Macroscelides Proboscideus – Karoo Round-Eared Sengi
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Petrodromus Tetradactylus – Four-Toed Sengi
Petrodromus tetradactylus – Four-toed Sengi Specialist Group web site and www.sengis.org for additional information. This genus specifically is in need of a taxonomic revision that would assess the currently recognized 10 subspecies. Subspecies are characterised mainly by pelage colour and bristles under the tail. Two subspecies occur within the assessment region, P. t. schwanni in north-eastern Limpopo and P. t. warreni in northern KwaZulu-Natal. The subspecies in KwaZulu-Natal (P. t. warreni) lacks tail bristles, as opposed to other forms (Rathbun 2013). For general biological information, please consult Perrin and Rathbun (2013), Rathbun (2013) and Rathbun (2005). Galen Rathbun (c) California Academy of Sciences Assessment Rationale Regional Red List status (2016) Near Threatened This species is at the edge of its range within the B2ab(ii,iii,v)* assessment region where two disjunct subspecies occur: National Red List status (2004) Endangered D P. t. schwanni in north-eastern Limpopo and P. t. warreni in northern KwaZulu-Natal, both being restricted to intact Reasons for change Non-genuine: riparian and coastal forest. The estimated area of New information occupancy for P. t. schwanni and P. t. warreni, based on remaining forest habitat, is 72 and 192 km2 respectively. Global Red List status (2015) Least Concern Although P. t. warreni at least may represent a South TOPS listing (NEMBA) None African endemic, further taxonomic resolution is required before we assess it separately. Overall, the species CITES listing None qualifies for Endangered B2ab(ii,iii,v) based on restricted Endemic Edge of Range area of occupancy (264 km2 in South Africa) presumed small population size, and a continuing decline in *Watch-list Data woodland habitat as a result of human expansion over the past decade. -
Genus Rhynchocyon)
RECONSTRUCTING THE MOLECULAR PHYLOGENY OF GIANT SENGIS (GENUS RHYNCHOCYON) A Thesis submitted to the faculty of A6 San Francisco State University 3(? In partial fulfillment of zo\5 the requirements for the Degree Ib'oL Master of Science In Biology: Ecology, Evolution, and Conservation Biology by Elizabeth Jane Carlen San Francisco, California August 2015 Copyright by Elizabeth Jane Carlen 2015 CERTIFICATION OF APPROVAL I certify that I have read Reconstructing the Molecular Phylogeny o f Giant Sengis (genus Rhynchocyon) by Elizabeth Jane Carlen, and that in my opinion this work meets the criteria for approving a thesis submitted in partial fulfillment of the requirement for the degree Master of Science in Biology: Ecology, Evolution, and Conservation Biology at San Francisco State University. Research Fellow California Academy of Sciences RECONSTRUCTING THE MOLECULAR PHYLOGENY OF GIANT SENGIS (GENUS RHYNCHOCYON) Elizabeth Jane Carlen San Francisco, California 2015 Giant sengis (genus Rhynchocyon), also known as giant elephant-shrews, are approximately 500 g forest floor mammals that range from Central to East Africa. Previous work on giant sengi taxonomy has focused primarily on pelage color, pelage pattern, and the geographic distributions of the groups. Because there is complex phenotypic variation and large geographic ranges within some species, I chose to use genetic work to evaluate the phylogeny and classification of the genus. Genetic data were used to investigate the four currently recognized species (R. chrysopygus, R. cirnei, R. petersi, and R. udzungwensis) and seven of the eight currently recognized subspecies (R. cirnei cirnei, R. cirnei macrurus, R. cirnei reichardi, R. cirnei shirensis, R. cirnei stuhlmanni, R. -
The Evolution of Micro-Cursoriality in Mammals
© 2014. Published by The Company of Biologists Ltd | The Journal of Experimental Biology (2014) 217, 1316-1325 doi:10.1242/jeb.095737 RESEARCH ARTICLE The evolution of micro-cursoriality in mammals Barry G. Lovegrove* and Metobor O. Mowoe* ABSTRACT Perissodactyla) in response to the emergence of open landscapes and In this study we report on the evolution of micro-cursoriality, a unique grasslands following the Eocene Thermal Maximum (Janis, 1993; case of cursoriality in mammals smaller than 1 kg. We obtained new Janis and Wilhelm, 1993; Yuanqing et al., 2007; Jardine et al., 2012; running speed and limb morphology data for two species of elephant- Lovegrove, 2012b; Lovegrove and Mowoe, 2013). shrews (Elephantulus spp., Macroscelidae) from Namaqualand, Loosely defined, cursorial mammals are those that run fast. South Africa, which we compared with published data for other However, more explicit definitions of cursoriality remain obscure mammals. Elephantulus maximum running speeds were higher than because locomotor performance is influenced by multiple variables, those of most mammals smaller than 1 kg. Elephantulus also including behaviour, biomechanics, physiology and morphology possess exceptionally high metatarsal:femur ratios (1.07) that are (Taylor et al., 1970; Garland, 1983a; Garland, 1983b; Garland and typically associated with fast unguligrade cursors. Cursoriality evolved Janis, 1993; Stein and Casinos, 1997; Carrano, 1999). In an in the Artiodactyla, Perissodactyla and Carnivora coincident with evaluation of these definition problems, Carrano (Carrano, 1999) global cooling and the replacement of forests with open landscapes argued that ‘…morphology should remain the fundamental basis for in the Oligocene and Miocene. The majority of mammal species, making distinctions between locomotor performance…’. -
Mammalian Species 117
MAMMALIANSPECIES No. 117, pp. 14, 5 figs. Rhynchocyon chrysopygus. BY Galen B. Rathbun Published 8 June 1979 by the American Society of Mammalogists Rhynchocyon Peters, 1847 cyon chrysopygus apparently does not occur in the gallery forests of the Tana River, in the ground-water forest at Witu, or in the Rhynchocyon Peters, 1W7:36, type species Rhynchocyon cirnei dry bushlands between the Galana and Tana rivers. This ele- Peters by monotypy. phant-shrew's habitat is being cleared for exotic forest plantations Rhir~onaxThomas, 1918:370, type species Rh~nchoc~onchr~so- and agriculture all along the coast, resulting in a discontinuous pygus Gunther. and reduced distribution. It will re-occupy fallow agricultural land that is allowed to become overgrown with dense bush (Rathbun, CONTEXT AND CONTENT. Order Macroscelidea, Fam- ily Macroscelididae, Subfamily Rhynch~c~oninae.Corbet and unpublished data)' Hanks (1968) recognized three allopatric species of Rhynchocyon FOSSIL RECORD. As far as is known, the Macrosceli- (figure 1) for which they wrote the following key: didae have always been endemic to Africa (Patterson, 1%5). But- ler and Hopwood (1957) described Rhynchocyon clarki from the 1 Rump straw-colored, contrasting sharply with surround- early Miocene beds of Songhor, Kenya (near Lake Victoria). Ad- ing rufous pelage ----------.-------.-------R. chrysopygus ditional Miocene material from Rusinga Island, Kenya, has been Rump not straw-colored ---------.------.-------------------2 referred to this extinct form (Patterson, 1%5), which was smaller 2(1) Rump and posterior half of back with a pattern of dark than the extant species of Rhynchocyon. R. clarki contributes lines or spots on a yellowish-brown or rufous ground; significantly to the forest related fossil mammal fauna from Ru- top of head without a rufous tinge ._._._....._._R. -
AFROTHERIAN CONSERVATION Newsletter of the IUCN/SSC Afrotheria Specialist Group
AFROTHERIAN CONSERVATION Newsletter of the IUCN/SSC Afrotheria Specialist Group Number 10 Edited by PJ Stephenson September 2014 Afrotherian Conservation is published annually by the Speaking of our website, it was over ten years old IUCN Species Survival Commission Afrotheria Specialist and suffering from outdated material and old technology, Group to promote the exchange of news and inform- making it very difficult to maintain. Charles Fox, who ation on the conservation of, and applied research into, does our web maintenance at a hugely discounted cost golden moles, sengis, hyraxes, tenrecs and the aardvark. (many thanks Charles), has reworked the site, especially the design of the home page and conservation page Published by IUCN, Gland, Switzerland. (thanks to Rob Asher for his past efforts with the latter © 2014 International Union for Conservation of Nature material, which is still the basis for the new conservation and Natural Resources page). Because some of the hyrax material was dated, Lee ISSN: 1664-6754 Koren and her colleagues completely updated the hyrax material, and we have now linked our websites. A similar Find out more about the Group on our website at update is being discussed by Tom Lehmann and his http://afrotheria.net/ASG.html and follow us on colleagues for the aardvark link. The sengi web material is Twitter @Tweeting_Tenrec largely unchanged, with the exception of updating various pages to accommodate the description of a new species from Namibia (go to the current topics tab in the Message from the Chair sengi section). Galen Rathbun Although a lot of effort has focused on our Chair, IUCN/SSC Afrotheria Specialist Group group's education goals (logo, website, newsletter), it has not over-shadowed one of the other major functions that There has been a long time gap since our last newsletter our specialist group performs: the periodic update of the was produced in October 2012. -
Elephantulus Pilicaudus – Karoo Rock Sengi
Elephantulus pilicaudus – Karoo Rock Sengi the order Eulipotyphla. See www.afrotheria.net for additional information. For general biological information on all sengi species, consult accounts in Rathbun (2005, 2013) and Perrin and Rathbun (2013). For current and more technical information, search the on-line bibliography at www.sengis.org. Assessment Rationale This species was described in 2008, based almost entirely on molecular genetics, with weak support from external morphology. Thus, it is a highly cryptic species. It is considered a sister species of the Cape Rock Sengi, Galen Rathbun (c) California Academy of Sciences Elephantulus edwardii. There are only five known locations (with a total of 17 specimens), with two of these locations based on trapping after the year 2000, the other three are Red List status (2016) Data Deficient* based on older museum specimens. Based on these five Red List status (2004) Not Evaluated locations, this species mainly occurs in boulder habitats, but a sample of five locations is not sufficient to be Reasons for change Non genuine change conclusive. The five locations fall within an area of about Global Red List status (2015) Data Deficient 23,000 km2, but this area may include areas not occupied by the species, and thus a fragmented distribution is TOPS listing (NEMBA) None possible. All sengi species studied to date occur at low CITES listing None densities, which suggests relatively few animals per unit area. Recent trapping efforts for this species indicate that Endemic Yes this may be the case here. Without actual abundance and *Watch-list Data density data, more locations, habitat associations, and a proper assessment of habitat condition, there are not This is a recently described new species of sengi enough data to justify anything but a Data Deficient endemic to South Africa (Smit et al. -
Aspects of the Reproductive Biology of Sengis (Macroscelidea) in General
Aspects of the Reproductive Biology of Sengis (Macroscelidea) in general and the Postnatal Development of the Short-eared Sengi (Macroscelides proboscideus) in particular Inaugural-Dissertation zur Erlangung des Doktorgrades Dr. rer.nat. des Fachbereiches Biologie und Geographie an der Universität Duisburg-Essen Vorgelegt von Gea Olbricht aus Leipzig Juli 2009 Die der vorliegenden Arbeit zugrunde liegenden Experimente wurden im Zoologischen Garten der Stadt Wuppertal, im Zentralafrikanischen Museum Tervuren, Belgien, im Museum Alexander Koenig, Bonn und in der Anatomischen Anstalt der Universität München, sowie in den südafrikanischen Museen McGregor in Kimberley und Amathole in King Williams Town durchgeführt. 1. GUTACHTER: Prof. Dr. H. Burda, Universität Duisburg-Essen 2. GUTACHTER: Prof. Dr. B. Sures, Universität Duisburg-Essen 3. GUTACHTER: Dr. R. Asher, Universität Cambridge, GB VORSITZENDER DES PRÜFUNGSAUSSCHUSSES: Prof. Dr. D. Hering, Universität Duisburg-Essen Tag der Disputation: 03. 07. 2009 When we try to pick anything for itself, then it turns out that it is linked to everything else in the universe. John Muir Was wir wissen, ist ein Tropfen; was wir nicht wissen, ein Ozean. Isaac Newton Es ist nicht schwer zu komponieren. Aber es ist fabelhaft schwer, die überflüssigen Noten unter den Tisch fallen zu lassen. Johannes Brahms Meiner Familie gewidmet, Dr. Alexander Sliwa mit Leona, Feline und Olivia ACKNOWLEDGMENTS Six years came and went in the blink of an eye. Through it all, I´ve had a great deal of fun and it is a great pleasure for me to acknowledge all those who´ve helped me in this endeavour. In 2002 I approached Professor Hynek Burda of the Department of General Zoology at the University of Duisburg-Essen with the idea of initiating a study on the reproductive biology of sengis after I have had the unique opportunity of observing short- eared sengis during my time as curator at Wuppertal Zoo. -
Elephant-Shrew) Bibliography, Citations Listed Alphabetically by Author
Sengi (elephant-shrew) bibliography, citations listed alphabetically by author. Assembed by Galen Rathbun, current to 15 July 2015 For searchable version go to www.sengis.org • Adaci, M., R. Tabuce, F. Mebroukc, M. Bensalah, P. Fabre, L. Hautier, J. Jaeger, V. Lazzari, M. Mahboubic, L. Marivaux, O. Otero, S. Peigné, and H. Tong. 2007. Nouveaux sites à vertébrés paléogènes dans la région des Gour Lazib (Sahara nord- occidental, Algérie). Comptes Rendus Palevo 6:535-544. • Agacino, E. M. 1935. Sobre algunos insectivoros de Saint Joseph de Luluabourg (Congo Belge). Boletin de la Sociedad Espanola de Historia Natural 35:17-23. • Agacino, E. M. 1940. Additions a la fauna mastozoologique du territoire d'Ifni. Mammalia 4:59-62. • Aggundey, I. R., and D. A. Schlitter. 1986. Annotated checklist of the mammals of Kenya. II: Insectivora and Macroscelidea. Annals of Carnegie Museum 55:325-347. • Agnelli, P., M. L. Azzaroli, and A. M. Simonetta. 1990. Some remarks on the mammals of Somalia. Biogeographia (New Series) 14:499-513. • Alibhai, S. K., and G. Key. 1985. A preliminary investigation of small mammal biology in the Kora National Reserve, Kenya. Journal of Tropical Ecology 1:321-327. • Alibhai, S. K., and G. Key. 1986. Biology of small mammals in the Kora National Reserve. Pages 303-317 in M. Coe and N. M. Collins, editors. Kora: an ecological inventory of the Kora National Reserve, Kenya. Royal Geographical Society, London. • Allard, M. W., B. E. McNiff, and M. M. Miyamoto. 1996. Support for interordinal relationships with an emphasis on primates and their archontan relatives. Molecular Phylogenetics and Evolution 5:78-88. -
Review Article Why Is There Discordant Diversity in Sengi
Review article Why is there discordant diversity in sengi (Mammalia: Afrotheria: Macroscelidea) taxonomy and ecology? Galen B. Rathbun* Department of Ornithology and Mammalogy, California Academy of Sciences (San Francisco), c ⁄ o P.O. Box 202, Cambria, CA 93428, U.S.A. allant de de´serts coˆtiers a` des foreˆts de montagne. En raison Abstract de leur isolement sur le continent africain tre`s vite apre`sla The seventeen species of sengis or elephant-shrews form a scission du Gondwana, les sengis ont the´oriquement well-defined clade of mammals endemic to Africa that e´volue´ au de´part sans qu’il existe beaucoup de compe´tition occupy the extremes of terrestrial habitats, from coastal avec les radiations d’autres placentaires. Les caracte´ris- deserts to montane forests. Because of their isolation on tiques de leur histoire incluent de la myrme´cophagie, des Africa soon after the break-up of Gondwanaland, theo- de´placements par bonds, un usage de nids limite´, voire retically sengis initially evolved with little competition inexistant, la monogamie sociale, de petites porte´es de from other placental radiations. Their life history features jeunes pre´coces et l’inexistence de soins maternels pour les include myrmecophagy, saltatorial gaits, no or limited nouveau-ne´s. Toutes ces caracte´ristiques sont uniques use of nests, social monogamy, small litters of precocial pour les Macrosce´lide´s et repre´sentent un regroupement de young and absentee maternal care of neonates. These caracte´ristiques d’habitude associe´es a` de petites antilopes traits together are unique to the Macroscelidea and rep- ou a` des fourmiliers. -
Elephantulus Rufescens. by Fred W. Koontz and Nancy I. Roeper Published 15 December 1983 by the American Society of Mammalogists
Elephantulus rufescens. BY Fred W. Koontz and Nancy I. Roeper Published 15 December 1983 by The American Society of Mammalogists Elephantulus Thomas and Schwann, 1906 Macroscelides boranus Thomas, 1901 a:802. Type locality "Mega, Western Boran Galla, south east of Lake Rudolf." Moreau et Elephantulus Thomas and Schwann, 1906:577. Type species ~Wac- al. (1946) stated that this locality was "doubtless Mega, at 4' roscelides rupestris Smith, 1831, by original designation. N, in Abvssinia (Ethiooia). not Kenya Colony, and east of the .hlasilio Thomas and Schwann, 1906:578. Type species Macrosce- middle of Lake iiudod.= lides brachyrhynchus Smith, 1836, by original designation. ~Vacroscelidespeasei Thomas, 1901 b: 154. Type locality "Hoolul, Elephantomys Broom, 1937:758. Type species Elephantomys lan- ~bvssinia'; (30 miles northwest of Harar.-~thio~ia:koreau et gi Broom, 1937, by original designation. al.: 1946). ' ~Vacroscelidessornalicus Thomas, 1901c:255. Type locality "Ar- CONTEXT AND CONTENT. Order Macroscelidea, Fam- absiyo, Somaliland" (25 miles northwest of Hargeisa, Somalia; ily Macroscelididae, Subfamily Macroscelidinae. Elephantulus in- Moreau et al., 1946). cludes 10 extant species confined to the African continent; the Elephantulus dundasi Dollman, 1910:95. Type locality "Harich, following key, modified from Corbet (1971). should aid in their near Lake Baringo, British East Africa" (Kenya). identification. Elephantulus phaeus Heller, 1910:8. Type locality "Njoro 0 So- 1 Sternal (pectoral) gland present, a naked or short-haired lali, Sotik District, British East Africa" (Kenya). patch in center of thor Eleohantulus delicatus Dollman. 1911:652. Tvoe,a locality "Orr Sternal gland absent Valley, Mt. Nyiro" (Kenya). 2 (1) Prominent brown m Elephantulus ocularis Kershaw, 1921:563. -
Protein Sequence Signatures Support the African Clade of Mammals
Protein sequence signatures support the African clade of mammals Marjon A. M. van Dijk*, Ole Madsen*, Franc¸ois Catzeflis†, Michael J. Stanhope‡, Wilfried W. de Jong*§¶, and Mark Pagel¶ʈ *Department of Biochemistry, University of Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands; †Institut des Sciences de l’E´ volution, Universite´Montpellier 2, 34095 Montpellier, France; ‡Queen’s University of Belfast, Biology and Biochemistry, Belfast BT9 7BL, United Kingdom; §Institute for Systematics and Population Biology, University of Amsterdam, 1090 GT Amsterdam, The Netherlands; and ʈSchool of Animal and Microbial Sciences, University of Reading, Whiteknights, Reading RG6 6AJ, United Kingdom Edited by Elwyn L. Simons, Duke University Primate Center, Durham, NC, and approved October 9, 2000 (received for review May 12, 2000) DNA sequence evidence supports a superordinal clade of mammals subfamily living outside of Madagascar. To assess the signifi- that comprises elephants, sea cows, hyraxes, aardvarks, elephant cance of the candidate signatures, we use likelihood methods shrews, golden moles, and tenrecs, which all have their origins in (20) to reconstruct their most probable ancestral states at the Africa, and therefore are dubbed Afrotheria. Morphologically, this basal node of the Afrotherian clade. These calculations use a appears an unlikely assemblage, which challenges—by including phylogeny reconstructed independently of the protein under golden moles and tenrecs—the monophyly of the order Lipotyphla investigation. We further use likelihood and combinatorial meth- (Insectivora). We here identify in three proteins unique combina- ods to estimate the probability of the signatures on three tions of apomorphous amino acid replacements that support this alternative morphology-based trees that are incompatible with clade. -
List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34.