Figures
Abstract
We here describe the endocranial cast of the Eocene archaic ungulate Hyopsodus lepidus AMNH 143783 (Bridgerian, North America) reconstructed from X-ray computed microtomography data. This represents the first complete cranial endocast known for Hyopsodontinae. The Hyopsodus endocast is compared to other known “condylarthran” endocasts, i. e. those of Pleuraspidotherium (Pleuraspidotheriidae), Arctocyon (Arctocyonidae), Meniscotherium (Meniscotheriidae), Phenacodus (Phenacodontidae), as well as to basal perissodactyls (Hyracotherium) and artiodactyls (Cebochoerus, Homacodon). Hyopsodus presents one of the highest encephalization quotients of archaic ungulates and shows an “advanced version” of the basal ungulate brain pattern, with a mosaic of archaic characters such as large olfactory bulbs, weak ventral expansion of the neopallium, and absence of neopallium fissuration, as well as more specialized ones such as the relative reduction of the cerebellum compared to cerebrum or the enlargement of the inferior colliculus. As in other archaic ungulates, Hyopsodus midbrain exposure is important, but it exhibits a dorsally protruding largely developed inferior colliculus, a feature unique among “Condylarthra”. A potential correlation between the development of the inferior colliculus in Hyopsodus and the use of terrestrial echolocation as observed in extant tenrecs and shrews is discussed. The detailed analysis of the overall morphology of the postcranial skeleton of Hyopsodus indicates a nimble, fast moving animal that likely lived in burrows. This would be compatible with terrestrial echolocation used by the animal to investigate subterranean habitat and/or to minimize predation during nocturnal exploration of the environment.
Citation: Orliac MJ, Argot C, Gilissen E (2012) Digital Cranial Endocast of Hyopsodus (Mammalia, “Condylarthra”): A Case of Paleogene Terrestrial Echolocation? PLoS ONE 7(2): e30000. https://doi.org/10.1371/journal.pone.0030000
Editor: Anjali Goswami, University College London, United Kingdom
Received: October 14, 2011; Accepted: December 8, 2011; Published: February 10, 2012
Copyright: © 2012 Orliac et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work has been conducted with the support of the ANR (ERC programme Palasiafrica (ANR-08-JCJC-0017-01). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
A major function of the brain is the maintenance of physiological condition (homeostasy). By collecting and processing sensory information, it insures optimal behavioral responses in a given environment. Therefore, several brain structures are molded by the ecophysiological situation of the animal within its niche [1]–[4]. The increased use of computed tomography (CTscan) recently gave an unprecedented access to internal structures of fossils, and triggered new interest for vertebrate cranial endocast studies (e.g., [5]–[14]). These recent works are building upon fundamental studies performed during the second half of the 20th century (e.g., [15]–[20]) and cranial endocast anatomy is now documented for major mammalians clades.
The brain and associated soft tissues such as meninges, nerves, veins and arteries are sheltered in the neurocranium and leave imprints on its tabula interna. The study of the endocranial cast is the only means to reach an understanding about the nervous and sensory system of extinct species. Edinger [21] and Jerison [17] demonstrated that analysis of mammalian endocasts can provide a good approximation of the relative size of the major encephalic subdivisions and accordingly, comparative studies of fossil mammalian endocasts largely contributed to our knowledge of brain evolutionary history (e.g., [6], [17], [22]–[25]).
In the history of mammals, ‘Condylarthra’ consists of a para – or polyphyletic assemblage of Paleocene-Eocene early diverging ungulates that potentially played a crucial role in the onset of crown ungulate clades such as Perissodactyla, Artiodactyla, Cetacea, Proboscidea, Sirenia, and Hyracoidea (e.g., [26]–[29]). The braincase of several groups of these early diverging ungulates has been described in the literature and major families are documented: Arctocyonidae (Arctocyon, [30], [31]; Artocyonides, [31]), Phenacodontidae (Phenacodus, [15], [30], [32], [33]; Meniscotherium, [34]), Periptychidae (Periptychus, [30]), Hyopsodontidae (Hyopsodus, [35]), and Pleuraspidotheriidae (Pleuraspidotherium, [31]). The diversity of these groups is also reflected in the disparity of brain morphologies. The phylogenetic relationships of archaic ungulates remain a current topic of investigation. A recent hypothesis of relationships among basal ungulates mammals [36] including most of the ‘condylarthran’ taxa for which the endocranial cast is known is presented in figure 1.
In this work, we describe the endocast of Hyopsodus following 3D virtual reconstruction based on CT scan data. Hyopsodus is the most common mammal in several Early and Middle Eocene faunas from western North America ([35], [37]). It first appeared in the North American record in the early Wasatchian (or latest Clarkforkian, i.e. around the Paleocene-Eocene transition) and is recorded until the late early Chadronian (latest Eocene, [37], [38]). Gazin [35] provided the most extensive morphological revision of the genus. He described the endocranial features of Hyopsodus based on a partial cranial endocast of H. miticulus (USNM 23745) reconstructed from assembled cranial fragments of the same individual originating from Wyoming (Knight Member, Wasatch Formation, Green River Basin). This reconstruction documents the cerebellum and the midbrain as well as the posterior part of the telencephalon. A natural cast of the olfactory lobes of the same species is also described by the same author [35]. The ventral portion of the endocranial cavity of Hyopsodus is known from a specimen of H. paulus from the Bridger Formation (late Early, early Middle Eocene, Wyoming) in which the base of the endocranium was exposed [35]. The endocranial structures of Hyopsodus are thus only partially known from Gazin's work, and from fragmentary individuals belonging to distinct species. The relative proportions of the various brain parts, especially most of the forebrain including the extension of the neopallium, remained undescribed. In this study, we document the first complete endocranial cast of Hyopsodus, bringing crucial information about the relative proportions of the various encephalic structures. We detail forebrain morphology and sinuses network, and compare the endocast of Hyopsodus to those of other early diverging ungulates. The peculiar structure of endocranial cast of Hyopsodus is compared to its postcranial anatomy and used to discuss its ecology, especially its putative ability of using terrestrial echolocation to progress in burrows or to avoid nocturnal predators.
Results and Discussion
Digital cranial endocast of Hyopsodus
The braincase of AMNH 143783 is broken in two parts at the base of the olfactory bulbs. The two fragments match perfectly and the neurocranium is complete (Figure 2). The skull has undergone a slight dorso-ventral compression and the braincase is slightly deformed by a lateral shift. Measurements of the endocast are provided in Table 1. The various parts of the brain, olfactory bulbs, cerebral hemisphere and cerebellum are aligned within the same plane and serially arranged (Figure 3A, C). The vermis of the cerebellum constitutes the highest point of the brain. The cerebrum is relatively flat compared with the cerebellum. The shape of the cerebrum is correlated to the almost complete absence of telencephalic flexure. The maximal width is at the level of the piriform lobes (Figure 3B). The development of the olfactory peduncles and bulbs is important and their length represents approximately half of the total length of the cerebrum (Figs. 2B, 3B). The forebrain length represents approximately 2/3 of the total length of the endocast (Figure 3B).
Specimen illustrated in lateral (A), dorsal (B), and ventral (C) views. Scale bar = 1 cm.
Reconstruction illustrated in left lateral (A), dorsal (B), right lateral (C), ventral with basicranium (D), ventral without basicranium (E), and posterior views. Abbreviations: cas, cavernous sinus; cc, condyloid canal; cdf, condyloid foramen; ci, colliculi inferior; cf, condylar foramen; cs, colliculi superior; fl, paraflocculus; flm, foramen lacerum medium; flp, foramen lacerum posterius; fo, foramen ovale; fp, fissure prima; hy, hypophysis; ips,inferior petrosal sinus; lal, lateral lobe of cerebellum; las, lateral sinus (or transverse sinus); los, longitudinal sinus; mf, mastoid foramen; mo, medulla oblongata; ms, mesencephalon; mv, mastoid vein; np, neopallium; ob, olfactory bulb; oc, occipital condyle; op, olfactory peduncle; os, occipital sinus; ot, olfactory tubercle; pb, petrosal bone; pgf, postglenoid foramen; pil, piriform lobe; rhp, rhinal fissure; sc, sinusal canal; tf, temporal foramen; ts, temporal sinus; vc, vermis cerebelli. Scale bar = 1 cm.
Rhinencephalon.
The specimen AMNH 143783 gives access to the complete extension of the rhinencephalon. The latter is strongly developed, as it almost represents half of the forebrain. The bulging olfactory lobes are of large size. Their combined diameters equal the width of the dorsal roof of the skull in the posterior half of the orbits (Figure 2B). The two lobes are elongated and contiguous. They are prolonged by long olfactory fibers spreading into the anterior part of the orbits and beyond (not reconstructed on the 3D model because of bad preservation of the specimen). The olfactory bulbs directly extend the olfactory peduncles. Both structures are aligned with the rest of the telencephalon. The location of the olfactory tubercles is not clear on the right side of the skull because of postmortem deformation. It is observable on the left side, although weakly prominent (Figure 3A). The piriform lobes represent most of the cerebral hemispheres; they are visible in dorsal view in the posterolateral part of the cerebrum where they constitute the greatest width of the brain. They are dorsally delimited by the posterior rhinal fissure located in the dorsal third of the cerebrum height. A sinus might be present in the posterolateral part of the piriform lobe, but there is no trace of its anterior extension.
Neopallium.
In the description of the Hyopsodus braincase provided by Gazin [35], a considerable portion of the forebrain was missing and the telencephalon was only partially described. Especially, the location of the rhinal fissure was unknown. In the specimen described here, the posterior rhinal fissure is shallow but clearly present on both sides of the telencephalon (Figure 3 A–C). It is located in the dorsal third of the hemisphere and delimits the posteroventral border of the neopallium. The anterior rhinal fissure is difficult to locate. When present, it is limited to the anteriormost part of the cerebrum and does not abut on the posterior rhinal fissure. The neopallium thus forms a reduced cap on the cerebral hemisphere. The neopallium is smooth or lissencephalic, suggesting that there were no gyri or sulci (neither the lateral sulcus nor the suprasylvian sulcus). Only a subtle convexity lays on the dorsoposterior part of the neopallium, slightly posterior to the location of the gyrus 3 described in earliest artiodactyls ([16]; Orliac pers. obs). This structure marks the highest point of the cerebrum, with its dorsal part being flat and anteriorly sloping. The neopallium is distinctly narrower in its anterior portion. Between the medial margins of the neopallium, the longitudinal sinus in Hyopsodus is deep and clearly sets apart the two cerebral hemispheres. The lateral or transverse sinuses separate just ahead of the superior colliculi.
Midbrain.
The posterior limit of the neopallium is far apart from the lobes of the cerebellum, and the tectum of the midbrain is broadly exposed on the dorsal surface. The midbrain exposure is accentuated by the anterior divergence of the two cerebral hemispheres.
The corpora quadrigemina (colliculi) are clearly visible. The inferior colliculus is especially important, and its development occupies most of the exposed midbrain. This special feature is also observed in the specimen described by Gazin [35]. On x-ray radiographies, quasi perpendicular to the tabula interna, the tentorium cerebelli is a thick crest of bone separating the cerebrum from the cerebellum.
Cerebellum.
The cerebellum is large and exhibits a well delimited vermis, cerebellar hemispheres (lateral lobes) and paraflocculus. The vermis of the cerebellum is wide and elevated; its dorsal extension is pointed and reaches the same level as the dorsal face of the telencephalon. The fissura prima is located in the posterior third of the vermis. The cerebellar hemispheres are separated from the cerebrum by a broad and shallow paramedian fissure. The former are moderately developed and not inflated, sloping anteriorly. Their dorsal surface is almost flat. In dorsal view, their posterior extension does not reach that of the vermis, with the posterior part of the latter forming a wide bulge. On both ventrolateral surfaces, the paraflocculi are observable. They consist of two rounded and large sized lobes that project outwards, downwards and somewhat backwards.
Nerves and sinuses.
The superior petrosal sinus is located underneath the cerebellar hemispheres, a continuation of the transverse or lateral sinus system. The posterior part of the sinus system cannot be described because most of the occipital surface of the skull is eroded and the bone is not preserved. The anterior part of the lateral sinus system, or temporal sinus, is partially reconstructed in blue on figure 3. It extends ventrally and leads to the postglenoid foramen (path for the external jugular vein). Dorsally, it leads to several small foramina indicating vascular communication with the temporal surface. Posteriorly, the occipital sinus runs external to the petrosal bone and opens on the occipital surface at the level of the mastoid foramen (path for the mastoid vein). Ventrally, the petrosal sinus curves slightly forward to the foramen lacerum posterius (internal jugular vein). Just ventral to this flexure, and before the sinus reaches the foramen lacerum posterius, a small posterior sinus corresponding to the condyloid canal opens in the internal aspect of the occipital condyle. Posteroventral to it, on the side of the medulla oblongata, lies the condylar foramen (or hypoglossal foramen) which corresponds to the path of the nerve XII.
Ventromedial to the paraflocullus there is the prominence representing the internal auditory meatus with the cast of the facial nerve (VII), and of the auditory nerve (VIII) located more posteroventrally. The elongated foramen lacerum medium, medial to the internal auditory meatus, connects posteriorly the foramen lacerum posterius by a discrete inferior petrosal sinus. The foramen ovale lies posterolateral to the cavernous sinus and contains the third branch of the trigeminal nerve (V3). The surface of the hypophysis or pituitary body cannot be delimited with precision due to deformation and partial preservation of the bone; however, it might be present on the right side of the specimen, medial to the foramen ovale (Figure 3E). The two cavernous sinuses are prominent like in the specimen described by Gazin [35]. They terminate at the position of the posterior aperture to the sphenoidale fissure, and, as suggested by Gazin [35], comprise a complex of vascular structures and cranial nerves (III to VI except V3).
Pattern of Hyopsodus cranial endocast compared to that of other archaic ungulates
Endocast volume and encephalization quotient.
The estimated volume (EV) of the endocast of the specimen of H. lepidus (AMNH 143783) described here is 2.79 cm3 (sinuses reconstructed in blue on figure 2 not included). Based on external observation of the specimen US 23745 described by Gazin [35], Jerison [17] proposed an endocast volume estimate of 3.2 cm3 for H. miticulus. The corresponding encephalization quotient (EQ) calculated with an estimated body mass (EM) of 630 g (based on head and body length), is of 0.36 using the equation proposed by Jerison [17] (EQ = EV/0.12(EM)2/3), and of 0.49 with the equation of Eisenberg [39] (EQ = EV/0.055(EM)0.74). Damuth [40] discussed the problem of estimating body weights of archaic ungulates which greatly differ from extant members of the group. Indeed, the body shape and proportions of Hyopsodus are markedly different from those of extant ungulates from which the correlations between dental measurements and body weight are estimated, making it difficult to propose plausible estimates. With its elongated body and relatively short limbs, Hyopsodus has been described as a rat-sized animal morphologically close to the weasel [35]. We used different formulas to estimate AMNH 143783 body size: Legendre [41] regressions for ungulates and for mammals, and Damuth [40] regressions for non-selenodont ungulates using m1 area and m1 length. Depending of the formula used, the estimated body weight of AMNH 143783 ranges between 412 and 854 g. Indeed, differences in body weight estimations have important repercussions on EQ estimates (Table 2). Damuth [40] considers that the use of m1 area overestimates the body mass of basal ungulates because they have larger teeth for their body size than do the average modern ones. This assumption gives more credit to the body weight estimate based on the m1 length (412 g). Given the morphological divergence between Hyopsodus and extant ungulates, we consider a body weight estimate comprised between 326 g and 412 g, which corresponds to an EQ between 0.48 and 0.41 following the equation of [17], [20], and between 0.59 and 0.70 according to Eisenberg's equation [39]. These EQ values are slightly superior to the estimate of Jerison ([17]; EQ = 0.36) based on a heavier body weight estimate. According to the EQ estimates calculated by Jerison [17] and Radinsky [20], Hyopsodus has one of the highest EQ of basal ungulates (Tab. 2): higher values are only observed for the mesonychian Mesonyx (“flesh-eater”) and for “advanced ungulates” such as Homacodon [20].
Development of the neopallium.
By its structure, the neopallium of Hyopsodus is rather simple among archaic ungulates. There is no junction between the posterior and anterior rhinal fissures, the location of the latter being even difficult to determine with precision (Figure 3). Pleuraspidotherium, Arctocyon and Meniscotherium have a more clearly marked rhinal fissure (Figure 4), with a junction between the anterior and posterior parts. In Hyopsodus, the ventral extension of the neopallium is weak and it does not reach the level of what is interpreted here as a vascular sinus. It is comparable to that of Pleuraspidotherium or Arctocyon. Meniscotherium has a more important development of the neopallium; it even exhibits an anterior inflection of the rhinal fissure that might delineate the frontal lobe ventrally (Figure 4D). This inflection is also observed in early artiodactyls (Cebochoerus) and perissodactyls (Hyracotherium). The neopallium of Hyopsodus is devoid of fissures and has no trace of suprasylvia or a lateral sulcus, it only exhibits a slight inflation of the posterior part of the neopallium. The same morphology is observed in Meniscotherium (AMNH 48082; Gazin, 1965), which shows a more important posterior inflation of the neopallium. This is in contrast with the neopallium of Phenacodus, Arctocyon and Pleuraspidotherium, which present clear sulci. Phenacodus bears a long lateral sulcus and another small more ventral depression possibly representing the suprasylvia. After verification on the original endocasts (MNHN CR 956, CR 700) Arctocyon presents both the lateral and the suprasylvian sulci (accordingly to [31]). Pleuraspidotherium only presents one oblique sulcus in a rather posterior and external position (AMNH 39266), interpreted as the suprasylvia by Russell and Sigogneau [31]. In the basalmost perissodactyl Hyracotherium (AMNH 55267), there are three well distinct sulci (suprasylvian, ectolateral and lateral, [42]), whereas the simplest artiodactyl endocast presents only two sulci (lateral sulcus and the suprasylvia, [16]). By its proportions, the neopallium of Hyopsodus is rather advanced as its antero-posterior extension almost covers half of the total length of the brain.
Reconstructions made after the original cranial endocasts of: (A) Hyopsodus lepidus (AMNH 143783), (B) Pleuraspidotherium (MNHN CR 252, 963; cast AMNH 39266); (C) Phenacodus (AMNH 4369); (D) Meniscotherium (AMNH 49082; USNM 19509); (E) Arctocyon (MNHN CR 700), modified after Russell and Sigogneau (1965). Not to scale. Abbreviations: same as Figure 2.
Midbrain exposure.
Midbrain exposure has often been correlated with a weak neocortical expansion [43]. It is wide in the pleuraspidotheriid Pleuraspidotherium, and the arctocyonids Artocyon and Artocyonides in which it represents one third of the length of the cerebral hemispheres. In these taxa, however, the corpora quadrigemina do not leave imprints on the skull roof. In the description of the endocast of Artocyon, Russel and Sigogneau [31] mentioned that a part of the corpora quadrigemina might be visible on the left side of the endocast (MNHN CR 700); however, there is no trace of this structure on the other specimen (MNHN CRL 956) and its location would be too low and too lateral to correspond to the corpora quadrigemina. Meniscotherium also presents a wide exposure of the midbrain. Gazin [34] suggested that the lateral sinuses of Meniscotherium might correspond to the corpora quadrigemina, but that their direct continuity with the sagittal sinus rather indicates that it is highly improbable. Hyopsodus midbrain exposure is as important as in other archaic ungulates, but its structure is more derived by the presence of inflated inferior colliculi protruding dorsally. To sum up, Hyopsodus is the only “basal ungulate” with hypertrophied inferior colliculus known so far.
Relative proportions of brain components.
Despite their simple lissencephalic structure, the antero-posterior extension of the cerebral hemispheres is important in Hyopsodus and represents more than 40% of the total brain length. By the proportions of the different parts of its brain, Hyopsodus is closer to “advanced ungulates” like basal perissodactyls (e.g. Hyracotherium, [42]) or artiodactyls (e.g. Cebochoerus, [16]), than to phenacodontids or arctocyonids (Figure 5). The extension of the neocortex (in red Figure 5) is important compared to that of the cerebellum (in green Figure 4); a feature also observed in “advanced ungulates”. Hyopsodus midbrain exposure is as important as in other archaic ungulates, but its structure is more derived. The reduction of the cerebrum relative to the total length of the endocast in Hyopsodus is most probably correlated with the development of the inferior colliculi. It is noticeable that the morphology of the vermis itself, with a posterior location of the fissure prima, is primitive [16], despite its reduced antero-posterior extension. Hyopsodus presents one of the highest EQs among archaic ungulates, a statement congruent with the derived general proportions of its brain. Hyopsodus presents an “advanced version” of the basal ungulate brain pattern, with a mosaic of archaic (large olfactory bulbs, weak ventral expansion of the neopallium, absence of neopallium fissuration) and highly derived (relative reduction of the cerebellum compared to cerebrum; enlargement of the inferior colliculus) characters.
Reconstructions made after the original cranial endocasts of: (A) Phenacodus (AMNH 4369), (B), Meniscotherium (AMNH 49082), (C) Hyopsodus (AMNH 143783), (D) Pleuraspidotherium (MNHN CR 252, 963), (E) Arctocyon (MNHN CR 700), (F) Cebochoerus (MNHN 34–1967), (G) Hyracotherium (AMNH 55267). All specimens normalized on the neopallium length. Proportions of the different parts indicated in percent of the total endocast length: black, rhinencephalon; red, neopallium; blue, mesencephalon; green, cerebellum. Not to scale.
Paleoecological inference based on cranial endocast morphology
The most significant feature observed in Hyopsodus is the clear delineation of the corpora quadrigemina, and especially the large development of the inferior colliculus. The superior colliculus receives major inputs from the retina but is more than just a visual processing structure. One of its major functions is to localize a stimulus and to cause the animal to orient to the stimulus by moving its neck and/or its eyes [44]. In contrast to the role of the superior colliculus within the visual system, the inferior colliculus is the principal source of input to the auditory thalamus, which relays auditory information to the primary auditory cortex [45]. Moreover, the inferior colliculus probably also represents a major output to premotor pathways that initiate or regulate sound evoked motor behavior [46].
While exposure of the midbrain may be a primitive feature of mammals correlated to the weak development of the cerebral hemispheres, it has also been argued that midbrain exposure may result from secondary sensory specialization, especially when the development of the colliculi is involved as in extant and extinct chiropterans (bats, [43]). Such a claim has also been made for the exposure of the colliculi in dermopterans (flying lemurs, [47], [48]). It is noteworthy that the inferior colliculus of Hyopsodus is elevated above the midbrain plane which indicates that inferior colliculi are basically exposed because of their development and not because of a lack of posterior extension of the cerebral hemispheres. Gazin [35] argued that the neopallium of Hyopsodus was very simple and might not have been able to process complex information. However, in extant mammals, the colliculi have descending projections to the paramedian pontine reticular formation and spinal cord, and thus can be involved in response to stimuli faster than cortical processing would allow. Their development is thus independent from neocortical complexity. In particular, the auditory system is unique among sensory systems with its highly complex network of pathways in the lower brainstem and a significant amount of processing accomplished in the inferior colliculus, prior to the level of the thalamus and the cerebral cortex [49]. The relative size of the inferior colliculus in Hyopsodus suggests a high level of development of acoustic reflexes. Development of auditory sense is commonly observed in animals where visual sense is reduced such as in some nocturnal animals or fossorial animals (e.g., [50]).
Mammalian echolocation is mostly associated with cetaceans in aquatic environments and bats in aerial environments (e.g., Microchiroptera and Megachiroptera; [51]–[52]). Echolocation, however, has also been demonstrated in terrestrial mammals such as Soricomorpha (shrews) and Tenrecomorpha (tenrecs), mostly in association with subterranean environments or nocturnal habits [53]. The use of low-intensity, short-duration ultrasonic pulses for echolocation has been described in soricid shrews, including the common shrew Sorex araneus and the short-tailed shrew Blarina brevicauda [54]–[58]. Although discussed, the ecological significance of echolocation in shrews was proposed to aid the search for protective cover or for detecting obstacles in subterranean tunnels. Evidence for echolocation by means of tongue clicks has also been observed in three Tenrecidae both under experimental and natural conditions, and correlated to nocturnal exploration of new environments [53]. Those two insectivorous mammals, although phylogenetically distant (e.g., [59], [60]) present a rather simple brain structure. However, like in bats, both show a well developed inferior colliculus; the latter being largely exposed in the Tenrecidae Tenrec (Figure 6) and Geogale [61], [62].
Scale bar = 5 mm.
Among edentate placentals, the Xenarthra Chlamyphorus (pink fairy armadillo, or “pichiciego” which means “short-sighted”) has a subterranean life. It shows a huge enlargement of the posterior (inferior) colliculus [43] compared to the optic midbrain colliculi. Edinger [43] parallels the peculiar morphology of the brain of Chlamyphorus and its highly derived forelimbs, specialized for digging. Moreover, she relates the large size of the posterior (inferior) colliculus to the unique faculty of Chlamyphorus among armadillos to have a “voice” [63], [64]. The fact that this mammal is fossorial suggests that the latter, as shrews and tenrecs, might be another example of underground echolocation in extant terrestrial mammals.
Although no strict relationship between echolocation and the development of inferior colliculus has been demonstrated in extant terrestrial mammals, the inferior colliculus size in Hyopsodus could indicate that the latter used terrestrial echolocation to investigate subterranean environment and/or to minimize predation during nocturnal exploration of the environment as concluded for extant shrews [55]–[57].
Postcranial ecological signal vs cranial endocast morphology
Hyopsodus was a weasel-sized mammal with a long body, shortened limbs and clawed feet. The postcranium of Hyopsodus has been extensively described and figured in Gazin [35] and this animal has either been considered as partly living in trees [65], or adapted to digging or rooting [35] and was likely an herbivorous ground and tree dweller [66]. Gazin interpreted Hyopsodus skull shape, dentition and postcranial morphology as clues of rooting and digging habits. Rose [29] describes Hyopsodus as having the body shape of a weasel or a prairie dog, and as being capable of climbing or digging but with not apparent specialization for any particular mode of life. Indeed, Hyopsodus postcranium is not particularly adapted to digging. The olecranon of the ulna and anterior ungual phalanges are not particularly elongated, the manus is not transformed and the humerus does not show any characteristic specialization related to fossorial ability: the deltopectoral crest is long but not prominent anteriorly, the diaphysis is thin and smooth, and the entepicondyle projects medially more than in Erinaceus and Rhynchocyon, reaching or overpassing that of Solenodon, Spermophilus, and Eocene leptictids [67]. However, the scapula bears a very high spine shifted posteriorly, and the elbow stabilization, together with the reduction of supination movements, could indicate some digging abilities for Hyopsodus. Rose [67] mentions the following as forelimb traits associated with terrestrial, and possibly digging behaviour: a nearly flat ulnar facet on the radius allowing little supination, separate scaphoid and lunar facets on the distal radius promoting stability at the wrist, and prominent extensor tubercles on the metacarpals and ungual phalanges, all features that can be observed in Hyopsodus (see [35] plate 10). As mentioned by Gazin [35], the femur possesses a greater trochanter that does not project proximally beyond the head and a very distal location of the third trochanter, interpreted by this author as an adaptation for abducting the limb, a position consistent with digging. However, in extant mammals, the position of the third trochanter is not necessarily correlated to the extension of the gluteus superficialis it supports, which impedes any functional interpretation of this character. On the other hand, the dorsally prominent tuberosity of the ischion (where the extensors of the hip joint originate) and the well-defined femur trochlea between sharp crests suggest that Hyopsodus could move swiftly. The femoral trochlea is better defined in Hyopsodus than in Tenrec, Tupaia, and Erinaceus, but less deep anteroposteriorly than in Rhynchocyon and Eocene leptictids [67], and the tibia and fibula are not fused. The overall morphology of the postcranial skeleton of Hyopsodus suggests a nimble, fast moving animal, with digging abilities and able, then, to live in burrows like small extant mustelids.
Matthews [65] regarded Hyopsodus as semi-arboreal. Even if its general morphology and the amplitude of its movements allowed Hyopsodus to climb in trees like extant mustelids, its postcranial morphology indicates that it was not particularly adapted to arboreal life: the stabilization of the elbow joint, characterized by the deep trochlea of the humerus, the perforated olecranon fossa, the reduced lateral epicondylar crest and an elongated humeral head and twisted proximal extremity of the humerus, differs greatly from what is observed in extant arboreal mammals such as primates and carnivorans (Argot, pers obs.). The oval shape of the head of the radius, and the reduced supination capabilities suggested by the tight radius-ulna contact, also indicates that Hyopsodus was not particularly adapted to arboreal life. Only the medially prominent entepicondyle and shape of the ulna, posteriorly convex, may be found in arboreal mammals.
Morphology and proportions of the endocranial cast of Hyopsodus suggest a developed auditory sense, possibly associated with terrestrial echolocation. The overall morphology of the postcranial skeleton of Hyopsodus, suggesting a nimble, fast moving animal likely to live in burrows, would be compatible with terrestrial echolocation and/or with nocturnal habits. The occurrence of a highly specialized behavior such as terrestrial echolocation could be put in question by the archaic neocortical structure of Hyopsodus. However, the high encephalization quotient of the latter and the relative proportions of the different brain segments, close to more advanced ungulates, make Hyopsodus brain outstanding among basal ungulates. Its advanced brain structure might have played a role in the long temporal range of this taxon; Hyopsodus persists in the fossil record until the Late Eocene and is among the last “condylarths” to go extinct in North America [38].
Materials and Methods
This study is based on the complete Hyopsodus skull AMNH 143783 housed at the American Museum of Natural History. The specimen consists in a complete cranium only lacking I1-2 on the left side and C, I3-1 on the right side. The mandible preserves a complete dentition. Its posterior part is broken and the angle, as well as the ascending ramus of the mandible, are missing on both sides. The size of the specimen, intermediate between H. paulus and H. minusculus, and its primitive dental morphology (as described by Flynn [68]; characters include: absence of molarization of the p4, well developed m1–2 hypoconid, absence of strong preprotocrista on P3–4, absence of strong hypocone on M1–2, absence of strong molar lophodonty) allows referring AMNH 143783 to Hyopsodus lepidus Matthew, 1909. Both a 3D reconstruction of the dentition (Figure S1) and dental measurements (Table S1) are provided in online supporting information. The exact provenance of this specimen remains uncertain, however, the known temporal range of Hyopsodus lepidus is Bridgerian (late Early – early Middle Eocene, [68]). To our knowledge, this skull has never been figured nor described prior to the present study.
The skull AMNH 143783 was scanned with a high resolution CT-scanner at the American Museum of Natural History. The scans resulted in 1300 slices with dimensions of 990 by 1000 pixels. The slices have a 60.83201 µm thickness and are spaced 60.83201 µm apart; two-dimensional slices were reconstructed from X-rays using Vgstudiomax® (version 1.2; VolumeGraphics GmbH, 2004). The 3D segmentation of bone, endocast and sinuses was performed using Aviso® (VSG); endocast volume has been calculated by surface integration. Measurements were taken with Aviso following the protocol of Macrini [69], endocast flexure was measured following the protocol of Macrini et al. [14]. Encephalization quotient was calculated both with the equation defined by Jerison [17] and Radinsky [20]: EQ = EV/0.12 (EM)0.67, and with the equation defined by Eisenberg [39]: EQ = EV/0.055 (EM)0.74. This latter equation is based on a regression analysis of empirical data from a large sample of extant placental mammal species and confirmed the now widely accepted exponent value of about 0.75 for the scaling of brain size to body size among mammals generally.
Supporting Information
Figure S1.
Digital reconstruction of AMNH 143783 left dentition. A, upper and lower cheek teeth in occlusion, lateral view; B–D, c-m3 in (B) occlusal, (C) lingual, (D) labial views; E–F, C-M3 in (E) occlusal, and (F) lingual views. Scale bar = 5 mm.
https://doi.org/10.1371/journal.pone.0030000.s001
(TIF)
Table S1.
Dental measurements of AMNH 143783 referred to Hyopsodus lepidus (given in mm). Measurements are base don the 3D reconstruction of the dentition.
https://doi.org/10.1371/journal.pone.0030000.s002
(DOC)
Acknowledgments
We are particularly grateful to R. O'Leary for her help and access to the AMNH collections. Many thanks to J. Thostenson and M. Hill for access to CT scan facilities and acquisition of the CT scan raw data. This is ISE-M publication 2011–151. This work has been possible thanks to the high resolution CT-scanner facility of the AMNH funded by the NSF MR1–R2 0959384 granted to N. Landman, Co-PIs: D. Ebel, D. Frost.
Author Contributions
Conceived and designed the experiments: MJO. Analyzed the data: MJO CA EG. Contributed reagents/materials/analysis tools: MJO CA EG. Wrote the paper: MJO CA EG.
References
- 1.
Allman JM (1999) Evolving brains. New York: W.H. Freeman and Company. 98 p.
- 2. Catania KC (2000) Cortical organization in Insectivora: the parallel evolution of the sensory periphery and the brain. Brain Behav Evol 55(6): 311–321.
- 3. Catania KC (2005) Evolution of sensory specializations in insectivores. The Anat Rec A 287A: 1038–1050.
- 4. Catania KC, Henry EC (2006) Touching on somatosensory specializations in mammals. Curr Opin Neurobiol 16: 467–473.
- 5.
Rowe TB, Carlson W, Bottorff W (1995) Thrinaxodon: Digital atlas of the skull. Austin: Univ. of Texas Press, CD-ROM, ed. 2.
- 6. Rowe TB, Macrini TE, Luo ZX (2011) Fossil evidence on origin of the mammalian brain. Science 332: 955–957.
- 7. Brochu CA (2000) A digitally rendered endocast for Tyrannosaurus rex. J Vertebr Paleontol 20: 1–6.
- 8. Larsson HCE, Sereno PC, Wilson JA (2000) Forebrain enlargement among nonavian theropod dinosaurs. J Vertebr Paleontol 30: 615–618.
- 9. Witmer LM, Chatterjee S, Franzosa J, Rowe T (2003) Neuroanatomy of flying reptiles and implications for flight, posture and behavior. Nature 425: 950–953.
- 10. Maisey JG (2005) Braincase of the Upper Devonian shark Cladoides wildungensis (Chondrichthyes, Elasmobranchii), with observations on the braincase in early chondrichthyans. Bull Am Mus Nat Hist 288: 1–103.
- 11. Marino L, Uhen MD, Frohlich B, Aldag JM, Blane C, et al. (2000) Endocranial volume of Mid-Late Eocene archaeocetes (Order: Cetacea) revealed by computed tomography: implications for cetacean brain evolution. J Mammal Evol 7(2): 81–94.
- 12. Marino L, Uhen MD, Pyenson ND, Frohlich B (2003) Reconstructing cetacean brain evolution using computed tomography. Anat rec 272B: 107–117.
- 13. Franzosa J, Rowe T (2005) Cranial endocast of the Cretaceous theropod dinosaur Acrocanthosaurus atokensis. J Vertebr Paleontol 25: 859–864.
- 14. Macrini TE, Muizon C, Cifelli RL, Rowe T (2007) Digital cranial endocast of Pucadelphys andinus, a Paleocene metatherian. J Vertebr Paleontol 27: 99–107.
- 15. Simpson GG (1933) Braincasts of Phenacodus, Notostylops, and Rhyphodon. Am Mus Nov 622: 1–19.
- 16. Dechaseaux C (1969) Moulages endocrâniens d'artiodactyles primitifs, essai sur l'histoire du néopallium. Annls Paleont (Vert) 55(2): 195–248.
- 17.
Jerison HJ (1973) Evolution of brain and intelligence. New York: Academic Press. 482 p.
- 18. Edinger T (1975) Paleoneurology 1804–1966. An annotated bibliography. Adv Anat Embryol Cell Biol 49: 1–258.
- 19. Radinsky LB (1977) Brains of early carnivores. Paleobiology 3: 333–349.
- 20. Radinsky LB (1978) Evolution of brain size in carnivorous and ungulates. Am Nat 112(987): 815–831.
- 21. Edinger T (1948) Evolution of the horse brain. Geol Soc Am Mem 25: 1–177.
- 22.
Jerison HJ (2009) How can fossils tell us about the evolution of the neocortex. In: Kaas JH, editor. Evolutionary Neuroscience. Amsterdam: Elsevier. pp. 497–508.
- 23. Radinsky LB (1968) A new approach to mammalian cranial analysis, illustrated by examples of prosimian primates. J Morphol 124: 167–180.
- 24. Radinsky LB (1973) Evolution of the canid brain. Brain Behav Evol 7(3): 169–202.
- 25. Radinsky LB (1976a) The brain of Mesonyx, A Middle Eocene mesonychid condylarth. Fieldiana Geol 33(18): 323–337.
- 26. Van Valen L (1978) The beginning of the age of mammals. Evol Theory 4: 45–80.
- 27.
Prothero DR, Manning EM, Fischer M (1988) The phylogeny of the ungulates. In: Benton MJ, editor. The phylogeny and classification of the tetrapods, Volume 2: Mammals. Oxford: Clarendon Press. pp. 201–234.
- 28.
Archibald JD (1998) Archaic ungulates (“Condylarthra”). In: Janis CM, Scott KM, Jacobs LL, editors. Evolution of Tertiary mammals of North America. Volume 1: Terrestrial carnivores, ungulates, and ungulatelike mammals. Cambridge: Cambridge University Press. pp. 292–331.
- 29.
Rose KD (2006) The beginning of the age of mammals. In: Rose KD, editor. Baltimore: The John Hopkins University Press. 428 p.
- 30. Edinger T (1929) Die fossilen Gehirne. Zeits Gesam Anat AbtIII 28: 1–249.
- 31. Russell DE, Sigogneau D (1965) Etude de moulages endocrâniens de mammifères paléocènes. Mem Mus Natl Hist Nat C 16(1): 1–34.
- 32.
Cope ED (1884) The vertebrata of the Tertiary Formation of the West. Rept US Geol Surv Terr, III.
- 33. Tilney F (1933) Fossil brains of some early tertiary mammals of North America. Bull Neurol Inst New York 1: 430–505.
- 34. Gazin LC (1965) A study of the Early Tertiary condylarthran mammal Meniscotherium. Smithson Misc Collect 149(4–2): 1–98.
- 35. Gazin LC (1968) A study of the Eocene condylarthran mammal Hyopsodus. Smithson Misc Collect 153(4): 1–90.
- 36. Ladevèze S, Missiaen P, Smith T (2010) First skull of Orthaspidotherium edwardsi (Mammalia, “Condylarthra”) from the late Paleocene of Berru (France) and phylogenetic affinities of the enigmatic European family Pleuraspidotheriidae. J Vertebr Paleontol 30(5): 1559–1578.
- 37. Rose KD (1980) Clarkforkian land-mammal age: revised definition, zonation, and tentative intercontinental correlations. Science 208: 744–746.
- 38.
Janis CM, Archibald DJ, Cifelli RL, Lucas SG, Schaff CR, et al. (1998) Part III: Archaic ungulates and ungulatelike mammals. In: Janis CM, editor. Evolution of Tertiary mammals of North America. Cambridge: Cambridge University Press. pp. 247–259.
- 39.
Eisenberg JF (1981) The mammalian radiations. Chicago: University of Chicago Press. 610 p.
- 40.
Damuth J (1990) Problems in estimating body masses of archaic ungulates using dental measurements in body size in mammalian paleobiology. In: Damuth J, MacFadden BJ, editors. Estimation and biological implications. Cambridge: Cambridge University Press. pp. 229–253.
- 41. Legendre S (1989) Les communautés de mammifères du Paléogène (Eocène supérieur et Oligocène) d'Europe occidentale: structure, milieux et évolution. Müncher Geowiss AbhA 16: 1–110.
- 42. Radinsky LB (1976b) Oldest horse brains: more advanced than previously realized. Science 194: 626–627.
- 43. Edinger T (1964) Midbrain exposure and overlap in mammals. Amer Zool 4: 5–19. 43.
- 44.
Butler AB, Hodos W (1996) Comparative vertebrate neuroanatomy. Evolution and adaptation. New York: Wiley-Liss. 514 p.
- 45. Malmierca MS, Merchán M, Henkel CK, Oliver DL (2002) Direct projections from cochlear nucleus complex to auditory thalamus in the rat. J Neurosci 22: 10891–10897.
- 46.
Casseday JH, Fremouw T, Covey E (2002) The inferior colliculus: a hub for the central auditory system. In: Oertel D, Popper AN, Fay RR, editors. Springer Handbook of Auditory Research. New York: Springer. pp. 238–318.
- 47. Starck D (1963) “Freiliegendes Tectum mesencephali” ein Kennzeichen des primitiven Säugetiergehirns? Zool Anz 171: 350–359.
- 48. Ginguerich PD, Gunnel GF (2005) Brain of Plesiadapis cookei (Mammalia, Proprimates): surface morphology and encephalization compared to those of Primates and Dermoptera. Contrib Mus Paleontol Univ Mich 31(8): 185–195.
- 49. Malmierca MS (2004) The inferior colliculus: A center for convergence of ascending and descending auditory information. Neuroembryol Aging 3: 215–229.
- 50. Barton RA, Purvis A, Harvey PH (1995) Evolutionary radiation of visual and olfactory brain systems in primates, bats and insectivores. Phil Trans R Soc Lond B 348: 381–392.
- 51. Jones G, Teeling EC (2006) The evolution of echolocation in bats. Trends Ecol Evol 21(3): 149–156.
- 52. Teeling EC (2009) Hear, hear: the convergent evolution of echolocation in bats? Trends Ecol Evol 24(7): 351–354.
- 53. Gould E (1965) Evidence for echolocation in the tenrecidae of Madagascar. Proc Amer Phil Soc 109: 352–360.
- 54. Gould E (1969) Communication in three genera of shrews (Soricidae) : Suncus, Blarina, Cryptotis. Communs Behav Biol(A) 3: 11–31.
- 55. Gould E, Negus N, Krech D (1964) Evidence for echolocation in shrews. J exp Zool 156: 19–38.
- 56. Buchler ER (1976) The use of echolocation in the wandering shrew Sorex vagrans. Anim Behav 24: 858–873.
- 57. Tomasi TE (1979) Echolocation by the short-tailed shrew Blarina brevicauda. J Mammal 60: 751–759.
- 58. Forsman KA, Malmquist MG (1988) Evidence for echolocation in the common shrew, Sorex araneus. J Zool 216: 655–662.
- 59. Douady CJ, Douzery EJ (2003) Molecular estimation of eulipotyphlan divergence timesand the evolution of “Insectivora”. Mol Phyl Evol 28: 285–296.
- 60. Symonds MRE (2005) Phylogeny and life histories of the ‘Insectivora’: controversies and consequences. Biol Rev 80: 93–128.
- 61.
Stephan H, Baron G, Frahm HD (1991) Comparative brain research in mammals Volume 1. Insectivora. New York: Springer Verlag. 573 p.
- 62. Rehkämper G, Stephan H, Poduschka W (1986) The brain of Geogale aurita Milne-Edwards and Grandidier 1872 (Tenrecidae, Insectivora). J Hirnforsch 27(4): 391–399.
- 63. Jakobs C (1943) El pichiciego. Un capitolo biogeográphico misterioso de la argentina. Rev Geogr Am 19: 307–314.
- 64. Minoprio JDL (1954) Sobre el Chlamyphorus truncatus Harlan. Acta Zool Lilloana 3: 5–58.
- 65. Matthews (1928) The evolution of the mammals in the Eocene. Proc Zool Soc London 1927: 947–985.
- 66. Williamson TE, Lucas SG (1992) Meniscotherium (Mammalia, “Condylarthra”) from the Paleocene-Eocene of Western North America. New Mexico Mus Nat Hist Sci Bull 1: 1–87.
- 67. Rose KD (1999) Postcranial skeleton of Eocene Leptictidae (Mammalia), and its implications for behavior and relationships. J Vertebr Paleontol 19: 355–372.
- 68. Flynn JJ (1991) Hyopsodus (Mammalia) from the Tepee Trail Formation (Eocene), Northwestern Wyoming. Amer Mus Nov 3007: 1–19.
- 69. Macrini TE (2009) Description of a digital cranial endocast of Bathygenys reevesi (Merocoidodontidae, Oreodontoidea) and implications for apomorphy based diagnosis of isolated, natural endocasts. J Vert Paleont 29(4): 1199–1211.