Sporobolus cynosuroides

Details Top

Internal ID UUID6440617036977402192353
Scientific name Sporobolus cynosuroides
Authority (L.) P.M.Peterson & Saarela
First published in Taxon 63: 1236 (2014)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Cynodon cynosuroides (L.) Raspail Ann. Sci. Nat. (Paris) 5: 303 (1825)
Limnetis cynosuroides (L.) Rich. Syn. Pl. 1: 72 (1895)
Limnetis polystachya (Michx.) Rich. Syn. Pl. 1: 72 (1805)
Paspalum cynosuroides (L.) Brot. Fl. Lusit. 1: 85 (1804)
Poa lagopoides Steud. Nomencl. Bot. [Steudel], ed. 2. ii. 360.
Spartina cynosuroides var. polystachya (Michx.) Beal Grass. N. Amer. 2: 698 (1896)
Spartina polystachya Willd. Enum. Pl. : 81 (1809)
Trachynotia cynosuroides (L.) Michx. Fl. Bor.-Amer. 1: 64 (1803)
Trachynotia polystachya Michx. Fl. Bor.-Amer. 1: 64 (1803)
Triodia cynosuroides Spreng. Syst. Veg. 1: 628 (1824)
Dactylis cynosuroides L. Sp. Pl. : 71 (1753)
Spartina cynosuroides (L.) Roth Catal. Bot. 3: 10 (1806)

Common names Top

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Language Common/alternative name
English big cordgrass
English salt reedgrass
Arabic عشب الحبل الكبير
Swedish jättemarskgräs
Chinese 大繩草
Chinese 大绳草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northeast
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New Jersey
      • New York
      • Pennsylvania
      • Rhode Island
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001341455
Florida Plant Atlas 930
USDA Plants SPCY
Tropicos 25512525
KEW urn:lsid:ipni.org:names:1217139-2
The Plant List kew-443765
Nature Serve 2.134582
IPNI 1217139-2
iNaturalist 145478
GBIF 5290042
Freebase /m/0j_7hmt
EPPO SPTCY
EOL 1114692
USDA GRIN 103563
Wikipedia Sporobolus_cynosuroides
Flora of Alabama 5044
Tropicos 100408197
KEW urn:lsid:ipni.org:names:77144710-1
Open Tree Of Life 422340
NCBI Taxonomy 180097
IPNI 77144710-1
iNaturalist 773033
GBIF 9531396
CMAUP NPO21594
Open Tree Of Life 422340

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Fauna Associated with American Alligator (Alligator mississippiensis) Nests in Coastal South Carolina, USA Rainwater TR, Singh R, Tuten CA, Given AM, Gibbons PW, Song B, Platt SG, Wilkinson PM, Bodinof Jachowski CM Animals (Basel) 14-Feb-2024
PMCID:PMC10886190
doi:10.3390/ani14040620
PMID:38396588
Fungal Biodiversity in Salt Marsh Ecosystems Calabon MS, Jones EB, Promputtha I, Hyde KD J Fungi (Basel) 09-Aug-2021
PMCID:PMC8399140
doi:10.3390/jof7080648
PMID:34436187
Belowground productivity varies by assessment technique, vegetation type, and nutrient availability in tidal freshwater forested wetlands transitioning to marsh From AS, Krauss KW, Noe GB, Cormier N, Stagg CL, Moss RF, Whitbeck JL PLoS One 16-Jul-2021
PMCID:PMC8284669
doi:10.1371/journal.pone.0253554
PMID:34270570
Natural Sources and Bioactivities of 2,4-Di-Tert-Butylphenol and Its Analogs Zhao F, Wang P, Lucardi RD, Su Z, Li S Toxins (Basel) 06-Jan-2020
PMCID:PMC7020479
doi:10.3390/toxins12010035
PMID:31935944
High Genetic Diversity With Weak Phylogeographic Structure of the Invasive Spartina alterniflora (Poaceae) in China Shang L, Li LF, Song ZP, Wang Y, Yang J, Wang CC, Qiu SY, Huang JX, Nie M, Wolfe LM, Li B Front Plant Sci 20-Nov-2019
PMCID:PMC6896949
doi:10.3389/fpls.2019.01467
PMID:31850008
Retreating marsh shoreline creates hotspots of high-marsh plant diversity Elsey-Quirk T, Mariotti G, Valentine K, Raper K Sci Rep 08-Apr-2019
PMCID:PMC6453922
doi:10.1038/s41598-019-42119-8
PMID:30962472
Quantitative acoustic differentiation of cryptic species illustrated with King and Clapper rails Stiffler LL, Schroeder KM, Anderson JT, McRae SB, Katzner TE Ecol Evol 20-Nov-2018
PMCID:PMC6309001
doi:10.1002/ece3.4711
PMID:30619585
Dynamic responses and implications to coastal wetlands and the surrounding regions under sea level rise Alizad K, Hagen SC, Medeiros SC, Bilskie MV, Morris JT, Balthis L, Buckel CA PLoS One 12-Oct-2018
PMCID:PMC6185723
doi:10.1371/journal.pone.0205176
PMID:30312304
Complete host specificity test plant list and associated data to assess host specificity of Archanara geminipuncta and Archanara neurica, two potential biocontrol agents for invasive Phragmites australis in North America Blossey B, Häfliger P, Tewksbury L, Dávalos A, Casagrande R Data Brief 26-Jun-2018
PMCID:PMC6141379
doi:10.1016/j.dib.2018.06.068
PMID:30229049
Genetic architecture of photosynthesis in Sorghum bicolor under non-stress and cold stress conditions Ortiz D, Hu J, Salas Fernandez MG J Exp Bot 18-Aug-2017
PMCID:PMC5853419
doi:10.1093/jxb/erx276
PMID:28981780
Higher Novel L-Cys Degradation Activity Results in Lower Organic-S and Biomass in Sarcocornia than the Related Saltwort, Salicornia Kurmanbayeva A, Bekturova A, Srivastava S, Soltabayeva A, Asatryan A, Ventura Y, Khan MS, Salazar O, Fedoroff N, Sagi M Plant Physiol 25-Jul-2017
PMCID:PMC5580768
doi:10.1104/pp.17.00780
PMID:28743765
Density-dependent role of an invasive marsh grass, Phragmites australis, on ecosystem service provision Theuerkauf SJ, Puckett BJ, Theuerkauf KW, Theuerkauf EJ, Eggleston DB PLoS One 24-Feb-2017
PMCID:PMC5325552
doi:10.1371/journal.pone.0173007
PMID:28235024
Tidal Marshes across a Chesapeake Bay Subestuary Are Not Keeping up with Sea-Level Rise Beckett LH, Baldwin AH, Kearney MS PLoS One 28-Jul-2016
PMCID:PMC4965100
doi:10.1371/journal.pone.0159753
PMID:27467784
Environmental costs and benefits of growing Miscanthus for bioenergy in the UK McCalmont JP, Hastings A, McNamara NP, Richter GM, Robson P, Donnison IS, Clifton‐Brown J Glob Change Biol Bioenergy 18-Aug-2015
PMCID:PMC5340280
doi:10.1111/gcbb.12294
PMID:28331551
Species-specific enzymatic tolerance of sulfide toxicity in plant roots Martin NM, Maricle BR Plant Physiol Biochem 23-Jan-2015
PMCID:PMC4339417
doi:10.1016/j.plaphy.2015.01.007
PMID:25635761

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1021/NP50028A035
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP50028A035
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50028A035
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP50028A035
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP50028A035
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
3',5'-di-O-methyltricetin(1-) 46878516 Click to see COC1=CC(=CC(=C1[O-])OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 329.28 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1021/NP50028A035
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database

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