Some Algae in Lakes Hume and Mulwala Victoria
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Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho
Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho To cite this version: James Umen, Susana Coelho. Algal Sex Determination and the Evolution of Anisogamy. Annual Review of Microbiology, Annual Reviews, 2019, 73 (1), 10.1146/annurev-micro-020518-120011. hal- 02187088 HAL Id: hal-02187088 https://hal.sorbonne-universite.fr/hal-02187088 Submitted on 17 Jul 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Annu. Rev. Microbiol. 2019. 73:X–X https://doi.org/10.1146/annurev-micro-020518-120011 Copyright © 2019 by Annual Reviews. All rights reserved Umen • Coelho www.annualreviews.org • Algal Sexes and Mating Systems Algal Sex Determination and the Evolution of Anisogamy James Umen1 and Susana Coelho2 1Donald Danforth Plant Science Center, St. Louis, Missouri 63132, USA; email: [email protected] 2Sorbonne Université, UPMC Université Paris 06, CNRS, Algal Genetics Group, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, CS 90074, F-29688, Roscoff, France [**AU: Please write the entire affiliation in French or write it all in English, rather than a combination of English and French**] ; email: [email protected] Abstract Algae are photosynthetic eukaryotes whose taxonomic breadth covers a range of life histories, degrees of cellular and developmental complexity, and diverse patterns of sexual reproduction. -
Detergent-Extracted Volvox Model Exhibits an Anterior–Posterior Gradient in Flagellar Ca2+ Sensitivity
Detergent-extracted Volvox model exhibits an PNAS PLUS + anterior–posterior gradient in flagellar Ca2 sensitivity Noriko Uekia and Ken-ichi Wakabayashia,1 aLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama-shi, Kanagawa 226-8503, Japan Edited by Krishna K. Niyogi, Howard Hughes Medical Institute, University of California, Berkeley, CA, and approved December 8, 2017 (received for review September 1, 2017) Volvox rousseletii is a multicellular spheroidal green alga contain- suggested by studies using demembranated and reactivated cells ing ∼5,000 cells, each equipped with two flagella (cilia). This or- and flagella (5, 6). ganism shows striking photobehavior without any known Multicellular spheroidal species of Volvocales, including Volvox intercellular communication. To help understand how the behav- species, have often been regarded as colonial Chlamydomonas. ior of flagella is regulated, we developed a method to extract the However, alignment of Chlamydomonas cells on the surface of a whole organism with detergent and reactivate its flagellar motil- spheroid, with each cell displaying breaststroke-like flagellar ity. Upon addition of ATP, demembranated flagella (axonemes) in beating, would result in spheroids unable to swim in one direction. the spheroids actively beat and the spheroids swam as if they Unlike a C. reinhardtii cell, each cell in a Volvox spheroid has two + were alive. Under Ca2 -free conditions, the axonemes assumed flagella beating in the same direction. A Volvox spheroid has an planar and asymmetrical waveforms and beat toward the poste- anterior–posterior (A–P) axis, and its ∼10,000 flagella beat toward rior pole, as do live spheroids in the absence of light stimulation. -
Lateral Gene Transfer of Anion-Conducting Channelrhodopsins Between Green Algae and Giant Viruses
bioRxiv preprint doi: https://doi.org/10.1101/2020.04.15.042127; this version posted April 23, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 5 Lateral gene transfer of anion-conducting channelrhodopsins between green algae and giant viruses Andrey Rozenberg 1,5, Johannes Oppermann 2,5, Jonas Wietek 2,3, Rodrigo Gaston Fernandez Lahore 2, Ruth-Anne Sandaa 4, Gunnar Bratbak 4, Peter Hegemann 2,6, and Oded 10 Béjà 1,6 1Faculty of Biology, Technion - Israel Institute of Technology, Haifa 32000, Israel. 2Institute for Biology, Experimental Biophysics, Humboldt-Universität zu Berlin, Invalidenstraße 42, Berlin 10115, Germany. 3Present address: Department of Neurobiology, Weizmann 15 Institute of Science, Rehovot 7610001, Israel. 4Department of Biological Sciences, University of Bergen, N-5020 Bergen, Norway. 5These authors contributed equally: Andrey Rozenberg, Johannes Oppermann. 6These authors jointly supervised this work: Peter Hegemann, Oded Béjà. e-mail: [email protected] ; [email protected] 20 ABSTRACT Channelrhodopsins (ChRs) are algal light-gated ion channels widely used as optogenetic tools for manipulating neuronal activity 1,2. Four ChR families are currently known. Green algal 3–5 and cryptophyte 6 cation-conducting ChRs (CCRs), cryptophyte anion-conducting ChRs (ACRs) 7, and the MerMAID ChRs 8. Here we 25 report the discovery of a new family of phylogenetically distinct ChRs encoded by marine giant viruses and acquired from their unicellular green algal prasinophyte hosts. -
Utah Wetlands Progre
Ecological and Beneficial Use Assessment of Farmington Bay Wetlands: Assessment and Site-Specific Nutrient Criteria Methods Development Phase I Progress Report to EPA, Region VIII and Final Report for Grant: CD988706-03 Submitted by Theron G. Miller, Ph.D. Utah DEQ, Division of Water Quality and Heidi M. Hoven, Ph.D. The Institute for Watershed Sciences April 10, 2007 Table of Contents Section Page Executive Summary ………………………………………………………………….. 1 Background and Purpose of study…………………………………………….. …….. 2 Plant Community Responses to Water Quality at Impounded and Sheetflow Sites … 3 Macroinvertebrate Response to Water Quality ……………………………………… 3 Shorebird Nesting Success and Prey Selection ……………………………………… 4 Nutrient Dynamics and Sediment Phosphorus Studies ……………………………… 4 Preliminary Conclusions …………………………………………………………….. 5 Potential metrics for wetlands assessment …………………………………………... 5 1.0 Introduction ……………………………………………………………………... 6 2.0 Methods and Study Design……………………………………………………... 8 3.0 Results and Discussion …………………………………………………………. 11 3.1Vegetative Community Response ………………………………………. 11 3.1.1 Impounded sites ……………………………………………………. 12 3.1.2 Vegetative Community Response at Sheetflow Sites …….. 21 3.1.3 Summary of Data Gaps …………………………………………. 27 3.1.3.1 Impounded …………………………………………………… 27 3.1.3.2 Sheetflow ……………………………………………………… 28 3.2 Macroinvertebrate Communities ……………………………………… 28 3.3 Shorebird Studies …………………………………………………………. 33 3.4 Water Column and Sediment Phosphorus Dynamics ……………. 40 3.5 Water-Sediment Interactions …………………………………………... 44 3.6 Conclusions …………………………………………………………………. 47 4.0 Literature Cited ………………………………………………………………….. 50 ii List of Figures Figure Page Figure 1.1. Great Salt Lake images during high water of 1988 and low water (2002). …….. 7 Figure 2.1.1. Sampling sites in Farmington Bay wetlands. …………………………………. 9 Figure 2.1.2. Wetland reference sites located in the Public Shooting Grounds …………….. 10 Figure 3.1.1. Seasonal changes in percent cover of SAV……………………………………. -
Kenneth G. Karol the Lewis B
Kenneth G. Karol The Lewis B. and Dorothy Cullman Program for Molecular Systematics Studies The New York Botanical Garden Bronx, New York 10458-5126 telephone: (718) 817-8615 e-mail: [email protected] Education Ph.D., Plant Biology. 2004. University of Maryland, College Park, MD Bachelor of Science, Botany. 1992. University of Wisconsin, Madison, WI Professional Experience Assistant Curator. 2007-Present. Cullman Program, The New York Botanical Garden, Bronx, NY Doctoral Faculty. 2007-Present. City University of New York, Plant Sciences Ph.D. Subprogram, Lehman College, Bronx, NY Chair - Phycological Section, Botanical Society of America. 2006-Present. Postdoctoral Fellow. 2006-2007. National Institutes of Health - National Research Service Award, Genomics/Biology, University of Washington, Seattle, WA LBNA Guest Researcher. 2005-present. Department of Energy Joint Genome Institute, Walnut Creek, CA Appointment runs concurrently with ongoing genome projects. Research Associate (post-doc). 2004-2006. US National Science Foundation Tree of Life Program, Biology, University of Washington, Seattle, WA Graduate Student. 1998-2004. Cell Biology and Molecular Genetics, University of Maryland, College Park, MD Research Assistant. 1999-2003. US NSF PEET Program, University of Maryland, College Park, MD Graduate Admissions Committee. 2001 & 2002. Cell Biology and Molecular Genetics, University of Maryland, College Park, MD Executive Committee. 1999-2000. Green Plant Phylogeny Research Coordination Group Biological Research Technician. 1997-1998. Laboratory of Molecular Systematics, National Museum of Natural History, Smithsonian Institution, Washington, DC Contract Researcher. 1997. Laboratory of Molecular Systematics, National Museum of Natural History, Smithsonian Institution, Smithsonian Institution, Washington, DC Research Technician. 1993-1996. Biological Sciences, DePaul University, Chicago, IL Visiting Scientist. -
Evolution Der Algen Und Plastiden (T
Georg-August-Universität Göttingen Vorlesung 63052 Biodiversität: Evolution der Algen EvolutionEvolution derder AlgenAlgen undund PlastidenPlastiden Teil 5: Viridiplantae Thomas Friedl Abteilung Experimentelle Phykologie undund Sammlung von Algenkulturen Albrecht-von-Haller-Institut für Pflanzenwissenschaften www.epsag.uni-goettingen.de Biodiversität: Evolution der Algen WS 2007/8 Mi 12:15 - 13:00 im Seminarraum 1.213 oder kleinen Hörsaal Evolution der Algen und Plastiden (T. Friedl) 17.10. Einführung, Übersicht über die Algen, Vorstellung der Abteilung EPSAG 24.10. Cyanobakterien 31.10. - Besichtigung der Abteilung und SAG (I. Lang) - 07.11. -- 14.11. Primäre Endosymbiose 21.11. Glaucophyta, Rotalgen 28.11. Grünalgen und Entstehung der Landpflanzen 05.12. Sekundäre Endosymbiose, Cryptophyta, Chlorarachniophyta 12.12. Stramenopiles + Haptophyta = "Chromista"? 19.12. Alveolates,Euglenozoa, Abschlußbetrachtung 09.01. Imke Lang: Cryokonservierung 16.01. Imke Lang: Anwendung von Algen in der Biotechnologie 23.01 Kathrin Mohr: Erfassen von Algenbiodiversität mit molekularen Methoden. I 30.01 Kathrin Mohr: Erfassen von Algenbiodiversität mit molekularen Methoden. II Benutzername: evolution Passwort: ers01ter www.epsag.uni-goettingen.de Primary endosymbiosis Secondary endosymbiosis Tertiary endosymbiosis Cyanobacterium Ciliates primary host Rhodophyta Sporozoa Glaucophyta Chlorophyta secondary host peridinin-containing Dinoflagellates Heterokontophyta, secondary host Haptophyta tertiary host fucoxanthin-containing Dinoflagellates Oomycetes heteroloboseid -
Freshwater Algae in Britain and Ireland - Bibliography
Freshwater algae in Britain and Ireland - Bibliography Floras, monographs, articles with records and environmental information, together with papers dealing with taxonomic/nomenclatural changes since 2003 (previous update of ‘Coded List’) as well as those helpful for identification purposes. Theses are listed only where available online and include unpublished information. Useful websites are listed at the end of the bibliography. Further links to relevant information (catalogues, websites, photocatalogues) can be found on the site managed by the British Phycological Society (http://www.brphycsoc.org/links.lasso). Abbas A, Godward MBE (1964) Cytology in relation to taxonomy in Chaetophorales. Journal of the Linnean Society, Botany 58: 499–597. Abbott J, Emsley F, Hick T, Stubbins J, Turner WB, West W (1886) Contributions to a fauna and flora of West Yorkshire: algae (exclusive of Diatomaceae). Transactions of the Leeds Naturalists' Club and Scientific Association 1: 69–78, pl.1. Acton E (1909) Coccomyxa subellipsoidea, a new member of the Palmellaceae. Annals of Botany 23: 537–573. Acton E (1916a) On the structure and origin of Cladophora-balls. New Phytologist 15: 1–10. Acton E (1916b) On a new penetrating alga. New Phytologist 15: 97–102. Acton E (1916c) Studies on the nuclear division in desmids. 1. Hyalotheca dissiliens (Smith) Bréb. Annals of Botany 30: 379–382. Adams J (1908) A synopsis of Irish algae, freshwater and marine. Proceedings of the Royal Irish Academy 27B: 11–60. Ahmadjian V (1967) A guide to the algae occurring as lichen symbionts: isolation, culture, cultural physiology and identification. Phycologia 6: 127–166 Allanson BR (1973) The fine structure of the periphyton of Chara sp. -
2013 Program Brochure START
!"#$%&'$()!#*)+!(,)+-$.,-.,/$0,)1#*#)0#$ 2345$6789$:$+3;389$6<'=$%>76$ University of New Brunswick, Fredericton New Brunswick, Canada SCOPE This is the second (http://www2.unb.ca/vip/IVC2013/) of what we hope to be a long series of Volvox meetings to be held every other year. The idea of a meeting on everything about Volvox and its relatives (aka Volvocales or volvocine algae) reflects both an increase in the size of the Volvox community and the realization that many researchers from fields traditionally not associated with Volvox research (e.g., physics, theoretical biology) are interested in various aspects of the system. Indeed, volvocine algae have become an important model system for the evolution of multicellularity, development and cellular differentiation, and lately have yielded important results in fields as diverse as genomics, hydrodynamics, and social evolution. We hope that these meetings will continue to foster exchange of ideas and expertise, and will initiate new collaborations. Furthermore, with these meetings we wish to attract new people and to build a stronger Volvox community. CONFERENCE ORGANIZER Aurora M. Nedelcu, University of New Brunswick, Canada ORGANIZING COMMITTEE Matthew Herron, University of Montana, USA Erik Hanschen, University of Arizona, USA David Smith, University of Western Ontario, Canada Hisayoshi Nozaki, University of Tokyo, Japan James Umen, Donald Danforth Plant Science Center, USA Stephen Miller, University of Maryland Baltimore County, USA Annette Coleman, Brown University USA Aurelia Honerkamp-Smith, -
An Unrecognized Ancient Lineage of Green Plants Persists in Deep Marine Waters
FAU Institutional Repository http://purl.fcla.edu/fau/fauir This paper was submitted by the faculty of FAU’s Harbor Branch Oceanographic Institute. Notice: ©2010 Phycological Society of America. This manuscript is an author version with the final publication available at http://www.wiley.com/WileyCDA/ and may be cited as: Zechman, F. W., Verbruggen, H., Leliaert, F., Ashworth, M., Buchheim, M. A., Fawley, M. W., Spalding, H., Pueschel, C. M., Buchheim, J. A., Verghese, B., & Hanisak, M. D. (2010). An unrecognized ancient lineage of green plants persists in deep marine waters. Journal of Phycology, 46(6), 1288‐1295. (Suppl. material). doi:10.1111/j.1529‐8817.2010.00900.x J. Phycol. 46, 1288–1295 (2010) Ó 2010 Phycological Society of America DOI: 10.1111/j.1529-8817.2010.00900.x AN UNRECOGNIZED ANCIENT LINEAGE OF GREEN PLANTS PERSISTS IN DEEP MARINE WATERS1 Frederick W. Zechman2,3 Department of Biology, California State University Fresno, 2555 East San Ramon Ave, Fresno, California 93740, USA Heroen Verbruggen,3 Frederik Leliaert Phycology Research Group, Ghent University, Krijgslaan 281 S8, 9000 Ghent, Belgium Matt Ashworth University Station MS A6700, 311 Biological Laboratories, University of Texas at Austin, Austin, Texas 78712, USA Mark A. Buchheim Department of Biological Science, University of Tulsa, Tulsa, Oklahoma 74104, USA Marvin W. Fawley School of Mathematical and Natural Sciences, University of Arkansas at Monticello, Monticello, Arkansas 71656, USA Department of Biological Sciences, North Dakota State University, Fargo, North Dakota 58105, USA Heather Spalding Botany Department, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA Curt M. Pueschel Department of Biological Sciences, State University of New York at Binghamton, Binghamton, New York 13901, USA Julie A. -
Green Algae and the Origins of Multicellularity in the Plant Kingdom
Downloaded from http://cshperspectives.cshlp.org/ on October 8, 2021 - Published by Cold Spring Harbor Laboratory Press Green Algae and the Origins of Multicellularity in the Plant Kingdom James G. Umen Donald Danforth Plant Science Center, St. Louis, Missouri 63132 Correspondence: [email protected] The green lineage of chlorophyte algae and streptophytes form a large and diverse clade with multiple independent transitions to produce multicellular and/or macroscopically complex organization. In this review, I focus on two of the best-studied multicellular groups of green algae: charophytes and volvocines. Charophyte algae are the closest relatives of land plants and encompass the transition from unicellularity to simple multicellularity. Many of the innovations present in land plants have their roots in the cell and developmental biology of charophyte algae. Volvocine algae evolved an independent route to multicellularity that is captured by a graded series of increasing cell-type specialization and developmental com- plexity. The study of volvocine algae has provided unprecedented insights into the innova- tions required to achieve multicellularity. he transition from unicellular to multicellu- and rotifers that are limited by prey size (Bell Tlar organization is considered one of the ma- 1985; Boraas et al. 1998). Reciprocally, increased jor innovations in eukaryotic evolution (Szath- size might also entail advantages in capturing ma´ry and Maynard-Smith 1995). Multicellular more or larger prey. organization can be advantageous for several There is some debate about how easy or reasons. Foremost among these is the potential difficult it has been for unicellular organisms for cell-type specialization that enables more to evolve multicellularity (Grosberg and Strath- efficient use of scarce resources and can open mann 2007). -
IUCN 00 Inner Page.Cdr
Biodiversity of Tanguar Haor: A Ramsar Site of Bangladesh Volume II: Flora Biodiversity of Tanguar Haor: A Ramsar Site of Bangladesh Volume II: Flora Research and Compilation Dr. Istiak Sobhan A. B. M. Sarowar Alam Mohammad Shahad Mahabub Chowdhury Technical Editor Dr. Sarder Nasir Uddin Md. Aminur Rahman Ishtiaq Uddin Ahmad The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, administration, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication are authors' personal views and do not necessarily reflect those of IUCN. Publication of this book is mandated and supported by Swiss Agency for Development and Cooperation (SDC) under the 'Community Based Sustainable Management of Tanguar Haor Project' of Ministry of Environment and Forest (MoEF) of Government of Bangladesh. Published by: IUCN (International Union for Conservation of Nature) Copyright: © 2012 IUCN, International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Sobhan, I., Alam, A. B. M. S. and Chowdhury, M. S. M. 2012. Biodiversity of Tanguar Haor: A Ramsar Site of Bangladesh, Volume II: Flora. IUCN Bangladesh Country Office, Dhaka, Bangladesh, Pp. xii+236. ISBN: 978-984-33-2973-8 Layout: Sheikh Asaduzzaman Cover Photo: Front Cover: Barringtonia acutangula, Nymphoides indicum, Clerodendrum viscosum, Rosa clinophylla,Back Cover: Millettia pinnata, Crataeva magna Cover Photo by: A. -
The Flagellar Photoresponse in Volvox Species (Volvocaceae, Chlorophyceae)1
J. Phycol. 47, ***–*** (2011Diana) Ó 2011Diana Phycological Society of America DOI: 10.1111/j.1529-8817.2011.00983.x NOTE THE FLAGELLAR PHOTORESPONSE IN VOLVOX SPECIES (VOLVOCACEAE, CHLOROPHYCEAE)1 Cristian A. Solari2 CONICET, Departamento de Biodiversidad y Biologı´a Experimental (FCEyN), Laboratorio de Biologı´a Comparada de Protistas, Universidad de Buenos Aires, Buenos Aires C1428EHA, Argentina Knut Drescher and Raymond E. Goldstein Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge CB3 0WA, UK Steering their swimming direction toward the light specialization, each of the Chlamydomonas-like somatic is crucial for the viability of Volvox colonies, the lar- cells is positioned at the surface of the extracellular ger members of the volvocine algae. While it is matrix, with its two flagella oriented outward, while known that this phototactic steering is achieved by a the germ cells grow inside the colony. Volvox species difference in behavior of the flagella on the illumi- with germ-soma separation have evolved several times nated and shaded sides, conflicting reports suggest independently from quite different colonial ancestors that this asymmetry arises either from a change in with no cellular differentiation (Coleman 1999, No- beating direction or a change in beating frequency. zaki et al. 1999, 2006, Nozaki 2003, Herron and Mi- Here, we report direct observations of the flagellar chod 2008). These species with different phyletic behavior of various Volvox species with different phy- origin have been classified within the volvocine algae letic origin in response to light intensity changes and into different sections ⁄ groups (Smith 1944, Nozaki thereby resolve this controversy: Volvox barberi W.