A Very Large Spawning Aggregation of a Deep-Sea Eel: Magnitude and Status
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Hikurangi Plateau: Crustal Structure, Rifted Formation, and Gondwana Subduction History
Article Geochemistry 3 Volume 9, Number 7 Geophysics 3 July 2008 Q07004, doi:10.1029/2007GC001855 GeosystemsG G ISSN: 1525-2027 AN ELECTRONIC JOURNAL OF THE EARTH SCIENCES Published by AGU and the Geochemical Society Click Here for Full Article Hikurangi Plateau: Crustal structure, rifted formation, and Gondwana subduction history Bryan Davy Institute of Geological and Nuclear Sciences, P.O. Box 30368, Lower Hutt, New Zealand ([email protected]) Kaj Hoernle IFM-GEOMAR, Wischhofstraße 1-3, D-24148 Kiel, Germany Reinhard Werner Tethys Geoconsulting GmbH, Wischhofstraße 1-3, D-24148 Kiel, Germany [1] Seismic reflection profiles across the Hikurangi Plateau Large Igneous Province and adjacent margins reveal the faulted volcanic basement and overlying Mesozoic-Cenozoic sedimentary units as well as the structure of the paleoconvergent Gondwana margin at the southern plateau limit. The Hikurangi Plateau crust can be traced 50–100 km southward beneath the Chatham Rise where subduction cessation timing and geometry are interpreted to be variable along the margin. A model fit of the Hikurangi Plateau back against the Manihiki Plateau aligns the Manihiki Scarp with the eastern margin of the Rekohu Embayment. Extensional and rotated block faults which formed during the breakup of the combined Manihiki- Hikurangi plateau are interpreted in seismic sections of the Hikurangi Plateau basement. Guyots and ridge- like seamounts which are widely scattered across the Hikurangi Plateau are interpreted to have formed at 99–89 Ma immediately following Hikurangi Plateau jamming of the Gondwana convergent margin at 100 Ma. Volcanism from this period cannot be separately resolved in the seismic reflection data from basement volcanism; hence seamount formation during Manihiki-Hikurangi Plateau emplacement and breakup (125–120 Ma) cannot be ruled out. -
Hoplostethus Atlanticus Fisheries Relating to the South Pacific Regional Fishery Management Organisation
SP-07-SWG-INF-09 Chile 13 May 2009 Information describing orange roughy Hoplostethus atlanticus fisheries relating to the South Pacific Regional Fishery Management Organisation WORKING DRAFT 04 MAY 2007 1. Overview ................................................................................................................ 2 2. Taxonomy .............................................................................................................. 3 2.1 Phylum ............................................................................................................. 3 2.2 Class ................................................................................................................. 3 2.3 Order ................................................................................................................ 3 2.4 Family .............................................................................................................. 3 2.5 Genus and species ............................................................................................ 3 2.6 Scientific synonyms ......................................................................................... 3 2.7 Common names ............................................................................................... 3 2.8 Molecular (DNA or biochemical) bar coding .................................................. 3 3. Species characteristics ........................................................................................... 4 3.1 Global distribution and depth range -
Crappie and Crappie Fishing
Crappie & Crappie Fishing Crappie are among the most popular sport fishes in Texas. They are known by various names including white perch, sac-a-lait, calico bass, and paper-mouth. Two species are found in Texas, the white crappie (Pomoxis annularis) and black crappie (P. nigromaculatus). Black crap pie have irregular dark speck les and blotches on their sides. On white crappie, the dark markings consist of regularly arranged vertical bars. When in doubt, count the number of sharp dorsal spines at the front of a crappie’s dorsal fin. Black crappie have seven or eight spines while white crappie Young crappie feed on microscopic crustaceans called have five or six. During the spawning season, males of zooplankton. Juveniles and adults feed primarily on both species develop dark markings over most of the small threadfin and gizzard shad and insect larvae, es body, causing many anglers to misidentify male white pecially mayflies. Their diet also includes minnows, crappie as black crappie. silversides, other crappie and any other fish small enough to swallow. Black crappie are more numerous in the clear, acidic to slightly alkaline waters of East Texas. White crappie are found state In lakes with low bass populations, crappie often wide. Fish of both species may live up to eight years and overpopulate and become stunted. For crappie to reach become sexually mature at one to two years. Crappie belong larger sizes, populations must experience high total mor to the same family as the sunfishes and black basses; like tality to keep their numbers within the carrying capacity their cousins, crappie are nest builders. -
Fish Spawning Aggregations
Fish Spawning Aggregations a focal point of fisheries management and marine conservation in Mexico Photo: Octavio Aburto Authorship Brad Erisman – Coastal Fisheries Research Program, University of Texas Marine Science Institute, 750 Channel View Drive, Port Aransas, TX 78373 William Heyman – LGL Ecological Research Associates, Inc., 4103 S. Texas Avenue, Bryan TX 77802 Stuart Fulton – Comunidad y Biodiversidad, Isla del Peruano 215, Lomas de Miramar, Guaymas, Sonora, Mexico Timothy Rowell – Gulf of California Marine Program, Scripps Institution of Oceanography, 9500 Gilman Drive, La Jolla, CA 92037 Illustrations – Larry Allen and Madeline Wukusick Graphic Design – Madeline Wukusick | www.communique.design Photography – Octavio Aburto, Richard Barnden, Douglas David Seifert, Walt Stearns, Cristina Limonta, Alfredo Barroso Citation – Erisman, B., W.D. Heyman, S. Fulton, and T.Rowell 2018. Fish spawning aggregations: a focal point of fisheries management and marine conservation in Mexico. Gulf of California Marine Program, La Jolla, CA. 24 p. Email Contact: Brad Erisman, [email protected] Fish Spawning Aggregations // 2 Contents > Introduction .................................................................................................................................................................. 4 > What are fish spawning aggregations (FSAs)? ............................................................................................................ 5 > What kinds of fishes form FSAs? ................................................................................................................................ -
Early Stages of Fishes in the Western North Atlantic Ocean Volume
ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation. -
Inside:The Pleistocene Cooling Built
THE PLEISTOCENE COOLING BUILT CHALLENGER MOUND, A DEEP-WATER CORAL MOUND IN THE NE ATLANTIC: INSIDE: SYNTHESIS FROM IODP EXPEDITION 307 PLUS: COUNCIL’S COMMENTS 2011 SPRING SEPM SECTION MEETINGS Special Publication #95 Cenozoic Carbonate Systems of Australasia Edited by: William A. Morgan, Annette D. George, Paul M. (Mitch) Harris, Julie A. Kupecz, and J.F. (Rick) Sarg The Cenozoic carbonate systems of Australasia are the product of a diverse assortment of depositional and post- depositional processes, reflecting the interplay of eustasy, tectonics (both plate and local scale), climate, and evolutionary trends that influenced their initiation and development. These systems, which comprise both land- attached and isolated platforms, were initiated in a wide variety of tectonic settings (including rift, passive margin, and arc-related) and under warm and cool-water conditions where, locally, siliciclastic input affected their development. The lithofacies, biofacies, growth morphology, diagenesis, and hydrocarbon reservoir potential of these systems are products of these varying influences. The studies reported in this volume range from syntheses of tectonic and depositional factors influencing carbonate deposition and controls on reservoir formation and petroleum system development, to local studies from the South China Sea, Indonesia, Kalimantan, Malaysia, the Marion Plateau, the Philippines, Western Australia, and New Caledonia that incorporate outcrop and subsurface data, including 3-D seismic imaging of carbonate platforms and facies, to understand the interplay of factors affecting the development of these systems under widely differing circumstances. This volume will be of importance to geoscientists interested in the variability of Cenozoic carbonate systems and the factors that controlled their formation, and to those wanting to understand the range of potential hydrocarbon reservoirs discovered in these carbonates and the events that led to favorable reservoir and trap development. -
From Marine Fishes Off New Caledonia, with a Key to Species of Cucullanus from Anguilliformes
Parasite 25, 51 (2018) Ó F. Moravec and J.-L. Justine, published by EDP Sciences, 2018 https://doi.org/10.1051/parasite/2018050 urn:lsid:zoobank.org:pub:FC92E481-4FF7-4DD8-B7C9-9F192F373D2E Available online at: www.parasite-journal.org RESEARCH ARTICLE OPEN ACCESS Three new species of Cucullanus (Nematoda: Cucullanidae) from marine fishes off New Caledonia, with a key to species of Cucullanus from Anguilliformes František Moravec1 and Jean-Lou Justine2,* 1 Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, Branišovská 31, 370 05 Cˇ eské Budeˇjovice, Czech Republic 2 Institut Systématique, Évolution, Biodiversité (ISYEB), Muséum national d’Histoire naturelle, CNRS, Sorbonne Université, EPHE, CP 51, 57 rue Cuvier, 75005 Paris, France Received 16 July 2018, Accepted 8 August 2018, Published online 20 September 2018 Abstract – Based on light and scanning electron microscopical studies of nematode specimens from the digestive tract of some rarely collected anguilliform and perciform fishes off New Caledonia, three new species of Cucullanus Müller, 1777 (Cucullanidae) are described: C. austropacificus n. sp. from the longfin African conger Conger cinereus (Congridae), C. gymnothoracis n. sp. from the lipspot moray Gymnothorax chilospilus (Muraenidae), and C. incog- nitus n. sp. from the seabream Dentex fourmanoiri (Sparidae). Cucullanus austropacificus n. sp. is characterized by the presence of cervical alae, ventral sucker, alate spicules 1.30–1.65 mm long, conspicuous outgrowths of the ante- rior and posterior cloacal lips and by elongate-oval eggs measuring 89–108 · 48–57 lm; C. gymnothoracis n. sp. is similar to the foregoing species, but differs from it in the absence of cervical alae and the posterior cloacal outgrowth, in the shape and size of the anterior cloacal outgrowth and somewhat shorter spicules 1.12 mm long; C. -
Clean &Unclean Meats
Clean & Unclean Meats God expects all who desire to have a relationship with Him to live holy lives (Exodus 19:6; 1 Peter 1:15). The Bible says following God’s instructions regarding the meat we eat is one aspect of living a holy life (Leviticus 11:44-47). Modern research indicates that there are health benets to eating only the meat of animals approved by God and avoiding those He labels as unclean. Here is a summation of the clean (acceptable to eat) and unclean (not acceptable to eat) animals found in Leviticus 11 and Deuteronomy 14. For further explanation, see the LifeHopeandTruth.com article “Clean and Unclean Animals.” BIRDS CLEAN (Eggs of these birds are also clean) Chicken Prairie chicken Dove Ptarmigan Duck Quail Goose Sage grouse (sagehen) Grouse Sparrow (and all other Guinea fowl songbirds; but not those of Partridge the corvid family) Peafowl (peacock) Swan (the KJV translation of “swan” is a mistranslation) Pheasant Teal Pigeon Turkey BIRDS UNCLEAN Leviticus 11:13-19 (Eggs of these birds are also unclean) All birds of prey Cormorant (raptors) including: Crane Buzzard Crow (and all Condor other corvids) Eagle Cuckoo Ostrich Falcon Egret Parrot Kite Flamingo Pelican Hawk Glede Penguin Osprey Grosbeak Plover Owl Gull Raven Vulture Heron Roadrunner Lapwing Stork Other birds including: Loon Swallow Albatross Magpie Swi Bat Martin Water hen Bittern Ossifrage Woodpecker ANIMALS CLEAN Leviticus 11:3; Deuteronomy 14:4-6 (Milk from these animals is also clean) Addax Hart Antelope Hartebeest Beef (meat of domestic cattle) Hirola chews -
Size-Based Responses of Prey to Piscivore Exclusion in a Species-Rich Neotropical River
Ecology, 85(5), 2004,pp. 1311-1320 @ 2004 by the Ecological Society of America SIZE-BASED RESPONSES OF PREY TO PISCIVORE EXCLUSION IN A SPECIES-RICH NEOTROPICAL RIVER CRAIG A. LAYMAN! AND KIRK O. WINEMILLER Section of Ecology and Evolutionary Biology, Department of Wildlife and Fisheries Sciences, 210 Nagle Hall, Texas A&M University, College Station, Texas 77843-2258 USA Abstract. Characteristics used to group species, and thus generalize ecological inter': actions, can aid in constructing predictive models in species-rich food webs. We tested whether size could be used to predict a behavioral response of multiple prey species (n > 50) to exclusion of large-bodied fishes, including seven abundant piscivore species, in a lowland Neotropical river. A randomized block design (n = 6) included three experimental treatments constructed on sandbank habitats: large fish exclusion, cage control (barrier with gaps), and natural reference plot (no barrier). Exclosures prevented passage of all large- bodied fishes, but the mesh size allowed passage of prey fishes. After two weeks, exper- imental areas were sampled once during the day and once at night. Total abundance of prey fishes was not significantly different among treatments, and effects on specie~density were variable. Analyses based on fish size class, however, demonstrated significant size- based effects of large-fish exclusion. Abundance of medium fishes (40-110 mm) in exclu. sion treatments increased significantly relative to controls in day (248%) and night (91 %) samples, and this trend was apparent for many species (n > 13). Species density of medium fishes increased significantly in exclusion treatments. There was evidence of an intraspecific, size-dependent response for the three most common species. -
Southwest Guide: Your Use to Word
BEST CHOICES GOOD ALTERNATIVES AVOID How to Use This Guide Arctic Char (farmed) Clams (US & Canada wild) Bass: Striped (US gillnet, pound net) Bass (US farmed) Cod: Pacific (Canada & US) Basa/Pangasius/Swai Most of our recommendations, Catfish (US) Crab: Southern King (Argentina) Branzino (Mediterranean farmed) including all eco-certifications, Clams (farmed) Lobster: Spiny (US) Cod: Atlantic (gillnet, longline, trawl) aren’t on this guide. Be sure to Cockles Mahi Mahi (Costa Rica, Ecuador, Cod: Pacific (Japan & Russia) Cod: Pacific (AK) Panama & US longlines) Crab (Asia & Russia) check out SeafoodWatch.org Crab: King, Snow & Tanner (AK) Oysters (US wild) Halibut: Atlantic (wild) for the full list. Lobster: Spiny (Belize, Brazil, Lionfish (US) Sablefish/Black Cod (Canada wild) Honduras & Nicaragua) Lobster: Spiny (Mexico) Salmon: Atlantic (BC & ME farmed) Best Choices Mahi Mahi (Peru & Taiwan) Mussels (farmed) Salmon (CA, OR & WA) Octopus Buy first; they’re well managed Oysters (farmed) Shrimp (Canada & US wild, Ecuador, Orange Roughy and caught or farmed responsibly. Rockfish (AK, CA, OR & WA) Honduras & Thailand farmed) Salmon (Canada Atlantic, Chile, Sablefish/Black Cod (AK) Squid (Chile & Peru) Norway & Scotland) Good Alternatives Salmon (New Zealand) Squid: Jumbo (China) Sharks Buy, but be aware there are Scallops (farmed) Swordfish (US, trolls) Shrimp (other imported sources) Seaweed (farmed) Tilapia (Colombia, Honduras Squid (Argentina, China, India, concerns with how they’re Shrimp (US farmed) Indonesia, Mexico & Taiwan) Indonesia, -
Morphology and Significance of the Luminous Organs in Alepocephaloid Fishes
Uiblein, F., Ott, J., Stachowitsch,©Akademie d. Wissenschaften M. (Eds), Wien; 1996: download Deep-sea unter www.biologiezentrum.at and extreme shallow-water habitats: affinities and adaptations. - Biosystematics and Ecology Series 11:151-163. Morphology and significance of the luminous organs in alepocephaloid fishes Y. I. SAZONOV Abstract: Alepocephaloid fishes, or slickheads (two families, Alepocephalidae and Platytroctidae), are deep-sea fishes distributed in all three major oceans at depths of ca. 100-5000 m, usually between ca. 500 and 3000 m. Among about 150 known species, 13 alepocephalid and all (ca. 40) platytroctid species have diverse light organs: 1) postcleithral luminous gland (all platytroctids); it releases a luminescent secredon which presumably startles or blinds predators and allows the fish to escape; 2) relatively large, regulär photophores on the head and ventral parts of the body in the alepocephalid Microphotolepis and in 6 (of 14) platytroctid genera. These organs may serve for countershading and possibly for giving signals to other individuals of the same species; 3) small "simple" or "secondary" photophores covering the whole body and fins in 5 alepocephalid genera, and a few such structures in 1 platytroctid; these organs may be used for Camouflage in the glow of spontaneous bioluminescence; 4) the mental light organ in 2 alepocephalid genera from the abyssal zone (Bathyprion and Mirognathus) may be used as a Iure to attract prey. Introduction Alepocephaloid fishes, or slickheads, comprise two families of isospondyl- ous fishes (Platytroctidae and Alepocephalidae). The group is one of the most diverse among oceanic bathypelagic fishes (about 35 genera with 150 species), and these fishes play a significant role in the communities of meso- and bathypelagic animals. -
Conger Oceanicus
Conger Eel − Conger oceanicus Overall Vulnerability Rank = High Biological Sensitivity = Moderate Climate Exposure = Very High Data Quality = 62% of scores ≥ 2 Expert Data Expert Scores Plots Conger oceanicus Scores Quality (Portion by Category) Low Moderate Stock Status 2.4 0.5 High Other Stressors 2.5 1.2 Very High Population Growth Rate 2.1 0.8 Spawning Cycle 2.9 2.4 Complexity in Reproduction 2.4 1.9 Early Life History Requirements 2.5 1.8 Sensitivity to Ocean Acidification 1.2 1.3 Prey Specialization 1.6 2.1 Habitat Specialization 2.4 3.0 Sensitivity attributes Sensitivity to Temperature 1.6 2.8 Adult Mobility 1.5 1.8 Dispersal & Early Life History 1.3 2.8 Sensitivity Score Moderate Sea Surface Temperature 4.0 3.0 Variability in Sea Surface Temperature 1.0 3.0 Salinity 2.4 3.0 Variability Salinity 1.2 3.0 Air Temperature 4.0 3.0 Variability Air Temperature 1.0 3.0 Precipitation 1.3 3.0 Variability in Precipitation 1.4 3.0 Ocean Acidification 4.0 2.0 Exposure variables Variability in Ocean Acidification 1.0 2.2 Currents 2.2 1.0 Sea Level Rise 2.4 1.5 Exposure Score Very High Overall Vulnerability Rank High Conger Eel (Anguilla oceanica) Overall Climate Vulnerability Rank: High (93% certainty from bootstrap analysis). Climate Exposure: Very High. Three exposure factors contributed to this score: Ocean Surface Temperature (4.0), Ocean Acidification (4.0) and Air Temperature (4.0). Conger Eel are semelparous: spawning in the ocean, developing in marine and estuarine habitats, then feeding growing, and maturing in marine and estuarine habitats.