Marine Invertebrate Species Sponges
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Buzzle – Zoology Terms – Glossary of Biology Terms and Definitions Http
Buzzle – Zoology Terms – Glossary of Biology Terms and Definitions http://www.buzzle.com/articles/biology-terms-glossary-of-biology-terms-and- definitions.html#ZoologyGlossary Biology is the branch of science concerned with the study of life: structure, growth, functioning and evolution of living things. This discipline of science comprises three sub-disciplines that are botany (study of plants), Zoology (study of animals) and Microbiology (study of microorganisms). This vast subject of science involves the usage of myriads of biology terms, which are essential to be comprehended correctly. People involved in the science field encounter innumerable jargons during their study, research or work. Moreover, since science is a part of everybody's life, it is something that is important to all individuals. A Abdomen: Abdomen in mammals is the portion of the body which is located below the rib cage, and in arthropods below the thorax. It is the cavity that contains stomach, intestines, etc. Abscission: Abscission is a process of shedding or separating part of an organism from the rest of it. Common examples are that of, plant parts like leaves, fruits, flowers and bark being separated from the plant. Accidental: Accidental refers to the occurrences or existence of all those species that would not be found in a particular region under normal circumstances. Acclimation: Acclimation refers to the morphological and/or physiological changes experienced by various organisms to adapt or accustom themselves to a new climate or environment. Active Transport: The movement of cellular substances like ions or molecules by traveling across the membrane, towards a higher level of concentration while consuming energy. -
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. -
Invertebrate Biology Wileyonlinelibrary.Com/Journal/Ivb VOLUME 134 | NUMBER 3 | 2015
ivb_134_3_oc_OC.qxd 8/18/2015 10:23 AM Page 1 Invertebrate Invertebrate Biology wileyonlinelibrary.com/journal/ivb VOLUME 134 | NUMBER 3 | 2015 VOLUME 134 NUMBER 3 2015 | | Biology CONTENTS 181–188 Ultrastructure of the rotifer integument: peculiarities of Sinantherina socialis (Monogononta: Invertebrate Biology Gnesiotrocha) Rick Hochberg, Adele Hochberg, and Courtney Chan 189–202 Linking zebra mussel growth and survival with two cellular stress indicators during chronic VOLUME temperature stress Jennifer A. Jost, Emily N. Soltis, Marshall R. Moyer, and Sarah S. Keshwani 134 203–213 Sex‐specific reproductive investment of summer spawners of Illex argentinus in the southwest | NUMBER Atlantic Dongming Lin, Xinjun Chen, Yong Chen, and Zhou Fang 3 – | 214 230 Immunohistochemical investigations of the development of Scoloplos armiger (“intertidalis clade”) 2015 indicate a paedomorphic origin of Proscoloplos cygnochaetus (Annelida, Orbiniidae) Conrad Helm, Anne Krause, and Christoph Bleidorn 231–241 Effects of tidal height and wave exposure on cirrus and penis morphology of the acorn barnacle Tetraclita stalactifera J. Matthew Hoch and Kevin V. Reyes 242–251 The distribution of cave twilight‐zone spiders depends on microclimatic features and trophic supply Raoul Manenti, Enrico Lunghi, and Gentile Francesco Ficetola 252–259 A non‐destructive tissue sampling technique for holothurians to facilitate extraction of DNA for genetic analysis Samantha J. Nowland, Dean R. Jerry, and Paul C. Southgate 260 Erratum COVER ILLUSTRATION Cave habitats are unusual among terrestrial habitats because most of their trophic resources are ultimately derived by transport from surface communities. The amount and distribution of these resources in caves may have strong effects on the biology of cave-dwelling species. -
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. -
Glossary - Zoology - Intro
1 Glossary - Zoology - Intro Abdomen: Posterior part of an arthropoda’ body; in vertebrates: abdomen between thorax and pelvic girdle. Acoelous: See coelom. Amixia: A restriction that prevents general intercrossing in a species leading to inbreeding. Anabiosis: Resuscitation after apparent death. Archenteron: See coelom. Aulotomy: Capacity of separating a limb; followed by regeneration; used also for asexual reproduction; see also fissipary (in echinodermata and platyhelminthes). Basal Lamina: Basal plate of developing neural tube; the noncellular, collagenous layer that separates an epithelium from an underlying layer of tissue; also basal membrane. Benthic: Organisms that live on ocean bottoms. Blastocoel: See coelom. Blastula: Stage of embryonic development, at / near the end of cleavage, preceding gastrulation; generally consisting of a hollow ball of cells (coeloblastula); if no blastoceol is present it is termed stereoblastulae (arise from isolecithal and moderately telolecithal ova); in meroblastic cleavage (only the upper part of the zygote is divided), the blastula consists of a disc of cells lying on top of the yolk mass; the blastocoel is reduced to the space separating the cells from the yolk mass. Blastoporus: The opening into the archenteron (the primitive gastric cavity of the gastrula = gastrocoel) developed by the invagination of the blastula = protostoma. Cephalisation: (Gk. kephale, little head) A type of animal body plan or organization in which one end contains a nerve-rich region and functions as a head. Cilium: (pl. cilia, long eyelash) A short, centriole-based, hairlike organelle: Rows of cilia propel certain protista. Cilia also aid the movement of substances across epithelial surfaces of animal cells. Cleavage: The zygote undergoes a series of rapid, synchronous mitotic divisions; results in a ball of many cells. -
Vertebrates and Invertebrates
Vertebrates and invertebrates The animal kingdom is divided into two groups: vertebrates and invertebrates. Vertebrates have been around for millions of years but have evolved and changed over time. The word vertebrate means “having a backbone." Many animals have backbones. You have a backbone. So does a cow, a whale, a fish, a frog, and a bird. Vertebrates are animals that have a backbone. Most animals have a backbone that is made of bones joined together to form a skeleton. Our skeleton gives us our shape and allows us to move. Mammals, fish, birds, reptiles, and amphibians have Vertebrae backbones so they are all vertebrates. Each bone that makes up the backbone Scientists classify vertebrates into five classes: is called a vertebra. These are the • Mammals building blacks that form the backbone, • Fish also known as the spinal cord. The • Birds vertebrae protect and support your • Reptiles spine. Without a backbone, you would not • Amphibians be able to move any part of your body. Animals without a backbone are called invertebrates. Most The human animals are invertebrates. In fact, 95% of all living creatures backbone has 26 on Earth are invertebrates. vertebrae. Arthropods are the largest group of invertebrates. Insects make up a large part of this group. All insects, such as ladybugs, ants, grasshoppers, and bumblebees have three body sections and six legs. Most arthropods live on land, but some of these fascinating creatures live in water. Lobsters, crabs, and shrimp are arthropods that live in the oceans. Many invertebrates have skeletons on the outside of their A frog only has bodies called exoskeletons. -
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. -
OREGON ESTUARINE INVERTEBRATES an Illustrated Guide to the Common and Important Invertebrate Animals
OREGON ESTUARINE INVERTEBRATES An Illustrated Guide to the Common and Important Invertebrate Animals By Paul Rudy, Jr. Lynn Hay Rudy Oregon Institute of Marine Biology University of Oregon Charleston, Oregon 97420 Contract No. 79-111 Project Officer Jay F. Watson U.S. Fish and Wildlife Service 500 N.E. Multnomah Street Portland, Oregon 97232 Performed for National Coastal Ecosystems Team Office of Biological Services Fish and Wildlife Service U.S. Department of Interior Washington, D.C. 20240 Table of Contents Introduction CNIDARIA Hydrozoa Aequorea aequorea ................................................................ 6 Obelia longissima .................................................................. 8 Polyorchis penicillatus 10 Tubularia crocea ................................................................. 12 Anthozoa Anthopleura artemisia ................................. 14 Anthopleura elegantissima .................................................. 16 Haliplanella luciae .................................................................. 18 Nematostella vectensis ......................................................... 20 Metridium senile .................................................................... 22 NEMERTEA Amphiporus imparispinosus ................................................ 24 Carinoma mutabilis ................................................................ 26 Cerebratulus californiensis .................................................. 28 Lineus ruber ......................................................................... -
Onychophorology, the Study of Velvet Worms
Uniciencia Vol. 35(1), pp. 210-230, January-June, 2021 DOI: http://dx.doi.org/10.15359/ru.35-1.13 www.revistas.una.ac.cr/uniciencia E-ISSN: 2215-3470 [email protected] CC: BY-NC-ND Onychophorology, the study of velvet worms, historical trends, landmarks, and researchers from 1826 to 2020 (a literature review) Onicoforología, el estudio de los gusanos de terciopelo, tendencias históricas, hitos e investigadores de 1826 a 2020 (Revisión de la Literatura) Onicoforologia, o estudo dos vermes aveludados, tendências históricas, marcos e pesquisadores de 1826 a 2020 (Revisão da Literatura) Julián Monge-Nájera1 Received: Mar/25/2020 • Accepted: May/18/2020 • Published: Jan/31/2021 Abstract Velvet worms, also known as peripatus or onychophorans, are a phylum of evolutionary importance that has survived all mass extinctions since the Cambrian period. They capture prey with an adhesive net that is formed in a fraction of a second. The first naturalist to formally describe them was Lansdown Guilding (1797-1831), a British priest from the Caribbean island of Saint Vincent. His life is as little known as the history of the field he initiated, Onychophorology. This is the first general history of Onychophorology, which has been divided into half-century periods. The beginning, 1826-1879, was characterized by studies from former students of famous naturalists like Cuvier and von Baer. This generation included Milne-Edwards and Blanchard, and studies were done mostly in France, Britain, and Germany. In the 1880-1929 period, research was concentrated on anatomy, behavior, biogeography, and ecology; and it is in this period when Bouvier published his mammoth monograph. -
Fun Facts: Incredible Invertebrates 40 Minutes Age 7-11
Fun Facts: Incredible Invertebrates 40 minutes Age 7-11 1. Invertebrates are animals that do not have a backbone. Some common invertebrates are worms, snails, corals, sponges, insects, jellyfish, and crustaceans (Brsuca and Brusca, 2003). 2. Invertebrates first evolved during the Cambrian Period, over 540 million years ago (Brusca and Brusca, 2003) 3. Over 95% of the 1.4 million known animal species are invertebrates (Smithsonian, 2018) 4. The largest invertebrate is the colossal squid which can weigh over 500kg and reach lengths of up to 14m (Ravaiolo and Youngster, 2012). 5. Corals are sessile invertebrates, meaning they are fixed in one place and unable to relocate. Corals grow at different rates, with some growing up to 10cm in one year and others only growing 0.3cm in one year (Barnes, 1987). 6. Many species of marine worms, such as feather duster and Christmas tree worms, survive by hiding their body in a tube attached to the reef. They feed by extending their gills into the water and catching phytoplankton and other microscopic organisms in the water column (NOAA, 2020). 7. Sea stars and sea urchins are some important species of invertebrates that have specialized organs called tube feet, which allow them to move and feed. The tube feet have two special types of cells. The first type of cell releases a glue-like substance that allows the tube feet to stick and hold onto different structures. The second type of cell releases a substance that breaks down the glue-like substance and allows the tube feet to release from the structure (Flammang et al., 2005). -
Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans
biology Review Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans Maria Giovanna Parisi 1,* , Daniela Parrinello 1, Loredana Stabili 2 and Matteo Cammarata 1,* 1 Department of Earth and Marine Sciences, University of Palermo, 90128 Palermo, Italy; [email protected] 2 Department of Biological and Environmental Sciences and Technologies, University of Salento, 73100 Lecce, Italy; [email protected] * Correspondence: [email protected] (M.G.P.); [email protected] (M.C.) Received: 10 August 2020; Accepted: 4 September 2020; Published: 11 September 2020 Abstract: Anthozoa is the most specious class of the phylum Cnidaria that is phylogenetically basal within the Metazoa. It is an interesting group for studying the evolution of mutualisms and immunity, for despite their morphological simplicity, Anthozoans are unexpectedly immunologically complex, with large genomes and gene families similar to those of the Bilateria. Evidence indicates that the Anthozoan innate immune system is not only involved in the disruption of harmful microorganisms, but is also crucial in structuring tissue-associated microbial communities that are essential components of the cnidarian holobiont and useful to the animal’s health for several functions including metabolism, immune defense, development, and behavior. Here, we report on the current state of the art of Anthozoan immunity. Like other invertebrates, Anthozoans possess immune mechanisms based on self/non-self-recognition. Although lacking adaptive immunity, they use a diverse repertoire of immune receptor signaling pathways (PRRs) to recognize a broad array of conserved microorganism-associated molecular patterns (MAMP). The intracellular signaling cascades lead to gene transcription up to endpoints of release of molecules that kill the pathogens, defend the self by maintaining homeostasis, and modulate the wound repair process. -
Phylum Onychophora
Lab exercise 6: Arthropoda General Zoology Laborarory . Matt Nelson phylum onychophora Velvet worms Once considered to represent a transitional form between annelids and arthropods, the Onychophora (velvet worms) are now generally considered to be sister to the Arthropoda, and are included in chordata the clade Panarthropoda. They are no hemichordata longer considered to be closely related to echinodermata the Annelida. Molecular evidence strongly deuterostomia supports the clade Panarthropoda, platyhelminthes indicating that those characteristics which the velvet worms share with segmented rotifera worms (e.g. unjointed limbs and acanthocephala metanephridia) must be plesiomorphies. lophotrochozoa nemertea mollusca Onychophorans share many annelida synapomorphies with arthropods. Like arthropods, velvet worms possess a chitinous bilateria protostomia exoskeleton that necessitates molting. The nemata ecdysozoa also possess a tracheal system similar to that nematomorpha of insects and myriapods. Onychophorans panarthropoda have an open circulatory system with tardigrada hemocoels and a ventral heart. As in arthropoda arthropods, the fluid-filled hemocoel is the onychophora main body cavity. However, unlike the arthropods, the hemocoel of onychophorans is used as a hydrostatic acoela skeleton. Onychophorans feed mostly on small invertebrates such as insects. These prey items are captured using a special “slime” which is secreted from large slime glands inside the body and expelled through two oral papillae on either side of the mouth. This slime is protein based, sticking to the cuticle of insects, but not to the cuticle of the velvet worm itself. Secreted as a liquid, the slime quickly becomes solid when exposed to air. Once a prey item is captured, an onychophoran feeds much like a spider.