Symphoricarpos albus - Unknown
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Details Top

Internal ID UUID643ffd0b2fd40891244152
Scientific name Symphoricarpos albus
Authority (L.) S.F.Blake
First published in Rhodora 16: 118. 1914

Description Top

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Synonyms Top

Scientific name Authority First published in
Lonicera alba (L.) Druce Rep. Bot. Exch. Club Soc. Brit. Isles 3: 420 (1913 publ. 1914)
Vaccinium album L. Sp. Pl. : 350 (1753)
Xylosteon album (L.) Moldenke Revista Sudamer. Bot. 5: 3 (1936 publ. 1937)
Symphoria heterophylla Raf. New Fl. 3: 21 (1838)
Symphoria albus Raf. New Fl. 3: 21 (1838)
Symphoria elongata Torr. & A.Gray Fl. N. Amer. 2: 3 (1841)
Symphoria glauca hort. ex Lavallée Énum. Arbres : 142 (1877)
Symphoria leucocarpa hort. ex DC. Prodr. 4: 339 (1830)
Symphoria macrocarpa hort. ex Lavallée Énum. Arbres : 142 (1877)
Symphoricarpos heterophyllus Presl ex DC. Prodr. 4: 339 (1830)
Symphoricarpos leucocarpus hort. ex K.Koch Dendrologie 2(1): 49 (1872)
Symphoricarpos elongatus Presl ex DC. Prodr. 4: 339 (1830)
Symphoricarpos leucocarpa M'Mahon in True Proc. Amer. Philos. Soc. 67: 14 (1928)
Symphoricarpos racemosus Michx. Fl. Bor.-Amer. 1: 107 (1803)
Lonicera racemosa Auct. ex Steud. Nomencl. Bot. , ed. 2, 2: 67 (1841)
Symphoria racemosa Pursh Fl. Amer. Sept. 1: 162 (1813)
Symphoricarpos racemosus var. pauciflorus Robbins Manual , ed. 5: 203 (1867)
Symphoricarpos pauciflorus Britton Mem. Torrey Bot. Club 5: 105 (1894)
Symphoricarpos albus var. pauciflorus S.F.Blake Rhodora 16: 119 (1914)
Symphoricarpos albus var. ovatus Rehder in L.H.Bailey Stand. Cycl. Hort. 6: 3293 (1917)

Common names Top

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Language Common/alternative name
English common snowberry
English snowberry
Arabic حب الثلج الأبيض
Azerbaijani ağ qargiləmeyvə
Belarusian Снежная ягада гронкавая
Belarusian Снягулькі
Belarusian Снежнаягаднік белы
Bulgarian бял снежноплодник
Czech pámelník bílý
Welsh llusen eira llus eira
Danish almindelig snebær
German gewöhnliche schneebeere
German schneebeere
German knallerbsenstrauch
German knackbeere
German weiße schneebeere
Estonian harilik lumimari
Persian مروارید سفید
Finnish valkolumimarja
Finnish amerikanlumimarja
French vaccinium album
French symphorine
Croatian bijeli biserak
Upper Sorbian běły sněženc
Hungarian fehér hóbogyó
Kazakh Ақ қаржеміс
Korean 인동딸기
Lithuanian baltauogė meškytė
Norwegian Bokmål vanlig snøbær
Norwegian Bokmål snøbær
Dutch sneeuwbes
Norwegian Nynorsk snøbær
nv dzidzéłgaii
Polish Śnieguliczka biała
Polish Śnieguliczka białoowocowa
Polish śnieguliczka biała
Russian Снежноягодник белый
Swedish snöbär
Chinese 雪果
Chinese 白雪果
Chinese 白毛核木
Chinese 总序毛核木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Symphoricarpos albus var. laevigatus S.F.Blake Rhodora 16: 119 (1914)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

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

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Database ID/link to page
World Flora Online wfo-0000439047
UNII 55DP96JT7A
Cornell Woody Plants 442
Canadensys 4233
USDA Plants SYAL
UConn 481
Tropicos 6000055
INPN 125324
Flora of Italy 5148
KEW urn:lsid:ipni.org:names:149485-1
The Plant List kew-2486129
Missouri Botanical Garden 278944
Open Tree Of Life 717590
Observations.org 7529
NCBI Taxonomy 13702
NBN Atlas NHMSYS0000464104
Nature Serve 2.148250
IPNI 247027-2
iNaturalist 48524
iNaturalist 48523
iNaturalist 48525
GBIF 2888634
Freebase /m/0dgsjrl
WisFlora 5179
FEIS plants/shrub/symalb
EPPO SYPAL
EOL 488109
Elurikkus 7614
Calflora (Californian flora) 10399
USDA GRIN 36006
Wikipedia Symphoricarpos_albus
PaleoBotany 34894

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
Assessing silvopasture management as a strategy to reduce fuel loads and mitigate wildfire risk Batcheler M, Smith MM, Swanson ME, Ostrom M, Carpenter-Boggs L Sci Rep 12-Mar-2024
PMCID:PMC10928111
doi:10.1038/s41598-024-56104-3
PMID:38467773
Epidemiology and Clinical Characteristics of Acute Plant Exposure in Patients Aged between 0 and 18 Years—A Six-Year Retrospective Study Nițescu GV, Grama A, Turcu T, Strătulă A, Dragomirescu A, Pană ES, Baciu A, Baconi DL, Crăciun MD, Ulmeanu CE Children (Basel) 21-Feb-2024
PMCID:PMC10969538
doi:10.3390/children11030271
PMID:38539306
The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M Sci Rep 21-Dec-2023
PMCID:PMC10739867
doi:10.1038/s41598-023-49696-9
PMID:38129458
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Polyphenolic profiles of a variety of wild berries from the Pacific Northwest region of North America Higbee J, Brownmiller C, Solverson P, Howard L, Carbonero F Curr Res Food Sci 16-Aug-2023
PMCID:PMC10474376
doi:10.1016/j.crfs.2023.100564
PMID:37664004
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Developmental Biology and Identification of a Garden Pest, Otiorhynchus (Podoropelmus) smreczynskii Cmoluch, 1968 (Coleoptera, Curculionidae, Entiminae), with Comments on Its Origin and Distribution Gosik R, Sprick P, Wrzesień M, Dzyr A, Krstić O, Toševski I Insects 04-Apr-2023
PMCID:PMC10147090
doi:10.3390/insects14040360
PMID:37103175
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 09-Jan-2023
PMCID:PMC9827234
doi:10.2903/j.efsa.2023.7726
PMID:36628332
Postfire futures in southwestern forests: Climate and landscape influences on trajectories of recovery and conversion Coop JD Ecol Appl 13-Oct-2022
PMCID:PMC10078526
doi:10.1002/eap.2725
PMID:36054332
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Temporal variation in climatic factors influences phenotypic diversity of Trochulus land snails Proćków M, Kuźnik-Kowalska E, Żeromska A, Mackiewicz P Sci Rep 19-Jul-2022
PMCID:PMC9296580
doi:10.1038/s41598-022-16638-w
PMID:35853920
Different factors limit early‐ and late‐season windows of opportunity for monarch development Yang LH, Swan K, Bastin E, Aguilar J, Cenzer M, Codd A, Gonzalez N, Hayes T, Higgins A, Lor X, Macharaga C, McMunn M, Oto K, Winarto N, Wong D, Yang T, Afridi N, Aguilar S, Allison A, Ambrose‐Winters A, Amescua E, Apse M, Avoce N, Bastin K, Bolander E, Burroughs J, Cabrera C, Candy M, Cavett A, Cavett M, Chang L, Claret M, Coleman D, Concha J, Danzer P, DaRosa J, Dufresne A, Duisenberg C, Earl A, Eckey E, English M, Espejo A, Faith E, Fang A, Gamez A, Garcini J, Garcini J, Gilbert‐Igelsrud G, Goedde‐Matthews K, Grahn S, Guerra P, Guerra V, Hagedorn M, Hall K, Hall G, Hammond J, Hargadon C, Henley V, Hinesley S, Jacobs C, Johnson C, Johnson T, Johnson Z, Juchau E, Kaplan C, Katznelson A, Keeley R, Kubik T, Lam T, Lansing C, Lara A, Le V, Lee B, Lee K, Lemmo M, Lucio S, Luo A, Malakzay S, Mangney L, Martin J, Matern W, McConnell B, McHale M, McIsaac G, McLennan C, Milbrodt S, Mohammed M, Mooney‐McCarthy M, Morgan L, Mullin C, Needles S, Nunes K, O'Keeffe F, O'Keeffe O, Osgood G, Padilla J, Padilla S, Palacio I, Panelli V, Paulson K, Pearson J, Perez T, Phrakonekham B, Pitsillides I, Preisler A, Preisler N, Ramirez H, Ransom S, Renaud C, Rocha T, Saris H, Schemrich R, Schoenig L, Sears S, Sharma A, Siu J, Spangler M, Standefer S, Strickland K, Stritzel M, Talbert E, Taylor S, Thomsen E, Toups K, Tran K, Tran H, Tuqiri M, Valdes S, VanVorhis G, Vue S, Wallace S, Whipple J, Yang P, Ye M, Yo D, Zeng Y Ecol Evol 11-Jul-2022
PMCID:PMC9273743
doi:10.1002/ece3.9039
PMID:35845370
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2021 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 15-Jun-2022
PMCID:PMC9198695
doi:10.2903/j.efsa.2022.7356
PMID:35734284
Emigration effects on estimates of age‐ and sex‐specific survival of two sciurids Weldy MJ, Lesmeister DB, Epps CW Ecol Evol 23-Apr-2022
PMCID:PMC9034453
doi:10.1002/ece3.8833
PMID:35475177

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 / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine 197810 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
Chelidonine (+) 10147 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
Chelidonine, (-)- 978315 Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6 353.40 unknown https://doi.org/10.1016/S0031-9422(00)94615-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Bauerenol 287684 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Bauerenol 111220 Click to see CC1CCC2(CCC3(C4=CCC5C(C(CCC5(C4CCC3(C2C1C)C)C)O)(C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lanosterol 246983 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
31-Norlanosterol 102179328 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC=C(C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Lophenol 160482 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylene-cycloartanol 9547213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenecycloartanol 94204 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
31-Norcycloartenol 14524546 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC=C(C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
24-Methylenelophenol 5283640 Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCC(=C)C(C)C)C)C)O 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Obtusifoliol 65252 Click to see CC1C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> 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/10.1016/S0031-9422(00)80074-6
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
5,25-Stigmastadienol 286499 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Clerosterol 5283638 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80074-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/0-387-28822-8_5

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