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Defining the Molecular Pathologies in Cloaca Malformation: Similarities Between Mouse and Human Laura A
© 2014. Published by The Company of Biologists Ltd | Disease Models & Mechanisms (2014) 7, 483-493 doi:10.1242/dmm.014530 RESEARCH ARTICLE Defining the molecular pathologies in cloaca malformation: similarities between mouse and human Laura A. Runck1, Anna Method1, Andrea Bischoff2, Marc Levitt2, Alberto Peña2, Margaret H. Collins3, Anita Gupta3, Shiva Shanmukhappa3, James M. Wells1,4 and Géraldine Guasch1,* ABSTRACT INTRODUCTION Anorectal malformations are congenital anomalies that form a Anorectal malformations are congenital anomalies that encompass spectrum of disorders, from the most benign type with excellent a wide spectrum of diseases and occur in ~1 in 5000 live births functional prognosis, to very complex, such as cloaca malformation (Levitt and Peña, 2007). The anorectal and urogenital systems arise in females in which the rectum, vagina and urethra fail to develop from a common transient embryonic structure called the cloaca that separately and instead drain via a single common channel into the exists from the fourth week of intrauterine development in humans perineum. The severity of this phenotype suggests that the defect (Fritsch et al., 2007; Kluth, 2010) and between days 10.5-12.5 post- occurs in the early stages of embryonic development of the organs fertilization in mice (Seifert et al., 2008). By the sixth week in derived from the cloaca. Owing to the inability to directly investigate humans the embryonic cloaca is divided, resulting in a ventral human embryonic cloaca development, current research has relied urogenital sinus and a separate dorsal hindgut. By the twelfth week, on the use of mouse models of anorectal malformations. However, the anal canal, vaginal and urethral openings are established. -
Pond-Breeding Amphibian Guild
Supplemental Volume: Species of Conservation Concern SC SWAP 2015 Pond-breeding Amphibians Guild Primary Species: Flatwoods Salamander Ambystoma cingulatum Carolina Gopher Frog Rana capito capito Broad-Striped Dwarf Siren Pseudobranchus striatus striatus Tiger Salamander Ambystoma tigrinum Secondary Species: Upland Chorus Frog Pseudacris feriarum -Coastal Plain only Northern Cricket Frog Acris crepitans -Coastal Plain only Contributors (2005): Stephen Bennett and Kurt A. Buhlmann [SCDNR] Reviewed and Edited (2012): Stephen Bennett (SCDNR), Kurt A. Buhlmann (SREL), and Jeff Camper (Francis Marion University) DESCRIPTION Taxonomy and Basic Descriptions This guild contains 4 primary species: the flatwoods salamander, Carolina gopher frog, dwarf siren, and tiger salamander; and 2 secondary species: upland chorus frog and northern cricket frog. Primary species are high priority species that are directly tied to a unifying feature or habitat. Secondary species are priority species that may occur in, or be related to, the unifying feature at some time in their life. The flatwoods salamander—in particular, the frosted flatwoods salamander— and tiger salamander are members of the family Ambystomatidae, the mole salamanders. Both species are large; the tiger salamander is the largest terrestrial salamander in the eastern United States. The Photo by SC DNR flatwoods salamander can reach lengths of 9 to 12 cm (3.5 to 4.7 in.) as an adult. This species is dark, ranging from black to dark brown with silver-white reticulated markings (Conant and Collins 1991; Martof et al. 1980). The tiger salamander can reach lengths of 18 to 20 cm (7.1 to 7.9 in.) as an adult; maximum size is approximately 30 cm (11.8 in.). -
Evaluating and Treating the Reproductive System
18_Reproductive.qxd 8/23/2005 11:44 AM Page 519 CHAPTER 18 Evaluating and Treating the Reproductive System HEATHER L. BOWLES, DVM, D ipl ABVP-A vian , Certified in Veterinary Acupuncture (C hi Institute ) Reproductive Embryology, Anatomy and Physiology FORMATION OF THE AVIAN GONADS AND REPRODUCTIVE ANATOMY The avian gonads arise from more than one embryonic source. The medulla or core arises from the meso- nephric ducts. The outer cortex arises from a thickening of peritoneum along the root of the dorsal mesentery within the primitive gonadal ridge. Mesodermal germ cells that arise from yolk-sac endoderm migrate into this gonadal ridge, forming the ovary. The cells are initially distributed equally to both sides. In the hen, these germ cells are then preferentially distributed to the left side, and migrate from the right to the left side as well.58 Some avian species do in fact have 2 ovaries, including the brown kiwi and several raptor species. Sexual differ- entiation begins by day 5 in passerines and domestic fowl and by day 11 in raptor species. Differentiation of the ovary is characterized by development of the cortex, while the medulla develops into the testis.30,58 As the embryo develops, the germ cells undergo three phases of oogenesis. During the first phase, the oogonia actively divide for a defined time period and then stop at the first prophase of the first maturation division. During the second phase, the germ cells grow in size to become primary oocytes. This occurs approximately at the time of hatch in domestic fowl. During the third phase, oocytes complete the first maturation division to 18_Reproductive.qxd 8/23/2005 11:44 AM Page 520 520 Clinical Avian Medicine - Volume II become secondary oocytes. -
Ontogenetic Evidence for the Paleozoic Ancestry of Salamanders
EVOLUTION & DEVELOPMENT 5:3, 314–324 (2003) Ontogenetic evidence for the Paleozoic ancestry of salamanders Rainer R. Schocha and Robert L. Carrollb aStaatlilches Museum für Naturkunde, Rosenstein 1, D-70191 Stuttgart, Germany bRedpath Museum, McGill University, Montréal, Québec, Canada, H3A 2K6 Authors for correspondence (e-mail: [email protected], [email protected]) SUMMARY The phylogenetic positions of frogs, sala- tire developmental sequence from hatching to metamor- manders, and caecilians have been difficult to establish. phosis is revealed in an assemblage of over 600 Data matrices based primarily on Paleozoic taxa support a specimens from a single locality, all belonging to the genus monophyletic origin of all Lissamphibia but have resulted in Apateon. Apateon forms the most speciose genus of the widely divergent hypotheses of the nature of their common neotenic temnospondyl family Branchiosauridae. The se- ancestor. Analysis that concentrates on the character quence of ossification of individual bones and the changing states of the stem taxa of the extant orders, in contrast, configuration of the skull closely parallel those observed in suggests a polyphyletic origin from divergent Paleozoic the development of primitive living salamanders. These clades. Comparison of patterns of larval development in fossils provide a model of how derived features of the sala- Paleozoic and modern amphibians provides a means to mander skull may have evolved in the context of feeding test previous phylogenies based primarily on adult charac- specializations that appeared in early larval stages of mem- teristics. This proves to be highly informative in the case of bers of the Branchiosauridae. Larvae of Apateon share the origin of salamanders. -
Early Stages of Fishes in the Western North Atlantic Ocean Volume
ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation. -
2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon
INFORMATION REPORTS NUMBER 2010-05 FISH DIVISION Oregon Department of Fish and Wildlife 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Oregon Department of Fish and Wildlife prohibits discrimination in all of its programs and services on the basis of race, color, national origin, age, sex or disability. If you believe that you have been discriminated against as described above in any program, activity, or facility, or if you desire further information, please contact ADA Coordinator, Oregon Department of Fish and Wildlife, 3406 Cherry Drive NE, Salem, OR, 503-947-6000. This material will be furnished in alternate format for people with disabilities if needed. Please call 541-757-4263 to request 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Sharon E. Tippery Brian L. Bangs Kim K. Jones Oregon Department of Fish and Wildlife Corvallis, OR November, 2010 This project was financed with funds administered by the U.S. Fish and Wildlife Service State Wildlife Grants under contract T-17-1 and the Oregon Department of Fish and Wildlife, Oregon Plan for Salmon and Watersheds. Citation: Tippery, S. E., B. L Bangs and K. K. Jones. 2010. 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon. Information Report 2010-05, Oregon Department of Fish and Wildlife, Corvallis. CONTENTS FIGURES....................................................................................................................................... -
Mayan Cichlid (Cichlasoma Urophthalmum) Ecological Risk Screening Summary
U.S. Fish and Wildlife Service Mayan Cichlid (Cichlasoma urophthalmum) Ecological Risk Screening Summary Web Version – 11/01/2012 Photo: Alexander Calder 1 Native Range, and Status in the United States Native Range From Robins (2001): The Mayan cichlid is native to the Central American Atlantic slope waters of southeastern Mexico (including the Yucatán Peninsula), Belize, Guatemala, Honduras, and Nicaragua. Nonindigenous Occurrences From Schofield et al. (2011): “This species was first documented in Florida when specimens were observed and collected and observed in Everglades National Park in 1983; it is established in several areas in and around the park (Loftus 1987; Lorenz et al. 1997; Smith-Vaniz, personal communication [not cited]; Tilmant 1999) and Big Cypress National Preserve (Nico, unpublished data; Tilmant 1999).” “On the east side of Florida it has been recorded from Canal C-111 north to the Little River Canal (C-7 Canal) (Shafland 1995).” Cichlasoma urophthalmus Ecological Risk Screening Summary U.S. Fish and Wildlife Service – Web Version – 11/1/2012 “A single specimen was taken from a rock pit in Manatee County in October 1975 (Smith- Vaniz, personal communication [not cited]).” “Mayan ciclids have also been collected in Lake Okeechobee and Lake Osbourne, Palm Beach County in 2003 (Cocking 2003; Werner 2003).” “A new population was found in Charlotte Harbor in the summer of 2003 (Adams and Wolfe 2007; Associated Press 2003; Charlotte Harbor NEP 2004; Byrley, personal communication [not cited]). This is the most northern population known.” Reported established in Florida Panther National Wildlife Refuge (2005).” “A specimen was collected in Holiday Park in Broward County (International Game Fishing Association 2000).” “In 2006, this species was found to be established in Mobbly Bayou in Tampa Bay and in canals on Merritt Island in 2007 (Paperno et al. -
Blackchin Tilapia (Sarotherodon Melanotheron) Ecological Risk Screening Summary
U.S. Fish and Wildlife Service Blackchin Tilapia (Sarotherodon melanotheron) Ecological Risk Screening Summary Web Version – 10/01/2012 Photo: © U.S. Geological Survey From Nico and Neilson (2014). 1 Native Range and Nonindigenous Occurrences Native Range From Nico and Neilson (2014): “Tropical Africa. Brackish estuaries and lagoons from Senegal to Zaire (Trewavas 1983).” Nonindigenous Occurrences From Nico and Neilson (2014): “Established in Florida and Hawaii. Evidence indicates it is spreading rapidly in both fresh and salt water around island of Oahu, Hawaii (Devick 1991b).” “The first documented occurrence of this species in Florida was a specimen gillnetted by commercial fishermen in Hillsborough Bay near Tampa, Hillsborough County, in 1959 (Springer and Finucane 1963). Additional records for the western part of the state indicate that this species is established in brackish and freshwaters in eastern Tampa Bay and in adjoining drainages in Hillsborough County, ranging from the Alafia River south to Cockroach Bay. The species has been recorded from the Alafia River from its mouth up to Lithia Springs; from the Hillsborough River, Bullfrog Creek, the Palm River, and the Little Manatee River; and from various western drainage and irrigation ditches (Springer and Finucane 1963; Finucane and Rinckey 1967; Buntz Sarotherodon melanotheron Ecological Risk Screening Summary U.S. Fish and Wildlife Service – Web Version – 10/01/2012 and Manooch 1969; Lachner et al. 1970; Courtenay et al. 1974; Courtenay and Hensley 1979; Courtenay and Kohler 1986; Lee et al. 1980 et seq.; Courtenay and Stauffer 1990; DNR collections; UF museum specimens). There are two records of this species from the west side of Tampa Bay, in Pinellas County: a collection from Lake Maggiore in St. -
Respiratory Disorders of Fish
This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository. Authors requiring further information regarding Elsevier’s archiving and manuscript policies are encouraged to visit: http://www.elsevier.com/copyright Author's personal copy Disorders of the Respiratory System in Pet and Ornamental Fish a, b Helen E. Roberts, DVM *, Stephen A. Smith, DVM, PhD KEYWORDS Pet fish Ornamental fish Branchitis Gill Wet mount cytology Hypoxia Respiratory disorders Pathology Living in an aquatic environment where oxygen is in less supply and harder to extract than in a terrestrial one, fish have developed a respiratory system that is much more efficient than terrestrial vertebrates. The gills of fish are a unique organ system and serve several functions including respiration, osmoregulation, excretion of nitroge- nous wastes, and acid-base regulation.1 The gills are the primary site of oxygen exchange in fish and are in intimate contact with the aquatic environment. In most cases, the separation between the water and the tissues of the fish is only a few cell layers thick. Gills are a common target for assault by infectious and noninfectious disease processes.2 Nonlethal diagnostic biopsy of the gills can identify pathologic changes, provide samples for bacterial culture/identification/sensitivity testing, aid in fungal element identification, provide samples for viral testing, and provide parasitic organisms for identification.3–6 This diagnostic test is so important that it should be included as part of every diagnostic workup performed on a fish. -
Book Review: Fishing Into Our Past
Evolutionary Psychology www.epjournal.net – 2008. 6(2): 365-368 ¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯¯ Book Review Fishing into our Past A review of Neil Shubin, Your Inner Fish: A Journey into the 3.5 Billion-Year History of the Human Body. Allen Lane: London, 2008, 229pp, UK£20, ISBN13: 9780713999358 (Hardcover) Robert King, Department of Psychology, Birkbeck College, University of London, UK. Email: [email protected] I am sure that many of us vividly remember the first time we started to get evolutionary psychology. For me it was like coming out of the optician’s with new glasses and realizing that I had been making do with a terribly short-sighted blur for ages. There is a sort of vertigo attendant on appreciating that the self is not just a few decades old or, as the cultural determinists claimed, centuries old. The realization that our selves could be understood only on the scale of millions of years creates dizziness. It is like that first time lying on one’s back staring into the time machine that is the star-filled night sky and it’s hitting you that many of those stars are now long dead. Those in Evolutionary Psychology (EP) are used to the concept of Deep Time. Some new term needs to be invented for what is stressed in Neil Shubin’s Your Inner Fish. Bottomless Time? Unfathomable Time? Shubin invites us to pan back our usual EP scale by three orders of magnitude from the savannah ape and consider ourselves from the perspective of 3.5 billion years. Of course, in doing this, Shubin is taking us back well beyond the “inner fish” of the title, but it is fish that made Shubin famous. -
Updated Checklist of Marine Fishes (Chordata: Craniata) from Portugal and the Proposed Extension of the Portuguese Continental Shelf
European Journal of Taxonomy 73: 1-73 ISSN 2118-9773 http://dx.doi.org/10.5852/ejt.2014.73 www.europeanjournaloftaxonomy.eu 2014 · Carneiro M. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:9A5F217D-8E7B-448A-9CAB-2CCC9CC6F857 Updated checklist of marine fishes (Chordata: Craniata) from Portugal and the proposed extension of the Portuguese continental shelf Miguel CARNEIRO1,5, Rogélia MARTINS2,6, Monica LANDI*,3,7 & Filipe O. COSTA4,8 1,2 DIV-RP (Modelling and Management Fishery Resources Division), Instituto Português do Mar e da Atmosfera, Av. Brasilia 1449-006 Lisboa, Portugal. E-mail: [email protected], [email protected] 3,4 CBMA (Centre of Molecular and Environmental Biology), Department of Biology, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal. E-mail: [email protected], [email protected] * corresponding author: [email protected] 5 urn:lsid:zoobank.org:author:90A98A50-327E-4648-9DCE-75709C7A2472 6 urn:lsid:zoobank.org:author:1EB6DE00-9E91-407C-B7C4-34F31F29FD88 7 urn:lsid:zoobank.org:author:6D3AC760-77F2-4CFA-B5C7-665CB07F4CEB 8 urn:lsid:zoobank.org:author:48E53CF3-71C8-403C-BECD-10B20B3C15B4 Abstract. The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. -
New Zealand Fishes a Field Guide to Common Species Caught by Bottom, Midwater, and Surface Fishing Cover Photos: Top – Kingfish (Seriola Lalandi), Malcolm Francis
New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing Cover photos: Top – Kingfish (Seriola lalandi), Malcolm Francis. Top left – Snapper (Chrysophrys auratus), Malcolm Francis. Centre – Catch of hoki (Macruronus novaezelandiae), Neil Bagley (NIWA). Bottom left – Jack mackerel (Trachurus sp.), Malcolm Francis. Bottom – Orange roughy (Hoplostethus atlanticus), NIWA. New Zealand fishes A field guide to common species caught by bottom, midwater, and surface fishing New Zealand Aquatic Environment and Biodiversity Report No: 208 Prepared for Fisheries New Zealand by P. J. McMillan M. P. Francis G. D. James L. J. Paul P. Marriott E. J. Mackay B. A. Wood D. W. Stevens L. H. Griggs S. J. Baird C. D. Roberts‡ A. L. Stewart‡ C. D. Struthers‡ J. E. Robbins NIWA, Private Bag 14901, Wellington 6241 ‡ Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, 6011Wellington ISSN 1176-9440 (print) ISSN 1179-6480 (online) ISBN 978-1-98-859425-5 (print) ISBN 978-1-98-859426-2 (online) 2019 Disclaimer While every effort was made to ensure the information in this publication is accurate, Fisheries New Zealand does not accept any responsibility or liability for error of fact, omission, interpretation or opinion that may be present, nor for the consequences of any decisions based on this information. Requests for further copies should be directed to: Publications Logistics Officer Ministry for Primary Industries PO Box 2526 WELLINGTON 6140 Email: [email protected] Telephone: 0800 00 83 33 Facsimile: 04-894 0300 This publication is also available on the Ministry for Primary Industries website at http://www.mpi.govt.nz/news-and-resources/publications/ A higher resolution (larger) PDF of this guide is also available by application to: [email protected] Citation: McMillan, P.J.; Francis, M.P.; James, G.D.; Paul, L.J.; Marriott, P.; Mackay, E.; Wood, B.A.; Stevens, D.W.; Griggs, L.H.; Baird, S.J.; Roberts, C.D.; Stewart, A.L.; Struthers, C.D.; Robbins, J.E.