The Occurrence of Black Necrotic Disease in Crab Species from the West of Scotland
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Report of the Working Group on the Biology and Life History of Crabs (WGCRAB)
ICES WGCRAB REPORT 2012 SCICOM STEERING GROUP ON ECOSYSTEM FUNCTIONS ICES CM 2012/SSGEF:08 REF. SSGEF, SCICOM, ACOM Report of the Working Group on the Biology and Life History of Crabs (WGCRAB) 14–18 May 2012 Port Erin, Isle of Man, UK International Council for the Exploration of the Sea Conseil International pour l’Exploration de la Mer H. C. Andersens Boulevard 44–46 DK-1553 Copenhagen V Denmark Telephone (+45) 33 38 67 00 Telefax (+45) 33 93 42 15 www.ices.dk [email protected] Recommended format for purposes of citation: ICES. 2012. Report of the Working Group on the Biology and Life History of Crabs (WGCRAB), 14–18 May 2012. ICES CM 2012/SSGEF:08 80pp. For permission to reproduce material from this publication, please apply to the Gen- eral Secretary. The document is a report of an Expert Group under the auspices of the International Council for the Exploration of the Sea and does not necessarily represent the views of the Council. © 2012 International Council for the Exploration of the Sea ICES WGCRAB Report 2012 | i Contents Executive summary ................................................................................................................ 1 1 Introduction .................................................................................................................... 2 2 Adoption of the agenda ................................................................................................ 2 3 Terms of reference 2011 ................................................................................................ 2 4 -
The Tail Flip Escape Response of the Brown Shrimp Crangon Crangon (L.) in the Context of Predator-Prey Interactions
The tail flip escape response of the brown shrimp Crangon crangon (L.) in the context of predator-prey interactions Stephen Andrew Arnott This thesis is presented for the degree of Doctor of Philosophy at the University of Glasgow, Institute of Biomedical & Life Sciences, Division of Environmental & Evolutionary Biology. November 1996 ProQuest Number: 11007907 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 11007907 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 Iq U! S' ^LASCOw' ©NIVERSIfS’ I h b b a r y I Declaration: I declare that this thesis represents, except where a note is made to the contrary, work carried out by myself. The text was composed by myself. Stephen Andrew Amott. November 1996. ACKNOWLEDGEMENTS There are many people who have helped me in all manner of ways during the period of my PhD, and I am extremely grateful for all of the assistance which they have given me. First and foremost, I would like to thank my supervisors Dr. Douglas Neil and Dr. Alan Ansell for offering me the opportunity to undertake this project, for the excellent guidance they have provided through all stages of my laboratory and field work, and especially for their speedy and productive feed-back during my writing up period. -
First Record of Dromia Neogenica Müller, 1979 (Decapoda, Brachyura, Dromiidae) from Neogene Strata in the Southern North Sea Basin
FIRST RECORD OF DROMIA NEOGENICA MÜLLER, 1979 (DECAPODA, BRACHYURA, DROMIIDAE) FROM NEOGENE STRATA IN THE SOUTHERN NORTH SEA BASIN BY RENÉ H.B. FRAAIJE1,4), BARRY W.M. VAN BAKEL1,2,5) and JOHN W.M. JAGT3,6) 1) Oertijdmuseum De Groene Poort, Bosscheweg 80, NL-5283 Boxtel, The Netherlands 2) Nederlands Centrum voor Biodiversiteit (Naturalis), P.O. Box 9517, NL-2300 RA Leiden, The Netherlands 3) Natuurhistorisch Museum Maastricht, de Bosquetplein 6-7, NL-6211 KJ Maastricht, The Netherlands ABSTRACT The sponge crab Dromia neogenica Müller, 1979 (Dromiidae) is recorded for the first time from strata of Neogene (late Miocene-early Pliocene) age in the southern North Sea Basin, on the basis of two concretion-preserved carapaces from Bemmel (north of Nijmegen, province of Gelderland, The Netherlands). The presence of this species, which was previously known from the middle-upper Miocene of Hungary and Algeria, suggests relatively higher seawater temperatures in the North Sea during the late Miocene-early Pliocene. Morphological differences (extraorbital and anterolateral teeth, development of cervical and branchiocardiac grooves) between D. neogenica and extant D. personata (Linnaeus, 1758) are relatively minor. This observation, coupled with the absence of the former species in mid-Pliocene and younger strata, and with the robust record of the latter in the mid-Pliocene to upper Pleistocene of Italy, would indicate that D. neogenica and D. personata are closely related, and probably represent the same lineage. RÉSUMÉ La dromie éponge Dromia neogenica Müller, 1979 (Dromiidae) est signalée pour la premiére fois dans les strates du Néogène (fin du Miocène-début du Pliocène) du sud du bassin de la mer du Nord. -
Identification and Characterization of a Luteinizing Hormone
International Journal of Molecular Sciences Article Identification and Characterization of a Luteinizing Hormone Receptor (LHR) Homolog from the Chinese Mitten Crab Eriocheir sinensis Li-Juan Yuan 1,2,3,4,†, Chao Peng 1,2,3,4,†, Bi-Hai Liu 1,2,3,4,†, Jiang-Bin Feng 1,2,3,4,† and Gao-Feng Qiu 1,2,3,4,*,† 1 National Demonstration Center for Experimental Fisheries Science Education, Shanghai Ocean University, Shanghai 201306, China; [email protected] (L.-J.Y.); [email protected] (C.P.); [email protected] (B.-H.L.); [email protected] (J.-B.F.) 2 Key Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Ministry of Education, Shanghai Ocean University, Shanghai 201306, China 3 Key Laboratory of Freshwater Aquatic Genetic Resources, Ministry of Agriculture, Shanghai Ocean University, Shanghai 201306, China 4 Shanghai Engineering Research Center of Aquaculture, Shanghai Ocean University, Shanghai 201306, China * Correspondence: [email protected]; Tel./Fax: +86-21-61900436 † These authors contributed equally to this work. Received: 6 March 2019; Accepted: 4 April 2019; Published: 8 April 2019 Abstract: Luteinizing hormone (LH), a pituitary gonadotropin, coupled with LH receptor (LHR) is essential for the regulation of the gonadal maturation in vertebrates. Although LH homolog has been detected by immunocytochemical analysis, and its possible role in ovarian maturation was revealed in decapod crustacean, so far there is no molecular evidence for the existence of LHR. In this study, we cloned a novel LHR homolog (named EsLHR) from the Chinese mitten crab Eriocheir sinensis. The complete sequence of the EsLHR cDNA was 2775bp, encoding a protein of 924 amino acids, sharing 71% amino acids identity with the ant Zootermopsis nevadensis LHR. -
Belgian Register of Marine Species
BELGIAN REGISTER OF MARINE SPECIES September 2010 Belgian Register of Marine Species – September 2010 BELGIAN REGISTER OF MARINE SPECIES, COMPILED AND VALIDATED BY THE VLIZ BELGIAN MARINE SPECIES CONSORTIUM VLIZ SPECIAL PUBLICATION 46 SUGGESTED CITATION Leen Vandepitte, Wim Decock & Jan Mees (eds) (2010). Belgian Register of Marine Species, compiled and validated by the VLIZ Belgian Marine Species Consortium. VLIZ Special Publication, 46. Vlaams Instituut voor de Zee (VLIZ): Oostende, Belgium. 78 pp. ISBN 978‐90‐812900‐8‐1. CONTACT INFORMATION Flanders Marine Institute – VLIZ InnovOcean site Wandelaarkaai 7 8400 Oostende Belgium Phone: ++32‐(0)59‐34 21 30 Fax: ++32‐(0)59‐34 21 31 E‐mail: [email protected] or [email protected] ‐ 2 ‐ Belgian Register of Marine Species – September 2010 Content Introduction ......................................................................................................................................... ‐ 5 ‐ Used terminology and definitions ....................................................................................................... ‐ 7 ‐ Belgian Register of Marine Species in numbers .................................................................................. ‐ 9 ‐ Belgian Register of Marine Species ................................................................................................... ‐ 12 ‐ BACTERIA ............................................................................................................................................. ‐ 12 ‐ PROTOZOA ........................................................................................................................................... -
Influence of Infection by Sacculina Carcini (Cirripedia, Rhizocephala)
Journal of Experimental Marine Biology and Ecology 446 (2013) 209–215 Contents lists available at SciVerse ScienceDirect Journal of Experimental Marine Biology and Ecology journal homepage: www.elsevier.com/locate/jembe Influence of infection by Sacculina carcini (Cirripedia, Rhizocephala) on consumption rate and prey size selection in the shore crab Carcinus maenas Martin H. Larsen a, Jens T. Høeg b, Kim N. Mouritsen a,⁎ a Department of Bioscience, Marine Ecology, University of Aarhus, Ole Worms Allé 1, DK-8000 Aarhus C, Denmark b Department of Biology, Marine Biology Section, University of Copenhagen, Universitetsparken 4, DK-2100 Copenhagen, Denmark article info abstract Article history: Parasites generally influence the feeding behavior of their host and may therefore indirectly impact ecosystem Received 26 March 2013 structure and functioning if the host plays an ecological key role. The ecologically important shore crab Received in revised form 30 May 2013 (Carcinus maenas) is commonly infected by the rhizocephalan parasite Sacculina carcini that aside from Accepted 31 May 2013 inflicting behavioral change, castration and ceased molting, also feminizes its male host morphologically. Available online xxxx The latter results in reduced cheliped size, and, together with the other parasite-induced effects, this may potentially impact host feeding behavior. In two separate laboratory experiments, we offered infected and Keywords: Community structure uninfected adult male crabs respectively ad libitum small, easy-to-handle blue mussels (Mytilus edulis) Feeding behavior (10–15 mm in shell-length), and a limited, size-structured prey population (15–45 mm in shell-length; Feminization seven size-classes, ten mussels per class) during 10–15 days. -
Behavioural Effects of Hypersaline Exposure on the Lobster Homarus Gammarus (L) and the Crab Cancer Pagurus (L)
Journal of Experimental Marine Biology and Ecology (2014) 457: 208–214 http://dx.doi.org/10.1016/j.jembe.2014.04.016 Behavioural effects of hypersaline exposure on the lobster Homarus gammarus (L) and the crab Cancer pagurus (L) Katie Smyth 1,*, Krysia Mazik1,, Michael Elliott1, 1 Institute of Estuarine and Coastal Studies, University of Hull, Hull HU6 7RX, United Kingdom * Corresponding author. E-mail address: [email protected] (K. Smyth). Suggested citation: Smyth, K., Mazik, K., and Elliott, M., 2014. Behavioural effects of hypersaline exposure on the lobster Homarus gammarus (L) and the crab Cancer pagurus (L). Journal of Experimental Marine Biology and Ecology 457: 208- 214 Abstract There is scarce existing information in the literature regarding the responses of any marine species, especially commercially valuable decapod crustaceans, to hypersalinity. Hypersaline discharges due to solute mining and desalination are increasing in temperate areas, hence the behavioural responses of the edible brown crab, Cancer pagurus, and the European lobster, Homarus gammarus, were studied in relation to a marine discharge of highly saline brine using a series of preference tests. Both species had a significant behavioural response to highly saline brine, being able to detect and avoid areas of hypersalinity once their particular threshold salinity was reached (salinity 50 for C. pagurus and salinity 45 for H. gammarus). The presence of shelters had no effect on this response and both species avoided hypersaline areas, even when shelters were provided there. If the salinity of commercial effluent into the marine environment exceeds the behavioural thresholds found here, it is likely that adults of these species will relocate to areas of more favourable salinity. -
Crangon Franciscorum Class: Multicrustacea, Malacostraca, Eumalacostraca
Phylum: Arthropoda, Crustacea Crangon franciscorum Class: Multicrustacea, Malacostraca, Eumalacostraca Order: Eucarida, Decapoda, Pleocyemata, Caridea Common gray shrimp Family: Crangonoidea, Crangonidae Taxonomy: Schmitt (1921) described many duncle segment (Wicksten 2011). Inner fla- shrimp in the genus Crago (e.g. Crago fran- gellum of the first antenna is greater than ciscorum) and reserved the genus Crangon twice as long as the outer flagellum (Kuris et for the snapping shrimp (now in the genus al. 2007) (Fig. 2). Alpheus). In 1955–56, the International Mouthparts: The mouth of decapod Commission on Zoological Nomenclature crustaceans comprises six pairs of appendag- formally reserved the genus Crangon for the es including one pair of mandibles (on either sand shrimps only. Recent taxonomic de- side of the mouth), two pairs of maxillae and bate revolves around potential subgeneric three pairs of maxillipeds. The maxillae and designation for C. franciscorum (C. Neocran- maxillipeds attach posterior to the mouth and gon franciscorum, C. franciscorum francis- extend to cover the mandibles (Ruppert et al. corum) (Christoffersen 1988; Kuris and Carl- 2004). Third maxilliped setose and with exo- ton 1977; Butler 1980; Wicksten 2011). pod in C. franciscorum and C. alaskensis (Wicksten 2011). Description Carapace: Thin and smooth, with a Size: Average body length is 49 mm for single medial spine (compare to Lissocrangon males and 68 mm for females (Wicksten with no gastric spines). Also lateral (Schmitt 2011). 1921) (Fig. 1), hepatic, branchiostegal and Color: White, mottled with small black spots, pterygostomian spines (Wicksten 2011). giving gray appearance. Rostrum: Rostrum straight and up- General Morphology: The body of decapod turned (Crangon, Kuris and Carlton 1977). -
Systematics, Phylogeny, and Taphonomy of Ghost Shrimps (Decapoda): a Perspective from the Fossil Record
73 (3): 401 – 437 23.12.2015 © Senckenberg Gesellschaft für Naturforschung, 2015. Systematics, phylogeny, and taphonomy of ghost shrimps (Decapoda): a perspective from the fossil record Matúš Hyžný *, 1, 2 & Adiël A. Klompmaker 3 1 Geological-Paleontological Department, Natural History Museum Vienna, Burgring 7, 1010 Vienna, Austria; Matúš Hyžný [hyzny.matus@ gmail.com] — 2 Department of Geology and Paleontology, Faculty of Natural Sciences, Comenius University, Mlynská dolina, Ilkovičova 6, SVK-842 15 Bratislava, Slovakia — 3 Florida Museum of Natural History, University of Florida, 1659 Museum Road, PO Box 117800, Gaines- ville, FL 32611, USA; Adiël A. Klompmaker [[email protected]] — * Correspond ing author Accepted 06.viii.2015. Published online at www.senckenberg.de/arthropod-systematics on 14.xii.2015. Editor in charge: Stefan Richter. Abstract Ghost shrimps of Callianassidae and Ctenochelidae are soft-bodied, usually heterochelous decapods representing major bioturbators of muddy and sandy (sub)marine substrates. Ghost shrimps have a robust fossil record spanning from the Early Cretaceous (~ 133 Ma) to the Holocene and their remains are present in most assemblages of Cenozoic decapod crustaceans. Their taxonomic interpretation is in flux, mainly because the generic assignment is hindered by their insufficient preservation and disagreement in the biological classification. Fur- thermore, numerous taxa are incorrectly classified within the catch-all taxonCallianassa . To show the historical patterns in describing fos- sil ghost shrimps and to evaluate taphonomic aspects influencing the attribution of ghost shrimp remains to higher level taxa, a database of all fossil species treated at some time as belonging to the group has been compiled: 250 / 274 species are considered valid ghost shrimp taxa herein. -
Theses Digitisation: This Is a Digitised
https://theses.gla.ac.uk/ Theses Digitisation: https://www.gla.ac.uk/myglasgow/research/enlighten/theses/digitisation/ This is a digitised version of the original print thesis. Copyright and moral rights for this work are retained by the author A copy can be downloaded for personal non-commercial research or study, without prior permission or charge This work cannot be reproduced or quoted extensively from without first obtaining permission in writing from the author The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the author When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given Enlighten: Theses https://theses.gla.ac.uk/ [email protected] THE AGONISTIC BEHAVIOUR OF THE VELVET SWIMMING CRAB, LIOCARCINUS PUBER (L.) (BRACHYURA, PORTUNIDAE) Ian Philip Smith BSc (Wales) Department of Zoology, The University, Glasgow, G12 8QQ and University Marine Biological Station, Millport, Isle of Cumbrae, KA28 OEG A thesis submitted for the degree of Doctor of Philosophy to the Faculty of Science at the University of Glasgow, November 1990. ProQuest Number: 11007588 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 11007588 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. -
High-Pressure Processing for the Production of Added-Value Claw Meat from Edible Crab (Cancer Pagurus)
foods Article High-Pressure Processing for the Production of Added-Value Claw Meat from Edible Crab (Cancer pagurus) Federico Lian 1,2,* , Enrico De Conto 3, Vincenzo Del Grippo 1, Sabine M. Harrison 1 , John Fagan 4, James G. Lyng 1 and Nigel P. Brunton 1 1 UCD School of Agriculture and Food Science, University College Dublin, Belfield, D04 V1W8 Dublin, Ireland; [email protected] (V.D.G.); [email protected] (S.M.H.); [email protected] (J.G.L.); [email protected] (N.P.B.) 2 Nofima AS, Muninbakken 9-13, Breivika, P.O. Box 6122, NO-9291 Tromsø, Norway 3 Department of Agricultural, Food, Environmental and Animal Sciences, University of Udine, I-33100 Udine, Italy; [email protected] 4 Irish Sea Fisheries Board (Bord Iascaigh Mhara, BIM), Dún Laoghaire, A96 E5A0 Co. Dublin, Ireland; [email protected] * Correspondence: Federico.Lian@nofima.no; Tel.: +47-77629078 Abstract: High-pressure processing (HPP) in a large-scale industrial unit was explored as a means for producing added-value claw meat products from edible crab (Cancer pagurus). Quality attributes were comparatively evaluated on the meat extracted from pressurized (300 MPa/2 min, 300 MPa/4 min, 500 MPa/2 min) or cooked (92 ◦C/15 min) chelipeds (i.e., the limb bearing the claw), before and after a thermal in-pack pasteurization (F 10 = 10). Satisfactory meat detachment from the shell 90 was achieved due to HPP-induced cold protein denaturation. Compared to cooked or cooked– Citation: Lian, F.; De Conto, E.; pasteurized counterparts, pressurized claws showed significantly higher yield (p < 0.05), which was Del Grippo, V.; Harrison, S.M.; Fagan, possibly related to higher intra-myofibrillar water as evidenced by relaxometry data, together with J.; Lyng, J.G.; Brunton, N.P. -
Shell Disease in Crangon Crangon (Linnaeus, 1758): the Interaction of T Temperature and Stress Response ⁎ Alexandra Segelken-Voigta, , Gabrielle M
Journal of Experimental Marine Biology and Ecology 500 (2018) 105–111 Contents lists available at ScienceDirect Journal of Experimental Marine Biology and Ecology journal homepage: www.elsevier.com/locate/jembe Shell disease in Crangon crangon (Linnaeus, 1758): The interaction of T temperature and stress response ⁎ Alexandra Segelken-Voigta, , Gabrielle M. Millera, Gabriele Gerlacha,b,c a Institute of Biology and Environmental Sciences, Carl von Ossietzky University Oldenburg, Carl von Ossietzky Str. 9-11, 26111 Oldenburg, Germany b Helmholtz Institute for Functional Marine Biodiversity Oldenburg (HIFMB), Germany c School of Marine and Tropical Biology and ARC Centre of Excellence for Coral Reef Studies, James Cook University, Queensland, Australia ARTICLE INFO ABSTRACT Keywords: The prevalence of black spot shell disease is increasing among marine crustaceans worldwide. Rising seawater Black spot disease temperatures – often stressful for ectothermic species – are assumed to enhance the occurrence of shell disease. Climate warming In the North Sea > 50% of local populations of the brown shrimp (Crangon crangon) are affected by the disease. Crustacea While fisheries are suffering because diseased crustaceans are barely merchantable, the impact of shell disease Metabolism on life history traits of crustaceans is little understood. To determine the role of temperature on the development Molting of black spots and its implications for survival and physiology in the brown shrimp, a prolonged (3 months) Survival thermal stress experiment was performed. We measured the increment of shell disease and the effect of molting in shrimps kept at control (15 °C = equivalent to the seafloor temperature in the North Sea during sampling) and increased temperature (20 °C = according to predictions for the end of the century).