Commonwealth of Massachusetts Interdepartmental Service Agreement ISAEQE22309702ENV15A

Total Page:16

File Type:pdf, Size:1020Kb

Commonwealth of Massachusetts Interdepartmental Service Agreement ISAEQE22309702ENV15A Commonwealth of Massachusetts Interdepartmental Service Agreement ISAEQE22309702ENV15A Wetlands Monitoring and Assessment Salt Marsh Data Collection and Processing Report 2015-2016 Northeast Basin Group Parker and Ipswich Basins December 30, 2016 Prepared for: Massachusetts Department of Environmental Protection Wetlands Program 1 Winter Street Boston, MA 02108 Prepared by: Massachusetts Office of Coastal Zone Management 251 Causeway Street, Suite 800 Boston, MA 02114 This report describes work performed under an Interagency Service Agreement (ISA) (ISAEQE22309702ENV15A) by the Massachusetts Office of Coastal Zone Management (CZM), for the Massachusetts Department of Environmental Protection (DEP) from 2015-2016. CZM was contracted to collect data on vegetation and macroinvertebrates at twenty salt marsh sites in the DEP Surface Water Monitoring Program’s Northeast Basin Group in 2015—specifically, the Parker and Ipswich basins. Work was extended to 2016 due to unforeseen circumstances (e.g., one key staff member on maternity leave, and another with a knee injury preventing fieldwork). All data were collected following a Quality Assurance Project Plan (QAPP) previously approved by DEP and the U.S. Environmental Protection Agency (EPA). Sampling Design CZM staff selected sites using a stratified random design in coordination with DEP staff. Index of Ecological Integrity (IEI) values from the Conservation Assessment and Prioritization System (CAPS) were averaged for salt marshes within each sub-watershed of the target basins. A random point generator was used to identify over 100 points within the sub-watersheds with the lowest average IEI scores (< 0.5), and 25 points (> 0.8) within those with the highest average IEI values. The random point generator was specified with a 500-meter buffer to allow for geographic variability. Points were manually assessed to ensure that they meet the following sampling criteria, with the goal of identifying 15 sites within the “low IEI” sub-watersheds, and 5 sites within the “high IEI” sub-watersheds (Figure 1). Sampling Criteria The point is within 200 meters of a salt marsh creek (each sampling point will be moved not more than 200 m to the nearest tidal creek suitable for sampling); The creek is suitable for auger and D-Net macroinvertebrate sampling (e.g., channel width is at least 2 m, bank height is at least 1 m, and bank height and/or condition does not compromise safety); The point is not deemed inaccessible due to physical barriers; The point is not deemed inaccessible due to legal barriers (i.e., permission to access private property is granted). Permitting CZM sought and received permission to access and sample vegetation and macroinvertebrates on properties owned by the U.S. Fish and Wildlife Service (USFWS), The Trustees of Reservations (TTOR), Essex County Greenbelt Association, and private commercial or residential landowners (e.g., Perley’s Marina, Rowley). Special Use Permits were required by TTOR and USFWS. Data Collection and Processing Data were collected following the protocols described in the current standard operating procedures document (SOP), Appendix A of the salt marsh assessment QAPP approved by DEP and EPA. The SOP also includes information on the processing of macroinvertebrate specimens, including sorting, identification, and QA/QC testing. 2 Figure 1. Salt marsh site level assessment sites in the North Coastal Basin—specifically the Parker and Ipswich River sub-basins—selected by stratified random sampling design. Fifteen sites were randomly selected within the sub- watersheds with the lowest average IEI scores (< 0.5) for salt marshes. Five sites were randomly selected within the sub-watersheds with the highest average IEI scores > (0.8). Data were entered into spreadsheets with the same formatting used to report CAPS site-level assessment data to UMass for inclusion in the CAPS project database for development of Indices of Biological Integrity (IBIs). Two spreadsheets are included: caps_saltmarsh_vegetation_2015-2016.xlsx and caps_saltmarsh_macroinvertebrates_2015-2016.xlsx. The vegetation spreadsheet includes worksheets containing information on sampling methods, plot records (GPS locations, dates and times of sampling, etc.), vegetation data, nomenclature changes, collector codes, and a database dictionary / metadata record. The macroinvertebrate spreadsheet includes sample records, macroinvertebrate data, collector codes, an updated bench form (master list of taxa recorded since CAPS project inception), and a database dictionary / metadata record. Results Summary Twenty-four vascular plant taxa were recorded along 60 salt marsh transects (three per site), and 65 macroinvertebrate taxa were recorded in 40 dip net samples, 40 auger samples, and 40 quadrat observations (two samples of each type per site). 3 YrPlotID PlotID Phylum Class Subclass Order SubOrder Family Genus Species FinalID A1 A2 D1 D2 Q1 Q2 Notes 150802 8-2 Arthropoda Malacostraca Amphipoda Talitridae Talitridae 0 0 0 0 16 31 150802 8-2 Mollusca Gastropoda Ellobiidae Melampus bidentatus Melampus bidentatus 0 0 0 0 17 8 150802 8-2 Arthropoda Insecta Hemiptera Auchenorrhyncha Auchenorrhyncha 0 0 0 0 2 1 150802 8-2 Arthropoda Arachnida Araneae Araneae 0 0 0 0 6 1 150802 8-2 Arthropoda Arachnida Acari Acari 0 0 0 0 0 3 150802 8-2 Arthropoda Insecta Diptera Diptera 0 0 0 0 3 0 150802 8-2 Arthropoda (larvae) Insecta (larvae) Diptera (larvae) Diptera (larvae) 0 0 1 1 1 0 150802 8-2 Arthropoda Insecta Hemiptera Auchenorrhyncha Delphacidae Delphacidae 1 0 0 0 0 0 150802 8-2 Arthropoda Malacostraca Tanaidacea Tanaidacea 4 4 82 0 0 0 150802 8-2 Arthropoda Malacostraca Amphipoda Corophiidae Corophiidae 18 22 2 0 0 0 150802 8-2 Arthropoda Malacostraca Eumalacostraca Amphipoda Gammaridea Melitidae Melitidae 5 1 0 0 0 0 150802 8-2 Arthropoda Malacostraca Isopoda Anthuridae Anthuridae 2 0 2 0 0 0 D1: most spionids and 150802 8-2 Annelida Polychaeta Spionida Spionidae Spionidae 0 1 109 0 0 0 some ampharetidae missing tentacles D1: most spionids and 150802 8-2 Annelida Polychaeta Terebellida Ampharetidae Ampharetidae 0 1 20 0 0 0 some ampharetidae missing tentacles D1: Sabellidae very small, 150802 8-2 Annelida Polychaeta Sabellida Sabellidae Sabellidae 0 0 4 0 0 0 difficult to remove from tube - in 2 pieces 150802 8-2 Mollusca Gastropoda Littorinimorpha Hydrobiidae Hydrobiidae 0 0 4 0 0 0 150802 8-2 Mollusca Gastropoda Littorinimorpha Littorinidae Littorinidae 0 0 3 0 0 0 150802 8-2 Mollusca Bivalvia Myoida Myidae Myidae 0 0 1 0 0 0 150802 8-2 Annelida Clitellata Hirudinea Hirudinea 0 0 10 0 0 0 150802 8-2 Nematoda Nematoda 0 0 7 0 0 0 150802 8-2 Arthropoda Insecta Hymenoptera Hymenoptera 0 0 1 0 0 0 150802 8-2 Arthropoda Insecta Orthoptera Orthoptera 0 0 2 0 0 0 150802 8-2 Arthropoda Malacostraca Cumacea Cumacea 0 0 1 0 0 0 150802 8-2 Arthropoda Malacostraca Amphipoda Gammaridae Gammaridae 0 0 3 0 0 0 150802 8-2 Arthropoda Malacostraca Isopoda Idoteidae Idoteidae 0 0 2 0 0 0 150802 8-2 Arthropoda Malacostraca Decapoda Palaemonidae Palaemonetes pugio Palaemonetes pugio 0 0 2 1 0 0 150802 8-2 Arthropoda Insecta Hemiptera Heteroptera Corixidae Corixidae 0 0 0 1 0 0 150807 8-7 Arthropoda Malacostraca Amphipoda Talitridae Talitridae 0 0 0 0 21 85 150807 8-7 Mollusca Bivalvia Mytiloida Mytilidae Geukensia demissa Geukensia demissa 0 0 0 0 6 2 150807 8-7 Mollusca Gastropoda Littorinimorpha Littorinidae Littorina saxatilis 0 0 0 0 2 25 150807 8-7 Arthropoda Insecta Hemiptera Auchenorrhyncha Auchenorrhyncha 0 0 0 0 14 43 150807 8-7 Arthropoda Arachnida Araneae Araneae 0 0 0 0 10 21 150807 8-7 Arthropoda Arachnida Acari Acari 0 0 0 0 1 0 150807 8-7 Arthropoda Insecta Diptera Diptera 0 0 0 0 0 2 150807 8-7 Annelida Polychaeta Phyllodocida Nereididae Nereididae 1 0 0 0 0 0 150807 8-7 Annelida Annelida (Capitellidae/Oligochaeta type) 0 2 0 0 0 0 150807 8-7 Annelida Polychaeta Scolecida Orbiniidae Orbiniidae 0 1 0 0 0 0 150807 8-7 Annelida Polychaeta Phyllodocida Phyllodocidae Phyllodocidae 0 3 0 0 0 0 150807 8-7 Mollusca Gastropoda Littorinimorpha Littorinidae Littorinidae 0 0 0 4 0 0 151202 12-2 Arthropoda Malacostraca Amphipoda Talitridae Talitridae 0 0 0 0 5 1 151202 12-2 Mollusca Gastropoda Ellobiidae Melampus bidentatus Melampus bidentatus 0 0 0 0 8 5 151202 12-2 Arthropoda Arachnida Araneae Araneae 0 0 0 1 1 2 151202 12-2 Arthropoda Insecta Coleoptera Coleoptera 0 0 0 0 3 1 151202 12-2 Arthropoda (larvae) Insecta (larvae) Coleoptera (larvae) Coleoptera (larvae) 0 0 0 0 0 1 151202 12-2 Annelida Polychaeta Phyllodocida Nereididae Nereididae 1 0 0 0 0 0 151202 12-2 Annelida Polychaeta Terebellida Ampharetidae Ampharetidae 1 0 0 0 0 0 151202 12-2 Arthropoda Malacostraca Tanaidacea Tanaidacea 1 1 0 0 0 0 151202 12-2 Annelida Annelida (unknown) 0 1 0 0 0 0 A2: Heavily damaged 151202 12-2 Arthropoda Malacostraca Amphipoda Aoridae Aoridae 0 1 0 0 0 0 151202 12-2 Arthropoda Insecta Hemiptera Sternorrhyncha Aphididae Aphididae 0 0 3 0 0 0 151202 12-2 Arthropoda Malacostraca Amphipoda Corophiidae Corophiidae 0 0 0 2 0 0 151202 12-2 Arthropoda Malacostraca Eumalacostraca Amphipoda Gammaridea Melitidae Melitidae 0 0 0 3 0 0 151203 12-3 Arthropoda Malacostraca Amphipoda Talitridae Talitridae 0 0 0 0 2 18 151203 12-3 Mollusca Gastropoda Ellobiidae Melampus bidentatus Melampus bidentatus 0 0 0 0 3 13 151203 12-3 Arthropoda Arachnida Araneae Araneae 0 0 0 0 0 3 151203 12-3 Arthropoda Insecta Hymenoptera Formicidae Formicidae 0 0 0 0 0 1 151203 12-3 Annelida Polychaeta Terebellida Ampharetidae Ampharetidae 0 0 1 0 0 0 151203
Recommended publications
  • (Gastropoda: Littorinidae) in the Temperate Southern Hemisphere: the Genera Nodilittorina, Austrolittorina and Afrolittorina
    © Copyright Australian Museum, 2004 Records of the Australian Museum (2004) Vol. 56: 75–122. ISSN 0067-1975 The Subfamily Littorininae (Gastropoda: Littorinidae) in the Temperate Southern Hemisphere: The Genera Nodilittorina, Austrolittorina and Afrolittorina DAVID G. REID* AND SUZANNE T. WILLIAMS Department of Zoology, The Natural History Museum, London SW7 5BD, United Kingdom [email protected] · [email protected] ABSTRACT. The littorinine gastropods of the temperate southern continents were formerly classified together with tropical species in the large genus Nodilittorina. Recently, molecular data have shown that they belong in three distinct genera, Austrolittorina, Afrolittorina and Nodilittorina, whereas the tropical species are members of a fourth genus, Echinolittorina. Austrolittorina contains 5 species: A. unifasciata in Australia, A. antipodum and A. cincta in New Zealand, and A. fernandezensis and A. araucana in western South America. Afrolittorina contains 4 species: A. africana and A. knysnaensis in southern Africa, and A. praetermissa and A. acutispira in Australia. Nodilittorina is monotypic, containing only the Australian N. pyramidalis. This paper presents the first detailed morphological descriptions of the African and Australasian species of these three southern genera (the eastern Pacific species have been described elsewhere). The species-level taxonomy of several of these has been confused in the past; Afrolittorina africana and A. knysnaensis are here distinguished as separate taxa; Austrolittorina antipodum is a distinct species and not a subspecies of A. unifasciata; Nodilittorina pyramidalis is separated from the tropical Echinolittorina trochoides with similar shell characters. In addition to descriptions of shells, radulae and reproductive anatomy, distribution maps are given, and the ecological literature reviewed.
    [Show full text]
  • Shell Classification – Using Family Plates
    Shell Classification USING FAMILY PLATES YEAR SEVEN STUDENTS Introduction In the following activity you and your class can use the same techniques as Queensland Museum The Queensland Museum Network has about scientists to classify organisms. 2.5 million biological specimens, and these items form the Biodiversity collections. Most specimens are from Activity: Identifying Queensland shells by family. Queensland’s terrestrial and marine provinces, but These 20 plates show common Queensland shells some are from adjacent Indo-Pacific regions. A smaller from 38 different families, and can be used for a range number of exotic species have also been acquired for of activities both in and outside the classroom. comparative purposes. The collection steadily grows Possible uses of this resource include: as our inventory of the region’s natural resources becomes more comprehensive. • students finding shells and identifying what family they belong to This collection helps scientists: • students determining what features shells in each • identify and name species family share • understand biodiversity in Australia and around • students comparing families to see how they differ. the world All shells shown on the following plates are from the • study evolution, connectivity and dispersal Queensland Museum Biodiversity Collection. throughout the Indo-Pacific • keep track of invasive and exotic species. Many of the scientists who work at the Museum specialise in taxonomy, the science of describing and naming species. In fact, Queensland Museum scientists
    [Show full text]
  • North American Hydrobiidae (Gastropoda: Rissoacea): Redescription and Systematic Relationships of Tryonia Stimpson, 1865 and Pyrgulopsis Call and Pilsbry, 1886
    THE NAUTILUS 101(1):25-32, 1987 Page 25 . North American Hydrobiidae (Gastropoda: Rissoacea): Redescription and Systematic Relationships of Tryonia Stimpson, 1865 and Pyrgulopsis Call and Pilsbry, 1886 Robert Hershler Fred G. Thompson Department of Invertebrate Zoology Florida State Museum National Museum of Natural History University of Florida Smithsonian Institution Gainesville, FL 32611, USA Washington, DC 20560, USA ABSTRACT scribed) in the Southwest. Taylor (1966) placed Tryonia in the Littoridininae Taylor, 1966 on the basis of its Anatomical details are provided for the type species of Tryonia turreted shell and glandular penial lobes. It is clear from Stimpson, 1865, Pyrgulopsis Call and Pilsbry, 1886, Fonteli- cella Gregg and Taylor, 1965, and Microamnicola Gregg and the initial descriptions and subsequent studies illustrat- Taylor, 1965, in an effort to resolve the systematic relationships ing the penis (Russell, 1971: fig. 4; Taylor, 1983:16-25) of these taxa, which represent most of the generic-level groups that Fontelicella and its subgenera, Natricola Gregg and of Hydrobiidae in southwestern North America. Based on these Taylor, 1965 and Microamnicola Gregg and Taylor, 1965 and other data presented either herein or in the literature, belong to the Nymphophilinae Taylor, 1966 (see Hyalopyrgus Thompson, 1968 is assigned to Tryonia; and Thompson, 1979). While the type species of Pyrgulop- Fontelicella, Microamnicola, Nat ricola Gregg and Taylor, 1965, sis, P. nevadensis (Stearns, 1883), has not received an- Marstonia F. C. Baker, 1926, and Mexistiobia Hershler, 1985 atomical study, the penes of several eastern species have are allocated to Pyrgulopsis. been examined by Thompson (1977), who suggested that The ranges of both Tryonia and Pyrgulopsis include parts the genus may be a nymphophiline.
    [Show full text]
  • Supplementary Tales
    Metabarcoding reveals different zooplankton communities in northern and southern areas of the North Sea Jan Niklas Macher, Berry B. van der Hoorn, Katja T. C. A. Peijnenburg, Lodewijk van Walraven, Willem Renema Supplementary tables 1-5 Table S1: Sampling stations and recorded abiotic variables recorded during the NICO 10 expedition from the Dutch Coast to the Shetland Islands Sampling site name Coordinates (°N, °E) Mean remperature (°C) Mean salinity (PSU) Depth (m) S74 59.416510, 0.499900 8.2 35.1 134 S37 58.1855556, 0.5016667 8.7 35.1 89 S93 57.36046, 0.57784 7.8 34.8 84 S22 56.5866667, 0.6905556 8.3 34.9 220 S109 56.06489, 1.59652 8.7 35 79 S130 55.62157, 2.38651 7.8 34.8 73 S156 54.88581, 3.69192 8.3 34.6 41 S176 54.41489, 4.04154 9.6 34.6 43 S203 53.76851, 4.76715 11.8 34.5 34 Table S2: Species list and read number per sampling site Class Order Family Genus Species S22 S37 S74 S93 S109 S130 S156 S176 S203 Copepoda Calanoida Acartiidae Acartia Acartia clausi 0 0 0 72 0 170 15 630 3995 Copepoda Calanoida Acartiidae Acartia Acartia tonsa 0 0 0 0 0 0 0 0 23 Hydrozoa Trachymedusae Rhopalonematidae Aglantha Aglantha digitale 0 0 0 0 1870 117 420 629 0 Actinopterygii Trachiniformes Ammodytidae Ammodytes Ammodytes marinus 0 0 0 0 0 263 0 35 0 Copepoda Harpacticoida Miraciidae Amphiascopsis Amphiascopsis cinctus 344 0 0 992 2477 2500 9574 8947 0 Ophiuroidea Amphilepidida Amphiuridae Amphiura Amphiura filiformis 0 0 0 0 219 0 0 1470 63233 Copepoda Calanoida Pontellidae Anomalocera Anomalocera patersoni 0 0 586 0 0 0 0 0 0 Bivalvia Venerida
    [Show full text]
  • New Insights in the Biogeographical Distributions of Two Spionidae (Annelida) from the NE Atlantic and Mediterranean French Coasts
    Zoosymposia 19: 173–184 (2020) ISSN 1178-9905 (print edition) https://www.mapress.com/j/zs ZOOSYMPOSIA Copyright © 2020 · Magnolia Press ISSN 1178-9913 (online edition) https://doi.org/10.11646/zoosymposia.19.1.18 http://zoobank.org/urn:lsid:zoobank.org:pub:7CF4D06E-47F9-48C5-9703-5CECFD9C1491 New insights in the biogeographical distributions of two Spionidae (Annelida) from the NE Atlantic and Mediterranean French coasts JÉRÔME JOURDE1,5*, NICOLAS LAVESQUE2,7, CÉLINE LABRUNE3,10, JEAN-MICHEL AMOUR- OUX3,12, PAULO BONIFÁCIO3,11, SUZIE HUMBERT2,8, BASTIEN LAMARQUE2,9, PIERRE-GUY SAURIAU1,6 & KARIN MEIßNER4,13 1La Rochelle Université, CNRS, UMR 7266 LIENSs, 2 rue Olympe de Gouges 17000 La Rochelle, France 2Université de Bordeaux, CNRS, UMR 5805 EPOC, Station Marine d’Arcachon, 2 rue du Professeur Jolyet, 33120 Arcachon, France 3Sorbonne Université, CNRS, UMR LECOB 8222, Laboratoire d’Ecogéochimie des Environnements Benthiques, Observatoire Océanologique de Banyuls, Avenue Pierre Fabre, 66650 Banyuls-sur-Mer, France 4Senckenberg Forschungsinstitute und Naturmuseen (SFN), Deutsches Zentrum für Marine Biodiversitätsforschung, Biozentrum Grindel, Martin-Luther-King-Platz 3, D-20146 Hamburg, Germany 5 [email protected], https://orcid.org/0000-0001-7260-8419 6 [email protected], https://orcid.org/0000-0002-5360-8728 7 [email protected], https://orcid.org/0000-0001-5701-2393 8 [email protected], https://orcid.org/0000-0003-4254-3567 9 [email protected], https://orcid.org/0000-0002-1418-9049 10 [email protected],
    [Show full text]
  • BASTERIA, 101-113, 1998 Hydrobia (Draparnaud, 1805) (Gastropoda
    BASTERIA, Vol 61: 101-113, 1998 Note on the occurrence of Hydrobia acuta (Draparnaud, 1805) (Gastropoda, Prosobranchia: Hydrobiidae) in western Europe, with special reference to a record from S. Brittany, France D.F. Hoeksema Watertoren 28, 4336 KC Middelburg, The Netherlands In August 1992 samples of living Hydrobia acuta (Draparnaud, 1805) have been collected in the Baie de Quiberon (Morbihan, France). The identification is elucidated. Giusti & Pezzoli (1984) and Giusti, Manganelli& Schembri (1995) suggested that Hydrobia minoricensis (Paladilhe, of H. The features ofthe 1875) and Hydrobia neglecta Muus, 1963, are junior synomyms acuta. material from Quiberon support these suggestions: it will be demonstrated that H. minoricensis and H. neglecta fit completely in the conception of H. acuta. H. acuta, well known from the be also distributed in and northwestern Mediterranean, appears to widely western Europe. Key words: Gastropoda,Prosobranchia, Hydrobiidae,Hydrobia acuta, distribution, France. Europe. INTRODUCTION In favoured localities often hydrobiid species are very abundant, occurring in dense populations. Some species prefer fresh water, others brackish or sea-water habitats. in the distributionof Although salinity preferences play a part determining each species, most species show a broad tolerance as regards the degree of salinity. Frequently one live in the habitat with Some hydrobiid species may same another. hydrobiid species often dealt with are in publications on marine species as well in those on non-marine Cachia Giusti species (e.g. et al., 1996, and et al., 1995). Many hydrobiid species are widely distributed, but often in genetically isolated populations; probably due to dif- ferent circumstances ecological the species may show a considerablevariability, especially as to the dimensions and the shape of the shell and to the pigmentation of the body.
    [Show full text]
  • Boccardia Proboscidea Class: Polychaeta, Sedentaria, Canalipalpata
    Phylum: Annelida Boccardia proboscidea Class: Polychaeta, Sedentaria, Canalipalpata Order: Spionida, Spioniformia A burrowing spionid worm Family: Spionidae Taxonomy: Boccardia proboscidea’s senior Trunk: subjective synonym, Polydora californica Posterior: Pygidium is a round, flaring (Treadwell, 1914) and an un-typified name, disc with four unequal lobes where dorsal Spio californica (Fewkes, 1889) were both lobes are smaller (Fig. 4) (Hartman 1969). suppressed in 2012 by the International Parapodia: Biramous after first setiger. Commission on Zoological Nomenclature Podia on the first setiger are not lobed, small (ICZN, case 3520). The widely cited and and inconspicuous. The second setiger's used name, Boccardia proboscidea parapodial lobes become twice as large as (Hartman, 1940) was conserved (ICZN the first's, and continue to worm posterior. 2012). Setae (chaetae): All setae are simple and in- clude bunches of short, capillary spines to se- Description tiger six (except for modified setiger five) Size: Specimens up to 30–35 mm in length (Figs. 5a, b). A transverse row of and 1.5 mm in width, where length extends approximately eight neuropodial uncini with age (Hartman 1940). The illustrated (hooded hooks) with bifid (two-pronged) tips specimen has approximately 130 segments begins on setiger seven and continues to (Fig. 1). posterior end (Fig. 5e), with bunches of Color: Yellow-orange with red branchiae capillary setae below them (until setiger 11). and dusky areas around prostomium and Notosetae of setiger five are heavy, dark and parapodia (Hartman 1969). Sato-Okoshi arranged vertically in two rows of five with and Okoshi (1997) report black pigment fol- pairs of long, falcate spines (Fig.
    [Show full text]
  • Mild Osmotic Stress in Intertidal Gastropods Littorina Saxatilis and Littorina Obtusata (Mollusca: Caenogastropoda): a Proteomic Analysis
    CORE Metadata, citation and similar papers at core.ac.uk Provided by Saint PetersburgFULL State University COMMUNICATION PHYSIOLOGY Mild osmotic stress in intertidal gastropods Littorina saxatilis and Littorina obtusata (Mollusca: Caenogastropoda): a proteomic analysis Olga Muraeva1, Arina Maltseva1, Marina Varfolomeeva1, Natalia Mikhailova1,2, and Andrey Granovitch1 1 Department of Invertebrate Zoology, Faculty of Biology, Saint Petersburg State University, Universitetskaya nab. 7–9, St. Petersburg, 199034, Russian Federation; 2 Center of Cell Technologies, Institute of Cytology RAS, Tikhoretsky prospect, 4, St. Petersburg, 194064, Russian Federation Address correspondence and requests for materials to Arina Maltseva, [email protected] Abstract Salinity is a crucial abiotic environmental factor for marine animals, affecting their physiology and geographic ranges. Deviation of environmental salin- ity from the organismal optimum range results in an osmotic stress in osmo- conformers, which keep their fluids isotonic to the environment. The ability to overcome such stress is critical for animals inhabiting areas with considerable salinity variation, such as intertidal areas. In this study, we compared the reac- tion to mild water freshening (from 24 to 14 ‰) in two related species of inter- tidal snails, Littorina saxatilis and L. obtusata, with respect to several aspects: survival, behavior and proteomic changes. Among these species, L. saxatilis is Citation: Muraeva, O., Maltseva, A., Varfolomeeva, M., Mikhailova, N., more tolerant to low salinity and survives in estuaries. We found out that the Granovitch, A. 2017. Mild osmotic response of these species was much milder (with no mortality or isolation re- stress in intertidal gastropods Littorina saxatilis and Littorina obtusata (Mollusca: action observed) and involved weaker proteomic changes than during acute Caenogastropoda): a proteomic analysis.
    [Show full text]
  • Marine Ecology Progress Series 502:219
    The following supplement accompanies the article Spatial patterns in early post-settlement processes of the green sea urchin Strongylocentrotus droebachiensis L. B. Jennings*, H. L. Hunt Department of Biology, University of New Brunswick, PO Box 5050, Saint John, New Brunswick E2L 4L5, Canada *Corresponding author: [email protected] Marine Ecology Progress Series 502: 219–228 (2014) Supplement. Table S1. Average abundance of organisms in the cages for the with-suite treatments at the end of the experiment at the 6 sites in 2008 Birch Dick’s Minister’s Tongue Midjic Clark’s Cove Island Island Shoal Bluff Point Amphipod Corophium 38.5 37.5 21.5 21.6 52.1 40.7 Amphipod Gammaridean 1.4 1.8 3.8 16.2 19.8 16.4 Amphipod sp. 0.5 0.4 0.0 0.0 0.1 0.0 Amphiporus angulatus 0.0 0.0 0.0 0.0 0.2 0.1 Amphitrite cirrata 0.0 0.0 0.1 0.0 0.0 0.0 Amphitrite ornata 0.1 0.0 0.0 0.0 0.0 0.0 Anenome sp. 1 0.0 0.0 0.0 0.4 0.3 0.0 Anenome sp. 2 0.0 0.1 0.3 0.0 0.0 3.7 Anomia simplex 47.6 28.7 25.2 25.2 10.3 10.4 Anomia squamula 3.2 1.6 0.8 1.1 0.1 0.2 Arabellid unknown 0.0 0.1 0.0 0.0 0.0 0.1 Ascidian sp. 0.0 0.0 0.0 0.1 0.0 0.0 Astarte sp.
    [Show full text]
  • Mollusca: Veneridae) in the Western Pacific Ocean1
    Genetic Relationships among Species of Meretrix (Mollusca: Veneridae) in the Western Pacific Ocean1 Ayako Yashiki Yamakawa,2,3,6 Masashi Yamaguchi,4,5 and Hideyuki Imai4 Abstract: We compared allozymes at 12 loci in 12 populations of six species of Meretrix: M. lusoria ( Japan, Korea, and Taiwan), M. petechialis (China and Ko- rea), M. ovum (Thailand and Mozambique), M. lyrata (China), M. lamarckii ( Ja- pan), and Meretrix sp. A (Okinawa, Japan). Our allozyme results were generally consistent with the major groupings currently recognized within the genus based on morphological characters. However, we found two cryptic or un- described species: Meretrix sp. A from Okinawa and M. cf. lusoria from Taiwan. The shell characters of Meretrix sp. A were similar to those of M. lamarckii, but the species was genetically distinct (Nei’s genetic distance D > 0.845) from all other species examined. The Taiwanese Meretrix population was morphologi- cally indistinguishable from Japanese M. lusoria, although the genetic distance between the Taiwanese and Japanese populations showed a high degree of ge- netic differentiation (D > 0.386). Meretrix lusoria seedlings were introduced into Taiwan from Japan in the 1920s, and Japanese M. lusoria was previously thought to be established as a cultured stock. However, our results suggest that the Taiwanese population may represent a sibling or cryptic species of M. lusoria. Asianhardclams, genus Meretrix (Vener- (Yoosukh and Matsukuma 2001). These idae), are commercially important bivalves clams inhabit the tidal flats, estuaries, and in East and Southeast Asia and East Africa sandy beaches of the Indian Ocean, including East Africa and Southeast Asia, and the west- ern Pacific along the Chinese coast, Korean 1 Financial support was provided from the 21st Peninsula, and Japanese Archipelago.
    [Show full text]
  • Annelida, Polychaeta, Chaetopteridae), with Re- Chaetopteridae), with Re-Description of M
    2 We would like to thank the Zoological Journal of the Linnean Society, The Linnean Society of London and Blackwell Publishing for accepting our manuscript entitled “Description of a Description of a new species of Mesochaetopterus (Annelida, Polychaeta, new species of Mesochaetopterus (Annelida, Polychaeta, Chaetopteridae), with re- Chaetopteridae), with re-description of M. xerecus and an approach to the description of M. xerecus and an approach to the phylogeny of the family”, which has phylogeny of the family been published in the Journal issue Zool. J. Linnean Soc. 2008, 152: 201–225. D. MARTIN1,* J. GIL1, J. CARRERAS-CARBONELL1 and M. BHAUD2 By posting this version of the manuscript (i.e. pre-printed), we agree not to sell or reproduce the Article or any part of it for commercial purposes (i.e. for monetary gain on your own 1Centre d'Estudis Avançats de Blanes (CSIC), Carrer d’accés a la Cala Sant Francesc 14, account or on that of a third party, or for indirect financial gain by a commercial entity), and 17300 Blanes (Girona), Catalunya (Spain). we expect the same from the users. 2 Observatoire Océanologique de Banyuls, Université P. et M. Curie - CNRS, BP 44, 66650 As soon as possible, we will add a link to the published version of the Article at the editors Banyuls-sur-Mer, Cedex, France. web site. * Correspondence author: Daniel Martin. Centre d'Estudis Avançats de Blanes (CSIC), Carrer Daniel Martin, Joao Gil, Michel Bhaud & Josep Carreras-Carbonell d’accés a la Cala Sant Francesc 14, 17300 Blanes (Girona), Catalunya (Spain). Tel. +34972336101; Fax: +34 972337806; E-mail: [email protected].
    [Show full text]
  • Littorina Littorea Class
    . Easily seen year round along the Littorina littorea shore line of Burntcoat Class: Gastropoda Head. Order: Neotaenioglossa Family: Littorinidae Genus: Littorina Distribution The Littorinidae family is a In the genus Littorina is the species L.littorea commonly known group of over 200 known as the edible periwinkle. It is native to the north-eastern coasts species of sea snails, of the Atlantic Ocean, including northern Spain, France, commonly referred to as England, Scotland, Ireland, Scandinavia and Russia and has been periwinkles. They have a introduced to the Atlantic coast of North America. It is now a global distribution. Within predominant mollusc from New Jersey to Newfoundland. In this family of periwinkles Canada, their range includes New Brunswick, Nova Scotia, there are several genera, Quebec, Newfoundland and Labrador. one of which is Litttorina. They are plentiful at Burntcoat Head. Habitat Though most abundant on rocky substrates and common in tide In the Atlantic it is found pools, it is a habitat generalist that also occurs on muddy or on both open coast and sandy bottoms. They are found along the entire coast, on estuary habitats from the breakwaters, dikes, piers, etc. In favourable habitats, it reaches upper intertidal zone to densities of up to 200-800 individuals per square metre. about 40 metres deep, and Since its arrival in North America it has become the most can tolerate salinities down abundant shallow-water herbivorous snail from Nova Scotia to to around 13 ppt. Long Island Sound. Food Although primarily an algae grazer, it also feeds on small L. littorea is a mostly invertebrates such as barnacle larvae.
    [Show full text]