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Why Some Metazoan Mucus Secretions are More Susceptible to Microbial Attack than Others

1979; University of Chicago Press; Volume: 114; Issue: 1 Linguagem: Inglês

10.1086/283460

1537-5323

Peter Calow,

Cephalopods and Marine Biology

Previous articleNext article No AccessNotes and CommentsWhy Some Metazoan Mucus Secretions are More Susceptible to Microbial Attack than OthersP. CalowP. Calow Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 114, Number 1Jul., 1979 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/283460 Views: 7Total views on this site Citations: 29Citations are reported from Crossref Copyright 1979 The University of ChicagoPDF download Crossref reports the following articles citing this article:Michael S. Bodri TURBELLARIANS, (Dec 2021): 129–150.https://doi.org/10.1002/9781119569831.ch7Maria Giovanna Parisi, Daniela Parrinello, Loredana Stabili, Matteo Cammarata Cnidarian Immunity and the Repertoire of Defense Mechanisms in Anthozoans, Biology 9, no.99 (Sep 2020): 283.https://doi.org/10.3390/biology9090283Loredana Stabili, Lucia Rizzo, Lorena Basso, Marinella Marzano, Bruno Fosso, Graziano Pesole, Stefano Piraino The Microbial Community Associated with Rhizostoma pulmo: Ecological Significance and Potential Consequences for Marine Organisms and Human Health, Marine Drugs 18, no.99 (Aug 2020): 437.https://doi.org/10.3390/md18090437Benjamin Wilden, Nabil Majdi, Ute Kuhlicke, Thomas R. Neu, Walter Traunspurger Flatworm mucus as the base of a food web, BMC Ecology 19, no.11 (Mar 2019).https://doi.org/10.1186/s12898-019-0231-2Lorena Basso, Lucia Rizzo, Marinella Marzano, Marianna Intranuovo, Bruno Fosso, Graziano Pesole, Stefano Piraino, Loredana Stabili Jellyfish summer outbreaks as bacterial vectors and potential hazards for marine animals and humans health? The case of Rhizostoma pulmo (Scyphozoa, Cnidaria), Science of The Total Environment 692 (Nov 2019): 305–318.https://doi.org/10.1016/j.scitotenv.2019.07.155Loredana Stabili, Margherita Licciano, Adriana Giangrande, Carmela Gerardi, Sandra Angelica De Pascali, Francesco Paolo Fanizzi First Insight on the Mucus of the Annelid Myxicola infundibulum (Polychaeta, Sabellidae) as a Potential Prospect for Drug Discovery, Marine Drugs 17, no.77 (Jul 2019): 396.https://doi.org/10.3390/md17070396Gary G. Martin, Abby K. Bailey, Seth Cohen, Yeraldi Loera, Anne M. Crooke, Stephanie Stamnes, Naomi Field, Zain Natha, Nisha Ramesh, Kasey Rose Morphology and function of the skin epithelium covering the giant keyhole limpet Megathura crenulata, Invertebrate Biology 137, no.22 (Jun 2018): 151–170.https://doi.org/10.1111/ivb.12213Loredana Stabili, Roberto Schirosi, Maria Parisi, Stefano Piraino, Matteo Cammarata The Mucus of Actinia equina (Anthozoa, Cnidaria): An Unexplored Resource for Potential Applicative Purposes, Marine Drugs 13, no.88 (Aug 2015): 5276–5296.https://doi.org/10.3390/md13085276Loredana Stabili, Roberto Schirosi, Margherita Licciano, Adriana Giangrande Role of Myxicola infundibulum (Polychaeta, Annelida) mucus: From bacterial control to nutritional home site, Journal of Experimental Marine Biology and Ecology 461 (Dec 2014): 344–349.https://doi.org/10.1016/j.jembe.2014.09.005Loredana Stabili, Adriana Giangrande, Graziano Pizzolante, Giorgia Caruso, Pietro Alifano Characterization of Vibrios Diversity in the Mucus of the Polychaete Myxicola infundibulum (Annellida, Polichaeta), Microbial Ecology 67, no.11 (Nov 2013): 186–194.https://doi.org/10.1007/s00248-013-0312-2KATHLEEN R. GORBACH, M. ERIC BENBOW, MOLLIE D. McINTOSH, ALBERT J. BURKY Dispersal and upstream migration of an amphidromous neritid snail: implications for restoring migratory pathways in tropical streams, Freshwater Biology 57, no.88 (Jun 2012): 1643–1657.https://doi.org/10.1111/j.1365-2427.2012.02826.xMEGUMU FUJIBAYASHI, WOO-SEOK SHIN, YUMI NAGAHAMA, YOSHIO AIKAWA, OSAMU NISHIMURA The effect of pedal mucus of pond snail, Bellamya chinensis on decomposition of organic matter in paddy field sediments, Japanese Journal of Water Treatment Biology 48, no.44 (Jan 2012): 141–144.https://doi.org/10.2521/jswtb.48.141Michael S. Bodri Turbellarians, (Oct 2011): 77–93.https://doi.org/10.1002/9780470960806.ch5Catherine Mouneyrac, Priscilla Leung, Kenneth Leung Cost of Tolerance, (Feb 2011): 265–297.https://doi.org/10.1201/b10519-15Michael S. Bodri Turbellarians, (Feb 2008): 53–64.https://doi.org/10.1002/9780470344606.ch4Franz Riemann, Elisabeth Helmke Symbiotic Relations of Sediment-Agglutinating Nematodes and Bacteria in Detrital Habitats: The Enzyme-Sharing Concept, Marine Ecology 23, no.22 (Jul 2002): 93–113.https://doi.org/10.1046/j.1439-0485.2002.02765.xMark S. Davies, S.J. Hawkins Mucus from Marine Molluscs, (Jan 1998): 1–71.https://doi.org/10.1016/S0065-2881(08)60210-2Alan D. Steinman Effects of Grazers on Freshwater Benthic Algae, (Jan 1996): 341–373.https://doi.org/10.1016/B978-012668450-6/50041-2Mark S. Davies, S.J. Hawkins, Hugh D. Jones Pedal mucus and its influence on the microbial food supply of two intertidal gastropods, Patella vulgata L. and Littorina littorea (L.), Journal of Experimental Marine Biology and Ecology 161, no.11 (Oct 1992): 57–77.https://doi.org/10.1016/0022-0981(92)90190-LMark S. Davies, Hugh D. Jones, S. J. Hawkins Physical factors affecting the fate of pedal mucus produced by the common limpet Patella vulgata, Journal of the Marine Biological Association of the United Kingdom 72, no.33 (May 2009): 633–643.https://doi.org/10.1017/S0025315400059403P. Calow Physiological costs of combating chemical toxicants: Ecological implications, Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 100, no.1-21-2 (Jan 1991): 3–6.https://doi.org/10.1016/0742-8413(91)90110-FAnne E. Hershey Snail populations in arctic lakes: competition mediated by predation?, Oecologia 82, no.11 (Jan 1990): 26–32.https://doi.org/10.1007/BF00318529P. CALOW Platyhelminthes and Rhynchocoela, with Special Reference to the Triclad Turbellarians, (Jan 1987): 121–158.https://doi.org/10.1016/B978-0-12-544791-1.50008-XDAVID M. LODGE Macrophyte-gastropod associations: observations and experiments on macrophyte choice by gastropods, Freshwater Biology 15, no.66 (Dec 1985): 695–708.https://doi.org/10.1111/j.1365-2427.1985.tb00243.x The feeding strategies of juvenile and adult Biomphalaria glabrata (Say) under simulated natural conditions and their relevance to ecological theory and snail control, Proceedings of the Royal Society of London. Series B. Biological Sciences 226, no.12431243 (Jan 1997): 177–209.https://doi.org/10.1098/rspb.1985.0090Valerie M. Connor, James F. Quinn Stimulation of Food Species Growth by Limpet Mucus, Science 225, no.46644664 (Aug 1984): 843–844.https://doi.org/10.1126/science.225.4664.843P. Calow, A. F. Davidson, A. S. Woollhead Life‐cycle and feeding strategies of freshwater triclads: a synthesis, Journal of Zoology 193, no.22 (Aug 2009): 215–237.https://doi.org/10.1111/j.1469-7998.1981.tb03441.xP. Calow Acquisition, (Jan 1981): 20–62.https://doi.org/10.1007/978-1-4757-0331-3_2P. CALOW FEEDING IN FRESHWATER TRICLADS - ADAPTATIONAL ASPECTS, (Jan 1980): 15–31.https://doi.org/10.1016/B978-0-08-025904-8.50005-5