Baleen Whales Are Also Called Great Whales – Not Because They Are Any Greater Than Other Whales, but Because They Are Usually Much, Much Bigger Than Toothed Whales
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Toothed Vs. Baleen Whales Monday
SPOT THE DIFFERENCE: TOOTHED VS. BALEEN WHALES MONDAY Their classifications help to give you the answer, so what do you think the most obvious difference is in a toothed whale versus a baleen whale? Your clues are in the close-up photos, below! PHOTO: TASLI SHAW PHOTO: CINDY HANSEN Answer: The most obvious difference between a toothed whale and a baleen whale is the way that they feed and what’s inside their mouth. Toothed whales (including all dolphins and porpoises) have teeth, like we do, and they actively hunt fish, squid, and other sea creatures. Their teeth help them capture, bite, and tear their food into smaller pieces before swallowing. Baleen whales have several hundred plates that hang from their upper jaw, instead of teeth. These plates are made of keratin, the same substance as our hair and fingernails, and are used to filter food from the water or the sediment. Once the food has been trapped in the baleen plates, the whales will use their massive tongues to scrape the food off and swallow it. SPOT THE DIFFERENCE: TOOTHED VS. BALEEN WHALES TUESDAY The photos provided show specific prey types for resident orcas and for the gray whales that stop to feed in Saratoga Passage in the spring. Besides being two different species, what is another difference between these prey types? Who eats what and what makes you think that? Answer: The photos show Chinook salmon and ghost shrimp. Other than being two different species, their main difference is size! A toothed whale, like a resident orca, uses their teeth to capture, bite, and tear Chinook salmon into smaller pieces to be shared with other orcas in their family. -
History-Of-Whaling-Museum.Pdf
WHALING MUSEUM Hadwen & Barney Oil and Candle Factory as the Whaling Museum, 1967 JACK E. BOUCHER, LIBRARY OF CONGRESS, PRINTS AND PHOTOGRAPHS DIVISION, HABS MA-908-2 100 Nantucket Historical Association WHALING MUSEUM Whaling Museum The Whaling Museum is the flagship site of the Nantucket Historical Association’s fleet of properties. From its origin in 1930 in the Hadwen ADDRESS & Barney Oil and Candle Factory, 13–15 Broad Street where the story of the industry that TH made Nantucket a celebrated place CONSTRUCTED . BIKE PA CLIFF CLIFF RD RD. BIKE Hulbert Ave. PA was told THthrough a collection of whal- Hadwen & Barney Oil ing implements, to its twenty-first-cen - and Candle Factory Civil War Brant Point Monument Tristram Con East Lincoln Ave. tury reinterpretation andHomesite expansion, Marker the 1847 W illard St Wa museum has consistentlyCli Road been a major PeterCornish Foulger St Museum N. Beach St . lsh St Swain St attraction for residents and visitors. 1971 . Easton Street . OldestWilliam House Hadwen and Nathaniel Whaling Museum N & Kitchen orth Ave. N. Centre St Way BarneyGarden were partners in one of the larg- 2005. Kite Hill MacKay Way Chester St est whale-oil manufacturing firms on Harborview S. Beach St Nantucket Harbor . N. Water St theSunset island Hill inLane the mid-nineteenth. cen- West Chester St tury, Hadwen & Barney. In 1848, they . North Liberty St . Sea St . Steamboat purchased the oil and candle factory Centre St NHA Whaling Museum Step Ln. Wharf Wyers Way Franklin St. Lily Pond Park & Museum Shop building on Broad Street at the head Ash St. -
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. -
Curiosityat Home Whale Feeding
CURIOSITY AT HOME WHALE FEEDING Did you know that whales feed in two different ways? There are toothed whales, called Odontocetes, such as orca and sperm whales, as well as baleen whales, called Mysticetes, such as grey and humpback whales. Can you find what type of food each kind of whale likes based on how it eats? MATERIALS • Large container that holds water, filled half way with Odontocetes water, such as baking pan or large bowl • Something to represent plankton, such as parsley, grass, or pieces of leaves • Something to represent fish, such as small plastic toys, candy, large cereal pieces, or packing peanuts • Something to represent baleen whales, such as fine-tooth comb or toothbrush • Something to represent toothed whales, such as tweezers, binder clips, or chopsticks • Activity location that can get a little wet • Cups Mysticetes • Stopwatch or other time keeping device PROCEDURE WHAT’S HAPPENING • Fill a large container halfway with water. Drop in This activity shows that whales evolved two different “plankton” and “fish” and scatter around. methods for feeding. Toothed whales, such as orcas • Decide which type of whale to be first. Toothed use their teeth to catch bigger food like fish. They whales get tweezers as teeth and baleen whales are fast and agile swimmers in order to swim after get a comb as baleen. and catch this kind of food. Baleen whales, such as humpback whales, use their filter to scoop up and • Time out 30 seconds and collect as much food as trap tiny organisms called plankton, like krill. Baleen is you can and place it into your cup. -
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. -
Educator's Guide
Educator’s Guide Inside: • Suggestions to Help You Come Prepared • Essential Questions for Student Inquiry • Strategies for Teaching in the Exhibition • Map of the Exhibition • Online Resources • Standards Correlation • Glossary The Museum gratefully acknowledges the sdnat.org/whales County of San Diego and the City of San Diego Commission for Arts and Culture. ESSENTIAL Questions What is a whale? Many populations remain endangered. National and intergovernmental organizations collaborate to establish Whales are mammals; they breathe air and live their and enforce regulations that protect whale populations, whole lives in water. People often use the word “whale” to and some are showing recovery from whaling. The most refer to large species like sperm and humpback whales, effective whale protection programs involve the whole life but dolphins and porpoises are also whales since they’re cycle, from monitoring migration routes to conserving all members of the order Cetacea. Cetaceans evolved important breeding habitats and feeding grounds. from hoofed animals that walked on four legs, and their closest living relatives are hippos. Living whales are divided into two groups: baleen whales (Mysticeti, or How do scientists study whales? filter feeders) and toothed whales (Odontoceti, which Many kinds of scientists — conservation biologists, hunt larger prey). Whales inhabit all of the world’s major paleontologists, taxonomists, anatomists, ecologists, oceans, and even some of its rivers. Some species are geneticists — work together to learn more about these widespread, while others are localized. Many migrate magnificent creatures. Fossil specimens provide a long distances, with some species feeding in polar glimpse back some 50 million years, to whales’ waters and mating in warmer ones during the winter land-dwelling ancestors. -
Lunge Filter Feeding Biomechanics Constrain Rorqual Foraging Ecology Across Scale S
© 2020. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2020) 223, jeb224196. doi:10.1242/jeb.224196 RESEARCH ARTICLE Lunge filter feeding biomechanics constrain rorqual foraging ecology across scale S. R. Kahane-Rapport1,*, M. S. Savoca1, D. E. Cade1,2, P. S. Segre1, K. C. Bierlich3, J. Calambokidis4, J. Dale3, J. A. Fahlbusch1, A. S. Friedlaender2, D. W. Johnston3, A. J. Werth5 and J. A. Goldbogen1 ABSTRACT morphological scaling (Haldane, 1926), resulting in functional Fundamental scaling relationships influence the physiology of vital trade-offs that ultimately impact evolution and ecology. rates, which in turn shape the ecology and evolution of organisms. For The physiological advantages and disadvantages associated with diving mammals, benefits conferred by large body size include different body sizes have wide-ranging effects, from behavior to life reduced transport costs and enhanced breath-holding capacity, history. For example, the smallest animals have the lowest absolute thereby increasing overall foraging efficiency. Rorqual whales feed energetic demands (Kelt and Van Vuren, 1999), yet they may also by engulfing a large mass of prey-laden water at high speed and struggle with thermoregulation and be forced to compensate by filtering it through baleen plates. However, as engulfment capacity increasing their metabolism (Scholander et al., 1950; Taylor et al., increases with body length (engulfment volume∝body length3.57), the 1980). Small size enables high performance maneuverability and surface area of the baleen filter does not increase proportionally agility (Domenici, 2001), but may limit maximum attainable speeds (baleen area∝body length1.82), and thus the filtration time of larger (Carrier, 1994; Hirt et al., 2017). -
Mandible Allometry in Extant and Fossil Balaenopteridae (Cetacea: Mammalia): the Largest Vertebrate Skeletal Element and Its Role in Rorqual Lunge Feeding
bs_bs_banner Biological Journal of the Linnean Society, 2013, 108, 586–599. With 6 figures Mandible allometry in extant and fossil Balaenopteridae (Cetacea: Mammalia): the largest vertebrate skeletal element and its role in rorqual lunge feeding NICHOLAS D. PYENSON1,2*, JEREMY A. GOLDBOGEN3 and ROBERT E. SHADWICK4 1Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC, 20013-7013, USA 2Departments of Mammalogy and Paleontology, Burke Museum of Natural History and Culture, Seattle, WA 98195, USA 3Cascadia Research Collective, 218½ West 4th Avenue, Olympia, WA, USA 4Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, BC, Canada V6T 1Z4 Received 4 July 2012; revised 10 September 2012; accepted for publication 10 September 2012 Rorqual whales (crown Balaenopteridae) are unique among aquatic vertebrates in their ability to lunge feed. During a single lunge, rorquals rapidly engulf a large volume of prey-laden water at high speed, which they then filter to capture suspended prey. Engulfment biomechanics are mostly governed by the coordinated opening and closing of the mandibles at large gape angles, which differentially exposes the floor of the oral cavity to oncoming flow. The mouth area in rorquals is delimited by unfused bony mandibles that form kinetic linkages to each other and with the skull. The relative scale and morphology of these skeletal elements have profound consequences for the energetic efficiency of foraging in these gigantic predators. Here, we performed a morphometric study of rorqual mandibles using a data set derived from a survey of museum specimens. Across adult specimens of extant balaenopterids, mandibles range in size from ~1–6 m in length, and at their upper limit they represent the single largest osteological element of any vertebrate, living or extinct. -
Why Japan Supports Whaling
An edited version of this paper has been accepted for publication in the Journal of International Wildlife and Policy WHY JAPAN SUPPORTS WHALING Keiko Hirata* 1. INTRODUCTION Japan is one of the few states in the world that adamantly supports whaling. For decades, Tokyo has steadfastly maintained its right to whale and has aggressively lobbied the International Whaling Commission (IWC) for a resumption of commercial whaling. Japan’s pro-whaling stance has invited strong international criticism from both environmental groups and Western governments, many of which view Tokyo as obstructing international efforts to protect whales. Why has Japan adhered to a pro-whaling policy that has brought the country international condemnation? Its defiant pro-whaling stance is not consistent with its internationally cooperative position on other environmental matters. For the past decade, Tokyo has been a key player in international environmental regimes, such as those to combat ozone depletion and global warming.1 If Japan is serious about environmental protection and desires to play a role as a ‘green contributor,’2 why hasn’t it embraced the anti-whaling norm, 3 thereby joining other states in wildlife protection and assuming a larger role in global environmental leadership? *Research Fellow, Center for the Study of Democracy, University of California, Irvine, California, USA. E-mail: [email protected]. 1 Isao Miyaoka, 1980s and Early 1990s: Changing from an Eco-outlaw to a Green Contributor, 16 NEWSL. INST. SOC. SCI. U. TOKYO, 7-10 (1999). 2 Id. at 7. 3 Robert L. Friedheim, Introduction: The IWC as a Contested Regime, in TOWARD A SUSTAINABLE WHALING REGIME, 1-45 (Robert L. -
On the Sperm Whale (Physeter Macrocephalus) Ecology, Sociality and Behavior Off Ischia Island (Italy): Patterns of Sound Production and Acoustically Measured Growth
DEPARTMENT OF ENVIRONMENTAL BIOLOGY “CHARLES DARWIN” SAPIENZA UNIVERSITY OF ROME PHD IN ENVIRONMENTAL AND EVOLUTIONARY BIOLOGY ANIMAL BIOLOGY CURRICULUM XXVIII CYCLE On the sperm whale (Physeter macrocephalus) ecology, sociality and behavior off Ischia Island (Italy): patterns of sound production and acoustically measured growth by Daniela Silvia Pace Tutor: Prof. Giandomenico Ardizzone, Sapienza University of Rome, Italy External Reviewer: Prof. Gianni Pavan, University of Pavia, Italy Rome, November 2016 Table of contents _____________________________________________________________________________________________________ List of Figures List of Tables Goals and thesis outline Chapter 1 – Sperm whale biology 1.1 General anatomy ……………………………………………………………………………………………………………... 1 1.2 Abundance, distribution and movements ………………………………………………………………………….. 2 1.3 Reproduction and social structure ……………………………………………………………………………………. 5 1.4 Feeding and main prey …………………………………………………………………………………………………….. 7 1.5 Diving behavior …………………………………………………….…………………………………………………………. 8 1.6 Threats and conservation ………………………………………………………………………………………………… 9 Chapter 2 – Sperm whale acoustics 2.1 The spermaceti organ …………………………………………………………………………………………….……… 12 2.2 Click structure ………………………………………………………………………………………………………………. 14 2.3 Type of sounds ……………………………………………………………………………………………………………… 16 2.3.1 Usual clicks ………………………………………………………………………….…….………………..…… 16 2.3.2 Creaks …………………………………………………..……………………………………………………..…. 17 2.3.3 Codas …………………………………………….……………………………………………………………..… 19 -
Rorqual Whale (Balaenopteridae) Surface Lunge-Feeding Behaviors: Standardized Classification, Repertoire Diversity, and Evolutionary Analyses
MARINE MAMMAL SCIENCE, 30(4): 1335–1357 (October 2014) © 2014 Society for Marine Mammalogy DOI: 10.1111/mms.12115 Rorqual whale (Balaenopteridae) surface lunge-feeding behaviors: Standardized classification, repertoire diversity, and evolutionary analyses BRIAN W. KOT,1 Department of Ecology and Evolutionary Biology, University of California, 621 Charles E. Young Drive South, Los Angeles, California 90095-1606 U.S.A. and Mingan Island Cetacean Study, Inc., 378 Bord de la Mer, Longue-Pointe-de-Mingan, Quebec G0G 1V0, Canada; RICHARD SEARS, Mingan Island Cetacean Study, Inc., 378 Bord de la Mer, Longue-Pointe-de-Mingan, Quebec G0G 1V0, Canada; DANY ZBINDEN, Meriscope Marine Research Station, 7 chemin de la Marina, Portneuf-sur-Mer, Quebec G0T 1P0, Canada; ELIZABETH BORDA, Department of Marine Biology, Texas A&M University, 200 Seawolf Parkway, Galveston, Texas 77553, U.S.A.; MALCOLM S. GORDON, Department of Ecology and Evolutionary Biology, University of California, 621 Charles E. Young Drive South, Los Angeles, California 90095-1606, U.S.A. Abstract Rorqual whales (Family: Balaenopteridae) are the world’s largest predators and sometimes feed near or at the sea surface on small schooling prey. Most rorquals cap- ture prey using a behavioral process known as lunge-feeding that, when occurring at the surface, often exposes the mouth and head above the water. New technology has recently improved historical misconceptions about the natural variation in rorqual lunge-feeding behavior yet missing from the literature is a dedicated study of the identification, use, and evolution of these behaviors when used to capture prey at the surface. Here we present results from a long-term investigation of three rorqual whale species (minke whale, Balaenoptera acutorostrata; fin whale, B.