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Calypogeia muelleriana

Calypogeia muelleriana - 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 UUID64404ffae3a9f236333441
Scientific name Calypogeia muelleriana
Authority (Schiffner) K.Müller
First published in Beih. Bot. Centralbl. 10: 217 1901

Description Top

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Synonyms Top

Scientific name Authority First published in
Kantius muellerianus Schiffner Sitzungsber. Deutsch. Naturwiss.-Med. Vereins Böhmen "Lotos" Prag 48: 344 1900

Common names Top

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Language Common/alternative name
Czech kryjnice müllerova
Welsh codlys mueller
German müllers bartkelchmoos
Estonian mülleri kottsammal
Finnish loukkopaanusammal
Dutch gaaf buidelmos
Swedish sumpsäckmossa
Chinese 芽胞护蒴苔

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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Name Authority First published in
Calypogeia muelleriana f. paludosa (Warnst.) Schljakov Novosti Syst. Niza. Rast. 15: 241 1978
Calypogeia muelleriana f. sphagnicola (Arnell & J.Perss.) Schljakov Novosti Syst. Niza. Rast. 15: 241 1978

Germination/Propagation Top

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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

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Database ID/link to page
World Flora Online wfo-0001196166
USDA Plants CAMU21
Tropicos 35184879
INPN 6637
The Plant List tro-35184879
Open Tree Of Life 126779
NCBI Taxonomy 56915
NBN Atlas NHMSYS0000309536
Nature Serve 2.122606
iNaturalist 56487
GBIF 2689329
EPPO QLPMU
EOL 604574
Elurikkus 3316

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
Liverworts of Magadan: Life on the Edge of Beringia Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 22-Nov-2023
PMCID:PMC10708503
doi:10.3390/plants12233928
PMID:38068565
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
Initial ecological change in plant and arthropod community composition after wildfires in designated areas of upland peatlands Kelly R, Montgomery WI, Reid N Ecol Evol 11-Feb-2023
PMCID:PMC9919495
doi:10.1002/ece3.9771
PMID:36789349
Super-Mitobarcoding in Plant Species Identification? It Can Work! The Case of Leafy Liverworts Belonging to the Genus Calypogeia Ślipiko M, Myszczyński K, Buczkowska K, Bączkiewicz A, Sawicki J Int J Mol Sci 08-Dec-2022
PMCID:PMC9779425
doi:10.3390/ijms232415570
PMID:36555212
The Taxonomically Richest Liverwort Hemiboreal Flora in Eurasia Is in the South Kurils Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 25-Aug-2022
PMCID:PMC9460601
doi:10.3390/plants11172200
PMID:36079582
Calypogeia (Calypogeiaceae, Marchantiophyta) in Pacific Asia: Updates from Molecular Revision with Particular Attention to the Genus in North Indochina Bakalin VA, Maltseva YD, Müller F, Klimova KG, Nguyen VS, Choi SS, Troitsky AV Plants (Basel) 04-Apr-2022
PMCID:PMC9002642
doi:10.3390/plants11070983
PMID:35406962
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Liverwort flora of Ayan – a gained link between subarctic and hemiboreal floras in West Okhotiya (Pacific Russia) Bakalin V, Klimova K, Bakalin D, Choi SS Biodivers Data J 01-Apr-2021
PMCID:PMC8032650
doi:10.3897/BDJ.9.e65199
PMID:33841022
The complete chloroplast genome of Douinia plicata (Lindb.) Konstant. & Vilnet (Scapaniaceae, Jungermanniales) Bum HM, Kim HK, Kim NS, Kwon W, Park J Mitochondrial DNA B Resour 09-Nov-2020
PMCID:PMC7655068
doi:10.1080/23802359.2020.1832599
PMID:33367065
The complete chloroplast genome of Scapania ampliata Steph., 1897 (Scapaniaceae, Jungermanniales) Choi SS, Kwon W, Park J Mitochondrial DNA B Resour 20-Jul-2020
PMCID:PMC7782855
doi:10.1080/23802359.2020.1791011
PMID:33457990
Molecular delimitation of European leafy liverworts of the genus Calypogeia based on plastid super-barcodes Ślipiko M, Myszczyński K, Buczkowska K, Bączkiewicz A, Szczecińska M, Sawicki J BMC Plant Biol 28-May-2020
PMCID:PMC7257191
doi:10.1186/s12870-020-02435-y
PMID:32466772
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512
A Persistent and Diverse Airway Microbiota Present during Chronic Obstructive Pulmonary Disease Exacerbations Huang YJ, Kim E, Cox MJ, Brodie EL, Brown R, Wiener-Kronish JP, Lynch SV OMICS 01-Feb-2010
PMCID:PMC3116451
doi:10.1089/omi.2009.0100
PMID:20141328
Conservative ecological and evolutionary patterns in liverwort–fungal symbioses Bidartondo MI, Duckett JG Proc Biol Sci 07-Oct-2009
PMCID:PMC2842645
doi:10.1098/rspb.2009.1458
PMID:19812075
Sesquiterpene constituents of the liverwort Calypogeia muelleriana. Warmers U, Wihstutz K, Bülow N, Fricke C, König WA Phytochemistry 20-Nov-1998
doi:10.1016/S0031-9422(98)00283-0
PMID:11711089

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(+)-Eudesma-5,7(11)-diene 6428860 Click to see CC1CCCC2(C1=CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(R)-3-Methylene-6-((S)-1,2,2-trimethylcyclopentyl)cyclohex-1-ene 25202927 Click to see CC1(CCCC1(C)C2CCC(=C)C=C2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(S)-gamma-Calacorene 5315609 Click to see CC1CC=C(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
alpha-Calacorene 12302243 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Bourbon-11-ene 91749842 Click to see CC1CCC2C1C3C2(CCC3C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Cadalene 10225 Click to see CC1=CC2=C(C=CC(=C2C=C1)C)C(C)C 198.30 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
gamma-Calacorene 14038842 Click to see CC1CC=C(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
gamma-Gurjunene 90805 Click to see CC1CCC(C=C2C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Aristolene 530421 Click to see CC1CCCC2=CCC3C(C12C)C3(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Globulol 12304982 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(1aS,4R,4aR,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7b-hexahydro-1aH-cyclopropa[e]azulen-4-ol 100927813 Click to see CC1=C2C(CC1)C(CCC3C2C3(C)C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(1aS,6R,7R,7aS,7bS)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulen-6-ol 100927812 Click to see CC1C(CC2=C(CCC3C(C12)C3(C)C)C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
1,1,4,7-Tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulen-6-ol 101417907 Click to see CC1C(CC2=C(CCC3C(C12)C3(C)C)C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Anastreptene 91746864 Click to see CC1=CCC2C13C2(CCC4C3C4(C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
beta-Spathulene 15923779 Click to see CC1=CCC2C1C3C(C3(C)C)CCC2=C 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Ent-Spathulenol 13854255 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1R,2R,3R,6R)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane 101973934 Click to see CC(=C)C1C2C(C2(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1aS,3aR,7aR,7bS)-1,1,3a,7-tetramethyl-2,3,4,5,7a,7b-hexahydro-1aH-cyclopropa[a]naphthalene 102361380 Click to see CC1=CCCC2(C1C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
(1aS,3aS,7aS,7bS)-1,1,3a,7-tetramethyl-2,3,7a,7b-tetrahydro-1aH-cyclopropa[a]naphthalene 162877912 Click to see CC1=CC=CC2(C1C3C(C3(C)C)CC2)C 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
delta-Selinene 520383 Click to see CC1=C2C=C(CCC2(CCC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Maalialcohol 10944069 Click to see CC1(C2C1C3C(CCCC3(C)O)(CC2)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1beta,4alpha,5beta,6alpha,7alpha)-9-Aromadendrene 13892025 Click to see CC1CCC2C1C3C(C3(C)C)CC=C2C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00283-0

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