Cephalopods Between Science, Art, and Engineering: a Contemporary Synthesis
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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 -
Through the Looking Glass
THROUGH THE LOOKING-GLASS OF CEPHALOPOD COLOUR PATTERNS A skin-diver's guide to the Octopus brain. A. PACKARD Dept. of Zoology, University of Naples "Federico II ", Via Mezzocannone 8, Napoli 80134 and Stazione Zoologica "Anton Dohrn", I-Napoli 80121, Italy Dept. of Psychology, University of Edinburgh, 7 George Square, Edinburgh EH8 9JZ, Scotland. 1. Introduction Our supporting organisation, NATO, has shown itself ready to revise its military thinkingin face of the latest facts. As scientists we should be equally flexible. In the zoological realm,what had long been quoted as the most brilliant example of analogous structures and of convergent evolution - the similarity of the vertebrate and the cephalopod eye, despite their separate phylogenetic histories - is now revealed as having within it the seeds of an ancienthomology: perhaps as ancient as animal life itself. I refer to the recent discovery [38] that the same Homeobox gene family responsible for morphogenesis in the eye primordia of insects and of vertebrates is also contained in the germ cells of squids. It invites us to consider that the rules of Vision operating in the field of evolution - not so very different from the military field - are universal rules that have to do less with the nature of light and optics than with the tasks that can be performed with information extractable from an illuminated world. Emphasis on tasks, in turn suggests that the skin of cephalopods - clearly a successful group of animals- might be a very convenient way of arriving at these rules. Its capacity for colour change and its repertoire of signals andcompositions have, over millions of years, been directed at and tuned by the eyes that occupy behaviour space [29]. -
Eye Development in Sepia Officinalis Embryo: What the Uncommon Gene
ORIGINAL RESEARCH published: 24 August 2017 doi: 10.3389/fphys.2017.00613 Eye Development in Sepia officinalis Embryo: What the Uncommon Gene Expression Profiles Tell Us about Eye Evolution Boudjema Imarazene 1, Aude Andouche 1, Yann Bassaglia 1, 2, Pascal-Jean Lopez 1 and Laure Bonnaud-Ponticelli 1* 1 UMR Biologie des Organismes et Ecosystèmes Aquatiques, Museum National d’Histoire Naturelle, Sorbonne Universités, Centre National de la Recherche Scientifique (CNRS 7208), Université Pierre et Marie Curie (UPMC), Université de Caen Normandie, Institut de Recherche Pour le Développement (IRD207), Université des Antilles, Paris, France, 2 Université Paris Est Créteil-Val de Marne, Paris, France In metazoans, there is a remarkable diversity of photosensitive structures; their shapes, physiology, optical properties, and development are different. To approach the evolution of photosensitive structures and visual function, cephalopods are particularly interesting organisms due to their most highly centralized nervous system and their camerular Edited by: eyes which constitute a convergence with those of vertebrates. The eye morphogenesis Frederike Diana Hanke, in numerous metazoans is controlled mainly by a conserved Retinal Determination University of Rostock, Germany Gene Network (RDGN) including pax, six, eya, and dac playing also key developmental Reviewed by: Shuichi Shigeno, roles in non-retinal structures and tissues of vertebrates and Drosophila. Here we have Stazione Zoologica Anton Dohrn, Italy identified and explored the role of Sof-dac, Sof-six1/2, Sof-eya in eye morphogenesis, Oleg Simakov, University of Vienna, Austria and nervous structures controlling the visual function in Sepia officinalis. We compare *Correspondence: that with the already shown expressions in eye development of Sof-otx and Sof-pax Laure Bonnaud-Ponticelli genes. -
Biodiversity Has Been a “Fashionable” Word During Invertebrate Becoming Extinct During the Past Hundred the Last Decade
Cephalopod Biodiversity, Ecology and Evolution Payne, A. I. L., Lipi´nski, M. R., Clarke, M. R. and M. A. C. Roeleveld (Eds). S. Afr. J. mar. Sci. 20: 165–173 1998 165 BIODIVERSITY AND SYSTEMATICS IN CEPHALOPODS: UNRESOLVED PROBLEMS REQUIRE AN INTEGRATED APPROACH K. N. NESIS* Some problems of cephalopod biodiversity are discussed. Many squid species are represented by 2–4 intraspecies groupings that may be wholly or partly sympatric, but differ in spawning season and size at maturity. They may be genetically distinct stock units, but their taxonomic status remains unresolved. Discovery of a biochemical or molecular key to distinguish between intra- and interspecific differences may help to solve the problem of subspecific taxa in cephalopods, as stated by G. L. Voss in 1977. Electrophoretic study of al- lozyme differentiation is a good method for clearing up relationships between taxa within a family, but this method cannot be used in situations when the concept of subgenus or subfamily is necessary. The problem of suprafamilial taxa needs urgent attention. However, restructuring only one family or group of families leaving others unrevised may lead to skewing the entire system. Examples are splitting the Enoploteuthidae into three families (as proposed by M. R. Clarke in 1988) and raising the rank of the Sepiidae and the Sepiolidae to ordinal, a proposal by P. Fioroni in 1981. In such cases the method of common level should be applied: subdivisions in a large taxon shall be separated by approximately similar characters. Many attempts to select natural groups of families, for example in the Oegopsida, failed primarily because they were based on analysis of a single organ or system of organs when study of other organs/systems may lead to different natural groupings. -
Compensation for Longitudinal Chromatic Aberration in the Eye of the firefly Squid, Watasenia Scintillans
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Vision Research 44 (2004) 2129–2134 www.elsevier.com/locate/visres Compensation for longitudinal chromatic aberration in the eye of the firefly squid, Watasenia scintillans Ronald H.H. Kroger€ *, Anna Gislen Department of Cell and Organism Biology, Lund Vision Group, Zoology Building, Lund University, Helgonava€gen 3, 22362 Lund, Sweden Received 31 October 2003; received in revised form 26 March 2004 Abstract The camera eyes of fishes and cephalopods have come forth by convergent evolution. In a variety of vertebrates capable of color vision, longitudinal chromatic aberration (LCA) of the optical system is corrected for by the exactly tuned longitudinal spherical aberration (LSA) of the crystalline lens. The LSA leads to multiple focal lengths, such that several wavelengths can be focused on the retina. We investigated whether that is also the case in the firefly squid (Watasenia scintillans), a cephalopod species that is likely to have color vision. It was found that the lens of W. scintillans is virtually free of LSA and uncorrected for LCA. However, the eye does not suffer from LCA because of a banked retina. Photoreceptors sensitive to short and long wavelengths are located at appropriate distances from the lens, such that they receive well-focused images. Such a design is an excellent solution for the firefly squid because a large area of the retina is monochromatically organized and it allows for double use of the surface area in the dichromatically organized part of the retina. -
Dynamic Skin Patterns in Cephalopods
How, M. , Norman, M., Finn, J., Chung, W-S., & Marshall, N. J. (2017). Dynamic Skin Patterns in Cephalopods. Frontiers in Physiology, 8, [393]. https://doi.org/10.3389/fphys.2017.00393 Publisher's PDF, also known as Version of record License (if available): CC BY Link to published version (if available): 10.3389/fphys.2017.00393 Link to publication record in Explore Bristol Research PDF-document This is the final published version of the article (version of record). It first appeared online via Frontiers Media at http://journal.frontiersin.org/article/10.3389/fphys.2017.00393/full. Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/red/research-policy/pure/user-guides/ebr-terms/ ORIGINAL RESEARCH published: 19 June 2017 doi: 10.3389/fphys.2017.00393 Dynamic Skin Patterns in Cephalopods Martin J. How 1*, Mark D. Norman 2 †, Julian Finn 2 †, Wen-Sung Chung 3 and N. Justin Marshall 3 1 Ecology of Vision Group, School of Biological Sciences, University of Bristol, Bristol, United Kingdom, 2 Marine Sciences, Museum Victoria, Melbourne, VIC, Australia, 3 Sensory Neurobiology Group, Queensland Brain Institute, University of Queensland, Brisbane, QLD, Australia Cephalopods are unrivaled in the natural world in their ability to alter their visual appearance. These mollusks have evolved a complex system of dermal units under neural, hormonal, and muscular control to produce an astonishing variety of body patterns. -
Anti-Predator Responses of Squid Throughout Ontogeny
Old Dominion University ODU Digital Commons Biological Sciences Theses & Dissertations Biological Sciences Spring 2016 Anti-Predator Responses of Squid Throughout Ontogeny Carly Anne York Old Dominion University, [email protected] Follow this and additional works at: https://digitalcommons.odu.edu/biology_etds Part of the Biology Commons, and the Physiology Commons Recommended Citation York, Carly A.. "Anti-Predator Responses of Squid Throughout Ontogeny" (2016). Doctor of Philosophy (PhD), Dissertation, Biological Sciences, Old Dominion University, DOI: 10.25777/twms-7w98 https://digitalcommons.odu.edu/biology_etds/9 This Dissertation is brought to you for free and open access by the Biological Sciences at ODU Digital Commons. It has been accepted for inclusion in Biological Sciences Theses & Dissertations by an authorized administrator of ODU Digital Commons. For more information, please contact [email protected]. ANTI-PREDATOR RESPONSES OF SQUID THROUGHOUT ONTOGENY by Carly Anne York B.S. December 2007, Elon University M.S. August 2011, Western Kentucky University A Dissertation Submitted to the Faculty of Old Dominion University in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY ECOLOGICAL SCIENCES OLD DOMINION UNIVERSITY May 2016 Approved by: Ian Bartol (Director) Lisa Horth (Member) Kent Carpenter (Member) Sara Maxwell (Member) Paul Krueger (Member) Joseph Thompson (Member) ABSTRACT ANTI-PREDATOR BEHAVIOR OF SQUID THROUGHOUT ONTOGENY Carly Anne York Old Dominion University, 2016 Director: Dr. Ian K. Bartol Multiple sensory modalities and a complex array of escape behaviors have evolved as components of anti-predator responses in squids. The goals of this study include: (1) examine the role of the lateral line analogue and vision in successful predator evasion; (2) measure kinematics of escape jetting; (3) document how chromatic patterning, posturing and inking in squid change in response to predators; and (4) investigate escape jet hydrodynamics of squid. -
Phylum Mollusca (연체동물문) I
Phylum Mollusca (연체동물문) I. Coelomate Phyla A. True coelom - body cavity lined by mesoderm B. More efficient arrangement of internal organs C. Gastrovascular system surrounded by muscle II. Phylum Mollusca A. L. molluscus, soft B. Mol-lus' ka, Mollusca or Molluska C. At least to Cambrian Period (600 MY) D. 100,000 living species ; 35,000 extinct species E. Bilateral symmetry F. To 18m long, most small • Malacology; study of living molluscs; • Conchology; study of shells only, shell collector • Often have valves; none to 8 • Shell of CaCo3 • Most have gills • Usually open circulatory system • Most have kidney (nephridia) A very ومط تلورىStomach with crystalline style • long gelatinous crystalline style rotates against the gastric shield and releases digestive enzymes into the stomach lumen • Feeding; herbivores, carnivores, detrivores, filter feeders, deposit feeders Phylum Mollusca – Body Structure G. 3 embryonic germ layers: endoderm, mesoderm, ectoderm H. Organ level of organization I. Extracellular digestion in complete gastrovascular system J. coelom K. Excretory system with kidneys (metanephridia) L. Often with special respiratory structures: gills, lungs, mantle surface Phylum Mollusca – Systems M. Open circulatory system with multi-chambered heart N. Nervous system varies, based on ganglia at key points in some bivalves اقل جطوراLeast sophisticated .1 2. More sophisticated in cephalopods, with nerve ring surrounding pharynx O. Various sense organs 1. Eyes of cephalopods most advanced among invertebrates Phylum Mollusca – Body Surface & Skeleton P. Cilia on certain body surfaces 1. Highly advanced on gill surfaces in bivalves Q. Skeletal systems vary: 1. Some have none 2. Some have exoskeleton (shell) 3. Some have endoskeleton (cuttlebone) لسان الثحر Phylum Mollusca – Unique Structures R. -
Scaros Baratte 2018.Pdf
Research Article Cite This: ACS Chem. Neurosci. 2018, 9, 2074−2088 pubs.acs.org/chemneuro Immunohistochemical Approach to Understanding the Organization of the Olfactory System in the Cuttlefish, Sepia officinalis † † ‡ Alexia T. Scaros, Roger P. Croll, and Sebastień Baratte*, † Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada ‡ Sorbonne Universite,́ MNHN, UNICAEN, UA, CNRS, IRD, Biologie des Organismes et Ecosystemes̀ Aquatiques (BOREA), Paris 75005, France ABSTRACT: Cephalopods are nontraditional but captivating models of invertebrate neurobiology, particularly in evolu- tionary comparisons. Cephalopod olfactory systems have striking similarities and fundamental differences with verte- brates, arthropods, and gastropods, raising questions about the ancestral origins of those systems. We describe here the organization and development of the olfactory system of the common cuttlefish, Sepia officinalis, using immunohistochem- istry and in situ hybridization. FMRFamide and/or related peptides and histamine are putative neurotransmitters in olfactory sensory neurons. Other neurotransmitters, including serotonin and APGWamide within the olfactory and other brain lobes, suggest efferent control of olfactory input and/or roles in the processing of olfactory information. The distributions of neurotransmitters, along with staining patterns of phalloidin, anti-acetylated α-tubulin, and a synaptotagmin riboprobe, help to clarify the structure of the olfactory lobe. We discuss a key difference, the lack of identifiable olfactory glomeruli, in cuttlefish in comparison to other models, and suggest its implications for the evolution of olfaction. KEYWORDS: Cephalopod, olfaction, glomerulus, neurotransmitters, immunohistochemistry, in situ hybridization ■ INTRODUCTION the brains of these animals are organized to mediate their 7−9 While not generally considered traditional models in neuro- remarkable intelligence.