A New Basal Hadrosauroid Dinosaur from the Lower Cretaceous Khok Kruat Formation in Nakhon Ratchasima Province,Northeastern Thailand

A new basal hadrosauroid dinosaur from the Lower Cretaceous Khok Kruat Formation of Thailand, Sirindhorna khoratensis gen. et sp. nov is described. The new taxon is based on composite skull and mandible including premaxilla, maxilla, jugal, quadrate, braincases, predentary, dentaries, surangular, and maxillary and dentary teeth. It is diagnostic by such characters as, sagittal crest extending along entire dorsal surface of the parietal and reaching the frontoparietal suture (autapomorphy), transversely straight frontoparietal suture, caudodorsally faced supraoccipital, no participation of the supraoccipital in the foramen magnum, mesiodistally wide leaf-shaped dentary tooth with primary and secondary ridges on the lingual surface of the crown, perpendicularly-erected and large coronoid process of dentary, and nonvisible antorbital fossa of the maxilla in lateral view. Phylogenetic analysis revealed S. khoratensis as among the most basal hadrosauroids. Sirindhorna khoratensis is the best-preserved iguanodontian ornithopod in Southeast Asia and sheds new light to resolve the evolution of basal hadrosauriforms.     

Characteristics of dentition in gekkonid lizards of the genus <Emphasis Type="Italic">Teratoscincus</Emphasis> and other Gekkota (Sauria,Reptilia)

The dentition and tooth crown microstructure of gekkonids and eublepharids are examined. Scanning electron microscopy shows that the lingual surface of teeth in these lizards has one, two, or, occasionally, several cusps separated by grooves. The teeth of geckoes usually have two (lingual and labial) cusps in the apical region. With respect to the number of teeth, the majority of Gekkota fall into two groups. The first includes a few species with many teeth (50 or more) in the dentary and maxilla, the eublepharids Goniurosaurus and Aeluroscalabotes, and the gekkonid Cyrtopodion louisiadensis. The second group, comprising most of the species, is subdivided into two subgroups, species with 20–30 or 30–40 teeth in jaw bones. Teratoscincus belongs to the first subgroup of the second group.     

New triconodontids (Mammalia) from the Lower Cretaceous Shahai and Fuxin formations, northeastern China

The first triconodontids from Asia have been discovered from the Lower Cretaceous (Aptian to Albian) Shahai and Fuxin formations in Liaoning Province, northeastern China: Meiconodon lii gen. and sp. nov. and M. setoguchii gen. and sp. nov. M. lii is characterized by molariform teeth with a developed cusp d, an m3 with taller cusp a, an m4 with three primary cusps of subequal height, the posteriorly decreasing transverse width of the m4, and a considerably reduced m5. M. setoguchii is slightly larger than M. lii, and characterized by a sharp labial cingulum on the m4, and a less developed cusp d on the molariform teeth than M. lii. The extensive interlocking system between molariforms, posteriorly recumbent primary molariform cusps, and their great degree of asymmetry in occlusal view with rounded labial faces and more angulate lingual faces in lateral view, indicate that Meiconodon belongs to the triconodontid subfamily Alticonodontinae. These new taxa are the first record of Triconodontidae from Asia, and of Alticonodontinae outside North America, suggesting the occurrence of mammalian faunal exchange between North America and Asia during or before the Aptian-Albian.     

Redescription, palaeobiogeography and palaeoecology of Coniasaurus crassidens Owen, 1850 (Squamata) from the Lower Chalk (Cretaceous; Cenomanian) of SE England

Type and referred specimens of Coniasaurus crassidens from the Lower Chalk (Upper Cretaceous; Cenomanian) of southeast England, are re-described. The type is a left maxilla associated with 14 dorsal vertebrae. The maxilla is elongate, bears a low ascending process, and has a long and posteriorly positioned external narial margin. The first maxillary tooth is pointed and bears a groove on the labial face; more posterior maxillary teeth are increasingly rounded and bulbous, and have a single groove on the labial face. Mandibles assigned to Coniasaurus cf. C. crassidens possess teeth of similar form; mandibular bones include the dentary, splenial, angular, coronoid, prearticular, and surangular. A number of features show important similarities to later mosasaurs and contemporaneous groups such as dolichosaurs. These new data provide a very different picture of coniasaurs and their mode of life in the early Upper Cretaceous. The functional morphology of coniasaur teeth is unique and shows occlusion between the lingual platforms of the upper teeth with the crowns of the lower teeth. Coniasaurs can be considered as analgous to small sauropterygians in terms of general morphology, habitats, and trophic structure. Coniasaur distributions in the Cenomanian and Turonian of Europe and North America are similar to the palaeobiogeographic patterns of other organisms living in the Tethys and SuperTethys Seaway.     

Structure, attachment, replacement and growth of teeth in bluefish, Pomatomus saltatrix (), a teleost with deeply socketed teeth

Tooth replacement poses many questions about development, pattern formation, tooth attachment mechanisms, functional morphology and the evolution of vertebrate dentitions. Although most vertebrate species have polyphyodont dentitions, detailed knowledge of tooth structure and replacement is poor for most groups, particularly actinopterygians. We examined the oral dentition of the bluefish, Pomatomus saltatrix, a pelagic and coastal marine predator, using a sample of 50 individuals. The oral teeth are located on the dentary and premaxillary bones, and we scored each tooth locus in the dentary and premaxillary bones using a four-part functional classification: absent (A), incoming (I), functional (F=fully ankylosed) or eroding (E). The homodont oral teeth of Pomatomus are sharp, deeply socketed and firmly ankylosed to the bone of attachment. Replacement is intraosseus and occurs in alternate tooth loci with long waves of replacement passing from rear to front. The much higher percentage of functional as opposed to eroding teeth suggests that replacement rates are low but that individual teeth are quickly lost once erosion begins. Tooth number increases ontogenetically, ranging from 15–31 dentary teeth and 15–39 premaxillary teeth in the sample studied. Teeth increase in size with every replacement cycle. Remodeling of the attachment bone occurs continuously to accommodate growth. New tooth germs originate from a discontinuous dental lamina and migrate from the lingual (dentary) or labial (premaxillary) epithelium through pores in the bone of attachment into the resorption spaces beneath the existing teeth. Pomatomus shares unique aspects of tooth replacement with barracudas and other scombroids and this supports the interpretation that Pomatomus is more closely related to scombroids than to carangoids.     

Larinus berti sp. n. (Coleoptera,Curculionidae, Lixinae) from North Africa

A new species, Larinus berti sp. n. is described from Morocco and assigned to subgenus Cryphopus Petri, 1907 (Curculionidae: Lixinae; Lixini). Diagnostic characters of the new species are large size, elongate-ovate body, bisulcate sub-quadrangular rostrum, triangularly raised dorsum of rostrum, flat subgena and submentum, Y-shaped apodeme of sternite VIII of female and thin nodulus of spermatheca.     

Dentition and Jaw of Kokopellia juddi, a Primitive Marsupial or Near-Marsupial from the Medial Cretaceous of Utah

We add to the knowledge of the dentition and lower jaw of the primitive marsupial or near marsupial, Kokopellia juddi, based on newly collected materials from the medial Cretaceous (Albian–Cenomanian) of central Utah. The dental formula, i4 c1 p3 m4, is primitive for (or with respect to) Marsupialia, as are a number of features of the dentary and dentition: presence of a labial mandibular foramen, ?an inflected angle, ?and a trace of the meckelian groove; lack of “staggering” of the lower incisor series; lack of “twinning” between entoconid and hypoconulid on lower molars; incompletely lingual position of lower molar paraconid; upper molar protocone relatively small and mesiodistally narrow; and conules placed about halfway between the protocone and the paracone–metacone. Other than the stylocone, cusps are lacking from the stylar shelf; we argue that this represents the primitive marsupial condition based on the economy of character change and the stratigraphic record of marsupials in the Cretaceous of North America. Recent discoveries of early marsupials, eutherians, and therians of metatherian–eutherian grade provide data indicating that some derived features of the dentary and dentition (e.g., loss of coronoid, meckelian groove, and labial mandibular foramen; acquisition of strong, “winged” conules, double rank postvallum/prevallid shearing, and stylar cusp D) probably arose independently, in some cases more than once, among the major groups of tribosphenic mammals. In turn, this suggests that a common ancestor for marsupials and placentals was more primitive than has generally been appreciated.     

Early Cretaceous mammals of Western Siberia: 2. Tegotheriidae

New specimens of the tegotheriid docodont Sibirotherium rossicum Maschenko et al., 2003, including a maxillary fragment with two posterior teeth, an isolated upper molar, and mandibular fragments with teeth from the Early Cretaceous Shestakovo locality are described. The dental formula of Sibirotherium is I_{1 + ?}C1P₆M_6?. The upper molars of Sibirotherium, with two main labial and three lingual cusps, are convergently similar to the molars of tribosphenic mammals. In the dentary, the symphysis is short and Meckel’s groove is reduced. Sibirotherium is similar in the structure of lower teeth to Tegotherium from the Upper Jurassic of Mongolia; it is the latest known representative of Docodonta.     

Functional Morphology and Sexual Dimorphism of Mouthparts of the Short-Faced Scorpionfly Panorpodes kuandianensis (Mecoptera: Panorpodidae)

Mouthparts are closely associated with the feeding behavior and feeding habits of insects. The features of mouthparts frequently provide important traits for evolutionary biologists and systematists. The short-faced scorpionflies (Panorpodidae) are distinctly different from other families of Mecoptera by their extremely short rostrum. However, their feeding habits are largely unknown so far. In this study, the mouthpart morphology of Panorpodes kuandianensis Zhong et al., 2011 was investigated using scanning electron microscopy and histological techniques. The mandibulate mouthparts are situated at the tip of the short rostrum. The clypeus and labrum are short and lack distinct demarcation between them. The epipharynx is furnished with sublateral and median sensilla patches. The blade-shaped mandibles are sclerotized and symmetrical, bearing apical teeth and serrate inner margins. The maxilla and labium retain the structures of the typical pattern of biting insects. The hirsute galea, triangular pyramid-shaped lacinia, and labial palps are described in detail at ultrastructural level for the first time. Abundant sensilla are distributed on the surface of maxillary and labial palps. The sexual dimorphism of mouthparts is found in Panorpodes for the first time, mainly exhibiting on the emargination of the labrum and apical teeth of mandibles. Based on the features of mouthparts, the potential feeding strategy and feeding mechanism are briefly discussed in Panorpodes.     

Juvenile ornithopod (Dinosauria: Rhabdodontidae) remains from the Upper Cretaceous (Lower Campanian, Gosau Group) of Muthmannsdorf (Lower Austria)

The fragmentary remains of a juvenile rhabdodontid ornithopod from the Coal-bearing Complex of the Gosau Group (Lower Campanian, Grünbach syncline) at Muthmannsdorf near Wiener Neustadt, Lower Austria are revised. The material, probably belonging to a single individual, includes a right dentary (lectotype of Iguanodon suessi Bunzel, 1871, designated herein), teeth, a fragmentary parietal, fragments of scapula, ?radius, femur, tibia, two vertebrae (lost) and a manual ungual.The lectotype dentary does not provide clear autapomorphies or sufficient diagnostic features to determine its position within the Rhabdodontidae at generic level. By this “Iguanodon suessi” Bunzel, 1871 and the genus “Mochlodon” Seeley, 1881, to which it was latter referred as type species, cannot be characterized sufficiently by differential diagnosis and these are best considered nomina dubia. Based upon combined character comparisons (mainly postcranial features) the Muthmannsdorf ornithopod is referred herein to Zalmoxes Weishampel, Jianu, Csiki and Norman, 2003, a genus so far known from the late Maastrichtian of Romania. It probably but not evidently represents a yet unnamed species, most closely related to Zalmoxes shqiperorum Weishampel, Jianu, Csiki and Norman, 2003. At the present state of knowledge the Austrian material is not further diagnostic at the species level and kept in open nomenclature as Zalmoxes sp.     

A juvenile skull of Acerorhinus yuanmouensis (Mammalia: Rhinocerotidae) from the Late Miocene hominoid fauna of the Yuanmou Basin (Yunnan,China)

A unique juvenile skull bearing both milk premolars and unerupted but fully developed permanent premolars and molars (observed using X-ray microcomputed tomography), and some isolated upper cheek teeth, all from the Late Miocene hominoid fauna of the Yuanmou Basin (Yunnan, China), closely resemble craniodental material of Acerorhinus yuanmouensis Zong, 1998 from the same locality, and are referred to this species. A phylogenetic analysis based on 214 craniodental morphological characters scored for 31 terminal taxa reveals that A. yuanmouensis should be assigned to the genus Acerorhinus indeed. The newly discovered specimens improve our understanding of this species, especially with respect to the morphology of the milk premolars and premolars. Two intraspecific variations in the upper premolars are noted: a lingual bridge may be present or absent, and the lingual cingulum continuous or reduced. The analysis also indicates that: the phylogenetic status of Acerorhinus lufengensis Deng and Qi, 2009 should be reconsidered; “Aceratherium” huadeensis Qiu, 1979 does neither belong to Aceratherium nor Acerorhinus, and its phylogenetic status remains debatable.     

A new species of Sturisoma (Loricariidae: Loricariinae) from the Madre de Dios River basin,Peru, with a key to all congeners and comments on the type series of Sturisoma rostratum

A new species of the genus Sturisoma from the Madre de Dios River, upper Madeira, Peru, is described. The new species can be differentiated from its congeners by the following characteristics: dorsolateral stripe reaching to less than half, or only half length of caudal peduncle (v. absence of dorsolateral stripe or, if present, spanning more than half caudal‐peduncle length); premaxillary teeth longer than dentary teeth (v. dentary teeth longer); sexually mature adult males having well‐developed odontodes on the sides of the head and a broader snout (v. adult males lacking well‐developed hypertrophied odontodes or, if present, rostrum is same width as females' or immature males'); by having the ventral portion of the rostrum conspicuously darker than ventral surface of the body (v. rostrum light, with same colour as ventral portion of body, except in Sturisoma barbatum); by lacking the lateral process of the sphenotic (v. lateral process of sphenotic well‐developed, except in Sturisoma tenuirostre); a dark spot on the first three branched pectoral‐fin rays (v. brown spot absent, except in S. barbatum); and the frontal bone contributing less than half of dorsal border of the orbital ridge (v. extensive participation of the frontal, except in Sturisoma guentheri). Furthermore, the new species has 18–20 plates in the median series, which differentiates it from Sturisoma rostratum (21–22), and Sturisoma monopelte (21); and 14–15 coalescent plates, which differentiates it from S. tenuirostre (16–17). It is further differentiated from Sturisoma brevirostre by presence of an enlarged rostrum (v. rostrum not enlarged). A discussion regarding status of the type series and geographic distribution of Sturisoma rostratum is offered, and an identification key for all Sturisoma species is presented.     

Tooth development and replacement in the Atlantic Cutlassfish,Trichiurus lepturus,with comparisons to other Scombroidei

Atlantic Cutlassfish, Trichiurus lepturus, have large, barbed, premaxillary and dentary fangs, and sharp dagger-shaped teeth in their oral jaws. Functional teeth firmly ankylose to the dentigerous bones. We used dry skeletons, histology, SEM, and micro-CT scanning to study 92 specimens of T. lepturus from the western North Atlantic to describe its dentition and tooth replacement. We identified three modes of intraosseous tooth replacement in T. lepturus depending on the location of the tooth in the jaw. Mode 1 relates to replacement of premaxillary fangs, in which new tooth germs enter the lingual surface of the premaxilla, develop horizontally, and rotate into position. We suggest that growth of large fangs in the premaxilla is accommodated by this horizontal development. Mode 2 occurs for dentary fangs: new tooth germs enter the labial surface of the dentary, develop vertically, and erupt into position. Mode 3 describes replacement of lateral teeth, in which new tooth germs enter a trench along the crest of the dentigerous bone, develop vertically, and erupt into position. Such distinct modes of tooth replacement in a teleostean species are unknown. We compared modes of replacement in T. lepturus to 20 species of scombroids to explore the phylogenetic distribution of these three replacement modes. Alternate tooth replacement (in which new teeth erupt between two functional teeth), ankylosis, and intraosseous tooth development are plesiomorphic to Bluefish + other Scombroidei. Our study highlights the complexity and variability of intraosseous tooth replacement. Within tooth replacement systems, key variables include sites of formation of tooth germs, points of entry of tooth germs into dentigerous bones, coupling of tooth germ migration and bone erosion, whether teeth develop horizontally or immediately beneath the tooth to be replaced, and how tooth eruption and ankylosis occur. Developmentally different tooth replacement processes can yield remarkably similar dentitions.     

Cranial anatomy of Shunosaurus, a basal sauropod dinosaur from the Middle Jurassic of China

Shunosaurus, from the Middle Jurassic of China, is probably the best‐known basal sauropod and is represented by several complete skeletons. It is unique among sauropods in having a small, bony club at the end of its tail. New skull material provides critical information about its anatomy, brain morphology, tooth replacement pattern, feeding habits and phylogenetic relationships. The skull is akinetic and monimostylic. The brain is relatively small, narrow and primitively designed. The tooth replacement pattern exhibits back to front replacement waves in alternating tooth position. The teeth are spatulate, stout and show well‐developed wear facets indicative of coarser plant food. Upper and lower tooth rows interdigitate and shear past each other. Tooth morphology, skull architecture, and neck posture indicate that Shunosaurus was adapted to ground feeding or low browsing. Shunosaurus exhibits the following cranial autapomorphies: emargination of the ventral margin of the jugal/quadratojugal bar behind the tooth row; postorbital contains a lateral pit; vomers do not participate in the formation of the choanae; pterygoid is extremely slender and small with a dorsal fossa; quadrate ramus of the pterygoid is forked; quadratojugal participates in the jaw articulation; tooth morphology is a combination of cylindrical and spatulate form; basipterygoid process is not wrapped by the caudal process of the pterygoid; trochlear nerve has two exits; occlusal level of the maxillary tooth row is convex downward, whereas that of the dentary is concave upward, acting like a pair of garden shears; dentary tooth count is 25 or more; and the replacing teeth invade the labial side of the functional teeth. Cranial characters among the basal sauropods are reviewed. As Shunosaurus is the earliest sauropod for which cranial remains are known, it occupies an important position phylogenetically, showing the modification of skull morphology from the prosauropod condition. Although the skull synapomorphies of Sauropoda are unknown at present, 27 cranial synapomorphies are known for the clade Eusauropoda. © 2002 The Linnean Society of London, Zoological Journal of the Linnean Society, 2002, 136 , 145?169.     

Structure, attachment, replacement and growth of teeth in bluefish, Pomatomus saltatrix (Linnaeus, 1776), a teleost with deeply socketed teeth

Tooth replacement poses many questions about development, pattern formation, tooth attachment mechanisms, functional morphology and the evolution of vertebrate dentitions. Although most vertebrate species have polyphyodont dentitions, detailed knowledge of tooth structure and replacement is poor for most groups, particularly actinopterygians. We examined the oral dentition of the bluefish, Pomatomus saltatrix, a pelagic and coastal marine predator, using a sample of 50 individuals. The oral teeth are located on the dentary and premaxillary bones, and we scored each tooth locus in the dentary and premaxillary bones using a four-part functional classification: absent (A), incoming (I), functional (F=fully ankylosed) or eroding (E). The homodont oral teeth of Pomatomus are sharp, deeply socketed and firmly ankylosed to the bone of attachment. Replacement is intraosseus and occurs in alternate tooth loci with long waves of replacement passing from rear to front. The much higher percentage of functional as opposed to eroding teeth suggests that replacement rates are low but that individual teeth are quickly lost once erosion begins. Tooth number increases ontogenetically, ranging from 15–31 dentary teeth and 15–39 premaxillary teeth in the sample studied. Teeth increase in size with every replacement cycle. Remodeling of the attachment bone occurs continuously to accommodate growth. New tooth germs originate from a discontinuous dental lamina and migrate from the lingual (dentary) or labial (premaxillary) epithelium through pores in the bone of attachment into the resorption spaces beneath the existing teeth. Pomatomus shares unique aspects of tooth replacement with barracudas and other scombroids and this supports the interpretation that Pomatomus is more closely related to scombroids than to carangoids.     

An early juvenile specimen of Bolong yixianensis (Ornithopoda: Iguanodontia) from the Lower Cretaceous of Ningcheng County,Nei Mongol,China

We describe an early juvenile specimen (ZMNH M8812) of Bolong yixianensis from the Yixian Formation (Lower Cretaceous) of Ningcheng County, Nei Mongol, China. The specimen consists of an almost complete skeleton preserved two-dimensionally on a slab. The short and deep skull proportions and unfused neurocentral sutures in most preserved vertebrae suggest that the ZMNH M8812 is a juvenile individual. Osteohistological study confirms a very early developmental stage. The study reveals the ontogenetic changes of Bolong for the first time. The specimen revealed one additional autapomorphy for Bolong yixianensis: the lingual face of the maxillary crown is bounded by thickened mesial and distal margins and bisected by a prominent median principal ridge. The study revealed the following ontogenetic trends of Bolong: increased tooth rows in both maxilla and dentary, increased robustness of the jugal and scapula, the radius and ulna become more robust and shorter relative to the hindlimb and the metatarsals become proportionally shorter. ZMNH M8812 represents the first juvenile non-hadrosaurid iguanodontian specimen described from the Lower Cretaceous of eastern Asia.     

Anatomical study of the skull of amphisbaenian Diplometopon zarudnyi (Squamata,Amphisbaenia)

This study investigates the amphisbaenian species skull which includes cranium, lower jaw and hyoid apparatus. The medial dorsal bones comprise the premaxilla, nasal, frontal and parietal. The premaxilla carries a large medial tooth and two lateral ones. The nasals are paired bones and separated by longitudinal suture. Bones of circumorbital series are frontal, orbitosphenoid and maxilla. The occipital ring consists of basioccipital, supraoccipital and exooccipital. Supraoccipital and basioccipital are single bones while the exo-occipitals are paired. The bones of the palate comprise premaxilla, maxilla, septomaxilla, palatine, pterygoid, ectopterygoid, basisphenoid, parasphenoid, orbitosphenoid and laterosphenoid. Prevomer and pterygoid teeth are absent. Palatine represent by two separate bones. The temporal bones are clearly visible. The lower jaw consists of the dentary, articular, coronoid, supra-angular, angular and splenial. The hyoid apparatus is represented by a Y-shaped structure. The mandible is long and is suspended from the braincase via relatively short quadrate. There is an extensive contact between the long angular and the large triangular coronoid. Thus inter-mandibular joint is bridged completely by the angular and consequently, the lower jaws are relatively rigid and kinetic. The maxillae are suspended from the braincase largely by ligaments and muscles rather than through bony articulation. In conclusion, the skull shape affects feeding strategy in Diplometopon zarudnyi. The prey is ingested and transported via a rapid maxillary raking mechanism.     

A revision of chamaeleonids from the Lower Miocene of the Czech Republic with description of a new species of Chamaeleo (Squamata, Chamaeleonidae)

A revision of Chamaeleo caroliquarti Moody and Ro?ek is presented. The comparisons of the holotypic left dentary with those of specimens subsequently assigned to C. caroliquarti and of the Recent species of Chamaeleo, Furcifer and Calumma is carried out. It is shown that the type dentaries of C. caroliquarti include two different morphotypes with the absence of unique features. Within the Recent chameleons, the exact determination of the individual species merely on the basis of the dentaries is impossible. The holotypic dentary of C. caroliquarti is basically identical with that of C. calyptratus. However, the same morphology of the dentary as present in C. caroliquarti is also present in other species of different genera such as Calumma globifer and Furcifer pardalis. The paratypic dentaries of C. caroliquarti have a different morphology to the holotype and are indistinguishable from that in the Recent C. chamaeleon. On the other hand, a new species of the genus Chamaeleo, C. andrusovi, is described on the basis of isolated cranial elements, which possess clear autapomorphic features. This material comes from the Lower Miocene (Ottnangian) zone MN 4 in the Dolnice locality of the Czech Republic, and it differs from Recent and fossil chameleons in the following combination of characters: (1) its typically developed strongly pustular ornamentation and its distribution on the external surfaces of the skull roofing bones; (2) the frontoparietal suture is digitiform with a well-developed, anteriorly directed mesial spine, and (3) the parietal bone narrows posteriorly at its midlength, it is not bowed dorsally and it does not contribute posteriorly to a dorsal sagittal crest. This new material expands our knowledge of the cranial anatomy of Lower Miocene chameleons.     

First detailed description of Hispanomys bijugatus Mein and Freudenthal, 1971 (Rodentia, Cricetodontinae) from the Upper Aragonian of La Grive-Saint Alban (France): Biostratigraphical implications

The material of Hispanomys bijugatus (Rodentia, Cricetodontinae) from La Grive-Saint Alban (carrière Lechartier, fissure L3) is described for the first time and compared with all species of the genus known to date. As common in the Upper Aragonian populations of Hispanomys, this taxon evidences a low variability. H. bijugatus shows some progressive characters with respect to the remaining Aragonian congeneric species, such as the absence of labial and lingual cingula surrounding the upper and lower molar valleys respectively, the increase in the number of roots on the second lower molar, and the lost of mesolophs. This suggests that H. bijugatus, in spite of being one of the oldest species of the genus, is relatively derived with regard to the coeval congeneric species. Because H. bijugatus and H. decedens are believed to be closely related species within the same lineage, the fact that the former shows a more progressive dental morphology than the latter suggests that the unnamed fissure-fillings from La Grive and La Grive M (with H. decedens only) are older than La Grive L3 (with H. bijugatus only). The coexistence of both species at locality L5 suggests an intermediate age.