“Coastal Marine Biodiversity of Vietnam: Regional and Local Challenges and Coastal Zone Management for Sustainable Development”
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A Classification of Living and Fossil Genera of Decapod Crustaceans
RAFFLES BULLETIN OF ZOOLOGY 2009 Supplement No. 21: 1–109 Date of Publication: 15 Sep.2009 © National University of Singapore A CLASSIFICATION OF LIVING AND FOSSIL GENERA OF DECAPOD CRUSTACEANS Sammy De Grave1, N. Dean Pentcheff 2, Shane T. Ahyong3, Tin-Yam Chan4, Keith A. Crandall5, Peter C. Dworschak6, Darryl L. Felder7, Rodney M. Feldmann8, Charles H. J. M. Fransen9, Laura Y. D. Goulding1, Rafael Lemaitre10, Martyn E. Y. Low11, Joel W. Martin2, Peter K. L. Ng11, Carrie E. Schweitzer12, S. H. Tan11, Dale Tshudy13, Regina Wetzer2 1Oxford University Museum of Natural History, Parks Road, Oxford, OX1 3PW, United Kingdom [email protected] [email protected] 2Natural History Museum of Los Angeles County, 900 Exposition Blvd., Los Angeles, CA 90007 United States of America [email protected] [email protected] [email protected] 3Marine Biodiversity and Biosecurity, NIWA, Private Bag 14901, Kilbirnie Wellington, New Zealand [email protected] 4Institute of Marine Biology, National Taiwan Ocean University, Keelung 20224, Taiwan, Republic of China [email protected] 5Department of Biology and Monte L. Bean Life Science Museum, Brigham Young University, Provo, UT 84602 United States of America [email protected] 6Dritte Zoologische Abteilung, Naturhistorisches Museum, Wien, Austria [email protected] 7Department of Biology, University of Louisiana, Lafayette, LA 70504 United States of America [email protected] 8Department of Geology, Kent State University, Kent, OH 44242 United States of America [email protected] 9Nationaal Natuurhistorisch Museum, P. O. Box 9517, 2300 RA Leiden, The Netherlands [email protected] 10Invertebrate Zoology, Smithsonian Institution, National Museum of Natural History, 10th and Constitution Avenue, Washington, DC 20560 United States of America [email protected] 11Department of Biological Sciences, National University of Singapore, Science Drive 4, Singapore 117543 [email protected] [email protected] [email protected] 12Department of Geology, Kent State University Stark Campus, 6000 Frank Ave. -
The New South Wales Cancellariidae
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Laseron, C. F., 1955. The New South Wales Cancellariidae. Records of the Australian Museum 23(5): 267–272. [1 September 1955]. doi:10.3853/j.0067-1975.23.1955.635 ISSN 0067-1975 Published by the Australian Museum, Sydney naturenature cultureculture discover discover AustralianAustralian Museum Museum science science is is freely freely accessible accessible online online at at www.australianmuseum.net.au/publications/www.australianmuseum.net.au/publications/ 66 CollegeCollege Street,Street, SydneySydney NSWNSW 2010,2010, AustraliaAustralia THE NEW SOUTH WALES CANCELLARIIDAE* By OHARLES F. LASERON, F.R.Z.S. ilonorary Correspondent, Australian Museum. (Figures 1-13.) INTRODUOTION. Hedley in his Oheck List in 1918 recorded six '3pecies of this family as occurring in New South vVales. Since that time considerable revision in nomenclature has taken place, and some further material has come to hand. As descriptions and references to the family are very scattered in literature, the opportunity is now taken to bring them together, and to illustrate not only species new to science, but also all those which have already been described. It is felt that such papers are of great convenience to conchologists and form a base on which future work can be under taken. The complete check list of species from the Peronian zoogeographical province will now read as follows: Sydaphera ren01)atn Iredale obniJ';a Iredale anxifer Iredale deZicosa Laseron " scobina Hedley Trigonaphera vinn11,Za Iredale " interZaevis Laseron. A rizelostoma Zaseroni Iredale Pepta stricto. Iredale Microsveltia recessa Iredale PaUidonia simo[!Zex Laseron. All types, as well as specimens illustrated, are being presented to the Australian :Museum, Sydney. -
MARINE FAUNA and FLORA of BERMUDA a Systematic Guide to the Identification of Marine Organisms
MARINE FAUNA AND FLORA OF BERMUDA A Systematic Guide to the Identification of Marine Organisms Edited by WOLFGANG STERRER Bermuda Biological Station St. George's, Bermuda in cooperation with Christiane Schoepfer-Sterrer and 63 text contributors A Wiley-Interscience Publication JOHN WILEY & SONS New York Chichester Brisbane Toronto Singapore ANTHOZOA 159 sucker) on the exumbrella. Color vari many Actiniaria and Ceriantharia can able, mostly greenish gray-blue, the move if exposed to unfavorable condi greenish color due to zooxanthellae tions. Actiniaria can creep along on their embedded in the mesoglea. Polyp pedal discs at 8-10 cm/hr, pull themselves slender; strobilation of the monodisc by their tentacles, move by peristalsis type. Medusae are found, upside through loose sediment, float in currents, down and usually in large congrega and even swim by coordinated tentacular tions, on the muddy bottoms of in motion. shore bays and ponds. Both subclasses are represented in Ber W. STERRER muda. Because the orders are so diverse morphologically, they are often discussed separately. In some classifications the an Class Anthozoa (Corals, anemones) thozoan orders are grouped into 3 (not the 2 considered here) subclasses, splitting off CHARACTERISTICS: Exclusively polypoid, sol the Ceriantharia and Antipatharia into a itary or colonial eNIDARIA. Oral end ex separate subclass, the Ceriantipatharia. panded into oral disc which bears the mouth and Corallimorpharia are sometimes consid one or more rings of hollow tentacles. ered a suborder of Scleractinia. Approxi Stomodeum well developed, often with 1 or 2 mately 6,500 species of Anthozoa are siphonoglyphs. Gastrovascular cavity compart known. Of 93 species reported from Ber mentalized by radially arranged mesenteries. -
Preliminary Report on the Octocorals (Cnidaria: Anthozoa: Octocorallia) from the Ogasawara Islands
国立科博専報,(52), pp. 65–94 , 2018 年 3 月 28 日 Mem. Natl. Mus. Nat. Sci., Tokyo, (52), pp. 65–94, March 28, 2018 Preliminary Report on the Octocorals (Cnidaria: Anthozoa: Octocorallia) from the Ogasawara Islands Yukimitsu Imahara1* and Hiroshi Namikawa2 1Wakayama Laboratory, Biological Institute on Kuroshio, 300–11 Kire, Wakayama, Wakayama 640–0351, Japan *E-mail: [email protected] 2Showa Memorial Institute, National Museum of Nature and Science, 4–1–1 Amakubo, Tsukuba, Ibaraki 305–0005, Japan Abstract. Approximately 400 octocoral specimens were collected from the Ogasawara Islands by SCUBA diving during 2013–2016 and by dredging surveys by the R/V Koyo of the Tokyo Met- ropolitan Ogasawara Fisheries Center in 2014 as part of the project “Biological Properties of Bio- diversity Hotspots in Japan” at the National Museum of Nature and Science. Here we report on 52 lots of these octocoral specimens that have been identified to 42 species thus far. The specimens include seven species of three genera in two families of Stolonifera, 25 species of ten genera in two families of Alcyoniina, one species of Scleraxonia, and nine species of four genera in three families of Pennatulacea. Among them, three species of Stolonifera: Clavularia cf. durum Hick- son, C. cf. margaritiferae Thomson & Henderson and C. cf. repens Thomson & Henderson, and five species of Alcyoniina: Lobophytum variatum Tixier-Durivault, L. cf. mirabile Tixier- Durivault, Lohowia koosi Alderslade, Sarcophyton cf. boletiforme Tixier-Durivault and Sinularia linnei Ofwegen, are new to Japan. In particular, Lohowia koosi is the first discovery since the orig- inal description from the east coast of Australia. -
Amphipholis Squamata MICHAEL P
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Aug. 1990, p. 2436-2440 Vol. 56, No. 8 0099-2240/90/082436-05$02.00/0 Copyright C) 1990, American Society for Microbiology Description of a Novel Symbiotic Bacterium from the Brittle Star, Amphipholis squamata MICHAEL P. LESSERt* AND RICHARD P. BLAKEMORE Department of Microbiology, University of New Hampshire, Durham, New Hampshire 03824 Received 8 November 1989/Accepted 3 June 1990 A gram-negative, marine, facultatively anaerobic bacterial isolate designated strain AS-1 was isolated from the subcuticular space of the brittle star, Amphipholis squamata. Its sensitivity to 0/129 and novobiocin, overall morphology, and biochemical characteristics and the moles percent guanine-plus-cytosine composition of its DNA (42.9 to 44.4) suggest that this isolate should be placed in the genus Vibrio. Strain AS-1 was not isolated from ambient seawater and is distinct from described Vibrio species. This symbiotic bacterium may assist its host as one of several mechanisms of nutrient acquisition during the brooding of developing embryos. The biology of bacterium-invertebrate symbiotic associa- isopropyl alcohol for 30 s and two rinses in sterile ASW. tions has elicited considerable interest, particularly since the Logarithmic dilutions were plated on Zobell modified 2216E discoveries during the past decade of chemoautotrophic medium (ASW, 1 g of peptone liter-1, 1 g of yeast extract symbiotic bacteria associated with several invertebrate spe- liter-' [pH 7.8 to 8.4]) (29), as were samples of ambient cies in sulfide-rich habitats (4, 5). Bacterial-invertebrate seawater from the site of collection and ASW controls. All symbioses (mutualistic) have been reported from many materials and equipment were sterilized, and all procedures invertebrate taxa, examples of which include cellulolytic were performed by aseptic techniques. -
Crustacea: Amphipoda: Dogielinotidae) from the Nipa Palm in Thailand, with an Updated Key to the Genera
RESEARCH ARTICLE Discovery of a new genus and species of dogielinotid amphipod (Crustacea: Amphipoda: Dogielinotidae) from the Nipa palm in Thailand, with an updated key to the genera 1,2 3 4 Koraon WongkamhaengID *, Pongrat Dumrongrojwattana , Myung-Hwa Shin a1111111111 a1111111111 1 Department of Zoology, Faculty of Science, Kasetsart University, Bangkok, Thailand, 2 Coastal Oceanography and Climate Change Research Center, Prince of Songkla University, Hatyai, Songkhla, a1111111111 Thailand, 3 Department of Biology, Faculty of Science, Burapha University, Bangsaen, Chonburi, Thailand, a1111111111 4 National Marine Biodiversity Institute of Korea, Seocheon, South Korea a1111111111 * [email protected] Abstract OPEN ACCESS Citation: Wongkamhaeng K, Dumrongrojwattana During a scientific survey, a new genus of the dogielinotid amphipoda was found in the Nipa P, Shin M (2018) Discovery of a new genus and palm (Nypa fruticans) in Bang Krachao Urban Oasis, Samut Prakan Province, Thailand. We species of dogielinotid amphipod (Crustacea: placed this new genus, Allorchestoides gen. nov., within the family Dogielinotidae. The new Amphipoda: Dogielinotidae) from the Nipa palm in Thailand, with an updated key to the genera. PLoS taxa can be easily distinguished from the remaining genera by differences in the incisor of ONE 13(10): e0204299. https://doi.org/10.1371/ the left and right mandibles, apical robust setae of the maxilla 1, and the large coxa and journal.pone.0204299 strong obtuse palm in the female gnathopod 1. The type species of Allorchestoides gen. Editor: Feng Zhang, Nanjing Agricultural University, nov., Allorchestoides rosea n. sp., is described here in, with an updated key to the genera of CHINA the family Dogielinotidae. -
ECOLOGICAL ENERGETICS of TROPICAL LIMPET Cellana Testudinaria (Linnaeus, 1758) LIVING on the ROCKY SHORE of OHOIWAIT, SOUTHEAST MOLUCCAS, INDONESIA
Journal of Coastal Deveolpment ISSN : 1410-5217 Volume 11, Number 2, February 2008 : 89-96 ECOLOGICAL ENERGETICS OF TROPICAL LIMPET Cellana testudinaria (Linnaeus, 1758) LIVING ON THE ROCKY SHORE OF OHOIWAIT, SOUTHEAST MOLUCCAS, INDONESIA Abraham Seumel Khouw Faculty of Fisheries and Marine Sciences, Pattimura University, Ambon Indonesia Received : November, 2, 2007 ; Accepted :January,4, 2008 ABSTRACT Study on ecological energetics of tropical limpet C. testudinaria has been carried out at approximately one year from October 2001 to September 2002. Population energy budgets estimated on the assumption of steady state conditions for C. testudinaria (Linnaeus, 1758) on the rocky shore of Ohoiwait, are presented. Large difference in population structure, and hence energetics, occurred at different localities along the rocky shore. Relatively high proportions (98 %) of the assimilated energy was lost via metabolism. Assimilation efficiency is 39 %, net growth efficiency is 1.8 %, and ecological efficiency 0.3 %. Production (P), energy flow (A) and total energy consumption (C) were expressed as functions of animal size, in order to facilitate gross estimations of the energy component for which data on size frequency and density are available. Key words: ecological energetics, cellana testudinaria, energy components Correspondence: Phone : +6281343044295, e-mail: [email protected] INTRODUCTION Cellana testudinaria is intertidal, grazing Little has been published on the gastropod abundant on medium to very ecology of C. testudinaria. Khouw (2002) exposed rocky shores of Ohoiwait. The discussed their growth pattern and shell species shows marked zonation, with only a shape variation in relation to zonal little overlap between zones. C. testudinaria distribution. Distribution, abundance, and occurs at several spatial and temporal scales biomass were investigated by Khouw from the extreme low water spring tide (2006a) and presented evidence for the (ELWST) to the extreme high water spring effects of drying. -
Title Biogeography in Cellana (Patellogastropoda, Nacellidae) with Special Emphasis on the Relationships of Southern Hemisphere
Biogeography in Cellana (Patellogastropoda, Nacellidae) with Title Special Emphasis on the Relationships of Southern Hemisphere Oceanic Island Species González-Wevar, Claudio A.; Nakano, Tomoyuki; Palma, Author(s) Alvaro; Poulin, Elie Citation PLOS ONE (2017), 12(1) Issue Date 2017-01-18 URL http://hdl.handle.net/2433/218484 © 2017 González-Wevar et al. This is an open access article distributed under the terms of the Creative Commons Right Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Type Journal Article Textversion publisher Kyoto University RESEARCH ARTICLE Biogeography in Cellana (Patellogastropoda, Nacellidae) with Special Emphasis on the Relationships of Southern Hemisphere Oceanic Island Species Claudio A. GonzaÂlez-Wevar1,2*, Tomoyuki Nakano3, Alvaro Palma4, Elie Poulin1 1 GAIA-AntaÂrtica, Universidad de Magallanes, Punta Arenas, Chile, 2 Instituto de EcologõÂa y Biodiversidad Ä a1111111111 (IEB), Departamento de Ciencias EcoloÂgicas, Facultad de Ciencias, Universidad de Chile, Nuñoa, Santiago, Chile, 3 Seto Marine Biological Laboratory, Field Science Education and Research Centre, Kyoto University, a1111111111 Nishimuro, Wakayama, Japan, 4 Universidad Gabriela Mistral, Facultad de IngenierõÂa y Negocios, a1111111111 Providencia, Santiago, Chile a1111111111 a1111111111 * [email protected] Abstract OPEN ACCESS Oceanic islands lacking connections to other land are extremely isolated from sources of Citation: GonzaÂlez-Wevar CA, Nakano T, Palma A, potential colonists and have acquired their biota mainly through dispersal from geographi- Poulin E (2017) Biogeography in Cellana cally distant areas. Hence, isolated island biota constitutes interesting models to infer bio- (Patellogastropoda, Nacellidae) with Special geographical mechanisms of dispersal, colonization, differentiation, and speciation. Limpets Emphasis on the Relationships of Southern Hemisphere Oceanic Island Species. -
The Genus Phlyctenodes Milne Edwards, 1862 (Crustacea: Decapoda: Xanthidae) in the Eocene of Europe
350 RevistaBusulini Mexicana et al. de Ciencias Geológicas, v. 23, núm. 3, 2006, p. 350-360 The genus Phlyctenodes Milne Edwards, 1862 (Crustacea: Decapoda: Xanthidae) in the Eocene of Europe Alessandra Busulini1,*, Giuliano Tessier2, and Claudio Beschin3 1 c/o Museo di Storia Naturale, S. Croce 1730, I - 30125, Venezia, Italia. 2 via Barbarigo 10, I – 30126, Lido di Venezia, Italia. 3 Associazione Amici del Museo Zannato, Piazza Marconi 15, I - 36075, Montecchio Maggiore (Vicenza), Italia. * [email protected] ABSTRACT A systematic review of the crab genus Phlyctenodes Milne Edwards, 1862 is carried out. Based on carapace features, this taxon is placed in the subfamily Actaeinae, family Xanthidae MacLeay, 1838. Species attributed to this genus are known from Eocene reef environments in Europe. Preservation of crustacean remains in this kind of environment is very rare, and it could explain scarcity of specimens of this genus. For the fi rst time, pictures of types of this genus described during the XIX century and the fi rst decades of the XX century are presented. A study of recently collected specimens from the Eocene of Veneto (Italy) allows to clarify relationships between Phlyctenodes krenneri Lörenthey, 1898 and P. dalpiazi Fabiani, 1911. Presence of P. tuberculosus Milne Edwards, 1862 among the new material is documented. The other known species of this genus, P. hantkeni Lörenthey, 1898 is placed in Pseudophlyctenodes new genus on the basis of differences in morphological features. Key words: Crustacea, Decapoda, Phlyctenodes, systematic review, Eocene, Italy. RESUMEN Se presenta una revisión sistemática del género de cangrejo Phlyctenodes Milne Edwards, 1862. Con base en las características del caparazón, este taxon es ubicado en la subfamilia Actaeinae, familia Xanthidae MacLeay, 1838. -
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. -
Atoll Research Bulletin No. 588 Spatio-Temporal
ATOLL RESEARCH BULLETIN NO. 588 SPATIO-TEMPORAL DISTRIBUTION OF ASSEMBLAGES OF BRACHYURAN CRABS AT LAAMU ATOLL, MALDIVES BY A. A. J. KUMAR AND S. G. WESLEY ISSUED BY NATIONAL MUSEUM OF NATURAL HISTORY SMITHSONIAN INSTITUTION WASHINGTON, D.C., U.S.A. DECEMBER 2010 A N B C Figure l. A) The Maldives (7°10′N and 0°4′S and 72°30′ and 73°40′E) showing Laamu atoll; B) Laamu atoll (2°08′N and 1°47′N) showing Maavah (inside the circle); C) Maavah (1°53′08.92′′N and 73°14′35.61′′E) showing the study sites. SPATIO-TEMPORAL DISTRIBUTION OF ASSEMBLAGES OF BRACHYURAN CRABS AT LAAMU ATOLL, MALDIVES BY A. A. J. KUMAR AND S. G. WESLEY ABSTRACT A spatio-temporal study of the brachyuran assemblages at five marine habitats at Maavah Island, Laamu atoll, Maldives, was conducted for a period of two years from April 2001 to March 2003. Forty-seven species and a sub-species were collected from the study sites. An analysis of the species diversity of the study sites revealed that distributions of families and species were site-specific although some species have wider distributions than others and that there were seasonal variations at some of the sites. The highest species richness (S = 32) and the highest diversity index was shown by a site at north lagoon, which has complex and heterogeneous habitats. The south-east beach brachyuran community, which was low in species richness, exhibited the lowest evenness. An analysis of the constancy index of the different brachyuran communities revealed that the ratio of the species number and abundance of the constant species were considerably higher than the accessory and accidental species. -
Fauna of Australia 4A Phylum Sipuncula
FAUNA of AUSTRALIA Volume 4A POLYCHAETES & ALLIES The Southern Synthesis 5. PHYLUM SIPUNCULA STANLEY J. EDMONDS (Deceased 16 July 1995) © Commonwealth of Australia 2000. All material CC-BY unless otherwise stated. At night, Eunice Aphroditois emerges from its burrow to feed. Photo by Roger Steene DEFINITION AND GENERAL DESCRIPTION The Sipuncula is a group of soft-bodied, unsegmented, coelomate, worm-like marine invertebrates (Fig. 5.1; Pls 12.1–12.4). The body consists of a muscular trunk and an anteriorly placed, more slender introvert (Fig. 5.2), which bears the mouth at the anterior extremity of an introvert and a long, recurved, spirally wound alimentary canal lies within the spacious body cavity or coelom. The anus lies dorsally, usually on the anterior surface of the trunk near the base of the introvert. Tentacles either surround, or are associated with the mouth. Chaetae or bristles are absent. Two nephridia are present, occasionally only one. The nervous system, although unsegmented, is annelidan-like, consisting of a long ventral nerve cord and an anteriorly placed brain. The sexes are separate, fertilisation is external and cleavage of the zygote is spiral. The larva is a free-swimming trochophore. They are known commonly as peanut worms. AB D 40 mm 10 mm 5 mm C E 5 mm 5 mm Figure 5.1 External appearance of Australian sipunculans. A, SIPUNCULUS ROBUSTUS (Sipunculidae); B, GOLFINGIA VULGARIS HERDMANI (Golfingiidae); C, THEMISTE VARIOSPINOSA (Themistidae); D, PHASCOLOSOMA ANNULATUM (Phascolosomatidae); E, ASPIDOSIPHON LAEVIS (Aspidosiphonidae). (A, B, D, from Edmonds 1982; C, E, from Edmonds 1980) 2 Sipunculans live in burrows, tubes and protected places.