Details Top

Internal ID UUID644019b46ee0e500155446
Scientific name Hymenocallis rotata
Authority (Ker Gawl.) Herb.
First published in Appendix : 44 (1821)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Hymenocallis rotata is cultivated as an ornamental bulbous perennial. The principal commercial products are dormant bulbs sold for spring planting, potted plants for landscape or container use, and cut‑flower stems for the florist trade. The plant is marketed under common names such as “spider lily” or “pine lily” and appears in the catalogs of North American bulb growers and horticultural nurseries.

Properties relevant to use:
The species forms tunicated, fleshy bulbs that store carbohydrates and enable rapid vegetative propagation by division. Its foliage consists of basal, linear leaves that persist through the growing season, providing a green backdrop. The flower spike bears several large, white, fragrant blossoms with a conspicuous cup and six tepals; the fragrance is attributed to volatile aromatic compounds such as benzyl acetate and linalool, which are attractive to pollinators and valued by the ornamental market. The plant is adapted to USDA hardiness zones 8–10, tolerates moderate drought once established, and naturalizes readily in suitable climates, making it suitable for low‑maintenance garden plantings and for cut‑flower production where a vase life of several days is required.

Sustainability and sourcing:
All commercial material of H. rotata is derived from cultivated stock; wild harvest is not common and the species is listed as “secure” in the USDA PLANTS database. Bulb production follows standard horticultural propagation methods (seed sowing, bulb division, and tissue culture) and complies with national plant‑health regulations (e.g., USDA APHIS import/export rules). Because the taxon is not listed under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), international trade is unrestricted subject to routine phytosanitary certification. The reliance on cultivated propagation reduces pressure on native populations and supports sustainable sourcing for the ornamental industry.

Synonyms Top

Scientific name Authority First published in
Hymenocallis disciformis (DC.) M.Roem. Fam. Nat. Syn. Monogr. 4: 174. 1847
Hymenocallis floridana (Raf.) C.V.Morton Year Book Amer. Amaryllis Soc. 2: 81 (1935)
Hymenocallis floridana subsp. amplifolia Traub Pl. Life 23: 67 (1967)
Hymenocallis lacera var. minor Chapm. Fl. South. U.S. , ed. 3: 494 (1897)
Hymenocallis laciniata Small Man. S.E. Fl. : 323 (1933)
Hymenocallis mexicana (L.) Herb. Appendix : 44 (1821)
Hymenocallis rotata var. disciformis (Redouté) Herb. Amaryllidaceae : 217 (1837)
Hymenocallis rotata var. quadrifolia Herb. Amaryllidaceae 217 1837
Ismene knightii Knowles & Westc. Fl. Cab. 2: 51 (1838)
Pancratium disciforme Redouté Liliac. [Redouté] 3(pt. 26): t. 155. 1806 [Apr 1806]
Pancratium rotatum Ker Gawl. Bot. Mag. 21: t. 827 (1805)
Tomodon rotatum (Ker Gawl.) Raf. Fl. Tellur. 4: 22 (1838)
Tomodon floridanum Raf. Fl. Tellur. 4: 22 (1838)
Pancratium rotatum var. pluriflorum Ker Gawl. in Curtis Bot. Mag. 27: t. 1082 (1808)
Pancratium rotatum var. biflorum Ker Gawl. Bot. Mag. 27: t. 1082 (1808)
Hymenocallis paludosa Salisb. Trans. Hort. Soc. London 1: 338 (1812)
Pancratium carribaeum Mill. Gard. Dict. ed. 8 : n.º 4 (1768)

Common names Top

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Language Common/alternative name
English streambank spiderlily

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000667750
Florida Plant Atlas 4098
Flora of Alabama 5319
USDA Plants HYRO2
KEW urn:lsid:ipni.org:names:1204176-2
The Plant List kew-278898
Open Tree Of Life 442885
NCBI Taxonomy 1234395
Nature Serve 2.128893
IPNI 1204176-2
iNaturalist 163918
GBIF 2860322
Freebase /m/0_fqgzw
EOL 1001658
USDA GRIN 19511
Wikipedia Hymenocallis_rotata

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Phylogenomics of the Andean Tetraploid Clade of the American Amaryllidaceae (Subfamily Amaryllidoideae): Unlocking a Polyploid Generic Radiation Abetted by Continental Geodynamics Meerow AW, Gardner EM, Nakamura K Front Plant Sci 05-Nov-2020
PMCID:PMC7674842
doi:10.3389/fpls.2020.582422
PMID:33250911
Alkaloidal constituents of Hymenocallis rotata Herb. (Amaryllidaceae). MASARU KIHARA, TOMOMI KOIKE, YASUHIRO IMAKURA, KIYOSHI KIDA, TETSURO SHINGU, SHIGERU KOBAYASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.35.1070
Alkaloide aus Hymenocallis-Arten Hans-G. Boit, Werner D�pke Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00622237

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 / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine 443693 Click to see 271.31 unknown https://doi.org/10.1248/CPB.35.1070
(1R,13R,15S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 398938 Click to see 271.31 unknown https://doi.org/10.1248/CPB.35.1070
(1S,13R,15S,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol 162950863 Click to see 287.31 unknown https://doi.org/10.1248/CPB.35.1070
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1248/CPB.35.1070
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1248/CPB.35.1070
Hemanthamine 441593 Click to see 301.34 unknown https://doi.org/10.1248/CPB.35.1070
Vittatine, 11-hydroxy- 602595 Click to see 287.31 unknown https://doi.org/10.1248/CPB.35.1070
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1248/CPB.35.1070
(1R,12S,14S)-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 21826140 Click to see 275.34 unknown https://doi.org/10.1248/CPB.35.1070
(1S,12S,14S)-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 102065728 Click to see 275.34 unknown https://doi.org/10.1248/CPB.35.1070
1,2-Dihydrogalanthamine 625595 Click to see 289.40 unknown https://doi.org/10.1248/CPB.35.1070
9-Methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9-trien-14-ol 16666692 Click to see 275.34 unknown https://doi.org/10.1248/CPB.35.1070
Epi Norgalanthamine 11357792 Click to see 273.33 unknown https://doi.org/10.1248/CPB.35.1070
Galantamin 3449 Click to see 287.35 unknown https://doi.org/10.1248/CPB.35.1070
Lycoramine 443723 Click to see 289.40 unknown https://doi.org/10.1248/CPB.35.1070
N-Desmethylgalantamine 9838394 Click to see 273.33 unknown https://doi.org/10.1248/CPB.35.1070
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Homolycorine 160473 Click to see 315.40 unknown https://doi.org/10.1007/BF00622237
Lycorenan-7-one,9,10-dimethoxy-1-methyl- 573128 Click to see 315.40 unknown https://doi.org/10.1007/BF00622237
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
3,3a-Didehydrolycoran-1alpha,2beta-diol 3978 Click to see 287.31 unknown https://doi.org/10.1248/CPB.35.1070
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.1248/CPB.35.1070
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Ismine 188957 Click to see 257.28 unknown https://doi.org/10.1248/CPB.35.1070
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-11-ol 162894672 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 443682 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 11873227 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
3-Epimacronine 375117 Click to see 329.30 unknown https://doi.org/10.1248/CPB.35.1070
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol 419046 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-one 500134 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(=O)O2)OCO5 329.30 unknown https://doi.org/10.1248/CPB.35.1070
Pretazettine 73360 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
Sekisanin 271607 Click to see 331.40 unknown https://doi.org/10.1248/CPB.35.1070
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1248/CPB.35.1070
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
6-Hydroxy-7,8-dimethoxy-2-(2-oxopropyl)-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one 71436822 Click to see CC(=O)CC1CC2C(O1)C3=CC(=C(C(=C3C(=O)O2)O)OC)OC 322.31 unknown https://doi.org/10.1248/CPB.35.1070
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see 273.33 unknown https://doi.org/10.1248/CPB.35.1070
4-Methoxy-9-azatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-5,12-diol 494912 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown https://doi.org/10.1248/CPB.35.1070
Demethylmaritidine 72695824 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown https://doi.org/10.1248/CPB.35.1070

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