Sphinctospermum

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Sphinctospermum
Contributions from the U.S. National Herbarium (1906) (20660267756).jpg
Status TNC G4.svg
Apparently Secure  (NatureServe) [1]
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Fabales
Family: Fabaceae
Subfamily: Faboideae
Tribe: Robinieae
Genus: Sphinctospermum
Rose (1906)
Species:
S. constrictum
Binomial name
Sphinctospermum constrictum
(S.Watson) Rose (1906)
Synonyms [2]
  • Cracca constricta(S.Watson) Tidestr. (1935)
  • Tephrosia constrictaS.Watson (1889)

Sphinctospermum is a genus of flowering plants in the legume family, Fabaceae. It belongs to the subfamily Faboideae. It is a monotypic genus, containing the single species Sphinctospermum constrictum. It is native to North America, where it occurs in western and central Mexico and in Arizona in the southwestern United States. [2] [1] [3] The plant is known by the common name hourglass peaseed. [4]

Contents

This species occurs in grasslands and dry forests. It grows in sandy soils and is more common in wet years. [1]

Related Research Articles

<span class="mw-page-title-main">Mimosoideae</span> Subfamily of legumes

The Mimosoideae are a traditional subfamily of trees, herbs, lianas, and shrubs in the pea family (Fabaceae) that mostly grow in tropical and subtropical climates. They are typically characterized by having radially symmetric flowers, with petals that are twice divided (valvate) in bud and with numerous showy, prominent stamens.

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

The Fabaceae or Leguminosae, commonly known as the legume, pea, or bean family, are a large and agriculturally important family of flowering plants. It includes trees, shrubs, and perennial or annual herbaceous plants, which are easily recognized by their fruit (legume) and their compound, stipulate leaves. The family is widely distributed, and is the third-largest land plant family in number of species, behind only the Orchidaceae and Asteraceae, with about 765 genera and nearly 20,000 known species.

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

The Faboideae are a subfamily of the flowering plant family Fabaceae or Leguminosae. An acceptable alternative name for the subfamily is Papilionoideae, or Papilionaceae when this group of plants is treated as a family.

<i>Phaseolus</i> Genus of legumes

Phaseolus is a genus of herbaceous to woody annual and perennial vines in the family Fabaceae containing about 70 plant species, all native to the Americas, primarily Mesoamerica.

<i>Acacia</i> Genus of plants

Acacia, commonly known as wattles or acacias, is a genus of about 1084 species of shrubs and trees in the subfamily Mimosoideae of the pea family Fabaceae. Initially, it comprised a group of plant species native to Africa, South America and Australasia, but is now reserved for species mainly from Australia, with others from New Guinea, Southeast Asia and the Indian Ocean. The genus name is Neo-Latin, borrowed from the Greek ἀκακία, a term used by Dioscorides for a preparation extracted from the leaves and fruit pods of Vachellia nilotica, the original type of the genus. In his Pinax (1623), Gaspard Bauhin mentioned the Greek ἀκακία from Dioscorides as the origin of the Latin name.

<i>Centrolobium</i> Genus of legumes

Centrolobium is a Neotropical genus of flowering plants in the family Fabaceae, assigned to the informal monophyletic Pterocarpus clade of the Dalbergieae. The genus comprises mostly large trees to 30 m tall, characterised by an abundance of orange peltate glands that cover most parts of the plant, and fruits that are large winged samaras to 30 cm long with a spiny basal seed chamber.

<span class="mw-page-title-main">Crotalarieae</span> Tribe of legumes

Crotalarieae is a tribe of flowering plants belonging to the family Fabaceae. It includes rooibos (Aspalathus linearis), which is harvested for sale as a tisane.

<span class="mw-page-title-main">Cercidoideae</span> Subfamily of legumes

Cercidoideae is a subfamily in the pea family, Fabaceae. Well-known members include Cercis (redbuds), including species widely cultivated as ornamental trees in the United States and Europe, Bauhinia, widely cultivated as an ornamental tree in tropical Asia, and Tylosema, a semi-woody genus of Africa. The subfamily occupies a basal position within the Fabaceae and is supported as monophyletic in many molecular phylogenies. At the 6th International Legume Conference, the Legume Phylogeny Working Group proposed elevating the tribe Cercidae to the level of subfamily within the Leguminosae (Fabaceae). The consensus agreed to the change, which was fully implemented in 2017. It has the following clade-based definition:

The most inclusive crown clade containing Cercis canadensisL. and Bauhinia divaricataL. but not Poeppigia proceraC.Presl, Duparquetia orchidaceaBaill., or Bobgunnia fistuloides(Harms) J.H.Kirkbr. & Wiersema.

<i>Luetzelburgia</i> Genus of legumes

Luetzelburgia is a genus of flowering plants in the legume family, Fabaceae. It includes 14 species of trees and shrubs native to Brazil, Bolivia, and Colombia. Typical habitat is seasonally-dry tropical lowland woodland and wooded grassland, and occasionally lowland rain forests. The genus belongs to the subfamily Faboideae. It was traditionally assigned to the tribe Sophoreae, mainly on the basis of flower morphology; recent molecular phylogenetic analyses assigned Luetzelburgia into an informal, monophyletic clade called the "vataireoids". Keys for the different species of Luetzelburgia have been published.

<i>Strophostyles</i> Genus of legumes

Strophostyles is monophyletic three-species genus of flowering plants in the family Fabaceae, subfamily Faboideae. Common names for the genus include wild bean and fuzzybean. It consists of annual and perennial herbaceous vines, ranging in their native distribution from Nevada, east to Florida, and north to the Great Lakes and eastern Canada. The etymology of the name is strophe (turning) + stylos (style), referring to the curve of the style within the keel petal.

Hiroyoshi Ohashi is a botanist formerly at the University of Tokyo and Tohoku University. He began publishing on Japanese Arisaema in the early 1960s. He published a couple of miscellaneous notes on Arisaema in 1963 and 1964 and these were followed by a revision of the genus for Japan jointly published in 1980 with J. Murata, and by the Araceae treatment for the Wildflowers of Japan.

<span class="mw-page-title-main">Brongniartieae</span> Tribe of legumes

The tribe Brongniartieae is one of the subdivisions of the plant family Fabaceae, primarily found in tropical regions of the Americas and in Australia The members of this tribe consistently form a monophyletic clade in molecular phylogenetic analyses. The tribe does not currently have a node-based definition, but morphological synapomorphies have been identified:

"stamens united by filaments in an adaxially open tube; anthers alternately long and basifixed, short and versatile; anther connective inconspicuous; septa present between seeds in pods; aril lateral lobe present and fitting into heel of funicle; fine red glandular processes present in axils; and pollen tricolporate with opercula and no definite endoaperture."

<span class="mw-page-title-main">Indigofereae</span> Tribe of legumes

The tribe Indigofereae is a subdivision of the plant family Fabaceae. It is consistently recovered as a monophyletic clade in molecular phylogenies. The Indigofereae arose 30.0 ± 3.3 million years ago.

<span class="mw-page-title-main">Psoraleeae</span> Tribe of legumes

The tribe Psoraleeae is one of the subdivisions of the plant family Fabaceae. Recent phylogenetics has this tribe nested within tribe Phaseoleae.

<span class="mw-page-title-main">Sophoreae</span> Tribe of legumes

The tribe Sophoreae is one of the subdivisions of the plant family Fabaceae. Traditionally this tribe has been used as a wastebasket taxon to accommodate genera of Faboideae which exhibit actinomorphic, rather than zygomorphic floral symmetry and/or incompletely differentiated petals and free stamens. Various morphological and molecular analyses indicated that Sophoreae as traditionally circumscribed was polyphyletic. This led to a re-circumscription of Sophoreae, which resulted in the transfer of many genera to other tribes. This also necessitated the inclusion of two former tribes, Euchresteae and Thermopsideae, in the new definition of Sophoreae. Tribe Sophoreae, as currently circumscribed, consistently forms a monophyletic clade in molecular phylogenetic analyses. The Sophoreae arose 40.8 ± 2.4 million years ago.

<span class="mw-page-title-main">Swartzieae</span> Clade of legumes

The tribe Swartzieae is an early-branching monophyletic clade of the flowering plant subfamily Faboideae or Papilionaceae. Traditionally this tribe has been used as a wastebasket taxon to accommodate genera of Faboideae which exhibit actinomorphic, rather than zygomorphic floral symmetry and/or incompletely differentiated petals and free stamens. It was recently revised and most of its genera were redistributed to other tribes. Under its new circumscription, this clade is consistently resolved in molecular phylogenies. Members of this tribe possess "non-papilionate swartzioid flowers[…]largely characterized by a tendency to lack petals combined with a profusion and elaboration of free stamens" and a "lack of unidirectional order in the initiation of the stamens". They also have "complete or near complete fusion of sepals resulting from intercalary growth early in development, relatively numerous stamens, and a single or no petal, with other petals not at all apparent in development." The tribe is predicted to have diverged from the other legume lineages 48.9±2.8 million years ago.

<span class="mw-page-title-main">Robinioids</span> Clade of legumes

The robinioids are one of the four major clades in subfamily Faboideae of the plant family Fabaceae (Leguminosae). It is composed of the traditional tribes Loteae, Sesbanieae and Robinieae. It is a large and important clade that is distributed in mostly temperate areas. Species in this clade share a unique determinate root nodule structure. The clade is predicted to have diverged from the other legume lineages 48.3±1.0 million years ago.

<span class="mw-page-title-main">Inverted repeat-lacking clade</span> Group of flowering plants

The inverted repeat-lacking clade(IRLC) is a monophyletic clade of the flowering plant subfamily Faboideae (or Papilionaceae). Faboideae includes the majority of agriculturally-cultivated legumes. The name of this clade is informal and is not assumed to have any particular taxonomic rank like the names authorized by the ICBN or the ICPN. The clade is characterized by the loss of one of the two 25-kb inverted repeats in the plastid genome that are found in most land plants. It is consistently resolved in molecular phylogenies. The clade is predicted to have diverged from the other legume lineages 39.0±2.4 million years ago (in the Eocene). It includes several large, temperate genera such as AstragalusL., HedysarumL., MedicagoL., OxytropisDC., SwainsonaSalisb., and TrifoliumL..

<span class="mw-page-title-main">Exostyleae</span> Clade of legumes

The tribe Exostyleae is an early-branching monophyletic clade of the flowering plant subfamily Faboideae that are mostly found in Neotropical rainforests.

<span class="mw-page-title-main">Genisteae</span> Tribe of legumes

Genisteae is a tribe of trees, shrubs and herbaceous plants in the subfamily Faboideae of the family Fabaceae. It includes a number of well-known plants including broom, lupine (lupin), gorse and laburnum.

References

Further reading

Lavin, M. 1990. The genus Sphinctospermum (Leguminosae): Taxonomy and tribal relationships as inferred from a cladistic analysis of traditional data. Systematic Botany Vol. 15, No. 4 pp. 544–559