Extracts Characterization and in Vitro Evaluation of Potential Immunomodulatory Activities of the Moss Hypnum Cupressiforme Hedw
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A Revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1
Revision of Schoenobryum 147 Tropical Bryology 24: 147-159, 2003 A revision of Schoenobryum (Cryphaeaceae, Bryopsida) in Africa1 Brian J. O’Shea 141 Fawnbrake Avenue, London SE24 0BG, U.K. Abstract. The nine species and two varieties of Schoenobryum reported for Africa were investigated, and no characters were found that uniquely identified any of the taxa to be other than the pantropical Schoenobryum concavifolium. The following nine names become new synonyms of S. concavifolium: Cryphaea madagassa, C. subintegra, Acrocryphaea robusta, A. latifolia, A. subrobusta, A. tisserantii, A. latifolia var. microspora, A. plicatula and A. subintegra var. idanreense; a lectotype is selected for Acrocryphaea latifolia var. microspora P.de la Varde. INTRODUCTION as the majority have not been examined since the type description, and many have never been A recent checklist of Sub-Saharan Africa illustrated. (O’Shea, 1999) included nine species and two varieties of Schoenobryum, most of quite limited The purpose of this paper is to provide an distribution. Recent collecting in both Malawi overview of the genus worldwide, and to review (O’Shea et al., 2001) and Uganda (Wigginton et the taxonomic position of the African taxa. al., 2001) has shown the genus to be not uncommon, although there was only one CRYPHAEACEAE SCHIMP. 1856. previously published collection from the two countries (O’Shea, 1993). Apart from one Cryphaeaceae Schimp., Coroll. Bryol. Eur. 97. African taxon occurring in nine countries, the 1856 [‘1855’]. Type: Cryphaea D.Mohr in other 10 occurred in an average of 1.7 countries. F.Weber This particular profile is typical of unrevised genera in Africa, and indicative of a possible A brief review of the circumscription and need for revision (O’Shea, 1997), particularly systematics of the family, and the distinctions from related families (e.g. -
Anthocerotophyta
Glime, J. M. 2017. Anthocerotophyta. Chapt. 2-8. In: Glime, J. M. Bryophyte Ecology. Volume 1. Physiological Ecology. Ebook 2-8-1 sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 5 June 2020 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 2-8 ANTHOCEROTOPHYTA TABLE OF CONTENTS Anthocerotophyta ......................................................................................................................................... 2-8-2 Summary .................................................................................................................................................... 2-8-10 Acknowledgments ...................................................................................................................................... 2-8-10 Literature Cited .......................................................................................................................................... 2-8-10 2-8-2 Chapter 2-8: Anthocerotophyta CHAPTER 2-8 ANTHOCEROTOPHYTA Figure 1. Notothylas orbicularis thallus with involucres. Photo by Michael Lüth, with permission. Anthocerotophyta These plants, once placed among the bryophytes in the families. The second class is Leiosporocerotopsida, a Anthocerotae, now generally placed in the phylum class with one order, one family, and one genus. The genus Anthocerotophyta (hornworts, Figure 1), seem more Leiosporoceros differs from members of the class distantly related, and genetic evidence may even present -
Fossil Mosses: What Do They Tell Us About Moss Evolution?
Bry. Div. Evo. 043 (1): 072–097 ISSN 2381-9677 (print edition) DIVERSITY & https://www.mapress.com/j/bde BRYOPHYTEEVOLUTION Copyright © 2021 Magnolia Press Article ISSN 2381-9685 (online edition) https://doi.org/10.11646/bde.43.1.7 Fossil mosses: What do they tell us about moss evolution? MicHAEL S. IGNATOV1,2 & ELENA V. MASLOVA3 1 Tsitsin Main Botanical Garden of the Russian Academy of Sciences, Moscow, Russia 2 Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia 3 Belgorod State University, Pobedy Square, 85, Belgorod, 308015 Russia �[email protected], https://orcid.org/0000-0003-1520-042X * author for correspondence: �[email protected], https://orcid.org/0000-0001-6096-6315 Abstract The moss fossil records from the Paleozoic age to the Eocene epoch are reviewed and their putative relationships to extant moss groups discussed. The incomplete preservation and lack of key characters that could define the position of an ancient moss in modern classification remain the problem. Carboniferous records are still impossible to refer to any of the modern moss taxa. Numerous Permian protosphagnalean mosses possess traits that are absent in any extant group and they are therefore treated here as an extinct lineage, whose descendants, if any remain, cannot be recognized among contemporary taxa. Non-protosphagnalean Permian mosses were also fairly diverse, representing morphotypes comparable with Dicranidae and acrocarpous Bryidae, although unequivocal representatives of these subclasses are known only since Cretaceous and Jurassic. Even though Sphagnales is one of two oldest lineages separated from the main trunk of moss phylogenetic tree, it appears in fossil state regularly only since Late Cretaceous, ca. -
Vertical Distribution of Epiphytic Bryophytes Depends on Phorophyte Type; a Case Study from Windthrows in Kampinoski National Park (Central Poland)
Folia Cryptog. Estonica, Fasc. 57: 59–71 (2020) https://doi.org/10.12697/fce.2020.57.08 Vertical distribution of epiphytic bryophytes depends on phorophyte type; a case study from windthrows in Kampinoski National Park (Central Poland) Barbara Fojcik1*, Damian Chmura2 1Institute of Biology, Biotechnology and Environmental Protection, University of Silesia, 28 Jagiellońska St., 40-032 Kato- wice, Poland. E-mail: [email protected] 2Institute of Environmental Protection and Engineering, University of Bielsko-Biala, 2 Willowa St., 43-309 Bielsko-Biała, Poland. E-mail: [email protected] *Author for correspondence Abstract: The vertical distribution of epiphytic bryophytes in European forests are still relatively poorly understood. The aim of the study was to analyse the diversity and vertical zonation of epiphytic mosses and liverworts on selected tree types (Quercus petraea, Betula pendula and Pinus sylvestris) within windthrow areas in the Kampinoski National Park (Central Poland). The investigations were performed in five parts of the trees: the tree base, lower trunk, upper trunk, lower crown, and upper crown. Deciduous trees have more species than pine trees (13 on Quercus and Betula, 8 on Pinus). The type of phorophyte was crucial for the differences in the species composition from the tree base to the upper crown that was observed. The highest richness of bryophytes was recorded on the tree bases, while the lowest was recorded in the upper parts of the crowns. The variability of the habitat conditions in the vertical gradient on the trunk that affected the patterns of the occurrence of species with different ecological preferences was determined using the Ellenberg indicator values. -
Bryophytes of Adjacent Serpentine and Granite Outcrops on the Deer Isles, Maine, U.S.A
RHODORA, Vol. 111, No. 945, pp. 1–20, 2009 E Copyright 2009 by the New England Botanical Club BRYOPHYTES OF ADJACENT SERPENTINE AND GRANITE OUTCROPS ON THE DEER ISLES, MAINE, U.S.A. LAURA R. E. BRISCOE The Field Museum, 1400 South Lakeshore Drive, Chicago, IL 60605 TANNER B. HARRIS University of Massachusetts, Fernald Hall, 270 Stockbridge Road, Amherst, MA 01003 WILLIAM BROUSSARD University of Maine, 421 Estabrooke Hall, Orono, ME 04469 1 EVA DANNENBERG,FRED C. OLDAY, AND NISHANTA RAJAKARUNA College of the Atlantic, 105 Eden Street, Bar Harbor, ME 04609 1Author for Correspondence; Current Address: Department of Biological Sciences, One Washington Square, San Jose´ State University, San Jose´, CA 95192-0100 e-mail: [email protected] ABSTRACT. The serpentine-substrate effect is well documented for vascular plants, but the literature for bryophytes is limited. The majority of literature on bryophytes in extreme geoedaphic habitats focuses on the use of species as bioindicators of industrial pollution. Few attempts have been made to characterize bryophyte floras on serpentine soils derived from peridotite and other ultramafic rocks. This paper compares the bryophyte floras of both a peridotite and a granite outcrop from the Deer Isles, Hancock County, Maine, and examines tissue elemental concentrations for select species from both sites. Fifty-five species were found, 43 on serpentine, 26 on granite. Fourteen species were shared in common. Twelve species are reported for the first time from serpentine soils. Tissue analyses indicated significantly higher Mg, Ni, and Cr concentrations and significantly lower Ca:Mg ratios for serpentine mosses compared to those from granite. -
Flora of New Zealand Mosses
FLORA OF NEW ZEALAND MOSSES BRACHYTHECIACEAE A.J. FIFE Fascicle 46 – JUNE 2020 © Landcare Research New Zealand Limited 2020. Unless indicated otherwise for specific items, this copyright work is licensed under the Creative Commons Attribution 4.0 International licence Attribution if redistributing to the public without adaptation: "Source: Manaaki Whenua – Landcare Research" Attribution if making an adaptation or derivative work: "Sourced from Manaaki Whenua – Landcare Research" See Image Information for copyright and licence details for images. CATALOGUING IN PUBLICATION Fife, Allan J. (Allan James), 1951- Flora of New Zealand : mosses. Fascicle 46, Brachytheciaceae / Allan J. Fife. -- Lincoln, N.Z. : Manaaki Whenua Press, 2020. 1 online resource ISBN 978-0-947525-65-1 (pdf) ISBN 978-0-478-34747-0 (set) 1. Mosses -- New Zealand -- Identification. I. Title. II. Manaaki Whenua-Landcare Research New Zealand Ltd. UDC 582.345.16(931) DC 588.20993 DOI: 10.7931/w15y-gz43 This work should be cited as: Fife, A.J. 2020: Brachytheciaceae. In: Smissen, R.; Wilton, A.D. Flora of New Zealand – Mosses. Fascicle 46. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/w15y-gz43 Date submitted: 9 May 2019 ; Date accepted: 15 Aug 2019 Cover image: Eurhynchium asperipes, habit with capsule, moist. Drawn by Rebecca Wagstaff from A.J. Fife 6828, CHR 449024. Contents Introduction..............................................................................................................................................1 Typification...............................................................................................................................................1 -
Molecular Phylogeny of Chinese Thuidiaceae with Emphasis on Thuidium and Pelekium
Molecular Phylogeny of Chinese Thuidiaceae with emphasis on Thuidium and Pelekium QI-YING, CAI1, 2, BI-CAI, GUAN2, GANG, GE2, YAN-MING, FANG 1 1 College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China. 2 College of Life Science, Nanchang University, 330031 Nanchang, China. E-mail: [email protected] Abstract We present molecular phylogenetic investigation of Thuidiaceae, especially on Thudium and Pelekium. Three chloroplast sequences (trnL-F, rps4, and atpB-rbcL) and one nuclear sequence (ITS) were analyzed. Data partitions were analyzed separately and in combination by employing MP (maximum parsimony) and Bayesian methods. The influence of data conflict in combined analyses was further explored by two methods: the incongruence length difference (ILD) test and the partition addition bootstrap alteration approach (PABA). Based on the results, ITS 1& 2 had crucial effect in phylogenetic reconstruction in this study, and more chloroplast sequences should be combinated into the analyses since their stability for reconstructing within genus of pleurocarpous mosses. We supported that Helodiaceae including Actinothuidium, Bryochenea, and Helodium still attributed to Thuidiaceae, and the monophyletic Thuidiaceae s. lat. should also include several genera (or species) from Leskeaceae such as Haplocladium and Leskea. In the Thuidiaceae, Thuidium and Pelekium were resolved as two monophyletic groups separately. The results from molecular phylogeny were supported by the crucial morphological characters in Thuidiaceae s. lat., Thuidium and Pelekium. Key words: Thuidiaceae, Thuidium, Pelekium, molecular phylogeny, cpDNA, ITS, PABA approach Introduction Pleurocarpous mosses consist of around 5000 species that are defined by the presence of lateral perichaetia along the gametophyte stems. Monophyletic pleurocarpous mosses were resolved as three orders: Ptychomniales, Hypnales, and Hookeriales (Shaw et al. -
Hypnaceaeandpossiblyrelatedfn
Hikobial3:645-665.2002 Molecularphylo窪enyOfhypnobrJ/aleanmOssesasin化rredfroma lar淫e-scaledatasetofchlOroplastlbcL,withspecialre他rencetothe HypnaceaeandpOssiblyrelatedfnmilies1 HIRoMITsuBoTA,ToMoTsuGuARIKAwA,HIRoYuKIAKIYAMA,EFRAINDELuNA,DoLoREs GoNzALEz,MASANoBuHIGucHIANDHIRoNoRIDEGucHI TsuBoTA,H、,ARIKAwA,T,AKIYAMA,H,,DELuNA,E,GoNzALEz,,.,HIGucHI,M 4 &DEGucHI,H、2002.Molecularphylogenyofhypnobryaleanmossesasinferred fiPomalarge-scaledatasetofchloroplastr6cL,withspecialreferencetotheHypnaceae andpossiblyrelatedfamiliesl3:645-665. ▲ Phylogeneticrelationshipswithinthehypnobryaleanmosses(ie,theHypnales,Leuco- dontales,andHookeriales)havebeenthefbcusofmuchattentioninrecentyears Herewepresentphylogeneticinfierencesonthislargeclade,andespeciallyonthe Hypnaceaeandpossiblyrelatedftlmilies,basedonmaximumlikelihoodanalysisof l81r6cLsequences、Oursmdycorroboratesthat(1)theHypnales(sstr.[=sensu Vittl984])andLeucodontalesareeachnotmonophyleticentities、TheHypnalesand LeucodontalestogethercompriseawellsupportedsistercladetotheHookeriales;(2) theSematophyllaceae(s」at[=sensuTsubotaetaL2000,2001a,b])andPlagiothecia‐ ceae(s・str.[=sensupresentDareeachresolvedasmonophyleticgroups,whileno particularcladeaccommodatesallmembersoftheHypnaceaeandCryphaeaceae;and (3)theHypnaceaeaswellasitstypegenusノリDlwz"川tselfwerepolyphyletioThese resultsdonotconcurwiththesystemsofVitt(1984)andBuckandVitt(1986),who suggestedthatthegroupswithasinglecostawouldhavedivergedfiFomthehypnalean ancestoratanearlyevolutionarystage,fbllowedbythegroupswithadoublecosta (seealsoTsubotaetall999;Bucketal2000)OurresultsfiPomlikelihoodanalyses -
Volume 1, Chapter 2-7: Bryophyta
Glime, J. M. 2017. Bryophyta – Bryopsida. Chapt. 2-7. In: Glime, J. M. Bryophyte Ecology. Volume 1. Physiological Ecology. Ebook 2-7-1 sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 10 January 2019 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 2-7 BRYOPHYTA – BRYOPSIDA TABLE OF CONTENTS Bryopsida Definition........................................................................................................................................... 2-7-2 Chromosome Numbers........................................................................................................................................ 2-7-3 Spore Production and Protonemata ..................................................................................................................... 2-7-3 Gametophyte Buds.............................................................................................................................................. 2-7-4 Gametophores ..................................................................................................................................................... 2-7-4 Location of Sex Organs....................................................................................................................................... 2-7-6 Sperm Dispersal .................................................................................................................................................. 2-7-7 Release of Sperm from the Antheridium..................................................................................................... -
Estimation of Plant Sampling Uncertainty: an Example Based on Chemical Analysis of Moss Samples
Environ Sci Pollut Res DOI 10.1007/s11356-016-7477-4 RESEARCH ARTICLE Estimation of plant sampling uncertainty: an example based on chemical analysis of moss samples Sabina Dołęgowska1 Received: 18 April 2016 /Accepted: 15 August 2016 # The Author(s) 2016. This article is published with open access at Springerlink.com Abstract In order to estimate the level of uncertainty arising Keywords Pleurozium schreberi (Brid.) Mitt . Trace from sampling, 54 samples (primary and duplicate) of the elements . Sampling uncertainty . Statistical methods moss species Pleurozium schreberi (Brid.) Mitt. were collect- ed within three forested areas (Wierna Rzeka, Piaski, Posłowice Range) in the Holy Cross Mountains (south-central Introduction Poland). During the fieldwork, each primary sample com- posed of 8 to 10 increments (subsamples) was taken over an Since the 1960s, monitoring studies using living organisms has area of 10 m2 whereas duplicate samples were collected in the been one of the most popular methods used to measure re- same way at a distance of 1–2 m. Subsequently, all samples sponse of individual organism to pollutants and to assess the were triple rinsed with deionized water, dried, milled, and environmental quality (Čeburnis and Steinnes 2000;Gerhardt digested (8 mL HNO3 (1:1) + 1 mL 30 % H2O2) in a closed 2002; Wolterbeek 2002; Szczepaniak and Biziuk 2003; Burger microwave system Multiwave 3000. The prepared solutions 2006; Samecka-Cymerman et al. 2006; Zechmeister et al. were analyzed twice for Cu, Fe, Mn, and Zn using FAAS and 2006). Among the wide and spread group of organisms, some GFAAS techniques. All datasets were checked for normality moss species, e.g., Pleurozium schreberi, Hylocomium and for normally distributed elements (Cu from Piaski, Zn splendens, Hypnum cupressiforme,andPseudoscleropodium from Posłowice, Fe, Zn from Wierna Rzeka). -
A New Genus Austrohondaella (Bryopsida, Hypnaceae) from Australasia
Telopea 12(3) 361–369 A new genus Austrohondaella (Bryopsida, Hypnaceae) from Australasia Zen Iwatsuki1, H. P. Ramsay2 and A. J. Fife3 1 The Hattori Botanical Laboratory, Okazaki Branch, 10–3 Mutsuna-shin-machi, Okazaki-shi, Aichi-ken 444–0846, Japan. 2 National Herbarium of New South Wales, Royal Botanic Gardens, Sydney 2000 NSW Australia. 3 Manaaki Whenua - Landcare Research, P.O. Box 40, Lincoln 7640, New Zealand. Author for correspondence: [email protected] Abstract The taxonomic position of Isopterygium limatum (Hook.f. & Wilson) Broth. has been re- evaluated. Some morphological characters, such as cylindric capsules, conic and non-rostrate opercula, well-differentiated annuli, pseudoparaphyllia shape, and axillary, papillose rhizoids suggest that the species should be excluded from the genus Isopterygium. A new genus, Austrohondaella Z.Iwats., H.P.Ramsay & Fife is therefore described here for Isopterygium limatum. This new genus should be classified in the family Hypnaceae. Introduction During studies on the genus Isopterygium for the floras of Australia and of New Zealand, it was noted separately by Fife and Iwatsuki that certain characteristics such as the erect capsule and operculum form, presence of an annulus, form of pseudoparaphyllia, and axillary and papillose rhizoids in Isopterygium limatum were not characteristic of the genus Isopterygium as outlined by Iwatsuki (1970, 1987) and Iwatsuki and Ramsay (2009). The common morphological features such as lanceolate leaves with a usually entire leaf margin, papillose axillary rhizoids and a differentiated annulus suggest that it might be a species of Isopterygiopsis (Fife in Seppelt 2004: 186). However, other features of I. limatum such as its erect capsules, bluntly conic opercula, narrowly foliose pseudoparaphyllia, etc are not consistent with this suggestion. -
Fontinalis Antipyretica Greater Water-Moss Key 324
Hypnales Fontinalis antipyretica Greater Water-moss Key 324 Sharply keeled leaf 4 mm Sharply keeled leaf in cross- section 0.5 mm 4 mm Identification This is our largest aquatic moss, with shoots (1.5–) 5–8 mm wide and often exceeding 15 cm in length. The leaves are 4–5 mm long and strongly folded inwards along the midline, with the fold-line forming a prominent keel. The shoots are usually 3-sided, with the keels forming the angles and the overlapping halves of adjacent leaves forming the sides. The leaf lacks a nerve (though it is not easy to unfold the keel and demonstrate this) and its tip is bluntly pointed and untoothed. Capsules are very uncommon, and almost hidden amongst the leaves, occurring only on plants which have undergone a period of exposure above the water. Similar species No other aquatic mosses have strongly keeled leaves like those of F. antipyretica. Like many aquatics, however, the species is very variable and not all plants have shoots which are as neatly 3-sided as the illustrated plants. However, even slender forms and those with more distantly spaced leaves have at least a moderately well- developed keel. Habitat F. antipyretica grows in a wide range of still, slowly or rapidly flowing water bodies, including lakes and ponds, canals, streams and rivers. Plants are usually attached to stones, rocks or waterside trees, but sometimes occur in loose masses on the bottom of shallow, still waters. It tolerates a wide range of water quality, but is usually replaced by F. squamosa (p.