Red algae

Red algae, or Rhodophyta (/roʊˈdɒfɪtə/, /ˌroʊdəˈfaɪtə/; from Ancient Greek ῥόδον (rhódon) 'rose', and φυτόν (phutón) 'plant'), are one of the oldest groups of eukaryotic algae.[3] The Rhodophyta comprises one of the largest phyla of algae, containing over 7,000 currently recognized species with taxonomic revisions ongoing.[4] The majority of species (6,793) are found in the Florideophyceae (class), and mostly consist of multicellular, marine algae, including many notable seaweeds.[4][5] Red algae are abundant in marine habitats but relatively rare in freshwaters.[6] Approximately 5% of red algae species occur in freshwater environments, with greater concentrations found in warmer areas.[7] Except for two coastal cave dwelling species in the asexual class Cyanidiophyceae, there are no terrestrial species, which may be due to an evolutionary bottleneck in which the last common ancestor lost about 25% of its core genes and much of its evolutionary plasticity.[8][9]

Red algae
Temporal range:
A-D : Chondrus crispus Stackhouse,
E-F : Mastocarpus stellatus J.Ag.
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
(unranked): Archaeplastida
Division: Rhodophyta
Wettstein, 1922
Clades

The red algae form a distinct group characterized by having eukaryotic cells without flagella and centrioles, chloroplasts that lack external endoplasmic reticulum and contain unstacked (stroma) thylakoids, and use phycobiliproteins as accessory pigments, which give them their red color.[10] But despite their name, red algae can vary greatly in color from bright green, soft pink, resembling brown algae, to shades of red and purple, and may be almost black at greater depths.[11][12] Unlike green algae, red algae store sugars outside the chloroplasts as floridean starch, a type of starch that consists of highly branched amylopectin without amylose,[13] as food reserves outside their plastids. Most red algae are also multicellular, macroscopic, marine, and reproduce sexually. The life history of red algae is typically an alternation of generations that may have three generations rather than two.[14] The coralline algae, which secrete calcium carbonate and play a major role in building coral reefs, belong here. Red algae such as Palmaria palmata (dulse) and Porphyra species (laver/nori/gim) are a traditional part of European and Asian cuisines and are used to make other products such as agar, carrageenans and other food additives.[15]

Evolution
Botryocladia occidentalis scale bar: 2 cm

Chloroplasts probably evolved following an endosymbiotic event between an ancestral, photosynthetic cyanobacterium and an early eukaryotic phagotroph.[16] This event (termed primary endosymbiosis) is at the origin of the red and green algae (including the land plants or Embryophytes which emerged within them)) and the glaucophytes, which together make up the oldest evolutionary lineages of photosynthetic eukaryotes, the Archaeplastida.[17] A secondary endosymbiosis event involving an ancestral red alga and a heterotrophic eukaryote resulted in the evolution and diversification of several other photosynthetic lineages such as Cryptophyta, Haptophyta, Stramenopiles (or Heterokontophyta), and Alveolata.[17] In addition to multicellular brown algae, it is estimated that more than half of all known species of microbial eukaryotes harbor red-alga-derived plastids.[18]

Red algae are divided into the Cyanidiophyceae, a class of unicellular and thermoacidophilic extremophiles found in sulphuric hot springs and other acidic environments,[19] an adaptation partly made possible by horizontal gene transfers from prokaryotes,[20] with about 1% of their genome having this origin,[21] and two sister clades called SCRP (Stylonematophyceae, Compsopogonophyceae, Rhodellophyceae and Porphyridiophyceae) and BF (Bangiophyceae and Florideophyceae), which are found in both marine and freshwater environments. The SCRP clade are microalgae, consisting of both unicellular forms and multicellular microscopic filaments and blades. The BF are macroalgae, seaweed that usually do not grow to more than about 50 cm in length, but a few species can reach lengths of 2 m.[22] Most rhodophytes are marine with a worldwide distribution, and are often found at greater depths compared to other seaweeds. While this was formerly attributed to the presence of pigments (such as phycoerythrin) that would permit red algae to inhabit greater depths than other macroalgae by chromatic adaption, recent evidence calls this into question (e.g. the discovery of green algae at great depth in the Bahamas).[23] Some marine species are found on sandy shores, while most others can be found attached to rocky substrata.[24] Freshwater species account for 5% of red algal diversity, but they also have a worldwide distribution in various habitats;[7] they generally prefer clean, high-flow streams with clear waters and rocky bottoms, but with some exceptions.[25] A few freshwater species are found in black waters with sandy bottoms [26] and even fewer are found in more lentic waters.[27] Both marine and freshwater taxa are represented by free-living macroalgal forms and smaller endo/epiphytic/zoic forms, meaning they live in or on other algae, plants, and animals.[10] In addition, some marine species have adopted a parasitic lifestyle and may be found on closely or more distantly related red algal hosts.[28][29]

Taxonomy
Further information: Wikispecies:Rhodophyta

In the classification system of Adl et al. 2005, the red algae are classified in the Archaeplastida, along with the glaucophytes and the green algae plus land plants (Viridiplantae or Chloroplastida). The authors use a hierarchical arrangement where the clade names do not signify rank; the class name Rhodophyceae is used for the red algae. No subdivisions are given; the authors say, "Traditional subgroups are artificial constructs, and no longer valid."[30] Many subsequent studies provided evidence that is in agreement for monophyly in the Archaeplastida (including red algae).[31][32][33][34] However, other studies have suggested Archaeplastida is paraphyletic.[35][36] As of January 2011, the situation appears unresolved.

Below are other published taxonomies of the red algae using molecular and traditional alpha taxonomic data; however, the taxonomy of the red algae is still in a state of flux (with classification above the level of order having received little scientific attention for most of the 20th century).[37]

  • If the kingdom Plantae is defined as the Archaeplastida, then red algae will be part of that group.
  • If Plantae are defined more narrowly, to be the Viridiplantae, then the red algae might be excluded.

A major research initiative to reconstruct the Red Algal Tree of Life (RedToL) using phylogenetic and genomic approach is funded by the National Science Foundation as part of the Assembling the Tree of Life Program.

Classification comparison
Classification system according to
Saunders and Hommersand 2004[37]		 Classification system according to
Hwan Su Yoon et al. 2006[38]		 Orders Multicelluar? Pit plugs? Example
 Cyanidiales No No Cyanidioschyzon merolae
  • Subphylum Rhodophytina subphylum novus
Rhodellales No No Rhodella
Compsopogonales, Rhodochaetales, Erythropeltidales Yes No Compsopogon
 Rufusiales, Stylonematales Yes No Stylonema

Bangiales

 Yes Yes Bangia, "Porphyra"

Porphyridiales

 No No Porphyridium cruentum
Hildenbrandiales Yes Yes Hildenbrandia
 Batrachospermales, Balliales, Balbianiales, Nemaliales, Colaconematales, Acrochaetiales, Palmariales, Thoreales Yes Yes Nemalion
Rhodogorgonales, Corallinales Yes Yes Corallina officinalis
  • Subclass Ahnfeltiophycidae
 Ahnfeltiales, Pihiellales Yes Yes Ahnfeltia
 Bonnemaisoniales, Gigartinales, Gelidiales, Gracilariales, Halymeniales, Rhodymeniales, Nemastomatales, Plocamiales, Ceramiales Yes Yes Gelidium

Some sources (such as Lee) place all red algae into the class "Rhodophyceae". (Lee's organization is not a comprehensive classification, but a selection of orders considered common or important.[39])

A subphylum - Proteorhodophytina - has been proposed to encompass the existing classes Compsopogonophyceae, Porphyridiophyceae, Rhodellophyceae and Stylonematophyceae.[40] This proposal was made on the basis of the analysis of the plastid genomes.

See also: Eukaryote § Phylogeny

Species of red algae

Over 7,000 species are currently described for the red algae,[4] but the taxonomy is in constant flux with new species described each year.[37][38] The vast majority of these are marine with about 200 that live only in fresh water.

Some examples of species and genera of red algae are:

Morphology

Red algal morphology is diverse ranging from unicellular forms to complex parenchymatous and non- parenchymatous thallus.[41] Red algae have double cell walls.[42] The outer layers contain the polysaccharides agarose and agaropectin that can be extracted from the cell walls as agar by boiling.[42] The internal walls are mostly cellulose.[42] They also have the most gene-rich plastid genomes known.[43]

Cell structure

Red algae do not have flagella and centrioles during their entire life cycle. The distinguishing characters of red algal cell structure include the presence of normal spindle fibres, microtubules, un-stacked photosynthetic membranes, phycobilin pigment granules,[44] pit connection between cells, filamentous genera, and the absence of chloroplast endoplasmic reticulum.[45]

Chloroplasts

The presence of the water-soluble pigments called phycobilins (phycocyanobilin, phycoerythrobilin, phycourobilin and phycobiliviolin), which are localized into phycobilisomes, gives red algae their distinctive color.[46] Their chloroplasts contain evenly spaced and ungrouped thylakoids[47] and contain the pigments chlorophyll a, α- and β-carotene, lutein and zeaxanthin. Their chloroplasts are enclosed in a double membrane, lack grana and phycobilisomes on the stromal surface of the thylakoid membrane.[48]

Storage products

The major photosynthetic products include floridoside (major product), D‐isofloridoside, digeneaside, mannitol, sorbitol, dulcitol etc.[49] Floridean starch (similar to amylopectin in land plants), a long-term storage product, is deposited freely (scattered) in the cytoplasm.[50] The concentration of photosynthetic products are altered by the environmental conditions like change in pH, the salinity of medium, change in light intensity, nutrient limitation etc.[51] When the salinity of the medium increases the production of floridoside is increased in order to prevent water from leaving the algal cells.

Pit connections and pit plugs
Main article: Pit connection

Pit connections

Pit connections and pit plugs are unique and distinctive features of red algae that form during the process of cytokinesis following mitosis.[52][53] In red algae, cytokinesis is incomplete. Typically, a small pore is left in the middle of the newly formed partition. The pit connection is formed where the daughter cells remain in contact.

Shortly after the pit connection is formed, cytoplasmic continuity is blocked by the generation of a pit plug, which is deposited in the wall gap that connects the cells.

Connections between cells having a common parent cell are called primary pit connections. Because apical growth is the norm in red algae, most cells have two primary pit connections, one to each adjacent cell.

Connections that exist between cells not sharing a common parent cell are labelled secondary pit connections. These connections are formed when an unequal cell division produced a nucleated daughter cell that then fuses to an adjacent cell. Patterns of secondary pit connections can be seen in the order Ceramiales.[53]

Pit plugs

After a pit connection is formed, tubular membranes appear. A granular protein called the plug core then forms around the membranes. The tubular membranes eventually disappear. While some orders of red algae simply have a plug core, others have an associated membrane at each side of the protein mass, called cap membranes. The pit plug continues to exist between the cells until one of the cells dies. When this happens, the living cell produces a layer of wall material that seals off the plug.

Function

The pit connections have been suggested to function as structural reinforcement, or as avenues for cell-to-cell communication and transport in red algae, however little data supports this hypothesis.[54]

Reproduction

The reproductive cycle of red algae may be triggered by factors such as day length.[3] Red algae reproduce sexually as well as asexually. Asexual reproduction can occur through the production of spores and by vegetative means (fragmentation, cell division or propagules production).[55]

Fertilization

Red algae lack motile sperm. Hence, they rely on water currents to transport their gametes to the female organs – although their sperm are capable of "gliding" to a carpogonium's trichogyne.[3] Animals also help with the dispersal and fertilization of the gametes. The first species discovered to do so is the isopod Idotea balthica.[56]

The trichogyne will continue to grow until it encounters a spermatium; once it has been fertilized, the cell wall at its base progressively thickens, separating it from the rest of the carpogonium at its base.[3]

Upon their collision, the walls of the spermatium and carpogonium dissolve. The male nucleus divides and moves into the carpogonium; one half of the nucleus merges with the carpogonium's nucleus.[3]

The polyamine spermine is produced, which triggers carpospore production.[3]

Spermatangia may have long, delicate appendages, which increase their chances of "hooking up".[3]

Life cycle

They display alternation of generations. In addition to a gametophyte generation, many have two sporophyte generations, the carposporophyte-producing carpospores, which germinate into a tetrasporophyte – this produces spore tetrads, which dissociate and germinate into gametophytes.[3] The gametophyte is typically (but not always) identical to the tetrasporophyte.[57]

Carpospores may also germinate directly into thalloid gametophytes, or the carposporophytes may produce a tetraspore without going through a (free-living) tetrasporophyte phase.[57] Tetrasporangia may be arranged in a row (zonate), in a cross (cruciate), or in a tetrad.[3]

The carposporophyte may be enclosed within the gametophyte, which may cover it with branches to form a cystocarp.[57]

The two following case studies may be helpful to understand some of the life histories algae may display:

In a simple case, such as Rhodochorton investiens:

In the carposporophyte: a spermatium merges with a trichogyne (a long hair on the female sexual organ), which then divides to form carposporangia – which produce carpospores.
Carpospores germinate into gametophytes, which produce sporophytes. Both of these are very similar; they produce monospores from monosporangia "just below a cross-wall in a filament"[3] and their spores are "liberated through the apex of sporangial cell."[3]
The spores of a sporophyte produce either tetrasporophytes. Monospores produced by this phase germinates immediately, with no resting phase, to form an identical copy of the parent. Tetrasporophytes may also produce a carpospore, which germinates to form another tetrasporophyte.[3]
The gametophyte may replicate using monospores, but produces sperm in spermatangia, and "eggs"(?) in carpogonium.[3]

A rather different example is Porphyra gardneri:

In its diploid phase, a carpospore can germinate to form a filamentous "conchocelis stage", which can also self-replicate using monospores. The conchocelis stage eventually produces conchosporangia. The resulting conchospore germinates to form a tiny prothallus with rhizoids, which develops to a cm-scale leafy thallus. This too can reproduce via monospores, which are produced inside the thallus itself.[3] They can also reproduce via spermatia, produced internally, which are released to meet a prospective carpogonium in its conceptacle.[3]

Chemistry
Algal group δ13C range[58]
HCO3-using red algae −22.5‰ to −9.6‰
CO2-using red algae −34.5‰ to −29.9‰
Brown algae −20.8‰ to −10.5‰
Green algae −20.3‰ to −8.8‰

The δ13C values of red algae reflect their lifestyles. The largest difference results from their photosynthetic metabolic pathway: algae that use HCO3 as a carbon source have less negative δ13C values than those that only use CO2.[58] An additional difference of about 1.71‰ separates groups intertidal from those below the lowest tide line, which are never exposed to atmospheric carbon. The latter group uses the more 13C-negative CO2 dissolved in sea water, whereas those with access to atmospheric carbon reflect the more positive signature of this reserve.

Photosynthetic pigments of Rhodophyta are chlorophylls a and d. Red algae are red due to phycoerythrin. They contain the sulfated polysaccharide carrageenan in the amorphous sections of their cell walls, although red algae from the genus Porphyra contain porphyran. They also produce a specific type of tannin called phlorotannins, but in a lower amount than brown algae do.

Genomes and transcriptomes of red algae

As enlisted in realDB,[59] 27 complete transcriptomes and 10 complete genomes sequences of red algae are available. Listed below are the 10 complete genomes of red algae.

Fossil record

One of the oldest fossils identified as a red alga is also the oldest fossil eukaryote that belongs to a specific modern taxon. Bangiomorpha pubescens, a multicellular fossil from arctic Canada, strongly resembles the modern red alga Bangia and occurs in rocks dating to 1.05 billion years ago.[2]

Two kinds of fossils resembling red algae were found sometime between 2006 and 2011 in well-preserved sedimentary rocks in Chitrakoot, central India. The presumed red algae lie embedded in fossil mats of cyanobacteria, called stromatolites, in 1.6 billion-year-old Indian phosphorite – making them the oldest plant-like fossils ever found by about 400 million years.[71]

Red algae are important builders of limestone reefs. The earliest such coralline algae, the solenopores, are known from the Cambrian period. Other algae of different origins filled a similar role in the late Paleozoic, and in more recent reefs.

Calcite crusts that have been interpreted as the remains of coralline red algae, date to the Ediacaran Period.[72] Thallophytes resembling coralline red algae are known from the late Proterozoic Doushantuo formation.[73]

Relationship to other algae

Chromista and Alveolata algae (e.g., chrysophytes, diatoms, phaeophytes, dinophytes) seem to have evolved from bikonts that have acquired red algae as endosymbionts. According to this theory, over time these endosymbiont red algae have evolved to become chloroplasts. This part of endosymbiotic theory is supported by various structural and genetic similarities.[74]

Human consumption

Red algae have a long history of use as a source of nutritional, functional food ingredients and pharmaceutical substances.[75] They are a source of antioxidants including polyphenols, and phycobiliproteins and contain proteins, minerals, trace elements, vitamins and essential fatty acids.[76][77] Traditionally red algae are eaten raw, in salads, soups, meal and condiments. Several species are food crops, in particular dulse (Palmaria palmata)[78] and members of the genus Porphyra, variously known as nori (Japan), gim (Korea), zicai 紫菜 (China), and laver (British Isles).[79] Some of the red algal species like Gracilaria and Laurencia are rich in polyunsaturated fatty acids (eicopentaenoic acid, docohexaenoic acid, arachidonic acid)[80] and have protein content up to 47% of total biomass.[75] Where a big portion of world population is getting insufficient daily iodine intake, a 150 ug/day requirement of iodine is obtained from a single gram of red algae.[81] Red algae, like Gracilaria, Gelidium, Euchema, Porphyra, Acanthophora, and Palmaria are primarily known for their industrial use for phycocolloids (agar, algin, furcellaran and carrageenan) as thickening agent, textiles, food, anticoagulants, water-binding agents etc.[82] Dulse (Palmaria palmata) is one of the most consumed red algae and is a source of iodine, protein, magnesium and calcium.[83] China, Japan, Republic of Korea are the top producers of seaweeds.[84] In East and Southeast Asia, agar is most commonly produced from Gelidium amansii. These rhodophytes are easily grown and, for example, nori cultivation in Japan goes back more than three centuries.

Rhodophyta (red algae)

See also

References
  1. N. J. Butterfield (2000). "Bangiomorpha pubescens n. gen., n. sp.: implications for the evolution of sex, multicellularity, and the Mesoproterozoic/Neoproterozoic radiation of eukaryotes". Paleobiology. 26 (3): 386–404. doi:10.1666/0094-8373(2000)026<0386:BPNGNS>2.0.CO;2. ISSN 0094-8373. S2CID 36648568.
  2. T.M. Gibson (2018). "Precise age of Bangiomorpha pubescens dates the origin of eukaryotic photosynthesis". Geology. 46 (2): 135–138. Bibcode:2018Geo....46..135G. doi:10.1130/G39829.1.
  3. Lee, R.E. (2008). Phycology (4th ed.). Cambridge University Press. ISBN 978-0-521-63883-8.
  4. Guiry, M.D.; Guiry, G.M. (2016). "Algaebase". www.algaebase.org. Retrieved November 20, 2016.
  5. D. Thomas (2002). Seaweeds. Life Series. Natural History Museum, London. ISBN 978-0-565-09175-0.
  6. Dodds, Walter K. (Walter Kennedy), 1958- (7 May 2019). Freshwater ecology : concepts and environmental applications of limnology. Whiles, Matt R. (Third ed.). London, United Kingdom. ISBN 9780128132555. OCLC 1096190142.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: multiple names: authors list (link)
  7. Sheath, Robert G. (1284). "The biology of freshwater red algae". Progress Phycological Research. 3: 89–157.
  8. Why don't we live on a red planet?
  9. Azua-Bustos, A; González-Silva, C; Arenas-Fajardo, C; Vicuña, R (2012). "Extreme environments as potential drivers of convergent evolution by exaptation: the Atacama Desert Coastal Range case". Front Microbiol. 3: 426. doi:10.3389/fmicb.2012.00426. PMC 3526103. PMID 23267354.
  10. W. J. Woelkerling (1990). "An introduction". In K. M. Cole; R. G. Sheath (eds.). Biology of the Red Algae. Cambridge University Press, Cambridge. pp. 1–6. ISBN 978-0-521-34301-5.
  11. Campbell Biology Australian and New Zealand Edition
  12. Introduction to the Biology of Marine Life
  13. Viola, R.; Nyvall, P.; Pedersén, M. (2001). "The unique features of starch metabolism in red algae". Proceedings of the Royal Society of London B. 268 (1474): 1417–1422. doi:10.1098/rspb.2001.1644. PMC 1088757. PMID 11429143.
  14. "Algae". autocww.colorado.edu. Archived from the original on 2012-03-15. Retrieved 2012-11-30.
  15. M. D. Guiry. "Rhodophyta: red algae". National University of Ireland, Galway. Archived from the original on 2007-05-04. Retrieved 2007-06-28.
  16. Gould, S.B.; Waller, R.F.; McFadden, G.I. (2008). "Plastid Evolution". Annual Review of Plant Biology. 59: 491–517. doi:10.1146/annurev.arplant.59.032607.092915. PMID 18315522. S2CID 30458113.
  17. McFadden, G.I. (2001). "Primary and Secondary Endosymbiosis and the Evolution of Plastids". Journal of Phycology. 37 (6): 951–959. doi:10.1046/j.1529-8817.2001.01126.x. S2CID 51945442.
  18. Steal My Sunshine | The Scientist Magazine
  19. Ciniglia, C.; Yoon, H.; Pollio, A.; Bhattacharya, D. (2004). "Hidden biodiversity of the extremophilic Cyanidiales red algae". Molecular Ecology. 13 (7): 1827–1838. doi:10.1111/j.1365-294X.2004.02180.x. PMID 15189206. S2CID 21858509.
  20. Plants and animals sometimes take genes from bacteria, study of algae suggests - Sciencemag.org
  21. The genomes of polyextremophilic cyanidiales contain 1% horizontally transferred genes with diverse adaptive functions
  22. Brawley, SH (2017). "Insights into the red algae and eukaryotic evolution from the genome of Porphyra umbilicalis (Bangiophyceae, Rhodophyta)". Proceedings of the National Academy of Sciences of the United States of America. 114 (31): E6361–E6370. Bibcode:2017PNAS..114E6361B. doi:10.1073/pnas.1703088114. PMC 5547612. PMID 28716924.
  23. Norris, J. N.; Olsen, J. L. (1991). "Deep-water green algae from the Bahamas, including Cladophora vandenhoekii sp. nov. (Cladophorales)". Phycologia. 30 (4): 315–328. doi:10.2216/i0031-8884-30-4-315.1. ISSN 0031-8884.
  24. Kain, J.M.; Norton, T.A. (1990). "Marine Ecology". In Cole, J.M.; Sheath, R.G. (eds.). Biology of the Red Algae. Cambridge, U.K.: Cambridge University Press. pp. 377–423. ISBN 978-0521343015.
  25. Eloranta, P.; Kwandrans, J. (2004). "Indicator value of freshwater red algae in running waters for water quality assessment" (PDF). International Journal of Oceanography and Hydrobiology. XXXIII (1): 47–54. ISSN 1730-413X. Archived from the original (PDF) on 2011-07-27.
  26. Vis, M.L.; Sheath, R.G.; Chiasson, W.B. (2008). "A survey of Rhodophyta and associated macroalgae from coastal streams in French Guiana". Cryptogamie Algologie. 25: 161–174.
  27. Sheath, R.G.; Hambrook, J.A. (1990). "Freshwater Ecology". In Cole, K.M.; Sheath, R.G. (eds.). Biology of the Red Algae. Cambridge, U.K.: Cambridge University Press. pp. 423–453. ISBN 978-0521343015.
  28. Goff, L.J. (1982). "The biology of parasitic red algae". Progress Phycological Research. 1: 289–369.
  29. Salomaki, E.D.; Lane, C.E. (2014). "Are all red algal parasites cut from the same cloth?". Acta Societatis Botanicorum Poloniae. 83 (4): 369–375. doi:10.5586/asbp.2014.047.
  30. Adl, Sina M.; et al. (2005). "The New Higher Level Classification of Eukaryotes with Emphasis on the Taxonomy of Protists". Journal of Eukaryotic Microbiology. 52 (5): 399–451. doi:10.1111/j.1550-7408.2005.00053.x. PMID 16248873. S2CID 8060916.
  31. Fabien Burki; Kamran Shalchian-Tabrizi; Marianne Minge; Åsmund Skjæveland; Sergey I. Nikolaev; Kjetill S. Jakobsen; Jan Pawlowski (2007). Butler, Geraldine (ed.). "Phylogenomics Reshuffles the Eukaryotic Supergroups". PLOS ONE. 2 (8): e790. Bibcode:2007PLoSO...2..790B. doi:10.1371/journal.pone.0000790. PMC 1949142. PMID 17726520.
  32. Burki, Fabien; Inagaki, Yuji; Bråte, Jon; Archibald, John M.; Keeling, Patrick J.; Cavalier-Smith, Thomas; Sakaguchi, Miako; Hashimoto, Tetsuo; Horak, Ales; Kumar, Surendra; Klaveness, Dag; Jakobsen, Kjetill S.; Pawlowski, Jan; Shalchian-Tabrizi, Kamran (2009). "Large-Scale Phylogenomic Analyses Reveal That Two Enigmatic Protist Lineages, Telonemia and Centroheliozoa, Are Related to Photosynthetic Chromalveolates". Genome Biology and Evolution. 1: 231–8. doi:10.1093/gbe/evp022. PMC 2817417. PMID 20333193.
  33. Cavalier-Smith, Thomas (2009). "Kingdoms Protozoa and Chromista and the eozoan root of the eukaryotic tree". Biology Letters. 6 (3): 342–5. doi:10.1098/rsbl.2009.0948. PMC 2880060. PMID 20031978.
  34. Rogozin, I.B.; Basu, M.K.; Csürös, M. & Koonin, E.V. (2009). "Analysis of Rare Genomic Changes Does Not Support the Unikont–Bikont Phylogeny and Suggests Cyanobacterial Symbiosis as the Point of Primary Radiation of Eukaryotes". Genome Biology and Evolution. 1: 99–113. doi:10.1093/gbe/evp011. PMC 2817406. PMID 20333181.
  35. Kim, E.; Graham, L.E. & Graham, Linda E. (2008). Redfield, Rosemary Jeanne (ed.). "EEF2 analysis challenges the monophyly of Archaeplastida and Chromalveolata". PLOS ONE. 3 (7): e2621. Bibcode:2008PLoSO...3.2621K. doi:10.1371/journal.pone.0002621. PMC 2440802. PMID 18612431.
  36. Nozaki, H.; Maruyama, S.; Matsuzaki, M.; Nakada, T.; Kato, S.; Misawa, K. (2009). "Phylogenetic positions of Glaucophyta, green plants (Archaeplastida) and Haptophyta (Chromalveolata) as deduced from slowly evolving nuclear genes". Molecular Phylogenetics and Evolution. 53 (3): 872–880. doi:10.1016/j.ympev.2009.08.015. PMID 19698794.
  37. G. W. Saunders & M. H. Hommersand (2004). "Assessing red algal supraordinal diversity and taxonomy in the context of contemporary systematic data". American Journal of Botany. 91 (10): 1494–1507. doi:10.3732/ajb.91.10.1494. PMID 21652305. S2CID 9925890.
  38. Hwan Su Yoon; K. M. Müller; R. G. Sheath; F. D. Ott & D. Bhattacharya (2006). "Defining the major lineages of red algae (Rhodophyta)" (PDF). Journal of Phycology. 42 (2): 482–492. doi:10.1111/j.1529-8817.2006.00210.x. S2CID 27377549. Archived from the original (PDF) on 2016-03-04. Retrieved 2011-12-09.
  39. Robert Edward Lee (2008). Phycology. Cambridge University Press. pp. 107. ISBN 978-0-521-68277-0. Retrieved 31 January 2011.
  40. Muñoz-Gómez, SA; Mejía-Franco, FG; Durnin, K; Colp, M; Grisdale, CJ; Archibald, JM; Ch, Slamovits (2017). "The new red algal subphylum Proteorhodophytina comprises the largest and most divergent plastid genomes known". Curr Biol. 27 (11): 1677–1684. doi:10.1016/j.cub.2017.04.054. PMID 28528908.
  41. Goff, L. J.; Coleman, A. W. (1986). "A Novel Pattern of Apical Cell Polyploidy, Sequential Polyploidy Reduction and Intercellular Nuclear Transfer in the Red Alga Polysiphonia". American Journal of Botany. 73 (8): 1109–1130. doi:10.1002/j.1537-2197.1986.tb08558.x.
  42. Fritsch, F. E. (1945), The structure and reproduction of the algae, Cambridge: Cambridge Univ. Press, ISBN 0521050421, OCLC 223742770
  43. Janouškovec, Jan; Liu, Shao-Lun; Martone, Patrick T.; Carré, Wilfrid; Leblanc, Catherine; Collén, Jonas; Keeling, Patrick J. (2013). "Evolution of Red Algal Plastid Genomes: Ancient Architectures, Introns, Horizontal Gene Transfer, and Taxonomic Utility of Plastid Markers". PLOS ONE. 8 (3): e59001. Bibcode:2013PLoSO...859001J. doi:10.1371/journal.pone.0059001. PMC 3607583. PMID 23536846.
  44. W. J. Woelkerling (1990). "An introduction". In K. M. Cole; R. G. Sheath (eds.). Biology of the Red Algae. Cambridge University Press, Cambridge. pp. 1–6. ISBN 978-0-521-34301-5.
  45. Scott, J.; Cynthia, B.; Schornstein, K.; Thomas, J. (1980). "Ultrastructure of Cell Division and Reproductive Differentiation of Male Plants in the Florideophyceae (Rhodophyta): Cell Division in Polysiphonia1". Journal of Phycology. 16 (4): 507–524. doi:10.1111/j.1529-8817.1980.tb03068.x. S2CID 83062611.
  46. Gantt, E (1969). "Properties and Ultrastructure of Phycoerythrin From Porphyridium cruentum12". Plant Physiology. 44 (11): 1629–1638. doi:10.1104/pp.44.11.1629. PMC 396315. PMID 16657250.
  47. "The Fine Structure of Algal Cells - 1st Edition". shop.elsevier.com. Retrieved 2023-08-16.
  48. Tsekos, I.; Reiss, H.-D.; Orfanidis, S.; Orologas, N. (1996). "Ultrastructure and supramolecular organization of photosynthetic membranes of some marine red algae". New Phytologist. 133 (4): 543–551. doi:10.1111/j.1469-8137.1996.tb01923.x.
  49. Karsten, U.; West, J. A.; Zuccarello, G. C.; Engbrodt, R.; Yokoyama, A.; Hara, Y.; Brodie, J. (2003). "Low Molecular Weight Carbohydrates of the Bangiophycidae (Rhodophyta)1". Journal of Phycology. 39 (3): 584–589. doi:10.1046/j.1529-8817.2003.02192.x. S2CID 84561417.
  50. Lee, R. E. (1974). Chloroplast structure and starch grain production as phylogenetic indicators in the lower Rhodophyceae. British Phycological Journal, 9(3), 291–295. doi:10.1080/00071617400650351
  51. Eggert, Anja; Karsten, Ulf (2010), Seckbach, Joseph; Chapman, David J. (eds.), "Low Molecular Weight Carbohydrates in Red Algae – an Ecophysiological and Biochemical Perspective", Red Algae in the Genomic Age, Cellular Origin, Life in Extreme Habitats and Astrobiology, Dordrecht: Springer Netherlands, vol. 13, pp. 443–456, doi:10.1007/978-90-481-3795-4_24, ISBN 978-90-481-3795-4, retrieved 2023-08-16
  52. Clinton JD, Scott FM, Bowler E (November–December 1961). "A Light- and Electron-Microscopic Survey of Algal Cell Walls. I. Phaeophyta and Rhodophyta". American Journal of Botany. 48 (10): 925–934. doi:10.2307/2439535. JSTOR 2439535.
  53. Lee RE (2008). Phycology (4th ed.). Cambridge University Press. ISBN 978-0-521-63883-8.
  54. "Pit Plugs". FHL Marine Botany. Retrieved 2016-06-30.
  55. In Archibald, J. M., In Simpson, A. G. B., & In Slamovits, C. H. (2017). Handbook of the protists.
  56. Tamisiea, Jack. "In a First, Tiny Crustaceans Are Found to 'Pollinate' Seaweed like Bees of the Sea". Scientific American. Retrieved 2023-08-16.
  57. Kohlmeyer, J. (February 1975). "New Clues to the Possible Origin of Ascomycetes". BioScience. 25 (2): 86–93. doi:10.2307/1297108. JSTOR 1297108.
  58. Maberly, S. C.; Raven, J. A.; Johnston, A. M. (1992). "Discrimination between 12C and 13C by marine plants". Oecologia. 91 (4): 481. doi:10.1007/BF00650320. JSTOR 4220100.
  59. Chen, Fei; Zhang, Jiawei; Chen, Junhao; Li, Xiaojiang; Dong, Wei; Hu, Jian; Lin, Meigui; Liu, Yanhui; Li, Guowei; Wang, Zhengjia; Zhang, Liangsheng (2018-01-01). "realDB: a genome and transcriptome resource for the red algae (phylum Rhodophyta)". Database. 2018. doi:10.1093/database/bay072. ISSN 1758-0463. PMC 6051438. PMID 30020436.
  60. Matsuzaki; et al. (April 2004). "Genome sequence of the ultrasmall unicellular red alga Cyanidioschyzon merolae 10D". Nature. 428 (6983): 653–657. Bibcode:2004Natur.428..653M. doi:10.1038/nature02398. PMID 15071595.
  61. Nozaki; et al. (2007). "A 100%-complete sequence reveals unusually simple genomic features in the hot-spring red alga Cyanidioschyzon merolae". BMC Biology. 5: 28. doi:10.1186/1741-7007-5-28. PMC 1955436. PMID 17623057.
  62. Schönknecht; et al. (March 2013). "Gene transfer from bacteria and archaea facilitated evolution of an extremophilic eukaryote". Science. 339 (6124): 1207–1210. Bibcode:2013Sci...339.1207S. doi:10.1126/science.1231707. PMID 23471408. S2CID 5502148.
  63. Nakamura; et al. (2013). "The first symbiont-free genome sequence of marine red alga, Susabi-nori (Pyropia yezoensis)". PLOS ONE. 8 (3): e57122. Bibcode:2013PLoSO...857122N. doi:10.1371/journal.pone.0057122. PMC 3594237. PMID 23536760.
  64. Collen; et al. (2013). "Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida". PNAS. 110 (13): 5247–5252. Bibcode:2013PNAS..110.5247C. doi:10.1073/pnas.1221259110. PMC 3612618. PMID 23503846.
  65. Bhattacharya; et al. (2013). "Genome of the red alga Porphyridium purpureum". Nature Communications. 4: 1941. Bibcode:2013NatCo...4.1941B. doi:10.1038/ncomms2931. PMC 3709513. PMID 23770768.
  66. Brawley, SH; Blouin, NA; Ficko-Blean, E; Wheeler, GL; et al. (1 August 2017). "Insights into the red algae and eukaryotic evolution from the genome of Porphyra umbilicalis (Bangiophyceae, Rhodophyta)". Proceedings of the National Academy of Sciences of the United States of America. 114 (31): E6361–E6370. Bibcode:2017PNAS..114E6361B. doi:10.1073/pnas.1703088114. PMC 5547612. PMID 28716924.
  67. Ho, C.-L.; Lee, W.-K.; Lim, E.-L. (2018). "Unraveling the nuclear and chloroplast genomes of an agar producing red macroalga, Gracilaria changii (Rhodophyta, Gracilariales)". Genomics. 110 (2): 124–133. doi:10.1016/j.ygeno.2017.09.003. PMID 28890206.
  68. Qiu, H.; Price, D. C.; Weber, A. P. M.; Reeb, V.; Yang, E. C.; Lee, J. M.; Bhattacharya, D. (2013). "Adaptation through horizontal gene transfer in the cryptoendolithic red alga Galdieria phlegrea". Current Biology. 23 (19): R865–R866. doi:10.1016/j.cub.2013.08.046. PMID 24112977.
  69. Zhou, W.; Hu, Y.; Sui, Z.; Fu, F.; Wang, J.; Chang, L.; Li, B. (2013). "Genome Survey Sequencing and Genetic Background Characterization of Gracilariopsis lemaneiformis (Rhodophyta) Based on Next-Generation Sequencing". PLOS ONE. 8 (7): e69909. Bibcode:2013PLoSO...869909Z. doi:10.1371/journal.pone.0069909. PMC 3713064. PMID 23875008.
  70. JunMo Lee, Eun Chan Yang, Louis Graf, Ji Hyun Yang, Huan Qiu, Udi Zelzion, Cheong Xin Chan, Timothy G Stephens, Andreas P M Weber, Ga Hun Boo, Sung Min Boo, Kyeong Mi Kim, Younhee Shin, Myunghee Jung, Seung Jae Lee, Hyung-Soon Yim, Jung-Hyun Lee, Debashish Bhattacharya, Hwan Su Yoon, "Analysis of the Draft Genome of the Red Seaweed Gracilariopsis chorda Provides Insights into Genome Size Evolution" in Rhodophyta, Molecular Biology and Evolution, Volume 35, Issue 8, August 2018, pp. 1869–1886, doi:10.1093/molbev/msy081
  71. Bengtson, S; Sallstedt, T; Belivanova, V; Whitehouse, M (2017). "Three-dimensional preservation of cellular and subcellular structures suggests 1.6 billion-year-old crown-group red algae". PLOS Biol. 15 (3): e2000735. doi:10.1371/journal.pbio.2000735. PMC 5349422. PMID 28291791.
  72. Grant, S. W. F.; Knoll, A. H.; Germs, G. J. B. (1991). "Probable Calcified Metaphytes in the Latest Proterozoic Nama Group, Namibia: Origin, Diagenesis, and Implications". Journal of Paleontology. 65 (1): 1–18. Bibcode:1991JPal...65....1G. doi:10.1017/S002233600002014X. JSTOR 1305691. PMID 11538648. S2CID 26792772.
  73. Yun, Z.; Xun-lal, Y. (1992). "New data on multicellular thallophytes and fragments of cellular tissues from Late Proterozoic phosphate rocks, South China". Lethaia. 25 (1): 1–18. doi:10.1111/j.1502-3931.1992.tb01788.x.
  74. Summarised in Cavalier-Smith, Thomas (April 2000). "Membrane heredity and early chloroplast evolution". Trends in Plant Science. 5 (4): 174–182. doi:10.1016/S1360-1385(00)01598-3. PMID 10740299.
  75. Wang, T., Jónsdóttir, R., Kristinsson, H. G., Hreggvidsson, G. O., Jónsson, J. Ó., Thorkelsson, G., & Ólafsdóttir, G. (2010). "Enzyme-enhanced extraction of antioxidant ingredients from red algae Palmaria palmata". LWT – Food Science and Technology, 43(9), 1387–1393. doi:10.1016/j.lwt.2010.05.010
  76. MacArtain, P.; Gill, C. I. R.; Brooks, M.; Campbell, R.; Rowland, I. R. (2007). "Nutritional Value of Edible Seaweeds". Nutrition Reviews. 65 (12): 535–543. doi:10.1111/j.1753-4887.2007.tb00278.x. PMID 18236692. S2CID 494897.
  77. Becker, E.W. (March 2007). "Micro-algae as a source of protein". Biotechnology Advances. 25 (2): 207–210. doi:10.1016/j.biotechadv.2006.11.002. PMID 17196357.
  78. "Dulse: Palmaria palmata". Quality Sea Veg. Archived from the original on 2012-02-22. Retrieved 2007-06-28.
  79. T. F. Mumford & A. Muira (1988). "Porphyra as food: cultivation and economics". In C. A. Lembi & J. Waaland (eds.). Algae and Human Affairs. Cambridge University Press, Cambridge. ISBN 978-0-521-32115-0.
  80. Gressler, V., Yokoya, N. S., Fujii, M. T., Colepicolo, P., Filho, J. M., Torres, R. P., & Pinto, E. (2010). "Lipid, fatty acid, protein, amino acid and ash contents in four Brazilian red algae species". Food Chemistry, 120(2), 585–590. doi:10.1016/j.foodchem.2009.10.028
  81. Hoek, C. van den, Mann, D.G. and Jahns, H.M. (1995). Algae An Introduction to Phycology. Cambridge University Press, Cambridge. ISBN 0521304199
  82. Dhargalkar VK, Verlecar XN. "Southern Ocean Seaweeds: a resource for exploration in food and drugs". Aquaculture 2009; 287: 229–242.
  83. "On the human consumption of the red seaweed dulse (Palmaria palmata (L.) Weber & Mohr)". researchgate.net. December 2013.
  84. Manivannan, K., Thirumaran, G., Karthikai, D.G., Anantharaman. P., Balasubramanian, P. (2009). "Proximate Composition of Different Group of Seaweeds from Vedalai Coastal Waters (Gulf of Mannar): Southeast Coast of India". Middle-East J. Scientific Res., 4: 72–77.
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