Student Worksheet Achoo! Pollen Does More Than Make Us Sneeze
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"Lophophorates" Brachiopoda Echinodermata Asterozoa
Deuterostomes Bryozoa Phoronida "lophophorates" Brachiopoda Echinodermata Asterozoa Stelleroidea Asteroidea Ophiuroidea Echinozoa Holothuroidea Echinoidea Crinozoa Crinoidea Chaetognatha (arrow worms) Hemichordata (acorn worms) Chordata Urochordata (sea squirt) Cephalochordata (amphioxoius) Vertebrata PHYLUM CHAETOGNATHA (70 spp) Arrow worms Fossils from the Cambrium Carnivorous - link between small phytoplankton and larger zooplankton (1-15 cm long) Pharyngeal gill pores No notochord Peculiar origin for mesoderm (not strictly enterocoelous) Uncertain relationship with echinoderms PHYLUM HEMICHORDATA (120 spp) Acorn worms Pharyngeal gill pores No notochord (Stomochord cartilaginous and once thought homologous w/notochord) Tornaria larvae very similar to asteroidea Bipinnaria larvae CLASS ENTEROPNEUSTA (acorn worms) Marine, bottom dwellers CLASS PTEROBRANCHIA Colonial, sessile, filter feeding, tube dwellers Small (1-2 mm), "U" shaped gut, no gill slits PHYLUM CHORDATA Body segmented Axial notochord Dorsal hollow nerve chord Paired gill slits Post anal tail SUBPHYLUM UROCHORDATA Marine, sessile Body covered in a cellulose tunic ("Tunicates") Filter feeder (» 200 L/day) - perforated pharnx adapted for filtering & repiration Pharyngeal basket contractable - squirts water when exposed at low tide Hermaphrodites Tadpole larvae w/chordate characteristics (neoteny) CLASS ASCIDIACEA (sea squirt/tunicate - sessile) No excretory system Open circulatory system (can reverse blood flow) Endostyle - (homologous to thyroid of vertebrates) ciliated groove -
Number of Living Species in Australia and the World
Numbers of Living Species in Australia and the World 2nd edition Arthur D. Chapman Australian Biodiversity Information Services australia’s nature Toowoomba, Australia there is more still to be discovered… Report for the Australian Biological Resources Study Canberra, Australia September 2009 CONTENTS Foreword 1 Insecta (insects) 23 Plants 43 Viruses 59 Arachnida Magnoliophyta (flowering plants) 43 Protoctista (mainly Introduction 2 (spiders, scorpions, etc) 26 Gymnosperms (Coniferophyta, Protozoa—others included Executive Summary 6 Pycnogonida (sea spiders) 28 Cycadophyta, Gnetophyta under fungi, algae, Myriapoda and Ginkgophyta) 45 Chromista, etc) 60 Detailed discussion by Group 12 (millipedes, centipedes) 29 Ferns and Allies 46 Chordates 13 Acknowledgements 63 Crustacea (crabs, lobsters, etc) 31 Bryophyta Mammalia (mammals) 13 Onychophora (velvet worms) 32 (mosses, liverworts, hornworts) 47 References 66 Aves (birds) 14 Hexapoda (proturans, springtails) 33 Plant Algae (including green Reptilia (reptiles) 15 Mollusca (molluscs, shellfish) 34 algae, red algae, glaucophytes) 49 Amphibia (frogs, etc) 16 Annelida (segmented worms) 35 Fungi 51 Pisces (fishes including Nematoda Fungi (excluding taxa Chondrichthyes and (nematodes, roundworms) 36 treated under Chromista Osteichthyes) 17 and Protoctista) 51 Acanthocephala Agnatha (hagfish, (thorny-headed worms) 37 Lichen-forming fungi 53 lampreys, slime eels) 18 Platyhelminthes (flat worms) 38 Others 54 Cephalochordata (lancelets) 19 Cnidaria (jellyfish, Prokaryota (Bacteria Tunicata or Urochordata sea anenomes, corals) 39 [Monera] of previous report) 54 (sea squirts, doliolids, salps) 20 Porifera (sponges) 40 Cyanophyta (Cyanobacteria) 55 Invertebrates 21 Other Invertebrates 41 Chromista (including some Hemichordata (hemichordates) 21 species previously included Echinodermata (starfish, under either algae or fungi) 56 sea cucumbers, etc) 22 FOREWORD In Australia and around the world, biodiversity is under huge Harnessing core science and knowledge bases, like and growing pressure. -
The Plankton Lifeform Extraction Tool: a Digital Tool to Increase The
Discussions https://doi.org/10.5194/essd-2021-171 Earth System Preprint. Discussion started: 21 July 2021 Science c Author(s) 2021. CC BY 4.0 License. Open Access Open Data The Plankton Lifeform Extraction Tool: A digital tool to increase the discoverability and usability of plankton time-series data Clare Ostle1*, Kevin Paxman1, Carolyn A. Graves2, Mathew Arnold1, Felipe Artigas3, Angus Atkinson4, Anaïs Aubert5, Malcolm Baptie6, Beth Bear7, Jacob Bedford8, Michael Best9, Eileen 5 Bresnan10, Rachel Brittain1, Derek Broughton1, Alexandre Budria5,11, Kathryn Cook12, Michelle Devlin7, George Graham1, Nick Halliday1, Pierre Hélaouët1, Marie Johansen13, David G. Johns1, Dan Lear1, Margarita Machairopoulou10, April McKinney14, Adam Mellor14, Alex Milligan7, Sophie Pitois7, Isabelle Rombouts5, Cordula Scherer15, Paul Tett16, Claire Widdicombe4, and Abigail McQuatters-Gollop8 1 10 The Marine Biological Association (MBA), The Laboratory, Citadel Hill, Plymouth, PL1 2PB, UK. 2 Centre for Environment Fisheries and Aquacu∑lture Science (Cefas), Weymouth, UK. 3 Université du Littoral Côte d’Opale, Université de Lille, CNRS UMR 8187 LOG, Laboratoire d’Océanologie et de Géosciences, Wimereux, France. 4 Plymouth Marine Laboratory, Prospect Place, Plymouth, PL1 3DH, UK. 5 15 Muséum National d’Histoire Naturelle (MNHN), CRESCO, 38 UMS Patrinat, Dinard, France. 6 Scottish Environment Protection Agency, Angus Smith Building, Maxim 6, Parklands Avenue, Eurocentral, Holytown, North Lanarkshire ML1 4WQ, UK. 7 Centre for Environment Fisheries and Aquaculture Science (Cefas), Lowestoft, UK. 8 Marine Conservation Research Group, University of Plymouth, Drake Circus, Plymouth, PL4 8AA, UK. 9 20 The Environment Agency, Kingfisher House, Goldhay Way, Peterborough, PE4 6HL, UK. 10 Marine Scotland Science, Marine Laboratory, 375 Victoria Road, Aberdeen, AB11 9DB, UK. -
Check List of Plankton of the Northern Red Sea
Pakistan Journal of Marine Sciences, Vol. 9(1& 2), 61-78,2000. CHECK LIST OF PLANKTON OF THE NORTHERN RED SEA Zeinab M. El-Sherif and Sawsan M. Aboul Ezz National Institute of Oceanography and Fisheries, Kayet Bay, Alexandria, Egypt. ABSTRACT: Qualitative estimation of phytoplankton and zooplankton of the northern Red Sea and Gulf of Aqaba were carried out from four sites: Sharm El-Sheikh, Taba, Hurghada and Safaga. A total of 106 species and varieties of phytoplankton were identified including 41 diatoms, 53 dinoflagellates, 10 cyanophytes and 2 chlorophytes. The highest number of species was recorded at Sharm El-Sheikh (46 spp), followed by Safaga (40 spp), Taba (30 spp), and Hurghada (23 spp). About 95 of the recorded species were previously mentioned by different authors in the Red Sea and Gulf of Suez. Eleven species are considered new to the Red Sea. About 115 species of zooplankton were recorded from the different sites. They were dominated by four main phyla namely: Arthropoda, Protozoa, Mollusca, and Urochordata. Sharm El-Sheikh contributed the highest number of species (91) followed by Safaga (47) and Taba (34). Hurghada contributed the least (26). Copepoda dominated the other groups at the four sites. The appearances of Spirulina platensis, Pediastrum simplex, and Oscillatoria spp. of phyto plankton in addition to the rotifer species and the protozoan Difflugia oblongata of zooplankton impart a characteristic feature of inland freshwater discharge due to wastewater dumping at sea in these regions resulting from the expansion of cities and hotels along the coast. KEY WORDS: Plankton, Northern Red Sea, Check list. -
Chaetognatha: a Phylum of Uncertain Affinity Allison Katter, Elizabeth Moshier, Leslie Schwartz
Chaetognatha: A Phylum of Uncertain Affinity Allison Katter, Elizabeth Moshier, Leslie Schwartz What are Chaetognaths? Chaetognaths are in a separate Phylum by themselves (~100 species). They are carnivorous marine invertebrates ranging in size from 2-120 mm. There are also known as “Arrow worms,” “Glass worms,” and “Tigers of the zooplankton.” Characterized by a slender transparent body, relatively large caudal fins, and anterior spines on either side of the mouth, these voracious meat-eaters catch large numbers of copepods, swallowing them whole. Their torpedo-like body shape allows them to move quickly through the water, and the large spines around their mouth helps them grab and restrain their prey. Chaetognaths alternate between swimming and floating. The fins along their body are not used to swim, but rather to help them float. A Phylogenetic mystery: The affinities of the chaetognaths have long been debated, and present day workers are far from reaching any consensus of opinion. Problems arise because of the lack of morphological and physiological diversity within the group. In addition, no unambiguous chaetognaths are preserved as fossils, so nothing about this groups evolutionary origins can be learned from the fossil record. During the past 100 years, many attempts have been made to ally the arrow worms to a bewildering variety of taxa. Proposed relatives have included nematodes, mollusks, various arthropods, rotifers, and chordates. Our objective is to analyze the current views regarding “arrow worm” phylogeny and best place them in the invertebrate cladogram of life. Phylogeny Based on Embryology and Ultrastructure Casanova (1987) discusses the possibility that the Hyman, Ducret, and Ghirardelli have concluded chaetognaths are derived from within the mollusks. -
The Relation Between the Distribution of Zooplankton Predators and Anchovy Larvae
ALVARINO: DISTRIBUTION OF ZOOPLANKTON PREDATORS AND ANCHOVY LARVAE CalCOFI Rep., Vol. XXI, 1980 THE RELATION BETWEEN THE DISTRIBUTION OF ZOOPLANKTON PREDATORS AND ANCHOVY LARVAE ANGELES ALVARINO National Oceanic and Atmospheric Administration National Marine Fisheries Sewice Southwest Fisheries Center La Jolla. CA 92038 ABSTRACT dores y las correspondientes muestras de plancton han Monthly CalCOFI cruises of 1954, 1956, and 1958 demostrado que cuando abundaban en el plancton cope- were analyzed for abundance of populations of species of podos y eufausidos, 10s depredadores ingerian menos Chaetognatha, Siphonophorae, Chondrophorae, Medusae, larvas de peces. and Ctenophora. Data were also noted on other abun- dant zooplankters in the samples (copepods, euphausiids, INTRODUCTION decapod larvae, pteropods, heteropods, polychaetes, salps, Mortality of pelagic marine fish larvae can result from doliolids, and pyrosomes). Information was grouped into a variety of causes, both biotic and abiotic. Among the three categories of abundance of anchovy larvae per stan- more important biotic causes are starvation, predation, dard haul (more than 241 anchovy larvae, from 1 to 240, parasites, and disease; among the abiotic causes are and absence of larvae). In general, concentration of pre- storms, currents, ultraviolet radiation, temperature, sa- dators was inversely related to aggregations of anchovy linity, oxygen, and pollution. It was the consensus of larvae. Absence of anchovy larvae coincided with pro- participants in a Colloquium on Larval Fish Mortality chordates, decapod larvae, pteropods, heteropods, and Studies, held in La Jolla during January of 1975, “that polychaetes, and abundance of anchovy larvae concurred the major causes of larval mortality are starvation and with abundance of copepods and/or euphausiids. -
1409 Lab Manual
The Diversityof Life Lab Manual Stephen W. Ziser Department of Biology Pinnacle Campus for BIOL 1409 General Biology: The Diversity of Life Lab Activities, Homework & Lab Assignments 2017.6 Biol 1409: Diversity of Life – Lab Manual, Ziser, 2017.6 1 Biol 1409: Diversity of Life Ziser - Lab Manual Table of Contents 1. Overview of Semester Lab Activities Laboratory Activities . 3 2. Introduction to the Lab & Safety Information . 5 3. Laboratory Exercises Microscopy . 13 Taxonomy and Classification . 14 Cells – The Basic Units of Life . 18 Asexual & Sexual Reproduction . 23 Development & Life Cycles . 27 Ecosystems of Texas . 30 The Bacterial Kingdoms . 33 The Protists . 43 The Fungi . 51 The Plant Kingdom . 60 The Animal Kingdom . 90 4. Lab Reports (to be turned in - deadline dates as announced) Taxonomy & Classification . 16 Ecosystems of Texas. 31 The Bacterial Kingdoms . 40 The Protists . 47 The Fungi . 55 Leaf Identification Exercise . 69 The Plant Kingdom . 82 Identifying Common Freshwater Invertebrates . 105 The Animal Kingdom . 148 Biol 1409: Diversity of Life – Lab Manual, Ziser, 2017.6 2 Biol 1409: Diversity of Life Semester Activities Lab Exercises The schedule for the lab activities is posted in the Course Syllabus and on the instructor’s website. Changes will be announced ahead of time. The Photo Atlas is used as a visual guide to the activities described in this lab manual Introduction & Use of Compound Microscope & Dissecting Scope be able to identify and use the various parts of a compound microscope be able to use a magnifying -
Systema Naturae. the Classification of Living Organisms
Systema Naturae. The classification of living organisms. c Alexey B. Shipunov v. 5.601 (June 26, 2007) Preface Most of researches agree that kingdom-level classification of living things needs the special rules and principles. Two approaches are possible: (a) tree- based, Hennigian approach will look for main dichotomies inside so-called “Tree of Life”; and (b) space-based, Linnaean approach will look for the key differences inside “Natural System” multidimensional “cloud”. Despite of clear advantages of tree-like approach (easy to develop rules and algorithms; trees are self-explaining), in many cases the space-based approach is still prefer- able, because it let us to summarize any kinds of taxonomically related da- ta and to compare different classifications quite easily. This approach also lead us to four-kingdom classification, but with different groups: Monera, Protista, Vegetabilia and Animalia, which represent different steps of in- creased complexity of living things, from simple prokaryotic cell to compound Nature Precedings : doi:10.1038/npre.2007.241.2 Posted 16 Aug 2007 eukaryotic cell and further to tissue/organ cell systems. The classification Only recent taxa. Viruses are not included. Abbreviations: incertae sedis (i.s.); pro parte (p.p.); sensu lato (s.l.); sedis mutabilis (sed.m.); sedis possi- bilis (sed.poss.); sensu stricto (s.str.); status mutabilis (stat.m.); quotes for “environmental” groups; asterisk for paraphyletic* taxa. 1 Regnum Monera Superphylum Archebacteria Phylum 1. Archebacteria Classis 1(1). Euryarcheota 1 2(2). Nanoarchaeota 3(3). Crenarchaeota 2 Superphylum Bacteria 3 Phylum 2. Firmicutes 4 Classis 1(4). Thermotogae sed.m. 2(5). -
Introduction to the Bilateria and the Phylum Xenacoelomorpha Triploblasty and Bilateral Symmetry Provide New Avenues for Animal Radiation
CHAPTER 9 Introduction to the Bilateria and the Phylum Xenacoelomorpha Triploblasty and Bilateral Symmetry Provide New Avenues for Animal Radiation long the evolutionary path from prokaryotes to modern animals, three key innovations led to greatly expanded biological diversification: (1) the evolution of the eukaryote condition, (2) the emergence of the A Metazoa, and (3) the evolution of a third germ layer (triploblasty) and, perhaps simultaneously, bilateral symmetry. We have already discussed the origins of the Eukaryota and the Metazoa, in Chapters 1 and 6, and elsewhere. The invention of a third (middle) germ layer, the true mesoderm, and evolution of a bilateral body plan, opened up vast new avenues for evolutionary expan- sion among animals. We discussed the embryological nature of true mesoderm in Chapter 5, where we learned that the evolution of this inner body layer fa- cilitated greater specialization in tissue formation, including highly specialized organ systems and condensed nervous systems (e.g., central nervous systems). In addition to derivatives of ectoderm (skin and nervous system) and endoderm (gut and its de- Classification of The Animal rivatives), triploblastic animals have mesoder- Kingdom (Metazoa) mal derivatives—which include musculature, the circulatory system, the excretory system, Non-Bilateria* Lophophorata and the somatic portions of the gonads. Bilater- (a.k.a. the diploblasts) PHYLUM PHORONIDA al symmetry gives these animals two axes of po- PHYLUM PORIFERA PHYLUM BRYOZOA larity (anteroposterior and dorsoventral) along PHYLUM PLACOZOA PHYLUM BRACHIOPODA a single body plane that divides the body into PHYLUM CNIDARIA ECDYSOZOA two symmetrically opposed parts—the left and PHYLUM CTENOPHORA Nematoida PHYLUM NEMATODA right sides. -
Redalyc.Functional Response of Sagitta Setosa (Chaetognatha) And
Revista de Biología Marina y Oceanografía ISSN: 0717-3326 [email protected] Universidad de Valparaíso Chile Vergara-Soto, Odette; Calliari, Danilo; Tiselius, Peter; Escribano, Rubén; González, M. Lorena; Soto- Mendoza, Samuel Functional response of Sagitta setosa (Chaetognatha) and Mnemiopsis leidyi (Ctenophora) under variable food concentration in the Gullmar fjord, Sweden Revista de Biología Marina y Oceanografía, vol. 45, núm. 1, abril, 2010, pp. 35-42 Universidad de Valparaíso Viña del Mar, Chile Available in: http://www.redalyc.org/articulo.oa?id=47915589003 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Revista de Biología Marina y Oceanografía 45(1): 35-42, abril de 2010 Functional response of Sagitta setosa (Chaetognatha) and Mnemiopsis leidyi (Ctenophora) under variable food concentration in the Gullmar fjord, Sweden Respuesta funcional de Sagitta setosa (Chaetognatha) y Mnemiopsis leidyi (Ctenophora) bajo una concentración de alimento variable en el fiordo Gullmar, Suecia Odette Vergara-Soto1, Danilo Calliari2,3, Peter Tiselius3, Rubén Escribano1, 5, M. Lorena González4 and Samuel Soto-Mendoza6 1Pelagic Laboratory and Mesozooplankton (PLAMZ) of COPAS Center, Marine Biology Station,Universidad de Concepción, P.O. Box 42, Dichato, Concepción, Chile 2Sección Oceanología, Facultad de Ciencias, Universidad de la República, Iguá 4225, CP 11400 Montevideo, Uruguay 3Sven-Loven Centre for Marine Research-Kristineberg, Marine Ecology Dept., Göteborg University, S-450 34 Fiskebäckskil, Göteborg, Sweden 4Program for Regional Studies in Physical Oceanography and Climate (PROFC), Universidad de Concepción, Box 160-C. -
Harmful Algae News
1 The Intergovernmental Oceanographic Commission of UNESCO May 2008 HARMFUL ALGAE NEWS An IOC Newsletter on toxic algae and algal blooms http://ioc.unesco.org/hab/news.htm No. 36 • Turkey Mucilage event associated with diatoms and dinoflagellates in Sea of Marmara, Turkey The massive presence of consisting of white gelatinous material mid-autumn 2007 along the north- mucilaginous organic matter, resulting initially suspended at the surface and in eastern part of Marmara Sea with from planktonic and benthic algal the water column was noticed along the temperatures 18.4±1.0oC. It extended blooms, has become more frequent in Turkish coast of the Marmara Sea from Izmit Bay to the Dardanelles during many coastal waters around Europe, (especially Izmit Bay). Marmara Sea the calm weather period; it was denser especially in the Adriatic. The has a rather complex hydrological and of longer duration in Izmit Bay, appearance of mucilage in the Adriatic system, in a zone of transition between which is affected by intense industrial Sea has been reported periodically since dense (salinity 37- 38.5 ‰) and warmer activity, and which has a weaker 1800, with major mucus blooms during waters originating in the Mediterranean circulation compared to Marmara Sea. the 1990s [1]. The mucilage Sea, and cold, lower-salinity water (20- To identify phytoplankton species phenomenon of the Adriatic Sea had 22 ‰) coming from the Black Sea. The responsible for the mucilage, water usually been related to extracellular pycnocline lies at 10 to 30 m depth and samples were collected from surface organic matter of phytoplanktonic origin. varies seasonally [2]. -
An Illustrated Key to the Chaetognatha of the Northern Gulf of Mexico with Notes on Their Distribution
Gulf and Caribbean Research Volume 8 Issue 2 January 1989 An Illustrated Key to the Chaetognatha of the Northern Gulf of Mexico with Notes on their Distribution Jerry A. McLelland Gulf Coast Research Laboratory Follow this and additional works at: https://aquila.usm.edu/gcr Part of the Marine Biology Commons Recommended Citation McLelland, J. A. 1989. An Illustrated Key to the Chaetognatha of the Northern Gulf of Mexico with Notes on their Distribution. Gulf Research Reports 8 (2): 145-172. Retrieved from https://aquila.usm.edu/gcr/vol8/iss2/7 DOI: https://doi.org/10.18785/grr.0802.07 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Gulf and Caribbean Research by an authorized editor of The Aquila Digital Community. For more information, please contact [email protected]. Guy Research Reports, Vol. 8, No. 2, 145-172, 1989 Manuscript received August 5, 1988: accepted September 28, 1988 AN ILLUSTRATED KEY TO THE CHAETOGNATHA OF THE NORTHERN GULF OF MEXICO WITH NOTES ON THEIR DISTRIBUTION A. McLELLAND InvertebrateJERRY Zoology Section, Gulf Coast Research Laboratory, P.O. Box 7000, Ocean Springs, Mississippi 39564-7000 ABSTRACT A key is provided to facilitate the identification of 24 species in nine genera of Chaetognatha occurring in the northem Gulf of Mexico. Included are the deep-water species, Eukrohnia proboscidea, E. calliops, Mesosagitta sibogae, and Sagitta megalophthalma, all recent additions to the known fauna of the region. Meristic data, brief descriptions, ecological notes, Gulf of Mexico records, and illustrations are also presented.