Beroe abyssicola | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Ctenophora |
Class: | Nuda |
Order: | Beroida |
Family: | Beroidae |
Genus: | Beroe |
Species: | B. abyssicola |
Binomial name | |
Beroe abyssicola Mortensen, 1927 | |
Beroe abyssicola is a species of beroid ctenophore, or comb jelly. [1] It is largely found in deep waters in the North Pacific Ocean, and is common in Japan and the Arctic Ocean. A predator, B. abyssicola feeds mostly on other ctenophores by swallowing them whole. Like other ctenophores, B. abyssicola has a simple nervous system in the form of a nerve net, which it uses to direct its movement, feeding, and hunting behaviors.
Beroe abyssicola is a pelagic ctenophore species that inhabits the North Pacific. [2] Like other Beroida, B. abyssicola has a very different body plan from other Ctenophores, namely the lack of any tentacles in any life stage. [2] B. abyssicola has a muscular, flat, and cylindrical body. It can grow up to 7 cm long, shorter than other beroids, but larger than most ctenophores. [3] Its body is more opaque than other ctenophores and can have coloration red or purple. When not feeding, the large mouth is kept closed using adhesive bands of epithelial cells that stick together, holding the mouth closed. [2]
Beroe abyssicola is a ctenophore with a flexible, highly muscular body. Being a predator, B. abyssicola uses its muscular body along with its ctene rows to swim and capture its prey, and uses its wide mouth to swallow its prey whole. [2] When not feeding, the mouth is held closed using bands of adhesive epithelial cells paired for each mouth. [4] The mesoglea of Beroe have large smooth muscle fibers, which allows the ctenophore the flexibility to swallow much of its prey whole. [2]
The nervous system of B. abyssicola does not have a central nervous system, but rather consists of a nerve net. The largest concentration of nervous function is concentrated in the aboral organ, located opposite the mouth. Beroe has a defense response that retracts the entire aboral organ inside the body of itself for protection. This organ mediates swimming, gravity sensing and possibly more functions. The nerve net extends out from this organ, covering the surface and pharyngeal surface, as well as a separate system of neurons in the mesoglea.
There is a band of sensory cells surrounding the mouth of abyssicola that can detect chemical and mechanical stimuli. These "lips" can be used by Beroe to detect prey and assist with feeding. [2]
The nervous system of Beroe abyssicola, along with other Ctenophora, is different to those of other animals. Almost no neurotransmitters but glutamate are shared between ctenophore nervous systems and others, as well as lacking many of the same pathways involved in other nervous systems. [5] It has been hypothesized that the nervous systems of Beroe abyssicola, along with other Ctenophores, evolved independently of those of other animals. [5]
Beroe abyssicola, like other members of the class Nuda, are predatory ctenophores, whose diet consists mainly of smaller ctenophores. [6] The primary prey of B. abyssicola is Bolinopsis infundibulum . [2] Beroe has a set of large cilia on the inside of its mouth called macrocilia. [7] These macrocilia are large enough to function as teeth, used to keep prey inside and even tear the tissue of the gelatinous prey. Using its "lips" to detect prey, Beroe opens its mouth and swallows its prey whole. B. abyssicola possesses a large pharynx that spans nearly the length of the body to digest its food, using pharyngeal muscles and macrocilia to keep its mouth closed and prey inside. Once digested, the food then moves through the gastrovascular system in canals, which supplies nutrients throughout the mesoglea.
Beroe's swimming is powered by 8 comb rows of joined cilia, swimming mouth-first. They swim constantly and strongly to search for prey, and swallow their prey blindly when they do. [8] Their swimming is controlled largely by the aboral organ. [2]
Beroe abyssicola can be found throughout the Northern Pacific Ocean. [1] Abyssicola can be found up to 2000 meters below the ocean surface, [9] and is common in the waters around Japan, as well as the Arctic Ocean, [10] mostly found below 400 meters. [11]
Like other ctenophores, B. abyssicola has a rainbow effect on its comb rows caused by light refraction, but it also possesses bioluminescence. Bioluminescence in Beroe is caused by calcium activated photoproteins, similar to hydromedusae. This photoprotein is called berovin, and differs from photoproteins used by hydromedusa in that it is sensitive to visible and UV light, and largely has a different genetic sequence. [12] However both types of photoprotein have a similar EF-Hand structure despite the sequence differences between the two proteins.
Beroe abyssicola is a ctenophore in the genus Beroe, in the class Nuda. It is classified here because of its lack of tentacles placing it into the Nuda class, and its cylindrical body shape classifying it as Beroe. Ctenophore phylogeny is complicated and not agreed upon entirely. Recent evidence [13] suggests that the Beroida order may be polyphyletic, with Beroe abyssicola being outside of the clade including all other Beroe species. This also suggests B. abyssicola evolved a loss of tentacles independently of other beroid species.
Cnidaria is a phylum under kingdom Animalia containing over 11,000 species of aquatic invertebrates found both in fresh water and marine environments, including jellyfish, hydroids, sea anemones, corals and some of the smallest marine parasites. Their distinguishing features are a decentralized nervous system distributed throughout a gelatinous body and the presence of cnidocytes or cnidoblasts, specialized cells with ejectable flagella used mainly for envenomation and 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 are also some of the few animals that can reproduce both sexually and asexually.
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.
A nerve net consists of interconnected neurons lacking a brain or any form of cephalization. While organisms with bilateral body symmetry are normally associated with a condensation of neurons or, in more advanced forms, a central nervous system, organisms with radial symmetry are associated with nerve nets, and are found in members of the Ctenophora, Cnidaria, and Echinodermata phyla, all of which are found in marine environments. In the Xenacoelomorpha, a phylum of bilaterally symmetrical animals, members of the subphylum Xenoturbellida also possess a nerve net. Nerve nets can provide animals with the ability to sense objects through the use of the sensory neurons within the nerve net.
Beroidae is a family of ctenophores or comb jellies more commonly referred to as the beroids. It is the only known family within the monotypic order Beroida and the class Nuda. They are distinguished from other comb jellies by the complete absence of tentacles, in both juvenile and adult stages. Species of the family Beroidae are found in all the world's oceans and seas and are free-swimmers that form part of the plankton.
Lobata is an order of transparent marine invertebrates belonging to the phylum of Ctenophora in the class Tentaculata, and are commonly referred to as comb jellies or sea gooseberries. There are currently 19 extant known species in the order of Lobata. Members of Lobata exhibit a compressed body in the vertical plane and a pair of oral lobes. They are known to inhabit marine pelagic surfaces and the marine shores.
Mesoglea refers to the extracellular matrix found in cnidarians like coral or jellyfish as well as ctenophores that functions as a hydrostatic skeleton. It is related to but distinct from mesohyl, which generally refers to extracellular material found in sponges.
Mnemiopsis leidyi, the warty comb jelly or sea walnut, is a species of tentaculate ctenophore. It is native to western Atlantic coastal waters, but has become established as an invasive species in European and western Asian regions. Three species have been named in the genus Mnemiopsis, but they are now believed to be different ecological forms of a single species M. leidyi by most zoologists.
Phacellophora, commonly known as the fried egg jellyfish or egg-yolk jellyfish, is a very large jellyfish in the monotypic family Phacellophoridae containing a single species Phacellophora camtschatica. This genus can be easily identified by the yellow coloration in the center of its body which closely resembles an egg yolk, hence 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.
Ocyropsis, a genus within the comb jelly phylum Ctenophora, belonging to the family of Ocyropsidae, are characterized by their prominent muscular lobes and four auricles. These pale, translucent organisms inhabit a wide range of oceanic environments, from warm tropical waters to the cold depths. Unlike many other ctenophores, which are relatively slow-moving, Ocyropsis species are agile predators, utilizing their powerful lobes for rapid propulsion. Additionally, they possess the ability to secrete bioluminescent mucus, a defense mechanism that can disorient and deter potential threats. To capture prey, Ocyropsis employ their muscular lobes to seize and manipulate food items, subsequently transferring them to their prehensile mouths for ingestion.
Cydippida is an order of comb jellies. They are distinguished from other comb jellies by their spherical or oval bodies, and the fact their tentacles are branched, and can be retracted into pouches on either side of the pharynx. The order is not monophyletic, that is, more than one common ancestor is believed to exist.
Pleurobrachia bachei is a member of the phylum Ctenophora and is commonly referred to as the Pacific sea gooseberry. These comb jellies are often mistaken for medusoid Cnidaria, but lack stinging cells.
Mertensia ovum, also known as the Arctic comb jelly or sea nut, is a cydippid comb jelly or ctenophore first described as Beroe ovum by Johan Christian Fabricius in 1780. It is the only species in the genus Mertensia. Unusually among ctenophores, which normally prefer warmer waters, it is found in the Arctic and adjacent polar seas, mostly in surface waters down to 50 metres (160 ft).
Beroe, commonly known as the cigar comb jellies, is a genus of comb jellies in the family Beroidae. Beroe exhibits bioluminescence.
Beroe ovata is a comb jelly in the family Beroidae. It is found in the South Atlantic Ocean and the Mediterranean Sea and has been introduced into the Black Sea, the Aegean Sea, the Sea of Azov and the Caspian Sea. It was first described by the French physician and zoologist Jean Guillaume Bruguière in 1789.
Beroe cucumis is a species of comb jelly in the family Beroidae. It is found in the Atlantic Ocean. It was first described by the Danish missionary and naturalist Otto Fabricius in 1780.
Pleurobrachia pileus is a species of comb jelly, commonly known as a sea gooseberry. It is found in open water in the northern Atlantic Ocean, the North Sea, the Baltic Sea and the Black Sea, and was first described by the Danish zoologist Otto Friedrich Müller in 1776.
Edwardsiella lineata, the lined anemone, is a species of sea anemone in the family Edwardsiidae. It is native to the northwestern Atlantic Ocean where it occurs in the subtidal zone.
Neis is a genus of nudan ctenophores. It is a monotypic genus containing the single species Neis cordigera. It occurs only near Australia. As all beroids, it is a free-swimmer that form part of the plankton.
Euplokamis is a genus of ctenophores, or comb jellies, belonging to the monotypic family Euplokamididae. It shares the common name sea gooseberry with species of the genus Pleurobrachia. After being originally described by Chun (1879), the family Euplokamididae was expanded by Mills (1987) due to the discovery of a new species, Euplokamis dunlapae. Further research indicated that Euplokamis should be identified from Mertensiidae due to the rows of combs and some compression. They may also be distinguished from the genus Pleurobrachia due to their more elongated shape. Additionally, various adaptations of Euplokamis have been observed such as the use of tentacles for movement/feeding, a complex nervous system, and bioluminescent capabilities. Other characteristics including a defined mesoderm, lack of stinging cells, developmental differences, and symmetry supported the reclassification of these organisms.
Beroe gracilis is a species of comb jelly in the family Beroidae. It is a free-swimming species found in the North Sea, the Atlantic Ocean and the Mediterranean Sea.