First Finding of Diffalaba Vitrea (Sowerby III, 1915) (Gastropoda
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National Monitoring Program for Biodiversity and Non-Indigenous Species in Egypt
UNITED NATIONS ENVIRONMENT PROGRAM MEDITERRANEAN ACTION PLAN REGIONAL ACTIVITY CENTRE FOR SPECIALLY PROTECTED AREAS National monitoring program for biodiversity and non-indigenous species in Egypt PROF. MOUSTAFA M. FOUDA April 2017 1 Study required and financed by: Regional Activity Centre for Specially Protected Areas Boulevard du Leader Yasser Arafat BP 337 1080 Tunis Cedex – Tunisie Responsible of the study: Mehdi Aissi, EcApMEDII Programme officer In charge of the study: Prof. Moustafa M. Fouda Mr. Mohamed Said Abdelwarith Mr. Mahmoud Fawzy Kamel Ministry of Environment, Egyptian Environmental Affairs Agency (EEAA) With the participation of: Name, qualification and original institution of all the participants in the study (field mission or participation of national institutions) 2 TABLE OF CONTENTS page Acknowledgements 4 Preamble 5 Chapter 1: Introduction 9 Chapter 2: Institutional and regulatory aspects 40 Chapter 3: Scientific Aspects 49 Chapter 4: Development of monitoring program 59 Chapter 5: Existing Monitoring Program in Egypt 91 1. Monitoring program for habitat mapping 103 2. Marine MAMMALS monitoring program 109 3. Marine Turtles Monitoring Program 115 4. Monitoring Program for Seabirds 118 5. Non-Indigenous Species Monitoring Program 123 Chapter 6: Implementation / Operational Plan 131 Selected References 133 Annexes 143 3 AKNOWLEGEMENTS We would like to thank RAC/ SPA and EU for providing financial and technical assistances to prepare this monitoring programme. The preparation of this programme was the result of several contacts and interviews with many stakeholders from Government, research institutions, NGOs and fishermen. The author would like to express thanks to all for their support. In addition; we would like to acknowledge all participants who attended the workshop and represented the following institutions: 1. -
ED45E Rare and Scarce Species Hierarchy.Pdf
104 Species 55 Mollusc 8 Mollusc 334 Species 181 Mollusc 28 Mollusc 44 Species 23 Vascular Plant 14 Flowering Plant 45 Species 23 Vascular Plant 14 Flowering Plant 269 Species 149 Vascular Plant 84 Flowering Plant 13 Species 7 Mollusc 1 Mollusc 42 Species 21 Mollusc 2 Mollusc 43 Species 22 Mollusc 3 Mollusc 59 Species 30 Mollusc 4 Mollusc 59 Species 31 Mollusc 5 Mollusc 68 Species 36 Mollusc 6 Mollusc 81 Species 43 Mollusc 7 Mollusc 105 Species 56 Mollusc 9 Mollusc 117 Species 63 Mollusc 10 Mollusc 118 Species 64 Mollusc 11 Mollusc 119 Species 65 Mollusc 12 Mollusc 124 Species 68 Mollusc 13 Mollusc 125 Species 69 Mollusc 14 Mollusc 145 Species 81 Mollusc 15 Mollusc 150 Species 84 Mollusc 16 Mollusc 151 Species 85 Mollusc 17 Mollusc 152 Species 86 Mollusc 18 Mollusc 158 Species 90 Mollusc 19 Mollusc 184 Species 105 Mollusc 20 Mollusc 185 Species 106 Mollusc 21 Mollusc 186 Species 107 Mollusc 22 Mollusc 191 Species 110 Mollusc 23 Mollusc 245 Species 136 Mollusc 24 Mollusc 267 Species 148 Mollusc 25 Mollusc 270 Species 150 Mollusc 26 Mollusc 333 Species 180 Mollusc 27 Mollusc 347 Species 189 Mollusc 29 Mollusc 349 Species 191 Mollusc 30 Mollusc 365 Species 196 Mollusc 31 Mollusc 376 Species 203 Mollusc 32 Mollusc 377 Species 204 Mollusc 33 Mollusc 378 Species 205 Mollusc 34 Mollusc 379 Species 206 Mollusc 35 Mollusc 404 Species 221 Mollusc 36 Mollusc 414 Species 228 Mollusc 37 Mollusc 415 Species 229 Mollusc 38 Mollusc 416 Species 230 Mollusc 39 Mollusc 417 Species 231 Mollusc 40 Mollusc 418 Species 232 Mollusc 41 Mollusc 419 Species 233 -
Revision of the Systematic Position of Lindbergia Garganoensis
Revision of the systematic position of Lindbergia garganoensis Gittenberger & Eikenboom, 2006, with reassignment to Vitrea Fitzinger, 1833 (Gastropoda, Eupulmonata, Pristilomatidae) Gianbattista Nardi Via Boschette 8A, 25064 Gussago (Brescia), Italy; [email protected] [corresponding author] Antonio Braccia Via Ischia 19, 25100 Brescia, Italy; [email protected] Simone Cianfanelli Museum System of University of Florence, Zoological Section “La Specola”, Via Romana 17, 50125 Firenze, Italy; [email protected] & Marco Bodon c/o Museum System of University of Florence, Zoological Section “La Specola”, Via Romana 17, 50125 Firenze, Italy; [email protected] Nardi, G., Braccia, A., Cianfanelli, S. & Bo- INTRODUCTION don, M., 2019. Revision of the systematic position of Lindbergia garganoensis Gittenberger & Eiken- Lindbergia garganoensis Gittenberger & Eikenboom, 2006 boom, 2006, with reassignment to Vitrea Fitzinger, is the first species of the genus, Lindbergia Riedel, 1959 to 1833 (Gastropoda, Eupulmonata, Pristilomatidae). be discovered in Italy. The genus Lindbergia encompasses – Basteria 83 (1-3): 19-28. Leiden. Published 6 April 2019 about ten different species, endemic to the Greek mainland, Crete, the Cycladic islands, Dodecanese islands, northern Aegean islands, and southern Turkey (Riedel, 1992, 1995, 2000; Welter-Schultes, 2012; Bank & Neubert, 2017). Due to Lindbergia garganoensis Gittenberger & Eikenboom, 2006, lack of anatomical data, some of these species remain ge- a taxon with mainly a south-Balkan distribution, is the only nerically questionable. Up to now, L. garganoensis was only Italian species assigned to the genus Lindbergia Riedel, 1959. known by the presence of very fine spiral striae on the tel- The assignment to this genus, as documented by the pecu- eoconch and by the general shape of its shell. -
Pelagic Sargassum Community Change Over a 40-Year Period: Temporal and Spatial Variability
Mar Biol (2014) 161:2735–2751 DOI 10.1007/s00227-014-2539-y ORIGINAL PAPER Pelagic Sargassum community change over a 40-year period: temporal and spatial variability C. L. Huffard · S. von Thun · A. D. Sherman · K. Sealey · K. L. Smith Jr. Received: 20 May 2014 / Accepted: 3 September 2014 / Published online: 14 September 2014 © The Author(s) 2014. This article is published with open access at Springerlink.com Abstract Pelagic forms of the brown algae (Phaeo- ranging across the Sargasso Sea, Gulf Stream, and south phyceae) Sargassum spp. and their conspicuous rafts are of the subtropical convergence zone. Recent samples also defining characteristics of the Sargasso Sea in the western recorded low coverage by sessile epibionts, both calcifying North Atlantic. Given rising temperatures and acidity in forms and hydroids. The diversity and species composi- the surface ocean, we hypothesized that macrofauna asso- tion of macrofauna communities associated with Sargas- ciated with Sargassum in the Sargasso Sea have changed sum might be inherently unstable. While several biological with respect to species composition, diversity, evenness, and oceanographic factors might have contributed to these and sessile epibiota coverage since studies were con- observations, including a decline in pH, increase in sum- ducted 40 years ago. Sargassum communities were sam- mer temperatures, and changes in the abundance and distri- pled along a transect through the Sargasso Sea in 2011 and bution of Sargassum seaweed in the area, it is not currently 2012 and compared to samples collected in the Sargasso possible to attribute direct causal links. Sea, Gulf Stream, and south of the subtropical conver- gence zone from 1966 to 1975. -
THE LISTING of PHILIPPINE MARINE MOLLUSKS Guido T
August 2017 Guido T. Poppe A LISTING OF PHILIPPINE MARINE MOLLUSKS - V1.00 THE LISTING OF PHILIPPINE MARINE MOLLUSKS Guido T. Poppe INTRODUCTION The publication of Philippine Marine Mollusks, Volumes 1 to 4 has been a revelation to the conchological community. Apart from being the delight of collectors, the PMM started a new way of layout and publishing - followed today by many authors. Internet technology has allowed more than 50 experts worldwide to work on the collection that forms the base of the 4 PMM books. This expertise, together with modern means of identification has allowed a quality in determinations which is unique in books covering a geographical area. Our Volume 1 was published only 9 years ago: in 2008. Since that time “a lot” has changed. Finally, after almost two decades, the digital world has been embraced by the scientific community, and a new generation of young scientists appeared, well acquainted with text processors, internet communication and digital photographic skills. Museums all over the planet start putting the holotypes online – a still ongoing process – which saves taxonomists from huge confusion and “guessing” about how animals look like. Initiatives as Biodiversity Heritage Library made accessible huge libraries to many thousands of biologists who, without that, were not able to publish properly. The process of all these technological revolutions is ongoing and improves taxonomy and nomenclature in a way which is unprecedented. All this caused an acceleration in the nomenclatural field: both in quantity and in quality of expertise and fieldwork. The above changes are not without huge problematics. Many studies are carried out on the wide diversity of these problems and even books are written on the subject. -
List of the Shells of Cuba in the . . . Museum
£> • £!~ - ? -6 LIST / OF THE SHELLS OF CUBA THE COLLECTION OF THE BRITISH MUSEUM, & BY M. RAMON DE LA SAGRA. DESCRIBED BY Prof. ALCIDE D’ORBIGNY, In the “ Histoire de l’lle de Cuba.” LONDON: PRINTED BY ORDER OF THE TRUSTEES. 1854. PRINTED BY TAYEOR AND FRANCIS, RED LION COUkT, FLEET STREET. PREP AC E. The specimens of Shells in the following list marked B.M. were received from Professor Alcide d’Orbigny, as the type specimens described by him in the Mollusca part of the “ Histoire physique, politique et naturelle de Pile de Cuba, par M. Ramon de la Sagra, Directeur du Jardin botanique de la Havane, Correspondant de Plnstitut Royal de France.” Paris, 8 vo, with a folio Atlas. The specimens are on their original cartoons, named by M. d’Orbigny, and marked with their special habitats. JGPIN EDWARD GRAY. Sept. 1, 1854. LIST OF THE SHELLS OF CUBA. Class I. CEPHALOPODA CRYPTODIBRANCHIATA. Order I. ACETABULIEERA. Suborder I. Octopoda. Fam. 1. OCTOPID^L 1. Octopus vulgaris, Linn., Ramon de la Sagra , Moll. 11. t. l.f. 1. Sepia octopodia, Linn. Polypus octopodia, Leach, Octopus appendiculatus, Blainv. 2. Octopus tuberculatus, Blainv ., Ramon de la Sagra, Moll. 15. Octopus ruber, Rajinq.l B . 2 SHELLS OF CUBA. 3. Octopus rugosus, d’Orb., Ramon de la Sagra, Moll. 18. Sepia rugosa, Bose. Octopus granulatus, Ramie. Sepia granulosa, Bose. Octopus Bakeri, Feruss Octopus americanus, Blainv. 4. Philonexis Quoyanus, d’Orb., Ramon de la Sagra , Hist, de Cuba3 21. 5. Argonauta Argo, Linn., Sagra3 Cuba , 24. Ocythoe tuberculata, Rafinq. Ocythoe antiquorum, Leach. Octopus antiquorum, Blainv. -
Memorial to Katherine Van Winkle Palmer 1895-1982 KENNETH E
Memorial to Katherine Van Winkle Palmer 1895-1982 KENNETH E. CASTER Department o f Geology, University o f Cincinnati, Cincinnati, OH 45221-0013 Katherine (Evangeline Hilton) Van Winkle Palmer, illustrious Tertiary paleontologist and long-time (1952— 1978) director and Life Trustee of the Paleontological Research Institution, died on September 12, 1982. In November a memorial service was held at the Dewitt Historical Society of Tompkins County, Ithaca, New York. At that time her notable career in scientific, academic, and civic affairs was celebrated. She was the widow of Ephraim Laurence Palmer, famous professor of nature study at Cornell University. Their son Robin survives her. Katherine was the lineal descendant of Jacob Walingen Van Winkle who came to New Amsterdam in 1634. He was one of the “First Twelve Men” who helped form the first official representative body of New York and New Jersey in 1641. Eph’s earliest American ancestor was a founder of the Massachusetts Bay Colony in 1629. I first knew Katherine as a paleontologist 300 years after Ephraim’s ancestor landed, but I had known Eph as my scout master for about ten years by then. Katherine was the senior paleontologist in the well-known paleontological laboratory of G. D. Harris at Cornell University when I first made her acquaintance as a scientist; her widely known doctoral study on veneracean lamellibranchs (1927, 1929) was an example to emulate for all of us aspiring students of paleontology. As Harris often remarked. “After God made Katherine. He broke the mold.” Katherine Palmer’s paleontological career began at the University of Washington (B.S., 1918) under the inspiring teaching of Charles E. -
The Journal of Molluscan Studies
Downloaded from https://academic.oup.com/mollus/issue/55/1 by guest on 30 September 2021 The Journal of Molluscan Studies Edited by J. Taylor INDEX FOR VOLUME 55 1989 Downloaded from https://academic.oup.com/mollus/issue/55/1 by guest on 30 September 2021 Contents for Volume 55, 1989 Journal of Molluscan Studies VOLUME 55, 1989 Part 1, pp. 1-147 (published 3 March 1989) Part 2, pp. 149-311 (published 10 May 1989) Part 3, pp. 313-^*29 (published 10 August 1989) Part 4, pp. 431-553 (published 1 November 1989) CONTENTS page AGUIRRE, A., see VICARIO et al. ALLANSON, B.R., see VILLIERS & ALLANSON Downloaded from https://academic.oup.com/mollus/issue/55/1 by guest on 30 September 2021 BAILEY, S.E.R. Foraging behaviour of terrestrial gastropods: integrating field and labora- tory studies 263 BARKAI, A. & BRANCH, G.M. Growth and mortality of the mussels Choromytilus meridionalis (Krauss) and Aulacomya ater (Molina) as indicators of biotic conditions 329 BAUR, B. Growth and reproduction of the minute land snail Punctum pygmaeum (Drapamaud) 383 BERNARD, R.T.F., see HODGSON & BERNARD BERRY, A.J. Spawning season and egg production in Forth estuary Retusa obtusa (Opisthobranchia: Retusidae) 455 BODE, A. Production of the intertidal chiton Acanlhochitona crinita within a community of CoraUina tlongato (Rhodophyta) 37 BOUCHET, P. A review of poecilogony in gastropods 67 BOUKRAA, A., see GOMOT et al. BRANCH, G.M., see BARKAI & BRANCH BRONMARK, C. Interactions between epiphytes, macrophytes and freshwater snails: a review 299 BROWN, A.C., see TRUEMAN & BROWN BROWN, A.C., see VAN W1JK et al. -
Malacologia, 1993, 35(2); 261-313
^;^2_ MALACOLOGIA, 1993, 35(2); 261-313 PHYLOGENETIC RELATIONSHIPS AND GENERIC REVIEW OF THE BITTIINAE (PROSOBRANCHIA: GERITHIOIDEA) Richard S. Houbrick Department of Invertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20560, U.S.A. ABSTRACT The anatomy of seven members of the Bittium group is described, clarifying the status of the genus-level taxa comprising it. Bittium reticulatum, the type species of Bittium Gray, is described in depth, thereby establishing criteria for comparisons with other taxa of Bitliinae. The type species of Stylidium Dell and LirobiWum Bartsch, and representatives of Bittiolum Cossmann and Cacozeliana Strand are examined and compared with Bittium, s.s. Results of anatomical studies and a phylogenetic analysis using the Hennig86 and CLADOS programs, with Cehtt)ium as an outgroup, establish monophyly for Bitliinae Cossmann and reveal six different genus-level taxa. A new genus, ittibittium, from the Indo-Pacific, is proposed. Synonymies of each genus- level taxon and representative species examined are presented. Brief accounts of the ecology and zoogeography of each taxon are given. Two taxa formerly attributed to the 6/ff/um-group are herein excluded from it and referred to Cerithium Bruguière. These are Cerithium zebrum Kiener, 1841, and Cerithium boeticum Pease, 1861. The subfamily Bittiinae Cossmann, 1906, is thought to comprise nine genera (four of which were not included in phylogenetic analyses) : Bittium Gray, 1847; Bittiolum Cossmann, 1906; Ittibittium gen. n., Stylidium Dalí, 1907; Lirobit- tium Bartsch, 1911 ; Cacozeliana Strand, 1928; Argyropeza Melvill & Standen, 1901 ; Varicopeza Gründel, 1976; Zebittium Finlay, 1927. The genus Cassiella Gofas, 1987, of uncertain place- ment, is included as a possible member of the group. -
An Annotated Checklist of the Marine Macroinvertebrates of Alaska David T
NOAA Professional Paper NMFS 19 An annotated checklist of the marine macroinvertebrates of Alaska David T. Drumm • Katherine P. Maslenikov Robert Van Syoc • James W. Orr • Robert R. Lauth Duane E. Stevenson • Theodore W. Pietsch November 2016 U.S. Department of Commerce NOAA Professional Penny Pritzker Secretary of Commerce National Oceanic Papers NMFS and Atmospheric Administration Kathryn D. Sullivan Scientific Editor* Administrator Richard Langton National Marine National Marine Fisheries Service Fisheries Service Northeast Fisheries Science Center Maine Field Station Eileen Sobeck 17 Godfrey Drive, Suite 1 Assistant Administrator Orono, Maine 04473 for Fisheries Associate Editor Kathryn Dennis National Marine Fisheries Service Office of Science and Technology Economics and Social Analysis Division 1845 Wasp Blvd., Bldg. 178 Honolulu, Hawaii 96818 Managing Editor Shelley Arenas National Marine Fisheries Service Scientific Publications Office 7600 Sand Point Way NE Seattle, Washington 98115 Editorial Committee Ann C. Matarese National Marine Fisheries Service James W. Orr National Marine Fisheries Service The NOAA Professional Paper NMFS (ISSN 1931-4590) series is pub- lished by the Scientific Publications Of- *Bruce Mundy (PIFSC) was Scientific Editor during the fice, National Marine Fisheries Service, scientific editing and preparation of this report. NOAA, 7600 Sand Point Way NE, Seattle, WA 98115. The Secretary of Commerce has The NOAA Professional Paper NMFS series carries peer-reviewed, lengthy original determined that the publication of research reports, taxonomic keys, species synopses, flora and fauna studies, and data- this series is necessary in the transac- intensive reports on investigations in fishery science, engineering, and economics. tion of the public business required by law of this Department. -
Florida Keys Species List
FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P. -
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.