New Alien Mediterranean Biodiversity Records (March 2020)
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High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project
High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project AEA Technology, Environment Contract: W/35/00632/00/00 For: The Department of Trade and Industry New & Renewable Energy Programme Report issued 30 August 2002 (Version with minor corrections 16 September 2002) Keith Hiscock, Harvey Tyler-Walters and Hugh Jones Reference: Hiscock, K., Tyler-Walters, H. & Jones, H. 2002. High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project. Report from the Marine Biological Association to The Department of Trade and Industry New & Renewable Energy Programme. (AEA Technology, Environment Contract: W/35/00632/00/00.) Correspondence: Dr. K. Hiscock, The Laboratory, Citadel Hill, Plymouth, PL1 2PB. [email protected] High level environmental screening study for offshore wind farm developments – marine habitats and species ii High level environmental screening study for offshore wind farm developments – marine habitats and species Title: High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project. Contract Report: W/35/00632/00/00. Client: Department of Trade and Industry (New & Renewable Energy Programme) Contract management: AEA Technology, Environment. Date of contract issue: 22/07/2002 Level of report issue: Final Confidentiality: Distribution at discretion of DTI before Consultation report published then no restriction. Distribution: Two copies and electronic file to DTI (Mr S. Payne, Offshore Renewables Planning). One copy to MBA library. Prepared by: Dr. K. Hiscock, Dr. H. Tyler-Walters & Hugh Jones Authorization: Project Director: Dr. Keith Hiscock Date: Signature: MBA Director: Prof. S. Hawkins Date: Signature: This report can be referred to as follows: Hiscock, K., Tyler-Walters, H. -
Diversity of Norwegian Sea Slugs (Nudibranchia): New Species to Norwegian Coastal Waters and New Data on Distribution of Rare Species
Fauna norvegica 2013 Vol. 32: 45-52. ISSN: 1502-4873 Diversity of Norwegian sea slugs (Nudibranchia): new species to Norwegian coastal waters and new data on distribution of rare species Jussi Evertsen1 and Torkild Bakken1 Evertsen J, Bakken T. 2013. Diversity of Norwegian sea slugs (Nudibranchia): new species to Norwegian coastal waters and new data on distribution of rare species. Fauna norvegica 32: 45-52. A total of 5 nudibranch species are reported from the Norwegian coast for the first time (Doridoxa ingolfiana, Goniodoris castanea, Onchidoris sparsa, Eubranchus rupium and Proctonotus mucro- niferus). In addition 10 species that can be considered rare in Norwegian waters are presented with new information (Lophodoris danielsseni, Onchidoris depressa, Palio nothus, Tritonia griegi, Tritonia lineata, Hero formosa, Janolus cristatus, Cumanotus beaumonti, Berghia norvegica and Calma glau- coides), in some cases with considerable changes to their distribution. These new results present an update to our previous extensive investigation of the nudibranch fauna of the Norwegian coast from 2005, which now totals 87 species. An increase in several new species to the Norwegian fauna and new records of rare species, some with considerable updates, in relatively few years results mainly from sampling effort and contributions by specialists on samples from poorly sampled areas. doi: 10.5324/fn.v31i0.1576. Received: 2012-12-02. Accepted: 2012-12-20. Published on paper and online: 2013-02-13. Keywords: Nudibranchia, Gastropoda, taxonomy, biogeography 1. Museum of Natural History and Archaeology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway Corresponding author: Jussi Evertsen E-mail: [email protected] IntRODUCTION the main aims. -
E Urban Sanctuary Algae and Marine Invertebrates of Ricketts Point Marine Sanctuary
!e Urban Sanctuary Algae and Marine Invertebrates of Ricketts Point Marine Sanctuary Jessica Reeves & John Buckeridge Published by: Greypath Productions Marine Care Ricketts Point PO Box 7356, Beaumaris 3193 Copyright © 2012 Marine Care Ricketts Point !is work is copyright. Apart from any use permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission of the publisher. Photographs remain copyright of the individual photographers listed. ISBN 978-0-9804483-5-1 Designed and typeset by Anthony Bright Edited by Alison Vaughan Printed by Hawker Brownlow Education Cheltenham, Victoria Cover photo: Rocky reef habitat at Ricketts Point Marine Sanctuary, David Reinhard Contents Introduction v Visiting the Sanctuary vii How to use this book viii Warning viii Habitat ix Depth x Distribution x Abundance xi Reference xi A note on nomenclature xii Acknowledgements xii Species descriptions 1 Algal key 116 Marine invertebrate key 116 Glossary 118 Further reading 120 Index 122 iii Figure 1: Ricketts Point Marine Sanctuary. !e intertidal zone rocky shore platform dominated by the brown alga Hormosira banksii. Photograph: John Buckeridge. iv Introduction Most Australians live near the sea – it is part of our national psyche. We exercise in it, explore it, relax by it, "sh in it – some even paint it – but most of us simply enjoy its changing modes and its fascinating beauty. Ricketts Point Marine Sanctuary comprises 115 hectares of protected marine environment, located o# Beaumaris in Melbourne’s southeast ("gs 1–2). !e sanctuary includes the coastal waters from Table Rock Point to Quiet Corner, from the high tide mark to approximately 400 metres o#shore. -
Phylum MOLLUSCA
285 MOLLUSCA: SOLENOGASTRES-POLYPLACOPHORA Phylum MOLLUSCA Class SOLENOGASTRES Family Lepidomeniidae NEMATOMENIA BANYULENSIS (Pruvot, 1891, p. 715, as Dondersia) Occasionally on Lafoea dumosa (R.A.T., S.P., E.J.A.): at 4 positions S.W. of Eddystone, 42-49 fm., on Lafoea dumosa (Crawshay, 1912, p. 368): Eddystone, 29 fm., 1920 (R.W.): 7, 3, 1 and 1 in 4 hauls N.E. of Eddystone, 1948 (V.F.) Breeding: gonads ripe in Aug. (R.A.T.) Family Neomeniidae NEOMENIA CARINATA Tullberg, 1875, p. 1 One specimen Rame-Eddystone Grounds, 29.12.49 (V.F.) Family Proneomeniidae PRONEOMENIA AGLAOPHENIAE Kovalevsky and Marion [Pruvot, 1891, p. 720] Common on Thecocarpus myriophyllum, generally coiled around the base of the stem of the hydroid (S.P., E.J.A.): at 4 positions S.W. of Eddystone, 43-49 fm. (Crawshay, 1912, p. 367): S. of Rame Head, 27 fm., 1920 (R.W.): N. of Eddystone, 29.3.33 (A.J.S.) Class POLYPLACOPHORA (=LORICATA) Family Lepidopleuridae LEPIDOPLEURUS ASELLUS (Gmelin) [Forbes and Hanley, 1849, II, p. 407, as Chiton; Matthews, 1953, p. 246] Abundant, 15-30 fm., especially on muddy gravel (S.P.): at 9 positions S.W. of Eddystone, 40-43 fm. (Crawshay, 1912, p. 368, as Craspedochilus onyx) SALCOMBE. Common in dredge material (Allen and Todd, 1900, p. 210) LEPIDOPLEURUS, CANCELLATUS (Sowerby) [Forbes and Hanley, 1849, II, p. 410, as Chiton; Matthews. 1953, p. 246] Wembury West Reef, three specimens at E.L.W.S.T. by J. Brady, 28.3.56 (G.M.S.) Family Lepidochitonidae TONICELLA RUBRA (L.) [Forbes and Hanley, 1849, II, p. -
Hawai`I's Sea Creatures P. 1
Changes for revised ed - Hawai`i’s Sea Creatures p. 1 Below are the changes made to HAWAII'S SEA CREATURES for the Revised Editiion 11-02-2005 Text to remove is in red strikethrough. Text to add is in blue Sometimes I use blue underlined to show where something is inserted, or to highlight a small change of one or two characters. Boxed paragraphs show complete species accounts in final form after all individual corrections have been made. However I did not do boxed paragraphs for most of the species. ==================================================================================================================== change Copyright 199 8 to Copyright 199 9 -Replace First printing March 1998 with March 1999 p. iv: Add at bottom: Note to the Revised Edition. This revision attempts to bring the book taxonomically up to date as of October 2005. In addition, errors have been corrected, photos improved, new information incorporated, and several species added. For continuing updates please visit http://www.hawaiisfishes.com . Special thanks to Gustav Paulay, Cory Pittman, Pauline Fiene, Chela Zabin, Richard Mooi, Ray Caldwell, Christopher Mah, Alain Crosnier, Alexander Bruce, Leslie Newman, Junji Okuno, Christine Huffard, Mark Norman, Daphne Fautin, Jerry Crow, Ralph DeFelice, Colin McLay, Peter Castro, Arthur Anker, Daryl Feldman and Dale Calder for taxonomical help. This revised edition is dedicated to the memory to Darrell Takaoka, who contributed so much to the first edition. p. vi -line 15: Delete "Pauline Fiene Severns , Kihei, Maui." Should be "Pauline Fiene, Kihei, Maui." p. x -line 1: Replace “There are 30-33 named phyla” with “There are 30-33 named phyla of multicelled animals ” p. -
Phyllodesmium Tuberculatum Tritonia Sp. 3 Doto Sp. H Facelina Sp. A
Austraeolis stearnsi Hermosita hakunamatata Learchis poica Phidiana militaris Protaeolidiella juliae Moridilla brockii Noumeaella sp. 4 Cerberilla bernadettae Cerberilla sp. A Noumeaella sp. B Facelina sp. A Tritonia nilsodhneri Tritoniella belli Flabellina babai Notaeolidia depressa Tethys fimbria Armina californica Tritonia sp. F Tritonia antarctica Tritonia pickensi Leminda millecra Marianina rosea Scyllaea pelagica Pteraeolidia ianthina Limenandra sp. B 1 1 Limenandra fusiformis Limenandra sp. C 0.99 Limenandra sp. A Baeolidia nodosa 1 Spurilla sargassicola 0.82 Spurilla neapolitana 0.75 Spurilla sp. A Spurilla braziliana 1 Protaeolidiella atra Caloria indica 1 Aeolidia sp. B 0.92 Aeolidia sp. A Aeolidia papillosa 1 Glaucus atlanticus Glaucus marginatus 1 Tritonia diomedea Tritonia festiva 0.99 Hancockia californica 1 Hancockia uncinata Hancockia cf. uncinata 0.99 Spurilla creutzbergi 1 Berghia verrucicornis 0.98 Berghia coerulescens 0.91 Aeolidiella stephanieae 1 Berghia rissodominguezi 0.9 Berghia columbina Berghia sp. A 0.99 Aeolidiella sanguinea Aeolidiella alderi 0.99 Phidiana hiltoni Phidiana lynceus Armina lovenii 0.98 Armina sp. 3 Armina sp. 9 Dermatobranchus semistriatus Dermatobranchus sp. A 1 Armina semperi 0.89 Armina sp. 0.98 Dermatobranchus sp. 12 1 Dermatobranchus sp. 7 0.86 Dermatobranchus sp. 17 Dermatobranchus pustulosus 0.72 Dermatobranchus sp. 16 Dermatobranchus sp. 21 0.97 Dirona albolineata Charcotia granulosa 0.95 Baeolidia moebii 0.85 Aeolidiopsis ransoni 0.75 Baeolidia sp. A 1 Berghia salaamica 0.98 0.51 Berghia cf. salaamica 0.97 Baeolidia sp. B 0.94 Baeolidia japonica Baeolidia sp. C 0.95 Noumeaella sp. 3 Noumeaella rehderi 0.91 Cerberilla sp. B 0.57 Cerberilla sp. -
South Carolina Department of Natural Resources
FOREWORD Abundant fish and wildlife, unbroken coastal vistas, miles of scenic rivers, swamps and mountains open to exploration, and well-tended forests and fields…these resources enhance the quality of life that makes South Carolina a place people want to call home. We know our state’s natural resources are a primary reason that individuals and businesses choose to locate here. They are drawn to the high quality natural resources that South Carolinians love and appreciate. The quality of our state’s natural resources is no accident. It is the result of hard work and sound stewardship on the part of many citizens and agencies. The 20th century brought many changes to South Carolina; some of these changes had devastating results to the land. However, people rose to the challenge of restoring our resources. Over the past several decades, deer, wood duck and wild turkey populations have been restored, striped bass populations have recovered, the bald eagle has returned and more than half a million acres of wildlife habitat has been conserved. We in South Carolina are particularly proud of our accomplishments as we prepare to celebrate, in 2006, the 100th anniversary of game and fish law enforcement and management by the state of South Carolina. Since its inception, the South Carolina Department of Natural Resources (SCDNR) has undergone several reorganizations and name changes; however, more has changed in this state than the department’s name. According to the US Census Bureau, the South Carolina’s population has almost doubled since 1950 and the majority of our citizens now live in urban areas. -
Nudibranch Range Shifts Associated with the 2014 Warm Anomaly in the Northeast Pacific
Bulletin of the Southern California Academy of Sciences Volume 115 | Issue 1 Article 2 4-26-2016 Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific Jeffrey HR Goddard University of California, Santa Barbara, [email protected] Nancy Treneman University of Oregon William E. Pence Douglas E. Mason California High School Phillip M. Dobry See next page for additional authors Follow this and additional works at: https://scholar.oxy.edu/scas Part of the Marine Biology Commons, Population Biology Commons, and the Zoology Commons Recommended Citation Goddard, Jeffrey HR; Treneman, Nancy; Pence, William E.; Mason, Douglas E.; Dobry, Phillip M.; Green, Brenna; and Hoover, Craig (2016) "Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific," Bulletin of the Southern California Academy of Sciences: Vol. 115: Iss. 1. Available at: https://scholar.oxy.edu/scas/vol115/iss1/2 This Article is brought to you for free and open access by OxyScholar. It has been accepted for inclusion in Bulletin of the Southern California Academy of Sciences by an authorized editor of OxyScholar. For more information, please contact [email protected]. Nudibranch Range Shifts associated with the 2014 Warm Anomaly in the Northeast Pacific Cover Page Footnote We thank Will and Ziggy Goddard for their expert assistance in the field, Jackie Sones and Eric Sanford of the Bodega Marine Laboratory for sharing their observations and knowledge of the intertidal fauna of Bodega Head and Sonoma County, and David Anderson of the National Park Service and Richard Emlet of the University of Oregon for sharing their respective observations of Okenia rosacea in northern California and southern Oregon. -
Phidiana Lynceus Berghia Coerulescens Doto Koenneckeri
Cuthona abronia Cuthona divae Austraeolis stearnsi Flabellina exoptata Flabellina fusca Calma glaucoides Hermosita hakunamatata Learchis poica Anteaeolidiella oliviae Aeolidiopsis ransoni Phidiana militaris Baeolidia moebii Facelina annulicornis Protaeolidiella juliae Moridilla brockii Noumeaella isa Cerberilla sp. 3 Cerberilla bernadettae Aeolidia sp. A Aeolidia sp. B Baeolidia sp. A Baeolidia sp. B Cerberilla sp. A Cerberilla sp. B Cerberilla sp. C Facelina sp. C Noumeaella sp. A Noumeaella sp. B Facelina sp. A Marionia blainvillea Aeolidia papillosa Hermissenda crassicornis Flabellina babai Dirona albolineata Doto sp. 15 Marionia sp. 10 Marionia sp. 5 Tritonia sp. 4 Lomanotus sp. E Piseinotecus sp. Dendronotus regius Favorinus elenalexiarum Janolus mirabilis Marionia levis Phyllodesmium horridum Tritonia pickensi Babakina indopacifica Marionia sp. B Godiva banyulensis Caloria elegans Favorinus brachialis Flabellina baetica 1 Facelinidae sp. A Godiva quadricolor 0.99 Limenandra fusiformis Limenandra sp. C 0.71 Limenandra sp. B 0.91 Limenandra sp. A Baeolidia nodosa 0.99 Crosslandia daedali Scyllaea pelagica Notobryon panamica Notobryon thompsoni 0.98 Notobryon sp. B Notobryon sp. C Notobryon sp. D Notobryon wardi 0.97 Tritonia sp. 3 Marionia arborescens 0.96 Hancockia cf. uncinata Hancockia californica 0.94 Spurilla chromosoma Pteraeolidia ianthina 0.92 Noumeaella sp. 3 Noumeaella rehderi 0.92 Nanuca sebastiani 0.97 Dondice occidentalis Dondice parguerensis 0.92 Pruvotfolia longicirrha Pruvotfolia pselliotes 0.88 Marionia sp. 14 Tritonia sp. G 0.87 Bonisa nakaza 0.87 Janolus sp. 2 0.82 Janolus sp. 1 Janolus sp. 7 Armina sp. 3 0.83 Armina neapolitana 0.58 Armina sp. 9 0.78 Dermatobranchus sp. 16 0.52 Dermatobranchus sp. 21 0.86 Dermatobranchus sp. -
Cuthona Sp. 7 Notobryon Sp. C Dendronotus Rufus Limenandra Sp
Austraeolis stearnsi Hermosita hakunamatata Learchis poica Phidiana militaris Protaeolidiella juliae Moridilla brockii Noumeaella sp. 4 Cerberilla bernadettae Cerberilla sp. A Cerberilla sp. C Noumeaella sp. B Facelina sp. A Cratena peregrina Tritonia nilsodhneri Tritoniella belli Facelina bostoniensis Notaeolidia depressa Tethys fimbria Armina californica Tritonia sp. F Tritonia antarctica Tritonia pickensi Leminda millecra Marianina rosea Spurilla major Caloria elegans Flabellina bilas Baeolidia australis Favorinus sp. Pteraeolidia ianthina 1 Tritonia diomedea Tritonia festiva 1 Aeolidia sp. B 0.92 Aeolidia sp. A Aeolidia papillosa 1 Glaucus atlanticus Glaucus marginatus 1 Spurilla sargassicola 0.8 Spurilla neapolitana 0.74 Spurilla sp. A Spurilla braziliana 1 Hancockia californica 1 Hancockia uncinata Hancockia cf. uncinata 1 Facelina annulicornis Facelina punctata Limenandra sp. B 1 1 Limenandra fusiformis Limenandra sp. C 0.99 Limenandra sp. A Baeolidia nodosa 0.99 Protaeolidiella atra Caloria indica 0.99 Anteaeolidiella sp. B 0.91 Anteaeolidiella sp. A 0.62 Anteaeolidiella takanosimensis 0.82 Anteaeolidiella cacaotica 0.91 Anteaeolidiella saldanhensis Anteaeolidiella lurana 0.99 Pruvotfolia longicirrha Pruvotfolia pselliotes 0.98 Phidiana hiltoni Phidiana lynceus 0.98 Aeolidiella sanguinea Aeolidiella alderi Armina neapolitana Armina sp. 3 Armina sp. 9 Dermatobranchus semistriatus 0.97 Dermatobranchus sp. A 1 Armina semperi 0.75 Armina sp. 0.98 Dermatobranchus sp. 12 0.99 Dermatobranchus sp. 7 0.98 0.87 Dermatobranchus sp. 17 Dermatobranchus pustulosus 0.67 Dermatobranchus sp. 16 Dermatobranchus sp. 21 0.65 Armina maculata Armina lovenii 0.97 Spurilla creutzbergi 1 Berghia verrucicornis 0.98 Berghia coerulescens 0.9 Berghia columbina 1 Berghia sp. A 0.88 Aeolidiella stephanieae Berghia rissodominguezi Bornella hermanni 0.96 0.8 Bornella calcarata Bornella valdae 0.58 0.8 Bornella anguilla Bornella sarape 0.6 Bornella stellifer Bornella johnsonorum 0.95 Noumeaella sp. -
Table of Contents
ALL INDIA CO-ORDINATED PROJECT ON TAXONOMY OF MOLLUSCA ANNUAL REPORT (December 2016 – May 2018) GUJARAT STATE BOMBAY NATURAL HISTORY SOCIETY Dr. Deepak Apte Director Dr. Dishant Parasharya Dr. Bhavik Patel Scientist – B Scientist – B All India Coordinated Project on Taxonomy – Mollusca , Gujarat State Acknowledgements We are thankful to the Department of Forest and Environment, Government of Gujarat, Mr. G. K. Sinha, IFS HoFF and PCCF (Wildlife) for his guidance and cooperation in the work. We are thankful to then CCF Marine National Park and Sanctuary, Mr. Shyamal Tikader IFS, Mr. S. K. Mehta IFS and their team for the generous support, We take this opportunity to thank the entire team of Marine National Park and Sanctuary. We are thankful to all the colleagues of BNHS who directly or indirectly helped us in our work. We specially thank our field assistant, Rajesh Parmar who helped us in the field work. All India Coordinated Project on Taxonomy – Mollusca , Gujarat State 1. Introduction Gujarat has a long coastline of about 1650 km, which is mainly due to the presence of two gulfs viz. the Gulf of Khambhat (GoKh) and Gulf of Kachchh (GoK). The coastline has diverse habitats such as rocky, sandy, mangroves, coral reefs etc. The southern shore of the GoK in the western India, notified as Marine National Park and Sanctuary (MNP & S), harbours most of these major habitats. The reef areas of the GoK are rich in flora and fauna; Narara, Dwarka, Poshitra, Shivrajpur, Paga, Boria, Chank and Okha are some of these pristine areas of the GoK and its surrounding environs. -
The Jewels of Neptune
88 Spotlight A portrait of Chromodoris kuniei feeding on a sponge offers a clear view of its frontal rhinophores and dorsal, exposed gills. NUDIBRANCHS THE JEWELS OF NEPTUNE Much loved and sought after by underwater photographers, these toxic marine slugs come in a dazzling variety of colors and shapes GOOGLE EARTH COORDINATES HERE 89 TEXT BY ANDREA FERRARI A pair of PHOTOS BY ANDREA & ANTONELLA FERRARI Hypselodoris apolegma prior to mating. Nudibranchs espite their being utilize their Dquite common in worldwide gaudy temperate and tropical waters and aposematic most of the times being quite coloration to spectacularly shaped and colored, advertise their nudibranchs – or “nudis” in divers toxicity to parlance – are still a mysterious lot to would-be predators. plenty of people. What are those technicolored globs crawling in the muck? Have they got a head? Eyes, anyone? Where’s the front, and where the back? Do those things actually eat? Well, to put it simply, they’re slugs – or snails without an external shell. About forty Families in all, counting literally hundreds of different species: in scientific lingo – which is absolutely fundamental even if most divers shamefully skip it – they’re highly evolved gastropods (gastro=stomach, pod=foot: critters crawling on their belly), belonging to the Class Opistobranchia (opisto=protruding, branchia=gills: with external gills), ie close relatives of your common land-based, lettuce- eating garden snails. Like those drably colored pests, nudibranchs are soft-bodied mollusks which move on the substrate crawling on a fleshy belly which acts like an elegantly undulating foot (if disturbed, some of them can even “swim” some distance continued on page 93 › 90 A telling sample of the stunning variety in shape and colors offered by the nudibranch tribe.