Algae, Lichens and Bryophyta [B.Sc
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RED ALGAE · RHODOPHYTA Rhodophyta Are Cosmopolitan, Found from the Artic to the Tropics
RED ALGAE · RHODOPHYTA Rhodophyta are cosmopolitan, found from the artic to the tropics. Although they grow in both marine and fresh water, 98% of the 6,500 species of red algae are marine. Most of these species occur in the tropics and sub-tropics, though the greatest number of species is temperate. Along the California coast, the species of red algae far outnumber the species of green and brown algae. In temperate regions such as California, red algae are common in the intertidal zone. In the tropics, however, they are mostly subtidal, growing as epiphytes on seagrasses, within the crevices of rock and coral reefs, or occasionally on dead coral or sand. In some tropical waters, red algae can be found as deep as 200 meters. Because of their unique accessory pigments (phycobiliproteins), the red algae are able to harvest the blue light that reaches deeper waters. Red algae are important economically in many parts of the world. For example, in Japan, the cultivation of Pyropia is a multibillion-dollar industry, used for nori and other algal products. Rhodophyta also provide valuable “gums” or colloidal agents for industrial and food applications. Two extremely important phycocolloids are agar (and the derivative agarose) and carrageenan. The Rhodophyta are the only algae which have “pit plugs” between cells in multicellular thalli. Though their true function is debated, pit plugs are thought to provide stability to the thallus. Also, the red algae are unique in that they have no flagellated stages, which enhance reproduction in other algae. Instead, red algae has a complex life cycle, with three distinct stages. -
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. -
Red Algae (Bangia Atropurpurea) Ecological Risk Screening Summary
Red Algae (Bangia atropurpurea) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, February 2014 Revised, March 2016, September 2017, October 2017 Web Version, 6/25/2018 1 Native Range and Status in the United States Native Range From NOAA and USGS (2016): “Bangia atropurpurea has a widespread amphi-Atlantic range, which includes the Atlantic coast of North America […]” Status in the United States From Mills et al. (1991): “This filamentous red alga native to the Atlantic Coast was observed in Lake Erie in 1964 (Lin and Blum 1977). After this sighting, records for Lake Ontario (Damann 1979), Lake Michigan (Weik 1977), Lake Simcoe (Jackson 1985) and Lake Huron (Sheath 1987) were reported. It has become a major species of the littoral flora of these lakes, generally occupying the littoral zone with Cladophora and Ulothrix (Blum 1982). Earliest records of this algae in the basin, however, go back to the 1940s when Smith and Moyle (1944) found the alga in Lake Superior tributaries. Matthews (1932) found the alga in Quaker Run in the Allegheny drainage basin. Smith and 1 Moyle’s records must have not resulted in spreading populations since the alga was not known in Lake Superior as of 1987. Kishler and Taft (1970) were the most recent workers to refer to the records of Smith and Moyle (1944) and Matthews (1932).” From NOAA and USGS (2016): “Established where recorded except in Lake Superior. The distribution in Lake Simcoe is limited (Jackson 1985).” From Kipp et al. (2017): “Bangia atropurpurea was first recorded from Lake Erie in 1964. During the 1960s–1980s, it was recorded from Lake Huron, Lake Michigan, Lake Ontario, and Lake Simcoe (part of the Lake Ontario drainage). -
Algae & Marine Plants of Point Reyes
Algae & Marine Plants of Point Reyes Green Algae or Chlorophyta Genus/Species Common Name Acrosiphonia coalita Green rope, Tangled weed Blidingia minima Blidingia minima var. vexata Dwarf sea hair Bryopsis corticulans Cladophora columbiana Green tuft alga Codium fragile subsp. californicum Sea staghorn Codium setchellii Smooth spongy cushion, Green spongy cushion Trentepohlia aurea Ulva californica Ulva fenestrata Sea lettuce Ulva intestinalis Sea hair, Sea lettuce, Gutweed, Grass kelp Ulva linza Ulva taeniata Urospora sp. Brown Algae or Ochrophyta Genus/Species Common Name Alaria marginata Ribbon kelp, Winged kelp Analipus japonicus Fir branch seaweed, Sea fir Coilodesme californica Dactylosiphon bullosus Desmarestia herbacea Desmarestia latifrons Egregia menziesii Feather boa Fucus distichus Bladderwrack, Rockweed Haplogloia andersonii Anderson's gooey brown Laminaria setchellii Southern stiff-stiped kelp Laminaria sinclairii Leathesia marina Sea cauliflower Melanosiphon intestinalis Twisted sea tubes Nereocystis luetkeana Bull kelp, Bullwhip kelp, Bladder wrack, Edible kelp, Ribbon kelp Pelvetiopsis limitata Petalonia fascia False kelp Petrospongium rugosum Phaeostrophion irregulare Sand-scoured false kelp Pterygophora californica Woody-stemmed kelp, Stalked kelp, Walking kelp Ralfsia sp. Silvetia compressa Rockweed Stephanocystis osmundacea Page 1 of 4 Red Algae or Rhodophyta Genus/Species Common Name Ahnfeltia fastigiata Bushy Ahnfelt's seaweed Ahnfeltiopsis linearis Anisocladella pacifica Bangia sp. Bossiella dichotoma Bossiella -
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 -
Coral Reef Algae
Coral Reef Algae Peggy Fong and Valerie J. Paul Abstract Benthic macroalgae, or “seaweeds,” are key mem- 1 Importance of Coral Reef Algae bers of coral reef communities that provide vital ecological functions such as stabilization of reef structure, production Coral reefs are one of the most diverse and productive eco- of tropical sands, nutrient retention and recycling, primary systems on the planet, forming heterogeneous habitats that production, and trophic support. Macroalgae of an astonish- serve as important sources of primary production within ing range of diversity, abundance, and morphological form provide these equally diverse ecological functions. Marine tropical marine environments (Odum and Odum 1955; macroalgae are a functional rather than phylogenetic group Connell 1978). Coral reefs are located along the coastlines of comprised of members from two Kingdoms and at least over 100 countries and provide a variety of ecosystem goods four major Phyla. Structurally, coral reef macroalgae range and services. Reefs serve as a major food source for many from simple chains of prokaryotic cells to upright vine-like developing nations, provide barriers to high wave action that rockweeds with complex internal structures analogous to buffer coastlines and beaches from erosion, and supply an vascular plants. There is abundant evidence that the his- important revenue base for local economies through fishing torical state of coral reef algal communities was dominance and recreational activities (Odgen 1997). by encrusting and turf-forming macroalgae, yet over the Benthic algae are key members of coral reef communities last few decades upright and more fleshy macroalgae have (Fig. 1) that provide vital ecological functions such as stabili- proliferated across all areas and zones of reefs with increas- zation of reef structure, production of tropical sands, nutrient ing frequency and abundance. -
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..................................................................................................... -
Brown Algae and 4) the Oomycetes (Water Molds)
Protista Classification Excavata The kingdom Protista (in the five kingdom system) contains mostly unicellular eukaryotes. This taxonomic grouping is polyphyletic and based only Alveolates on cellular structure and life styles not on any molecular evidence. Using molecular biology and detailed comparison of cell structure, scientists are now beginning to see evolutionary SAR Stramenopila history in the protists. The ongoing changes in the protest phylogeny are rapidly changing with each new piece of evidence. The following classification suggests 4 “supergroups” within the Rhizaria original Protista kingdom and the taxonomy is still being worked out. This lab is looking at one current hypothesis shown on the right. Some of the organisms are grouped together because Archaeplastida of very strong support and others are controversial. It is important to focus on the characteristics of each clade which explains why they are grouped together. This lab will only look at the groups that Amoebozoans were once included in the Protista kingdom and the other groups (higher plants, fungi, and animals) will be Unikonta examined in future labs. Opisthokonts Protista Classification Excavata Starting with the four “Supergroups”, we will divide the rest into different levels called clades. A Clade is defined as a group of Alveolates biological taxa (as species) that includes all descendants of one common ancestor. Too simplify this process, we have included a cladogram we will be using throughout the SAR Stramenopila course. We will divide or expand parts of the cladogram to emphasize evolutionary relationships. For the protists, we will divide Rhizaria the supergroups into smaller clades assigning them artificial numbers (clade1, clade2, clade3) to establish a grouping at a specific level. -
727-735 Issn 2077-4613
Middle East Journal of Applied Volume : 08 | Issue :03 |July-Sept.| 2018 Sciences Pages: 727-735 ISSN 2077-4613 Antifungal bio-efficacy of the red algae Gracilaria confervoides extracts against three pathogenic fungi of cucumber plant Amira Sh. Soliman1, A.Y. Ahmed2, Siham E. Abdel-Ghafour2, Mostafa M. El-Sheekh3 and Hassan M. Sobhy1 1Natural Resources Department, Institute of African Research and Studies, Cairo University, Giza, Egypt. 2Plant Pathology Research Institute, Agricultural Research Center, Giza, Egypt. 3Botany Department, Faculty of Science, Tanta University, Tanta, Egypt. Received: 07 May 2018 / Accepted: 26 June 2018 / Publication date: 15 July 2018 ABSTRACT In this study, the potential of the macroalgae Gracilaria confervoides red algae extracts and powder were evaluated as a bioagent source of the three soil-borne pathogenic fungi of cucumber namely; Rhizoctonia solani, Fusarium solani and Macrophomina phaseolina in Egypt. Five organic solvents; Ethyl acetate, Methanol, Acetone, Benzene, and Chloroform, in addition to water were used for the extraction to evaluate their bioeffecinecy on mycelium growth reduction of the three fungal pathogens on potato dextrose agar (PDA). Radial growth reduction of the pathogens was noticed in R. solani and F. solani with all solvents and water extraction. In case of the fungus M. phaseolinae all solvents and water extractions malformatted the fungal growth (aerial mycelium and no microsclerotia). The highest reduction (100%) obtained on R. solani when chloroform extraction was used followed by ethyl acetate extraction (50%). In the greenhouse experiment, macroalgae powder was used to evaluate its effect on disease incidence which indicated about (70%) decrease for diseases. The highest total yield (133.2g) was obtained from plants infected with M. -
Bangor University DOCTOR of PHILOSOPHY Biosystematic and Cytological Studies of Mosses and Liverworts. Abderrahman, Salim Moh'd
Bangor University DOCTOR OF PHILOSOPHY Biosystematic and cytological studies of mosses and liverworts. Abderrahman, Salim Moh'd Mansur Award date: 1981 Link to publication General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal ? Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 05. Oct. 2021 In the name of GOD Most Gracious Most Merciful -ii iä -0 Thanking Him with a full heart and devoted tongue ST COPY AVAILA L TEXT IN ORIGINAL IS CLOSETO THE EDGE OF THE PAGE BIOSYSTE14ATIC'AND'CYTOLOGICAL', STUDIES'OF 'MOSSES'AND 'LIVERWORTS A thesis Presented for the &gree pf- PhiloSophiae Doctor in the University of Wales by Salim Moh'd Mansur Abderrahmano B. Sc. Biology & Ed. Cý (Kuwait University) School of Plant Biology, University College of North Wales, Bangor M. K. ), I hereby declare that the work herein, now submitted as a thesis for the degree of Philosophiae Doctor of the University of Wales, is the result of my own investigations and that all references to ideas and work of other resefrchers has been specifically acknoFledged. -
Axenically Culturing the Bryophytes: Establishment and Propagation of the Moss Hypnum Cupressiforme Hedw. (Bryophyta, Hypnaceae) in in Vitro Conditions
35 (1): (2011) 71-77 Original Scientifi c Paper Axenically culturing the bryophytes: establishment and propagation of the moss Hypnum cupressiforme Hedw. (Bryophyta, Hypnaceae) in in vitro conditions Milorad Vujičić✳, Aneta Sabovljević and Marko Sabovljević Institute of Botany and Garden, Faculty of Biology, University of Belgrade, Takovska 43, 11000 Belgrade, Serbia ABSTRACT: Th e study gives the fi rst report of in vitro culture of the pleurocarpous moss Hypnum cupressiforme and on the problems of axenicaly culturing this bryophyte and the conditions for establishment and propagation. Problems of surface sterilization are elaborated regarding sporophyte vs. gametophyte. Th e infl uence of nutrient, light length and temperature on diff erent developmental stages is discussed. Th e best conditions for micro-propagation from shoots are slightly lower temperature (18-20°C), on MS-sugar free medium irrelevant of day length. Th is moss is a counterpart of some rare and endangered mosses from the same genus and data presented should be taken into account of conservation and propagation of its counterparts as well. Its propagation is valuable for horticultural, pharmaceutical and bioindication purposes, as well. Key words: moss, Hypnum cupressiforme, in vitro, development, propagation Received 29 October 2010 Revision accepted 27 December 2010 UDK 582.325.23:575.2.085.2 INTRODUCTION establishment in axenic culture, it is oft en problem of material availability, genetic variability of material, disposal Bryophytes (comprising hornworts, liverworts and of axenic organisms leaving on bryophytes and low level mosses) are the second largest group of higher plants aft er of species biology knowledge (e.g. Duckett et al. -
(Bryopsida: Splachnaceae). Lily Roberta Lewis University of Connecticut, [email protected]
University of Connecticut OpenCommons@UConn Doctoral Dissertations University of Connecticut Graduate School 5-7-2015 Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae). Lily Roberta Lewis University of Connecticut, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/dissertations Recommended Citation Lewis, Lily Roberta, "Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae)." (2015). Doctoral Dissertations. 747. https://opencommons.uconn.edu/dissertations/747 Resolving Amphitropical Phylogeographic Histories in the Common Dung Moss Tetraplodon (Bryopsida: Splachnaceae). Lily Roberta Lewis, PhD University of Connecticut, 2015 Many plants have geographic disjunctions, with one of the more rare, yet extreme being the amphitropical, or bipolar disjunction. Bryophytes (namely mosses and liverworts) exhibit this pattern more frequently relative to other groups of plants and typically at or below the level of species. The processes that have shaped the amphitropical disjunction have been infrequently investigated, with notably a near absence of studies focusing on mosses. This dissertation explores the amphitropical disjunction in the dung moss Tetraplodon, with a special emphasis on the origin of the southernmost South American endemic T. fuegianus. Chapter 1 delimits three major lineages within Tetraplodon with distinct yet overlapping geographic ranges, including an amphitropical lineage containing the southernmost South American endemic T. fuegianus. Based on molecular divergence date estimation and phylogenetic topology, the American amphitropical disjunction is traced to a single direct long-distance dispersal event across the tropics. Chapter 2 provides the first evidence supporting the role of migratory shore birds in dispersing bryophytes, as well as other plant, fungal, and algal diaspores across the tropics.