Paleontology and horses is a field of study that investigates the evolutionary history and fossil record of equids, the family of mammals that includes modern horses, zebras, and donkeys. This area of research explores the morphological changes and adaptations that have occurred over millions of years, leading to the diverse species we see today. Fossil evidence provides insights into the anatomical and ecological transformations of ancient equids, such as changes in limb structure, dentition, and body size, which are associated with shifts in habitat and diet. This page compiles peer-reviewed research studies and scholarly articles that examine the fossil record, evolutionary pathways, and paleoecological contexts of horses and their ancestors.
Eronen JT, Evans AR, Fortelius M, Jernvall J.One of the classic examples of faunal turnover in the fossil record is the Miocene transition from faunas dominated by anchitheriine horses with low-crowned molar teeth to faunas with hipparionine horses characterized by high-crowned teeth. The spread of hipparionine horses is associated with increased seasonality and the expansion of open habitats. It is generally accepted that anchitheriine horses did not display an evolutionary increase in tooth crown height prior to their extinction. Nevertheless, to test whether anchitheriines showed any changes interpretable as adaptation to local condit...
Carter AM.Recently a fossil of one of the earliest jawed fishes was found with a fetal skeleton and the remains of a cord. It was from the Devonian period and takes the history of vertebrate placentation back to 380 million years ago. This and later fossil evidence for viviparity in marine reptiles and early mammals is reviewed. Of particular interest are the fossils of horses as they document that a reproductive strategy with a single precocial newborn was evolved early on. In one instance there is sufficient representation of soft tissue to imply that early horses had a diffuse placenta, much as had b...
Solow AR, Roberts DL, Robbirt KM.The fossil record has been used to shed light on the late Pleistocene megafaunal extinctions in North America and elsewhere. It is therefore important to account for variability due to the incompleteness of the fossil record and error in dating fossil remains. Here, a joint confidence region for the extinction times of horses and mammoths in Alaska is constructed. The results suggest that a prior claim that the extinction of horses preceded the arrival of humans cannot be made with confidence.
Weinstock J, Willerslev E, Sher A, Tong W, Ho SY, Rubenstein D, Storer J, Burns J, Martin L, Bravi C, Prieto A, Froese D, Scott E, Xulong L, Cooper A.The rich fossil record of horses has made them a classic example of evolutionary processes. However, while the overall picture of equid evolution is well known, the details are surprisingly poorly understood, especially for the later Pliocene and Pleistocene, c. 3 million to 0.01 million years (Ma) ago, and nowhere more so than in the Americas. There is no consensus on the number of equid species or even the number of lineages that existed in these continents. Likewise, the origin of the endemic South American genus Hippidion is unresolved, as is the phylogenetic position of the "stilt-legged"...
Pichardo M.Analysis of the morphological characters in North and South American horses present during Paleoindian time indicates that at least eight Equus ecospecies occurred in North America. In South America, Equus had radiated into four ecospecies, Hippidion had one, and Onohippidium had three geographically separate ecospecies. These species are found in archeological deposits ranging from ca. 13,000 to 8,000 yr B.P., in tropical habitats as well as in the high Andean and Patagonian colder ecotopes.
Vollmerhaus B, Roos H, Gerhards H, Knospe C.The canine teeth of the horse developed phylogenically from the simple, pointed, short-rooted tooth form of the leaf eating, in pairs living, Eocene horse Hyracotherium and served up to the Oligocene as a means of defense (self preservation). In the Miocene the living conditions of the Merychippus changed and they took to eating grass and adopted as a new behavior the life in a herd. The canine teeth possibly played an important role in fights for social ranking; they changed from a crown form to knife-like shape. In the Pliohippus the canine tooth usually remained in male horses and since the...
Kaiser TM, Fortelius M.A new approach of reconstructing ungulate diet, the mesowear method, was recently introduced by Fortelius and Solounias ([2000] Am Mus Novitat 3301:1-36). Mesowear is based on facet development on the occlusal surfaces of the teeth. Restricting mesowear investigation to maxillary cheek teeth would allow mesowear investigation only in assemblages of large numbers of individuals and therefore would generally restrict this method to relatively few assemblages of recent and fossil ungulates. Most of the fossil, subfossil, and recent ungulate osteological assemblages that may be assigned to a singl...
Pichardo M.Greater precision in North American Pleistocene equid taxonomy makes it now possible to exploit the ubiquitous horse remains in Paleoindian sites as ecological index-fossils. The horses of Central Mexico and the Southern Plains can be sorted by tooth size alone, except for two rare large horses of the Southern Plains. The species endemic to these grasslands and south to Central Mexico are Equus pacificus (large), E. conversidens (small), E. francisci (smallest). The Southern Plains were also occupied by a specialized grazer E. excelsus (Burnet and Sandia caves) and E. occidentalis (Dry and San...
Science (New York, N.Y.)February 5, 1999
Volume 283, Issue 5403 824-827 doi: 10.1126/science.283.5403.824
MacFadden BJ, Solounias N, Cerling TE.Six sympatric species of 5-million-year-old (late Hemphillian) horses from Florida existed during a time of major global change and extinction in terrestrial ecosystems. Traditionally, these horses were interpreted to have fed on abrasive grasses because of their high-crowned teeth. However, carbon isotopic and tooth microwear data indicate that these horses were not all C4 grazers but also included mixed feeders and C3 browsers. The late Hemphillian Florida sister species of the modern genus Equus was principally a browser, unlike the grazing diet of modern equids. Late Hemphillian horse exti...
Vagedes K.The bone finds from the neolithic settlement in Pestenacker (near Landsberg am Lech) date back to the second half of the 4th millennium BC (Altheim). Like in any other late neolithic horse bones, the question we have to deal with is whether they represent the remains of wild horse or early domestic horse, as we do not know for certain yet the date of the earliest domestic horses' occurrence in Middle Europe. The post pleistocene distribution of the wild horse is described. For a long time people thought that hardly any wild horses existed in post pleistocene Middle Europe any longer, due to th...
Klide AM.Lumbar and thoracic vertebrae of the extinct horse, Equus occidentalis, were examined for gross and radiographic evidence of overriding spinous processes. Of 2,661 vertebrae examined, 580 had intact spinous processes. Thirty-six intact spinous processes, which appeared grossly similar to overriding spinous processes in the modern domestic horse, E caballus caballus, were radiographed. Of these 36 vertebrae, 2 had radiographic signs compatible with a radiographic diagnosis of overriding spinous processes, ie, radiographically observed lysis and/or sclerosis. Seemingly, weight bearing or other s...
Science (New York, N.Y.)June 24, 1983
Volume 220, Issue 4604 1403-1404 doi: 10.1126/science.220.4604.1403
Berger J.The identities, sexes, and reproductive status of groups of wild horses (Equus caballus) living in the Great Basin Desert of North America were known prior to their deaths on ridgelines. Another group of very young horses died on a quagmire. Snow accumulation or drought was apparently responsible for the mass deaths. These data have implications for reconstructing some aspects of the social structure of fossil mammals on the basis of skewed sex or age ratios in bone assemblages.
Science (New York, N.Y.)November 5, 1976
Volume 194, Issue 4265 626-627 doi: 10.1126/science.790567
Radinsky L.Previous interpretations of early horse brains were based on an incorrectly identified fossil endocast, now believed to be from a condylarth. Newly prepared endocasts of Hyracotherium, the oldest horse and one of the earliest perissodactyls, reveal a relatively larger brain, with a more expanded neocortex, than existed in the condylarth ancestors of perissodactyls. Fifty million years ago, horse brains had suprasylvian, ectolateral, and lateral sulci, but the frontal lobe was undeveloped.
Science (New York, N.Y.)May 2, 1969
Volume 164, Issue 3879 543-547 doi: 10.1126/science.164.3879.543
Jepsen GL, Woodburne MO.A lower jaw of an eohippus (Hyracotherium cf. H. angustidens) from late Paleocene strata in Wyoming has extended the geological record of fossil horses into pre-Eocene time and suggests that the order Perissodactyla had an origin earlier than that heretofore conjectured. This specimen, together with equid teeth also possibly of late Paleocene age from Baja California, indicates that early perissodactyls were widespread on the North American continent before the Eocene epoch. Late Paleocene and early Eocene deposits of northwestern Wyoming have yielded many vertebrate rarities and "first or ear...
Vollmerhaus B, Roos H, Gerhards H, Knospe C.The canine teeth of the horse developed phylogenically from the simple, pointed, short-rooted tooth form of the leaf eating, in pairs living, Eocene horse Hyracotherium and served up to the Oligocene as a means of defense (self preservation). In the Miocene the living conditions of the Merychippus changed and they took to eating grass and adopted as a new behavior the life in a herd. The canine teeth possibly played an important role in fights for social ranking; they changed from a crown form to knife-like shape. In the Pliohippus the canine tooth usually remained in male horses and since the...
Klide AM.Lumbar and thoracic vertebrae of the extinct horse, Equus occidentalis, were examined for gross and radiographic evidence of overriding spinous processes. Of 2,661 vertebrae examined, 580 had intact spinous processes. Thirty-six intact spinous processes, which appeared grossly similar to overriding spinous processes in the modern domestic horse, E caballus caballus, were radiographed. Of these 36 vertebrae, 2 had radiographic signs compatible with a radiographic diagnosis of overriding spinous processes, ie, radiographically observed lysis and/or sclerosis. Seemingly, weight bearing or other s...
MacFadden BJ.The dispersal of Equus into South America during the Great American Biotic Interchange (GABI) represented a major event for Pleistocene land-mammal age chronology on that continent. It has been argued that this dispersal occurred during the late Pleistocene, ∼0.125 Ma, and it defines the base of the Lujanian South American Land Mammal Age (SALMA). In this scenario, Equus dispersed during the fourth and latest recognized phase of the interchange, i.e., GABI 4. Although Equus was widely distributed in South America during the Pleistocene, only a few localities are calibrated by independent chr...
Vincelette AR, Renders E, Scott KM, Falkingham PL, Janis CM.The traditional story of the evolution of the horse (family Equidae) has been in large part about the evolution of their feet. How did modern horses come to have a single toe (digit III), with the hoof bearing a characteristic V-shaped keratinous frog on the sole, and what happened to the other digits? While it has long been known that the proximal portions of digits II and IV are retained as the splint bones, a recent hypothesis suggested that the distal portion of these digits have also been retained as part of the frog, drawing upon the famous Laetoli footprints of the tridactyl (three-toed...
Vershinina AO, Kapp JD, Baryshnikov GF, Shapiro B.Museum collections are essential for reconstructing and understanding past biodiversity. Many museum specimens are, however, challenging to identify. Museum samples may be incomplete, have an unusual morphology, or represent juvenile individuals, all of which complicate accurate identification. In some cases, inaccurate identification can lead to false biogeographic reconstructions with cascading impacts on paleontological and paleoecological research. Here, we analyzed an unusual Equid mandible found in the Far North of the Taymyr peninsula that was identified morphologically as Equus hemionu...
Vagedes K.The bone finds from the neolithic settlement in Pestenacker (near Landsberg am Lech) date back to the second half of the 4th millennium BC (Altheim). Like in any other late neolithic horse bones, the question we have to deal with is whether they represent the remains of wild horse or early domestic horse, as we do not know for certain yet the date of the earliest domestic horses' occurrence in Middle Europe. The post pleistocene distribution of the wild horse is described. For a long time people thought that hardly any wild horses existed in post pleistocene Middle Europe any longer, due to th...
MacLaren JA.Locomotion in terrestrial tetrapods is reliant on interactions between distal limb bones (e.g. metapodials and phalanges). The metapodial-phalangeal joint in horse (Equidae) limbs is highly specialized, facilitating vital functions (shock absorption; elastic recoil). While joint shape has changed throughout horse evolution, potential drivers of these modifications have not been quantitatively assessed. Here, I examine the morphology of the forelimb metacarpophalangeal (MCP) joint of horses and their extinct kin (palaeotheres) using geometric morphometrics and disparity analyses, within a phylo...
Kalmykov NP.This report analyzes a find of fossils of Pliocene three-toed horse (Hipparion tchicoicum) in western Transbaikalia. The age of the mammalian fauna from red-brown clay in the Udunga locality indicates that Chikoi hipparion lived in the south of Eastern Siberia as early as the second half of the Early Pliocene; its remains in this area were known only from the red beds of the Upper Pliocene. This find made it possible to fill the existing hiatus (Early Pliocene) in its stratigraphic distribution: Late Miocene-Late Pliocene. The range of this three-toed horse species did not go beyond the border...
Pichardo M.Analysis of the morphological characters in North and South American horses present during Paleoindian time indicates that at least eight Equus ecospecies occurred in North America. In South America, Equus had radiated into four ecospecies, Hippidion had one, and Onohippidium had three geographically separate ecospecies. These species are found in archeological deposits ranging from ca. 13,000 to 8,000 yr B.P., in tropical habitats as well as in the high Andean and Patagonian colder ecotopes.
Science (New York, N.Y.)May 2, 1969
Volume 164, Issue 3879 543-547 doi: 10.1126/science.164.3879.543
Jepsen GL, Woodburne MO.A lower jaw of an eohippus (Hyracotherium cf. H. angustidens) from late Paleocene strata in Wyoming has extended the geological record of fossil horses into pre-Eocene time and suggests that the order Perissodactyla had an origin earlier than that heretofore conjectured. This specimen, together with equid teeth also possibly of late Paleocene age from Baja California, indicates that early perissodactyls were widespread on the North American continent before the Eocene epoch. Late Paleocene and early Eocene deposits of northwestern Wyoming have yielded many vertebrate rarities and "first or ear...
Kalmykov NP.Morphological features of the teeth were studied in the three-toed horse Hipparion tchicoicum from the Pliocene of Western Transbaikalia (Russia). Several diagnostic signs of the Chicoi hipparion were described for the first time to provide criteria for distinguishing the taxon among other fossils of three-toed horses and estimating their real diversity at the final stage of their distribution in Inner Asia.
Julien MA, Rivals F, Serangeli J, Bocherens H, Conard NJ.It is often difficult to differentiate between archaeological bonebeds formed by one event such as a mass kill of a single herd, and those formed by multiple events that occurred over a longer period of time. The application of high temporal resolution studies such as intra-tooth isotopic profiles on archaeological mammal cohorts offers new possibilities for exploring this issue, allowing investigators to decipher between single and multiple accumulation events. We examined (18)O and (13)C isotopic variations from the enamel carbonate of 23 horse third molars from the Middle Pleistocene archae...
Landry Z, Roloson MJ, Fraser D.The metapodials of extinct horses have long been regarded as one of the most useful skeletal elements to determine taxonomic identity. However, recent research on both extant and extinct horses has revealed the possibility for plasticity in metapodial morphology, leading to notable variability within taxa. This calls into question the reliability of metapodials in species identification, particularly for species identified from fragmentary remains. Here, we use ten measurements of metapodials from 203 specimens of four Pleistocene horse species from eastern Beringia to test whether there are s...
Jones KE.The specialization of equid limbs for cursoriality is a classic case of adaptive evolution, but the role of the axial skeleton in this famous transition is not well understood. Extant horses are extremely fast and efficient runners, which use a stiff-backed gallop with reduced bending of the lumbar region relative to other mammals. This study tests the hypothesis that stiff-backed running in horses evolved in response to evolutionary increases in body size by examining lumbar joint shape from a broad sample of fossil equids in a phylogenetic context. Lumbar joint shape scaling suggests that st...
Pichardo M.Greater precision in North American Pleistocene equid taxonomy makes it now possible to exploit the ubiquitous horse remains in Paleoindian sites as ecological index-fossils. The horses of Central Mexico and the Southern Plains can be sorted by tooth size alone, except for two rare large horses of the Southern Plains. The species endemic to these grasslands and south to Central Mexico are Equus pacificus (large), E. conversidens (small), E. francisci (smallest). The Southern Plains were also occupied by a specialized grazer E. excelsus (Burnet and Sandia caves) and E. occidentalis (Dry and San...
