Flatworms and Ribbon Worms I
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Flatworms Phylum Platyhelminthes
Flatworms Phylum Platyhelminthes The flatworms include more than 13,000 species of free-living and parasitic species.There are 3 classes of flat- worms, the planarians, flukes and tapeworms. General Physical Traits (Anatomy): Flatworms are bilaterally symmetrical. This means that they can only be cut them length-wise to produce two mirror-image halves. They have a distinct right and left half. This is differ- ent from radially symmetrical animals, like the anemones, which can be cut anywhere top to bottom to get two similar halves. Flatworms have 3 tissue layers, compared to the 2 layers in sponges and cnidarians (jellyfishes, anemones and corals). They also have only one opening for food to enter and waste to leave, like the sponges and cnidarians. This is called a “sac” body plan. Planarian (class Tubellaria) Habitat: They live mostly in saltwater (marine) habitats, but are also found in freshwater. Habits: They are free-living flatworms (not parasites). Physical Traits (Anatomy): Planarians are small - less than a centimeter long. They have a head, brain and sense organs. This is called “cephalization.” The sense organs – called eyespots – look like eyes and are sensitive to light changes, but are not like human eyes. They are made up of simple nerve cells that respond to stimuli, like light. When many nerve cells are gathered in one place, they are called a “ganglion,” so the two eyespots are actually ganglia. They also have points on either side of the head that look a bit like ears, called “sensory lobes” or auricles. They do not hear, but can sense food. -
Platyhelminthes, Nemertea, and "Aschelminthes" - A
BIOLOGICAL SCIENCE FUNDAMENTALS AND SYSTEMATICS – Vol. III - Platyhelminthes, Nemertea, and "Aschelminthes" - A. Schmidt-Rhaesa PLATYHELMINTHES, NEMERTEA, AND “ASCHELMINTHES” A. Schmidt-Rhaesa University of Bielefeld, Germany Keywords: Platyhelminthes, Nemertea, Gnathifera, Gnathostomulida, Micrognathozoa, Rotifera, Acanthocephala, Cycliophora, Nemathelminthes, Gastrotricha, Nematoda, Nematomorpha, Priapulida, Kinorhyncha, Loricifera Contents 1. Introduction 2. General Morphology 3. Platyhelminthes, the Flatworms 4. Nemertea (Nemertini), the Ribbon Worms 5. “Aschelminthes” 5.1. Gnathifera 5.1.1. Gnathostomulida 5.1.2. Micrognathozoa (Limnognathia maerski) 5.1.3. Rotifera 5.1.4. Acanthocephala 5.1.5. Cycliophora (Symbion pandora) 5.2. Nemathelminthes 5.2.1. Gastrotricha 5.2.2. Nematoda, the Roundworms 5.2.3. Nematomorpha, the Horsehair Worms 5.2.4. Priapulida 5.2.5. Kinorhyncha 5.2.6. Loricifera Acknowledgements Glossary Bibliography Biographical Sketch Summary UNESCO – EOLSS This chapter provides information on several basal bilaterian groups: flatworms, nemerteans, Gnathifera,SAMPLE and Nemathelminthes. CHAPTERS These include species-rich taxa such as Nematoda and Platyhelminthes, and as taxa with few or even only one species, such as Micrognathozoa (Limnognathia maerski) and Cycliophora (Symbion pandora). All Acanthocephala and subgroups of Platyhelminthes and Nematoda, are parasites that often exhibit complex life cycles. Most of the taxa described are marine, but some have also invaded freshwater or the terrestrial environment. “Aschelminthes” are not a natural group, instead, two taxa have been recognized that were earlier summarized under this name. Gnathifera include taxa with a conspicuous jaw apparatus such as Gnathostomulida, Micrognathozoa, and Rotifera. Although they do not possess a jaw apparatus, Acanthocephala also belong to Gnathifera due to their epidermal structure. ©Encyclopedia of Life Support Systems (EOLSS) BIOLOGICAL SCIENCE FUNDAMENTALS AND SYSTEMATICS – Vol. -
I FLATWORM PREDATION on JUVENILE FRESHWATER
FLATWORM PREDATION ON JUVENILE FRESHWATER MUSSELS A Thesis Presented to the Graduate College of Southwest Missouri State University In Partial Fulfillment of the Requirements for the Master of Science Degree By Angela Marie Delp July 2002 i FLATWORM PREDATION OF JUVENILE FRESHWATER MUSSELS Biology Department Southwest Missouri State University, July 27, 2002 Master of Science in Biology Angela Marie Delp ABSTRACT Free-living flatworms (Phylum Platyhelminthes, Class Turbellaria) are important predators on small aquatic invertebrates. Macrostomum tuba, a predominantly benthic species, feeds on juvenile freshwater mussels in fish hatcheries and mussel culture facilities. Laboratory experiments were performed to assess the predation rate of M. tuba on newly transformed juveniles of plain pocketbook mussel, Lampsilis cardium. Predation rate at 20 oC in dishes without substrate was 0.26 mussels·worm-1·h-1. Predation rate increased to 0.43 mussels·worm-1·h-1 when a substrate, polyurethane foam, was present. Substrate may have altered behavior of the predator and brought the flatworms in contact with the mussels more often. An alternative prey, the cladoceran Ceriodaphnia reticulata, was eaten at a higher rate than mussels when only one prey type was present, but at a similar rate when both were present. Finally, the effect of flatworm size (0.7- 2.2 mm long) on predation rate on mussels (0.2 mm) was tested. Predation rate increased with predator size. The slope of this relationship decreased with increasing predator size. Predation rate was near zero in 0.7 mm worms. Juvenile mussels grow rapidly and can escape flatworm predation by exceeding the size of these tiny predators. -
Mapping and Distribution of Sabella Spallanzanii in Port Phillip Bay Final
Mapping and distribution of Sabellaspallanzanii in Port Phillip Bay Final Report to Fisheries Research and Development Corporation (FRDC Project 94/164) G..D. Parry, M.M. Lockett, D.P. Crookes, N. Coleman and M.A. Sinclair May 1996 Mapping and distribution of Sabellaspallanzanii in Port Phillip Bay Final Report to Fisheries Research and Development Corporation (FRDC Project 94/164) G.D. Parry1, M. Lockett1, D. P. Crookes1, N. Coleman1 and M. Sinclair2 May 1996 1Victorian Fisheries Research Institute Departmentof Conservation and Natural Resources PO Box 114, Queenscliff,Victoria 3225 2Departmentof Ecology and Evolutionary Biology Monash University Clayton Victoria 3068 Contents Page Technical and non-technical summary 2 Introduction 3 Background 3 Need 4 Objectives 4 Methods 5 Results 5 Benefits 5 Intellectual Property 6 Further Development 6 Staff 6 Final cost 7 Distribution 7 Acknow ledgments 8 References 8 Technical and Non-technical Summary • The sabellid polychaete Sabella spallanzanii, a native to the Mediterranean, established in Port Phillip Bay in the late 1980s. Initially it was found only in Corio Bay, but during the past fiveyears it has spread so that it now occurs throughout the western half of Port Phillip Bay. • Densities of Sabella in many parts of the bay remain low but densities are usually higher (up to 13/m2 ) in deeper water and they extend into shallower depths in calmer regions. • Sabella larvae probably require a 'hard' surface (shell fragment, rock, seaweed, mollusc or sea squirt) for initial attachment, but subsequently they may use their own tube as an anchor in soft sediment . • Changes to fish communities following the establishment of Sabella were analysed using multidimensional scaling and BACI (Before, After, Control, Impact) design analyses of variance. -
Phylum Chordata
Phylum Chordata 48,000 species very diverse phylum but still more unity in major characteristics than in most other phyla most advanced phylum of animal kingdom one to which we belong along with fish, amphibians reptiles, birds and other mammals some of the largest or most massive animals true coelom 4 major identifying characteristics: 1. Notochord flexible rodlike structure enclosed by a fibrous sheath extends the length of the body in larva and/or adult provides basic support and serves as main axis for muscle attachments to permit “fishlike” undulatory movements first part of skeleton to form in embryo in primitive chordates the notochord persists through life Animals: Chordates & Introduction to Vertebrates; Ziser Lecture Notes, 2006 1 in most chordates the notochord is replaced by a vertebral column of bone remnants of the notochord remain as “intervertebral discs” 2. Dorsal tubular nerve cord in most invert groups; nerve cord is ventral & paired in chordates the nerve cord is a single dorsal hollow nerve cord front end usually enlarged to form brain 3. Pharyngeal (gill) slits slit-like opening sleading from throat to outside first evolved as a filter feeding apparatus still used by some to filter water for food in others as gills in some groups they are only found in embryo and lost as adults 4. endostyle or thyroid gland specific kind of tissue found only in chordates was originally part of the feeding apparatus endostyle secretes mucus and traps food inside the pharyngeal cavity eg. lamprey larva in most chordates the same tissue has become an endocrine Animals: Chordates & Introduction to Vertebrates; Ziser Lecture Notes, 2006 2 gland in the neck region that helps control metabolism 5. -
Comparative Neuroanatomy of Mollusks and Nemerteans in the Context of Deep Metazoan Phylogeny
Comparative Neuroanatomy of Mollusks and Nemerteans in the Context of Deep Metazoan Phylogeny Von der Fakultät für Mathematik, Informatik und Naturwissenschaften der RWTH Aachen University zur Erlangung des akademischen Grades einer Doktorin der Naturwissenschaften genehmigte Dissertation vorgelegt von Diplom-Biologin Simone Faller aus Frankfurt am Main Berichter: Privatdozent Dr. Rudolf Loesel Universitätsprofessor Dr. Peter Bräunig Tag der mündlichen Prüfung: 09. März 2012 Diese Dissertation ist auf den Internetseiten der Hochschulbibliothek online verfügbar. Contents 1 General Introduction 1 Deep Metazoan Phylogeny 1 Neurophylogeny 2 Mollusca 5 Nemertea 6 Aim of the thesis 7 2 Neuroanatomy of Minor Mollusca 9 Introduction 9 Material and Methods 10 Results 12 Caudofoveata 12 Scutopus ventrolineatus 12 Falcidens crossotus 16 Solenogastres 16 Dorymenia sarsii 16 Polyplacophora 20 Lepidochitona cinerea 20 Acanthochitona crinita 20 Scaphopoda 22 Antalis entalis 22 Entalina quinquangularis 24 Discussion 25 Structure of the brain and nerve cords 25 Caudofoveata 25 Solenogastres 26 Polyplacophora 27 Scaphopoda 27 i CONTENTS Evolutionary considerations 28 Relationship among non-conchiferan molluscan taxa 28 Position of the Scaphopoda within Conchifera 29 Position of Mollusca within Protostomia 30 3 Neuroanatomy of Nemertea 33 Introduction 33 Material and Methods 34 Results 35 Brain 35 Cerebral organ 38 Nerve cords and peripheral nervous system 38 Discussion 38 Peripheral nervous system 40 Central nervous system 40 In search for the urbilaterian brain 42 4 General Discussion 45 Evolution of higher brain centers 46 Neuroanatomical glossary and data matrix – Essential steps toward a cladistic analysis of neuroanatomical data 49 5 Summary 53 6 Zusammenfassung 57 7 References 61 Danksagung 75 Lebenslauf 79 ii iii 1 General Introduction Deep Metazoan Phylogeny The concept of phylogeny follows directly from the theory of evolution as published by Charles Darwin in The origin of species (1859). -
A Phylum-Wide Survey Reveals Multiple Independent Gains of Head Regeneration Ability in Nemertea
bioRxiv preprint doi: https://doi.org/10.1101/439497; this version posted October 11, 2018. 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 4.0 International license. A phylum-wide survey reveals multiple independent gains of head regeneration ability in Nemertea Eduardo E. Zattara1,2,5, Fernando A. Fernández-Álvarez3, Terra C. Hiebert4, Alexandra E. Bely2 and Jon L. Norenburg1 1 Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington, DC, USA 2 Department of Biology, University of Maryland, College Park, MD, USA 3 Institut de Ciències del Mar, Consejo Superior de Investigaciones Científicas, Barcelona, Spain 4 Institute of Ecology and Evolution, University of Oregon, Eugene, OR, USA 5 INIBIOMA, Consejo Nacional de Investigaciones Científicas y Tecnológicas, Bariloche, RN, Argentina Corresponding author: E.E. Zattara, [email protected] Abstract Animals vary widely in their ability to regenerate, suggesting that regenerative abilities have a rich evolutionary history. However, our understanding of this history remains limited because regeneration ability has only been evaluated in a tiny fraction of species. Available comparative regeneration studies have identified losses of regenerative ability, yet clear documentation of gains is lacking. We surveyed regenerative ability in 34 species spanning the phylum Nemertea, assessing the ability to regenerate heads and tails either through our own experiments or from literature reports. Our sampling included representatives of the 10 most diverse families and all three orders comprising this phylum. -
Xenacoelomorpha's Significance for Understanding Bilaterian Evolution
Available online at www.sciencedirect.com ScienceDirect Xenacoelomorpha’s significance for understanding bilaterian evolution Andreas Hejnol and Kevin Pang The Xenacoelomorpha, with its phylogenetic position as sister biology models are the fruitfly Drosophila melanogaster and group of the Nephrozoa (Protostomia + Deuterostomia), plays the nematode Caenorhabditis elegans, in which basic prin- a key-role in understanding the evolution of bilaterian cell types ciples of developmental processes have been studied in and organ systems. Current studies of the morphological and great detail. It might be because the field of evolutionary developmental diversity of this group allow us to trace the developmental biology — EvoDevo — has its origin in evolution of different organ systems within the group and to developmental biology and not evolutionary biology that reconstruct characters of the most recent common ancestor of species under investigation are often called ‘model spe- Xenacoelomorpha. The disparity of the clade shows that there cies’. Criteria for selected representative species are cannot be a single xenacoelomorph ‘model’ species and primarily the ease of access to collected material and strategic sampling is essential for understanding the evolution their ability to be cultivated in the lab [1]. In some cases, of major traits. With this strategy, fundamental insights into the a supposedly larger number of ancestral characters or a evolution of molecular mechanisms and their role in shaping dominant role in ecosystems have played an additional animal organ systems can be expected in the near future. role in selecting model species. These arguments were Address used to attract sufficient funding for genome sequencing Sars International Centre for Marine Molecular Biology, University of and developmental studies that are cost-intensive inves- Bergen, Thormøhlensgate 55, 5008 Bergen, Norway tigations. -
The Effect of Caffeine and Ethanol on Flatworm Regeneration
East Tennessee State University Digital Commons @ East Tennessee State University Electronic Theses and Dissertations Student Works 8-2007 The ffecE t of Caffeine nda Ethanol on Flatworm Regeneration. Erica Leighanne Collins East Tennessee State University Follow this and additional works at: https://dc.etsu.edu/etd Part of the Chemical and Pharmacologic Phenomena Commons Recommended Citation Collins, Erica Leighanne, "The Effect of Caffeine nda Ethanol on Flatworm Regeneration." (2007). Electronic Theses and Dissertations. Paper 2028. https://dc.etsu.edu/etd/2028 This Thesis - Open Access is brought to you for free and open access by the Student Works at Digital Commons @ East Tennessee State University. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Digital Commons @ East Tennessee State University. For more information, please contact [email protected]. The Effect of Caffeine and Ethanol on Flatworm Regeneration ____________________ A thesis presented to the faculty of the Department of Biological Sciences East Tennessee State University In partial fulfillment of the requirements for the degree Master of Science in Biology ____________________ by Erica Leighanne Collins August 2007 ____________________ Dr. J. Leonard Robertson, Chair Dr. Thomas F. Laughlin Dr. Kevin Breuel Keywords: Regeneration, Planarian, Dugesia tigrina, Flatworms, Caffeine, Ethanol ABSTRACT The Effect of Caffeine and Ethanol on Flatworm Regeneration by Erica Leighanne Collins Flatworms, or planarian, have a high potential for regeneration and have been used as a model to investigate regeneration and stem cell biology for over a century. Chemicals, temperature, and seasonal factors can influence planarian regeneration. Caffeine and ethanol are two widely used drugs and their effect on flatworm regeneration was evaluated in this experiment. -
Animal Phylum Poster Porifera
Phylum PORIFERA CNIDARIA PLATYHELMINTHES ANNELIDA MOLLUSCA ECHINODERMATA ARTHROPODA CHORDATA Hexactinellida -- glass (siliceous) Anthozoa -- corals and sea Turbellaria -- free-living or symbiotic Polychaetes -- segmented Gastopods -- snails and slugs Asteroidea -- starfish Trilobitomorpha -- tribolites (extinct) Urochordata -- tunicates Groups sponges anemones flatworms (Dugusia) bristleworms Bivalves -- clams, scallops, mussels Echinoidea -- sea urchins, sand Chelicerata Cephalochordata -- lancelets (organisms studied in detail in Demospongia -- spongin or Hydrazoa -- hydras, some corals Trematoda -- flukes (parasitic) Oligochaetes -- earthworms (Lumbricus) Cephalopods -- squid, octopus, dollars Arachnida -- spiders, scorpions Mixini -- hagfish siliceous sponges Xiphosura -- horseshoe crabs Bio1AL are underlined) Cubozoa -- box jellyfish, sea wasps Cestoda -- tapeworms (parasitic) Hirudinea -- leeches nautilus Holothuroidea -- sea cucumbers Petromyzontida -- lamprey Mandibulata Calcarea -- calcareous sponges Scyphozoa -- jellyfish, sea nettles Monogenea -- parasitic flatworms Polyplacophora -- chitons Ophiuroidea -- brittle stars Chondrichtyes -- sharks, skates Crustacea -- crustaceans (shrimp, crayfish Scleropongiae -- coralline or Crinoidea -- sea lily, feather stars Actinipterygia -- ray-finned fish tropical reef sponges Hexapoda -- insects (cockroach, fruit fly) Sarcopterygia -- lobed-finned fish Myriapoda Amphibia (frog, newt) Chilopoda -- centipedes Diplopoda -- millipedes Reptilia (snake, turtle) Aves (chicken, hummingbird) Mammalia -
Echinoderms for Dummies Colwyn Sleep Echinoderm Classification and Examples
ECHINODERMS FOR DUMMIES COLWYN SLEEP ECHINODERM CLASSIFICATION AND EXAMPLES What exactly is an Echinoderm? Echinoderms (or “Echinodermata”) are a group of animals which exist only in a marine (ocean) environment. Their name comes from the Greek word for "spiny skin". They inhabit a diverse range of marine habitats and are found on the sea floor from the intertidal zone to great ocean depths. In the following slides we will explore echinoderms and look into their body systems and structures more closely. A FEW EXAMPLES OF ECHINODERMS Sea star Kingdom: Animalia Phylum: Echinodermata Class: Asteroidea Feather Star Kingdom: Animalia Phylum: Echinodermata Subphylum: Crinozoa Class: Crinoidea Probably one of the best known echinoderms This lesser-known star, the feather star gains is the easily recognized sea star. The its name from its featherlike arms, which it echinoderm phylum contains many more uses to swim through the water. Like all species, in fact there are around 7000 known echinoderms, they are “Deuterostomes.” echinoderms. Later, we will investigate the This means that during their embryonic sea star and it’s classification as an development the first embryonic opening echinoderm in greater detail. becomes the anus and the second becomes the mouth. Because of this, biologists believe that echinoderms are more evolutionarily advanced than some of the other animals. A FEW MORE… Sea cucumber Kingdom: Animalia Phylum: Echinodermata Class: Holothuroidea Sea Urchin Kingdom: Animalia Phylum: Echinodermata Class: Echinoidea Related to Jabba the Hutt in appearance Like other echinoderms, the sea urchin has only, the sea cucumber is actually another radial symmetry. Its pointed spines offer example of an echinoderm. -
King George Whiting (Sillaginodes Punctatus)
Parasites of King George whiting (Sillaginodes punctatus) Name: Echinocephalus sp. (larval stage), a nematode Microhabitat: Lives in the intestinal tract Appearance: Rows of spines around the head and a single hook on the tail Pathology: Unknown Curiosity: As Echinocephalus species mature they grow more rows of spines Name: Cardicola sp., digenean flukes commonly called ‘blood fluke’ Microhabitat: Lives in the circulatory system Appearance: Adult worms are ~2mm long Pathology: Unknown Curiosity: This is the first record of these worms from King George whiting and only 2 adults have been found in over 1000 specimens examined Name: A juvenile isopod from the family Gnathiidae Microhabitat: Attaches to the gills of hosts while feeding Appearance: Small, transparent body that becomes red when feeding on blood Pathology: Unknown Curiosity: Only the larval and juvenile stages are parasitic Name: Anaclavella sillaginoides, a parasitic copepod, or ‘sea-louse’ Microhabitat: Attach to the gill arch Appearance: Small, white, circular-shaped body with long trunk-like attachment; females have a pair of egg strings Pathology: Unknown Name: A juvenile acanthocephalan from the family Polymorphidae, commonly called spiny headed worms Microhabitat: Lives in the intestinal track Appearance: Small, neck and head covered in a number of spines (can be retracted inside the body) Pathology: Unknown Curiosity: The shape of the head (proboscis) and the number of spines does not change during development Name: Polylabris sillaginae, flatworm parasites commonly called ‘gill fluke’ Microhabitat: Lives on the gills and feed on blood Appearance: Small, brown coloured worm that has two rows of microscopic clamps Pathology: Unknown. Gill flukes have been associated with anaemia in other fish hosts Further contact: A research initiative supported by: Conditions of use: ----------------------------------------------------- ----------------------------------------------------- ----------------------------------------------------- Emma L.