Sinotherium Temporal range: | |
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Skull of Sinotherium | |
A drawing showing Sinotherium lagrelii | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Perissodactyla |
Family: | Rhinocerotidae |
Subfamily: | † Elasmotheriinae |
Genus: | † Sinotherium Ringstrom, 1923 |
Type species | |
†Sinotherium lagrelii Ringstrom, 1923 | |
Other species | |
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Sinotherium ("Chinese Beast") is an extinct genus of single-horned elasmotheriine rhinocerotids that lived from the late Miocene (Tortonian - Messinian) to Early Pliocene. It was ancestral to Elasmotherium, demonstrating a very important evolutionary transition from nasal-horned elasmotheriines to frontal-horned elasmotheriines. Its fossils have been found in the Karabulak Formation of Kazakhstan, lower jaw and teeth have been found in Mongolia, and a partial skull is known from the upper part of the Liushu Formation of western China. Sinotherium diverged from the ancestral genus, Iranotherium , first found in Iran, during the early Pliocene. Some experts prefer to lump Sinotherium, and Iranotherium into Elasmotherium .
The type species of Sinotherium is S. lagrelii. It is also known to have an additional species from the Zaisan depression of Kazakhstan called S. zaisanensis, however, doubt has been raised on its validity. [1]
Finds of Sinotherium are rather rare and often only fragmentary. The first fossils, which also led to the description of the rhinoceros genus, came to light at the beginning of the 20th century and were discovered by JG Andersson in the Baode district in the Chinese province of Shanxi in deposits from the Upper Miocene. These mainly consisted of isolated teeth, an upper jaw fragment with the preserved row of teeth from the second premolar to the penultimate molar, and a lower jaw fragment. [2] [3] From north-western Mongolia near Chono-Khariakha, a 72 cm long, well-preserved lower jaw was discovered which dates to the Lower Pliocene. [4] Other individual finds are known from Kazakhstan, including a rear part of the skull with part of the teeth and several skeletal elements of the body. [1] The most complete skull to date was found in the upper area of the Liushu Formation near Houaigou in the Guanghe District of Gansu Province. The Liushu Formation is about 100 m thick and over wide ranges of Linxia basin digested. This section is dated to about 7 to 6.4 million years and thus belongs to the end of the Miocene. The geological deposits of the Linxia Basin have already produced numerous well-preserved fossil rhinoceros remains, including numerous representatives of the Elasmotheriinae. Only the part of the snout is missing from the skull and it provided evidence of the location of the horns in Sinotherium. [5]
The horns of older elasmotheriines are present on their nasals (nose), whereas the horn of Sinotherium's descendant Elasmotherium is present on its frontals (forehead), Sinotherium shows a unique condition in which its horn is present in an intermediate "naso-frontal" position. [5] This represents the horn shifting from its ancestral nasal position to the derived frontal position, eventually resulting in the completely frontal restricted position of Elasmotherium . [5]
In addition to the nasofrontal horn, Sinotherium also preserves a rugosity on its forehead, just behind the nasofrontal horn, which implies that the animal had two horns.
Early elasmotheriine genera of the line leading to Elasmotherium , have a dolichocephalic skull supporting a horn growing on their nose, just like any other Rhinocerotid, however, Elasmotherium was the sole member of Elasmotheriinae that had a brachycephalic skull and supported a horn on its forehead instead. [5] A transition between this state of nose-horned to forehead-horned elasmotheriines remained missing until 2012, when the first cranial remains of Sinotherium lagrelii, (specimen IVPP V 18539, a partial skull housed at the Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences in Beijing) was described, demonstrating a very important transition from nose-horned elasmotheriines like Ningxiatherium to forehead-horned elasmotheriines like Elasmotherium . [5]
While the horns of Ningxiatherium -like elasmotheriines are present on their nasals, and the horn of Elasmotherium on its frontals, Sinotherium shows its horn to be present in a "nasofrontal" position, (present on both the nose and the forehead). [5] This shows the horn shifting from its ancestral nasal position to a more derived frontal position, eventually resulting in the completely frontal restricted position of Elasmotherium . [5]
Sinotherium first appeared during the Late Miocene, occupying east Asian and Mid-Asian regions, but remains dating to the Early Pliocene can be found from eastern Asia to as far as the Kumo-Manych depression of South-Western Russia. [6] This showed that at the beginning of the Pliocene (5.3–4.8 Mya), Sinotherium had significantly expanded its range westward. [6] Sinotherium is known from Pliocene to Late Miocene deposits of Kazakhstan, Mongolia, and China.
In China, the species S. lagrelii is known from an age of 7 Ma from the red clays of the Late Miocene Liushu Formation in the Linxia Basin, Gansu Province, accompanying one bear ( Ursavus sp.), one badger-like mustelid ( Parataxidea sinensis), three hyenas ( Hyaenictitherium wongii, H. hyaenoides, and Ictitherium sp.), three felids ( Amphimachairodus giganteus , Metailurus major, and Felis sp.), one chalicothere ( Ancylotherium sp. ), one three-toed horse ( Hipparion coelophyes ), one deer ( Dicrocerus sp. ), one giraffid ( Palaeotragus microdon ), and three bovids ( Sinotragus wimani, Tsaidamotherium hedini and Protoryx sp. ). Of these, the combination of H. coelophyes , S. wimani , and Protoryx sp . strongly support a late Late Miocene age. Pollen analysis of the Liushu Formation showed that grasses increased significantly and became dominant, especially xerophilous and sub-xerophilous grasses, along with some broad leaves of temperate and warm temperate zones, suggesting that the vegetation of the Liushu Formation belonged to a subarid or arid steppe. [5]
In Kazakhstan, Sinotherium zaisanensis is known from the Karabulak formation which dates to 6.3–6.5 Ma (Late Miocene). It coexisted with four caniforms ( Martes sp., Promeles sp., Plesiogulo crassa Teilhard, Indarctos punjabiensis ), three feliforms ( Adcrocuta eximia, Hyaenictitherium hyaenoides orlovi, Amphimachairodus kurteni), three perissodactyls (Hipparion hippidiodus, H. elegans , Chilotherium sp.), and six artiodactyls ( Cervavitus novorossiae, Procapreolus latifrons, Samotherium cf. irtyshense, Paleotragus (Yuorlovia) asiaticus, Tragoportax sp., Gazella dorcadoides ). The climate that Sinotherium zaisanensis lived in was mild and arid. It was a habitat of wide, open steppes. [7]
Elasmotherium is an extinct genus of large rhinoceros endemic to Eastern Europe and Central Asia with isolated finds from East Asia during Late Miocene through to the Late Pleistocene, with the youngest reliable dates around 39,000 years ago. It was the last surviving member of Elasmotheriinae, a distinctive group of rhinoceroses separate from the group that contains living rhinoceros (Rhinocerotinae).
A rhinoceros, commonly abbreviated to rhino, is a member of any of the five extant species of odd-toed ungulates in the family Rhinocerotidae; it can also refer to a member of any of the extinct species of the superfamily Rhinocerotoidea. Two of the extant species are native to Africa, and three to South and Southeast Asia.
Diceros is a genus of rhinoceros containing the extant black rhinoceros (Diceros bicornis) and several extinct species.
Dicerorhinus is a genus of the family Rhinocerotidae, consisting of a single extant species, the two-horned Sumatran rhinoceros, and several extinct species. The genus likely originated from the Late Miocene of central Myanmar. Many species previously placed in this genus probably belong elsewhere.
Iranotherium is an extinct genus of large elasmotheriine rhinocerotids, comparable in size to a modern white rhino. It is known from the Late Miocene (Tortonian) of Maragha, Iran and the middle part of the Liushu formation of northwestern China. It was a precursor to the related Sinotherium and may have been ultimately outcompeted by its descendant. This species is most well known for showing unique sexual dimorphism among rhinos.
Subhyracodon is an extinct genus of hornless rhinocerotids. With a length of 2.4 m and an estimated weight of 381 kg (840 lb) in S. mitis, it was a tapir-sized herbivore on the plains of early Oligocene South Dakota 33 million years ago. It coexisted with other perissodactyls such as horses, brontotheres, and chalicotheres. Subhyracodon had no horns, relying more on its speed to escape from predators, but a species found at Wind Cave National Park had a pair of bony nasal ridges. The genus Caenopus and species originally referred to as Aceratherium were synonymized into Subhyracodon. It has been suggested to be one of the oldest known members of the subfamily Elasmotheriinae by some studies, though other studies place it firmly outside the Rhinocerotinae-Elasmotheriinae split.
Chilotherium is an extinct genus of rhinocerotids endemic to Eurasia during the Miocene through Pliocene living for 13.7—3.4 mya, existing for approximately 10.3 million years.
Euthecodon is an extinct genus of long-snouted crocodile. It was common throughout much of Africa during the Neogene, with fossils being especially common in Kenya, Ethiopia, and Libya. Although superficially resembling that of gharials, the long snout was a trait developed independently from that of other crocodilians and suggests a diet of primarily fish. Euthecodon coexisted with a wide range of other crocodiles in the areas it inhabited before eventually going extinct during the Pleistocene.
Ceratotherium neumayri is a fossil species of rhinoceros from the Late Miocene (Vallesian-Turolian) of the Balkans and Western Asia, with remains known from Greece, Bulgaria, Iran, and Anatolia in Turkey.
Stephanorhinus is an extinct genus of two-horned rhinoceros native to Eurasia and North Africa that lived during the Late Pliocene to Late Pleistocene. Species of Stephanorhinus were the predominant and often only species of rhinoceros in much of temperate Eurasia, especially Europe, for most of the Pleistocene. The last two species of Stephanorhinus – Merck's rhinoceros and the narrow-nosed rhinoceros – went extinct during the last glacial period.
Victoriaceros is an extinct genus of elasmotheriine rhinoceros known from the Miocene of Maboko Island, Kenya.
Rusingaceros or Dicerorhinus leakeyi is an extinct genus of rhinocerotid known from the Miocene of Rusinga Island, Kenya.
Deng Tao is a Chinese palaeontologist at the Institute of Vertebrate Paleontology and Paleoanthropology (IVPP), Chinese Academy of Sciences, who has made important fossil discoveries on Cenozoic mammals. He is a professor of vertebrate palaeontology, deputy director of the Academic Committee, and deputy director of Key Laboratory of Evolutionary Systematics of Vertebrates at IVPP.
Tsaidamotherium is an extinct genus of Late Miocene ovibovinid caprine from the Tibetan Plateau of Northwestern China. Both known species are extremely unusual in that the horns are of unequal sizes: the left horn core is several times smaller than the right horn core. Although it is originally considered that it belongs to the tribe Ovibovini, close to the muskox, Ovibos moschatus, a study in 2022 posits Tsaidamotherium as a giraffoidean genus in the family Prolibytheriidae together with Prolibytherium and Discokeryx.
Forstercooperia is an extinct genus of forstercooperiine paraceratheriid rhinocerotoids from the Middle Eocene of Asia.
Pappaceras is an extinct genus of rhinocerotoids from the Early Eocene of Asia belonging to Paraceratheriidae.
The Liushu Formation is a geological formation in Gansu province, China that spans up to 100 m thick and is widely distributed within the Linxia Basin, with a paleomagnetic age between 11 and 6.4 mya.
Dihoplus is an extinct genus of rhinoceros that lived in Eurasia from the Late Miocene to Pliocene.
Eoazara xerrii is a species of extinct elasmotheriine rhinoceros from the upper Miocene of Morocco, the first definitive representative of the subfamily in North Africa. It is known from a well preserved skull and postcranial material, preserving the most complete late Miocene rhino skull found in Africa.
Pliorhinus is an extinct genus of rhinoceros known from the Late Miocene and Pliocene of Eurasia. The type species, Pliorhinus megarhinus, was previously assigned to Dihoplus.
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