Nesting Emergences by the Kemp's Ridley Sea Turtle
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Beach Dynamics and Impact of Armouring on Olive Ridley Sea Turtle (Lepidochelys Olivacea) Nesting at Gahirmatha Rookery of Odisha Coast, India
Indian Journal of Geo-Marine Sciences Vol. 45(2), February 2016, pp. 233-238 Beach dynamics and impact of armouring on olive ridley sea turtle (Lepidochelys olivacea) nesting at Gahirmatha rookery of Odisha coast, India Satyaranjan Behera1, 2, Basudev Tripathy3*, K. Sivakumar2, B.C. Choudhury2 1Odisha Biodiversity Board, Regional Plant Resource Centre Campus, Nayapalli, Bhubaneswar-15 2Wildlife Institute of India, Dehradun, PO Box 18, Chandrabani, Dehradun – 248 001, India. 3Zoological Survey of India, Prani Vigyan Bhawan, M-Block, New Alipore, Kolkata-700 053 (India) *[E. mail:[email protected]] Received 28 March 2014; revised 18 September 2014 Gahirmatha arribada beach are most dynamic and eroding at a faster rate over the years from 2008-09 to 2010-11, especially during the turtles breeding seasons. Impact of armouring cement tetrapod on olive ridley sea turtle nesting beach at Gahirmatha rookery of Odisha coast has also been reported in this study. This study documented the area of nesting beach has reduced from 0.07 km2to 0.06 km2. Due to a constraint of nesting space, turtles were forced to nest in the gap of cement tetrapods adjacent to the arribada beach and get entangled there, resulting into either injury or death. A total of 209 and 24 turtles were reported to be injured and dead due to placement of cement tetrapods in their nesting beach during 2008-09 and 2010-11 respectively. Olive ridley turtles in Odisha are now exposed to many problems other than fishing related casualty and precautionary measures need to be taken by the wildlife and forest authorities to safeguard the Olive ridleys and their nesting habitat at Gahirmatha. -
World Bank Document
LatIN AMERIca & CARIBBEAN REGION Environment & Water Resources Uncertain Future, Robust Decisions OCCASIONAL PAPER SERIES The Case of Climate Change Public Disclosure Authorized Adaptation in Campeche, Mexico Public Disclosure Authorized Public Disclosure Authorized Public Disclosure Authorized © 2013 International Bank for Reconstruction and Development / The World Bank 1818 H Street NW Washington DC 20433 Telephone: 202-473-1000 Internet: www.worldbank.org This work is a product of the staff of The World Bank with external contributions. The findings, interpretations, and conclusions expressed in this work do not necessarily reflect the views of The World Bank, its Board of Executive Directors, or the governments they represent. The World Bank does not guarantee the accuracy of the data included in this work. The boundaries, colors, denominations, and other information shown on any map in this work do not imply any judgment on the part of The World Bank concerning the legal status of any territory or the endorsement or acceptance of such boundaries. The Environment and Water Resources Occasional Paper Series was developed under the direction of Karin Kemper, Sector Manager for Environment and Water Resources in the Latin America and Caribbean Region (LCSEN) of the World Bank. The publications in this Series were designed and produced by GRC Direct under the supervision of Emilia Battaglini and Rachel Pasternack (LCSEN). A list of the most recent papers is on the back cover of this publication. For electronic copies of all our LAC Environment & Water Resources Occasional Papers please visit our website: www.worldbank.org/lac Rights and Permissions The material in this work is subject to copyright. -
AN INTRODUCTION to Texas Turtles
TEXAS PARKS AND WILDLIFE AN INTRODUCTION TO Texas Turtles Mark Klym An Introduction to Texas Turtles Turtle, tortoise or terrapin? Many people get confused by these terms, often using them interchangeably. Texas has a single species of tortoise, the Texas tortoise (Gopherus berlanderi) and a single species of terrapin, the diamondback terrapin (Malaclemys terrapin). All of the remaining 28 species of the order Testudines found in Texas are called “turtles,” although some like the box turtles (Terrapene spp.) are highly terrestrial others are found only in marine (saltwater) settings. In some countries such as Great Britain or Australia, these terms are very specific and relate to the habit or habitat of the animal; in North America they are denoted using these definitions. Turtle: an aquatic or semi-aquatic animal with webbed feet. Tortoise: a terrestrial animal with clubbed feet, domed shell and generally inhabiting warmer regions. Whatever we call them, these animals are a unique tie to a period of earth’s history all but lost in the living world. Turtles are some of the oldest reptilian species on the earth, virtually unchanged in 200 million years or more! These slow-moving, tooth less, egg-laying creatures date back to the dinosaurs and still retain traits they used An Introduction to Texas Turtles | 1 to survive then. Although many turtles spend most of their lives in water, they are air-breathing animals and must come to the surface to breathe. If they spend all this time in water, why do we see them on logs, rocks and the shoreline so often? Unlike birds and mammals, turtles are ectothermic, or cold- blooded, meaning they rely on the temperature around them to regulate their body temperature. -
Background on Sea Turtles
Background on Sea Turtles Five of the seven species of sea turtles call Virginia waters home between the months of April and November. All five species are listed on the U.S. List of Endangered and Threatened Wildlife and Plants and classified as either “Threatened” or “Endangered”. It is estimated that anywhere between five and ten thousand sea turtles enter the Chesapeake Bay during the spring and summer months. Of these the most common visitor is the loggerhead followed by the Kemp’s ridley, leatherback and green. The least common of the five species is the hawksbill. The Loggerhead is the largest hard-shelled sea turtle often reaching weights of 1000 lbs. However, the ones typically sighted in Virginia’s waters range in size from 50 to 300 lbs. The diet of the loggerhead is extensive including jellies, sponges, bivalves, gastropods, squid and shrimp. While visiting the Bay waters the loggerhead dines almost exclusively on horseshoe crabs. Virginia is the northern most nesting grounds for the loggerhead. Because the temperature of the nest dictates the sex of the turtle it is often thought that the few nests found in Virginia are producing predominately male offspring. Once the male turtles enter the water they will never return to land in their lifetime. Loggerheads are listed as a “Threatened” species. The Kemp’s ridley sea turtle is the second most frequent visitor in Virginia waters. It is the smallest of the species off Virginia’s coast reaching a maximum weight of just over 100 lbs. The specimens sited in Virginia are often less than 30 lbs. -
Estaciã³n De Investigaciones Marinas El Carmen, Universidad Nacional
Gulf of Mexico Science Volume 28 Article 5 Number 1 Number 1/2 (Combined Issue) 2010 Estación de Investigaciones Marinas El Carmen, Universidad Nacional Autónoma de México Elva Escobar Briones Universidad Nacional Autónoma de México Raymundo Lecuanda Universidad Nacional Autónoma de México DOI: 10.18785/goms.2801.05 Follow this and additional works at: https://aquila.usm.edu/goms Recommended Citation Briones, E. E. and R. Lecuanda. 2010. Estación de Investigaciones Marinas El Carmen, Universidad Nacional Autónoma de México. Gulf of Mexico Science 28 (1). Retrieved from https://aquila.usm.edu/goms/vol28/iss1/5 This Article is brought to you for free and open access by The Aquila Digital Community. It has been accepted for inclusion in Gulf of Mexico Science by an authorized editor of The Aquila Digital Community. For more information, please contact [email protected]. Briones and Lecuanda: Estación de Investigaciones Marinas El Carmen, Universidad Nacion Gulf of Mexico Science, 2010(1–2), pp. 22–35 ESTACIO´ N DE INVESTIGACIONES MARINAS EL CARMEN UNIVERSIDAD NACIONAL AUTO´ NOMA DE ME´ XICO ELVA ESCOBAR BRIONES AND RAYMUNDO LECUANDA BACKGROUND AND SETTING FOR THE CREATION OF tions. The extraction of shrimp through artisanal UNAM’s FIELD STATION IN CIUDAD DEL CARMEN and offshore fisheries had been a major source of income and development of infrastructure in The Estacio´n de Investigaciones Marinas El Ciudad del Carmen from 1945 until the mid Carmen (the Station of Marine Research in 1970s. Shipyards, canneries, and freezing indus- Ciudad del Carmen) is a subunit of the Instituto tries flourished through at least three decades. -
American Horseshoe Crabs, Limulus Polyphemus, in Mexico: Open Possibilities
American Horseshoe Crabs, Limulus polyphemus, in Mexico: Open Possibilities Jaime Zaldı´ var-Rae, Rene´ Elı´ as Sapie´ n-Silva, Martha Rosales-Raya, and H. Jane Brockmann Abstract Little is known about Mexican Limulus polyphemus, the southern- most population of the species. We present an overview of work on Mexican horseshoe crabs, their situation, and perceived threats and opportunities regarding the conservation of the species. Horseshoe crabs occur along the western, northern, and eastern coasts of the Yucata´ n peninsula, and are geneti- cally distinct from populations in the United States. Spawning aggregations and nests are found continuously throughout the year, commonly in protected lagoons where mangrove (Rhizophora mangle, Laguncularia racemosa, Avicen- nia germinans, and Conocarpus erectus) and sea grass (Thalassia testudinum) communities proliferate. Populations are thought to be dwindling since the 1960s and Limulus is listed as ‘‘in danger of extinction’’ in Mexican legislation since 1994. The most important localities are within protected areas. Direct exploitation is not an important threat, but coastline modification (especially of mangrove areas and coastal lagoons) for housing and tourism is a major concern. Additional potential threats are the oil industry and shrimp fishery in the southern Gulf of Mexico, but their effects on horseshoe crab populations have not been assessed. 1 Introduction Knowledge about the biology and ecology of Mexican Limulus polyphemus, the southernmost population of the species, is scant (Escalante et al. 1980; Gomez-´ Aguirre 1980; Bonilla-Gonza´ lez et al. 1986; Anderson and Shuster 2003). This chapter aims at providing an overview of the available information on the biology of horseshoe crabs in Mexico and our perspective on potential threats and opportunities for the study and conservation of these animals in Mexico. -
Issue Number 118 October 2007 ISSN 0839-7708 in THIS
Issue Number 118 October 2007 Green turtle hatchling from Turkey with extra carapacial scutes (see pp. 6-8). Photo by O. Türkozan IN THIS ISSUE: Editorial: Conservation Conflicts, Conflicts of Interest, and Conflict Resolution: What Hopes for Marine Turtle Conservation?..........................................................................................L.M. Campbell Articles: From Hendrickson (1958) to Monroe & Limpus (1979) and Beyond: An Evaluation of the Turtle Barnacle Tubicinella cheloniae.........................................................A. Ross & M.G. Frick Nest relocation as a conservation strategy: looking from a different perspective...................O. Türkozan & C. Yılmaz Linking Micronesia and Southeast Asia: Palau Sea Turtle Satellite Tracking and Flipper Tag Returns......S. Klain et al. Morphometrics of the Green Turtle at the Atol das Rocas Marine Biological Reserve, Brazil...........A. Grossman et al. Notes: Epibionts of Olive Ridley Turtles Nesting at Playa Ceuta, Sinaloa, México...............................L. Angulo-Lozano et al. Self-Grooming by Loggerhead Turtles in Georgia, USA..........................................................M.G. Frick & G. McFall IUCN-MTSG Quarterly Report Announcements News & Legal Briefs Recent Publications Marine Turtle Newsletter No. 118, 2007 - Page 1 ISSN 0839-7708 Editors: Managing Editor: Lisa M. Campbell Matthew H. Godfrey Michael S. Coyne Nicholas School of the Environment NC Sea Turtle Project A321 LSRC, Box 90328 and Earth Sciences, Duke University NC Wildlife Resources Commission Nicholas School of the Environment 135 Duke Marine Lab Road 1507 Ann St. and Earth Sciences, Duke University Beaufort, NC 28516 USA Beaufort, NC 28516 USA Durham, NC 27708-0328 USA E-mail: [email protected] E-mail: [email protected] E-mail: [email protected] Fax: +1 252-504-7648 Fax: +1 919 684-8741 Founding Editor: Nicholas Mrosovsky University of Toronto, Canada Editorial Board: Brendan J. -
Reproductive Physiology of Nesting Leatherback Turtles (Dermochelys Coriacea) at Las Baulas National Park, Costa Rica
Chelolliall COllserwuioll (lnd Biology, 1996,2(2):230- 236 © 1996 by Chelonian Research Foundation Reproductive Physiology of Nesting Leatherback Turtles (Dermochelys coriacea) at Las Baulas National Park, Costa Rica i 2 3 4 DAVID C. ROSTAL , FRANK V. PALADIN0 , RHONDA M. PATTERSON , AND JAMES R. SPOTILA I Department of Biology, Georgia Southern Uni versity, Statesboro, Georgia 30460 USA [Fax: 912-681-0845; E-mail: [email protected]}; 2Department of Biology, Indiana-Purdue University, Fort Wayne, Indiana 46805 USA ; 3Department of Biology, Texas A&M University, College Station, Texas 77843 USA ; 4Department o{Bioscience and Biotechnology, Drexel University, Philadelphia, Pennsylvania 19104 USA ABSTRACT. - The reproductive physiology of nesting leatherback turtles (Dermochelys coriacea) was studied at Playa Grande, Costa Rica, from 1992 to 1994 during November, December, and January. Ultrasonography indicated that 82 % of nesting females had mature preovulatory ovaries in November, 40 % in December, and 23 % in January. Mean follicular diameter was 3.33 ±0.02 cm and did not vary significantly through the nesting season. Plasma testosterone and estradiol levels measured by radioimmunoassay correlated strongly with reproductive condition. No correlation, however, was observed between reproductive condition and plasma progesterone levels. Testoster one declined from 2245 ± 280 pglml at the beginning of the nesting cycle to 318 ± 89 pglml at the end of the nesting cycle. Estradiol declined in a similar manner. Plasma calcium levels were constant throughout the nesting cycle. Vitellogenesis appeared complete prior to the arrival of the female at the nesting beach. Dermochelys coriacea is a seasonal nester displaying unique variations (e.g., 9 to 10 day internesting interval, yolkless eggs) on the basic chelonian pattern. -
OLIVE RIDLEY SEA TURTLE (Lepidochelys Olivacea)
OLIVE RIDLEY SEA TURTLE (Lepidochelys olivacea) General Characteristics The name of the olive ridley originates from the olive color of the adult’s carapace. Its head is triangular in shape, measuring up to 13 cm (5.1 in.) wide, with two pairs of prefrontal scales. Their carapace is circular and flat with a uniquely high and variable number (six to nine pairs) of costal scutes, and ranges from olive green to dark grey in color. The plastron is cream colored and has a small and distinct pore close to the rear margin of each of the four inframarginal scutes. Its body is deeper than the Kemp’s Ridley (L. kempii), which is found primarily in the Gulf of Mexico and along the eastern coast of the USA. Size The olive ridley is one of the smallest sea turtles; the length of the carapaces is approximately 65 cm (2 ft.) and reaches up to 50 kg. (110 lbs.). Both the front and rear flippers have one, or sometimes two, claws. Habitat Olive ridleys are found throughout the tropical waters of the Pacific, Indian and southern Atlantic Oceans. In the eastern Pacific they range from Mexico to Colombia and are sometimes found off the southwestern coast of the United States. Non-nesting individuals are often found in Isla de Margarita (Venezuela) and Trinidad & Tobago; however, they rarely go deeper into the Caribbean. They typically forage offshore in surface waters, primarily in bays and estuaries. They may dive to depths of 150 meters (500 ft.) to feed on bottom- dwelling crustaceans. Diet Their large and powerful jaws are adapted to their diet of mostly fish, mussels and crustaceans, particularly shrimp. -
King and Spanish Hackerel Higration and Stock Assessment Study in the Southern Gulf of Mexico
KING AND SPANISH HACKEREL HIGRATION AND STOCK ASSESSMENT STUDY IN THE SOUTHERN GULF OF MEXICO Contract No. NA90AA-H -MFI00 (MARFIN) 1990 Quarter V (January I-Mar ch 31, 1991) Report Submitted to : Dr. Donald Ekberg Regional Oirector National Marine Fisheries Servi ce Duval Building 9450 Koger Bou l evard St. Petersburg, FL 33702 Mote Marine Laboratory 1600 Thompson Parkway Sarasota, FL 34236 (813) 388-4441 ~;5~ Richard H. Pierce, Ph.D. Karen M. Burns Director of Research Principal Investigator Jay M. Sprinkel Data Manager April I , 1991 TAB LE OF CONTENTS Cover Table of Contents .j List of Fi gures i ; list of Tables i i Acknowledgements iii Pre face/ Prefac i 0 iv INTROOUCTION/ INTROOUCCION I. MOVEMENT AND MIG RATIO N OF MA CKER EL 1 A. Tagging Synopsis, Yucatan and Quintana Roo 4 B. Tag Returns 4 C. Publ ic Information Program I ! II. LENGTH/ FREQUENCY DISTRIBUTION OF MACKEREL 15 III. HISTORICAL LANDINGS DATA 17 IV . STOCK IDENTIFICATION 17 A. Specimen Collection for Electrophoresis 17 B. Oto l ith Co ll ection 17 V. RESULTS 18 LIST OF FIGURES Figure 1. Spanish mackerel tag release locations , 1990 - 1991. Figure 2 . Mackerel length/frequency and catch per unit effort (CPUE) locations , 1990-1991. Figure 3 . King mackerel Quarter V winter tag returns. 12 Figure 4. Number of mackerel tagged off Mexican Gulf Coast States (1986 - 1991). 13 Figure 5. Significant long di stance tag returns between the U. S. and Mexico (1986 - 1991). Figure 6. Significant tag returns within Mexico and from VeraCrlJ 7\ Mexico to the u.s. -
Olive Ridley Turtle)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Lepidochelys olivacea (Olive Ridley Turtle) Family: Cheloniidae (Sea Turtles) Order: Testudines (Turtles and Tortoises) Class: Reptilia (Reptiles) Fig. 1. Olive ridley turtle, Lepidochelys olivacea. [http://www.nathab.com/central-america/mexico-sea-turtle-tour/, downloaded 9 March 2016] TRAITS. Lepidochelys olivacea or the olive ridley turtle is named due to the greenish coloration of its skin and carapace, and is one of the smallest sea turtles (Fig. 1). Mature turtles typically weigh around 30-50 kg and grow to be around 60-75cm in length (Eckert, 1999). The carapace or protective shell of Lepidochelys olivacea has a short but wide structure that has high vertebral projections in juvenile turtles, and is smooth with an elevated tectiform (roof-like) shape in adult turtles. The carapace is also known to have an inconstant amount of lateral scutes, ranging between six to ten pairs. In addition to this, eight pores are found on the scutes of the ventral surface of the shell (Marcovaldi, 1999). The head of Lepidochelys olivacea is relatively larger than most turtles, with an average width of 13cm, and has two pairs of prefrontal scales. Male olive ridleys can be distinguished from females by their long tails, relatively soft and concave plastron, as well as sturdy talons found on their anterior limbs (Wibbels et al., 1991). DISTRIBUTION. Olive ridleys are found only in warm waters such as the southern Atlantic Ocean, Pacific Ocean and Indian Ocean (Fig. 2). There are a few records of Lepidochelys olivacea being found in areas of the western Atlantic Ocean such as off the coast of Trinidad and Tobago, Brazil, Venezuela and Suriname (Schulz, 1975). -
Congenital Malformations in Sea Turtles: Puzzling Interplay Between Genes and Environment
animals Review Congenital Malformations in Sea Turtles: Puzzling Interplay between Genes and Environment Rodolfo Martín-del-Campo 1, María Fernanda Calderón-Campuzano 2, Isaías Rojas-Lleonart 3, Raquel Briseño-Dueñas 2,4 and Alejandra García-Gasca 5,* 1 Department of Oral Health Sciences, Faculty of Dentistry, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z3, Canada; [email protected] 2 Marine Turtle Programme, Instituto de Ciencias del Mar y Limnología-UNAM-FONATUR, Mazatlán, Sinaloa 82040, Mexico; [email protected] (M.F.C.-C.); [email protected] (R.B.-D.) 3 Universidad Central “Martha Abreu” de las Villas (IRL), CUM Remedios, Villa Clara 52700, Cuba; [email protected] 4 Banco de Información sobre Tortugas Marinas (BITMAR), Unidad Académica Mazatlán, Instituto de Ciencias del Mar y Limnología-UNAM, Mazatlán, Sinaloa 82040, Mexico 5 Laboratory of Molecular and Cellular Biology, Centro de Investigación en Alimentación y Desarrollo, Mazatlán, Sinaloa 82112, Mexico * Correspondence: [email protected]; Tel.: +52-669-989-8700 Simple Summary: Congenital malformations can lead to embryonic mortality in many species, and sea turtles are no exception. Genetic and/or environmental alterations occur during early develop- ment in the embryo, and may produce aberrant phenotypes, many of which are incompatible with life. Causes of malformations are multifactorial; genetic factors may include mutations, chromosomal aberrations, and inbreeding effects, whereas non-genetic factors may include nutrition, hyperthermia, low moisture, radiation, and contamination. It is possible to monitor and control some of these Citation: Martín-del-Campo, R.; Calderón-Campuzano, M.F.; factors (such as temperature and humidity) in nesting beaches, and toxic compounds in feeding Rojas-Lleonart, I.; Briseño-Dueñas, R.; areas, which can be transferred to the embryo through their lipophilic properties.