Euplokamis

Euplokamis is a genus of ctenophores, or comb jellies, belonging to the monotypic family Euplokamididae.[2] It shares the common name sea gooseberry with species of the genus Pleurobrachia. Despite living for hundreds of millions of years in marine environments, there is minimal research regarding Euplokamis, because they are uncommon. Research on the evolution of the basic body structures of diploblastic metazoans revealed that there are four major phyla, including the Ctenophores.[3] Although the morphology of Euplokamis often resembles the medusa stage of Cnidarians, their eight rows of combs are one distinguishing feature that led to the official classification of Ctenophores.[4] 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.[5] Further research indicated that Euplokamis should be identified from Mertensiidae due to the rows of combs and some compression.[6] They may also be distinguished from the genus Pleurobrachia due to their more elongated shape.[6] 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.[7]

Euplokamis
Temporal range:
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Ctenophora
Class: Tentaculata
Order: Cydippida
Family: Euplokamididae
Mills, 1987
Genus: Euplokamis
Chun, 1879
Synonyms[1]

Euplokamidae Mills, 1987

Distribution & Habitat

Euplokamis have been found in fossil records dating back to the Cambrian period, part of the Paleozoic Era, and it is estimated that some species may have evolved before this period.[3] Originally, Cnidarians and Ctenophores were classified under the same phyla, Coelenterata. Ctenophore bodies are made up of a gelatin substance, similar to Cnidarians, but the multiple rows of combs present in fossil records are unique to ctenophores.[8] Records of Euplokamis sp. indicate they are distributed widely around the world, but are most often found in warm coastal waters.[9] Euplokamis prefer marine, or saltwater, environments and are classified as free swimmers, due to their ability to move through the water column.[4] They have been identified in the Mediterranean Sea, the North Pacific, the Gulf of Maine, and off the coast of Sweden.[10][5] However, since this genus was originally grouped in the family Pleurobrachiidae, there is limited information regarding their actual distribution and habitat.

Figure 1. Pelagic ctenophores: (a) Beroe ovata, (b) unidentified cydippid (c) "Tortugas red" cydippid, (d) Bathocyroe fosteri, (e) Mnemiopsis leidyi, and (f) Ocyropsis sp. from Wikipedia Commons

Anatomy & Morphology
Figure 2. Euplokamis sp. from Wikipedia Commons

Ctenophores are divided into two classes based on either the presence(Tentaculat)) or the lack (Nuda) of tentacles.[9] Within each class, there are multiple orders to further distinguish their structures and characteristics. The class Tentaculata contains the following orders: Cydippida, Lobata, and Cestida.[11] The genus Euplokamis is part of the class tentaculate, which indicates that tentacles are present.[7] They are also part of the order Cydippida, distinguished by their tentacles and their round body shape.[7] Euplokamis tentacles are long, with side branches, and have a sheath allowing them to be retracted inside of the body.[9] The tentacle side branches are known as tentilla, which in the case of Euplokamis are held tightly in coils except during the act of prey capture.[12] Further, the widely spaced tentillia droplets allow for organisms to be classified to the genus level and are one of the only examples of striated muscle found in ctenophores.[13]

Additionally, these organisms have bi-radial symmetry with a mouth on their front end and a statocyst, or sense organ, at the other end.[7] The sides of their stomachs are lined with distinct bulbs, shaped like tadpoles,[12] and unlike other well-known jellyfish, Euplokamis do not have any nematocytes, known as stinging cells. The mouth is connected to the digestive tract via the pharynx. The digestive system, or gastrovascular cavity, is made up of intricate canals that allow for both digestion and circulation to occur.[7] They also lack an anus but are able to excrete some waste through pores on the adoral end. Typically, Euplokamis are small, only growing up to approximately 20 millimeters (mm) in length.[12]

Another distinct feature of this genus is the eight rows of combs present. While they are known as comb plates, they are actually made up of large cilia, which are hair-like structures.[13] These plates are unique because they consist of some of the largest known cilia found on any organism.[13] Additionally, the combs primarily function in movement, allowing some species to move forward and backward.[4] Since their bodies are made of the mesoglea—a translucent, gelatin-like substance—the 8 comb rows can be easily identified. These combs function in movement, due to their large ciliary structures.[13]

Behaviors & Adaptations

Tentacles: Movement and Feeding Behavior
Figure 3. Structure of Ctenophora: Order Cypiddia from Wikipedia Commons

Euplokamis have long tentacles with branches that are used for feeding and movement. These branches are known as tentilla and are held tightly in coils, forming droplet shapes.[12] The tentilla are usually held in coils but can be uncoiled to aid in movement.[14] Further, these organisms can move their tentilla in slow spontaneous movements or in rapid extensions.[14] According to research, Euplokamis are carnivorous, like all other known species of Ctenophores.[15] They are known to feed primarily on rotifers and other small crustaceans: including copepods, amphipods, and some planktonic larvae.[15] To catch prey, they will extend the tentilla and wrap them around copepods.[16] The tentilla are covered in sticky colloblasts, which keep the prey stuck in place.[14] Not only can the tentilla be released at high velocities to quickly capture prey, but they also can be released in a slow and controlled manner, likely to attract prey.[14] Additionally, the cilia that make up the comb plate move by making a stroke in a certain direction. After capturing prey, they can reverse the stroke, or beat, in the other direction on two rows, while the other rows continue to beat in the normal direction.[13] They are then able to push the prey to their mouth in a sweeping motion, and the ciliary reversal causes the organism to rotate, which tangles the prey further into its mouth.[13]

Nervous System

Despite their simple exterior, research on the nervous system of Euplokamis sp. indicates the use of more complex systems, including axons. The use of these axons has allowed some species of Euplokamis sp. to swim backward rapidly. The direction of the cilia comb plate may be reversed causing them to move backward.[10] These organisms are unique due to the presence of giant axons in their combs that allow for a rapid escape response.[17] Additionally, Euplokamis sp. has an aboral sensory organ, which is bypassed to produce this escape response.[18]

Bioluminescence
Figure 4. Bioluminescent Euplokamis sp. from Wikipedia Commons

Another adaptation that many ctenophores have developed is bioluminescence, or the ability to produce light. For example, Euplokamis dunlapae were found to produce light off the coast of Washington when exposed to stimuli.[10] After physical stimulation, they produced bright flashes of light, consistent with bioluminescence. According to research, bioluminescence in Euplokamis sp. is both intrinsic and extrinsic, because light can appear in the comb rows or as bursts of light in the water.[19] Additionally, off the coast of Maine, Euplokamis sp. was found to be one of the two brightest species to have bioluminescence.[20] Research suggests that bioluminescence in Euplokamis sp. may function as a defense mechanism.[20] The bursts of light were only observed directly in response to a disturbance or stimulation, likely to distract or blind predators when they are sensed.[21] Additionally, some produce light as a warning signal, or to expose nearby predators. The various strategies may impact predator-prey relationships or other the population dynamics in an area.[20]

Taxonomy[11]

References
  1. "Euplokamididae". WoRMS. World Register of Marine Species. Retrieved 13 May 2021.
  2. "Euplokamididae". Global Biodiversity Information Facility. Retrieved 13 May 2021.
  3. Giribet, Gonzalo (2002-09-01). "Current advances in the phylogenetic reconstruction of metazoan evolution. A new paradigm for the Cambrian explosion?". Molecular Phylogenetics and Evolution. 24 (3): 345–357. doi:10.1016/S1055-7903(02)00206-3. PMID 12220976.
  4. Minni, M. (2021). "Phylum Ctenophora – Characteristics, Classification & Examples". Embibe Exams.
  5. Mills, Claudia E. (1987). "Revised classification of the genus Euplokamis Chun, 1880 (Ctenophora: Cydippida: Euplokamidae n. fam.) with a description of the new species Euplokamis dunlapae". Canadian Journal of Zoology. 65 (11): 2661–2668. doi:10.1139/z87-404.
  6. RITTER, WILLIAM (1906). Zoology: Volume II. Berkley the University Press: University of California Publications. p. 46. ISBN 048477736X.
  7. Britannica, T. (2013). "Ctenophore: Marine invertebrate". www.britannica.com. Encyclopedia Britannica.
  8. Parry, Luke A.; Lerosey-Aubril, Rudy; Weaver, James C. & Ortega-Hernández, Javier (2021-09-24). "Cambrian comb jellies from Utah illuminate the early evolution of nervous and sensory systems in ctenophores". iScience. 24 (9): 102943. Bibcode:2021iSci...24j2943P. doi:10.1016/j.isci.2021.102943. PMC 8426560. PMID 34522849.
  9. Shah, R (2016). "Phylum Ctenophora: Features, Characters and Other Details". Biology Discussion.
  10. Haddock, Steven H. D. & Case, James F. (1995). "Not all ctenophores are bioluminescent: Pleurobrachia". Biological Bulletin. 189 (3): 356–362. doi:10.2307/1542153. JSTOR 1542153. PMID 29244577.
  11. World Register of Marine Species, WoRMS (2022). "WoRMS taxon details: Euplokamis". www.marinespecies.org.
  12. Gershwin, L; Lewis, M; Gowlett-Holmes, K & Kloser, R (2014). "The Ctenophores". Pelagic Invertebrates of South-Eastern Australia: A field reference guide. Hobart: CSIRO Marine and Atmospheric Research. pp. 5–6.
  13. Tamm, Sidney L. (2014). "Cilia and the life of ctenophores". Invertebrate Biology. 133 (1): 1–46. doi:10.1111/ivb.12042. JSTOR 24697149.
  14. Mackie, G. O.; Mills, C. E. & Singla, C. L. (1988). "Structure and function of the prehensile tentilla of Euplokamis (Ctenophora, Cydippida)". Zoomorphology. 107 (6): 319–337. doi:10.1007/bf00312216. S2CID 317017.
  15. Wright, Jeremy. "Ctenophora (comb jellies)". Animal Diversity Web. Retrieved 2022-04-10.
  16. Haddock, Steven H. D. (2007). "Comparative feeding behavior of planktonic ctenophores". Integrative and Comparative Biology. 47 (6): 847–853. doi:10.1093/icb/icm088. JSTOR 4540225. PMID 21669763.
  17. Mackie, G. O.; Mills, C. E. & Singla, C. L. (1992). "Giant axons and escape swimming in Euplokamis dunlapae (Ctenophora: Cydippida)". The Biological Bulletin. 182 (2): 248–256. doi:10.2307/1542118. JSTOR 1542118. PMID 29303667.
  18. Norekian, Tigran P. & Moroz, Leonid L. (2019). "Comparative neuroanatomy of ctenophores: Neural and muscular systems in Euplokamis dunlapae and related species". Journal of Comparative Neurology. 528 (3): 481–501. doi:10.1002/cne.24770. PMID 31498892. S2CID 202407426.
  19. Widder, Edith (January 2002). "Bioluminescence and the Pelagic Visual Environment". Marine and Freshwater Behaviour and Physiology. 35 (1–2): 1–26. doi:10.1080/10236240290025581. S2CID 85259393.
  20. Widder, E.A.; Greene, C.H. & Youngbluth, M.J. (1992). "Bioluminescence of sound-scattering layers in the Gulf of Maine". Journal of Plankton Research. 14 (11): 1607–1624. doi:10.1093/plankt/14.11.1607.
  21. Dybas, Cheryl (2013). "RIPPLE MARKS—The Story Behind the Story". Oceanography. 26 (2). doi:10.5670/oceanog.2013.23.
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