What Are Algae? What Are Algae?

Total Page:16

File Type:pdf, Size:1020Kb

What Are Algae? What Are Algae? Marine botany – Algae– the study of aquatic plants and algae that live in seawater have chlorophyll as their primary photosynthetic pigment of the open ocean and the littoral zone and in brackish and lack a sterile covering of cells around their reproductive waters of estuaries cells Macroalgae Phycology-study of algae - Rhodophyta, Chlorophyta, Ochrophyta Microalgae (Phytoplankton) alga (singular) : “I study Silvetia, the intertidal alga” - Dinophyta , Haptophyta, Ochrophyta algae (plural): “Algae rock my world” Angiosperms algal (adj.): Algal lunch, algal skirt, algal growth rate -Mangroves, Marsh Plants, Seagrasses “algaes” (wrong!) Cyanobacteria 21 22 What are algae? What are algae? • Polyphyletic group = different ancestors, different evolutionary histories A B C D E A B C D E A B C D E A B C D E monophyletic polyphyletic paraphyletic or Algae encompassing various distinctly related groups of clade aquatic photosynthetic eukaryotes & bacteria. 23 24 1 Eukaryota Groups DOMAIN Groups (Kingdom) 1.Bacteria- cyanobacteria 2.Archae Alveolates- dinoflagellates 3.Eukaryota 1. Alveolates- unicellular,plasma membrane supported by Stramenopiles- diatoms, ochrophyta flattened vesicles Rhizaria 2. Stramenopiles- two unequal flagella, chloroplasts 4 Excavates membranes 3. Rhizaria- unicellular amoeboids Plantae- rhodophyta, chlorophyta, seagrasses Amoebozoans 4. Excava tes- unilllicellular fllltflagellates Fungi 5. Plantae- most broadly defined plant group Choanoflagellates Animals 6. Amoebozoans- pseudopods for movement & eating 7. Fungi- heterotrophs with extracellular digestion 8. Choanoflagellates- unicellular withsingle flagella 25 26 9. Animals- multicellular heterotrophs DOMAIN Groups (Kingdom) 1.Bacteria- cyanobacteria (blue green algae) Defining characteristics of Algae: 2.Archae “Algae” Photosynthesis (photoautotrophic, usually), using Chl a as 3.Eukaryotes 1. Alveolates- dinoflagellates primary pigment 2. Stramenopiles- diatoms, ochrophyta BUT: Limited cellular differentiation compared to 3. Rhizaria- unicellular amoeboids terrestrial plants 4. Excavates- unicellular flagellates No “real” vascular system 5. Plantae- rhodophyta, chlorophyta, seagrasses Sex organs unicellular, or all cells capable of reproduction (no sterile layer of cells 6. Amoebozoans- slimemolds surrounding sex organs aka NO FLOWERS) 7. Fungi- heterotrophs with extracellular digestion Much greater diversity of photosynthetic pigments 8. Choanoflagellates- unicellular and life histories 9. Animals- multicellular heterotrophs 27 28 2 Algae show tremendous diversity of A Vascular plant An Alga form, habitat, and lifestyle flower sorus blade stem photo Pete Dal Ferro stipe leaf holdfast roots Thallophyte- plants that lack roots, stems & leaves29 30 Free-living and unattached Gymnodinium – planktonic dinoflagellates Rhodoliths - benthic macroalgae photo: Morgan Bond Found in all bodies of water (freshwater, marine intertidal and subtidal) as well as terrestrial systems with enough moisture31 32 3 Free-living and attached to the substrate Epiphytic Parasitic Postelsia palmaeformis “saxicolous”, or “saxiphytic” Caulerpa taxifolia “psammophtyic” Smithora naiadum on Trentepohlia on 33 Phyllospadix torreyi Monterey Cypress 34 Symbiotic and Endoymbiotic Ecological importance of algae Lichen = close association of an alga and a fungus - Primary production; role in species interactions - Ecosystem engineers: e.g. kelp forests, rhodolith beds, coral Marine: Zooxanthellae in corals, anemonies, reefs = Create structure that defines the habitat type nudibranchs, flatworms Radiolarians, Foramaniferans = ameoba + alga fH2O too!: Zoochlorellae in hydras, sponges, etc.35 36 4 Allochthonous input – external source, not from the same ecosystem Nutrient input into terrestrial systems & deep sea Direct importance of algae to human beings Origin’s of the world’s oil supplies (dinoflagellates,coccolithophores,diatoms) Used in biological and medical research (e.g. Cyanobacteria, Chlamydomonas; fucoids); One product of red algae (e.g. Gelidium, Gigartina) = agar; produces gel at low temperatures, used in gel electrophoresis. (HUGE in genetics) Eaten “as itself” (e.g. nori, Spirulina) Products of algae are everywhere: carrageenan (from red algae) and alginates (from brown algae, e.g. Macrocystis, Laminaria) from polysaccharides in cell walls, act as thickening agents Ice cream, mayonnaise, chocolate milk, soy milk, toothpaste, salad dressings, 37 shaving cream, fertilizers, rubber, paint, hair products 38 Algal Taxonomy Algal Taxonomy Hierarchical system of classification: Hierarchical system of classification: Level: suffix: Level: suffix: example: Domain/Empire Domain Eukaryote Kingdom/Group Kingdom/Group Plantae Phylum/Division -phyta Phylum/Division -phyta Chlorophyta Class -ppyhyceae Class -ppyhyceae Ulvoppyhyceae Order -ales Order -ales Ulvales Family -aceae Family -aceae Ulvaceae Genus Genus Ulva species species fenestrata • King Phillip Came Over For Good Spaghetti • Keep Dishes Clean Or Family Gets Sick 39 40 5 DOMAIN Groups (Kingdom) Algal Taxonomy 1.Bacteria- cyanobacteria (blue green algae) Hierarchical system of classification: 2.Archae 3.Eukaryotes 1. Alveolates- dinoflagellates, coccolithophore Level: suffix: example: Chromista 2. Stramenopiles- diatoms, ochrophyta Domain Eukaryote Kingdom/Group Chromista 3. Rhizaria- unicellular amoeboids Phylum/Division -phyta Ochrophyta Class -ppyhyceae Phaeoppyhyceae 4. Excavates- unicellular flagellates Order -ales Laminariales 5. Plantae- rhodophyta, chlorophyta, seagrasses Family -aceae Alariaceae Genus Egregia 6. Amoebozoans- slimemolds species menziesii 7. Fungi- heterotrophs with extracellular digestion 8. Choanoflagellates- unicellular 41 9. Animals- multicellular heterotrophs 42 Algal Nomenclature- acknowledges the first and last person to describe the species 1753, Linneaus divided all life into two Phyla = Plants and Animals for example: Linnaeus called this Fucus pyriferus; later Within the plants, he recognized renamed Macrocystis pyrifera by Carl Adardh, so: • Cryptogams – hidden gametes…land plants • Thallogams – unspecialized gametes … the algae Macrocystis pyrifera (Linnaeus) Adardh Only three genera originally recognized: Fucus-fleshy Ulva- membranous Conferva- filamentous 43 44 6 -Taxonomy/systematics constantly under revision Division % marine ~# species Cyanophyta (blue-green algae) 8 4,500 - Depending on who you ask, between 50,000 and Rhodophyta (red algae) 98 7,000 Chlorophyta (green algae) 13 6,000 10 million different algal spp! Ochrophyta 16,758 Phaeophyceae (brown algae) 99 2,000 Bacillario/Coscinodiscophyceae(diatoms) 50 12,000 Dinop hy ta (dino flage llat es) 90 3, 000 - Biological species concept? Bryophyta Mosses, liverworts 0 25,000 -Morphology? Vascular plants Ferns, horsetail, club moss 0.1 13,018 - Genetics? Gymnosperms 0 722 Angiosperms 0.09 285,000 45 46 Mastocarpus species complex Petrocelis Mastocarpus papillatus + 2N 2N ‘Petrocelis’ crust (sporophyte) 1N 47 1N fronds 48 (gametophytes) 7 Algal Evolution: Endosymbiotic theory of organelle acquisition: 3.9 bya = Cyanobacteria appear and introduce photosynthesis (L. Margolis) 2.5 bya = Eukaryotes appeared (nuclear envelope and ER thought to come from invagination of plasma membrane) - Heterotrophic eukaryote eats heterotrophic bacteria 1.6 bya = Multicellular algae -Rhodophyta (Red algae) &Chlorophyta (proteobacteria) lead to the (Green algae) formation of mitochondria 900 mya= Dinoflagellates & Invertebrates appear -Heterotroppyhic eukaryote eats a photosynthetic bacteria 490 mya = Phaeophyceae (Brown algae) & land plants & coralline algae & (cyanobacteria) lead to the formation crustaceans & mulluscs of a chloroplast 408mya= Insects & Fish -Bacteria not digested but becomes an organelle 362 mya = Coccolithophores & Amphibians & Reptiles 290mya- Gymnosperms Support of Endosymbiotic Theory 49 -Genetic material of the 2 membranes that surround the50 145 mya = Diatoms & Angiosperms organelle Primary Endosymbiosis: Secondary endosymbiotic events 1. Heterotrophic eukaryote eats photosynthetic bacteria 1. Heterotrophic eukaryote eats (cyanobacterium). photosynthetic eukaryote 2. Results in photosynthetic eukaryote. 2. Nucleus from photosynthetic Chloroplast has 2 membranes eukaryote is lost 3. Chloroplast ends up with 4 mmbmembrane s 51 52 8 Secondary endosymbiotic events Secondary Endosymbiosis: 1. Heterotrophic eukaryote eats 1. Heterotrophic eukaryote eats photosynthetic eukaryote photosynthetic eukaryote 2. Nucleus from photosynthetic 2. Nucleus from photosynthetic eukaryote is lost eukaryote is lost 3. Chloroplast ends up with 4 3. Results in photosynthetic eukaryote. mmbmembrane s Chlorop last has 4 membranes. Tertiary endosymbiotic events occur in dinoflagellates 53 54 Details of Endosymbiotic origins - Loss of plastids What is agreed upon: e.g. Parasitic algae on seaweeds: no pigments, all white ? • Each algal division is a Plocamiocolax = Parasite on Rhodophyte alga Plocamium monophyletic group • Reds and Greens – 1 event-2 membranes • Browns – 2 events- 4 membranes Plocamiocolax on Plocamium Plocamium Adapted From Palmer 2003 55 56 9 Three main divisions (phyla) of seaweeds: - Loss of plastids e.g. Heterotrophic algae Chlorophyta: green algae Toxoplasma gondii = parasite in mammal muscular tissues 1 endosymbiotic event = 2 plastid membranes - Apicomplexan, closely related to dinoflagellates ~1.6bya ~6,000 species, 13% marine Ochrophyta: brown algae & diatoms 2 endosymbiotic events = 4 plastid membranes ~490 mya ~2,000, 99% marine & 12,000, 50% Rhodophyta: red algae 1 endosymbiotic event = 2 plastid membranes ~0.9 bya ~60% of domestic cats are infected; ~7,000, 98% marine toxoplasmosis in pregnant women… caused by an alga! 57 58 Paper Discussion on thursday: Lubchenco and Cubit. 1980. Heteromorphic life histories of certain marine algae as adaptations to variations in herbivory. Ecology 61(3): 676-687 Abstract Introduction Graphs & Figures Methods Results Discussion Sign up for paper you would like to lead. 59 60 10.
Recommended publications
  • Basal Body Structure and Composition in the Apicomplexans Toxoplasma and Plasmodium Maria E
    Francia et al. Cilia (2016) 5:3 DOI 10.1186/s13630-016-0025-5 Cilia REVIEW Open Access Basal body structure and composition in the apicomplexans Toxoplasma and Plasmodium Maria E. Francia1* , Jean‑Francois Dubremetz2 and Naomi S. Morrissette3 Abstract The phylum Apicomplexa encompasses numerous important human and animal disease-causing parasites, includ‑ ing the Plasmodium species, and Toxoplasma gondii, causative agents of malaria and toxoplasmosis, respectively. Apicomplexans proliferate by asexual replication and can also undergo sexual recombination. Most life cycle stages of the parasite lack flagella; these structures only appear on male gametes. Although male gametes (microgametes) assemble a typical 9 2 axoneme, the structure of the templating basal body is poorly defined. Moreover, the rela‑ tionship between asexual+ stage centrioles and microgamete basal bodies remains unclear. While asexual stages of Plasmodium lack defined centriole structures, the asexual stages of Toxoplasma and closely related coccidian api‑ complexans contain centrioles that consist of nine singlet microtubules and a central tubule. There are relatively few ultra-structural images of Toxoplasma microgametes, which only develop in cat intestinal epithelium. Only a subset of these include sections through the basal body: to date, none have unambiguously captured organization of the basal body structure. Moreover, it is unclear whether this basal body is derived from pre-existing asexual stage centrioles or is synthesized de novo. Basal bodies in Plasmodium microgametes are thought to be synthesized de novo, and their assembly remains ill-defined. Apicomplexan genomes harbor genes encoding δ- and ε-tubulin homologs, potentially enabling these parasites to assemble a typical triplet basal body structure.
    [Show full text]
  • Early Photosynthetic Eukaryotes Inhabited Low-Salinity Habitats
    Early photosynthetic eukaryotes inhabited PNAS PLUS low-salinity habitats Patricia Sánchez-Baracaldoa,1, John A. Ravenb,c, Davide Pisanid,e, and Andrew H. Knollf aSchool of Geographical Sciences, University of Bristol, Bristol BS8 1SS, United Kingdom; bDivision of Plant Science, University of Dundee at the James Hutton Institute, Dundee DD2 5DA, United Kingdom; cPlant Functional Biology and Climate Change Cluster, University of Technology Sydney, Ultimo, NSW 2007, Australia; dSchool of Biological Sciences, University of Bristol, Bristol BS8 1TH, United Kingdom; eSchool of Earth Sciences, University of Bristol, Bristol BS8 1TH, United Kingdom; and fDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138 Edited by Peter R. Crane, Oak Spring Garden Foundation, Upperville, Virginia, and approved July 7, 2017 (received for review December 7, 2016) The early evolutionary history of the chloroplast lineage remains estimates for the origin of plastids ranging over 800 My (7). At the an open question. It is widely accepted that the endosymbiosis that same time, the ecological setting in which this endosymbiotic event established the chloroplast lineage in eukaryotes can be traced occurred has not been fully explored (8), partly because of phy- back to a single event, in which a cyanobacterium was incorpo- logenetic uncertainties and preservational biases of the fossil re- rated into a protistan host. It is still unclear, however, which cord. Phylogenomics and trait evolution analysis have pointed to a Cyanobacteria are most closely related to the chloroplast, when the freshwater origin for Cyanobacteria (9–11), providing an approach plastid lineage first evolved, and in what habitats this endosym- to address the early diversification of terrestrial biota for which the biotic event occurred.
    [Show full text]
  • 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.
    [Show full text]
  • 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).
    [Show full text]
  • Supplementary Table S2: New Taxonomic Assignment of Sequences of Basal Fungal Lineages
    Supplementary Table S2: New taxonomic assignment of sequences of basal fungal lineages. Fungal sequences were subjected to BLAST-N analysis and checked for their taxonomic placement in the eukaryotic guide-tree of the SILVA release 111. Sequences were classified depending on combined results from the methods mentioned above as well as literature searches. Accession Name New classification Clustering of the sequence in the Best BLAST-N hit number based on combined results eukaryotic guide tree of SILVA Name Accession number E.value Identity AB191431 Uncultured fungus Chytridiomycota Chytridiomycota Basidiobolus haptosporus AF113413.1 0.0 91 AB191432 Unculltured eukaryote Blastocladiomycota Blastocladiomycota Rhizophlyctis rosea NG_017175.1 0.0 91 AB252775 Uncultured eukaryote Chytridiomycota Chytridiomycota Blastocladiales sp. EF565163.1 0.0 91 AB252776 Uncultured eukaryote Fungi Nucletmycea_Fonticula Rhizophydium sp. AF164270.2 0.0 87 AB252777 Uncultured eukaryote Chytridiomycota Chytridiomycota Basidiobolus haptosporus AF113413.1 0.0 91 AB275063 Uncultured fungus Chytridiomycota Chytridiomycota Catenomyces sp. AY635830.1 0.0 90 AB275064 Uncultured fungus Chytridiomycota Chytridiomycota Endogone lactiflua DQ536471.1 0.0 91 AB433328 Nuclearia thermophila Nuclearia Nucletmycea_Nuclearia Nuclearia thermophila AB433328.1 0.0 100 AB468592 Uncultured fungus Basal clone group I Chytridiomycota Physoderma dulichii DQ536472.1 0.0 90 AB468593 Uncultured fungus Basal clone group I Chytridiomycota Physoderma dulichii DQ536472.1 0.0 91 AB468594 Uncultured
    [Show full text]
  • 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
    [Show full text]
  • Phylogenetic Classification of Life
    Proc. Natl. Accad. Sci. USA Vol. 93, pp. 1071-1076, February 1996 Evolution Archaeal- eubacterial mergers in the origin of Eukarya: Phylogenetic classification of life (centriole-kinetosome DNA/Protoctista/kingdom classification/symbiogenesis/archaeprotist) LYNN MARGULIS Department of Biology, University of Massachusetts, Amherst, MA 01003-5810 Conitribluted by Lynnl Marglulis, September 15, 1995 ABSTRACT A symbiosis-based phylogeny leads to a con- these features evolved in their ancestors by inferable steps (4, sistent, useful classification system for all life. "Kingdoms" 20). rRNA gene sequences (Trichomonas, Coronympha, Giar- and "Domains" are replaced by biological names for the most dia; ref. 11) confirm these as descendants of anaerobic eu- inclusive taxa: Prokarya (bacteria) and Eukarya (symbiosis- karyotes that evolved prior to the "crown group" (12)-e.g., derived nucleated organisms). The earliest Eukarya, anaero- animals, fungi, or plants. bic mastigotes, hypothetically originated from permanent If eukaryotes began as motility symbioses between Ar- whole-cell fusion between members of Archaea (e.g., Thermo- chaea-e.g., Thermoplasma acidophilum-like and Eubacteria plasma-like organisms) and of Eubacteria (e.g., Spirochaeta- (Spirochaeta-, Spirosymplokos-, or Diplocalyx-like microbes; like organisms). Molecular biology, life-history, and fossil ref. 4) where cell-genetic integration led to the nucleus- record evidence support the reunification of bacteria as cytoskeletal system that defines eukaryotes (21)-then an Prokarya while
    [Show full text]
  • Plant Evolution an Introduction to the History of Life
    Plant Evolution An Introduction to the History of Life KARL J. NIKLAS The University of Chicago Press Chicago and London CONTENTS Preface vii Introduction 1 1 Origins and Early Events 29 2 The Invasion of Land and Air 93 3 Population Genetics, Adaptation, and Evolution 153 4 Development and Evolution 217 5 Speciation and Microevolution 271 6 Macroevolution 325 7 The Evolution of Multicellularity 377 8 Biophysics and Evolution 431 9 Ecology and Evolution 483 Glossary 537 Index 547 v Introduction The unpredictable and the predetermined unfold together to make everything the way it is. It’s how nature creates itself, on every scale, the snowflake and the snowstorm. — TOM STOPPARD, Arcadia, Act 1, Scene 4 (1993) Much has been written about evolution from the perspective of the history and biology of animals, but significantly less has been writ- ten about the evolutionary biology of plants. Zoocentricism in the biological literature is understandable to some extent because we are after all animals and not plants and because our self- interest is not entirely egotistical, since no biologist can deny the fact that animals have played significant and important roles as the actors on the stage of evolution come and go. The nearly romantic fascination with di- nosaurs and what caused their extinction is understandable, even though we should be equally fascinated with the monarchs of the Carboniferous, the tree lycopods and calamites, and with what caused their extinction (fig. 0.1). Yet, it must be understood that plants are as fascinating as animals, and that they are just as important to the study of biology in general and to understanding evolutionary theory in particular.
    [Show full text]
  • Pharmacognosy 1
    PHARMACOGNOSY 1 Dr. Dima MUHAMMAD 0 References: 1. Trease and Evans Pharmacognosy, William C. Evans, Saunders Elsevier, 2009, sixteenth ed., ISBN 978-0 -7020 -2934 9 2. textbook of pharmacognosy & phytochemistry, Biren Shah & A.K. Seth, Elsevier, 2010, 1st ed, ISBN: 978-81-312-2298-0 3. Medicinal Natural Products: A Biosynthetic Approach. Paul M Dewick, John Wiley & Sons, 2009,3rd Edition, ISBN 978-0-470-74168-9. 4. Martins, A., Vieira, H., Gaspar, H., & Santos, S. (2014). Marketed Marine Natural Products in the Pharmaceutical and Cosmeceutical Industries: Tips for Success. Marine Drugs, 12(2) 1 1. MEANING OF PHARMACOGNOSY Pharmacognosy, known initially as materia medica, may be defined as the study of crude drugs obtained from plants, animals and mineral kingdom and their constituents. There is a historical misinformation about who created the term pharmacognosy. According to some sources, it was C. A. Seydler, a medical student at Halle, Germany, in 1815; he wrote his doctoral thesis titled Analectica Pharmacognostica. However, recent historical research has found an earlier usage of this term. The physician J. A. Schmidt (Vienna) used that one in his Lehrbuch der materia medica in 1811, to describe the study of medicinal plants and their properties. The word pharmacognosy is derived from two Latin words pharmakon, ‘a drug,’ and gignoso, ‘to acquire knowledge of’. It means ‘knowledge or science of drugs. Crude drugs are plants or animals, or their parts which after collection are subjected only to drying or making them into transverse or longitudinal slices or peeling them in some cases. Most of the crude drugs used in medicine are obtained from plants, and only a small number comes from animal and mineral kingdoms.
    [Show full text]
  • Protocols for Monitoring Harmful Algal Blooms for Sustainable Aquaculture and Coastal Fisheries in Chile (Supplement Data)
    Protocols for monitoring Harmful Algal Blooms for sustainable aquaculture and coastal fisheries in Chile (Supplement data) Provided by Kyoko Yarimizu, et al. Table S1. Phytoplankton Naming Dictionary: This dictionary was constructed from the species observed in Chilean coast water in the past combined with the IOC list. Each name was verified with the list provided by IFOP and online dictionaries, AlgaeBase (https://www.algaebase.org/) and WoRMS (http://www.marinespecies.org/). The list is subjected to be updated. Phylum Class Order Family Genus Species Ochrophyta Bacillariophyceae Achnanthales Achnanthaceae Achnanthes Achnanthes longipes Bacillariophyta Coscinodiscophyceae Coscinodiscales Heliopeltaceae Actinoptychus Actinoptychus spp. Dinoflagellata Dinophyceae Gymnodiniales Gymnodiniaceae Akashiwo Akashiwo sanguinea Dinoflagellata Dinophyceae Gymnodiniales Gymnodiniaceae Amphidinium Amphidinium spp. Ochrophyta Bacillariophyceae Naviculales Amphipleuraceae Amphiprora Amphiprora spp. Bacillariophyta Bacillariophyceae Thalassiophysales Catenulaceae Amphora Amphora spp. Cyanobacteria Cyanophyceae Nostocales Aphanizomenonaceae Anabaenopsis Anabaenopsis milleri Cyanobacteria Cyanophyceae Oscillatoriales Coleofasciculaceae Anagnostidinema Anagnostidinema amphibium Anagnostidinema Cyanobacteria Cyanophyceae Oscillatoriales Coleofasciculaceae Anagnostidinema lemmermannii Cyanobacteria Cyanophyceae Oscillatoriales Microcoleaceae Annamia Annamia toxica Cyanobacteria Cyanophyceae Nostocales Aphanizomenonaceae Aphanizomenon Aphanizomenon flos-aquae
    [Show full text]
  • Kingdom Animalia: Phylum Summary Table
    KINGDOM ANIMALIA: PHYLUM SUMMARY TABLE Phylum PORIFERA CNIDARIA PLATYHELMINTHES (flatworms) NEMATODA (roundworms) ANNELIDA (segmented worms) Examples Sponges Sea jellies, Hydra, coral Planaria, tapeworm Trichinella, hookworm, Earthworm, polychaete worms, colonies, sea anemones nematode leech Body type Asymmetry Radial symmetry Bilateral symmetry Bilateral symmetry Bilateral symmetry (Symmetry) Ecological roles Food source Food source Food source Food source Food source home / shelter Reef- home, protect Parasitic Parasitic Parasitic symbiotic with shores Eat dead animals – Aerate soil Aerate soil bacteria Chem. – anticancer saprophyte Breakdown material Breakdown material Body organization 2 germ layers 2 layers: ecto & endo 3 layers: ectoderm, mesoderm, 3 layers: ectoderm, 3 layers: ectoderm, mesoderm, (# germ layers) Ectoderm, endoderm With mesoglea between endoderm mesoderm, endoderm endoderm Body cavity Acoelom Acoelom Acoelom Pseudocoelom Coelom Digestive system Filter feed: collar cells, Gastrovascular cavity, Mouth and gastrovascular Complete digestive Complete digestive system: food vacuoles, mouth, and cavity system: mouth & anus mouth & anus osculum nematocysts to capture food Mouth also serves as anus Special organs Special organs Reproduction Sexual: Sexual: male & female Sexual: hermaphroditic – Sexual: separate sexes = Sexual: hermaphroditic – heramaphroditic – medusa – gametes fuse cross fertilization dioecious cross fertilization gametes released in H2O Asexual: budding, Asexual: fragmentation Asexual: budding, regeneration
    [Show full text]
  • The Moss-Back Alga (Cladophorophyceae, Chlorophyta) on Two Species of Freshwater Turtles in the Kimberleys
    Telopea 12(2) 279–284 The moss-back alga (Cladophorophyceae, Chlorophyta) on two species of freshwater turtles in the Kimberleys Stephen Skinner1,2, Nancy FitzSimmons3 and Timothy J. Entwisle1 1National Herbarium of New South Wales, Mrs Macquaries Road, Sydney NSW 2000 Australia 2Southern ACT Catchment Group Inc., PO Box 2056, Kambah, ACT Author for correspondence: [email protected] 3Institute for Applied Ecology, School of Resource, Environmental & Heritage Sciences, University of Canberra, Canberra, ACT 2601, Australia Abstract The range of the Australian freshwater alga Basicladia ramulosa Ducker is extended, both in its turtle hosts (Chelodina burrungandjii Thomson et al.; Emydura australis (Grey)) and in geography, to tropical northern Western Australia. Along with further morphological observations, sporangia are described for the first time in this taxon. Introduction Moss-back turtles (Fig. 1) have fascinated biologists for many years. While the carapace of a potentially amphibious turtle would be a challenging habitat for most aquatic organisms, it is perhaps surprising there are only a handful of attached algae reported from such sites. Edgren et al. (1953) detailed the range of host turtles then known in North America and the range of epizoic algae that included Rhizoclonium and Cladophora. Two further genera in the Cladophoraceae are the only macroalgae widely reported on turtle carapaces: the prostrate, spreading, endozoic (and possibly disease causing) Dermatophyton radicans Peter, and species of the heterotrichous genus Basicladia, responsible for the name ‘moss-back’. In the United States, Basicladia is considered a small epizoic genus on turtles and water snails, of three to four taxa (John 2003). Hamilton (1948) described sexual reproduction in North American species of Basicladia involving the fusion of biflagellate zooids as is commonly the case in the Cladophoraceae.
    [Show full text]