Section 21 Environmental Risk Assessment Guidance for Marine Coastal Environments
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MARINE LIFE PROFILE: HAWAIIAN LIMPET SNAIL Classification
Waikïkï Aquarium Education Department MARINE LIFE PROFILE: HAWAIIAN LIMPET SNAIL Hawaiian name: ‘opihi Scientific name: Cellana exarata and others Distribution: Hawaiian Islands Size: up to 3 inches (7.5 cm) Diet: algae Limpets are common snails found on rocky shores throughout the world. But the four species which occur in Hawaii are endemic, found here and no where else! The most common species is the "blackfoot" ‘opihi (Cellana exarata) which occurs on basalt shorelines, from the splash zone high on the shore, seaward to the level of the mean low tide where crust-like pink calcareous algae forms a band on the rocks. Like other snails, limpets have: (1) a head with eyes and tentacles, a mouth on a protrusible proboscis (mouth tube); (2) a broad muscular foot for clinging and crawling; and (3) a soft body mass (containing the internal organs) which is protected by their shell. Living on this part of the shore, the ‘opihi must withstand periods of drying exposure during low tides, as well as heavy surge and pounding waves at high tide. They cling firmly to the rock surface with the muscular foot that acts like a suction cup to keep them from being torn off the rocks. The cap-shaped shell has a low profile and low center of gravity so that the snail presents little resistance to the water as it pounds and pours over the shore. The ribs and grooves in the shell help spread the force of the crashing waves by channeling water down the sides of the shell. Each ‘opihi lives in a shallow depression on the rock that it makes itself, possibly by rasping at the rock with its radula. -
The Native Stream Fishes of Hawaii
Summer 2014 American Currents 2 THE NATIVE STREAM FISHES OF HAWAII Konrad Schmidt St. Paul, MN [email protected] Several years ago at the University of Minnesota a poster The “uniqueness” of these species is due not only to the about Hawaii’s native freshwater fishes caught my eye. I high degree of endemism, but also includes their habitat, life was astonished to learn that for a tropical zone the indige- cycle, and evolutionary adaptations. Hawaii’s watersheds nous freshwater ichthyofauna (traditionally and collectively are typically short and small. The healthiest fish populations known as ‘o’opu) is incredibly rich in uniqueness, but very generally inhabit perennial streams located on the windward poor in species diversity, comprising only four gobies and (northeast) side of islands which are drenched with 100-300 one sleeper. Four of the five are endemic to Hawaii. How- inches of rainfall annually. Frequent and turbid flash floods, ever, recent research suggests the ‘o’opu nākea of Hawaii is called freshets, occur on a regular basis; between events, a distinct species from the Pacific River Goby, and is, there- however, stream visibility can exceed 30 feet. On the lee- fore, also endemic. In addition to these fishes, there are only ward, drier sides, populations do persist in some intermit- two native euryhaline species that venture from the ocean tent streams at higher elevations even though lower reaches into the lower and slower reaches of streams not far above may be dry for months or years. These dynamic streams are their mouths: Hawaiian Flagtail (Kuhlia sandvicensis) and continually and naturally in a state of recovery. -
Pu'u Wa'awa'a Biological Assessment
PU‘U WA‘AWA‘A BIOLOGICAL ASSESSMENT PU‘U WA‘AWA‘A, NORTH KONA, HAWAII Prepared by: Jon G. Giffin Forestry & Wildlife Manager August 2003 STATE OF HAWAII DEPARTMENT OF LAND AND NATURAL RESOURCES DIVISION OF FORESTRY AND WILDLIFE TABLE OF CONTENTS TITLE PAGE ................................................................................................................................. i TABLE OF CONTENTS ............................................................................................................. ii GENERAL SETTING...................................................................................................................1 Introduction..........................................................................................................................1 Land Use Practices...............................................................................................................1 Geology..................................................................................................................................3 Lava Flows............................................................................................................................5 Lava Tubes ...........................................................................................................................5 Cinder Cones ........................................................................................................................7 Soils .......................................................................................................................................9 -
Section 3.9 Fish
3.9 Fish MARIANA ISLANDS TRAINING AND TESTING FINAL EIS/OEIS MAY 2015 TABLE OF CONTENTS 3.9 FISH .................................................................................................................................. 3.9-1 3.9.1 INTRODUCTION .............................................................................................................................. 3.9-2 3.9.1.1 Endangered Species Act Species ................................................................................................ 3.9-2 3.9.1.2 Taxonomic Groups ..................................................................................................................... 3.9-3 3.9.1.3 Federally Managed Species ....................................................................................................... 3.9-5 3.9.2 AFFECTED ENVIRONMENT ................................................................................................................ 3.9-9 3.9.2.1 Hearing and Vocalization ......................................................................................................... 3.9-10 3.9.2.2 General Threats ....................................................................................................................... 3.9-12 3.9.2.3 Scalloped Hammerhead Shark (Sphyrna lewini) ...................................................................... 3.9-14 3.9.2.4 Jawless Fishes (Orders Myxiniformes and Petromyzontiformes) ............................................ 3.9-15 3.9.2.5 Sharks, Rays, and Chimaeras (Class Chondrichthyes) -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
Availability and Distribution of Low Flow in Anahola Stream, Kaua I
Prepared in cooperation with the State of Hawaiÿi Department of Hawaiian Home Lands Availability and Distribution of Low Flow in Anahola Stream, Kauaÿi, Hawaiÿi Scientific Investigations Report 2012–5264 U.S. Department of the Interior U.S. Geological Survey Cover: Kalalea Mountains in northeast Kauaÿi, Hawaiÿi. Photographed by Chui Ling Cheng. Availability and Distribution of Low Flow in Anahola Stream, Kauaÿi, Hawaiÿi By Chui Ling Cheng and Reuben H. Wolff Prepared in cooperation with the State of Hawaiÿi Department of Hawaiian Home Lands Scientific Investigations Report 2012–5264 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2012 For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web: http://www.usgs.gov Telephone: 1-888-ASK-USGS For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod Suggested citation: Cheng, C.L., and Wolff, R.H., 2012, Availability and distribution of low flow in Anahola Stream, Kauaÿi, Hawaiÿi: U.S. Geological Survey Scientific Investigations Report 2012-5264, 32 p. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this information product, for the most part, is in the public domain, it also may contain copyrighted materials as noted in the text. Permission to reproduce copyrighted items must be secured from the copyright owner. -
Aspects of the Behavioral Ecology, Life History, Genetics, and Morophology
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2002 Aspects of the behavioral ecology, life history, genetics, and morophology of the Hawaiian kuhliid fishes Lori Keene Benson Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Recommended Citation Benson, Lori Keene, "Aspects of the behavioral ecology, life history, genetics, and morophology of the Hawaiian kuhliid fishes" (2002). LSU Doctoral Dissertations. 1890. https://digitalcommons.lsu.edu/gradschool_dissertations/1890 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]. ASPECTS OF THE BEHAVIORAL ECOLOGY, LIFE HISTORY, GENETICS, AND MORPHOLOGY OF THE HAWAIIAN KUHLIID FISHES 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 Biological Sciences by Lori Keene Benson B.S., University of Tampa, 1995 December 2002 ACKNOWLEDGMENTS I would like to first thank my major professor, Dr. Mike Fitzsimons, for being a wonderful adviser on matters both scientific and unscientific. He was supportive when I left Baton Rouge during my final year of graduate school to pursue a job opportunity. I feel that I couldn’t have successfully juggled all of these responsibilities without him. I am also especially grateful for all of the help I received from my fellow graduate students at LSU. -
Comparative Ecology, Morphology, and Population Genetics of Black Triggerfish, Melichthys Niger
W&M ScholarWorks Dissertations, Theses, and Masters Projects Theses, Dissertations, & Master Projects 1991 Comparative Ecology, Morphology, and Population Genetics of Black Triggerfish, Melichthys niger Kathryn D. Kavanagh College of William and Mary - Virginia Institute of Marine Science Follow this and additional works at: https://scholarworks.wm.edu/etd Part of the Genetics Commons, Marine Biology Commons, Oceanography Commons, and the Zoology Commons Recommended Citation Kavanagh, Kathryn D., "Comparative Ecology, Morphology, and Population Genetics of Black Triggerfish, Melichthys niger" (1991). Dissertations, Theses, and Masters Projects. Paper 1539617624. https://dx.doi.org/doi:10.25773/v5-pf9s-f194 This Thesis is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Dissertations, Theses, and Masters Projects by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. COMPARATIVE ECOLOGY, MORPHOLOGY, AND POPULATION GENETICS OF BLACK TRIGGERFISH, MELICHTHYS NIGER A Thesis Presented to The Faculty of the School of Marine Science The College of William and Mary in Virginia In Partial Fulfillment of the Requirements for the Degree of Master of Arts by Kathryn Diane Kavanagh 1991 This thesis is submitted in partial fulfillment the requirements for the degree of Master of Arts Approved, December 1991 John Olney, M.A. Comm e Chairman/Adviso John A. Musick, Ph.D. TABLE OF CONTENTS Page ACKNOWLEDGMENTS.............................................. iv LIST OF TABLES............................................... v LIST OF FIGURES.............................................. vi ABSTRACT.....................................................vii INTRODUCTION................................................. 2 METHODS............. 7 Study sites............................................. 7 Density Estimation, Community Survey, and Behavior... 9 Collection and Storage of Specimens................... -
Energetic Costs of Chronic Fish Predation on Reef-Building Corals
ResearchOnline@JCU This file is part of the following reference: Cole, Andrew (2011) Energetic costs of chronic fish predation on reef-building corals. PhD thesis, James Cook University. Access to this file is available from: http://researchonline.jcu.edu.au/37611/ The author has certified to JCU that they have made a reasonable effort to gain permission and acknowledge the owner of any third party copyright material included in this document. If you believe that this is not the case, please contact [email protected] and quote http://researchonline.jcu.edu.au/37611/ The energetic costs of chronic fish predation on reef-building corals Thesis submitted by Andrew Cole BSc (Hons) September 2011 For the degree of Doctor of Philosophy in Marine Biology ARC Centre of Excellence for Coral Reef Studies and the School of Marine and Tropical Biology James Cook University Townsville, Queensland, Australia Statement of Access I, the undersigned, the author of this thesis, understand that James Cook University will make it available for use within the University Library and via the Australian Digital Thesis Network for use elsewhere. I understand that as an unpublished work this thesis has significant protection under the Copyright Act and I do not wish to put any further restrictions upon access to this thesis. 09/09/2011 (signature) (Date) ii Statement of Sources Declaration I declare that this thesis is my own work and has not been submitted in any form for another degree or diploma at my university or other institution of tertiary education. Information derived from the published or unpublished work of others has been acknowledged in the text and a list of references is given. -
Langston R and H Spalding. 2017
A survey of fishes associated with Hawaiian deep-water Halimeda kanaloana (Bryopsidales: Halimedaceae) and Avrainvillea sp. (Bryopsidales: Udoteaceae) meadows Ross C. Langston1 and Heather L. Spalding2 1 Department of Natural Sciences, University of Hawai`i- Windward Community College, Kane`ohe,¯ HI, USA 2 Department of Botany, University of Hawai`i at Manoa,¯ Honolulu, HI, USA ABSTRACT The invasive macroalgal species Avrainvillea sp. and native species Halimeda kanaloana form expansive meadows that extend to depths of 80 m or more in the waters off of O`ahu and Maui, respectively. Despite their wide depth distribution, comparatively little is known about the biota associated with these macroalgal species. Our primary goals were to provide baseline information on the fish fauna associated with these deep-water macroalgal meadows and to compare the abundance and diversity of fishes between the meadow interior and sandy perimeters. Because both species form structurally complex three-dimensional canopies, we hypothesized that they would support a greater abundance and diversity of fishes when compared to surrounding sandy areas. We surveyed the fish fauna associated with these meadows using visual surveys and collections made with clove-oil anesthetic. Using these techniques, we recorded a total of 49 species from 25 families for H. kanaloana meadows and surrounding sandy areas, and 28 species from 19 families for Avrainvillea sp. habitats. Percent endemism was 28.6% and 10.7%, respectively. Wrasses (Family Labridae) were the most speciose taxon in both habitats (11 and six species, respectively), followed by gobies for H. kanaloana (six Submitted 18 November 2016 species). The wrasse Oxycheilinus bimaculatus and cardinalfish Apogonichthys perdix Accepted 13 April 2017 were the most frequently-occurring species within the H. -
Life History, Mating Behavior, and Multiple Paternity in Octopus
LIFE HISTORY, MATING BEHAVIOR, AND MULTIPLE PATERNITY IN OCTOPUS OLIVERI (BERRY, 1914) (CEPHALOPODA: OCTOPODIDAE) A DISSERTATION SUBMITTED TO THE GRADUATE DIVISION OF THE UNIVERSITY OF HAWAI´I AT MĀNOA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN ZOOLOGY DECEMBER 2014 By Heather Anne Ylitalo-Ward Dissertation Committee: Les Watling, Chairperson Rob Toonen James Wood Tom Oliver Jeff Drazen Chuck Birkeland Keywords: Cephalopod, Octopus, Sexual Selection, Multiple Paternity, Mating DEDICATION To my family, I would not have been able to do this without your unending support and love. Thank you for always believing in me. ii ACKNOWLEDGMENTS I would like to thank all of the people who helped me collect the specimens for this study, braving the rocks and the waves in the middle of the night: Leigh Ann Boswell, Shannon Evers, and Steffiny Nelson, you were the hard core tako hunters. I am eternally grateful that you sacrificed your evenings to the octopus gods. Also, thank you to David Harrington (best bucket boy), Bert Tanigutchi, Melanie Hutchinson, Christine Ambrosino, Mark Royer, Chelsea Szydlowski, Ily Iglesias, Katherine Livins, James Wood, Seth Ylitalo-Ward, Jessica Watts, and Steven Zubler. This dissertation would not have happened without the support of my wonderful advisor, Dr. Les Watling. Even though I know he wanted me to study a different kind of “octo” (octocoral), I am so thankful he let me follow my foolish passion for cephalopod sexual selection. Also, he provided me with the opportunity to ride in a submersible, which was one of the most magical moments of my graduate career. -
Reproductive Biology of Acanthurus Coeruleus (Bloch & Schneider, 1801) (Perciformes: Acanthuridae) in the North Coast of the State of Pernambuco, Brazil
Reproductive biology of Acanthurus coeruleus (Bloch & Schneider, 1801) (Perciformes: Acanthuridae) in the north coast of the State of Pernambuco, Brazil RAILMA MARIA VILANOVA QUEIROZ1, MARIANA GOMEZ DO RÊGO2, FABIO HISSA VIEIRA HAZIN1 & PAULO GUILHERME VASCONCELOS DE OLIVEIRA1 1 Universidade Federal Rural de Pernambuco, Departamento de Pesca e Aqüicultura, Av. Dom Manoel de Medeiros s/n, Dois Irmãos, 52171-900, Recife, Pernambuco, Brasil. 2 Universidade Federal Rural de Pernambuco, Departamento de Morfologia e Fisiologia Animal, Av. Dom Manoel de Medeiros s/n, Dois Irmãos, 52171-900, Recife, Pernambuco, Brasil. *Corresponding author: [email protected] Abstract. The objective of this work was to determine aspects of reproductive biology of Blue tang surgeonfish, Acanthurus coeruleus. 496 specimens were sampled, between January 2013 and December 2015, out of which, 235 were male and 261 were female. Sexual ratio did not significanlty differ among genders, and a ratio of 1.11 females per 1 male was found. Total length frequency distribution ranged from 14 to 41.7 cm with predominance of females in the 24-32 cm classes and of males in the 26- 32 cm classes. The estimated allometric coefficient (2.7695), suggests that the species presents negative allometric growth. According to the GSI and the gonads histological analysis, the reproductive period of the species occurs from June to January with periods of greater reproductive activity from August. The oocyte diameter-frequency distribution analysis revealed a multimodal distribution, confirming the evidence of multiple spawning and batch fecundity varied from 20000 to 55000 oocytes. Spawning frequency estimates, based on the hydrated oocytes (HO) method indicated that the species spawns once every 3.8 days, while the estimates based on the post-ovulatory follicle (POF) method indicated a spawning every 3.4 days, during a 6-month spawning season lasting from August to January.