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  • 1
    Online Resource
    Online Resource
    Dordrecht :Springer Netherlands,
    Keywords: Crustacea. ; Introduced organisms. ; Electronic books.
    Description / Table of Contents: This book provides a unique view into the story of how shrimps, crabs, and lobsters have been distributed around the world by human activity, and the profound implications of this global reorganization of biodiversity for marine conservation biology.
    Type of Medium: Online Resource
    Pages: 1 online resource (713 pages)
    Edition: 1st ed.
    ISBN: 9789400705913
    Series Statement: Invading Nature - Springer Series in Invasion Ecology Series ; v.6
    Language: English
    Note: Intro -- In the Wrong Place - Alien Marine Crustaceans: Distribution, Biology and Impacts -- Preface -- Contents -- Contributors -- Part I: In the Beginning -- The Global Dispersal of Marine and Estuarine Crustaceans -- 1 Introduction -- 2 Vectors -- 3 History of Recognition of Human-Altered Biogeography of Marine Crustaceans -- 4 The Scale of Modern-Day Recognition of Crustacean Invasions -- 5 Discussion -- References -- Part II: Global Dispersal -- Human-Mediated Spread of Alien Crabs -- 1 Introduction -- 2 Alien Marine Crabs -- 3 Regional Invasions (See Table 3, Fig. 6) -- 3.1 The North Sea -- 3.2 North Atlantic -- 3.3 Mediterranean and Black Sea -- 3.4 South Atlantic -- 3.5 Indian Ocean -- 3.6 North West Pacific -- 3.7 South West Pacific -- 3.8 North East Pacific -- 3.9 Hawaiian Islands -- 3.10 South East Pacific -- 3.11 Southern Ocean -- 4 Vectors and Routes (Fig. 7) -- 5 Most Significant Alien Crab Species Worldwide -- 5.1 Callinectes sapidus Rathbun, 1896, Blue Crab -- 5.1.1 Distribution -- 5.1.2 Habitat -- 5.1.3 Biology -- 5.1.4 Impact -- 5.2 Carcinus aestuarii Nardo, 1847, Mediterranean Green Crab -- 5.2.1 Distribution -- 5.2.2 Habitat -- 5.2.3 Biology -- 5.2.4 Impact -- 5.3 Carcinus maenas (Linnaeus, 1758), European Shore Crab, Green Crab -- 5.3.1 Distribution -- 5.3.2 Habitat -- 5.3.3 Biology -- 5.3.4 Impact -- 5.3.5 Management -- 5.4 Charybdis (Charybdis) hellerii (A. Milne Edwards, 1867) -- 5.4.1 Distribution -- 5.4.2 Habitat -- 5.4.3 Biology -- 5.4.4 Impact -- 5.5 Charybdis (Charybdis) japonica (A. Milne Edwards, 1861), Asian Paddle Crab, Lady Crab -- 5.5.1 Distribution -- 5.5.2 Habitat -- 5.5.3 Biology -- 5.5.4 Uses -- 5.5.5 Impact -- 5.6 Chionoecetes opilio (Fabricius, 1788), Snow Crab -- 5.6.1 Distribution -- 5.6.2 Habitat -- 5.6.3 Biology -- 5.6.4 Impact -- 5.7 Eriocheir sinensis H. Milne Edwards, 1853, Chinese mitten crab. , 5.7.1 Distribution -- 5.7.2 Habitat -- 5.7.3 Biology -- 5.7.4 Impact -- 5.7.5 Management -- 5.8 Hemigrapsus sanguineus (de Haan, 1853), Japanese, Asian Shore Crab -- 5.8.1 Distribution -- 5.8.2 Habitat -- 5.8.3 Biology -- 5.8.4 Impact -- 5.8.5 Management -- 5.9 Hemigrapsus takanoi Asakura and Watanabe, 2005 -- 5.9.1 Distribution -- 5.9.2 Habitat -- 5.9.3 Biology -- 5.9.4 Impact -- 5.10 Metacarcinus novaezelandiae (Hombron and Jacquinot, 1846), Pie-Crust Crab -- 5.10.1 Distribution -- 5.10.2 Habitat -- 5.10.3 Biology -- 5.10.4 Impact -- 5.11 Pachygrapsus marmoratus (Fabricius, 1787), Marbled Crab -- 5.11.1 Distribution -- 5.11.2 Habitat -- 5.11.3 Biology -- 5.11.4 Impact -- 5.12 Paralithodes camtschaticus (Tilesius, 1815), Red King Crab -- 5.12.1 Distribution -- 5.12.2 Habitat -- 5.12.3 Biology -- 5.12.4 Impact -- 5.13 Percnon gibbesi (H. Milne Edwards, 1853), Sally Lightfoot -- 5.13.1 Distribution -- 5.13.2 Habitat -- 5.13.3 Biology -- 5.13.4 Impact -- 5.14 Petrolisthes armatus (Gibbes, 1850), Green Porcelain Crab -- 5.14.1 Distribution -- 5.14.2 Habitat -- 5.14.3 Biology -- 5.14.4 Impact -- 5.15 Portunus (Portunus) pelagicus (Linnaeus, 1758), Blue Swimming Crab -- 5.15.1 Distribution -- 5.15.2 Habitat -- 5.15.3 Biology -- 5.15.4 Impact -- 5.16 Pyromaia tuberculata (Lockington, 1877), Spider Crab -- 5.16.1 Distribution -- 5.16.2 Habitat -- 5.16.3 Biology -- 5.16.4 Impact -- 5.17 Rhithropanopeus harrisii (Gould, 1841), Dwarf Crab, Harris Mud Crab -- 5.17.1 Distribution -- 5.17.2 Habitat -- 5.17.3 Biology -- 5.17.4 Impact -- 5.17.5 Management -- 5.18 Scylla serrata (Forskål, 1775), Mangrove Crab -- 5.18.1 Distribution -- 5.18.2 Invasion History -- 5.18.3 Habitat -- 5.18.4 Biology -- 5.18.5 Impact -- 6 Life History Trends and Body Size of Alien Crabs -- 7 Discussion -- 7.1 Regional Observations -- 7.2 Dominant Alien Brachyuran Groups (Fig. 10). , 7.3 Invasion Dynamics of Alien Brachyurans -- 7.4 Alien Crab Fisheries -- 7.4.1 Cancer pagurus -- 7.4.2 Chionoecetes opilio -- 7.4.3 Eriocheir sinensis -- 7.4.4 Paralithodes camtschaticus -- 7.4.5 Portunus pelagicus -- 7.4.6 Scylla serrata -- 7.5 Role of Live Exports and the Aquarium Trade in the Spread of Alien Crabs -- 7.6 Pest Management Options for Alien Brachyuran Crabs -- 8 Summary -- References -- The Global Spread of the Chinese Mitten Crab Eriocheir sinensis -- 1 Introduction -- 2 Life History and Physiology -- 3 Routes of Introduction and Capacity to Spread -- 4 The Chinese Mitten Crab in Continental Europe -- 5 Introduction to the UK -- 6 Introduction to West Coast USA -- 7 Recent Introductions and Rate of Spread -- 8 Economic Importance and Transmission of Human Pathogens -- 9 Riparian Degradation -- 10 The Future -- References -- The Japanese Skeleton Shrimp Caprella mutica (Crustacea, Amphipoda): A Global Invader of Coastal Waters -- 1 Introduction -- 2 Biology and Ecology of Caprella mutica -- 2.1 Morphology -- 2.2 Life History and Seasonal Population Dynamics -- 2.3 Habitat Preference -- 2.4 Environmental Tolerance Limits -- 2.5 Feeding -- 2.6 Intraspecific Behaviour and Aggression -- 2.7 Interspecific Interactions -- 3 Distribution and Dispersal -- 3.1 Current Distribution -- 3.2 Dispersal Vectors -- 3.3 Future Spread -- 4 Risk Assessment and Potential Management Options -- 5 Conclusions -- References -- Part III: Alien Faunas by Region -- Barnacle Invasions: Introduced, Cryptogenic, and Range Expanding Cirripedia of North and South America -- 1 Introduction -- 2 Vectors That Transport Barnacles Across and Between Oceans -- 3 Introduced and Cryptogenic Cirripedia of the Americas -- 4 Balanomorpha: Balanidae: Amphibalaninae -- 4.1 Status of Amphibalanus eburneus and Amphibalanus improvisus on the Atlantic Coast of South America. , 4.2 Amphibalanus amphitrite (Darwin, 1854) -- 4.3 Amphibalanus eburneus (Gould, 1841) -- 4.4 Amphibalanus improvisus (Darwin, 1854) -- 4.5 Amphibalanus reticulatus (Utinomi, 1967) -- 4.6 Amphibalanus subalbidus (Henry, 1974) -- 4.7 Fistulobalanus pallidus (Darwin, 1854) -- 5 Balanomorpha: Balanidae: Balaninae -- 5.1 Balanus glandula Darwin, 1854 -- 5.2 Balanus trigonus (Darwin, 1854) -- 5.3 Balanus calidus Pilsbry, 1916 and Balanus spongicola Brown, 1844 -- 6 Balanomorpha: Balanidae: Megabalaninae -- 6.1 Megabalanus coccopoma (Darwin, 1854) -- 6.2 Megabalanus tintinnabulum (Linnaeus, 1758) -- 7 Balanomorpha: Balanidae: Archaeobalanidae -- 7.1 Striatobalanus amaryllis (Darwin, 1854) -- 8 Rhizocephala: Sacculinidae -- 8.1 Loxothylacus panopaei (Gissler, 1884) -- 9 Intracontinental Range Expansions -- 9.1 Balanidae: Amphibalanus subalbidus (Henry, 1974) -- 9.2 Chthamalidae: Chthamalus fragilis Darwin, 1854 -- 9.3 Archaeobalanidae: Semibalanus balanoides (Linnaeus, 1758) -- 9.4 Tetraclitidae: Tetraclita rubescens (Darwin, 1854) -- 10 Balanidae Species Removed from Further Consideration -- 10.1 Paraconcavus pacificus (Pilsbry, 1916) -- 10.2 Balanus crenatus Bruguière, 1789 -- 11 Discussion -- 11.1 Temporal Patterns -- 11.2 Temporal Patterns: Post-Discovery Spreading -- 11.3 Temporal-Geographic Patterns -- 11.4 Geographic Patterns: Diversity and Origins -- 11.5 Geographic Patterns: Regional Diversity of Invaders -- 11.6 Galapagos Islands -- 11.7 The Panama Canal -- 11.8 Future Invasions -- References -- Marine Crustacean Invasions in North America: A Synthesis of Historical Records and Documented Impacts -- 1 Introduction -- 2 Taxonomic and Geographic Distribution of Non-native Crustaceans -- 2.1 Number of Species by Coast -- 2.2 Salinity Distribution of Species by Coast -- 2.3 Taxonomic Distribution by Coast -- 2.4 Native Region by Coast. , 3 Impacts of Non-native Crustaceans -- 3.1 Impact Type -- 3.2 Information Type and Effect Magnitude -- 3.3 Certainty -- 4 Conclusions -- Appendix 1 -- Appendix 2 -- Appendix 3 -- References -- Alien Decapod Crustaceans in the Southwestern Atlantic Ocean -- 1 Introduction -- 2 Established Alien Decapods -- 2.1 Charybdis hellerii (A. Milne-Edwards, 1867) (Fig. 1b) -- 2.2 Eurypanopeus depressus (Smith, 1869) -- 2.3 Palaemon macrodactylus Rathbun, 1902 -- 2.4 Pyromaia tuberculata (Lockington, 1877) (Fig. 2a) -- 2.5 Rhithropanopeus harrisii (Gould, 1841) (Fig. 2b) -- 3 Penaeid Shrimp Farming -- 3.1 Marsupenaeus japonicus (Bate, 1888) -- 3.2 Penaeus monodon (Fabricius, 1798) -- 3.3 Fenneropenaeus penicillatus (Alcock, 1905) -- 3.4 Litopenaeus stylirostris (Stimpson, 1874) -- 3.5 Litopenaeus vannamei (Boone, 1931) -- 4 Discussion -- 4.1 Taxonomic Resolution and Patterns of Diversity and Geographic Distribution -- 4.2 Detection, Regulations and Management -- References -- The Alien and Cryptogenic Marine Crustaceans of South Africa -- 1 Introduction -- 2 Inventory -- 3 Temporal Trends -- 4 Biogeographic Patterns -- 5 Main Pathways -- 5.1 Wood Boring -- 5.2 Dry Ballast -- 5.3 Fouling -- 5.4 Ballast Water -- 5.5 Aquaculture -- 6 Economic and Ecological Impacts -- 7 Future Trends -- References -- The Snow Crab, Chionoecetes opilio (Decapoda, Majoidea, Oregoniidae) in the Barents Sea -- 1 Introduction -- 2 The Barents Sea: Short Description -- 3 Distribution of Snow Crab in the Barents Sea -- 4 Size Distribution -- 5 Reproductive Characteristics -- 6 Predators -- 7 Diet -- 8 Genetics -- 9 Discussion -- References -- Alien Malacostracan Crustaceans in the Eastern Baltic Sea: Pathways and Consequences -- 1 Introduction -- 2 The Study Area -- 3 Invasion History of Crustaceans in the Gulf of Finland, Curonian and Vistula Lagoons -- 4 Amphipods -- 5 Mysids. , 6 Isopods.
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  • 2
    Type of Medium: Book
    Pages: 146 S
    Series Statement: ICES cooperative research report 224
    Language: English
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  • 3
    Book
    Book
    Washington, D.C. [u.a.] : Island Pr.
    Keywords: Biological invasions ; Nonindigenous pests ; Biodiversity conservation ; Nonindigenous pests Control ; Biological invasions ; Biological invasions Management ; Bibliografie ; Invasive Art ; Invasion ; Schädling ; Artenschutz
    Type of Medium: Book
    Pages: XIII, 518 S , graph. Darst., Kt
    ISBN: 1559639024 , 1559639032
    DDC: 577/.18
    RVK:
    Language: English
    Note: Includes bibliographical references and index
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  • 4
    Publication Date: 2024-03-05
    Description: Underlying established alien species lists for three recipeint regions: Great Lakes-St. Lawrence River (GLSL), North and Baltic Seas (NBS), and Chesapeake Bay (CB). Each species entry is recorded against its taxonomic grouping and geographic origin.
    Keywords: Class; Kingdom; Ocean and sea region; Origin; Phylum; Species
    Type: Dataset
    Format: text/tab-separated-values, 1956 data points
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  • 5
    Publication Date: 2024-03-05
    Description: A comprehensive dataset of non-native species (NNS) was assembled by combining the SInAS database of alien species occurrences (Seebens, 2021) with several other publicly available databases and NNS lists to examine NNS diversity globally (Bailey et al., 2020; Campbell et al., 2016; Carlton & Eldredge, 2009; Casties et al., 2016; Eldredge & Carlton, 2015; Hewitt et al., 2002, 2004; Lambert, 2002; Meyer, 2000; NEMESIS, 2017, 2020; Paulay et al., 2002; Richardson et al., 2020; Schwindt et al., 2020; Sturtevant et al., 2019; U.S. Geological Survey, 2017; Wonham & Carlton, 2005) to examine NNS diversity globally. The SInAS_AlienSpeciesDB_2.4.1 file was used as the base file for our dataset. Species without assignment of invaded country/region were removed from the dataset. Then, species assigned only as CASUAL and ABSENT in the columns degreeOfEstablishment (N) and occurrenceStatus (L), respectively, were also removed due to their undetermined non-native establishment status in those particular regions (Groom et al., 2019). Following, species from other publicly available databases and NNS lists that had not been listed for particular region/s in the SInAS database were added to the file. The species that were both native and NNS within a continent were retained in the dataset. Accordingly, the dataset consisted 36 822 species established outside of their native regions, out of which 36 326 came from Seebens (2021) and 496 species from other databases and NNS lists. Binominal scientific names, phylum, class, and family levels were assigned to each species based on the SInAS_AlienSpeciesDB_2.4.1_FullTaxaList file that was originally determined following Global Biodiversity Information Facility (GBIF). When a species was not automatically assigned to binominal scientific name and/or taxonomic level, an additional manual search of GBIF, World Register of Marine Species (WoRMS) and a general internet search engine was conducted in June and July 2022, and September 2023. Also, to examine NNS diversity among different habitats (i.e., terrestrial, freshwater, and marine), we assigned one or more habitats for each species based on the Step2_StandardTerms_GRIIS file; habitat data in the Step2_StandardTerms_GRIIS file originated from the Global Register of Introduced and Invasive Species (GRIIS). Again, if habitat(s) was(were) not automatically assigned to a species, an additional manual search of WoRMS and a general internet search engine was conducted from July to September 2022. We emphasize that due to the great number of species in our dataset and changing information availability over time, there is a possibility that we did not list all potential habitats for all species. Brackish habitats were defined as marine based on the Venice System (1958). Regions were assigned based on the geographic continental definitions (i.e., North America, South America, Europe, Africa, Asia, and Australia), with Pacific islands as a separate region due to their unclear/undefined continental affiliations (National Geographic Society, 2022). Finally, global estimated biodiversity (i.e., numbers of species per taxonomic group) of each particular phylum, class, and family was obtained from the GBIF in October 2022 (GBIF, 2022).
    Keywords: Area/locality; Class; Code; Family; Habitat; Identification; Phylum; Reference/source; Scientific name; Taxon/taxa
    Type: Dataset
    Format: text/tab-separated-values, 664480 data points
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  • 6
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Ecology, Evolution, and Systematics 30 (1999), S. 515-538 
    ISSN: 0066-4162
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Ecology, Evolution, and Systematics 31 (2000), S. 481-531 
    ISSN: 0066-4162
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Notes: Abstract Biological invasions of marine habitats have been common, and many patterns emerge from the existing literature. In North America, we identify 298 nonindigenous species (NIS) of invertebrates and algae that are established in marine and estuarine waters, generating many "apparent patterns" of invasion: (a) The rate of reported invasions has increased exponentially over the past 200 years; (b) Most NIS are crustaceans and molluscs, while NIS in taxonomic groups dominated by small organisms are rare; (c) Most invasions have resulted from shipping; (d) More NIS are present along the Pacific coast than the Atlantic and Gulf coasts; (e) Native and source regions of NIS differ among coasts, corresponding to trade patterns. The validity of these apparent patterns remains to be tested, because strong bias exists in the data. Overall, the emergent patterns reflect interactive effects of propagule supply, invasion resistance, and sampling bias. Understanding the relative contribution of each component remains a major challenge for invasion ecology and requires standardized, quantitative measures in space and time that we now lack.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Biological invasions 1 (1999), S. 1-1 
    ISSN: 1573-1464
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-1464
    Keywords: Atlantic ; ballast water ; Chesapeake Bay ; exotic species ; North America ; physiological tolerance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The relationships between invasion pressure, post-transport inoculant survival, and regional susceptibility to invasion are poorly understood. In marine ecosystems, the movement and release of ballast water from ocean-going ships provides a model system by which to examine the interplay among these factors. One of the largest estuaries in North America, the Chesapeake Bay, receives tremendous amounts of foreign ballast water annually and thus should be at high invasion risk. To date, however, few introductions in Chesapeake Bay have been attributed to ballast release. To understand better the dynamics of this invasion process, we (1) characterized and quantified the biota arriving to Chesapeake Bay in foreign ballast water, (2) compared temperatures and salinities of ballast water and harbor water in upper Chesapeake Bay, and (3) tested experimentally survival of organisms collected from ballast water in temperatures and salinities characteristic of the region. From 1993 to 1994, we sampled planktonic and benthic organisms from 60 foreign vessels arriving to Chesapeake Bay. Our data show that the estuary is being inoculated by a diverse assemblage of aquatic organisms from around the world. Furthermore, the short transit time (≤15 d) for most vessels ensured that substantial numbers of larval and post-larval organisms were being deballasted alive. Most of the ballast water discharged into the upper Chesapeake Bay, however, was significantly higher in salinity (〉20‰) than that of the receiving harbor. In laboratory tolerance experiments, ballast water organisms perished under such conditions. Thus, a mismatch in physical conditions between donor and receiver regions may explain the dearth of invasions in the upper Bay. It is likely that the lower Chesapeake Bay, which is more saline, remains at higher risk to ballast water invasion. Recognition of such intraregional differences should allow more focused predictions for monitoring and management.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2022-10-27
    Description: Author Posting. © Ecological Society of America, 2019. This article is posted here by permission of Ecological Society of America for personal use, not for redistribution. The definitive version was published in Ecology (2019): e02863, doi:10.1002/ecy.2863.
    Description: In 2014, a DNA‐based phylogenetic study confirming the paraphyly of the grass subtribe Sporobolinae proposed the creation of a large monophyletic genus Sporobolus, including (among others) species previously included in the genera Spartina, Calamovilfa, and Sporobolus. Spartina species have contributed substantially (and continue contributing) to our knowledge in multiple disciplines, including ecology, evolutionary biology, molecular biology, biogeography, experimental ecology, biological invasions, environmental management, restoration ecology, history, economics, and sociology. There is no rationale so compelling to subsume the name Spartina as a subgenus that could rival the striking, global iconic history and use of the name Spartina for over 200 yr. We do not agree with the subjective arguments underlying the proposal to change Spartina to Sporobolus. We understand the importance of both the objective phylogenetic insights and of the subjective formalized nomenclature and hope that by opening this debate we will encourage positive feedback that will strengthen taxonomic decisions with an interdisciplinary perspective. We consider that the strongly distinct, monophyletic clade Spartina should simply and efficiently be treated as the genus Spartina.
    Description: We are grateful to the many colleagues, students and eight anonymous expert taxonomists from Argentina, United States, Spain, UK, and Uruguay for sharing their opinions, perspectives, and ideas, improving our reasoning and encouraging us to initiate this debate. The authors’ positions are personal, and do not necessarily reflect the organizations or networks they represent or with which they are affiliated. We are also deeply grateful to two anonymous reviewers as well as to the Editor‐in‐Chief Don Strong who supplied excellent insight that truly improved our work.
    Keywords: Botanical nomenclature ; Coastal ecology ; Cordgrass ; Integrative analysis ; Interdisciplinary decisions ; Salt marsh
    Repository Name: Woods Hole Open Access Server
    Type: Article
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