2019. Gada Darbības Pārskats
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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, -
Monograph of the Cyprinid Fis~Hes of the Genus Garra Hamilton (173)
MONOGRAPH OF THE CYPRINID FIS~HES OF THE GENUS GARRA HAMILTON By A. G. K. MENON, Zoologist, ,Zoological Surt1ey of India, Oalcutta. (With 1 Table, 29 Text-figs. and 6 Plates) CONTENTS Page I-Introduction 175 II-Purpose and general results 176 III-Methods and approaches 176 (a) The definition of Measurements 176 (b) The analysis of Intergradation 178 (c) The recognition of subspecies. 179 (d) Procedures in the paper 180 (e) Evaluation of systematic characters 181 (I) Abbreviations of names of Institutions 181 IV-Historical sketch 182 V-Definition of the genus 187 VI-Systematic section 188 (a) The variabilis group 188 (i) The variabilis Complex 188 1. G. variabilis 188 2. G. rossica 189 (b) The tibanica group 191 (i) The tibanica Complex 191 3. G. tibanica. 191 4. G. quadrimaculata 192 5. G. ignestii 195 6. G. ornata 196 7. G. trewavasi 198 8. G. makiensis 198 9. G. dembeensis 199 10. G. ethelwynnae 202 (ii) The rufa complex 203 11. G. rufa rufa 203 12. G. rufa obtusa 205 13. O. barteimiae 206 (iii) The lamta complex 208 14. G. lamta 208 15. G. mullya 212 16. G. 'ceylonensis ceylonensis 216 17. G. c. phillipsi 216 18. G. annandalei 217 (173) 174 page (iv) The lissorkynckus complex 219 19. G. lissorkynchus 219 20. G. rupecula 220 ~ (v) The taeniata complex 221 21. G. taeniata. 221 22" G. borneensis 224 (vi) The yunnanensis complex 224 23. G. yunnanensis 225 24. G. gracilis 229 25. G. naganensis 226 26. G. kempii 227 27. G. mcOlellandi 228 28. G. -
Safety and Hygiene of Ichthyotherapy with G. Rufa Fish
Arch Phys Glob Res 2019; 23 (2): 37-44 ORIGINAL PAPER DOI 10.15442/apgr.23.2.5 Safety and hygiene of ichthyotherapy with G. rufa fish Małgorzata Gorzel*, Anna Kiełtyka-Dadasiewicz** * Faculty of Health Sciences, Vincent Pol University, ** Research and Science Innovation Center, Lublin Abstract Today, biotherapies (therapies using animals, plants or their secretions) are becoming increasingly popular. In medicine and cosmetology, leeches, fish, insect larvae, mucus fromH. aspersa snail, bee products are used. Among them, ichthyotherapy - therapy with the use of Garra rufa (Heckel 1843), which is gaining popularity not only in the exotic resorts of Turkey, Iran and Jordan, but also in Poland, deserves attention. In view of the growing interest in ichthyotherapy, the question arises: Are cosmetic and therapeutic procedures using this vertebrate completely safe for humans? This question became a contribution to taking up this topic of study. Ichthyotherapy is the use of freshwater, sedentary benthopelagic fish of the cyprinid family, red garra (G. rufa), commercially referred to as “the doctor fish”. This fish has a suction apparatus that allows removal of calloused epidermis in patients undergoing therapy. This treatment has been used mainly in cosmetics as so-called fish pedicure, but also in medicine. Scientific reports indicate that this fish may be helpful in treating some skin diseases, i.e. in alleviating the symptoms of psoriasis or atopic dermatitis. Treatments using the red garra have to be performed in full compliance with hygiene rules. In 2011, the British Health Protect Agency (BHPA) published the guidelines for carrying out treatments using these fish. It specified the indications and contraindications for performing the procedure, the way it should be performed, as well as the threats that could result from possible non-compliance with the principles of occupational health and safety during the procedures. -
A Review of Freshwater Fish Fauna in Jordan
Libyan Agriculture Research Center Journal International 1 (5): 320-324, 2010 ISSN 2219-4304 © IDOSI Publications, 2010 A Review of Freshwater Fish Fauna in Jordan Saleh Ahmad Al-Quran Department of Biology, Faculty of Science, Mutah University, Karak, Jordan Abstract: A total of 27 fish species belonging to ten families were recorded. The fish fauna distribution in two rivers (Jordan and Yarmouk) and some dams and tributaries in Jordan was examined. The rivers surveyed were generally shallow, fast flowing with clear water and rocky and sandy substrate. At the time of survey, the rivers gave excellent water quality data. Cyprinidae has the highest diversity 0.296% with 8 species; while the lowest one are Anguillidae, Blennidae, Clariidae, Mugilidae and Pseudocrenilabrinae; each represented only by one species (0.037%). Cichlidae represented by 6 species (0.222%), Balitoridae and Cyprinodontidae are represented by three species (0.111%) and finally Acanthuridae is represented by two species (0.074%). Key words: Review % Freshwater % Fish % Fauna % Jordan INTRODUCTION drains into the Dead Sea which, at 407 meters below sea level, is the lowest point on earth. The river is between Location, Topography and Climate: Jordan is a relatively 20 and 30 meters wide near its endpoint. Its flow has been small country situated at the junction of the Levantine much reduced and its salinity increased because and Arabian areas of the Middle East. The country is significant amounts have been diverted for irrigational bordered on the north by Syria, to the east by Iraq and by uses. Several degrees warmer than the rest of the country, Saudi Arabia on the east and south. -
Attacked from Above and Below, New Observations of Cooperative and Solitary Predators on Roosting Cave Bats
bioRxiv preprint doi: https://doi.org/10.1101/550582; this version posted February 17, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Attacked from above and below, new observations of cooperative and solitary predators on roosting cave bats Krizler Cejuela. Tanalgo1, 2, 3, 7*, Dave L. Waldien4, 5, 6, Norma Monfort6, Alice Catherine Hughes1, 3* 1Landscape Ecology Group, Centre for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China 2International College, University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China 3Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China 4Harrison Institute, Bowerwood House, 15 St Botolph’s Road, Sevenoaks, Kent, TN13 3AQ, United Kingdom 5Christopher Newport University, 1 Avenue of the Arts, Newport News, VA 23606, United States of America 6Philippine Bats for Peace Foundation Inc., 5 Ramona Townhomes, Guadalupe Village, Lanang, Davao City 7Department of Biological Sciences, College of Arts and Sciences, University of Southern Mindanao, Kabacan 9407, North Cotabato, the Republic of the Philippines Corresponding authors: ACH ([email protected]) and KCT ([email protected]) Landscape Ecology Group, Centre for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China Abstract Predation of bats in their roosts has previously only been attributed to a limited number of species such as various raptors, owls, and snakes. -
Coordinated Hunting by Cuban Boas
ABC 2017, 4(1):24-29 Animal Behavior and Cognition DOI: 10.12966/abc.02.02.2017 ©Attribution 3.0 Unported (CC BY 3.0) Coordinated Hunting by Cuban Boas Vladimir Dinets1,* 1University of Tennessee, Knoxville, TN *Corresponding author (Email: [email protected]) Citation – Dinets, V. (2017). Coordinated hunting by Cuban boas. Animal Behavior and Cognition, 4(1), 24–29. doi: 10.12966/abc.02.02.2017 Abstract - Coordinated hunting, in which individual predators relate in time and space to each other’s actions, is uncommon in animals, and is often difficult to distinguish from simply hunting in non-coordinated groups, which is much more common. The author tested if Cuban boas (Chilabothrus angulifer) hunting bats in cave passages take into account other boas’ positions when choosing hunting sites, and whether their choices increase hunting efficiency. Snakes arriving to the hunting area were significantly more likely to position themselves in the part of the passage where other snakes were already present, forming a “fence” across the passage and thus more effectively blocking the flight path of the prey, significantly increasing hunting efficiency. This is the first study to test for coordination between hunting reptiles, rather than assume such coordination based on perceived complexity of hunting behavior. Keywords – Boidae, Chilabothrus angulifer, Cooperative hunting, Cuba, Predation, Social behavior Coordinated hunting, in which individual predators relate in time and space to each other’s actions, is uncommon but widespread in animals (Bailey, -
Fish-Released Kairomones Affect Culiseta Longiareolata Oviposition and Larval Life History
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.22.423951; this version posted December 22, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Fish-released kairomones affect Culiseta longiareolata oviposition and larval life history Alon Silberbush Department of Biology and the Environment, Faculty of Natural Sciences, University of Haifa, Israel Abstract: Several species of mosquitoes respond to the presence of kairomones released by larval predators during oviposition habitat selection and larval development. These responses may differ among mosquito species and do not always correlate with larval survival. This study examined the responses of the mosquito Culiseta longiareolata Macquart to kairomones released by three species of fish during oviposition, Gambusia affinis Baird and Girard, Aphanius mento Heckel and Garra rufa Heckel. In addition, the study examined the effects of kairomones released by G. affinis on larval development. Results show that ovipositing female avoided cues from larvivorous, but not algivorous fish. In addition, developing larvae metamorphosed slower and showed increased mortality when exposed to fish-released kairomones. Results suggest that the responses of this mosquito species to fish-released kairomones may be explained by its competitive ability. Keywords: Predator-released kairomones, life history, oviposition habitat selection. Introduction: Semiochemicals indicating the presence of predators are often an important part of predator detection mechanisms in addition to visual, audio and tactical cues (Kats and Dill 1998). Aquatic organisms often rely specifically on kairomones or other predator associated semiochemicals, bioRxiv preprint doi: https://doi.org/10.1101/2020.12.22.423951; this version posted December 22, 2020. -
Training Manual Series No.15/2018
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CMFRI Digital Repository DBTR-H D Indian Council of Agricultural Research Ministry of Science and Technology Central Marine Fisheries Research Institute Department of Biotechnology CMFRI Training Manual Series No.15/2018 Training Manual In the frame work of the project: DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals 2015-18 Training Manual In the frame work of the project: DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals 2015-18 Training Manual This is a limited edition of the CMFRI Training Manual provided to participants of the “DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals” organized by the Marine Biotechnology Division of Central Marine Fisheries Research Institute (CMFRI), from 2nd February 2015 - 31st March 2018. Principal Investigator Dr. P. Vijayagopal Compiled & Edited by Dr. P. Vijayagopal Dr. Reynold Peter Assisted by Aditya Prabhakar Swetha Dhamodharan P V ISBN 978-93-82263-24-1 CMFRI Training Manual Series No.15/2018 Published by Dr A Gopalakrishnan Director, Central Marine Fisheries Research Institute (ICAR-CMFRI) Central Marine Fisheries Research Institute PB.No:1603, Ernakulam North P.O, Kochi-682018, India. 2 Foreword Central Marine Fisheries Research Institute (CMFRI), Kochi along with CIFE, Mumbai and CIFA, Bhubaneswar within the Indian Council of Agricultural Research (ICAR) and Department of Biotechnology of Government of India organized a series of training programs entitled “DBT sponsored Three Months National Training in Molecular Biology and Biotechnology for Fisheries Professionals”. -
Výroční Zpráva
2017 VÝROČNÍ ZPRÁVA Zoologická a botanická zahrada města Plzně / VÝROČNÍ ZPRÁVA 2017 Zoologická a botanická zahrada města Plzně Zoological and Botanical Garden Pilsen/ Annual Report 2017 Provozovatel ZOOLOGICKÁ A BOTANICKÁ ZAHRADA MĚSTA PLZNĚ, příspěvková organizace ZOOLOGICKÁ A BOTANICKÁ ZAHRADA MĚSTA PLZNĚ POD VINICEMI 9, 301 00 PLZEŇ, CZECH REPUBLIC tel.: 00420/378 038 325, fax: 00420/378 038 302 e-mail: [email protected], www.zooplzen.cz Vedení zoo Management Ředitel Ing. Jiří Trávníček Director Ekonom Jiřina Zábranská Economist Provozní náměstek Ing. Radek Martinec Assistent director Vedoucí zoo. oddělení Bc. Tomáš Jirásek Head zoologist Zootechnik Svatopluk Jeřáb Zootechnicist Zoolog Ing. Lenka Václavová Curator of monkeys, carnivores Jan Konáš Curator of reptiles Miroslava Palacká Curator of ungulates Botanický náměstek, zoolog Ing. Tomáš Peš Head botanist, curator of birds, small mammals Botanik Mgr. Václava Pešková Botanist Propagace, PR Mgr. Martin Vobruba Education and PR Sekretariát Alena Voráčková Secretary Privátní veterinář MVDr. Jan Pokorný Veterinary Celkový počet zaměstnanců Total Employees (k 31. 12. 2017) 130 Zřizovatel Plzeň, statutární město, náměstí Republiky 1, Plzeň IČO: 075 370 tel.: 00420/378 031 111 Fotografie: Kateřina Misíková, Jiří Trávníček, Tomáš Peš, Miroslav Volf, Martin Vobruba, Jiřina Pešová, archiv Zoo a BZ, DinoPark, Oživená prehistorie a autoři článků Redakce výroční zprávy: Jiří Trávníček, Martin Vobruba, Tomáš Peš, Alena Voráčková, Kateřina Misíková, Pavel Toman, David Nováček a autoři příspěvků 1 výroční -
Systematics of Quaternary Squamata from Cuba
UNIVERSIDADE DE SÃO PAULO MUSEU DE ZOOLOGIA Ernesto Aranda Pedroso Systematics of Quaternary Squamata from Cuba Sistemática dos Squamata Quaternários de Cuba Corrected version Dissertation presented to the PostGraduate Program of the Museu de Zoologia da Universidade de São Paulo to obtain the degree of Master of Science (Systematics, Animal Taxonomy and Biodiversity) Advisor: Hussam El Dine Zaher Co-Advisor: Luis Manuel Díaz Beltrán São Paulo 2019 Resumo Aranda E. (2019). Sistemática dos Squama do Quaternário de Cuba. (Dissertação de Mestrado). Museu de Zoologia, Universidade de São Paulo, São Paulo. A paleontologia de répteis no Caribe é um tema de grande interesse para entender como a fauna atual da área foi constituída a partir da colonização e extinção dos seus grupos. O maior número de fósseis pertence a Squamata, que vá desde o Eoceno até nossos dias. O registro abrange todas as ilhas das Grandes Antilhas, a maioria das Pequenas Antilhas e as Bahamas. Cuba, a maior ilha das Antilhas, tem um registro fóssil de Squamata relativamente escasso, com 11 espécies conhecidas de 10 localidades, distribuídas no oeste e centro do país. No entanto, existem muitos outros fósseis depositados em coleções biológicas sem identificação que poderiam esclarecer melhor a história de sua fauna de répteis. Um total de 328 fósseis de três coleções paleontológicas foi selecionado para sua análise, a busca de características osteológicas diagnosticas do menor nível taxonômico possível, e compará-los com outros fósseis e espécies recentes. No presente trabalho, o registro fóssil de Squamata é aumentado, tanto em número de espécies quanto em número de localidades. O registro é estendido a praticamente todo o território cubano. -
1 ¡Cuba! Opens at the American Museum of Natural History
Media Inquiries: Kendra Snyder, Department of Communications 212-496-3419, [email protected] www.amnh.org _____________________________________________________________________________________ November 2016 ¡CUBA! OPENS AT THE AMERICAN MUSEUM OF NATURAL HISTORY NEW EXHIBITION EXPLORES THE ISLAND’S RICH BIODIVERSITY AND CULTURE Cuba is a place of exceptional biodiversity and cultural richness, and now a new bilingual exhibition at the American Museum of Natural History will offer visitors fresh insights into this island nation just 94 miles from Florida’s shores. With a close look at Cuba’s unique natural history, including its native species, highly diverse ecosystems, and geology, ¡Cuba! also explores Cuba’s history, traditions, and contemporary Cuban voices to inspire novel perspectives on this dynamic country. ¡Cuba! opens for a weekend of Member previews on Friday, November 18, and will be on view from Monday, November 21, 2016, to August 13, 2017. “American Museum of Natural History scientists have worked in collaboration with colleagues in Cuba for many decades, studying the extraordinary biological diversity and endemism of this island nation,” said Ellen V. Futter, President of the American Museum of Natural History. “We are delighted now to work in collaboration with the National Natural History Museum in Havana in a groundbreaking partnership to present this major exhibition exploring Cuba’s amazing and unique nature and culture, especially at a time when cultural understanding and education are critically important.” Technically an archipelago of more than 4,000 islands and keys, Cuba is the largest island nation in the Caribbean—and one of the region’s most ecologically diverse countries. About 50 percent of its plants and 32 percent of its vertebrate animals are endemic, meaning they are found only on the island. -
DNA-Validated Parthenogenesis: First Case in a Captive Cuban Boa (Chilabothrus Angulifer)
SALAMANDRA 56(1): 83–86 SALAMANDRA 15 February 2020 ISSN 0036–3375 Correspondence German Journal of Herpetology Correspondence DNA-validated parthenogenesis: first case in a captive Cuban boa (Chilabothrus angulifer) Fernanda Seixas1, Francisco Morinha2, Claudia Luis3, Nuno Alvura3 & Maria dos Anjos Pires1 1) Laboratório de Histologia e Anatomia Patológica, Escola de Ciências Agrárias e Veterinárias, CECAV, Quinta de Prados, 5000-801 Vila Real, Portugal 2) Department of Evolutionary Ecology, National Museum of Natural Sciences (MNCN), Spanish National Research Council (CSIC), José Gutiérrez Abascal 2, 28006 Madrid, Spain 3) Zoo da Maia, Rua da Igreja, S/N, 4470-184 Maia, Portugal Corresponding author: Maria dos Anjos Pires, e-mail: [email protected] Manuscript received: 24 September 2019 Accepted: 15 December 2019 by Arne Schulze Parthenogenesis is a natural form of asexual reproduction FP has been reported in various species of major vertebrate in which offspring are produced from unfertilised eggs groups including reptiles, birds and elasmobranchs (sharks (Neaves & Baumann 2011, van der Kooi & Schwander and rays) (Booth & Schuett 2016, Harmon et al. 2016, 2015). This uncommon reproductive strategy has been re- Dudgeon et al. 2017, Ramachandran & McDaniel, ported in less than 0.1% of vertebrate species, neverthe- 2018). Most FP events were documented in captive females less including a wide range of taxa (i.e. fishes, amphibians, after long periods without contact with male conspecifics reptiles, birds and mammals), even in wild populations during their reproductive lifetime (Lampert 2008, Booth (Neaves & Baumann 2011, Booth et al. 2012, van der & Schuett 2016). However, parthenogenesis has recently Kooi & Schwander 2015, Dudgeon et al.