scholarly journals Questioning hagfish affinities of the enigmatic Devonian vertebrate Palaeospondylus

2017 ◽  
Vol 4 (7) ◽  
pp. 170214 ◽  
Author(s):  
Zerina Johanson ◽  
Moya Smith ◽  
Sophie Sanchez ◽  
Tim Senden ◽  
Kate Trinajstic ◽  
...  

Palaeospondylus gunni Traquair, 1890 is an enigmatic Devonian vertebrate whose taxonomic affinities have been debated since it was first described. Most recently, Palaeospondylus has been identified as a stem-group hagfish (Myxinoidea). However, one character questioning this assignment is the presence of three semicircular canals in the otic region of the cartilaginous skull, a feature of jawed vertebrates. Additionally, new tomographic data reveal that the following characters of crown-group gnathostomes (chondrichthyans + osteichthyans) are present in Palaeospondylus : a longer telencephalic region of the braincase, separation of otic and occipital regions by the otico-occipital fissure, and vertebral centra. As well, a precerebral fontanelle and postorbital articulation of the palatoquadrate are characteristic of certain chondrichthyans. Similarities in the structure of the postorbital process to taxa such as Pucapampella , and possible presence of the ventral cranial fissure, both support a resolution of Pa. gunni as a stem chondrichthyan. The internally mineralized cartilaginous skeleton in Palaeospondylus may represent a stage in the loss of bone characteristic of the Chondrichthyes.

2017 ◽  
Vol 91 (4) ◽  
pp. 767-780 ◽  
Author(s):  
Jeffrey R. Thompson ◽  
Elizabeth Petsios ◽  
David J. Bottjer

AbstractThe Permian is regarded as one of the most crucial intervals during echinoid evolution because crown group echinoids are first widely known from the Permian. New faunas provide important information regarding the diversity of echinoids during this significant interval as well as the morphological characterization of the earliest crown group and latest stem group echinoids. A new fauna from the Capitanian Lamar Member of the Bell Canyon Formation in the Guadalupe Mountains of West Texas comprises at least three new taxa, includingEotiaris guadalupensisThompson n. sp. an indeterminate archaeocidarid, andPronechinus? sp. All specimens represented are silicified and known from disarticulated or semiarticulated interambulacral and ambulacral plates and spines. This assemblage is one of the most diverse echinoid assemblages known from the Permian and, as such, informs the paleoecological setting in which the earliest crown group echinoids lived. This new fauna indicates that crown group echinoids occupied the same environments as stem group echinoids of the Archaeocidaridae and Proterocidaridae. Furthermore, the echinoids described herein begin to elucidate the order of character transitions that likely took place between stem group and crown group echinoids. At least one of the morphological innovations once thought to be characteristic of early crown group echinoids, crenulate tubercles, was in fact widespread in a number of stem group taxa from the Permian as well. Crenulate tubercles are reported from two taxa, and putative cidaroid style U-shaped teeth are present in the fauna. The presence of crenulate tubercles in the archaeocidarid indicates that crenulate tubercles were present in stem group echinoids, and thus the evolution of this character likely preceded the evolution of many of the synapomorphies that define the echinoid crown group.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Richard J. Howard ◽  
Gregory D. Edgecombe ◽  
Xiaomei Shi ◽  
Xianguang Hou ◽  
Xiaoya Ma

Abstract Background Ecdysozoa are the moulting protostomes, including arthropods, tardigrades, and nematodes. Both the molecular and fossil records indicate that Ecdysozoa is an ancient group originating in the terminal Proterozoic, and exceptional fossil biotas show their dominance and diversity at the beginning of the Phanerozoic. However, the nature of the ecdysozoan common ancestor has been difficult to ascertain due to the extreme morphological diversity of extant Ecdysozoa, and the lack of early diverging taxa in ancient fossil biotas. Results Here we re-describe Acosmia maotiania from the early Cambrian Chengjiang Biota of Yunnan Province, China and assign it to stem group Ecdysozoa. Acosmia features a two-part body, with an anterior proboscis bearing a terminal mouth and muscular pharynx, and a posterior annulated trunk with a through gut. Morphological phylogenetic analyses of the protostomes using parsimony, maximum likelihood and Bayesian inference, with coding informed by published experimental decay studies, each placed Acosmia as sister taxon to Cycloneuralia + Panarthropoda—i.e. stem group Ecdysozoa. Ancestral state probabilities were calculated for key ecdysozoan nodes, in order to test characters inferred from fossils to be ancestral for Ecdysozoa. Results support an ancestor of crown group ecdysozoans sharing an annulated vermiform body with a terminal mouth like Acosmia, but also possessing the pharyngeal armature and circumoral structures characteristic of Cambrian cycloneuralians and lobopodians. Conclusions Acosmia is the first taxon placed in the ecdysozoan stem group and provides a constraint to test hypotheses on the early evolution of Ecdysozoa. Our study suggests acquisition of pharyngeal armature, and therefore a change in feeding strategy (e.g. predation), may have characterised the origin and radiation of crown group ecdysozoans from Acosmia-like ancestors.


2019 ◽  
Vol 187 (4) ◽  
pp. 1061-1077 ◽  
Author(s):  
Russell D C Bicknell ◽  
Lisa Amati ◽  
Javier Ortega-Hernández

Abstract Vision allows animals to interact with their environment. Aquatic chelicerates dominate the early record of lateral compound eyes among non-biomineralizing crown-group euarthropods. Although the conservative morphology of lateral eyes in Xiphosura is potentially plesiomorphic for Euarthropoda, synziphosurine eye organization has received little attention despite their early diverging phylogenetic position. Here, we re-evaluate the fossil evidence for lateral compound eyes in the synziphosurines Bunodes sp., Cyamocephalus loganensis, Legrandella lombardii, Limuloides limuloides, Pseudoniscus clarkei, Pseudoniscus falcatus and Pseudoniscus roosevelti. We compare these data with lateral eyes in the euchelicerates Houia yueya, Kasibelinurus amicorum and Lunataspis aurora. We find no convincing evidence for lateral eyes in most studied taxa, and Pseudoniscus roosevelti and Legrandella lombardii are the only synziphosurines with this feature. Our findings support two scenarios for euchelicerate lateral eye evolution. The elongate-crescentic lateral eyes of Legrandella lombardii might represent the ancestral organization, as suggested by the phylogenetic position of this taxon in stem-group Euchelicerata. Alternatively, the widespread occurrence of kidney-shaped lateral eyes in stem-group Xiphosura and stem-group Arachnida could represent the plesiomorphic condition; Legrandella lombardii eyes would therefore be derived. Both evolutionary scenarios support the interpretation that kidney-shaped lateral eyes are ancestral for crown-group Euchelicerata and morphologically conserved in extant Limulus polyphemus.


2003 ◽  
Vol 77 (4) ◽  
pp. 784-789 ◽  
Author(s):  
Dario G. Lazo ◽  
Marcela Cichowolski

Plesiosaurs constitute a monophyletic group whose stratigraphical range is uppermost Triassic to uppermost Cretaceous (Brown, 1981). They were large predatory marine reptiles, highly adapted for submarine locomotion, with powerful paddle-like limbs and heavily reinforced limb girdles (Saint-Seine, 1955; Romer, 1966; Carroll, 1988; Benton, 1990). The Plesiosauria clade belongs to the Sauropterygia, which has recently been hypothesized as the sister-group of the Ichthyosauria. Together with that clade they form the Euryapsida (Caldwell, 1997). The Sauropterygia can be subdivided into relatively plesiomorphic stem-group taxa from the Triassic (Placodonts, Nothosauroids, and Pistosauroids), and the obligatorily marine crown-group Plesiosauria (Rieppel, 1999). Plesiosaurs are traditionally divided into two superfamilies: Plesiosauroidea, with usually small heads and long necks; and Pliosauroidea, with larger heads and shorter necks (Welles, 1943; Persson, 1963; Brown, 1981). Plesiosauroidea contains three families: Plesiosauridae, Cryptoclididae, and Elasmosauridae (Brown, 1981; Brown and Cruickshank, 1994). The validity of the Polycotylidae Cope, 1869, has long been questioned and its phylogenetic position among Plesiosauria debated, as many consider it to be related to the Pliosauridae or to be a sister-group of the Elasmosauridae (Sato and Storrs, 2000; O'Keefe, 2001).


2004 ◽  
Vol 10 ◽  
pp. 35-50 ◽  
Author(s):  
Susannah M. Porter

The Cambrian explosion can be thought of as the culmination of a diversification of eukaryotes that had begun several hundred million years before. Eukaryotes - one of the three domains of life — originated by late Archean time, and probably underwent a long period of stem group evolution during the Paleoproterozoic Era. A suite of taxonomically resolved body fossils and biomarkers, together with estimates of acritarch and compression fossil diversity, suggest that while divergences among major eukaryotic clades or 'super-groups' may have occurred as early as latest Paleoproterozoic through Mesoproterozoic time, the main phase of eukaryotic diversification took place several hundred million years later, during the middle Neoproterozoic Era. Hypotheses for Neoproterozoic diversification must therefore explain why eukaryotic diversification is delayed several hundred million years after the origin of the eukaryotic crown group, and why diversification appears to have occurred independently within several eukaryotic super-groups at the same time. Evolutionary explanations for eukaryotic diversification (the evolution of sex; the acquisition of plastids) fail to account for these patterns, but ecological explanations (the advent of microbial predators) and environmental explanations (changes in ocean chemistry) are both consistent with them. Both ecology and environment may have played a role in triggering or at least fueling Neoproterozoic eukaryotic diversification.


2015 ◽  
Vol 112 (28) ◽  
pp. 8678-8683 ◽  
Author(s):  
Jie Yang ◽  
Javier Ortega-Hernández ◽  
Sylvain Gerber ◽  
Nicholas J. Butterfield ◽  
Jin-bo Hou ◽  
...  

We describe Collinsium ciliosum from the early Cambrian Xiaoshiba Lagerstätte in South China, an armored lobopodian with a remarkable degree of limb differentiation including a pair of antenna-like appendages, six pairs of elongate setiferous limbs for suspension feeding, and nine pairs of clawed annulated legs with an anchoring function. Collinsium belongs to a highly derived clade of lobopodians within stem group Onychophora, distinguished by a substantial dorsal armature of supernumerary and biomineralized spines (Family Luolishaniidae). As demonstrated here, luolishaniids display the highest degree of limb specialization among Paleozoic lobopodians, constitute more than one-third of the overall morphological disparity of stem group Onychophora, and are substantially more disparate than crown group representatives. Despite having higher disparity and appendage complexity than other lobopodians and extant velvet worms, the specialized mode of life embodied by luolishaniids became extinct during the Early Paleozoic. Collinsium and other superarmored lobopodians exploited a unique paleoecological niche during the Cambrian explosion.


2014 ◽  
Vol 1 (4) ◽  
pp. 498-520 ◽  
Author(s):  
Shuhai Xiao ◽  
A. D. Muscente ◽  
Lei Chen ◽  
Chuanming Zhou ◽  
James D. Schiffbauer ◽  
...  

Abstract The rise of multicellularity represents a major evolutionary transition and it occurred independently in multiple eukaryote clades. Although simple multicellular organisms may have evolved in the Mesoproterozoic Era or even earlier, complex multicellular eukaryotes began to diversify only in the Ediacaran Period, just before the Cambrian explosion. Thus, the Ediacaran fossil record can provide key paleontological evidence about the early radiation of multicellular eukaryotes that ultimately culminated in the Cambrian explosion. The Ediacaran Weng'an biota in South China hosts exceptionally preserved eukaryote fossils, including various acanthomorphic acritarchs, pseudoparenchymatous thalli, tubular microfossils, and spheroidal fossils such as Megasphaera, Helicoforamina, Spiralicellula, and Caveasphaera. Many of these fossils have been interpreted as multicellular eukaryotes, although alternative interpretations have also been proposed. In this review, we critically examine these various interpretations, focusing particularly on Megasphaera, which has been variously interpreted as a sulfur-oxidizing bacterium, a unicellular protist, a mesomycetozoean-like holozoan, a volvocine green alga, a stem-group animal, or a crown-group animal. We conclude that Megasphaera is a multicellular eukaryote with evidence for cell-to-cell adhesion, a flexible membrane unconstrained by a rigid cell wall, spatial cellular differentiation, germ–soma separation, and programmed cell death. These features are inconsistent with the bacterium, unicellular protist, and mesomycetozoean-like holozoan interpretations. Thus, the surviving hypotheses, particularly the stem-group animal and algal interpretations, should be further tested with additional evidence. The Weng'an biota also hosts cellularly differentiated pseudoparenchymatous thalli with specialized reproductive structures indicative of an affinity with florideophyte red algae. The other Weng'an fossils reviewed here may also be multicellular eukaryotes, although direct cellular evidence is lacking in some and phylogenetic affinities are poorly constrained in others. The Weng'an biota offers many research opportunities to resolve the life histories and phylogenetic diversity of early multicellular eukaryotes and to illuminate the evolutionary prelude to the Cambrian explosion.


2015 ◽  
Vol 11 (10) ◽  
pp. 20150763 ◽  
Author(s):  
Luke Parry ◽  
Jakob Vinther ◽  
Gregory D. Edgecombe

The oldest fossil annelids come from the Early Cambrian Sirius Passet and Guanshan biotas and Middle Cambrian Burgess Shale. While these are among the best preserved polychaete fossils, their relationship to living taxa is contentious, having been interpreted either as members of extant clades or as a grade outside the crown group. New morphological observations from five Cambrian species include the oldest polychaete with head appendages, a new specimen of Pygocirrus from Sirius Passet, and an undescribed form from the Burgess Shale. We propose that the palps of Canadia are on an anterior segment bearing neuropodia and that the head of Phragmochaeta is formed of a segment bearing biramous parapodia and chaetae. The unusual anatomy of these taxa suggests that the head is not differentiated into a prostomium and peristomium, that palps are derived from a modified parapodium and that the annelid head was originally a parapodium-bearing segment. Canadia , Phragmochaeta and the Marble Canyon annelid share the presence of protective notochaetae, interpreted as a primitive character state subsequently lost in Pygocirrus and Burgessochaeta , in which the head is clearly differentiated from the trunk.


2015 ◽  
Vol 66 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Peter Vršanský ◽  
Günter Bechly

Abstract We describe a new extinct lineage Manipulatoridae (new family) of cockroaches from the Upper Cretaceous (Cenomanian) amber of Myanmar. Manipulator modificaputis gen. et sp. n. is a morphologically unique extinct cockroach that represents the first (of a total of 29 known worldwide) cockroach family reported exclusively from the Myanmar amber. This family represents an early side branch of the stem group of Mantodea (most probably a sister group of Eadiidae within Blattaria/Corydioidea) because it has some synapomorphies with the Mantodea (including the stem group and Eadiidae). This family also retains symplesiomorphies that exclude a position in the crown group, and furthermore has unique autapomorphies that exclude a position as a direct ancestor of Mantodea. The unique adaptations such as strongly elongated extremities and freely movable head on a long neck suggest that these animals were pursuit predators. Five additional specimens (including two immatures) reported from the Myanmar amber suggest that this group was relatively rare but belonged to the indigenous and autochthonous inhabitants of the ancient amber forest of the Myanmar region.


Author(s):  
Per Erik Ahlberg ◽  
Jennifer A. Clack

AbstractThe lower jaw of the Devonian tetrapod Acanthostega is described for the first time. Redescriptions are provided for the lower jaws of the elpistostegid Panderichthys, the Devonian tetrapods Elginerpeton, Obruchevichthys, Metaxygnathus, Ventastega and Ichthyostega, and the Carboniferous tetrapods Crassigyrinus, Megalocephalus and Gephyrostegus. The character distri- butions thus revealed differ considerably from previous accounts, particularly in the wide distribution of certain primitive characters. Meckelian ossification in the middle part of the jaw is widespread among Devonian tetrapods, being demonstrably absent only in Acanthostega. Among Carboniferous tetrapods, a tooth-bearing parasymphysial plate is shown to be present in Crassigyrinus and Megalocephalus (having already been demonstrated by other authors in Whatcheeria and Greererpeton). A phylogenetic analysis of 26 early tetrapods including all the aforementioned genera, scored for 51 lower jaw characters, produces at least 2,500 equally parsimonious trees. However, the lack of resolution lies largely in a big top end polychotomy containing anthracosaurs, temnospondyls, seymouriamorphs, microsaurs and a nectridean-amniote clade. Below this polycho- tomy, which may correspond approximately to the tetrapod crown group, there is a well-resolved stem-group containing, in descending order, Megalocephalus, Greererpeton, Crassigyrinus, (jaws associated with) Tulerpeton, Whatcheeria, Acanthostega, Metaxygnathus, Ichthyostega, Ventastega and Metaxygnathus (unresolved), an Elginerpeton-Obruchevichthys clade, and Panderichthys. This conflicts with recently published phylogenies by Coates and Lebedev & Coates, which place Tulerpeton and all post-Devonian tetrapods in the amphibian or amniote branches of the tetrapod crown group.


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