A new ceratopsid dinosaur (Ornithischia) from the uppermost Horseshoe Canyon Formation (upper Maastrichtian), Alberta, Canada

2007 ◽  
Vol 44 (9) ◽  
pp. 1243-1265 ◽  
Author(s):  
Xiao-chun Wu ◽  
Donald B Brinkman ◽  
David A Eberth ◽  
Dennis R Braman

A skeleton of a new ceratopsid dinosaur, Eotriceratops xerinsularis gen. et sp. nov., is described in this paper. It is the first associated vertebrate skeleton found within the upper 20 m of the Horseshoe Canyon Formation. Eotriceratops xerinsularis is a large chasmosaurine that differs from other chasmosaurines in a unique set of features in the premaxilla, nasal horn core, squamosal frill, and epijugal. The most striking of those features includes an extremely tall, non-recessed narial process of the premaxilla; the presence of greatly elongate, spindle-shaped epoccipitals on the squamosal frill; a deep, well-demarcated fossa on the anteroventral surface of the squamosal frill; a sharply conical epijugal with a pronounced proximoposterior process and separate fossa-like facets for the jugal and quadratojugal; and the presence of an obliquely extending vascular trace meeting a transverse vascular trace ventrally on the anterior surface of the nasal horn core. Our phylogenetic analysis suggests that E. xerinsularis is nested within a clade including Triceratops, Diceratops, and Torosaurus, which are all from late Maastrichtian deposits. The upper 20 m of the Horseshoe Canyon Formation comprises a coal-rich interval (Carbon–Thompson coal zone, unit 5), which previously has been assigned to upper Maastrichtian magnetochrons 31n and 30r, and the Mancicorpus gibbus miospore subzone. The ceratopsid specimen was collected from between the Carbon and Thompson coal seams, and thus, is inferred to (1) occur near the top of magnetochron 31n and (2) have an age of 67.6–68.0 Ma. Large chasmosaurine ceratopsids, such as Triceratops and Torosaurus, have not previously been described from the Horseshoe Canyon Formation or from magnetochron 31n or the M. gibbus miospore subzone. Thus, Eotriceratops is distinctly older than any other ceratopsid in the Triceratops group, and the discovery of E. xerinsularis helps fill a biostratigraphic gap between early and late Maastrichtian chasmosaurines.

2014 ◽  
Vol 51 (6) ◽  
pp. 618-634 ◽  
Author(s):  
Jordan C. Mallon ◽  
Robert Holmes ◽  
Jason S. Anderson ◽  
Andrew A. Farke ◽  
David C. Evans

Arrhinoceratops brachyops is a poorly understood chasmosaurine ceratopsid from the Upper Cretaceous Horseshoe Canyon Formation of Alberta, previously described on the basis of only a single skull. Here, we report on a second specimen attributable to this species, including a relatively complete skull, syncervical, and partial left forelimb. This second specimen clarifies aspects of morphology not visible in the holotype, and also elucidates variation in A. brachyops. The species is distinguished by a square-shaped triangular process of the premaxilla, a steeply inclined triturating surface of the predentary, and a triangular nasal horncore in horizontal section. The dentary is also distinctive in bearing a bony lateral ridge similar to that of Anchiceratops ornatus, but more strongly developed. Phylogenetic analysis cannot resolve the relationships of Arrhinoceratops beyond the level of Chasmosaurinae, owing to both missing data and conflicting characters. However, we do find some support for a deep split within Chasmosaurinae, contrary to conventional topologies. We also report on other fragmentary specimens plausibly attributable to A. brachyops that suggest a minimum age range of approximately 750 ka for this species.


2019 ◽  
Vol 94 (1) ◽  
pp. 145-164 ◽  
Author(s):  
P. González Ruiz ◽  
M. S. de la Fuente ◽  
M.S. Fernández

AbstractNeusticemys neuquina (Fernández and de la Fuente, 1988) is a turtle from the Upper Jurassic of the Neuquén Basin, Patagonia, Argentina. Here we describe in detail a new skull, lower jaw, and a vertebra, utilizing both traditional anatomical description and computed tomography (CT). New diagnostic cranial characters of Neusticemys neuquina are: a round depression on the ventral surface of the basisphenoid, a relatively larger oval foramen nervi trigemini, and reduced and steepened triturating surfaces on both the maxilla and dentary. The new morphological information presented in this study was included in a phylogenetic analysis, the primary result of which was recovery of Neusticemys neuquina within Thalassochelydia. Characters recognized as synapomorphies of this clade include: (1) anterolateral recess of the anterior surface of the quadrate positioned lateral to the processus trochlearis oticum, (2) presence of a fossa on the supraoccipital-opisthotic-exoccipital contact area, (3) foramina anterius caroticus cerebralis located close together but independently perforating the basisphenoid, and (4) the presence of the splenial in the mandible. Two contrasting dispersal scenarios could explain how this species of Thalassochelydia can be found outside of Europe. The presence of Neusticemys neuquina in the Neuquén Basin could be the consequence of an early dispersion event, for which we lack intermediate forms, or it could be the result of a later event once the clade was already established in Europe.


2020 ◽  
Vol 141 ◽  
pp. 39-46
Author(s):  
MD Dorjievna Batueva ◽  
X Pan ◽  
J Zhang ◽  
X Liu ◽  
W Wei ◽  
...  

In the present study, we provide supplementary data for Myxidium cf. rhodei Léger, 1905 based on morphological, histological and molecular characterization. M. cf. rhodei was observed in the kidneys of 918 out of 942 (97%) roach Rutilus rutilus (Linnaeus, 1758). Myxospores of M. cf. rhodei were fusiform with pointed ends, measuring 12.7 ± 0.1 SD (11.8-13.4) µm in length and 4.6 ± 0.1 (3.8-5.4) µm in width. Two similar pear-shaped polar capsules were positioned at either ends of the longitudinal axis of the myxospore: each of these capsules measured 4.0 ± 0.1 (3.1-4.7) µm in length and 2.8 ± 0.1 (2.0-4.0) µm in width. Polar filaments were coiled into 4 to 5 turns. Approximately 18-20 longitudinal straight ridges were observed on the myxospore surface. The suture line was straight and distinctive, running near the middle of the valves. Histologically, the plasmodia of the present species were found in the Bowman’s capsules, and rarely in the interstitium of the host. Phylogenetic analysis revealed that M. cf. rhodei was sister to M. anatidum in the Myxidium clade including most Myxidium species from freshwater hosts.


2012 ◽  
Vol 3 (3) ◽  
pp. 302-304
Author(s):  
G. D.Sharma G. D.Sharma ◽  
◽  
* Dhritiman Chanda ◽  
D.K. Jha D.K. Jha

2014 ◽  
Vol 8 (1) ◽  
pp. 55-60
Author(s):  
V Buzylo ◽  
◽  
O Koshka ◽  
S Poimanov ◽  
D Malashkevych ◽  
...  
Keyword(s):  

2020 ◽  
Vol 62 (1-2) ◽  
pp. 69-108
Author(s):  
S. Y. Kondratyuk ◽  
D. K. Upreti ◽  
G. K. Mishra ◽  
S. Nayaka ◽  
K. K. Ingle ◽  
...  

Eight species, new for science, i.e.: Lobothallia gangwondoana S. Y. Kondr., J.-J. Woo et J.-S. Hur and Phyllopsora dodongensis S. Y. Kondr. et J.-S. Hur from South Korea, Eastern Asia, Ioplaca rinodinoides S. Y. Kondr., K. K. Ingle, D. K. Upreti et S. Nayaka, Letrouitia assamana S. Y. Kondr., G. K. Mishra et D. K. Upreti, and Rusavskia indochinensis S. Y. Kondr., D. K. Upreti et S. Nayaka from India and China, South Asia, Caloplaca orloviana S. Y. Kondr. and Rusavskia drevlyanica S. Y. Kondr. et O. O. Orlov from Ukraine, Eastern Europe, as well as Xanthoria ibizaensis S. Y. Kondr. et A. S. Kondr. from Ibiza Island, Spain, Mediterranean Europe, are described, illustrated and compared with closely related taxa. Fominiella tenerifensis S. Y. Kondr., Kärnefelt, A. Thell et Feuerer is for the first time recorded from Mediterranean Europe, Huriella loekoesiana S. Y. Kondr. et Upreti is provided from Russia for the first time, and H. pohangensis S. Y. Kondr., L. Lőkös et J.-S. Hur for the first time from China, Phoma candelariellae Z. Kocakaya et Halıcı is new to Ukraine, and Staurothele frustulenta Vain. is recorded from the Forest Zone of Ukraine for the first time. Twelve new combinations, i.e.: Bryostigma apotheciorum (for Sphaeria apotheciorum A. Massal.), Bryostigma biatoricola (for Arthonia biatoricola Ihlen et Owe-Larss.), Bryostigma dokdoense (for Arthonia dokdoensis S. Y. Kondr., L. Lőkös, B. G. Lee, J.-J. Woo et J.-S. Hur), Bryostigma epiphyscium (for Arthonia epiphyscia Nyl.), Bryostigma lobariellae (for Arthonia lobariellae Etayo), Bryostigma lapidicola (for Lecidea lapidicola Taylor), Bryostigma molendoi (for Tichothecium molendoi Heufl. ex Arnold), Bryostigma neglectulum (for Arthonia neglectula Nyl.), Bryostigma parietinarium (for Arthonia parietinaria Hafellner et Fleischhacker), Bryostigma peltigerinum (for Arthonia vagans var. peltigerina Almq.), Bryostigma phaeophysciae (for Arthonia phaeophysciae Grube et Matzer), Bryostigma stereocaulinum (for Arthonia nephromiaria var. stereocaulina Ohlert), are proposed based on results of combined phylogenetic analysis based on mtSSU and RPB2 gene sequences. Thirty-one new combinations for members of the genus Polyozosia (i.e.: Polyozosia actophila (for Lecanora actophila Wedd.), Polyozosia agardhiana (for Lecanora agardhiana Ach.), Polyozosia altunica (for Myriolecis altunica R. Mamut et A. Abbas), Polyozosia antiqua (for Lecanora antiqua J. R. Laundon), Polyozosia bandolensis (for Lecanora bandolensis B. de Lesd.), Polyozosia behringii (for Lecanora behringii Nyl.), Polyozosia caesioalutacea (for Lecanora caesioalutacea H. Magn.), Polyozosia carlottiana (for Lecanora carlottiana C. J. Lewis et Śliwa), Polyozosia congesta (for Lecanora congesta Clauzade et Vězda), Polyozosia eurycarpa (for Lecanora eurycarpa Poelt, Leuckert et Cl. Roux), Polyozosia expectans (Lecanora expectans Darb.), Polyozosia flowersiana (Lecanora flowersiana H. Magn.), Polyozosia fugiens (for Lecanora fugiens Nyl.), Polyozosia invadens (for Lecanora invadens H. Magn.), Polyozosia juniperina (for Lecanora juniperina Śliwa), Polyozosia latzelii (for Lecanora latzelii Zahlbr.), Polyozosia liguriensis (for Lecanora liguriensis B. de Lesd.), Polyozosia massei (for Myriolecis massei M. Bertrand et J.-Y. Monnat), Polyozosia mons-nivis (for Lecanora mons-nivis Darb.), Polyozosia oyensis (for Lecanora oyensis M.-P. Bertrand et Cl. Roux), Polyozosia percrenata (for Lecanora percrenata H. Magn.), Polyozosia persimilis (for Lecanora hagenii subsp. persimilis Th. Fr.), Polyozosia poeltiana (for Lecanora poeltiana Clauzade et Cl. Roux), Polyozosia prominens (for Lecanora prominens Clauzade et Vězda), Polyozosia prophetae-eliae (for Lecanora prophetae-eliae Sipman), Polyozosia salina (for Lecanora salina H. Magn.), Polyozosia schofieldii (for Lecanora schofieldii Brodo), Polyozosia sverdrupiana (for Lecanora sverdrupiana Øvstedal), Polyozosia torrida (for Lecanora torrida Vain.), Polyozosia wetmorei (for Lecanora wetmorei Śliwa), Polyozosia zosterae (for Lecanora subfusca? zosterae Ach.)) are proposed.


2020 ◽  
Vol 40 (10) ◽  
pp. 818-823
Author(s):  
Juliana F.V. Braga ◽  
Rodrigo M. Couto ◽  
Marcelo C. Rodrigues ◽  
Roselene Ecco

ABSTRACT: Avipoxvirus is the etiological agent of the avian pox, a well-known disease of captive and wild birds, and it has been associated with tumor-like lesions in some avian species. A white-faced whistling duck (Dendrocygna viduata) raised in captivity was referred to a Veterinary Teaching Hospital in Northeast due to cutaneous nodules present in both wings. A few days after the clinical examination, the animal died naturally. Once submitted to necropsy, histopathological evaluation of the lesions revealed clusters of proliferating epithelial cells expanding toward the dermis. Some of these cells had round, well-defined, intracytoplasmic eosinophilic material suggestive of poxvirus inclusion (Bollinger bodies). PCR performed on the DNA extracted from tissue samples amplified a fragment of the 4b core protein gene (fpv167), which was purified and sequenced. This fragment of Avipoxvirus DNA present in these tumor-like lesions showed high genetic homology (100.0%) with other poxviruses detected in different avian species in several countries, but none of them were related to tumor-like lesions or squamous cell carcinoma. This is the first report of Avipoxvirus detected in tumor-like lesions of a white-faced whistling duck with phylogenetic analysis of the virus.


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