Alloteropsis

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Alloteropsis
Alloteropsis cimicina W IMG 1708.jpg
Alloteropsis cimicina
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Monocots
Clade: Commelinids
Order: Poales
Family: Poaceae
Subfamily: Panicoideae
Supertribe: Panicodae
Tribe: Paniceae
Subtribe: Boivinellinae
Genus: Alloteropsis
C.Presl [1]
Type species
Alloteropsis distachya
(syn. of A. semialata)
Synonyms [3]
  • CoridochloaNees
  • BluffiaNees
  • HolosetumSteud.
  • PterochlaenaChiov.
  • MezochloaButzin

Alloteropsis (from the Greek allotrios ("strange") and opsis ("appearance")) is a genus of Old World plants in the grass family. [4] [5] [6] [7] [8] [2] [9] [10]

Contents

The group is widely distributed in tropical and subtropical parts of Africa, Asia and Australia, as well as on certain islands in the Indian and Pacific Oceans. [11] The genus is unusual among plants in that it includes species with both C3 and C4 photosynthetic pathways, and ongoing research is investigating these taxa as a case study in how carbon concentrating mechanisms for photosynthesis evolve in land plants. [12]

Photosynthetic pathway evolution

Most of the species of Alloteropsis use variants of the C4 photosynthetic pathway, but A. semialata ssp. eckloniana uses the C3 photosynthetic pathway. Phylogenetic reconstructions of the evolutionary relationships between these species have led to two hypotheses about how photosynthetic pathways have evolved within the group. First, C4 photosynthesis evolved in three lineages within this group, leading to independently derived realisations of this pathway (the hypothesis of multiple C4 origins). [13] [14] Secondly, that there was a single origin of C4 photosynthesis within the genus, and the C3 taxon, A. s. ecklonia, was subsequently derived from a C4 ancestor (the reversion hypothesis). [12] [13] Since C4 photosynthesis is a complex trait, its evolution followed by a reversion to the ancestral type of C3 photosynthesis would represent an exception to Dollo's law.

The reversion hypothesis is the most parsimonious explanation of phylogenetic relationships within Alloteropsis. [12] However, direct evidence for the hypothesis, in the form of C4 genes or pseudogenes in the C3 taxon, is currently lacking. [13] [15] Instead, two pieces of evidence better support the hypothesis of multiple C4 origins. First, different variants of C4 leaf anatomy are found in three different Alloteropsis lineages. [13] Secondly, key C4 enzymes (PEPC and PEPCK) were recruited multiple times to function in C4 biochemistry across independent lineages. [15]

C4 photosynthetic pathway evolution in Alloteropsis also represents an example of adaptive evolution via horizontal gene transfer in eukaryotes. [15] It is the first such example of gene transfer between plant species that are not in direct physical contact (as in a host-parasite relationship). In each case, genes adapted for an important function in C4 photosynthesis have been transferred from grass lineages that diverged from Alloteropsis more than 20 million years ago, [15] and independently evolved C4 photosynthesis. Horizontally inherited genes encode the photosynthesis enzymes PEPC and PEPCK. All other genes expressed in the mature C4 leaf of A. s. semialata were vertically inherited from a common ancestor with the C3 taxon A. s. eckloniana. [15]

Diversity

Accepted species [3] [16]
Formerly included [3]

see Mayariochloa Scutachne

See also

Related Research Articles

<span class="mw-page-title-main">Photosynthesis</span> Biological process to convert light into chemical energy

Photosynthesis is a biological process used by many cellular organisms to convert light energy into chemical energy, which is stored in organic compounds that can later be metabolized through cellular respiration to fuel the organism's activities. The term usually refers to oxygenic photosynthesis, where oxygen is produced as a byproduct, and some of the chemical energy produced is stored in carbohydrate molecules such as sugars, starch and cellulose, which are synthesized from endergonic reaction of carbon dioxide with water. Most plants, algae and cyanobacteria perform photosynthesis; such organisms are called photoautotrophs. Photosynthesis is largely responsible for producing and maintaining the oxygen content of the Earth's atmosphere, and supplies most of the biological energy necessary for complex life on Earth.

<span class="mw-page-title-main">Amaranthaceae</span> Family of flowering plants

Amaranthaceae is a family of flowering plants commonly known as the amaranth family, in reference to its type genus Amaranthus. It includes the former goosefoot family Chenopodiaceae and contains about 165 genera and 2,040 species, making it the most species-rich lineage within its parent order, Caryophyllales.

<span class="mw-page-title-main">RuBisCO</span> Key enzyme of the photosynthesis involved in carbon fixation

Ribulose-1,5-bisphosphate carboxylase/oxygenase, commonly known by the abbreviations RuBisCo, rubisco, RuBPCase, or RuBPco, is an enzyme involved in light-independent part of photosynthesis, including the carbon fixation by which atmospheric carbon dioxide is converted by plants and other photosynthetic organisms to energy-rich molecules such as glucose. It emerged approximately four billion years ago in primordial metabolism prior to the presence of oxygen on earth. It is probably the most abundant enzyme on Earth. In chemical terms, it catalyzes the carboxylation of ribulose-1,5-bisphosphate.

C<sub>4</sub> carbon fixation Photosynthetic process in some plants

C4 carbon fixation or the Hatch–Slack pathway is one of three known photosynthetic processes of carbon fixation in plants. It owes the names to the 1960s discovery by Marshall Davidson Hatch and Charles Roger Slack that some plants, when supplied with 14CO2, incorporate the 14C label into four-carbon molecules first.

<span class="mw-page-title-main">Photorespiration</span> Process in plant metabolism

Photorespiration (also known as the oxidative photosynthetic carbon cycle or C2 cycle) refers to a process in plant metabolism where the enzyme RuBisCO oxygenates RuBP, wasting some of the energy produced by photosynthesis. The desired reaction is the addition of carbon dioxide to RuBP (carboxylation), a key step in the Calvin–Benson cycle, but approximately 25% of reactions by RuBisCO instead add oxygen to RuBP (oxygenation), creating a product that cannot be used within the Calvin–Benson cycle. This process lowers the efficiency of photosynthesis, potentially lowering photosynthetic output by 25% in C3 plants. Photorespiration involves a complex network of enzyme reactions that exchange metabolites between chloroplasts, leaf peroxisomes and mitochondria.

C<sub>3</sub> carbon fixation Most common pathway in photosynthesis

C3 carbon fixation is the most common of three metabolic pathways for carbon fixation in photosynthesis, the other two being C4 and CAM. This process converts carbon dioxide and ribulose bisphosphate (RuBP, a 5-carbon sugar) into two molecules of 3-phosphoglycerate through the following reaction:

<span class="mw-page-title-main">Gomphrenoideae</span> Subfamily of flowering plants

The Gomphrenoideae are a subfamily of the Amaranthaceae.

<span class="mw-page-title-main">Evolutionary history of plants</span> History of plants

The evolution of plants has resulted in a wide range of complexity, from the earliest algal mats, through multicellular marine and freshwater green algae, terrestrial bryophytes, lycopods and ferns, to the complex gymnosperms and angiosperms of today. While many of the earliest groups continue to thrive, as exemplified by red and green algae in marine environments, more recently derived groups have displaced previously ecologically dominant ones; for example, the ascendance of flowering plants over gymnosperms in terrestrial environments.

<i>Axonopus</i> Genus of grasses

Axonopus is a genus of plants in the grass family, known generally as carpet grass. They are native primarily to the tropical and subtropical regions of the Americas with one species in tropical Africa and another on Easter Island. They are sometimes rhizomatous and many are tolerant of periodic submersion.

<span class="mw-page-title-main">BOP clade</span> Clade of grasses

The BOP clade (sometimes BEP clade) is one of two major lineages (or clades) of undefined taxonomic rank in the grasses (Poaceae), containing more than 5,400 species, about half of all grasses. Its sister group is the PACMAD clade; contrary to many species of that group who have evolved C4 photosynthesis, the BOP grasses all use the C3 photosynthetic pathway.

<i>Alloteropsis semialata</i> Species of grass

Alloteropsis semialata, known commonly as black seed grass, cockatoo grass, donkersaad gras, swartsaadgras, tweevingergras, and isi quinti, is a perennial grass distributed across much of tropical and subtropical Africa, Asia and Australia, as well as Papuasia and Madagascar. The genus name Allopteropsis comes from the Greek words "allotrios", meaning "belonging to another", and "opsis", meaning appearance. The specific epithet semialata comes from the Latin "semi" (half) and "ala" (wing), referring to the winged margins of the upper glume.

<span class="mw-page-title-main">Oryzoideae</span> Subfamily of plants

Oryzoideae (syn. Ehrhartoideae) is a subfamily of the true grass family Poaceae. It has around 120 species in 19 genera, notably including the major cereal crop rice. Within the grasses, this subfamily is one of three belonging to the species-rich BOP clade, which all use C3 photosynthesis; it is the basal lineage of the clade.

<span class="mw-page-title-main">PACMAD clade</span> A major clade in the grass family Poaceae

The PACMAD clade (previously PACCMAD, PACCAD, or PACC) is one of two major lineages (or clades) of the true grasses (Poaceae), regrouping six subfamilies and about 5700 species, more than half of all true grasses. Its sister group is the BOP clade. The PACMAD lineage is the only group within the grasses in which the C4 photosynthesis pathway has evolved; studies have shown that this happened independently multiple times.

<span class="mw-page-title-main">Paniceae</span> Tribe of grasses

Paniceae is a large tribe of the subfamily Panicoideae in the grasses (Poaceae), the only in the monotypic supertribe Panicodae. It includes roughly 1,500 species in 84 genera, primarily found in tropical and subtropical regions of the world. Paniceae includes species using either of the C4 and C3 photosynthetic pathways, as well as presumably intermediate species. Most of the millets are members of tribe Paniceae.

The evolution of photosynthesis refers to the origin and subsequent evolution of photosynthesis, the process by which light energy is used to assemble sugars from carbon dioxide and a hydrogen and electron source such as water. The process of photosynthesis was discovered by Jan Ingenhousz, a Dutch-born British physician and scientist, first publishing about it in 1779.

<span class="mw-page-title-main">Cathestecum</span> Genus of grasses

Cathestecum is a genus of the North American plants in the grass family.

<span class="mw-page-title-main">Micrairoideae</span> Subfamily of plants

Micrairoideae is a subfamily of the grass family Poaceae, distributed in tropical and subtropical regions. Within the PACMAD clade, it is sister to subfamily Arundinoideae.

<i>Euploca</i> Genus of flowering plants in the borage family Boraginaceae

Euploca is an almost cosmopolitan genus of plants with around 100 species. It was first described by Thomas Nuttall in 1837. While part of the broadly defined Boraginaceae in the APG IV system from 2016, a revision of the order Boraginales from the same year includes Euploca in the separate family Heliotropiaceae. Its species used to be classified in the genera Hilgeria and Schleidenia and in Heliotropium sect. Orthostachys, but were found to form an independent lineage in a molecular phylogenetic analysis, more closely related to Myriopus than to Heliotropium. While many species use the C4 photosynthetic pathway, there are also C3–C4 intermediate species. Species have leaves with a C4-typical Kranz anatomy.

References

  1. Haenke, Thaddeus; Presl, Carolus Bor. (1830). Reliquiae Haenkeanae (in Latin). Vol. 1. pp. 343–344 via Biodiversity Heritage Library.
  2. 1 2 Hitchcock, A. S. 1909. Catalogue of the Grasses of Cuba. Contributions from the United States National Herbarium 12(6): 183–258, vii–xi Alloteropsis on pages 210-211
  3. 1 2 3 Kew World Checklist of Selected Plant Families
  4. Watson, L. and M. J. Dallwitz. (2008). "Alloteropsis". The Grass Genera of the World. Retrieved 2009-08-19.
  5. Presl, Jan Svatopluk 1830. Reliquiae Haenkeanae 1(4–5): 343-344 in Latin
  6. Presl, Jan Svatopluk 1830. Reliquiae Haenkeanae 1(4–5): plate XLVII (47) line drawing of Alloteropsis distachya (syn of A. semialata)
  7. Flora of China Vol. 22 Page 519 毛颖草属 mao ying cao shu Alloteropsis Presl, Reliq. Haenk. 1: 343. 1830.
  8. Atlas of Living Australia, Alloteropsis C.Presl
  9. Bor, N. L. 1960. Grasses of Burma, Ceylon, India and Pakistan (excluding Bambuseae). Pergamon Press, Oxford
  10. Clayton, W. D. & S. A. Renvoize. 1982. Gramineae (Part 3). 451–898. In W. B. Turrill & R. M. Polhill (ed.), Flora of Tropical East Africa . A. A. Balkema, Rotterdam
  11. Clayton, W. D.; et al. (2006). "Alloteropsis Description". Kew GrassBase - The Online World Grass Flora. Retrieved 2013-03-08.
  12. 1 2 3 Ibrahim, D. G., et al. (2009). A molecular phylogeny of the genus Alloteropsis (Panicoideae, Poaceae) suggests an evolutionary reversion from C4 to C3 photosynthesis. Annals of Botany 103(1): 127–136. PMID   18974099.
  13. 1 2 3 4 Christin, P., et al. (2010). Can phylogenetics identify C4 origins and reversals? Trends in Ecology and Evolution 25(7): 403–09.
  14. Grass Phylogeny Working Group II. (2012). New grass phylogeny resolves deep evolutionary relationships and discovers C4 origins. New Phytologist 193(2): 304–12. PMID   22115274.
  15. 1 2 3 4 5 Christin, P., et al. (2012). Adaptive evolution of C4 photosynthesis through recurrent lateral gene transfer. Current Biology 22(5): 445–49. PMID   22342748.
  16. The Plant List search for Alloteropsis
  17. Biota of North America Program 2013 county distribution map, Alloteropsis cimicina

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