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Archidiskodon Pohlig, Family Elephantidae Gray Cranium,jrg. 15, nr. l.pag. 15-20,juli 1998 Is there a genus Archidiskodon Pohlig, 1885, of the family Elephantidae Gray, 1821? Wadim+E. Garutt Summary In 1885 Pohlig established the elephant genus Archidiskodon. The earliest representatives of the genus appeared at the begin- ning of the Pliocene in Africa. Representatives of the genus migrated to Eurasia and North America where they gave rise to Substantial climatic in the in the Pleistocene led the of the Mam- several new species. change Holarctic to emergence genera muthus Brookes, 1828, and Parelephas Osborn, 1924, in Eurasia and North America, respectively. Some paleontologists con- of others it valid. In end the sider Archidiskodon a junior synonym Mammuthus, regard as an attempt to put an to Archidiskodon disagreement, I here undertake a detailed comparison of the skeleton and teeth identified as and Mammuthus. of the Archidiskodon. There are 23 differentfeatures and only 10 shared ones, which confirms the validity genus Samenvatting Pohlig beschreef in 1885 het olifantengeslacht Archidiskodon. De oudste vertegenwoordigers van dit genus verschijnen aan in Afrika. Vanuit Afrika Archidiskodon Eurazië Noord het begin van het Plioceen migreerde naar en Amerika, waar ver- scheidene nieuwe soorten ontstonden. De grootschalige Pleistocene klimaatsveranderingen op het noordelijk halfrond waren 1924 in de oorzaak van het ontstaan van de geslachten Mammuthus Brookes, 1828 en Parelephas Osbom, respectievelijk Eu- is Archidiskodon anderen razië en Noord Amerika. Volgens sommige paleontologen een junior synoniem van Mammuthus, te beslechten dit artikel beschouwen het als een goed genus. In een poging om het pleit geeft een gedetailleerde vergelijking tussen skeletten en kiezen die als Archidiskodon en Mammuthus gedetermineerd zijn. Er zijn 23 verschillen en 10 overeen- komsten gevonden, hetgeen de geldigheid van het geslacht Archidiskodon bevestigt. Introduction "steppic" one and the species composing the specific bio- cenosis of the periglacial landscape dispersed over se- all the extant and extinct elephants (Family Ele- Initially veral continents. in the phantidae Gray, 1821) were placed genus Elephas Linnaeus, 1758. As early as 1828 Brookes distinguished Environmental change forced the archidiskodonts to adapt Mammuthus as a separate genus, including the woolly to a vegetation of shrubs and grasses. During this period mammoth, M. primigenius (Blumenbach), 1799. In 1885 Archidiskodon evolved into the genera Mammuthus and Pohlig established the genus Archidiskodon. The latter in- Parelephas, morphologically different from their ancestor described the of environment The cluded (FALCONER & CAUTLEY), 1845, on a more temperate (GARUTT, 1986). fossils and A. earliest ofthe basis of from the northern Himalayas, representative genus Mammuthus in Eurasia meridionalis (Nesti, 1825) from Eurasia. Dispite simila- is the steppe mammoth, M. trogontherii Pohlig, 1885, rity in molar structure, these two species differ sharply in known from Middle Pleistocene deposits of Europe, Cen- craniological features, GARUTT (1957a) referred A. plani- tral Asia, the Ural Mountains, Siberia and the Far East. frons to the new genus Protelephas, but left A. meridio- Some paleontologists, 1945; nalis in Archidiskodon. e.g. SIMPSON, AGUIRRE, 1968, 1969; MAGLIO, 1973; GUTH, 1982; COPPENS & BEDEN, Archidiskodon for The elephants of the genus appeared 1982; HOOIJER, 1984; MOL & ESSEN, 1992; AGENBROAD, first time in Africa in the Pliocene. lived in not the early They 1994, do recognize the genusArchidiskodon, but con- savanna environments and fed mainly on twigs and leaves, sider it a junior synonym of Mammuthus. SIMPSON (1945) indicated their dental as by morphology (GARUTT, 1977). and BELYAEVA (1948), however retain Archidiskodon as a second half of the Pliocene archidiskodont ele- In the subgenus. Others acknowledge Archidiskodon as a valid phants dispersed to Eurasia and to North America, where genus, e.g. POHLIG, 1885, 1888; OSBORN, 1925, 1942; DU- to number of they gave rise a new species (GARUTT, BININ & GARUTT, 1952; GARUTT, 1954, 1957a, 1957b, 1986). The latest and most advanced representative of the 1964a, 1964b, 1971, 1977, 1985, 1986; GARUTT & ALEK- genus was A. tamanensis Dubrovo, 1964, considered by SEEVA, 1964; GARUTT & SAFRONOV, 1965; GARUTT, ALEK- ofA. meridionalis. this its author a subspecies Probably at SEEVA & BAIGUSHEVA, 1975; GARUTT & FORONOVA 1976; Archidiskodon into North America. stage penetrated GARUTT & BAIGUSHEVA, 1981; GARUTT & VANGENGEIM, 1982; GARUTT & URBANAS, 1986; GARUTT & NIK.OLSKAYA, The cooling and aridization of the climate in the Pleisto- 1988; GARUTT et al., 1990; DUBROVO, 1957, 1960, 1962, cene led to a decrease ofthe forest and to broad expansion 1964, 1989; BAIGUSHEVA, 1959, 1964, 1984; BAIGUSHEVA of open landscapes, i.e. arctic steppe, forest-steppe, forest- & GARUTT, 1987; VANGENGE1M, 1961, 1977; GABUNYA, tundra and tundra. Following this climatic and vegetational 1961; GABUNYA & VEK.UA, 1963, 1967; GABUNYA & DUB- change, the Pleistocene mammalian faunabecame a more ROVO, 1990; DUBROVO & BAIGUSHEVA, 1964; APOSTOL, 15 1965, 1974; ALEKSEEVA & GARUTT, 1965; ALEKSEEVA, column or between the third and seventh thoracal verte- 1977, 1984; KONSTANTINOVA, 1965; MULLER, 1970; LE- brae, but gradually declining towards the lumbar section. BEDEVA, 1972; VISLOBOKOVA, 1974a, 1974b; The ribs in the 9. (costae) are oval cross section, except ZHYLK.IBAEV, 1975; BOEF, 1976; GROMOV, 1977; AZ- first and second pair which are flattened. ZAROLI, 1977, 1983; VOROS, 1979; DATUEV & LEBEDEVA, 1981; GUENTHER, 1986. Below a detailed comparison is 10. The wings of the iliac bones (ala ossis ilii) have given of the skeletons and teeth identified as Archidisko- straight rims. don and Mammuthus. Distinguishing skeletal and dental characters of Archidis- Comparison kodon and Mammuthus: Skeletal and dental morphology shared by Archidiskodon 1. The relative length of the skull. The skull of Archidis- and Mammuthus: kodon is relatively low and elongated in sagittal direction: from to the the length/height ratio ranges 86.1 78.9%. As 1. The top of the skull when viewed from the front or back Mammuthinievolved the skull became shorter. In Mam- incisura cranii is absent. is convex semi-circular in shape; muthus the length/height ratio ofthe skull is 78.0-68.2%. Mammuthini show small In single cases the tribe may a depression on the top of the skull. This should be consi- 2. The occipital proportions. The relative height of the oc- dered an atavism, as in the assumed ancestral tribe Pha- ciput gradually increased in the Mammuthini. In Ar- nagoroloxodontini Garutt, 1991, this feature is clearly chidiskodon the height/width ratio varies between 68.4- marked (GARUTT, 1957c, 1958, 1986, 1991, 1992, 1995). 78.0%, in Mammuthusbetween 70.2-83.9%. 2. Facies frontalis is considerably narrowed from both 3. In Archidiskodon the surface of the occiput is flat, due sides and in the middle, it is concave in sagittal and to the development of the occipital tubercles, paired cone- direction. slightly convex (seldom straight) in transversal shaped protuberances situated on both sides of the fossa is The tuber frontalis in its proximal part more pro- nuchales. These protuberances are especially pronounced nounced in the male than the female. in the male. In Mammuthus the occipital tubercles are weak. 3. The nasal opening (orificum nasalis extemus) is wide and crescent-shaped, its lateral rims are sharpened and di- 4. The occipital condyli in Archidiskodon project slightly rected down in the male, narrower with rounded rims in above the occipital surface; in Mammuthus they project the female. still less. 4. The processus nasalis is triangular with a pointed end. 5. During the evolution of the Mammuthini the concavity Its external surface is flat, while the inner surface is in sagittal direction ofthe facies frontalis decreased. slightly concave with a weak longitudinal ridge near its base. 6. The relative width of the forehead increased during the evolution of the Mammuthini: in Archidiskodon the ratio 5. The fossae temporales have indistinct borders. minimum width of the frontal surface/width of the occiput varies from 29.0 to 47.1%, in Mammuthus from 31.8 to 6. The intermaxillar bones (intermaxillaria) are bent and 54.3%. when viewed from the front or back form a figure resem- bling an X. They are wide at the level of the infraorbital Archidiskodon 7. In the supraorbital processes are short foramina, gradually narrowing towards their middle part of and the width the skull in the region of the processes is and then widening again towards their distal end, where smaller than the width of the occiput. In the former width the tusks emerge from the alveoli. either exceeds that of the occiput (in males) or equals it (in On the surface of the intermaxillarbones there is females). upper a longitudinal depression, which is narrow and deep in Archidiskodon 8. In the orbits as a rule do not project rela- males, shallow with sloping rims in females. The reliefof tive to the skull profile, but in Mammuthus they some- the depression depends on the degree of development of times do. the tusks. 9. Archidiskodon the In lacrymal tubercles are poorly de- 7. The tusks are characterized by pronounced twisting. On whereas in Mammuthus veloped, they are more pro- from the alveoli directed emerging they are downand out, nounced, especially in males. then turn up and in towards one another. The twisting is more pronounced and the tusks more massive in males 10. In Archidiskodon the lowerrim ofthe nasal opening is than females. situated than level higher or on a with the upper rims of the orbits. In Mammuthus the nasal opening is shifted The 8. thoracal vertebrae have pronounced spinous pro- downward so that its lower rim is on a level with a line cesses, longest and most massive in the anterior part ofthe drawn horizontally through the orbits. Analogous down- 16 of 22. The of Archidiskodon is characterized the shifting of the nasal opening occurs also in other groups manus by serial of the i.e. each elephants. arrangement carpal bones, proximal carpal bone articulates directly with a corresponding bone nasalis to 11.
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