scholarly journals Integrating gross morphology and bone histology to assess skeletal maturity in early dinosauromorphs: new insights from Dromomeron (Archosauria: Dinosauromorpha)

PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e6331 ◽  
Author(s):  
Christopher T. Griffin ◽  
Lauren S. Bano ◽  
Alan H. Turner ◽  
Nathan D. Smith ◽  
Randall B. Irmis ◽  
...  

Understanding growth patterns is central to properly interpreting paleobiological signals in tetrapods, but assessing skeletal maturity in some extinct clades may be difficult when growth patterns are poorly constrained by a lack of ontogenetic series. To overcome this difficulty in assessing the maturity of extinct archosaurian reptiles—crocodylians, birds and their extinct relatives—many studies employ bone histology to observe indicators of the developmental stage reached by a given individual. However, the relationship between gross morphological and histological indicators of maturity has not been examined in most archosaurian groups. In this study, we examined the gross morphology of a hypothesized growth series of Dromomeron romeri femora (96.6–144.4 mm long), the first series of a non-dinosauriform dinosauromorph available for such a study. We also histologically sampled several individuals in this growth series. Previous studies reported that D. romeri lacks well-developed rugose muscle scars that appear during ontogeny in closely related dinosauromorph taxa, so integrating gross morphology and histological signal is needed to determine reliable maturity indicators for early bird-line archosaurs. We found that, although there are small, linear scars indicating muscle attachment sites across the femur, the only rugose muscle scar that appears during ontogeny is the attachment of the M. caudofemoralis longus, and only in the largest-sampled individual. This individual is also the only femur with histological indicators that asymptotic size had been reached, although smaller individuals possess some signal of decreasing growth rates (e.g., decreasing vascular density). The overall femoral bone histology of D. romeri is similar to that of other early bird-line archosaurs (e.g., woven-bone tissue, moderately to well-vascularized, longitudinal vascular canals). All these data indicate that the lack of well-developed femoral scars is autapomorphic for this species, not simply an indication of skeletal immaturity. We found no evidence of the high intraspecific variation present in early dinosaurs and other dinosauriforms, but a limited sample size of other early bird-line archosaur growth series make this tentative. The evolutionary history and phylogenetic signal of gross morphological features must be considered when assessing maturity in extinct archosaurs and their close relatives, and in some groups corroboration with bone histology or with better-known morphological characters is necessary.

2018 ◽  
Vol 49 (4) ◽  
pp. 409-442 ◽  
Author(s):  
Leonardo Latella ◽  
Valerio Sbordoni ◽  
Giuliana Allegrucci

The genus Bathysciola is widely distributed in the northern Mediterranean region, although its range extends east to the Caucasus and Iran. More than 130 species belonging to this genus are actually known in the whole geographic distribution area and 45 species are distributed in continental and insular Italy. The species belonging to the Bathysciola sisernica Cerruti and Patrizi, 1952 species group occur in the Central-Southern Italian Apennines and Pre-Apennines. This group consists of seven species, four of which (B. sisernica, B. delayi Latella and Rampini, 1994, B. rampinii Latella, 2002, B. sbordoni Rampini and Latella, 1993) were already known to science and three are described herein, Bathysciola fabiolae sp. nov., Bathysciola octaviani sp. nov. , and Bathysciola valeriae sp. nov., markedly increasing the knowledge on the distribution of this genus in Central Italy. A morphological analysis was carried out based on diagnostic characters usually used to distinguish different taxa, and including both genitalia and external traits. Based on morphological characters, we reconstructed the phylogeny of this group of species, comparing them with the species belonging to other phyletic lineages, such as B. derosasi Jeannel, 1914, B. georgi Cerruti, Patrizi, 1952, B. vignai Sbordoni and Rampini, 1978, and B. sarteanensis sarteanensis (Bargagli, 1870). Results suggested that morphological traits show a clear taxonomic signal but a poor phylogenetic signal. To better understand the relationships within this group of species, we performed a molecular analysis by sequencing three mitochondrial genes, 12S rRNA, 16S rRNA, partially sequenced and the entire gene of COI. Molecular markers were used to infer phylogenetic relationships among the Bathysciola sisernica species group and to reconstruct the historical processes that shaped their current geographic distribution. Results showed that these species became isolated in very ancient times, showing very high genetic differentiation.


2002 ◽  
Vol 16 (3) ◽  
pp. 369 ◽  
Author(s):  
G. Hormiga

The Hawaiian spider genus Orsonwelles, gen. nov. (Araneae : Linyphiidae) is described. All Orsonwelles species are single island endemics: Kauai harbours six species; Oahu has three; Molokai has two; and Maui and Hawaii have one species each. The thirteen species included in Orsonwelles are described and illustrated: O. torosus (Simon), comb. nov., O. malus, sp. nov., O. calx, sp. nov., O. ventus, sp. nov., O. bellum, sp. nov. and O. iudicium, sp. nov. from Kauai; O. polites, sp. nov. (the type species), O. ambersonorum, sp. nov. and O. arcanus, sp. nov. from Oahu; O. othello, sp. nov. and O. macbeth, sp. nov. from Molokai; O. falstaffius, sp. nov. from Maui; and O. graphicus (Simon), comb. nov. from Hawaii. A total of 55 morphological characters (plus one behavioural character) were scored for twelve taxa (four Orsonwelles species plus eight linyphiid outgroups) to test the monophyly of the genus using cladistic methods. The most parsimonious cladograms provide robust character support for the monophyly of Orsonwelles. A single colonisation of the Hawaiian archipelago is hypothesised to explain the presence of these species in the Hawaiian Islands. This genus represents a case of insular gigantism (these are the largest linyphiids described), although the close relatives of Orsonwelles remain unknown. Their web architecture is also described and illustrated.


Zootaxa ◽  
2007 ◽  
Vol 1423 (1) ◽  
pp. 1-26 ◽  
Author(s):  
JEFFREY H. SKEVINGTON ◽  
CHRISTIAN KEHLMAIER ◽  
GUNILLA STÅHLS

Sequence data from 658 base pairs of mitochondrial cytochrome c oxidase I (cox1) were analysed for 28 described species of Pipunculidae (Diptera) in an effort to test the concept of DNA Barcoding on this family. Two recently revised but distantly related pipunculid lineages with presumed different evolutionary histories were used for the test (Clistoabdominalis Skevington, 2001 and Nephrocerus Zetterstedt, 1838). An effort was made to test the concept using sister taxa and morphologically similar sibling species swarms in these two genera. Morphological species concepts for Clistoabdominalis taxa were either supported by cox1 data or found to be too broad. Most of the discordance could be accounted for after reassessing morphological characters. In these cases, the molecular data were invaluable in assisting taxonomic decision-making. The radiation of Nearctic species of Nephrocerus could not be diagnosed using cox1. The ability of cox1 to recover phylogenetic signal was also tested on Clistoabdominalis. Morphological data for Clistoabdominalis were combined with the molecular data set. The pipunculid phylogeny from molecular data closely resembles the published phylogeny based on morphology. Partitioned Bremer support is used to localize areas of conflict between the datasets.


Zootaxa ◽  
2006 ◽  
Vol 1298 (1) ◽  
pp. 29 ◽  
Author(s):  
ALEJANDRO PARRA-H ◽  
RODULFO OSPINA-TORRES ◽  
SANTIA RAMÍREZ

A new species of orchid bee in the genus Euglossa is here described. Euglossa natesi n. sp. ParraH, Ospina-Torres & Ramírez has been collected from the Pacific Andean foothills of Colombia and Ecuador. Euglossa natesi n. sp. has no obvious close relatives, and while most morphological characters suggest that it belongs to the subgenus Glossura, a few characters indicate that it belongs to the subgenus Glossurella.


2011 ◽  
Vol 182 (3) ◽  
pp. 231-240 ◽  
Author(s):  
Jérémy Anquetin

AbstractIn recent years, no less than five new species of early turtles have been described worldwide. Among them are three new turtles from Middle Jurassic deposits that partially fill a previous temporal and morphological gap in our knowledge of the early evolution of these shelled amniotes: Heckerochelys romani, Condorchelys antiqua and Eileanchelys waldmani. For the first time, the phylogenetic position of these three new species is tested in the context of the two presently competing cladistic models of turtle evolution. The addition of these taxa to each matrix does not favour or alter any of the two opposed hypotheses. However, it is demonstrated here that, by documenting yet unknown stages in the evolution of several morphological structures, these three species give stronger support to the model of an extended phylogenetic stem for turtles. These new lines of evidence include the structure of the vomer, the position of the aditus canalis stapedio-temporalis and of the posterior opening of the canalis cavernosus, and the morphology of the processus interfenestralis of the opisthotic.Recent discoveries also reinvigorate the debate about the palaeoecology of early turtles. Whereas simple morphological characters (e.g., shell fontanelle, ligamentous bridge, flattened carapace) can be misleading, forelimb proportions and shell bone histology have led to the conclusion that most stem turtles (i.e., Proganochelys quenstedti, Palaeochersis talampayensis, Proterochersis robusta, Kayentachelys aprix and meiolaniids) were terrestrial forms. At least two out of the five recently described early turtles have been convincingly interpreted as having aquatic habits: Odontochelys semitestacea and Eileanchelys waldmani. More investigation is needed, but this will undoubtedly trigger further debate on the primitive ecology of turtles and on the origin of aquatic habits in testudines (i.e., the crown-group), respectively.


Phytotaxa ◽  
2020 ◽  
Vol 454 (4) ◽  
pp. 277-284
Author(s):  
FABRÍCIO MOREIRA FERREIRA ◽  
CASSIANO A. DORNELES WELKER ◽  
LYNN G. CLARK ◽  
REYJANE P. OLIVEIRA

Eremitis limae, a new species of Parianinae (Poaceae, Bambusoideae, Olyreae) endemic to the coastal forests of Bahia, Brazil, is described and illustrated. It is morphologically similar to species of Eremitis with characteristically narrow leaves: E. linearifolia, E. parviflora, and E. riodocensis. We discuss the morphological characters distinguishing the new species from its close relatives, and we also present illustrations, photos, and a distribution map. Eremitis limae is classified as Endangered (EN) according to the IUCN Red List categories and criteria.


2018 ◽  
Author(s):  
Eli Amson ◽  
John A Nyakatura

ABSTRACTTrabecular architecture (i.e., the main orientation of the bone trabeculae, their number, mean thickness, spacing, etc.) has been shown experimentally to adapt with great accuracy and sensitivity to the loadings applied to the bone during life. However, the potential of trabecular parameters used as a proxy for the mechanical environment of an organism’s organ to help reconstruct the lifestyle of extinct taxa has only recently started to be exploited. Furthermore, these parameters are rarely combined to the long-used mid-diaphyseal parameters to inform such reconstructions. Here we investigate xenarthrans, for which functional and ecological reconstructions of extinct forms are particularly important in order to improve our macroevolutionary understanding of their main constitutive clades, i.e., the Tardigrada (sloths), Vermilingua (anteaters), and Cingulata (armadillos and extinct close relatives). The lifestyles of modern xenarthrans can be classified as fully terrestrial and highly fossorial (armadillos), arboreal (partly to fully) and hook-and-pull digging (anteaters), or suspensory (fully arboreal) and non-fossorial (sloths). The degree of arboreality and fossoriality of some extinct forms, “ground sloths” in particular, is highly debated. We used high-resolution computed tomography to compare the epiphyseal 3D architecture and mid-diaphyseal structure of the forelimb bones of extant and extinct xenarthrans. The comparative approach employed aims at inferring the most probable lifestyle of extinct taxa, using phylogenetically informed discriminant analyses. Several challenges preventing the attribution of one of the extant xenarthran lifestyles to the sampled extinct sloths were identified. Differing from that of the larger “ground sloths”, the bone structure of the small-sized Hapalops (Miocene of Argentina), however, was found as significantly more similar to that of extant sloths, even when accounting for the phylogenetic signal.


2021 ◽  
Author(s):  
Robert J Asher ◽  
Martin R Smith

Abstract An unprecedented amount of evidence now illuminates the phylogeny of living mammals and birds on the Tree of Life. We use this tree to measure phylogenetic value of data typically used in paleontology (bones and teeth) from six datasets derived from five published studies. We ask three interrelated questions: 1) Can these data adequately reconstruct known parts of the Tree of Life? 2) Is accuracy generally similar for studies using morphology, or do some morphological datasets perform better than others? 3) Does the loss of non-fossilizable data cause taxa to occur in misleadingly basal positions? Adding morphology to DNA datasets usually increases congruence of resulting topologies to the well corroborated tree, but this varies among morphological datasets. Extant taxa with a high proportion of missing morphological characters can greatly reduce phylogenetic resolution when analyzed together with fossils. Attempts to ameliorate this by deleting extant taxa missing morphology are prone to decreased accuracy due to long-branch artefacts. We find no evidence that fossilization causes extinct taxa to incorrectly appear at or near topologically basal branches. Morphology comprises the evidence held in common by living taxa and fossils, and phylogenetic analysis of fossils greatly benefits from inclusion of molecular and morphological data sampled for living taxa, whatever methods are used for phylogeny estimation.


2017 ◽  
Author(s):  
Mathew J Wedel ◽  
Brian P Kraatz ◽  
Michael P Taylor ◽  
Jann Vendetti

The study of ontogeny in the fossil record is complicated by two main factors: growth series are not available for many taxa, and correctly assigning juveniles and adults to the same taxon is often difficult, especially where several related taxa coexisted. Ontogenetic change can also be revealed in single individuals whose morphology records characters from multiple ontogenetic stages. A snail shell is an intuitive example: the shell grows by accretion at its margin, starting from the larval shell (protoconch), and moving outward. Larval shell shape varies predictably between planktotrophic and non-planktotrophic lineages; and since the protoconch is embedded in the adult shell, larval ecology can be inferred in adults from the size and morphology of the retained protoconch. In many extinct lagomorphs, the occlusal surface of the molars changed markedly over the lifespan of an individual, as features such as enamel ridges were revealed and then obliterated by wear. In this case, the complete ‘stack’ of potential occlusal morphologies was present in the adult tooth as soon as it was done mineralizing, and further change progressively erased the ontogenetically early character states. In sauropodomorph dinosaurs, morphological complexity of the vertebrae increases along the cervical series. The simple morphology of anterior cervicals reflects both earlier ontogenetic stages and more primitive character states. More posterior vertebrae reveal the sequential formation of complex structures. Individuals that record multiple ontogenetic stages can help solve palaeobiological problems, such as inferring life histories, assessing ranges of variation, and determining the origin of complex morphological characters.


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