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 Daur and Oroqen peoples of northeastern China, the roots and rhizomes of Iris tenuifolia have been taken as a mild decoction for colds, fever, and sore throat (Huang et al., 2008; Jilin Provincial Herbs Survey, 1984). In parts of Tibet, the plant’s rhizomes and young leaves are simmered as a decoction or infused as a tea to ease coughs and minor respiratory irritation (Zhang et al., 2009; Tibetan Medicine Board, 2014). In Inner Mongolia, the aboveground parts are sometimes boiled into a bitter decoction and drunk to calm gastrointestinal upset and loss of appetite (Shao et al., 2007).

One practical way to prepare a mild decoction is to simmer 10 g of fresh or dried roots and rhizomes in 500 ml of water for 20–30 minutes, let the liquid cool slightly, and sip a small cup (about 50–100 ml) two to three times daily for short-term relief of cough or sore throat (Chinese Materia Medica, 2009). A 1:5 ethanol tincture can also be made by macerating 20 g of dried roots and rhizomes in 100 ml of 45–50% ethanol for 3–4 weeks, shaking daily, then straining; typical drops are 10–20 in water as needed (Tibetan Medicine Board, 2014). Iris species contain isoflavonoids such as irisflorentin and resveratrol-type stilbenes, which are well reported from I. tenuifolia and plausibly underlie the observed anti-inflammatory and antimicrobial activities (Zhang et al., 2006; Wu et al., 2012).

Several journal studies have examined extracts and isolated compounds for antibacterial and antitubercular activity against clinically relevant bacteria (Zhang et al., 2006; Zhou et al., 2011), indicating growing scientific interest despite the plant’s limited commercial profile in China. While small decoctions remain in current folk practice in the regions mentioned, use is conservative and seasonal; avoid during pregnancy and seek professional advice if taking other medicines.

General Uses Top

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Common products:
- Ornamental garden plant, especially valued in rock‑garden and alpine plantings; marketed by specialist nurseries for its compact habit, low water demand, and early‑summer bloom.

Properties relevant to use:
- Rhizomatous habit: short, thickened rhizomes spread laterally, facilitating rapid clump formation and division for propagation.
- Foliage: narrow, linear leaves 1–3 mm wide that form low mounds up to about 30 cm tall, suitable for foreground placement.
- Flowering: violet‑blue to lilac tepals, 3–5 cm in diameter, appearing in late May to early June, providing early seasonal color.
- Habitat preference: naturally occurs on well‑drained, sandy or gritty soils of dry slopes and steppe margins, indicating good drought adaptation.
- Geographic distribution: native to Central Asia (e.g., Xinjiang, Mongolia, Kazakhstan), informing climate‑appropriate horticultural use.
- Cold hardiness: documented as hardy in USDA zones 5–8, tolerating temperatures down to –20 °C with modest snow cover.
- Propagation: commercial production relies almost exclusively on vegetative division of mature rhizomes, preserving cultivar traits and ensuring clonal consistency.

Sustainability and sourcing:
- Cultivation is almost entirely via division of cultivated stock, eliminating the need for wild harvesting.
- The species is not currently assessed by the IUCN Red List, indicating a stable global status.
- Low commercial demand results in small‑scale nursery production; most stock originates from locally sourced divisions, reducing transport‑related carbon footprints.
- Seed set is limited and of low commercial value; growers primarily use division, preserving genetic identity and minimizing introgression risk.
- Trade follows standard horticultural plant‑health regulations (e.g., EU Plant Passport system, US Phytosanitary Certificate) for all commercial shipments of the plant material.

Synonyms Top

Scientific name	Authority	First published in
Cryptobasis tenuifolia	(Pall.) Nevski	Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 4: 244 (1937)
Iris acaulis	Pall.	Reise Russ. Reich. 3: 213 (1776)
Iris regelii	Maxim ex Regel	Trudy Imp. S.-Peterburgsk. Bot. Sada vi. (1879) 495.
Joniris tenuifolia	Klatt	Bot. Zeitung (Berlin) 30: 502 (1872)
Neubeckia tenuifolia	Alef.	Bot. Zeitung (Berlin) 21: 297 (1863)
Xiphion tenuifolium	Schrank	Flora 7(2 Beibl.): 19 (1824)
Cryptobasis mariae	Mavrodiev	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 107(5): 78 (2002)
Cryptobasis regelii	(Maxim. ex Regel) M.B.Crespo, Mart.-Azorín & Mavrodiev	Phytotaxa 232: 61 (2015)

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	nazikyarpaq süsən
Bulgarian	тънколистен ирис
mn	Нарийн цахилдаг
Russian	Ирис тонколистный
Chinese	丝叶马蔺
Chinese	细叶马蔺
Chinese	细叶鸢尾
Chinese	老牛拽
Chinese	老牛揣
Chinese	细叶莺尾
Chinese	老牛揣子

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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No forms added yet.

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

Asia-temperate click to expand
- China
  - China North-central
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Siberia
  - Chita
- Western Asia
  - Afghanistan
  - Iran

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Europe click to expand
- Eastern Europe
  - East European Russia
  - South European Russia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000783952
Tropicos	16602071
KEW	urn:lsid:ipni.org:names:439173-1
The Plant List	kew-322479
Plantarium	20835
Open Tree Of Life	43090
Observations.org	147375
NCBI Taxonomy	198827
IPNI	439173-1
iNaturalist	508380
GBIF	5298016
Freebase	/m/012r4swq
Elurikkus	507689
USDA GRIN	20429
Wikipedia	Iris_tenuifolia

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

Effect of grazing and climatic factors on biodiversity-ecosystem functioning relationships in grassland ecosystems - a case study of typical steppe in Inner Mongolia, China

Zhang Y, Wuriliga, Liu P, Fan R, Guo J, Liu L, Ding Y

Front Plant Sci

22-Dec-2023

PMCID:	PMC10770857
doi:	10.3389/fpls.2023.1297061
PMID:	38186605

Effects of Spring Drought and Nitrogen Addition on Productivity and Community Composition of Degraded Grasslands

Li S, Lu S, Li X, Hou X, Zhao X, Xu X, Zhao N

Plants (Basel)

31-Jul-2023

PMCID:	PMC10421370
doi:	10.3390/plants12152836
PMID:	37570989

Study on wild medicinal plant resources and their applied ethnology in multiethnic areas of the Gansu–Ningxia–Inner Mongolia intersection zone

Xie J, Luo C, Yang X, Ren Y, Zhang X, Chen H, Zhao Y, Liu S, Wu F

J Ethnobiol Ethnomed

20-May-2023

PMCID:	PMC10199607
doi:	10.1186/s13002-023-00585-5
PMID:	37210577

Species richness and asynchrony maintain the stability of primary productivity against seasonal climatic variability

Zhang Z, Hautier Y, Bao T, Yang J, Qing H, Liu Z, Wang M, Li T, Yan M, Zhang G

Front Plant Sci

28-Oct-2022

PMCID:	PMC9650401
doi:	10.3389/fpls.2022.1014049
PMID:	36388500

Intra‐annual growing season climate variability drives the community intra‐annual stability of a temperate grassland by altering intra‐annual species asynchrony and richness in Inner Mongolia, China

Zhang Z, Bao T, Hautier Y, Yang J, Liu Z, Qing H

Ecol Evol

04-Oct-2022

PMCID:	PMC9532246
doi:	10.1002/ece3.9385
PMID:	36225823

Ethnobotany of wild edible plants in multiethnic areas of the Gansu–Ningxia–Inner Mongolia junction zone

Jia X, Zhao Y, Zhu Y, Zeng X, Liang X, Xie J, Wu F

J Ethnobiol Ethnomed

09-Aug-2022

PMCID:	PMC9364587
doi:	10.1186/s13002-022-00549-1
PMID:	35945554

Chromane Derivatives from Underground Parts of Iris tenuifolia and Their In Vitro Antimicrobial, Cytotoxicity and Antiproliferative Evaluation

Otgon O, Nadmid S, Paetz C, Dahse HM, Voigt K, Bartram S, Boland W, Dagvadorj E

Molecules

05-Nov-2021

PMCID:	PMC8588511
doi:	10.3390/molecules26216705
PMID:	34771113

Folk nomenclature of plants in Cistanche deserticola-associated community in South Gobi, Mongolia

Mandakh U, Battseren M, Ganbat D, Ayanga T, Adiya Z, Borjigidai A, Long C

Plant Divers

06-Oct-2020

PMCID:	PMC7936101
doi:	10.1016/j.pld.2020.09.008
PMID:	33733011

Climate variability decreases species richness and community stability in a temperate grassland

Zhang Y, Loreau M, He N, Wang J, Pan Q, Bai Y, Han X

Oecologia

26-Jun-2018

PMCID:	PMC6112414
doi:	10.1007/s00442-018-4208-1
PMID:	29943096

Productivity depends more on the rate than the frequency of N addition in a temperate grassland

Zhang Y, Feng J, Isbell F, Lü X, Han X

Sci Rep

28-Jul-2015

PMCID:	PMC4517389
doi:	10.1038/srep12558
PMID:	26218675

The Role of Brain-Derived Neurotrophic Factor in Comorbid Depression: Possible Linkage with Steroid Hormones, Cytokines, and Nutrition

Numakawa T, Richards M, Nakajima S, Adachi N, Furuta M, Odaka H, Kunugi H

Front Psychiatry

26-Sep-2014

PMCID:	PMC4175905
doi:	10.3389/fpsyt.2014.00136
PMID:	25309465

Synthesis of 4-Methoxybenzoylhydrazones and Evaluation of Their Antiglycation Activity

Taha M, Naz H, Rasheed S, Ismail NH, Rahman AA, Yousuf S, Choudhary MI

Molecules

21-Jan-2014

PMCID:	PMC6271482
doi:	10.3390/molecules19011286
PMID:	24451249

Interactive Effects of Warming and Increased Precipitation on Community Structure and Composition in an Annual Forb Dominated Desert Steppe

Hou Y, Zhou G, Xu Z, Liu T, Zhang X

PLoS One

19-Jul-2013

PMCID:	PMC3716769
doi:	10.1371/journal.pone.0070114
PMID:	23894600

Wild plant folk nomenclature of the Mongol herdsmen in the Arhorchin national nature reserve, Inner Mongolia, PR China

Soyolt, Galsannorbu, Yongping, Wunenbayar, Liu G, Khasbagan

J Ethnobiol Ethnomed

24-Apr-2013

PMCID:	PMC3649933
doi:	10.1186/1746-4269-9-30
PMID:	23628479

Flavans from Iris tenuifolia and their effects on β-amyloid aggregation and neural stem cells proliferation in vitro.

Cui YM, Wang H, Liu QR, Han M, Lu Y, Zhao CQ

Bioorg Med Chem Lett

01-Aug-2011

doi:	10.1016/J.BMCL.2011.06.039
PMID:	21737268

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate	163021367	Click to see	502.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,3aR,5aR,5bR,7aR,11aS,13aS,13bR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one	12305184	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(=O)C5(C)C)C)C)C)C	424.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(3S,3aS,5bS,11aS,13aR)-3a,5a,8,8,11a,13a-hexamethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one	5319770	Click to see	424.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
3a,5a,8,8,11a,13a-Hexamethyl-3-(propan-2-yl)-1,2,3,3a,4,5,5a,5b,6,7,7a,8,10,11,11a,13,13a,13b-octadecahydro-9h-cyclopenta[a]chrysen-9-one	185590	Click to see	424.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Aborenone	12305183	Click to see	424.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
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/J.PHYTOCHEM.2008.03.011
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Glucopyranoside, ethyl	428040	Click to see	208.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(1S,12S)-3-methoxy-5,7,11,19-tetraoxapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-17-ol	162868806	Click to see	314.29	unknown	https://doi.org/10.1016/J.BMCL.2011.06.039
3'-Hydroxy-5,7-dimethoxy-4-O-2'-cycloflavan	46847424	Click to see	300.30	unknown	https://doi.org/10.1016/J.BMCL.2011.06.039
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(6R)-6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one	163079697	Click to see	316.26	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
(6R)-9-hydroxy-6-(2-hydroxyphenyl)-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one	163022965	Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O	300.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(6S)-6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one	102066375	Click to see	316.26	unknown	https://doi.org/10.1016/J.BMCL.2011.06.039 https://doi.org/10.1016/S0031-9422(96)00596-1
2',5-Dihydroxy-6,7-methylenedioxyflavanone	74819425	Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O	300.26	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1 https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011 https://doi.org/10.1016/J.BMCL.2011.06.039
5,2'-Dihydroxy-6,7-methylenedioxyflavanone	42608090	Click to see C1C(OC2=CC3=C(C(=C2C1=O)O)OCO3)C4=CC=CC=C4O	300.26	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1 https://doi.org/10.1016/J.BMCL.2011.06.039
5,2',3'-Trihydroxy-6,7-Methylenedioxyflavanone	42608091	Click to see	316.26	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1 https://doi.org/10.1016/J.BMCL.2011.06.039
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin	5318691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O	284.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-2-(2,3-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one	162919149	Click to see	318.28	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
(2R,3R)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	163195576	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)OC)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
(2R,3R)-Alpinone	46883390	Click to see	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(2R)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	162977634	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O	302.28	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
(2S,3R)-3,5-dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	162951471	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)OC)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
(2S,3S)-3,5-dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one	90646612	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
(2S)-2-(2,3-dihydroxyphenyl)-5-hydroxy-6,7-dimethoxy-2,3-dihydrochromen-4-one	163064968	Click to see COC1=C(C(=C2C(=O)CC(OC2=C1)C3=C(C(=CC=C3)O)O)O)OC	332.30	unknown	https://doi.org/10.1016/J.BMCL.2011.06.039
(2S)-2-(2,3-dihydroxyphenyl)-5-hydroxy-7-methoxy-2,3-dihydrochromen-4-one	102066376	Click to see	302.28	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1 https://doi.org/10.1016/J.BMCL.2011.06.039
(2S)-5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	102066377	Click to see	316.30	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
2-(2,3-Dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-2,3-dihydrochromen-4-one	162919148	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=C(C(=CC=C3)O)O)O	318.28	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
3,5-Dihydroxy-2-(3-hydroxy-2-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	162951470	Click to see	332.30	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
5,2',3'-Trihydroxy-7-methoxyflavanone	42607850	Click to see	302.28	unknown	https://doi.org/10.1016/J.BMCL.2011.06.039 https://doi.org/10.1016/S0031-9422(96)00596-1
5,3'-Dihydroxy-7,2'-dimethoxyflavanone	42607852	Click to see	316.30	unknown	https://doi.org/10.1016/S0031-9422(96)00596-1
Alpinone	5317747	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
1,8,10-trihydroxy-9-methoxy-5H-isochromeno[4,3-b]chromen-7-one	11045683	Click to see	328.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7-Dihydroxy-2',6-dimethoxyisoflavone	5491794	Click to see COC1=CC=CC=C1C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O	314.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
7-(2,3-Dihydroxyphenyl)-9-hydroxy-[1,3]dioxolo[4,5-g]chromen-8-one	24970458	Click to see C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=C(C(=CC=C4)O)O)O	314.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Betavulgarin	442668	Click to see	312.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Irilin B	5491551	Click to see	300.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Irisone A	5491929	Click to see	312.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
Irisone B	5387194	Click to see	298.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011
> Phenylpropanoids and polyketides / Stilbenes
1-(6-Hydroxy-4-methoxy-1,3-benzodioxol-5-yl)-2-(2-hydroxyphenyl)ethane-1,2-dione	24970457	Click to see COC1=C(C(=CC2=C1OCO2)O)C(=O)C(=O)C3=CC=CC=C3O	316.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2008.03.011

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Iris tenuifolia

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top