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Articles de revues sur le sujet « Anastrophyllum »

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Auteur : Grafiati
Publié le 27 juillet 2024
Mis à jour le 29 juillet 2024

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1

Alvaro Alba, Wilson Ricardo, et Jaime Uribe Meléndez. « Revisión taxonómica del género Anastrophyllum (Marchantiophyta, Anastrophyllaceae) para Colombia ». Caldasia 39, no 2 (1 juillet 2017) : 269–91. http://dx.doi.org/10.15446/caldasia.v39n2.63100.

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En el estudio taxonómico del género Anastrophyllum para Colombia se registran cinco especies. A. auritum, A. nigrescens, A. piligerum, A. stellatum y A. tubulosum. El género Anastrophyllum presenta pigmentación pardo-rojiza, rojo-negruzca, ocasionalmente verde; tallos con corteza y médula diferenciadas; ramificación terminal tipo Frullania, lateral tipo Plagiochila y ventral tipo Bazzania; hojas bífidas, cóncavas, asimétricas, margen entera; células con trígonos pequeños a conspicuos. Dioicas; perianto emergente, cilindrico, plegado desde la base o solamente en la parte distal, con la boca hialina. Anastrophyllum leptodictyon es pasado a la sinonimia de A. auritum. Para cada una de las especies se proporciona una descripción detallada, ilustraciones, mapas de distribución y una clave donde se destacan principalmente caracteres del gametofito.
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Hong, Won Shic. « Anastrophyllum in Western North America ». Bryologist 99, no 1 (1996) : 85. http://dx.doi.org/10.2307/3244444.

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Buchanan, Malcolm S., Joseph D. Connolly et David S. Rycroft. « Sphenolobane diterpenoids from the liverwort Anastrophyllum donnianum ». Phytochemistry 43, no 6 (décembre 1996) : 1297–301. http://dx.doi.org/10.1016/s0031-9422(96)00466-9.

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4

Pohjamo, Maria, et Sanna Laaka-Lindberg. « Reproductive modes in the epixylic hepatic Anastrophyllum hellerianum ». Perspectives in Plant Ecology, Evolution and Systematics 6, no 3 (janvier 2003) : 159–68. http://dx.doi.org/10.1078/1433-8319-00074.

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Zapp, Josef, Gunther Burkhardt et Hans Becker. « Sphenolobane and fusicoccane diterpenoids from the liverwort Anastrophyllum auritum ». Phytochemistry 37, no 3 (novembre 1994) : 787–93. http://dx.doi.org/10.1016/s0031-9422(00)90359-5.

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Mamontov, S. Yu, et A. A. Vilnet. « Anastrophyllum astorgae (Anastrophyllaceae, Marchantiophyta), a new species from Chile ». Arctoa 32, no 2 (décembre 2023) : 158–70. http://dx.doi.org/10.15298/arctoa.32.13.

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7

Mamontov, Yuriy S., Jochen Heinrichs, Jiří Váňa et Michael S. Ignatov. « Hepatics from Rovno amber (Ukraine), 3. Anastrophyllum rovnoi sp. nov. » Arctoa 24, no 1 (septembre 2015) : 43–46. http://dx.doi.org/10.15298/arctoa.24.08.

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Beyer, Jürgen, Hans Becker, Masao Toyota et Yoshinori Asakawa. « Diterpenoids with a novel skeleton from the liverwort Anastrophyllum minutum ». Phytochemistry 26, no 4 (janvier 1987) : 1085–89. http://dx.doi.org/10.1016/s0031-9422(00)82355-9.

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Nagashima, Fumihiro, et Yoshinori Asakawa. « Diterpenoids From the Argentine and Malaysian Liverworts Anastrophyllum and Jungermannia Species ». Natural Product Communications 14, no 12 (1 décembre 2019) : 1934578X1989478. http://dx.doi.org/10.1177/1934578x19894786.

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We are engaged in the ongoing investigation into the chemical constituents of liverworts in our search for novel compounds and biologically active substances. In the present study, two new rosane diterpenoids were isolated from the Argentine liverwort Anastrophyllum species, together with known aromadendrane sesqui- and rosane diterpenoids. Two new ent-kaurene and 4 ent-kaurene diterpenoids were isolated from the Malaysian liverwort Jungermannia species. Their structures were determined using nuclear magnetic resonance spectroscopy techniques, circular dichroism spectroscopy, and chemical transformation.
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10

Váňa, Jíri, Lars Söderström, Anders Hagborg et Matt Von Konrat. « Notes on Early Land Plants Today. 45. A correction ». Phytotaxa 152, no 1 (11 décembre 2013) : 48. http://dx.doi.org/10.11646/phytotaxa.152.1.4.

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Váňa et al. (2013) elevated Anastrophyllum subgen. Schizophyllum (Schuster 1969: 739) to generic rank as Schizophyllum (R.M.Schust.) Váňa & L.Söderstr. (2013: 16), overlooking the genus Schizophyllum Nuttall (1841: 452; Asteraceae) and, thereby creating an illegitimate later homonym. This is corrected here by publication of the new genus Schizophyllopsis and the transfer of all species of Schizophyllum (R.M.Schust.) Váňa et al. to that genus. Despite the generic name itself being illegitimate, names published under Schizophyllum (R.M.Schust.) Váňa & L.Söderstr. are legitimate under ICN Art. 55.1 (see below).
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11

Müller, Frank. « Additions to the bryophyte flora of Réunion (East African Islands) ». Bryophyte Diversity and Evolution 18, no 1 (31 décembre 2000) : 91–95. http://dx.doi.org/10.11646/bde.18.1.12.

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Nineteen species of bryophytes are reported for the first time for Réunion. Especially remarkable are the first African record of Anastrophyllum leucocephalum (Tayl.) Steph. and the first records for the East African Islands of Cephaloziella cf. vaginans Steph., Fossombronia foveolata Lindb., Riccia huebeneriana Lindenb., Barbula unguiculata Hedw., Bryum pseudotriquetrum (Hedw.) Schwägr., Chenia leptophylla (Müll.Hal.) R.H.Zander, Dicranella subsubulata (Hampe ex Müll.Hal.) A.Jaeger, Ditrichum punctulatum Mitt., Physcomitrium spathulatum (Hornsch.) Müll.Hal. var. spathulatum and Trichostomum crispulum Bruch var. crispulum. Brachymenium gemmiferum A.J.Shaw & W.R.Buck is regarded as synonymous with Brachymenium exile (Dozy & Molk.) Bosch & Sande Lac.
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12

Ahrens, Matthias. « The liverwort Anastrophyllum michauxii (F. Web.) Buch in the Black Forest (Southwestern Germany) ». Herzogia 10 (21 décembre 1994) : 115–19. http://dx.doi.org/10.1127/herzogia/10/1994/115.

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13

Majumdar, Shuvadeep, et David Long. « Two New Synonyms and Extended Distribution of Anastrophyllum ellipticum Inoue (Anastrophyllaceae : Marchantiophyta) ». Cryptogamie, Bryologie 41, no 4 (11 mars 2020) : 49. http://dx.doi.org/10.5252/cryptogamiebryologie2020v41a4.

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Mamontov, Yuriy S., et Anna А. Vilnet. « Anastrophyllum ellipticum Inoue (Jungermanniales, Marchantiophyta), a new species for Russian liverwort flora ». Arctoa 22, no 1 (décembre 2013) : 151–58. http://dx.doi.org/10.15298/arctoa.22.24.

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Pohjamo, Maria, Sanna Laaka-Lindberg, Otso Ovaskainen et Helena Korpelainen. « Dispersal potential of spores and asexual propagules in the epixylic hepatic Anastrophyllum hellerianum ». Evolutionary Ecology 20, no 5 (septembre 2006) : 415–30. http://dx.doi.org/10.1007/s10682-006-0011-2.

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16

Gradstein, S. R., et J. Florschütz-de Waard. « RESULTS OF A BOTANICAL EXPEDITION TO MOUNT RORAIMA, GUYANA. I. BRYOPHYTES ». Bryophyte Diversity and Evolution 1, no 1 (31 décembre 1989) : 25–54. http://dx.doi.org/10.11646/bde.1.1.6.

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A bryological inventory of the Upper Mazaruni District, Guyana (former British Guiana) yielded almost three hundred species, including 2 genera and 11 species new to science and 130 species new to the Guianas. The densely forested and very humid north slope of Mount Roraima (500-2300 m.) proved to be the richest area for bryophytes and most of the novelties were found there. The present paper provides an enumeration of the species collected with a brief characterization of their habitat. The following species are described as new: Haesselia acuminata Gradst., Plagiochila gymnocalyx Inoue, Radula gradsteinii Yamada, Radula guyanensis Yamada, Radula mazarunensis Yamada and Stenorrhipis grollei Gradst. Anastrophyllum subg. Vanaea Inoue & Gradst. from Mount Roraima is elevated to generic rank.
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17

Hedderson, Terry A., et Guy R. Brassard. « The bryophytes of Nachvak, northern Labrador, with additional records from Saglek ». Canadian Journal of Botany 64, no 9 (1 septembre 1986) : 2028–36. http://dx.doi.org/10.1139/b86-265.

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One hundred and thirty-four species of mosses and 18 species of liverworts are reported from Nachvak Fiord and 22 mosses are reported from Saglek Fiord. Nineteen of the mosses had not previously been reported from Labrador and 49 are new to northern Labrador. Seven of the liverworts are new to Labrador. Brophyte species new to eastern North America are Anastrophyllum assimile, Hygrophypnum cochlearifolium (possibly) and Lophozia cavifolia. The record of Lophozia cavifolia represents an addition to the hepatic flora of North America (excluding Greenland). The North American distributions of Hydrogrimmia mollis, Marsupella revoluta and Trichostomum arcticum are mapped. The high incidence of disjunct species in the bryoflora of the Torngat Mountains is discussed in relation to the proposed glacial history of the area.
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18

СОФРОНОВА, Е. В. « ПЕЧЕНОЧНИКИ ГОРНЫХ ЕЛОВЫХ ЛЕСОВ ЯКУТИИ, "БОТАНИЧЕСКИЙ ЖУРНАЛ" ». Ботанический журнал, no 8 (2013) : 1007–13. http://dx.doi.org/10.1134/s1234567813080053.

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Впервые приводятся данные по печеночникам, произрастающим в еловых лесах горных территорий Северо-Восточной Якутии (хребты Орулган, Сетте-Дабан, Юдомо-Майское нагорье) и Южной Якутии (хребты Токинский Становик, Удокан, Алданское нагорье). Хотя еловые леса в Якутии занимают менее 1—2 % лесопокрытой площади, здесь выявлено 56 видов печеночников, относящихся к 33 родам и 19 семействам. В лесах из ели сибирской выявлено 28 видов из 18 родов, 12 семейств, в аянских ельниках — 46 видов из 30 родов и 17 семейств. Шесть видов — Anastrophyllum michauxii, Frullania koponenii, F. parvistipula, Mylia taylorii, Scapania apiculata, S. glaucocephala — относятся к редко встречающимся на территории Якутии печеночникам. Представленный в таблице список аннотирован данными по распределению видов по типам ельников, геоморфологическим подразделениям Якутии, субстратам. Кроме того, приведены данные по характеру роста видов и структурам, связанным с размножением.
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19

Pohjamo, Maria, et Sanna Laaka-Lindberg. « Demographic population structure of a leafy epixylic hepatic Anastrophyllum hellerianum (Nees ex Lindenb.) R.M.Schust ». Plant Ecology (formerly Vegetatio) 173, no 1 (juillet 2004) : 73–81. http://dx.doi.org/10.1023/b:vege.0000026330.62021.0a.

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20

Majumdar, Shuvadeep, et D. K. Singh. « First Report of Anastrophyllum lignicola (Anastrophyllaceae, Marchantiophyta) from Arunachal Pradesh in Eastern Himalaya of India ». National Academy Science Letters 40, no 6 (13 novembre 2017) : 439–44. http://dx.doi.org/10.1007/s40009-017-0580-3.

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21

Jessup, Steven L. « Hepaticae of the Klamath Mountains : I. Anastrophyllum minutum in the Siskiyou Mountains of Oregon and California ». Evansia 17, no 4 (2000) : 137–40. http://dx.doi.org/10.5962/p.346503.

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22

Daniels, A. E. D., D. G. Long, K. C. Kariyappa et P. Daniel. « Anastrophyllum aristatum(Herzog ex N.Kitag.) A.E.D. Danielset al.,comb. et stat. nov. (Marchantiophyta : Anastrophyllaceae) from India and China ». Journal of Bryology 34, no 2 (juin 2012) : 146–49. http://dx.doi.org/10.1179/1743282012y.0000000002.

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23

Potemkin, A. D., et E. I. Rozantseva. « New and little-known for the Leningrad Region liverworts (Marchantiophyta) from Hogland Island (Gulf of Finland, Baltic Sea) ». Novosti sistematiki nizshikh rastenii 49 (2015) : 369–81. http://dx.doi.org/10.31111/nsnr/2015.49.369.

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Brief description of the history of investigation of liverwort flora of Hog land Island is provided. The list of 24 species newly recorded for the island (Anastrophyllum michauxii, Bazzania trilobata, Calypogeia fissa, Cephalozia loitlesbergeri, C. macounii, Cephaloziella elegans, C. hampeana, C. rubella, Diplophyllum obtusifolium, Isopaches alboviridis, Kurzia pauciflora, Lophozia sudetica, Metzgeria furcata, Mylia taylori, Nardia scalaris, Odontoschisma francisci, Orthocaulis floerkei, Riccardia chamedryfolia, R. incurvata, Scapania nemorea, Schistichilopsis laxa, Tetralophozia setiformis) is annotated by data on coordinates of their locations, habitats, growth pattern, associated species, known locations on adjacent territories, presence of structures associated with reproduction (gem. — gemmae and brood bodies, per. — perianths and other protecting structures of developing sporophytes, juv. caps. — juvenile capsules, caps. — mature capsules, anth. — antheridia). Species marked in the list by one asterisk (*) are published for the first time for the island, species marked by two asterisks (**) (Calypogeia fissa, Cephaloziella elegans, Isopaches alboviridis, Tetralophozia setiformis) — for the first time for the Leningrad Region, records marked in the list by exclamation mark (!) (Isopaches alboiviridis, Lophozia sudetica, Tetralophozia setiformis) are the most southern records for European Russia. Specificity of the liverwort flora of Hogland Island is demonstrated on the basis of analysis of frequency and activity of the rare species.
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Dulin, M. « Contribution to the liverwort flora of the Koigorodsky National park (Komi republic, Russia) ». Proceedings of the Komi Science Centre of the Ural Division of the Russian Academy of Sciences, no 4 (3 novembre 2022) : 14–21. http://dx.doi.org/10.19110/1994-5655-2022-4-14-21.

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The Koigorodsky National Park (56.7 thousand hectares) was established on December 7, 2019. It is located on the border of the Komi Republic and the Kirov region. An annotated list of liverworts collected in the Koigorodsky National Park has been presented in the article for the first time. The list includes 38 species and one subspecies of 28 genera, 21 families, seven orders (Blasiales, Jungermanniales, Marchantiales, Metzgeriales, Pelliales, Porellales, Ptilidiales), and two classes (Marchantiopsida and Jungermanniopsida). For each species, the article provides data on structures associated with reproductuion, geographical locations, substrate and the species habitats. Three liverworts species listed in the Red Data Book of the Komi Republic such as Anastrophyllum michauxii, Lophozia ascendens, and Scapania apiculata have been found in the flora. Indicator species of old-growth forests such as Calypogeia suecica, Crossocalyx hellerianus, Riccardia latifrons, and Syzygiella autumnalis have been found. The rare epiphytic liverwort Frullania oakesiana has been discovered in the Komi Republic flora for the first time. 23 species that can potentially be found within the Koygorodsky National Park have been identified on the Tulashor site adjacent territory (the Nurgush Nature Reserve). At present, the taxonomic diversity of the studied flora is probably 62%. The floras of the Koigorodsky National Park and the Tulashor site are parts of a single flora covering a large old-growth spruce forests array and, accordingly, are similar in structure. Forest habitats and spruce forests are characterized by the highest taxonomic diversity: 33 or 87% and 27 or 71% species, respectively. Liverworts prefer to grow on rotting wood due to reduced competition from vascular plants. About 79 % of the identified species form reproductive structures. This indicates that growth conditions are favorable. The remote southwestern part of the national park is promising for further research.
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Srivastava, Smita, S. C. Srivastava et K. K. Rawat. « Status of Family Lophoziaceae (Hepaticae) in India ». Nelumbo, 1 décembre 2013, 113–52. http://dx.doi.org/10.20324/nelumbo/v55/2013/73297.

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Status of family Lophoziaceae in India has been discussed in the light of recent investigations and our own observations on Indian taxa. A total of 19 taxa have been recognised under eight genera including Isopaches Buch., Lophozia (Dumort.) Dumort., Schistochilopsis (N. Kitag.) Konstant., Anastrepta (Lindb.) Schiffn., Anastrophyllum (Spruce) Schiffn., Tritomaria Schiffn. ex Loeske, Tetralophozia (R.M. Schust.) Schljakov and Plicanthus R.M. Schust. Four taxa viz., Anastrophyllum minutum var. himalayanum var. nov., Lophozia udarii sp. nov., Lophozia indica sp. nov. and Schistochilopsis incisa var. himalayana var. nov., have been described as new to science. Sphenolobus longkyrdumii A.P. Singh&V. Nath is proposed as synonym under Metahygrobiella albula (Mitt.) Grolle (family Cephaloziaceae Mig.), hence excluded.
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VÁŇA, JIŘÍ, LARS SÖDERSTRÖM, ANDERS HAGBORG et MATT VON KONRAT. « Notes on Early Land Plants Today. 30. Transfer of some taxa from Anastrophyllum (Anastrophyllaceae, Marchantiophyta) ». Phytotaxa 81, no 1 (19 février 2013). http://dx.doi.org/10.11646/phytotaxa.81.1.6.

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Zhu, Mingzhu, Yinghui Gao, Yi Li, Feng Xie, Jinchuan Zhou, Lintao Xu, Dongxue Lv et al. « Novel Diterpenoids Incorporating Rearranged Labdanes from the Chinese Liverwort Anastrophyllum joergensenii and Their Anti-inflammatory Activity ». Journal of Agricultural and Food Chemistry, 30 novembre 2023. http://dx.doi.org/10.1021/acs.jafc.3c06235.

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Górski, Piotr, Grzegorz Vončina, Antoni Zięba, Michał Smoczyk, Adam Stebel, Marcin Wilhelm, Wojciech Ciurzycki et Robert Zubel. « Liverworts collected in the Tatra Mountains during the 19th Field Workshop of the Bryological Section of the Polish Botanical Society ». Wiadomości Botaniczne 67 (26 septembre 2023). http://dx.doi.org/10.5586/wb/168300.

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Niniejszy artykuł prezentuje wyniki badań florystycznych przeprowadzonych w trakcie warsztatów terenowych Sekcji Briologicznej Polskiego Towarzystwa Botanicznego w Tatrach w 2022 roku. Eksploracje prowadzono w czterech obszarach, po dwa w Tatrach Wysokich i Zachodnich. Łącznie zinwentaryzowano 82 gatunki wątrobowców. Największą bioróżnorodność odnotowano w Tatrach Wysokich, w Waksmundzkim Żlebie i na północnych stokach Mięguszowieckich Szczytów. Po raz pierwszy w polskiej części Tatr Wysokich odnaleziono dwie rośliny – <i>Jungermannia polaris</i> i <i>Scapania calcicola</i>. Dla trzech gatunków ustalono nowe maksima wysokościowe w skali całego masywu tatrzańskiego. Są to: <i>Bazzania flaccida</i> (2201 m n.p.m.), <i>Mesoptychia heterocolpos</i> (2201 m n.p.m.) oraz <i>Solenostoma confertissimum</i> (2254 m n.p.m.). Jeden arktyczno-alpejski gatunek, <i>Scapania cuspiduligera</i>, odnotowano na nowym minimum wysokościowym (1027 m n.p.m.). W prezentowanym wykazie 11 wątrobowców znajduje się na polskiej, czerwonej liście gatunków zagrożonych. Do tej grupy należą: <i>Anastrophyllum michauxii</i> (kategoria VU), <i>Bazzania flaccida</i> (VU), <i>Calypogeia suecica</i> (VU), <i>Eremonotus myriocarpus</i> (VU), <i>Frullania tamarisci</i> (VU), <i>Lophoziopsis longidens</i> (VU), <i>Marsupella boeckii</i> (VU), <i>Metzgeria conjugata</i> (VU), <i>M. pubescens</i> (VU), <i>Neoorthocaulis binsteadii</i> (VU) oraz <i>Schljakovianthus quadrilobus</i> (VU). W puli stwierdzonych wątrobowców siedem ma swoje jedyne stanowiska w Polsce na terenie Tatr, a 19 to rośliny arktyczno(subarktyczno)-alpejskie.
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FELDBERG, KATHRIN, S. ROBBERT GRADSTEIN, CARSTEN GRÖHN, JOCHEN HEINRICHS†, MATT VON KONRAT, YURIY S. MAMONTOV, MATT A. M. RENNER et al. « Checklist of fossil liverworts suitable for calibrating phylogenetic reconstructions ». Bryophyte Diversity and Evolution 43, no 1 (30 juin 2021). http://dx.doi.org/10.11646/bde.43.1.6.

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The number of available liverwort fossils substantially increased within the past decade, which is mainly due to new findings from Cretaceous and Cenozoic amber deposits. Many of them, however, are fragmentary and not predestined for consideration in evolutionary analyses. Here, we list those liverwort fossils that we suggest as suitable for calibrating phylogenetic reconstructions, along with brief descriptions, justification of their use, and age information. Our recommendations are based on thorough microscopic investigation of available fossils from worldwide amber collections including recent findings. We recommend that the following 42 fossil taxa can be used as confident minimum age constraints in phylogenetic reconstructions: Acrolejeunea ucrainica (35 Ma), Anastrophyllum rovnoi (35 Ma), Bazzania polyodus (34 Ma), Blepharolejeunea obovata (15 Ma), the genus Bryopteris with B. bispinosa and B. succinea (15 Ma), Calypogeia stenzeliana (34 Ma), Cephaloziella nadezhdae (35 Ma), the genus Ceratolejeunea with C. antiqua, C. palaeomexicana, and C. sublaetefusca (15 Ma), Cheilolejeunea latiloba (34 Ma), Cheirorhiza brittae (158 Ma), Cololejeunea sp. (15 Ma), Cyclolejeunea archaica (15 Ma), Dibrachiella grollei (15 Ma), Diettertia montanensis (112 Ma), Drepanolejeunea eogena (15 Ma), the genus Frullania with F. baerlocheri, F. cretacea, and F. partita (99 Ma), Frullania subgen. Frullania with F. casparyi (34 Ma) and F. riclefgrollei (35 Ma), F. subgen. Trachycolea with F. rovnoi (35 Ma) and F. schumannii (34 Ma), Gackstroemia cretacea (99 Ma), Geocalyx heinrichsii (34 Ma), the genus Lejeunea with L. hamatiloba, L. miocenica, L. resinata, and L. urbanioides (15 Ma), Lopholejeunea subnigricans (15 Ma), Marchantites cyathodoides (228 Ma), Marchesinia brachiata (15 Ma), Metzgeriothallus sharonae (383 Ma), Microlejeunea nyiahae (52 Ma), Neurolejeunea macrostipula (15 Ma), Nipponolejeunea europaea (34 Ma), Notoscyphus balticus (34 Ma), Odontoschisma (sect. Iwatsukia) dimorpha (34 Ma), Plagiochila groehnii (34 Ma), Porella subgrandiloba (34 Ma), Protolophozia kutscheri (34 Ma), Radula (subgen. Odontoradula) cretacea (99 Ma), R. (subgen. Amentuloradula) heinrichsii (99 Ma), Scapania hoffeinsiana (34 Ma), Solenostoma berendtii (34 Ma), Spruceanthus polonicus (34 Ma), Stictolejeunea squamata (15 Ma), Tetralophozia groehnii (34 Ma), Thysananthus auriculatus (15 Ma), Thysananthus contortus (34 Ma). Furthermore, we transfer Lophozia kutscheri to Protolophozia, Archilejeunea grollei to Dibrachiella, Frullania ucrainica to Acrolejeunea, and Mastigolejeunea extincta to Spruceanthus, based on new fossil evidence and morphological revisions.
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