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Akashiwo sanguinea

Akashiwo sanguinea is a species of marine dinoflagellates well known for forming blooms that result in red tides.[1] The organism is unarmored (naked). Therefore, it lacks a thick cellulose wall, the theca, common in other genera of dinoflagellates. Reproduction of the phytoplankton species is primarily asexual.[2]

Akashiwo sanguinea
Scientific classification
Domain:
(unranked):
(unranked):
Phylum:
Class:
Order:
Family:
Genus:
Akashiwo
Species:
A. sanguinea
Binomial name
Akashiwo sanguinea
(K. Hirasaka) Hansen & Moestrup

Recently recognized as mixotrophic, A. sanguinea is capable of preying on various organisms.[3] For example, A. sanguinea is found to be capable of ingesting the cyanobacterium Synechococcus sp. at values comparable to other heterotrophic phytoplankton. This suggests implications it may have on the grazing impact of Synechococcus.[4]

Description edit

Despite its lack of thecal plates, a prominent feature helpful in identifying armored flagellates, A. sanguinea is relatively large and easily recognizable. Like most dinoflagellates, one flagellum is complex, wrapping around the equator of the cell in a groove. The other flagellum extends out from the cell to help aid its movement through the water.[5] A. sanguinea’s most prominent features are the lack of a nuclear envelope chamber and the apical groove's large, clockwise path when viewed from the front of the cell. These features, along with observations and data from LSU rDNA sequencing, recently helped declare a new genus for this species (Hansen & Moestrup).[6]

Etymology edit

The genus name akashiwo is Japanese for red tide.[6]

Distribution edit

Akashiwo sanguinea covers a broad range of distributions.[7] Frequent blooms exist off the coast of Florida and Southern California.[5][8] Blooms dominated by this species have also been observed in Narragansett Bay, Rhode Island.[9]

Behavior and physiology edit

Akashiwo sanguinea exhibits a diurnal vertical migration pattern, observed to move toward the sun in field experiments even before the start of the light cycle. In laboratory settings, the migration is light dependent but the direction of movement is not solely explained by positive phototaxis. It has also been shown to swim across large gradients in temperature. However, more study is needed to determine the organisms’ migratory behavior.[10]

Akashiwo sanguinea responds to certain changes in the water column by forming subsurface chlorophyll maximum layers in the marine environment.[11] A study off of Southern California's coast observed a subsurface layer when nitrate was limiting to the organism.[10] A. sangiunea's subsurface chlorophyll maximum layer has contributed to the success of larval anchovy growth on California's coastline. The larva have been observed to ingest this organism and not other species such as Chaetoceros spp. and Thalassiosira spp. suggesting a preference for A. sanguinea over other dinoflagellates.[8]

Context and content edit

Synonyms Gymnodinium splendens (Lebour), Gymnodinium sanguineum (Hirasaka), Gymnodinium nelsoni (Martin)

The names listed above were used during prior research on the organism. The genus is now redefined into four new genera. Gymnodinium was one of many dinoflagellate genera declared when taxonomic nomenclature was limited to features only visible with the light microscope. In 2000, Hansen and Moestrup analyzed ultrastructural details of the organism using large-subunit (LSU) rDNA sequencing. Aided by this new technology, the scientists were able to declare variations in the path of the apical groove of the organism (found on the flagellar apparatus). Since the apical groove varies among species, the scientists used it to indicate differences between the unarmored flagellates. Akashiwo was one of four new genera that was redefined using the analysis.[1]

HAB implications edit

Akashiwo sanguinea has been correlated to harmful algal blooms (HABs), but more study is needed to make sense of the blooms.

The protist can produce mycosporine-like amino acids (MAAs) which are water-soluble surfactants. A red tide caused by A. sanguinea was coincident with widespread seabird mortality across fourteen different species of birds in November–December 2007 in Northeastern Monterey Bay, California. Plankton samples showed A. sanguinea as the dominant flagellate in the bloom. Affected birds accumulated a proteinaceous material on their feathers, causing a loss in the natural water repellency. However no toxins, such as domoic acid, saxitoxin or brevetoxin was detected in the water. It was the first documented case of its tide causing harm to birds.[7] In 2009 a huge foam event blamed on Akashiwo sanguinea killed vast quantities of sea birds from the northern Oregon coast to the tip of the Olympic Peninsula in Washington state.[12]

The species’ blooms have also been linked to coral bleaching. More research is needed before predictions of HAB events that may be linked with this species.[7]

References edit

  1. ^ a b Hargraves, P. E. (June 14, 2011). "Akashiwo sanguinea". Protists of the Indian River Lagoon. Smithsonian Institution. Retrieved October 27, 2011.
  2. ^ Lalli, Carol M.; Parsons, Timothy R. (1993). Biological Oceanography: an Introduction (2nd ed.). Elsevier Butterworth-Heinemann. pp. 42–45. ISBN 0-7506-3384-0.
  3. ^ Bockstahler, K. R.; Coats, D. W. (1993). "Grazing of the mixotrophic dinoflagellate Gymnodinium sanguineum on ciliate populations of Chesapeake Bay". Marine Biology. 116 (3): 477–487. Bibcode:1993MarBi.116..477B. doi:10.1007/BF00350065. S2CID 84468485.
  4. ^ Jeong, Hae Jin; Park, Jae Yeon; Nho, Jae Hoon; Park, Myung Ok; Ha, Jeong Hyun; Seong, Kyeong Ah; Jeng, Chang; Seong, Chi Nam; Lee, Kwang Ya; Yih, Won Ho (2005). "Feeding by red-tide dinoflagellates on the cyanobacterium Synechococcus". Aquatic Microbial Ecology. 41 (2): 131–143. doi:10.3354/ame041131.
  5. ^ a b Miller, Charles B. (2004). Biological Oceanography. Blackwell. pp. 26–32. ISBN 0-632-05536-7.
  6. ^ a b Daugbjerg, Niels; Hansen, Gert; Larsen, Jacob; Moestrup, Øjvind (2000). "Phylogeny of some of the major genera of dinoflagellates based on ultrastructure and partial LSU rDNA sequence data, including the erection of three new genera of unarmoured dinoflagellates" (PDF). Phycologia. 39 (4): 302–317. Bibcode:2000Phyco..39..302D. doi:10.2216/i0031-8884-39-4-302.1. S2CID 86456565.
  7. ^ a b c Jessup, David A.; Miller, Melissa A.; Ryan, John P.; Nevins, Hannah M.; Kerkering, Heather A.; Mekebri, Abdou; Crane, David B.; Johnson, Tyler A.; Kudela, Raphael M. (2009). "Mass stranding of marine birds caused by a surfactant-producing red tide". PLoS ONE. 4 (2): e4550. Bibcode:2009PLoSO...4.4550J. doi:10.1371/journal.pone.0004550. PMC 2641015. PMID 19234604.
  8. ^ a b Lasker, Reuben (1975). "Field criteria for survival of anchovy larvae: the relation between inshore chlorophyll maximum layers and successful first feeding" (PDF). Fishery Bulletin. 73 (3): 453–462.
  9. ^ Smayda, Theodore J. (1957). "Phytoplankton studies in Lower Narragansett Bay". Limnology and Oceanography. 2 (4): 342–359. Bibcode:1957LimOc...2..342S. doi:10.1002/lno.1957.2.4.0342. JSTOR 2832835.
  10. ^ a b Cullen, J. J.; Horrigan, S. G. (1981). "Effects of nitrate on the diurnal vertical migration, carbon to nitrogen ratio, and the photosynthetic capacity of the dinoflagellate Gymnodinium splendens". Marine Biology. 62 (2–3): 81–89. Bibcode:1981MarBi..62...81C. doi:10.1007/BF00388169. S2CID 82258412.
  11. ^ Reid, F. M. H.; Stewart, E.; Eppley, R. W.; Goodman, D. (1978). "Spatial distribution of phytoplankton species in chlorophyll maximum layers off Southern California". Limnology and Oceanography. 23 (2): 219–226. Bibcode:1978LimOc..23..219R. doi:10.4319/lo.1978.23.2.0219. JSTOR 2835393.
  12. ^ Terry, Lynne (October 22, 2009). "Foam from ocean algae bloom killing thousands of birds". OregonLive. Retrieved 2017-03-03.

Further reading edit

  • Badylak, Susan; Philips, Edward; Mathews, Loren; Kelley, Karen (September 2014). "Akashiwo sanguinea (Dinophyceae) extruding mucous from pores on the cell surface". Algae. 29 (3): 197–201. doi:10.4490/algae.2014.29.3.197.
  • Matsubara, Tadashi; Nagasoe, Sou; Yamasaki, Yasuhiro; Shikata, Tomoyuki; Shimasaki, Yohei; Oshima, Yuji; Honjo, Tsuneo (16 April 2007). "Effects of temperature, salinity, and irradiance on the growth of the dinoflagellate Akashiwo sanguinea". Journal of Experimental Marine Biology and Ecology. 342 (2): 226–230. doi:10.1016/j.jembe.2006.09.013.
  • Yang, Caiyun; Li, Yi; Zhou, Yanyan (December 2012). "Bacterial community dynamics during a bloom caused by Akashiwo sanguinea in the Xiamen sea area, China". Harmful Algae. 20: 132–141. doi:10.1016/j.hal.2012.09.002.

akashiwo, sanguinea, species, marine, dinoflagellates, well, known, forming, blooms, that, result, tides, organism, unarmored, naked, therefore, lacks, thick, cellulose, wall, theca, common, other, genera, dinoflagellates, reproduction, phytoplankton, species,. Akashiwo sanguinea is a species of marine dinoflagellates well known for forming blooms that result in red tides 1 The organism is unarmored naked Therefore it lacks a thick cellulose wall the theca common in other genera of dinoflagellates Reproduction of the phytoplankton species is primarily asexual 2 Akashiwo sanguineaScientific classificationDomain Eukaryota unranked SAR unranked AlveolataPhylum DinoflagellataClass DinophyceaeOrder GymnodinialesFamily GymnodiniaceaeGenus AkashiwoSpecies A sanguineaBinomial nameAkashiwo sanguinea K Hirasaka Hansen amp MoestrupRecently recognized as mixotrophic A sanguinea is capable of preying on various organisms 3 For example A sanguinea is found to be capable of ingesting the cyanobacterium Synechococcus sp at values comparable to other heterotrophic phytoplankton This suggests implications it may have on the grazing impact of Synechococcus 4 Contents 1 Description 2 Etymology 3 Distribution 4 Behavior and physiology 5 Context and content 6 HAB implications 7 References 7 1 Further readingDescription editDespite its lack of thecal plates a prominent feature helpful in identifying armored flagellates A sanguinea is relatively large and easily recognizable Like most dinoflagellates one flagellum is complex wrapping around the equator of the cell in a groove The other flagellum extends out from the cell to help aid its movement through the water 5 A sanguinea s most prominent features are the lack of a nuclear envelope chamber and the apical groove s large clockwise path when viewed from the front of the cell These features along with observations and data from LSU rDNA sequencing recently helped declare a new genus for this species Hansen amp Moestrup 6 Etymology editThe genus name akashiwo is Japanese for red tide 6 Distribution editAkashiwo sanguinea covers a broad range of distributions 7 Frequent blooms exist off the coast of Florida and Southern California 5 8 Blooms dominated by this species have also been observed in Narragansett Bay Rhode Island 9 Behavior and physiology editAkashiwo sanguinea exhibits a diurnal vertical migration pattern observed to move toward the sun in field experiments even before the start of the light cycle In laboratory settings the migration is light dependent but the direction of movement is not solely explained by positive phototaxis It has also been shown to swim across large gradients in temperature However more study is needed to determine the organisms migratory behavior 10 Akashiwo sanguinea responds to certain changes in the water column by forming subsurface chlorophyll maximum layers in the marine environment 11 A study off of Southern California s coast observed a subsurface layer when nitrate was limiting to the organism 10 A sangiunea s subsurface chlorophyll maximum layer has contributed to the success of larval anchovy growth on California s coastline The larva have been observed to ingest this organism and not other species such as Chaetoceros spp and Thalassiosira spp suggesting a preference for A sanguinea over other dinoflagellates 8 Context and content editSynonyms Gymnodinium splendens Lebour Gymnodinium sanguineum Hirasaka Gymnodinium nelsoni Martin The names listed above were used during prior research on the organism The genus is now redefined into four new genera Gymnodinium was one of many dinoflagellate genera declared when taxonomic nomenclature was limited to features only visible with the light microscope In 2000 Hansen and Moestrup analyzed ultrastructural details of the organism using large subunit LSU rDNA sequencing Aided by this new technology the scientists were able to declare variations in the path of the apical groove of the organism found on the flagellar apparatus Since the apical groove varies among species the scientists used it to indicate differences between the unarmored flagellates Akashiwo was one of four new genera that was redefined using the analysis 1 HAB implications editAkashiwo sanguinea has been correlated to harmful algal blooms HABs but more study is needed to make sense of the blooms The protist can produce mycosporine like amino acids MAAs which are water soluble surfactants A red tide caused by A sanguinea was coincident with widespread seabird mortality across fourteen different species of birds in November December 2007 in Northeastern Monterey Bay California Plankton samples showed A sanguinea as the dominant flagellate in the bloom Affected birds accumulated a proteinaceous material on their feathers causing a loss in the natural water repellency However no toxins such as domoic acid saxitoxin or brevetoxin was detected in the water It was the first documented case of its tide causing harm to birds 7 In 2009 a huge foam event blamed on Akashiwo sanguinea killed vast quantities of sea birds from the northern Oregon coast to the tip of the Olympic Peninsula in Washington state 12 The species blooms have also been linked to coral bleaching More research is needed before predictions of HAB events that may be linked with this species 7 References edit a b Hargraves P E June 14 2011 Akashiwo sanguinea Protists of the Indian River Lagoon Smithsonian Institution Retrieved October 27 2011 Lalli Carol M Parsons Timothy R 1993 Biological Oceanography an Introduction 2nd ed Elsevier Butterworth Heinemann pp 42 45 ISBN 0 7506 3384 0 Bockstahler K R Coats D W 1993 Grazing of the mixotrophic dinoflagellate Gymnodinium sanguineum on ciliate populations of Chesapeake Bay Marine Biology 116 3 477 487 Bibcode 1993MarBi 116 477B doi 10 1007 BF00350065 S2CID 84468485 Jeong Hae Jin Park Jae Yeon Nho Jae Hoon Park Myung Ok Ha Jeong Hyun Seong Kyeong Ah Jeng Chang Seong Chi Nam Lee Kwang Ya Yih Won Ho 2005 Feeding by red tide dinoflagellates on the cyanobacterium Synechococcus Aquatic Microbial Ecology 41 2 131 143 doi 10 3354 ame041131 a b Miller Charles B 2004 Biological Oceanography Blackwell pp 26 32 ISBN 0 632 05536 7 a b Daugbjerg Niels Hansen Gert Larsen Jacob Moestrup Ojvind 2000 Phylogeny of some of the major genera of dinoflagellates based on ultrastructure and partial LSU rDNA sequence data including the erection of three new genera of unarmoured dinoflagellates PDF Phycologia 39 4 302 317 Bibcode 2000Phyco 39 302D doi 10 2216 i0031 8884 39 4 302 1 S2CID 86456565 a b c Jessup David A Miller Melissa A Ryan John P Nevins Hannah M Kerkering Heather A Mekebri Abdou Crane David B Johnson Tyler A Kudela Raphael M 2009 Mass stranding of marine birds caused by a surfactant producing red tide PLoS ONE 4 2 e4550 Bibcode 2009PLoSO 4 4550J doi 10 1371 journal pone 0004550 PMC 2641015 PMID 19234604 a b Lasker Reuben 1975 Field criteria for survival of anchovy larvae the relation between inshore chlorophyll maximum layers and successful first feeding PDF Fishery Bulletin 73 3 453 462 Smayda Theodore J 1957 Phytoplankton studies in Lower Narragansett Bay Limnology and Oceanography 2 4 342 359 Bibcode 1957LimOc 2 342S doi 10 1002 lno 1957 2 4 0342 JSTOR 2832835 a b Cullen J J Horrigan S G 1981 Effects of nitrate on the diurnal vertical migration carbon to nitrogen ratio and the photosynthetic capacity of the dinoflagellate Gymnodinium splendens Marine Biology 62 2 3 81 89 Bibcode 1981MarBi 62 81C doi 10 1007 BF00388169 S2CID 82258412 Reid F M H Stewart E Eppley R W Goodman D 1978 Spatial distribution of phytoplankton species in chlorophyll maximum layers off Southern California Limnology and Oceanography 23 2 219 226 Bibcode 1978LimOc 23 219R doi 10 4319 lo 1978 23 2 0219 JSTOR 2835393 Terry Lynne October 22 2009 Foam from ocean algae bloom killing thousands of birds OregonLive Retrieved 2017 03 03 Further reading edit Badylak Susan Philips Edward Mathews Loren Kelley Karen September 2014 Akashiwo sanguinea Dinophyceae extruding mucous from pores on the cell surface Algae 29 3 197 201 doi 10 4490 algae 2014 29 3 197 Matsubara Tadashi Nagasoe Sou Yamasaki Yasuhiro Shikata Tomoyuki Shimasaki Yohei Oshima Yuji Honjo Tsuneo 16 April 2007 Effects of temperature salinity and irradiance on the growth of the dinoflagellate Akashiwo sanguinea Journal of Experimental Marine Biology and Ecology 342 2 226 230 doi 10 1016 j jembe 2006 09 013 Yang Caiyun Li Yi Zhou Yanyan December 2012 Bacterial community dynamics during a bloom caused by Akashiwo sanguinea in the Xiamen sea area China Harmful Algae 20 132 141 doi 10 1016 j hal 2012 09 002 Retrieved from https en wikipedia org w index php title Akashiwo sanguinea amp oldid 1213433422, wikipedia, wiki, book, books, library,

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