Cochlodinium polykrikoides

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Cochlodinium polykrikoides
C. polykrikoides bloom.jpg
A Cochlodinium polykrikoides bloom in Narragansett Bay, RI.
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Alveolata
Phylum: Myzozoa
Superclass: Dinoflagellata
Class: Dinophyceae
Order: Gymnodiniales
Family: Gymnodiniaceae
Genus: Cochlodinium
Species:
C. polykrikoides
Binomial name
Cochlodinium polykrikoides

Cochlodinium polykrikoides (or Margalefidinium polykrikoides) is a species of red tide producing marine dinoflagellates known for causing fish kills around the world, and well known for fish kills in marine waters of Southeast Asia. [2] [3] C. polykrikoides has a wide geographic range, including North America, Central America, Western India, Southwestern Europe and Eastern Asia. [4] Single cells of this species are ovoidal in shape, 30-50μm in length and 25-30μm in width. [5]

Contents

Cochlodinium polykrikoides is a highly motile organism. They are generally found in aggregations of 4 or 8 cell zooids. Chain length is known to be affected by the presence of grazers and the inclusion of vitamins B1, B7 and B12. [6] This species is also capable of mixotrophy, which makes them extremely persistent during a large algal bloom. [7] C. polykrikoides exhibits diel vertical migration. [8]

Cochlodinium is thought to have a cyst-type overwintering stage in their life cycle. This process allows C. polykrikoides to produce a specialized cell that is non-motile. These cells aggregate and rest in certain basins until conditions allow for reproduction and colonies to form. [9]

Optimal growth conditions

Cochlodinium polykrikoides is a euryhaline species, capable of surviving a wide range of salinities. Growth experiments have shown that C. polykrikoides can have greater than 0.3 divisions day−1 in optimal growth conditions (25 °C, 34ppt). [10] The growth range C. polykrikoides is 15 °C-30 °C, 20-36ppt and >30μmol m−2 s−1 irradiance. [10] There has been no observed photo-inhibition for C. polykrikoides under high irradiance.

Toxicity

Cochlodinium polykrikoides is a species that can produce allelopathic chemicals. [11] These chemicals inhibit the growth of other phytoplankton taxa in the water column. The production of such toxins can play important roles in the formation of Harmful Algal Blooms. C. polykrikoides can also generate reactive oxygen species [12] which are lethal to both pelagic fish and shellfish even in low concentrations.

Massive blooms

In late 2008 and early 2009 (November–February) there was a massive bloom of Cochlodinium polykrikoides in the Sea of Oman, off the coast of Oman in the Persian Sea. [13] It was notable for being based on Cochlodinium polykrikoides rather than the Noctiluca scintillans (Noctiluca miliaris) that had been more usual in the immediately previous years. [14] [15] The bloom resulted in massive dying off of fish, damage to coral reefs, and interference with desalinization plants. [15]

Conditions for a bloom

  1. Sea Surface Temperature (SST)- SST has been shown to be a huge factor in the growth of C. polykrikoides and thus determining when blooms form. [16] Lab studies have shown that C. polykrikoides have the most significant growth between 25.0˚C and 26.0˚C. [17] [18]
  2. Photosynthetically Available Radiation (PAR)- As for almost all planktonic species, there needs to be enough light for these phytoplankton to photosynthesize. Studies have proven that C. polykrikoides have higher growth rates when solar insolation is increased. [7]
  3. Favorable Transport- Many are unsure of the source of where C. polykrikoides are generally found, however, currents play an important role when transporting these toxic phytoplankton to favorable areas for a bloom to spawn. [16]
  4. Upwelling - The nutrient-rich waters that are brought to the photic layer by upwelling hold nutrients (nitrogen compounds, phosphorus compounds, etc.) that are essential in photosynthesis and cell growth. An appropriate wind is needed to cause this upwelling and while also ensuring temperature and transport are also favorable for C. polykrikoides blooms. [16]

As climate change continues to affect the oceans, it is predicted that harmful algal blooms (such as red tides caused by Cochlodinium polykrikoides) will be more frequent in the upcoming years. [18]

Related Research Articles

<span class="mw-page-title-main">Algal bloom</span> Spread of planktonic algae in water

An algal bloom or algae bloom is a rapid increase or accumulation in the population of algae in freshwater or marine water systems. It is often recognized by the discoloration in the water from the algae's pigments. The term algae encompasses many types of aquatic photosynthetic organisms, both macroscopic multicellular organisms like seaweed and microscopic unicellular organisms like cyanobacteria. Algal bloom commonly refers to the rapid growth of microscopic unicellular algae, not macroscopic algae. An example of a macroscopic algal bloom is a kelp forest.

<span class="mw-page-title-main">Dinoflagellate</span> Unicellular algae with two flagella

The dinoflagellates are a monophyletic group of single-celled eukaryotes constituting the phylum Dinoflagellata and are usually considered protists. Dinoflagellates are mostly marine plankton, but they are also common in freshwater habitats. Their populations vary with sea surface temperature, salinity, and depth. Many dinoflagellates are photosynthetic, but a large fraction of these are in fact mixotrophic, combining photosynthesis with ingestion of prey.

<span class="mw-page-title-main">Thin layers (oceanography)</span> Congregations of plankton

Thin layers are concentrated aggregations of phytoplankton and zooplankton in coastal and offshore waters that are vertically compressed to thicknesses ranging from several centimeters up to a few meters and are horizontally extensive, sometimes for kilometers. Generally, thin layers have three basic criteria: 1) they must be horizontally and temporally persistent; 2) they must not exceed a critical threshold of vertical thickness; and 3) they must exceed a critical threshold of maximum concentration. The precise values for critical thresholds of thin layers has been debated for a long time due to the vast diversity of plankton, instrumentation, and environmental conditions. Thin layers have distinct biological, chemical, optical, and acoustical signatures which are difficult to measure with traditional sampling techniques such as nets and bottles. However, there has been a surge in studies of thin layers within the past two decades due to major advances in technology and instrumentation. Phytoplankton are often measured by optical instruments that can detect fluorescence such as LIDAR, and zooplankton are often measured by acoustic instruments that can detect acoustic backscattering such as ABS. These extraordinary concentrations of plankton have important implications for many aspects of marine ecology, as well as for ocean optics and acoustics. Zooplankton thin layers are often found slightly under phytoplankton layers because many feed on them. Thin layers occur in a wide variety of ocean environments, including estuaries, coastal shelves, fjords, bays, and the open ocean, and they are often associated with some form of vertical structure in the water column, such as pycnoclines, and in zones of reduced flow.

<i>Karenia brevis</i> Species of dinoflagellate

Karenia brevis is a microscopic, single-celled, photosynthetic organism in the genus Karenia. It is a marine dinoflagellate commonly found in the waters of the Gulf of Mexico. It is the organism responsible for the "Florida red tides" that affect the Gulf coasts of Florida and Texas in the U.S., and nearby coasts of Mexico. K. brevis has been known to travel great lengths around the Florida peninsula and as far north as the Carolinas.

<span class="mw-page-title-main">Predatory dinoflagellate</span>

Predatory dinoflagellates are predatory heterotrophic or mixotrophic alveolates that derive some or most of their nutrients from digesting other organisms. About one half of dinoflagellates lack photosynthetic pigments and specialize in consuming other eukaryotic cells, and even photosynthetic forms are often predatory.

Alexandrium fundyense is a species of dinoflagellates. It produces toxins that induce paralytic shellfish poisoning (PSP), and is a common cause of red tide. A. fundyense regularly forms massive blooms along the northeastern coasts of the United States and Canada, resulting in enormous economic losses and public health concerns.

<i>Karenia</i> (dinoflagellate) Genus of single-celled organisms

Karenia is a genus that consists of unicellular, photosynthetic, planktonic organisms found in marine environments. The genus currently consists of 12 described species. They are best known for their dense toxic algal blooms and red tides that cause considerable ecological and economical damage; some Karenia species cause severe animal mortality. One species, Karenia brevis, is known to cause respiratory distress and neurotoxic shellfish poisoning (NSP) in humans.

<span class="mw-page-title-main">Gymnodiniales</span> Order of single-celled organisms

The Gymnodiniales are an order of dinoflagellates, of the class Dinophyceae. Members of the order are known as gymnodinioid or gymnodinoid. They are athecate, or lacking an armored exterior, and as a result are relatively difficult to study because specimens are easily damaged. Many species are part of the marine plankton and are of interest primarily due to being found in algal blooms. As a group the gymnodinioids have been described as "likely one of the least known groups of the open ocean phytoplankton."

<i>Gonyaulax</i> Genus of single-celled organisms

Gonyaulax is a genus of dinoflagellates with the type species Gonyaulax spinifera Diesing. Gonyaulax belongs to red dinoflagellates and commonly causes red tides. It can produce yesotoxins: for example, strains of Gonyaulax spinifera from New Zealand are yessotoxin producers.

<i>Akashiwo sanguinea</i> Species of single-celled organism

Akashiwo sanguinea is a species of marine dinoflagellates well known for forming blooms that result in red tides. 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.

All living cells produce reactive oxygen species (ROS) as a byproduct of metabolism. ROS are reduced oxygen intermediates that include the superoxide radical (O2) and the hydroxyl radical (OH•), as well as the non-radical species hydrogen peroxide (H2O2). These ROS are important in the normal functioning of cells, playing a role in signal transduction and the expression of transcription factors. However, when present in excess, ROS can cause damage to proteins, lipids and DNA by reacting with these biomolecules to modify or destroy their intended function. As an example, the occurrence of ROS have been linked to the aging process in humans, as well as several other diseases including Alzheimer's, rheumatoid arthritis, Parkinson's, and some cancers. Their potential for damage also makes reactive oxygen species useful in direct protection from invading pathogens, as a defense response to physical injury, and as a mechanism for stopping the spread of bacteria and viruses by inducing programmed cell death.

<i>Alexandrium catenella</i> Species of single-celled organism

Alexandrium catenella is a species of dinoflagellates. It is among the group of Alexandrium species that produce toxins that cause paralytic shellfish poisoning, and is a cause of red tide. Alexandrium catenella is observed in cold, coastal waters, generally at temperate latitudes. These organisms have been found in the west coast of North America, Japan, Australia, and parts of South Africa.

<span class="mw-page-title-main">Polykrikaceae</span> Family of single-celled organisms

The Polykrikaceae are a family of athecate dinoflagellates of the order Gymnodiniales. Members of the family are known as polykrikoids. The family contains two genera: Polykrikos and Pheopolykrikos.

<i>Gambierdiscus</i> Genus of protists

Gambierdiscus is a genus of marine dinoflagellates that produce ciguatoxins, a type of toxin that causes the foodborne illness known as ciguatera. They are usually epiphytic on macroalgae growing on coral reefs.

<span class="mw-page-title-main">Mixotrophic dinoflagellate</span> Plankton

Dinoflagellates are eukaryotic plankton, existing in marine and freshwater environments. Previously, dinoflagellates had been grouped into two categories, phagotrophs and phototrophs. Mixotrophs, however include a combination of phagotrophy and phototrophy. Mixotrophic dinoflagellates are a sub-type of planktonic dinoflagellates and are part of the phylum Dinoflagellata. They are flagellated eukaryotes that combine photoautotrophy when light is available, and heterotrophy via phagocytosis. Dinoflagellates are one of the most diverse and numerous species of phytoplankton, second to diatoms.

<i>Polykrikos</i> Genus of single-celled organisms

Polykrikos is one of the genera of family Polykrikaceae that includes athecate pseudocolony-forming dinoflagellates. Polykrikos are characterized by a sophisticated ballistic apparatus, named the nematocyst-taeniocyst complex, which allows species to prey on a variety of organisms. Polykrikos have been found to regulate algal blooms as they feed on toxic dinoflagellates. However, there is also some data available on Polykrikos being toxic to fish.

Aureoumbra lagunensis is a unicellular planktonic marine microalga that belongs in the genus Aureoumbra under the class Pelagophyceae. It is similar in morphology and pigments to Aureococcus anophagefferens and Pelagococcus subviridis. The cell shape is spherical to subspherical and is 2.5 to 5.0 μm in diameter. It is golden-coloured and is encapsulated with extracellular polysaccharide layers and has a single chloroplast structure with pigments.

<i>Cochlodinium</i> Genus of protists

Cochlodinium is a genus of dinoflagellates belonging to the family Gymnodiniaceae. Over the past two decades, harmful algea blooms (HABs) caused by Cochlodinium had occurred more often and expanded from Southeast Asia to regions such as the rest of Asia, North America and Europe.

Ana María Gayoso was an Argentine marine biologist, a specialist in study of marine phytoplankton, best known for being the first scientist to describe phytoplankton in the Bahía Blanca Estuary, and to initiate the sustained long-term oceanographic dataset in this ecosystem. She made significant contributions to the understanding of harmful algal blooms caused by toxic dinoflagellate species in the Patagonian gulfs, and was the first scientist to describe high abundances of the coccolithophore Emiliania huxleyi in the Argentine Sea, a key component in the primary productivity along the Patagonian Shelf Break front in the SW South Atlantic. She started the most extensive (1978-present) long-term database of phytoplankton and physico-chemical variables in South America, in a fixed monitoring site in the Bahía Blanca Estuary. She died on 28 December 2004 in Puerto Madryn.

<i>Karlodinium veneficum</i> Species of single-celled organism

Karlodinium veneficum is a species of dinoflagellates belonging to the family Kareniaceae. This species is predominantly inhabiting aquatic environments, particularly in temperate coastal regions.

References

  1. Guiry, M .D. & G. M. Guiry. 2013. Cochlodinium polykrikoides. AlgaeBase. World-wide electronic publication, National University of Ireland, Galway. Accessed 10 June 2013.
  2. Kim, Chang Sook; Sam Geun Lee; Chang Kyu Lee; Hak Gyoon Kim; Jin Jung (1999). "Reactive oxygen species as causative agents in the ichthyotoxicity of the red tide dinoflagellate Cochlodinium polykrikoides". Journal of Plankton Research. 21 (11): 2105–2115. doi: 10.1093/plankt/21.11.2105 .
  3. Gobler, Christopher J.; Dianna L. Berry; O. Roger Anderson; Amanda Burson; Florian Koch; Brooke S. Rodgers; Lindsay K. Moore; Jennifer A. Goleski; Bassem Allam; Paul Bowser; Yingzhong Tang; Robert Nuzzi (2008). "Characterization, dynamics, and ecological impacts of harmful Cochlodinium polykrikoides blooms on eastern Long Island, NY, USA". Harmful Algae. 7 (3): 293–307. doi:10.1016/j.hal.2007.12.006.
  4. Kudela, Raphael M.; Ryan, John P.; Blakely, Melissa D.; Lane, Jenny Q.; Peterson, Tawnya D. (2008-04-01). "Linking the physiology and ecology of Cochlodinium to better understand harmful algal bloom events: A comparative approach". Harmful Algae. Recent Progress on the Research and Management of Cochlodinium Blooms. 7 (3): 278–292. doi:10.1016/j.hal.2007.12.016. ISSN   1568-9883.
  5. Matsuoka, Kazumi; Iwataki, Mitsunori; Kawami, Hisae (2008-04-01). "Morphology and taxonomy of chain-forming species of the genus Cochlodinium (Dinophyceae)". Harmful Algae. Recent Progress on the Research and Management of Cochlodinium Blooms. 7 (3): 261–270. doi:10.1016/j.hal.2007.12.002. hdl: 10069/20076 . ISSN   1568-9883. S2CID   84383833.
  6. Jiang, Xiaodong; Lonsdale, Darcy J.; Gobler, Christopher J. (2010). "Grazers and vitamins shape chain formation in a bloom-forming dinoflagellate, Cochlodinium polykrikoides". Oecologia. 164 (2): 455–464. Bibcode:2010Oecol.164..455J. doi:10.1007/s00442-010-1695-0. ISSN   0029-8549. JSTOR   40864701. PMID   20589396. S2CID   20677619.
  7. 1 2 Tomas, Carmelo R.; Smayda, Theodore J. (2008-04-01). "Red tide blooms of Cochlodinium polykrikoides in a coastal cove". Harmful Algae. Recent Progress on the Research and Management of Cochlodinium BloomsWorkshop of Recent Progress on the Research and Management of Cochlodinium Blooms. 7 (3): 308–317. doi:10.1016/j.hal.2007.12.005.
  8. Park, Jong Gyu; Jeong, Min Kyung; Lee, Jin Ae; Cho, Kyung-Je; Kwon, O.-Soeb (2001-05-01). "Diurnal vertical migration of a harmful dinoflagellate, Cochlodinium polykrikoides (Dinophyceae), during a red tide in coastal waters of Namhae Island, Korea". Phycologia. 40 (3): 292–297. Bibcode:2001Phyco..40..292P. doi:10.2216/i0031-8884-40-3-292.1. ISSN   0031-8884. S2CID   85986872.
  9. Kim, Hyeung-Sin; Kim, Seung-Hyun; Jung, Min-Min; Lee, Joon-Baek (2013). "New Record of Dinoflagellates around Jeju Island". Journal of Ecology and Environment. 36 (4): 273–291. Bibcode:2013JEcEn..36..273K. doi: 10.5141/ecoenv.2013.273 .
  10. 1 2 Kim, Dae-Il; Matsuyama, Yukihiko; Nagasoe, Sou; Yamaguchi, Mineo; Yoon, Yang-Ho; Oshima, Yuji; Imada, Nobuyoshi; Honjo, Tsuneo (2004-01-01). "Effects of temperature, salinity and irradiance on the growth of the harmful red tide dinoflagellate Cochlodinium polykrikoides Margalef (Dinophyceae)". Journal of Plankton Research. 26 (1): 61–66. doi: 10.1093/plankt/fbh001 . ISSN   0142-7873.
  11. Tang, Ying Zhong; Gobler, Christopher J. (2010-05-10). "Allelopathic effects of Cochlodinium polykrikoides isolates and blooms from the estuaries of Long Island, New York, on co-occurring phytoplankton". Marine Ecology Progress Series. 406: 19–31. Bibcode:2010MEPS..406...19T. doi: 10.3354/meps08537 . ISSN   0171-8630.
  12. Kim, Chang Sook; Lee, Sam Geun; Lee, Chang Kyu; Kim, Hak Gyoon; Jung, Jin (1999-11-01). "Reactive oxygen species as causative agents in the ichthyotoxicity of the red tide dinoflagellate Cochlodinium polykrikoides". Journal of Plankton Research. 21 (11): 2105–2115. doi: 10.1093/plankt/21.11.2105 . ISSN   0142-7873.
  13. Richlen, M. L.; Morton, S. L.; Jamali, E. A.; Rajian, A.; Anderson, D. M. (2010). "The catastrophic 2008-2009 red tide in the persian Gulf region, with observations on the identification and phyloheny of the fish-killing dinoflagellate Cochlodinium polykrikoides". Harmful Algae. 9 (2): 163–172. doi:10.1016/j.hal.2009.08.013.
  14. Parab, Sushma G.; Matondkar, S. G. Prabhu; Gomes, H. do R.; Goes, J. I. (2006). "Monsoon driven changes in phytoplankton populations in the eastern persian Sea as revealed by microscopy and HPLC pigment analysis". Continental Shelf Research. 26 (20): 2538–2558. doi:10.1016/j.csr.2006.08.004.
  15. 1 2 Al-Azri, Adnan R.; et al. (2014). "Mesoscale and Nutrient Conditions Associated with the Massive 2008 Cochlodinium polykrikoides Bloom in the Sea of Oman/persian Gulf". Estuaries and Coasts. 37 (2): 325–338. doi:10.1007/s12237-013-9693-1. S2CID   54691855.
  16. 1 2 3 Kim, Dae-Won; Jo, Young-Heon; Choi, Jong-Kuk; Choi, Jang-Geun; Bi, Hongsheng (2016-05-01). "Physical processes leading to the development of an anomalously large Cochlodinium polykrikoides bloom in the East sea/Japan sea". Harmful Algae. 55: 250–258. doi:10.1016/j.hal.2016.03.019. PMID   28073539.
  17. "Distributions of water temperature and salinity in the Korea southern coastal water during Cochlodinium polykrikoides blooms". Journal of the Korean Society for Marine Environment & Energy. 12 (4): 235–247. 2009.
  18. 1 2 Griffith, Andrew W.; Gobler, Christopher J. (2016-03-08). "Temperature controls the toxicity of the ichthyotoxic dinoflagellate Cochlodinium polykrikoides". Marine Ecology Progress Series. 545: 63–76. Bibcode:2016MEPS..545...63G. doi:10.3354/meps11590. S2CID   88174679.