Tetrodotoxin - Distribution and Accumulation in Aquatic Organisms, and Title Cases of Human Intoxication
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Environmental Risk Limits for Triphenyltin in Water
Environmental risk limits for triphenyltin in water RIVM report 601714018/2012 R. van Herwijnen | C.T.A. Moermond | P.L.A. van Vlaardingen | F.M.W. de Jong | E.M.J. Verbruggen National Institute for Public Health and the Environment P.O. Box 1 | 3720 BA Bilthoven www.rivm.com Environmental risk limits for triphenyltin in water RIVM Report 601714018/2012 RIVM Report 601714018 Colophon © RIVM 2012 Parts of this publication may be reproduced, provided acknowledgement is given to the 'National Institute for Public Health and the Environment', along with the title and year of publication. R. van Herwijnen C.T.A. Moermond P.L.A. van Vlaardingen F.M.W. de Jong E.M.J. Verbruggen Contact: René van Herwijnen Expertise Centre for Substances [email protected] This investigation has been performed by order and for the account of the Ministry of Infrastructure and the Environment, Directorate for Sustainability, within the framework of the project 'Chemical aspects of the Water Framework Directive and the Directive on Priority Substances'. Page 2 of 104 RIVM Report 601714018 Abstract Environmental risk limits for triphenyltin in water RIVM has, by order of the Ministry of Infrastructure and the Environment, derived environmental risk limits for triphenyltin. This was necessary because the current risk limts have not been derived according to the most recent methodology. Main uses of triphenyltin were for wood preservation and as antifouling on ships. The use as antifouling has been banned within Europe since 2003. The Dutch Steering Committee for Substances will set new standards on the basis of the scientific advisory values in this report. -
Taricha Rivularis) in California Presents Conservation Challenges Author(S): Sean B
Discovery of a New, Disjunct Population of a Narrowly Distributed Salamander (Taricha rivularis) in California Presents Conservation Challenges Author(s): Sean B. Reilly, Daniel M. Portik, Michelle S. Koo, and David B. Wake Source: Journal of Herpetology, 48(3):371-379. 2014. Published By: The Society for the Study of Amphibians and Reptiles DOI: http://dx.doi.org/10.1670/13-066 URL: http://www.bioone.org/doi/full/10.1670/13-066 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Journal of Herpetology, Vol. 48, No. 3, 371–379, 2014 Copyright 2014 Society for the Study of Amphibians and Reptiles Discovery of a New, Disjunct Population of a Narrowly Distributed Salamander (Taricha rivularis) in California Presents Conservation Challenges 1 SEAN B. REILLY, DANIEL M. PORTIK,MICHELLE S. KOO, AND DAVID B. WAKE Museum of Vertebrate Zoology and Department of Integrative Biology, University of California, 3101 Valley Life Sciences Building, Berkeley, California 94720 USA ABSTRACT. -
Assessing the Presence of Chitinases in the Digestive Tract and Their Relationship to Diet and Morphology in Freshwater Fish
Assessing the Presence of Chitinases in the Digestive Tract and their Relationship to Diet and Morphology in Freshwater Fish Word count: 25 157 Andy Vervaet Student number: 01000500 Supervisor: Prof. dr. Ir. Geert Janssens Supervisor: Dr. Arturo Muñoz Saravia A dissertation submitted to Ghent University in partial fulfilment of the requirements for the degree of Master of Veterinary Medicine Academic year: 2018 - 2019 Ghent University, its employees and/or students, give no warranty that the information provided in this thesis is accurate or exhaustive, nor that the content of this thesis will not constitute or result in any infringement of third-party rights. Ghent University, its employees and/or students do not accept any liability or responsibility for any use which may be made of the content or information given in the thesis, nor for any reliance which may be placed on any advice or information provided in this thesis. ACKNOWLEDGEMENTS Writing this work would not have been possible without all the guidance, help and motivation I received during the process. I offer my sincerest gratitude to all the people who played a role in finishing the thesis. First, I would like to thank both my promotors; prof. dr. ir. Geert Janssens and dr. Arturo Muñoz Saravia. For offering me the opportunity to work on this exciting subject and allowing me to get an invaluable experience of learning to work in challenging conditions abroad. Their guidance and expertise on different issues were integral to finishing this work. Secondly, I would like to thank all the people who helped me during certain parts of the study; the people at IDP-Pacu who made their lab facilities for me in Bolivia, Donna Vanhauteghem for helping me to process my samples, and Stefania Magnusdottir and Joanna Wolthuis of UMC Utrecht for performing the data analysis of the DI-MS samples. -
Monitoring Aquatic Amphibians and Invasive Species in the Mediterranean Coast Network, 2013 Project Report Santa Monica Mountains National Recreation Area
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science Monitoring Aquatic Amphibians and Invasive Species in the Mediterranean Coast Network, 2013 Project Report Santa Monica Mountains National Recreation Area Natural Resource Data Series NPS/MEDN/NRDS—2014/715 ON THE COVER California newt (Taricha torosa) Photograph by: National Park Service Monitoring Aquatic Amphibians and Invasive Species in the Mediterranean Coast Network, 2012 Project Report Santa Monica Mountains National Recreation Area Natural Resource Data Series NPS/MEDN/NRDS—2014/715 Kathleen Semple Delaney Seth P. D. Riley National Park Service 401 W. Hillcrest Dr. Thousand Oaks, CA 91360 October 2014 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 Data Series is intended for the timely release of basic data sets and data summaries. Care has been taken to assure accuracy of raw data values, but a thorough analysis and interpretation of the data has not been completed. Consequently, the initial analyses of data in this report are provisional and subject to change. All manuscripts in the series receive the appropriate level of peer review to ensure that the information is scientifically credible, technically accurate, appropriately written for the intended audience, and designed and published in a professional manner. -
OSTRACIIDAE Boxfishes by K
click for previous page 3948 Bony Fishes OSTRACIIDAE Boxfishes by K. Matsuura iagnostic characters: Small to medium-sized (to 40 cm) fishes; body almost completely encased Din a bony shell or carapace formed of enlarged, thickened scale plates, usually hexagonal in shape and firmly sutured to one another; no isolated bony plates on caudal peduncle. Carapace triangular, rectangular, or pentangular in cross-section, with openings for mouth, eyes, gill slits, pectoral, dorsal, and anal fins, and for the flexible caudal peduncle. Scale-plates often with surface granulations which are prolonged in some species into prominent carapace spines over eye or along ventrolateral or dorsal angles of body. Mouth small, terminal, with fleshy lips; teeth moderate, conical, usually less than 15 in each jaw. Gill opening a moderately short, vertical to oblique slit in front of pectoral-fin base. Spinous dorsal fin absent; most dorsal-, anal-, and pectoral-fin rays branched; caudal fin with 8 branched rays; pelvic fins absent. Lateral line inconspicuous. Colour: variable, with general ground colours of either brown, grey, or yellow, usually with darker or lighter spots, blotches, lines, and reticulations. carapace no bony plates on caudal peduncle 8 branched caudal-fin rays Habitat, biology, and fisheries: Slow-swimming, benthic-dwelling fishes occurring on rocky and coral reefs and over sand, weed, or sponge-covered bottoms to depths of 100 m. Feed on benthic invertebrates. Taken either by trawl, other types of nets, or traps. Several species considered excellent eating in southern Japan, although some species are reported to have toxic flesh and are also able to secrete a substance when distressed that is highly toxic, both to other fishes and themselves in enclosed areas such as holding tanks. -
Fishes Collected During the 2017 Marinegeo Assessment of Kāne
Journal of the Marine Fishes collected during the 2017 MarineGEO Biological Association of the ā ‘ ‘ ‘ United Kingdom assessment of K ne ohe Bay, O ahu, Hawai i 1 1 1,2 cambridge.org/mbi Lynne R. Parenti , Diane E. Pitassy , Zeehan Jaafar , Kirill Vinnikov3,4,5 , Niamh E. Redmond6 and Kathleen S. Cole1,3 1Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian Institution, PO Box 37012, MRC 159, Washington, DC 20013-7012, USA; 2Department of Biological Sciences, National University of Singapore, Original Article Singapore 117543, 14 Science Drive 4, Singapore; 3School of Life Sciences, University of Hawai‘iatMānoa, 2538 McCarthy Mall, Edmondson Hall 216, Honolulu, HI 96822, USA; 4Laboratory of Ecology and Evolutionary Biology of Cite this article: Parenti LR, Pitassy DE, Jaafar Aquatic Organisms, Far Eastern Federal University, 8 Sukhanova St., Vladivostok 690091, Russia; 5Laboratory of Z, Vinnikov K, Redmond NE, Cole KS (2020). 6 Fishes collected during the 2017 MarineGEO Genetics, National Scientific Center of Marine Biology, Vladivostok 690041, Russia and National Museum of assessment of Kāne‘ohe Bay, O‘ahu, Hawai‘i. Natural History, Smithsonian Institution DNA Barcode Network, Smithsonian Institution, PO Box 37012, MRC 183, Journal of the Marine Biological Association of Washington, DC 20013-7012, USA the United Kingdom 100,607–637. https:// doi.org/10.1017/S0025315420000417 Abstract Received: 6 January 2020 We report the results of a survey of the fishes of Kāne‘ohe Bay, O‘ahu, conducted in 2017 as Revised: 23 March 2020 part of the Smithsonian Institution MarineGEO Hawaii bioassessment. We recorded 109 spe- Accepted: 30 April 2020 cies in 43 families. -
Annotated Checklist of the Fish Species (Pisces) of La Réunion, Including a Red List of Threatened and Declining Species
Stuttgarter Beiträge zur Naturkunde A, Neue Serie 2: 1–168; Stuttgart, 30.IV.2009. 1 Annotated checklist of the fish species (Pisces) of La Réunion, including a Red List of threatened and declining species RONALD FR ICKE , THIE rr Y MULOCHAU , PA tr ICK DU R VILLE , PASCALE CHABANE T , Emm ANUEL TESSIE R & YVES LE T OU R NEU R Abstract An annotated checklist of the fish species of La Réunion (southwestern Indian Ocean) comprises a total of 984 species in 164 families (including 16 species which are not native). 65 species (plus 16 introduced) occur in fresh- water, with the Gobiidae as the largest freshwater fish family. 165 species (plus 16 introduced) live in transitional waters. In marine habitats, 965 species (plus two introduced) are found, with the Labridae, Serranidae and Gobiidae being the largest families; 56.7 % of these species live in shallow coral reefs, 33.7 % inside the fringing reef, 28.0 % in shallow rocky reefs, 16.8 % on sand bottoms, 14.0 % in deep reefs, 11.9 % on the reef flat, and 11.1 % in estuaries. 63 species are first records for Réunion. Zoogeographically, 65 % of the fish fauna have a widespread Indo-Pacific distribution, while only 2.6 % are Mascarene endemics, and 0.7 % Réunion endemics. The classification of the following species is changed in the present paper: Anguilla labiata (Peters, 1852) [pre- viously A. bengalensis labiata]; Microphis millepunctatus (Kaup, 1856) [previously M. brachyurus millepunctatus]; Epinephelus oceanicus (Lacepède, 1802) [previously E. fasciatus (non Forsskål in Niebuhr, 1775)]; Ostorhinchus fasciatus (White, 1790) [previously Apogon fasciatus]; Mulloidichthys auriflamma (Forsskål in Niebuhr, 1775) [previously Mulloidichthys vanicolensis (non Valenciennes in Cuvier & Valenciennes, 1831)]; Stegastes luteobrun- neus (Smith, 1960) [previously S. -
University of California, San Diego Global
UNIVERSITY OF CALIFORNIA, SAN DIEGO GLOBAL ASSESSMENT OF THE STATUS OF CORAL REEF HERBIVOROUS FISHES: EVIDENCE FOR FISHING EFFECTS A Thesis submitted in partial satisfaction of the requirements for the degree Master of Science in Biology by Clinton Brook Edwards Committee in charge: Professor Jennifer Smith, Chair Professor Jonathan Shurin, Co-Chair Professor Joshua Kohn Professor Stuart Sandin 2013 The Thesis of Clinton Brook Edwards is approved and it is acceptable in quality and form for publication on microfilm and electronically: _____________________________________________________________________ _____________________________________________________________________ _____________________________________________________________________ Co-Chair _____________________________________________________________________ Chair University of California, San Diego 2013 iii Dedication To my sister Katee, who never had the opportunity to grow old and define new dreams as old ones were reached. I will carry your purple spirit with me wherever I go. To my sister Shannon…nobody makes me more mad or proud!!!! I love you!! To Brandon…..my co-conspirator, brother and best friend. You taught me to be proud of being smart, to be bold in my opinions and to truly love people. Thank you. To Seamus, Nagy, Neil, Pete, Pat, Mikey B and Spence dog. Learning to surf with you guys has been one of the true honors of my life. To the madmen, Ed, Sean, Garth, Pig Dog and Theo. Not sure if thanking you guys is necessarily the most appropriate course of action but I am certain that I would not be here without you guys…. To my parents and Rozy…..this is as much your thesis as it is mine. iv Epigraph No man is an island, Entire of itself. -
Review of the Sharpnose Pufferfishes (Subfamily Canthigasterinae) of the Indo-Pacific
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Allen, Gerald R., and J. E. Randall, 1977. Review of the sharpnose pufferfishes (Subfamily Canthigasterinae) of the Indo-Pacific. Records of the Australian Museum 30(17): 475–517. [31 December 1977]. doi:10.3853/j.0067-1975.30.1977.192 ISSN 0067-1975 Published by the Australian Museum, Sydney naturenature cultureculture discover discover AustralianAustralian Museum Museum science science is is freely freely accessible accessible online online at at www.australianmuseum.net.au/publications/www.australianmuseum.net.au/publications/ 66 CollegeCollege Street,Street, SydneySydney NSWNSW 2010,2010, AustraliaAustralia REVIEW OF THE SHARPNOSE PUFFERFISHES (SUBFAMILY CANTHIGASTERINAE) OF THE INDO-PAClFIC GERALD R. ALLEN Department of Fishes, Western Australian Museum, Perth and JOHN E. RANDALL Fish Division, Bernice P. Bishop Museum, Honolulu SUMMARY Twenty-two species of Canthigaster (Tetraodontidae; Canthigasterinae), including seven which are described as new, are recognized from the tropical Indo-Pacific: C. amboinensis (widespread Indo-Pacific), C. bennetti (widespread Indo-W. Pacific), C. callisterna (New South Wales; Lord Howe, Norfolk, and Kermadec islands; northern New Zealand), C. compressa (E. Indies; Melanesia; Philippine Islands), C. coronata (widespread Indo-W. Pacific), C. epilampra (W. Pacific), C. inframacula n. sp. (Hawaiian Islands), C. investigatoris (Andaman Islands), C. jactator (Hawaiian Islands), C. janthinoptera (widespread Indo-W. Pacific), C. margaritata (Red Sea), C. marquesensis n. sp. (Marquesas Islands), C. nata/ensis (Mauritius; South Africa), C. ocellicincta n. sp. (Melanesia; Great Barrier Reef), C. punctatissima (eastern Pacific), C. pygmaea n. sp. (Red Sea), C. rapaensis n. sp. (Rapa), C. rivulata (widespread Indo-W. Pacific), C. smithae n.sp. (Mauritius, and South Africa), C. -
Effects of Introduced Mosquitofish and Bullfrogs on the Threatened California Red-Legged Frog
Effects of Introduced Mosquitofish and Bullfrogs on the Threatened California Red-Legged Frog SHARON P. LAWLER,*‡ DEBORAH DRITZ,* TERRY STRANGE,† AND MARCEL HOLYOAK* *Department of Entomology, University of California, Davis, CA 95616–8584, U.S.A. †San Joaquin County Mosquito and Vector Control District, 7759 South Airport Way, Stockton, CA 95206, U.S.A. Abstract: Exotic species have frequently caused declines of native fauna and may contribute to some cases of amphibian decline. Introductions of mosquitofish (Gambusia affinis) and bullfrogs (Rana catesbeiana) are suspected to have caused the decline of California red-legged frogs (Rana aurora draytonii). We tested the ef- fects of mosquitofish and bullfrog tadpoles on red-legged frog tadpoles in spatially complex, speciose commu- nities. We added 720 hatchling red-legged frog tadpoles to each of 12 earthen ponds. Three ponds were con- trols, 3 were stocked with 50 bullfrog tadpoles, 3 with 8 adult mosquitofish, and 3 with 50 bullfrogs plus 8 mosquitofish. We performed tests in aquaria to determine whether red-legged frog tadpoles are preferred prey of mosquitofish. Mosquitofish fed on a mixture of equal numbers of tadpoles and either mosquitoes, Daphnia, or corixids until , 50% of prey were eaten; then we calculated whether there was disproportionate predation on tadpoles. We also recorded the activity of tadpoles in the presence and absence of mosquitofish to test whether mosquitofish interfere with tadpole foraging. Survival of red-legged frogs in the presence of bullfrog tadpoles was less than 5%; survival was 34% in control ponds. Mosquitofish did not affect red-legged frog sur- vival, even though fish became abundant (approximately 1011 per pond). -
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group SIERRA NEWT Taricha sierrae Family: SALAMANDRIDAE Order: CAUDATA Class: AMPHIBIA A075 Written by: S. Morey Reviewed by: T. Papenfuss Updated by: CWHR Staff May 2013 and Dec 2018 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The Sierra newt is found the length of the Sierra, primarily in the foothills; an isolated population also occurs near the headwaters of Shasta Reservoir in Shasta Co. A few populations are also known from the floor of the Central Valley. Occurs primarily in valley- foothill hardwood, valley-foothill hardwood-conifer, coastal scrub and mixed chaparral, but is also known from annual grassland and mixed conifer types. Elevation range extends from near sea level to about 1830 m (6000 ft) (Jennings and Hayes 1994). SPECIFIC HABITAT REQUIREMENTS Feeding: Postmetamorphic juveniles and terrestrial adults take earthworms, snails, slugs, sowbugs, and insects (Stebbins 1972). Adult males at breeding ponds have been shown to take the eggs and hatching larvae of their own species (Kaplan and Sherman 1980) late in the breeding season, the eggs of other amphibians and trout, as well as adult and larval aquatic insects, small crustaceans, snails, and clams (Borell 1935). Aquatic larvae eat many small aquatic organisms, especially crustaceans. Cover: Terrestrial individuals seek cover under surface objects such as rocks and logs, within hollowed out trees, or in mammal burrows, rock fissures, or human-made structures such as wells. Aquatic larvae find cover beneath submerged rocks, logs, debris, and undercut banks. Reproduction: Eggs are laid in small firm clusters on the submerged portion of emergent vegetation, on submerged vegetation, rootwads, unattached sticks, and on the underside of cobbles off the bottom. -
Co-Occurrence of Tetrodotoxin and Saxitoxins and Their Intra-Body Distribution in the Pufferfish Canthigaster Valentini
toxins Article Co-Occurrence of Tetrodotoxin and Saxitoxins and Their Intra-Body Distribution in the Pufferfish Canthigaster valentini Hongchen Zhu 1, Takayuki Sonoyama 2, Misako Yamada 1, Wei Gao 1, Ryohei Tatsuno 3, Tomohiro Takatani 1 and Osamu Arakawa 1,* 1 Graduate School of Fisheries and Environmental Sciences, Nagasaki University. 1-14, Bunkyo-machi, Nagasaki, Nagasaki 852-8521, Japan; [email protected] (H.Z.); [email protected] (M.Y.); [email protected] (W.G.); [email protected] (T.T.) 2 Shimonoseki Marine Science Museum. 6-1, Arcaport, Shimonoseki, Yamaguchi 750-0036, Japan; [email protected] 3 Department of Food Science and Technology, National Fisheries University, Japan Fisheries Research and Education Agency. 2-7-1, Nagatahonmachi, Shimonoseki, Yamaguchi 759-6595, Japan; tatsuno@fish-u.ac.jp * Correspondence: [email protected]; Tel.: +81-95-819-2844 Received: 9 June 2020; Accepted: 2 July 2020; Published: 3 July 2020 Abstract: Pufferfish of the family Tetraodontidae possess tetrodotoxin (TTX) and/or saxitoxins (STXs), but the toxin ratio differs, depending on the genus or species. In the present study, to clarify the distribution profile of TTX and STXs in Tetraodontidae, we investigated the composition and intra-body distribution of the toxins in Canthigaster valentini. C. valentini specimens (four male and six female) were collected from Amami-Oshima Island, Kagoshima Prefecture, Japan, and the toxins were extracted from the muscle, liver, intestine, gallbladder, gonads, and skin. Analysis of the extracts for TTX by liquid chromatography tandem mass spectrometry and of STXs by high-performance liquid chromatography with post-column fluorescence derivatization revealed TTX, as well as a large amount of STXs, with neoSTX as the main component and dicarbamoylSTX and STX itself as minor components, in the skin and ovary.