Minke Whale Populations in the North Atlantic – an Overview with Special Reference to UK Waters
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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. -
List of Marine Mammal Species and Subspecies Written by The
List of Marine Mammal Species and Subspecies Written by the Committee on Taxonomy The Ad-Hoc Committee on Taxonomy , chaired by Bill Perrin, has produced the first official SMM list of marine mammal species and subspecies. Consensus on some issues was not possible; this is reflected in the footnotes. This list will be revisited and possibly revised every few months reflecting the continuing flux in marine mammal taxonomy. This list can be cited as follows: “Committee on Taxonomy. 2009. List of marine mammal species and subspecies. Society for Marine Mammalogy, www.marinemammalscience.org, consulted on [date].” This list includes living and recently extinct species and subspecies. It is meant to reflect prevailing usage and recent revisions published in the peer-reviewed literature. Author(s) and year of description of the species follow the Latin species name; when these are enclosed in parentheses, the species was originally described in a different genus. Classification and scientific names follow Rice (1998), with adjustments reflecting more recent literature. Common names are arbitrary and change with time and place; one or two currently frequently used in English and/or a range language are given here. Additional English common names and common names in French, Spanish, Russian and other languages are available at www.marinespecies.org/cetacea/ . The cetaceans genetically and morphologically fall firmly within the artiodactyl clade (Geisler and Uhen, 2005), and therefore we include them in the order Cetartiodactyla, with Cetacea, Mysticeti and Odontoceti as unranked taxa (recognizing that the classification within Cetartiodactyla remains partially unresolved -- e.g., see Spaulding et al ., 2009) 1. -
Balaenoptera Bonaerensis – Antarctic Minke Whale
Balaenoptera bonaerensis – Antarctic Minke Whale compared to B. bonaerensis. This smaller form, termed the “Dwarf” Minke Whale, may be genetically different from B. bonaerensis, and more closely related to the North Pacific Minke Whales, and thus has been classified B. acutorostrata (Wada et al. 1991; IWC 2001). This taxonomic position, although somewhat controversial, has been accepted by the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), and the Convention on Migratory Species (CMS). Assessment Rationale The current IWC global estimate of abundance of Antarctic Dr. Meike Scheidat Minke Whales is about 500,000 individuals. The abundance estimates declined from about 700,000 for the second circumpolar set of abundance survey cruises Regional Red List status (2016) Least Concern* (1985/86 to 1990/91) to about 500,000 for the third National Red List status (2004) Least Concern (1991/92 to 2003/04). Although this decline was not statistically significant, the IWC Scientific Committee does Reasons for change No change consider these results to reflect a change. However, Global Red List status (2008) Data Deficient whether this change is genuine or attributed to greater proportions of pack ice limiting the survey extent, has not TOPS listing (NEMBA) (2007) None yet been determined. More detailed results from an CITES listing (1986) Appendix I assessment model are available for the mid-Indian to the mid-Pacific region, and suggest that the population Endemic No increased to a peak in 1970 and then declined, with it *Watch-list Data being unclear whether this decline has levelled off or is still continuing past 2000. -
Understanding Harbour Porpoise (Phocoena Phocoena) and Fisheries Interactions in the North-West Iberian Peninsula
20th ASCOBANS Advisory Committee Meeting AC20/Doc.6.1.b (S) Warsaw, Poland, 27-29 August 2013 Dist. 11 July 2013 Agenda Item 6.1 Project Funding through ASCOBANS Progress of Supported Projects Document 6.1.b Project Report: Understanding harbour porpoise (Phocoena phocoena) and fisheries interactions in the north-west Iberian Peninsula Action Requested Take note Submitted by Secretariat / University of Aberdeen NOTE: DELEGATES ARE KINDLY REMINDED TO BRING THEIR OWN COPIES OF DOCUMENTS TO THE MEETING Final report to ASCOBANS (SSFA/ASCOBANS/2010/4) Understanding harbour porpoise (Phocoena phocoena) and fishery interactions in the north-west Iberian Peninsula Fiona L. Read1,2, M. Begoña Santos2,3, Ángel F. González1, Alfredo López4, Marisa Ferreira5, José Vingada5,6 and Graham J. Pierce2,3,6 1) Instituto de Investigaciones Marinas (C.S.I.C), Eduardo Cabello 6, 36208 Vigo, Spain 2) School of Biological Sciences (Zoology), University of Aberdeen, Tillydrone Avenue, Aberdeen, AB24 2TZ, Aberdeen, United Kingdom 3) Instituto Español de Oceanografía, Centro Oceanográfico de Vigo, PO Box 1552, 36200, Vigo, Spain 4) CEMMA, Apdo. 15, 36380, Gondomar, Spain 5) CBMA/SPVS, Departamento de Biologia, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal 6) CESAM, Departamento de Biologia, Universidade do Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal Coordinated by: In collaboration with: 1 Final report to ASCOBANS (SSFA/ASCOBANS/2010/4) Introduction The North West Iberian Peninsula (NWIP), as defined for the present project, consists of Galicia (north-west Spain), and north-central Portugal as far south as Peniche (Figure 1). Due to seasonal upwelling (Fraga, 1981), the NWIP sustains high productivity and high biodiversity, including almost 300 species of fish (Solørzano et al., 1988) and over 75 species of cephalopods (Guerra, 1992). -
FC Inshore Cetacean Species Identification
Falklands Conservation PO BOX 26, Falkland Islands, FIQQ 1ZZ +500 22247 [email protected] www.falklandsconservation.com FC Inshore Cetacean Species Identification Introduction This guide outlines the key features that can be used to distinguish between the six most common cetacean species that inhabit Falklands' waters. A number of additional cetacean species may occasionally be seen in coastal waters, for example the fin whale (Balaenoptera physalus), the humpback whale (Megaptera novaeangliae), the long-finned pilot whale (Globicephala melas) and the dusky dolphin (Lagenorhynchus obscurus). A full list of the species that have been documented to date around the Falklands can be found in Appendix 1. Note that many of these are typical of deeper, oceanic waters, and are unlikely to be encountered along the coast. The six species (or seven species, including two species of minke whale) described in this document are observed regularly in shallow, nearshore waters, and are the focus of this identification guide. Questions and further information For any questions about species identification then please contact the Cetaceans Project Officer Caroline Weir who will be happy to help you try and identify your sighting: Tel: 22247 Email: [email protected] Useful identification guides If you wish to learn more about the identification features of various species, some comprehensive field guides (which include all cetacean species globally) include: Handbook of Whales, Dolphins and Porpoises by Mark Carwardine. 2019. Marine Mammals of the World: A Comprehensive Guide to Their Identification by Thomas A. Jefferson, Marc A. Webber, and Robert L. Pitman. 2015. Whales, Dolphins and Seals: A Field Guide to the Marine Mammals of the World by Hadoram Shirihai and Brett Jarrett. -
A Brief Review of the Genetic Studies on Dwarf Minke Whale Based on Jarpa Samples
SC/D06/J8 A BRIEF REVIEW OF THE GENETIC STUDIES ON DWARF MINKE WHALE BASED ON JARPA SAMPLES Luis A. Pastene Institute of Cetacean Research, Toyomi-cho 4-5, Chuo-ku, Tokyo 104-0055, Japan ABSTRACT Prior to the JARPA surveys ‘dwarf’ minke whales were only believed to be found between 7-41°S. However the locality of the JARPA catches in Areas IV and V was mainly between 55-62°S (one animal was caught at 65°S), showing that the ‘dwarf’ minke whale is found much further south than shown by the previous data. A total of 16 ‘dwarf’ minke whales were sampled by JARPA and these animals were examined genetically with the purpose to investigate their relationship to the southern ‘ordinary’ minke whale and to minke whales in the Northern Hemisphere. Early studies showed that the degree of mtDNA divergence between both southern minke whales was large and similar to that found between southern ‘ordinary’ minke whale and Northern Hemisphere minke whales. Phylogenetic analyses showed that the ‘dwarf’ minke whale was more closely related to Northern Hemisphere minke whales. In 1993 the Scientific Committee recommended the inclusion of the ‘dwarf’ minke whale in the Schedule, so that catch limits for Antarctic minke whales recognise the distinction between the two southern minke whales. The genetic analysis conducted using JARPA samples of the southern ‘ordinary’ and ‘dwarf’ minke whales assisted greatly to the taxonomic review of minke whale conducted by Rice (1998), which confirmed the existence of two species, the larger, Antarctic minke whale Balaenoptera bonaerensis confined to the Southern Hemisphere, and the smaller, common minke whale B. -
Sc/F16/Jr/42
SC/63/RMP10 SATELLITE TRACKING OF A COMMON MINKE WHALE IN THE COASTAL WATERS OFF HOKKAIDO, NORTHERN JAPAN IN 2010 Toshiya Kishiro and Tomio Miyashita National Research Institute of Far Seas Fisheries, 2-12-4 Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-8648, Japan Contact e-mail: [email protected] ABSTRACT Using a research vessel, Shonan-maru No.2, the sighting and satellite tagging survey for common minke whales was conducted in the coastal waters off Kushiro, southeastern coast of Hokkaido, northern Japan in 2010 autumn season. The period of survey was from 6 September to 4 October. During the survey, a total of 878.2 n. miles was searched with the restricted closing mode, and 28 schools/ 30 individuals of common minke whales were sighted (primary sightings: 20/21, secondly sightings: 8/9). Using a handy air gun, a satellite tag (Argos transmitter) was attached on one common minke whale in the 15 n. miles offing of Kiritappu on 13 September. The estimated body length of the whale was 7.8m. The electric wave reception by the satellite was started on 15 September, and the movement of the whale was tracked for a period of 27 days. Estimated position of the tagged whale was located in the west coast off the cape of Erimo, and moved to east –west courses along the coastline. These results suggested that the tagged whale stayed in the coastal waters off Kushiro, for at least four weeks in autumn season. The tracking results were not contradicted with the expected migration routes of the whales. -
Habitat Modelling of Harbour Porpoise (Phocoena Phocoena) in the Northern Gulf of St
Living among giants: Habitat modelling of Harbour porpoise (Phocoena phocoena) in the Northern Gulf of St. Lawrence By Raquel Soley Calvet Masters Research in Marine Mammal Science Supervision by: Dr. Sonja Heinrich Dr. Debbie J. Russell Sea Mammal Research Unit, August 2011 Table of contents Abstract .................................................................................................................................i 1. Introduction 1.1 Cetacean habitat modelling....................................................................................1 1.2 Ocean Models........................................................................................................2 1.3 The Gulf of St. Lawrence......................................................................................3 1.4 Biology of Harbour Porpoises...............................................................................4 1.5 Aims.......................................................................................................................6 2. Materials and Methods 2.1 Study Area..............................................................................................................7 2.2 Data collection........................................................................................................8 2.3 Generating pseudo-absences.................................................................................10 2.4 Analysis.................................................................................................................11 -
The Possible Reasons for Bottlenose Dolphins (Tursiops Truncatus) Participating In
The possible reasons for bottlenose dolphins (Tursiops truncatus) participating in non-predatory aggressive interactions with harbour porpoises (Phocoena phocoena) in Cardigan Bay, Wales Leonora Neale Student ID: 4103778 BSc Zoology Supervised by Dr Francis Gilbert Word count: 5335 Contents Page Page: ABSTRACT……………………………………………………………………….......1 INTRODUCTION…………………………………………………..............................3 METHODS………………………………………………………………....................9 Study species………………………………………………………………......9 Study area………………………………………………………………….…10 Methods of data collection………………………………………...................10 Methods of data analysis………………………………………......................13 RESULTS………………………………………………………………………........14 Geographical distribution……………………………………………….......14 Object-oriented play……………………………………………………........15 DISCUSSION………………………………………………………………….…….18 Geographical distribution……………………………………………………18 Object-oriented play…………………………………………………….........18 Diet………………………………………………………………...................21 CONCLUSION………………………………………………………………………23 ACKNOWLEDGEMENTS………………………………………………………….25 REFERENCES………………………………………………………………………26 APPENDIX……………………………………………………………………..........33 CBMWC sightings………………………...………………………………….…33 CBMWC sightings form guide………………...………………………….….34 CBMWC excel spreadsheet equations……………………………………......35 Abstract Between 1991 and 2011, 137 harbour porpoises (Phocoena phocoena) died as a result of attacks by bottlenose dolphins (Tursiops truncatus) in Cardigan Bay. The suggested reasons for these non-predatory aggressive interactions -
Range-Dependent Flexibility in the Acoustic Field of View Of
RESEARCH ARTICLE elifesciences.org Range-dependent flexibility in the acoustic field of view of echolocating porpoises (Phocoena phocoena) Danuta M Wisniewska1,2*, John M Ratcliffe3,4, Kristian Beedholm1, Christian B Christensen1, Mark Johnson5, Jens C Koblitz6, Magnus Wahlberg3,7,8, Peter T Madsen1 1Zoophysiology, Department of Bioscience, Aarhus University, Aarhus, Denmark; 2Marine Mammal Research, Department of Bioscience, Aarhus University, Roskilde, Denmark; 3Sound and Behaviour Group, Institute of Biology, University of Southern Denmark, Odense, Denmark; 4Department of Biology, University of Toronto Mississauga, Mississauga, Canada; 5Scottish Oceans Institute, University of St Andrews, St Andrews, Scotland; 6Animal Physiology, Institute for Neurobiology, University of Tubingen,¨ Tubingen,¨ Germany; 7Marine Biological Research Centre, University of Southern Denmark, Kerteminde, Denmark; 8Fjord and Belt, Kerteminde, Denmark Abstract Toothed whales use sonar to detect, locate, and track prey. They adjust emitted sound intensity, auditory sensitivity and click rate to target range, and terminate prey pursuits with high- repetition-rate, low-intensity buzzes. However, their narrow acoustic field of view (FOV) is considered stable throughout target approach, which could facilitate prey escape at close-range. Here, we show that, like some bats, harbour porpoises can broaden their biosonar beam during the terminal phase of attack but, unlike bats, maintain the ability to change beamwidth within this phase. Based on video, MRI, and acoustic-tag recordings, we propose this flexibility is modulated by the melon and implemented to accommodate dynamic spatial relationships with prey and acoustic complexity of surroundings. Despite independent evolution and different means of sound generation *For correspondence: danuta. and transmission, whales and bats adaptively change their FOV, suggesting that beamwidth [email protected] flexibility has been an important driver in the evolution of echolocation for prey tracking. -
Cetaceans Evolution: Insights from the Genome Sequences of Common Minke Whales', BMC Genomics, Vol
Edinburgh Research Explorer Cetaceans evolution Citation for published version: Park, JY, An, Y-R, Kanda, N, An, C-M, An, HS, Kang, J-H, Kim, EM, An, D-H, Jung, H, Joung, M, Park, MH, Yoon, SH, Lee, B-Y, Lee, T, Kim, K-W, Park, WC, Shin, DH, Lee, YS, Kim, J, Kwak, W, Kim, HJ, Kwon, Y-J, Moon, S, Kim, Y, Burt, DW, Cho, S & Kim, H 2015, 'Cetaceans evolution: insights from the genome sequences of common minke whales', BMC Genomics, vol. 16, 13. https://doi.org/10.1186/s12864-015- 1213-1 Digital Object Identifier (DOI): 10.1186/s12864-015-1213-1 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: BMC Genomics Publisher Rights Statement: © 2015 Park et al.; licensee Biomed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. -
WWF FACTSHEET 12Th Meeting of the Conference of the Parties to CITES Santiago, 3-15 November 2002
CITES 2002 www.panda.org/species/CITES WWF FACTSHEET 12th Meeting of the Conference of the Parties to CITES Santiago, 3-15 November 2002 Northern and Southern minke whales Balaenoptera acutorostrata and B. bonaerensis I. Species Facts History, appearance and distribution The minke whale has been known under this name since the beginning of the 20th century. It is thought that a Norwegian whaler called Meincke, mistook a group of this species for blue whales. Up until the 1930s, no-one in the whaling industry bothered about minke whales because their larger relatives, such as fin and blue whales, were plentiful and brought a higher profit per catch. However, when populations of the larger whales started being seriously depleted, with several species being brought close to extinction, attention turned to minkes. In 1949, Norway alone caught no fewer than 4,000 of this species. By the time the International Whaling Commission’s (IWC) moratorium on commercial whaling was agreed in 1982, minkes were the most important species for whaling in both the North Atlantic and the Antarctic. In 2000, whale scientists agreed that there are in fact two separate species of minke whales, Northern (or Common) Minke whale (Balaenoptera acutorostrata) in the Northern hemisphere, and the larger Southern (or Antarctic) minke whale (Balaenoptera bonaerensis) in the Southern Hemisphere. Having been around for millions of years, these mammals are cetaceans which belong to the Mysticeti suborder and the Balaenopteridae family (they have baleen plates and ventral grooves). Although the smallest of the rorquals, they may still reach 10 metres (females usually being bigger than males) and weigh up to 10 tonnes.