Cargando…
Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle
The holotype (MHM-K2) of the Eocene cheloniine Tasbacka danica is arguably one of the best preserved juvenile fossil sea turtles on record. Notwithstanding compactional flattening, the specimen is virtually intact, comprising a fully articulated skeleton exposed in dorsal view. MHM-K2 also preserves...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645316/ https://www.ncbi.nlm.nih.gov/pubmed/29042651 http://dx.doi.org/10.1038/s41598-017-13187-5 |
_version_ | 1783271861941960704 |
---|---|
author | Lindgren, Johan Kuriyama, Takeo Madsen, Henrik Sjövall, Peter Zheng, Wenxia Uvdal, Per Engdahl, Anders Moyer, Alison E. Gren, Johan A. Kamezaki, Naoki Ueno, Shintaro Schweitzer, Mary H. |
author_facet | Lindgren, Johan Kuriyama, Takeo Madsen, Henrik Sjövall, Peter Zheng, Wenxia Uvdal, Per Engdahl, Anders Moyer, Alison E. Gren, Johan A. Kamezaki, Naoki Ueno, Shintaro Schweitzer, Mary H. |
author_sort | Lindgren, Johan |
collection | PubMed |
description | The holotype (MHM-K2) of the Eocene cheloniine Tasbacka danica is arguably one of the best preserved juvenile fossil sea turtles on record. Notwithstanding compactional flattening, the specimen is virtually intact, comprising a fully articulated skeleton exposed in dorsal view. MHM-K2 also preserves, with great fidelity, soft tissue traces visible as a sharply delineated carbon film around the bones and marginal scutes along the edge of the carapace. Here we show that the extraordinary preservation of the type of T. danica goes beyond gross morphology to include ultrastructural details and labile molecular components of the once-living animal. Haemoglobin-derived compounds, eumelanic pigments and proteinaceous materials retaining the immunological characteristics of sauropsid-specific β-keratin and tropomyosin were detected in tissues containing remnant melanosomes and decayed keratin plates. The preserved organics represent condensed remains of the cornified epidermis and, likely also, deeper anatomical features, and provide direct chemical evidence that adaptive melanism – a biological means used by extant sea turtle hatchlings to elevate metabolic and growth rates – had evolved 54 million years ago. |
format | Online Article Text |
id | pubmed-5645316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56453162017-10-26 Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle Lindgren, Johan Kuriyama, Takeo Madsen, Henrik Sjövall, Peter Zheng, Wenxia Uvdal, Per Engdahl, Anders Moyer, Alison E. Gren, Johan A. Kamezaki, Naoki Ueno, Shintaro Schweitzer, Mary H. Sci Rep Article The holotype (MHM-K2) of the Eocene cheloniine Tasbacka danica is arguably one of the best preserved juvenile fossil sea turtles on record. Notwithstanding compactional flattening, the specimen is virtually intact, comprising a fully articulated skeleton exposed in dorsal view. MHM-K2 also preserves, with great fidelity, soft tissue traces visible as a sharply delineated carbon film around the bones and marginal scutes along the edge of the carapace. Here we show that the extraordinary preservation of the type of T. danica goes beyond gross morphology to include ultrastructural details and labile molecular components of the once-living animal. Haemoglobin-derived compounds, eumelanic pigments and proteinaceous materials retaining the immunological characteristics of sauropsid-specific β-keratin and tropomyosin were detected in tissues containing remnant melanosomes and decayed keratin plates. The preserved organics represent condensed remains of the cornified epidermis and, likely also, deeper anatomical features, and provide direct chemical evidence that adaptive melanism – a biological means used by extant sea turtle hatchlings to elevate metabolic and growth rates – had evolved 54 million years ago. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5645316/ /pubmed/29042651 http://dx.doi.org/10.1038/s41598-017-13187-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lindgren, Johan Kuriyama, Takeo Madsen, Henrik Sjövall, Peter Zheng, Wenxia Uvdal, Per Engdahl, Anders Moyer, Alison E. Gren, Johan A. Kamezaki, Naoki Ueno, Shintaro Schweitzer, Mary H. Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title | Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title_full | Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title_fullStr | Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title_full_unstemmed | Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title_short | Biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
title_sort | biochemistry and adaptive colouration of an exceptionally preserved juvenile fossil sea turtle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645316/ https://www.ncbi.nlm.nih.gov/pubmed/29042651 http://dx.doi.org/10.1038/s41598-017-13187-5 |
work_keys_str_mv | AT lindgrenjohan biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT kuriyamatakeo biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT madsenhenrik biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT sjovallpeter biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT zhengwenxia biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT uvdalper biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT engdahlanders biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT moyeralisone biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT grenjohana biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT kamezakinaoki biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT uenoshintaro biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle AT schweitzermaryh biochemistryandadaptivecolourationofanexceptionallypreservedjuvenilefossilseaturtle |