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Journal articles on the topic 'Conocephalum salebrosum'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

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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2

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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3

Zhang, Chi, Xinlu Chen, Barbara Crandall-Stotler, et al. "Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase." Phytochemistry 164 (August 31, 2019): 50–59. https://doi.org/10.1016/j.phytochem.2019.04.013.

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Zhang, Chi, Chen, Xinlu, Crandall-Stotler, Barbara, Qian, Ping, Köllner, Tobias G., Guo, Hong, Chen, Feng (2019): Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase. Phytochemistry 164: 50-59, DOI: 10.1016/j.phytochem.2019.04.013, URL: http://dx.doi.org/10.1016/j.phytochem.2019.04.013

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4

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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5

Szweykowski, J., K. Buczkowska, and I. J. Odrzykoski. "Conocephalum salebrosum (Marchantiopsida, Conocephalaceae) – a new Holarctic liverwort species." Plant Systematics and Evolution 253, no. 1-4 (2005): 133–58. http://dx.doi.org/10.1007/s00606-005-0301-0.

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6

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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7

Montserrat, Brugués, Infante Marta, and M. Cros Rosa. "Anotaciones sobre hepáticas de España." Boletín de la Sociedad Española de Briología, no. 36(30) (May 1, 2011): 3–8. http://dx.doi.org/10.58469/bseb.2011.52.91.002.

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Se justifican los motivos por los que 22 especies de hepáticas fueron excluidas, añadidas o confirmadas en el último catálogo de las hepáticas españolas (Casas et al., 2009) en relación a los catálogos previos (Casas, 1998; Ros et al., 2007). Fundamentalmente como resultado de la revisión de las muestras de las especies consideradas dudosas, se excluyeron: Acrobolbus wilsonii, Cephalozia catenulata, Cephaloziella elachista, C. phyllacantha, Jungermannia paroica, J. subelliptica, Lophozia capitata, Mannia triandra, Marsupella boeckii, M. sparsifolia, Radula aquilegia, Riccia canaliculata, Riell

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8

Zhang, Chi, Xinlu Chen, Barbara Crandall-Stotler, et al. "Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase." Phytochemistry 164 (August 2019): 50–59. http://dx.doi.org/10.1016/j.phytochem.2019.04.013.

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9

Potemkin, A. D., and G. Ya Doroshina. "To the liverwort flora of the Russian part of Caucasus." Novosti sistematiki nizshikh rastenii 43 (2009): 377–91. http://dx.doi.org/10.31111/nsnr/2009.43.377.

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Identification of over 300 specimens collected by G. Ya. Doroshina (Ukrainskaya) in Stavropol and Krasnodar territories, Kabardino-Balkar, Karachay-Cherkess and Adygea Republics resulted in list of 72 liverwort species. Barbilophozia barbata, Cephalozia bicuspidata, Chiloscyphus minor, Conocephalum cf. salebrosum, Frullania dilatata, Leiocolea heterocolpos, Liochlaena subulata, Metzgeria furcata, Pellia neesiana, Porella cordaeana, Preissia quadrata, Radula complanata, Scapania calcicola, S. helvetica, S. mucronata subsp. praetervisa are new for Stavropol Territory; Blasia pusilla, Blepharosto

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10

Poponessi, Silvia, Michele Aleffi, Marko S. Sabovljević, and Roberto Venanzoni. "Bryophyte diversity hotspot: the Marmore Waterfalls Regional Park (Umbria, central Italy)." Italian Botanist 10 (September 30, 2020): 33–45. http://dx.doi.org/10.3897/italianbotanist.10.54885.

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A study of the bryophyte of Marmore Waterfall Natural Park a very peculiar territory for its geological, biogeographical and bioclimatic traits, was carried out. The reported data were collected in the valley area of ‘Parco Fluviale del Nera’ Regional Park, where the waters are flowing and the humidity of the rocks is oozing. Research led to the identification of 101 taxa of bryophytes (21 liverworts and 80 mosses), among which two liverwort and 10 moss species are new records for the Umbria region, while four are confirmed. The study offers new outcomes on neglected aspects of the flora of ce

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11

Poponessi, Silvia, Michele Aleffi, Marko S. Sabovljević, and Roberto Venanzoni. "Bryophyte diversity hotspot: the Marmore Waterfalls Regional Park (Umbria, central Italy)." Italian Botanist 10 (September 30, 2020): 33–45. https://doi.org/10.3897/italianbotanist.10.54885.

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A study of the bryophyte of Marmore Waterfall Natural Park a very peculiar territory for its geological, biogeographical and bioclimatic traits, was carried out. The reported data were collected in the valley area of 'Parco Fluviale del Nera' Regional Park, where the waters are flowing and the humidity of the rocks is oozing. Research led to the identification of 101 taxa of bryophytes (21 liverworts and 80 mosses), among which two liverwort and 10 moss species are new records for the Umbria region, while four are confirmed. The study offers new outcomes on neglected aspects of the flora of ce

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12

Zhang, Chi, Xinlu Chen, Barbara Crandall-Stotler, et al. "Corrigendum to “Biosynthesis of methyl (E)-cinnamate in the liverwort Conocephalum salebrosum and evolution of cinnamic acid methyltransferase” [Phytochemistry 164 (2019) 50–59]." Phytochemistry 166 (October 2019): 112074. http://dx.doi.org/10.1016/j.phytochem.2019.112074.

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13

Crous, Pedro, M.J. Wingfield, Ž. Jurjević, et al. "Fungal Planet description sheets: 1697–1780." Fungal Systematics and Evolution 14 (December 30, 2024): 325–577. https://doi.org/10.3114/fuse.2024.14.19.

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Novel species of fungi described in this study include those from various countries as follows: <strong>Antarctica,</strong> <em>Leuconeurospora bharatiensis</em> from accumulated snow sediment sample. <strong>Argentina,</strong> <em>Pseudocercospora quetri</em> on leaf spots of <em>Luma apiculata.</em> <strong>Australia,</strong> <em>Polychaetomyces verrucosus</em> on submerged decaying wood in sea water, <em>Ustilaginoidea cookiorum</em> on <em>Scleria levis, Xylaria guardiae</em> as endophyte from healthy leaves of <em>Macaranga tanarius.</em> <strong>Belgium,</strong> <em>Iodophanus taxi</

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14

Sawicki, Jakub, Łukasz Nadolski, Michał Hościk, and Roman Zielinski. "Identification of Conocephalum conicum and C. salebrosum (Hepaticophyta) based on DNA markers." July 8, 2008. https://doi.org/10.5281/zenodo.824548.

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Conocephalum conicum (L.) Dumort. is one of the most common thallose liverworts in Poland. Enzymatic protein electrophoresis allowed to identify sibling species S and L within Conocephalum conicum at the end of the 1970s. Morphological and anatomi-cal analyses resulted in determining the features permitting the identification of the species S and L and enabled to describe the species S as Conocephalum salebrosum Szweykowski, Buczkowska & Odrzykoski. Despite long-term investigations, Conocephalum species have not been analyzed with DNA markers so far. The aim of the present study was to fin

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15

Rossell, Irene M., Simon Barrie, Alan L. Hobbs, Alyssa S. Melton, and Janet M. Weaver. "Ecology of Conocephalum salebrosum (Snakeskin Liverwort) in Western North Carolina Streams." Southeastern Naturalist 23, no. 2 (2024). http://dx.doi.org/10.1656/058.023.0202.

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16

Schott, Rena T., Martin Nebel, and Anita Roth-Nebelsick. "Comparison of the freezing behavior of two liverwort species – Conocephalum salebrosum and Marchantia polymorpha subsp. ruderalis." Lindbergia 2021, no. 1 (2021). http://dx.doi.org/10.25227/linbg.01135.

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17

Hattori, Takefumi, Megumi Katayama, Hiromitsu Tsuzuki, et al. "S-Adenosyl-l-methionine-dependent cinnamic acid carboxyl methyltransferase from the basidiomycete Tricholoma matsutake, which has low identity but similar overall structure to plant SABATH-family enzymes." Journal of Wood Science 71, no. 1 (2025). https://doi.org/10.1186/s10086-025-02179-z.

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Abstract We have cloned cDNA encoding an S-adenosyl-l-methionine (SAM)-dependent cinnamic acid carboxyl methyltransferase from the basidiomycete Tricholoma matsutake. For cloning, we focused on four conserved motifs in SABATH (Salicylic Acid, Benzoic Acid and THeobromine)-family proteins, including the cinnamic acid carboxyl methyltransferases from Ocimum basillicum (ObCCMT1) and Conocephalum salebrosum (CsCAMT), not their full amino acid sequences. On the basis of the homology of the motifs between ObCCMT1 and putative SAM-dependent methyltransferases predicted in RNA-Seq data for T. matsutak

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18

Crous, P. W., M. J. Wingfield, Ž. Jurjević, et al. "Fungal Planet description sheets: 1697–1780." Fungal Systematics and Evolution, 2024. https://doi.org/10.3114/fuse.2024.14.19.

Full text

Abstract:

Novel species of fungi described in this study include those from various countries as follows: Antarctica, Leuconeurospora bharatiensis from accumulated snow sediment sample. Argentina, Pseudocercospora quetri on leaf spots of Luma apiculata. Australia, Polychaetomyces verrucosus on submerged decaying wood in sea water, Ustilaginoidea cookiorum on Scleria levis, Xylaria guardiae as endophyte from healthy leaves of Macaranga tanarius. Belgium, Iodophanus taxi on leaf of Taxus baccata. Belize, Hygrocybe mirabilis on soil. Brazil, Gongronella irregularis from soil, Linodochium splendidum on deca

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