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§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
Research Funding (Total $2,552,481) $15,000 2019
CURRICULUM VITAE TENNESSEE AQUARIUM CONSERVATION INSTITUTE 175 BAYLOR SCHOOL RD CHATTANOOGA, TN 37405 RESEARCH FUNDING (TOTAL $2,552,481) $15,000 2019. Global Wildlife Conservation. Rediscovering the critically endangered Syr-Darya Shovelnose Sturgeon. $10,000 2019. Tennessee Wildlife Resources Agency. Propagation of the Common Logperch as a host for endangered mussel larvae. $8,420 2019. Tennessee Wildlife Resources Agency. Monitoring for the Laurel Dace. $4,417 2019. Tennessee Wildlife Resources Agency. Examining interactions between Laurel Dace (Chrosomus saylori) and sunfish $12,670 2019. Trout Unlimited. Southern Appalachian Brook Trout propagation for reintroduction to Shell Creek. $106,851 2019. Private Donation. Microplastic accumulation in fishes of the southeast. $1,471. 2019. AZFA-Clark Waldram Conservation Grant. Mayfly propagation for captive propagation programs. $20,000. 2019. Tennessee Valley Authority. Assessment of genetic diversity within Blotchside Logperch. $25,000. 2019. Riverview Foundation. Launching Hidden Rivers in the Southeast. $11,170. 2018. Trout Unlimited. Propagation of Southern Appalachian Brook Trout for Supplemental Reintroduction. $1,471. 2018. AZFA Clark Waldram Conservation Grant. Climate Change Impacts on Headwater Stream Vertebrates in Southeastern United States $1,000. 2018. Hamilton County Health Department. Step 1 Teaching Garden Grants for Sequoyah School Garden. $41,000. 2018. Riverview Foundation. River Teachers: Workshops for Educators. $1,000. 2018. Tennessee Valley Authority. Youth Freshwater Summit $20,000. 2017. Tennessee Valley Authority. Lake Sturgeon Propagation. $7,500 2017. Trout Unlimited. Brook Trout Propagation. $24,783. 2017. Tennessee Wildlife Resource Agency. Assessment of Percina macrocephala and Etheostoma cinereum populations within the Duck River Basin. $35,000. 2017. U.S. Fish and Wildlife Service. Status surveys for conservation status of Ashy (Etheostoma cinereum) and Redlips (Etheostoma maydeni) Darters. -
Catalogue of the Amphibians of Venezuela: Illustrated and Annotated Species List, Distribution, and Conservation 1,2César L
Mannophryne vulcano, Male carrying tadpoles. El Ávila (Parque Nacional Guairarepano), Distrito Federal. Photo: Jose Vieira. We want to dedicate this work to some outstanding individuals who encouraged us, directly or indirectly, and are no longer with us. They were colleagues and close friends, and their friendship will remain for years to come. César Molina Rodríguez (1960–2015) Erik Arrieta Márquez (1978–2008) Jose Ayarzagüena Sanz (1952–2011) Saúl Gutiérrez Eljuri (1960–2012) Juan Rivero (1923–2014) Luis Scott (1948–2011) Marco Natera Mumaw (1972–2010) Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 13(1) [Special Section]: 1–198 (e180). Catalogue of the amphibians of Venezuela: Illustrated and annotated species list, distribution, and conservation 1,2César L. Barrio-Amorós, 3,4Fernando J. M. Rojas-Runjaic, and 5J. Celsa Señaris 1Fundación AndígenA, Apartado Postal 210, Mérida, VENEZUELA 2Current address: Doc Frog Expeditions, Uvita de Osa, COSTA RICA 3Fundación La Salle de Ciencias Naturales, Museo de Historia Natural La Salle, Apartado Postal 1930, Caracas 1010-A, VENEZUELA 4Current address: Pontifícia Universidade Católica do Río Grande do Sul (PUCRS), Laboratório de Sistemática de Vertebrados, Av. Ipiranga 6681, Porto Alegre, RS 90619–900, BRAZIL 5Instituto Venezolano de Investigaciones Científicas, Altos de Pipe, apartado 20632, Caracas 1020, VENEZUELA Abstract.—Presented is an annotated checklist of the amphibians of Venezuela, current as of December 2018. The last comprehensive list (Barrio-Amorós 2009c) included a total of 333 species, while the current catalogue lists 387 species (370 anurans, 10 caecilians, and seven salamanders), including 28 species not yet described or properly identified. Fifty species and four genera are added to the previous list, 25 species are deleted, and 47 experienced nomenclatural changes. -
FAMILY Gasteropelecidae Bleeker, 1859 - Freshwater Hatchetfishes [=Gasteropelecini, Carnegiellidi, Thoracocharacini] Notes: Gasteropelecini Bleeker, 1859:XXXII [Ref
FAMILY Gasteropelecidae Bleeker, 1859 - freshwater hatchetfishes [=Gasteropelecini, Carnegiellidi, Thoracocharacini] Notes: Gasteropelecini Bleeker, 1859:XXXII [ref. 371[ (stirps) Gasteropelecus [family name sometimes seen as Gastropelecidae] Carnegiellidi Fowler, 1958b:9 [ref. 1470] (tribe) Carnegiella Thoracocharacini Weitzman, 1960:220 [ref. 9611] (tribe) Thoracocharax GENUS Carnegiella Eigenmann, 1909 - freshwater hatchefishes [=Carnegiella Eigenmann [C. H.], 1909:13] Notes: [ref. 1222]. Fem. Gasteropelecus strigatus Günther, 1864. Type by original designation (also monotypic). •Valid as Carnegiella Eigenmann, 1909 – (Weitzman 1960:225 [ref. 9611], Géry 1977:247 [ref. 1597], Vari 1983:5 [ref. 5419], Weitzman & Palmer in Reis et al. 2003:101 [ref. 27061], Mirande 2009:6 [ref. 30267] in Gasteropelecidae, Mirande 2010:466 [ref. 31006] in Gasteropeledidae, Oliveira et al. 2011:13 [ref. 31685] in Gasteropelecidae). Current status: Valid as Carnegiella Eigenmann, 1909. Gasteropelecidae. Species Carnegiella marthae Myers, 1927 - blackwing hatchetfish [=Carnegiella marthae Myers [G. S.], 1927:119-120] Notes: [Bulletin of the Museum of Comparative Zoology v. 68 (no. 3); ref. 3096] Caño de Quiribana, near Caicara, Venezuela. Current status: Valid as Carnegiella marthae Myers, 1927. Gasteropelecidae. Distribution: Negro and upper Orinoco River basins: Brazil and Venezuela. Habitat: freshwater. Species Carnegiella myersi Fernández-Yépez, 1950 - dwarf hatchetfish [=Carnegiella myersi Fernández-Yépez [A.], 1950:175, Figs. 3, 3a-d] Notes: [Stanford Ichthyological Bulletin v. 3 (no. 4); ref. 12321] Creek near Yurimaguas, Peru. Current status: Valid as Carnegiella myersi Fernández-Yépez, 1950. Gasteropelecidae. Distribution: Amazon River basin, Peru. Habitat: freshwater. Species Carnegiella schereri Fernández-Yépez, 1950 - dwarf hatchetfish [=Carnegiella schereri Fernández-Yépez [A.], 1950:178, Figs. 5, 5a-d] Notes: [Stanford Ichthyological Bulletin v. 3 (no. 4); ref. -
Zootaxa, Molecular Phylogeny, Classification, and Biogeography Of
Zootaxa 2067: 1–28 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Molecular phylogeny, classification, and biogeography of West Indian racer snakes of the Tribe Alsophiini (Squamata, Dipsadidae, Xenodontinae) S. BLAIR HEDGES1, ARNAUD COULOUX2, & NICOLAS VIDAL3,4 1Department of Biology, 208 Mueller Lab, Pennsylvania State University, University Park, PA 16802-5301 USA. E-mail: [email protected] 2Genoscope. Centre National de Séquençage, 2 rue Gaston Crémieux, CP5706, 91057 Evry Cedex, France www.genoscope.fr 3UMR 7138, Département Systématique et Evolution, Muséum National d’Histoire Naturelle, CP 26, 57 rue Cuvier, 75005 Paris, France 4Corresponding author. E-mail : [email protected] Abstract Most West Indian snakes of the family Dipsadidae belong to the Subfamily Xenodontinae and Tribe Alsophiini. As recognized here, alsophiine snakes are exclusively West Indian and comprise 43 species distributed throughout the region. These snakes are slender and typically fast-moving (active foraging), diurnal species often called racers. For the last four decades, their classification into six genera was based on a study utilizing hemipenial and external morphology and which concluded that their biogeographic history involved multiple colonizations from the mainland. Although subsequent studies have mostly disagreed with that phylogeny and taxonomy, no major changes in the classification have been proposed until now. Here we present a DNA sequence analysis of five mitochondrial genes and one nuclear gene in 35 species and subspecies of alsophiines. Our results are more consistent with geography than previous classifications based on morphology, and support a reclassification of the species of alsophiines into seven named and three new genera: Alsophis Fitzinger (Lesser Antilles), Arrhyton Günther (Cuba), Borikenophis Hedges & Vidal gen. -
A New Locality for Correlophus Ciliatus and Rhacodactylus Leachianus (Sauria: Diplodactylidae) from Néhoué River, Northern New Caledonia
Herpetology Notes, volume 8: 553-555 (2015) (published online on 06 December 2015) A new locality for Correlophus ciliatus and Rhacodactylus leachianus (Sauria: Diplodactylidae) from Néhoué River, northern New Caledonia Mickaël Sanchez1, Jean-Jérôme Cassan2 and Thomas Duval3,* Giant geckos from New Caledonia (Pacific Ocean) We observed seven native gecko species: Bavayia are charismatic nocturnal lizards. This paraphyletic (aff.) cyclura (n=1), Bavayia (aff.) exsuccida (n=1), group is represented by three genera, Rhacodactylus, Correlophus ciliatus (n=1), Dierrogekko nehoueensis Correlophus and Mniarogekko, all endemic to Bauer, Jackman, Sadlier and Whitaker, 2006 (n=1), New Caledonia (Bauer et al., 2012). Rhacodactylus Eurydactylodes agricolae Henkel and Böhme, 2001 leachianus (Cuvier, 1829) is largely distributed on the (n=1), Mniarogekko jalu Bauer, Whitaker, Sadlier and Grande Terre including the Île des Pins and its satellite Jackman, 2012 (n=1) and Rhacodactylus leachianus islands, whereas Correlophus ciliatus Guichenot, 1866 (n=1). Also, the alien Hemidactylus frenatus Dumeril is mostly known in the southern part of the Grande and Bibron, 1836 (n=3) has been sighted. The occurrence Terre, the Île des Pins and its satellite islands (Bauer of C. ciliatus and R. leachianus (Fig. 2 and 3) represent et al., 2012). Here, we report a new locality for both new records for this site. Both gecko species were species in the north-western part of Grande Terre, along observed close to the ground, at a height of less than the Néhoué River (Fig. 1). 1.5 m. The Néhoué River is characterized by gallery forests It is the first time that R. leachianus is recorded in the growing on deep alluvial soils. -
Amorphometric and Meristic Study of the Halfbeak, Hyporhamphus
W&M ScholarWorks Dissertations, Theses, and Masters Projects Theses, Dissertations, & Master Projects 1993 Amorphometric and Meristic Study of the Halfbeak, Hyporhamphus unifasciatus (Teleostei: Hemiramphidae) from the Western Atlantic, with the Description of a New Species Heidi M. Banford College of William and Mary - Virginia Institute of Marine Science Follow this and additional works at: https://scholarworks.wm.edu/etd Part of the Marine Biology Commons, and the Oceanography Commons Recommended Citation Banford, Heidi M., "Amorphometric and Meristic Study of the Halfbeak, Hyporhamphus unifasciatus (Teleostei: Hemiramphidae) from the Western Atlantic, with the Description of a New Species" (1993). Dissertations, Theses, and Masters Projects. Paper 1539617658. https://dx.doi.org/doi:10.25773/v5-pbsc-sy52 This Thesis is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Dissertations, Theses, and Masters Projects by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. A MORPHOMETRIC AND MERISTIC STUDY OF THE HALFBEAK, HYPORHAMPHUS UNIFASCIATUS (TELEOSTEI: HEMIRAMPHIDAE) FROM THE WESTERN ATLANTIC, WITH THE DESCRIPTION OF A NEW SPECIES A Thesis Presented to The Faculty of the School of Marine Science The College of William and Mary in Virginia In Partial Fulfillment Of the Requirements for the Degree of Master of Arts by Heidi M. Banford 1993 This thesis is submitted in partial fulfillment of the requirements for the degree of Master of Arts Heidi M. Banford Approved, July 1993 Jojm A. Musick,' Ph.D. flmittee Chairman/Advisor ~ t M . ^ Herbert M. Austin, Ph.D. -
Evolutionary Genomics of a Plastic Life History Trait: Galaxias Maculatus Amphidromous and Resident Populations
EVOLUTIONARY GENOMICS OF A PLASTIC LIFE HISTORY TRAIT: GALAXIAS MACULATUS AMPHIDROMOUS AND RESIDENT POPULATIONS by María Lisette Delgado Aquije Submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy at Dalhousie University Halifax, Nova Scotia August 2021 Dalhousie University is located in Mi'kma'ki, the ancestral and unceded territory of the Mi'kmaq. We are all Treaty people. © Copyright by María Lisette Delgado Aquije, 2021 I dedicate this work to my parents, María and José, my brothers JR and Eduardo for their unconditional love and support and for always encouraging me to pursue my dreams, and to my grandparents Victoria, Estela, Jesús, and Pepe whose example of perseverance and hard work allowed me to reach this point. ii TABLE OF CONTENTS LIST OF TABLES ............................................................................................................ vii LIST OF FIGURES ........................................................................................................... ix ABSTRACT ...................................................................................................................... xii LIST OF ABBREVIATION USED ................................................................................ xiii ACKNOWLEDGMENTS ................................................................................................ xv CHAPTER 1. INTRODUCTION ....................................................................................... 1 1.1 Galaxias maculatus .................................................................................................. -
Distribution, Abundance, and Biomass of Giant Sea Bass (Stereolepis Gigas) Off Santa Catalina Island, California, 2014-2015
Bull. Southern California Acad. Sci. 115(1), 2016, pp. 1–14 E Southern California Academy of Sciences, 2016 The Return of the King of the Kelp Forest: Distribution, Abundance, and Biomass of Giant Sea Bass (Stereolepis gigas) off Santa Catalina Island, California, 2014-2015 Parker H. House*, Brian L.F. Clark, and Larry G. Allen California State University, Northridge, Department of Biology, 18111 Nordhoff St., Northridge, CA, 91330 Abstract.—It is rare to find evidence of top predators recovering after being negatively affected by overfishing. However, recent findings suggest a nascent return of the critically endangered giant sea bass (Stereolepis gigas) to southern California. To provide the first population assessment of giant sea bass, surveys were conducted during the 2014/2015 summers off Santa Catalina Island, CA. Eight sites were surveyed on both the windward and leeward side of Santa Catalina Island every two weeks from June through August. Of the eight sites, three aggregations were identified at Goat Harbor, The V’s, and Little Harbor, CA. These three aggregation sites, the largest containing 24 individuals, contained a mean stock biomass of 19.6 kg/1000 m2 over both summers. Over the course of both summers the giant sea bass population was primarily made up of 1.2 - 1.3 m TL individuals with several small and newly mature fish observed in aggregations. Comparison to historical data for the island suggests giant sea bass are recovering, but have not reached pre-exploitation levels. The giant sea bass (Stereolepis gigas) is the largest teleost to inhabit nearshore rocky reefs and kelp forests in the northeastern Pacific (Hawk and Allen 2014). -
Endangered Species
FEATURE: ENDANGERED SPECIES Conservation Status of Imperiled North American Freshwater and Diadromous Fishes ABSTRACT: This is the third compilation of imperiled (i.e., endangered, threatened, vulnerable) plus extinct freshwater and diadromous fishes of North America prepared by the American Fisheries Society’s Endangered Species Committee. Since the last revision in 1989, imperilment of inland fishes has increased substantially. This list includes 700 extant taxa representing 133 genera and 36 families, a 92% increase over the 364 listed in 1989. The increase reflects the addition of distinct populations, previously non-imperiled fishes, and recently described or discovered taxa. Approximately 39% of described fish species of the continent are imperiled. There are 230 vulnerable, 190 threatened, and 280 endangered extant taxa, and 61 taxa presumed extinct or extirpated from nature. Of those that were imperiled in 1989, most (89%) are the same or worse in conservation status; only 6% have improved in status, and 5% were delisted for various reasons. Habitat degradation and nonindigenous species are the main threats to at-risk fishes, many of which are restricted to small ranges. Documenting the diversity and status of rare fishes is a critical step in identifying and implementing appropriate actions necessary for their protection and management. Howard L. Jelks, Frank McCormick, Stephen J. Walsh, Joseph S. Nelson, Noel M. Burkhead, Steven P. Platania, Salvador Contreras-Balderas, Brady A. Porter, Edmundo Díaz-Pardo, Claude B. Renaud, Dean A. Hendrickson, Juan Jacobo Schmitter-Soto, John Lyons, Eric B. Taylor, and Nicholas E. Mandrak, Melvin L. Warren, Jr. Jelks, Walsh, and Burkhead are research McCormick is a biologist with the biologists with the U.S. -
Ostariophysi: Characiformes: Anostomidae)
Neotropical Ichthyology, 4(1):27-44, 2006 Copyright © 2006 Sociedade Brasileira de Ictiologia Revision of the South American freshwater fish genus Laemolyta Cope, 1872 (Ostariophysi: Characiformes: Anostomidae) Kelly Cristina Mautari and Naércio Aquino Menezes The anostomid genus Laemolyta Cope, 1872, is redefined.Various morphological, especially osteological characters in addi- tion to the commonly utilized features of dentition proved useful for its characterization. A taxonomic revision of all species was made using meristics, morphometrics and color pattern. Five species are recognized: Laemolyta fernandezi Myers, 1950, from the río Orinoco (Venezuela) and the sub-basins Tocantins/Araguaia and Xingu, L. orinocensis (Steindachner, 1879), restricted to the río Orinoco, L. garmani (Borodin, 1931) and L. proxima (Garman, 1890), from the Amazon basin with the latter also occurring in the Essequibo River (Guiana), and L. taeniata (Kner, 1859), from the Amazon and Orinoco basins. Laemolyta garmani macra is considered a synonym of L. garmani, L. petiti a synonym of L. fernandezi, and L. nitens and L. varia synonyms of L. proxima. Lectotypes are designated herein for L. orinocencis and L. taeniata. O gênero Laemolyta Cope, 1872 da família Anostomidae é redefinido e além das características da dentição usualmente utilizadas, outros caracteres morfológicos, principalmente osteológicos, também se revelaram úteis para sua conceituação. Foi feita a revisão taxonômica de todas as espécies utilizando-se dados morfométricos, merísticos e padrão de colorido. Cinco espécies são reconhecidas: Laemolyta fernandezi Myers, 1950 do rio Orinoco (Venezuela) e rios Tocantins/Araguaia e Xingu, Laemolyta orinocensis (Steindachner, 1879) restrita ao rio Orenoco, L. garmani (Borodin, 1931) e Laemolyta proxima (Garman, 1890) da bacia Amazônica, esta última ocorrendo também no rio Essequibo (Guianas) e Laemolyta taeniata (Kner, 1859) da bacia Amazônica e rio Orenoco. -
Vii Fishery-At-A-Glance: California Sheephead
Fishery-at-a-Glance: California Sheephead (Sheephead) Scientific Name: Semicossyphus pulcher Range: Sheephead range from the Gulf of California to Monterey Bay, California, although they are uncommon north of Point Conception. Habitat: Both adult and juvenile Sheephead primarily reside in kelp forest and rocky reef habitats. Size (length and weight): Male Sheephead can grow up to a length of three feet (91 centimeters) and weigh over 36 pounds (16 kilograms). Life span: The oldest Sheephead ever reported was a male at 53 years. Reproduction: As protogynous hermaphrodites, all Sheephead begin life as females, and older, larger females can develop into males. They are batch spawners, releasing eggs and sperm into the water column multiple times during their spawning season from July to September. Prey: Sheephead are generalist carnivores whose diet shifts throughout their growth. Juveniles primarily consume small invertebrates like tube-dwelling polychaetes, bryozoans and brittle stars, and adults shift to consuming larger mobile invertebrates like sea urchins. Predators: Predators of adult Sheephead include Giant Sea Bass, Soupfin Sharks and California Sea Lions. Fishery: Sheephead support both a popular recreational and a commercial fishery in southern California. Area fished: Sheephead are fished primarily south of Point Conception (Santa Barbara County) in nearshore waters around the offshore islands and along the mainland shore over rocky reefs and in kelp forests. Fishing season: Recreational anglers can fish for Sheephead from March 1through December 31 onboard boats south of Point Conception and May 1 through December 31 between Pigeon Point and Point Conception. Recreational divers and shore-based anglers can fish for Sheephead year round.