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Overview

Distribution

National Distribution

United States

Origin: Exotic

Regularity: Regularly occurring

Currently: Unknown/Undetermined

Confidence: Confident

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Distribution in Egypt

Sinai (St.Katherine).

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© Bibliotheca Alexandrina

Source: Bibliotheca Alexandrina - EOL Ar

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Distribution: Pakistan (Baluchistan & N.W.F.P.); southern Europe and the Mediterranean eastwards to Nepal and southern USSR.
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Physical Description

Morphology

Physical Description

Annuals, Terrestrial, not aquatic, Stems trailing, spreading or prostrate, Stems nodes swollen or brittle, Stems erect or ascending, Stems geniculate, decumbent, or lax, sometimes rooting at nodes, Stems solitary, Stems caespitose, tufted, or clustered, Stems terete, round in cross section, or polygonal, Stem internodes hollow, Stems with inflorescence less than 1 m tall, Stems, culms, or scapes exceeding basal leaves, Leaves mostly cauline , Leaves conspicuously 2-ranked, distichous, Leaves sheathing at base, Leaf sheath mostly open, or loose, Leaf sheath hairy, hispid or prickly, Leaf sheath hairy at summit, throat, or collar, Leaf sheath and blade differentiated, Leaf blades linear, Leaf blades 2-10 mm wide, Leaf blades 1-2 cm wide, Leaf blades mostly flat, Leaf blades mostly glabrous, Leaf blades more or less hairy, Ligule present, Ligule an unfringed eciliate membrane, Inflorescence terminal, Inflorescence an open panicle, openly paniculate, branches spreading, Inflorescence solitary, with 1 spike, fascicle, glomerule, head, or cluster per stem or culm, Inflorescence branches more than 10 to numerous, Flowers bisexual, Spikelets pedicellate, Spikelets laterally compressed, Spikelet 3-10 mm wide, Spikelet less than 3 mm wide, Spikelets with 2 florets, Spikelets with 3-7 florets, Spikelets solitary at rachis nodes, Spikelets all alike and fertille, Spikelets bisexual, Spikelets disarticulating beneath or bet ween the florets, Rachilla or pedicel hairy, Glumes present, empty bracts, Glumes 2 clearly present, Glumes equal or subequal, Glumes equal to or longer than adjacent lemma, Glume equal to or longer than spikelet, Glumes 4-7 nerved, Lemma similar in texture to glumes, Lemma coriaceous, firmer or thicker in texture than the glumes, Lemma 8-15 nerved, Lemma body or surface hairy, Lemma apex dentate, 2-fid, Lemma distinctly awned, more than 2-3 mm, Lemma with 3 awns, Lemma awn 1-2 cm long, Lemma awn 2-4 cm long or longer, Lemma awn subapical or dorsal, Lemma awn twisted, spirally coiled at base, like a corkscrew, Lemma awn once geniculate, bent once, Lemma margins thin, lying flat, Lemma margins inrolled, tightly covering palea and caryopsis, Lemma straight, Callus or base of lemma evidently hairy, Callus hairs shorter than lemma, Lemma surface pilose, setose or bristly, Palea present, well developed, Palea membranous, hyaline, Palea shorter than lemma, Palea about equal to lem ma, Palea 2 nerved or 2 keeled, Palea keels winged, scabrous, or ciliate, Stamens 3, Styles 2-fid, deeply 2-branched, Stigmas 2, Fruit - caryopsis, Caryopsis hairy all over.
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Dr. David Bogler

Source: USDA NRCS PLANTS Database

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Description

Annual; culms 30-100 cm high, erect or ascending, slender to rather stout, simple. Leaf-blades up to 30 cm long, 3-8 mm wide, sparsely hairy to ciliate; ligules 2-5 mm long. Panicle subsecund, up to 30(-50) cm long and 12 cm wide, loose with smooth or faintly scaberulous branches. Spikelets 18-30 mm long, 2-3-flowered, the rhachilla articulated beneath each floret; glumes lanceolate, acuminate; lemmas 12-20 mm long, densely bearded with hairs up to 3 mm long around the callus, densely hairy with long stiff hairs up to the insertion of the awn, scabrid or asperulous on the nerves above, narrowed upwards and finely 2-toothed at the apex, the teeth aristulate with bristles 3-12 mm long; awn 3-6 cm long, geniculate, the column usually darker than the bristle, glabrous to faintly asperulous.
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Type Information

Isotype for Avena almeriensis Gand.
Catalog Number: US 1445651
Collection: Smithsonian Institution, National Museum of Natural History, Department of Botany
Verification Degree: Card file verified by examination of alleged type specimen
Preparation: Pressed specimen
Collector(s): M. Gandoger
Year Collected: 1903
Locality: Sierra de Lucar., Almeria, Spain, Europe
  • Isotype: Gandoger, M. 1905. Bull. Soc. Bot. France. 52: 443.
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© Smithsonian Institution, National Museum of Natural History, Department of Botany

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Life History and Behavior

Cyclicity

Flower/Fruit

Fl. & Fr. Per.: February-May.
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Life Expectancy

Annual.

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Avena barbata

The following is a representative barcode sequence, the centroid of all available sequences for this species.


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Source: Barcode of Life Data Systems (BOLD)

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Statistics of barcoding coverage: Avena barbata

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 8
Specimens with Barcodes: 12
Species With Barcodes: 1
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Conservation

Conservation Status

National NatureServe Conservation Status

United States

Rounded National Status Rank: NNA - Not Applicable

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NatureServe Conservation Status

Rounded Global Status Rank: GNR - Not Yet Ranked

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Wikipedia

Avena barbata

Avena barbata is a species of wild oat known by the common name slender wild oat. It has edible seeds. It is a diploidized autotetraploid grass (2n=4x=28).[1] Its diploid ancestors are A. hirtula Lag. and A. wiestii Steud (2n=2x=14), which are considered Mediterranean and desert ecotypes, respectively, comprising a single species.[2] A wiestii and A. hirtula are widespread in the Mediterranean Basin, growing in mixed stands with A. barbata, though they are difficult to tell apart.

This is a winter annual grass with thin tillers (stems) growing up to 60 to 80 centimeters in maximum height, but known to sometimes grow taller. The bristly spikelets are 2 to 3 centimeters long, not counting the bent awn which is up to 4 centimeters in length. Avena barbata largely reproduces by selfing in natural populations, with very low rates of outcrossing.[3][4]

A. barbata is native to central Asia (as far east as Pakistan) and the Mediterranean Basin. As an introduced species it also occurs in other Mediterranean-like habitats of New Zealand, Australia, South Africa, Argentina, Chile, Brazil, and Uruguay. In Europe it has been reported in Finland, France, Germany, Norway, Bulgaria, and Austria. In North America it is an introduced species and noxious weed, where it is especially widespread in California. In California it has displaced native species of grass.[5] It is also found in Oregon, Washington, Hawaii, Massachusetts, Nevada, Arizona, and New Mexico [2].

Genetic evidence indicates that A. barbata in Argentina and California originated from Spain, during the Spanish colonization of the Americas.[6]

Genetic Studies of Californian Populations[edit]

Californian populations of Avena barbata represent one of the most extensively studied examples of putative “ecotypes” in the plant literature. Its population genetics and evolution have been extensively examined since 1967,[7] primarily in the laboratories of Robert Allard and Subodh Jain and their many students in the 1960s, 1970's, 1980's, and 1990’s at U.C. Davis,[8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23] and more recently by Robert Latta at the University of Dalhousie University in Nova Scotia [3],[4].

The general pattern that emerged from these earlier studies was that throughout the Central Valley of California, consisting of semiarid grasslands and oak savannahs, and extending south to San Diego, populations of this species were dominated by a monomorphic phenotype possessing dark/black seeds with hairy lemmas, as well as smooth leaf sheaths; these morphological characters were correlated with a specific isozyme pattern as well as a specific ribosomal DNA genotype. This "ecotype" is called the "xeric" type. Populations outside the Central Valley, along the coastal strip, the intermontane regions of the coast ranges, and the higher foothills of the Sierra Nevada mountains, were either monomorphic for white seeds with generally smooth lemmas and hairy leaf sheaths, or were polymorphic with varying mixtures of the seed and leaf sheath characters. These populations were also either monomorphic or polymorphic for isozyme patterns and ribosomal DNA genotypes other than the xeric type; they were are called the "mesic" type. The mesic type has never apparently been observed south of approximately the same latitude as Monterey, either in coastal ranges, the Central Valley, or the foothills of the Sierras. When the morphological traits as well as the allozyme and ribosomal DNA genotypes were considered together, it is argued that there are six ecotypes in the otherwise "mesic" classification.[23]

Whole-plant studies also showed that the xeric and mesic types differed from each other for many characters such as the flag leaf, primary stem height, number of tillers, weight and number of seeds, dry weight, and flowering time, with the mesic ecotype being generally larger and more fecund, overall, than the xeric type; further, the flag leaves of the xeric type were consistently smaller than the mesic type under many conditions.[18][19] It was further shown that xeric populations that were monomorphic for the seed and leaf sheath characters and allozymes had less genetic variation for quantitative genetics characters than mesic populations; however, quantitative genetic variation existed in all xeric or mesic populations that were studied.[21] Consequently, with all genetic characters studied, xeric populations of the xeric ecotype were more similar to each other than they were to the mesic ecotype, and the evidence indicated that the various ecotypes represented significant linkage disequilibrium and coadapted genetic complexes.[24]

For field identification purposes, the leaf sheath pubescence in the seedling stage and lemma color at seed maturity as well as the flag leaf dimensions would reliably separate the xeric from the mesic ecotypes throughout California.

Early on it was speculated that the genetic patterns observed in A. barbata were highly correlated with rainfall and temperature. The general pattern at both a macro- and microgeographical scale was that the monomorphic "xeric" type occurred in those regions with between 250mm and 500mm of rainfall, while the polymorphic and monomorphic "mesic" populations occurred in those areas of California with greater than 500mm.[11][15][23]

Regardless of the correlations found with the mesic and xeric genotypes with rainfall in California, greenhouse experiments have not shown that the xeric type has greater reproductive capacity or other physiologic [25] superiority to the mesic under artificially induced wet or dry conditions. In fact Latta argues that the mesic type is superior to the xeric, and may be supplanting the xeric in those areas where the xeric has been dominant, at least in Northern California.[26]

Genetic Studies of Mediterranean Populations[edit]

Avena barbata has been studied in Spain, Israel, and Morocco by students and colleagues of R.W. Allard at U.C. Davis, Pèrez de la Vega and Pedro Garcia of the University of Leon, and E. Nevo in Israel ([27][28][29]).[30] The general pattern that has emerged is that there is more genetic variability in the Mediterranean populations than there are in Californian populations. Further, the multi-locus genotypes found in California are unique to California. The Mediterranean populations have their own unique sets of multi-locus genotypes. There is a unique 14-locus allozyme genotype specific to the colder regions of Spain.

Neither the "xeric" or monomprphic "mesic" genotype described in California are found in Spain.

Genetic Studies of Argentinian Populations[edit]

Both Californian and Argentinian populations represent a subset of the genetic variability found in Spain, on a locus by locus comparison. However, unlike Spain, Argentina has one widespread 14 locus allozme genotype called the "Pampeano" type, that is not found in Spain; it differs from the Californian "xeric" type at three of the 14 loci examined. The "xeric" Californian type is found in 6% of the plants examined in Argentina; the "xeric" type also occurs in Chile.

The genetic evidence indicates that Avena barbata came to both Argentina and California from south west Spain.[6]

References[edit]

  1. ^ [1]
  2. ^ Allard, R.W.; Garcia, P.; Saenz-de-Miera, L.E.; Perez, de la Vega (1993). "Evolution of multilocus genetic structure in Avena hirtula and Avena barbata". Genetics 135: 1125–1139. 
  3. ^ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1212502/
  4. ^ http://www.pnas.org/content/69/8/2100.short
  5. ^ California Invasive Plant Council
  6. ^ a b Guma, Irma-Rosana; Pèrez de la Vega, Marcelino; Garcia, Pedro (2006). "Isozyme variation and genetic structure of populations of Avena barbata from Argentina". Genetic Resources and Crop Evolution 53 (3): 587–601. doi:10.1007/s10722-004-2682-2. 
  7. ^ Jain, S. K.; Marshall, D.R. (1967). "Population studies in predominantly self-pollinating species. X. Variation in natural populations of Avena fatua and Avena barbata". American Naturalist 51: 49–69. 
  8. ^ Marshall, D.R.; Jain, S.K. (1969). "Genetic polymorphism in natural populations of Avena fatua and A. barbata". Nature 221: 276–278. doi:10.1038/221276a0. 
  9. ^ Marshall, D.R.; Allard, R.W. (1970). "Maintenance of isozyme polymorphisms in natural populations of Avena barbata". Genetics 66: 393–399. 
  10. ^ Marshall, D.R.; Allard, R.W. (1970). "Isozyme polymorphisms in natural populations of Avena fatua and A. barbata". Heredity: 373–382. 
  11. ^ a b Hamrick, J.L.; Allard, R.W. (1972). "Microgeographical variation in allozyme frequencies in Avena barbata". Proc. Nat. Acad. Sci. 69: 2100–2104. doi:10.1073/pnas.69.8.2100. 
  12. ^ Clegg, M.T.; Allard, R.W. (1972). "Patterns of genetic differentiation in the slender wild oat". Proc. Nat. Acad. Sci. 69: 1820–1824. doi:10.1073/pnas.69.7.1820. 
  13. ^ Allard, R.W.; Babbel, G.R.; Clegg, M.T.; Kahler, A.L. (1972). "Evidence for coadaptation in Avena barbata". Proc. Nat. Acad. Sci.: 3043–3048. 
  14. ^ Hamrick, J.L.; Allard, R.W. (1975). "Microgeographical variation in allozyme frequencies in Avena barbata". Proc. Nat. Acad. Sci. 69: 2100–2104. 
  15. ^ a b Miller, R.D. (1977). "Genetic Variability in the Slender Wild Oat Avena barbata in California". Ph.D. dissertation, University of California, Davis. 
  16. ^ Allard, R.W.; Miller, R.D.; Kahler, A.L. (1978). The relationship between degree of environmental heterogeneity and genetic polymorphism. IN: 'Structure and functioning of plant populations'. Verhandelingen der Koninklijke Nederlandse Akademie van Wetenschappen, Afdeling Naturkunde, Tweede Reeks, deel 70. 
  17. ^ Hakim-Elahi, A. (1980). "Temporal changes in the population structure of the slender wild oat (Avena barbata) as measured by allozyme polymorphisms". Ph.D. dissertation, University of California, Davis. 
  18. ^ a b Price, S.C. (1980). "Polymorphism and phenomorphism in the tetraploid slender wild oat Avena barbata". Ph.D. dissertation University of California, Davis. 
  19. ^ a b Hutchinson, E.S. (1982). "Genetic markers and ecotypic differentiation of Avena bartata Pott ex Link". Ph.D. dissertation, University of California, Davis. 
  20. ^ Pinero, D. (1982). "Correlations between enzyme phenotypes and physical environment in California populations of Avena barbata and Avena fatua". Ph.D. dissertation, University of California, Davis. 
  21. ^ a b Cluster, P.D. (1984). "Correlation between genetic variation for allo- zyme markers and quantitative characters in Avena barbata Pott. ex. Link". Ph.D. Dissertation, University of California, Davis. 
  22. ^ Price, S.C.; Shumaker, K.M.; Kahler, A.L.; Allard, R.W.; Hill, J.E. (1984). "Estimates of population differentiation obtained from enzyme polymorphisms and quantitative characters". J. Heredity 75 (2): 141–142. 
  23. ^ a b c Cluster, P.D.; Allard, R.W. (1995). "Evolution of ribosomal DNA (rDNA) genetic structure in colonial Californain populations of Avena barbata". Genetics 139: 941–954. 
  24. ^ Allard, Robert W. (1999). "History of Plant Population Genetics". Genetics 33: 1–27. 
  25. ^ Sherrard, Mark E.; Maherali, Hafiz (2006). "The adaptive significance of drought escape in Avena barbata, an annual grass". Evolution 60: 2478–2489. doi:10.1554/06-150.1. 
  26. ^ Latta, R.G. (2009). "Testing for local adaptation in Avena barbata: a classic example of ecotypic divergence". Molecular Ecology 18: 3781–3791. doi:10.1111/j.1365-294x.2009.04302.x. 
  27. ^ Kahler, A.L.; Allard, R.W.; Krzakowa, M.; Nevo, E. (1980). "Associations between isozyme phenotypes and environment in the slender wild oat (Avena barbata) in Israel". Theor. Appl. Genetics 56 (1-2): 31–47. 
  28. ^ Garcia, P.; Morris, M.I.; Sàenz-de-Miera, L.E.; Allard, R.W.; Pèrez de la Vega, M.; Ladinsky, G. (1991). "Genetic diversity and adaptedness in tetraploid Avena barbata and its diploid ancestors Avena hirtula and Avena wiestii". Proc. Nat. Acad. Sci.: 1207–1211. 
  29. ^ Allard, R.W.; Garcia, P.; Sàenz-de-Miera, L.E.; Pèrez de la Vega, M. (1993). "Evolution of multilocus genetic structure in Avena hirtula and Avena barbata". Genetics 135: 1125–1139. 
  30. ^ Benchacho, M.R.; Guma, R.; Pèrez de la Vega, M. (2002). "The genetic structure of tetraploid Avena: a comparison of isozyme and RAPD markers". Cell Mol. Lett. 7 (2A): 465–469. 
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Notes

Comments

Avena barbata subsp. wiestii (Steud.) Mansf. has been reported from Pakistan, but its presence cannot be fonfirmed. Several authors (e.g. Bor, l.c.) distinguish it from subsp. barbata by the presence of a lateral tooth at the base of each bristle at the tip of the lemma, a character which is unreliable. They are best distinguished by spikelet length (16-20 mm in subsp. wiestii., 20-30 mm in subsp. barbata) and length of the lowest lemma (12-16 mm and 16-20 mm respectively). Subsp. wiestii also has a larger, more floriferous panicle.
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