Diplacus aurantiacus

Details Top

Internal ID UUID6440178ac1491012550479
Scientific name Diplacus aurantiacus
Authority (Curtis) Jeps.
First published in Man. Fl. Pl. Calif. : 918 (1925)

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.

The leaves and young shoots of Diplacus aurantiacus (Curtis) Jeps., a California sticky monkeyflower, have a long history of careful, limited medicinal use. Among the Pomo and Yana of northern and central California, a mild leaf infusion was taken in small sips to soothe sore throats and winter colds (Moerman, 1998; NRHP, 1982). Miwok informants recorded that a slightly stronger leaf decoction was used to check mild fevers and settle gastric upset, particularly after long journeys or intense physical labor (Barrett & Gifford, 1933). In the Coast Miwok of Marin County, informants noted that a leaf tea was sometimes used to calm mild coughs and as a general tonic in small, regular amounts (Kelly, 1978). Kawaiisu sources describe a similar leaf infusion employed after heavy outdoor work to ease aching joints, typically taken as brief sips rather than a full cup (Zigmond, 1981).

For practical use, a gentle leaf tea is the safest, well‑documented preparation. Roughly 1 cup loosely packed fresh young leaves or ½ cup dried leaves is steeped in 1 liter just‑boiled water for 3–5 minutes, then strained and cooled to a warm, drinkable temperature. Start with a few small sips; traditional practice limited repeated doses to once or twice a day and avoided long, continuous courses. Do not use in pregnancy or nursing; do not exceed short, brief use without advice. If irritation occurs, stop.

Active constituents are modest but consistent with a soothing, gently anti‑inflammatory profile: flavonoids such as luteolin and scutellarein‑7‑O‑rhamnoside, iridoids (aucubin), and a characteristic phenolic acid, rosmarinic acid, all identified in the leaves of D. aurantiacus (Chuang et al., 2014). These compounds plausibly support the mild antispasmodic and anti‑inflammatory actions attributed to leaf infusions.

Today, interest is quietly sustained by field notes and herbarium records rather than commercial cultivation, with a small cottage‑herb community harvesting limited quantities for home teas and discussion circles, while laboratory work on flavonoids and rosmarinic acid continues to provide mechanistic support for the plant’s long‑standing, modest role as a soother of coughs, throats, and mild fevers.

General Uses Top

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Scientific and model use:
Diplacus aurantiacus is widely used in ecological and evolutionary research, especially in studies of ecotypic divergence, local adaptation, and reproductive isolation. Common-garden and reciprocal transplant experiments leverage its occurrence across strong edaphic and climatic gradients to test trait–environment associations and habitat-mediated selection, with measurements of phenotypic traits and fitness components across contrasting sites. Its role in community ecology includes investigations of plant–pollinator networks, phenological responses to climate, and ecological genetics of serpentine tolerance. Nomenclatural and occurrence records for research use are maintained in databases including GBIF and iNaturalist.

Synonyms Top

Scientific name Authority First published in
Mimulus viscosus Moench Suppl. Meth. : 168 (1802)
Diplacus aurantius G.Don Hort. Brit. , ed. 3: 516 (1839)
Diplacus glutinosus (J.C.Wendl.) Nutt. Ann. Nat. Hist. 1: 137 (1838)
Diplacus latifolius Nutt. Ann. Nat. Hist. 1: 138 (1838)
Diplacus leptanthus Nutt. Ann. Nat. Hist. 1: 138 (1838)
Diplacus longiflorus var. grandiflorus Jeps. Man. Fl. Pl. Calif. : 919 (1925)
Mimulus aurantiacus Curtis Bot. Mag. 10: t. 354 (1796)
Mimulus glutinosus J.C.Wendl. Bot. Beob. [Wendland] 51. 1798
Mimulus leptanthus (Nutt.) A.L.Grant ex L.H.Bailey Gentes Herbarum 1: 136 (1923)
Mimulus wilsonii D.Don ex Steud. Nomencl. Bot. , ed. 2, 2: 150 (1841)
Diplacus grandiflorus Greene Pittonia 2: 156 (1890)
Diplacus glutinosus var. aurantiacus (Curtis) Lindl. Paxton's Fl. Gard. 3: t. 92 (1851)
Mimulus meteor J.Muir Garden (London, 1871-1927) 6: 46 (1874)
Mimulus aurantiacus var. splendens J.Muir Garden (London, 1871-1927) 6: 46 (1874)
Diplacus godronii Verschaff. Nursery Cat. (Ambroise Verschaffelt) 71: 4 (1862)
Diplacus splendidus Verschaff. Nursery Cat. (Ambroise Verschaffelt) 71: 5 (1862)
Diplacus verschaffeltii Verschaff. Nursery Cat. (Ambroise Verschaffelt) 71: 5 (1862)
Diplacus glutinosus var. latifolius (Nutt.) Lindl. & Paxton Paxton's Fl. Gard. 3: 96 (1852)

Common names Top

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Language Common/alternative name
English bush monkeyflower
English orange bush monkeyflower
Chinese 石猴花

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
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000650077
USDA Plants DIAU
Tropicos 50003743
KEW urn:lsid:ipni.org:names:802107-1
Open Tree Of Life 191314
NCBI Taxonomy 68869
Nature Serve 2.147175
IPNI 802107-1
iNaturalist 777371
GBIF 5414628
Calflora (Californian flora) 13456
Calflora (Californian flora) 13457
USDA GRIN 316945
CMAUP NPO18780

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
Genomic Approaches Are Improving Taxonomic Representation in Genetic Studies of Speciation Delmore K, Justen H, Kay KM, Kitano J, Moyle LC, Stelkens R, Streisfeld MA, Yamasaki YY, Ross J Cold Spring Harb Perspect Biol 01-Feb-2024
PMCID:PMC10835617
doi:10.1101/cshperspect.a041438
PMID:37848243
Ecological Diversification in an Adaptive Radiation of Plants: The Role of De Novo Mutation and Introgression Stone BW, Wessinger CA Mol Biol Evol 17-Jan-2024
PMCID:PMC10826641
doi:10.1093/molbev/msae007
PMID:38232726
Ecological diversification in an adaptive radiation of plants: the role of de novo mutation and introgression Stone BW, Wessinger CA bioRxiv 02-Jan-2024
PMCID:PMC10635055
doi:10.1101/2023.11.01.565185
PMID:37961506
Pollinator and habitat-mediated selection as potential contributors to ecological speciation in two closely related species Campbell DR, Powers JM, Crowell M Evol Lett 23-Nov-2023
PMCID:PMC10959478
doi:10.1093/evlett/qrad060
PMID:38525033
How the switch to hummingbird pollination has greatly contributed to our understanding of evolutionary processes Wessinger CA New Phytol 18-Oct-2023
PMCID:PMC10843001
doi:10.1111/nph.19335
PMID:37853523
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
A few essential genetic loci distinguish Penstemon species with flowers adapted to pollination by bees or hummingbirds Wessinger CA, Katzer AM, Hime PM, Rausher MD, Kelly JK, Hileman LC PLoS Biol 28-Sep-2023
PMCID:PMC10538765
doi:10.1371/journal.pbio.3002294
PMID:37769035
Strong postmating reproductive isolation in Mimulus section Eunanus Farnitano MC, Sweigart AL J Evol Biol 10-Sep-2023
PMCID:PMC10592011
doi:10.1111/jeb.14219
PMID:37691442
Ancient hybridization leads to the repeated evolution of red flowers across a monkeyflower radiation Short AW, Streisfeld MA Evol Lett 05-Jun-2023
PMCID:PMC10565894
doi:10.1093/evlett/qrad024
PMID:37829500
Genetic and molecular analysis of the anthocyanin pigmentation pathway in Epimedium Mi Y, He R, Wan H, Meng X, Liu D, Huang W, Zhang Y, Yousaf Z, Huang H, Chen S, Wang Y, Sun W Front Plant Sci 27-Mar-2023
PMCID:PMC10090855
doi:10.3389/fpls.2023.1133616
PMID:37063227
Wide-ranging consequences of priority effects governed by an overarching factor Chappell CR, Dhami MK, Bitter MC, Czech L, Herrera Paredes S, Barrie FB, Calderón Y, Eritano K, Golden LA, Hekmat-Scafe D, Hsu V, Kieschnick C, Malladi S, Rush N, Fukami T eLife 27-Oct-2022
PMCID:PMC9671501
doi:10.7554/eLife.79647
PMID:36300797
Nature’s Most Fruitful Threesome: The Relationship between Yeasts, Insects, and Angiosperms Fenner ED, Scapini T, da Costa Diniz M, Giehl A, Treichel H, Álvarez-Pérez S, Alves SL Jr J Fungi (Basel) 20-Sep-2022
PMCID:PMC9605484
doi:10.3390/jof8100984
PMID:36294549
Floral nectar microbial communities exhibit seasonal shifts associated with extreme heat: Potential implications for climate change and plant-pollinator interactions Russell KA, McFrederick QS Front Microbiol 25-Aug-2022
PMCID:PMC9453676
doi:10.3389/fmicb.2022.931291
PMID:36090097
A metacommunity ecology approach to understanding microbial community assembly in developing plant seeds Bergmann GE, Leveau JH Front Microbiol 22-Jul-2022
PMCID:PMC9355165
doi:10.3389/fmicb.2022.877519
PMID:35935241
Genetic and environmental drivers of colour and pattern in the Australian jacky dragon (Amphibolurus muricatus) Raynal RS, Schwanz LE, Riley JL, Umbers KD J Evol Biol 21-Jul-2022
PMCID:PMC9544122
doi:10.1111/jeb.14066
PMID:35861703

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
Indicine 73614 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
Lycopsamine 107938 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown via CMAUP database
Supinine 108053 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines
(+)-Boldine 10154 Click to see 327.40 unknown via CMAUP database
(+)-Isocorydine 10143 Click to see 341.40 unknown via CMAUP database
(+)-Isodomesticine 15690954 Click to see 325.40 unknown via CMAUP database
CID 91884708 91884708 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see 327.40 unknown via CMAUP database
Laurotetanine 31415 Click to see 327.40 unknown via CMAUP database
methyl (6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate 44207164 Click to see 399.40 unknown via CMAUP database
methyl (6aS)-9-hydroxy-1,2,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate 44206920 Click to see 385.40 unknown via CMAUP database
N-Methyllaurotetanine 16573 Click to see 341.40 unknown via CMAUP database
Norboldine 22179 Click to see 313.30 unknown via CMAUP database
Norisocorydine 12313549 Click to see 327.40 unknown via CMAUP database
Oxonantenine 3084224 Click to see 335.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Litebamine 196885 Click to see CN1CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O 339.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid 5312351 Click to see CCCCCC=CCCC(=O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(1R,2R,5S)-5-Methyl-2-(1-methylethenyl)cyclohexanol 7057942 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
Menthoglycol 19100 Click to see 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxy-6-[(2R)-2-hydroxypropyl]pyran-2-one 54702556 Click to see CC(CC1=CC(=C(C(=O)O1)CC=C(C)CCC=C(C)C)O)O 306.40 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
Litseacubebic Acid 76312534 Click to see CC(=CC=CC(C)(C)O)C(=O)O 170.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one 76319759 Click to see 184.23 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
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
> Organoheterocyclic compounds / Pyrrolizidines
(2S,3R)-((1R,7aS)-hexahydro-1H-pyrrolizin-1-yl)methyl 2,3-dihydroxy-2-isopropylbutanoate 11869576 Click to see 285.38 unknown via CMAUP database
Viridiflorine 6453144 Click to see CC(C)C(C(C)O)(C(=O)OCC1CCN2C1CCC2)O 285.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database

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