scholarly journals Yuanansuchus maopingchangensissp. nov., the second capitosauroid temnospondyl from the Middle Triassic Badong Formation of Yuanan, Hubei, China

PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e1903 ◽  
Author(s):  
Jun Liu

A second species ofYuanansuchus,Y. maopingchangensis, is erected for new temnospondyl material from the Maopingchang site, Yuanan County, Hubei Province, China. These specimens are from the same horizon that producedY. laticeps, the type species.Y. maopingchangensisshares the following features withY. laticeps: postorbital portion of skull occupied more than 1/3 of skull length; tabular horn directed laterally; lateral line sulci continuous, well impressed; supraorbital sensory canal enters lacrimal; preorbital projection of jugal less than half length of snout; and vomerine plate short. However,Y. maopingchangensisdiffers fromY. laticepsin having an elongated skull, frontal extending posteriorly to the level of the posterior orbital margin, closed otic fenestra, cultriform process of parasphenoid extending to the level of the anterior margin of the interpterygoid vacuities, and absence of fodina vomeralis. Analysis of a new capitosaur phylogenetic data matrix, containing 56 characters and 29 species, confirms that the two species from Yuanan are sister taxa and that Capitosauroidea can be divided into two major clades: one includingParotosuchus,Eryosuchus, CalmasuchusandCherninia, and another includingMastodonsaurus,Yuanansuchus,Stanocephalosaurus,Procyclotosaurus,Paracyclotosaurus,Antarctosuchus,Eocyclotosaurus,Quasicyclotosaurus,TatrasuchusandCyclotosaurus.

Zootaxa ◽  
2018 ◽  
Vol 4524 (1) ◽  
pp. 77 ◽  
Author(s):  
KEIJI BABA ◽  
SHANE T. AHYONG ◽  
KAREEN E. SCHNABEL

The chirostyloidean squat lobster genus Gastroptychus Caullery, 1896 is revised and is split into two genera: Gastroptychus sensu stricto (type species, Ptychogaster spinifer A. Milne-Edwards, 1880) and Sternostylus new genus (type species, Ptychogaster formosus Filhol, 1884). Gastroptychus sensu stricto, is restricted to nine species with a sternal plastron, at sternite 3, abruptly demarcated from the preceding sternites (excavated sternum) by a distinct step forming a well-defined transverse or concave anterior margin at the articulation with maxillipeds 3, the maxillipeds 3 widely separated, with the distal parts accommodated in the excavated sternum between the left and right maxillipeds 3 when folded, and the P2–4 dactyli with the terminal spine demarcated by a suture. Sternostylus new genus, represented by 12 species, has the sternite 3 anteriorly bluntly produced medially and steeply sloping anterodorsally to the anterior sternite, with a pair of spines directly behind the anterior margin, the left and right maxillipeds 3 adjacent, and the P2–4 dactyli ending in an indistinctly demarcated corneous spine. The above-mentioned characters of Gastroptychus are consistent with Chirostylidae sensu stricto. Published molecular phylogenies indicate, however, that Sternostylus is the sister group to all the other Chirostylidae, and is designated the type genus of a new family, Sternostylidae. 


Zootaxa ◽  
2009 ◽  
Vol 2052 (1) ◽  
pp. 1-31 ◽  
Author(s):  
CHRISTIANA KLINGENBERG ◽  
C. ROBERTO F. BRANDÃO

Based on the morphology of workers, gynes and males, we revise the taxonomy of nominal taxa traditionally included by authors in the fungus-growing ant genus Mycetophylax. Our results indicate that Mycetophylax Emery (Myrmicocrypta brittoni Wheeler, 1907, type species, by designation of Emery, 1913; junior synonym of Cyphomyrmex conformis Mayr, 1884 by Kempf, 1962) includes M. conformis, M. simplex (Emery, 1888), and M. morschi (Emery, 1888) new combination (formerly in Cyphomyrmex), with several synonymies. Mycetophylax bruchi (Santschi, 1916) does not belong to the same genus and is diagnosed, in addition to other characters, by a psammophore arising at the anterior margin of the clypeus. For this species we are resurrecting from synonymy Paramycetophylax Kusnezov, 1956 (Mycetophylax bruchi as type species, by original designation, with M. cristulatus as its new synonym). Myrmicocrypta emeryi Forel, 1907 is the only attine in which females lack the median clypeal seta and have the antennal insertion areas very much enlarged and anteriorly produced, with the psammophore setae arising from the middle of the clypeus and not at its anterior margin as in Paramycetophylax. Notwithstanding its inclusion in Mycetophylax by recent authors, it is here recognized as belonging to a hitherto undescribed, thus far monotypic genus, Kalathomyrmex new genus (Myrmicocrypta emeryi as its type species, here designated). We redescribe workers, gynes and males of all species in the


The rhynchosaur Rhynchosaurus articeps Owen, 1842, from the Middle Triassic of Grinshill, northern Shropshire, England, was a small reptile, about 0.5 m long. About 17 individual animals are represented by skulls, complete skeletons and partial skeletons, and these have permitted detailed restorations. The skull (60-80 mm long) is low and broad at the back, and it shows all of the typical rhynchosaur features of beak-like premaxillae, single median naris, fused parietal, broad maxillary tooth plate and dentary, both with multiple rows of teeth, and a deep lower jaw. The skeleton shows adaptations for fast terrestrial locomotion with a semi-erect hindlimb posture and for scratch-digging with the hind-foot. The skeleton is relatively more slender than that of most other middle and late Triassic rhynchosaurs, but this is probably an allometric effect of its much smaller size (they are typically 1-2 m long). A further species of Rhynchosaurus from Warwick, named here R. brodiei , is represented by 15 specimens of partial skulls, tooth-bearing elements, and isolated postcranial bones. It was slightly larger than R. articeps , with a typical skull length of 90 mm, and estimated body length of 0.6 m, but the skull length ranged up to 140 mm. It differs from R. articeps in having a much larger jugal in the cheek area, and in the greater height and breadth of the skull. The isolated maxillary fragments from Bromsgrove probably also belong to R. brodiei . The third species of Rhynchosaurus from Devon, named here R. spenceri , is now known from numerous specimens of at least 25 individuals, most of which were collected recently. These show a range in estimated skull length from 40 to 170 mm, but most specimens are at the upper end of that range, with an average skull length of 140 mm, and an estimated total body length of 0.9-1.0 m R. spenceri differs from R. articeps and R. brodiei in having a skull that is broader than it is long (otherwise a character of late Triassic rhynchosaurs), and it shares the large jugal character with R. brodiei . Teeth are not well preserved in R. articeps, but several specimens of R. brodiei and R. spenceri give detailed information. The pattern of wear, and the nature of the jaw joint, suggest that Rhynchosaurus had a precision-shear bite, as in other rhynchosaurs, with no back and forwards motion. The maxilla had two grooves, a major and a minor one, which received two matching ridges of the dentary on occlusion. The multiple rows of teeth on maxilla and dentary, and the surrounding bone, wore down as uniform units. The diet was probably tough vegetation, which was dug up by scratch-digging, raked together with the hands or the premaxillary beak, and manipulated in the mouth by a strong tongue. Rhynchosaurus is found variously in fluvial-intertidal deposits with evidence of desiccation (Grinshill, Warwick, Bromsgrove), and fluvial-aeolian deposits laid down in arid conditions with occasional flash floods (Devon). The bones have generally been transported (Warwick, Bromsgrove, Devon), but the Grinshill specimens are largely complete and undisturbed. The associated floras and faunas at Warwick, Bromsgrove, and Devon include pteridophytes, gymnospermopsids, bivalves, scorpions, freshwater fish, temnospondyl amphibians and reptiles (macrocnemids, thecodontians, ?procolophonids). Rhynchosaurs are archosauromorph diapsids, possibly related to the enigmatic Trilophosaurus, and a sister group to Prolacertiformes + Archosauria. A cladistic analysis of Rhynchosauria reveals one major subgroup, the Hyperodapedontinae ( Hyperodapedonand and Scaphonyx ), which is late Triassic in age. The earlier rhynchosaurs, including the middle Triassic Stenaulorhynchus and Rhynchosaurus , appear to form successively closer outgroups to the Hyperodapedontinae. The three species of Rhynchosaurus share only one possible synapomorphy in comparison with Stenaluorhynchus : The dentary is well over half the length of the lower jaw. The ‘Rhynchosaurinae’ ( Stenaulorhynchus and Rhynchosaurus ) was not established as a monophyletic group in the present analysis. These two genera share two postulated synapomorphies: the occipital condyle lies well in front of the quadrates, and there are two grooves on the maxilla and two ridges on the dentary. A third postulated synapomorphy, the presence of a single row of teeth on the pterygoid, has not been confirmed in this study for either Rhynchosaurus or Stenaulorhynchus . However, these postulated synapomorphies are outweighed by the synapomorphies that Rhynchosaurus shares with the Hyperodapedontinae. The specimens of Rhynchosaurus have been used as biostratigraphic indicators for the English middle Triassic, indicating Anisian to early Ladinian ages. The three species can be arranged in a sequence from ‘most prim itive’ to ‘most advanced’, but this cannot be used confidently to give a stratigraphic sequence.


2020 ◽  
Vol 298 (1) ◽  
pp. 9-15
Author(s):  
Vittorio Pieroni ◽  
Alexander Nützel

A monospecific mass occurrence of the new gastropod species Freboldia carinii sp. nov. is described from the Middle Triassic Esino Limestone of the Brembana Valley, Southern Alps, Italy. It is the second species assigned to the genus Freboldia that was initially described from the Early Jurassic of Ellesmere Island, Canadian Arctic. This gastropod is unusual in being planispiral and inflated with a nearly bilateral symmetrical shape and in having a very thin shell. Like the Canadian type species of Freboldia, the new Triassic species is interpreted as a possibly holoplanktonic gastropod. If true, it would be the oldest known example of this life style in Gastropoda.


Zootaxa ◽  
2007 ◽  
Vol 1446 (1) ◽  
pp. 31-42 ◽  
Author(s):  
HORÁCIO HIGUCHI ◽  
JOSÉ L.O. BIRINDELLI ◽  
LEANDRO M. SOUSA ◽  
HERALDO A. BRITSKI

Merodoras nheco, new genus and species of Doradidae (Siluriformes) is described from Rio Paraguay basin, Brazil. The new genus belongs to the new subfamily Astrodoradinae, a monophyletic group formally named herein that includes, besides Merodoras, Amblydoras, Anadoras, Astrodoras, Hypodoras, Physopyxis, and Scorpiodoras. This group is diagnosed by the possession of: lacrimal serrated and participating in the orbital margin, four to seven pleural ribs; spines on the postcleithral process; postero-inferior portion of the coracoid exposed.  Merodoras nheco, new species, is distinguished from other doradids by the unique combination of the following characteristics: 1) tips of retrorse spines on the midlateral scutes ventrally oriented in adults; 2) incomplete lateral line, with only a few midlateral scutes anteriorly; 3) pectoral girdle entirely exposed ventrally, with the opening of the arrector ventralis inferior reduced to a small fossae on the anterior edge of the coracoid; 4) caudal fin truncate; 5) dorsal-fin spine smooth, without serrae on both faces; 5) lacrimal serrated; 6) lateral ethmoid serrated.  Merodoras nheco inhabits the “Pantanal Matogrossense,” a flooded portion of the upper Rio Paraguay basin in western Brazil.


1992 ◽  
Vol 6 ◽  
pp. 202-202 ◽  
Author(s):  
Ricardo N. Martínez ◽  
Catherine A. Forster ◽  
Cathleen L. May

Two skulls representing new forms of carnivorous cynodonts were discovered recently in the Upper Triassic (Carnian) Ischigualasto Formation of northwestern Argentina. These specimens are the first complete carnivorous cynodonts described from the Late Triassic of Argentina, and provide critical evidence for the evolution of cranial form between well known Middle Triassic cynodonts, such as Probainognathus, and the first mammals in the latest Triassic.The first skull (PVSJ 422) is proportionately long, with a posterior skull width only 35 per cent of basal skull length (9.5 cm.). Other distinctive features of the skull include the form of the postcanine crowns, which have two cusps posterior to the principal cusp and fine serations on their leading edges, and which overlap each other in an imbricate pattern. Postcanines 5-7 are subequal in size, overlap the dentary laterally, and are substantially larger than postcanines 2-4. The dental formula in the upper jaw is I4-C1-PC7, with the small first postcanine separated fore and aft by small diastemas. As in other advanced eucynodonts, no pineal foramen is present. Some postcranial elements, as yet unstudied, were also found with this specimen.The second skull (PVSJ 411) has broader proportions, the width between quadrates almost half that of basal skull length (7.5 cm.). These proportions, in combination with deep, curved zygomatic arches, resemble other Middle Triassic cynodonts such as Probelesodon. Distinctive features of this skull include bicusped postcanines in the upper jaw similar to those of Probelesodon, and a mandibular symphysis that extends back to the level of the fourth postcanine. The dental formula in the upper jaw is I4-C1-PC6. As in the first skull, a pineal foramen is absent.Several advanced cranial features, such as a fused mandibular symphysis, occur in both skulls and strongly suggest that these new forms belong within the Eucynodontia (Hopson, 1991). Other advanced features, such as the absence of a pineal foramen, further suggest that these new forms are closer to mammals than are traversodontid cynodonts. In contrast, other characters appear to be curiosly primitive, such as a short hard palate in the first skull. These new cynodonts thus may introduce previously unseen features and character combinations to the study of cynodont cranial evolution.


Paleobiology ◽  
1992 ◽  
Vol 18 (1) ◽  
pp. 50-79 ◽  
Author(s):  
Benjamin J. Greenstein

The class Echinoidea apparently originated during the Ordovician Period and diversified slowly through the Paleozoic Era. The clade then mushroomed in diversity beginning in Late Triassic time and continued expanding into the present. Although this evolutionary history is generally accepted, the taphonomic overprint affecting it has not been explored. To gain a more accurate perception of the evolutionary history of the group, I have compared the diversity history of the family Cidaridae (Echinodermata: Echinoidea) with the preservational style of fossil type species using literature-derived data. The Cidaridae apparently originated in Middle Triassic time and diversified slowly through the Neocomian (Early Cretaceous). Diversity was maintained through the remainder of the Cretaceous and Tertiary Periods, reflecting the diversity history of the subclass. Characterization of the preservational style of type fossil material for the family revealed the following breakdown of preservational states: 60% of species were described on the basis of disarticulated skeletal material, primarily spines; 20% based on intact coronas denuded of spines, apical system, Aristotle's lantern and peristomial plates; 10% based on large coronal fragments; and 10% based on other skeletal elements. This distribution may represent the effect of a disarticulation threshold on the condition of echinoid carcasses before final burial and suggests that preservation of intact specimens may be very unlikely. For cidaroids, previous work has suggested that this threshold is likely to be reached after 7 days of decay.Comparison of the diversity history of the Cidaridae with the preservation data reveals that characteristic patterns of taphonomic overprint have affected the group since its origination in Middle Triassic time, and the nature of that overprint has changed over time: the early diversity history of the group is characterized by occurrences of fragmented fossil material, with spines predominant; further radiation of the group in mid-Jurassic time coincided with an increase in modes of preservation, ranging between exceptionally well-preserved material and disarticulated skeletal elements. Finally, type material is more rarely described from younger stratigraphic intervals (Miocene–Pleistocene) and consists predominantly of disarticulated skeletal elements and coronal fragments larger than an interambulacrum in size. Intact, denuded coronas are noticeably lacking.The number of type species of Cidaridae described in each stratigraphic interval has not been consistent during post-Paleozoic time. Middle Triassic, Malm (Upper Jurassic), Senonian (Upper Cretaceous) and Eocene series yielded significantly (α = .05) higher numbers of type specimens per million years, while the Lias (Lower Jurassic), Dogger (Mid-Jurassic), Lower Cretaceous and Paleocene yielded significantly (α = .05) lower numbers of type specimens per million years. This may be the result of a combination of taxonomic, sampling, and geographical biases.


Zootaxa ◽  
2018 ◽  
Vol 4374 (2) ◽  
pp. 263
Author(s):  
NARENGBAM RONI ◽  
WAIKHOM VISHWANATH

Garra substrictorostris, a new labeonine species, is described from the Barak River drainage in Manipur, India. It is distinguished from its congeners by the combination of the following characters: a prominent unilobed antrorse proboscis, with 3–5 medium to large multicuspid tubercles on its anterior margin; 4–6 multicuspid tubercles on its anteroventral margin; a prominent transverse lobe with 14–20 multicuspid tubercles; the lateral surface of the snout slightly elevated, lobular with 7–11 small tubercles; 5½ transverse scale rows above the lateral line and 3½ or 4½ scale rows between lateral line and anal-fin origin. 


Fossil Record ◽  
2020 ◽  
Vol 23 (2) ◽  
pp. 197-204
Author(s):  
Andrei A. Legalov ◽  
Markus J. Poschmann

Abstract. The new weevil genus Igneonasus gen. nov. (type species: I. rudolphi sp. nov.) of the tribe Ceutorhynchini (Curculionidae: Conoderinae: Ceutorhynchitae) is described from the late Oligocene of Fossillagerstätte Enspel, Germany. The new genus differs from the similar genus Stenocarus Thomson, 1859 in the anterior margin of the pronotum, which is not raised, a pronotum without tubercles on the sides, and a femur without teeth. This weevil is the largest representative of this supertribe and the first fossil Curculionidae species described from the paleolake Enspel. In this ancient ecosystem, weevils were at least sometimes an important food resource for the cyprinid fish Palaeorutilus enspelensis.


Zootaxa ◽  
2011 ◽  
Vol 2994 (1) ◽  
pp. 1 ◽  
Author(s):  
JUAN MARCOS MIRANDE ◽  
GASTÓN AGUILERA ◽  
MARÍA DE LAS MERCEDES AZPELICUETA

Oligosarcus itau n. sp. is described. This species is the sister group of the remaining analyzed species of Oligosarcus and this relationship is supported by seven morphological synapomorphies: 1) well developed temporal fossa, 2) absence of a dorsal expansion on the rhinosphenoid, 3) posteroventrally angled articulation between second and third infraorbitals, 4) presence of ectopterygoid teeth on a row, 5) laterally displaced cartilage on the ectopterygoid, 6) presence of bony lamellae bordering laterosensory canal of suprapreopercle, and 7) presence of two pairs of uroneurals. The new species is diagnosed by the following combination of characters: 1) two distinct premaxillary rows of teeth, 2) tricuspidate and pentacuspidate teeth on dentary and posterior premaxillary row, 3) presence of a row of 3–4 tricuspidate to conical ectopterygoid teeth, 4) possession of v-vi,21–23 anal-fin rays, and 5) presence of 41–42 perforated scales on lateral line. Oligosarcus itau n. sp. was previously considered as an Astyanacinus. Astyanacinus moorii (Boulenger), type species of the genus, is included in the Astyanax clade and Astyanacinus platensis Messner is transferred to Oligosarcus.


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