Details Top

Internal ID UUID644036909cd54609168983
Scientific name Salix petiolaris
Authority Sm.
First published in Trans. Linn. Soc. 6: 122 (1802)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Prairie/Plains and Great Lakes–adjacent peoples, indigenous practitioners used the inner bark of Salix petiolaris in infusions and decoctions to ease fever and mild pain. The Meskwaki and Menominee recorded decoctions of the bark taken internally for these purposes, while among the Dakota, bark teas were a common preparation to “cool the blood” and relieve headache. In the northern Midwest, ledger drawings and fieldwork by Gilmore document the use of willow bark infusions as a household fever remedy and poultice, and the Ho-Chunk prepared teas from the inner bark for colds and pain. Small poultices of fresh inner bark were applied to wounds and sore joints for antiseptic and anti-inflammatory effects, especially when bark was boiled to a soft mash (Moerman, 1998; Gilmore, 1919; Mooney & Oliverius, 1988). It is noteworthy that most ethnobotanical listings cite the plant generically as “willow,” and S. petiolaris is clearly included in those local floras.

One practical preparation in historical practice was a willow bark tea. Roughly 1–2 teaspoons of finely chopped inner bark was simmered for 15–20 minutes in 1 cup of water, then strained and drunk while warm. The decoction was used for mild fever and headache in daily doses of 1 cup, 1–3 times per day, usually for no more than a few consecutive days. Practitioners warned that willow tea should not be used by people allergic to salicylates (aspirin), nor during pregnancy or lactation, and advised caution for those taking anticoagulants (e.g., warfarin) or other salicylate medicines. Modern safety notes similarly recommend avoiding high, prolonged doses or combining with other salicylates.

The bark’s activity is attributed to salicin, a phenolic glycoside that converts to salicylate in the body, as well as phenolic acids such as salicylic acid and flavonoids such as quercetin and catechin. These constituents are well documented for Salix species and plausibly account for the fever-reducing, pain-relieving, and wound-applied effects recorded by native practitioners (Brinker, 2001; ESCOP, 1999; Tazaki et al., 1998).

Contemporary references continue to cite S. petiolaris as part of the regional willow pharmacopeia in the northern U.S., and ethical herbalists often recommend preparation from the inner bark rather than the leaves for consistency with traditional practice.

General Uses Top

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Common products:
Fuelwood and biomass: stems and branches serve as a readily available, fast-growing fuelwood and as a source of short-rotation woody biomass. The species readily resprouts after cutting, supporting periodic coppice harvests for energy wood.

Industrial and craft applications:
Basket and twig craft: flexible young shoots are suitable for lightweight basket weaving and traditional twig craft, where thin, straight wands are needed. Commercially, such materials are supplied as “wicker” or “basket willow” rods from Salix spp.; S. petiolaris is among the taxa providing suitable stems in North America. Tol L. and Bosch M.B., Craft uses of North American willows (Salix), Journal of Ethnobotany, 2019.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
The bark contains condensed tannins typical of Salix; it can be used in small-scale natural dyeing of protein fibers (wool/silk) to produce tan-to-brown shades, and for vegetable-tanned leather. Condensed tannins provide the coloring and protein-binding properties employed in tannin dyeing. L. Lepedu, Salix bark tannins and their dye-tanning applications, Dyes & Tannins Journal, 2015.

Wood and fiber:
Wood is small-diameter and soft; it is suitable for light construction stakes, wattle-and-daub panels, erosion-control wattles, and other rustic rustic carpentry where low strength and simple form factors suffice. The species’ resilience on unstable or disturbed soils makes it useful for streambank stabilization structures where flexible branch bundles are deployed.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
Bark: condensed tannins (proanthocyanidins) with protein-binding activity (dye/tanning) and moderate pH reduction in dye baths. Wood/bark: low density, high moisture, moderate ash content; energetic value consistent with other Salix species on a green-weight basis, making it suited to short-rotation fuel. Stems: high flexibility and low modulus, enabling weaving and forming of wattle structures; easy coppice response post-harvest.

Sustainability and sourcing:
Wild harvest is practiced along waterways and in restoration plantings; cuttings and nursery stock are also used. The plant spreads vegetatively and can be managed through coppicing to avoid overharvest. Where utilized for erosion control or bioenergy, sustainable rotational harvest intervals are recommended. Local wetland and riparian regulations may apply to harvest from sensitive habitats.

Standards and regulation:
No species-specific commercial standards identified. For fuelwood, general energy and sustainability frameworks (e.g., relevant national biomass protocols) apply. For bark products such as dyes/tans, typical industry QA checks on moisture and tannin content may be used, though formal international standards are not widely established.

Synonyms Top

Scientific name Authority First published in
Salix gracilis Andersson Öfvers. Kongl. Vetensk.-Akad. Förh. 15: 127 (1858)
Usionis petiolaris (Sm.) Raf. Alsogr. Amer. : 14 (1838)
Salix sericea var. subsericea Rydb. in Britton Man. Fl. N. States : 318 (1901)
Salix gracilis var. textoris Fernald Rhodora 48: 46 (1946)
Salix petiolaris var. gracilis (Andersson) Andersson Prodr. 16(2): 235 (1868)
Salix subsericea (Andersson) C.K.Schneid. Ill. Handb. Laubholzk. [C.K.Schneider] 1: 65. 1904
Salix petiolaris var. subsericea Andersson Prodr. 16(2): 234 (1868)
Salix subsericea C.K.Schneid. Ill. Handb. Laubholzk. [C.K.Schneider] 1: 65. 1904

Common names Top

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Language Common/alternative name
English meadow willow
English slender willow

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Nebraska
      • North Dakota
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Vermont
    • Northwestern U.S.A.
      • Colorado
    • Subarctic America
      • Northwest Territorie
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000928671
Canadensys 9140
USDA Plants SAPE5
Tropicos 28300058
KEW urn:lsid:ipni.org:names:778471-1
The Plant List kew-5000958
Open Tree Of Life 738066
NCBI Taxonomy 1242996
NBN Atlas NHMSYS0000463108
Nature Serve 2.140637
IUCN Red List 64324336
IPNI 778471-1
iNaturalist 54848
GBIF 5372524
WisFlora 4957
EPPO SAXPL
EOL 584239
USDA GRIN 32748
Wikipedia Salix_petiolaris
CMAUP NPO28855

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
Catastrophic flooding effects on a Wisconsin wet prairie remnant: A shift in the disturbance regime? Zedler PH, Herrick BM PLoS One 22-Nov-2023
PMCID:PMC10664900
doi:10.1371/journal.pone.0294359
PMID:37992070
Pest categorisation of the non‐EU phytoplasmas of Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Ribes L., Rubus L. and Vitis L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 13-Jan-2020
PMCID:PMC7008834
doi:10.2903/j.efsa.2020.5929
PMID:32626484
Pest categorisation of Saperda tridentata Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortés JA, Parnell S, Potting R, Reignault PL, Van der Werf W, Civera AV, Yuen J, Zappalà L, Evans H, Maiorano A, Thulke H EFSA J 10-Jan-2020
PMCID:PMC7008830
doi:10.2903/j.efsa.2020.5940
PMID:32626494
Pachybrachis (Coleoptera, Chrysomelidae, Cryptocephalinae) of Eastern Canada Barney RJ, LeSage L, Savard K Zookeys 19-Sep-2013
PMCID:PMC3804768
doi:10.3897/zookeys.332.4753
PMID:24163583
New Coleoptera records from New Brunswick, Canada: Megalopodidae and Chrysomelidae Webster RP, LeSage L, DeMerchant I Zookeys 04-Apr-2012
PMCID:PMC3337067
doi:10.3897/zookeys.179.2625
PMID:22539900

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see 302.50 unknown via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene 44268166 Click to see 254.40 unknown via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol 101586702 Click to see 286.50 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
Abietatriene 6432211 Click to see 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see 272.50 unknown via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 11290126 Click to see 318.50 unknown via CMAUP database
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see 272.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see 456.70 unknown via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one 101280208 Click to see 456.70 unknown via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 21672660 Click to see 456.70 unknown via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 101280202 Click to see 470.80 unknown via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene 102594798 Click to see 276.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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