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Journal articles on the topic 'Conocephalum conicum'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Ghani, Nurunajah Ab, Agnieszka Ludwiczuk, Nor Hadiani Ismail, and Yoshinori Asakawa. "Volatile Components of the Stressed Liverwort Conocephalum Conicum." Natural Product Communications 11, no. 1 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100130.

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The Type-II Japanese Conocephalum conicum, which is known to have (+)-bornyl acetate as a marker compound, was put in the stressed condition to start biosynthesis of a phenyl propanoid, trans-methyl cinnamate. Analysis of the HS-SPME GC/MS of stressed C. conicum showed trans-methyl cinnamate as a major component. This phenomenon results in some confusion from the chemotype perspective since trans-methyl cinnamate is only present in type-III Japanese C. conicum.

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2

Toyota, Masao, Tetsuya Saito, and Yoshinori Asakawa. "A phenethyl glycoside from Conocephalum conicum." Phytochemistry 43, no. 5 (1996): 1087–88. http://dx.doi.org/10.1016/s0031-9422(96)00504-3.

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3

Shimamura, Masaki, Tomio Yamaguchi, and Hironori Deguchi. "Airborne sperm of Conocephalum conicum (Conocephalaceae)." Journal of Plant Research 121, no. 1 (2007): 69–71. http://dx.doi.org/10.1007/s10265-007-0128-6.

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4

Masao, Toyota, Nagashima Fumihiro, Fukuyama Yoshiyasu, Honda Shoko, and Asakawa Yoshinori. "Bicyclogermacrene type sesquiterpenoid from the liverwort Conocephalum conicum." Phytochemistry 27, no. 10 (1988): 3317–19. http://dx.doi.org/10.1016/0031-9422(88)80054-2.

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5

Piippo, Sinikka, and Timo Koponen. "Bryophyte Flora of Hunan Province, China. 16. Complex Thalloids (Marchantiopsida, Hepaticae)." Polish Botanical Journal 58, no. 1 (2013): 179–92. http://dx.doi.org/10.2478/pbj-2013-0017.

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Abstract The occurrence of 13 species belonging to eight complex thalloid genera and six families are reported for Hunan. Conocephalum japonicum (Thunb.) Grolle, C. salebrosum Szweykowski et al. and Dumortiera hirsuta (Sw.) Nees are moderately common in Hunan, Conocephalum conicum (L.) Dumort., Marchantia palaecea Bertol. and M. emarginata Reinw. et al. subsp. tosana (Steph.) Bischler are rather rare, M. polymorpha L., Plagiochasma pterospermum Mass., Reboulia hemisphaerica (L.) Raddi, and Wiesnerella denutata (Mitt.) Steph. are rare and Asterella khasyana (Griff.) Pandé et al., Plagiochasma a

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6

AKIYAMA, HIROYUKI, and IRENEUSZ J. ODRZYKOSKI. "Phylogenetic re-examination of the genus Conocephalum Hill. (Marchantiales: Conocephalaceae)." Bryophyte Diversity and Evolution 42, no. 1 (2020): 1–18. http://dx.doi.org/10.11646/bde.42.1.1.

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Inter-relationship among the cryptic species in the genus Conocephalum Hill was studied using rbcL + rps4 sequences as well as morphological features. Samples used in this study originated from 1) the long-cultivated strains from Europe, North America, and Asia used for previous allozymes and molecular studies and 2) newly gathered plants mainly from Japan and Taiwan used for both molecular and morphological study. For the C. conicum/ salebrosum complex, a total of six species were confirmed, including a new species previously recognized as R type or Chemotype III (Toyota 1994, Kim et al. 2001

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7

Trebacz, K., and T. Zawadzki. "Light-triggered action potentials in the liverwort Conocephalum conicum." Physiologia Plantarum 64, no. 4 (1985): 482–86. http://dx.doi.org/10.1111/j.1399-3054.1985.tb08526.x.

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8

Melching, S. "Two aromadendrane type alcohols from the liverwort Conocephalum conicum." Phytochemistry 51, no. 2 (1999): 277–80. http://dx.doi.org/10.1016/s0031-9422(98)00768-7.

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9

TOYOTA, Masao. "Phytochemical Study of Liverworts Conocephalum conicum and Chiloscyphus polyanthos." YAKUGAKU ZASSHI 120, no. 12 (2000): 1359–72. http://dx.doi.org/10.1248/yakushi1947.120.12_1359.

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10

Ritchie, Raymond J. "Photosynthetic Electron Transport in the Liverwort Conocephalum conicum (Marchantiales)." Journal of Botanical Research 6, no. 3 (2025): 1–17. https://doi.org/10.30564/jbr.v6i3.9222.

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Photosynthetic Electron Transport Rate (ETR) of Conocephalum conicum (Snakeskin Liverwort) was measured using PAM technology modelled using the Waiting-in-Line model. Plants were grown in greenhouses which had irregular sunflecks of full sunlight and in a culture room under LED lights. Plants grown in the greenhouse had photosynthetic maxima about 1/3 to ½ of sunlight, but very low optimum light requirements when grown in a culture room under LED lights. Chl a content was ≈ 241 mg Chl a m-2 (Chl b/a ≈ 0.216). Mid-morning (10:30 solar time): Ymax ≈ 0.629, irradiance ½ point for Yield ≈ 231 μmol

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11

Maresca, Viviana, Gennaro Lettieri, Sergio Sorbo, Marina Piscopo, and Adriana Basile. "Biological Responses to Cadmium Stress in Liverwort Conocephalum conicum (Marchantiales)." International Journal of Molecular Sciences 21, no. 18 (2020): 6485. http://dx.doi.org/10.3390/ijms21186485.

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Oxidative damage (production and localization of reactive oxygen species) and related response mechanisms (activity of antioxidant enzymes), and induction of Heat Shock Protein 70 expression, have been studied in the toxi-tolerant liverwort Conocephalum conicum (Marchantiales) in response to cadmium stress using two concentrations (36 and 360 µM CdCl2). Cadmium dose-dependent production of reactive oxygen species (ROS) and related activity of antioxidant enzymes was observed. The expression level of heat shock protein (Hsp)70, instead, was higher at 36 µM CdCl2 in comparison with the value obt

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12

Craft, Jonathan D., Daniel Harrelson, and William N. Setzer. "Chemotypic Variation of Conocephalum salebrosum in the Southeastern Appalachian Range: A Search for Cryptic Plant Biodiversity Around the Tennessee River Valley." Natural Product Communications 11, no. 7 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100735.

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The chemotaxonomy of the Conocephalum spp. complex, based on GC-MS analysis of the volatile compositions, has helped to reveal cryptic biodiversity and delineate actual distribution patterns of chemotypes. In the Appalachian Mountains, two samples from eastern central part of the range were previously shown to be C. salebrosum. Additionally, it has recently come to light that stress can alter the volatile composition of C. conicum. This study address a previously unsampled region of the southeastern Appalachians, a region that is a biodiversity epicenter, to determine if more chemotypic divers

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13

Szweykowski, Jerzy, and Maria Anna Bobowicz. "Variability of ventral scales in polish populations of Conocephalum conicum (L.) Dum. (Hepaticae, Marchantiales)." Acta Societatis Botanicorum Poloniae 47, no. 4 (2015): 417–27. http://dx.doi.org/10.5586/asbp.1978.038.

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Samples taken from 6 natural populations of the liverwort species <i>Conocephalum conicum</i> were cultivated in a glasshouse and the variability of 9 ventral scale characters was studied in them. Genetic differences were discovered between population samples but all the attempts to correlate them with the geographic distribution and/or habitat ecology have failed so far.

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14

Melching, Stephanie, and Wilfried A. König. "Sesquiterpenes from the essential oil of the liverwort Conocephalum conicum." Phytochemistry 51, no. 4 (1999): 517–23. http://dx.doi.org/10.1016/s0031-9422(98)00769-9.

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15

Valterová, Irena, C. Rikard Unelius, Jan Vrkoč, and Torbjörn Norin. "Enantiomeric composition of monoterpene hydrocarbons from the liverwort Conocephalum conicum." Phytochemistry 31, no. 9 (1992): 3121–23. http://dx.doi.org/10.1016/0031-9422(92)83457-a.

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16

Ivkovic, Ivana, Danka Bukvicki, Miroslav Novakovic, et al. "Antibacterial properties of thalloid liverworts Marchantia polymorpha L., Conocephalum conicum (L.) Dum. and Pellia endiviifolia (Dicks.) Dumort." Journal of the Serbian Chemical Society 86, no. 12 (2021): 1249–58. http://dx.doi.org/10.2298/jsc210728084i.

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The antimicrobial activity of methanol extracts of three thalloid liverworts, Marchantia polymorpha, Conocephalum conicum and Pellia endiviifolia and bis-bibenzyl marchantin A, the most dominant compound in the methanol extract of M. polymorpha, have been investigated in this research. 1H-NMR spectroscopy revealed that the M. polymorpha and P. endiviifolia extracts of liverwort contain terpenes, oils, sugars and bis-bibenzyls, while these specific macrocyclic compounds were absent in the C. conicum extract. The antimicrobial potential was tested on eight bacterial strains. Antimicrobial effect

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17

Kim, Hong Nam, and Tsuneyuki Yamazaki. "Nonconcerted evolution of histone 3 genes in a liverwort, Conocephalum conicum." Genes & Genetic Systems 79, no. 6 (2004): 331–44. http://dx.doi.org/10.1266/ggs.79.331.

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18

Pawlikowska-Pawlęga, Bożena, Elżbieta Król, Kazimierz Trębacz, and Antoni Gawron. "Genistein and changes of resting and action potentials in Conocephalum conicum." Journal of Plant Physiology 166, no. 7 (2009): 712–19. http://dx.doi.org/10.1016/j.jplph.2008.09.014.

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19

Krol, Elzbieta, Halina Dziubinska, and Kazimierz Trebacz. "Low-Temperature Induced Transmembrane Potential Changes in the Liverwort Conocephalum conicum." Plant and Cell Physiology 44, no. 5 (2003): 527–33. http://dx.doi.org/10.1093/pcp/pcg070.

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20

Toyota, Masao. "ChemInform Abstract: Phytochemical Study of Liverworts Conocephalum conicum and Chiloscyphus polyanthos." ChemInform 32, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.200122227.

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21

Borovichev, Evgeny A., Nijole Kalinauskaite, and Nadezhda A. Konstantinova. "On the distribution of Conocephalum conicum and C. salebrosum (Marchanthiophyta) in Russia." Arctoa 18, no. 1 (2009): 115–20. http://dx.doi.org/10.15298/arctoa.18.04.

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22

Zawadzki, T., and K. Trebacz. "Extra- and intracellular measurements of action potentials in the liverwort Conocephalum conicum." Physiologia Plantarum 64, no. 4 (1985): 477–81. http://dx.doi.org/10.1111/j.1399-3054.1985.tb08525.x.

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23

Trebacz, K., R. Tarnecki, and T. Zawadzki. "Characteristics of the light-induced generator potentials in the liverwort Conocephalum conicum." Physiologia Plantarum 75, no. 1 (1989): 20–23. http://dx.doi.org/10.1111/j.1399-3054.1989.tb02057.x.

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24

Harinantenaina, Liva, Shyoko Kida, and Yoshinori Asakawa. "Phytochemistry of three selected liverworts: Conocephalum conicum, Plagiochila barteri and P. terebrans." Arkivoc 2007, no. 7 (2006): 22–29. http://dx.doi.org/10.3998/ark.5550190.0008.704.

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25

Trebacz, K., G. Schonknecht, H. Dziubinska, and A. Hanaka. "Characteristics of Anion Channels in the Tonoplast of the Liverwort Conocephalum conicum." Plant and Cell Physiology 48, no. 12 (2007): 1747–57. http://dx.doi.org/10.1093/pcp/pcm147.

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26

Krol, E., and K. Trebacz. "Calcium-Dependent Voltage Transients Evoked by Illumination in the Liverwort Conocephalum conicum." Plant and Cell Physiology 40, no. 1 (1999): 17–24. http://dx.doi.org/10.1093/oxfordjournals.pcp.a029470.

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27

Dakskobler, Igor, Andrej Martinčič, and Daniel Rojšek. "Phytosociological Analysis Of Communities With Adiantum Capillusveneris In The Foothills Of The Julian Alps (Western Slovenia)." Hacquetia 13, no. 2 (2014): 235–58. http://dx.doi.org/10.2478/hacq-2014-0016.

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Abstract We conducted a phytosociological study of the communities hosting the rare and endangered fern Adiantum capillus-veneris in the foothills of the Julian Alps, in Karst and in Istria. Based on a comparison with similar communities elsewhere in the southern Alps (northern Italy) we classified most of the recorded stands into the syntaxa Eucladio-Adiantetum eucladietosum and -cratoneuretosum commutati. Releves from the southern Julian Alps, located in comparatively slightly colder and moister local climate and the dolomite bedrock are classified into the new subassociation -hymenostylieto

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28

Castaldo-Cobianchi, R., S. Giordano, A. Basile, and U. Violante. "Occurrence of antibiotic activity in Conocephalum conicum, Mnium undulatum and Leptodictyum riparium (Bryophytes)." Giornale botanico italiano 122, no. 5-6 (1988): 303–11. http://dx.doi.org/10.1080/11263508809429412.

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29

Ludwiczuk, Agnieszka, Ireneusz J. Odrzykoski, and Yoshinori Asakawa. "Identification of cryptic species within liverwort Conocephalum conicum based on the volatile components." Phytochemistry 95 (November 2013): 234–41. http://dx.doi.org/10.1016/j.phytochem.2013.06.011.

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30

Pawlikowska-Pawlěga, Bożena, Kazimierz Trěbacz, Elżbieta Król, and Antoni Gawron. "Effects of quercetin and verapamil on membrane potential in the liverwort Conocephalum conicum." Acta Physiologiae Plantarum 22, no. 1 (2000): 61–67. http://dx.doi.org/10.1007/s11738-000-0009-2.

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31

Pawlikowska-Pawlęga, Bożena, Elżbieta Król, Kazimierz Trębacz, and Antoni Gawron. "Quercetin and genistein hindering effect of neomycin action in the liverwort Conocephalum conicum." Acta Physiologiae Plantarum 33, no. 4 (2010): 1335–44. http://dx.doi.org/10.1007/s11738-010-0666-8.

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32

Król, Elżbieta, Maria Stolarz, Halina Dziubińska, and Kazimierz Trębacz. "Receptory glutaminianu u roślin." Acta Universitatis Lodziensis. Folia Biologica et Oecologica 3 (January 1, 2006): 67–73. http://dx.doi.org/10.18778/1730-2366.03.09.

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Badania prowadzone na pobudliwych plechach wątrobowca Conocephalum conicum wykazały, że podanie 5 mM roztworu glutaminianu (Glu) bądź glicyny (Gly) wywołuje serie potencjałów czynnościowych (AP), którym towarzyszy napływ wapnia do cytoplazmy pobudzonej komórki. Otrzymane wyniki są zgodne z istniejącą hipotezą że międzykomórkowy signalling oparty na aminokwasach jest obecny w królestwie roślin i zwierząt. Jak dotąd opublikowane dane eksperymentalne z równoległych pomiarów wewnątrzkom órkowego stężenia Ca"+ i poziomu potencjału transmem branowego izolowanych komórek liści (M eyerhoff et al. 2004

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33

Dziubinska, H., K. Trebacz, and T. Zawadzki. "The effect of excitation on the rate of respiration in the liverwort Conocephalum conicum." Physiologia Plantarum 75, no. 3 (1989): 417–23. http://dx.doi.org/10.1111/j.1399-3054.1989.tb04648.x.

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34

Trebacz, K. "Measurements of intra-and extracellular pH in the liverwort Conocephalum conicum during action potentials." Physiologia Plantarum 84, no. 3 (1992): 448–52. http://dx.doi.org/10.1111/j.1399-3054.1992.tb04689.x.

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35

Trebacz, K. "Measurements of intra- and extracellular pH in the liverwort Conocephalum conicum during action potentials." Physiologia Plantarum 84, no. 3 (1992): 448–52. http://dx.doi.org/10.1034/j.1399-3054.1992.840319.x.

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36

Kim, Hong Nam, Eiji Nitasaka, I. J. Odrzykoski, and Tsuneyuki Yamazaki. "Phylogenetic relationships among taxa of the liverwort Conocephalum conicum (Conocephalaceae) revealed by psbA sequence." Genes & Genetic Systems 76, no. 5 (2001): 279–88. http://dx.doi.org/10.1266/ggs.76.279.

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37

Pawlikowska-Pawlęga, Bożena, Elżbieta Król, Kazimierz Trębacz, and Antoni Gawron. "The influence of apigenin on membrane and action potential in the liverwort Conocephalum conicum." Acta Physiologiae Plantarum 29, no. 2 (2007): 143–49. http://dx.doi.org/10.1007/s11738-006-0018-x.

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38

Wood, William F., William C. Lancaster, Christoph O. Fisher, and Raymond E. Stotler. "Trans-methyl cinnamate: The major volatile from some populations of the liverwort, Conocephalum conicum." Phytochemistry 42, no. 1 (1996): 241–42. http://dx.doi.org/10.1016/0031-9422(96)83287-0.

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39

Imada, Yume, Atsushi Kawakita, and Makoto Kato. "Allopatric distribution and diversification without niche shift in a bryophyte-feeding basal moth lineage (Lepidoptera: Micropterigidae)." Proceedings of the Royal Society B: Biological Sciences 278, no. 1721 (2011): 3026–33. http://dx.doi.org/10.1098/rspb.2011.0134.

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The Lepidoptera represent one of the most successful radiations of plant-feeding insects, which predominantly took place within angiosperms beginning in the Cretaceous period. Angiosperm colonization is thought to underlie the evolutionary success of the Lepidoptera because angiosperms provide an enormous range of niches for ecological speciation to take place. By contrast, the basal lepidopteran lineage, Micropterigidae, remained unassociated with angiosperms since Jurassic times but nevertheless achieved a modest diversity in the Japanese Archipelago. We explored the causes and processes of

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40

Pannequin, Anaïs, Erik Laurini, Laurent Giordano, Alain Muselli, Sabrina Pricl, and Aura Tintaru. "Caution: Chemical Instability of Natural Biomolecules During Routine Analysis." Molecules 25, no. 14 (2020): 3292. http://dx.doi.org/10.3390/molecules25143292.

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Natural products (NPs) constitute a significant source of active biomolecules widely used in medicine, pharmacology and cosmetics. However, NPs structural characterization has the drawback of their chemical instability during the extraction steps and their likely transformation during the analytical protocol. In particular, tamariscol and conocephalenol are two compounds largely used in the cosmetic industry for their odorant properties. Thus, in the present study, we focused on the evolution of these two metabolites (extracted from Frullania tamarisci and Conocephalum conicum, respectively),

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41

Maresca, Viviana, Giovanna Salbitani, Federica Moccia, et al. "Antioxidant response to heavy metal pollution of Regi Lagni freshwater in Conocephalum conicum L. (Dum.)." Ecotoxicology and Environmental Safety 234 (April 2022): 113365. http://dx.doi.org/10.1016/j.ecoenv.2022.113365.

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42

Trebacz, K., W. Simonis, and G. Schonknecht. "Effects of Anion Channel Inhibitors on Light-Induced Potential Changes in the Liverwort Conocephalum conicum." Plant and Cell Physiology 38, no. 5 (1997): 550–57. http://dx.doi.org/10.1093/oxfordjournals.pcp.a029204.

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43

Satô, Syôiti, and Misuzu Nagano-Baba. "Electron microscope studies on spermatids in Conocephalum conicum by freeze-fracture replicas and ultrathin sections." CYTOLOGIA 50, no. 2 (1985): 373–85. http://dx.doi.org/10.1508/cytologia.50.373.

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44

Kirn, Hong Nam, Ko Harada, and Tsuneyuki Yamazaki. "Isozyme polymorphism and genetic structure of a liverwort Conocephalum conicum in natural populations of Japan." Genes & Genetic Systems 71, no. 4 (1996): 225–35. http://dx.doi.org/10.1266/ggs.71.225.

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45

Toyota, Masao, Tetsuya Saito, Junko Matsunami, and Yoshinori Asakawa. "A comparative study on three chemo-types of the liverwort Conocephalum conicum using volatile constituents." Phytochemistry 44, no. 7 (1997): 1265–70. http://dx.doi.org/10.1016/s0031-9422(96)00723-6.

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46

Krol, Elzbieta, Halina Dziubinska, Kazimierz Trebacz, Mateusz Koselski, and Maria Stolarz. "The influence of glutamic and aminoacetic acids on the excitability of the liverwort Conocephalum conicum." Journal of Plant Physiology 164, no. 6 (2007): 773–84. http://dx.doi.org/10.1016/j.jplph.2006.04.015.

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47

Bhagat, Madhu, Anil Sharma, and Anima Langer. "<i>Conocephalum conicum</i> (L.) Dumort: A Case of Unique Reproductive Biology." American Journal of Plant Sciences 03, no. 08 (2012): 1145–49. http://dx.doi.org/10.4236/ajps.2012.38138.

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48

Tori, Motoo, Masakazu Sono, Katsuyuki Nakashima, Yoko Nakaki, and Yoshinori Asakawa. "Synthesis and relative structure of conocephalenol, a sesquiterpene alcohol isolated from the european liverwort Conocephalum conicum." Journal of the Chemical Society, Perkin Transactions 1, no. 2 (1991): 447. http://dx.doi.org/10.1039/p19910000447.

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49

Thiel, Rolf, and Klaus Peter Adam. "Incorporation of [1- 13 C]1-deoxy- d -xylulose into isoprenoids of the liverwort Conocephalum conicum." Phytochemistry 59, no. 3 (2002): 269–74. http://dx.doi.org/10.1016/s0031-9422(01)00453-8.

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50

Radulović, Niko S., Sonja I. Filipović, Milan S. Nešić, et al. "Immunomodulatory Constituents of Conocephalum conicum (Snake Liverwort) and the Relationship of Isolepidozenes to Germacranes and Humulanes." Journal of Natural Products 83, no. 12 (2020): 3554–63. http://dx.doi.org/10.1021/acs.jnatprod.0c00585.

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