Ontogeny and cranial morphology of the tympanic region of the Tupaiidae, with special reference to Ptilocercus

The structure of the tympanic region of the skull of Ptilocercus lowii was studied in an embryo of 30 mm crown-rump length and in 5 osteocrania. As in Tupaia, the anterior wall of the bulla of Ptilocercus is not completed by a tympanic process of the alisphenoid, contrary to earlier reports. Ptilocercus resembles Tupaia in the following derived characters. The ventral wall of the tympanic cavity is formed by a rostral entotympanic and by a caudal tympanic process of the petrosal. The entotympanic develops in primary connection with the tubal cartilage. The tympanic aperture of the auditory tube is bordered by the entotympanic. The ring-shaped tympanicum is covered by the entotympanicum and is aphaneric. The musculus tensor tympani is lacking. Among mammals, these characters can be regarded as synapomorphic for the Tupaiidae, that is, to have been present in the common ancestor of the two subfamilies. From the evidence of the tympanic region, the Tupaiidae, therefore, form a monophyletic group. Besides these synapomorphies, there are remarkable differences between Ptilocercus and Tupaia in the structure of the bulla. In Ptilocercus the bulla is smaller and less pneumatized than in Tupaia. An anterior intrabullar septum, present in Tupaia, is lacking in Ptilocercus. The epitympanic wing of the alisphenoid is smaller in Ptilocercus than in Tupaia. A lateral prefacial commissure of the tegmen tympani is present in Ptilocercus, but absent in Tupaia. The caudal tympanic process of the petrosal is larger in Ptilocercus than in Tupaia. These characters are autapomorphic for the Ptilocercinae and for the Tupaiinae, respectively. They demonstrate that the auditory bulla of Ptilocercus and that of Tupaia have evolved independently to a considerable extent. An early phylogenetic separation of their respective ancestors seems likely. The tympanic region of the skull provides no evidence for close relationships of the tree shrews to the primates or to any other eutherians. The classification of the Tupaiidae in a separate order, Scandentia, is supported.     

Morphology and development of the cranium of Felis silvestris f. catus Linné 1758--a contribution to the comparative anatomy of the Carnivora. III: Ear region and occipital region

In Felis, the otic region of younger embryonic stages up to Felis 1 is characterized by extremely medial extended cochleae, compressing the basal plate to a slender trabeculum. As a result of a quite strong rostrad convergence of the long axis of the ear capsules, the Commissura praefacialis fuses with the Commissura orbitoparietalis laterally. Until now, this has been found in whales only. Continuing embryogenesis towards Felis 2, the cochlea moves laterally and slightly ventrally, so the angle of convergence between the whole Capsula otica and the skull base decreases. The problem of interpreting these positional changes of the Capsula otica during phylogenesis and ontogenesis is discussed in detail. Up to recent literature, there is a discussion about homology of the Foramen perilymphaticum and allied structures in reptiles referring to the openings in the Capsula otica in mammals. Configuration of these structures in fissiped carnivores and the appearance of a "limitating membrane" in Felis 2, gives reason for a new discussion of these problems. Composition of the Bulla tympani is a very important feature for investigation of phylogeny and systematics in fissiped carnivores. In Felis 2, there appears a caudal entotympanic, consisting of young cartilaginous tissue. The development of the caudal entotympanic has impact on 2 structures in the occipital region: The Lamina alaris and the Processus paracondyloideus. Felis 1 shows a distinct Lamina alaris and a short Processus paracondyloideus. With Felis 2, either element is reduced largely, probably to the extent as the caudal entotympanic develops.     

The entotympanic in late fetal artiodactyla (Mammalia)

The entotympanic is a neomorphic component of the bulla tympanica of placental mammals. Ontogenetically, its rostral component seems to be derived from the tubal cartilage, whereas its caudal component is normally connected with the sheath of the tympanohyal; the present study indicates additional sources of the caudal entotympanic. The entotympanics develop in late fetal or early postnatal life as cartilaginous structures, but in most taxa they ossifiy endochondrally as “os bullae”. This skeletal element is absent only in a few placental orders, among them the Artiodactyla. Because it is present in their sister taxa within the Scrotifera, it is likely to be reduced secondarily in the even‐toed mammals. The study of histological serial sections of late fetal stages of several artiodactyl species shows that vestigial cartilaginous homologues of the entotympanics are invariably present, contrary to statements in the literature. In a few perinatal stages even secondary ossifications or calcifications of the entotympanic cartilages can be observed. The tubal cartilage of artiodactyls also continues into an anterior tegmen tympani (new term) that forms the floor of the fossa muscularis major. J. Morphol. 274:926–939, 2013. © 2013 Wiley Periodicals, Inc.     

Changes in the composition of the auditory bulla in southern Solomon Islands populations of the grey cuscus, Phalanger orientalis breviceps (Marsupialia, Phalangeridae)

The auditory bulla is a much-scrutinized taxonomic character of mammals, which is generally regarded as showing a high degree of structural consistency within higher taxa. Observations of bulla variability in populations of the marsupial Phalanger orientalis from the Solomon Islands demonstrate considerable flexibility in bulla makeup, with variable incorporation of the squamosal into the tympanic floor. Studies of the ontogeny of the bulla in Phalanger show the presence of three ossification centres, including an entotympanic. Squamosal invasion of one of these ossificiation centres is seen as a possible result of inbreeding, arising from the mode of colonization of the Solomon Islands by this species. This suggests that, under certain conditions, considerable morphological plasticity may be induced within the selective constraints of bulla function.     

Morphologische Untersuchungen am Mittelohr der Marsupialial

Morphological studies on the auditory bulla of marsupials The resent study on the comparative anatomy of the marsupial auditory bulla starts with that of the didelphids; ontogenetic data are included. It becomes clear from these comparisons, that the marsupial bulla is throughout composed of the same skeletal elements. Contrary to widespread opinion, there exists no good evidence for the existence of an entotympanic in any marsupial. The tympanic process of the petrosal develops relatively late in ontogeny as ‘additional bone’ (“Zuwachsknochen” of Starck ); the same holds true for the tympanic process of the alisphe-noid. Biometric study of the tymanic ring in didelhids reveals that the tympanic membrane does only slightly increase with skull size (pronounced negative allometry). It is surprising, however, that the data of the tympanic diameter do arrane at two distinct levels of regression. Several taxa of didelphids must have jumped at this level independently. The possible functional meanings of these data are briefly discussed.     

新疆准噶尔盆地北缘铁尔斯哈巴合晚渐新世两种啮形类耳区的形态研究

我们曾描述过一块与本文描述的标本产自同一地点和层位、可能为Ａｍｐｈｅｃｈｉｎｕｓ的猬类岩骨标本（孟津等,１９９９）。后来新发现的与牙齿属同一个体的Ａｍｐｈｅｃｈｉｎｕｓ岩骨标本证明我们根据单体岩骨的分类鉴定无误。此例说明,在一定的条件下,耳区标本在某些哺乳动物类群中可以鉴定到属,甚至种。因此在形态学、生物地层学上都有一定的意义,而且会因有关标本的不断积累而越来越重要。本文记述了另外两块产自新疆准噶尔盆地北缘铁尔斯哈巴合晚渐新世地层中的岩骨。有关地层、地点资料及所用术语见孟津等（１９９９）以及其中…     

The petrosal of Omomys carteri and the evolution of the primate basicranium

The first omomyine petrosals, those of Omomys carteri, are described. Omomys probably had a tympanic bulla and canals for the intratympanic carotid circulation derived from the petrosal bone. The stapedial and promontory canals were complete, large and subequal. The posterior carotid foramen entered the bulla posteromedially. The intratympanic portion of the facial nerve was fully enclosed in bone, the stapedius fossa is extrabullar and the parotic fissure is patent. The mastoid was pneumatized from the epitympanic recess and a supracochlear cavity may have been present. The Omomys petrosals exhibit a generic omomyiform morphology, exhibiting no features that can be interpreted as autapomorphies and only one feature shared with adapiforms. The monophyly of Omomyiformes is based on other cranial characters, dental and postcranial characters assessed elsewhere. The similarity of the Shanghuang petrosal to the petrosals of omomyiforms, as well as the ambiguous evidence of its association, suggest that an omomyiform affinity for that petrosal cannot be ruled out.     

Relationship of Nandinia binotata (Gray) to the Superfamily Feloidea (Mammalia, Carnivora)

The phylogenetic relationship between Nandinia binotata and Feloidea is analysed by the cladistic method, based on a literature review of osteological characters used in systematic works on carnivores for more than a century. The reduced or lost postglenoid foramen is a synapomorphy that define Nandinia and Feloidea as a monophyletic group. Nandinia does not have an ectotympanic septum in the bulla nor a paroccipital process nested with the posterior wall of the bulla, which are autapomorphies for the Feloidea. Thus it is hypothesized that Nandinia binotata has a sister-group relation to Feloidea. The cartilaginous caudal entotympanic is an autapomorphy for Nandinia.     

First Description of the Auditory Region of a Tremarctinae (Ursidae,Mammalia) Bear: The Case of Arctotherium angustidens

Here we present the first detailed morphological study of the auditory region of a tremarctine bear, the South American giant short-faced bear Arctotherium angustidens. We compared 19 specimens of A. angustidens with other tremarctines and ursines. Through the use of CT scans, we confirmed the presence of a recesus epitympanicus and an anterior incomplete septum of uncertain homology, not related with the septum bullae nor with the longitudinal septum formed by the ecto- and the entotympanic. A secondary crus formed by the lateral semicircular canal (LSC) with the posterior semicircular canal (PSC) of the inner ear was observed in A. angustidens, A. bonariense, Tremarctos ornatus, Ursus spelaeus, and Ursus arctos. This secondary crus was not previously reported for ursids. We also observed that the intraspecific variation in the auditory region of A. angustidens is related to 1) the position of the foramen postglenoideum, 2) the anterior projection of the bulla tympanica over the foramen lacerum and over the opening of the Eustachian tube (medial process of the bulla tympanica), and 3) the projection of the bulla tympanica over the posterior surface of the processus postglenoideus (tympanic process). In addition to this variation, we also identified the presence of interspecific variation in the external auditory region among Tremarctinae and Ursidae. These differences are related to the size of the processus mastoideus and the processus paraoccipitalis, the position of the foramen postglenoideum, and the presence/absence of contact between the bulla tympanica and the processus paraoccipitalis.     

Cranial anatomy of the Paleocene plesiadapiform Carpolestes simpsoni (Mammalia, Primates) using ultra high-resolution X-ray computed tomography, and the relationships of plesiadapiforms to Euprimates

Central to issues surrounding the origin of euprimates, affinities of Paleocene Carpolestidae have been controversial. Carpolestids have been classified as plesiadapoid primates, tarsiiform euprimates, dermopterans, or the sister taxon of euprimates to the exclusion of other plesiadapiforms, based exclusively on dental or postcranial data. Newly discovered crania of Carpolestes simpsoni from the latest Paleocene of the Clarks Fork Basin, Wyoming, are the first described for the family Carpolestidae. The two best preserved skulls were studied using ultra high-resolution X-ray computed tomography. Comparison of these specimens to those of other stem primates (Plesiadapiformes) demonstrates that the diversity of cranial morphology in this group is greater than previously thought. Carpolestes differs from euprimates and is similar to other plesiadapiforms (Ignacius and Plesiadapis) in lacking a postorbital bar and having a relatively long rostrum. Carpolestes is similar to fossil euprimates and Plesiadapis in having a bullar morphology consistent with a petrosal origin, and differs from Ignacius, in which the bulla is composed of the entotympanic. Carpolestes differs from primitive euprimates and all other known plesiadapiforms in possessing a two-chambered auditory bulla, similar to that of modern Tarsius. However, Carpolestes had an internal carotid artery (ICA) that took a transpromontorial route from a posteromedially positioned posterior carotid foramen (pcf), unlike Tarsius, in which this artery takes a perbullar route from an anterolaterally positioned pcf. Carpolestes has clear grooves on the promontorium for both the promontorial and stapedial arteries, indicating that it had an unreduced internal carotid circulation, similar to that of early euprimates. Carpolestes differs from primitive euprimates and some specimens of Ignacius in not having bony tubes surrounding the branches of the ICA. Cladistic analysis of cranial data fails to support a close relationship of Carpolestidae to either tarsiiform euprimates or extant Dermoptera, but suggests a close relationship between Carpolestidae, Plesiadapidae, and Euprimates.     

The entotympanic of Equus caballus (Perissodactyla,Mammalia)

In the majority of extant placental mammals the bulla tympanica is composed of two skeletal elements, the entotympanic and the ectotympanic. Former studies revealed that the presence of an entotympanic in the bulla tympanica of extant Perissodactyla is restricted to Rhinocerotidae. The existence of the entotympanic in Tapiridae and Equidae remained speculative. Here we present the first evidence of an entotympanic, strictly speaking rostral entotympanic, in the domestic horse, Equus caballus. The enchondrally ossified entotympanic can be easily separated from the desmal ectotympanic by its greater thickness and by its cancellous bone texture in a late fetal stage. Both elements are separated by a suture that is in the process of coalescence. The complete fusion of the two elements and the unification of bone texture are almost accomplished at birth but the entotympanic and ectotympanic assume the same thickness obviously not until early postnatal development. Based on modern phylogenetic hypotheses we can conclude that the common ancestor of Perissodactyla must have possessed a well-developed entotympanic, probably only evident in their fetal life. This must be considered as a plesiomorphic character state of this order, because the entotympanic is a neomorphic apomorphy of placental mammals. However, the prenatal fusion of the entotympanic and the ectotympanic is an apomorphy of Equus caballus and possibly of the Equidae as a whole.     

The angular process of Monodelphis domestica (Didelphidae, Marsupialia) and its relation to the middle ear: an ontogenetic and evolutionary morphologic study

In most marsupials, the angular process is inflected medially. By using an ontogenetic series of Monodelphis domestica, the development of this characteristic structure has been described. In contrast with the eutherian mammals, in marsupials there is retained a close connection between the dentale and the tympanicum and goniale; it is well known that these 2 elements of the middle ear are derived from the angulare and prearticulare of the reptilian lower jaw. At the neonatal stage, the dentale and tympanicum are both relatively vertically orientated; during the following 2 weeks, they take an increasingly oblique position, which is primarily caused by the rapid growth of the braincase. Only after the eruption of the first teeth, the ascending ramus of the dentale takes a more and more vertical position, whereas the angular process remains with its tip near the medioventral floor of the tympanic bulla. The bulla shows at this place a rectangular fenestra which is covered by a membrane of loose connective tissue; the tip of the angular process, which is always free of muscular insertions, maintains contacts with this fenestra throughout life. During juvenile and adult life stages, the process becomes somewhat removed from the fenestra for obvious reasons, but at a gape of about 40 to 50 degrees it inevitably must touch the "inferior tympanic membrane" and possibly also the tympanic ring. It is speculated that the relationship between the angular process and the tympanic bulla represents a specific form-function complex for sound transmission, which may be a modified retention from archaic mammalian conditions. Further details of the ontogenetic development of the tympanic region have been described which may be of some relevance for the evolutionary morphology of mammals: The tympanic process of the petrosal, which fixes the posterior end of the tympanic ring, is formed by 'Zuwachsknochen' (additional bone) but not by cartilage. The styloid process remains cartilaginous throughout life: its free tip ends in the lateral wall of the tympanic cavity and it is closely connected with the collum mallei and the posterior end of the tympanicum; it guides the chorda tympani and may therefore be homologous with the cartilage of Spence. The cartilage of Paauw is interpreted in terms of functional morphology. A model of evolutionary transformation of the dentale-tympanicum complex in mesozoic mammals in outlined on the basis of the ontogenetic findings in Monodelphis and other didelphid and dasyurid marsupials.     

经豚鼠下鼓道口记录耳蜗电图

豚鼠是听觉机能研究最常应用的动物,在其颅骨的鼓泡上,有一卵圆形的小孔,称为下鼓道口,在此插入电极,可抵鼓岬部,能够很好地记录出耳蜗电图。此方法简便、可靠,不需要打开乳突,是从鼓岬部记录耳蜗电图的一种新途径,在听觉机能研究及生理学实验教学中具有广泛的应用价值。     

Cranial circulation of the pen-tailed tree shrewPtilocercus lowii and relationships of Scandentia

The major cranial arteries and veins are described for a 30-mm crown-rump length fetus of the pen-tailed tree shrewPtilocercus lowii, and comparisons are made with cranial vessels reported in the tree shrewTupaia and with the vascular pattern reconstructed for primitive eutherians.Ptilocercus shares a number of derived features of the cranial circulation withTupaia, which, therefore, represent synapomorphies of tree shrews (Tupaiidae, Scandentia). Included are (1) the enclosure of the intratympanic portion of the internal carotid artery in a bony canal that is floored proximally and distally by the entotympanic and by the petrosal in between, (2) the enclosure of the intratympanic portion of the stapedial artery by the petrosal in a canal on the promontorium and within the epitympanic crest beneath the tympanic roof, (3) the absence of an exit for the arteria diploëtica magna, (4) an alisphenoid canal, (5) a maxillary artery that passes medial to the mandibular nerve beneath foramen ovale, and (6) a laryngeopharyngeal artery. Some of these derived features, however, are also found in certain other eutherians (e.g., numbers 2, 3, and 6 in Euprimates) and, therefore, may be used in future studies to assess the higher-level affinities of Scandentia.     

菱臼齿兽((犭亚)目、哺乳纲)耳区的骨骼结构

本文详细描述了菱臼齿兽耳区各个部分的基本结构;并指出了耳区结构与某些啮齿类的相似性,以及中耳鼓泡组成成份与戈壁(犭亚)兽(Anagale gobiensis)的区别。     

New notharctine (primates,adapiformes) skull from the Uintan (middle Eocene) of San Diego County,California

A new genus and species of notharctine primate, Hesperolemur actius, is described from Uintan (middle Eocene) aged rocks of San Diego County, California. Hesperolemur differs from all previously described adapiforms in having the anterior third of the ectotympanic anulus fused to the internal lateral wall of the auditory bulla. In this feature Hesperolemur superficially resembles extant cheirogaleids. Hesperolemur also differs from previously known adapiforms in lacking bony canals that transmit the internal carotid artery through the tympanic cavity. Hesperolemur, like the later occurring North American cercamoniine Mahgarita stevensi, appears to have lacked a stapedial artery. Evidence from newly discovered skulls of Notharctus and Smilodectes, along with Hesperolemur, Mahgarita, and Adapis, indicates that the tympanic arterial circulatory pattern of these adapiforms is characterized by stapedial arteries that are smaller than promontory arteries, a feature shared with extant tarsiers and anthropoids and one of the characteristics often used to support the existence of a haplorhine-strepsirhine dichotomy among extant primates. The existence of such a dichotomy among Eocene primates is not supported by any compelling evidence. Hesperolemur is the latest occurring notharctine primate known from North America and is the only notharctine represented among a relatively diverse primate fauna from southern California. The coastal lowlands of southern California presumably served as a refuge area for primates during the middle and later Eocene as climates deteriorated in the continental interior. Hesperolemur probably was an immigrant taxon that entered California from either the northern (Wyoming/Utah) or southern (New Mexico) western interior during the middle Eocene © 1995 Wiley-Liss, Inc.     

Cranial Morphology of a Pantolestid Eutherian Mammal from the Eocene Bridger Formation,Wyoming, USA: Implications for Relationships and Habitat

Pantolestinae is a eutherian subfamily of mammals whose members are known from the middle early Paleocene through at least the beginning of the Oligocene of North America. They are also known from Europe, and possibly Africa. A lack of information on pantolestine skulls has prevented the use of cranial anatomy in evaluation of this group’s enigmatic higher-level phylogenetic relationships. Conversely, postcranial skeletons are well known and locomotor interpretations based on them are robust. The most complete known skull of a pantolestine, Pantolestes longicaudus (YPM 13525), is described here and compared to potential close fossil relatives and extant mammals. Semicircular canal morphology is used to test locomotor hypotheses. YPM 13525 lacks an ossified bulla. It has a mediolaterally broad basioccipital, a large entoglenoid process, and a deeply incised glaserian fissure of the squamosal, caudal and rostral tympanic processes on the petrosal, a foramen for an internal carotid artery (ICA) that entered the tympanic cavity from a posteromedial position, bony tubes enclosing the main stem and transpromontorial branch of the ICA, a large anterior carotid foramen formed within the basisphenoid, evidence of a stapedial artery ramus superior, a groove on the dorsal aspect of the basisphenoid leading to the piriform fenestra possibly for drainage of the cavernous sinus to an extracranial inferior petrosal sinus, a dorsum sellae with well-developed posterior clinoid processes, a foramen rotundum within the alisphenoid, and a sphenorbital fissure between the alisphenoid and orbitosphenoid. Overall, the morphology is not strikingly similar to any potential close relative and the phylogenetic position of Pantolestinae cannot be estimated without cladistic analysis of a character matrix that includes this new morphology and broadly samples extant and extinct eutherian taxa. Semicircular canal morphology differs from that of two likely terrestrial Paleocene mammals, Aphronorus (another pantolestid) and Eoryctes (a palaeoryctid), suggesting a different, possibly semi-aquatic, lifestyle for Pantolestes.     

Congenital anomalies of the ear resulting from cyclophosphamide treatment in the rat

A single dose of cyclophosphamide (20 mg/kg) administered on day 12 of gestation to CF rats resulted in microtia in 97.5% of fetuses at term. The ears of affected fetuses were low set and dorsally placed. Histological examination revealed persistence of meatal plug, branching of the primordium of external acoustic meatus, periotic hemorrhages, narrowing of tympanic cavity, presence of only one to two primordia of middle ear ossicles, hypoplasia of stapedial artery, a maximum of two turns of cochlea and under differentiation of the organ of Corti and the semicircular ducts. Hemorrhages in and around the region of the ear were extensive. Bilaterally symmetrical distribution of microtia and consistency of associated anomalies suggest that this is a good animal model for further investigation into the pathogenetic mechanisms of these ear anomalies.     

Ontogenetic and phylogenetic transformations of the ear ossicles in marsupial mammals

This study is based on the examination of histological sections of specimens of different ages and of adult ossicles from macerated skulls representing a wide range of taxa and aims at addressing several issues concerning the evolution of the ear ossicles in marsupials. Three-dimensional reconstructions of the ear ossicles based on histological series were done for one or more stages of Monodelphis domestica, Caluromys philander, Sminthopsis virginiae, Trichosurus vulpecula, and Macropus rufogriseus. Several common trends were found. Portions of the ossicles that are phylogenetically older develop earlier than portions representing more recent evolutionary inventions (manubrium of the malleus, crus longum of the incus). The onset of endochondral ossification in the taxa in which this was examined followed the sequence; first malleus, then incus, and finally stapes. In M. domestica and C. philander at birth the yet precartilaginous ossicles form a supportive strut between the lower jaw and the braincase. The cartilage of Paauw develops relatively late in comparison with the ear ossicles and in close association to the tendon of the stapedial muscle. A feeble artery traverses the stapedial foramen of the stapes in the youngest stages of M. domestica, C. philander, and Sminthopsis virginiae examined. Presence of a large stapedial foramen is reconstructed in the groundplan of the Didelphidae and of Marsupialia. The stapedial foramen is absent in all adult caenolestids, dasyurids, Myrmecobius, Notoryctes, peramelids, vombatids, and phascolarctids. Pouch young of Perameles sp. and Dasyurus viverrinus show a bicrurate stapes with a sizeable stapedial foramen. Some didelphids examined to date show a double insertion of the Tensor tympani muscle. Some differences exist between M. domestica and C. philander in adult ossicle form, including the relative length of the incudal crus breve and of the stapes. Several differences exist between the malleus of didelphids and that of some phalangeriforms, the latter showing a short neck, absence of the lamina, and a ventrally directed manubrium. Hearing starts in M. domestica at an age in which the external auditory meatus has not yet fully developed, the ossicles are not fully ossified, and the middle ear space is partially filled with loose mesenchyme. The ontogenetic changes in hearing abilities in M. domestica between postnatal days 30 and 40 may be at least partially related to changes in middle ear structures.     

Ontogeny and morphology of the round window and aqueduct of cochlea in Tupaia and other mammals

Studied the morphogenesis of the Fenestra rotunda and of the Aquaeductus cochleae in a series of 23 dated embryos and postnatal stages of Tupaia belangeri. The ontogeny of the Fenestra rotunda is the result of the caudal growth of the Processus recessus (DE BEER 1937). The Processus arises from the caudal ridge of the floor of the cochlear part of the otic capsule. On the 28th d of ontogeny (the gestation period of Tupaia belangeri is 43 d), it is fused with the lateral edge of the parachordal plate. On the 40th d, the Processus recessus joins the ventral surface of the canalicular part of the otic capsule, which develops a small cartilaginous process to meet it. In Tupaia, the Processus recessus is a large cartilaginous plate in a nearly horizontal position. It does not reach the plane of the Foramen perilymphaticum. The Processus recessus can be regarded as a part of the parachordal plate that was shifted laterally together with the Recessus scalae tympani by the enlargement of the cochlear part of the otic capsule in the ancestors of living mammals. The Processus forms the floor of the Aquaeductus cochleae, by which the laterally shifted Recessus scalae tympani of mammals remains connected with the cranial cavity. The Aquaeductus cochleae contains the Ductus perilymphaticus connecting the Cavum perilymphaticum of the inner ear with the Cavum leptomeningeum. The Fenestra rotunda of mammals is homologous with the lateral aperture of the Recessus scalae tympani of reptiles. In some mammals (e.g. Micropotamogale), the Membrana tympani secundaria spans the lateral aperture of the Recessus scalae tympani, as in many reptiles. Both the Membrana tympani secundaria of reptiles and that of mammals are homologous. Secondarily, in a large number of therian mammals (e.g. Myotis [Frick 1952]), the tympanic cavity extends into the Recessus scalae tympani displacing the Membrana tympani secundaria medially from the lateral aperture of the Recessus scalae tympani (= Fenestra rotunda of mammals) and even into the plane of the Foramen perilymphaticum. Thereby the Fossula fenestrae rotundae is formed, which in bounded medially by the Membrana tympani secundaria.