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Hexactinellid

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Glass sponges
Temporal range: Late Ediacaran–present[1]
"Hexactinellae" from Ernst Haeckel's Kunstformen der Natur, 1904
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Porifera
Class: Hexactinellida
Schmidt, 1870
Subgroups

See text.

Synonyms
  • Hyalospongiae
Bolosoma stalked glass sponge

Hexactinellid sponges are sponges with a skeleton made of four- and/or six-pointed siliceous spicules, often referred to as glass sponges. They are usually classified along with other sponges in the phylum Porifera, but some researchers consider them sufficiently distinct to deserve their own phylum, Symplasma. Some experts believe glass sponges are the longest-lived animals on earth;[2] these scientists tentatively estimate a maximum age of up to 15,000 years.

Biology

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Glass sponges are relatively uncommon and are mostly found at depths from 450 to 900 metres (1,480 to 2,950 ft) below sea level. Although the species Oopsacas minuta has been found in shallow water, others have been found much deeper. They are found in all oceans of the world, although they are particularly common in Antarctic and Northern Pacific waters.[3]

They are more-or-less cup-shaped animals, ranging from 10 to 30 centimetres (3.9 to 11.8 in) in height, with sturdy skeletons made of glass-like silica spicules, fused to form a lattice.[4][5] In some glass sponges such as members of the genus Euplectela, these structures are aided by a protein called glassin. It helps accelerate the production of silicas from the silicic acid absorbed from the surrounding seawater.[6] The body is relatively symmetrical, with a large central cavity that, in many species, opens to the outside through a sieve formed from the skeleton. Some species of glass sponges are capable of fusing together to create reefs or bioherms. They are generally pale in colour, ranging from white to orange.[3]

Much of the body is composed of syncitial tissue, extensive regions of multinucleate cytoplasm. The epidermal cells characteristic of other sponges are absent, being replaced by a syncitial net of amoebocytes, through which the spicules penetrate. Unlike other sponges, they do not possess the ability to contract.[3]

Their body comprises three parts: the inner and outer peripheral trabecular networks, and the choanosome, which is used for feeding purposes. The choanosome acts as the mouth for the sponge while the inner and outer canals that meet at the choanosome are passages for the food, creating a consumption path for the sponge.[7]

All hexactinellids have the potential to grow to different sizes, but the average maximum growth is estimated to be around 32 centimeters long. Some grow past that length and continue to extend their length up to 1 meter long. The estimated life expectancy for hexactinellids that grow around 1 meter is approximately 200 years (Plyes).

The glass sponge Euplectella.[8]: 83 Fig. 5–7 
  Water flow
  Main syncitium
  Spicules
  Choanosyncitium and collar bodies showing interior

Glass sponges possess a unique system for rapidly conducting electrical impulses across their bodies, making it possible for them to respond quickly to external stimuli.[9] In the case Rhabdocalyptus dawsoni, the sponge uses electrical neuron signaling to detect outside stimuli, such as sediments, and then send a signal through its body system to alert the organism to no longer be actively feeding. Another glass sponge species in the same experiment of R. dawsoni, showed that the electrical conduction system for this class of sponges all has its own threshold of how much outside stimuli, sediments, etc., it can endure before it will stop its feeding process.[10] Species like "Venus' flower basket" have a tuft of fibers that extends outward like an inverted crown at the base of their skeleton. These fibers are 50 to 175 millimetres (2.0 to 6.9 in) long and about the thickness of a human hair.

Syncytia

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Bodies of glass sponges are different from those other sponges in various other ways. For example, most of their cytoplasm is not divided into separate cells by membranes, but forms a syncytium or continuous mass of cytoplasm with many nuclei (e.g., Reiswig and Mackie, 1983); it is held suspended like a cobweb by a scaffolding-like framework made of silica spicules.[8] The remaining cells are connected to the syncytium by bridges of cytoplasmic "rivers" that transport nuclei, organelles ("organs" within cells) and other substances.[11] Instead of choanocytes, these bridges have further syncytia, known as choanosyncytia, which form bell-shaped chambers where water enters via perforations. The insides of these chambers are lined with "collar bodies", each consisting of a collar and flagellum but without a nucleus of its own. The motion of the flagella sucks water through passages in the "cobweb" and expels it via the open ends of the bell-shaped chambers.[8]

Some types of cells have a single nucleus and membrane each but are connected to other single-nucleus cells and to the main syncytium by "bridges" made of cytoplasm. The sclerocytes that build spicules have multiple nuclei, and in glass sponge larvae they are connected to other tissues by cytoplasm bridges; such connections between sclerocytes have not so far been found in adults, but this may simply reflect the difficulty of investigating such small-scale features. The bridges are controlled by "plugged junctions" that apparently permit some substances to pass while blocking others.[11]

This physiology is what allows for a greater flow of ions and electrical signals to move throughout the organism, with around 75% of the sponge tissue being fused in this way.[6] Another way is their role in the nutrient cycles of deep-sea environments. One species for example, Vazella pourtalesii, has an abundance of symbiotic microbes which aid in the nitrification and denitrification of the communities in which they are present. These interactions help the sponges survive in the low-oxygen conditions of the depths.[12]

Longevity

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Venus' flower basket, Euplectella aspergillum
Euplectella aspergillum

These creatures are long-lived, but the exact age is hard to measure; one study based on modelling gave an estimated age of a specimen of Scolymastra joubini as 23,000 years (with a range from 13,000 to 40,000 years). However, due to changes in sea levels since the Last Glacial Maximum, its maximum age is thought to be no more than 15,000 years,[13] hence its listing of c. 15,000 years in the AnAge Database.[14] The shallow-water occurrence of hexactinellids is rare worldwide. In the Antarctic, two species occur as shallow as 33 meters under the ice. In the Mediterranean, one species occurs as shallow as 18 metres (59 ft) in a cave with deep water upwelling (Boury-Esnault & Vacelet (1994))

  • Staurocalyptus sp.
    Staurocalyptus sp.
  • Various hexactinellid sponges.
    Various hexactinellid sponges.
  • Hexactinellid sponge on a xenophorid gastropod.
    Hexactinellid sponge on a xenophorid gastropod.
  • Pattersonia ulrichi Rauff, 1894; an Ordovician hexactinellid sponge from near Cincinnati, Ohio.
    Pattersonia ulrichi Rauff, 1894; an Ordovician hexactinellid sponge from near Cincinnati, Ohio.

Reefs

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The sponges form reefs (called sponge reefs) off the coast of British Columbia, southeast Alaska and Washington state,[15] which are studied in the Sponge Reef Project. In the case of Sarostegia oculata, this species almost always hosts symbiotic zoanthids, which cause the hexactinellid sponge to imitate the appearance and structure of coral reefs.[16] Only 33 species of this sponge have ever been reported in the South Atlantic until 2017 when the Shinkai 6500 submersible went on an expedition through the Rio Grande Rise.[16] Reefs discovered in Hecate Strait, British Columbia, have grown to up to 7 kilometres long and 20 metres high. Prior to these discoveries, sponge reefs were thought to have died out in the Jurassic period.[17][18]

Reports of glass sponges have also been recorded on the HMCS Saskatchewan and HMCS Cape Breton wrecks off the coast of Vancouver Island. Species of zoantharin that rely on hexactinellid have also been found off the coast of the Japanese island of Minami-Torishima. Unidentified species of zoanthids have also been found in Australian waters, if these are identified as the same as the ones found in Minami-Torishima, this could potentially be proof of hexactinellids existing in all of the Pacific Ocean.[19]

Conservation

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Most hexactinellids live in deep waters that are not impacted by human activities. However, there are glass sponge reefs off the coast of British Columbia. The Canadian government designated 2140 km2 of the Hecate strait and Queen Charlotte sound as a marine protected area. This area contains four glass sponge reefs. The new regulations prohibit bottom contact fishing within 200 meters of the sponge reefs.[20] Although human activities only affect a small portion of glass sponges, they are still subject to the threat of climate changes. Experiments using the species Aphrocallistes vastus have shown that increases in temperature and acidification can lead to weakened skeletal strength and stiffness.[21] In 1995, an Antarctic ice shelf collapsed due to climate change. Since then, studies of the area have shown that hexactinellid reefs have been increasing in size despite the changes in climate.[22]

Classification

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The earliest known hexactinellids are from the earliest Cambrian or late Neoproterozoic eras. They are fairly common relative to demosponges as fossils, but this is thought to be, at least in part, because their spicules are sturdier than spongin and fossilize better. Like almost all sponges, the hexactinellids draw water in through a series of small pores by the whip-like beating of a series of hairs or flagella in chambers which in this group line the sponge wall.

The class is divided into two subclasses and several orders:[23]

Class Hexactinellida

See also

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References

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  1. ^ Brasier, Martin; Green, Owen; Shields, Graham (April 1997). "Ediacarian sponge spicule clusters from southwestern Mongolia and the origins of the Cambrian fauna" (PDF). Geology. 25 (4): 303–306. Bibcode:1997Geo....25..303B. doi:10.1130/0091-7613(1997)025<0303:ESSCFS>2.3.CO;2.
  2. ^ "Hexactinellid sponge (Scolymastra joubini) longevity, ageing, and life history". genomics.senescence.info. Retrieved 2 March 2023.
  3. ^ a b c Barnes, Robert D. (1982). Invertebrate Zoology. Philadelphia: Holt-Saunders International. p. 104. ISBN 978-0-03-056747-6.
  4. ^ "Glass Sponges, the Living Ornaments of the Deep Sea". Schmidt Ocean Institute. 2020-10-01. Retrieved 2023-06-11.
  5. ^ US Department of Commerce, National Oceanic and Atmospheric Administration. "What is a glass sponge?". oceanservice.noaa.gov. Retrieved 2023-06-11.
  6. ^ a b Nishi, Michika; Kobayashi, Hiroki; Amano, Taro; Sakate, Yuto; Bito, Tomohiro; Arima, Jiro; Shimizu, Katsuhiko (2020-12-01). "Identification of the Domains Involved in Promotion of Silica Formation in Glassin, a Protein Occluded in Hexactinellid Sponge Biosilica, for Development of a Tag for Purification and Immobilization of Recombinant Proteins". Marine Biotechnology. 22 (6): 739–747. Bibcode:2020MarBt..22..739N. doi:10.1007/s10126-020-09967-2. ISSN 1436-2236. PMID 32291549. S2CID 215761084.
  7. ^ "Gale - Institution Finder".
  8. ^ a b c Ruppert RE, Fox RS, Barnes RD (2004). Invertebrate Zoology (7th ed.). Brooks / COLE Publishing. pp. 76–97. ISBN 978-0-03-025982-1.
  9. ^ Lawrence, Eleanor (1999). "Nervous sponge". Nature. doi:10.1038/news990415-5.
  10. ^ Tompkins-MacDonald, Gabrielle J.; Leys, Sally P. (2008-05-15). "Glass sponges arrest pumping in response to sediment: implications for the physiology of the hexactinellid conduction system". Marine Biology. 154 (6): 973–984. Bibcode:2008MarBi.154..973T. doi:10.1007/s00227-008-0987-y. ISSN 0025-3162. S2CID 54079172.
  11. ^ a b Leys SP (February 2003). "The significance of syncytial tissues for the position of the hexactinellida in the metazoa". Integrative and Comparative Biology. 43 (1): 19–27. doi:10.1093/icb/43.1.19. PMID 21680406.
  12. ^ Maldonado, Manuel; López-Acosta, María; Busch, Kathrin; Slaby, Beate M.; Bayer, Kristina; Beazley, Lindsay; Hentschel, Ute; Kenchington, Ellen; Rapp, Hans Tore (2021). "A Microbial Nitrogen Engine Modulated by Bacteriosyncytia in Hexactinellid Sponges: Ecological Implications for Deep-Sea Communities". Frontiers in Marine Science. 8. doi:10.3389/fmars.2021.638505. hdl:10261/235467. ISSN 2296-7745.
  13. ^ Susanne Gatti (2002). "The Role of Sponges in High-Antarctic Carbon and Silicon Cycling - a Modelling Approach" (PDF). Ber. Polarforsch. Meeresforsch. 434. ISSN 1618-3193. Archived from the original (PDF) on 2011-07-24. Retrieved 2009-05-25.
  14. ^ "Hexactinellid information from the AnAge Database".
  15. ^ Stiffler, Lisa (2007-07-27). "Reef of glass sponges found off Washington's coast". Seattle Post-Intelligencer.
  16. ^ a b Hajdu, Eduardo; Castello-Branco, Cristiana; Lopes, Daniela A.; Sumida, Paulo Yukio Gomes; Perez, Jose Angel Alvarez (December 2017). "Deep-sea dives reveal an unexpected hexactinellid sponge garden on the Rio Grande Rise (SW Atlantic). A mimicking habitat?". Deep Sea Research Part II: Topical Studies in Oceanography. 146: 93–100. Bibcode:2017DSRII.146...93H. doi:10.1016/j.dsr2.2017.11.009.
  17. ^ "B.C.'s Reefs Among Science's Great Finds". Georgia Straight Vancouver's News & Entertainment Weekly. 2005-02-24. Retrieved 2017-05-22.
  18. ^ "Diving deep for glass sponges". CBC Radio. Retrieved 2017-05-22.
  19. ^ Kise, Hiroki; Nishijima, Miyuki; Iguchi, Akira; Minatoya, Junpei; Yokooka, Hiroyuki; Ise, Yuji; Suzuki, Atsushi (2023-03-24). "A new hexactinellid-sponge-associated zoantharian (Porifera, Hexasterophora) from the northwestern Pacific Ocean". ZooKeys (1156): 71–85. Bibcode:2023ZooK.1156...71K. doi:10.3897/zookeys.1156.96698. ISSN 1313-2970. PMC 10208231. PMID 37234793.
  20. ^ Government of Canada, Fisheries and Oceans Canada (2019-09-18). "Hecate Strait/Queen Charlotte Sound Glass Sponge Reefs Marine Protected Area (HS/QCS MPA)". www.dfo-mpo.gc.ca. Retrieved 2023-10-06.
  21. ^ Stevenson, A.; Archer, S. K.; Schultz, J. A.; Dunham, A.; Marliave, J. B.; Martone, P.; Harley, C. D. G. (2020-05-18). "Warming and acidification threaten glass sponge Aphrocallistes vastus pumping and reef formation". Scientific Reports. 10 (1): 8176. Bibcode:2020NatSR..10.8176S. doi:10.1038/s41598-020-65220-9. ISSN 2045-2322. PMC 7235243. PMID 32424237.
  22. ^ Fillinger, Laura; Janussen, Dorte; Lundalv, Tomas; Richter, Claudio (July 22, 2013). "Rapid glass sponge expansion after climate-induce Antarctic ice shelf collapse". Current Biology. 23 (14): 1330–1334. Bibcode:2013CBio...23.1330F. doi:10.1016/j.cub.2013.05.051. PMID 23850279. S2CID 18142746.
  23. ^ "Hexactinellida". WoRMS. World Register of Marine Species.
  24. ^ a b Treatise on Invertebrate Paleontology Part E, Revised. Porifera, Volume 3: Classes Demospongea, Hexactinellida, Heteractinida & Calcarea, xxxi + 872 p., 506 fig., 1 table, 2004, available here. ISBN 0-8137-3131-3.
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