Cargando…

The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans

Understanding the role of biology in planetary evolution remains an outstanding challenge to geobiologists. Progress towards unravelling this puzzle for Earth is hindered by the scarcity of well‐preserved rocks from the Archean (4.0 to 2.5 Gyr ago) and Proterozoic (2.5 to 0.5 Gyr ago) Eons. In addit...

Descripción completa

Detalles Bibliográficos
Autores principales: Hamilton, Trinity L., Bryant, Donald A., Macalady, Jennifer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019231/
https://www.ncbi.nlm.nih.gov/pubmed/26549614
http://dx.doi.org/10.1111/1462-2920.13118
_version_ 1782453020183756800
author Hamilton, Trinity L.
Bryant, Donald A.
Macalady, Jennifer L.
author_facet Hamilton, Trinity L.
Bryant, Donald A.
Macalady, Jennifer L.
author_sort Hamilton, Trinity L.
collection PubMed
description Understanding the role of biology in planetary evolution remains an outstanding challenge to geobiologists. Progress towards unravelling this puzzle for Earth is hindered by the scarcity of well‐preserved rocks from the Archean (4.0 to 2.5 Gyr ago) and Proterozoic (2.5 to 0.5 Gyr ago) Eons. In addition, the microscopic life that dominated Earth's biota for most of its history left a poor fossil record, consisting primarily of lithified microbial mats, rare microbial body fossils and membrane‐derived hydrocarbon molecules that are still challenging to interpret. However, it is clear from the sulfur isotope record and other geochemical proxies that the production of oxygen or oxidizing power radically changed Earth's surface and atmosphere during the Proterozoic Eon, pushing it away from the more reducing conditions prevalent during the Archean. In addition to ancient rocks, our reconstruction of Earth's redox evolution is informed by our knowledge of biogeochemical cycles catalysed by extant biota. The emergence of oxygenic photosynthesis in ancient cyanobacteria represents one of the most impressive microbial innovations in Earth's history, and oxygenic photosynthesis is the largest source of O (2) in the atmosphere today. Thus the study of microbial metabolisms and evolution provides an important link between extant biota and the clues from the geologic record. Here, we consider the physiology of cyanobacteria (the only microorganisms capable of oxygenic photosynthesis), their co‐occurrence with anoxygenic phototrophs in a variety of environments and their persistence in low‐oxygen environments, including in water columns as well as mats, throughout much of Earth's history. We examine insights gained from both the rock record and cyanobacteria presently living in early Earth analogue ecosystems and synthesize current knowledge of these ancient microbial mediators in planetary redox evolution. Our analysis supports the hypothesis that anoxygenic photosynthesis, including the activity of metabolically versatile cyanobacteria, played an important role in delaying the oxygenation of Earth's surface ocean during the Proterozoic Eon.
format Online
Article
Text
id pubmed-5019231
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-50192312016-09-23 The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans Hamilton, Trinity L. Bryant, Donald A. Macalady, Jennifer L. Environ Microbiol Minireviews Understanding the role of biology in planetary evolution remains an outstanding challenge to geobiologists. Progress towards unravelling this puzzle for Earth is hindered by the scarcity of well‐preserved rocks from the Archean (4.0 to 2.5 Gyr ago) and Proterozoic (2.5 to 0.5 Gyr ago) Eons. In addition, the microscopic life that dominated Earth's biota for most of its history left a poor fossil record, consisting primarily of lithified microbial mats, rare microbial body fossils and membrane‐derived hydrocarbon molecules that are still challenging to interpret. However, it is clear from the sulfur isotope record and other geochemical proxies that the production of oxygen or oxidizing power radically changed Earth's surface and atmosphere during the Proterozoic Eon, pushing it away from the more reducing conditions prevalent during the Archean. In addition to ancient rocks, our reconstruction of Earth's redox evolution is informed by our knowledge of biogeochemical cycles catalysed by extant biota. The emergence of oxygenic photosynthesis in ancient cyanobacteria represents one of the most impressive microbial innovations in Earth's history, and oxygenic photosynthesis is the largest source of O (2) in the atmosphere today. Thus the study of microbial metabolisms and evolution provides an important link between extant biota and the clues from the geologic record. Here, we consider the physiology of cyanobacteria (the only microorganisms capable of oxygenic photosynthesis), their co‐occurrence with anoxygenic phototrophs in a variety of environments and their persistence in low‐oxygen environments, including in water columns as well as mats, throughout much of Earth's history. We examine insights gained from both the rock record and cyanobacteria presently living in early Earth analogue ecosystems and synthesize current knowledge of these ancient microbial mediators in planetary redox evolution. Our analysis supports the hypothesis that anoxygenic photosynthesis, including the activity of metabolically versatile cyanobacteria, played an important role in delaying the oxygenation of Earth's surface ocean during the Proterozoic Eon. John Wiley and Sons Inc. 2016-02 2015-12-21 /pmc/articles/PMC5019231/ /pubmed/26549614 http://dx.doi.org/10.1111/1462-2920.13118 Text en © 2015 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Minireviews
Hamilton, Trinity L.
Bryant, Donald A.
Macalady, Jennifer L.
The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title_full The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title_fullStr The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title_full_unstemmed The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title_short The role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen Proterozoic oceans
title_sort role of biology in planetary evolution: cyanobacterial primary production in low‐oxygen proterozoic oceans
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019231/
https://www.ncbi.nlm.nih.gov/pubmed/26549614
http://dx.doi.org/10.1111/1462-2920.13118
work_keys_str_mv AT hamiltontrinityl theroleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans
AT bryantdonalda theroleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans
AT macaladyjenniferl theroleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans
AT hamiltontrinityl roleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans
AT bryantdonalda roleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans
AT macaladyjenniferl roleofbiologyinplanetaryevolutioncyanobacterialprimaryproductioninlowoxygenproterozoicoceans