Volume 3 Issue 1: Apr. 2002
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Aphanotorulus Ammophilus ERSS
Aphanotorulus ammophilus (a catfish, no common name) Ecological Risk Screening Summary U.S. Fish & Wildlife Service, August 2011 Revised, August 2018 Web Version, 8/31/2018 1 Native Range and Status in the United States Native Range From Froese and Pauly (2018a): “South America: Portuguesa River basin [Colombia, Venezuela].” From Ray and Armbruster (2016): “Type locality: Venezuela, Estado Cojedes, Río San Carlos, R. Portuguesa drainage at Caño Hondo, 2 km west of Las Vegas on the road from Las Vegas to Campo Allegre – 9º31'51"N, 68º39'39"W.” From Armbruster and Page (1996): “Rio Orinoco drainage of Venezuela […]; mainly known from the Rio Apure system.” 1 Status in the United States No records of Aphanotorulus ammophilus in trade or in the wild in the United States were found. Means of Introductions in the United States No records of Aphanotorulus ammophilus in the wild in the United States were found. Remarks Information searches were conducted using the accepted species name, Aphanotorulus ammophilus, and the synonym Hypostomus ammophilus. 2 Biology and Ecology Taxonomic Hierarchy and Taxonomic Standing According to Eschmeyer et al. (2018), Aphanotorulus ammophilus (Armbruster and Page 1996) is the valid name for this species; Hypostomus ammophilus (Armbruster and Page 1996) used to be a valid name for this species and now is a synonym. From Froese and Pauly (2018b): “Kingdom Animalia Phylum Chordata Class Actinopterygii Order Siluriformes Family Loricariidae Genus Aphanotorulus” Size, Weight, and Age Range From Froese and Pauly (2018a): “Max length : 16.1 cm SL male/unsexed; [Weber 2003]” Environment From Froese and Pauly (2018a): “Freshwater; benthopelagic.” Climate/Range From Froese and Pauly (2018a): “Tropical” 2 Distribution Outside the United States Native From Froese and Pauly (2018a): “South America: Portuguesa River basin [Colombia and Venezuela].” From Ray and Armbruster (2016): “Type locality: Venezuela, Estado Cojedes, Río San Carlos, R. -
§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, -
Modifications of the Digestive Tract for Holding Air in Loricariid and Scoloplacid Catfishes
Copeia, 1998(3), pp. 663-675 Modifications of the Digestive Tract for Holding Air in Loricariid and Scoloplacid Catfishes JONATHAN W. ARMBRUSTER Loricariid catfishes have evolved several modifications of the digestive tract that • appear to fWIction as accessory respiratory organs or hydrostatic organs. Adapta tions include an enlarged stomach in Pterygoplichthys, Liposan:us, Glyptoperichthys, Hemiancistrus annectens, Hemiancistrus maracaiboensis, HyposWmus panamensis, and Lithoxus; a U-shaped diverticulum in Rhinelepis, Pseudorinelepis, Pogonopoma, and Po gonopomoides; and a ringlike diverticulum in Otocinclus. Scoloplacids, closely related to loricariids, have enlarged, clear, air-filled stomachs similar to that of Lithoxus. The ability to breathe air in Otocinclus was confirmed; the ability of Lithoxus and Scoloplax to breathe air is inferred from morphology. The diverticula of Pogonopomoides and Pogonopoma are similar to swim bladders and may be used as hydrostatic organs. The various modifications of the stomach probably represent characters that define monophyletic clades. The ovaries of Lithoxus were also examined and were sho~ to have very few (15--17) mature eggs that were large (1.6-2.2 mm) for the small size of the fish (38.6-41.4 mm SL). Los bagres loricariid an desarrollado varias modificaciones del canal digestivo que aparentan fWIcionar como organos accesorios de respiracion 0 organos hidrostati cos. Las adaptaciones incluyen WI estomago agrandado en Pterygoplichthys, Liposar cus, Glyproperichthys, Hemiancistrus annectens, Hemiancistrus maracaiboensis, Hyposto mus panamensis, y Lithoxus; WI diverticulum en forma de U en Rhinelepis, Pseudori nelepis, Pogonopoma, y Pogonopomoides; y WI diverticulum en forma de circulo en Otocinclus. Scoloplacids, de relacion cercana a los loricariids, tienen estomagos cla ros, agrandados, llenos de aire similares a los de Lithoxus. -
FAMILY Loricariidae Rafinesque, 1815
FAMILY Loricariidae Rafinesque, 1815 - suckermouth armored catfishes SUBFAMILY Lithogeninae Gosline, 1947 - suckermoth armored catfishes GENUS Lithogenes Eigenmann, 1909 - suckermouth armored catfishes Species Lithogenes valencia Provenzano et al., 2003 - Valencia suckermouth armored catfish Species Lithogenes villosus Eigenmann, 1909 - Potaro suckermouth armored catfish Species Lithogenes wahari Schaefer & Provenzano, 2008 - Cuao suckermouth armored catfish SUBFAMILY Delturinae Armbruster et al., 2006 - armored catfishes GENUS Delturus Eigenmann & Eigenmann, 1889 - armored catfishes [=Carinotus] Species Delturus angulicauda (Steindachner, 1877) - Mucuri armored catfish Species Delturus brevis Reis & Pereira, in Reis et al., 2006 - Aracuai armored catfish Species Delturus carinotus (La Monte, 1933) - Doce armored catfish Species Delturus parahybae Eigenmann & Eigenmann, 1889 - Parahyba armored catfish GENUS Hemipsilichthys Eigenmann & Eigenmann, 1889 - wide-mouthed catfishes [=Upsilodus, Xenomystus] Species Hemipsilichthys gobio (Lütken, 1874) - Parahyba wide-mouthed catfish [=victori] Species Hemipsilichthys nimius Pereira, 2003 - Pereque-Acu wide-mouthed catfish Species Hemipsilichthys papillatus Pereira et al., 2000 - Paraiba wide-mouthed catfish SUBFAMILY Rhinelepinae Armbruster, 2004 - suckermouth catfishes GENUS Pogonopoma Regan, 1904 - suckermouth armored catfishes, sucker catfishes [=Pogonopomoides] Species Pogonopoma obscurum Quevedo & Reis, 2002 - Canoas sucker catfish Species Pogonopoma parahybae (Steindachner, 1877) - Parahyba -
Reproductive Behavior, Development and Eye Regression in the Cave
Neotropical Ichthyology, 7(3):479-490, 2009 Copyright © 2009 Sociedade Brasileira de Ictiologia Reproductive behavior, development and eye regression in the cave armored catfish, Ancistrus cryptophthalmus Reis, 1987 (Siluriformes: Loricariidae), breed in laboratory Sandro Secutti and Eleonora Trajano The troglobitic armored catfish, Ancistrus cryptophthalmus (Loricariidae, Ancistrinae) is known from four caves in the São Domingos karst area, upper rio Tocantins basin, Central Brazil. These populations differ in general body shape and degree of reduction of eyes and of pigmentation. The small Passa Três population (around 1,000 individuals) presents the most reduced eyes, which are not externally visible in adults. A small group of Passa Três catfish, one male and three females, reproduced spontaneously thrice in laboratory, at the end of summertime in 2000, 2003 and 2004. Herein we describe the reproductive behavior during the 2003 event, as well as the early development of the 2003 and 2004 offsprings, with focus on body growth and ontogenetic regression of eyes. The parental care by the male, which includes defense of the rock shelter where the egg clutch is laid, cleaning and oxygenation of eggs, is typical of many loricariids. On the other hand, the slow development, including delayed eye degeneration, low body growth rates and high estimated longevity (15 years or more) are characteristic of precocial, or K-selected, life cycles. In the absence of comparable data for close epigean relatives (Ancistrus spp.), it is not possible to establish whether these features are an autapomorphic specialization of the troglobitic A. cryptophthalmus or a plesiomorphic trait already present in the epigean ancestor, possibly favoring the adoption of the life in the food-poor cave environment. -
Jadas De Dientes Bilobulados, Con Cúspides Bífidas Asimétricas, Setiformes O En Forma De Cuchara, Aunque Pueden Faltar O Ser Rudimentarios En La Quijada Superior
FAUNA de agua dulce de la República JA _ a VOLUMEN 40 Argentina DIPLOM YSTIDAE D ire cto r. fascículos ZULMA A. DE CASTELLANOS lor icar hdaeancistr inae FAUNA DE AGUA DULCE DE LA REPUBLICA ARGENTINA Esta obra se realiza con el auspicio y financiación del Consejo Nacional de Investigaciones Científicas y Técnicas de la República Argentina. © 1994 PROFADU (CONICET) Programa cié Fauna cié Agua Dulce Museo de La Plata La Plata Paseo del Bosque República Argentina LOS ANCISTRINAE (PISCES: LORICARIIDAE) DE ARGENTINA Amalia M. Miquelarena, Hugo L. López y Adriana E. Aquino VOLUMEN 40 PISCES FASCICULO 5 LORICARIIDAE ANCISTRINAE AGRADECIMIENTOS Los autores agradecen a Sonia Muller dei Museum d’ Histoire naturelle, Genéve, y al personal del Programa Estudios Limnológicos Regionales (UNaM) por el material donado. LOS ANCISTRINAE (PISCES: LORICARIIDAE) DE ARGENTINA1 Amalia M. Miquelarena2, Hugo L. López3 y Adriana E. Aquino4 I. INTRODUCCION A. GENERALIDADES Y OBJETIVOS La subfamilia Ancistrinae contiene alrededor de 28 géneros (Isbrücker y Nijssen, 1992) y 127 especies (Isbrücker, 1980; Boeseman, 1982; Heitmans, et al., 1983; Rapp Py-Daniel, 1985, 1991; Nijssen e Isbrücker, 1985, 1987, 1990; Ferraris etal., 1986; Reis, 1987; Isbrücker y Nijssen, 1988, 1989, 1991; Isbrücker et al., 1988; Muller, 1989; Mullere Isbrücker, 1993) distribuidos en los grandes sistemas hidrográficos de la Región Neotropical. Su límite norte se encuentra en Panamá y la Isla de Puerto Rico mientras que el meridional está dado por su presencia en el Río de la Plata interior y arro yos afluentes de dicho curso. Dentro de la familia existen especies que ha bitan áreas de alta montaña (e.g., Ancistrus bufonius en el río Apurimac, Perú, a más de 2000 m de altura) y también zonas insulares (Ancistrus cirrhosus y Lasíancistrus trinitatus en Isla Trinidad y Lasiancistrus guacharote en la Isla de Puerto Rico, las dos últimas mencionadas con reservas por Isbrücker, 1980). -
THE SOUTH AMERICAN NEMATOGNATHI of the MUSEUMS at LEIDEN and AMSTERDAM by J. W. B. VAN DER STIQCHEL the Collections of the South
THE SOUTH AMERICAN NEMATOGNATHI OF THE MUSEUMS AT LEIDEN AND AMSTERDAM by J. W. B. VAN DER STIQCHEL (Museum voor het OnderwSs, 's-Gravenhage) The collections of the South American Nematognathi in the Rijksmuseum van Natuurlijke Historie at Leiden, referred to in this publication as "Mu• seum Leiden", and of those in the Zoologisch Museum at Amsterdam, referred to as "Museum Amsterdam", consist of valuable material, which for a very important part has not been studied yet. I feel very much obliged to Prof. Dr. H. Boschma who allowed me to start with the study of the Leiden collections and whom I offer here my sincere thanks. At the same time I want to express my gratitude towards Prof. Dr. L. F. de Beaufort, who has been so kind to place the collection of the Zoological Museum at Amsterdam at my disposal. Furthermore I am greatly indebted to Dr. F. P. Koumans at Leiden for his assistance and advice to solve the various problems which I met during my study. The material dealt with here comes from a large number of collections of different collectors, from various areas of South America, it consists of 125 species, belonging to 14 families of the order Nematognathi. Contrary to the original expectations no adequate number of specimens from Surinam could be obtained to get a sufficient opinion about the occurrence of the various species, and, if possible, also about their distribution in this tropical American part of the Netherlands. On the whole the collections from Surinam were limited to the generally known species only. -
A New Black Baryancistrus with Blue Sheen from the Upper Orinoco (Siluriformes: Loricariidae)
Copeia 2009, No. 1, 50–56 A New Black Baryancistrus with Blue Sheen from the Upper Orinoco (Siluriformes: Loricariidae) Nathan K. Lujan1, Mariangeles Arce2, and Jonathan W. Armbruster1 Baryancistrus beggini, new species, is described from the upper Rı´o Orinoco and lower portions of its tributaries, the Rı´o Guaviare in Colombia and Rı´o Ventuari in Venezuela. Baryancistrus beggini is unique within Hypostominae in having a uniformly dark black to brown base color with a blue sheen in life, and the first three to five plates of the midventral series strongly bent, forming a distinctive keel above the pectoral fins along each side of the body. It is further distinguished by having a naked abdomen, two to three symmetrical and ordered predorsal plate rows including the nuchal plate, and the last dorsal-fin ray adnate with adipose fin via a posterior membrane that extends beyond the preadipose plate up to half the length of the adipose-fin spine. Se describe una nueva especie, Baryancistrus beggini, del alto Rı´o Orinoco y las partes bajas de sus afluentes: el rı´o Guaviare en Colombia, y el rı´o Ventuari en Venezuela. Baryancistrus beggini es la u´ nica especie entre los Hypostominae que presenta fondo negro oscuro a marro´ n sin marcas, con brillo azuloso en ejemplares vivos. Las primeras tres a cinco placas de la serie medioventral esta´n fuertemente dobladas, formando una quilla notable por encima de las aletas pectorales en cada lado del cuerpo. Baryancistrus beggini se distingue tambie´n por tener el abdomen desnudo, dos o tres hileras de placas predorsales sime´tricas y ordenadas (incluyendo la placa nucal) y el u´ ltimo radio de la aleta dorsal adherido a la adiposa a trave´s de una membrana que se extiende posteriormente, sobrepasando la placa preadiposa y llegando hasta la mitad de la espina adiposa. -
Panaque (Panaque), with Descriptions of Three New Species from the Amazon Basin (Siluriformes, Loricariidae)
Copeia 2010, No. 4, 676–704 Revision of Panaque (Panaque), with Descriptions of Three New Species from the Amazon Basin (Siluriformes, Loricariidae) Nathan K. Lujan1, Max Hidalgo2, and Donald J. Stewart3 The Panaque nigrolineatus group (subgenus Panaque) is revised; three nominal species—P. cochliodon, P. nigrolineatus, and P. suttonorum—are redescribed and three new species are described. Panaque armbrusteri, new species, is widespread in the Tapajo´ s River and its tributaries in Brazil and is distinguished by having a supraoccipital hump, higher numbers of jaw teeth and an ontogenetic increase in interpremaxillary and intermandibular tooth-row angles, relatively short paired-fin spines, and dorsal margin of infraorbital six flared laterally. Panaque schaeferi, new species, is widespread in main-channel habitats of the upper Amazon (Solimo˜es) River basin in Brazil and Peru; it is distinguished by having a coloration consisting of dark or faded black spots evenly distributed on a pale gray to brown base, and by its large adult body size (.570 mm SL). Panaque titan, new species, is distributed in larger, lowland to piedmont rivers of the Napo River basin in Ecuador, and is distinguished by having a postorbital pterotic region bulged beyond the ventral pterotic margin, coloration consisting of irregular and widely spaced dark gray to brown stripes on light brown to tan base, and large adult body size (.390 mm SL). A relatively large pterotic, indicative of an enlarged gas bladder and gas bladder capsule, and allometric increases in tooth number are hypothesized to be synapomorphies uniting members of the subgenus Panaque. Se reviso´ el grupo Panaque nigrolineatus (subge´nero Panaque); se redescriben tres especies nominales—P. -
Amazon Alive: a Decade of Discoveries 1999-2009
Amazon Alive! A decade of discovery 1999-2009 The Amazon is the planet’s largest rainforest and river basin. It supports countless thousands of species, as well as 30 million people. © Brent Stirton / Getty Images / WWF-UK © Brent Stirton / Getty Images The Amazon is the largest rainforest on Earth. It’s famed for its unrivalled biological diversity, with wildlife that includes jaguars, river dolphins, manatees, giant otters, capybaras, harpy eagles, anacondas and piranhas. The many unique habitats in this globally significant region conceal a wealth of hidden species, which scientists continue to discover at an incredible rate. Between 1999 and 2009, at least 1,200 new species of plants and vertebrates have been discovered in the Amazon biome (see page 6 for a map showing the extent of the region that this spans). The new species include 637 plants, 257 fish, 216 amphibians, 55 reptiles, 16 birds and 39 mammals. In addition, thousands of new invertebrate species have been uncovered. Owing to the sheer number of the latter, these are not covered in detail by this report. This report has tried to be comprehensive in its listing of new plants and vertebrates described from the Amazon biome in the last decade. But for the largest groups of life on Earth, such as invertebrates, such lists do not exist – so the number of new species presented here is no doubt an underestimate. Cover image: Ranitomeya benedicta, new poison frog species © Evan Twomey amazon alive! i a decade of discovery 1999-2009 1 Ahmed Djoghlaf, Executive Secretary, Foreword Convention on Biological Diversity The vital importance of the Amazon rainforest is very basic work on the natural history of the well known. -
Multilocus Molecular Phylogeny of the Suckermouth Armored Catfishes
Molecular Phylogenetics and Evolution xxx (2014) xxx–xxx Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Multilocus molecular phylogeny of the suckermouth armored catfishes (Siluriformes: Loricariidae) with a focus on subfamily Hypostominae ⇑ Nathan K. Lujan a,b, , Jonathan W. Armbruster c, Nathan R. Lovejoy d, Hernán López-Fernández a,b a Department of Natural History, Royal Ontario Museum, 100 Queen’s Park, Toronto, Ontario M5S 2C6, Canada b Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, Ontario M5S 3B2, Canada c Department of Biological Sciences, Auburn University, Auburn, AL 36849, USA d Department of Biological Sciences, University of Toronto Scarborough, Toronto, Ontario M1C 1A4, Canada article info abstract Article history: The Neotropical catfish family Loricariidae is the fifth most species-rich vertebrate family on Earth, with Received 4 July 2014 over 800 valid species. The Hypostominae is its most species-rich, geographically widespread, and eco- Revised 15 August 2014 morphologically diverse subfamily. Here, we provide a comprehensive molecular phylogenetic reap- Accepted 20 August 2014 praisal of genus-level relationships in the Hypostominae based on our sequencing and analysis of two Available online xxxx mitochondrial and three nuclear loci (4293 bp total). Our most striking large-scale systematic discovery was that the tribe Hypostomini, which has traditionally been recognized as sister to tribe Ancistrini based Keywords: on morphological data, was nested within Ancistrini. This required recognition of seven additional tribe- Neotropics level clades: the Chaetostoma Clade, the Pseudancistrus Clade, the Lithoxus Clade, the ‘Pseudancistrus’ Guiana Shield Andes Mountains Clade, the Acanthicus Clade, the Hemiancistrus Clade, and the Peckoltia Clade. -
Great Lakes Fish Health Committee
GREAT LAKES FISH HEALTH COMMITTEE 2006 Annual Meeting Madison, Wisconsin February 21-23, 2006 Minutes (with attachments) Submitted By: Andrew D. Noyes New York State Department of Environmental Conservation The data, results, and discussions herein are considered provisional; permission to cite the contents of this report must be requested from the authors or their agency GREAT LAKES FISHERY COMMISSION 2100 Commonwealth Blvd Ann Arbor, Michigan 48105-1563 Great Lakes Fish Health Committee 2006 Annual Meeting Madison, WI February 21-23, 2006 Table of Contents List of Attendees ..................................................................................................................2 Meeting Agenda ...................................................................................................................4 Minutes ................................................................................................................................6 Appendix 1: Great Lakes Fish Disease Control Policy and Model Program ...................10 Appendix 2: Factors Controlling the Susceptibility of Chinook Salmon to Bacterial Kidney Disease ...................................................................................70 Appendix 3: Evaluation of Immune Function in Thiamine Deficient Lake Trout ..........118 Appendix 4: Heterosporis sp. (Microspora: Pleistophoridae): A parasite from Perca flavescens, Stizostedion vitreum, and Esox lucius in Minnesota, Wisconsin and Lake Ontario ................................................................................150