Pathogens of Dikerogammarus Haemobaphes Regulate Host Activity and Survival, but Also Threaten Native Amphipod Populations in the UK
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The Killer Shrimp, Dikerogammarus Villosus (Sowinsky, 1894), Is Spreading in Italy
Aquatic Invasions (2010) Volume 5, Issue 2: 211-214 This is an Open Access article; doi: 10.3391/ai.2010.5.2.14 Open Access © 2010 The Author(s). Journal compilation © 2010 REABIC Short communication The killer shrimp, Dikerogammarus villosus (Sowinsky, 1894), is spreading in Italy Elena Tricarico, Giuseppe Mazza, Gabriele Orioli, Claudia Rossano, Felicita Scapini and Francesca Gherardi* Dipartimento di Biologia Evoluzionistica “Leo Pardi”, Università di Firenze, via Romana 17, 50125 Firenze, Italy E-mail: [email protected] (ET), [email protected] (GM), [email protected] (GO), [email protected] (CR), [email protected] (FS), [email protected] (FG) * Corresponding author Received: 23 November 2009 / Accepted: 11 January 2010 / Published online: 21 January 2009 Abstract In 2008, the killer shrimp, Dikerogammarus villosus, native to the Ponto-Caspian region, was found for the first time in Central Italy, in Bilancino, an artificial lake situated in the watershed of the River Arno (Tuscany). This new record shows that this species’ range is expanding in Italy. It is thus imperative to identify the pathways and vectors of spread of this species in order to halt this invasion process. Key words: Dikerogammarus villosus, inland waters, Italy Because of its predatory voracity and aggressive Devin et al. 2003; Brooks et al. 2009) and adapts behaviour, Dikerogammarus villosus (Sowinsky, to several types of substrate (Devin et al. 2003), 1894) is called the ‘‘killer shrimp’’. It is a favoured in this by its polymorphic pigmentation crustacean amphipod native to the Ponto-Caspian (Devin et al. 2004a). Its aggressive behaviour region. After the opening of the Danube-Main- and voracity cause the replacement of indigenous Rhine canal in 1992, as the result of both natural gammarids (Dick and Platvoet 2000; Van Riel et expansion and transportation in ballast waters al. -
Crustacea-Arthropoda) Fauna of Sinop and Samsun and Their Ecology
J. Black Sea/Mediterranean Environment Vol. 15: 47- 60 (2009) Freshwater and brackish water Malacostraca (Crustacea-Arthropoda) fauna of Sinop and Samsun and their ecology Sinop ve Samsun illeri tatlısu ve acısu Malacostraca (Crustacea-Arthropoda) faunası ve ekolojileri Mehmet Akbulut1*, M. Ruşen Ustaoğlu2, Ekrem Şanver Çelik1 1 Çanakkale Onsekiz Mart University, Fisheries Faculty, Çanakkale-Turkey 2 Ege University, Fisheries Faculty, Izmir-Turkey Abstract Malacostraca fauna collected from freshwater and brackishwater in Sinop and Samsun were studied from 181 stations between February 1999 and September 2000. 19 species and 4 subspecies belonging to 15 genuses were found in 134 stations. In total, 23 taxon were found: 11 Amphipoda, 6 Decapoda, 4 Isopoda, and 2 Mysidacea. Limnomysis benedeni is the first time in Turkish Mysidacea fauna. In this work at the first time recorded group are Gammarus pulex pulex, Gammarus aequicauda, Gammarus uludagi, Gammarus komareki, Gammarus longipedis, Gammarus balcanicus, Echinogammarus ischnus, Orchestia stephenseni Paramysis kosswigi, Idotea baltica basteri, Idotea hectica, Sphaeroma serratum, Palaemon adspersus, Crangon crangon, Potamon ibericum tauricum and Carcinus aestuarii in the studied area. Potamon ibericum tauricum is the most encountered and widespread species. Key words: Freshwater, brackish water, Malacostraca, Sinop, Samsun, Turkey Introduction The Malacostraca is the largest subgroup of crustaceans and includes the decapods such as crabs, mole crabs, lobsters, true shrimps and the stomatopods or mantis shrimps. There are more than 22,000 taxa in this group representing two third of all crustacean species and contains all the larger forms. *Corresponding author: [email protected] 47 Malacostracans play an important role in aquatic ecosystems and therefore their conservation is important. -
A Review of Potential Methods to Control and Eradicate the Invasive Gammarid, Dikerogammarus Villosus from UK Waters
Cefas contract report C5525 A review of potential methods to control and eradicate the invasive gammarid, Dikerogammarus villosus from UK waters Paul Stebbing, Stephen Irving, Grant Stentiford and Nicola Mitchard For Defra, Protected Species and Non-native Species Policy Group Commercial in confidence Executive Summary The killer shrimp, Dikerogammarus villosus (Dv) is a large gammarid of Ponto-Caspian origin Dv has invaded and spread over much of mainland Europe where it has out-competed a number of native species. Dv was discovered at Grafham Water, Cambridgeshire, England, in September 2010 and subsequently in Wales in Cardiff Bay and Eglwys Nunydd near Port Talbot. In early 2012 it was found in the Norfolk Broads, the full extent of its distribution in the area is still being determined. The main objective of this work was to review the potential approaches for the control/eradication of invasive Dv populations in the UK. The approaches reviewed include physical removal (e.g. trapping), physical control (e.g. drainage, barriers), biological control (e.g. predation, disease), autocides (e.g. male sterilization and pheromone control) and biocides (the use of chemical pesticides). It should be noted that there have been no specific studies looking at the control and/or eradication of this particular species. The examples presented within this study are therefore primarily related to control of other invasive/pest species or are speculative. Recommendation made and potential applications of techniques are therefore based on expert opinion, but are limited by a relative lack of understanding of the basic life history of D. villosus within its invasive range. -
Influence of Intraspecific Competition and Effects on Intermediate Host
Dianne et al. Parasites & Vectors 2012, 5:166 http://www.parasitesandvectors.com/content/5/1/166 RESEARCH Open Access Larval size in acanthocephalan parasites: Influence of intraspecific competition and effects on intermediate host behavioural changes Lucile Dianne1*, Loïc Bollache1, Clément Lagrue1,2, Nathalie Franceschi1 and Thierry Rigaud1 Abstract Background: Parasites often face a trade-off between exploitation of host resources and transmission probabilities to the next host. In helminths, larval growth, a major component of adult parasite fitness, is linked to exploitation of intermediate host resources and is influenced by the presence of co-infecting conspecifics. In manipulative parasites, larval growth strategy could also interact with their ability to alter intermediate host phenotype and influence parasite transmission. Methods: We used experimental infections of Gammarus pulex by Pomphorhynchus laevis (Acanthocephala), to investigate larval size effects on host behavioural manipulation among different parasite sibships and various degrees of intra-host competition. Results: Intra-host competition reduced mean P. laevis cystacanth size, but the largest cystacanth within a host always reached the same size. Therefore, all co-infecting parasites did not equally suffer from intraspecific competition. Under no intra-host competition (1 parasite per host), larval size was positively correlated with host phototaxis. At higher infection intensities, this relationship disappeared, possibly because of strong competition for host resources, -
Cucumispora Ornata N. Sp. (Fungi: Microsporidia) Infecting Invasive 1 ‘Demon Shrimp’
This is a repository copy of Cucumispora ornata n. sp. (Fungi: Microsporidia) infecting invasive 1 ‘demon shrimp’. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/85921/ Version: Accepted Version Article: Bojko, J, Dunn, A, Stebbing, PD et al. (3 more authors) (2015) Cucumispora ornata n. sp. (Fungi: Microsporidia) infecting invasive 1 ‘demon shrimp’. Journal of Invertebrate Pathology, 128. 22 - 30. ISSN 0022-2011 https://doi.org/10.1016/j.jip.2015.04.005 © 2015, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ *Manuscript Click here to view linked References 1 Cucumispora ornata n. -
Dikerogammarus Villosus)
Management of Biological Invasions (2018) Volume 9, Issue 2: 101–113 DOI: https://doi.org/10.3391/mbi.2018.9.2.04 Open Access © 2018 The Author(s). Journal compilation © 2018 REABIC Research Article A preliminary investigation into biosecurity treatments to manage the invasive killer shrimp (Dikerogammarus villosus) Marion Sebire*, Georgina Rimmer, Ruth Hicks, Sarah-Jane Parker and Paul D. Stebbing Centre for Environment, Fisheries and Aquaculture Science (Cefas), Weymouth, DT4 8UB, UK Author e-mails: [email protected] (MS), [email protected] (GR), [email protected] (RH), [email protected] (SJP), [email protected] (PDS) *Corresponding author Received: 11 April 2017 / Accepted: 18 December 2017 / Published online: 4 February 2018 Handling editor: Calum MacNeil Abstract Following the detection of the invasive killer shrimp, Dikerogammarus villosus (Dv) at two sites in the UK in September 2010, an effective biosecurity system is required to prevent further spread. This study investigated the application of several treatments as potential biosecurity measures with a view to their application on Dv-infected fomites. For each treatment, adult Dv were submerged for 15 minutes at different concentrations to determine the maximum lethal concentration, and for each effective treatment for different times to assess a minimal lethal time (LT50). Sodium hypochlorite (50,000 mg/Lmg/L), FAM30® (6 ml/l), Virkon S® (1% solution) and water at high temperature (45 °C) were found to cause 100% mortality within 15-min exposure, while carbonated water caused narcosis in 100% of animals within a few seconds of exposure. -
Molecular Data Suggest Multiple Origins and Diversification Times Of
www.nature.com/scientificreports OPEN Molecular data suggest multiple origins and diversifcation times of freshwater gammarids on the Aegean archipelago Kamil Hupało1,3*, Ioannis Karaouzas2, Tomasz Mamos1,4 & Michał Grabowski1 Our main aim was to investigate the diversity, origin and biogeographical afliations of freshwater gammarids inhabiting the Aegean Islands by analysing their mtDNA and nDNA polymorphism, thereby providing the frst insight into the phylogeography of the Aegean freshwater gammarid fauna. The study material was collected from Samothraki, Lesbos, Skyros, Evia, Andros, Tinos and Serifos islands as well as from mainland Greece. The DNA extracted was used for amplifcation of two mitochondrial (COI and 16S) and two nuclear markers (28S and EF1-alpha). The multimarker time- calibrated phylogeny supports multiple origins and diferent diversifcation times for the studied taxa. Three of the sampled insular populations most probably represent new, distinct species as supported by all the delimitation methods used in our study. Our results show that the evolution of freshwater taxa is associated with the geological history of the Aegean Basin. The biogeographic afliations of the studied insular taxa indicate its continental origin, as well as the importance of the land fragmentation and the historical land connections of the islands. Based on the fndings, we highlight the importance of studying insular freshwater biota to better understand diversifcation mechanisms in fresh waters as well as the origin of studied Aegean freshwater taxa. Te Mediterranean islands are considered natural laboratories of evolution, exhibiting high levels of diversity and endemism, making them a vital part of one of the globally most precious biodiversity hotspots and a model system for studies of biogeography and evolution1–4. -
Continental-Scale Patterns of Hyper-Cryptic Diversity
www.nature.com/scientificreports OPEN Continental‑scale patterns of hyper‑cryptic diversity within the freshwater model taxon Gammarus fossarum (Crustacea, Amphipoda) Remi Wattier1*, Tomasz Mamos2,3, Denis Copilaş‑Ciocianu4, Mišel Jelić5, Anthony Ollivier1, Arnaud Chaumot6, Michael Danger7, Vincent Felten7, Christophe Piscart8, Krešimir Žganec9, Tomasz Rewicz2,10, Anna Wysocka11, Thierry Rigaud1 & Michał Grabowski2* Traditional morphological diagnoses of taxonomic status remain widely used while an increasing number of studies show that one morphospecies might hide cryptic diversity, i.e. lineages with unexpectedly high molecular divergence. This hidden diversity can reach even tens of lineages, i.e. hyper cryptic diversity. Even well‑studied model‑organisms may exhibit overlooked cryptic diversity. Such is the case of the freshwater crustacean amphipod model taxon Gammarus fossarum. It is extensively used in both applied and basic types of research, including biodiversity assessments, ecotoxicology and evolutionary ecology. Based on COI barcodes of 4926 individuals from 498 sampling sites in 19 European countries, the present paper shows (1) hyper cryptic diversity, ranging from 84 to 152 Molecular Operational Taxonomic Units, (2) ancient diversifcation starting already 26 Mya in the Oligocene, and (3) high level of lineage syntopy. Even if hyper cryptic diversity was already documented in G. fossarum, the present study increases its extent fourfold, providing a frst continental‑scale insight into its geographical distribution and establishes several diversifcation hotspots, notably south‑eastern and central Europe. The challenges of recording hyper cryptic diversity in the future are also discussed. In many areas of biology, including biodiversity assessments, eco-toxicology, environmental monitoring, and behavioural ecology, the species status of the studied organisms relies only on a traditional morphological defnition1. -
Disease of Aquatic Organisms 136:121
Vol. 136: 121–132, 2019 DISEASES OF AQUATIC ORGANISMS Published online October 2 https://doi.org/10.3354/dao03355 Dis Aquat Org Contribution to DAO Special 8 ‘Amphipod disease: model systems, invasions and systematics’ OPENPEN ACCESSCCESS REVIEW Amphipod parasites may bias results of ecotoxicological research Daniel Grabner1,*, Bernd Sures1,2 1Aquatic Ecology and Centre for Water and Environmental Research, University of Duisburg-Essen, 45141 Essen, Germany 2Department of Zoology, University of Johannesburg, PO Box 524, Auckland Park 2006, Johannesburg, South Africa ABSTRACT: Amphipods are commonly used test organisms in ecotoxicological studies. Neverthe- less, their naturally occurring parasites have mostly been neglected in these investigations, even though several groups of parasites can have a multitude of effects, e.g. on host survival, physiol- ogy, or behavior. In the present review, we summarize the knowledge on the effects of Micro - sporidia and Acanthocephala, 2 common and abundant groups of parasites in amphipods, on the outcome of ecotoxicological studies. Parasites can have significant effects on toxicological end- points (e.g. mortality, biochemical markers) that are unexpected in some cases (e.g. down-regula- tion of heat shock protein 70 response in infected individuals). Therefore, parasites can bias the interpretation of results, for example if populations with different parasite profiles are compared, or if toxicological effects are masked by parasite effects. With the present review, we would like to encourage ecotoxicologists to consider parasites as an additional factor if field-collected test organisms are analyzed for biomarkers. Additionally, we suggest intensification of research activ- ities on the effects of parasites in amphipods in connection with other stressors to disentangle par- asite and pollution effects and to improve our understanding of parasite effects in this host taxon. -
Dikerogammarus Villosus) Ecological Risk Screening Summary
Killer Shrimp (Dikerogammarus villosus) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, September 2014 Revised, June 2015 and September 2016 Web Version, 09/14/2017 Photo: S. Giesen, NOAA Great Lakes Environmental Research Laboratory 1 Native Range, and Status in the United States Native Range From CABI (2015): “The amphipod is native to the lower reaches of the rivers discharging into the Black Sea and Caspian Sea (Dedju, 1967; Nesemann et al., 1995; Vaate et al., 2002).” Status in the United States From Dettloff et al. (2015): “Not established in North America” Means of Introductions in the United States From Dettloff et al. (2015): “Due to its high tolerance to varying levels of salinity, oxygen and temperature, D. villosus is considered a highly likely candidate for introduction to the Great Lakes through ballast water 1 transport from European ships ([Bruijs] et al. 2001, Dick and Platvoet 2001, Dick et al. 2002, Grigorovich et al. 2002, MacIsaac 1999, Mills et al. 1993, Ricciardi and Rasmussen 1998).” Remarks From Dettloff et al. (2015): “Dikerogammarus bispinosus was originally described as a subspecies of D. villosus (Martynov 1925), but a more recent genetic study by Müller et al. (2002) demonstrated that these two taxa should be considered to be separate species.” “Obesogammarus aralensis, listed by Grigorovich et al 2003 as having a high probability of invading the Great Lakes, is most likely a synonym for Dikerogammarus villosus.” 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing From CABI (2015): “Domain: Eukaryota Kingdom: Metazoa Phylum: Arthropoda Subphylum: Crustacea Class: Malacostraca Subclass: Eumalacostraca Order: Amphipoda Suborder: Gammaridea Family: Gammaridae Genus: Dikerogammarus Species: Dikerogammarus villosus Dikerogammarus villosus Sowinsky 1894 is a valid amphipod species.” Size, Weight, and Age Range From CABI (2015): “The maximum reported body length is 30 mm.” From Dettloff et al. -
Benthic Invertebrate Fauna, Small Streams
Benthic Invertebrate Fauna, Small Streams J Bruce Wallace, University of Georgia, Athens, GA, USA S L Eggert, USDA Forest Service, Northern Research Station, Grand Rapids, MN, USA ã 2009 Elsevier Inc. All rights reserved. Introduction invertebrate taxa have been recorded in a mountain stream on Bougainville Island, Papua New Guinea. Small streams (first- through third-order streams) Incredibly, there are many headwater invertebrate spe- make up >98% of the total number of stream seg- cies that remain undescribed in both isolated and popu- ments and >86% of stream length in many drainage lated regions of the world. networks. Small streams occur over a wide array of With the great diversity of foods available for con- climates, geology, and biomes, which influence tem- sumption by invertebrates (i.e., deposited and retained perature, hydrologic regimes, water chemistry, light, on substrates, or suspended in the water column), it is substrate, stream permanence, a basin’s terrestrial not surprising that invertebrates have evolved diverse plant cover, and food base of a given stream. Small morphobehavioral mechanisms for exploiting food streams are generally most abundant in the upper resources. Their diverse feeding behaviors have been reaches of a basin, but they can also be found through- lumped into a broad functional classification scheme, out the basin and may enter directly into larger rivers. which is based on mechanisms used by invertebrates to They have maximum interface with the terrestrial acquire foods. These functional groups are as follows: environment, and in most temperate and tropical cli- scrapers, animals adapted to graze or scrape materials mates they may receive large inputs of terrestrial, or (periphyton, or attached algae, fine particulate organic allochthonous, organic matter (e.g., leaves, wood) matter, and its associated microbiota) from mineral from the surrounding plant communities. -
Horizon Scan of Invasive Alien Species for the Island of Ireland
Management of Biological Invasions (2020) Volume 11, Issue 2: 155–177 CORRECTED PROOF Research Article Horizon scan of invasive alien species for the island of Ireland Frances E. Lucy1,*, Eithne Davis1,*, Roy Anderson2, Olaf Booy3, Ken Bradley4, J. Robert Britton5, Colin Byrne6, Joseph M. Caffrey7, Neil E. Coughlan8, Kate Crane8, Ross N. Cuthbert8, Jaimie T.A. Dick8, James W.E. Dickey8, Jeffrey Fisher9, Cathal Gallagher10, Simon Harrison11, Matthew Jebb12, Mark Johnson13, Colin Lawton13, Dave Lyons14, Tim Mackie4, Christine Maggs5, Ferdia Marnell14, Tom McLoughlin15, Dan Minchin16, Oonagh Monaghan15, Ian Montgomery8, Niall Moore3, Liam Morrison13, Rose Muir4, Brian Nelson14, Art Niven17, Colette O’Flynn18, Bruce Osborne19, Ruth M. O’Riordan11, Neil Reid8, Helen Roy20, Rory Sheehan1, Dorothy Stewart15, Monica Sullivan21, Paula Tierney22, Paula Treacy23, Elena Tricarico24 and Wayne Trodd15 1Centre for Environmental Research, Innovation and Sustainability, Dept. of Environmental Science, Institute of Technology, Ash Lane, Sligo, Ireland, 2Royal Entomological Society, Belfast, Northern Ireland, 3GB Non-native Species Secretariat, Sand Hutton, York, UK, 4Department of Agriculture, Environment and Rural Affairs, Dundonald House, Upper Newtownards Road, Ballymiscaw, Belfast, Northern Ireland, 5University of Bournemouth, Poole UK, 6Dept of Housing, Planning and Local Govt., Custom House, Dublin, Ireland, 7INVAS Biosecurity Ltd., 82 Lakelands Close, Stillorgan, Co Dublin, Ireland, 8Institute for Global Food Security, School of Biological Sciences,