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Breeding of wild and some domestic animals at regional zoological institutions in 2013

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P I S C E S

ВОББЕЛОНГООБРАЗНЫЕ ORECTOLOBIFORMES

Сем. Азиатские кошачьи акулы (Бамбуковые акулы) Hemiscyllidae

Коричневополосая бамбуковая акула – Chiloscyllium punctatum

Brownbanded bambooshark

IUCN (NT)

Sevastopol 20

ХВОСТОКОЛООБРАЗНЫЕ DASYATIFORMES

Сем. Речные хвостоколы Potamotrygonidae

Глазчатый хвостокол (Моторо) – Potamotrygon motoro

Ocellate river stingray

IUCN (DD)

Sevastopol - ?

КАРПООБРАЗНЫЕ CYPRINIFORMES

Сем. Цитариновые Citharinidae

Серебристый дистиход – Distichodusaffinis (noboli)

Silver distichodus

Novosibirsk 40

Сем. Пираньевые – Serrasalmidae

Серебристый метиннис – Metynnis argenteus

Silver dollar

Yaroslavl 10 Обыкновенный метиннис – Metynnis schreitmuelleri (hypsauchen)

Plainsilver dollar

Nikolaev 4; Novosibirsk 100; Kharkov 20

Пятнистый метиннис – Metynnis maculatus

Spotted metynnis

Novosibirsk 50

Пиранья Наттерера – Serrasalmus nattereri

Red piranha

Novosibirsk 80; Kharkov 30

4

Сем. Харацидовые – Characidae

Красноплавничный афиохаракс – Aphyocharax anisitsi (rubripinnis)

Bloodfin tetra

Киев 5; Perm 10

Парагвайский афиохаракс – Aphyocharax paraquayensis

Whitespot tetra

Perm 11

Рубиновый афиохаракс Рэтбина – Aphyocharax rathbuni

Redflank bloodfin

Perm 10

Эквадорская тетра – Astyanax sp.

Tetra

Perm 17 Слепая рыбка – Astyanax fasciatus mexicanus (Anoptichthys jordani)

Mexican tetra

Kharkov 10 Рублик-монетка – Ctenobrycon spilurus (+ С. spilurusvar. albino)

Silver tetra

Kharkov 20

Тернеция (Траурная тетра) – Gymnocorymbus ternetzi

Black tetra

Minsk 1; Novosibirsk 150; Perm 11; Kharkov 70

Тетра Блехера – Hemigrammus bleheri

Firehead tetra

Novosibirsk 290

Тетрагоноптерус (Тетра-плотвичка) – Hemigrammus caudovittatus

Buenos Aires tetra

(+ H. caudovittatus var. albino)
Novosibirsk 118; Perm15; Kharkov 20

Грацилис (Тетра-светлячок) – Hemigrammus erythrozonus

Glowlight tetra

Novosibirsk 350; Perm 12

Зелёный неон (Костело) – Hemigrammus hyanuary

January tetra

Perm 19

Медная рыбка (Хасемания) – Hemigrammus (Hasemania) nanus

Silvertip tetra

Nikolaev 5; Novosibirsk 150; Perm 16

Фонарик – Hemigrammus ocellifer

Head-and-taillight

Perm 18

5

Пульхер – Hemigrammus pulcher

Garnet tetra

Perm 15

Красноносая тетра – Hemigrammus rhodostomus

Rummy-nose tetra

Nikolaev 5; Perm 22; Kharkov 10

Тетра Аманды – Hyphessobrycon amandae

Ember tetra

Perm 16 Обыкновенный орнатус – Hyphessobrycon bentosi bentosi (оrnatus)

Ornate tetra

Nikolaev 5

Минор (Красня тетра) – Hyphessobrycon callistus minor

Jewe ltetra

Nikolaev 7; Novosibirsk 130; Perm 15

Эквадорский хифессобрикон – Hyphessobrycon ecuadoriensis

Tetra

Novosibirsk 100

Тетра-фон-рио (Пламенная тетра) – Hyphessobrycon flammeus

Flame tetra

Perm 16; Kharkov 20 Черный неон – Hyphessobrycon herbertaxelrodi

Blackneon tetra

Omsk 10; Perm 15

Лимонная тетра – Hyphessobrycon pulchripinnis

Lemon tetra

Perm 11; Kharkov 20

Тетра Шольца – Hyphessobrycon scholzei

Blackline tetra

Perm 15

Ложная королевская тетра (Кери)– Inpaichthys kerri

Royal tetra

Perm 25

Чёрный орнатус – Megalamphodus megalopterus

Blackphantom tetra

Nikolaev 15; Perm 14

Желто-красный мегаламфодус – Megalamphodus roseus

Tetra

Perm 12

Красный фантом (Красный орнатус) – Megalamphodus sweglesi

Redphantom tetra

Perm 15

6

Бриллиантовая моенкаузия – Moenkhausia pittieri

Diamond tetra

Perm 30

Филомена (Красноглазая моенкаузия) – Moenkhausia sanctaefilomenae

Redeye tetra

Perm 8; Kharkov 20

Королевская тетра – Nematobrycon palmeri

Emperor tetra

Perm 20; Kharkov 30; Yaroslavl 10 Красный неон – Paracheirodon (Cheirodon) axelrodi

Cardinal tetra

Nikolaev 15; Novosibirsk 260; Perm 24

Голубой неон (Неоновая рыбка Инесса) – Paracheirodon innesi

Neon tetra

Novosibirsk 250; Perm 40

Стеклянная тетра (Прионобрама) – Prionobrama filigera

Glass bloodfin

Perm 12; Kharkov 30 Пристелла – Pristella maxillaris (riddlei)

X-ray tetra

Perm 10

Косая тайерия (Обликва) – Thayeria boehlkei

Blackline penguinfish

Nikolaev 3; Perm 12

Сем. Пиррулиновые (Лебиасиновые) – Pyrrhulinidae (Lebiasinidae)

Нанностомус Бекфорда – Nannostomus beckfordi

Golden pencilfish

Perm 9

Карликовый нанностомус – Nannostomus marginatus

Dwarf pencilfish

Perm 10 Пецилобрикон – Poecilobrycon (Nannobrycon) eques

Brown pencilfish

Perm 6

Сем. Африканские тетры (Алестовые) Alestidae

Конго-тетра – Phenacogrammus (Micralestis) interruptus

Congo tetra

Perm 25

7

Сем. Аптероновые Apterоnotidae

Чёрный нож (белолобый) – Apteronotus albifrons

Black ghost

Novosibirsk 70; Perm 12

Сем. Карповые Cyprinidae

Глянцевый усач (Барбус арулиус) – Barbus arulius

Arulius barb

Kharkov 20

Синештриховый (тигровый) барбус – Barbus bariloides

Africanbanded barb

Nikolaev 5; Perm 18 Огненный барбус – Barbus (Cuvier) conchonius, c. var.

Rosy barb

Grodno 50; Novosibirsk 150; Perm 20;Surgut110;Kharkov55

Барбус-клоун Эверетта – Barbus everetti

Clown barb

Perm 15

Полосатый барбус – Barbus fasciatus

Striped barb

Perm 10

Оливковый клоун (Барбус филаментоза) – Barbus filamentosus

Blackspot barb

Perm 15; Kharkov 30

Крестовый барбус (латеристRiga) – Barbus lateristriga

Spanner barb

Novosibirsk 100

Чёрный барбус – Barbus nigrofasciatus

IUCN (LC)

Blackruby barb

Nikolaev 25; Novosibirsk 80; Perm 23; Kharkov 10

ОстRovnoй усач (Барбус олиголепис) – Barbus oligolepis

Island barb (Checker barb)

Perm 12

Пятиполосый барбус (Пентазона) – Barbus pentazona

Fiveband barb

Perm 20

Ромбополосый барбус – Barbus rhomboocellatus

Barb

Perm 28

Зелёный барбус – Barbus semifasciolatus

Chinese barb (Green barb)

Nikolaev 30; Novosibirsk 60

8

Барбус Шуберта (порода зеленого барбуса) – Barbus (Capoeta) s. “schuberti”

Schuberti barb

Киев 10; Novosibirsk 70; Perm 17; Kharkov 20

Суматранский барбус – Barbus tetrazona

Sumatra barb

Voronezh (Zoo) 80; Grodno 350; Nikolaev 10; Novosibirsk 200; Omsk 10; Perm 30; Surgut 150; Kharkov 65; Yaroslavl 50

Барбус мутант, альбинос и т.п. – Barbus tetrazona var.

Tiger barb

Kharkov 5

Алый барбус (Одесский) – Barbus ticto (“Odessae”)

Ticto barb

Nikolaev 5; Omsk 3; Perm 10;Kharkov 60

Вишнёвый барбус – Barbus (Capoeta) titteya

Cherry barb

IUCN (LC)

Nikolaev 10; Perm 40

Барбус – Barbus sp.

Barb

Perm 10

Розовый данио – Brachydanio albolineatus

Pearl danio

Grodno 115; Novosibirsk 170; Perm 15

Леопардовый данио – Brachydanio “frankei”

Leopard danio

Grodno 135; Nikolaev 35; Surgut 40; Kharkov70

Данио рерио – Brachydanio rerio + В. var.

Zebra danio

Grodno 80; Киев 25; Nikolaev 15; Omsk 30; Perm 30; Surgut 50; Kharkov 175

Золотая рыбка – Carassius auratus var. dom.

(вуалехвост, телескоп, жемчужинка, оранда, комета красная шапочка и др.)

Gold fish

Almaty 50; Grodno 18; Novosibirsk 180; Perm 36; Rostov-on-Don 60; Kharkov 40

Цветной карп (Кои) – Cyprinus carpio var. koi

Japanese carp (Koi, Nishiki goi)

Almaty 70; Voronezh (Zoo) 60; Киев 30; Nikolaev 6; Novosibirsk 40; Kharkov 20 Малабарский данио – Danio aequipinnatus (malabaricus)

Malabar danio

IUCN (DD)

Lodz 20; Novosibirsk 70; Perm 14

Гарра – Garra rufa

Garra

Novosibirsk 100; Surgut 10

9

Двухцветный лабео – Labeo (Epalzeorhynchus) bicolor

Redtail sharkminnow

IUCN (EW)

Novosibirsk 140

Микрорасбора маргинатус – Microrasbora marginatus

Rasbora

Perm 15

Расбора Хенгеля – Rasbora hengeli

Glowlight rasbora

Nikolaev 2

Клинопятнистая расбора – Rasbora heteromorpha

Harlequin rasbora

Nikolaev 10; Perm 10 Пятнистая расбора – Rasbora maculata (Boraras maculatus) Perm 15

Краснополосая расбора – Rasbora pauciperforata

Redstripe rasbora

Perm 13

Трёхлинейная расбора – Rasbora trilineata

Three-lined rasbora

Perm 10 Расбора Бригтты – Rasbora brigittae (Boraras brigittae) Perm 14 Кардинал – Tanichthys albonubes

White cloud mountain minnow

Nikolaev 8; Novosibirsk 145; Perm 15; Kharkov 50

Сем. Вьюновые Cobitidae

Мраморная боция – Botia lohachata

Reticulate loach

Novosibirsk 70

СОМООБРАЗНЫЕ SILURIFORMES

Сем. Косатковые – Bagridae

Павлиний глаз (Хорабагрус) – Horabagrus brachysoma

Günther's catfish

Novosibirsk 270

Сиамская косатка – Leiocassis siamensis

Asian bumblebee catfish

Novosibirsk 160

10

Косатка - перевертыш – Mystus (Heterobagrus) leucophasis

Asian upside down catfish

Novosibirsk 225

Индийская синяя косатка (Сомик тенгара) – Mystus tengara

Tengara catfish

Novosibirsk 160

Сем. Перистоусые (Бахромчатоусые) сомы Mochokidae

Бурый (крапчатый) синодонт – Synodontis nigrita

Common syno

IUCN (DD)

Novosibirsk 150

Сем. Бокочешуйниковые (Броняковые) сомы Doradidae

Полосатый платидор – Platydoras costatus

Raphael catfish

Novosibirsk 330

Сем. Панцирные сомы Callichthyidae

Золотистый сомик – Corydoras aeneus

Bronze corydoras

Novosibirsk 170

Крапчатый сомик – Corydoras paleatus

Peppered corydoras

Grodno 85; Novosibirsk180; Perm10; Kharkov 10

Сомик-панда– Corydoras panda

Panda corydoras

Grodno10

Чернолинейный сомик (пигмей)– Corydoras pygmaeus

Pygmy corydoras

Novosibirsk 50

Сомик Штербы – Corydoras sterbai

Sterba`s catfish

Novosibirsk 45; Perm 5

Обыкновенный хоплостернум – Hoplosternum (Megalechis) thoracatum

Spotted hoplo catfish

Novosibirsk140; Perm 5

Сем. Кольчужные сомы Loricariidae

Обыкновенный анцистр – Ancistrus dolichopterus

Spottedhoplo catfish

Kaunas 20; Krasnoyarsk («Roev Ruchey») 5; Minsk 23; Nikolaev 15; Novosibirsk 100; Omsk 10; Perm 20; Rostov-on-Don 10; Surgut 40; Kharkov 10

11

Звездчатый анцистр – Ancistrus hoplogenys

Spotted bristle-nosed pleco

Perm 10

Обыкновенная лорикария– Dasyloricaria filamentosa

Whiptail catfish

Perm 4

Панамская стурисома – Sturisoma panamense

Panama catfish

Perm 10

КАРПОЗУБООБРАЗНЫЕCYPRINODONTIFORMES

Сем. Карпозубые Cyprinodontidae

Щучка линеатус (Полосатый аплохейл) – Aplocheilus lineatus

Striped panchax

Perm 10

Сем. Гамбузиевые (Пецилиевые) Poeciliidae

Гирардинус – Girardinus metallicus

Topminnow

Lodz 10

Формоза – Heterandria formosa

Least killifish

Lodz 35

Шарфовая пецилия (Моллинезия) – Poecilia (Mollienesia) latipinna

Sailfin molly

Almaty 15; Perm 15 Гуппи – Poecilia (Lebistes) reticulata

Guppy

Grodno 1496; Киев 1140; Krasnoyarsk («Roev Ruchey») 10; Lipetsk 300; Nikolaev 40; Novosibirsk 160; Perm 40; Riga 250; Rostov-on-Don 340; Semey 10; Surgut 80; Kharkov 305

Моллинезия сфенопс (Чёрная лира-молли) – Poecilia (Mollienesia) sphenops

Blackfish molly

Kaunas 16; Киев 600; Krasnoyarsk («Roev Ruchey») 10; Lipetsk 100; Nikolaev 10; Novosibirsk 95; Perm 30; Riga 180; Rostov-on-Don 10; Kharkov 15; Yaroslavl 10

Велифера (Парусная моллинезия) – Poecilia (Mollienesia) velifera

Sailfin molly

Krasnoyarsk («Roev Ruchey») 10; Nikolaev 5; Perm 12; Kharkov 10

12

Крапчатая пецилия – Poecilia vittata

Cuban limia

Perm 15

Гуппи (пецилия) Эндлера– Poecilia wingei

Guppy

Riga 20

Пецилия – Poecilia sp.

Yaroslavl 10

Обыкновенный (зеленый) меченосец – Xiphophorus helleri

Swordtail

Киев 390; Kosice 1; Krasnoyarsk («Roev Ruchey») 10; Lipetsk 100; Nikolaev 105; Novosibirsk 110; Omsk 10; Perm 25; Riga 500; Rostov-on-Don 35; Surgut 80; Tashkent 2000; Kharkov 20

Пятнистая плятипецилия – Xiphophorus maculatus

Spotted platyfish

Krasnoyarsk («Roev Ruchey») 10; Lodz 20; Perm 10

Многоцветная (обыкновенная) плятипецилия – Xiphophorus variatus

Sunset platyfish

Krasnoyarsk («Roev Ruchey») 10; Nikolaev 5; Perm 15; Tashkent 1500

АТЕРИНООБРАЗНЫЕ ATHERINIFORMES

Сем. Бедоциевые – Bedotiidae

Бедоция – Bedotia geayi (madagascariensis)

Madagascar rainbowfish

Perm 10

IUCN (VU) IUCN (VU)

Сем. Радужницы Melanotaeniidae

Красная атерина – Glossolepis incisus

Red rainbowfish

Nikolaev 5; Perm 19; Kharkov 120

Голубоватый уанамский глоссолепис – Glossolepis wanamensis IUCN (CR)

Rainbowfish

Lodz 9

Ириатерина Вернера – Iriaterina werneri

Threadfin rainbowfish

Perm 10

Двухцветная атерина (Атерина Боесмена) – Melanotaenia boesmani

Boesemann`s rainbowfish

IUCN (EN)

Lodz 30; Perm 18

13

Меланотения Аксельрода – Melanotaenia herbertaxelrodi

Lake Tebera yellow raimbowfish

Perm 15

Бирюзовая (смарагдовая) атерина – Melanotaenia lacustris

Lake Kutubu rainbowfish

IUCN (DD) IUCN (VU)

Lodz 7; Perm 14

Радужная рыбка Маккулоха – Melanotaenia maccullochi

Dwarf Australian rainbowfish

Kharkov 20

Меланотения папуа – Melanotaenia papua

Papuan rainbowfish

Perm 8

Меланотения Паркинсона – Melanotaenia parkinsoni

Parkinson`s rainbowfish

Lodz 22; Perm 10

IUCN (LC) IUCN (DD)

Неоновая радужница – Melanotaenia praecox

Neon dwarf rainbowfish

Novosibirsk 80

Горбатая атерина – Melanotaenia splendida

Australian rainbowfish

Perm 8; Kharkov20

Трёхполосая радужница (Трёхполосая атерина) – Melanotaenia trifasciata

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    Cambodian Journal of Natural History

    Cambodian Journal of Natural History Artisanal Fisheries Tiger Beetles & Herpetofauna Coral Reefs & Seagrass Meadows June 2019 Vol. 2019 No. 1 Cambodian Journal of Natural History Editors Email: [email protected], [email protected] • Dr Neil M. Furey, Chief Editor, Fauna & Flora International, Cambodia. • Dr Jenny C. Daltry, Senior Conservation Biologist, Fauna & Flora International, UK. • Dr Nicholas J. Souter, Mekong Case Study Manager, Conservation International, Cambodia. • Dr Ith Saveng, Project Manager, University Capacity Building Project, Fauna & Flora International, Cambodia. International Editorial Board • Dr Alison Behie, Australia National University, • Dr Keo Omaliss, Forestry Administration, Cambodia. Australia. • Ms Meas Seanghun, Royal University of Phnom Penh, • Dr Stephen J. Browne, Fauna & Flora International, Cambodia. UK. • Dr Ou Chouly, Virginia Polytechnic Institute and State • Dr Chet Chealy, Royal University of Phnom Penh, University, USA. Cambodia. • Dr Nophea Sasaki, Asian Institute of Technology, • Mr Chhin Sophea, Ministry of Environment, Cambodia. Thailand. • Dr Martin Fisher, Editor of Oryx – The International • Dr Sok Serey, Royal University of Phnom Penh, Journal of Conservation, UK. Cambodia. • Dr Thomas N.E. Gray, Wildlife Alliance, Cambodia. • Dr Bryan L. Stuart, North Carolina Museum of Natural Sciences, USA. • Mr Khou Eang Hourt, National Authority for Preah Vihear, Cambodia. • Dr Sor Ratha, Ghent University, Belgium. Cover image: Chinese water dragon Physignathus cocincinus (© Jeremy Holden). The occurrence of this species and other herpetofauna in Phnom Kulen National Park is described in this issue by Geissler et al. (pages 40–63). News 1 News Save Cambodia’s Wildlife launches new project to New Master of Science in protect forest and biodiversity Sustainable Agriculture in Cambodia Agriculture forms the backbone of the Cambodian Between January 2019 and December 2022, Save Cambo- economy and is a priority sector in government policy.
  • Trade in Live Reptiles, Its Impact on Wild Populations, and the Role of the European Market

    Trade in Live Reptiles, Its Impact on Wild Populations, and the Role of the European Market

    BIOC-06813; No of Pages 17 Biological Conservation xxx (2016) xxx–xxx Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/bioc Review Trade in live reptiles, its impact on wild populations, and the role of the European market Mark Auliya a,⁎,SandraAltherrb, Daniel Ariano-Sanchez c, Ernst H. Baard d,CarlBrownd,RafeM.Browne, Juan-Carlos Cantu f,GabrieleGentileg, Paul Gildenhuys d, Evert Henningheim h, Jürgen Hintzmann i, Kahoru Kanari j, Milivoje Krvavac k, Marieke Lettink l, Jörg Lippert m, Luca Luiselli n,o, Göran Nilson p, Truong Quang Nguyen q, Vincent Nijman r, James F. Parham s, Stesha A. Pasachnik t,MiguelPedronou, Anna Rauhaus v,DannyRuedaCórdovaw, Maria-Elena Sanchez x,UlrichScheppy, Mona van Schingen z,v, Norbert Schneeweiss aa, Gabriel H. Segniagbeto ab, Ruchira Somaweera ac, Emerson Y. Sy ad,OguzTürkozanae, Sabine Vinke af, Thomas Vinke af,RajuVyasag, Stuart Williamson ah,1,ThomasZieglerai,aj a Department Conservation Biology, Helmholtz Centre for Environmental Conservation (UFZ), Permoserstrasse 15, 04318 Leipzig, Germany b Pro Wildlife, Kidlerstrasse 2, 81371 Munich, Germany c Departamento de Biología, Universidad del Valle de, Guatemala d Western Cape Nature Conservation Board, South Africa e Department of Ecology and Evolutionary Biology,University of Kansas Biodiversity Institute, 1345 Jayhawk Blvd, Lawrence, KS 66045, USA f Bosques de Cerezos 112, C.P. 11700 México D.F., Mexico g Dipartimento di Biologia, Universitá Tor Vergata, Roma, Italy h Amsterdam, The Netherlands
  • Sex Chromosome Translocations

    Sex Chromosome Translocations

    RESEARCH ARTICLE Rapid Karyotype Evolution in Lasiopodomys Involved at Least Two Autosome ± Sex Chromosome Translocations Olga L. Gladkikh1☯, Svetlana A. Romanenko1,2☯*, Natalya A. Lemskaya1, Natalya A. Serdyukova1, Patricia C. M. O'Brien3, Julia M. Kovalskaya4, Antonina V. Smorkatcheva5, Feodor N. Golenishchev6, Polina L. Perelman1,2, Vladimir A. Trifonov1,2, Malcolm A. Ferguson-Smith3, Fengtang Yang7, Alexander S. Graphodatsky1,2 a11111 1 Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia, 2 Novosibirsk State University, Novosibirsk, Russia, 3 Cambridge Resource Centre for Comparative Genomics, Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom, 4 Severtzov Institute of Ecology and Evolution, Russian Academy of Sciences, Moscow, Russia, 5 Department of Vertebrate Zoology, Saint Petersburg State University, Saint Petersburg, Russia, 6 Zoological Institute, Russian Academy of Sciences, Saint Petersburg, Russia, 7 Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, United Kingdom ☯ These authors contributed equally to this work. OPEN ACCESS * [email protected] Citation: Gladkikh OL, Romanenko SA, Lemskaya NA, Serdyukova NA, O'Brien PCM, Kovalskaya JM, et al. (2016) Rapid Karyotype Evolution in Abstract Lasiopodomys Involved at Least Two Autosome ± Sex Chromosome Translocations. PLoS ONE 11 The generic status of Lasiopodomys and its division into subgenera Lasiopodomys (L. man- (12): e0167653. doi:10.1371/journal. pone.0167653 darinus, L. brandtii) and Stenocranius (L. gregalis, L. raddei) are not generally accepted because of contradictions between the morphological and molecular data. To obtain cyto- Editor: Igor V. Sharakhov, Virginia Tech, UNITED STATES genetic evidence for the Lasiopodomys genus and its subgenera and to test the autosome to sex chromosome translocation hypothesis of sex chromosome complex origin in L.
  • Pterapogon Kauderni in Appendix II, in Accordance with Article II, Paragraph 2(A) of the Convention and Satisfying Criteria a and B in Annex 2A of Resolution Conf

    Pterapogon Kauderni in Appendix II, in Accordance with Article II, Paragraph 2(A) of the Convention and Satisfying Criteria a and B in Annex 2A of Resolution Conf

    Original language: English CoP17 Prop. XXX CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ____________________ Seventeenth meeting of the Conference of the Parties Johannesburg (South Africa), 24 September – 5 October 2016 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II A. Proposal Inclusion of Pterapogon kauderni in Appendix II, in accordance with Article II, paragraph 2(a) of the Convention and satisfying Criteria A and B in Annex 2a of Resolution Conf. 9.24 (Rev. CoP16). B. Proponent The European Union and its Member States* C. Supporting statement 1. Taxonomy 1.1 Class: Actinopterygii 1.2 Order: Perciformes 1.3 Family: Apogonidae 1.4 Genus, species or subspecies, including author and year: Pterapogon kauderni Koumans, 1933 1.5 Scientific synonyms: 1.6 Common names: English: Banggai Cardinalfish French: Poisson-cardinal de Banggai Spanish: Pez cardenal de Banggai 1.7 Code numbers: 2. Overview Pterapogon kauderni is a small marine fish endemic to the Banggai Archipelago off Central Sulawesi, eastern Indonesia (Allen and Steene, 2005; Vagelli and Erdmann, 2002). The species has an extremely restricted range of c. 5,500 km2 and occurs as isolated small populations in the shallows of 34 islands (Vagelli, 2011). The species has been subject to heavy collection pressure for the aquarium trade, with annual harvests reportedly having reached 900.000 fish/year in 2007 (Vagelli, 2008; 2011). The species’ biological characteristics make it vulnerable to overexploitation (low fecundity, extended parental care, and a lack of planktonic phase that precludes dispersal). A reported widespread decline in the abundance of * The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CITES Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries.
  • Further Evidence for Male Infanticide and Feticide in Captive Plains Zebra, Equus Burchelli

    Further Evidence for Male Infanticide and Feticide in Captive Plains Zebra, Equus Burchelli

    Folia Zool. – 54(3): 258–262 (2005) Further evidence for male infanticide and feticide in captive plains zebra, Equus burchelli Jan PLUHÁČEK1,2* and Luděk BARTOŠ1 1 Ethology Group, Research Institute of Animal Production, P. O. Box 1, 104 01 Praha 10 – Uhříněves, Czech Republic; e-mail: [email protected] 2 Department of Zoology, Faculty of Science, Charles University, Viničná 7, 128 44 Praha 2, Czech Republic; e-mail: [email protected] Received 3 January 2005; Accepted 21 July 2005 A b s t r a c t . The captive plains zebra are characterised by a high incidence of male infanticide and feticide. One of the most common reasons why infanticide and feticide occur is the introduction of a new male into a herd. In the present study, we used twice as much data, including nine plains zebra herds from four Czech zoos, compared to our previous study on this topic. As a result, both of the statistical models that we tested were significant. The probability of the death of a foal was greatest when a new male was introduced into the herd just after conception. The probability of a foal to die in the presence of the new male was nearly 100% during the first two months of age and decreased as the foal aged. The foal’s probability to die, depending on the timing of the introduction of a new male or the foal’s age, was neither affected by the zoo nor the subspecies. In this paper, we also describe a fourth case of male feticide in plains zebra.
  • A Rapid Biological Assessment of the Upper Palumeu River Watershed (Grensgebergte and Kasikasima) of Southeastern Suriname

    A Rapid Biological Assessment of the Upper Palumeu River Watershed (Grensgebergte and Kasikasima) of Southeastern Suriname

    Rapid Assessment Program A Rapid Biological Assessment of the Upper Palumeu River Watershed (Grensgebergte and Kasikasima) of Southeastern Suriname Editors: Leeanne E. Alonso and Trond H. Larsen 67 CONSERVATION INTERNATIONAL - SURINAME CONSERVATION INTERNATIONAL GLOBAL WILDLIFE CONSERVATION ANTON DE KOM UNIVERSITY OF SURINAME THE SURINAME FOREST SERVICE (LBB) NATURE CONSERVATION DIVISION (NB) FOUNDATION FOR FOREST MANAGEMENT AND PRODUCTION CONTROL (SBB) SURINAME CONSERVATION FOUNDATION THE HARBERS FAMILY FOUNDATION Rapid Assessment Program A Rapid Biological Assessment of the Upper Palumeu River Watershed RAP (Grensgebergte and Kasikasima) of Southeastern Suriname Bulletin of Biological Assessment 67 Editors: Leeanne E. Alonso and Trond H. Larsen CONSERVATION INTERNATIONAL - SURINAME CONSERVATION INTERNATIONAL GLOBAL WILDLIFE CONSERVATION ANTON DE KOM UNIVERSITY OF SURINAME THE SURINAME FOREST SERVICE (LBB) NATURE CONSERVATION DIVISION (NB) FOUNDATION FOR FOREST MANAGEMENT AND PRODUCTION CONTROL (SBB) SURINAME CONSERVATION FOUNDATION THE HARBERS FAMILY FOUNDATION The RAP Bulletin of Biological Assessment is published by: Conservation International 2011 Crystal Drive, Suite 500 Arlington, VA USA 22202 Tel : +1 703-341-2400 www.conservation.org Cover photos: The RAP team surveyed the Grensgebergte Mountains and Upper Palumeu Watershed, as well as the Middle Palumeu River and Kasikasima Mountains visible here. Freshwater resources originating here are vital for all of Suriname. (T. Larsen) Glass frogs (Hyalinobatrachium cf. taylori) lay their
  • Whole Genome Sequencing of the Asian Arowana (Scleropages Formosus) Provides Insights Into the Evolution of Ray-Finned Fishes

    Whole Genome Sequencing of the Asian Arowana (Scleropages Formosus) Provides Insights Into the Evolution of Ray-Finned Fishes

    GBE Whole Genome Sequencing of the Asian Arowana (Scleropages formosus) Provides Insights into the Evolution of Ray-Finned Fishes Christopher M. Austin1,2,y, Mun Hua Tan1,2,y, Larry J. Croft1,2,3, Michael P. Hammer4,and HanMingGan1,2,* 1School of Science, Monash University Malaysia, Petaling Jaya, Selangor, Malaysia 2Monash University Malaysia Genomics Facility, Monash University Malaysia, Petaling Jaya, Selangor, Malaysia 3Malaysian Genomics Resource Centre Berhad, Boulevard Signature Office, Kuala Lumpur, Malaysia 4Museum and Art Gallery of the Northern Territory, Darwin, NT, Australia *Corresponding author: E-mail: [email protected]. yThese authors contributed equally to this work. Accepted: September 28, 2015 Data deposition: This project has been deposited at DNA Data Bank of Japan/EMBL/GenBank under the accession JARO00000000. Abstract The Asian arowana (Scleropages formosus) is of commercial importance, conservation concern, and is a representative of one of the oldest lineages of ray-finned fish, the Osteoglossomorpha. To add to genomic knowledge of this species and the evolution of teleosts, the genome of a Malaysian specimen of arowana was sequenced. A draft genome is presented consisting of 42,110 scaffolds with a total size of 708 Mb (2.85% gaps) representing 93.95% of core eukaryotic genes. Using a k-mer-based method, a genome size of 900 Mb was also estimated. We present an update on the phylogenomics of fishes based on a total of 27 species (23 fish species and 4 tetrapods) using 177 orthologous proteins (71,360 amino acid sites), which supports established relationships except that arowana is placed as the sister lineage to all teleost clades (Bayesian posterior probability 1.00, bootstrap replicate 93%), that evolved after the teleost genome duplication event rather than the eels (Elopomorpha).
  • Chromosomal Polymorphism of Mandarin Vole, Microtus Mandarinus (Rodentia) J

    Chromosomal Polymorphism of Mandarin Vole, Microtus Mandarinus (Rodentia) J

    http://www.paper.edu.cn Hereditas 138: 47–53 (2003) Chromosomal polymorphism of mandarin vole, Microtus mandarinus (Rodentia) J. X. WANG1, X. F. ZHAO1, Y. DENG1,H.Y.QI1 and Z. J. WANG2 1School of Life Sciences, Shandong Uni6ersity, Jinan, P. R. China 2Plant Protection Center of Shandong Pro6ince, P. R. China Wang, J. X., Zhao, X. F., Deng, Y., Qi, H. Y. and Wang, Z. J. 2003. Chromosomal polymorphism of mandarin vole, Microtus mandarinus (Rodentia). — Hereditas 138: 47–53. Lund, Sweden. ISSN 0018-0661. Received May 8, 2002. Accepted January 21, 2003 The mitotic and meiotic chromosomes of mandarin vole, Microtus mandarinus Milne-Edwards, from Shandong Province of China were analyzed by conventional, G- and C-banding and Silver-staining techniques. We detected chromosomal polymorphism in the vole, exhibiting diploid chromosome numbers 2n=48–50 and variable morphology of the 1st pair, one medium sized telocentric pair and the X chromosomes. Four types of karyotypes were revealed in the population. According to banding analysis, there were pericentric inversion, Robertsonian fusion and translocation in M. mandarinus karyotype evolution. The X displayed two different morphologies, which could be explained by prericentric inversion and a telocentric autosome translocation. Jin-Xing Wang, Department of Biology, School of Life Sciences, Shandong Uni6ersity, Jinan 250100, Shandong, P. R. China. E-mail: [email protected] The small-sized subterranean rodent, mandarin vole, Cytological methods Microtus mandarinus (Milne-Edwards, 1871) is one of Each specimen was injected intraperitoneally with the harmful mice to farming, forestry and horticul- 1–2 mg colchicine per gram of animal 2 to 3 hours ture when its populations are high.