Cargando…

Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization

Exceptionally preserved fossils provide major insights into the evolutionary history of life. Microbial activity is thought to play a pivotal role in both the decay of organisms and the preservation of soft tissue in the fossil record, though this has been the subject of very little experimental inv...

Descripción completa

Detalles Bibliográficos
Autores principales: Butler, Aodhán D., Cunningham, John A., Budd, Graham E., Donoghue, Philip C. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455810/
https://www.ncbi.nlm.nih.gov/pubmed/25972468
http://dx.doi.org/10.1098/rspb.2015.0476
_version_ 1782374775272767488
author Butler, Aodhán D.
Cunningham, John A.
Budd, Graham E.
Donoghue, Philip C. J.
author_facet Butler, Aodhán D.
Cunningham, John A.
Budd, Graham E.
Donoghue, Philip C. J.
author_sort Butler, Aodhán D.
collection PubMed
description Exceptionally preserved fossils provide major insights into the evolutionary history of life. Microbial activity is thought to play a pivotal role in both the decay of organisms and the preservation of soft tissue in the fossil record, though this has been the subject of very little experimental investigation. To remedy this, we undertook an experimental study of the decay of the brine shrimp Artemia, examining the roles of autolysis, microbial activity, oxygen diffusion and reducing conditions. Our findings indicate that endogenous gut bacteria are the main factor controlling decay. Following gut wall rupture, but prior to cuticle failure, gut-derived microbes spread into the body cavity, consuming tissues and forming biofilms capable of mediating authigenic mineralization, that pseudomorph tissues and structures such as limbs and the haemocoel. These observations explain patterns observed in exceptionally preserved fossil arthropods. For example, guts are preserved relatively frequently, while preservation of other internal anatomy is rare. They also suggest that gut-derived microbes play a key role in the preservation of internal anatomy and that differential preservation between exceptional deposits might be because of factors that control autolysis and microbial activity. The findings also suggest that the evolution of a through gut and its bacterial microflora increased the potential for exceptional fossil preservation in bilaterians, providing one explanation for the extreme rarity of internal preservation in those animals that lack a through gut.
format Online
Article
Text
id pubmed-4455810
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-44558102015-06-12 Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization Butler, Aodhán D. Cunningham, John A. Budd, Graham E. Donoghue, Philip C. J. Proc Biol Sci Research Articles Exceptionally preserved fossils provide major insights into the evolutionary history of life. Microbial activity is thought to play a pivotal role in both the decay of organisms and the preservation of soft tissue in the fossil record, though this has been the subject of very little experimental investigation. To remedy this, we undertook an experimental study of the decay of the brine shrimp Artemia, examining the roles of autolysis, microbial activity, oxygen diffusion and reducing conditions. Our findings indicate that endogenous gut bacteria are the main factor controlling decay. Following gut wall rupture, but prior to cuticle failure, gut-derived microbes spread into the body cavity, consuming tissues and forming biofilms capable of mediating authigenic mineralization, that pseudomorph tissues and structures such as limbs and the haemocoel. These observations explain patterns observed in exceptionally preserved fossil arthropods. For example, guts are preserved relatively frequently, while preservation of other internal anatomy is rare. They also suggest that gut-derived microbes play a key role in the preservation of internal anatomy and that differential preservation between exceptional deposits might be because of factors that control autolysis and microbial activity. The findings also suggest that the evolution of a through gut and its bacterial microflora increased the potential for exceptional fossil preservation in bilaterians, providing one explanation for the extreme rarity of internal preservation in those animals that lack a through gut. The Royal Society 2015-06-07 /pmc/articles/PMC4455810/ /pubmed/25972468 http://dx.doi.org/10.1098/rspb.2015.0476 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Butler, Aodhán D.
Cunningham, John A.
Budd, Graham E.
Donoghue, Philip C. J.
Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title_full Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title_fullStr Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title_full_unstemmed Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title_short Experimental taphonomy of Artemia reveals the role of endogenous microbes in mediating decay and fossilization
title_sort experimental taphonomy of artemia reveals the role of endogenous microbes in mediating decay and fossilization
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455810/
https://www.ncbi.nlm.nih.gov/pubmed/25972468
http://dx.doi.org/10.1098/rspb.2015.0476
work_keys_str_mv AT butleraodhand experimentaltaphonomyofartemiarevealstheroleofendogenousmicrobesinmediatingdecayandfossilization
AT cunninghamjohna experimentaltaphonomyofartemiarevealstheroleofendogenousmicrobesinmediatingdecayandfossilization
AT buddgrahame experimentaltaphonomyofartemiarevealstheroleofendogenousmicrobesinmediatingdecayandfossilization
AT donoghuephilipcj experimentaltaphonomyofartemiarevealstheroleofendogenousmicrobesinmediatingdecayandfossilization