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Long-Duration Anesthetization of Squid (Doryteuthis Pealeii) T
Marine and Freshwater Behaviour and Physiology Vol. 43, No. 4, July 2010, 297–303 Long-duration anesthetization of squid (Doryteuthis pealeii) T. Aran Mooneya,b*, Wu-Jung Leeb and Roger T. Hanlona aMarine Resources Center, Marine Biological Laboratory, Woods Hole, MA 02543, USA; bWoods Hole Oceanographic Institution, Woods Hole, MA 02543, USA (Received 4 May 2010; final version received 15 June 2010) Cephalopods, and particularly squid, play a central role in marine ecosystems and are a prime model animal in neuroscience. Yet, the capability to investigate these animals in vivo has been hampered by the inability to sedate them beyond several minutes. Here, we describe methods to anesthetize Doryteuthis pealeii, the longfin squid, noninvasively for up to 5 h using a 0.15 mol magnesium chloride (MgCl2) seawater solution. Sedation was mild, rapid (54 min), and the duration could be easily controlled by repeating anesthetic inductions. The sedation had no apparent effect on physiological evoked potentials recorded from nerve bundles within the statocyst system, suggesting the suitability of this solution as a sedating agent. This simple, long-duration anesthetic technique opens the possibility for longer in vivo investigations on this and related cephalopods, thus expanding potential neuroethological and ecophysiology research for a key marine invertebrate group. Keywords: anesthesia; sedation; squid; Loligo; neurophysiology; giant axon Introduction Although cephalopods are key oceanic organisms used extensively as experimental animals in a variety of research fields (Gilbert et al. 1990), there is a relative paucity of information on maintaining them under anesthesia for prolonged durations. Lack of established protocols for sedation beyond several minutes constrains Downloaded By: [Hanlon, Roger T.] At: 12:46 19 August 2010 experimental conditions for many neurobiological and physiological preparations. -
Microchemistry of Juvenile Mercenaria Mercenaria Shell: Implications for Modeling Larval Dispersal
Vol. 465: 155–168, 2012 MARINE ECOLOGY PROGRESS SERIES Published September 28 doi: 10.3354/meps09895 Mar Ecol Prog Ser Microchemistry of juvenile Mercenaria mercenaria shell: implications for modeling larval dispersal A. M. Cathey1,*, N. R. Miller2, D. G. Kimmel3 1Department of Biology, East Carolina University, Greenville, North Carolina 27858, USA 2Department of Geological Sciences, The University of Texas at Austin, Austin, Texas 78712, USA 3Department of Biology, Institute for Coastal Science and Policy, East Carolina University, Greenville, North Carolina 27858, USA ABSTRACT: The elemental signature of trace and minor elements within biominerals has been used to investigate the larval dispersal of bivalves. We investigated the potential of this technique by examining elemental signals in juvenile shells of the hard clam Mercenaria mercenaria within an estuarine−lagoonal system near Cape Lookout, North Carolina, USA. We assessed the spatial distinction (~12 to 40 km) and temporal stability (fall versus spring) of elemental concentrations using inductively coupled plasma mass spectrometry (ICP-MS). Twelve minor and trace elements were present at detectable levels in all shell samples: calcium (Ca), manganese (Mn), aluminum (Al), titanium (Ti), cobalt (Co), copper (Cu), barium (Ba), magnesium (Mg), zinc (Zn), lead (Pb), nickel (Ni), and strontium (Sr). Discriminant function analyses (DFA) using metal to Ca ratios as independent variables correctly assigned hard clams to their site of collection with 100% success from both fall and spring sampling events. Mn:Ca ratio proved to be the most effective discrimi- nator explaining 91.2 and 71.9% of our among-group variance, respectively. Elemental concentra- tions within juvenile shell differed temporally. -
Life in the Fast Lane – from Hunted to Hunter Middle School Version
Life in the Fast Lane: From Hunted to Hunter Lab Activity: Dissection of a Squid-A Cephalopod Middle School Version Lesson by Kevin Goff Squid and octopi are cephalopods [say “SEFF-uh-luh-pods”]. The name means “head-foot,” because these animals have VIDEOS TO WATCH gripping, grasping arms that emerge straight from their heads. Watch this short clip on the Shape of Life At first glance, they seem totally different from every other website to become familiar with basic mollusc anatomy: creature on Earth. But in fact, they are molluscs, closely related • “Mollusc Animation: Abalone Body to snails, slugs, clams, oysters, mussels, and scallops. Like all Plan” (under Animation; 1.5 min) modern day molluscs, cephalopods descended from simple, Note the abalone’s foot, radula, and shell- snail-like ancestors. These ancient snails crept sluggishly on making mantle. These were present in the seafloor over 500 million years ago. Their shells resembled the snail-like ancestor of all molluscs an umbrella, probably to shield them from the sun’s intense ultraviolet radiation. When all sorts of new predators appeared on the scene, with powerful jaws or crushing claws, a thin shell was no match for such weapons. Over time, some snails evolved thicker shells, often coiled and spiky. These heavy shells did a better job of fending off predators, but they came with a price: They were costly to build and a burden to lug around. These snails sacrificed speed for safety. This lifestyle worked fine for many molluscs. And, still today, nearly 90% of all molluscs are heavily armored gastropods that crawl around at a snail’s pace. -
The Pax Gene Family: Highlights from Cephalopods Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, Yann Bassaglia
The Pax gene family: Highlights from cephalopods Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, Yann Bassaglia To cite this version: Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, et al.. The Pax gene family: Highlights from cephalopods. PLoS ONE, Public Library of Science, 2017, 12 (3), pp.e0172719. 10.1371/journal.pone.0172719. hal-01921138 HAL Id: hal-01921138 https://hal.archives-ouvertes.fr/hal-01921138 Submitted on 13 Nov 2018 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. Distributed under a Creative Commons Attribution| 4.0 International License RESEARCH ARTICLE The Pax gene family: Highlights from cephalopods Sandra Navet1☯, Auxane Buresi1☯, SeÂbastien Baratte1,2, Aude Andouche1, Laure Bonnaud-Ponticelli1, Yann Bassaglia1,3* 1 UMR BOREA MNHN/CNRS7208/IRD207/UPMC/UCN/UA, MuseÂum National d'Histoire Naturelle, Sorbonne UniversiteÂs, Paris, France, 2 Univ. Paris Sorbonne-ESPE, Sorbonne UniversiteÂs, Paris, France, 3 Univ. Paris Est CreÂteil-Val de Marne, CreÂteil, France ☯ These authors contributed equally to this work. * [email protected] a1111111111 a1111111111 a1111111111 a1111111111 Abstract a1111111111 Pax genes play important roles in Metazoan development. Their evolution has been exten- sively studied but Lophotrochozoa are usually omitted. -
Octopus Consciousness: the Role of Perceptual Richness
Review Octopus Consciousness: The Role of Perceptual Richness Jennifer Mather Department of Psychology, University of Lethbridge, Lethbridge, AB T1K 3M4, Canada; [email protected] Abstract: It is always difficult to even advance possible dimensions of consciousness, but Birch et al., 2020 have suggested four possible dimensions and this review discusses the first, perceptual richness, with relation to octopuses. They advance acuity, bandwidth, and categorization power as possible components. It is first necessary to realize that sensory richness does not automatically lead to perceptual richness and this capacity may not be accessed by consciousness. Octopuses do not discriminate light wavelength frequency (color) but rather its plane of polarization, a dimension that we do not understand. Their eyes are laterally placed on the head, leading to monocular vision and head movements that give a sequential rather than simultaneous view of items, possibly consciously planned. Details of control of the rich sensorimotor system of the arms, with 3/5 of the neurons of the nervous system, may normally not be accessed to the brain and thus to consciousness. The chromatophore-based skin appearance system is likely open loop, and not available to the octopus’ vision. Conversely, in a laboratory situation that is not ecologically valid for the octopus, learning about shapes and extents of visual figures was extensive and flexible, likely consciously planned. Similarly, octopuses’ local place in and navigation around space can be guided by light polarization plane and visual landmark location and is learned and monitored. The complex array of chemical cues delivered by water and on surfaces does not fit neatly into the components above and has barely been tested but might easily be described as perceptually rich. -
Giant Pacific Octopus (Enteroctopus Dofleini) Care Manual
Giant Pacific Octopus Insert Photo within this space (Enteroctopus dofleini) Care Manual CREATED BY AZA Aquatic Invertebrate Taxonomic Advisory Group IN ASSOCIATION WITH AZA Animal Welfare Committee Giant Pacific Octopus (Enteroctopus dofleini) Care Manual Giant Pacific Octopus (Enteroctopus dofleini) Care Manual Published by the Association of Zoos and Aquariums in association with the AZA Animal Welfare Committee Formal Citation: AZA Aquatic Invertebrate Taxon Advisory Group (AITAG) (2014). Giant Pacific Octopus (Enteroctopus dofleini) Care Manual. Association of Zoos and Aquariums, Silver Spring, MD. Original Completion Date: September 2014 Dedication: This work is dedicated to the memory of Roland C. Anderson, who passed away suddenly before its completion. No one person is more responsible for advancing and elevating the state of husbandry of this species, and we hope his lifelong body of work will inspire the next generation of aquarists towards the same ideals. Authors and Significant Contributors: Barrett L. Christie, The Dallas Zoo and Children’s Aquarium at Fair Park, AITAG Steering Committee Alan Peters, Smithsonian Institution, National Zoological Park, AITAG Steering Committee Gregory J. Barord, City University of New York, AITAG Advisor Mark J. Rehling, Cleveland Metroparks Zoo Roland C. Anderson, PhD Reviewers: Mike Brittsan, Columbus Zoo and Aquarium Paula Carlson, Dallas World Aquarium Marie Collins, Sea Life Aquarium Carlsbad David DeNardo, New York Aquarium Joshua Frey Sr., Downtown Aquarium Houston Jay Hemdal, Toledo -
Biology and Description of Antisabia Juliae Sp. Nov., New Hipponicid Gastropod Commensal on Turbo Spp
SCI. MAR., 61 (Supl. 2): 5-14 SCIENTIA MARINA 1997 ECOLOGY OF MARINE MOLLUSCS. J.D. ROS and A. GUERRA (eds.) Biology and description of Antisabia juliae sp. nov., new Hipponicid gastropod commensal on Turbo spp. in Laing Island (Papua New Guinea)* MATHIEU POULICEK1, JEAN-CLAUDE BUSSERS1 and PIERRE VANDEWALLE2 1Animal Ecology Laboratory and 2Functional Morphology Laboratory, Zoological Institute, Liège University. 22, Quai Van Beneden, B-4020 Liège. Belgium. SUMMARY: The gastropod family Hipponicidae comprises widely distributed but poorly known sedentary species. On the beach-rock of the coral reefs of Laing Island (Papua New Guinea) live rich populations of several gastropod Turbo species of which many specimens have attached to their shell a hipponicid gastropod attributed to a new species, Antisabia juliae. This new species, described in this paper, appears to have adapted its mode of life on live turbinids in several ways result- ing in morphological changes (thin basal plate loosely adherent to the supporting shell, functional eyes, very long snout, functional radula, small osphradium) and ethological changes (foraging behaviour: it appears to feed on the epiphytic com- munity growing on the host, in the vicinity of the “host” shell). Except for these characteristics, the mode of life appears quite similar to that of other hipponicid species with few big females surrounded by several much smaller males. Development occurs within the egg mass inside the female shell and a few young snails escape at the crawling stage. Key words: Mollusca, Gastropoda, ecology, Hipponicidae, Papua New Guinea, Indopacific. RESUMEN: BIOLOGÍA Y DESCRIPCIÓN DE ANTISABIA JULIAE SP. NOV., UN NUEVO GASTERÓPODO HIPONÍCIDO COMENSAL DE TURBO SPP. -
Annelids, Arthropods, Molluscs 2. Very Diverse, Mostly Marine B. Characteristics 1
Molluscs A. Introduction 1. Three big Protostome Phyla - Annelids, Arthropods, Molluscs 2. Very diverse, mostly marine B. Characteristics 1. Bilateral symmetrical, unsegmented with definite head 2. Muscular foot 3. Mantle - mantle cavity a. Secretes shell - Calcium carbonate 4. Ciliated epithelium 5. Coelom reduced - around heart 6. Open circulatory system 7. Gaseous exchange by gills, lung, or just body surface 8. Metanephridia - empty into mantle cavity C. Body Plan 1. Generalized mollusc a. Mantle - secreted shell b. Mantle - cavity has gills - posterior - location important 2. Head-foot a. Head - 1. Radula - rasping tongue a. Mostly for scraping - snails b. Some (Cone shells) modified to a dart and poison b. Foot - Variously modified 1. Ventral sole-like structure - movement 2. May be shaped for burrowing 3. Shell 1. Made of Calcium Carbonate Molluscs 2. Three layers a. Periostracum - organic layer - not always visible b. Prismatic layer - prim-shaped crystals of calcium carbonate 1. Secreted by gladular margin of mantle 2. Grows as animal grows c. Nacreous layer 1. Continuously secreted by mantle on interior of shell 2. Pearls 4. Reproduction a. Larval stages 1. Trochophore - first stage to hatch from egg 2. Veliger - planktonic larva of most marine snails and bivalves a. Beginnings of foot, shell and mantle D. Classes - problem of segmentation - is it the original body plan - have molluscs lost segementation? 1. Monoplacophora - genus Neopilina a. Serial repetition in body form b. Single shell c. Interesting story of discovery 2. Polyplacophora - chitons a. Segmented shell - plates b. Multiple gills down side of body - not like generalized plan c. Rock dwellers that use radula to scrape algae off rocks 3. -
Mollusca Three Classes
Mollusca Three Classes 1. Gastropoda (gastropods)~ slugs and snails 2. Bivalvia (bivalves) ~ clams and other two- shelled shellfish 3. Cephalopoda (cephalopods) ~ squids, octopuses and cuttlefish 1 Bodies of Mollusks • A mollusk has a soft body which is usually covered by a hard outer shell. • Exceptions: – Slugs and octopuses have lost their shells through evolution – Squids have very reduced shells Anatomy of a Mollusk • All mollusks have: – Foot ~ the muscular foot helps it move – Visceral mass ~ contains the gills, gut, and other organs – Mantle ~ covers the visceral mass to protect the mollusks without shells • Most mollusks have: – Shell ~ protects the mollusk from predators and keeps land mollusks from drying out. 2 Symmetry of Mollusks • Mollusks have bilateral symmetry. – The two halves of the body mirror each other. Anatomy of a Snail (gastropod) 3 Anatomy of a Clam (bivalve) Anatomy of a Squid (cephalopod) 4 Eating Behaviors • Bivalves (clams) ~ filter tiny plant and bacteria from the water • Gastropods (snails) ~ eat with a radula (tiny tongue covered with teeth. – The radula is used to scrape algae off rocks and pieces of leaves and seaweed • Cephalopods (squid) ~use tentacles to grab their prey and put it in their powerful jaws. Blue-ringed octopus 5 Market Squid Moon Snail chasing its food 6 Achatina fulica Giant African Land Snail The largest land snail known is the Giant African Land Snail. It can weigh up to 2 pounds and be 15 inches long. Commonly Eaten Mollusks cockles conch oysters clams scallops abalone whelks Mussels Pen shells 7. -
Squid Giant Axon (Glia/Neurons/Secretion)
Proc. Nat. Acad. Sci. USA Vol. 71, No. 4, pp. 1188-1192, April 1974 Transfer of Newly Synthesized Proteins from Schwann Cells to the Squid Giant Axon (glia/neurons/secretion) R. J. LASEK*, H. GAINERt, AND R. J. PRZYBYLSKI* Marine Biological Laboratory, Woods Hole, Massachusetts 02543 Communicated by Walle J. H. Nauta, November 28, 1973 ABSTRACT The squid giant axon is presented as a teins synthesized in the Schwann cells surrounding the axon model for the study of macromolecular interaction be- tween cells in the nervous system. When the isolated giant are subsequently transferred into the axoplasm. axon was incubated in sea water containing [3Hjleucine MATERIALS AND METHODS for 0.5-5 hr, newly synthesized proteins appeared in the sheath and axoplasm as demonstrated by: (i) radioautogra- Protein synthesis was studied in squid giant axons obtained phy, (ii) separation of the -sheath and axoplasm by extru- from live squid which were kept in a sea tank and used within sion, and (iii) perfusion of electrically excitable axons. hr of obtained The absence of ribosomal RNA in the axoplasm [Lasek, 48 capture. The giant axons were by decapitat- R. J. et al. (1973) Nature 244, 162-165] coupled with other ing the squid and dissecting the axons under a stream of run- evidence indicates that the labeled proteins that are found ning sea water. The axons, 4-6 cm long, were tied with thread in the axoplasm originate in the Schwann cells surrounding at both ends, removed from the mantle, and cleaned of ad- the axon. Approximately 50%70 of the newly synthesized hering connective tissue in a petri dish filled with sea water Schwann cell proteins are transferred to the giant axon. -
Effects of Temperature on Escape Jetting in the Squid Loligo Opalescens
The Journal of Experimental Biology 203, 547–557 (2000) 547 Printed in Great Britain © The Company of Biologists Limited 2000 JEB2451 EFFECTS OF TEMPERATURE ON ESCAPE JETTING IN THE SQUID LOLIGO OPALESCENS H. NEUMEISTER*,§, B. RIPLEY*, T. PREUSS§ AND W. F. GILLY‡ Hopkins Marine Station of Stanford University, Department of Biological Science, 120 Ocean View Boulevard, Pacific Grove, 93950 CA, USA *Authors have contributed equally ‡Author for correspondence (e-mail: [email protected]) §Present address: Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA Accepted 19 November 1999; published on WWW 17 January 2000 Summary In Loligo opalescens, a sudden visual stimulus (flash) giant and non-giant motor axons in isolated nerve–muscle elicits a stereotyped, short-latency escape response that is preparations failed to show the effects seen in vivo, i.e. controlled primarily by the giant axon system at 15 °C. We increased peak force and increased neural activity at low used this startle response as an assay to examine the effects temperature. Taken together, these results suggest that of acute temperature changes down to 6 °C on behavioral L. opalescens is able to compensate escape jetting and physiological aspects of escape jetting. In free- performance for the effects of acute temperature reduction. swimming squid, latency, distance traveled and peak A major portion of this compensation appears to occur in velocity for single escape jets all increased as temperature the central nervous system and involves alterations in the decreased. In restrained squid, intra-mantle pressure recruitment pattern of both the giant and non-giant axon transients during escape jets increased in latency, duration systems. -
2,3-Bisphosphoglycerate (2,3-BPG)
11-cis retinal 5.4.2 achondroplasia 19.1.21 active transport, salt 3.4.19 2,3-bisphosphoglycerate 11.2.2 acid-base balance 18.3.34 activity cycle, flies 2.2.2 2,4-D herbicide 3.3.22, d1.4.23 acid coagulation cheese 15.4.36 activity rhythms, locomotor 7.4.2 2,6-D herbicide, mode of action acid growth hypothesis, plant cells actogram 7.4.2 3.2.22 3.3.22 acute mountain sickness 8.4.19 2-3 diphosphoglycerate, 2-3-DPG, acid hydrolases 15.2.36 acute neuritis 13.5.32 in RBCs 3.2.25 acid in gut 5.1.2 acute pancreatitis 9.3.24 2C fragments, selective weedkillers acid rain 13.2.10, 10.3.25, 4.2.27 acyltransferases 11.5.39 d1.4.23 1.1.15 Adams, Mikhail 12.3.39 3' end 4.3.23 acid rain and NO 14.4.18 adaptation 19.2.26, 7.2.31 3D formula of glucose d16.2.15 acid rain, effects on plants 1.1.15 adaptation, chemosensory, 3-D imaging 4.5.20 acid rain, mobilization of soil in bacteria 1.1.27 3-D models, molecular 5.3.7 aluminium 3.4.27 adaptation, frog reproduction 3-D reconstruction of cells 18.1.16 acid rain: formation 13.2.10 17.2.17 3-D shape of molecules 7.2.19 acid 1.4.16 adaptations: cereals 3.3.30 3-D shapes of proteins 6.1.31 acid-alcohol-fast bacteria 14.1.30 adaptations: sperm 10.5.2 3-phosphoglycerate 5.4.30 acidification of freshwater 1.1.15 adaptive immune response 5' end 4.3.23 acidification 3.4.27 19.4.14, 18.1.2 5-hydroxytryptamine (5-HT) 12.1.28, acidification, Al and fish deaths adaptive immunity 19.4.34, 5.1.35 3.4.27 d16.3.31, 5.5.15 6-aminopenicillanic acid 12.1.36 acidification, Al and loss of adaptive radiation 8.5.7 7-spot ladybird