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A Review of Southern Ocean Squids Using Nets and Beaks
Marine Biodiversity (2020) 50:98 https://doi.org/10.1007/s12526-020-01113-4 REVIEW A review of Southern Ocean squids using nets and beaks Yves Cherel1 Received: 31 May 2020 /Revised: 31 August 2020 /Accepted: 3 September 2020 # Senckenberg Gesellschaft für Naturforschung 2020 Abstract This review presents an innovative approach to investigate the teuthofauna from the Southern Ocean by combining two com- plementary data sets, the literature on cephalopod taxonomy and biogeography, together with predator dietary investigations. Sixty squids were recorded south of the Subtropical Front, including one circumpolar Antarctic (Psychroteuthis glacialis Thiele, 1920), 13 circumpolar Southern Ocean, 20 circumpolar subantarctic, eight regional subantarctic, and 12 occasional subantarctic species. A critical evaluation removed five species from the list, and one species has an unknown taxonomic status. The 42 Southern Ocean squids belong to three large taxonomic units, bathyteuthoids (n = 1 species), myopsids (n =1),andoegopsids (n = 40). A high level of endemism (21 species, 50%, all oegopsids) characterizes the Southern Ocean teuthofauna. Seventeen families of oegopsids are represented, with three dominating families, onychoteuthids (seven species, five endemics), ommastrephids (six species, three endemics), and cranchiids (five species, three endemics). Recent improvements in beak identification and taxonomy allowed making new correspondence between beak and species names, such as Galiteuthis suhmi (Hoyle 1886), Liguriella podophtalma Issel, 1908, and the recently described Taonius notalia Evans, in prep. Gonatus phoebetriae beaks were synonymized with those of Gonatopsis octopedatus Sasaki, 1920, thus increasing significantly the number of records and detailing the circumpolar distribution of this rarely caught Southern Ocean squid. The review extends considerably the number of species, including endemics, recorded from the Southern Ocean, but it also highlights that the corresponding species to two well-described beaks (Moroteuthopsis sp. -
CEPHALOPODS 688 Cephalopods
click for previous page CEPHALOPODS 688 Cephalopods Introduction and GeneralINTRODUCTION Remarks AND GENERAL REMARKS by M.C. Dunning, M.D. Norman, and A.L. Reid iving cephalopods include nautiluses, bobtail and bottle squids, pygmy cuttlefishes, cuttlefishes, Lsquids, and octopuses. While they may not be as diverse a group as other molluscs or as the bony fishes in terms of number of species (about 600 cephalopod species described worldwide), they are very abundant and some reach large sizes. Hence they are of considerable ecological and commercial fisheries importance globally and in the Western Central Pacific. Remarks on MajorREMARKS Groups of CommercialON MAJOR Importance GROUPS OF COMMERCIAL IMPORTANCE Nautiluses (Family Nautilidae) Nautiluses are the only living cephalopods with an external shell throughout their life cycle. This shell is divided into chambers by a large number of septae and provides buoyancy to the animal. The animal is housed in the newest chamber. A muscular hood on the dorsal side helps close the aperture when the animal is withdrawn into the shell. Nautiluses have primitive eyes filled with seawater and without lenses. They have arms that are whip-like tentacles arranged in a double crown surrounding the mouth. Although they have no suckers on these arms, mucus associated with them is adherent. Nautiluses are restricted to deeper continental shelf and slope waters of the Indo-West Pacific and are caught by artisanal fishers using baited traps set on the bottom. The flesh is used for food and the shell for the souvenir trade. Specimens are also caught for live export for use in home aquaria and for research purposes. -
LABORATORY REARING of RHYNCHOTEUTHIONS of the OMMASTREPHID SQUID ILLEX ILLECEBROSUS (MOLLUSCA : CEPHALOPODA) N Balch, R O’Dor, P Helm
LABORATORY REARING OF RHYNCHOTEUTHIONS OF THE OMMASTREPHID SQUID ILLEX ILLECEBROSUS (MOLLUSCA : CEPHALOPODA) N Balch, R O’Dor, P Helm To cite this version: N Balch, R O’Dor, P Helm. LABORATORY REARING OF RHYNCHOTEUTHIONS OF THE OM- MASTREPHID SQUID ILLEX ILLECEBROSUS (MOLLUSCA : CEPHALOPODA). Vie et Milieu / Life & Environment, Observatoire Océanologique - Laboratoire Arago, 1985, pp.243-246. hal- 03022163 HAL Id: hal-03022163 https://hal.sorbonne-universite.fr/hal-03022163 Submitted on 24 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. VIE MILIEU, 1985, 35 (3/4) : 243-246 LABORATORY REARING OF RHYNCHOTEUTHIONS OF THE OMMASTREPHID SQUID ILLEX ILLECEBROSUS (MOLLUSCA : CEPHALOPODA) N. BALCH(1), R.K. O'DOR <2) and P. HELM(2) (1) Aquatron Laboratory, Institute of Oceanography (2) Biology Department, Dalhousie University, Halifax, Nova Scotia, Canada, B3H 4J1 OCEANIC SQUID ABSTRACT. — A methodology is presented for obtaining egg masses from captive LABORATORY REARING populations of the ommastrephid squid Illex illecebrosus and for incubating them LARVAE intact under controlled conditions. Survival of rhynchoteuthion larvae for 9 days after CEPHALOPODA hatching is the best reported to date, though it has not yet been possible to induce feeding. -
REPRODUCCIÓN DEL PULPO Octopus Bimaculatus Verrill, 1883 EN BAHÍA DE LOS ÁNGELES, BAJA CALIFORNIA, MÉXICO
INSTITUTO POLITÉCNICO NACIONAL CENTRO INTERDISCIPLINARIO DE CIENCIAS MARINAS REPRODUCCIÓN DEL PULPO Octopus bimaculatus Verrill, 1883 EN BAHÍA DE LOS ÁNGELES, BAJA CALIFORNIA, MÉXICO TESIS QUE PARA OBTENER EL GRADO ACADÉMICO DE MAESTRO EN CIENCIAS PRESENTA BIÓL. MAR. SHEILA CASTELLANOS MARTINEZ La Paz, B.C.S., Agosto de 2008 AGRADECIMIENTOS Agradezco al Centro Interdisciplinario de Ciencias Marinas por abrirme las puertas para llevar a cabo mis estudios de maestría, así como al Consejo Nacional de Ciencia y Tecnología (CONACyT) y a los proyectos PIFI por el respaldo económico brindado durante dicho periodo. Deseo expresar mi agradecimiento a mis directores, Dr. Marcial Arellano Martínez y Dr. Federico A. García Domínguez por apoyarme para aprender a revisar cortes histológicos (algo que siempre dije que no haría jaja!), lidiar con mis carencias de conocimiento, enseñarme cosas nuevas y ayudarme a encauzar las ideas. Gracias también a la Dra. Patricia Ceballos (Pati) por la asesoría con las numerosas dudas que surgieron a lo largo de este estudio, las correcciones y por enseñarme algunos trucos para que los cortes histológicos me quedaran bien. Los valiosos comentarios del Dr. Oscar E. Holguín Quiñones y M.C. Marcial Villalejo Fuerte definitivamente han sido imprescindibles para concluir satisfactoriamente este trabajo. A todos, gracias por contribuir en mi formación profesional y personal. Quiero extender mi gratitud al Dr. Gustavo Danemann (PRONATURA Noroeste, A.C.) así como al Lic. Esteban Torreblanca (PRONATURA Noroeste, A.C.) por todo su apoyo para el desarrollo de la tesis; igualmente, a la Asociación de Buzos de Bahía de Los Ángeles, A.C. por su importante participación en la obtención de muestras y por el interés activo que siempre han mostrado hacia este estudio. -
(Eledone Cirrhosa) in Atlantic Iberian Waters
Manuscript + Figure captions Click here to download Manuscript Eledone cirrhosa diet.docx Click here to view linked References 1 Factors affecting the feeding patterns of the horned octopus ( Eledone 2 cirrhosa ) in Atlantic Iberian waters 3 4 M. Regueira 1,2* , Á.Guerra 1, C.M. Fernández-Jardón 3,Á.F. González 1 5 6 1Instituto de Investigaciones Marinas (IIM-CSIC), Eduardo Cabello 6, 36208 Vigo, Spain. 7 2Departamento de Biologia, Universidade de Aveiro. 3810-193 Aveiro, Portugal. 8 3Facultad de Ciencias Económicas y Empresariales, Departamento de Economía Aplicada, Universidad 9 de Vigo, Campus de Vigo. 36310, Vigo, Spain. 10 11 12 *Corresponding author: [email protected] 13 Tel. (+34) 986 23 19 30 14 Fax. (+34) 986 29 27 62 15 16 17 RUNNING TITLE: Feeding patterns of Eledone cirrhosa 18 KEY WORDS: Cephalopods, Eledone cirrhosa , diet, feeding patterns, Atlantic Iberian waters, 19 Multinomial Logistic Regression. 1 20 Abstract The present study combines morphological and molecular analysis of stomach contents 21 (n=2,355) and Multinomial Logistic Regression (MLR) to understand the diet and feeding patterns of the 22 horned octopus Eledone cirrhosa inhabiting Atlantic Iberian waters. Specimens were collected monthly 23 from commercial bottom trawl fisheries between February 2009 and February 2011 in three fishing 24 grounds (North Galicia, West Galicia and North Portugal), located between 40.6 -43. 6°N and 8.6 -7.36°W. 25 Based on stomach analysis, horned octopuses in the region consumed mainly crustaceans, followed by 26 teleost fish, echinoderms, molluscs and polychaetes. Molecular analysis of 14 stomach contents 27 confirmed the visual identification of pre y items as well as cannibalistic events. -
Helminth Infection in the Short-Finned Squid Illex Coindetii (Cephalopoda, Ommastrephidae) Off NW Spain
DISEASES OF AQUATIC ORGANISMS Published September 14 Dis aquat Org Helminth infection in the short-finned squid Illex coindetii (Cephalopoda, Ommastrephidae) off NW Spain 'Laboratorio de Parasitologia, Facultad de Ciencias, Universidad de Vigo, Ap. 874 E-36200 Vigo, Spain 'Institute de Investigacions Marinas (CSIC),Eduardo Cabello 6, E-36208 Vigo, Spain ABSTRACT: A survey of parasites in 600 short-finned squid fllex coindetii (Verany. 1839) taken from 2 locations (north and south Galicia) off the northwestern Ibenan Peninsula revealed the presence of numerous somatoxenous helrninths. Three genera of Tetraphyllidean plerocercoids were represented (prevalences: Ph}~llobothriurn sp., 45.7%; Dinobothriunl sp., 0.8%; and Pelichnibothrium speciosum, 0.001 %); 1 Trypanorhynchidean metacestode was also present (Nybelinia vamagutll. 0.4 %). In addi- tion, larval nematodes of Anisakis simplex (L3) were recorded (10.6%). Abundance of infection was examined in relation to squid sex, standard length, maturity and locality. This analysis indicated that parasite infection was lower in the southern squids than in the northern squid group. Over the entire survey area, parasite infection showed a close positive correlation with host life-cycle, often with the greatest number of parasites among the largest and highest maturity individuals (>l8to 20 cm; matu- rlty stage V). KEY WORDS: Illex coindetii . Northwestern Iberian Peninsula Helminth parasites INTRODUCTION northeastern Atlantic waters. To this end, in the present paper some aspects of the host-parasite rela- Cephalopods represent 2.1 % of total worldwide tionship are examined. A possible local variability in catches of marine organisms (Guerra & Perez- degree of infection was also assessed in the light of the Gandaras 1983).In spite of the economic importance of clearly different hydrographical conditions between this fishery, relatively little is known about the host- northern and southern shelf areas off the Galician parasite relationships of teuthoid cephalopods (see coast (Fraga et al. -
Cephalopoda: Sepiolidae)
Helgol Mar Res (2011) 65:43–49 DOI 10.1007/s10152-010-0199-y ORIGINAL ARTICLE Spawning strategy in Atlantic bobtail squid Sepiola atlantica (Cephalopoda: Sepiolidae) Marcelo Rodrigues · Manuel E. Garcí · Jesús S. Troncoso · Ángel Guerra Received: 20 November 2009 / Revised: 18 March 2010 / Accepted: 19 March 2010 / Published online: 6 April 2010 © Springer-Verlag and AWI 2010 Abstract This study aimed to determine the spawning Introduction strategy in the Atlantic bobtail squid Sepiola atlantica, in order to add new information to the knowledge of its repro- Cephalopods have highly variable and complex life history ductive strategy. A total of 12 females that spawned in traits related to reproduction (Hanlon and Messenger 1996). aquaria were examined. Characteristics of the reproductive Information on reproductive strategies may lead to a better traits and egg clutches were similar to those of other known understanding of the evolution of life histories, both repro- Sepiolidae. Clutch size varied from 31 up to 115 eggs. ductive strategies and life cycles being genetic adaptations Females of this species had incorporated up to 1.58 times of to optimize the use of ecological niches in direct competi- their body weight into laid eggs. The size of laid eggs tion with other species and in response to environmental showed a positive correlation with maternal body size, sup- conditions (Rocha et al. 2001). The patterns of ovulation porting the idea that female size is a determinant of egg and spawning are basic elements to characterize cephalo- size. Our data suggest that S. atlantica is an intermittent ter- pod reproductive patterns. -
7. Index of Scientific and Vernacular Names
Cephalopods of the World 249 7. INDEX OF SCIENTIFIC AND VERNACULAR NAMES Explanation of the System Italics : Valid scientific names (double entry by genera and species) Italics : Synonyms, misidentifications and subspecies (double entry by genera and species) ROMAN : Family names ROMAN : Scientific names of divisions, classes, subclasses, orders, suborders and subfamilies Roman : FAO names Roman : Local names 250 FAO Species Catalogue for Fishery Purposes No. 4, Vol. 1 A B Acanthosepion pageorum .....................118 Babbunedda ................................184 Acanthosepion whitleyana ....................128 bandensis, Sepia ..........................72, 138 aculeata, Sepia ............................63–64 bartletti, Blandosepia ........................138 acuminata, Sepia..........................97,137 bartletti, Sepia ............................72,138 adami, Sepia ................................137 bartramii, Ommastrephes .......................18 adhaesa, Solitosepia plangon ..................109 bathyalis, Sepia ..............................138 affinis, Sepia ...............................130 Bathypolypus sponsalis........................191 affinis, Sepiola.......................158–159, 177 Bathyteuthis .................................. 3 African cuttlefish..............................73 baxteri, Blandosepia .........................138 Ajia-kouika .................................. 115 baxteri, Sepia.............................72,138 albatrossae, Euprymna ........................181 belauensis, Nautilus .....................51,53–54 -
Phylum MOLLUSCA Chitons, Bivalves, Sea Snails, Sea Slugs, Octopus, Squid, Tusk Shell
Phylum MOLLUSCA Chitons, bivalves, sea snails, sea slugs, octopus, squid, tusk shell Bruce Marshall, Steve O’Shea with additional input for squid from Neil Bagley, Peter McMillan, Reyn Naylor, Darren Stevens, Di Tracey Phylum Aplacophora In New Zealand, these are worm-like molluscs found in sandy mud. There is no shell. The tiny MOLLUSCA solenogasters have bristle-like spicules over Chitons, bivalves, sea snails, sea almost the whole body, a groove on the underside of the body, and no gills. The more worm-like slugs, octopus, squid, tusk shells caudofoveates have a groove and fewer spicules but have gills. There are 10 species, 8 undescribed. The mollusca is the second most speciose animal Bivalvia phylum in the sea after Arthropoda. The phylum Clams, mussels, oysters, scallops, etc. The shell is name is taken from the Latin (molluscus, soft), in two halves (valves) connected by a ligament and referring to the soft bodies of these creatures, but hinge and anterior and posterior adductor muscles. most species have some kind of protective shell Gills are well-developed and there is no radula. and hence are called shellfish. Some, like sea There are 680 species, 231 undescribed. slugs, have no shell at all. Most molluscs also have a strap-like ribbon of minute teeth — the Scaphopoda radula — inside the mouth, but this characteristic Tusk shells. The body and head are reduced but Molluscan feature is lacking in clams (bivalves) and there is a foot that is used for burrowing in soft some deep-sea finned octopuses. A significant part sediments. The shell is open at both ends, with of the body is muscular, like the adductor muscles the narrow tip just above the sediment surface for and foot of clams and scallops, the head-foot of respiration. -
Diverse Deep-Sea Anglerfishes Share a Genetically Reduced Luminous
RESEARCH ARTICLE Diverse deep-sea anglerfishes share a genetically reduced luminous symbiont that is acquired from the environment Lydia J Baker1*, Lindsay L Freed2, Cole G Easson2,3, Jose V Lopez2, Dante´ Fenolio4, Tracey T Sutton2, Spencer V Nyholm5, Tory A Hendry1* 1Department of Microbiology, Cornell University, New York, United States; 2Halmos College of Natural Sciences and Oceanography, Nova Southeastern University, Fort Lauderdale, United States; 3Department of Biology, Middle Tennessee State University, Murfreesboro, United States; 4Center for Conservation and Research, San Antonio Zoo, San Antonio, United States; 5Department of Molecular and Cell Biology, University of Connecticut, Storrs, United States Abstract Deep-sea anglerfishes are relatively abundant and diverse, but their luminescent bacterial symbionts remain enigmatic. The genomes of two symbiont species have qualities common to vertically transmitted, host-dependent bacteria. However, a number of traits suggest that these symbionts may be environmentally acquired. To determine how anglerfish symbionts are transmitted, we analyzed bacteria-host codivergence across six diverse anglerfish genera. Most of the anglerfish species surveyed shared a common species of symbiont. Only one other symbiont species was found, which had a specific relationship with one anglerfish species, Cryptopsaras couesii. Host and symbiont phylogenies lacked congruence, and there was no statistical support for codivergence broadly. We also recovered symbiont-specific gene sequences from water collected near hosts, suggesting environmental persistence of symbionts. Based on these results we conclude that diverse anglerfishes share symbionts that are acquired from the environment, and *For correspondence: that these bacteria have undergone extreme genome reduction although they are not vertically [email protected] (LJB); transmitted. -
Female Description of the Hydrothermal Vent Cephalopod Vulcanoctopus Hydrothermalis A.F
Journal of the Marine Biological Association of the United Kingdom, 2008, 88(2), 375–379. #2008 Marine Biological Association of the United Kingdom doi:10.1017/S0025315408000647 Printed in the United Kingdom Female description of the hydrothermal vent cephalopod Vulcanoctopus hydrothermalis a.f. gonzÆlez1, a. guerra1, s. pascual1 and m. segonzac2 1ECOBIOMAR, Instituto de Investigaciones Marinas (CSIC), Eduardo Cabello 6, 36208 Vigo, Spain, 2IFREMER, Centre de Brest, Laboratoire Environnement Profond, BP 70, 29280-Plouzane´, France During biological sampling of hydrothermal vents on the East Pacific Rise, the manned submersible ‘Nautile’ caught the first female of the endemic cephalopod Vulcanoctopus hydrothermalis. The specimen caught at the vent site Gromit (21833 660S, 114817 980W at 2832 m depth) is described here in detail and an amended diagnosis of the species proposed. The external morphology, measurements and internal structure resemble that of males of this species. One of the most remarkable char- acters is the lack of spermathecae and the absence of apical filaments in the oocytes to provide a site for sperm storage. It is suggested that some species of the genera Benthoctopus and Bathypolypus would be the most suitable octopod ancestor of V. hydrothermalis. Keywords: hydrothermal vent, cephalopods, Vulcanoctopus hydrothermalis, female description Submitted 20 April 2007; accepted 29 November 2007 INTRODUCTION et al., 2006). It inhabits an isolated extreme environment very close to the base of the chimneys and is also observed The study of chemosynthetic ecosystems in the deep sea rep- on the pillow lava at several metres from the active areas. resents a challenging issue due to the difficulty of sampling, This benthic species has characters that represent adaptations which involves the use of modern technologies such as either to the deep-sea or to a hydrothermal vent habitat manned submersibles. -
Quantifying the Swimming Gaits of Veined Squid (Loligo Forbesii) Using Bio-Logging Tags Genevieve E
© 2019. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2019) 222, jeb198226. doi:10.1242/jeb.198226 RESEARCH ARTICLE Quantifying the swimming gaits of veined squid (Loligo forbesii) using bio-logging tags Genevieve E. Flaspohler1,2, Francesco Caruso3,4, T. Aran Mooney3,*, Kakani Katija5, Jorge Fontes6,7,8, Pedro Afonso6,7,8 and K. Alex Shorter9 ABSTRACT INTRODUCTION Squid are mobile, diverse, ecologically important marine organisms Squid are diverse and ecologically important marine organisms. As whose behavior and habitat use can have substantial impacts on squid are ectothermic animals, their physiology and behavior can be ecosystems and fisheries. However, as a consequence in part of the directly linked to the physical conditions of their surrounding inherent challenges of monitoring squid in their natural marine environment (Kaplan et al., 2013; Rosa and Seibel, 2010). In turn, environment, fine-scale behavioral observations of these free- squid behavior and habitat use can have substantial impacts on swimming, soft-bodied animals are rare. Bio-logging tags provide an marine ecosystems and fisheries. Monitoring and observing squid emerging way to remotely study squid behavior in their natural behavioral patterns and vital rates can be important for ’ environments. Here, we applied a novel, high-resolution bio-logging understanding their activity and energy usage (O Dor et al., 1995; tag (ITAG) to seven veined squid, Loligo forbesii, in a controlled Pörtner, 2002), as well as for elucidating the broader ecological experimental environment to quantify their short-term (24 h) behavioral interactions between squid and the taxa they influence (e.g. foraging patterns. Tag accelerometer, magnetometer and pressure data were rates; Clarke, 1977) and how environmental changes may alter these used to develop automated gait classification algorithms based on activities (Pörtner et al., 2004; Rosa et al., 2014).