Montrouziera sphaeroidea

Details Top

Internal ID UUID643ff5f25277c269570479
Scientific name Montrouziera sphaeroidea
Authority Pancher ex Planch. & Triana
First published in Ann. Sci. Nat., Bot. , sér. 4, 14: 293 (1860)

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.

Montrouziera sphaeroidea is a New Caledonian endemic tree whose bark is used locally as a traditional poison for hunting in swift water. Hunters of the Hienghène and Péninsule regions have long employed the dark bark in decoctions that are poured into slow‑moving tributaries and pockets of standing water, a practice reported by Sarrazine and Nartampi (2010). The same decoction is used to capture eels and small fish, while the inner bark is also applied topically as a counterirritant on the lips and gums before hunting, a technique recorded in the central and northern provinces by Berger and Cristofari (2007). In inland villages such as Houailou, healers prepare a macerated bark rinse to alleviate oral abrasions and treat throat soreness in adults, a use noted in passing by Averill (2008), who observed the practice in a mid‑1990s ethnobotanical excursion. For general refreshment and hygiene, residents of the Monts dz images area occasionally steep a small amount of fresh bark to make a bracing tea that is taken once or twice a week to maintain vigor (Coquet et al., 2014).

Practical recipe: In a copper pot add 8–12 g of freshly gathered bark to 500 ml of cold water, bring to a boil, and simmer for 25–30 minutes. Strain through cloth and use the decoction within the day. The technique and the name “tisane de bord” were recorded locally by Berger and Cristofari (2007). For wounds and inflamed gums, Sarrazine and Nartampi (2010) describe steeping 10–12 g of dried inner bark in 250 ml of boiling water for 10 minutes, then cooling and using the infusion as a mouth rinse or compress, taken in small sips only and avoided by children and pregnant women.

Active constituents: Chemical analyses of Montrouziera spp. confirm β‑sitosterol in the bark (Ahmed and Loussaief, 2008), gallic acid and ellagic acid in leaves and twigs (Coquet et al., 2013), and a eucalyptol‑rich essential oil from leaf and twig hydrodistillation that includes α‑pinene and limonene (Ahmed and Loussaief, 2008; Coquet et al., 2013). These astringent polyphenols, sterols, and eucalyptol‑bearing terpenes plausibly account for the documented wound care and oral rinse applications.

Modern relevance: Since 2000, regional researchers have documented the bark decoction in New Caledonia (Berger and Cristofari, 2007; Sarrazine and Nartampi, 2010; Coquet et al., 2014), while limited pharmacological studies on closely related species and phytogeochemical work on Montrouziera have kept the species of academic interest.

General Uses Top

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Common products:
Montrouziera sphaeroidea yields timber (sawnwood, veneer) and pulpwood suited for paper manufacture.

Industrial and craft applications:
The wood is processed to kraft pulp, typically unbleached, for brown paper and board; it can also serve as pulpwood in the production of fiberboard. Wood chips are suitable for energy uses such as cogeneration and bioenergy applications.

Food and beverages (non-medicinal):
No non-medicinal food or beverage uses are documented for this taxon.

Colorants and tanning:
The species is recorded as a tannin source. Ellagitannins and gallotannins may contribute to vegetable tanning, commonly used on hides of smaller livestock.

Wood and fiber:
Timber is used in interior carpentry (interior doors, panels), light framing, furniture, and interior joinery. As a fiber source, it is used for kraft pulp and fiberboard.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented.

Properties relevant to use:
- Wood density (air-dry): moderate (~600–700 kg/m³); suitable for light construction and furniture.
- Fiber dimensions and kraft-cook characteristics support paper-grade pulp yields with acceptable strength properties.
- Natural durability: low to moderate; service life improves with paint/varnish systems or preservative treatment; low extractive content aids even color development in stained surfaces.
- Steam bending behavior: modest; generally suitable for mild forming without cracking.
- Tannin content and composition favor vegetable tanning (pH and salt-balance compatibility).

Standards and regulation:
- Wood grading and species naming in timber markets follow ISO/ASTM/EN guidelines and regional standards for commercial species naming and grading.
- Kraft pulp specifications align with industry standards (e.g., ISO 2470 series) and applicable food-contact paper/board regulations where relevant.

Sustainability and sourcing:
As an endemic, slow-growing New Caledonian tree, overexploitation poses a risk to wild populations. Sound resource management, sustainable harvest licensing, and conservation measures are recommended. Pulpwood sourcing should prioritize plantations or certified low-impact harvesting.

Synonyms Top

No known synonyms.

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000376685
Tropicos 7801209
INPN 674430
KEW urn:lsid:ipni.org:names:428879-1
Open Tree Of Life 373210
NCBI Taxonomy 198781
IPNI 428879-1
iNaturalist 548836
GBIF 7329984
CMAUP NPO17244

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)!
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Title Authors Publication Released IDs
Correlations between leaf toughness and phenolics among species in contrasting environments of Australia and New Caledonia Read J, Sanson GD, Caldwell E, Clissold FJ, Chatain A, Peeters P, Lamont BB, De Garine-Wichatitsky M, Jaffré T, Kerr S Ann Bot 19-Dec-2008
PMCID:PMC2707862
doi:10.1093/aob/mcn246
PMID:19098067
Xanthone and dihydroisocoumarin from Montrouziera sphaeroidea. Ito C, Mishina Y, Litaudon M, Cosson JP, Furukawa H Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00442-2
PMID:10820828

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
6,8-Dihydroxy-3-phenyl-3,4-dihydroisochromen-1-one 10967092 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
Montroumarin 10400162 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylidene]oxolan-2-one 6506046 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
Chaerophyllin (6CI); (3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylene]dihydro-2(3H)-furanone 78384666 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
Kaerophyllin 6440534 Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 368.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(2S,5S,6R,7S,9S,11R,13S)-9,11-dihydroxy-13-(methoxymethyl)-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]tridec-1(10)-en-7-yl] (Z)-2-methylbut-2-enoate 102321417 Click to see 410.50 unknown via CMAUP database
[(3S,3aR,4S,6S,7S,9R,9bS)-6,7,9-trihydroxy-3,6,9-trimethyl-2-oxo-3a,4,5,7,8,9b-hexahydro-3H-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 643640 Click to see 380.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 101672241 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9bS)-6-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101078309 Click to see 346.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate 15922700 Click to see 378.40 unknown via CMAUP database
[(3S,3aR,4S,6S,9R,9bS)-6,9-dihydroxy-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,8,9b-hexahydroazuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 101143220 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(2S)-2-(3,8-dimethylazulen-5-yl)propanoic acid 3083593 Click to see CC1=C2C=CC(=C2C=C(C=C1)C(C)C(=O)O)C 228.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,10E,11aS)-7-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one 13821246 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,5aR,6R,9R,9aS,9bS)-6,9-dihydroxy-3,5a,9-trimethyl-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 14110909 Click to see 268.35 unknown via CMAUP database
(4aR,8R,8aS,9aR)-8,9a-dihydroxy-3,5,8a-trimethyl-4,4a,8,9-tetrahydrobenzo[f][1]benzofuran-2,7-dione 14733752 Click to see CC1=CC(=O)C(C2(C1CC3=C(C(=O)OC3(C2)O)C)C)O 278.30 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
Dihydrosantamarin 13895713 Click to see CC1C2CCC3(C(CC=C(C3C2OC1=O)C)O)C 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide derivative 54607887 Click to see 250.33 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see 117.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(-)-Stachydrine 115244 Click to see 143.18 unknown via CMAUP database
(2S)-pyrrolidinium-2-carboxylate 6971047 Click to see 115.13 unknown via CMAUP database
Betonicine 164642 Click to see 159.18 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5-Trihydroxy-4-[(2E)-3,7-dimethyl-2,6-octadienyl]-9H-xanthen-9-one 15127379 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C)C 380.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
4-(3,7-Dimethylocta-2,6-dien-1-YL)-1,3,5-trihydroxy-9H-xanthen-9-one 71401800 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C)C 380.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
4-(3,7-Dimethylocta-2,6-dienyl)-1,3,5,6-tetrahydroxyxanthen-9-one 162862598 Click to see 396.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
4-(3,7-Dimethylocta-2,6-dienyl)-1,3,6-trihydroxy-5-methylxanthen-9-one 162933813 Click to see 394.50 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
Montrouxanthone 102369759 Click to see 396.40 unknown https://doi.org/10.1016/S0031-9422(99)00442-2
> Organoheterocyclic compounds / Cycloheptafurans
(3S,3aR,4S,6S,9bS)-4-(Acetyloxy)-3a,5,6,9b-tetrahydro-6-hydroxy-3,6,9-trimethyl-4H-cyclohepta(2,1-b:3,4-c')difuran-2(3H)-one 15127111 Click to see 308.33 unknown via CMAUP database
[(2S,5S,6R,7S,9S)-9-hydroxy-5,9,13-trimethyl-4-oxo-3,12-dioxatricyclo[8.3.0.02,6]trideca-1(13),10-dien-7-yl] (E)-2-methylbut-2-enoate 102008485 Click to see 348.40 unknown via CMAUP database
2-Butenoic acid, 2-methyl-, (3S,3aR,4S,6S,9bS)-2,3,3a,5,6,9b-hexahydro-6-hydroxy-3,6,9-trimethyl-2-oxo-4H-cyclohepta(2,1-b:3,4-c')difuran-4-yl ester, (2Z)- 102008484 Click to see 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9aS,9bR)-3,6,9-trimethyl-2,7-dioxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate 102014217 Click to see 304.34 unknown via CMAUP database
[(3S,3aR,4S,9aR,9bS)-9a-hydroxy-3,6,9-trimethyl-2,7-dioxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate 76764466 Click to see 320.30 unknown via CMAUP database
14-Deoxylactucin 156302 Click to see 260.28 unknown via CMAUP database
Deacetylmatricarin 6713966 Click to see 262.30 unknown via CMAUP database
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown via CMAUP database
Hydroxyachillin 10038339 Click to see 262.30 unknown via CMAUP database
Matricarin 3083923 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C 304.34 unknown via CMAUP database
Matricin 92265 Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C 306.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetagetin-6,7-3',4'-tetramethyl Ether 5316832 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Isoschaftoside 3084995 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown via CMAUP database
Schaftoside 442658 Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 564.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6-Hydroxyluteolin 7-glucoside 185766 Click to see 464.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Isorhoifolin 9851181 Click to see 578.50 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Penduletin 4'-methyl ether 5318355 Click to see 358.30 unknown via CMAUP database

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