Common Names in English:
, cespitose or not, rhizomatous
or not, stoloniferous
or not. Roots
, principally adventitious. Stems (culms
) usually trigonous
, occasionally terete
, rarely compressed
, usually solid, rarely hollow or septate
. Leaves basal and/or cauline, alternate, usually 3-ranked, rarely 2-ranked or multi-ranked, bases
enclosing stem, margins
usually fused; junction of sheaths and blades
often with adaxial
flaps of tissue
of hair (ligules) ; blades frequently absent from some basal leaves
, rarely from cauline leaves, when present divergent or ascending
, flat, folded, plicate
, rolled, or terete, linear
) a shortened axis; glumaceous
) 1-many, spirally arranged
, sometimes 2-ranked, usually appressed
or ascending; scales usually all fertile
, each subtending
a single flower, sometimes proximal
and/or distal scales empty; lateral
spikes often with basal, usually empty, usually 2-keeled scale (prophyll) ; occasionally prophyll subtending and enclosing rachilla, bearing 1 pistillate
, sometimes (0-) 3 staminate flowers
and empty scales (Carex, Cymophyllus, and Kobresia) . Secondary inflorescences panicles, often modified to corymb, pseudoumbel, cyme (anthela), raceme
, spike, or capitulum (head
), rarely single spike, usually subtended by foliaceous
or, less frequently, glumaceous bracts; secondary inflorescences sometimes simulating spikelets (Carex, Cymophyllus, and Kobresia) . Flowers hypogynous, bisexual
in most genera, unisexual
in Scleria, Carex, Cymophyllus, and Kobresia; perianth absent or with (1-) 3-6(-30) bristles
and/or scales, usually falling off with fruit; stamens usually (1-) 3, rarely more, usually distinct
; pistils 1, 2-3(-4) -carpellate, fused, locule 1; style undivided or branches 2-3(-4) ; stigma sometimes papillate
. Fruits achenes, usually trigonous or biconvex
; pericarps thin (except in Scleria) . Seeds 1; testa thin, free
from pericarp; embryo basal; endosperm abundant. x
= 5-ca. 100.
Genera ca. 100, species ca. 5000 (27 genera, 843 species in the flora ) : worldwide.
No consensus exists regarding the number of genera and the overall relationships of genera within Cyperaceae. The most recent account of the family (P. Goetghebeur 1998) recognized 104 genera distributed among 4 subfamilies and 14 tribes . That arrangement differs somewhat from that of J. Bruhl (1995) . With one minor exception the arrangement of the family here follows that of Goetghebeur.
The family is characterized by the occurrence of a number of unusual cytological features including: (1) chromosomes with diffuse centromeres , (2) post-reductional meiosis, and (3) pollen grains formed from tetrads in which 3 of the 4 microspores fail to develop. The first two features are found in at least some Juncaceae and are unique to the two families. Juncaceae also have pollen in tetrads, but in that family all four microspores produce pollen grains. Some species in some genera of Cyperaceae (particularly Eleocharis) possess chromosomes with localized centromeres (S. S. Bir et al. 1993) . The wide range of chromosome numbers found in Cyperaceae is largely because of agmatoploidy; polyploidy has been hypothesized for some genera, especially Eleocharis, although polyploidy has not been demonstrated unequivocally.
Because of morphologic similarities in vegetative and inflorescence characters, the family has commonly been associated with Poaceae. Cytological features discussed above clearly indicate that to be a superficial similarity . Data from rbcL studies also support the view that Cyperaceae and Poaceae are not closely related (M. R. Duvall et al. 1993b; G. M. Plunkett et al. 1995) ; they do support the concept of close relationship between Cyperaceae and Juncaceae.
For most families of flowering plants the phenological data given are flowering times. Because most Cyperaceae cannot be reliably identified when in flower, in this volume fruiting time is given for all species by season , sometimes qualified by early, mid, or late, or by months. The fruiting time has been interpreted broadly to include the period when the fruit is more or less fully formed but not yet ripe . The fruiting period provided covers the entire range of the taxon . Quite a difference between fruiting periods in different parts of the range of the species may well occur, especially for widespread species and species with extensive elevation range.
For a recent, comprehensive review of the economic importance of Cyperaceae, see D. A. Simpson and C. A. Inglis (2001) .
- Whittaker & Margulis,1978
- Haeckel, 1866
- Cavalier-Smith, 1981
- Sinnott, 1935 ex Cavalier-Smith, 1998
- Vascular Plants
- Kenrick & Crane, 1997
- Brongniart, 1843
- Takhtajan, 1967
- Superorder: Juncanae () - Takhtajan, 1967
- Subclass: Commelinidae () - Takhtajan, 1967
- Class: Spermatopsida () - Brongniart, 1843
- Infraphylum: Radiatopses () - Kenrick & Crane, 1997
- Subphylum: Euphyllophytina ()
- Phylum: Tracheophyta () - Sinnott, 1935 ex Cavalier-Smith, 1998 - Vascular Plants
- Subkingdom: Viridaeplantae () - Cavalier-Smith, 1981
- Kingdom: Plantae () - Haeckel, 1866 - Plants
Status: Accepted Name
Last scrutiny: 21-Jun-2005
Members of the genus Machaerina
ZipcodeZoo has pages for 5 species, subspecies, varieties, forms, and cultivars in this genus:
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- An annotated catalogue of types of the University of Illinois mycological collections (ILL) / Urbana: University of Illinois Press, c1997. url p. 136, p. 137, p. 333.
- Novon a journal of botanical nomenclature from the Missouri Botanical Garden. 11 2001 St. Louis, MO: Missouri Botanical Garden, url p. 151, p. 187, p. 282, p. 310.
- Bruhl, J. 1995. Sedge genera of the world: Relationships and a new classification of the Cyperaceae. Austral. Syst. Bot. 8: 125-305.
- Goetghebeur, P. 1998. Cyperaceae. In: K. Kubitzki et al., eds. 1990+. The Families and Genera of Vascular Plants. 4+ vols. Berlin etc. Vol. 4, pp. 141-190.
- Mackenzie, K. K. 1931-1935. Cyperaceae [in part]. In: N. L. Britton et al., eds. 1905+. North American Floraâ¦. 47+ vols. New York. Vol. 18, parts 1-7, pp. 1-478.
- Simpson, D. A. and C. A. Inglis. 2001. Cyperaceae of economic, ethnobotanical and horticultural importance: A checklist. Kew Bull. 56: 257-360.
- Svenson, H. K. 1957. Cyperaceae. Tribe 2, Scirpeae. In: N. L. Britton et al., eds. 1905+. North American Flora.... 47+ vols. New York. Vol. 18, pp. 505-556.
- Tucker, G. C. 1987. The genera of Cyperaceae in the southeastern United States. J. Arnold Arbor. 68: 361-445.
- Bisby, F.A., Y.R. Roskov, M.A. Ruggiero, T.M. Orrell, L.E. Paglinawan, P.W. Brewer, N. Bailly, J. van Hertum, eds (2007). Species 2000 & ITIS Catalogue of Life: 2007 Annual Checklist. Species 2000: Reading, U.K.
- Brands, S.J. (comp.) 1989-present. The Taxonomicon. Universal Taxonomic Services, Zwaag, The Netherlands. Accessed January 12, 2012.
- Global Biodiversity Information Facility. Accessed February 28, 2008. http://www.gbif.org Mediated distribution data from 2 providers.
- Ruggiero M., Gordon D., Bailly N., Kirk P., Nicolson D. (2011). The Catalogue of Life Taxonomic Classification, Edition 2, Part A. In: Species 2000 & ITIS Catalogue of Life: 2011 Annual Checklist (Bisby F.A., Roskov Y.R., Orrell T.M., Nicolson D., Paglinawan L.E., Bailly N., Kirk P.M., Bourgoin T., Baillargeon G., Ouvrard D., eds). DVD; Species 2000: Reading, UK.
- USDA, NRCS. 2005. The PLANTS Database, Version 3.5 (http://plants.usda.gov). National Plant Data Center, Baton Rouge, LA 70874-4490 USA.
- World Checklist of Selected Plant Families. Release date: November 27, 2009
Accessed through GBIF Data Portal February 28, 2008:
- Bernice Pauahi Bishop Museum: Bishop Museum Natural History Specimen Data
- USDA PLANTS: USDA PLANTS Database
- Biodiversity Heritage Library NamebankID: 2660721
- Catalogue of Life Accepted Name Code: Kew-252749
- Globally Unique Identifier: urn:lsid:ipni.org:names:310342-1
- Integrated Taxonomic Information System (ITIS) Taxonomic Serial Number (TSN): 40343
- Natural Heritage Network Species Identifier: PMCYP0J010
- U.S.D.A. Plant Symbol: MAAN
- Zipcode Zoo Species Identifier: 48763