Lagenorhynchus Obscurus – Dusky Dolphin
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EXTERNAL FEATURES of the DUSKY DOLPHIN Lagenorhynchus Obscurus (GRAY, 1828) from PERUVIAN WATERS Caracteristicas EXTERNAS DEL DE
Estud. Oceanol. 12: 37-53 1993 ISSN CL 0O71-173X EXTERNAL FEATURES OF THE DUSKY DOLPHIN Lagenorhynchus obscurus (GRAY, 1828) FROM PERUVIAN WATERS CARACTERisTICAS EXTERNAS DEL DELFiN OSCURO Lagenorhynchus obscurus (GRAY, 1828) DE AGUAS PERUANAS Koen Van Waerebeek Centro Peruano de Estudios Cetol6gicos (CEPEC), Asociaci6n de Ecologfa y Conservaci6n, Casilla 1536, Lima 18, Peru ABSTRACT Individual, sexual and developmental variation is quantified in the external morphology and colouration of the dusky dolphin Lagenorhynchus obscurus from Peruvian coastal waters. No significant difference in body length between sexes is found{p = 0.09) and, generally, little sexual dimorphism is present. However, males have a more anteriorly positioned genital slit and anus and their dorsal fin is more curved, has a broader base and a greater surface area than females Although the dorsal fin apparently serves as a secondary sexual character, the use of it for sexing free-ranging dusky dolphins is discouraged because of high overlap in values Relative growth in 25 body measurements is characterized for both sexes by multiplicative regression equations. The colouration pattern of the dorsal fin, flank patch, thoracic field, flipper stripe and possibly (x2, p = 008) the eye patch, are independent of maturity status. Flipper blaze and lower lip patch are less pigmented in juveniles than in adults No sexual dimorphism is found in the colour pattern The existence of a discrete "Fitzroy" colour form can not be confirmed from available data. Various cases of anomalous, piebald pigmentation are described, probably equivalent to so-called partial albinism Adult dusky dolphins from both SW Africa and New Zealand are 8-10 cm shorter than Peruvian specimens, supporting conclusions of separate populations from a recent skull variability study. -
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. -
Taxonomic Status of the Genus Sotalia: Species Level Ranking for “Tucuxi” (Sotalia Fluviatilis) and “Costero” (Sotalia Guianensis) Dolphins
MARINE MAMMAL SCIENCE, **(*): ***–*** (*** 2007) C 2007 by the Society for Marine Mammalogy DOI: 10.1111/j.1748-7692.2007.00110.x TAXONOMIC STATUS OF THE GENUS SOTALIA: SPECIES LEVEL RANKING FOR “TUCUXI” (SOTALIA FLUVIATILIS) AND “COSTERO” (SOTALIA GUIANENSIS) DOLPHINS S. CABALLERO Laboratory of Molecular Ecology and Evolution, School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand and Fundacion´ Omacha, Diagonal 86A #30–38, Bogota,´ Colombia F. TRUJILLO Fundacion´ Omacha, Diagonal 86A #30–38, Bogota,´ Colombia J. A. VIANNA Sala L3–244, Departamento de Biologia Geral, ICB, Universidad Federal de Minas Gerais, Avenida Antonio Carlos, 6627 C. P. 486, 31270–010 Belo Horizonte, Brazil and Escuela de Medicina Veterinaria, Facultad de Ecologia y Recursos Naturales, Universidad Andres Bello Republica 252, Santigo, Chile H. BARRIOS-GARRIDO Laboratorio de Sistematica´ de Invertebrados Acuaticos´ (LASIA), Postgrado en Ciencias Biologicas,´ Facultad Experimental de Ciencias,Universidad del Zulia, Avenida Universidad con prolongacion´ Avenida 5 de Julio, Sector Grano de Oro, Maracaibo, Venezuela M. G. MONTIEL Laboratorio de Ecologıa´ y Genetica´ de Poblaciones, Centro de Ecologıa,´ Instituto Venezolano de Investigaciones Cientıficas´ (IVIC), San Antonio de los Altos, Carretera Panamericana km 11, Altos de Pipe, Estado Miranda, Venezuela S. BELTRAN´ -PEDREROS Laboratorio de Zoologia,´ Colec¸ao˜ Zoologica´ Paulo Burheim, Centro Universitario´ Luterano de Manaus, Manaus, Brazil 1 2 MARINE MAMMAL SCIENCE, VOL. **, NO. **, 2007 M. MARMONTEL Sociedade Civil Mamiraua,´ Rua Augusto Correa No.1 Campus do Guama,´ Setor Professional, Guama,´ C. P. 8600, 66075–110 Belem,´ Brazil M. C. SANTOS Projeto Atlantis/Instituto de Biologia da Conservac¸ao,˜ Laboratorio´ de Biologia da Conservac¸ao˜ de Cetaceos,´ Departamento de Zoologia, Universidade Estadual Paulista (UNESP), Campus Rio Claro, Sao˜ Paulo, Brazil M. -
Morphometrics of the Dolphin Genus Lagenorhynchus: Deciphering A
Morphometrics of the dolphin genus Lagenorhynchus: deciphering a contested phylogeny Allison Galezo1,2 and Nicole Vollmer1,3 1 Department of Vertebrate Zoology, Smithsonian Institution National Museum of Natural History 2 Department of Biology, Georgetown University 3 NOAA National Systematics Laboratory Background Results & Analysis Discussion • Our morphological data support the hypothesis that Figure 1. Phenogram from cluster analysis of dolphin skull Figure 2. Species symbols key with sample sizes. measurements. Calculated using Euclidian distances and the genus Lagenorhynchus is not monophyletic, evident Height l La. acutus (24) p C. commersonii (5) a b c Ward’s method. from the separation in the phenogram of La. albirostris Height p C. eutropia (2) Recent phylogenetic studies1-7 have indicated that the Distance l La. albirostris (10) and La. acutus from the other Lagenorhynchus species, 0 2 4 6 8 p genus Lagenorhynchus, currently containing the species 0 2 4 6 8 l La. australis (7) C. heavisidii (1) u Li. borealis (11) and the mix of genera in the lowermost clade (Figure 1). L. obliquidensa, L. acutusb , L. albirostrisc, L. obscurusd , L. l La. obliquidens (28) p C. hectori (2) n Unknown (1) • Our results show that La. obscurus and La. obliquidens e f cruciger , and L. australis , is not monophyletic. These C. commersonii l La. obscurus (15) are very similar morphologically, which supports the C. commersonii species were originally grouped together because of C.C. cocommemmersoniirsonii C. commeC. hersoniictori hypothesis that they are closely related: they have C. commeC. hersoniictori similarities in external morphology and coloration, but C. commeC. hersoniictori Figure 3. -
Global Patterns in Marine Mammal Distributions
SUPPLEMENTARY INFORMATION I. TAXONOMIC DECISIONS In this work we followed Wilson and Reeder (2005) and Reeves, Stewart, and Clapham’s (2002) taxonomy. In the last 20 years several new species have been described such as Mesoplodon perrini (Dalebout 2002), Orcaella heinsohni (Beasley 2005), and the recognition of several species have been proposed for orcas (Perrin 1982, Pitman et al. 2007), Bryde's whales (Kanda et al. 2007), Blue whales (Garrigue et al. 2003, Ichihara 1996), Tucuxi dolphin (Cunha et al. 2005, Caballero et al. 2008), and other marine mammals. Since we used the conservation status of all species following IUCN (2011), this work is based on species recognized by this IUCN to keep a standardized baseline. II. SPECIES LIST List of the species included in this paper, indicating their conservation status according to IUCN (2010.4) and its range area. Order Family Species IUCN 2010 Freshwater Range area km2 Enhydra lutris EN A2abe 1,084,750,000,000 Mustelidae Lontra felina EN A3cd 996,197,000,000 Odobenidae Odobenus rosmarus DD 5,367,060,000,000 Arctocephalus australis LC 1,674,290,000,000 Arctocephalus forsteri LC 1,823,240,000,000 Arctocephalus galapagoensis EN A2a 167,512,000,000 Arctocephalus gazella LC 39,155,300,000,000 Arctocephalus philippii NT 163,932,000,000 Arctocephalus pusillus LC 1,705,430,000,000 Arctocephalus townsendi NT 1,045,950,000,000 Carnivora Otariidae Arctocephalus tropicalis LC 39,249,100,000,000 Callorhinus ursinus VU A2b 12,935,900,000,000 Eumetopias jubatus EN A2a 3,051,310,000,000 Neophoca cinerea -
SHORT-FINNED PILOT WHALE (Globicephala Macrorhynchus): Western North Atlantic Stock
February 2019 SHORT-FINNED PILOT WHALE (Globicephala macrorhynchus): Western North Atlantic Stock STOCK DEFINITION AND GEOGRAPHIC RANGE There are two species of pilot whales in the western North Atlantic - the long-finned pilot whale, Globicephala melas melas, and the short-finned pilot whale, G. macrorhynchus. These species are difficult to differentiate at sea and cannot be reliably visually identified during either abundance surveys or observations of fishery mortality without high-quality photographs (Rone and Pace 2012); therefore, the ability to separately assess the two species in U.S. Atlantic waters is complex and requires additional information on seasonal spatial distribution. Pilot whales (Globicephala sp.) in the western North Atlantic occur primarily along the continental shelf break from Florida to the Nova Scotia Shelf (Mullin and Fulling 2003). Long-finned and short- finned pilot whales overlap spatially along the mid-Atlantic shelf break between Delaware and the southern flank of Georges Bank (Payne and Heinemann 1993; Rone and Pace 2012). Long-finned pilot whales have occasionally been observed stranded as far south as South Carolina, and short- finned pilot whales have occasionally been observed stranded as far north as Massachusetts (Pugliares et al. 2016). The exact latitudinal ranges of the two species remain uncertain. However, south of Cape Hatteras most pilot whale sightings are expected to be short- Figure 1. Distribution of long-finned (open symbols), short-finned finned pilot whales, while north of (black symbols), and possibly mixed (gray symbols; could be ~42°N most pilot whale sightings are either species) pilot whale sightings from NEFSC and SEFSC expected to be long-finned pilot whales shipboard and aerial surveys during the summers of 1998, 1999, (Figure 1; Garrison and Rosel 2017). -
Riverine and Marine Ecotypes of Sotalia Dolphins Are Different Species
Marine Biology (2005) 148: 449–457 DOI 10.1007/s00227-005-0078-2 RESEARCH ARTICLE H.A. Cunha Æ V.M.F. da Silva Æ J. Lailson-Brito Jr M.C.O. Santos Æ P.A.C. Flores Æ A.R. Martin A.F. Azevedo Æ A.B.L. Fragoso Æ R.C. Zanelatto A.M. Sole´-Cava Riverine and marine ecotypes of Sotalia dolphins are different species Received: 24 December 2004 / Accepted: 14 June 2005 / Published online: 6 September 2005 Ó Springer-Verlag 2005 Abstract The current taxonomic status of Sotalia species cific status of S. fluviatilis ecotypes and their population is uncertain. The genus once comprised five species, but structure along the Brazilian coast. Nested-clade (NCA), in the twentieth century they were grouped into two phylogenetic analyses and analysis of molecular variance (riverine Sotalia fluviatilis and marine Sotalia guianensis) of control region sequences showed that marine and that later were further lumped into a single species riverine ecotypes form very divergent monophyletic (S. fluviatilis), with marine and riverine ecotypes. This groups (2.5% sequence divergence; 75% of total molec- uncertainty hampers the assessment of potential impacts ular variance found between them), which have been on populations and the design of effective conservation evolving independently since an old allopatric fragmen- measures. We used mitochondrial DNA control region tation event. This result is also corroborated by cyto- and cytochrome b sequence data to investigate the spe- chrome b sequence data, for which marine and riverine specimens are fixed for haplotypes that differ by 28 (out Communicated by J. P. -
Distribution and Movement Patterns of Killer Whales (Orcinus Orca) in the Northwest Atlantic. ICES CM 2008/B:20
ICES CM 2008/B:20 Distribution and Movement Patterns of Killer Whales (Orcinus orca) in the Northwest Atlantic Tara S. Stevens1,2 and Jack W. Lawson1 (1) Fisheries and Oceans Canada, NAFC, 80 East White Hills Road, St. John’s, Newfoundland and Labrador A1C 5X1, Canada (2) Memorial University of Newfoundland, Cognitive and Behavioural Ecology Program, St. John’s, Newfoundland and Labrador A1B 3X7, Canada Corresponding author e-mail: [email protected] ABSTRACT: Killer whales (Orcinus orca) occur throughout the northwest Atlantic. A sightings database and photographic catalogue, created mostly from opportunistic sources, is used to examine the occurrence of killer whales in Atlantic Canada. A majority of the sightings are from the Newfoundland and Labrador Region despite comparable observer coverage in adjacent areas such as the Gulf of St. Lawrence and Scotian Shelf, which suggests greater abundance in and habitat preference for Newfoundland and Labrador waters. Killer whales occur in all months of the year and in both near- and offshore regions, although particular sighting patterns may represent local observer effort and awareness. The distribution, movement, and residency patterns of killer whales may be closely linked to that of their prey; they have been observed harassing, attacking, and eating marine mammals, including minke whales (Balaenoptera acuterostrata), dolphins, and seals, and potentially eating fish. Some killer whales appear to remain year round in the Newfoundland and Labrador area and have been sighted during the spring within pack ice, potentially in association with breeding harp seals (Phoca groenlandica). Based on photographic records, individual killer whales in this area have been shown to move hundreds of kilometers within a year. -
A North Carolina Stranding of a White-Beaked Dolphin (Lagenorhynchus Albirostris), Family Delphinidae: a New Southerly Record Victoria G
Aquatic Mammals 2018, 44(1), 32-38 DOI 10.1578/AM.44.1.2018.32 A North Carolina Stranding of a White-Beaked Dolphin (Lagenorhynchus albirostris), Family Delphinidae: A New Southerly Record Victoria G. Thayer,1, 2 Craig A. Harms,3 Keith A. Rittmaster,4 David S. Rotstein,5 and John E. Hairr4 1North Carolina Division of Marine Fisheries, 3441 Arendell Street, Morehead City, NC 28557, USA E-mail: [email protected] 2North Carolina State University, Center for Marine Sciences and Technology, 303 College Circle, Morehead City, NC 28557, USA 3Department of Clinical Sciences, College of Veterinary Medicine and Center for Marine Sciences and Technology, North Carolina State University, 303 College Circle, Morehead City, NC 28557, USA 4North Carolina Maritime Museum, 315 Front Street, Beaufort, NC 28516, USA 5Marine Mammal Pathology Services, Olney, MD 20832, USA Abstract waters; and it is also seen in coastal waters (Kinze, 2002). The species is abundant and is listed as one An adult 273.7-kg, 266-cm male white-beaked of Least Concern by the International Union for dolphin (Lagenorhynchus albirostris) stranded Conservation of Nature (IUCN) as there have in Beaufort, North Carolina, on 16 April 2015 at been neither reported population declines nor 34.698125 N, -76.650476 W. Morphometrics, gross identified threats (Hammond et al., 2012). A pop- necropsy, and histopathologic evaluation were per- ulation minimum of several thousand is currently formed. Bilateral adrenal gland tumors (pheochro- estimated to exist in the northwestern Atlantic, mocytomas) were found and may have contributed and populations in the northeastern Atlantic may to stranding. This is the first recorded white-beaked be greater than 100,000 (Hammond et al., 2012). -
Extreme Physiological Adaptations As Predictors of Climatechange
MARINE MAMMAL SCIENCE, 27(2): 334–349 (April 2011) C 2010 by the Society for Marine Mammalogy DOI: 10.1111/j.1748-7692.2010.00408.x Extreme physiological adaptations as predictors of climate-change sensitivity in the narwhal, Monodon monoceros TERRIE M. WILLIAMS SHAWN R. NOREN Department of Ecology and Evolutionary Biology, University of California-Santa Cruz, Center for Ocean Health, 100 Shaffer Road, Santa Cruz, California 95060, U.S.A. E-mail: [email protected] MIKE GLENN Sea World of San Diego, 500 Sea World Drive, San Diego, California 92109, U.S.A. ABSTRACT Rapid changes in sea ice cover associated with global warming are poised to have marked impacts on polar marine mammals. Here we examine skeletal muscle charac- teristics supporting swimming and diving in one polar species, the narwhal, and use these attributes to further document this cetacean’s vulnerability to unpredictable sea ice conditions and changing ecosystems. We found that extreme morphological and physiological adaptations enabling year-round Arctic residency by narwhals limit behavioral flexibility for responding to alternations in sea ice. In contrast to the greyhound-like muscle profile of acrobatic odontocetes, the longissimus dorsi of narwhals is comprised of 86.8% ± 7.7% slow twitch oxidative fibers, resembling the endurance morph of human marathoners. Myoglobin content, 7.87 ± 1.72 g/100 g wet muscle, is one of the highest levels measured for marine mammals. Calculated maximum aerobic swimming distance between breathing holes in ice is <1,450 m, which permits routine use of only 2.6%–10.4% of ice-packed foraging grounds in Baffin Bay. -
Dusky Dolphin Nursery Groups Off Kaikoura, New
DUSKY DOLPHIN NURSERY GROUPS OFF KAIKOURA, NEW ZEALAND A Thesis by JODY SUZANNE WEIR Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE May 2007 Major Subject: Wildlife and Fisheries Sciences DUSKY DOLPHIN NURSERY GROUPS OFF KAIKOURA, NEW ZEALAND A Thesis by JODY SUZANNE WEIR Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Approved by: Chair of Committee, Bernd Würsig Committee Members, Jane Packard Wyndylyn von Zharen Head of Department, Delbert Gatlin May 2007 Major Subject: Wildlife and Fisheries Sciences iii ABSTRACT Dusky Dolphin Nursery Groups off Kaikoura, New Zealand. (May 2007) Jody Suzanne Weir, B.Sc., University of British Columbia Chair of Advisory Committee: Dr. Bernd Würsig The distribution, behaviours, and composition of dusky dolphin (Lagenorhynchus obscurus) nursery groups off Kaikoura, New Zealand, were examined. Data were collected during January–May 2005 and December 2005–April 2006 by systematic boat based surveys, group focal follows and photo-identification techniques. A total of 99 nursery groups were encountered on survey. Nursery groups were encountered in shallow water (<20 m) significantly more often than in deeper water (>20 m). Other group types (large groups, mating groups, adult non-mating groups) were not found in shallow water significantly more often than in deeper water. By staying in the shallower water, nursery groups may be protected from aggressive conspecifics and predators. More boats, especially private recreational boats, were found in the shallower waters, indicating that nursery groups are at greater risk from encounters with boat motors or recreational fishing gear in such areas. -
Marine Mammal Taxonomy
Marine Mammal Taxonomy Kingdom: Animalia (Animals) Phylum: Chordata (Animals with notochords) Subphylum: Vertebrata (Vertebrates) Class: Mammalia (Mammals) Order: Cetacea (Cetaceans) Suborder: Mysticeti (Baleen Whales) Family: Balaenidae (Right Whales) Balaena mysticetus Bowhead whale Eubalaena australis Southern right whale Eubalaena glacialis North Atlantic right whale Eubalaena japonica North Pacific right whale Family: Neobalaenidae (Pygmy Right Whale) Caperea marginata Pygmy right whale Family: Eschrichtiidae (Grey Whale) Eschrichtius robustus Grey whale Family: Balaenopteridae (Rorquals) Balaenoptera acutorostrata Minke whale Balaenoptera bonaerensis Arctic Minke whale Balaenoptera borealis Sei whale Balaenoptera edeni Byrde’s whale Balaenoptera musculus Blue whale Balaenoptera physalus Fin whale Megaptera novaeangliae Humpback whale Order: Cetacea (Cetaceans) Suborder: Odontoceti (Toothed Whales) Family: Physeteridae (Sperm Whale) Physeter macrocephalus Sperm whale Family: Kogiidae (Pygmy and Dwarf Sperm Whales) Kogia breviceps Pygmy sperm whale Kogia sima Dwarf sperm whale DOLPHIN R ESEARCH C ENTER , 58901 Overseas Hwy, Grassy Key, FL 33050 (305) 289 -1121 www.dolphins.org Family: Platanistidae (South Asian River Dolphin) Platanista gangetica gangetica South Asian river dolphin (also known as Ganges and Indus river dolphins) Family: Iniidae (Amazon River Dolphin) Inia geoffrensis Amazon river dolphin (boto) Family: Lipotidae (Chinese River Dolphin) Lipotes vexillifer Chinese river dolphin (baiji) Family: Pontoporiidae (Franciscana)