Information Resources on the Care and Use of Invertebrates, 2000
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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. -
LONG-LIVED AQUATIC INSECTS ACCUMULATE CALCIUM CARBONATE DEPOSITS in a MONTANE DESERT STREAM Eric K
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Papers in Natural Resources Natural Resources, School of 2016 CAUGHT BETWEEN A ROCK AND A HARD MINERAL ENCRUSTATION: LONG-LIVED AQUATIC INSECTS ACCUMULATE CALCIUM CARBONATE DEPOSITS IN A MONTANE DESERT STREAM Eric K. Moody Arizona State University Jessica R. Corman University of Nebraska - Lincoln, [email protected] Michael T. Bogan University of California - Berkeley Follow this and additional works at: http://digitalcommons.unl.edu/natrespapers Part of the Natural Resources and Conservation Commons, Natural Resources Management and Policy Commons, and the Other Environmental Sciences Commons Moody, Eric K.; Corman, Jessica R.; and Bogan, Michael T., "CAUGHT BETWEEN A ROCK AND A HARD MINERAL ENCRUSTATION: LONG-LIVED AQUATIC INSECTS ACCUMULATE CALCIUM CARBONATE DEPOSITS IN A MONTANE DESERT STREAM" (2016). Papers in Natural Resources. 796. http://digitalcommons.unl.edu/natrespapers/796 This Article is brought to you for free and open access by the Natural Resources, School of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Natural Resources by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Western North American Naturalist 76(2), © 2016, pp. 172–179 CAUGHT BETWEEN A ROCK AND A HARD MINERAL ENCRUSTATION: LONG-LIVED AQUATIC INSECTS ACCUMULATE CALCIUM CARBONATE DEPOSITS IN A MONTANE DESERT STREAM Eric K. Moody1, Jessica R. Corman1,2, and Michael T. Bogan3 ABSTRACT.—Aquatic ecosystems overlying regions of limestone bedrock can feature active deposition of calcium carbonate in the form of travertine or tufa. Although most travertine deposits form a cement-like layer on stream sub- strates, mineral deposits can also form on benthic invertebrates. -
Insects and Bobwhite Quail Brood Habitat Management
National Quail Symposium Proceedings Volume 1 Article 13 1972 Insects and Bobwhite Quail Brood Habitat Management George A. Hurst Department of Wildlife & Fisheries, Mississippi Follow this and additional works at: https://trace.tennessee.edu/nqsp Recommended Citation Hurst, George A. (1972) "Insects and Bobwhite Quail Brood Habitat Management," National Quail Symposium Proceedings: Vol. 1 , Article 13. Available at: https://trace.tennessee.edu/nqsp/vol1/iss1/13 This Technical Session I: Problems and Methods in Bobwhite Ecology is brought to you for free and open access by Volunteer, Open Access, Library Journals (VOL Journals), published in partnership with The University of Tennessee (UT) University Libraries. This article has been accepted for inclusion in National Quail Symposium Proceedings by an authorized editor. For more information, please visit https://trace.tennessee.edu/nqsp. I ! Hurst: Insects and Bobwhite Quail Brood Habitat Management I 65 I ! I 15. Stoddard, Herbert L. 1931. The bobwhite quail: its habits, pre servation and increase. Charles Scribner's Sons, New York. 559 p. ,I 16. Stoddard, Herbert L., and Ed. V. Komarek. 1941. The carrying capacity of Southeastern quail lands. Trans. N. Am. Wildl. I i Con£. 6:149-155. l I INSECTS AND BOBWHITE QUAIL BROOD HABITAT MANAGEMENT I George A. Hurst, Department of Wildlife & Fisheries, Mississippi State University, Mississippi State, Miss. Recipient of the "Wendell Bever" award presented by the Okla homa Wildlife Federation to the best paper of the Symposium. The award was in memorium to the late Wendell Bever, former Director of the Oklahoma Department of Wildlife Conservation and Regional Representative of the National Wildlife Federation. -
Scope: Munis Entomology & Zoology Publishes a Wide
790 _____________Mun. Ent. Zool. Vol. 8, No. 2, June 2013__________ LIFE CYCLE AND LABORATORY REARING OF LACCOTREPHES MACULATES (HEMIPTERA:NEPIDAE) FROM JAMMU (J & K, INDIA) Ramnik Kour*, J. S. Tara, Sheetal Sharma and Shivani Kotwal * Department of Zoology, University of Jammu (J & K), 180006, INDIA. E-mail: [email protected] [Kour, R., Tara, J. S., Sharma, S. & Kotwal, S. 2013. Life cycle and laboratory rearing of Laccotrephes maculates (Hemiptera: Nepidae) from Jammu (J & K, India). Munis Entomology & Zoology, 8 (2): 790-795] ABSTRACT: The life cycle of Laccotrephes maculates was studied by rearing from egg to adult in laboratory conditions at a temperature of 28.9± 1.08oC with description of immature stages. Individuals were reared on nymphs of Anisops sp. (Hemiptera: Notonectidae) and mosquito larvae. The incubation period averaged 12.6 days. Durations of five subsequent instars averaged 8.1, 10.0, 10.3, 11.3 and 9.1 days respectively. Total life cycle averaged 61.4 days. KEY WORDS: Anisops, Laccotrephes maculates, laboratory rearing, Hemiptera, Nepidae. Aquatic hemipterans play a significant role as the major predator of aquatic fauna (Blaustein, 1998). The members belonging to family nepidae feed on a variety of aquatic organisms such as aquatic insects and tadpoles (Menke, 1979). Laccotrephes maculates Fabr. commonly known as water scorpion belongs to family Nepidae of order Hemiptera is carnivorous and air breather. Though most of the time they live in water but sometimes emerge out of water on the ground or under stones in damp beds of recently dried streams. All legs are employed in swimming but they are not good swimmers. -
(Coleoptera: Curculionidae) for the Control of Salvinia
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2011 Introduction and Establishment of Cyrtobagous salviniae Calder and Sands (Coleoptera: Curculionidae) for the Control of Salvinia minima Baker (Salviniaceae), and Interspecies Interactions Possibly Limiting Successful Control in Louisiana Katherine A. Parys Louisiana State University and Agricultural and Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Part of the Entomology Commons Recommended Citation Parys, Katherine A., "Introduction and Establishment of Cyrtobagous salviniae Calder and Sands (Coleoptera: Curculionidae) for the Control of Salvinia minima Baker (Salviniaceae), and Interspecies Interactions Possibly Limiting Successful Control in Louisiana" (2011). LSU Doctoral Dissertations. 1565. https://digitalcommons.lsu.edu/gradschool_dissertations/1565 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. INTRODUCTION AND ESTABLISHMENT OF CYRTOBAGOUS SALVINIAE CALDER AND SANDS (COLEOPTERA: CURCULIONIDAE) FOR THE CONTROL OF SALVINIA MINIMA BAKER (SALVINIACEAE), AND INTERSPECIES INTERACTIONS POSSIBLY LIMITING SUCCESSFUL CONTROL IN LOUISIANA. A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Entomology By Katherine A. Parys B.A., University of Rhode Island, 2002 M.S., Clarion University of Pennsylvania, 2004 December 2011 ACKNOWLEDGEMENTS In pursing this Ph.D. I owe many thanks to many people who have supported me throughout this endeavor. -
And Lepidoptera Associated with Fraxinus Pennsylvanica Marshall (Oleaceae) in the Red River Valley of Eastern North Dakota
A FAUNAL SURVEY OF COLEOPTERA, HEMIPTERA (HETEROPTERA), AND LEPIDOPTERA ASSOCIATED WITH FRAXINUS PENNSYLVANICA MARSHALL (OLEACEAE) IN THE RED RIVER VALLEY OF EASTERN NORTH DAKOTA A Thesis Submitted to the Graduate Faculty of the North Dakota State University of Agriculture and Applied Science By James Samuel Walker In Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Major Department: Entomology March 2014 Fargo, North Dakota North Dakota State University Graduate School North DakotaTitle State University North DaGkroadtaua Stet Sacteho Uolniversity A FAUNAL SURVEYG rOFad COLEOPTERA,uate School HEMIPTERA (HETEROPTERA), AND LEPIDOPTERA ASSOCIATED WITH Title A FFRAXINUSAUNAL S UPENNSYLVANICARVEY OF COLEO MARSHALLPTERTAitl,e HEM (OLEACEAE)IPTERA (HET INER THEOPTE REDRA), AND LAE FPAIDUONPATLE RSUAR AVSESYO COIFA CTOEDLE WOIPTTHE RFRAA, XHIENMUISP PTENRNAS (YHLEVTAENRICOAP TMEARRAS),H AANLDL RIVER VALLEY OF EASTERN NORTH DAKOTA L(EOPLIDEAOCPTEEAREA) I ANS TSHOEC RIAETDE RDI VWEITRH V FARLALXEIYN UOSF P EEANSNTSEYRLNV ANNOICRAT HM DAARKSHOATALL (OLEACEAE) IN THE RED RIVER VAL LEY OF EASTERN NORTH DAKOTA ByB y By JAMESJAME SSAMUEL SAMUE LWALKER WALKER JAMES SAMUEL WALKER TheThe Su pSupervisoryervisory C oCommitteemmittee c ecertifiesrtifies t hthatat t hthisis ddisquisition isquisition complies complie swith wit hNorth Nor tDakotah Dako ta State State University’s regulations and meets the accepted standards for the degree of The Supervisory Committee certifies that this disquisition complies with North Dakota State University’s regulations and meets the accepted standards for the degree of University’s regulations and meetMASTERs the acce pOFted SCIENCE standards for the degree of MASTER OF SCIENCE MASTER OF SCIENCE SUPERVISORY COMMITTEE: SUPERVISORY COMMITTEE: SUPERVISORY COMMITTEE: David A. Rider DCoa-CCo-Chairvhiadi rA. -
Synaptophysin Regulates Activity-Dependent Synapse Formation in Cultured Hippocampal Neurons
Synaptophysin regulates activity-dependent synapse formation in cultured hippocampal neurons Leila Tarsa and Yukiko Goda* Division of Biology, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0366 Edited by Charles F. Stevens, The Salk Institute for Biological Studies, La Jolla, CA, and approved November 20, 2001 (received for review October 29, 2001) Synaptophysin is an abundant synaptic vesicle protein without a homogenotypic syp-mutant cultures, however, synapse forma- definite synaptic function. Here, we examined a role for synapto- tion is similar to that observed for wild-type cultures. Interest- physin in synapse formation in mixed genotype micro-island cul- ingly, the decrease in syp-mutant synapse formation is prevented tures of wild-type and synaptophysin-mutant hippocampal neu- when heterogenotypic cultures are grown in the presence of rons. We show that synaptophysin-mutant synapses are poor tetrodotoxin (TTX) or postsynaptic receptor blockers. Our donors of presynaptic terminals in the presence of competing results demonstrate a role for syp in activity-dependent com- wild-type inputs. In homogenotypic cultures, however, mutant petitive synapse formation. neurons display no apparent deficits in synapse formation com- pared with wild-type neurons. The reduced extent of synaptophy- Materials and Methods sin-mutant synapse formation relative to wild-type synapses in Hippocampal Cultures. Primary cultures of dissociated hippocam- mixed genotype cultures is attenuated by blockers of synaptic pal neurons were prepared from late embryonic (E18–19) or transmission. Our findings indicate that synaptophysin plays a newborn (P1) wild-type and syp-mutant mice as described (10). previously unsuspected role in regulating activity-dependent syn- Briefly, dissected hippocampi were incubated for 30 min in 20 apse formation. -
LYGAEOIDEA La Superfamila Lygaeoidea (Hemiptera: Heteroptera: Pentatomomorpha) Es Una De Las Mayores Y Más Diver- Sas, Con Más De 4000 Especies, De Heteroptera
| 421 Resumen LYGAEOIDEA La superfamila Lygaeoidea (Hemiptera: Heteroptera: Pentatomomorpha) es una de las mayores y más diver- sas, con más de 4000 especies, de Heteroptera. Los hábitats de las especies del grupo son variados, hay grupos arbóreos, geófilos y laminófilos. La mayoría se alimentan de semillas maduras, aunque las Blissidae y algunas Lygaeidae son succionadoras de savia, los Geocoridae son principalmente depredadoras y las Cle- radini (Rhyparochromidae) se alimentan de sangre de vertebrados. Las ninfas viven en los mismos hábitats que los adultos y se alimentan generalmente de las mismas plantas. Actualmente en los Lygaeoidea se reconocen 15 familias, de las cuales 12 han sido registradas de la región Neotropical y 11 de la Argentina: Berytidae, Blissidae, Colobathristidae, Cymidae, Geocoridae, Lygaeidae, Ninidae, Oxycarenidae, Pachygronthidae, Piesmatidae y Rhyparochromidae. Se presenta una breve historia taxonómica, aspectos filogenéticos y de la clasificación actual de la superfamilia, bibliografía de referencia y una clave para la identificación de las familias de la Argentina. Para cada familia se presenta una diagnosis, principales trabajos, aspectos de la bio- logía y la diversidad a nivel mundial y en la Argentina, así como claves para la determinación de los géneros presentes en el pais. Además, se reseña la importancia agroeconómica del grupo. Se adjunta un listado de las 154 especies citadas de Argentina. Pablo Matías DELLAPÉ Abstract The superfamily Lygaeoidea (Hemiptera: Heteroptera: División Entomología, Museo de La Plata, Paseo del Pentatomomorpha) is one of the most diverse within the Bosque, 1900 La Plata, Argentina. Heteroptera, with more than 4000 species described. [email protected] The Lygaeoid habitats are diverse; there are arboreal, geophile and laminophile species. -
John Wilson Moore
John Wilson Moore BORN: Winston-Salem, North Carolina November 1, 1920 EDUCATION: Davidson College, B.S. Physics (1941) University of Virginia, Ph.D. Physics (1945) APPOINTMENTS: Radio Corporation of America Laboratories (1945–1946) Assistant Professor of Physics, Medical College of Virginia (1946–1950) Biophysicist, Naval Medical Research Institute (1950–1954) Associate Chief, Laboratory of Biophysics, NINDB, NIH (1954–1961) Professor of Physiology & Pharmacology, Duke University (1961–1988) Professor of Neurobiology, Duke University (1988–1990) Professor Emeritus of Neurobiology, Duke University (1990–present) HONORS AND AWARDS (SELECTED): Dupont Fellowship, University of Virginia (1941–1945) Fellow: National Neurological Research Foundation for Scientists (1961) Biophysical Society, Council and Executive Board (1966–1969; 1977–1979) Biomedical Engineering Society, Board of Directors (1971–1975) Trustee and Executive Committee, Marine Biological Laboratory (1971–1979; 1981–1985) K. S. Cole Award, Biophysical Society (1981) Fight for Sight Citation for Achievement in Basic Research (1982) John Wilson Moore initially became known for elucidating the action of tetrodotoxin and other neurotoxins using his innovative sucrose gap method for voltage clamping squid axon. He also was a pioneer in the nascent area of computational neuroscience, using computer simulations in parallel with experiments to predict experimental results and thus validate the concepts used in modeling. Intrigued by the possibility of applying his knowledge of physics to learn how neurons employ electricity to generate and transmit signals, he led the fi eld in exploring how ion channels and neuronal morphology affect excitation and signal propagation. He developed electronic instrumentation of high precision for electrophysiology, the result of experience gained through an unconventional career path: early training in physics, assignments involving feedback in the Manhattan Project, and learning principles of operational amplifi ers at the RCA Laboratories. -
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