scholarly journals An assemblage of giant aquatic snakes (Serpentes, Palaeophiidae) from the Eocene of Togo

2021 ◽  
Vol 140 (1) ◽  
Author(s):  
Georgios L. Georgalis ◽  
Guillaume Guinot ◽  
Koffi Evenyon Kassegne ◽  
Yawovi Zikpi Amoudji ◽  
Ampah Kodjo C. Johnson ◽  
...  

AbstractWe here describe a monospecific assemblage of giant aquatic snakes from the middle Eocene of Kpogamé, Togo. The material, consisting of large isolated vertebrae, is referred to Palaeophis africanus, an enigmatic palaeophiid species, which was so far otherwise known only from a limited number of vertebrae from the middle Eocene of Nigeria and Angola. Material from the late Eocene of the eastern USA that had been referred to the same species, is here instead considered too fragmentary for species-level determination and Palaeophis africanus is thus so far restricted to Africa. With the aid of micro-CT scanning, we present 3D models of 17 vertebrae, pertaining to different portions of the vertebral column. We provide detailed comparisons of the new material with all named African species of the genus Palaeophis. A tentative diagnosis of Palaeophis africanus is provided. With more than 50 vertebrae, the new Togolese specimens represent the most abundant known material attributed to Palaeophis africanus and significantly enhance our knowledge of the vertebral anatomy and intracolumnar variation for this taxon. Furthermore, this adds to the, as yet, extremely scarce fossil record of squamates from central western Africa, a region where Paleogene herpetofaunas are only rather poorly known.

Author(s):  
Thomas Valenzuela ◽  
Jorge Zhingre Sanchez ◽  
Mikayle Holm ◽  
Tinen Iles ◽  
Paul Iaizzo

Abstract There are few medical devices currently utilized that have not had, at the very least, a second iteration. Medical device companies continually strive to improve their product to make it the best on the market. Medical devices are often optimized by defining the size of the device, making it more efficient and/or improving the device to tissue interface. Using the capabilities of the Visible Heart® Laboratories various cardiac devices can be implanted in reanimated swine and human hearts for the assessment of the various aforementioned parameters. After the implantation of these devices and assessment in functional anatomies, specimens were perfusion-fixed and then a micro-CT scanner was utilized to take high-resolution scans of the resultant device and tissue interfaces. These scans are used to generate high-resolution (∼20 microns) 3D models of the numerous implanted devices, measurement analyses, device simulations, and the creation of virtual reality scenes. All can then be used for detailed visual analyses. These abilities to render high-resolution models will allow medical device designers to closely evaluate their designs, in order to optimize their next iterations.


2021 ◽  
Author(s):  
Dominik Göldner ◽  
Fotios Alexandros Karakostis ◽  
Armando Falcucci

This protocol presents the first detailed step-by-step pipeline for the 3D scanning and post processing of large batches of lithic artefacts using a micro-computed tomography (micro-CT) scanner (i.e., a Phoenix v-tome-x S model by General Electronics MCC, Boston MA) and an Artec Space Spider scanner (Artec Inc., Luxembourg). This protocol was used to scan and analyze ca. 700 lithic artefacts from the Protoaurignacian layers at Fumane Cave in north-eastern Italy (Falcucci et al., in preparation). For this study several costly scanners and proprietary software packages were employed. Although it is not easy to find a low-budget alternative for the scanners, it is possible to use free and open-source software programs, such as 3D-Slicer (https://www.slicer.org/) or MorphoDig (https://morphomuseum.com/morphodig), to process CT data as well as MeshLab (Cignoni et al. 2008) to interact with the 3D models in general. However, if alternative software is used, the steps and their order described in this protocol might diverge significantly. A cost-effective alternative to create 3D models is digital photogrammetry using commercial cameras and freely available software like Meshroom (https://alicevision.org). Although photogrammetry is an affordable technique to create accurate 3D models of objects, this method might not be useful when scanning large batches of artefacts, as it will require a lot of computation time and processing capacity. Likewise, it could be difficult to generate accurate 3D models of very small and/or detailed tool shapes using 3D surface scanners because stone tools are often much smaller than the recommended minimum field of view. Similarly, the resolution of conventional medical CT scanners might not be sufficient to capture minor details of stone tools, such as the outline or dorsal scars. Thus, high-resolution micro-CT technology is the only reliable way to accurately capture the overall morphology of small stone tools. This protocol aims at providing the first detailed procedure dedicated to the scanning of small lithic implements for further three-dimensional analysis. Note that some of the steps must be repeated at different working stages throughout this protocol. In cases where a task must be done in the exact same way as described in a previous step, a reference to that step is provided. When slight changes were made, the step was modified and reported entirely. This protocol contains a few red and green colours (e.g., arrows or within-program colours) which might be perceived differently by people with dyschromatopsia. However, the display of these colours has been kept to a minimum. We recommend the reader to go over the entire protocol carefully, even if only some specific parts are required. A few points are in fact interdependent, and some of them must be applied simultaneously. Content: Part 1 – Styrofoam preparation Part 2 – Micro-CT scanning Part 3 – 3D model extraction of CT scanned stone artifacts using Avizo Part 4 – Cropping extracted surface model to separate Face A and B in Artec Studio Part 5 – Cropping Face A to separate the lines in Artec Studio Part 6 – Cropping each stone artefact from the lines in Artec Studio Part 7 – Virtually control measurements in MeshLab Part 8 – Artec scanning of larger artifacts Part 9 – Export meshes as non-binary ply models for successive analysis in geomorph Three-dimensional example (in ply format) of the effectivity of the StyroStone Protocol: You can download an example of one Styrofoam line in 3D obtained using our protocol to appreciate the result that can be achieved. We have selected a line where objects are characterized by different metric and morphological attributes. Notice the retouching well visible in the last five smaller artifacts (counting from the left when artifact are oriented with the dorsal face in front of the observer and the butt down), as well as the platforms and bulbs of all artifacts. For more information and examples, feel free to contact us!


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2639 ◽  
Author(s):  
Matthew R. Borths ◽  
Patricia A. Holroyd ◽  
Erik R. Seiffert

Hyaenodonta is a diverse, extinct group of carnivorous mammals that included weasel- to rhinoceros-sized species. The oldest-known hyaenodont fossils are from the middle Paleocene of North Africa and the antiquity of the group in Afro-Arabia led to the hypothesis that it originated there and dispersed to Asia, Europe, and North America. Here we describe two new hyaenodont species based on the oldest hyaenodont cranial specimens known from Afro-Arabia. The material was collected from the latest Eocene Locality 41 (L-41, ∼34 Ma) in the Fayum Depression, Egypt.Akhnatenavus nefertiticyonsp. nov. has specialized, hypercarnivorous molars and an elongate cranial vault. InA. nefertiticyonthe tallest, piercing cusp on M1–M2is the paracone.Brychotherium ephalmosgen. et sp. nov. has more generalized molars that retain the metacone and complex talonids. InB. ephalmosthe tallest, piercing cusp on M1–M2is the metacone. We incorporate this new material into a series of phylogenetic analyses using a character-taxon matrix that includes novel dental, cranial, and postcranial characters, and samples extensively from the global record of the group. The phylogenetic analysis includes the first application of Bayesian methods to hyaenodont relationships.B. ephalmosis consistently placed within Teratodontinae, an Afro-Arabian clade with several generalist and hypercarnivorous forms, andAkhnatenavusis consistently recovered in Hyainailourinae as part of an Afro-Arabian radiation. The phylogenetic results suggest that hypercarnivory evolved independently three times within Hyaenodonta: in Teratodontinae, in Hyainailourinae, and in Hyaenodontinae. Teratodontines are consistently placed in a close relationship with Hyainailouridae (Hyainailourinae + Apterodontinae) to the exclusion of “proviverrines,” hyaenodontines, and several North American clades, and we propose that the superfamily Hyainailouroidea be used to describe this relationship. Using the topologies recovered from each phylogenetic method, we reconstructed the biogeographic history of Hyaenodonta using parsimony optimization (PO), likelihood optimization (LO), and Bayesian Binary Markov chain Monte Carlo (MCMC) to examine support for the Afro-Arabian origin of Hyaenodonta. Across all analyses, we found that Hyaenodonta most likely originated in Europe, rather than Afro-Arabia. The clade is estimated by tip-dating analysis to have undergone a rapid radiation in the Late Cretaceous and Paleocene; a radiation currently not documented by fossil evidence. During the Paleocene, lineages are reconstructed as dispersing to Asia, Afro-Arabia, and North America. The place of origin of Hyainailouroidea is likely Afro-Arabia according to the Bayesian topologies but it is ambiguous using parsimony. All topologies support the constituent clades–Hyainailourinae, Apterodontinae, and Teratodontinae–as Afro-Arabian and tip-dating estimates that each clade is established in Afro-Arabia by the middle Eocene.


2021 ◽  
Vol 140 (1) ◽  
Author(s):  
Georgios L. Georgalis ◽  
Márton Rabi ◽  
Krister T. Smith

AbstractLarge constrictor snakes, referred to the genera Palaeopython and Paleryx, are an ecologically prominent part of the fauna of Europe during the Paleogene. Most species were named over a century ago and their taxonomy is largely based on isolated vertebrae. Furthermore, the majority of named taxa originate from imprecisely known localities within the Phosphorites du Quercy, in southern France, and thus their exact age is not known. We critically review and re-diagnose these genera based on personal examination of all existing type material, an array of new specimens, and a detailed literature review. We consider Palaeopython and Paleryx to be valid and propose vertebral characters to distinguish them. We recognize three valid species of Palaeopython, i.e. Palaeopythoncadurcensis (type species) from the Phosphorites du Quercy, Palaeopythonceciliensis from Geiseltal, and Palaeopythonhelveticus from Dielsdorf (Switzerland), and one valid species of Paleryx, i.e. Paleryxrhombifer (type species) from Hordle Cliff (England). Four other species, which were previously treated as members of Palaeopython and Paleryx, i.e. “Palaeopython” filholii and “Palaeopython” neglectus from the Phosphorites du Quercy, “Palaeopython” fischeri from Messel, and “Paleryx” spinifer from Geiseltal, are also considered as valid but pertain to other genera. Among these four taxa, “Palaeopython” fischeri has been recently assigned to its own genus, Eoconstrictor. A new genus, Phosphoroboa gen. nov. is established to accommodate “Palaeopython” filholii. We designate a lectotype for Palaeopythoncadurcensis and establish that the paralectotype maxilla and dentary are reasonably referred to this species. New material attributed to Palaeopythoncadurcensis is described from the old collections of the Phosphorites du Quercy. Paleryxcayluxi, another species established from the old collections of the Phosphorites du Quercy, is synonymized here with Palaeopythoncadurcensis. We further clarify important errors in the original description and figures of Paleryxcayluxi, identify the exact specimens that comprise the type series, and designate a lectotype. Much new material is described for Palaeopythonceciliensis from its type area in Geiseltal and intracolumnar variation is considered. We describe additional vertebral and cranial material of Paleryxrhombifer from its type area in Hordle Cliff. Based on this cranial material, we suggest non-booid affinities for Paleryxrhombifer. We designate a lectotype for Paleryxdepressus and agree with its previous suggested synonymy with Paleryxrhombifer. We re-describe the lectotype and paralectotypes of “Palaeopython” neglectus and refer and describe new material of this species from the Phosphorites du Quercy, paying special attention to intracolumnar variation; we also defer a decision on its generic relations until more abundant and complete material can be studied. We describe new vertebral material of the booid Eoconstrictor cf. fischeri from Geiseltal; similar material was previously known only from Messel and Dielsdorf. We determine that Eoconstrictorfischeri contains two distinct and unrelated species and describe intracolumnar variation in the nominotype. We clarify certain issues regarding the type series of Paleryxspinifer, designate a lectotype, and report previously unrecognized cranial material associated with the latter specimen; we transfer this species to Eoconstrictor based on cranial features and recombine it as Eoconstrictorspinifer comb. nov. We finally describe much new vertebral and cranial material of Phosphoroboafilholii comb. nov. from the Phosphorites du Quercy (both from the old collections but also from the late Eocene localities of Escamps A and C), paying special attention to intracolumnar variation. Based on this cranial material from Escamps, we identify Phosphoroboa gen. nov. as a booid. An analytical approach is undertaken in many isolated remains in order to quantify vertebral structures and assess intracolumnar variation, as well as associating isolated cranial elements to vertebral-based taxa. 3D models of the type material of the Geiseltal and Messel taxa are presented. The importance of vertebrae in the taxonomy of fossil Constrictores is addressed, although it is acknowledged that it is cranial material that can afford the most reliable phylogenetic conclusions. The diversity, distribution, biogeographic origins, and final demise and extinction of large Constrictores in the Paleogene of Europe are discussed.


2013 ◽  
Vol 82 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Ana Ivanović ◽  
Gregor Aljančič ◽  
Jan W. Arntzen

We performed an exploratory analysis of the morphology of the cranium in the white olm (Proteus anguinus anguinus) and the black olm (P. a. parkelj) with micro-CT scanning and geometric morphometrics. The mudpuppy (Necturus maculosus) was used as an outgroup. The black olm falls outside the white olm morphospace by a markedly wider skull, shorter vomers which are positioned further apart and by laterally positioned squamosals and quadrates relative to the palate (the shape of the buccal cavity). On account of its robust skull with more developed premaxillae a shorter otico-occipital region, the black olm is positioned closer to Necturus than are the studied specimens of the white olm. The elongated skull of the white olm, with an anteriorly positioned jaw articulation point, could be regarded as an adaptation for improved feeding success, possibly compensating for lack of vision. As yet, the alternative explanations on the evolution of troglomorphism in Proteus are an extensive convergence in white olms versus the reverse evolution towards less troglomorphic character states in the black olm. To further understand the evolutionary trajectories within Proteus we highlight the following hypotheses for future testing: i) morphological differentiation is smaller within than between genetically differentiated white olm lineages, and ii) ontogenetic shape changes are congruent with the shape changes between lineages. We anticipate that the morphological detail and analytical power that come with the techniques we here employed will assist us in this task.


2021 ◽  
Vol 11 (11) ◽  
pp. 5086
Author(s):  
Mazen F. Alkahtany ◽  
Saqib Ali ◽  
Abdul Khabeer ◽  
Shafqat A. Shah ◽  
Khalid H. Almadi ◽  
...  

This study aimed to investigate variations in the root canal morphology of maxillary second premolar (MSP) teeth using microcomputed tomography (micro-CT). Sixty (N = 60) human extracted MSPs were collected and prepared for micro-CT scanning. The duration for scanning a single sample ranged between 30 and 40 min and a three-dimensional (3-D) image was obtained for all the MSPs. The images were evaluated by a single observer who recorded the canal morphology type, number of roots, canal orifices, apical foramina(s), apical delta(s), and accessory canals. The root canal configuration was categorized in agreement with Vertucci’s classification, and any configuration not in agreement with Vertucci’s classification was reported as an “additional canal configuration”. Descriptive statistics (such as mean percentages) were calculated using SPSS software. The most common types agreeing with Vertucci’s classification (in order of highest to lowest incidence) were types I, III, V, VII, II, and VI. The teeth also exhibited four additional configurations that were different from Vertucci’s classification: types 2-3, 1-2-3, 2-1-2-1, and 1-2-1-3. A single root was found in 96.7% and the majority of the samples demonstrated two canals (73.3%). Further, 80% of the teeth showed one canal orifice. The number of apical foramina’s in the teeth was variable, with 56.7% having solitary apical foramen. The accessory canal was found in 33.3%, and apical delta was found in only 20% of the samples. Variable morphology of the MSPs was detected in our study. The canal configuration most prevalent was type 1; however, the results also revealed some additional canal types.


2021 ◽  
Vol 9 (1) ◽  
pp. 8
Author(s):  
Daisy (Jihyung) Ko ◽  
Tess Kelly ◽  
Lacey Thompson ◽  
Jasmene K. Uppal ◽  
Nasim Rostampour ◽  
...  

For humans and other mammals to eat effectively, teeth must develop properly inside the jaw. Deciphering craniodental integration is central to explaining the timely formation of permanent molars, including third molars which are often impacted in humans, and to clarifying how teeth and jaws fit, function and evolve together. A factor long-posited to influence molar onset time is the jaw space available for each molar organ to form within. Here, we tested whether each successive molar initiates only after a minimum threshold of space is created via jaw growth. We used synchrotron-based micro-CT scanning to assess developing molars in situ within jaws of C57BL/6J mice aged E10 to P32, encompassing molar onset to emergence. We compared total jaw, retromolar and molar lengths, and molar onset times, between upper and lower jaws. Initiation time and developmental duration were comparable between molar upper and lower counterparts despite shorter, slower-growing retromolar space in the upper jaw, and despite size differences between upper and lower molars. Timing of molar formation appears unmoved by jaw length including space. Conditions within the dental lamina likely influence molar onset much more than surrounding jaw tissues. We theorize that molar initiation is contingent on sufficient surface area for the physical reorganization of dental epithelium and its invagination of underlying mesenchyme.


Paleobiology ◽  
2021 ◽  
pp. 1-15
Author(s):  
Dana S. Friend ◽  
Brendan M. Anderson ◽  
Warren D. Allmon

Abstract Rates of speciation and extinction are often linked to many ecological factors, traits (emergent and nonemergent) such as environmental tolerance, body size, feeding type, and geographic range. Marine gastropods in particular have been used to examine the role of larval dispersal in speciation. However, relatively few studies have been conducted placing larval modes in species-level phylogenetic context. Those that have, have not incorporated fossil data, while landmark macroevolutionary studies on fossil clades have not considered both phylogenetic context and net speciation (speciation–extinction) rates. This study utilizes Eocene volutid Volutospina species from the U.S. Gulf Coastal Plain and the Hampshire Basin, U.K., to explore the relationships among larval mode, geographic range, and duration. Based on the phylogeny of these Volutospina, we calculated speciation and extinction rates in order to compare the macroevolutionary effects of larval mode. Species with planktotrophic larvae had a median duration of 9.7 Myr, which compared significantly to 4.7 Myr for those with non-planktotrophic larvae. Larval mode did not significantly factor into geographic-range size, but U.S. and U.K. species do differ, indicating a locality-specific component to maximum geographic-range size. Non-planktotrophs (NPTs)were absent among the Volutospina species during the Paleocene–early Eocene. The relative proportions of NPTs increased in the early middle Eocene, and the late Eocene was characterized by disappearance of planktotrophs (PTs). The pattern of observed lineage diversity shows an increasing preponderance of NPTs; however, this is clearly driven by a dramatic extinction of PTs, rather than higher NPT speciation rates during the late Eocene. This study adds nuance to paleontology's understanding of the macroevolutionary consequences of larval mode.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Damián A. Fernández ◽  
Luis Palazzesi ◽  
M. Sol González Estebenet ◽  
M. Cristina Tellería ◽  
Viviana D. Barreda

AbstractA major climate shift took place about 40 Myr ago—the Middle Eocene Climatic Optimum or MECO—triggered by a significant rise of atmospheric CO2 concentrations. The biotic response to this MECO is well documented in the marine realm, but poorly explored in adjacent landmasses. Here, we quantify the response of the floras from America’s southernmost latitudes based on the analysis of terrestrially derived spores and pollen grains from the mid-late Eocene (~46–34 Myr) of southern Patagonia. Robust nonparametric estimators indicate that floras in southern Patagonia were in average ~40% more diverse during the MECO than pre-MECO and post-MECO intervals. The high atmospheric CO2 and increasing temperatures may have favored the combination of neotropical migrants with Gondwanan species, explaining in part the high diversity that we observed during the MECO. Our reconstructed biota reflects a greenhouse world and offers a climatic and ecological deep time scenario of an ice-free sub-Antarctic realm.


1998 ◽  
Vol 11 (6) ◽  
pp. 711 ◽  
Author(s):  
Robert S. Hill ◽  
Leonie J. Scriven

A re-investigation of macrofossils previously referred to the extantpodocarpaceous genus Falcatifolium Laubenfels shows thatno records can be sustained. Falcatifolium australisD.R.Greenwood from Middle Eocene sediments in Victoria bears littleresemblance to extant species in the genus and is transferred to the newfossil genus Sigmaphyllum R.S.Hill & L.J.Scriven.Specimens from Early Oligocene sediments in Tasmania previously assigned toFalcatifolium are described as a second species ofSigmaphyllum, S. tasmanensisR.S.Hill & L.J.Scriven, and specimens from mid to late Eocene sediments inTasmania previously assigned to Falcatifolium do notbelong to that genus, although their true generic affinities are uncertain.Dispersed cuticle specimens from Late Eocene–Oligocene sediments inSouth Australia referred to Falcatifolium are notreliable records of the genus and require further investigation. However,Dacrycarpus eocenica D.R.Greenwood, from Middle Eocenesediments in Victoria is transferred to Falcatifolium,and is similar to the extant species F. angustumLaubenfels, which has a leaf morphology unusual for the genus.Falcatifolium eocenica (D.R.Greenwood) R.S.Hill & L.J.Scriven is the only reliable record of the genus in the Australian fossilrecord to date.


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