Cannonball Jellyfish June 2017
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The Jellyfish Fishery in Mexico
Vol.4, No.6A, 57-61 (2013) Agricultural Sciences http://dx.doi.org/10.4236/as.2013.46A009 The jellyfish fishery in Mexico Juana López-Martínez*, Javier Álvarez-Tello Centro de Investigaciones Biológicas del Noroeste, S.C. (CIBNOR), Unidad Sonora, Campus Guaymas, Guaymas, México; *Corresponding Author: [email protected] Received 26 April 2013; revised 26 May 2013; accepted 15 June 2013 Copyright © 2013 Juana López-Martínez, Javier Álvarez-Tello. This is an open access article distributed under the Creative Com- mons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT ure 1), because some species secrete painful neurotoxic, even deadly, venom. Globally there has been a slight Jellyfish has been captured in Asia for 1700 increase of individuals in this group of organisms during years, and it has been considered a delicacy. the last decades [1], but in some countries as Australia, Since the 70s important jellyfish fisheries have jellyfish is considered a plague, so in response the gov- developed in several parts of the world, with ernment developed programs to control them. Among the catches increasing exponentially, reaching possible causes of the increase of jellyfish population, an 500,000 tons per year in the mid-nineties. In increase in water temperature due to global warming Mexico, only the cannonball jellyfish Stomolo- [2,3], reduction of predators by overfishing, and water phus meleagris is captured commercially. Most pollution [4,5] have been mentioned. Waste discharge of the capture of this jellyfish species is ob- into the sea, and in general, the increment of pollution in tained within the Gulf of California, specifically in the state of Sonora. -
Impact of Scyphozoan Venoms on Human Health and Current First Aid Options for Stings
toxins Review Impact of Scyphozoan Venoms on Human Health and Current First Aid Options for Stings Alessia Remigante 1,2, Roberta Costa 1, Rossana Morabito 2 ID , Giuseppa La Spada 2, Angela Marino 2 ID and Silvia Dossena 1,* ID 1 Institute of Pharmacology and Toxicology, Paracelsus Medical University, Strubergasse 21, A-5020 Salzburg, Austria; [email protected] (A.R.); [email protected] (R.C.) 2 Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Viale F. Stagno D'Alcontres 31, I-98166 Messina, Italy; [email protected] (R.M.); [email protected] (G.L.S.); [email protected] (A.M.) * Correspondence: [email protected]; Tel.: +43-662-2420-80564 Received: 10 February 2018; Accepted: 21 March 2018; Published: 23 March 2018 Abstract: Cnidaria include the most venomous animals of the world. Among Cnidaria, Scyphozoa (true jellyfish) are ubiquitous, abundant, and often come into accidental contact with humans and, therefore, represent a threat for public health and safety. The venom of Scyphozoa is a complex mixture of bioactive substances—including thermolabile enzymes such as phospholipases, metalloproteinases, and, possibly, pore-forming proteins—and is only partially characterized. Scyphozoan stings may lead to local and systemic reactions via toxic and immunological mechanisms; some of these reactions may represent a medical emergency. However, the adoption of safe and efficacious first aid measures for jellyfish stings is hampered by the diffusion of folk remedies, anecdotal reports, and lack of consensus in the scientific literature. Species-specific differences may hinder the identification of treatments that work for all stings. -
Hermit Crabs - Paguridae and Diogenidae
Identification Guide to Marine Invertebrates of Texas by Brenda Bowling Texas Parks and Wildlife Department April 12, 2019 Version 4 Page 1 Marine Crabs of Texas Mole crab Yellow box crab Giant hermit Surf hermit Lepidopa benedicti Calappa sulcata Petrochirus diogenes Isocheles wurdemanni Family Albuneidae Family Calappidae Family Diogenidae Family Diogenidae Blue-spot hermit Thinstripe hermit Blue land crab Flecked box crab Paguristes hummi Clibanarius vittatus Cardisoma guanhumi Hepatus pudibundus Family Diogenidae Family Diogenidae Family Gecarcinidae Family Hepatidae Calico box crab Puerto Rican sand crab False arrow crab Pink purse crab Hepatus epheliticus Emerita portoricensis Metoporhaphis calcarata Persephona crinita Family Hepatidae Family Hippidae Family Inachidae Family Leucosiidae Mottled purse crab Stone crab Red-jointed fiddler crab Atlantic ghost crab Persephona mediterranea Menippe adina Uca minax Ocypode quadrata Family Leucosiidae Family Menippidae Family Ocypodidae Family Ocypodidae Mudflat fiddler crab Spined fiddler crab Longwrist hermit Flatclaw hermit Uca rapax Uca spinicarpa Pagurus longicarpus Pagurus pollicaris Family Ocypodidae Family Ocypodidae Family Paguridae Family Paguridae Dimpled hermit Brown banded hermit Flatback mud crab Estuarine mud crab Pagurus impressus Pagurus annulipes Eurypanopeus depressus Rithropanopeus harrisii Family Paguridae Family Paguridae Family Panopeidae Family Panopeidae Page 2 Smooth mud crab Gulf grassflat crab Oystershell mud crab Saltmarsh mud crab Hexapanopeus angustifrons Dyspanopeus -
JELLYFISH FISHERIES of the WORLD by Lucas Brotz B.Sc., The
JELLYFISH FISHERIES OF THE WORLD by Lucas Brotz B.Sc., The University of British Columbia, 2000 M.Sc., The University of British Columbia, 2011 A DISSERTATION SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in The Faculty of Graduate and Postdoctoral Studies (Zoology) THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) December 2016 © Lucas Brotz, 2016 Abstract Fisheries for jellyfish (primarily scyphomedusae) have a long history in Asia, where people have been catching and processing jellyfish as food for centuries. More recently, jellyfish fisheries have expanded to the Western Hemisphere, often driven by demand from buyers in Asia as well as collapses of more traditional local finfish and shellfish stocks. Despite this history and continued expansion, jellyfish fisheries are understudied, and relevant information is sparse and disaggregated. Catches of jellyfish are often not reported explicitly, with countries including them in fisheries statistics as “miscellaneous invertebrates” or not at all. Research and management of jellyfish fisheries is scant to nonexistent. Processing technologies for edible jellyfish have not advanced, and present major concerns for environmental and human health. Presented here is the first global assessment of jellyfish fisheries, including identification of countries that catch jellyfish, as well as which species are targeted. A global catch reconstruction is performed for jellyfish landings from 1950 to 2013, as well as an estimate of mean contemporary catches. Results reveal that all investigated aspects of jellyfish fisheries have been underestimated, including the number of fishing countries, the number of targeted species, and the magnitudes of catches. Contemporary global landings of jellyfish are at least 750,000 tonnes annually, more than double previous estimates. -
Species–Specific Crab Predation on the Hydrozoan Clinging Jellyfish Gonionemus Sp
Species–specific crab predation on the hydrozoan clinging jellyfish Gonionemus sp. (Cnidaria, Hydrozoa), subsequent crab mortality, and possible ecological consequences Mary R. Carman1, David W. Grunden2 and Annette F. Govindarajan1 1 Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA, United States of America 2 Town of Oak Bluffs Shellfish Department, Oak Bluffs, MA, United States of America ABSTRACT Here we report a unique trophic interaction between the cryptogenic and sometimes highly toxic hydrozoan clinging jellyfish Gonionemus sp. and the spider crab Libinia dubia. We assessed species–specific predation on the Gonionemus medusae by crabs found in eelgrass meadows in Massachusetts, USA. The native spider crab species L. dubia consumed Gonionemus medusae, often enthusiastically, but the invasive green crab Carcinus maenus avoided consumption in all trials. One out of two blue crabs (Callinectes sapidus) also consumed Gonionemus, but this species was too rare in our study system to evaluate further. Libinia crabs could consume up to 30 jellyfish, which was the maximum jellyfish density treatment in our experiments, over a 24-hour period. Gonionemus consumption was associated with Libinia mortality. Spider crab mortality increased with Gonionemus consumption, and 100% of spider crabs tested died within 24 h of consuming jellyfish in our maximum jellyfish density containers. As the numbers of Gonionemus medusae used in our experiments likely underestimate the number of medusae that could be encountered by spider crabs over a 24-hour period in the field, we expect that Gonionemus may be having a negative effect on natural Submitted 16 August 2017 Libinia populations. Furthermore, given that Libinia overlaps in habitat and resource Accepted 6 October 2017 use with Carcinus, which avoids Gonionemus consumption, Carcinus populations could Published 26 October 2017 be indirectly benefiting from this unusual crab–jellyfish trophic relationship. -
The State of World Fisheries and Aquaculture 2020
2018 2020 2018 2018 THE STATE OF WORLD FISHERIES AND AQUACULTURE SUSTAINABILITY IN ACTION This flagship publication is part of THE STATE OF THE WORLD series of the Food and Agriculture Organization of the United Nations. Required citation: FAO. 2020. The State of World Fisheries and Aquaculture 2020. Sustainability in action. Rome. https://doi.org/10.4060/ca9229en The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO) concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The designations employed and the presentation of material in the maps do not imply the expression of any opinion whatsoever on the part of FAO concerning the legal or constitutional status of any country, territory or sea area, or concerning the delimitation of frontiers. The mention of specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO in preference to others of a similar nature that are not mentioned. The views expressed in this information product are those of the author(s) and do not necessarily reflect the views or policies of FAO. ISSN 1020-5489 [PRINT] ISSN 2410-5902 [ONLINE] ISBN 978-92-5-132692-3 © FAO 2020 Some rights reserved. This work is made available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons.org/licenses/by-nc-sa/3.0/igo). -
Chapter Three Habitats of the Estuarine Reserve
77 Chapter Three Habitats of the Estuarine Reserve 78 Ocean Beaches Ocean Beaches The ocean beach that sunbathers love is only one part of the ocean beach habitats found at the Reserve sites. The beach in a sense begins underwater, extending in some places for miles offshore to the edge of the continental shelf. The water currents and patterns of sediment deposition along the shelf influence what a beach looks like – how it erodes, its Cannonball jellyfish size. Along the shore itself are three contrasting environments – the subtidal, intertidal and supratidal zones – which are populated by organisms specially adapted to the harsh characteristics of each area. Subtidal zone Starfish The shallow waters, breaking waves, and swirling sand of the subtidal zone are home to plankton, algae, jellyfish, starfish, mollusks, crustaceans and fish. The only plants that survive here are one-celled algae. The constant movement of water and sand prevents organisms that need to be attached to a hard surface (such as barnacles) from taking hold. Mole crab As the water rakes shell fragments and coarse sand across the bottom, each wave can injure or bury organisms. Coquina clam Great Southern White 79 Ocean Beaches Intertidal zone Animals living in the sandy environment of the intertidal zone are exposed to alternating periods of wave action and salt- laden drying breezes. Although Sand shrimp it may appear that the only creatures here are birds, millions of tiny worms, shrimp and other organisms live among the sand grains. Coquina clams, Donax spp., and mole crabs, Emerita talpoida, survive by burrowing into the sand and filtering plankton (microscopic plants and animals) from the waves that wash over them. -
Jellyfish (Cnidaria/Ctenophora)
JELLYFISH (CNIDARIA/CTENOPHORA) CARE MANUAL CREATED BY THE AZA AQUATIC INVERTEBRATE TAXON ADVISORY GROUP IN ASSOCIATION WITH THE AZA ANIMAL WELFARE COMMITTEE Jellyfish Care Manual Jellyfish Care Manual Published by the Association of Zoos and Aquariums in association with the AZA Animal Welfare Committee Formal Citation: AZA Aquatic Invertebrate TAG. (2013). Jellyfish Care Manual. Association of Zoos and Aquariums, Silver Spring, MD. p. 79. Authors and Significant Contributors: Jerry Crow, Waikiki Aquarium Michael Howard, Monterey Bay Aquarium Vincent Levesque, Birch Aquarium/Museum at Scripps Leslee Matsushige, Birch Aquarium/Museum at Scripps Steve Spina, New England Aquarium Mike Schaadt, Cabrillo Marine Aquarium Nancy Sowinski, Sunset Marine Labs Chad Widmer, Monterey Bay Aquarium Bruce Upton, Monterey Bay Aquarium Edited by: Mike Schaadt, Cabrillo Marine Aquarium Reviewers: Pete Mohan, Akron Zoo, AZA Aquatic Invertebrate TAG Chair Mackenzie Neale, Vancouver Aquarium Nancy Sowinski, Sunset Marine Labs Chad Widmer, Monterey Bay Aquarium Emma Rees (Cartwright), Weymouth Sealife Park Dr. Poh Soon Chow, Oceanis World Rebecca Helm, Brown University AZA Staff Editors: Maya Seamen, AZA ACM Intern Candice Dorsey, Ph.D., Director, Animal Conservation Cover Photo Credits: Gary Florin Illustrations: Celeste Schaadt Disclaimer: This manual presents a compilation of knowledge provided by recognized animal experts based on the current science, practice, and technology of animal management. The manual assembles basic requirements, best practices, and animal care recommendations to maximize capacity for excellence in animal care and welfare. The manual should be considered a work in progress, since practices continue to evolve through advances in scientific knowledge. The use of information within this manual should be in accordance with all local, state, and federal laws and regulations concerning the care of animals. -
Graham WOM Graham Web Only.Qxd
WM Graham et al. – Supplemental information (Requests for these materials in another format should be sent to the corresponding author, at [email protected]) WebPanel 1. Indirect impacts of jellyfish on fisheries WebPanel 2. Costs: fisheries and aquaculture Jellyfish can affect commercial species by preying directly on The 2010 landings of the top 20 net-based fisheries (purse egg and larval stages (Purcell and Arai 2001; Sabates et al. seine, gill net, and trawl) at 26.6 million metric tons represent 2010) and by reducing their consumption of foods via 35% of the total tonnage of marine capture fisheries (75.9 mil- intraguild predation (Suchman et al. 2008; Brodeur et al. 2008). lion metric tons). We calculated this percentage using capture In many cases, jellyfish and small coastal pelagic fishes feed at a fisheries production from all FAO areas, except “Inland similar trophic level (Purcell and Sturdevant 2001; Ruzicka et Waters” (FAO 2011). Species groups excluded were aquatic al. 2012), which is a proposed mechanism for jellyfish prolifer- plants, freshwater diadromous fish, and “Marine Mollusks nei” ation as exploited fish are removed (Lynam et al. 2006). (nei: not elsewhere identified). Interestingly, reduction of Mnemiopsis leidyi ctenophore popu- lations by gelatinous predators reduces predation pressure on oyster larvae and zooplankton that support fish populations (Purcell et al. 1991; Purcell and Decker 2005). Monetary costs of jellyfish as predators and competitors of important fishery species are difficult to assess. WebPanel 3. Response to jellyfish ingress into power plants Since the 1980s, some companies have developed gear to pre- vent jellyfish from entering the cooling system of power plants. -
Stable Isotopes Confirm a Foraging Dichotomy in Juvenile Loggerhead
Journal of Experimental Marine Biology and Ecology 387 (2010) 44–51 Contents lists available at ScienceDirect Journal of Experimental Marine Biology and Ecology journal homepage: www.elsevier.com/locate/jembe Stable isotopes confirm a foraging dichotomy in juvenile loggerhead sea turtles Catherine M. McClellan a,⁎, Joanne Braun-McNeill b, Larisa Avens b, Bryan P. Wallace a,c, Andrew J. Read a a Division of Marine Science and Conservation, Duke University Marine Laboratory, 135, Duke Marine Lab Road, Beaufort, NC 28516, USA b NOAA, National Marine Fisheries Service, Southeast Fisheries Science Center, Center for Coastal Fisheries and Habitat Research, 101 Pivers Island Road, Beaufort, NC 28516, USA c Center for Applied Biodiversity Science, Conservation International, 2011 Crystal Drive, Suite 500, Arlington, VA 22202, USA article info abstract Article history: Differential habitat use and foraging behaviors at various life-stages within a population can have profound Received 2 December 2009 consequences for survivorship, stage duration, and time to maturity. While evidence for plasticity within a Received in revised form 24 February 2010 given life-stage in marine species is mounting, factors that contribute to this diversity remain poorly Accepted 25 February 2010 understood. We used stable isotope analysis of consumer and prey tissues to describe the trophic niche Keywords: width of juvenile loggerhead turtles (Caretta caretta) that have been tracked and previously shown to have Life history variation significant variation in movement behaviors (oceanic versus neritic). Results of a Bayesian mixing model Loggerhead turtle indicated that whereas benthic invertebrates dominated the recent diet of neritic turtles (determined Migration through blood plasma), pelagic prey items contributed substantially to the diets of oceanic turtles. -
Ecological and Oceanographic Influences on Leatherback Turtle
The University of Southern Mississippi The Aquila Digital Community Dissertations Fall 12-2017 Ecological and Oceanographic Influences on Leatherback urT tle Behavior and Scyphozoan Jellyfish Distributions in the Gulf of Mexico Katrina Aleksa University of Southern Mississippi Follow this and additional works at: https://aquila.usm.edu/dissertations Part of the Biology Commons, Marine Biology Commons, Oceanography Commons, and the Population Biology Commons Recommended Citation Aleksa, Katrina, "Ecological and Oceanographic Influences on Leatherback urT tle Behavior and Scyphozoan Jellyfish Distributions in the Gulf of Mexico" (2017). Dissertations. 1476. https://aquila.usm.edu/dissertations/1476 This Dissertation is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Dissertations by an authorized administrator of The Aquila Digital Community. For more information, please contact [email protected]. ECOLOGICAL AND OCEANOGRAPHIC INFLUENCES ON LEATHERBACK TURTLE BEHAVIOR AND SCYPHOZOAN JELLYFISH DISTRIBUTIONS IN THE GULF OF MEXICO by Katrina T. Aleksa A Dissertation Submitted to the Graduate School, the College of Science and Technology, and the School of Ocean Science and Technology at The University of Southern Mississippi in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy December 2017 ECOLOGICAL AND OCEANOGRAPHIC INFLUENCES ON LEATHERBACK TURTLE BEHAVIOR AND SCYPHOZOAN JELLYFISH DISTRIBUTIONS IN THE GULF OF MEXICO by Katrina T. Aleksa December 2017 Approved by: ________________________________________________ Dr. William M. Graham, Committee Chair Professor, Ocean Science and Technology ________________________________________________ Dr. Scott P. Milroy, Committee Member Associate Professor, Ocean Science and Technology ________________________________________________ Dr. Jerry D. Wiggert, Committee Member Associate Professor, Ocean Science and Technology ________________________________________________ Dr. -
Cannonball Jellyfish Stomolophus Meleagris SCDNR Contributors (2005): Dubose B
Supplemental Volume: Species of Conservation Concern SC SWAP 2015 Cannonball Jellyfish Stomolophus meleagris SCDNR Contributors (2005): DuBose B. Griffin, Thomas M. Murphy, and Peter Kingsley-Smith [SCDNR] Reviewed and Edited (2013): DuBose B. Griffin, Pearse Webster, and Peter Kingsley-Smith [SCDNR] DESCRIPTION Cannonball jellyfish Taxonomy and Basic Description Cannonball, or cabbagehead, jellyfish (Stomolophus meleagris) (L. Agassiz 1860),are also known as jellyballs and belong to the class Scyphozoa and order Rhizostomeae. Agassiz (1860) described and illustrated the medusa of cannonballs using specimens collected from Wassaw Island, Georgia and Charleston, South Carolina. The hemisperical bell reaches 20 to 25 cm (8 to 10 in.) in size and is bordered with brown pigment. It has short, protruding oral arms with secondary mouth folds (scapulets) at the base of the bell covered with mucus for trapping small prey. Stomolophus meleagris means “many mouthed hunter.” The mucus is also thought to be a response to disturbance rather than for feeding (Phillips et al. 1969; Larson 1976). Status The cannonball jellyfish is not a state or federally listed species; however, cannonballs are ecologically important because they are the major prey base for the Endangered leatherback sea turtle (Dermochelys coriacea) and warrant conservation. POPULATION SIZE AND DISTRIBUTION Cannonball jellyfish have been reported in the western Atlantic from New England to Brazil (Kramp 1961; Larson 1976), in the eastern Pacific from southern California to Ecuador, and in the western Pacific from the Sea of Japan to the South China Sea (Kramp 1961; Omori 1978). They are one of the most abundant scyphomedusae along the Southeastern and Gulf Coasts of the United States (Mayer 1910; Kraeuter and Setzler 1975; Burke 1976; Calder and Hester 1978).