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(Gastropoda: Batillariidae) from Elkhorn Slough, California, USA
Mitochondrial DNA Part B Resources ISSN: (Print) 2380-2359 (Online) Journal homepage: https://www.tandfonline.com/loi/tmdn20 The complete mitogenome of the invasive Japanese mud snail Batillaria attramentaria (Gastropoda: Batillariidae) from Elkhorn Slough, California, USA Hartnell College Genomics Group, Paulina Andrade, Lisbeth Arreola, Melissa Belnas, Estefania Bland, Araceli Castillo, Omar Cisneros, Valentin Contreras, Celeste Diaz, Kevin T. Do, Carlos Donate, Estevan Espinoza, Nathan Frater, Garry G. Gabriel, Eric A. Gomez, Gino F. Gonzalez, Myrka Gonzalez, Paola Guido, Dylan Guidotti, Mishell Guzman Espinoza, Ivan Haro, Javier Hernandez Lopez, Caden E. Hernandez, Karina Hernandez, Jazmin A. Hernandez-Salazar, Jeffery R. Hughey, Héctor Jácome-Sáenz, Luis A. Jimenez, Eli R. Kallison, Mylisa S. King, Luis J. Lazaro, Feifei Zhai Lorenzo, Isaac Madrigal, Savannah Madruga, Adrian J. Maldonado, Alexander M. Medina, Marcela Mendez-Molina, Ali Mendez, David Murillo Martinez, David Orozco, Juan Orozco, Ulises Ortiz, Jennifer M. Pantoja, Alejandra N. Ponce, Angel R. Ramirez, Israel Rangel, Eliza Rojas, Adriana Roque, Beatriz Rosas, Colt Rubbo, Justin A. Saldana, Elian Sanchez, Alicia Steinhardt, Maria O. Taveras Dina, Judith Torres, Silvestre Valdez-Mata, Valeria Vargas, Paola Vazquez, Michelle M. Vazquez, Irene Vidales, Frances L. Wong, Christian S. Zagal, Santiago Zamora & Jesus Zepeda Amador To cite this article: Hartnell College Genomics Group, Paulina Andrade, Lisbeth Arreola, Melissa Belnas, Estefania Bland, Araceli Castillo, Omar Cisneros, Valentin Contreras, Celeste Diaz, Kevin T. Do, Carlos Donate, Estevan Espinoza, Nathan Frater, Garry G. Gabriel, Eric A. Gomez, Gino F. Gonzalez, Myrka Gonzalez, Paola Guido, Dylan Guidotti, Mishell Guzman Espinoza, Ivan Haro, Javier Hernandez Lopez, Caden E. Hernandez, Karina Hernandez, Jazmin A. -
Mineralogisch Museum Leiden”
collection, a label of the former museum is retained for all registered specimens. The names of museum in the labels are “Rijksmuseum van Geologie en Mineralogie”, “Rijksmuseum van Geologie Leiden”, or “Rijks Geologisch-Mineralogisch Museum Leiden”. Labels in Japanese letters: The limited number of specimens are accompanied by Japanese labels. In most cases, labels are directly pasted on specimens. Names are written in Katakana letters only (e.g. Fig. 1E) or both in Chinese and Katakana letters (e.g. Figs. 1B, 3C, 3F). Identification of a few specimens in Japanese label is different from current our recognition and interesting. “Ryôkotsu” in Figs. 3F and 3H means dragon bones, but they are actually fragments of molluscan shells and eroded mammalian bones, respectively. In China, fossil vertebrate bones are called “Longgu” which is written in the same Chinese characters as “Ryôkotsu” in Japan, and have been used as a crude medicine. “Mimizu-ishi” in Fig. 2E stands for an earthworm stone, and winding tubes on the rock are bore holes of boring bivalve (“Teredo” sp.) with interior lining. Other fossils were precisely identified at phylum or class level. Examples are fossil fish (“Sekigyo”: Fig. 1B), fossil of wood (“Moku-kwaseki”: Fig. 4A), stone clam (“Ishi-hamaguri”: Fig. 11A), and fossil of heart urchin (“Kaien-no-kwaseki”: Fig. 3A). Molluscan specimens in Siebold fossil collection The molluscs in the Siebold fossil collection consist of more than 40 species as described below (Figs. 5-14). This number, however, does not contain the shell fragments in sandstone (Figs. 1D-G, 2A). In the following accounts, the depository of the specimens is in the mineralogical collection in Naturalis, unless otherwise mentioned. -
Species Composition of the Free Living Multicellular Invertebrate Animals
Historia naturalis bulgarica, 21: 49-168, 2015 Species composition of the free living multicellular invertebrate animals (Metazoa: Invertebrata) from the Bulgarian sector of the Black Sea and the coastal brackish basins Zdravko Hubenov Abstract: A total of 19 types, 39 classes, 123 orders, 470 families and 1537 species are known from the Bulgarian Black Sea. They include 1054 species (68.6%) of marine and marine-brackish forms and 508 species (33.0%) of freshwater-brackish, freshwater and terrestrial forms, connected with water. Five types (Nematoda, Rotifera, Annelida, Arthropoda and Mollusca) have a high species richness (over 100 species). Of these, the richest in species are Arthropoda (802 species – 52.2%), Annelida (173 species – 11.2%) and Mollusca (152 species – 9.9%). The remaining 14 types include from 1 to 38 species. There are some well-studied regions (over 200 species recorded): first, the vicinity of Varna (601 spe- cies), where investigations continue for more than 100 years. The aquatory of the towns Nesebar, Pomorie, Burgas and Sozopol (220 to 274 species) and the region of Cape Kaliakra (230 species) are well-studied. Of the coastal basins most studied are the lakes Durankulak, Ezerets-Shabla, Beloslav, Varna, Pomorie, Atanasovsko, Burgas, Mandra and the firth of Ropotamo River (up to 100 species known). The vertical distribution has been analyzed for 800 species (75.9%) – marine and marine-brackish forms. The great number of species is found from 0 to 25 m on sand (396 species) and rocky (257 species) bottom. The groups of stenohypo- (52 species – 6.5%), stenoepi- (465 species – 58.1%), meso- (115 species – 14.4%) and eurybathic forms (168 species – 21.0%) are represented. -
The Evolution of Siphonophore Tentilla for Specialized Prey Capture in the Open Ocean
The evolution of siphonophore tentilla for specialized prey capture in the open ocean Alejandro Damian-Serranoa,1, Steven H. D. Haddockb,c, and Casey W. Dunna aDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520; bResearch Division, Monterey Bay Aquarium Research Institute, Moss Landing, CA 95039; and cEcology and Evolutionary Biology, University of California, Santa Cruz, CA 95064 Edited by Jeremy B. C. Jackson, American Museum of Natural History, New York, NY, and approved December 11, 2020 (received for review April 7, 2020) Predator specialization has often been considered an evolutionary makes them an ideal system to study the relationships between “dead end” due to the constraints associated with the evolution of functional traits and prey specialization. Like a head of coral, a si- morphological and functional optimizations throughout the organ- phonophore is a colony bearing many feeding polyps (Fig. 1). Each ism. However, in some predators, these changes are localized in sep- feeding polyp has a single tentacle, which branches into a series of arate structures dedicated to prey capture. One of the most extreme tentilla. Like other cnidarians, siphonophores capture prey with cases of this modularity can be observed in siphonophores, a clade of nematocysts, harpoon-like stinging capsules borne within special- pelagic colonial cnidarians that use tentilla (tentacle side branches ized cells known as cnidocytes. Unlike the prey-capture apparatus of armed with nematocysts) exclusively for prey capture. Here we study most other cnidarians, siphonophore tentacles carry their cnidocytes how siphonophore specialists and generalists evolve, and what mor- in extremely complex and organized batteries (3), which are located phological changes are associated with these transitions. -
Hydrozoa of the Eurasian Arctic Seas 397 S
THE ARCTIC SEAS CI imatology, Oceanography, Geology, and Biology Edited by Yvonne Herman IOm51 VAN NOSTRAND REINHOLD COMPANY ~ -----New York This work relates to Department of the Navy Grant NOOOI4-85- G-0252 issued by the Office of Naval Research. The United States Government has a royalty-free license throughout the world in all copyrightable material contained herein. Copyright © 1989 by Van Nostrand Reinhold Softcover reprint of the hardcover 1st edition 1989 Library of Congress Catalog Card Number 88-33800 ISBN-13 :978-1-4612-8022-4 e-ISBN-13: 978-1-4613-0677-1 DOI: 10.1007/978-1-4613-0677-1 All rights reserved. No part of this work covered by the copyright hereon may be reproduced or used in any form or by any means-graphic, electronic, or mechanical, including photocopying, recording, taping, or information storage and retrieval systems-without written permission of the publisher. Designed by Beehive Production Services Van Nostrand Reinhold 115 Fifth Avenue New York, New York 10003 Van Nostrand Reinhold (International) Limited 11 New Fetter Lane London EC4P 4EE, England Van Nostrand Reinhold 480 La Trobe Street Melbourne, Victoria 3000, Australia Nelson Canada 1120 Birchmount Road Scarborough, Ontario MIK 5G4, Canada 16 15 14 13 12 11 10 9 8 7 6 5 4 3 2 1 Library of Congress Cataloging in Publication Data The Arctic Seas. Includes index. 1. Oceanography-Arctic Ocean. 2. Geology-ArctiC Ocean. 1. Herman, Yvonne. GC401.A76 1989 551.46'8 88-33800 ISBN-13: 978-1-4612-8022-4 For Anyu Contents Preface / vii Contributors / ix 1. -
Clearance Rates of Jellyfish and Their Potential Predation Impact on Zooplankton and Fish Larvae in a Neritic Ecosystem (Limfjorden, Denmark)
MARINE ECOLOGY PROGRESS SERIES Vol. 304: 117–131, 2005 Published December 8 Mar Ecol Prog Ser Clearance rates of jellyfish and their potential predation impact on zooplankton and fish larvae in a neritic ecosystem (Limfjorden, Denmark) Lars Johan Hansson1,*, Ole Moeslund2, Thomas Kiørboe1, Hans Ulrik Riisgård2 1Danish Institute for Fisheries Research, Kavalergården 6, 2920 Charlottenlund, Denmark 2Marine Biological Research Centre (University of Southern Denmark) Hindsholmvej 11, 5300 Kerteminde, Denmark ABSTRACT: Clearance rates of the hydromedusae Sarsia tubulosa, Rathkea octopunctata and Bougainvillea superciliaris and the scyphomedusa Aurelia aurita were measured in the laboratory. Gut contents analyses of A. aurita were also collected in situ and subsequently used for estimation of clearance rate. The clearance rate of A. aurita varied widely with prey organisms. Large crustacean prey with low escape capabilities (Artemia salina nauplii and cirripede larvae) were cleared at high rates, whereas copepodites were cleared at lower rates, and clearance rates of small bivalve larvae and copepod nauplii were comparatively low. These data were used to assess the impact of jellyfish preda- tion upon zooplankton and fish larvae in Limfjorden, Denmark. Repeated sampling of zooplankton, fish larvae and medusae was undertaken during the first half of 2003. Nine taxa of hydromedusae and 4 taxa of scyphomedusae were identified. Abundance estimates were combined with estimated clear- ance rates of individual medusae to calculate potential jellyfish-induced mortality on prey in Limfjor- den. Copepoda was used as a model prey group to estimate the collective predation impact by all medusae. Medusa species with unknown clearance potential were given assumed clearance rate val- ues, but the collective predation potential by these species was evaluated to be small. -
Bering Sea Marine Invasive Species Assessment Alaska Center for Conservation Science
Bering Sea Marine Invasive Species Assessment Alaska Center for Conservation Science Scientific Name: Batillaria attramentaria Phylum Mollusca Common Name Japanese false cerith Class Gastropoda Order Neotaenioglossa Family Batillariidae Z:\GAP\NPRB Marine Invasives\NPRB_DB\SppMaps\BATATT.png 153 Final Rank 46.00 Data Deficiency: 12.50 Category Scores and Data Deficiencies Total Data Deficient Category Score Possible Points Distribution and Habitat: 12.25 23 7.50 Anthropogenic Influence: 6 10 0 Biological Characteristics: 17 25 5.00 Impacts: 5 30 0 Figure 1. Occurrence records for non-native species, and their geographic proximity to the Bering Sea. Ecoregions are based on the classification system by Spalding et al. (2007). Totals: 40.25 87.50 12.50 Occurrence record data source(s): NEMESIS and NAS databases. General Biological Information Tolerances and Thresholds Minimum Temperature (°C) -2 Minimum Salinity (ppt) 7 Maximum Temperature (°C) 40 Maximum Salinity (ppt) 33 Minimum Reproductive Temperature (°C) Minimum Reproductive Salinity (ppt) Maximum Reproductive Temperature (°C) Maximum Reproductive Salinity (ppt) Additional Notes Size of adult shells ranges from 10 to 34 mm. The shell is usually gray-brown, often with a white band below the suture, but can range from light brown to dirty-black. Historically introduced with the Pacific oyster, Crassostrea gigas, but in recent years, it has been found in areas where oysters are not cultivated. Nevertheless, its spread has been attributed to anthropogenic vectors rather than natural dispersal. Report updated on Wednesday, December 06, 2017 Page 1 of 13 1. Distribution and Habitat 1.1 Survival requirements - Water temperature Choice: Considerable overlap – A large area (>75%) of the Bering Sea has temperatures suitable for year-round survival Score: A 3.75 of High uncertainty? 3.75 Ranking Rationale: Background Information: Temperatures required for year-round survival occur over a large Based on its geographic distribution, B. -
Attachment Iii: Baseline Status and Cumulative Effects for the San Francisco Bay Listed Species
ATTACHMENT III: BASELINE STATUS AND CUMULATIVE EFFECTS FOR THE SAN FRANCISCO BAY LISTED SPECIES 1 TABLE OF CONTENTS 1: ALAMEDAWHIPSNAKE ............................................................................................ 6 1.1 CUMULATIVE EFFECTS ...................................................................................... 6 1.2 ENVIRONMENTAL BASELINE........................................................................... 6 1.2.1 Factors affecting species within the action area ............................................... 6 1.2.1.1 Urban development .................................................................................... 7 1.2.1.2 Fire suppression ......................................................................................... 9 1.2.1.3 Predation .................................................................................................... 9 1.2.1.4 Grazing practices ..................................................................................... 10 1.2.1.5 Non-native species ................................................................................... 10 1.2.2 Baseline Status ................................................................................................ 11 1.3 REFERENCES ...................................................................................................... 13 2: BAY CHECKERSPOT BUTTERFLY ....................................................................... 14 2.1 CUMULATIVE EFFECTS .................................................................................. -
Balanus Glandula Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia
Phylum: Arthropoda, Crustacea Balanus glandula Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia Order: Thoracica, Sessilia, Balanomorpha Acorn barnacle Family: Balanoidea, Balanidae, Balaninae Description (the plate overlapping plate edges) and radii Size: Up to 3 cm in diameter, but usually (the plate edge marked off from the parietes less than 1.5 cm (Ricketts and Calvin 1971; by a definite change in direction of growth Kozloff 1993). lines) (Fig. 3b) (Newman 2007). The plates Color: Shell usually white, often irregular themselves include the carina, the carinola- and color varies with state of erosion. Cirri teral plates and the compound rostrum (Fig. are black and white (see Plate 11, Kozloff 3). 1993). Opercular Valves: Valves consist of General Morphology: Members of the Cirri- two pairs of movable plates inside the wall, pedia, or barnacles, can be recognized by which close the aperture: the tergum and the their feathery thoracic limbs (called cirri) that scutum (Figs. 3a, 4, 5). are used for feeding. There are six pairs of Scuta: The scuta have pits on cirri in B. glandula (Fig. 1). Sessile barna- either side of a short adductor ridge (Fig. 5), cles are surrounded by a shell that is com- fine growth ridges, and a prominent articular posed of a flat basis attached to the sub- ridge. stratum, a wall formed by several articulated Terga: The terga are the upper, plates (six in Balanus species, Fig. 3) and smaller plate pair and each tergum has a movable opercular valves including terga short spur at its base (Fig. 4), deep crests for and scuta (Newman 2007) (Figs. -
Bryozoa of the Caspian Sea
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/339363855 Bryozoa of the Caspian Sea Article in Inland Water Biology · January 2020 DOI: 10.1134/S199508292001006X CITATIONS READS 0 90 1 author: Valentina Ivanovna Gontar Russian Academy of Sciences 58 PUBLICATIONS 101 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Freshwater Bryozoa View project Evolution of spreading of marine invertebrates in the Northern Hemisphere View project All content following this page was uploaded by Valentina Ivanovna Gontar on 19 February 2020. The user has requested enhancement of the downloaded file. ISSN 1995-0829, Inland Water Biology, 2020, Vol. 13, No. 1, pp. 1–13. © Pleiades Publishing, Ltd., 2020. Russian Text © The Author(s), 2020, published in Biologiya Vnutrennykh Vod, 2020, No. 1, pp. 3–16. AQUATIC FLORA AND FAUNA Bryozoa of the Caspian Sea V. I. Gontar* Institute of Zoology, Russian Academy of Sciences, St. Petersburg, Russia *e-mail: [email protected] Received April 24, 2017; revised September 18, 2018; accepted November 27, 2018 Abstract—Five bryozoan species of the class Gymnolaemata and a single Plumatella emarginata species of the class Phylactolaemata are found in the Caspian Sea. The class Gymnolaemata is represented by bryozoans of the orders Ctenostomatida (Amathia caspia, Paludicella articulata, and Victorella pavida) and Cheilostoma- tida (Conopeum grimmi and Lapidosella ostroumovi). Two species (Conopeum grimmi and Amatia caspia) are Caspian endemics. Lapidosella ostroumovi was identified in the Caspian Sea for the first time. The systematic position, illustrated morphological descriptions, and features of ecology of the species identified are pre- sented. -
Inland Fishes of California
Inland Fishes of California Revise d and Expanded PETER B. MO YL E Illustrations by Chris Ma ri van Dyck and Joe Tome ller i NIVERS ITyor ALfFORNJA PRESS Ikrkd cr I.", ..\ n~d e ' Lon don Universit }, 0 Ca lifornia Press Herkdey and Los Angeles, Ca lifornia Uni ve rsity of alifornia Press, Ltd. Lundun, England ~ 2002 by the Regents of the Unive rsi ty of Ca lifornia Library of Cungress ataloging-in -Publ ica tion Data j\·[oyk, Pen: r B. Inland fis hes of California / Peter B. Moyle ; illustrations by Chris Mari van D)'ck and Joe Tomell eri.- Rev. and expanded. p. cm. In lu de> bibl iographical refe rences (p. ). ISBN 0- 20-2.2754 -'1 (cl ot h: alk. papa) I. rreshw:ltcr lishes-Cali(ornia. I. Title. QL62S C2 M6H 2002 597 .17/i'097Q4-dc21 20010 27680 1\!UlIl.Ifaclu rcd in Canacla II 10 Q9 00 07 06 0 04 03 02 10 ' 1\ 7 b '; -\ 3 2 1 Th paper u!)ed in thi> public.ltiu(] 111l'd., the minimum requirements "fA SI / i': ISO Z39.4H-1992 (R 199;) ( Pmlllllh'/l e ofPa pcr) . e Special Thanks The illustrations for this book were made possible by gra nts from the following : California-Nevada Chapter, American Fi she ries Soc iety Western Di vision, Am erican Fi she ries Society California Department of Fish and Game Giles W. and El ise G. Mead Foundation We appreciate the generous funding support toward the publication of this book by the United Sta tes Environme ntal Protection Agency, Region IX, San Francisco Contents Pre(acc ix Salmon and Trout, Salmonidae 242 Ackl10 11'ledgl11 el1ts Xlll Silversides, Atherinopsidae 307 COlll'er,<iol1 ['actors xv -
Woodlice in Britain and Ireland: Distribution and Habitat Is out of Date Very Quickly, and That They Will Soon Be Writing the Second Edition
• • • • • • I att,AZ /• •• 21 - • '11 n4I3 - • v., -hi / NT I- r Arty 1 4' I, • • I • A • • • Printed in Great Britain by Lavenham Press NERC Copyright 1985 Published in 1985 by Institute of Terrestrial Ecology Administrative Headquarters Monks Wood Experimental Station Abbots Ripton HUNTINGDON PE17 2LS ISBN 0 904282 85 6 COVER ILLUSTRATIONS Top left: Armadillidium depressum Top right: Philoscia muscorum Bottom left: Androniscus dentiger Bottom right: Porcellio scaber (2 colour forms) The photographs are reproduced by kind permission of R E Jones/Frank Lane The Institute of Terrestrial Ecology (ITE) was established in 1973, from the former Nature Conservancy's research stations and staff, joined later by the Institute of Tree Biology and the Culture Centre of Algae and Protozoa. ITE contributes to, and draws upon, the collective knowledge of the 13 sister institutes which make up the Natural Environment Research Council, spanning all the environmental sciences. The Institute studies the factors determining the structure, composition and processes of land and freshwater systems, and of individual plant and animal species. It is developing a sounder scientific basis for predicting and modelling environmental trends arising from natural or man- made change. The results of this research are available to those responsible for the protection, management and wise use of our natural resources. One quarter of ITE's work is research commissioned by customers, such as the Department of Environment, the European Economic Community, the Nature Conservancy Council and the Overseas Development Administration. The remainder is fundamental research supported by NERC. ITE's expertise is widely used by international organizations in overseas projects and programmes of research.