scholarly journals Acherontiscus caledoniae : the earliest heterodont and durophagous tetrapod

2019 ◽  
Vol 6 (5) ◽  
pp. 182087 ◽  
Author(s):  
Jennifer A. Clack ◽  
Marcello Ruta ◽  
Andrew R. Milner ◽  
John E. A. Marshall ◽  
Timothy R. Smithson ◽  
...  

The enigmatic tetrapod Acherontiscus caledoniae from the Pendleian stage of the Early Carboniferous shows heterodontous and durophagous teeth, representing the earliest known examples of significant adaptations in tetrapod dental morphology. Tetrapods of the Late Devonian and Early Carboniferous (Mississippian), now known in some depth, are generally conservative in their dentition and body morphologies. Their teeth are simple and uniform, being cone-like and sometimes recurved at the tip. Modifications such as keels occur for the first time in Early Carboniferous Tournaisian tetrapods. Acherontiscus , dated as from the Pendleian stage, is notable for being very small with a skull length of about 15 mm, having an elongate vertebral column and being limbless. Cladistic analysis places it close to the Early Carboniferous adelospondyls, aïstopods and colosteids and supports the hypothesis of ‘lepospondyl’ polyphyly. Heterodonty is associated with a varied diet in tetrapods, while durophagy suggests a diet that includes hard tissue such as chitin or shells. The mid-Carboniferous saw a significant increase in morphological innovation among tetrapods, with an expanded diversity of body forms, skull shapes and dentitions appearing for the first time.

1983 ◽  
Vol 120 (1) ◽  
pp. 51-58 ◽  
Author(s):  
A. J. Boucot ◽  
C. H. C. Brunton ◽  
J. N. Theron

SummaryThe Devonian brachiopod Tropidoleptus is recognized for the first time in South Africa. It is present in the lower part of the Witteberg Group at four widely separated localities. Data regarding the stratigraphical range of the genus elsewhere, combined with information on recently described fossil plants and vertebrates from underlying strata of the upper Bokkeveld Group, suggest that a Frasnian or even Givetian age is reasonable for the lower part of the Witteberg Group. The recognition of Tropidoleptus in a shallow water, near-shore, molluscan association, at the top of the South African marine Devonian sequence, is similar to its occurrence in Bolivia, and suggests a common Malvinokaffric Realm history of shallowing, prior to later Devonian or early Carboniferous non-marine sedimentation. It is noteworthy that Tropidoleptus is now known to occur in ecologically suitable environments around the Atlantic, but is absent from these same environments in Asia and Australia. Tropidoleptus is an excellent example of dispersal in geological time — first appearing in northern Europe and Nova Scotia, then elsewhere in eastern North America and North Africa, followed by South America and South Africa, while continuing in North America.


2001 ◽  
Vol 75 (6) ◽  
pp. 1202-1213 ◽  
Author(s):  
Robert L. Carroll

The origin of tetrapods from sarcopterygian fish in the Late Devonian is one of the best known major transitions in the history of vertebrates. Unfortunately, extensive gaps in the fossil record of the Lower Carboniferous and Triassic make it very difficult to establish the nature of relationships among Paleozoic tetrapods, or their specific affinities with modern amphibians. The major lineages of Paleozoic labyrinthodonts and lepospondyls are not adequately known until after a 20–30 m.y. gap in the Early Carboniferous fossil record, by which time they were highly divergent in anatomy, ways of life, and patterns of development. An even wider temporal and morphological gap separates modern amphibians from any plausible Permo-Carboniferous ancestors. The oldest known caecilian shows numerous synapomorphies with the lepospondyl microsaur Rhynchonkos. Adult anatomy and patterns of development in frogs and salamanders support their origin from different families of dissorophoid labyrinthodonts. The ancestry of amniotes apparently lies among very early anthracosaurs.


Zootaxa ◽  
2011 ◽  
Vol 2963 (1) ◽  
pp. 1 ◽  
Author(s):  
SUSANNAH C. R. MAIDMENT ◽  
PAUL M. BARRETT

A previously undescribed chasmosaurine specimen excavated in 1919-1920 by William Cutler from the Dinosaur Park Formation of Alberta, Canada is referable to Chasmosaurus belli. The specimen comprises an almost complete skull in which, uniquely among Chasmosaurus, the cranial elements are disarticulated, allowing detailed examination of their morphology for the first time. The complete braincase is present and allows comparison with the braincase of other ceratopsians. The specimen also preserves an uncrushed and undistorted postcranium, including cervical, dorsal and sacral vertebrae and limb elements. The vertebral column of Chasmosaurus has never previously been described in detail, and NHMUK R4948 affords the opportunity to examine it because of the unparalleled state of vertebral preservation. A proliferation of new chasmosaurine genera has recently been described; many of them differ from each other only in details of frill and epiparietal morphology. Several of these are based on specimens previously referred to Chasmosaurus. As a result, the characters that distinguish Chasmosaurus from other Campanian chasmosaurines are unclear. However, the genus Chasmosaurus and species within the genus are diagnosable and valid based on unique combinations of characters and frill morphology. Detailed examination of the postcranial morphology of a variety of centrosaurines and chasmosaurines has highlighted previously undescribed synapomorphies for the two major ceratopsid clades, concentrated in the pectoral girdle and forelimb. Inconsistencies in the vertebral formula of specimens referred to Chasmosaurus belli suggests that the postcrania of ceratopsids may vary between species and genera far more than previously thought, and that postcranial characters should be incorporated into phylogenetic and taxonomic studies.


Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 552-565 ◽  
Author(s):  
PIERFILIPPO CERRETTI ◽  
THOMAS PAPE

A cladistic analysis of the genus Melanophora Meigen, 1803 (type-species: Musca grossificationis Linnaeus, 1758 [= Musca roralis Linnaeus, 1758]) is presented and the generic delimitation is critically redefined. The nominal genus-group taxon Bequaertiana Curran, 1929 (type-species: Bequaertiana argyriventris Curran, 1929) is synonymised with Melanophora Meigen syn. nov. The following new combinations are proposed: Melanophora argyriventris (Curran, 1929) comb. nov. and Melanophora basilewskyi (Peris, 1957) comb. nov. Melanophora chia sp. nov. from SW Sardinia is described, illustrated and compared with the other known species of the genus. The male of Melanophora asetosa Kugler, 1978 is described for the first time. Melanophora basilewskyi (Peris, 1957) is recorded from Kenya for the first time.


2019 ◽  
Vol 286 (1904) ◽  
pp. 20190409 ◽  
Author(s):  
David Michael Unwin ◽  
D. Charles Deeming

Recent fossil finds in China and Argentina have provided startling new insights into the reproductive biology and embryology of pterosaurs, Mesozoic flying reptiles. Nineteen embryos distributed among four species representing three distinct clades have been described and all are assumed to be at, or near, term. We show here how the application of four contrasting quantitative approaches allows a more precise identification of the developmental status of embryos revealing, for the first time to our knowledge, the presence of middle and late developmental stages as well as individuals that were at term. We also identify a predicted relationship between egg size and shape and the developmental stage of embryos contained within. Small elongate eggs contain embryos at an earlier stage of development than larger rounder eggs which contain more fully developed embryos. Changes in egg shape and size probably reflect the uptake of water, consistent with a pliable shell reported for several pterosaurs. Early ossification of the vertebral column, limb girdles and principal limb bones involved some heterochronic shifts in appearance times, most notably of manus digit IV, and facilitated full development of the flight apparatus prior to hatching. This is consistent with a super-precocial flight ability and, while not excluding the possibility of parental care in pterosaurs, suggests that it was not an absolute requirement.


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.


Zootaxa ◽  
2005 ◽  
Vol 846 (1) ◽  
pp. 1 ◽  
Author(s):  
CAROLINE SAYURI FUKUSHIMA ◽  
ROGÉRIO BERTANI ◽  
PEDRO ISMAEL DA SILVA

The genus Cyriocosmus Simon, 1903 is revised based on most types and additional material from Argentina, Brazil, Colombia, Tobago Island and Venezuela. Two species are newly described from Brazil: Cyriocosmus nogueira-netoi and Cyriocosmus fernandoi. The species Cyriocosmus fasciatus (Mello-Leitão, 1930), formerly synonymized with Cyriocosmus elegans, is revalidated. Metriopelma nigriventris (Mello-Leitão, 1939) and Cyriocosmus butantan Pérez-Miles, 1998 are transferred to Hapalopus Ausserer, 1875, proposing Hapalopus nigriventris (Mello-Leitão, 1939) new combination and Hapalopus butantan (Pérez-Miles, 1998) new combination. The female of Hapalopus butantan is described for the first time. All 11 species of Cyriocosmus are diagnosed and keyed. A cladistic analysis with 28 characters and 19 taxa was carried out. Searches using three phylogenetic packages found a single, totally resolved tree with the same topology.


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