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Mnium hornum

Mnium hornum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440886b77e09042473401
Scientific name Mnium hornum
Authority Hedw.
First published in Sp. Musc. Frond. 188 1801

Description Top

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It is native to Europe, Asia, and North America, where it is found in moist, shady habitats. It grows in dense, bright green tufts, and its leaves are ovate-lanceolate in shape. The leaves are typically 1-2 mm long, and have a smooth, glossy surface. The stems are reddish-brown in color, and the capsules are yellowish-brown.

Mnium hornum, commonly known as horn calcareous moss, is a species of moss native to Europe, Asia, and North America. It grows in moist, shady habitats in dense, bright green tufts. Its leaves are ovate-lanceolate in shape, 1-2 mm long, and have a smooth, glossy surface. The stems are reddish-brown and the capsules are yellowish-brown.

Synonyms Top

Scientific name Authority First published in
Mnium hornum var. schultzii Warnst. Krypt.-Fl. Brandenburg, Laubm. 544 1905
Mnium hornum var. sublaeve Milde Flora 53: 313 1870

Common names Top

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Language Common/alternative name
English horn calcareous moss
Czech měřík trsnatý
Welsh gruwfwsogl cyffredin
Danish brunfiltet stjernemos
German schwanenhals-sternmoos
Estonian hammas-tähtsammal
Finnish soukkalehväsammal
French mnie annuelle
Dutch gewoon sterrenmos
Swedish skuggstjärnmossa
Chinese 提灯藓

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001187550
USDA Plants MNHO
Tropicos 35170506
INPN 4917
The Plant List tro-35170506
Open Tree Of Life 199298
NCBI Taxonomy 41835
NBN Atlas NBNSYS0000036641
Nature Serve 2.126369
iNaturalist 165489
GBIF 5282688
EPPO MNMHO
EOL 928052
Elurikkus 5760
US Library of Congress sh95007281
Wikipedia Mnium_hornum
CMAUP NPO14435

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
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
Lakeshore vegetation: More resilient towards human recreation than we think? Meyer N, Swiatloch A, Dittrich S, von Oheimb G Ecol Evol 08-Jul-2023
PMCID:PMC10329258
doi:10.1002/ece3.10268
PMID:37424934
Fatty Acid Profiles of Some Siberian Bryophytes and Prospects of Their Use in Chemotaxonomy Filippova IP, Makhutova ON, Guseynova VE, Gladyshev MI Biomolecules 15-May-2023
PMCID:PMC10216562
doi:10.3390/biom13050840
PMID:37238711
Epiphytic Bryophytes in an Urban Landscape: Which Factors Determine Their Distribution, Species Richness, and Diversity? A Case Study in Wroclaw, Poland Żołnierz L, Fudali E, Szymanowski M Int J Environ Res Public Health 21-May-2022
PMCID:PMC9141403
doi:10.3390/ijerph19106274
PMID:35627811
Bryophyte Spores Tolerate High Desiccation Levels and Exposure to Cryogenic Temperatures but Contain Storage Lipids and Chlorophyll: Understanding the Essential Traits Needed for the Creation of Bryophyte Spore Banks Tiloca G, Brundu G, Ballesteros D Plants (Basel) 07-May-2022
PMCID:PMC9100633
doi:10.3390/plants11091262
PMID:35567263
Video recording and vegetation classification elucidate sheep foraging ecology in species‐rich grassland Hall SJ, Arney DR, Bunce RG, Vollmer E Ecol Evol 20-Oct-2021
PMCID:PMC8571568
doi:10.1002/ece3.8172
PMID:34765147
Habitat loss, predation pressure and episodic heat-shocks interact to impact arthropods and photosynthetic functioning of microecosystems Vanbergen AJ, Boissieres C, Gray A, Chapman DS Proc Biol Sci 07-Apr-2021
PMCID:PMC8059533
doi:10.1098/rspb.2021.0032
PMID:33823665
Natural Products as Fungicide and Their Role in Crop Protection Santra HK, Banerjee D Natural Bioactive Products in Sustainable Agriculture 12-May-2020
PMCID:PMC7212785
doi:10.1007/978-981-15-3024-1_9
Flood resilience, amenity and biodiversity benefits of an historic urban pond Krivtsov V, Birkinshaw S, Arthur S, Knott D, Monfries R, Wilson K, Christie D, Chamberlain D, Brownless P, Kelly D, Buckman J, Forbes H, Monteiro Y Philos Trans A Math Phys Eng Sci 17-Feb-2020
PMCID:PMC7061967
doi:10.1098/rsta.2019.0389
PMID:32063177
Valuable Fatty Acids in Bryophytes—Production, Biosynthesis, Analysis and Applications Lu Y, Eiriksson FF, Thorsteinsdóttir M, Simonsen HT Plants (Basel) 19-Nov-2019
PMCID:PMC6918284
doi:10.3390/plants8110524
PMID:31752421
Associations between shoot-level water relations and photosynthetic responses to water and light in 12 moss species Wang Z, Bader MY AoB Plants 24-May-2018
PMCID:PMC6012793
doi:10.1093/aobpla/ply034
PMID:29977488
Vascular plant and bryophyte species richness in response to water quality in lowland spring niches with different anthropogenic impacts Puczko K, Zieliński P, Jusik S, Kołakowska A, Jekatierynczuk-Rudczyk E Environ Monit Assess 10-May-2018
PMCID:PMC5945798
doi:10.1007/s10661-018-6703-6
PMID:29748822
A review on algae and plants as potential source of arachidonic acid Shanab SM, Hafez RM, Fouad AS J Adv Res 13-Mar-2018
PMCID:PMC6052662
doi:10.1016/j.jare.2018.03.004
PMID:30034871
The evolution of the stomatal apparatus: intercellular spaces and sporophyte water relations in bryophytes—two ignored dimensions Duckett JG, Pressel S Philos Trans R Soc Lond B Biol Sci 18-Dec-2017
PMCID:PMC5745334
doi:10.1098/rstb.2016.0498
PMID:29254963
A new microscopic method to analyse desiccation‐induced volume changes in aeroterrestrial green algae LAJOS K, MAYR S, BUCHNER O, BLAAS K, HOLZINGER A J Microsc 14-Apr-2016
PMCID:PMC4947386
doi:10.1111/jmi.12409
PMID:27075881

Phytochemical Profile Top

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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bR)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 6543710 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O 328.27 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Mallotucin B 101316809 Click to see CC1CC(C2=C(C13CC(OC3=O)C4=COC=C4)CCCC2(C(=O)OC)C(=O)OC)OC(=O)C 460.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13alpha,28R)-3alpha-(Benzoyloxy)-12beta,28-epoxy-28-methoxyursane 100973317 Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3OC)C 576.80 unknown via CMAUP database
(13alpha)-3alpha-(Benzoyloxy)-12beta-hydroxyursane-28-oic acid 28,12-lactone 100973316 Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3=O)C 560.80 unknown via CMAUP database
(13alpha)-3alpha-Hydroxyursan-28-oic acid 100973318 Click to see CC1CCC2(CCC3(C(C2C1C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O 458.70 unknown via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 7092625 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
3-Oxo-16alpha-hydroxy-D:A-friedoolean-27-oic acid 27,16-lactone 10928543 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C 454.70 unknown via CMAUP database
3alpha-(Benzoyloxy)-16alpha-hydroxy-D:A-friedoolean-27-oic acid 27,16-lactone 11060762 Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)OC(=O)C7=CC=CC=C7 560.80 unknown via CMAUP database
3beta,16alpha-Dihydroxy-D:A-friedoolean-27-oic acid 27,16-lactone 11070498 Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)O 456.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Methyl ursolate 636516 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Teucvin 179592 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown via CMAUP database
Teuflin 13071598 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
Mallorepine 13027 Click to see CN1C=CC(=O)C(=C1)C#N 134.14 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Dihydropyridines
1-Methyl-4-oxo-1,4-dihydropyridine-2-carbonitrile 45087607 Click to see CN1C=CC(=O)C=C1C#N 134.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,6-Dihydroxy-4-methoxyphenyl)-5,6-dihydroxybenzofuran-3-carboxylic acid 12444938 Click to see COC1=CC(=C(C(=C1)O)C2=C(C3=CC(=C(C=C3O2)O)O)C(=O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
2-[2-[(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-8-yl]-3,4-dihydroxyphenyl]-5,7-dihydroxychromen-4-one 163054611 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C(C=CC(=C3O)O)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)C6=CC(=C(C=C6)O)O 572.50 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
2-[2-[(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-8-yl]-3,4-dihydroxyphenyl]-5,7-dihydroxychromen-4-one 163054610 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C(C=CC(=C3O)O)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)C6=CC(=C(C=C6)O)O 572.50 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
2-[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-8-yl]-3,4-dihydroxyphenyl]-5,7-dihydroxychromen-4-one 15666671 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3=C(C=CC(=C3O)O)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)C6=CC(=C(C=C6)O)O 572.50 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Philonotisflavone 5469098 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4O)O)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 570.50 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
8-[6-(5,7-Dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenyl]-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 101039675 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4O)O)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 584.50 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3,8,9-Tetramethoxy-[1]benzofuro[3,2-c]chromen-6-one 346343 Click to see COC1=CC2=C(C(=C1)OC)C3=C(C4=CC(=C(C=C4O3)OC)OC)C(=O)O2 356.30 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
1,9-Dihydroxy-3,8-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 15895183 Click to see COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)OC)O)O 328.27 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
3,9-Dihydroxy-1,8-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 15895182 Click to see COC1=CC(=CC2=C1C3=C(C4=CC(=C(C=C4O3)O)OC)C(=O)O2)O 328.27 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
9-Hydroxy-1,3,8-trimethoxy-[1]benzofuro[3,2-c]chromen-6-one 15895184 Click to see COC1=CC2=C(C(=C1)OC)C3=C(C4=CC(=C(C=C4O3)O)OC)C(=O)O2 342.30 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
Demethylwedelolactone 5489605 Click to see C1=C(C=C2C(=C1O)C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)O 300.22 unknown https://doi.org/10.1016/S0031-9422(98)00514-7
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6-(6-carboxy-2,3,4-trihydroxyphenoxy)-7,8,11,12,13,22-hexahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate 21672437 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C7C(OC(=O)C8=CC(=C(C(=C78)O)O)O)C(=O)O 1137.80 unknown via CMAUP database
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate 21672435 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 969.60 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown via CMAUP database
Mallotinic acid 10056140 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O 802.60 unknown via CMAUP database
Punicafolin 5320800 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Wutxioakrfkqhk-bwpkhyersa- 21672436 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O 970.70 unknown via CMAUP database

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