An Introduction to the Japanese Groundwater Animals with Reference to Their Ecology and Hygienic Significance
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Anchialine Cave Biology in the Era of Speleogenomics Jorge L
International Journal of Speleology 45 (2) 149-170 Tampa, FL (USA) May 2016 Available online at scholarcommons.usf.edu/ijs International Journal of Speleology Off icial Journal of Union Internationale de Spéléologie Life in the Underworld: Anchialine cave biology in the era of speleogenomics Jorge L. Pérez-Moreno1*, Thomas M. Iliffe2, and Heather D. Bracken-Grissom1 1Department of Biological Sciences, Florida International University, Biscayne Bay Campus, North Miami FL 33181, USA 2Department of Marine Biology, Texas A&M University at Galveston, Galveston, TX 77553, USA Abstract: Anchialine caves contain haline bodies of water with underground connections to the ocean and limited exposure to open air. Despite being found on islands and peninsular coastlines around the world, the isolation of anchialine systems has facilitated the evolution of high levels of endemism among their inhabitants. The unique characteristics of anchialine caves and of their predominantly crustacean biodiversity nominate them as particularly interesting study subjects for evolutionary biology. However, there is presently a distinct scarcity of modern molecular methods being employed in the study of anchialine cave ecosystems. The use of current and emerging molecular techniques, e.g., next-generation sequencing (NGS), bestows an exceptional opportunity to answer a variety of long-standing questions pertaining to the realms of speciation, biogeography, population genetics, and evolution, as well as the emergence of extraordinary morphological and physiological adaptations to these unique environments. The integration of NGS methodologies with traditional taxonomic and ecological methods will help elucidate the unique characteristics and evolutionary history of anchialine cave fauna, and thus the significance of their conservation in face of current and future anthropogenic threats. -
Zootaxa 3266: 41–52 (2012) ISSN 1175-5326 (Print Edition) Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (Online Edition)
Zootaxa 3266: 41–52 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) Thalasseleotrididae, new family of marine gobioid fishes from New Zealand and temperate Australia, with a revised definition of its sister taxon, the Gobiidae (Teleostei: Acanthomorpha) ANTHONY C. GILL1,2 & RANDALL D. MOOI3,4 1Macleay Museum and School of Biological Sciences, A12 – Macleay Building, The University of Sydney, New South Wales 2006, Australia. E-mail: [email protected] 2Ichthyology, Australian Museum, 6 College Street, Sydney, New South Wales 2010, Australia 3The Manitoba Museum, 190 Rupert Ave., Winnipeg MB, R3B 0N2 Canada. E-mail: [email protected] 4Department of Biological Sciences, 212B Biological Sciences Bldg., University of Manitoba, Winnipeg MB, R3T 2N2 Canada Abstract Thalasseleotrididae n. fam. is erected to include two marine genera, Thalasseleotris Hoese & Larson from temperate Aus- tralia and New Zealand, and Grahamichthys Whitley from New Zealand. Both had been previously classified in the family Eleotrididae. The Thalasseleotrididae is demonstrably monophyletic on the basis of a single synapomorphy: membrane connecting the hyoid arch to ceratobranchial 1 broad, extending most of the length of ceratobranchial 1 (= first gill slit restricted or closed). The family represents the sister group of a newly diagnosed Gobiidae on the basis of five synapo- morphies: interhyal with cup-shaped lateral structure for articulation with preopercle; laterally directed posterior process on the posterior ceratohyal supporting the interhyal; pharyngobranchial 4 absent; dorsal postcleithrum absent; urohyal without ventral shelf. The Gobiidae is defined by three synapomorphies: five branchiostegal rays; expanded and medially- placed ventral process on ceratobranchial 5; dorsal hemitrich of pelvic-fin rays with complex proximal head. -
Changes in Species Composition of Haploniscidae (Crustacea Isopoda)
Progress in Oceanography 180 (2020) 102233 Contents lists available at ScienceDirect Progress in Oceanography journal homepage: www.elsevier.com/locate/pocean Changes in species composition of Haploniscidae (Crustacea: Isopoda) across T potential barriers to dispersal in the Northwest Pacific ⁎ Nele Johannsena,b, Lidia Linsa,b,c, Torben Riehla,b, Angelika Brandta,b, a Goethe University, Biosciences, Institute for Ecology, Evolution und Diversity, Max-von-Laue-Str. 13, 60438 Frankfurt am Main, Germany b Senckenberg Research Institute and Natural History Museum, Marine Zoology, Senckenberganlage 25, 60325 Frankfurt am Main, Germany c Ghent University, Marine Biology Research Group, Krijgslaan 281/S8, 9000 Ghent, Belgium ARTICLE INFO ABSTRACT Keywords: Speciation processes as drivers of biodiversity in the deep sea are still not fully understood. One potential driver Hadal for species diversification might be allopatry caused by geographical barriers, such as ridges or trenches, or Ecology physiological barriers associated with depth. We analyzed biodiversity and biogeography of 21 morphospecies of Sea of Okhotsk the deep-sea isopod family Haploniscidae to investigate barrier effects to species dispersal in the Kuril- Deep sea Kamchatka Trench (KKT) area in the Northwest (NW) Pacific. Our study is based on 2652 specimens from three Abyssal genera, which were collected during the German-Russian KuramBio I (2012) and II (2016) expeditions as well as Isopoda Kuril Kamchatka Trench the Russian-German SokhoBio (2015) campaign. The sampling area covered two potential geographical barriers Distribution (the Kuril Island archipelago and the Kuril-Kamchatka Trench), as well as three depth zones (bathyal, abyssal, Northwest Pacific hadal). We found significant differences in relative species abundance between abyssal and hadal depths. -
Platyhelminthes, Tricladida, Kenkiidae) from Great Smoky Mountains National Park
Journal of the North Carolina Academy of Science, 131(1), 2015, pp. 15–17 A CAVE PLANARIAN, SPHALLOPLANA PERCOECA, (PLATYHELMINTHES, TRICLADIDA, KENKIIDAE) FROM GREAT SMOKY MOUNTAINS NATIONAL PARK BENNY GLASGOW1 and PAULA PIERCE2 1Principal investigator, Park study GRSM-00341, 101 William Street, Vernon, AL 35592 Email: [email protected] 2Excalibur Pathology, Inc., 5830 N Blue Lake Dr., Norman OK 73069 Email: [email protected] Downloaded from http://meridian.allenpress.com/jncas/article-pdf/131/1/15/1818171/2167-5872-131_1_15.pdf by guest on 27 September 2021 Abstract: Five cave planarians collected from Gregory’s Cave, Blount Co., TN, Great Smoky Mountains National Park, were analyzed using stained serial sections and two are identified as Sphalloplana percoeca (Packard 1879). Notes on specimen characteristics and habitat are given, two photographs are provided, and the species’ taxonomy and distribution are discussed. Key Words: Sphalloplana percoeca; Kenkiidae; Gregory’s Cave. INTRODUCTION 1978, pers. comm. 2010). Aquatic amphipods may be The Great Smoky Mountains National Park’s ongo- food sources for cave planarians (Reeves 2000; Carpen- ing All Taxa Biodiversity Inventory, to determine ter 1982). Bats, amphibians, amphipods, millipedes, and presence and distribution of Park species or discover insects were observed in the cave during Park study new species, elicits this report on an obligate cave GRSM-00341 collections. Mays (2001) reported amphi- planarian belonging to family Kenkiidae (Hyman 1937). pods, millipedes, and spiders inhabiting the cave. Larvae Cave planarians are not well known and there could be of the Long-tailed Salamander (Eurycea longicauda) new species yet undiscovered. Gregory’s Cave was were reported in the cave’s rimstone pools (Dodd et al. -
Additions to and Revisions of the Amphipod (Crustacea: Amphipoda) Fauna of South Africa, with a List of Currently Known Species from the Region
Additions to and revisions of the amphipod (Crustacea: Amphipoda) fauna of South Africa, with a list of currently known species from the region Rebecca Milne Department of Biological Sciences & Marine Research Institute, University of CapeTown, Rondebosch, 7700 South Africa & Charles L. Griffiths* Department of Biological Sciences & Marine Research Institute, University of CapeTown, Rondebosch, 7700 South Africa E-mail: [email protected] (with 13 figures) Received 25 June 2013. Accepted 23 August 2013 Three species of marine Amphipoda, Peramphithoe africana, Varohios serratus and Ceradocus isimangaliso, are described as new to science and an additional 13 species are recorded from South Africa for the first time. Twelve of these new records originate from collecting expeditions to Sodwana Bay in northern KwaZulu-Natal, while one is an introduced species newly recorded from Simon’s Town Harbour. In addition, we collate all additions and revisions to the regional amphipod fauna that have taken place since the last major monographs of each group and produce a comprehensive, updated faunal list for the region. A total of 483 amphipod species are currently recognized from continental South Africa and its Exclusive Economic Zone . Of these, 35 are restricted to freshwater habitats, seven are terrestrial forms, and the remainder either marine or estuarine. The fauna includes 117 members of the suborder Corophiidea, 260 of the suborder Gammaridea, 105 of the suborder Hyperiidea and a single described representative of the suborder Ingolfiellidea. -
Syntopy in Rare Marine Interstitial Crustaceans (Amphipoda, Ingolfiellidae) from Small Coral Islands in the Molucca Sea, Indonesia
Mar Biodiv (2014) 44:163–172 DOI 10.1007/s12526-013-0193-0 ORIGINAL PAPER Syntopy in rare marine interstitial crustaceans (Amphipoda, Ingolfiellidae) from small coral islands in the Molucca Sea, Indonesia Ronald Vonk & Damià Jaume Received: 9 August 2013 /Revised: 19 November 2013 /Accepted: 19 November 2013 /Published online: 10 December 2013 # Senckenberg Gesellschaft für Naturforschung and Springer-Verlag Berlin Heidelberg 2013 Abstract Ingolfiella botoi, a new species of ingolfiellid am- (Stock 1979; Vonk and Schram 2003). Since their discovery phipod, is described in syntopy with the recently described in the frame of the deep-sea Danish ‘Ingolf’ expedition of I. moluccensis from the coarse coral sand interstitial medium 1895-1896 (Hansen 1903), only 48 species—most of them of the Gura Ici Islands (Molucca Sea, Indonesia). The new known from a single or very few specimens—have been taxon is unique among ingolfiellideans in the display of a described (Griffiths 1989, 1991; Vonk and Jaume 2013; multidenticulate unguis on P5–P6. The new species shares Iannilli and Vonk 2013). Locations rendering specimens are most character state resemblances with I. quadridentata Stock often placed widely apart and mainly in the tropics and sub- 1979, from coarse sublittoral sands up to 4 m depth in Curaçao tropics, mostly in interstitial or cave waters. Species ranges are (Leeward Antilles). This is the third record of syntopy among usually stated as reduced except in some cases where large members of this elusive group of stygobiont amphipods. areas have been methodically surveyed. Examples of species with presumed larger ranges than just pinpoint locations in- Keywords Ingolfiella botoi n. -
Two New Amphipod Crustaceans from Anchihaline Caves in Bermuda1)
Crustaceans 53 (1) 1987, E. J. Brill, Leiden TWO NEW AMPHIPOD CRUSTACEANS FROM ANCHIHALINE CAVES IN BERMUDA1) JAN H. STOCK Institute of Taxonomic Zoology, University of Amsterdam, P.O. Box 20125, 1000 HC Amsterdam. The Netherlands BORIS SKET Institut za biologijo, Univerza, p.p. 141, 61001 Ljubljana, Yugoslavia and THOMAS M. ILIFFE Bermuda Biological Station, Ferry Reach GE 01, Bermuda INTRODUCTION The two Amphipoda described in this paper are both rare in the anchihaline2) caves of the Walsingham area in Bermuda (see Sket s~ Iliffe, 1980). The occurrence of a bogidiellid amphipod was already noted by Sket s~ Iliffe, 1.c. The species in question was not described, but referred to as "Bogidiella martini Stock n. ssp." Recent sampling in Bermudian caves, during and after the International Symposium on Marine Caves (October 1984), has yielded some fresh specimens which form the basis for the following description. B. martini, from St. Martin in the Lesser Antilles, is indeed its closest relative, but the nature of the differenes is such that we prefer now to give the Bermudian material full specific rank. The presence of an ingolfiellid was briefly mentioned by Sket, 1979, and by Sket s~ Iliffe, 1980. Only a single specimen was originally collected and no new material has been found during subsequent sampling. The presence of an ingolfiellid in Bermudian cave waters is interesting enough to justify the des- cription of the species involved, even though it is based on a single female only. The ingolfiellids are an old group with a curious distribution pattern (Stock, 1977): (1) some species are bathyal or abyssal; (2) many species occur in inland groundwaters of old continental masses (Europe, Africa, South America); (3) many species occur in coastal groundwaters and interstitial waters. -
Ingolfiella Maldivensis Sp. N. (Crustacea, Amphipoda, Ingolfiellidae) from Coral Reef Sand Off Magoodhoo Island, Maldives
UvA-DARE (Digital Academic Repository) Ingolfiella maldivensis sp. n. (Crustacea, Amphipoda, Ingolfiellidae) from coral reef sand off Magoodhoo island, Maldives Vonk, R.; Jaume, D. DOI 10.3897/zookeys.449.8544 Publication date 2014 Document Version Final published version Published in ZooKeys License CC BY Link to publication Citation for published version (APA): Vonk, R., & Jaume, D. (2014). Ingolfiella maldivensis sp. n. (Crustacea, Amphipoda, Ingolfiellidae) from coral reef sand off Magoodhoo island, Maldives. ZooKeys, 449, 69-79. https://doi.org/10.3897/zookeys.449.8544 General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:24 Sep 2021 A peer-reviewed open-access journal ZooKeys 449: 69–79 (2014)Ingolfiella maldivensis sp. n. (Crustacea, Amphipoda, Ingolfiellidae) 69 doi: 10.3897/zookeys.449.8544 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Ingolfiella maldivensis sp. -
Patterns of Evolution in Gobies (Teleostei: Gobiidae): a Multi-Scale Phylogenetic Investigation
PATTERNS OF EVOLUTION IN GOBIES (TELEOSTEI: GOBIIDAE): A MULTI-SCALE PHYLOGENETIC INVESTIGATION A Dissertation by LUKE MICHAEL TORNABENE BS, Hofstra University, 2007 MS, Texas A&M University-Corpus Christi, 2010 Submitted in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY in MARINE BIOLOGY Texas A&M University-Corpus Christi Corpus Christi, Texas December 2014 © Luke Michael Tornabene All Rights Reserved December 2014 PATTERNS OF EVOLUTION IN GOBIES (TELEOSTEI: GOBIIDAE): A MULTI-SCALE PHYLOGENETIC INVESTIGATION A Dissertation by LUKE MICHAEL TORNABENE This dissertation meets the standards for scope and quality of Texas A&M University-Corpus Christi and is hereby approved. Frank L. Pezold, PhD Chris Bird, PhD Chair Committee Member Kevin W. Conway, PhD James D. Hogan, PhD Committee Member Committee Member Lea-Der Chen, PhD Graduate Faculty Representative December 2014 ABSTRACT The family of fishes commonly known as gobies (Teleostei: Gobiidae) is one of the most diverse lineages of vertebrates in the world. With more than 1700 species of gobies spread among more than 200 genera, gobies are the most species-rich family of marine fishes. Gobies can be found in nearly every aquatic habitat on earth, and are often the most diverse and numerically abundant fishes in tropical and subtropical habitats, especially coral reefs. Their remarkable taxonomic, morphological and ecological diversity make them an ideal model group for studying the processes driving taxonomic and phenotypic diversification in aquatic vertebrates. Unfortunately the phylogenetic relationships of many groups of gobies are poorly resolved, obscuring our understanding of the evolution of their ecological diversity. This dissertation is a multi-scale phylogenetic study that aims to clarify phylogenetic relationships across the Gobiidae and demonstrate the utility of this family for studies of macroevolution and speciation at multiple evolutionary timescales. -
Conservation Assessment for Hoffmaster's Cave Flatworm
Conservation Assessment for Hoffmaster’s Cave Flatworm (Macrocotyla hoffmasteri) (from Kenk, 1975) USDA Forest Service, Eastern Region December 2001 Julian J. Lewis, Ph.D. J. Lewis & Associates, Biological Consulting 217 W. Carter Avenue Clarksville, IN 47129 [email protected] This Conservation Assessment was prepared to compile the published and unpublished information on Macrocotyla hoffmasteri. It does not represent a management decision by the U.S. Forest Service. Though the best scientific information available was used and subject experts were consulted in preparation of this document, it is expected that new information will arise. In the spirit of continuous learning and adaptive management, if you have information that will assist in conserving the subject community and associated taxa, please contact the Eastern Region of the Forest Service Threatened and Endangered Species Program at 310 Wisconsin Avenue, Milwaukee, Wisconsin 53203. Conservation Assessment for Hoffmaster’s Cave Flatworm (Macrocotyla hoffmasteri) 2 Table of Contents EXECUTIVE SUMMARY .......................................................................... 4 NOMENCLATURE AND TAXONOMY .................................................. 4 DESCRIPTION OF SPECIES .................................................................... 4 LIFE HISTORY............................................................................................ 5 HABITAT ...................................................................................................... 5 DISTRIBUTION -
Platyhelminthes: Tricladida: Terricola) of the Australian Region
ResearchOnline@JCU This file is part of the following reference: Winsor, Leigh (2003) Studies on the systematics and biogeography of terrestrial flatworms (Platyhelminthes: Tricladida: Terricola) of the Australian region. PhD thesis, James Cook University. Access to this file is available from: http://eprints.jcu.edu.au/24134/ The author has certified to JCU that they have made a reasonable effort to gain permission and acknowledge the owner of any third party copyright material included in this document. If you believe that this is not the case, please contact [email protected] and quote http://eprints.jcu.edu.au/24134/ Studies on the Systematics and Biogeography of Terrestrial Flatworms (Platyhelminthes: Tricladida: Terricola) of the Australian Region. Thesis submitted by LEIGH WINSOR MSc JCU, Dip.MLT, FAIMS, MSIA in March 2003 for the degree of Doctor of Philosophy in the Discipline of Zoology and Tropical Ecology within the School of Tropical Biology at James Cook University Frontispiece Platydemus manokwari Beauchamp, 1962 (Rhynchodemidae: Rhynchodeminae), 40 mm long, urban habitat, Townsville, north Queensland dry tropics, Australia. A molluscivorous species originally from Papua New Guinea which has been introduced to several countries in the Pacific region. Common. (photo L. Winsor). Bipalium kewense Moseley,1878 (Bipaliidae), 140mm long, Lissner Park, Charters Towers, north Queensland dry tropics, Australia. A cosmopolitan vermivorous species originally from Vietnam. Common. (photo L. Winsor). Fletchamia quinquelineata (Fletcher & Hamilton, 1888) (Geoplanidae: Caenoplaninae), 60 mm long, dry Ironbark forest, Maryborough, Victoria. Common. (photo L. Winsor). Tasmanoplana tasmaniana (Darwin, 1844) (Geoplanidae: Caenoplaninae), 35 mm long, tall open sclerophyll forest, Kamona, north eastern Tasmania, Australia. -
And Peracarida
Contributions to Zoology, 75 (1/2) 1-21 (2006) The urosome of the Pan- and Peracarida Franziska Knopf1, Stefan Koenemann2, Frederick R. Schram3, Carsten Wolff1 (authors in alphabetical order) 1Institute of Biology, Section Comparative Zoology, Humboldt University, Philippstrasse 13, 10115 Berlin, Germany, e-mail: [email protected]; 2Institute for Animal Ecology and Cell Biology, University of Veterinary Medicine Hannover, Buenteweg 17d, D-30559 Hannover, Germany; 3Dept. of Biology, University of Washington, Seattle WA 98195, USA. Key words: anus, Pancarida, Peracarida, pleomeres, proctodaeum, teloblasts, telson, urosome Abstract Introduction We have examined the caudal regions of diverse peracarid and The variation encountered in the caudal tagma, or pancarid malacostracans using light and scanning electronic posterior-most body region, within crustaceans is microscopy. The traditional view of malacostracan posterior striking such that Makarov (1978), so taken by it, anatomy is not sustainable, viz., that the free telson, when present, bears the anus near the base. The anus either can oc- suggested that this region be given its own descrip- cupy a terminal, sub-terminal, or mid-ventral position on the tor, the urosome. In the classic interpretation, the telson; or can be located on the sixth pleomere – even when a so-called telson of arthropods is homologized with free telson is present. Furthermore, there is information that the last body unit in Annelida, the pygidium (West- might be interpreted to suggest that in some cases a telson can heide and Rieger, 1996; Grüner, 1993; Hennig, 1986). be absent. Embryologic data indicates that the condition of the body terminus in amphipods cannot be easily characterized, Within that view, the telson and pygidium are said though there does appear to be at least a transient seventh seg- to not be true segments because both structures sup- ment that seems to fuse with the sixth segment.