NPR 2016-17 Japan Small Cetaceans
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Evolutionary History of the Porpoises
bioRxiv preprint doi: https://doi.org/10.1101/851469; this version posted November 22, 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 The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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. 1 Evolutionary history of the porpoises (Phocoenidae) across the 2 speciation continuum: a mitogenome phylogeographic perspective 3 4 Yacine Ben Chehida1, Julie Thumloup1, Cassie Schumacher2, Timothy Harkins2, Alex 5 Aguilar3, Asunción Borrell3, Marisa Ferreira4, Lorenzo Rojas-Bracho5, Kelly M. Roberston6, 6 Barbara L. Taylor6, Gísli A. Víkingsson7, Arthur Weyna8, Jonathan Romiguier8, Phillip A. 7 Morin6, Michael C. Fontaine1,9* 8 9 1 Groningen Institute for Evolutionary Life Sciences (GELIFES), University of Groningen, PO Box 11103 CC, 10 Groningen, The Netherlands 11 2 Swift Biosciences, 674 S. Wagner Rd., Suite 100, Ann Arbor, MI 48103, USA 12 3 IRBIO and Department of Evolutive Biology, Ecology and Environmental Sciences, Faculty of Biology, 13 University of Barcelona, Diagonal 643, 08071 Barcelona, Spain 14 4 MATB-Sociedade Portuguesa de Vida Selvagem, Estação de Campo de Quiaios, Apartado EC Quiaios, 3080- 15 530 Figueira da Foz, Portugal & CPRAM-Ecomare, Estrada do Porto de Pesca Costeira, 3830-565 Gafanha da 16 Nazaré, Portugal 17 5 Instituto Nacional de Ecología, Centro de Investigación Científica y de Educación Superior de Ensenada, 18 Carretera Ensenada-Tijuana 3918, Fraccionamiento Zona Playitas, Ensenada, BC 22860, Mexico 19 6 Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA, 8901 La Jolla Shores Dr., La 20 Jolla, California 92037, USA 21 7 Marine and Freshwater Research Institute, PO Box 1390, 121 Reykjavik, Iceland 22 8 Institut des Sciences de l’Évolution (Université de Montpellier, CNRS UMR 5554), Montpellier, France 23 9 Laboratoire MIVEGEC (Université de Montpellier, UMR CNRS 5290, IRD 229), Centre IRD de Montpellier, 24 Montpellier, France 25 26 *Corresponding author: Michael C. -
Resolution 3.11 Conservation Plan for Black Sea Cetaceans
ACCOBAMS-MOP3/2007/Res.3.11 RESOLUTION 3.11 CONSERVATION PLAN FOR BLACK SEA CETACEANS The Meeting of the Parties to the Agreement on the Conservation of Cetaceans of the Black Sea, Mediterranean Sea and contiguous Atlantic area: On the recommendation of the ACCOBAMS Scientific Committee, Aware that all three Black Sea cetacean species, the harbour porpoise (Phocoena phocoena), the short-beaked common dolphin (Delphinus delphis) and the common bottlenose dolphin (Turpsiops truncatus), experienced a dramatic decline in abundance during the twentieth century, Taking into account that the International Union for the Conservation of Nature (IUCN)-ACCOBAMS workshop on the Red List Assessment of Cetaceans in the ACCOBAMS Area (Monaco, March 2006) concluded that the Black Sea populations of the harbour porpoise, common dolphin and bottlenose dolphin are endangered, Conscious that most of the factors responsible for their decline, such as current fisheries by-catches, extensive habitat degradation and other anthropogenic impacts, pose continuous threats to the existence of cetaceans in the Black Sea and contiguous waters, represented by the Sea of Azov, the Kerch strait and the Turkish straits system (including the Bosphorus strait, the Marmara Sea and the Dardanelles straits), Convinced that the plan is an integral component of discussions on Black Sea regional and national strategies, plans, programmes and projects concerned with the protection, exploration and management of the Black Sea environment, biodiversity, living resources, marine mammals -
Is Harbor Porpoise (Phocoena Phocoena) Exhaled Breath Sampling Suitable for Hormonal Assessments?
animals Article Is Harbor Porpoise (Phocoena phocoena) Exhaled Breath Sampling Suitable for Hormonal Assessments? Anja Reckendorf 1,2 , Marion Schmicke 3 , Paulien Bunskoek 4, Kirstin Anderson Hansen 1,5, Mette Thybo 5, Christina Strube 2 and Ursula Siebert 1,* 1 Institute for Terrestrial and Aquatic Wildlife Research, University of Veterinary Medicine Hannover, Werftstrasse 6, 25761 Buesum, Germany; [email protected] (A.R.); [email protected] (K.A.H.) 2 Centre for Infection Medicine, Institute for Parasitology, University of Veterinary Medicine Hannover, Buenteweg 17, 30559 Hannover, Germany; [email protected] 3 Clinic for Cattle, Working Group Endocrinology, University of Veterinary Medicine Hannover, Bischofsholer Damm 15, 30173 Hannover, Germany; [email protected] 4 Dolfinarium, Zuiderzeeboulevard 22, 3841 WB Harderwijk, The Netherlands; paulien.bunskoek@dolfinarium.nl 5 Fjord & Bælt, Margrethes Pl. 1, 5300 Kerteminde, Denmark; [email protected] * Correspondence: [email protected]; Tel.: +49-511-856-8158 Simple Summary: The progress of animal welfare in wildlife conservation and research calls for more non-invasive sampling techniques. In cetaceans, exhaled breath condensate (blow)—a mixture of cells, mucus and fluids expelled through the force of a whale’s exhale—is a unique sampling matrix for hormones, bacteria and genetic material, among others. Especially the detection of steroid hormones, such as cortisol, is being investigated as stress indicators in several species. As the only Citation: Reckendorf, A.; Schmicke, native cetacean in Germany, harbor porpoises (Phocoena phocoena) are of special conservation concern M.; Bunskoek, P.; Anderson Hansen, and research interest. So far, strandings and live captures have been the only method to obtain K.; Thybo, M.; Strube, C.; Siebert, U. -
Identifying Sexually Mature, Male Short-Beaked Common Dolphins (Delphinus Delphis) at Sea, Based on the Presence of a Postanal Hump
Aquatic Mammals 2002, 28.2, 181–187 Identifying sexually mature, male short-beaked common dolphins (Delphinus delphis) at sea, based on the presence of a postanal hump Dirk R. Neumann1, Kirsty Russell2, Mark B. Orams1, C. Scott Baker2, and Padraig Duignan3 1Coastal Marine Research Group, Massey University, Auckland, New Zealand 2Department of Biology, University of Auckland, New Zealand 3Department of Veterinary Science, Massey University, Palmerston North, New Zealand Abstract Introduction For detailed studies on the behaviour and social To fully comprehend the behaviour and social organization of a species, it is important to organization of a species, it is necessary to distinguish males and females. Many delphinid distinguish males and females. Long-term studies species show little sexual dimorphism. However, in of bottlenose dolphins (Tursiops truncatus, T. mature male spinner dolphins, Stenella longirostris aduncus), which tracked focal individuals of known (Perrin & Gilpatrick, 1994) and Fraser’s dolphins, sex, revealed sexual segregation of mature males Lagenodelphis hosei (Jefferson et al., 1997), tissue from females (Wells, 1991), the formation of male between the anus and the flukes forms a so-called coalitions (Wells, 1991; Connor et al., 1992), and peduncle keel, or postanal hump. We discovered an differences in the activity budgets of males and analogous feature in free-ranging short-beaked females (Waples et al., 1998). Many delphinid common dolphins, Delphinus delphis,offthe species show little sexual dimorphism, which makes north-eastern coast of New Zealand’s North Island. it exceedingly difficult to sex individuals at sea. For Genetic analysis of skin samples obtained from many species, the only individuals that can be sexed bow-riding individuals revealed that dolphins without capture are those that are consistently with a postanal hump were indeed always male. -
Marine Mammals of Hudson Strait the Following Marine Mammals Are Common to Hudson Strait, However, Other Species May Also Be Seen
Marine Mammals of Hudson Strait The following marine mammals are common to Hudson Strait, however, other species may also be seen. It’s possible for marine mammals to venture outside of their common habitats and may be seen elsewhere. Bowhead Whale Length: 13-19 m Appearance: Stocky, with large head. Blue-black body with white markings on the chin, belly and just forward of the tail. No dorsal fin or ridge. Two blow holes, no teeth, has baleen. Behaviour: Blow is V-shaped and bushy, reaching 6 m in height. Often alone but sometimes in groups of 2-10. Habitat: Leads and cracks in pack ice during winter and in open water during summer. Status: Special concern Beluga Whale Length: 4-5 m Appearance: Adults are almost entirely white with a tough dorsal ridge and no dorsal fin. Young are grey. Behaviour: Blow is low and hardly visible. Not much of the body is visible out of the water. Found in small groups, but sometimes hundreds to thousands during annual migrations. Habitat: Found in open water year-round. Prefer shallow coastal water during summer and water near pack ice in winter. Killer Whale Status: Endangered Length: 8-9 m Appearance: Black body with white throat, belly and underside and white spot behind eye. Triangular dorsal fin in the middle of the back. Male dorsal fin can be up to 2 m in high. Behaviour: Blow is tall and column shaped; approximately 4 m in height. Narwhal Typically form groups of 2-25. Length: 4-5 m Habitat: Coastal water and open seas, often in water less than 200 m depth. -
Southern Resident Killer Whales (Orcinus Orca) Cover: Aerial Photograph of a Mother and New Calf in SRKW J-Pod, Taken in September 2020
SPECIES in the SPOTLIGHT Priority Actions 2021–2025 Southern Resident killer whales (Orcinus orca) Cover: Aerial photograph of a mother and new calf in SRKW J-pod, taken in September 2020. The photo was obtained using a non-invasive octocopter drone at >100 ft. Photo: Holly Fearnbach (SR3, SeaLife Response, Rehab and Research) and Dr. John Durban (SEA, Southall Environmental Associates); collected under NMFS research permit #19091. Species in the Spotlight: Southern Resident Killer Whales | PRIORITY ACTIONS: 2021–2025 Central California Coast coho salmon adult, Lagunitas Creek. Photo: Mt. Tamalpais Photos. Passengers aboard a Washington State Ferry view Southern Resident killer whales in Puget Sound, an example of low-impact whale watching. Photo: NWFSC. The Species in the Spotlight Initiative In 2015, the National Marine Fisheries Service (NOAA Fisheries) launched the Species in the Spotlight initiative to provide immediate, targeted efforts to halt declines and stabilize populations, focus resources within and outside of NOAA on the most at-risk species, guide agency actions where we have discretion to make investments, increase public awareness and support for these species, and expand partnerships. We have renewed the initiative for 2021–2025. U.S. Department of Commerce | National Oceanic and Atmospheric Administration | National Marine Fisheries Service 1 Species in the Spotlight: Southern Resident Killer Whales | PRIORITY ACTIONS: 2021–2025 The criteria for Species in the Spotlight are that they partnerships, and prioritizing funding—providing or are endangered, their populations are declining, and leveraging more than $113 million toward projects that they are considered a recovery priority #1C (84 FR will help stabilize these highly at-risk species. -
Unsustainable Food Systems Threaten Wild Crop and Dolphin Species
INTERNATIONAL PRESS RELEASE Embargoed until: 07:00 GMT (16:00 JST) 5 December 2017 Elaine Paterson, IUCN Media Relations, t+44 1223 331128, email [email protected] Goska Bonnaveira, IUCN Media Relations, m +41 792760185, email [email protected] [In Japan] Cheryl-Samantha MacSharry, IUCN Media Relations, t+44 1223 331128, email [email protected] Download photographs here Download summary statistics here Unsustainable food systems threaten wild crop and dolphin species Tokyo, Japan, 5 December 2017 (IUCN) – Species of wild rice, wheat and yam are threatened by overly intensive agricultural production and urban expansion, whilst poor fishing practices have caused steep declines in the Irrawaddy Dolphin and Finless Porpoise, according to the latest update of The IUCN Red List of Threatened Species™. Today’s Red List update also reveals that a drying climate is pushing the Ringtail Possum to the brink of extinction. Three reptile species found only on an Australian island – the Christmas Island Whiptail-skink, the Blue- tailed Skink (Cryptoblepharus egeriae) and the Lister’s Gecko – have gone extinct, according to the update. But in New Zealand, conservation efforts have improved the situation for two species of Kiwi. “Healthy, species-rich ecosystems are fundamental to our ability to feed the world’s growing population and achieve the UN Sustainable Development Goal 2 – to end hunger by 2030,” says IUCN Director General Inger Andersen. “Wild crop species, for example, maintain genetic diversity of agricultural crops -
Anomalously Pigmented Common Dolphins (Delphinus Sp.) Off Northern New Zealand Karen A
Aquatic Mammals 2005, 31(1), 43-51, DOI 10.1578/AM.31.1.2005.43 Anomalously Pigmented Common Dolphins (Delphinus sp.) off Northern New Zealand Karen A. Stockin1 and Ingrid N. Visser2 1Coastal-Marine Research Group, Institute of Natural Resources, Massey University, Private Bag 102 904, North Shore MSC, Auckland, New Zealand 2Orca Research Trust, P.O. Box 1233, Whangarei, New Zealand Abstract New Zealand waters is provided by Bernal et al. (2003) who suggested that common dolphins exhib- Anomalous pigmentations have been recorded in iting long rostra, as photographed in New Zealand many cetacean species. However, typically only by Doak (1989; Plates 34A, 34B), are long-beaked one variation is reported from a population at common dolphins. However, as Amaha (1994) and a time (e.g., an albino). Here we record a spec- Jefferson & Van Waerebeek (2002) highlighted, trum of pigmentation from common dolphins neither New Zealand nor Australian common dol- (Delphinus sp.) off northern New Zealand. All- phins neatly fit the morphological description of black, dark-morph, pale-morph, and all-white either D. delphis or D. capensis. In the past, New individuals, as well as variations between these Zealand common dolphins have been identified have been recorded. Pale-coloured pectoral flip- from pigmentation patterns in the field and classi- pers are prevalent, and a number of individuals fied as short-beaked common dolphins (Bräger & with white “helmets” have been observed. Schneider, 1998; Gaskin, 1968; Neumann, 2001; Webb, 1973), although pigmentation alone may not Key Words: common dolphin, Delphinus delphis, be sufficient to positively identity these dolphins to Delphinus capensis, anomalous pigmentation, species. -
Cetacean Records Along a Coastal-Offshore Gradient in the Vitória
DOI: http://dx.doi.org/10.1590/1519-6984.21812 Cetacean records along a coastal-offshore gradient in the Vitória- Trindade Chain, western South Atlantic Ocean Wedekin, LL.a*, Rossi-Santos, MR.a, Baracho, C.a, Cypriano-Souza, AL.a,b and Simões-Lopes, PC.c aInstituto Baleia Jubarte, Rua Barão do Rio Branco, 125, CEP 45900-000, Caravelas, BA, Brazil bLaboratório de Biologia Genômica e Molecular, Faculdade de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul – PUCRS, Avenida Ipiranga, 6681, CEP 90619-900, Porto Alegre, RS, Brazil cLaboratório de Mamíferos Aquáticos – LAMAQ, Departamento de Ecologia e Zoologia, Universidade Federal de Santa Catarina – UFSC, Campus Universitário, CP 5102, Trindade, CEP 88040-970, Florianópolis, SC, Brazil *e-mail: [email protected] Received: November 2, 2012 – Accepted: December 27, 2012 – Distributed: February 28, 2014 (With 2 figures) Abstract Oceanic waters are difficult to assess, and there are many gaps in knowledge regarding cetacean occurrence. To fill some of these gaps, this article provides important cetacean records obtained in the winter of 2010 during a dedicated expedition to collect visual and acoustic information in the Vitória-Trindade seamounts. We observed 19 groups of cetaceans along a 1300-km search trajectory, with six species being identified: the humpback whale Megaptera( novaeangliae, N = 9 groups), the fin whale (Balaenoptera physalus, N = 1), the Antarctic minke whale (Balaenoptera bonaerensis, N = 1), the rough-toothed dolphin (Steno bredanensis, N = 1), the bottlenose dolphin (Tursiops truncatus, N = 2), and the killer whale (Orcinus orca, N = 1). Most humpback whale groups (N = 7; 78%) were observed in the Vitória-Trindade seamounts, especially the mounts close to the Abrolhos Bank. -
THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A
s l a m m a y t T i M S N v I i A e G t A n i p E S r a A C a C E H n T M i THE CASE AGAINST Marine Mammals in Captivity The Humane Society of the United State s/ World Society for the Protection of Animals 2009 1 1 1 2 0 A M , n o t s o g B r o . 1 a 0 s 2 u - e a t i p s u S w , t e e r t S h t u o S 9 8 THE CASE AGAINST Marine Mammals in Captivity Authors: Naomi A. Rose, E.C.M. Parsons, and Richard Farinato, 4th edition Editors: Naomi A. Rose and Debra Firmani, 4th edition ©2009 The Humane Society of the United States and the World Society for the Protection of Animals. All rights reserved. ©2008 The HSUS. All rights reserved. Printed on recycled paper, acid free and elemental chlorine free, with soy-based ink. Cover: ©iStockphoto.com/Ying Ying Wong Overview n the debate over marine mammals in captivity, the of the natural environment. The truth is that marine mammals have evolved physically and behaviorally to survive these rigors. public display industry maintains that marine mammal For example, nearly every kind of marine mammal, from sea lion Iexhibits serve a valuable conservation function, people to dolphin, travels large distances daily in a search for food. In learn important information from seeing live animals, and captivity, natural feeding and foraging patterns are completely lost. -
Description of a New Species of Beaked Whale (Berardius) Found in the North Pacific
www.nature.com/scientificreports OPEN Description of a new species of beaked whale (Berardius) found in the North Pacifc Received: 30 November 2018 Tadasu K. Yamada1, Shino Kitamura2,3, Syuiti Abe3, Yuko Tajima1, Ayaka Matsuda3, Accepted: 4 July 2019 James G. Mead4 & Takashi F. Matsuishi3,5 Published: xx xx xxxx Two types of Berardius are recognised by local whalers in Hokkaido, Japan. The frst is the ordinary Baird’s beaked whale, B. bairdii, whereas the other is much smaller and entirely black. Previous molecular phylogenetic analyses revealed that the black type is one recognisable taxonomic unit within the Berardius clade but is distinct from the two known Berardius species. To determine the characteristics of the black type, we summarised external morphology and skull osteometric data obtained from four individuals, which included three individuals from Hokkaido and one additional individual from the United States National Museum of Natural History collection. The whales difered from all of their congeners by having the following unique characters: a substantially smaller body size of physically mature individuals, proportionately shorter beak, and darker body colour. Thus, we conclude that the whales are a third Berardius species. Beaked whales (Family Ziphiidae, Odontoceti, Cetacea) include the second largest number of species among toothed whale families. Teir preference for deep ocean waters, elusive habits, and long dive capacity1 make beaked whales hard to see and inadequately understood. A total of 22 species are currently recognized in six genera (Berardius, Hyperoodon, Indopacetus, Mesoplodon, Tasmacetus, and Ziphius)2. Te genus Berardius has two species, Baird’s beaked whale Berardius bairdii, found in the North Pacifc and adjacent waters, and Arnoux’s beaked whale B. -
Genetic Structure of the Beaked Whale Genus Berardius in the North Pacific
MARINE MAMMAL SCIENCE, 33(1): 96–111 (January 2017) Published 2016. This article is a U.S. Government work and is in the public domain in the USA DOI: 10.1111/mms.12345 Genetic structure of the beaked whale genus Berardius in the North Pacific, with genetic evidence for a new species PHILLIP A. MORIN1, Marine Mammal and Turtle Division, Southwest Fisheries Science Cen- ter, National Marine Fisheries Service, NOAA, 8901 La Jolla Shores Drive, La Jolla, California 92037, U.S.A. and Scripps Institution of Oceanography, UCSD, 9500 Gilman Drive, La Jolla, California 92037, U.S.A.; C. SCOTT BAKER Marine Mammal Institute and Department of Fisheries and Wildlife, Oregon State University, 2030 SE Marine Science Drive, Newport, Oregon 07365, U.S.A.; REID S. BREWER Fisheries Technology, University of Alaska South- east, 1332 Seward Avenue, Sitka, Alaska 99835, U.S.A.; ALEXANDER M. BURDIN Kam- chatka Branch of the Pacific Geographical Institute, Partizanskaya Str. 6, Petropavlovsk- Kamchatsky, 683000 Russia; MEREL L. DALEBOUT School of Biological, Earth, and Environ- mental Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia; JAMES P. DINES Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, U.S.A.; IVAN D. FEDUTIN AND OLGA A. FILATOVA Faculty of Biology, Moscow State University, Moscow 119992, Russia; ERICH HOYT Whale and Dol- phin Conservation, Park House, Allington Park, Bridport, Dorset DT6 5DD, United King- dom; JEAN-LUC JUNG Laboratoire BioGEMME, Universite de Bretagne Occidentale, Brest, France; MORGANE LAUF Marine Mammal and Turtle Division, Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA, 8901 La Jolla Shores Drive, La Jolla, California 92037, U.S.A.; CHARLES W.