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MARINE TANK GUIDE About the Marine Tank
HOME EDITION MARINE TANK GUIDE About the Marine Tank With almost 34,000 miles of coastline, Alaska’s intertidal zones, the shore areas exposed and covered by ocean tides, are home to a variety of plants and animals. The Anchorage Museum’s marine tank is home to Alaskan animals which live in the intertidal zone. The plants and animals in the Museum’s marine tank are collected under an Alaska Department of Fish and Game Aquatic Resource Permit during low tide at various beaches in Southcentral and Southeast Alaska. Visitors are asked not to touch the marine animals. Touching is stressful for the animals. A full- time animal care technician maintains the marine tank. Since the tank is not located next to the ocean, ocean water cannot be constantly pumped through it. This means special salt water is mixed at the Museum. The tank is also cleaned regularly. Equipment which keeps the water moving, clean, chilled to 43°F and constantly monitored. Contamination from human hands would impact the cleanliness of the water and potentially hurt the animals. A second tank is home to the Museum’s king crab, named King Louie, and black rockfish, named Sebastian. King crab and black rockfish of Alaska live in deeper waters than the intertidal zone creatures. This guide shares information about some of the Museum’s marine animals. When known, the Dena’ina word for an animal is included, recognizing the thousands of years of stewardship and knowledge of Indigeneous people of the Anchorage area and their language. The Dena’ina & Marine Species The geographically diverse Dena’ina lands span both inland and coastal areas, including Anchorage. -
Biodiversity Risk and Benefit Assessment for Pacific Oyster (Crassostrea Gigas) in South Africa
Biodiversity Risk and Benefit Assessment for Pacific oyster (Crassostrea gigas) in South Africa Prepared in Accordance with Section 14 of the Alien and Invasive Species Regulations, 2014 (Government Notice R 598 of 01 August 2014), promulgated in terms of the National Environmental Management: Biodiversity Act (Act No. 10 of 2004). September 2019 Biodiversity Risk and Benefit Assessment for Pacific oyster (Crassostrea gigas) in South Africa Document Title Biodiversity Risk and Benefit Assessment for Pacific oyster (Crassostrea gigas) in South Africa. Edition Date September 2019 Prepared For Directorate: Sustainable Aquaculture Management Department of Environment, Forestry and Fisheries Private Bag X2 Roggebaai, 8001 www.daff.gov.za/daffweb3/Branches/Fisheries- Management/Aquaculture-and-Economic- Development Originally Prepared By Dr B. Clark (2012) Anchor Environmental Consultants Reviewed, Updated and Mr. E. Hinrichsen Recompiled By AquaEco as commisioned by Enterprises at (2019) University of Pretoria 1 | P a g e Biodiversity Risk and Benefit Assessment for Pacific oyster (Crassostrea gigas) in South Africa CONTENT 1. INTRODUCTION .............................................................................................................................. 9 2. PURPOSE OF THIS RISK ASSESSMENT ..................................................................................... 9 3. THE RISK ASSESSMENT PRACTITIONER ................................................................................. 10 4. NATURE OF THE USE OF PACIFIC OYSTER -
Marine Invertebrate Field Guide
Marine Invertebrate Field Guide Contents ANEMONES ....................................................................................................................................................................................... 2 AGGREGATING ANEMONE (ANTHOPLEURA ELEGANTISSIMA) ............................................................................................................................... 2 BROODING ANEMONE (EPIACTIS PROLIFERA) ................................................................................................................................................... 2 CHRISTMAS ANEMONE (URTICINA CRASSICORNIS) ............................................................................................................................................ 3 PLUMOSE ANEMONE (METRIDIUM SENILE) ..................................................................................................................................................... 3 BARNACLES ....................................................................................................................................................................................... 4 ACORN BARNACLE (BALANUS GLANDULA) ....................................................................................................................................................... 4 HAYSTACK BARNACLE (SEMIBALANUS CARIOSUS) .............................................................................................................................................. 4 CHITONS ........................................................................................................................................................................................... -
<I>Aplysia Californica</I>
Temperature Eff ects on Growth, Maturation, and Lifes- pan of the California Sea Hare (Aplysia californica) DUSTIN STOMMES, BLA, LYNNE A. FIEBER, PHD,* CHRISTINA BENO, ROBERT GERDES, MS, and THOMAS R. CAPO, BS We conducted a hatchery growth study to describe the variability in growth rates, spawning, and mortality of Aplysia californica in regard to rearing temperature. Animals were housed at a standard hatchery density of fi ve animals per cage, at temperatures of 13, 15, 18, and 21°C. Animals reared at 13 or 15°C grew as much as four times as large, lived twice as long, matured later, and spawned longer than did animals reared at 18 or 21°C. At age 170 to 205 days the fastest growth rates occurred at 18 and 21°C, and the slowest at 13°C. As animals at 18 and 21°C reached sexual maturity at ages 190 to 197 days, or ∼60% through their lifespans, their growth rates slowed such that by age 260 days, the fastest growth rate was at 13°C, and the slowest was at 21°C. Animals reared at 13 and 15°C reached sexual maturity at 242 and 208 days, respectively, or at ∼40% of their life spans. Lifespan and maximum average animal weight were signifi cantly inversely correlated with temperature (P ≤ 0.0001). However, there were no signifi cant diff erences at any temperature in the age at which maximum animal weight was reached when this age was expressed as a percentage of the life span: animals reached their maximum weight at ∼80% of their life span. -
Preliminary Mass-Balance Food Web Model of the Eastern Chukchi Sea
NOAA Technical Memorandum NMFS-AFSC-262 Preliminary Mass-balance Food Web Model of the Eastern Chukchi Sea by G. A. Whitehouse U.S. DEPARTMENT OF COMMERCE National Oceanic and Atmospheric Administration National Marine Fisheries Service Alaska Fisheries Science Center December 2013 NOAA Technical Memorandum NMFS The National Marine Fisheries Service's Alaska Fisheries Science Center uses the NOAA Technical Memorandum series to issue informal scientific and technical publications when complete formal review and editorial processing are not appropriate or feasible. Documents within this series reflect sound professional work and may be referenced in the formal scientific and technical literature. The NMFS-AFSC Technical Memorandum series of the Alaska Fisheries Science Center continues the NMFS-F/NWC series established in 1970 by the Northwest Fisheries Center. The NMFS-NWFSC series is currently used by the Northwest Fisheries Science Center. This document should be cited as follows: Whitehouse, G. A. 2013. A preliminary mass-balance food web model of the eastern Chukchi Sea. U.S. Dep. Commer., NOAA Tech. Memo. NMFS-AFSC-262, 162 p. Reference in this document to trade names does not imply endorsement by the National Marine Fisheries Service, NOAA. NOAA Technical Memorandum NMFS-AFSC-262 Preliminary Mass-balance Food Web Model of the Eastern Chukchi Sea by G. A. Whitehouse1,2 1Alaska Fisheries Science Center 7600 Sand Point Way N.E. Seattle WA 98115 2Joint Institute for the Study of the Atmosphere and Ocean University of Washington Box 354925 Seattle WA 98195 www.afsc.noaa.gov U.S. DEPARTMENT OF COMMERCE Penny. S. Pritzker, Secretary National Oceanic and Atmospheric Administration Kathryn D. -
Diversity and Life-Cycle Analysis of Pacific Ocean Zooplankton by Video Microscopy and DNA Barcoding: Crustacea
Journal of Aquaculture & Marine Biology Research Article Open Access Diversity and life-cycle analysis of Pacific Ocean zooplankton by video microscopy and DNA barcoding: Crustacea Abstract Volume 10 Issue 3 - 2021 Determining the DNA sequencing of a small element in the mitochondrial DNA (DNA Peter Bryant,1 Timothy Arehart2 barcoding) makes it possible to easily identify individuals of different larval stages of 1Department of Developmental and Cell Biology, University of marine crustaceans without the need for laboratory rearing. It can also be used to construct California, USA taxonomic trees, although it is not yet clear to what extent this barcode-based taxonomy 2Crystal Cove Conservancy, Newport Coast, CA, USA reflects more traditional morphological or molecular taxonomy. Collections of zooplankton were made using conventional plankton nets in Newport Bay and the Pacific Ocean near Correspondence: Peter Bryant, Department of Newport Beach, California (Lat. 33.628342, Long. -117.927933) between May 2013 and Developmental and Cell Biology, University of California, USA, January 2020, and individual crustacean specimens were documented by video microscopy. Email Adult crustaceans were collected from solid substrates in the same areas. Specimens were preserved in ethanol and sent to the Canadian Centre for DNA Barcoding at the Received: June 03, 2021 | Published: July 26, 2021 University of Guelph, Ontario, Canada for sequencing of the COI DNA barcode. From 1042 specimens, 544 COI sequences were obtained falling into 199 Barcode Identification Numbers (BINs), of which 76 correspond to recognized species. For 15 species of decapods (Loxorhynchus grandis, Pelia tumida, Pugettia dalli, Metacarcinus anthonyi, Metacarcinus gracilis, Pachygrapsus crassipes, Pleuroncodes planipes, Lophopanopeus sp., Pinnixa franciscana, Pinnixa tubicola, Pagurus longicarpus, Petrolisthes cabrilloi, Portunus xantusii, Hemigrapsus oregonensis, Heptacarpus brevirostris), DNA barcoding allowed the matching of different life-cycle stages (zoea, megalops, adult). -
Native Decapoda
NATIVE DECAPODA Dungeness crab - Metacarcinus magister DESCRIPTION This crab has white-tipped pinchers on the claws, and the top edges and upper pincers are sawtoothed with dozens of teeth along each edge. The last three joints of the last pair of walking legs have a comb-like fringe of hair on the lower edge. Also the tip of the last segment of the tail flap is rounded as compared to the pointed last segment of many other crabs. RANGE Alaska's Aleutian Islands south to Pt Conception in California SIZE Carapace width to 25 cm (9 inches), but typically less than 20 cm STATUS Native; see the full record at http://www.dfg.ca.gov/marine/dungeness_crab.asp COLOR Light reddish brown on the back, with a purplish wash anteriorly in some specimens. Underside whitish to light orange. HABITAT Rock, sand and eelgrass TIDAL HEIGHT Subtidal to offshore SALINITY Normal range 10–32ppt; 15ppt optimum for hatching TEMPERATURE Normally found from 3–19°C SIMILAR SPECIES Unlike the green crab, it has 10 spines on either side of the eye sockets and grows much larger. It can be distinguished from Metacarcinus gracilis which also has white claws, by the carapace being widest at the 10th tooth vs the 9th in M. gracilis . Unlike the red rock crab it has a tooth on the dorsal margin of its white tipped claw (this and other similar Cancer crabs have black tipped claws). ©Aaron Baldwin © bioweb.uwlax.edu red rock crab - note black tipped claws Plate Watch Monitoring Program . -
Draft Genome of the Peruvian Scallop Argopecten Purpuratus
GigaScience, 7, 2018, 1–6 doi: 10.1093/gigascience/giy031 Advance Access Publication Date: 2 April 2018 Data Note DATA NOTE Draft genome of the Peruvian scallop Argopecten Downloaded from https://academic.oup.com/gigascience/article/7/4/giy031/4958978 by guest on 29 September 2021 purpuratus Chao Li1, Xiao Liu2,BoLiu1, Bin Ma3, Fengqiao Liu1, Guilong Liu1, Qiong Shi4 and Chunde Wang 1,* 1Marine Science and Engineering College, Qingdao Agricultural University, Qingdao 266109, China, 2Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China, 3Qingdao Oceanwide BioTech Co., Ltd., Qingdao 266101, China and 4Shenzhen Key Lab of Marine Genomics, Guangdong Provincial Key Lab of Molecular Breeding in Marine Economic Animals, BGI Academy of Marine Sciences, BGI Marine, BGI, Shenzhen 518083, China *Correspondence address. Chunde Wang, Marine Science and Engineering College, Qingdao Agricultural University, Qingdao 266109, China. Tel: +8613589227997; E-mail: [email protected] http://orcid.org/0000-0002-6931-7394 Abstract Background: The Peruvian scallop, Argopecten purpuratus, is mainly cultured in southern Chile and Peru was introduced into China in the last century. Unlike other Argopecten scallops, the Peruvian scallop normally has a long life span of up to 7 to 10 years. Therefore, researchers have been using it to develop hybrid vigor. Here, we performed whole genome sequencing, assembly, and gene annotation of the Peruvian scallop, with an important aim to develop genomic resources for genetic breeding in scallops. Findings: A total of 463.19-Gb raw DNA reads were sequenced. A draft genome assembly of 724.78 Mb was generated (accounting for 81.87% of the estimated genome size of 885.29 Mb), with a contig N50 size of 80.11 kb and a scaffold N50 size of 1.02 Mb. -
Open Ocean Intake Effects Study
City of Santa Cruz Water Department & Soquel Creek Water District scwd2 Desalination Program Open Ocean Intake Effects Study December 2010 Submitted to: Ms. Heidi Luckenbach City of Santa Cruz 212 Locust Street Santa Cruz, CA 95060 Prepared by: Environmental ESLO2010-017.1 [Blank Page] ACKNOWLEDGEMENTS Tenera Environmental wishes to acknowledge the valuable contributions of the Santa Cruz Water Department, Soquel Creek Water District, and scwd² Task Force in conducting the Open Ocean Intake Effects Study. Specifically, Tenera would like to acknowledge the efforts of: City of Santa Cruz Water Department Soquel Creek Water District Bill Kocher, Director Laura Brown, General Manager Linette Almond, Engineering Manager Melanie Mow Schumacher, Public Information Heidi R. Luckenbach, Program Coordinator Coordinator Leah Van Der Maaten, Associate Engineer Catherine Borrowman, Professional and Technical scwd² Task Force Assistant Ryan Coonerty Todd Reynolds, Kennedy/Jenks and scwd² Bruce Daniels Technical Advisor Bruce Jaffe Dan Kriege Thomas LaHue Don Lane Cynthia Mathews Mike Rotkin Ed Porter Tenera’s project team included the following members: David L. Mayer, Ph.D., Tenera Environmental President and Principal Scientist John Steinbeck, Tenera Environmental Vice President and Principal Scientist Carol Raifsnider, Tenera Environmental Director of Operations and Principal Scientist Technical review and advice was provided by: Pete Raimondi, Ph.D., UCSC, Professor of Ecology and Evolutionary Biology in the Earth and Marine Sciences Dept. Gregor -
Omnibus Essential Fish Habitat (Efh) Amendment 2 Draft Environmental Impact Statement
New England Fishery Management Council 50 WATER STREET | NEWBURYPORT, MASSACHUSETTS 01950 | PHONE 978 465 0492 | FAX 978 465 3116 E.F. “Terry” Stockwell III, Chairman | Thomas A. Nies, Executive Director OMNIBUS ESSENTIAL FISH HABITAT (EFH) AMENDMENT 2 DRAFT ENVIRONMENTAL IMPACT STATEMENT Appendix D: The Swept Area Seabed Impact (SASI) approach: a tool for analyzing the effects of fishing on Essential Fish Habitat Appendix D: The Swept Area Seabed Impact Approach This document was prepared by the following members of the NEFMC Habitat Plan Development team, with feedback from the NEFMC Habitat Oversight Committee, NEFMC Habitat Advisory Panel, and interested members of the public. Michelle Bachman, NEFMC staff Peter Auster, University of Connecticut Chad Demarest, NOAA/Northeast Fisheries Science Center Steve Eayrs, Gulf of Maine Research Institute Kathyrn Ford, Massachusetts Division of Marine Fisheries Jon Grabowski, Gulf of Maine Research Institute Brad Harris, University of Massachusetts School of Marine Science and Technology Tom Hoff, Mid-Atlantic Fishery Management Council Mark Lazzari, Maine Department of Marine Resources Vincent Malkoski, Massachusetts Division of Marine Fisheries Dave Packer, NOAA/ Northeast Fisheries Science Center David Stevenson, NOAA/Northeast Regional Office Page Valentine, U.S. Geological Survey January 2011 Page 2 of 257 Appendix D: The Swept Area Seabed Impact Approach Table of Contents 1.0 OVERVIEW OF THE SWEPT AREA SEABED IMPACT MODEL ........... 13 2.0 DEFINING HABITAT ...................................................................................... -
Harbor Seal Species Profile Encyclopedia of Puget Sound June 9, 2014
(Photograph by G. E. Davis) Harbor seal species profile Encyclopedia of Puget Sound June 9, 2014 Jacqlynn C. Zier and Joseph K. Gaydos* SeaDoc Society / UC Davis’ Karen C. Drayer Wildlife Health Center Orcas Island Office 942 Deer Harbor Road, Eastsound, WA 98245 *Corresponding author [email protected] Table of Contents Introduction ............................................................................................................. 3 Distribution .............................................................................................................. 3 Global .............................................................................................................................................................................. 3 Local ................................................................................................................................................................................ 3 1 Populations .............................................................................................................. 4 Genetic diversity ........................................................................................................................................................ 4 Population size ........................................................................................................................................................... 5 Longevity and survival .......................................................................................................................................... -
1 Metagenetic Analysis of 2018 and 2019 Plankton Samples from Prince
Metagenetic Analysis of 2018 and 2019 Plankton Samples from Prince William Sound, Alaska. Report to Prince William Sound Regional Citizens’ Advisory Council (PWSRCAC) From Molecular Ecology Laboratory Moss Landing Marine Laboratory Dr. Jonathan Geller Melinda Wheelock Martin Guo Any opinions expressed in this PWSRCAC-commissioned report are not necessarily those of PWSRCAC. April 13, 2020 ABSTRACT This report describes the methods and findings of the metagenetic analysis of plankton samples from the waters of Prince William Sound (PWS), Alaska, taken in May of 2018 and 2019. The study was done to identify zooplankton, in particular the larvae of benthic non-indigenous species (NIS). Plankton samples, collected by the Prince William Sound Science Center (PWSSC), were analyzed by the Molecular Ecology Laboratory at the Moss Landing Marine Laboratories. The samples were taken from five stations in Port Valdez and nearby in PWS. DNA was extracted from bulk plankton and a portion of the mitochondrial Cytochrome c oxidase subunit 1 gene (the most commonly used DNA barcode for animals) was amplified by polymerase chain reaction (PCR). Products of PCR were sequenced using Illumina reagents and MiSeq instrument. In 2018, 257 operational taxonomic units (OTU; an approximation of biological species) were found and 60 were identified to species. In 2019, 523 OTU were found and 126 were identified to species. Most OTU had no reference sequence and therefore could not be identified. Most identified species were crustaceans and mollusks, and none were non-native. Certain species typical of fouling communities, such as Porifera (sponges) and Bryozoa (moss animals) were scarce. Larvae of many species in these phyla are poorly dispersing, such that they will be found in abundance only in close proximity to adult populations.