of particular foods or threats. Examples of such tentacles are the eyestalks of various kinds of snails. Some kinds of tentacles have both sensory and manipulatory functions.

<i>Chrysaora quinquecirrha</i> Species of jellyfish

The Atlantic sea nettle, also known as the East Coast sea nettle or US Atlantic sea nettle, is a species of jellyfish that inhabits the Atlantic coast of the United States. Historically it was confused with several Chrysaora species, resulting in incorrect reports of C. quinquecirrha from other parts of the Atlantic and other oceans. Most recently, C. chesapeakei of estuaries on the Atlantic coast of the United States, as well as the Gulf of Mexico, was only fully recognized as separate from C. quinquecirrha in 2017. It is smaller than the Pacific sea nettle, and has more variable coloration, but is typically pale, pinkish or yellowish, often with radiating more deeply colored stripes on the exumbrella, especially near the margin.

Symmetry in biology Geometric symmetry in living beings

Symmetry in biology refers to the symmetry observed in organisms, including plants, animals, fungi, and bacteria. External symmetry can be easily seen by just looking at an organism. For example, take the face of a human being which has a plane of symmetry down its centre, or a pine cone with a clear symmetrical spiral pattern. Internal features can also show symmetry, for example the tubes in the human body which are cylindrical and have several planes of symmetry.

<i>Velella</i> Species of cnidarian

Velella is a monospecific genus of hydrozoa in the Porpitidae family. Its only known species is Velella velella, a cosmopolitan free-floating hydrozoan that lives on the surface of the open ocean. It is commonly known by the names sea raft, by-the-wind sailor, purple sail, little sail, or simply Velella.

Medusozoa Clade of marine invertebrates

Medusozoa is a clade in the phylum Cnidaria, and is often considered a subphylum. It includes the classes Hydrozoa, Scyphozoa, Staurozoa and Cubozoa, and possibly the parasitic Polypodiozoa. Medusozoans are distinguished by having a medusa stage in their often complex life cycle, a medusa typically being an umbrella-shaped body with stinging tentacles around the edge. With the exception of some Hydrozoa, all are called jellyfish in their free-swimming medusa phase.

Mesoglea refers to the tissue found in cnidarians like coral or jellyfish that functions as a hydrostatic skeleton. It is related to but distinct from mesohyl, which generally refers to tissue found in sponges.

<i>Phacellophora camtschatica</i> Species of jellyfish

Phacellophora camtschatica, commonly known as the fried egg jellyfish or egg-yolk jellyfish, is a very large jellyfish in the family Phacellophoridae. This species can be easily identified by the yellow coloration in the center of its body which closely resembles an egg yolk, hence how it got its common name. Some individuals can have a bell close to 60 cm (2 ft) in diameter, and most individuals have 16 clusters of up to a few dozen tentacles, each up to 6 m (20 ft) long. A smaller jellyfish, Cotylorhiza tuberculata, typically found in warmer water, particularly in the Mediterranean Sea, is also popularly called a fried egg jellyfish. Also, P. camtschatica is sometimes confused with the Lion's mane jellyfish.

<i>Turritopsis dohrnii</i> Species of small, biologically immortal jellyfish

Turritopsis dohrnii, also known as the immortal jellyfish, is a species of small, biologically immortal jellyfish found worldwide in temperate to tropic waters. It is one of the few known cases of animals capable of reverting completely to a sexually immature, colonial stage after having reached sexual maturity as a solitary individual. Others include the jellyfish Laodicea undulata and species of the genus Aurelia.

<i>Chrysaora hysoscella</i> Species of jellyfish

Chrysaora hysoscella, the compass jellyfish, is a common species of jellyfish that inhabits coastal waters in temperate regions of the northeastern Atlantic Ocean, including the North Sea and Mediterranean Sea. In the past it was also recorded in the southeastern Atlantic, including South Africa, but this was caused by confusion with close relatives; C. africana, C. fulgida and an undescribed species tentatively referred to as "C. agulhensis".

Marine invertebrates

Marine invertebrates are the invertebrates that live in marine habitats. Invertebrate is a blanket term that includes all animals apart from the vertebrate members of the chordate phylum. Invertebrates lack a vertebral column, and some have evolved a shell or a hard exoskeleton. As on land and in the air, marine invertebrates have a large variety of body plans, and have been categorised into over 30 phyla. They make up most of the macroscopic life in the oceans.

Sea anemone Marine animals of the order Actiniaria


Sea anemones are the marine, predatory animals of the order Actiniaria. They are named after the anemone, a terrestrial flowering plant, because of the colourful appearance of many. Sea anemones are classified in the phylum Cnidaria, class Anthozoa, subclass Hexacorallia. As cnidarians, sea anemones are related to corals, jellyfish, tube-dwelling anemones, and Hydra. Unlike jellyfish, sea anemones do not have a medusa stage in their life cycle.