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Sorbus torminalis

Sorbus torminalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Sorbus torminalis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644040286c903714130421
Scientific name Sorbus torminalis
Authority (L.) Crantz
First published in Stirp. Austr. Fasc. 2: 45 (1763)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Aria torminalis (L.) Beck Fl. Nieder-Osterreich ii. (1892) 713.
Torminaria clusii M.Roem. Fam. Nat. Syn. Monogr. 3: 130 (1847)
Torminalis clusii (M.Roem.) K.R.Robertson & J.B.Phipps Syst. Bot. 16: 390 (1991)
Hahnia torminalis Medik. Gesch. Bot. : 81 (1793)
Sorbus orientalis Schönb.-Tem. Fl. Iranica 66: 47 (1969)
Crataegus torminalis L. Sp. Pl. : 476 (1753)
Pyrus torminalis Ehrh. Beitr. Naturk. 6: 92 (1791)

Common names Top

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Language Common/alternative name
English checkertree
English wild service tree
English wild service-tree
English torminalis glaberrima
English checker tree
English chequers
Spanish sorbo silvestre
Spanish mostajo de perucos
Arabic غبيراء ممغصة
Azerbaijani ağrıovunduran quşarmudu
Bulgarian брекина
Bulgarian Брекина
br kerzhin-bod
Catalan moixera de pastor
Czech jeřáb břek
Welsh cerddinen wyllt
Danish tarmvrid-røn
German elsbeere
German alzbeere
Esperanto adstringa sorbuso
Esperanto adstringa sorpujo
Estonian vahtralehine pihlakas
Basque basagurbe
Basque mazpil
Basque aizpil
Basque basa-gurbe
Basque maspil
Persian بارانک
Finnish etelänpihlaja
French alisier torminal
French sorbier torminal
Irish crann soirb fiáin
Manx billey greimmey
Hebrew בן-חוזרר לבנוני
Croatian brekinja
Upper Sorbian brěčica
Upper Sorbian brěčkowc
Hungarian barkócaberkenye
Armenian Խնձորենի արևելյան
Icelandic flipareynir
Italian sorbo ciaverdello
Italian torminalis glaberrima
Italian sorbo ciavardello
Japanese カエデバアズキナシ
Georgian თამელი
lb elsbier
lb ielenter
Macedonian Бреклинка
Macedonian бабилка
Macedonian бреклинка
Macedonian брекина
mzn الندری
Norwegian Bokmål tarmvriasal
Dutch elsbes
os Тамачъи
os Балгъондзы
os Балгъодзы
Polish jarząb brekinia
Polish jarząb brzęk
Polish brzęk
Polish brekinia
Romansh sorber grond
Romanian sorb
Russian Берека
Russian Глоговина
Russian Медвежья груша
Russian Рябина глоговина
Serbo-Croatian brekinja
Slovak jarabina brekyňová
Slovenian brek
Serbian Брекиња
Swedish tyskoxel
Turkish akçaağaç yapraklı üvez
Turkish elsbeere
Ukrainian Берека
Chinese 野生楸樹
Chinese 契克斯（水果）
Chinese 契克斯

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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20° x 2 weeks, then 4° until germinated - up to 30 weeks

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001014076
USDA Plants SOTO9
Tropicos 27800381
INPN 124346
Flora of Italy 2182
KEW urn:lsid:ipni.org:names:742021-1
The Plant List rjp-595
Missouri Botanical Garden 286408
Open Tree Of Life 846359
NCBI Taxonomy 106574
NBN Atlas NBNSYS0000003460
Nature Serve 2.961531
IUCN Red List 61957590
IPNI 742021-1
iNaturalist 198879
GBIF 3012567
Freebase /m/04hv51
EPPO SOUTO
EOL 249839
Elurikkus 7325
USDA GRIN 35071
Wikipedia Sorbus_torminalis
CMAUP NPO17358

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
Phenolic constituents of the inflorescences of Sorbus torminalis (L.) Crantz Monika A. Olszewska, Joanna Marta Roj Elsevier BV 07-Mar-2011
doi:10.1016/J.PHYTOL.2011.02.005
Chemotaxonomic survey of the genus Sorbus in Europe J. Challice, M. Kovanda Springer Science and Business Media LLC 11-Nov-2004
doi:10.1007/BF00440556

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
> Alkaloids and derivatives / Aporphines
(+)-1,2-Methylenedioxy-5,6,6aalpha,7-tetrahydro-4H-dibenzo[de,g]quinoline 26202781 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown via CMAUP database
1-[(12R)-16-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-11-yl]ethanone 10246449 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)OC)OCO3 337.40 unknown via CMAUP database
7H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline-7-carboxaldehyde,5,6,7a,8-tetrahydro-, (7aR)- 158516 Click to see C1CN(C2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5)C=O 293.30 unknown via CMAUP database
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown via CMAUP database
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
(12R,13S)-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaen-13-ol 15560530 Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O 281.30 unknown via CMAUP database
> Benzenoids / Anthracenes
10-hydroxy-2-methyl-4,4a,9a,10-tetrahydro-1H-anthracen-9-one 162971410 Click to see CC1=CCC2C(C1)C(=O)C3=CC=CC=C3C2O 228.29 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[1,1'-Biphenyl]-4-ol, 2'-methoxy-3,5'-di-2-propenyl- 11857938 Click to see COC1=C(C=C(C=C1)CC=C)C2=CC(=C(C=C2)O)CC=C 280.40 unknown via CMAUP database
4-O-Methylhonokiol 155160 Click to see COC1=C(C=C(C=C1)C2=C(C=CC(=C2)CC=C)O)CC=C 280.40 unknown via CMAUP database
Caryolanemagnolol 21726647 Click to see CC1(CC2C1CCC3(CC2(CCC3O)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C)C 486.70 unknown via CMAUP database
Honokiol 72303 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C 266.30 unknown via CMAUP database
Magnaldehyde E 5319190 Click to see C=CCC1=C(C=CC(=C1)C2=C(C=CC(=C2)C=O)O)O 254.28 unknown via CMAUP database
Magnolol 72300 Click to see C=CCC1=CC(=C(C=C1)O)C2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2,3,4-Trihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 71812224 Click to see C=CCC1=CC=C(C=C1)OC2=C(C(=C(C(=C2)C=O)O)O)O 286.28 unknown via CMAUP database
3-[3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)phenyl]prop-2-enal 134367 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
3,4-Dihydroxy-5-(4-prop-2-enylphenoxy)benzaldehyde 23259953 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=O 270.28 unknown via CMAUP database
5-[(E)-3-methoxyprop-1-enyl]-3-(4-prop-2-enylphenoxy)benzene-1,2-diol 71812222 Click to see COCC=CC1=CC(=C(C(=C1)OC2=CC=C(C=C2)CC=C)O)O 312.40 unknown via CMAUP database
Obovatal 6439677 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)C=CC=O 296.30 unknown via CMAUP database
Obovatol 100771 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C 282.30 unknown via CMAUP database
Phenol, 2-[3-hydroxy-4-(2-propenyl)phenoxy]-5-(2-propenyl)- 10016628 Click to see C=CCC1=CC(=C(C=C1)OC2=CC(=C(C=C2)CC=C)O)O 282.30 unknown via CMAUP database
Phenol, 4-(2-propenyl)-2-(4-(2-propenyl)phenoxy)- 159137 Click to see C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O 266.30 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Cadalene 10225 Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C 198.30 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanemagnolol 10323149 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)OC4=C(C=C(C=C4)CC=C)C5=C(C=CC(=C5)CC=C)O)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[2R-cis]-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol 91730386 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
2-[(2R,4aS,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 118976561 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown via CMAUP database
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Eudeshonokiol A 14587421 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)C4=C(C=CC(=C4)CC=C)O)CC=C 488.70 unknown via CMAUP database
Eudeshonokiol B 21726646 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=CC(=C(C=C4)O)CC=C 488.70 unknown via CMAUP database
Eudesmagnolol 14587417 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3)CC=C)C4=C(C=CC(=C4)CC=C)O 488.70 unknown via CMAUP database
Eudesobovatol A 442837 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=CC(=CC(=C3O)OC4=CC=C(C=C4)CC=C)CC=C 504.70 unknown via CMAUP database
Eudesobovatol B 10346031 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC3=C(C=C(C=C3OC4=CC=C(C=C4)CC=C)CC=C)O 504.70 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
Proximadiol 165258 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
Magnolianin 9918938 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC3=C2OC(C(O3)C4=CC(=C(C(=C4)OC5=CC=C(C=C5)CC=C)O)O)COC6=C(C=C(C=C6)CC=C)C7=C(C=CC(=C7)CC=C)O)CC=C 827.00 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-7-ol 6093330 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 21629882 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumanolignan 24796112 Click to see C=CCC1=CC(=C(C=C1)O)C2=C3C(=CC(=C2)CC=C)C=CC(=O)O3 318.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00440556
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1016/J.PHYTOL.2011.02.005
3-beta-d-Glucopyranosyloxy-4',5,7-trihydroxy-8-methoxyflavone 14307939 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O)O 478.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14186852 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
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 https://doi.org/10.1016/J.PHYTOL.2011.02.005
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 https://doi.org/10.1016/J.PHYTOL.2011.02.005
Isoquercetin 5280804 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 https://doi.org/10.1016/J.PHYTOL.2011.02.005
Isorhamnetin 3-galactoside 13245586 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 https://doi.org/10.1016/J.PHYTOL.2011.02.005
Limocitrin 3-O-beta-D-glucopyranoside 5319024 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.02.005

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