Ruppia

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Ruppia
Ruppia rostellata-brachypus-spiralis nf.jpg
Ruppia rostellata,
R. brachypus, + R. spiralis
[1]
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Monocots
Order: Alismatales
Family: Ruppiaceae
Horan. [2]
Genus: Ruppia
L.
Synonyms [3]
  • BucaferAdans.
  • BuccaferreaP.Micheli ex Petagna
  • DzieduszyckiaRehmann
Ruppia polycarpa Ruppia polycarpa (7597050858).jpg
Ruppia polycarpa

Ruppia, also known as the widgeonweeds, [4] ditch grasses or widgeon grass, is the only extant genus in the family Ruppiaceae, with eight known species. [5] These are aquatic plants widespread over much of the world. [3] The genus name honours Heinrich Bernhard Rupp, a German botanist (1688-1719). [6] They are widespread outside of frigid zones and the tropics.

Contents

Description

The leaf is simple and not rhizomatous. They can be annual (commonly) or perennial (rarely); stem growth is conspicuously sympodial, but sometimes is not. These species are adapted to be in brackish water (and salt marshes). The leaves are small or medium-sized. Their disposition can be alternate, opposite, or whorled (usually alternate except when subtending an inflorescence). Even, lamina keep entire and are setaceous or linear. The leaf just shows one vein without cross-venules. Stomata are not present. The mesophyll leaks calcium oxalate crystals. The minor leaf veins do not present phloem transfer cells and leaks vessels.

These plants have stems without secondary thickening and xylem without vessels. The sieve-tube plastids are P-type. The root xylem does not present vessels.

These plants are hermaphroditic, with anemophilous or hydrophilous pollination. The flowers are ebracteate, small, and regular. Commonly, the flowers are aggregated in ‘inflorescences’, but sometimes they are solitary. Often, they grow in racemes, spikes, or umbels. The scapiflorous inflorescences are terminal, in short spikes, or subumbelliform racemes, sometimes one- or few-flowered. They do not have hypogynous disks. These flowers do not have perianth absent, except when small staminal appendages are regarded as perianth segments. The androecial members are all equal. The androecium just presents two fertile stamens with sessile anthers dehiscing by longitudinal slits. The pollen is polysiphonous and its grains are three-celled and nonaperturate. The gynoecium (2–)4(–16) is superior, carpelled, and euapocarpous. The carpel is not stylate, apically stigmatic with the stigma peltate, or umbonate. These flowers only present one ovule pendulous, nonarillate, campylotropous, bitegmic, and crassinucellate. The placentation is apical and embryo-sac development is of the polygonum type. Before fertilization, they fuse polar nuclei. The fruit is drupaceous and fleshy, forming an aggregate. The fruiting carpel is indehiscent, commonly on a long, spirally twisted peduncle, with each drupelet becoming very long-stalked. The fruit contains one nonendospermic seed with starch. The embryo can be straight or slightly curved. Membranous testa do not have phytomelan.

Taxonomy

The Cronquist system of 1981 placed the family in order Najadales of subclass Alismatidae in class Liliopsida [=monocotyledons] in division Magnoliophyta [=angiosperms].

The APG II system of 2003 (unchanged from the APG system of 1998) does recognize such a family and places it in the order Alismatales, in the clade monocots.

According to the AP-Website the family is doubtfully distinct from the family Cymodoceaceae: the plants in the three families Cymodoceaceae, Posidoniaceae, and Ruppiaceae form a monophyletic group.

A genus-level taxonomy was briefly revised by Zhao and Wu, [7] including the following species in the world:

species [3]
  1. Ruppia bicarpa - Western Cape, South Africa [8]
  2. Ruppia cirrhosa * - temperate regions: Europe, Asia, north + south (but not tropical) Africa, North America, West Indies, Argentina *The name is a homotypic synonym of R. maritima [9]
  3. Ruppia didyma - Mexico, West Indies
  4. Ruppia drepanensis - western + central Mediterranean
  5. Ruppia filifolia - southern South America, Falkland Islands
  6. Ruppia maritima - seashores and lakeshores around the world
  7. Ruppia megacarpa - Australia, New Zealand, Asia (Korea, Japan, and Russia) [10] [11]
  8. Ruppia occidentalis - Canada, USA
  9. Ruppia polycarpa - Australia, New Zealand (incl Chatham Islands)
  10. Ruppia spiralis - seashores and lakeshores around the world [9]
  11. Ruppia tuberosa - Australia

Marine grasses families: Zosteraceae, Cymodoceaceae, Ruppiaceae and Posidoniaceae. Related families: Potamogetonaceae, Zannichelliaceae (not consistently).

Families and Genera crosses (Sea grasses)
Kubitzki (ed. 1998 [12] )Watson & Dallwitz (delta-intkey) [13] data.kew [14] APWeb (mobot.org) [15]
Zosteraceae
1. Zostera L. Zostera Zostera L. Zostera L. (including Heterozostera den Hartog, Macrozostera Tomlinson & Posluzny, Nanozostera Tomlinson & Posluzny, Zosterella J. K. Small)
2. Heterozostera den Hartog Heterozostera Heterozostera (Setch.) Hartog(in Zostera )
3. Phyllospadix Hook. Phyllospadix Phyllospadix Hook. Phyllospadix J. D. Hooker
Cymodoceaceae
1. Syringodium Kütz Syringodium Syringodium Kutz.(in Cymodocea )
2. Halodule Endl. Halodule Halodule Endl. Halodule Endlicher
3. Cymodocea König Cymodocea Cymodocea K.Koenig (including Phycoschoenus (Asch.) Nakai ) Cymodocea König (including Amphibolis Agardh ?, Syringodium Kütz. ?, Thalassodendron den Hartog ?)
4. Amphibolis Agardh Amphibolis Amphibolis C.Agardh (including Pectinella J.M.Black)(in Cymodocea )
5. Thalassodendron de Hartog(name not found) Thalassodendron Hartog(in Cymodocea )
Ruppiaceae
Ruppia L.Ruppia(in Ruppia L. in Potamogetonaceae)Ruppia L.
Posidoniaceae
Posidonia König Posidonia Posidonia K.Koenig Posidonia König
Families and Genera crosses (Potamogetonaceae)
Kubitzki (ed. 1998 [12] )Watson & Dallwitz (delta-intkey) [16] data.kew [17] APWeb (mobot.org) [18]
Potamogetonaceae
1. Potamogeton L. Potamogeton Potamogeton L. Potamogeton L. (including Coleogeton Les & Haynes, Stuckenia Börner)
2. Groenlandia J. Gray Groenlandia Groenlandia J.Gay Groenlandia J. Gay
(in Ruppia in Ruppiaceae)(in Ruppia in Ruppiaceae)Ruppia L.(in Ruppia in Ruppiaceae)
(in Althenia : Zannichelliaceae and Lepilaena : Zannichelliaceae)(in Althenia : Zannichelliaceae and Lepilaena : Zannichelliaceae)(in Althenia F.Petit: Zannichelliaceae and Lepilaena J.L.Drumm. ex Harv.:Zannichelliaceae) Althenia Petit (including Lepilaena Harvey)
(in Pseudalthenia including Vleisia : Zannichelliaceae)(in Pseudalthenia : Zannichelliaceae and Vleisia : Zannichelliaceae)( Pseudalthenia not found, Vleisia Toml. & Posl.: Zannichelliaceae) Pseudalthenia Nakai (including Vleisia Tomlinson & Posluszny)
(in Zannichellia L.: Zannichelliaceae)(in Zannichellia : Zannichelliaceae)(in Zannichellia L.: Zannichelliaceae) Zannichellia L.
Zannichelliaceae
1. Zannichellia L. Zannichellia Zannichellia L.(in Zannichellia L.: Potamogetonaceae)
2. Pseudalthenia Nakai (including Vleisia ) Pseudalthenia (excluding Vleisia )(name not found)(in Pseudalthenia : Potamogetonaceae)
3. Althenia Petit (excluding Lepilaena Drumm. ex. Harv.) Althenia (excluding Lepilaena ) Althenia F.Petit (excluding Lepilaena J.L.Drumm. ex Harv.) Althenia Petit (including Lepilaena Harvey)
4. Lepilaena Drumm. ex. Harv. Lepilaena Lepilaena J.L.Drumm. ex Harv.(in Althenia Petit)
(in Pseudalthenia ) Vleisia Vleisia Toml. & Posl.(in Pseudalthenia : Potamogetonaceae)

Phylogeny and evolution

The first molecular phylogeny of the monogeneric family discerned three distinct species, R. tuberosa, R. megacarpa, and R. polycarpa, and one species complex comprising six lineages. [10] The species complex, named R. maritima complex, [10] was later updated as a group of eight lineages. [19] These studies revealed that multiple hybridization and polyploidy events as well as chloroplast capture have occurred in the evolution of the genus.

Phytochemistry

These plants present an anatomy non-C4 type. Seven labdanes have been identified from this genus:

  • ent-14,15-Dinor-8(17)-labden-13-one
  • Methyl ester of (ent-12S)-15,16-Epoxy-12-hydroxy-12-oxo-8(17),13(16),14-labdatrien-19-oic acid.
  • (-)-15,16-epoxy-8(17),13(16),14-labdatrien-19-ol.
  • Methyl ester of (-)-15,16-epoxy-8(17),13(16),14-labdatrien-19-oic acid.
  • (-)-15,16-Epoxy-8(17),13(16),14-labdatrien-19-al.
  • (-)-15,16-Epoxy-8(17),13(16),14-labdatrien-19-yl acetate
  • (ent-13E)-8(17),13-Labdadien-15-ol

Three steroids have been also isolated:

  • (3β,5α,6β,7α,22E,24R)-Ergosta-8(14),22-diene-3,6,7-triol.
  • (3β,5α,6β,7α,22E,24R)-Ergosta-8,22-diene-3,6,7-triol
  • (24R)-Ergost-4-ene-3,6-dione.

Related Research Articles

<span class="mw-page-title-main">Alismatales</span> Order of herbaceous flowering plants of marshy and aquatic habitats

The Alismatales (alismatids) are an order of flowering plants including about 4,500 species. Plants assigned to this order are mostly tropical or aquatic. Some grow in fresh water, some in marine habitats. Perhaps the most important food crop in the order is the corm of the taro plant, Colocasia esculenta.

<span class="mw-page-title-main">Hydrocharitaceae</span> Family of aquatic plants

Hydrocharitaceae is a flowering plant family including 16 known genera with a total of ca 135 known species, that including a number of species of aquatic plant, for instance the tape-grasses, the well known Canadian waterweed, and frogbit.

<span class="mw-page-title-main">Potamogetonaceae</span> Family of aquatic plants

The Potamogetonaceae, commonly referred to as the pondweed family, is an aquatic family of monocotyledonous flowering plants. The roughly 110 known species are divided over six genera. The largest genus in the family by far is Potamogeton, which contains about 100 species.

<span class="mw-page-title-main">Zosteraceae</span> Family of aquatic plants

Zosteraceae is a family of marine perennial flowering plants found in temperate and subtropical coastal waters, with the highest diversity located around Korea and Japan. Most seagrasses complete their entire life cycle under water, having filamentous pollen especially adapted to dispersion in an aquatic environment and ribbon-like leaves that lack stomata. Seagrasses are herbaceous and have prominent creeping rhizomes. A distinctive characteristic of the family is the presence of characteristic retinacules, which are present in all species except members of Zostera subgenus Zostera.

Antitropicaldistribution is a type of disjunct distribution where a species or clade exists at comparable latitudes across the equator but not in the tropics. For example, a species may be found north of the Tropic of Cancer and south of the Tropic of Capricorn, but not in between. With increasing time since dispersal, the disjunct populations may be the same variety, species, or clade. How the life forms distribute themselves to the opposite hemisphere when they can't normally survive in the middle depends on the species; plants may have their seed spread through wind, animal, or other methods and then germinate upon reaching the appropriate climate, while sea life may be able to travel through the tropical regions in a larval state or by going through deep ocean currents with much colder temperatures than on the surface. For the American amphitropical distribution, dispersal has been generally agreed to be more likely than vicariance from a previous distribution including the tropics in North and South America.

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

Chrysobalanaceae is a family of flowering plants, consisting of trees and shrubs in 27 genera and about 700 species of pantropical distribution with a centre of diversity in the Amazon. Some of the species contain silica in their bodies for rigidity and so the mesophyll often has sclerenchymatous idioblasts. The widespread species Chrysobalanus icaco produces a plum-like fruit and the plant is commonly known as the coco plum.

<span class="mw-page-title-main">Najadales</span> Order of flowering plants

Najadales is the botanical name of an order of flowering plants. A well-known system that used this name is the Cronquist system (1981), which used this name for an order in subclass Alismatidae with this circumscription:

<span class="mw-page-title-main">Cymodoceaceae</span> Family of aquatic plants

Cymodoceaceae is a family of flowering plants, sometimes known as the "manatee-grass family", which includes only marine species.

<span class="mw-page-title-main">Nobuyuki Tanaka</span>

Nobuyuki Tanaka is an economic botanist at the Tokyo Metropolitan University, the Makino Botanical Garden in Kōchi Prefecture, Japan.

<i>Posidonia</i> Genus of aquatic plants

Posidonia is a genus of flowering plants. It contains nine species of marine plants ("seagrass"), found in the seas of the Mediterranean and around the south coast of Australia.

<i>Ruppia cirrhosa</i> Species of aquatic plant

Ruppia cirrhosa is a species of aquatic plant known by the common names spiral ditchgrass and spiral tasselweed. It is native to the Americas and Europe, where it grows in freshwater bodies, such as lakes. It is a thread-thin, grasslike perennial herb which grows from a rhizome anchored in the wet substrate. It produces a long, narrow inflorescence tipped with two tiny flowers. As the fruit develops the peduncle of the inflorescence curls into a neat spiral.

<i>Ruppia maritima</i> Species of aquatic plant

Ruppia maritima is an aquatic plant species commonly known as beaked tasselweed, beaked ditchgrass, ditch grass, tassel pondweed and widgeon grass. Despite its scientific name, it is not a marine plant; is perhaps best described as a salt-tolerant freshwater species. The generic name Ruppia was dedicated by Linnaeus to the German botanist Heinrich Bernhard Ruppius (1689–1719) and the specific name (maritima) translates to "of the sea".

Ruppia megacarpa is a submerged herb species in the genus Ruppia found in shallow brackish waters. It is a common on Australasian coasts, including Australia (NSW; SA; Vic; WA and New Zealand. Isolated populations have been currently found in East Asia, including Japan, Korea, and Far East Russia, hence, the species distribution exhibit latitudinally disjunct distribution between East Asia and Australasia.

<i>Ruppia tuberosa</i> Species of herb

Ruppia tuberosa is a submerged herb in the genus Ruppia found in shallow hypersaline waters in Australia.

Chloroplast capture is an evolutionary process through which inter-species hybridization and subsequent backcrosses yield a plant with new genetic combination of nuclear and chloroplast genomes. For instance, 1) species A's pollen hybridizes (backcross) to species B's ovule, yielding the 1st hybrid (F1) with chloroplast genome b and nuclear genome A (50%) and B (50%); 2) species A's pollen again hybridizes (backcross) to F1's ovule, yielding the 2nd hybrid (F2) with chloroplast genome b and nuclear genome A (75%) and B (25%); 3) species A's pollen again hybridizes (backcross) to F2's ovule, yielding the 3rd hybrid (F3) with chloroplast genome b and nuclear genome A (87.5%) and B (12.5%); 4) after further backcross generations, a plant is obtained with the new genetic combination.

Norio Tanaka is an aquatic botanist at Tsukuba Botanical Garden, National Science Museum, Tokyo, Japan.

<i>Najas tenuis</i> Species of aquatic plant

Najas tenuis is a species of aquatic plant found in freshwater habitats, especially still or slow-moving waters, like ponds and rice fields.

Ruppia bicarpa is an aquatic plant species in the genus Ruppia of Ruppiaceae. It is found in shallow waters.

Ruppia spiralis is an aquatic plant species in the genus Ruppia of the family Ruppiaceae. This name was synonymized under R. cirrhosa, but it has been resurrected for the species previously referred to as R. cirrhosa.

References

  1. painting by the Swedish botanist C. A. M. Lindman (1856–1928), taken from his book(s) Bilder ur Nordens Flora (first edition published 1901–1905, supplemented edition 1917–1926?)
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  8. Ito, Y., Nr. Tanaka, T. Ohi-Toma, J. Murata, and A.M. Muasya (2015) Phylogeny of Ruppia (Ruppiaceae) revisited: Molecular and morphological evidence for a new species from Western Cape, South Africa. Systematic Botany 40(4): 942-949. doi: 10.1600/036364415X689988
  9. 1 2 Ito, Y., T. Ohi-Toma, C. Nepi, A. Santangelo, A. Stinca, N. Tanaka, & J. Murata (2017) Towards a better understanding of the Ruppia maritima complex (Ruppiaceae): Notes on the correct application and typification of the names R. cirrhosa and R. spiralis Taxon 66: 167-171
  10. 1 2 3 Ito, Y., T. Ohi-Toma, J. Murata & Nr. Tanaka (2010) Hybridization and polyploidy of an aquatic plant, Ruppia (Ruppiaceae), inferred from plastid and nuclear DNA phylogenies American Journal of Botany 97: 1156-1167
  11. Ito, Y., T. Ohi-Toma, A. V. Skriptsova, M. Sasagawa, Nr. Tanaka, and J. Murata (2014) Ruppia megacarpa (Ruppiaceae): a new species to the floras of Japan, Korea, and Russia. Botanica Pacofica3: 49–52
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  15. VASCULAR PLANT FAMILIES and GENERA. List of Genera in CYMODOCEACEAE (accessed 2016-06-02) http://www.mobot.org/mobot/research/apweb/orders/alismatalesweb.htm#Cymodoceaceael
  16. Watson & Dallwitz. Potamogetonaceae. The families of flowering plants. http://delta-intkey.com/angio/www/potamoge.htm Archived 2021-04-17 at the Wayback Machine
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