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A Hitherto Unnoticed Adaptive Radiation: Epitoniid Species (Gastropoda: Epitoniidae) Associated with Corals (Scleractinia)
Contributions to Zoology, 74 (1/2) 125-203 (2005) A hitherto unnoticed adaptive radiation: epitoniid species (Gastropoda: Epitoniidae) associated with corals (Scleractinia) Adriaan Gittenberger and Edmund Gittenberger National Museum of Natural History, P.O. Box 9517, NL 2300 RA Leiden / Institute of Biology, University Leiden. E-mail: [email protected] Keywords: Indo-Pacific; parasites; coral reefs; coral/mollusc associations; Epitoniidae;Epitonium ; Epidendrium; Epifungium; Surrepifungium; new species; new genera; Scleractinia; Fungiidae; Fungia Abstract E. sordidum spec. nov. ....................................................... 155 Epifungium gen. nov. .............................................................. 157 Twenty-two epitoniid species that live associated with various E. adgranulosa spec. nov. ................................................. 161 hard coral species are described. Three genera, viz. Epidendrium E. adgravis spec. nov. ........................................................ 163 gen. nov., Epifungium gen. nov., and Surrepifungium gen. nov., E. adscabra spec. nov. ....................................................... 167 and ten species are introduced as new to science, viz. Epiden- E. hartogi (A. Gittenberger, 2003) .................................. 169 drium aureum spec. nov., E. sordidum spec. nov., Epifungium E. hoeksemai (A. Gittenberger and Goud, 2000) ......... 171 adgranulosa spec. nov., E. adgravis spec. nov., E. adscabra spec. E. lochi (A. Gittenberger and Goud, 2000) .................. -
(Gastropoda: Cerithiopsidae) from Bocas Del Toro, Panama
Caribbean Journal of Science, Vol. 40, No. 2, 192-197, 2004 Copyright 2004 College of Arts and Sciences University of Puerto Rico, Mayagu¨ez Development of Cerithiopsis gemmulosum (Gastropoda: Cerithiopsidae) from Bocas del Toro, Panama RACHEL COLLIN Smithsonian Tropical Research Institute, Unit 0948, APO AA 34002, USA e-mail: [email protected] ABSTRACT.—The relationships between the seven families in the Ptenoglossa and the relationships be- tween the Ptenoglossa and other gastropod groups have been based on anatomical features associated with feeding, and on developmental characters. However the embryonic development of several of these families remains undescribed. Here I describe the development of Cerithiopsis gemmulosum from Bocas del Toro Province, Panama. This species lives on and lays its thin-walled egg capsules in Halichondria melanadocia sponges. The 79 µm eggs have equal cleavage with a polar lobe. The ciliated “trochophore” stage is followed by an encapsulated veliger which has distinct embryonic kidneys and large granular cells that cover the head vesicle. The black eyes are large and develop early, but there is no pigmented mantle organ. At hatching the brown larval shell is a single whorl and 127 µm long, and each semicircular velar lobe is unpigmented. The velar lobes are equal in size at hatching, but as the shell grows and becomes high-spired the right lobe grows to twice the size of the left lobe. The late larval shell is smooth but has a prominent beak flanked by two distinct notches that fit the velar lobes. After 3 weeks in culture the velum begins to shrink, and larvae with 500 µm shell length metamorphose when exposed to host sponge. -
Marine Mollusca of Isotope Stages of the Last 2 Million Years in New Zealand
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/232863216 Marine Mollusca of isotope stages of the last 2 million years in New Zealand. Part 4. Gastropoda (Ptenoglossa, Neogastropoda, Heterobranchia) Article in Journal- Royal Society of New Zealand · March 2011 DOI: 10.1080/03036758.2011.548763 CITATIONS READS 19 690 1 author: Alan Beu GNS Science 167 PUBLICATIONS 3,645 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Integrating fossils and genetics of living molluscs View project Barnacle Limestones of the Southern Hemisphere View project All content following this page was uploaded by Alan Beu on 18 December 2015. The user has requested enhancement of the downloaded file. This article was downloaded by: [Beu, A. G.] On: 16 March 2011 Access details: Access Details: [subscription number 935027131] Publisher Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37- 41 Mortimer Street, London W1T 3JH, UK Journal of the Royal Society of New Zealand Publication details, including instructions for authors and subscription information: http://www.informaworld.com/smpp/title~content=t918982755 Marine Mollusca of isotope stages of the last 2 million years in New Zealand. Part 4. Gastropoda (Ptenoglossa, Neogastropoda, Heterobranchia) AG Beua a GNS Science, Lower Hutt, New Zealand Online publication date: 16 March 2011 To cite this Article Beu, AG(2011) 'Marine Mollusca of isotope stages of the last 2 million years in New Zealand. Part 4. Gastropoda (Ptenoglossa, Neogastropoda, Heterobranchia)', Journal of the Royal Society of New Zealand, 41: 1, 1 — 153 To link to this Article: DOI: 10.1080/03036758.2011.548763 URL: http://dx.doi.org/10.1080/03036758.2011.548763 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.informaworld.com/terms-and-conditions-of-access.pdf This article may be used for research, teaching and private study purposes. -
Smithsonian Miscellaneous Collections
SMITHSONIAN MISCELLANEOUS COLLECTIOXS. 227 AEEANGEMENT FAMILIES OF MOLLUSKS. PREPARED FOR THE SMITHSONIAN INSTITUTION BY THEODORE GILL, M. D., Ph.D. WASHINGTON: PUBLISHED BY THE SMITHSONIAN INSTITUTION, FEBRUARY, 1871. ^^1 I ADVERTISEMENT. The following list has been prepared by Dr. Theodore Gill, at the request of the Smithsonian Institution, for the purpose of facilitating the arrangement and classification of the Mollusks and Shells of the National Museum ; and as frequent applica- tions for such a list have been received by the Institution, it has been thought advisable to publish it for more extended use. JOSEPH HENRY, Secretary S. I. Smithsonian Institution, Washington, January, 1871 ACCEPTED FOR PUBLICATION, FEBRUARY 28, 1870. (iii ) CONTENTS. VI PAGE Order 17. Monomyaria . 21 " 18. Rudista , 22 Sub-Branch Molluscoidea . 23 Class Tunicata , 23 Order 19. Saccobranchia . 23 " 20. Dactjlobranchia , 24 " 21. Taeniobranchia , 24 " 22. Larvalia , 24 Class Braehiopoda . 25 Order 23. Arthropomata , 25 " . 24. Lyopomata , 26 Class Polyzoa .... 27 Order 25. Phylactolsemata . 27 " 26. Gymnolseraata . 27 " 27. Rhabdopleurse 30 III. List op Authors referred to 31 IV. Index 45 OTRODUCTIO^. OBJECTS. The want of a complete and consistent list of the principal subdivisions of the mollusks having been experienced for some time, and such a list being at length imperatively needed for the arrangement of the collections of the Smithsonian Institution, the present arrangement has been compiled for that purpose. It must be considered simply as a provisional list, embracing the results of the most recent and approved researches into the systematic relations and anatomy of those animals, but from which innova- tions and peculiar views, affecting materially the classification, have been excluded. -
Mollusc Fauna of Iskenderun Bay with a Checklist of the Region
www.trjfas.org ISSN 1303-2712 Turkish Journal of Fisheries and Aquatic Sciences 12: 171-184 (2012) DOI: 10.4194/1303-2712-v12_1_20 SHORT PAPER Mollusc Fauna of Iskenderun Bay with a Checklist of the Region Banu Bitlis Bakır1, Bilal Öztürk1*, Alper Doğan1, Mesut Önen1 1 Ege University, Faculty of Fisheries, Department of Hydrobiology Bornova, Izmir. * Corresponding Author: Tel.: +90. 232 3115215; Fax: +90. 232 3883685 Received 27 June 2011 E-mail: [email protected] Accepted 13 December 2011 Abstract This study was performed to determine the molluscs distributed in Iskenderun Bay (Levantine Sea). For this purpose, the material collected from the area between the years 2005 and 2009, within the framework of different projects, was investigated. The investigation of the material taken from various biotopes ranging at depths between 0 and 100 m resulted in identification of 286 mollusc species and 27542 specimens belonging to them. Among the encountered species, Vitreolina cf. perminima (Jeffreys, 1883) is new record for the Turkish molluscan fauna and 18 species are being new records for the Turkish Levantine coast. A checklist of Iskenderun mollusc fauna is given based on the present study and the studies carried out beforehand, and a total of 424 moluscan species are known to be distributed in Iskenderun Bay. Keywords: Levantine Sea, Iskenderun Bay, Turkish coast, Mollusca, Checklist İskenderun Körfezi’nin Mollusca Faunası ve Bölgenin Tür Listesi Özet Bu çalışma İskenderun Körfezi (Levanten Denizi)’nde dağılım gösteren Mollusca türlerini tespit etmek için gerçekleştirilmiştir. Bu amaçla, 2005 ve 2009 yılları arasında sürdürülen değişik proje çalışmaları kapsamında bölgeden elde edilen materyal incelenmiştir. -
Caenogastropoda
13 Caenogastropoda Winston F. Ponder, Donald J. Colgan, John M. Healy, Alexander Nützel, Luiz R. L. Simone, and Ellen E. Strong Caenogastropods comprise about 60% of living Many caenogastropods are well-known gastropod species and include a large number marine snails and include the Littorinidae (peri- of ecologically and commercially important winkles), Cypraeidae (cowries), Cerithiidae (creep- marine families. They have undergone an ers), Calyptraeidae (slipper limpets), Tonnidae extraordinary adaptive radiation, resulting in (tuns), Cassidae (helmet shells), Ranellidae (tri- considerable morphological, ecological, physi- tons), Strombidae (strombs), Naticidae (moon ological, and behavioral diversity. There is a snails), Muricidae (rock shells, oyster drills, etc.), wide array of often convergent shell morpholo- Volutidae (balers, etc.), Mitridae (miters), Buccin- gies (Figure 13.1), with the typically coiled shell idae (whelks), Terebridae (augers), and Conidae being tall-spired to globose or fl attened, with (cones). There are also well-known freshwater some uncoiled or limpet-like and others with families such as the Viviparidae, Thiaridae, and the shells reduced or, rarely, lost. There are Hydrobiidae and a few terrestrial groups, nota- also considerable modifi cations to the head- bly the Cyclophoroidea. foot and mantle through the group (Figure 13.2) Although there are no reliable estimates and major dietary specializations. It is our aim of named species, living caenogastropods are in this chapter to review the phylogeny of this one of the most diverse metazoan clades. Most group, with emphasis on the areas of expertise families are marine, and many (e.g., Strombidae, of the authors. Cypraeidae, Ovulidae, Cerithiopsidae, Triphori- The fi rst records of undisputed caenogastro- dae, Olividae, Mitridae, Costellariidae, Tereb- pods are from the middle and upper Paleozoic, ridae, Turridae, Conidae) have large numbers and there were signifi cant radiations during the of tropical taxa. -
Influence of Ecological Role on Bathymetric Patterns of Deep-Sea Species: Size Clines in Parasitic Gastropods
MARINE ECOLOGY PROGRESS SERIES Vol. 320: 161–167, 2006 Published August 29 Mar Ecol Prog Ser Influence of ecological role on bathymetric patterns of deep-sea species: size clines in parasitic gastropods Craig R. McClain1, 3,*, Jennifer Crouse2 1Department of Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA 2Department of Biology, University of Massachusetts, 100 Morrissey Blvd., Boston, Massachusetts 02125, USA 3Present address: Monterey Bay Aquarium Research Institute (MBARI), 7700 Sandholdt Road, Moss Landing, California 95039, USA ABSTRACT: How an organism’s phenotype responds to both its biotic and abiotic environment is a complex interplay of selection pressures and adaptive tradeoffs. Bathymetric patterns of body size in deep-sea organisms should also reflect both ecological role and taxon-specific constraints, as exem- plified in a variety of recent studies. Here, we examine bathymetric size clines in deep-sea ectopara- sites, a group that has received little attention in the literature compared to other deep-sea groups. Specifically, we focus on body size in 3 families (21 species) of ptenoglossate gastropods from the deep western North Atlantic, conducting analyses both within and among species. Both quantile and linear regression models yielded non-significant relationships for body size and depth for the 3 most abundant species. Two of the 3 families exhibited positive size–depth relationships, but only in mean size. The findings indicate that resource availability/host size may control parasite density, but dis- lodgement and predation risk may set a hard upper boundary on body size in deep-sea ectoparasites. Moreover, this study stresses the necessity of understanding the ecological role of species in investi- gating body size trends. -
Moluscos - Filo MOLLUSCA
Moluscos - Filo MOLLUSCA. Lista de especies registradas para Cuba (octubre de 2006). José Espinosa Sáez Instituto de Oceanología, Ave 1ª No. 18406, Playa, Ciudad de La Habana, C.P. 11200, Cuba [email protected] Zonas biogeográficas: (1) Zona suroriental – Costa sur de Oriente, (2) Zona surcentral - Archipiélago Jardines de la Reina, (3) Zona sur central - Costa al sur del Macizo de Guamuhaya, (4) Zona suroccidental - Golfo de Batabanó y Archipiélago de los, (5) Canarreos, (6) Zona suroccidental - Península de Guanahacabibes, (7) Zona noroccidental - Archipiélago de Los Colorados, (8) Zona noroccidental - Norte Habana-Matanzas, (9) Zona norte-central - Archipiélago Sabana - Camagüey, (10) Zona norte-oriental - Costa norte de Oriente Abreviaturas Especies Bioegiones Cu Pl Oc 1 2 3 4 5 6 7 8 9 Clase APLACOPHORA Subclase SOLENOGASTRES Orden CAVIBELONIA Familia Proneomeniidae Género Proneomenia Hubrecht, 1880 Proneomenia sp . R x Clase POLYPLACOPHORA Orden NEOLORICATA Suborden ISCHNOCHITONINA Familia Ischnochitonidae Subfamilia ISCHNOCHITONINAE Género Ischnochiton Gray, 1847 Ischnochiton erythronotus (C. B. Adams, 1845) C C C C C C C C x Ischnochiton papillosus (C. B. Adams, 1845) Nc Nc x Ischnochiton striolatus (Gray, 1828) Nc Nc Nc Nc x Género Ischnoplax Carpenter in Dall, 1879 x Ischnoplax pectinatus (Sowerby, 1832) C C C C C C C C x Género Stenoplax Carpenter in Dall, 1879 x Stenoplax bahamensis Kaas y Belle, 1987 R R x Stenoplax purpurascens (C. B. Adams, 1845) C C C C C C C C x Stenoplax boogii (Haddon, 1886) R R R R x Subfamilia CALLISTOPLACINAE Género Callistochiton Carpenter in Dall, 1879 x Callistochiton shuttleworthianus Pilsbry, 1893 C C C C C C C C x Género Ceratozona Dall, 1882 x Ceratozona squalida (C. -
ELENCO SISTEMATICO SCAPHOPODA , Forum
MANCOLISTA 10 Famiglia LEPIDOPLEURIDAE 1 30 Lepidopleurus (Leptochiton) asellus (Gmelin, 1791) 1 50 Lepidopleurus (Leptochiton) bedullii (Dell'Angelo & Palazzi, 1986) 1 60 Lepidopleurus (Leptochiton) cancellatus (Sowerby G.B.II, 1840) 1 80 Lepidopleurus (Leptochiton) geronensis (Kaas & Van Belle, 1985) 1 90 Lepidopleurus (Leptochiton) pepezamorai Carmona Zalvide, Urgorri & Garcia, 2004 1 100 Lepidopleurus (Lepidochitona) sarsi Kaas, 1981 1 120 Lepidopleurus (Leptochiton) xanthus (Kaas & van Belle, 1990) 1 130 Lepidopleurus (Parachiton) africanus Nierstrasz, 1906 140 Famiglia HANLEYIIDAE 1 150 Hanleya hanleyi (Bean in Thorpe, 1844) 160 Famiglia BATYCHITONIDAE 1 170 Bathychiton biondii Dell'Angelo & Palazzi, 1988 180 Famiglia ISCHNOCHITONIDAE 1 200 Ischnochiton (Ischnochiton) usticensis Dell'Angelo & Castriota, 1999 1 210 Ischnochiton (Stenosemus) dolii Van Belle & Dell'Angelo, 1998 1 220 Ischnochiton (Stenosemus) exaratus (Sars G.O., 1878) 1 230 Ischnochiton (Stenosemus) vanbellei Kaas, 1985 1 240 Ischnochiton (Haploplax) tsekosi Athanasios Koukouras & Par. Karachle, 2004 1 250 Callistochiton (Allerychiton) pachylasmae (Monterosato, 1878) 1 260 Callochiton calcatus Dell'Angelo & Palazzi, 1994 1 280 Lepidochitona (L.) canariensis (Thiele, 1909) 1 300 Lepidochitona (L.) cinerea (Linné, 1767) 1 310 Lepidochitona (L.) furtiva (Monterosato, 1879) 1 320 Lepidochitona (L.) kaasi Carmona Zaldive & García, 2000 1 330 Lepidochitona (L.) monterosatoi Kaas & Van Belle, 1981 1 340 Lepidochitona (L.) severianoi Carmona Zaldive & García, 2000 360 Famiglia CHITONIDAE 1 400 Chiton (Tegulaplax) hululensis (Smith E.A. in Gardiner, 1903) 560 Famiglia LEPETIDAE 1 590 Propilidium pertenue Jeffreys, 1883 1 600 Propilidium scabrosum Jeffreys, 1883 610 Famiglia COCCULINIDAE 1 620 Coccopigya spinigera (Jeffreys, 1883) 1 630 Coccopigya viminensis (Rocchini, 1990) 640 Famiglia BATHYSCIADIIDAE 1 650 Bathysciadium xylophagum Warén & Carrozza in Warén, 1996 1 660 Bathysciadium sp. -
Evolution, Distribution, and Phylogenetic Clumping of a Repeated Gastropod Innovation
Zoological Journal of the Linnean Society, 2017, 180, 732–754. With 5 figures. The varix: evolution, distribution, and phylogenetic clumping of a repeated gastropod innovation NICOLE B. WEBSTER1* and GEERAT J. VERMEIJ2 1Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9 2Department of Earth and Planetary Sciences, University of California, Davis, CA 95616, USA Received 27 June 2016; revised 4 October 2016; accepted for publication 25 October 2016 A recurrent theme in evolution is the repeated, independent origin of broadly adaptive, architecturally and function- ally similar traits and structures. One such is the varix, a shell-sculpture innovation in gastropods. This periodic shell thickening functions mainly to defend the animal against shell crushing and peeling predators. Varices can be highly elaborate, forming broad wings or spines, and are often aligned in synchronous patterns. Here we define the different types of varices, explore their function and morphological variation, document the recent and fossil distri- bution of varicate taxa, and discuss emergent patterns of evolution. We conservatively found 41 separate origins of varices, which were concentrated in the more derived gastropod clades and generally arose since the mid-Mesozoic. Varices are more prevalent among marine, warm, and shallow waters, where predation is intense, on high-spired shells and in clades with collabral ribs. Diversification rates were correlated in a few cases with the presence of varices, especially in the Muricidae and Tonnoidea, but more than half of the origins are represented by three or fewer genera. Varices arose many times in many forms, but generally in a phylogenetically clumped manner (more frequently in particular higher taxa), a pattern common to many adaptations. -
Results of the Rumphius Biohistorical Expedition to Ambon (1990) Part 2. an Unusual Triphorid (Mollusca: Gastropoda) from the Mo
Results of the Rumphius Biohistorical Expedition to Ambon (1990) Part 2. An unusual triphorid (Mollusca: Gastropoda) from the Moluccas, Indonesia B.A. Marshall Marshall, B.A. Results of the Rumphius Biohistorical Expedition to Ambon (1990). Part 2. An unusual triphorid (Mollusca: Gastropoda from the Moluccas, Indonesia. Zool. Med. Leiden 68 (4), 15.vii.1994: 39-43, figs. 1-6.— ISSN 0024-0672 B.A. Marshall, Museum of New Zealand Te Papa Tongarewa, P.O. Box 467, Wellington, New Zealand. Key words: Gastropoda, Triphoridae, new subgenus, Ambon, Indonesia. Costatophora is introduced as a new subgenus of Tetraphora Laseron, 1958 for Triforis seranus P.J. Fischer, 1927, a triphorid with distinctive teleoconch sculpture and radular morphology. Introduction The present contribution was initiated during a visit to Leiden in 1992 when I was invited by Mr Hermann Strack to view the Rumphius Biohistorical Expedition (1990) collections at the Nationaal Natuurhistorisch Museum (RMNH). A triphorid from Ambon drew my immediate attention because its sculpture was predominantly axial instead of reticulate as in the majority of the 500 or more living species of Triphoridae. A search of the literature revealed that it is probably conspecific with Triforis seranus RJ. Fischer, 1927, described as a Pliocene fossil from adjacent Seram (Seran or Ceram) Island, and hitherto unrecorded from the Recent fauna. Systematics Order Neotaenioglossa Haller, 1882 Suborder Ptenoglossa Gray, 1853 Superfamily Triphoroidea Gray, 1847 Family Triphoridae Gray, 1847 Subfamily Triphorinae Gray, 1847 Genus Tetraphora Laseron, 1958 Tetraphora Laseron, 1958: 625. Type species (by original designation): Tetraphora mapoonensis Laseron, 1958; Recent: Queensland. 40 Marshall. An unusual triphorid from the Moluccas. -
New Gastropod Records for the Eastern Mediterranean Sea and One New
Manousis and Galinou-Mitsoudi Journal of Biological Research-Thessaloniki 2014, 21:20 http://www.jbiolres.com/content/21/1/20 RESEARCH Open Access New gastropod records for the Eastern Mediterranean Sea and one new alien (Emarginula decorata Deshayes, 1863) for the Mediterranean Sea from NW Aegean Sea, Greece Thanasis Manousis1† and Sofia Galinou-Mitsoudi2*† Abstract Background: The NW Aegean Sea has a complex topography, high quality waters, oligotrophic to eutrophic conditions, is connected with estuaries and wetlands, is of high ecological interest, harbours all the types of human activities and yet few researchers work on its marine biodiversity. With this study, the contribution to the knowledge of the Hellenic and Eastern Mediterranean gastropod biodiversity of the studied families is continued, and an expansion of the search in other substrates and deeper waters of the NW Aegean Sea with emphasis on the minor in size species during the period from October 2008 to January 2014. Results: Thirty seven species belonging to seven families (Cerithiopsidae, Fissurellidae, Phasianellidae, Scissurellidae, Siliquariidae, Skeneidae, and Triphoridae) were identified and their biodiversity was compared with the current checklists of marine gastropod molluscs for the Hellenic Seas based on previous surveys. In this collection of gastropods, one species (Emarginula decorata Deshayes, 1863) is a new alien for the Mediterranean Sea, 14 species are new for the Eastern Mediterranean Sea and 16 species are new for the Hellenic fauna (with the one above mentioned alien species included). The main identification characteristics and ecological information such as habitat, distribution, alien expansion paths to the NW Aegean Sea and origin of the species are given and discussed.