===
Free pdf:
Salamanders and newts (urodeles) are often used as a model system to elucidate the evolution of tetrapod locomotion. Studies range from detailed descriptions of musculoskeletal anatomy and segment kinematics, to bone loading mechanics and central pattern generators. A further area of interest has been in vivo muscle activity patterns, measured through electromyography (EMG). However, most prior EMG work has primarily focused on muscles of the forelimb or hindlimb in specific species or the axial system in others. Here we present data on forelimb, hindlimb, and epaxial muscle activity patterns in one species, Salamandra salamandra, during steady state walking. The data are calibrated to limb stride cycle events (stance phase, swing phase), allowing direct comparisons to homologous muscle activation patterns recorded for other walking tetrapods (e.g. lizards, alligators, turtles, mammals). Results demonstrate that Salamandra has similar walking kinematics and muscle activity patterns to other urodele species, but that interspecies variation does exist. In the forelimb, both the m. dorsalis scapulae and m. latissimus dorsi are active for 80% of the forelimb swing phase, while the m. anconaeus humeralis lateralis is active at the swing-stance phase transition and continues through 86% of the stance phase. In the hindlimb, both the m. puboischiofemoralis internus and m. extensor iliotibialis anterior are active for 30% of the hindlimb swing phase, while the m. caudofemoralis is active 65% through the swing phase and remains active for most of the stance phase. With respect to the axial system, both the anterior and posterior m. dorsalis trunci display two activation bursts, a pattern consistent with stabilization and rotation of the pectoral and pelvic girdle. In support of previous assertions, comparison of Salamandra muscle activity timings to other walking tetrapods revealed broad-scale similarities, potentially indicating conservation of some aspects of neuromuscular function across tetrapods. Our data provides the foundation for building and testing dynamic simulations of fire salamander locomotor biomechanics to better understand musculoskeletal function. It could also be applied to future musculoskeletal simulations of extinct species to explore the evolution of tetrapod locomotion across deep-time.
=====
Anurans (frogs and toads) have a unique pelvic and hindlimb skeleton among tetrapods. Although their distinct body plan is primarily associated with saltation, anuran species vary in their primary locomotor mode (e.g., walkers, hoppers, jumpers, and swimmers) and are found in a wide array of microhabitats (e.g., burrowing, terrestrial, arboreal, and aquatic) with varying functional demands. Given their largely conserved body plan, morphological adaptation to these diverse niches likely results from more fine-scale morphological change. Our study determines how shape differences in Anura's unique pelvic and hindlimb skeletal structures vary with microhabitat, locomotor mode, and jumping ability. Using microCT scans of preserved specimens from museum collections, we added 3D landmarks to the pelvic and hindlimb skeleton of 230 anuran species. In addition, we compiled microhabitat and locomotor data from the literature for these species that span 52 of the 55 families of frogs and ~210 million years of anuran evolution. Using this robust dataset, we examine the relationship between pelvic and hindlimb morphology and phylogenetic history, allometry, microhabitat, and locomotor mode. We find pelvic and hindlimb changes associated with shifts in microhabitat ("ecomorphs"â) and locomotor mode ("locomorphs") and directly relate those morphological changes to the jumping ability of individual species. We also reveal how individual bones vary in evolutionary rate and their association with phylogeny, body size, microhabitat, and locomotor mode. Our findings uncover previously undocumented morphological variation related to anuran ecological and locomotor diversification and link that variation to differences in jumping ability among species.
====
Genome size variation in vertebrates reflects an amazing amount of genetic and genomic diversity. Câvalue (genome size) ranges from 0.4 picograms (pg) in pufferfish to 133âpg in the marbled lungfish. Most vertebrate lineages have characteristic average Câvalues with restricted ranges. Amphibia, in contrast, represent an extreme: Câvalues in salamanders range from around 13 to over 122âpg; in frogs, they range from under 1 to over 13âpg. Why would closely related lineages and species have such dramatic differences in Câvalue? A number of theories have been proposed to account for the extreme range in genome size found in all eukaryote taxa. The amphibia not only have a wide range of Câvalues, but they also have a correspondingly wide range of life history traits and other phenotypes such as neoteny and limb regeneration. This remarkable class of vertebrate thus provides a unique model system for addressing evolutionary and physiological hypotheses.
Key Concepts
Junk DNA (retroviruses and DNA transposons) infected the ancestral eukaryote cell and established, together with mitochondria, a symbiotic relationship from which all other eukaryotic life forms emerged.
The host response to the original infection was adaptive rather than purifyingly selective: junk DNA provided the conditions for the emergence of a checkpoint guardian of the genome and correspondingly enhanced genome stability.
As genome size expanded, DNA repair systems increased in efficiency, allowing for the acquisition of new genes and new adaptations.
DNA replication programs and gene transcription programs reorganised as genome size either increased or decreased over evolutionary time.
Species richness negatively correlates with genome stability and positively correlates with karyotype diversity within specific lineages.
DNA damage response and repair (DDR) programs have evolved differentially in r and Kâstrategists: large body organisms have enhanced DDRs compared to small body, shortâlived organisms, and hence they tend to have more deterministic and organised replication programs.
Junk DNA serves as a substrate for the DDR to protect the cell against âmitotic catastropheâ.
Junk DNA serves as a scaffold for the formation of facultative heterochromatin during development and speciation,and hence participates in the global tissueâspecific and speciesâdependent transcription programs.
=========
Free pdf:
Ilja Kogan, Andrea Tintori & Martin Licht (2020)
Locomotor function of scales and axial skeleton in Middle-Late Triassic species of Saurichthys (Actinopterygii).
Rivista Italiana di Paleontologia e Stratigrafia 126(2): 475-498
https://riviste.unimi.it/index.php/RIPS/article/view/13551Free pdf:
https://riviste.unimi.it/index.php/RIPS/article/view/13551/12651Starting in the Late Permian, the âTriassic osteichthyan revolutionâ gave rise to several new morphotypes of actinopterygians, including the iconic barracuda-shaped predator Saurichthys. About 50 species, from 10 cm to over 1.5 m long, are known from mainly marine deposits worldwide. Despite current interest in Saurichthys, freshwater species and those from late Middle to early Late Triassic remain understudied. We document the postcranial morphology of three small to mid-sized (15â45 cm) species from this timeframe represented by sufficiently complete individuals: Saurichthys orientalis Sytchevskaya, 1999, from lacustrine deposits of the Madygen Formation (late Ladinian/Carnian); S. striolatus (Bronn, 1858) from the fully marine Predil Limestone (early Carnian); and S. calcaratus Griffith, 1977, from the terrigenously influenced coastal environment of the Lunz Formation (middle Carnian). S. orientalis resembles early saurichthyids in having six rows of large, thick ganoid scales; fins with segmented lepidotrichia; and flank scales relating to dorsal vertebral elements as 1:2. S. calcaratus and S. striolatus share unsegmented fin rays and a reduced scale cover with well-ossified but narrow mid-dorsal and mid-ventral scales and small, thin flank scales, relating to the dorsal arcualia as 1:1. Ventral arcualia are first described for S. calcaratus and S. striolatus, where they change in shape and number at the abdominal-caudal transition. In all three species, force transmission to the tail fin is enhanced by the caudal peduncle strengthened by a stiff structure arising from interlocking or fusion of the last enlarged mid-dorsal and mid-ventral scales (scutes), while the vertebral column remains rather lightly built.
====
====
Free pdf:
David A. Kring, Sonia M. Tikoo, Martin Schmieder, Ulrich Riller, Mario Rebolledo-Vieyra, Sarah L. Simpson, Gordon R. Osinski, JÃrÃme Gattacceca, Axel Wittmann, Christina M. Verhagen, Charles S. Cockell, Marco J. L. Coolen, Fred J. Longstaffe, Sean P. S. Gulick, Joanna V. Morgan, Timothy J. Bralower, Elise Chenot, Gail L. Christeson, Philippe Claeys, Ludovic FerriÃre, Catalina Gebhardt, Kazuhisa Goto, Sophie L. Green, Heather Jones, Johanna Lofi, Christopher M. Lowery, RubÃn Ocampo-Torres, Ligia Perez-Cruz, Annemarie E. Pickersgill, H. Poelchau, Auriol S. P. Rae, Cornelia Rasmussen, Honami Sato, Jan Smit, Naotaka Tomioka, Jaime Urrutia-Fucugauchi, T. Whalen, Long Xiao and Kosei E. Yamaguchi (2020)
Probing the hydrothermal system of the Chicxulub impact crater.
Science Advances 6(22): eaaz3053
DOI: 10.1126/sciadv.aaz3053
https://advances.sciencemag.org/content/6/22/eaaz3053
Free pdf:
https://advances.sciencemag.org/content/6/22/eaaz3053/tab-pdfThe ~180-km-diameter Chicxulub peak-ring crater and ~240-km multiring basin, produced by the impact that terminated the Cretaceous, is the largest remaining intact impact basin on Earth. International Ocean Discovery Program (IODP) and International Continental Scientific Drilling Program (ICDP) Expedition 364 drilled to a depth of 1335 m below the sea floor into the peak ring, providing a unique opportunity to study the thermal and chemical modification of Earthâs crust caused by the impact. The recovered core shows the crater hosted a spatially extensive hydrothermal system that chemically and mineralogically modified ~1.4 Ã 105 km3 of Earthâs crust, a volume more than nine times that of the Yellowstone Caldera system. Initially, high temperatures of 300Â to 400ÂC and an independent geomagnetic polarity clock indicate the hydrothermal system was long lived, in excess of 106 years.
News:
A steaming cauldron follows the dinosaurs' demise