Parmales

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Parmales
Pentalamina corona.jpg
Pentalamina corona, scale bar = 1 μm
Scientific classification
Domain:
(unranked):
SAR
Superphylum:
Phylum:
Class:
Order:
Parmales
Family

The Parmales are an order of marine microalgae within the Bolidophyceae class. They are found worldwide and characterized by a cell wall composed of 5-8 interlocking silica plates with distinct forms. [1] They were initially thought to be loricate choanoflagellates [2] but were shown to be a separate phyla entirely upon the discovery of chloroplasts, placing it among the photosynthetic stramenopiles. [3]

Contents

The group is divided into two distinct morphologies- the naked and mobile bolidophyte form and the non-mobile and silica-plate covered parmalean form. The bolidophyte form lacks silica plates and has two unequal flagella inserted ventrally, vaguely reminiscent of Chlamydomonas . [3] The parmalean form is similar to the diatoms as it is coated in silicate plates. These silicate plates are used to divide the Parmales into separate genera based upon the number and location of the siliceous plates. Unlike the diatoms, the Parmales are able to grow in silica-limiting environments because the synthesis of the silica plates is not directly connected to growth or reproduction. [4]

The Parmales actively feed on nanophytoplankton such as Prochlorococcus and Synechococcus and are one of the most important grazers on these cyanobacteria in oligotrophic waters. [5] This heterotrophy serves as an important step in the foundation of the microbial loop.

Etymology

The name comes from the Latin word for a small, round shield carried by infantry and cavalry. It refers to the silica plates that the Parmales are covered by. [6]

Distribution

Parmales can be found in all the major world oceans. However, their density is consistently low (10-100 cells/ml) and they represent at most 3% of the phytoplankton present. [3] They are most abundant in polar and subarctic waters but are also capable of growing in tropical and subtropical locations. [7] [8]

Within the water column, Parmales are found in the upper, euphotic portion where they remain without difficulty due to their small size. It is currently unknown whether they have mechanisms to regulate buoyancy. [9]

Parmales have also been found as fossils in the Middle America Trench in sediments from the mid to late Quaternary period. [10] Older fossils have been reported but are unverifiable. [11]

Taxonomy

Although initially placed within the Chrysophyceae, Parmales were shown in 2016 to belong to the Bolidophyceae [6] [3]

Related Research Articles

<span class="mw-page-title-main">Diatom</span> Class of microalgae, found in the oceans, waterways and soils of the world

A diatom is any member of a large group comprising several genera of algae, specifically microalgae, found in the oceans, waterways and soils of the world. Living diatoms make up a significant portion of the Earth's biomass: they generate about 20 to 50 percent of the oxygen produced on the planet each year, take in over 6.7 billion tonnes of silicon each year from the waters in which they live, and constitute nearly half of the organic material found in the oceans. The shells of dead diatoms can reach as much as a half-mile deep on the ocean floor, and the entire Amazon basin is fertilized annually by 27 million tons of diatom shell dust transported by transatlantic winds from the African Sahara, much of it from the Bodélé Depression, which was once made up of a system of fresh-water lakes.

<span class="mw-page-title-main">Chert</span> Hard, fine-grained sedimentary rock composed of cryptocrystalline silica

Chert is a hard, fine-grained sedimentary rock composed of microcrystalline or cryptocrystalline quartz, the mineral form of silicon dioxide (SiO2). Chert is characteristically of biological origin, but may also occur inorganically as a chemical precipitate or a diagenetic replacement, as in petrified wood.

<span class="mw-page-title-main">Choanoflagellate</span> Group of eukaryotes considered the closest living relatives of animals

The choanoflagellates are a group of free-living unicellular and colonial flagellate eukaryotes considered to be the closest living relatives of the animals. Choanoflagellates are collared flagellates, having a funnel shaped collar of interconnected microvilli at the base of a flagellum. Choanoflagellates are capable of both asexual and sexual reproduction. They have a distinctive cell morphology characterized by an ovoid or spherical cell body 3–10 µm in diameter with a single apical flagellum surrounded by a collar of 30–40 microvilli. Movement of the flagellum creates water currents that can propel free-swimming choanoflagellates through the water column and trap bacteria and detritus against the collar of microvilli, where these foodstuffs are engulfed. This feeding provides a critical link within the global carbon cycle, linking trophic levels. In addition to their critical ecological roles, choanoflagellates are of particular interest to evolutionary biologists studying the origins of multicellularity in animals. As the closest living relatives of animals, choanoflagellates serve as a useful model for reconstructions of the last unicellular ancestor of animals.

<span class="mw-page-title-main">Golden algae</span> Class of algae

The Chrysophyceae, usually called chrysophytes, chrysomonads, golden-brown algae or golden algae, are a large group of algae, found mostly in freshwater. Golden algae is also commonly used to refer to a single species, Prymnesium parvum, which causes fish kills.

<span class="mw-page-title-main">Diatomaceous earth</span> Soft, siliceous sedimentary rock

Diatomaceous earth, diatomite, celite or kieselgur/kieselguhr is a naturally occurring, soft, siliceous sedimentary rock that can be crumbled into a fine white to off-white powder. It has a particle size ranging from more than 3 mm to less than 1 μm, but typically 10 to 200 μm. Depending on the granularity, this powder can have an abrasive feel, similar to pumice powder, and has a low density as a result of its high porosity. The typical chemical composition of oven-dried diatomaceous earth is 80–90% silica, with 2–4% alumina, and 0.5–2% iron oxide.

<span class="mw-page-title-main">Biogenic silica</span> Type of biogenic mineral

Biogenic silica (bSi), also referred to as opal, biogenic opal, or amorphous opaline silica, forms one of the most widespread biogenic minerals. For example, microscopic particles of silica called phytoliths can be found in grasses and other plants.

<span class="mw-page-title-main">Siliceous sponge</span> Clade of sponges

The siliceous sponges form a major group of the phylum Porifera, consisting of classes Demospongiae and Hexactinellida. They are characterized by spicules made out of silicon dioxide, unlike calcareous sponges.

<span class="mw-page-title-main">Marine sediment</span>

Marine sediment, or ocean sediment, or seafloor sediment, are deposits of insoluble particles that have accumulated on the seafloor. These particles either have their origins in soil and rocks and have been transported from the land to the sea, mainly by rivers but also by dust carried by wind and by the flow of glaciers into the sea, or they are biogenic deposits from marine organisms or from chemical precipitation in seawater, as well as from underwater volcanoes and meteorite debris.

<span class="mw-page-title-main">Bolidophyceae</span> Class of algae

Bolidophyceae is a class of photosynthetic heterokont picophytoplankton, and consist of less than 20 known species. They are distinguished by the angle of flagellar insertion and swimming patterns as well as recent molecular analyses. Bolidophyceae is the sister taxon to the diatoms (Bacillariophyceae). They lack the characteristic theca of the diatoms, and have been proposed as an intermediate group between the diatoms and all other heterokonts.

<span class="mw-page-title-main">Siliceous ooze</span> Biogenic pelagic sediment located on the deep ocean floor

Siliceous ooze is a type of biogenic pelagic sediment located on the deep ocean floor. Siliceous oozes are the least common of the deep sea sediments, and make up approximately 15% of the ocean floor. Oozes are defined as sediments which contain at least 30% skeletal remains of pelagic microorganisms. Siliceous oozes are largely composed of the silica based skeletons of microscopic marine organisms such as diatoms and radiolarians. Other components of siliceous oozes near continental margins may include terrestrially derived silica particles and sponge spicules. Siliceous oozes are composed of skeletons made from opal silica SiO2·nH2O, as opposed to calcareous oozes, which are made from skeletons of calcium carbonate (CaCO3·nH2O) organisms (i.e. coccolithophores). Silica (Si) is a bioessential element and is efficiently recycled in the marine environment through the silica cycle. Distance from land masses, water depth and ocean fertility are all factors that affect the opal silica content in seawater and the presence of siliceous oozes.

<span class="mw-page-title-main">Acanthoecidae</span> Family of protists

Acanthoecidae is a family of choanoflagellates. Its subgroups Diaphanoeca and Stephanoeca bear lorica composed of silica which possibly originate from diatoms via Horizontal gene transfer.

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

Triparma is a genus of unicellular algae in the family Triparmaceae in the order Parmales. They form siliceous plates on the cell surface that aid in identification. Triparma is distinguished by its possession of three shield plates, three triradiate girdle plates, a triradiate girdle plate with notched ends, and a small ventral plate. It was first described by Booth & Marchant in 1987 and the holotype is Triparma columacea.

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

Tetraparma is a genus of unicellular algae in the family Triparmaceae in the order Parmales. They form siliceous plates on the cell surface that aid in identification. Tetraparma is distinguished by its possession of three shield plates that may have everted rims, three triradiate girdle plates, a triradiate dorsal plate with notched ends, and a large ventral plate. It was first described by Booth & Marchant in 1987 and the holotype is Triparma columacea.

<span class="mw-page-title-main">Silica cycle</span> Biogeochemical cycle

The silica cycle is the biogeochemical cycle in which biogenic silica is transported between the Earth's systems. Silicon is considered a bioessential element and is one of the most abundant elements on Earth. The silica cycle has significant overlap with the carbon cycle and plays an important role in the sequestration of carbon through continental weathering, biogenic export and burial as oozes on geologic timescales.

<span class="mw-page-title-main">Protist shell</span> Protective shell of a type of eukaryotic organism

Many protists have protective shells or tests, usually made from silica (glass) or calcium carbonate (chalk). Protists are a diverse group of eukaryote organisms that are not plants, animals, or fungi. They are typically microscopic unicellular organisms that live in water or moist environments.

<i>Asterionella formosa</i> Species of single-celled organism

Asterionella formosa is a species of diatom belonging to the family Tabellariaceae.

<span class="mw-page-title-main">Silicification</span> Geological petrification process

In geology, silicification is a petrification process in which silica-rich fluids seep into the voids of Earth materials, e.g., rocks, wood, bones, shells, and replace the original materials with silica (SiO2). Silica is a naturally existing and abundant compound found in organic and inorganic materials, including Earth's crust and mantle. There are a variety of silicification mechanisms. In silicification of wood, silica permeates into and occupies cracks and voids in wood such as vessels and cell walls. The original organic matter is retained throughout the process and will gradually decay through time. In the silicification of carbonates, silica replaces carbonates by the same volume. Replacement is accomplished through the dissolution of original rock minerals and the precipitation of silica. This leads to a removal of original materials out of the system. Depending on the structures and composition of the original rock, silica might replace only specific mineral components of the rock. Silicic acid (H4SiO4) in the silica-enriched fluids forms lenticular, nodular, fibrous, or aggregated quartz, opal, or chalcedony that grows within the rock. Silicification happens when rocks or organic materials are in contact with silica-rich surface water, buried under sediments and susceptible to groundwater flow, or buried under volcanic ashes. Silicification is often associated with hydrothermal processes. Temperature for silicification ranges in various conditions: in burial or surface water conditions, temperature for silicification can be around 25°−50°; whereas temperatures for siliceous fluid inclusions can be up to 150°−190°. Silicification could occur during a syn-depositional or a post-depositional stage, commonly along layers marking changes in sedimentation such as unconformities or bedding planes.

Diaphanoeca grandis is a species of choanoflagellate in the family Acanthoecidae which is the type species of the genus Diaphanoeca. It is a unicellular micro-heterotroph with a large protective lorica that is found beneath sea ice in a wide distribution. The lorica is composed of silica and possibly originates from diatoms via Horizontal gene transfer.

Biogenous ooze is marine sediment that accumulates on the seafloor and is a byproduct of the death and sink of the skeletal remains of marine organisms.

References

  1. Konno, Susumu; Jordan, Richard W (2012). Parmales. doi:10.1002/9780470015902.a0023691. ISBN   978-0470016176.{{cite book}}: |journal= ignored (help)
  2. Silver, M. W.; Mitchell, J. G.; Ringo, D. L. (1980). "Siliceous nanoplankton. II. Newly discovered cysts and abundant choanoflagellates from the Weddell Sea, Antarctica". Marine Biology. 58 (3): 211–217. doi:10.1007/BF00391878. S2CID   84302442.
  3. 1 2 3 4 Ichinomiya, Mutsuo; dos Santos, Adriana Lopes; Gourvil, Priscillia; Yoshikawa, Shinya; Kamiya, Mitsunobu; Ohki, Kaori; Audic, Stéphane; de Vargas, Colomban; Noël, Mary-Hélène; Vaulot, Daniel; Kuwata, Akira (22 March 2016). "Diversity and oceanic distribution of the Parmales (Bolidophyceae), a picoplanktonic group closely related to diatoms". The ISME Journal. 10 (10): 2419–2434. doi:10.1038/ismej.2016.38. PMC   5030691 . PMID   27003244.
  4. Yamada, Kazumasa; Yoshikawa, Shinya; Ichinomiya, Mutsuo; Kuwata, Akira; Kamiya, Mitsunobu; Ohki, Kaori; Lovejoy, Connie (23 July 2014). "Effects of Silicon-Limitation on Growth and Morphology of Triparma laevis NIES-2565 (Parmales, Heterokontophyta)". PLOS ONE. 9 (7): e103289. Bibcode:2014PLoSO...9j3289Y. doi: 10.1371/journal.pone.0103289 . PMC   4108440 . PMID   25054645.
  5. Frias-Lopez, Jorge; Thompson, Anne; Waldbauer, Jacob; Chisholm, Sallie W. (February 2009). "Use of stable isotope-labelled cells to identify active grazers of picocyanobacteria in ocean surface waters". Environmental Microbiology. 11 (2): 512–525. doi:10.1111/j.1462-2920.2008.01793.x. PMC   2702499 . PMID   19196281.
  6. 1 2 Booth, Beatrice C.; Marchant, Harvey J. (June 1987). "Parmales, A New Order of Marine Chrysophytes, with Descriptions of Three New Genera and Seven New Species". Journal of Phycology. 23 (s2): 245–260. doi:10.1111/j.1529-8817.1987.tb04132.x. S2CID   84582735.
  7. Fujita, Ryohei; Jordan, Richard W. (September 2017). "Tropical Parmales (Bolidophyceae) assemblages from the Sulu Sea and South China Sea, including the description of five new taxa". Phycologia. 56 (5): 499–509. doi:10.2216/16-128.1. S2CID   90190189.
  8. Ichinomiya, M; Kuwata, A (6 July 2015). "Seasonal variation in abundance and species composition of the Parmales community in the Oyashio region, western North Pacific". Aquatic Microbial Ecology. 75 (3): 207–223. doi: 10.3354/ame01756 .
  9. Kuwata, A.; Jewson, D.H. (2015). "Ecology and evolution of marine diatoms and Parmales". In Ohtsuka, S.; Suzaki, T.; Horiguchi, T.; Suzuki, N; Not, F. (eds.). Marine Protists, Diversity and dynamics. Tokyo: Springer. pp. 251–275.
  10. Stradner, H.; Allram, F. (1982). "Notes on an enigmatic siliceous cyst, Middle America Trench, Deep Sea Drilling Project Hole 490". Deep Sea Drilling. Initial Reports of the Deep Sea Drilling Project. 66 (4): 641–642. doi: 10.2973/dsdp.proc.66.124.1982 .
  11. Konno, S.; Ohira, R.; Komuro, C.; Harada, N.; Jordan, R (2007). "Six new taxa of subarctic Parmales (Chrysophyceae)" (PDF). J. Nannoplankton Res. 29 (2): 108–128. doi:10.58998/jnr2153. S2CID   259979898. Archived from the original (PDF) on 13 April 2018. Retrieved 12 April 2018.
  12. M.D. Guiry (2016), AlgaeBase, World-wide electronic publication, National University of Ireland, Galway, retrieved 25 October 2016