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Purple False Brome

Brachypodium distachyon (L.) P. Beauv.

Distribution in Egypt

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Nile region, oases, Mediterranean region, eastern desert, Gebel Elba and Sinai.

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Global Distribution

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Mediterranean region, southwest Asia to Pakistan and central Asia.

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Habitat

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Sandy and gravelly soils, mostly as a weed of cultivation.

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Life Expectancy

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Annual.

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Description

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Annual. Culms tufted, usually ascending, infrequently erect, up to 15(–40) cm tall. Leaf sheaths loosely to densely pilose; leaf blades lanceolate, flat, rather stiff, glaucous, 1–12 cm, 3–4 mm wide, loosely pilose, margins scabrous-pectinate, apex acuminate; ligule ca. 1 mm. Raceme 2–4 cm, spikelets 1–3 crowded at apex of peduncle. Spikelets 2–3 cm, laterally compressed, florets 10–16; glumes pilose or glabrous, apex acute, lower glume lanceolate, 5–6 mm, 5-veined, upper glume lanceolate-oblong, 7–8 mm, 7-veined; lemmas 7.5–10 mm, glabrous, thinly setose or pubescent; awn 7–15 mm. Anthers 0.5–1 mm.
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
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Flora of China Vol. 22: 368 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of China @ eFloras.org
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Wu Zhengyi, Peter H. Raven & Hong Deyuan
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Description

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Tufted annual; culms up to 40 cm high, but usually much less, geniculately ascending, rarely erect, glabrous with the upper internodes smooth or scabrid or rarely pubescent throughout. Leaf-blades up to 12 cm long and 4 mm wide, flat, lanceolate-acuminate, rather stiff, glaucous; loosely pilose, scabrid-pectinate on the margins, sheaths loosely to densely pilose. Inflorescence with 1-3 spikelets crowded at the tip of the peduncle. Spikelets 2-3 cm long, slightly compressed, oblong-lanceolate, 10-16-flowered, glaucous; glumes unequal, hairy or glabrous, the lower lanceolate, acute, 5-6 mm long, 5-nerved, the upper lanceolate-oblong, acute, 7-8 mm long, 7-nerved; lemmas lanceolate-oblong, involute, 7.5-10 mm long, glabrous or with a few stiff bristles to pubescent, tipped by an awn up to 15 mm long; anthers 0.5-1 mm long.
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of Pakistan Vol. 0: 588 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of Pakistan @ eFloras.org
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S. I. Ali & M. Qaiser
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Distribution

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Distribution: Pakistan (Punjab, N.W.F.P. & Kashmir); Mediterranean region; South west and Central Asia; introduced elsewhere.
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
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Flora of Pakistan Vol. 0: 588 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of Pakistan @ eFloras.org
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S. I. Ali & M. Qaiser
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Flower/Fruit

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Fl. & Fr. Per.: April-May.
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
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Flora of Pakistan Vol. 0: 588 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of Pakistan @ eFloras.org
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S. I. Ali & M. Qaiser
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Habitat & Distribution

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Dry stony places. Xizang (Mainling) [Afghanistan, Pakistan, Tajikistan, Turkmenistan; N Africa, SW Asia, S Europe; introduced elsewhere].
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of China Vol. 22: 368 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of China @ eFloras.org
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Wu Zhengyi, Peter H. Raven & Hong Deyuan
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eFloras.org
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Synonym

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Bromus distachyos Linnaeus, Cent. Pl. 2: 8. 1756; Agro-pyron distachyon (Linnaeus) Chevallier; Festuca distachya (Linnaeus) Roth; Trachynia distachya (Linnaeus) Link; Zerna distachya (Linnaeus) Panzer ex B. D. Jackson.
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Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of China Vol. 22: 368 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
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Flora of China @ eFloras.org
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Wu Zhengyi, Peter H. Raven & Hong Deyuan
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eFloras.org
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Brief Summary

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Brachypodium distachyon has a native distribution including west Asia, tropical Asia, east Africa, southern Europe; occurs broadly as an alien species throughout North America. this taxon is found in a variety of habitats including forest edges, abandoned plantations, beaches, coastal dunes, orchards and waste places.

This annual grass, also known as Purple false brome, can attain a height of almost one half meter. The culm is terete in form (cylindrical tapering at the joints).

False purple brome has been pronounced as a model organism for molecular genetics experiments due to its unusually small genome, combined with short life cycle and compact growth form.
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Physical Description

provided by USDA PLANTS text
Annuals, Terrestrial, not aquatic, Stems nodes swolle n or brittle, Stems geniculate, decumbent, or lax, sometimes rooting at nodes, Stems caespitose, tufted, or clustered, Stems terete, round in cross section, or polygonal, Stem nodes bearded or hairy, 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 smooth, glabrous, Leaf sheath hairy, hispid or prickly, Leaf sheath and blade differentiated, Leaf blades linear, Leaf blades very narrow or filiform, less than 2 mm wide, Leaf blades 2-10 mm wide, Leaf blades mostly flat, Leaf blade margins folded, involute, or conduplicate, Leaf blades more or less hairy, Leaf blades scabrous, roughened, or wrinkled, Leaf blades glaucous, blue-green, or grey, or with white glands, Ligule present, Ligule an unfringed eciliate membrane, Inflorescence terminal, Inflorescence solitary, with 1 sp ike, fascicle, glomerule, head, or cluster per stem or culm, Inflorescence a panicle with narrowly racemose or spicate branches, Inflorescence with 2-10 branches, Flowers bisexual, Spikelets pedicellate, Spikelets laterally compressed, Spikelets dorsally compressed or terete, Spikelet less than 3 mm wide, Spikelets with 8-40 florets, Spikelets solitary at rachis nodes, Spikelets all alike and fertille, Spikelets bisexual, Spikelets disarticulating above the glumes, glumes persistent, Spikelets disarticulating beneath or between the florets, Spikelets closely appressed or embedded in concave portions of axis, Rachilla or pedicel glabrous, Glumes present, empty bracts, Glumes 2 clearly present, Glumes distinctly unequal, Glumes shorter than adjacent lemma, Glumes 4-7 nerved, Lemma similar in texture to glumes, Lemma coriaceous, firmer or thicker in texture than the glumes, Lemma 5-7 nerved, Lemma glabrous, Lemma body or surface hairy, Lemma apex acute or acuminate, Lemma disti nctly awned, more than 2-3 mm, Lemma with 1 awn, Lemma awn less than 1 cm long, Lemma awn 1-2 cm long, Lemma awned from tip, Lemma awns straight or curved to base, Lemma margins thin, lying flat, Lemma straight, Palea present, well developed, Palea membranous, hyaline, Palea about equal to lemma, Palea 2 nerved or 2 keeled, Stamens 3, Styles 2-fid, deeply 2-branched, Stigmas 2, Fruit - caryopsis, Caryopsis ellipsoid, longitudinally grooved, hilum long-linear, Caryopsis hairy at apex.
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USDA PLANTS text

Brachypodium distachyon

provided by wikipedia EN

Brachypodium distachyon, commonly called purple false brome[1] or stiff brome,[2] is a grass species native to southern Europe, northern Africa and southwestern Asia east to India. It is related to the major cereal grain species wheat, barley, oats, maize, rice, rye, sorghum, and millet. It has many qualities that make it an excellent model organism for functional genomics research in temperate grasses, cereals, and dedicated biofuel crops such as switchgrass. These attributes include small genome (~270 Mbp) diploid accessions, a series of polyploid accessions, a small physical stature, self-fertility, a short lifecycle, simple growth requirements, and an efficient transformation system. The genome of Brachypodium distachyon (diploid inbred line Bd21) has been sequenced and published in Nature in 2010.[3]

Model organism

Although Brachypodium distachyon has little or no direct agricultural significance, it has several advantages as an experimental model organism for understanding the genetic, cellular and molecular biology of temperate grasses. The relatively small size of its genome makes it useful for genetic mapping and sequencing. In addition, only ~21% of the Brachypodium genome consists of repetitive elements, compared to 26% in rice and ~80% in wheat, further simplifying genetic mapping and sequencing.[3] At about 272 million base pairs and with five chromosomes, it has a small genome for a grass species. Brachypodium distachyon's small size (15–20 cm) and rapid life cycle (eight to twelve weeks) are also advantageous for research purposes.[4] For early-flowering accessions it can take as little as three weeks from germination to flower (under an appropriate inductive photoperiod). The small size of some accessions makes it convenient for cultivation in a small space. As a weed it grows easily without specialized growing conditions.

This Brachypodium is emerging as a powerful model with a growing research community. The International Brachypodium Initiative (IBI) held its first genomics meeting and workshop at the PAG XIV conference in San Diego, California, in January 2006. The goal of the IBI is to promote the development of B. distachyon as a model system and will develop and distribute genomic, genetic, and bioinformatics resources such as reference genotypes, BAC libraries, genetic markers, mapping populations, and a genome sequence database. Recently, efficient Agrobacterium-mediated transformation systems have been developed for a range of Brachypodium genotypes,[5][6][7] enabling the development of T-DNA mutant collections.[6][8][9] The characterization and distribution of T-DNA insertion lines has been initiated to facilitate the understanding of gene function in grasses.[10]

By now, Brachypodium distachyon has established itself as an important tool for comparative genomics.[11] It is now emerging as a model for crop plant disease, facilitating the model-to-crop transfer of knowledge on disease resistance.[12] Brachypodium distachyon is also becoming a useful model system for studies of evolutionary developmental biology, in particular to contrast molecular genetic mechanisms with dicotyledon model systems, notably Arabidopsis thaliana.[13] The finding of higher genetic diversity in eastern Iberian populations occurring in basic soils suggests that these populations can be better adapted than those occurring in western areas of the Iberian Peninsula where the soils are more acidic and accumulate toxic Al ions.[14]

Notes

  1. ^ USDA, NRCS (n.d.). "Brachypodium distachyon". The PLANTS Database (plants.usda.gov). Greensboro, North Carolina: National Plant Data Team. Retrieved 10 January 2016.
  2. ^ BSBI List 2007 (xls). Botanical Society of Britain and Ireland. Archived from the original (xls) on 2015-06-26. Retrieved 2014-10-17.
  3. ^ a b The International Brachypodium Initiative (2010). "Genome sequencing and analysis of the model grass Brachypodium distachyon". Nature. 463 (7282): 763–8. Bibcode:2010Natur.463..763T. doi:10.1038/nature08747. PMID 20148030.
  4. ^ Li, Chuan; Rudi, Heidi; Stockinger, Eric J.; Cheng, Hongmei; Cao, Moju; Fox, Samuel E.; Mockler, Todd C.; Westereng, Bjørge; Fjellheim, Siri; Rognli, Odd Arne; Sandve, Simen R. (2012). "Comparative analyses reveal potential uses of Brachypodium distachyon as a model for cold stress responses in temperate grasses". BMC Plant Biol. 12 (65): 65. doi:10.1186/1471-2229-12-65. PMC 3487962. PMID 22569006.
  5. ^ Vogel, John P.; Garvin, David F.; Leong, Oymon M.; Hayden, Daniel M. (2006). "Agrobacterium-mediated transformation and inbred line development in the model grass Brachypodium distachyon". Plant Cell, Tissue and Organ Culture. 84 (2): 100179–91. doi:10.1007/s11240-005-9023-9. S2CID 23419929.
  6. ^ a b Vain, Philippe; Worland, Barbara; Thole, Vera; McKenzie, Neil; Alves, Silvia C.; Opanowicz, Magdalena; Fish, Lesley J.; Bevan, Michael W.; Snape, John W. (2008). "Agrobacterium-mediated transformation of the temperate grass Brachypodium distachyon (genotype Bd21) for T-DNA insertional mutagenesis". Plant Biotechnology Journal. 6 (5): 236–45. doi:10.1111/j.1467-7652.2007.00308.x. PMID 18004984.
  7. ^ Alves, Sílvia C; Worland, Barbara; Thole, Vera; Snape, John W; Bevan, Michael W; Vain, Philippe (2009). "A protocol for Agrobacterium-mediated transformation of Brachypodium distachyon community standard line Bd21". Nature Protocols. 4 (5): 638–49. doi:10.1038/nprot.2009.30. PMID 19360019. S2CID 21608193.
  8. ^ Thole, Vera; Alves, Sílvia C; Worland, Barbara; Bevan, Michael W; Vain, Philippe (2009). "A protocol for efficiently retrieving and characterising Flanking Sequence Tags (FSTs) in Brachypodium distachyon T-DNA insertional mutants". Nature Protocols. 4 (5): 650–61. doi:10.1038/nprot.2009.32. PMID 19360020. S2CID 24001172.
  9. ^ Thole, Vera; Peraldi, Antoine; Worland, Barbara; Nicholson, Paul; Doonan, John H.; Vain, Philippe (2012). "T-DNA mutagenesis in Brachypodium distachyon". J Exp Bot. 63 (2): 567–76. doi:10.1093/jxb/err333. PMID 22090444.
  10. ^ Thole, Vera; Worland, Barbara; Wright, Jonathan; Bevan, Michael W.; Vain, Philippe (2010). "Distribution and characterization of more than 1000 T-DNA tags in the genome of Brachypodium distachyon community standard line Bd21". Plant Biotechnology Journal. 8 (6): 734–47. doi:10.1111/j.1467-7652.2010.00518.x. PMID 20374523.
  11. ^ Huo, Naxin; Vogel, John P.; Lazo, Gerard R.; You, Frank M.; Ma, Yaqin; McMahon, Stephanie; Dvorak, Jan; Anderson, Olin D.; Luo, Ming-Cheng; Gu, Yong Q. (2009). "Structural characterization of Brachypodium genome and its syntenic relationship with rice and wheat". Plant Mol Biol. 70 (1–2): 47–61. doi:10.1007/s11103-009-9456-3. PMID 19184460.
  12. ^ Goddard, Rachel; Peraldi, Antoine; Ridout, Chris; Nicholson, Paul (2014). "Enhanced Disease Resistance Caused by BRI1 Mutation Is Conserved Between Brachypodium distachyon and Barley (Hordeum Vulgare)". Mol Plant Microbe Interact. 27 (10): 1095–1106. doi:10.1094/MPMI-03-14-0069-R. PMID 24964059.
  13. ^ Pacheco-Villalobos, David; Sankar, Martial; Ljung, Karin; Hardtke, Christian S. (2013). "Disturbed Local Auxin Homeostasis Enhances Cellular Anisotropy and Reveals Alternative Wiring of Auxin-ethylene Crosstalk in Brachypodium distachyon Seminal Roots". PLOS Genetics. 9 (6): e1003564. doi:10.1371/journal.pgen.1003564. PMC 3688705. PMID 23840182.
  14. ^ Marques, Isabel; Shiposha, Valeriia; López-Alvarez, Diana; Manzaneda, Antonio J.; Hernandez, Pilar; Olonova, Marina; Catalán, Pilar (2017-06-15). "Environmental isolation explains Iberian genetic diversity in the highly homozygous model grass Brachypodium distachyon". BMC Evolutionary Biology. 17 (1): 139. doi:10.1186/s12862-017-0996-x. ISSN 1471-2148. PMC 5472904. PMID 28619047.

References

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Brachypodium distachyon: Brief Summary

provided by wikipedia EN

Brachypodium distachyon, commonly called purple false brome or stiff brome, is a grass species native to southern Europe, northern Africa and southwestern Asia east to India. It is related to the major cereal grain species wheat, barley, oats, maize, rice, rye, sorghum, and millet. It has many qualities that make it an excellent model organism for functional genomics research in temperate grasses, cereals, and dedicated biofuel crops such as switchgrass. These attributes include small genome (~270 Mbp) diploid accessions, a series of polyploid accessions, a small physical stature, self-fertility, a short lifecycle, simple growth requirements, and an efficient transformation system. The genome of Brachypodium distachyon (diploid inbred line Bd21) has been sequenced and published in Nature in 2010.

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