Developmental constraint on the evolution of marsupial forelimb morphology

2010 ◽  
Vol 58 (1) ◽  
pp. 1 ◽  
Author(s):  
W. James Cooper ◽  
Scott J. Steppan

Compared with the placental mammals, marsupials are born at an almost embryonic stage, but nearly all of these neonates immediately climb or crawl to one of their mother’s teats using precociously developed forelimbs. Marsupial adults also exhibit limited forelimb shape diversity relative to the members of their sister group. That the functional requirements of this natal climb have imposed a developmental constraint on marsupial forelimb evolution represents a compelling and widely accepted hypothesis, yet its resulting predictions for the comparative patterns of mammal limb shape diversity have never been tested. In order to perform such tests we conducted extensive taxonomic sampling of mammal limb morphology (including fossil specimens), and then examined these data using morphometric methods, non-parametric analyses of anatomical disparity, and phylogenetic comparative analyses of evolutionary rates. Our results strongly support the constraint hypothesis, and indicate that the highly significant differences between marsupial and placental forelimb shape diversity has been strongly influenced by different rates of morphological evolution among the distal forelimb elements in these two important mammal lineages.

Paleobiology ◽  
2000 ◽  
Vol 26 (1) ◽  
pp. 56-79 ◽  
Author(s):  
Gunther J. Eble

Temporal asymmetries in clade histories have often been studied in lower Paleozoic radiations. Post-Paleozoic patterns, however, are less well understood. In this paper, disparity and diversity changes in Mesozoic heart urchins were analyzed at the ordinal level, with contrasts among the sister groups Holasteroida and Spatangoida, their paraphyletic stem group Disasteroida the more inclusive clade, the superorder Atelostomata. A 38-dimensional landmark-based morphospace representing test architecture was used to describe morphological evolution in terms of total variance and total range. Discordances between disparity and diversity were evident and were expressed both as deceleration in morphological diversification in all groups and as disproportionately higher disparity early in the histories of the Atelostomata, Holasteroida Spatangoida. The finding that the early atelostomate disparity peak coincides with the origin of the orders Holasteroida and Spatangoida lends support to the perception of orders as semi-independent entities in the biological hierarchy and as meaningful proxies for morphological distinctness.A comparison of holasteroid and spatangoid responses to the end-Cretaceous mass extinction revealed morphological selectivity. Paleocene spatangoid survivors showed no change in disparity relative to the Campanian-Maastrichtian sample, suggesting nonselectivity. Holasteroids suffered a pronounced loss in disparity (despite a rather high Late Cretaceous level of disparity), indicating morphological selectivity of extinction.Partitioning of disparity into plastral and nonplastral components, reflecting different degrees of developmental entrenchment and functionality, suggests that the origin of holasteroids and spatangoids is more consistent with an exploration of the developmental flexibility of nonplastral constructions than with uniform ecospace occupation. Within groups, several patterns were also most consistent with intrinsic controls. For plastral landmarks, there is an apparent increase in developmental modularity and decrease in developmental constraint from disasteroids to holasteroids and spatangoids. For nonplastral landmarks, no substantial change in disparity was observed from disasteroids to holasteroids and spatangoids, suggesting the maintenance of a developmental constraint despite the passage of time and ecological differentiation. More generally, this study suggests that certain topologies of disparity and evolutionary mechanisms potentially characteristic of the lower Paleozoic radiations of higher taxa (e.g., developmental flexibility) need not be confined to any given time period or hierarchical level.


2018 ◽  
Vol 98 (8) ◽  
pp. 1991-1998
Author(s):  
A. L. Ibáñez ◽  
L. A. Jawad

New Zealand rattail fish are of great interest both to biologists who study their phylogenetics and in fisheries. In contrast, their morphological evolution is little studied and poorly understood. Geometric morphometric methods based on scale shape were applied in this study to determine differences among species and genera. Scale shapes were described using seven landmarks, the coordinates of which were subjected to a generalized Procrustes analysis, followed by a principal components analysis. A cross-validated discriminant analysis was applied to assess and compare the size-shape (centroid size plus shape variables) efficacy in the species and the discrimination of the genera. Two main phenetic groups were identified: cluster no. 1 with eight species and cluster no. 2 with six species. Coelorhinchus aspercephalus and Mesovagus antipodum were more separated from the other species in the first cluster. The cross-validated canonical discriminant analysis correctly classified 74% at the genus level, with most misclassifications occurring between Coelorhinchus and Coryphaenoides, whereas the best classified genera were Mesovagus and Trachyrincus. The discrimination of correctly classified species ranged from 41.2 to 100%. The highest correct classification rates were recorded for Coryphaenoides armatus, Coelorhinchus innotabilis, Trachyrincus longirostris and Mesovagus antipodum.


1997 ◽  
Vol 66 (4) ◽  
pp. 263-268
Author(s):  
J.W. Arntzen ◽  
M. García-París

Three competing phylogenetic hypotheses for the genus Alytes (midwife toads) are evaluated. Based on quantitative coding of protein characters the most parsimonious solution shows a sister taxon relationship for Alytes dickhilleni and A. muletensis. The alternatives in which A. obstetricans has its sister group in either A. dickhilleni or A. muletensis lack support. Using calibrations derived from protein evolutionary rates, the vicariant events giving rise to A. obstetricans and the lineage leading to the A. muletensis and A. dickhilleni clade and the subsequent splitting between A. muletensis and A. dickhilleni cannot be placed much earlier than the Miocene-Pliocene boundary. Biogeographical scenarios invoking an earlier time of divergence should be rejected.


2020 ◽  
Vol 7 (2) ◽  
pp. 191936 ◽  
Author(s):  
Serjoscha W. Evers ◽  
Walter G. Joyce

Sandownidae is an enigmatic group of Cretaceous–Paleogene turtles with highly derived cranial anatomy. Although sandownid monophyly is not debated, relationships with other turtles remain unclear. Sandownids have been recovered in significantly different parts of the turtle tree: as stem-turtles, stem-cryptodires and stem-chelonioid sea turtles. Latest phylogenetic studies find sandownids as the sister-group of the Late Jurassic thalassochelydians and as stem-turtles. Here, we provide a detailed study of the cranial and mandibular anatomy of Sandownia harrisi from the Aptian of the Isle of Wight, based on high resolution computed tomography scanning of the holotype. Our results confirm a high number of anatomical similarities with thalassochelydians and particularly Solnhofia parsonsi , which is interpreted as an early member of the sandownid lineage. Sandownids + Solnhofia show many cranial modifications related to the secondary palate and a durophagous diet. Sandownia is additionally highly derived in features related to its arterial circulation and neuroanatomy, including the endosseous labyrinth. Our results imply rapid morphological evolution during the early history of sandownids. Sandownids likely evolved in central Europe from thalassochelydian ancestors during the Late Jurassic. The durophagous diet of sandownids possibly facilitated their survival of the Cretaceous/Paleogene mass extinction.


2012 ◽  
Vol 109 (44) ◽  
pp. 18006-18011 ◽  
Author(s):  
J. B. Smaers ◽  
D. K. N. Dechmann ◽  
A. Goswami ◽  
C. Soligo ◽  
K. Safi

2017 ◽  
Vol 31 (6) ◽  
pp. 765 ◽  
Author(s):  
Phillip Barden ◽  
Brendon Boudinot ◽  
Andrea Lucky

The distinctive ant genus Leptomyrmex Mayr, 1862 had been thought to be endemic to Australasia for over 150 years, but enigmatic Neotropical fossils have challenged this view for decades. The present study responds to a recent and surprising discovery of extant Leptomyrmex species in Brazil with a thorough evaluation of the Dominican Republic fossil material, which dates to the Miocene. In the first case study of direct fossil inclusion within Formicidae Latreille, 1809, we incorporated both living and the extinct Leptomyrmex species. Through simultaneous analysis of molecular and morphological characters in both Bayesian and parsimony frameworks, we recovered the fossil taxon as sister-group to extant Leptomyrmex in Brazil while considering the influence of taxonomic and character sampling on inferred hypotheses relating to tree topology, biogeography and morphological evolution. We also identified potential loss of signal in the binning of morphological characters and tested the impact of parameterisation on divergence date estimation. Our results highlight the importance of securing sufficient taxon sampling for extant lineages when incorporating fossils and underscore the utility of diverse character sources in accurate placement of fossil terminals. Specifically, we find that fossil placement in this group is influenced by the inclusion of male-based characters and the newly discovered Neotropical ‘Lazarus taxon’.


2019 ◽  
Vol 1 (1) ◽  
Author(s):  
E M Kelly ◽  
J D Marcot ◽  
L Selwood ◽  
K E Sears

Abstract The morphological interdependence of traits, or their integration, is commonly thought to influence their evolution. As such, study of morphological integration and the factors responsible for its generation form an important branch of the field of morphological evolution. However, most research to date on post-cranial morphological integration has focused on adult patterns of integration. This study investigates patterns of correlation (i.e., morphological integration) among skeletal elements of the fore- and hind limbs of developing marsupial and placental mammals. The goals of this study are to establish how patterns of limb integration vary over development in marsupials and placentals, and identify factors that are likely responsible for their generation. Our results indicate that although the overall pattern of correlation among limb elements is consistent with adult integration throughout mammalian development, correlations vary at the level of the individual element and stage. As a result, the relative integration among fore- and hind limb elements varies dynamically between stages during development in both marsupial and placental mammals. Therefore, adult integration studies of the limbs may not be indicative of developmental integration. Results are also consistent with integration during early limb development being more heavily influenced by genetic and developmental factors, and later by function. Additionally, results are generally consistent with a constraint on marsupial forelimb evolution caused by the functional requirements of the crawl to the teat that operates by limiting morphological variation before and at the time of birth, and not after.


2001 ◽  
Vol 33 (1) ◽  
pp. 63-72 ◽  
Author(s):  
Martin Grube ◽  
Ulf Arup

AbstractA phylogenetic hypothesis based on nuclear ITS sequence data is presented for the family Physciaceae based on various representatives of foliose and fruticose groups and a number of species selected from the crustose genera Rinodina and Buellia s.l. The analysis supports the monophyly of the Physcia- and the Buellia- groups. This is in agreement with existing morphological evidence, particularly ascus characters. The Physcia group in the analysis includes the genera Anaptychia, Heterodermia, Hyperphyscia, Mobergia, Phaeophyscia, Phaeorrhiza, Physcia, Physconia, Rinodina, and Rinodinella, while the Buellia group includes Amandinea, Buellia and Diploicia. The genera Physcia, Phaeophyscia, Phaeorrhiza and Rinodinella were well supported as monophyletic groups. The support for Physconia is low. Rinodina and Buellia are not supported as monophyletic genera. In agreement with ascus and ascospore characters, Buellia lindingeri is placed within the Rinodina group, close R. lecanorina. The genus Amandinea as currently circumscribed was not supported as a monophyletic group. The analysis confirms results from other lichen families that foliose members have evolved more than once from crustose lichens. Rinodina and Rinodinella species without chemical compounds in their thalli form the sister group to Phaeophyscia, and both groups form a monophyletic assemblage. A more detailed analysis of the Physcia group is presented. Whilst several of the foliose genera were well supported, there is only poor support for traditionally accepted crustose genera. The taxonomic implications of these findings are discussed.


Paleobiology ◽  
1986 ◽  
Vol 12 (4) ◽  
pp. 355-369 ◽  
Author(s):  
Bruce J. MacFadden

The evolution of body size in fossil horses is frequently depicted as a gradual, progressive trend toward increased body size (Cope's Law). Body size (actually body mass) was estimated for 40 species of fossil horses using dental and skeletal characters and regression equations derived from the same characters in extant species of Equus with known body mass. After body sizes were estimated, rates of morphological evolution, in darwins (d), were calculated between known ancestral and descendant fossil horse species. For the first half of horse evolution (from ca. 57 to 25 ma) body mass remained relatively static between about 25 and 50 kg with very slow evolutionary rates of 0.003–0.04 d. During the early–middle Miocene (from ca. 25 to 10 ma) there was a major diversification of body mass to about 75–400 kg and consistently higher evolutionary rates between 0.04 and 0.24 d. Since the late Miocene, body mass has generally increased with a maximum seen (in natural populations) in Equus scotti (ca. 500 kg) during the middle Pleistocene. Therefore, for horses, the traditional interpretation of gradual increase in body size through time is oversimplified because: (1) although the exception to the rule, 5 of 24 species lineages studied are characterized by dwarfism; and (2) the general trend seems to have been a long period (32 ma) of relative stasis followed by 25 ma of diversification and progressive (although not necessarily gradual) change in body size.


2014 ◽  
Vol 281 (1793) ◽  
pp. 20141278 ◽  
Author(s):  
Robin M. D. Beck ◽  
Michael S. Y. Lee

Analyses of a comprehensive morphological character matrix of mammals using ‘relaxed’ clock models (which simultaneously estimate topology, divergence dates and evolutionary rates), either alone or in combination with an 8.5 kb nuclear sequence dataset, retrieve implausibly ancient, Late Jurassic–Early Cretaceous estimates for the initial diversification of Placentalia (crown-group Eutheria). These dates are much older than all recent molecular and palaeontological estimates. They are recovered using two very different clock models, and regardless of whether the tree topology is freely estimated or constrained using scaffolds to match the current consensus placental phylogeny. This raises the possibility that divergence dates have been overestimated in previous analyses that have applied such clock models to morphological and total evidence datasets. Enforcing additional age constraints on selected internal divergences results in only a slight reduction of the age of Placentalia. Constraining Placentalia to less than 93.8 Ma, congruent with recent molecular estimates, does not require major changes in morphological or molecular evolutionary rates. Even constraining Placentalia to less than 66 Ma to match the ‘explosive’ palaeontological model results in only a 10- to 20-fold increase in maximum evolutionary rate for morphology, and fivefold for molecules. The large discrepancies between clock- and fossil-based estimates for divergence dates might therefore be attributable to relatively small changes in evolutionary rates through time, although other explanations (such as overly simplistic models of morphological evolution) need to be investigated. Conversely, dates inferred using relaxed clock models (especially with discrete morphological data and M r B ayes ) should be treated cautiously, as relatively minor deviations in rate patterns can generate large effects on estimated divergence dates.


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