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The 2014 Golden Gate National Parks Bioblitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 ON THIS PAGE Photograph of BioBlitz participants conducting data entry into iNaturalist. Photograph courtesy of the National Park Service. ON THE COVER Photograph of BioBlitz participants collecting aquatic species data in the Presidio of San Francisco. Photograph courtesy of National Park Service. The 2014 Golden Gate National Parks BioBlitz - Data Management and the Event Species List Achieving a Quality Dataset from a Large Scale Event Natural Resource Report NPS/GOGA/NRR—2016/1147 Elizabeth Edson1, Michelle O’Herron1, Alison Forrestel2, Daniel George3 1Golden Gate Parks Conservancy Building 201 Fort Mason San Francisco, CA 94129 2National Park Service. Golden Gate National Recreation Area Fort Cronkhite, Bldg. 1061 Sausalito, CA 94965 3National Park Service. San Francisco Bay Area Network Inventory & Monitoring Program Manager Fort Cronkhite, Bldg. 1063 Sausalito, CA 94965 March 2016 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Report Series is used to disseminate comprehensive information and analysis about natural resources and related topics concerning lands managed by the National Park Service. -
Settlement Patterns in Ascidians Concerning Have Been
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital.CSIC Larval settlement behaviour in six gregarious ascidians in relation to adult 2 distribution 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 Marc Rius1,2,*, George M. Branch2, Charles L. Griffiths1,2, Xavier Turon3 18 19 20 1 Centre for Invasion Biology, Zoology Department, University of Cape Town, 21 Rondebosch 7701, South Africa 22 23 2 Marine Biology Research Centre, Zoology Department, University of Cape Town, 24 Rondebosch 7701, South Africa 25 26 3 Center for Advanced Studies of Blanes (CEAB, CSIC), Accés Cala St. Francesc 14, 27 17300 Blanes (Girona), Spain 28 29 30 31 32 33 34 * Corresponding author: Marc Rius 35 Centre for Invasion Biology, Zoology Department, University of Cape Town, 36 Rondebosch 7701, South Africa 37 E-mail: [email protected] 38 Telephone: +27 21 650 4939 39 Fax: +27 21 650 3301 40 41 Running head: Settlement patterns of gregarious ascidians 42 43 44 1 45 ABSTRACT 46 Settlement influences the distribution and abundance of many marine organisms, 47 although the relative roles of abiotic and biotic factors influencing settlement are poorly 48 understood. Species that aggregate often owe this to larval behaviour, and we ask 49 whether this predisposes ascidians to becoming invasive, by increasing their capacity to 50 maintain their populations. We explored the interactive effects of larval phototaxis and 51 geotaxis and conspecific adult extracts on settlement rates of a representative suite of 52 six species of ascidians that form aggregations in the field, including four aliens with 53 global distributions, and how they relate to adult habitat characteristics. -
Crepidula Fornicata
NOBANIS - Marine invasive species in Nordic waters - Fact Sheet Crepidula fornicata Author of this species fact sheet: Kathe R. Jensen, Zoological Museum, Natural History Museum of Denmark, Universiteteparken 15, 2100 København Ø, Denmark. Phone: +45 353-21083, E-mail: [email protected] Bibliographical reference – how to cite this fact sheet: Jensen, Kathe R. (2010): NOBANIS – Invasive Alien Species Fact Sheet – Crepidula fornicata – From: Identification key to marine invasive species in Nordic waters – NOBANIS www.nobanis.org, Date of access x/x/201x. Species description Species name Crepidula fornicata, Linnaeus, 1758 – Slipper limpet Synonyms Patella fornicata Linnaeus, 1758; Crepidula densata Conrad, 1871; Crepidula virginica Conrad, 1871; Crepidula maculata Rigacci, 1866; Crepidula mexicana Rigacci, 1866; Crepidula violacea Rigacci, 1866; Crepidula roseae Petuch, 1991; Crypta nautarum Mörch, 1877; Crepidula nautiloides auct. NON Lesson, 1834 (ISSG Database; Minchin, 2008). Common names Tøffelsnegl (DK, NO), Slipper limpet, American slipper limpet, Common slipper snail (UK, USA), Østerspest (NO), Ostronpest (SE), Amerikanische Pantoffelschnecke (DE), La crépidule (FR), Muiltje (NL), Seba (E). Identification Crepidula fornicata usually sit in stacks on a hard substrate, e.g., a shell of other molluscs, boulders or rocky outcroppings. Up to 13 animals have been reported in one stack, but usually 4-6 animals are seen in a stack. Individual shells are up to about 60 mm in length, cap-shaped, distinctly longer than wide. The “spire” is almost invisible, slightly skewed to the right posterior end of the shell. Shell height is highly variable. Inside the body whorl is a characteristic calcareous shell-plate (septum) behind which the visceral mass is protected. -
Phlebobranchia of CTAW
PHLEBOBRANCHIA PHLEBOBRANCHIA The suborder Phlebobranchia (order Enterogona) is characterised by having unpaired gonads present only on the same side of the body as the gut. As in Stolidobranchia, the body is not divided into different sections (such as thorax, abdomen and posterior abdomen) as the gut is folded up in the parietal body wall outside the pharynx and the large branchial sac occupies the whole length of the body. Usually the branchial sac (which is flat, without folds) has internal longitudinal vessels (although only vestiges remain in Agneziidae). Epicardial sacs do not persist in adults as they do in Aplousobranchia, although excretory vesicles (nephrocytes) embedded in the body wall over the gut are known to originate from the embryonic epicardium in Ascidiidae and Corellidae. Most phlebobranchs are solitary. However, Plurellidae Kott, 1973 includes both solitary and colonial forms, and Perophoridae Giard, 1872 are all colonial. Replication in Perophoridae is from ectodermal epithelium (rather than endodermal or mesodermal tissue the mesodermal tissue of the vascular stolon (rather than the endodermal tissue as in most as in Aplousobranchia). The process of replication has not been investigated in Plurellidae. Phlebobranch taxa occurring in Australia are documented in Kott (1985). Family level taxa are characterised principally by the size and form of the branchial sac including the number of branchial vessels and form of the stigmata; the form, size and position of the gonads; and the habit (colonial or solitary) of the taxon. Berrill (1950) has discussed problems in assessing the phylogeny of Perophoridae. References Berrill, N.J. (1950). The Tunicata. Ray Soc. Publs 133: 1–354 Giard, A.M. -
The Ascidian Styela Plicata As a Potential Bioremediator of Bacterial and Algal Contamination of Marine Estuarine Waters
THE ASCIDIAN STYELA PLICATA AS A POTENTIAL BIOREMEDIATOR OF BACTERIAL AND ALGAL CONTAMINATION OF MARINE ESTUARINE WATERS by Lisa Denham Draughon A Dissertation Submitted to the Faculty of The Charles E. Schmidt College of Science In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Florida Atlantic University Boca Raton, Florida May, 2010 Copyright by Lisa Denham Draughon 2010 ii ACKNOWLEDGEMENTS I wish to express my sincerest gratitude to those who made this research possible; Ocean Restoration Corporation Associates (ORCA), the Link Foundation, and Florida Atlantic University (FAU) for their financial fellowships, and for the many hands that played a part in getting it all done. A special thank you goes to my committee members; Dr. James X. Hartmann (chairperson) and Dr. David Binninger of FAU, Dr. Ed Proffitt and Dr. John Scarpa of Harbor Branch Oceanographic Institute at FAU, and Dr. Ray Waldner of Palm Beach Atlantic University. You were all such an integral part of helping me achieve this goal. Special thanks also go to my friend Karen Halloway- Adkins who was always willing to help locate specimens and provide equipment when she had it. Mike Calinski of ORCA made trips from the Gulf Coast to deliver specimens to me. Sherry Reed of the Smithsonian Marine Station in Ft. Pierce was extremely helpful by keeping an eye out for the tunicates and at times gathering them for me. Dr. Patricia Keating was invaluable for her help in flow-cytometry analysis. Dr. Peter McCarthy of Harbor Branch Oceanographic Institute at FAU provided the bacteria for the filtration rate experiment. -
The American Slipper Limpet Crepidula Fornicata (L.) in the Northern Wadden Sea 70 Years After Its Introduction
Helgol Mar Res (2003) 57:27–33 DOI 10.1007/s10152-002-0119-x ORIGINAL ARTICLE D. W. Thieltges · M. Strasser · K. Reise The American slipper limpet Crepidula fornicata (L.) in the northern Wadden Sea 70 years after its introduction Received: 14 December 2001 / Accepted: 15 August 2001 / Published online: 25 September 2002 © Springer-Verlag and AWI 2002 Abstract In 1934 the American slipper limpet 1997). In the centre of its European distributional range Crepidula fornicata (L.) was first recorded in the north- a population explosion has been observed on the Atlantic ern Wadden Sea in the Sylt-Rømø basin, presumably im- coast of France, southern England and the southern ported with Dutch oysters in the preceding years. The Netherlands. This is well documented (reviewed by present account is the first investigation of the Crepidula Blanchard 1997) and sparked a variety of studies on the population since its early spread on the former oyster ecological and economic impacts of Crepidula. The eco- beds was studied in 1948. A field survey in 2000 re- logical impacts of Crepidula are manifold, and include vealed the greatest abundance of Crepidula in the inter- the following: tidal/subtidal transition zone on mussel (Mytilus edulis) (1) Accumulation of pseudofaeces and of fine sediment beds. Here, average abundance and biomass was 141 m–2 through the filtration activity of Crepidula and indi- and 30 g organic dry weight per square metre, respec- viduals protruding in stacks into the water column. tively. On tidal flats with regular and extended periods of This was reported to cause changes in sediments and emersion as well as in the subtidal with swift currents in near-bottom currents (Ehrhold et al. -
Ascidiacea (Chordata: Tunicata) of Greece: an Updated Checklist
Biodiversity Data Journal 4: e9273 doi: 10.3897/BDJ.4.e9273 Taxonomic Paper Ascidiacea (Chordata: Tunicata) of Greece: an updated checklist Chryssanthi Antoniadou‡, Vasilis Gerovasileiou§§, Nicolas Bailly ‡ Department of Zoology, School of Biology, Aristotle University of Thessaloniki, Thessaloniki, Greece § Institute of Marine Biology, Biotechnology and Aquaculture, Hellenic Centre for Marine Research, Heraklion, Greece Corresponding author: Chryssanthi Antoniadou ([email protected]) Academic editor: Christos Arvanitidis Received: 18 May 2016 | Accepted: 17 Jul 2016 | Published: 01 Nov 2016 Citation: Antoniadou C, Gerovasileiou V, Bailly N (2016) Ascidiacea (Chordata: Tunicata) of Greece: an updated checklist. Biodiversity Data Journal 4: e9273. https://doi.org/10.3897/BDJ.4.e9273 Abstract Background The checklist of the ascidian fauna (Tunicata: Ascidiacea) of Greece was compiled within the framework of the Greek Taxon Information System (GTIS), an application of the LifeWatchGreece Research Infrastructure (ESFRI) aiming to produce a complete checklist of species recorded from Greece. This checklist was constructed by updating an existing one with the inclusion of recently published records. All the reported species from Greek waters were taxonomically revised and cross-checked with the Ascidiacea World Database. New information The updated checklist of the class Ascidiacea of Greece comprises 75 species, classified in 33 genera, 12 families, and 3 orders. In total, 8 species have been added to the previous species list (4 Aplousobranchia, 2 Phlebobranchia, and 2 Stolidobranchia). Aplousobranchia was the most speciose order, followed by Stolidobranchia. Most species belonged to the families Didemnidae, Polyclinidae, Pyuridae, Ascidiidae, and Styelidae; these 4 families comprise 76% of the Greek ascidian species richness. The present effort revealed the limited taxonomic research effort devoted to the ascidian fauna of Greece, © Antoniadou C et al. -
1 Invasive Species in the Northeastern and Southwestern Atlantic
This is the author's accepted manuscript. The final published version of this work (the version of record) is published by Elsevier in Marine Pollution Bulletin. Corrected proofs were made available online on the 24 January 2017 at: http://dx.doi.org/10.1016/j.marpolbul.2016.12.048. This work is made available online in accordance with the publisher's policies. Please refer to any applicable terms of use of the publisher. Invasive species in the Northeastern and Southwestern Atlantic Ocean: a review Maria Cecilia T. de Castroa,b, Timothy W. Filemanc and Jason M Hall-Spencerd,e a School of Marine Science and Engineering, University of Plymouth & Plymouth Marine Laboratory, Prospect Place, Plymouth, PL1 3DH, UK. [email protected]. +44(0)1752 633 100. b Directorate of Ports and Coasts, Navy of Brazil. Rua Te filo Otoni, 4 - Centro, 20090-070. Rio de Janeiro / RJ, Brazil. c PML Applications Ltd, Prospect Place, Plymouth, PL1 3DH, UK. d Marine Biology and Ecology Research Centre, Plymouth University, PL4 8AA, UK. e Shimoda Marine Research Centre, University of Tsukuba, Japan. Abstract The spread of non-native species has been a subject of increasing concern since the 1980s when human- as a major vector for species transportation and spread, although records of non-native species go back as far as 16th Century. Ever increasing world trade and the resulting rise in shipping have highlighted the issue, demanding a response from the international community to the threat of non-native marine species. In the present study, we searched for available literature and databases on shipping and invasive species in the North-eastern (NE) and South-western (SW) Atlantic Ocean and assess the risk represented by the shipping trade between these two regions. -
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1 Mobilising molluscan models and genomes in biology 2 Angus Davison1 and Maurine Neiman2 3 1. School of Life Sciences, University Park, University of Nottingham, NG7 2RD, UK 4 2. Department of Biology, University of Iowa, Iowa City, IA, USA and Department of Gender, 5 Women's, and Sexuality Studies, University of Iowa, Iowa, City, IA, USA 6 Abstract 7 Molluscs are amongst the most ancient, diverse, and important of all animal taxa. Even so, 8 no individual mollusc species has emerged as a broadly applied model system in biology. 9 We here make the case that both perceptual and methodological barriers have played a role 10 in the relative neglect of molluscs as research organisms. We then summarize the current 11 application and potential of molluscs and their genomes to address important questions in 12 animal biology, and the state of the field when it comes to the availability of resources such 13 as genome assemblies, cell lines, and other key elements necessary to mobilising the 14 development of molluscan model systems. We conclude by contending that a cohesive 15 research community that works together to elevate multiple molluscan systems to ‘model’ 16 status will create new opportunities in addressing basic and applied biological problems, 17 including general features of animal evolution. 18 Introduction 19 Molluscs are globally important as sources of food, calcium and pearls, and as vectors of 20 human disease. From an evolutionary perspective, molluscs are notable for their remarkable 21 diversity: originating over 500 million years ago, there are over 70,000 extant mollusc 22 species [1], with molluscs present in virtually every ecosystem. -
Fecundity of the Invasive Marine Gastropod Crepidula Fornicata Near the Current Northern Extreme of Its Range
Invertebrate Biology 136(4): 394–402. © 2017, The American Microscopical Society, Inc. DOI: 10.1111/ivb.12194 Fecundity of the invasive marine gastropod Crepidula fornicata near the current northern extreme of its range Jan A. Pechenik,1,a Casey M. Diederich,1 Howard I. Browman,2 and Anders Jelmert3 1 Department of Biology, Tufts University, Medford, Massachusetts 02155, USA 2 Institute of Marine Research, Austevoll Research Station, Storebø, Norway 3 Institute of Marine Research, 5817 Bergen, Norway Abstract. The calyptraeid gastropod Crepidula fornicata is native to the eastern coast of the United States but has now become an extremely successful invader along much of the Euro- pean coastline. As the northern limit of its spread is thought to be determined by an inabil- ity of adults to tolerate prolonged exposure to low winter temperatures, this study sought to compare the fecundity of females collected from two sites along the Norwegian coastline with that of females collected from Rhode Island, USA. Few other studies have compared the fecundities of marine invertebrates from invasive populations with those found in native populations. For both populations studied, fecundities increased with increasing shell length. However, contrary to expectations, size-related fecundities were significantly higher for Norwegian females than for Rhode Island females, with Norwegian females producing larger egg capsules and a greater number of embryos per capsule, but not a greater number of egg capsules per brood. Current evidence suggests that at -
Assessing the Impact of Key Marine Invasive Non-Native Species on Welsh MPA Habitat Features, Fisheries and Aquaculture
Assessing the impact of key Marine Invasive Non-Native Species on Welsh MPA habitat features, fisheries and aquaculture. Tillin, H.M., Kessel, C., Sewell, J., Wood, C.A. Bishop, J.D.D Marine Biological Association of the UK Report No. 454 Date www.naturalresourceswales.gov.uk About Natural Resources Wales Natural Resources Wales’ purpose is to pursue sustainable management of natural resources. This means looking after air, land, water, wildlife, plants and soil to improve Wales’ well-being, and provide a better future for everyone. Evidence at Natural Resources Wales Natural Resources Wales is an evidence based organisation. We seek to ensure that our strategy, decisions, operations and advice to Welsh Government and others are underpinned by sound and quality-assured evidence. We recognise that it is critically important to have a good understanding of our changing environment. We will realise this vision by: Maintaining and developing the technical specialist skills of our staff; Securing our data and information; Having a well resourced proactive programme of evidence work; Continuing to review and add to our evidence to ensure it is fit for the challenges facing us; and Communicating our evidence in an open and transparent way. This Evidence Report series serves as a record of work carried out or commissioned by Natural Resources Wales. It also helps us to share and promote use of our evidence by others and develop future collaborations. However, the views and recommendations presented in this report are not necessarily those of -
Crepidula Formicatacrepidula Formicata
Crepidula formicataCrepidula formicata Easily seen Crepidula fornicata along the shoreline. Class: Gastropoda Order: Littorinimorpha Family: Calyptraeidae Genus: Crepidula Distribution It is native to the eastern This species has been introduced to several other countries, coast of North America. especially in Europe. It is considered to be an invasive, nuisance It occurs from the Gulf of species. The first known occurrence of Crepidula fornicata in St. Lawrence in the north Europe was in 1872. It was introduced accidently with imported all the way south to the American oysters. They have been repeatedly introduced ever Gulf of Mexico. since in ballast water and on ships’ hulls. Habitat They are most abundant in muddy or mixed muddy areas, This species occupies a reaching their highest densities in wave protected locations. variety of seabed surfaces. These include bays, estuaries and sheltered sides of wave- They also occur in a wide exposed islands. In Nova Scotia they are common in intertidal range of environmental and shallow subtidal regions. They attach themselves to almost conditions. any hard surface to be found (including each other and the shells of other living or dead hard-shelled invertebrates. Food They are active suspension feeders, generating a water current They live off of plankton through the mantle cavity by ciliary (hair-like) action and which they filter out of the trapping food particles on a mucous sheet lying across the front seawater. surface of the gill filament. Reproduction Being hermaphrodites they contain both male and female The Slipper limpet is a. reproductive organs. Sperm producing ability advances quicker protandric hermaphrodite.