Applied Ecology and Environmental Research (2015)
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Anchialine Cave Biology in the Era of Speleogenomics Jorge L
International Journal of Speleology 45 (2) 149-170 Tampa, FL (USA) May 2016 Available online at scholarcommons.usf.edu/ijs International Journal of Speleology Off icial Journal of Union Internationale de Spéléologie Life in the Underworld: Anchialine cave biology in the era of speleogenomics Jorge L. Pérez-Moreno1*, Thomas M. Iliffe2, and Heather D. Bracken-Grissom1 1Department of Biological Sciences, Florida International University, Biscayne Bay Campus, North Miami FL 33181, USA 2Department of Marine Biology, Texas A&M University at Galveston, Galveston, TX 77553, USA Abstract: Anchialine caves contain haline bodies of water with underground connections to the ocean and limited exposure to open air. Despite being found on islands and peninsular coastlines around the world, the isolation of anchialine systems has facilitated the evolution of high levels of endemism among their inhabitants. The unique characteristics of anchialine caves and of their predominantly crustacean biodiversity nominate them as particularly interesting study subjects for evolutionary biology. However, there is presently a distinct scarcity of modern molecular methods being employed in the study of anchialine cave ecosystems. The use of current and emerging molecular techniques, e.g., next-generation sequencing (NGS), bestows an exceptional opportunity to answer a variety of long-standing questions pertaining to the realms of speciation, biogeography, population genetics, and evolution, as well as the emergence of extraordinary morphological and physiological adaptations to these unique environments. The integration of NGS methodologies with traditional taxonomic and ecological methods will help elucidate the unique characteristics and evolutionary history of anchialine cave fauna, and thus the significance of their conservation in face of current and future anthropogenic threats. -
Balanus Glandula Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia
Phylum: Arthropoda, Crustacea Balanus glandula Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia Order: Thoracica, Sessilia, Balanomorpha Acorn barnacle Family: Balanoidea, Balanidae, Balaninae Description (the plate overlapping plate edges) and radii Size: Up to 3 cm in diameter, but usually (the plate edge marked off from the parietes less than 1.5 cm (Ricketts and Calvin 1971; by a definite change in direction of growth Kozloff 1993). lines) (Fig. 3b) (Newman 2007). The plates Color: Shell usually white, often irregular themselves include the carina, the carinola- and color varies with state of erosion. Cirri teral plates and the compound rostrum (Fig. are black and white (see Plate 11, Kozloff 3). 1993). Opercular Valves: Valves consist of General Morphology: Members of the Cirri- two pairs of movable plates inside the wall, pedia, or barnacles, can be recognized by which close the aperture: the tergum and the their feathery thoracic limbs (called cirri) that scutum (Figs. 3a, 4, 5). are used for feeding. There are six pairs of Scuta: The scuta have pits on cirri in B. glandula (Fig. 1). Sessile barna- either side of a short adductor ridge (Fig. 5), cles are surrounded by a shell that is com- fine growth ridges, and a prominent articular posed of a flat basis attached to the sub- ridge. stratum, a wall formed by several articulated Terga: The terga are the upper, plates (six in Balanus species, Fig. 3) and smaller plate pair and each tergum has a movable opercular valves including terga short spur at its base (Fig. 4), deep crests for and scuta (Newman 2007) (Figs. -
Molecular Species Delimitation and Biogeography of Canadian Marine Planktonic Crustaceans
Molecular Species Delimitation and Biogeography of Canadian Marine Planktonic Crustaceans by Robert George Young A Thesis presented to The University of Guelph In partial fulfilment of requirements for the degree of Doctor of Philosophy in Integrative Biology Guelph, Ontario, Canada © Robert George Young, March, 2016 ABSTRACT MOLECULAR SPECIES DELIMITATION AND BIOGEOGRAPHY OF CANADIAN MARINE PLANKTONIC CRUSTACEANS Robert George Young Advisors: University of Guelph, 2016 Dr. Sarah Adamowicz Dr. Cathryn Abbott Zooplankton are a major component of the marine environment in both diversity and biomass and are a crucial source of nutrients for organisms at higher trophic levels. Unfortunately, marine zooplankton biodiversity is not well known because of difficult morphological identifications and lack of taxonomic experts for many groups. In addition, the large taxonomic diversity present in plankton and low sampling coverage pose challenges in obtaining a better understanding of true zooplankton diversity. Molecular identification tools, like DNA barcoding, have been successfully used to identify marine planktonic specimens to a species. However, the behaviour of methods for specimen identification and species delimitation remain untested for taxonomically diverse and widely-distributed marine zooplanktonic groups. Using Canadian marine planktonic crustacean collections, I generated a multi-gene data set including COI-5P and 18S-V4 molecular markers of morphologically-identified Copepoda and Thecostraca (Multicrustacea: Hexanauplia) species. I used this data set to assess generalities in the genetic divergence patterns and to determine if a barcode gap exists separating interspecific and intraspecific molecular divergences, which can reliably delimit specimens into species. I then used this information to evaluate the North Pacific, Arctic, and North Atlantic biogeography of marine Calanoida (Hexanauplia: Copepoda) plankton. -
Rissoides Desmaresti INPN
1 La squille de Desmarest Rissoides desmaresti (Risso, 1816) Citation de cette fiche : Noël P., 2016. La squille de Desmarest Rissoides desmaresti (Risso, 1816). in Muséum national d'Histoire naturelle [Ed.], 5 décembre 2016. Inventaire national du Patrimoine naturel, pp. 1-10, site web http://inpn.mnhn.fr Contact de l'auteur : Pierre Noël, SPN et DMPA, Muséum national d'Histoire naturelle, 43 rue Buffon (CP 48), 75005 Paris ; e-mail [email protected] Résumé La squille de Desmarest est de taille moyenne, elle peut atteindre 10 cm de long. Son corps est très allongé, aplati. L'œil est très mobile. La griffe de sa patte ravisseuse porte 5 dents, dent apicale comprise. Le telson a une carène médiane bien marquée ; il est très épineux. Les mâles sont beige moucheté, et les femelles ont le centre du corps rose lorsqu'elles sont en vitellogenèse. La femelle tient ses œufs devant la bouche pendant l'incubation. Il y a neuf stades larvaires ; les larves sont planctoniques. La squille vit dans un terrier ayant une forme en "U". C'est un prédateur de petite faune vagile. Cette squille se rencontre dans l'Atlantique européen et dans toute la Méditerranée. Elle fréquente les herbiers de phanérogames marines et divers sédiments sableux jusqu'à une centaine de mètres de profondeur. Figure 1. Vue dorsale d'un spécimen catalan ; 4 mars 1975, Figure 2. Carte de distribution en France -7m, herbier du Racou (66). Photo © Jean Lecomte. métropolitaine. © P. Noël INPN-MNHN 2016. Classification : Phylum Arthropoda Latreille, 1829 > Sub-phylum Crustacea Brünnich, 1772 > Super-classe Multicrustacea Regier, Shultz, Zwick, Hussey, Ball, Wetzer, Martin & Cunningham, 2010 > Classe Malacostraca Latreille, 1802 > Sous-classe Eumalacostraca Grobben, 1892 > Super- ordre Hoplocarida Calman, 1904 > Ordre Stomatopoda Latreille, 1817 > Sous-ordre Unipeltata Latreille, 1825 > Super-famille Squilloidea Latreille, 1803 > Famille Squillidae Latreille, 1803 > Genre Rissoides Manning et Lewinsohn, 1982. -
Fish Species Inhabiting Lower Napa River and San Pablo Bay
APPENDIX E-5 Technical Memo: Fish Species Inhabiting Lower Napa River and San Pablo Bay Technical Memorandum Fish Species Inhabiting the lower Napa River and San Pablo Bay Prepared by: J. A. Johnson, T. Linder, D. George, and R. Isquith, Applied Marine Sciences, Inc. June 25, 2014 Pelagic (Open Water) Fish Community Seventeen species of pelagic fish have been documented inhabiting the deep and shallow water areas of San Pablo Bay and the Carquinez Strait adjacent to the Napa River mouth into San Pablo Bay (Table 1,). Six of these species account for over 96 percent of the total abundance, with the dominant species, Northern anchovy (Engraulis mordax), comprising 76.5 percent of the fish inhabiting the pelagic community. Pacific herring (Clupea pallasii) is the second most common fish species inhabiting the Napa River mouth, accounting for 14.4 percent of the total abundance. The remaining dominant fish species include American shad (Alosa sapidissima), Longfin smelt (Spirinchus thaleichthys), Striped bass (Morone saxatilis) and Bay goby (Lepidogobius lepidus) which together account for 5.3 percent of the total abundance inhabiting the water column. Additional pelagic species that are present in low abundance include Chinook salmon (Oncorhynchus tshawytscha), Plainfin midshipman (Porichthys notatus), Jacksmelt (Atherinopsis californiensis), Splittail (Pogonichthys macrolepidotus), Threadfin shad (Dorosoma petenense), Delta smelt (Hypomesus transpacificus), Threespine stickleback (Gasterosteus aculeatus), Pacific staghorn sculpin (Leptocottus armatus), English sole (Parophrys vetulus) and Starry flounder (Platichthys stellatus). Important managed, protected, or special status pelagic zone species that are found in the study area, either seasonally or year-round, include Northern anchovy, Pacific herring, longfin smelt, delta smelt, steelhead, and Chinook salmon (AMS 2014, IEP 2010-2012, USFWS 2013, CDFW 2014). -
4 National Approaches Used to Describe and Delineate Marine Ecosystems and Subregions in the North Pacific
Section 4 National Approaches 4 National Approaches Used to Describe and Delineate Marine Ecosystems and Subregions in the North Pacific Chris Harvey, Glen Jamieson, Patricia Livingston, Chang-Ik Zhang, Elena Dulepova, David Fluharty, Xianshi Jin, Tatsu Kishida, Jae Bong Lee, Mitsutaku Makino, R. Ian Perry, Vladimir Radchenko, Qisheng Tang, Inja Yeon and Elizabeth Fulton 4.1 Introduction With marine ecosystems facing increasing and often many of the large marine ecosystems (LMEs) in the unsustainable human demands, the need for PICES region (e.g., Sherman and Tang, 1999). Such comprehensive, integrated cross-sectoral resource spatio-temporal dynamics will likely be altered by management becomes ever clearer (Duda and global climate change, though in different ways in Sherman, 2002). Many hold that the most responsible different areas of the North Pacific. Second, marine strategy is ecosystem-based management (EBM), ecosystems typically extend hundreds of kilometers wherein factors such as ecological interactions, offshore and often beyond the exclusive economic socio-economic forces and human impacts are zone (EEZ) of a country. In many cases, the EEZs of explicit components of monitoring, assessment and multiple nations occupy the same ecosystem, often policy. While EBM has been variously defined by adjoining along extensive international borders. This many authors, some concepts are pervasive across all fact can limit the ability of a country to monitor the definitions: it is spatially discrete; it is adaptive; it full spatial extent of the ecosystem beyond its own incorporates dynamics, interactions and uncertainty territory, which in turn limits understanding of overall associated with physical, chemical and biological ecosystem function, structure and change. -
Biology, Stock Status and Management Summaries for Selected Fish Species in South-Western Australia
Fisheries Research Report No. 242, 2013 Biology, stock status and management summaries for selected fish species in south-western Australia Claire B. Smallwood, S. Alex Hesp and Lynnath E. Beckley Fisheries Research Division Western Australian Fisheries and Marine Research Laboratories PO Box 20 NORTH BEACH, Western Australia 6920 Correct citation: Smallwood, C. B.; Hesp, S. A.; and Beckley, L. E. 2013. Biology, stock status and management summaries for selected fish species in south-western Australia. Fisheries Research Report No. 242. Department of Fisheries, Western Australia. 180pp. Disclaimer The views and opinions expressed in this publication are those of the authors and do not necessarily reflect those of the Department of Fisheries Western Australia. While reasonable efforts have been made to ensure that the contents of this publication are factually correct, the Department of Fisheries Western Australia does not accept responsibility for the accuracy or completeness of the contents, and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of, or reliance on, the contents of this publication. Fish illustrations Illustrations © R. Swainston / www.anima.net.au We dedicate this guide to the memory of our friend and colleague, Ben Chuwen Department of Fisheries 3rd floor SGIO Atrium 168 – 170 St Georges Terrace PERTH WA 6000 Telephone: (08) 9482 7333 Facsimile: (08) 9482 7389 Website: www.fish.wa.gov.au ABN: 55 689 794 771 Published by Department of Fisheries, Perth, Western Australia. Fisheries Research Report No. 242, March 2013. ISSN: 1035 - 4549 ISBN: 978-1-921845-56-7 ii Fisheries Research Report No.242, 2013 Contents ACKNOWLEDGEMENTS ............................................................................................... -
Elaborating a Common Language
Elaborating a Common Language WP1 – Milestone 2, a glossary Contents Introduction ....................................................................................................................... 2 1. Why a Glossary? ................................................................................................................... 2 2. Methodology ........................................................................................................................ 2 3. Glossary structure ................................................................................................................ 3 GLOSSARY .......................................................................................................................... 4 Baseline ........................................................................................................................................... 4 Biodiversity ...................................................................................................................................... 4 Coastal zone .................................................................................................................................... 4 Connectivity .................................................................................................................................... 4 Continental Shelf ............................................................................................................................. 4 Ecosystem ...................................................................................................................................... -
Fossil Calibrations for the Arthropod Tree of Life
bioRxiv preprint doi: https://doi.org/10.1101/044859; this version posted June 10, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. FOSSIL CALIBRATIONS FOR THE ARTHROPOD TREE OF LIFE AUTHORS Joanna M. Wolfe1*, Allison C. Daley2,3, David A. Legg3, Gregory D. Edgecombe4 1 Department of Earth, Atmospheric & Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA 2 Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK 3 Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PZ, UK 4 Department of Earth Sciences, The Natural History Museum, Cromwell Road, London SW7 5BD, UK *Corresponding author: [email protected] ABSTRACT Fossil age data and molecular sequences are increasingly combined to establish a timescale for the Tree of Life. Arthropods, as the most species-rich and morphologically disparate animal phylum, have received substantial attention, particularly with regard to questions such as the timing of habitat shifts (e.g. terrestrialisation), genome evolution (e.g. gene family duplication and functional evolution), origins of novel characters and behaviours (e.g. wings and flight, venom, silk), biogeography, rate of diversification (e.g. Cambrian explosion, insect coevolution with angiosperms, evolution of crab body plans), and the evolution of arthropod microbiomes. We present herein a series of rigorously vetted calibration fossils for arthropod evolutionary history, taking into account recently published guidelines for best practice in fossil calibration. -
Balanus Nubilus Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia
Phylum: Arthropoda, Crustacea Balanus nubilus Class: Multicrustacea, Hexanauplia, Thecostraca, Cirripedia Order: Thoracica, Sessilia, Balanomorpha The giant barnacle Family: Balanoidea, Balanidae, Balaninae Description Plates: Calcareous, nearly coni- Size: Largest barnacle on the Pacific coast, cal and columnar. Six in family Balanidae. and probably in the world (Ricketts and Cal- Each plate is composed of parietes (exposed vin 1971), with individuals up to 100 mm in triangular part), alae (the plate overlapping diameter, and nearly as tall (Cornwall 1951). plate edges) and radii (the plate edge marked The illustrated specimen (from Coos Bay) is off from the parietes by a definite change in 90 mm in diameter. direction of growth lines) (Newman 2007). Color: Shell dirty white with interior of scuta The plates themselves include the carina, the and terga (see Plate 18, Kozloff 1993) buff carinolateral plates and the compound ros- and tergal beak usually purple tipped trum (see Fig. 3, Balanus glandula, this (Cornwall 1951). guide). Internal surfaces with fine horizontal General Morphology: Members of the Cirri- ribbing above and smooth near base, particu- pedia, or barnacles, can be recognized by larly in older specimens (Pilsbry 1916). Radii their feathery thoracic limbs (called cirri) that rather narrow (Darwin 1854). are used for feeding. There are six pairs of Opercular Valves: Thick and yellow- cirri in B. nubilus. Sessile barnacles are sur- ish, buff on interior but never white. Tergal rounded by a shell that is composed of a flat beaks project above orifice edge (Cornwall basis attached to the substratum, a wall 1977). Tergal and scutal adductor and de- formed by several articulated plates (six in pressor muscles are very thick in B. -
Seasonal Composition and Abundance of Juvenile And
SEASONAL COMPOSITION AND ABUNDANCE OF JUVENILE AND ADULT MARINE FINFISH AND CRAB SPECIES IN THE NEARSHORE ZONE OF KODIAK ISLAND’S EASTSIDE DURING APRIL 1978 THROUGH MARCH 1979 by James E. Blackburn and Peter B. Jackson Alaska Department of Fish and Game Final Report Outer Continental Shelf Environmental Assessment Program Research Unit 552 April 1982 377” TABLE OF CONTENTS E%?!2 List of Figures. 381 List of Tables . 385 List of Appendix Tables. 387 Summary of Objectives and Results with Respect to OCS Oil and Gas Development . 391 Introduction . 392 General Nature and Scope of Study . 392 Specific Objectives . 392 Relevance to Problems of Petroleum Development. 392 Acknowledgements. 392 Current State of Knowledge . 393 King Crab . 394 Tanner Crab . 394 Dungeness Crab. 397 Shrimp. 397 Scallops. 399 Salmon. 399 Herring . 411 Halibut . 412 Bottomfish. 413 Study Area . 413 Sources, Methods and Rationale of Data Collection. 419 Beach Seine . 420 Gill Net. 421 Trammel Net . 421 Tow Net . 421 Try Net . 421 Otter Trawl . 422 Sample Handling . 422 Stages of Maturity. 422 Sample Analysis . 423 Area Comparisons . 424 Diversity. 424 Species Association. 425 Data Limitations. 425 Results. 426 Relative Abundance. 430 Seasonality by Habitat. 437 Nearshore Habitat. 437 Pelagic Habitat. 443 Demersal Habitat . 443 Area Comparisons. 449 Species Associations . 463 Diversity . 465 Features of Distribution, Abundance, Migration, Growth and Reproduction of Prominent Taxa . 473 King Crab.. 473 Tanner Crab. 473 Pacific Herring. 473 Pink Salmon. 473 ChumSalnion. 482 CohoSalmon. 482 DollyVarden. 482 Capelin. 486 Pacific Cod. 486 PacificTomcod. ---- . 489 WalleyePollock. 489 Rockfish. 489 RockGreenling. 493 MaskedGreenling. 493 Whitespotted Greenling. 495 Seblefish. -
The Genome of the Crustacean Parhyale Hawaiensis, a Model For
TOOLS AND RESOURCES The genome of the crustacean Parhyale hawaiensis, a model for animal development, regeneration, immunity and lignocellulose digestion Damian Kao1†, Alvina G Lai1†, Evangelia Stamataki2†, Silvana Rosic3,4, Nikolaos Konstantinides5, Erin Jarvis6, Alessia Di Donfrancesco1, Natalia Pouchkina-Stancheva1, Marie Se´ mon 5, Marco Grillo5, Heather Bruce6, Suyash Kumar2, Igor Siwanowicz2, Andy Le2, Andrew Lemire2, Michael B Eisen7, Cassandra Extavour8, William E Browne9, Carsten Wolff10, Michalis Averof5, Nipam H Patel6, Peter Sarkies3,4, Anastasios Pavlopoulos2*, Aziz Aboobaker1* 1Department of Zoology, University of Oxford, Oxford, United Kingdom; 2Janelia Research Campus, Howard Hughes Medical Institute, Virginia, United States; 3MRC Clinical Sciences Centre, Imperial College London, London, United Kingdom; 4Clinical Sciences, Imperial College London, London, United Kingdom; 5Institut de Ge´ nomique Fonctionnelle de Lyon, Centre National de la Recherche Scientifique (CNRS) and E´ cole Normale Supe´ rieure de Lyon, Lyon, France; 6Department of Molecular and Cell Biology, University of California, Berkeley, United States; 7Molecular and Cell Biology, Howard Hughes Medical Institute, University of California, Berkeley, United States; 8Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, United States; 9Department of *For correspondence: Invertebrate Zoology, Smithsonian National Museum of Natural History, [email protected] 10 (AP); [email protected]. Washington, United States;