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[dinosaur] Oldest fossilized fish heart + Evolution of head-trunk interface in tetrapods (free pdfs)

Ben Creisler

New papers in open access:

Lara Maldanis, Murilo Carvalho, Mariana Ramos Almeida, Francisco Idalécio Freitas, José Artur Ferreira Gomes de Andrade, Rafael Silva Nunes, Carlos Eduardo Rochitte, Ronei Jesus Poppi, Raul Oliveira Freitas, Fábio Rodrigues, Sandra Siljeström, Frederico Alves Lima, Douglas Galante, Ismar S Carvalho, Carlos Alberto Perez, Marcelo Rodrigues de Carvalho, Jefferson Bettini, Vincent Fernandez & José Xavier-Neto  (2016)
Heart fossilization is possible and informs the evolution of cardiac outflow tract in vertebrates.
eLife 2016; 5:e14698
DOI: http: // dx.doi.org/10.7554/eLife.14698
https: // elifesciences.org/content/5/e14698v1/article-info

Elucidating cardiac evolution has been frustrated by lack of fossils. One celebrated enigma in cardiac evolution involves the transition from a cardiac outflow tract dominated by a multi-valved conus arteriosus in basal actinopterygians, to an outflow tract commanded by the non-valved, elastic, bulbus arteriosus in higher actinopterygians. We demonstrate that cardiac preservation is possible in the extinct fish Rhacolepis buccalis from the Brazilian Cretaceous. Using X-ray synchrotron microtomography, we show that Rhacolepis fossils display hearts with a conus arteriosus containing at least five valve rows. This represents a transitional morphology between the primitive, multivalvar, conal condition and the derived, monovalvar, bulbar state of the outflow tract in modern actinopterygians. Our data rescue a long-lost cardiac phenotype (119-113 Ma) and suggest that outflow tract simplification in actinopterygians is compatible with a gradual, rather than a drastic saltation event. Overall, our results demonstrate the feasibility of studying cardiac evolution in fossils.


https: // theconversation.com/the-first-fossilised-heart-ever-found-in-a-prehistoric-animal-57204


Elizabeth M Sefton,  Bhart-Anjan S Bhullar, Zahra Mohaddes & James Hanken (2016)
Evolution of the head-trunk interface in tetrapod vertebrates.
eLife 2016;5:e09972
DOI: http: // dx.doi.org/10.7554/eLife.09972
https: // elifesciences.org/content/5/e09972v1

Vertebrate neck musculature spans the transition zone between head and trunk. The extent to which the cucullaris muscle is a cranial muscle allied with the gill levators of anamniotes or is instead a trunk muscle is an ongoing debate. Novel computed tomography datasets reveal broad conservation of the cucullaris in gnathostomes, including coelacanth and caecilian, two sarcopterygians previously thought to lack it. In chicken, lateral plate mesoderm (LPM) adjacent to occipital somites is a recently identified embryonic source of cervical musculature. We fate-map this mesoderm in the axolotl (Ambystoma mexicanum), which retains external gills, and demonstrate its contribution to posterior gill-levator muscles and the cucullaris. Accordingly, LPM adjacent to the occipital somites should be regarded as posterior cranial mesoderm. The axial position of the head-trunk border in axolotl is congruent between LPM and somitic mesoderm, unlike in chicken and possibly other amniotes.


Also, NOT in open access:

J. Andrew Gillis & Brian K. Hall (2016)
A shared role for sonic hedgehog signalling in patterning chondrichthyan gill arch appendages and tetrapod limbs.
Development 2016 143: 1313-1317 
doi: 10.1242/dev.133884
http: // dev.biologists.org/content/143/8/1313

Chondrichthyans (sharks, skates, rays and holocephalans) possess paired appendages that project laterally from their gill arches, known as branchial rays. This led Carl Gegenbaur to propose that paired fins (and hence tetrapod limbs) originally evolved via transformation of gill arches. Tetrapod limbs are patterned by a sonic hedgehog (Shh)-expressing signalling centre known as the zone of polarising activity, which establishes the anteroposterior axis of the limb bud and maintains proliferative expansion of limb endoskeletal progenitors. Here, we use loss-of-function, label-retention and fate-mapping approaches in the little skate to demonstrate that Shh secretion from a signalling centre in the developing gill arches establishes gill arch anteroposterior polarity and maintains the proliferative expansion of branchial ray endoskeletal progenitor cells. These findings highlight striking parallels in the axial patterning mechanisms employed by chondrichthyan branchial rays and paired fins/limbs, and provide mechanistic insight into the anatomical foundation of Gegenbaur's gill arch hypothesis.