(Crustacea: Peracarida: Isopoda: Asellota), from Navassa Island, Northern Caribbean Sea

Total Page:16

File Type:pdf, Size:1020Kb

(Crustacea: Peracarida: Isopoda: Asellota), from Navassa Island, Northern Caribbean Sea PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON lI6(4):967-977. 2003. A new species of Stenetrium Haswell, 1881 (Crustacea: Peracarida: Isopoda: Asellota), from Navassa Island, Northern Caribbean Sea Joel W. Martin, Richard W. Heard, and Regina Wetzer (JWM, RW) Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, e-mail: [email protected]; [email protected] (RWH) Department of Coastal Sciences, The University of Southern Mississippi, RO. Box 7000, Ocean Springs, Mississippi ,39566-7000, e-mail: [email protected] Abstract.—A new species of the isopod genus Stenetrium Haswell, 1881, is described from Navassa Island, Caribbean Sea. The new species, S. kensleyi, is compared to S. serratum Hansen, 1905, the only congener known from the western Atlantic following recent revisions of the Stenetriidae (Serov and Wil­ son, 1995, 1999; Bolstad and Kensley, 1999), and to some members of the recently proposed genus Hansenium, with which it shares several characters. The new species differs from S. serratum (and from other members of the genus) in its possession of an unusual male first pereopod, which has a greatly inflated dactylus, broadly triangular propodus, and a medial sharply triangular shark-fin-shaped tooth on the propodal cutting border. In their comprehensive guide to isopods Serov and Wilson (1995) reviewed the of the Caribbean Sea and adjacent regions taxonomic status of the more than 60 nom­ of the northwestern Atlantic (Gulf of Mex­ inal species comprising the family Stenetri­ ico, Bahamas, and Bermuda), Kensley and idae Hansen, 1905. As part of their study, Schotte (1989) reported two genera of the they redescribed the type species, Stene­ family Stenetriidae Hansen: Stenetrium trium armatum Haswell, 1881, described Haswell, 1881, and Stenobermuda Schultz, the new species S. adrianae, and created 1979. The authors presented diagnoses, il­ four new genera to accommodate 23 spe­ lustrations, and keys to these two genera cies previously assigned to Stenetrium. Of and to the six species of Stenetrium {S. the seven northwestern Atlantic species for­ bowmani Kensley, 1984; S. minocule Men- merly assigned to Stenetrium, only S. ser­ zies and Glynn, 1968; S. patulipalma Ken­ ratum was recognized as a true member of sley, 1984; S. serratum Hansen, 1905; S. that genus by Serov and Wilson (1995). The spathulicarpus Kensley, 1984; and S. steb- remaining stenetriid species from the north­ bingi Richardson, 1902 [= S. untillense western Atlantic have been transferred to Hansen, 1905]) known at that time from the new genera (see Table 1) (and see Bolstad northwestern Atlantic. Since then, a seventh and Kensley, 1999, for a rediagnosis of Ser­ northwestern Atlantic species of Stene­ ov and Wilson's 1995 genus Hansenium). trium, S. caicosensis Kensley and Heard, Thus, as currently understood (i.e., follow­ 1991, was described from the Turks and ing Kensley and Schotte 1989; Kensley Caicos Islands. Additionally, Kensley 1994; Serov and Wilson 1995, 1999; Bol­ (1994) designated a second northwestern stad and Kensley 1999) the family Stene­ Atlantic species of Stenobermuda, S. ilijfei, triidae contains 9 genera and approximately a cave dwelling form that, like the type spe­ 67 species, 11 of which (in 6 genera) are cies Stenobermuda acutirostrata Schultz, currently known from the western Atlantic 1979, came from Bermuda. (Table 1). 968 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON Table I.—Northwestern Atlantic species of the isopod family Stenetriidae and their current status following Serov and Wilson (1995. 1999) and Kensley and Bolstad (1999), listed in alphabetical order. Former niimc New name Reference Lexceniiim poorei Unchanged since description Serov and Wilson, 1999 Stenetrium antillense* Transferred to Hansenium Serov and Wilson, 1995 Stenetrium bowmani Transferred to Hansenium Serov and Wilson, 1995 Stenetrium caicoensis Transferred to Hansenium Serov and Wilson, 1995 Stenetrium kensleyi Newly described, this study Stenetrium minocule Transferred to Liocoryphe Serov and Wilson, 1995 Stenetrium patulipalma Transferred to Mizothenar Serov and Wilson, 1995 Stenetrium serratum Unchanged since description Haswell, 1881 Stenetrium spathuUcarpus Transferred to Hansenium Serov and Wilson, 1995 Stenetrium stebbingi Transferred to Hansenium Serov and Wilson, 1995 Stenohermuda acutirostrata Unchanged since description Schultz, 1979 Stenohermuda iliffei Unchanged since description Kensley. 1994 * Considered a junior synonym of Stenetrium stebbingi by Kensley (1982) but listed as a valid member of Hansenium by Serov and Wilson (1995). As part of an ongoing biotic survey of terial examined during this study was col­ the cryptic marine invertebrates of certain lected by R. Wetzer and G. Hendler. The islands in the Caribbean (led by T. L. Zim­ specimens were fixed and preserved in 95% merman and J. W. Martin), we obtained nu­ ethanol. Total length equals the distance merous specimens, including adult males, from the tip of the rostrum to the posteri- of an undescribed asellote isopod referable ormost margin of the pleotelson. RW num­ to the genus Stenetrium Haswell, 1881, but bers refer to field collection stations of the also sharing some characters with the genus third author; LACM numbers are catalog Hansenium as described by Serov and Wil­ numbers in the Natural History Museum of son (1995) and Bolstad and Kensley Los Angeles County's collection of Crus­ (1999). The specimens came from waters tacea. surrounding Navassa Island, a United States Territory just off the southeastern coast of Stenetrium kensleyi, new species Cuba. Of the 18 species of Stenetrium rec­ Figs 1-4 ognized by Serov and Wilson (1995), the new species appears to have its closest af­ Material examined.—Holotype (LACM finities to S. serratum, the only other spe­ CR 2000-017.2): 1 ovigerous female, At­ cies of Stenetrium currently recognized (by lantic, Caribbean Sea, Navassa Island, Pin­ Serov and Wilson 1995, but see also Re­ nacles, 18°24.463'N, 75°01.094'W, SCU­ marks below) from the northwestern Atlan­ BA, — 19 m, Halimeda washes, R/V Coral tic. The species is also similar in some ways Reef II, 21 March 2000, RW00.070. Para- to Stenetrium caicosensis, a species that types: LACM CR 2000-017.1, 2 adult was treated as Hansenium (with spelling males (most appendages present), 2 ovig­ emended to H. caicosense) by Serov and erous females (lacking most appendages), Wilson (1995). 2 specimens (sex not determined), same The description of the new species of collection data as holotype. LACM CR Stenetrium, which is based solely on spec­ 2000-021.1, 4 females [2 females with imens collected from Navassa Island in the oostegites and 2 females without oostegi- tropical Northwest Atlantic (northern Ca­ tes; the latter 2 in poor condition]; 4 sub- ribbean Sea), is the subject of this report. adult males, Atlantic, Caribbean Sea, Na­ Unless otherwise indicated all of the ma­ vassa Island, NW Lulu Bay, 18°23.856'N, VOLUME 116. NUMBER 4 969 75°01.220'W, SCUBA, Halimeda washes, imately equal in length to peduncle and 3/ R/V Coral Reef II, 19 March 2000, NIP- 4 length of endopod. 2000-13, RW00.049. LACM CR 2000- Description of male.—Body (Fig. lA, 021.2, 1 subadult male, Atlantic, Caribbe­ B). Total length 3.6 mm, approximately 3.5 an Sea, Navassa Island NW Lulu Bay, times width, as measured across widest 18°23.856'N, 75°01.220'W, SCUBA, Hal­ (6th) pereonite. Pereonites 1-3 sharply an­ imeda washes. R/V Coral Reef II, 19 gled forward; pereonite 4 similar but less March 2000, NIP-2000-13, RW00.049 sharply angled; pereonites 5-7 directed pos­ (first left pereopod illustrated in fig. 3B). teriorly. All pereonites with at least one LACM CR 2000-020.1, 1 female without long lateral seta extending outward. oostegites (most appendages intact), Atlan­ Pigmentation (Fig. lA). Pattern some­ tic, Caribbean Sea, Navassa Island, near what similar to that described for S. serra- Lulu Bay, 18°23.791'N 75°01.195'W, tum Hansen, 1905 (see Kensley and Schot- SCUBA, ~9 m, rock rubble wash, R/V te, 1989, fig. 46F). Head with pigmentation Coral Reef II, 18 March 2000, coll. R. confined mostly to anterior third and be­ Wetzer and D. O'Foighel, RW00.044. tween the eyes. Pereonite 1 with pigment in LACM CR 2000-018.1, 1 adult male (most two narrow lateral bands running anterior appendages missing), Atlantic, Caribbean to posterior, with central region and antero­ Sea, Navassa Island, Tom's Rock, lateral corners unpigmented. Pereonite 4 18°23.655'N 75°01.094'W, SCUBA, rock mostly unpigmented. Pleotelson almost en­ and sponge washes, R/V Coral Reef II, 21 tirely pigmented except for horizontal un­ March 2000, RW00.074. LACM CR 2000- pigmented band at about midlength and for 019.1, 4 adult males (most with append­ outer posterior and posterolateral margins. ages missing but with chelipeds intact), At­ Other pereonites variously covered with re­ lantic, Caribbean Sea, Navassa Island, ticulated pigmentation broken up by open 18°23.655'N, 75°0I.094'W, RW00.074 and areas, as shown. RW00.051 (combined). Head (Fig. I A, B). Eyes located dorso- Diagnosis.—Stenetrium with short, wide, laterally, reniform, well pigmented, com­ distally truncate rostrum. Cephalon with posed of some 15—18 ommatidia. Antero­ well developed and acute anterolateral and lateral spines (anterolateral lobes) well de­ antennal spines subequal in length; antero­ veloped, acute, extending forward almost as lateral spine not quite reaching level of ros­ far as antennal spines, separated from an­ tral tip; antennal spine slightly longer and tennal spines by rounded gap extending extending anteriorly slightly beyond rostral backward toward eye. Antennal spine acute, tip. Eyes well pigmented, reniform. Pereon- extending anteriorly to level of rostrum. ites 1—3 with sharply angled anterolateral Rostrum broad, distally truncate. Outer (lat­ margins (less so on pereonite 4). Pleotelson eral) border of anterolateral lobes each with with lateral margins appearing serrate, with 2 long setae and scattered shorter setae as four movable spiniform setae and postero­ illustrated.
Recommended publications
  • Global Diversity of Marine Isopods (Except Asellota and Crustacean Symbionts)
    Collection Review Global Diversity of Marine Isopods (Except Asellota and Crustacean Symbionts) Gary C. B. Poore1*, Niel L. Bruce2,3 1 Museum Victoria, Melbourne, Victoria, Australia, 2 Museum of Tropical Queensland and School of Marine and Tropical Biology, James Cook University, Townsville, Queensland, Australia, 3 Department of Zoology, University of Johannesburg, Auckland Park, South Africa known from the supralittoral and intertidal to depths in excess of Abstract: The crustacean order Isopoda (excluding six kilometres. Isopods are a highly diverse group of crustaceans, Asellota, crustacean symbionts and freshwater taxa) with more than 10,300 species known to date, approximately comprise 3154 described marine species in 379 genera 6,250 of these being marine or estuarine. In the groups under in 37 families according to the WoRMS catalogue. The discussion here (about half the species) the vast majority of species history of taxonomic discovery over the last two centuries are known from depths of less than 1000 metres. is reviewed. Although a well defined order with the Peracarida, their relationship to other orders is not yet The Isopoda is one of the orders of peracarid crustaceans, that resolved but systematics of the major subordinal taxa is is, those that brood their young in a marsupium under the body. relatively well understood. Isopods range in size from less They are uniquely defined within Peracarida by the combination than 1 mm to Bathynomus giganteus at 365 mm long. of one pair of uropods attached to the pleotelson and pereopods of They inhabit all marine habitats down to 7280 m depth only one branch. Marine isopods are arguably the most but with few doubtful exceptions species have restricted morphologically diverse order of all the Crustacea.
    [Show full text]
  • 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.
    [Show full text]
  • The Coume Ouarnède System, a Hotspot of Subterranean Biodiversity in Pyrenees (France)
    diversity Article The Coume Ouarnède System, a Hotspot of Subterranean Biodiversity in Pyrenees (France) Arnaud Faille 1,* and Louis Deharveng 2 1 Department of Entomology, State Museum of Natural History, 70191 Stuttgart, Germany 2 Institut de Systématique, Évolution, Biodiversité (ISYEB), UMR7205, CNRS, Muséum National d’Histoire Naturelle, Sorbonne Université, EPHE, 75005 Paris, France; [email protected] * Correspondence: [email protected] Abstract: Located in Northern Pyrenees, in the Arbas massif, France, the system of the Coume Ouarnède, also known as Réseau Félix Trombe—Henne Morte, is the longest and the most complex cave system of France. The system, developed in massive Mesozoic limestone, has two distinct resur- gences. Despite relatively limited sampling, its subterranean fauna is rich, composed of a number of local endemics, terrestrial as well as aquatic, including two remarkable relictual species, Arbasus cae- cus (Simon, 1911) and Tritomurus falcifer Cassagnau, 1958. With 38 stygobiotic and troglobiotic species recorded so far, the Coume Ouarnède system is the second richest subterranean hotspot in France and the first one in Pyrenees. This species richness is, however, expected to increase because several taxonomic groups, like Ostracoda, as well as important subterranean habitats, like MSS (“Milieu Souterrain Superficiel”), have not been considered so far in inventories. Similar levels of subterranean biodiversity are expected to occur in less-sampled karsts of central and western Pyrenees. Keywords: troglobionts; stygobionts; cave fauna Citation: Faille, A.; Deharveng, L. The Coume Ouarnède System, a Hotspot of Subterranean Biodiversity in Pyrenees (France). Diversity 2021, 1. Introduction 13 , 419. https://doi.org/10.3390/ Stretching at the border between France and Spain, the Pyrenees are known as one d13090419 of the subterranean hotspots of the world [1].
    [Show full text]
  • From Ghost and Mud Shrimp
    Zootaxa 4365 (3): 251–301 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4365.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:C5AC71E8-2F60-448E-B50D-22B61AC11E6A Parasites (Isopoda: Epicaridea and Nematoda) from ghost and mud shrimp (Decapoda: Axiidea and Gebiidea) with descriptions of a new genus and a new species of bopyrid isopod and clarification of Pseudione Kossmann, 1881 CHRISTOPHER B. BOYKO1,4, JASON D. WILLIAMS2 & JEFFREY D. SHIELDS3 1Division of Invertebrate Zoology, American Museum of Natural History, Central Park West @ 79th St., New York, New York 10024, U.S.A. E-mail: [email protected] 2Department of Biology, Hofstra University, Hempstead, New York 11549, U.S.A. E-mail: [email protected] 3Department of Aquatic Health Sciences, Virginia Institute of Marine Science, College of William & Mary, P.O. Box 1346, Gloucester Point, Virginia 23062, U.S.A. E-mail: [email protected] 4Corresponding author Table of contents Abstract . 252 Introduction . 252 Methods and materials . 253 Taxonomy . 253 Isopoda Latreille, 1817 . 253 Bopyroidea Rafinesque, 1815 . 253 Ionidae H. Milne Edwards, 1840. 253 Ione Latreille, 1818 . 253 Ione cornuta Bate, 1864 . 254 Ione thompsoni Richardson, 1904. 255 Ione thoracica (Montagu, 1808) . 256 Bopyridae Rafinesque, 1815 . 260 Pseudioninae Codreanu, 1967 . 260 Acrobelione Bourdon, 1981. 260 Acrobelione halimedae n. sp. 260 Key to females of species of Acrobelione Bourdon, 1981 . 262 Gyge Cornalia & Panceri, 1861. 262 Gyge branchialis Cornalia & Panceri, 1861 . 262 Gyge ovalis (Shiino, 1939) . 264 Ionella Bonnier, 1900 .
    [Show full text]
  • Lazare Botosaneanu ‘Naturalist’ 61 Doi: 10.3897/Subtbiol.10.4760
    Subterranean Biology 10: 61-73, 2012 (2013) Lazare Botosaneanu ‘Naturalist’ 61 doi: 10.3897/subtbiol.10.4760 Lazare Botosaneanu ‘Naturalist’ 1927 – 2012 demic training shortly after the Second World War at the Faculty of Biology of the University of Bucharest, the same city where he was born and raised. At a young age he had already showed interest in Zoology. He wrote his first publication –about a new caddisfly species– at the age of 20. As Botosaneanu himself wanted to remark, the prominent Romanian zoologist and man of culture Constantin Motaş had great influence on him. A small portrait of Motaş was one of the few objects adorning his ascetic office in the Amsterdam Museum. Later on, the geneticist and evolutionary biologist Theodosius Dobzhansky and the evolutionary biologist Ernst Mayr greatly influenced his thinking. In 1956, he was appoint- ed as a senior researcher at the Institute of Speleology belonging to the Rumanian Academy of Sciences. Lazare Botosaneanu began his career as an entomologist, and in particular he studied Trichoptera. Until the end of his life he would remain studying this group of insects and most of his publications are dedicated to the Trichoptera and their environment. His colleague and friend Prof. Mar- cos Gonzalez, of University of Santiago de Compostella (Spain) recently described his contribution to Entomolo- gy in an obituary published in the Trichoptera newsletter2 Lazare Botosaneanu’s first contribution to the study of Subterranean Biology took place in 1954, when he co-authored with the Romanian carcinologist Adriana Damian-Georgescu a paper on animals discovered in the drinking water conduits of the city of Bucharest.
    [Show full text]
  • Zootaxa, Thylakogaster Namibiensis Sp. Nov. (Isopoda: Asellota
    Zootaxa 2096: 381–394 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Thylakogaster namibiensis sp. nov. (Isopoda: Asellota: Janiroidea), a new species of Haplomunnidae from the southeast Atlantic deep sea* NILS BRENKE1# & ANIKA BUSCHMANN2 1Abt. DZMB, Forschungsinstitut Senckenberg, Südstrand 44,26382 Wilhelmshaven, Germany 2Ruhr University of Bochum, Department of Animal Morphology and Systematics, Universitätsstraße 150, Building ND 05/753, 44780 Bochum, Germany # corresponding author: [email protected] * In: Brökeland, W. & George, K.H. (eds) (2009) Deep-sea taxonomy — a contribution to our knowledge of biodiversity. Zootaxa, 2096, 1–488. Abstract Thylakogaster namibiensis sp. nov., a new deep-sea species belonging to the family Haplomunnidae Wilson, 1976 is described from the southeast Atlantic Ocean. The differences of the new species to the other species of the genus Thylakogaster Wilson and Hessler, 1974 are discussed. Main characters distinguishing T. namibiensis sp. nov. from its congeners are the presence of cuticular spines on the lateral margins of the pereonites 1–7, the low number of spines on the pleotelson, and the number of five terminal flagellar articles bearing aesthetascs on the antenna 1 of the copulatory male. The new species, T. namibiensis, is the first member of this genus found in the southeast Atlantic Ocean and at a depth of 5415 m, it is also the deepest which a member of the genus has ever been found. Key words: Crustacea, Peracarida, Thylakogaster, taxonomy, Angola Basin, Me 48-1 / Diva 1, Me 63-2 / Diva 2 Introduction Over the last few decades the deep sea of the World ocean has generated increased scientific interest, especially with respect to biodiversity studies (Lambshead et al.
    [Show full text]
  • A Source‐Sink Hypothesis for Abyssal Biodiversity. Author(S): Michael A
    The University of Chicago A Source‐Sink Hypothesis for Abyssal Biodiversity. Author(s): Michael A. Rex, Craig R. McClain, Nicholas A. Johnson, Ron J. Etter, John A. Allen, Philippe Bouchet, and Anders Warén Source: The American Naturalist, Vol. 165, No. 2 (February 2005), pp. 163-178 Published by: The University of Chicago Press for The American Society of Naturalists Stable URL: http://www.jstor.org/stable/10.1086/427226 . Accessed: 11/07/2014 14:07 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. The University of Chicago Press, The American Society of Naturalists, The University of Chicago are collaborating with JSTOR to digitize, preserve and extend access to The American Naturalist. http://www.jstor.org This content downloaded from 152.3.68.115 on Fri, 11 Jul 2014 14:07:27 PM All use subject to JSTOR Terms and Conditions vol. 165, no. 2 the american naturalist february 2005 ൴ A Source-Sink Hypothesis for Abyssal Biodiversity Michael A. Rex,1,* Craig R. McClain,2,† Nicholas A. Johnson,3,‡ Ron J. Etter,1,§ John A. Allen,4,k Philippe Bouchet,5,# and Anders Ware´n6,** 1. Department of Biology, University of Massachusetts, Boston, organic carbon flux to the benthos with increasing depth and distance Massachusetts 02125; from productive coastal systems.
    [Show full text]
  • Isopoda, Asellota) with Some Phylogenetic Considerations Concerning Asellota
    Crustaceana 48 (2) 1985, E. J. Brill, Leiden A CONTRIBUTION TO THE GENERAL MORPHOLOGY OF PROTOJANIRIDAE (ISOPODA, ASELLOTA) WITH SOME PHYLOGENETIC CONSIDERATIONS CONCERNING ASELLOTA BY B. SKET Institut za biologijo, Univerza E. Kardelja v Ljubljani, p.p. 141, YU 61001 Ljubljana, Yugoslavia Since most representatives of the superfamily Gnathostenetroidoidea have been described only for "microtaxonomical" purposes, some important features and even peculiarities of the species and probably of the entire group have been overlooked. I took advantage of possessing a good sample of the comparatively very large representative, viz., Enckella lucei major Sket, 1982 (as well as some other species of the family Protojaniridae) to demonstrate some such features. Unfortunately, of the family Gnathostenetroididae I could study only specimens of an undescribed species from the Bahamas, while comparison with other representatives was possible only through illustrations. I abstained from comparing Enckella with the numerous and diverse Janiroidea, leaving this to a more versed student of that special group. I also abstained from discussing the remarkable idea about possible Asellotan nature of Microcerberidae (WageJe, J 980) which is anyway of little importance for the present subject. Cephalothorax ("head"). — With the exception of having two pairs of antennae, the Enckella's head bears greater resemblance to a prognathous in­ sect head than to an Asellid. The cephalic capsula is closed to a great extent, incorporating completely the first thoracomere. The capsula is closed and slightly sclerotised also behind the insertions of the maxillipeds, uniting them with the set of other mouth appendages. The clypeolabrum protrudes for­ wards, its inclination downwards is much less expressed than in most other groups of Isopoda.
    [Show full text]
  • Systematics, Zoogeography, Evolution and Biodiversity of Antarctic Deep-Sea Isopoda (Crustacea: Malacostraca)
    Systematics, zoogeography, evolution and biodiversity of Antarctic deep-sea Isopoda (Crustacea: Malacostraca) Dissertation zur Erlangung des Doktorgrades des Fachbereichs Biologie der Universität Hamburg vorgelegt von Wiebke Brökeland aus Essen Hamburg 2005 Our knowledge can only be finite, while our ignorance must necessarily be infinite. Karl Raimund Popper According to ICZN article 8.3 all names and nomenclatural acts in this thesis are disclaimed for nomenclatural purposes. Table of contents Summary..................................................................................................................................... i 1 Introduction............................................................................................................................ 1 1.1 The deep sea................................................................................................................................. 1 1.2 The Southern Ocean ................................................................................................................... 2 1.3 Deep-sea Isopoda......................................................................................................................... 3 1.4 Aims and questions ..................................................................................................................... 5 2 Material and Methods ............................................................................................................ 6 2.1 Sampling .....................................................................................................................................
    [Show full text]
  • Anatomical Glossary for Isopoda Asellota 1 09/20/13 GDF Wilson
    Anatomical glossary for Isopoda Asellota Glossary for anatomical terms of Asellota G.D.F. Wilson (20 September 2013) This glossary contains definitions of morphological terms originally used by Wilson (1985; 1989) with an emphasis on the family Munnopsidae in the asellotan superfamily Janiroidea and Wilson (1997) (more generally for Crustacea and Isopoda). Kensley & Schotte (1989) also provide a glossary for terms used in isopod systematics. Terminology of Hessler (1970), Wolff (1962) and homologies established in Wilson (2009) and Riehl and Wilson (in press) are employed throughout. Aesthetasc. A long, tubular sensory seta having thin cuticle, found on the antennula. Aesthetascs may have a chemosensory function, because males generally have many more than females. Ambulosome. The anterior part of the thorax (tagma) of munnopsid isopods that bears the walking legs. It consists of pereonites 1-4. Ambulosomite. A body segment of the ambulosome. Annulus (plural annuli). A distal segment of the either the antenna or antennula, generally tubular in form. Antenna (synonym, second antenna). The second, paired, cephalic appendage. It consists of four short, robust, proximal segments, two long, intermediate segments, and a series of tapering annuli, called the flagellum. The podomeric articles, using the terminology of Hansen (1893) The third basal segment bears a smaller, lateral appendage called the scale that is homologous to the exopod in other Crustacea. Antennula (synonyms first antenna, antennule). The first paired cephalic appendage. In most janiroidean isopods, it consists of a robust basal segment, two segments of intermediate thickness, and distal annular segments of varying lengths. The distal segments bear aesthetascs of varying number.
    [Show full text]
  • 332307 FULLTEXT01.Pdf
    THE MARINE ISOPOD CRUSTACEA OF THE TRISTAN DA CUNHA ARCHIPELAGO by Erling Sivertsen and Lipke B. Holthuis University of Trondheim The Royal Norwegian Society of Sciences and Letters, The Museum ISBN 82-7126-211-4 ISSN 0332-8554 CONTENTS INTRODUCTION ...................•........................ 7 GEOGRAPHICAL DISTRIBUTION 9 LrST OF STATIONS .........................•............. 10 SYSTEMATIC ACCOUNT OF THE SPECIES .....•............. 20 An thuridea 20 Tristanthura barnardi '" 21 Eisothistos minutus 25 Flabellifera 28 Anuropus aeronautus 28 Aega deshaysiana 33 Livoneca raynaudii 34 Isocladus tristensis 37 Dynamenella menziesi 41 Cassidinopsis tuberculata ~... 48 Phycolimnoria tristanensis 55 Valvifera 59 Paridotea apposita 59 Neastacilla tristanica 64 Asellota 68 Munna aculeata _ _ 68 Munna nana 70 Munna varians 73 Paramunna antarctica .. 83 Pleurogonium minutum 86 Pleurosignum chilense 86 Santia hispida '............. 89 Santia compacta 92 Joeropsis paulensis 97 Iathrippa tristani 99 Iais pubescens 103 Iais elongata 104 Neoj aera hirsuta 107 Ianiropsis longipes 109 Vermectias caudiculata 118 ACKNOWLEDGEMENTS ••.•••••••••••••••••••••••••.•••.••• 121 LITERATURE ••••••••••••.•••••••••••••••••••••••••••••• 122 Plate 1 127 Plate 2 128 ABSTRACT Sivertsen, Erling & Lipke B. Holthuis. 1979. The marine Isopod Crustacea of the Tristan da Cunha Archipel go. GWlnPl'ia 35: 1-128~) A review is given of the known species of marine Isopoda of Tristan da Cunha and the other islands of the Tristan da Cunha Archi­ pelago, based on the collections made by the 1937-1938 Norwegian Scientific Expedition in that island group. Most of the material was obtained in the intertidal zone, from the spray zone at sornc meters above the high water line to far out in the surf zone. Depths from 3 to 60 meters were explored by dredge and yielded much intC'l:r"sting material.
    [Show full text]
  • Isopoda, Asellota, Janiridae) from Korean Waters
    Anim. Syst. Evol. Divers. Vol. 37, No. 2: 146-153, April 2021 https://doi.org/10.5635/ASED.2021.37.2.006 Short communication Description of Janiralata sagamiensis (Isopoda, Asellota, Janiridae) from Korean Waters Sung Hoon Kim1, Seong Myeong Yoon2,3,* 1Division of Ocean Sciences, Korea Polar Research Institute, Incheon 21990, Korea 2Department of Biology, College of Natural Sciences, Chosun University, Gwangju 61452, Korea 3Educational Research Group for Age-associated Disorder Control Technology, Graduate School, Chosun University, Gwangju 61452, Korea ABSTRACT Janirid isopod, Janiralata sagamiensis Shimomura, 2006 is newly reported from Korean waters. This species can be distinguishable from its congeners by the following characteristics: the cephalon has a distinct anterolateral projection on the anterolateral margin; the frontal margin of the cephalon is lacking rostrum; the coxal plates are visible in dorsal view; the pleotelson is rounded distally without a posterolateral point; the first pleopod of the male has a pair of protrusions distally; the third pleopodal exopod is lacking plumose setae. In this paper, the detailed description and illustrations of the species are provided with a key to known Janiralata species in the surrounding waters of Korea, including China and Japan. Keywords: Janiralata, Janiridae, isopods, morphology, Korea INTRODUCTION ralata species have been known, including single record from Korea: J. chuni (Thielemann, 1910) from Japan; J. koreaensis The Janiralata Menzies, 1951, comprising 32 species, is the Jang, 1991 from Korea; J. sagamiensis Shimomura, 2006 third largest genus after the Jaera Leach, 1814 and Janira from Japan; J. shiinoi Kussakin, 1962 from the East China Leach, 1814 among 30 genera of the family Janiridae G.
    [Show full text]