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Disney•Pixar's “Finding Dory”
Educator’s Guide GRADES 2-6 Created in partnership with the Educational Team isney•Pixar’s “Finding Dory” welcomes back to the big convinced his biological sonar skills are on the fritz; and Dscreen everyone’s favorite forgetful blue tang Dory Destiny (voice of Kaitlin Olson), a nearsighted whale shark. (voice of Ellen DeGeneres), who’s living happily in the reef Deftly navigating the complex inner workings of the MLI, with Marlin (voice of Albert Brooks) and Nemo (voice Dory and her friends discover the magic within their flaws, of Hayden Rolence). When Dory suddenly remembers friendships and family. that she has a family out there who may be looking for Directed by Andrew Stanton (“Finding Nemo,” “WALL•E”), her, the trio takes off on a life-changing adventure across co-directed by Angus MacLane (“Toy Story OF TERROR!”), the ocean to California’s prestigious Marine Life Institute and produced by Lindsey Collins (co-producer “WALL•E”), (MLI), a rehabilitation center and aquarium. In an effort to Disney•Pixar’s “Finding Dory” swims home on Digital find her mom (voice of Diane Keaton) and dad (voice of HD October 25 and on Blu-ray™ November 15. For Eugene Levy), Dory enlists the help of three of the MLI’s more information, like us on Facebook, https://www. most intriguing residents: Hank (voice of Ed O’Neill), a facebook.com/PixarFindingDory, and follow us on Twitter, cantankerous octopus who frequently gives employees https://twitter.com/findingdory and Instagram, https:// the slip; Bailey (voice of Ty Burrell), a beluga whale who is instagram.com/DisneyPixar. -
Westminsterresearch Haemogregarina Bigemina
WestminsterResearch http://www.westminster.ac.uk/westminsterresearch Haemogregarina bigemina (Protozoa : Apicomplexa : Adeleorina) – Past, present and future Davies A.J., Smit N.J., Hayes P.M., Seddon A.M. and Wertheim D.F. This is the publisher version of an article published in Folia Parasitologica 51 (2/3) 99- 108 2004. The final definitive version is available online at:https://dx.doi.org/10.14411/fp.2004.015 © 2004 Parazitologický ústav AVČR. The WestminsterResearch online digital archive at the University of Westminster aims to make the research output of the University available to a wider audience. Copyright and Moral Rights remain with the authors and/or copyright owners. Whilst further distribution of specific materials from within this archive is forbidden, you may freely distribute the URL of WestminsterResearch: ((http://westminsterresearch.wmin.ac.uk/). In case of abuse or copyright appearing without permission e-mail [email protected] FOLIA PARASITOLOGICA 51: 99–108, 2004 REVIEW ARTICLE Haemogregarina bigemina (Protozoa: Apicomplexa: Adeleorina) – past, present and future Angela J. Davies1, Nico J. Smit2, Polly M. Hayes1, Alan M. Seddon1 and David Wertheim3 1School of Life Sciences and 3School of Computing, Kingston University, Penrhyn Road, Kingston upon Thames, Surrey, KT1 2EE, UK; 2Department of Zoology, Rand Afrikaans University, P.O. Box 524, Auckland Park 2006, South Africa Key words: Haemogregarina bigemina, haemogregarines, development, transmission, Gnathia, isopods Abstract. This paper reviews past, current and likely future research on the fish haemogregarine, Haemogregarina bigemina Laveran et Mesnil, 1901. Recorded from 96 species of fishes, across 70 genera and 34 families, this broad distribution for H. bigemina is questioned. -
Monitoring Functional Groups of Herbivorous Reef Fishes As Indicators of Coral Reef Resilience a Practical Guide for Coral Reef Managers in the Asia Pacifi C Region
Monitoring Functional Groups of Herbivorous Reef Fishes as Indicators of Coral Reef Resilience A practical guide for coral reef managers in the Asia Pacifi c Region Alison L. Green and David R. Bellwood IUCN RESILIENCE SCIENCE GROUP WORKING PAPER SERIES - NO 7 IUCN Global Marine Programme Founded in 1958, IUCN (the International Union for the Conservation of Nature) brings together states, government agencies and a diverse range of non-governmental organizations in a unique world partnership: over 100 members in all, spread across some 140 countries. As a Union, IUCN seeks to influence, encourage and assist societies throughout the world to conserve the integrity and diversity of nature and to ensure that any use of natural resources is equitable and ecologically sustainable. The IUCN Global Marine Programme provides vital linkages for the Union and its members to all the IUCN activities that deal with marine issues, including projects and initiatives of the Regional offices and the six IUCN Commissions. The IUCN Global Marine Programme works on issues such as integrated coastal and marine management, fisheries, marine protected areas, large marine ecosystems, coral reefs, marine invasives and protection of high and deep seas. The Nature Conservancy The mission of The Nature Conservancy is to preserve the plants, animals and natural communities that represent the diversity of life on Earth by protecting the lands and waters they need to survive. The Conservancy launched the Global Marine Initiative in 2002 to protect and restore the most resilient examples of ocean and coastal ecosystems in ways that benefit marine life, local communities and economies. -
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MARINE ECOLOGY PROGRESS SERIES Vol. 164: 263-271,1998 Published April 9 Mar Ecol Prog Ser Intraspecific and interspecific relationships between host size and the abundance of parasitic larval gnathiid isopods on coral reef fishes Alexandra S. Grutter 'l*, Robert poulin2 'Department of Parasitology, The University of Queensland. Brisbane, Queensland 4072, Australia 'Department of Zoology, University of Otago. PO Box 56. Dunedin. New Zealand ABSTRACT: Parasitic gnathud isopod larvae on coral reef teleosts and elasmobranchs were quantified at Lizard and Heron Islands (Great Barrier Reef), and Moreton Bay, Australia. The relationship between gnathlid abundance and host size was examined across and within species. Of the 56 species examined. 70 % had gnathiids, with counts ranging from 1 to 200 per fish and the elasmobranchs hav- ing the highest numbers. Pomacentrids rarely had gnathiids. In contrast, most labrids had gnathiids. Gnathiid abundance was positively correlated with host size in the species Chlorurus sordidus, Ctenochaetus stnatus, Hernigyrnnus melapterus, Siganus dollatus, and Thalassorna lunare, but not for Scolopsis b~lineatus.Mean gnathlid abundance per host species also correlated with host size across species, even after controlling for the potential confounding effects of uneven sampling effort and host phylogeny Thus host size explains much of the intraspecific and interspecific variation In gnathiid abundance on fish. KEY WORDS: Gnathiidae . Ectoparasites . Coral reef fish . Host-parasite interactions . Fish size . Great Barrier Reef INTRODUCTION gnathiids on fish (Grutter 1996a). When present in 'large' numbers (Paperna & Por 1977) and when fish Until recently, there was little evidence that para- have 'around a hundred' (Mugridge & Stallybrass sites were important in fish cleaning behavior (Losey 1983),gnathiids can cause fish mortality in captive fish 1987), however, current studies on the Great Barrier (Paperna & Por 1977). -
Patterns and Processes in the Evolutionary History of Parrotfishes
bs_bs_banner Biological Journal of the Linnean Society, 2012, ••, ••–••. With 5 figures Patterns and processes in the evolutionary history of parrotfishes (Family Labridae) JOHN. H. CHOAT1*, OYA. S. KLANTEN1†, LYNNE VAN HERWERDEN1, D. ROSS ROBERTSON2‡ and KENDALL D. CLEMENTS3 1School of Tropical and Marine Biology, James Cook University, Townsville, QLD, 4811, Australia 2Smithsonian Tropical Research Institute, Ancon, Balboa, Republic of Panama 3School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand Received 5 March 2012; revised 23 May 2012; accepted for publication 23 May 2012 Phylogenetic reconstruction of the evolutionary relationships among 61 of the 70 species of the parrotfish genera Chlorurus and Scarus (Family Labridae) based on mitochondrial and nuclear gene sequences retrieved 15 well-supported clades with mid Pliocene/Pleistocene diversification. Twenty-two reciprocally monophyletic sister- species pairs were identified: 64% were allopatric, and the remainder were sympatric. Age of divergence was similar for allopatric and sympatric species pairs. Sympatric sister pairs displayed greater divergence in morphol- ogy, ecology, and sexually dimorphic colour patterns than did allopatric pairs, suggesting that both genetic drift in allopatric species pairs and ecologically adaptive divergence between members of sympatric pairs have played a role in diversification. Basal species typically have small geographical ranges and are restricted to geographically and ecologically peripheral reef habitats. We found little evidence that a single dominant process has driven diversification, nor did we detect a pattern of discrete, sequential stages of diversification in relation to habitat, ecology, and reproductive biology. The evolution of Chlorurus and Scarus has been complex, involving a number of speciation processes. -
Hawaiian Parrotfishes (And a Few Wrasse Too!) Fishinar 11/15/2017 Questions? Feel Free to Contact Me at [email protected] Dr
Hawaiian Parrotfishes (and a few Wrasse too!) Fishinar 11/15/2017 Questions? Feel free to contact me at [email protected] Dr. Christy Pattengill-Semmens, Ph.D.– Instructor Director of Science- REEF Bullethead Parrotfish (Chlorurus sordidus) Symmetrical, bullet-shaped head profile. IP is reddish-brown to gray, double row of 4-5 white spots may mark the side and a broad white bar (which may contain a dark spot) often at the base of the tail. TP is variable in color but generally greenish with pale area on cheeks, typically has broad white saddle at tail base. Juveniles are b&w striped. Feed on both coral polyps and algae. Photo by: Bill Stohler Distribution/Size: Widespread throughout central and western Pacific. Up to 15” REEF Expert Sighting Frequency in Hawaii – 85% Photo by: Joyce Burek Palenose Parrotfish (Scarus psittacus) IP often found in schools, very drab in color (light gray to dark brownish gray) without distinctive markings. TP is green/blue, sometimes with large yellow patch on side. Dark blue patch on their nose. Juveniles look like tiny IP. Photo by: Ralph Turre Distribution/Size: Widespread throughout central and western Pacific. Up to 12” REEF Expert Sighting Frequency in Hawaii – 85% Photo by: Ralph Turre © 2017 Reef Environmental Education Foundation (REEF). All rights reserved. Redlip Parrotfish (Scarus rubroviolaceus) AKA Ember IPs often distinctly bi-colored with dark brownish-red front and paler in back, or overall reddish “textured” with white. IP often have algal mustache. TP are blue and green, often darker on front half, with blue mustache. TP and IP have squared-off head. -
National Prioritization of Key Vulnerable Reef Fish Species for Fiji, for Targeted Research
National prioritization of key vulnerable reef fish species for Fiji, for targeted research Coral reef fish and invertebrates sold at the Suva market. Photo by: Sangeeta Mangubhai/WCS Introduction The majority of Fiji’s population is coastal and therefore highly reliant on inshore fisheries for their subsistence and local economic needs (Hunt 1999). At least 33 percent of all animal protein consumed in Fiji comes from fish, and subsistence and artisanal fisheries contribute at least US$59.1 million to Fiji’s annual GDP (Gillett 2009). There is growing concerns for the impacts of present day harvesting rates and methods, especially for vulnerable fish and invertebrate species in Fiji. This is resulting in a progressive decline in fish belonging to higher trophic (feeding) groups, a pattern that is termed “fishing down food webs” (Pauly et al. 1998). Coral reef fish vary in their vulnerability to fishing pressure, and how well they can recover, if fishing is stopped or significantly reduced. Recovery potential relates to the rate at which a species can replace the individuals that are lost to natural mortality and to fishing. In general, the medium to larger carnivorous fish high in the food chain are thought to be more vulnerable to fishing (e.g. groupers) requiring in decades to recover, while smaller fish (e.g. herbivores such as rabbitfish) are thought be less vulnerable (Abesamis et al. 2014). Certain life history characteristics of fish species together can be good predictors of vulnerability at the population level to fishing pressure, including: (a) maximum size; (b) body growth rate; (c) lifespan; (d) natural mortality rates; (e) age at maturity; and (f) length at maturity (Abesamis et al. -
Check List of Fishes of the Gulf of Mannar Ecosystem, Tamil Nadu, India
Available online at: www.mbai.org.in doi: 10.6024/jmbai.2016.58.1.1895-05 Check list of fishes of the Gulf of Mannar ecosystem, Tamil Nadu, India K. K. Joshi*, Miriam Paul Sreeram, P. U. Zacharia, E. M. Abdussamad, Molly Varghese, O. M. M. J. Mohammed Habeeb1, K. Jayabalan1, K. P. Kanthan1, K. Kannan1, K. M. Sreekumar, Gimy George and M. S. Varsha ICAR-Central Marine Fisheries Research Institute, P. B. No.1603, Kochi - 682 018, Kerala, India. 1Tuticorin Research Centre of Central Marine Fisheries Research Institute, Tuticorin - 628 001, Tamil Nadu, India. *Correspondence e-mail: [email protected] Received: 10 Jan 2016, Accepted: 25 Jun 2016, Published: 30 Jun 2016 Original Article Abstract Introduction Gulf of Mannar Ecosystem (GOME) covers an area spread over Rameswaram and Kanyakumari for about 19000 km2 and lies between India is blessed with a vast region of coral reefs and 78°11’E and 79°15’ E longitude and 8°49’N and 9°15’N latitude. The mangroves and these regions support very rich fauna of flora 21 coral islands form a network of habitats for different kinds of fishes and constitute rich biodiversity of marine organisms. Gulf and marine organisms. Fish samples were collected during April 2005 of Mannar Ecosystem (GOME) covers an area spread over to March 2010 from different centers viz., Vembar, Tharuvaikulam, Rameswaram and Kanyakumari to about 19,000 km2. GOME Vellapatti, Therespuram, Tuticorin, Alangarathattu, Pazhaykayal, lies between 78°11’00” E and 79°15’00” E longitude and Punnakayal, Kayalpattinam, Veerapandiapattinam, Thiruchendur and 8°49’00” N and 9°15’00” N latitude. -
Introduced Marine Species in Pago Pago Harbor, Fagatele Bay and the National Park Coast, American Samoa
INTRODUCED MARINE SPECIES IN PAGO PAGO HARBOR, FAGATELE BAY AND THE NATIONAL PARK COAST, AMERICAN SAMOA December 2003 COVER Typical views of benthic organisms from sampling areas (clockwise from upper left): Fouling organisms on debris at Pago Pago Harbor Dry Dock; Acropora hyacinthus tables in Fagetele Bay; Porites rus colonies in Fagasa Bay; Mixed branching and tabular Acropora in Vatia Bay INTRODUCED MARINE SPECIES IN PAGO PAGO HARBOR, FAGATELE BAY AND THE NATIONAL PARK COAST, AMERICAN SAMOA Final report prepared for the U.S. Fish and Wildlife Service, Fagetele Bay Marine Sanctuary, National Park of American Samoa and American Samoa Department of Marine and Natural Resources. S. L. Coles P. R. Reath P. A. Skelton V. Bonito R. C. DeFelice L. Basch Bishop Museum Pacific Biological Survey Bishop Museum Technical Report No 26 Honolulu Hawai‘i December 2003 Published by Bishop Museum Press 1525 Bernice Street Honolulu, Hawai‘i Copyright © 2003 Bishop Museum All Rights Reserved Printed in the United States of America ISSN 1085-455X Contribution No. 2003-007 to the Pacific Biological Survey EXECUTIVE SUMMARY The biological communities at ten sites around the Island of Tutuila, American Samoa were surveyed in October 2002 by a team of four investigators. Diving observations and collections of benthic observations using scuba and snorkel were made at six stations in Pago Pago Harbor, two stations in Fagatele Bay, and one station each in Vatia Bay and Fagasa Bay. The purpose of this survey was to determine the full complement of organisms greater than 0.5 mm in size, including benthic algae, macroinvertebrates and fishes, occurring at each site, and to evaluate the presence and potential impact of nonindigenous (introduced) marine species. -
M590p155.Pdf
Vol. 590: 155–169, 2018 MARINE ECOLOGY PROGRESS SERIES Published March 12 https://doi.org/10.3354/meps12480 Mar Ecol Prog Ser OPENPEN ACCESSCCESS Constraining species−size class variability in rates of parrotfish bioerosion on Maldivian coral reefs: implications for regional-scale bioerosion estimates Robert T. Yarlett1,*, Chris T. Perry1, Rod W. Wilson2, Kate E. Philpot3 1Geography, College of Life and Environmental Sciences, University of Exeter, Exeter EX4 4RJ, UK 2Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter EX4 4QD, UK 3Ecology by Design Ltd, Unit 16, Hampden House, Monument Park, Chalgrove, Oxfordshire OX44 7RW, UK ABSTRACT: Parrotfish are important bioeroders on coral reefs, and thus influence reef carbonate budgets and generate large volumes of carbonate sand that contribute to local beach and reef island maintenance. However, despite the importance of this process, there is a paucity of data with which variations in bioerosion rates as a function of species, feeding modes, and body size of parrotfish can be constrained. There is, in addition, limited knowledge regarding how resultant rates may vary within and between reef-building regions. Here, direct estimates of parrotfish bio- erosion rates were quantified across different size classes of 6 common species of Maldivian par- rotfish. These species comprise both ‘scraper’ and ‘excavator’ taxa, and our data indicate marked variations in mean bioerosion rates among these species. We also note that all species exhibited an apparent bimodal feeding cycle, with peaks in the late morning and early afternoon. Highest bioerosion rates were found in the ‘excavator’ Chlorurus strongylocephalus (~460 kg ind.−1 yr−1), nearly 130 times greater than rates calculated for comparably sized (>45 cm) ‘scraper’ species. -
Trophic Classifications of Reef Fishes from the Tropical U.S
TROPHIC CLASSIFICATIONS OF REEF FISHES FROM THE TROPICAL U.S. PACIFIC (Version 1.0) Stuart A. Sandin Marine Biology Research Division Scripps Institution of Oceaongraphy 9500 Gilman Drive La Jolla, CA 92093-0202 [email protected] Completed in collaboration with: Ivor Williams Coral Reef Ecosystem Division NOAA, National Marine Fisheries Service Pacific Islands Fisheries Science Center 1125B Ala Moana Boulevard Honolulu, HI 96822, USA [email protected] Table 1 – List of fish taxa identified across surveys of the coral reef ecosystems of the U.S. Pacific islands. Taxa are organized alphabetically by family, and alphabetically within family by lowest identified level (typically species). Trophic classifications are provided in coarse groups based on major diet items integrated across the life stages of each species. The four groups are Primary Consumer (including herbivores and detritivores), Secondary Consumer (including invertivores, corallivores, and omnivores), Planktivores (primarily consuming zooplankton), and Piscivores (including species with fish as the dominant diet item). -
Shallow Water Records of Fish
Shallow water records of fish Collected from or observed at Howland Island from 1927-2002. Collected or compiled by Mundy et al. (2002). Scientific Name Common Name GINGLYMOSTOMATIDAE Nurse Sharks Nebrius ferrugineus nurse shark CARCHARHINIDAE Requiem Sharks Carcharhinus amblyrhynchos grey reef shark Carcharhinus melanopterus reef blacktip shark Galeocerdo cuvieri tiger shark HEMIGALEIDAE Weasel Sharks Triaenodon obesus reef whitetip shark SPHYRNIDAE Hammerhead Sharks Sphyrna lewini scalloped hammerhead shark DASYATIDAE Sand Rays Taeniura meyeni MYLIOBATIDIDAE Eagle Rays Aetobatus narinari spotted eagle ray MOBULIDAE Manta Rays Manta sp. manta MURAENIDAE Moray Eels Anarchias allardicei Allardice’s moray Anarchias cantonenesis Canton Island moray Echidna nebulosa snowflake moray Echidna polyzona barred moray Enchelycore pardalis Gymnomuraena zebra zebra moray Gymnothorax breedini Gymnothorax chilospilus Gymnothorax javanicus giant moray Gymnothorax flavimarginatus yellow-margined moray Gymnothorax marshallensis Marshall Island moray Gymnothorax meleagris white-mouth moray Gymnothorax picta peppered moray Gymnothorax rueppelliae yellow-headed moray Gymnothorax sp. Gymnothorax thyrsoideus Gymnothorax undulatus undulated moray Uropterygius sp. Uropterygius marmoratus marbled snake moray OPHICHTHIDAE Myrichthys maculosus spotted snake eel CONGRIDAE Conger Eel Conger sp. CHANIDAE Milkfish Chanos chanos milkfish SYNODONTIDAE Lizardfishes Synodus sp. HOLOCENTRIDAE Squirrelfishes Myripristis berndti bigscale soldierfish Sargocentron caudimaculatum