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Response of Antarctic cryoconite microbial communities to light
Microbial communities on polar glacier surfaces are found dispersed on the ice surface, or concentrated in cryoconite holes and cryolakes, which are accumulations of debris covered by a layer of ice for some or all of the year. The ice lid limits the penetration of photosynthetically available radia...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864406/ https://www.ncbi.nlm.nih.gov/pubmed/27095815 http://dx.doi.org/10.1093/femsec/fiw076 |
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author | Bagshaw, Elizabeth A. Wadham, Jemma L. Tranter, Martyn Perkins, Rupert Morgan, Alistair Williamson, Christopher J. Fountain, Andrew G. Fitzsimons, Sean Dubnick, Ashley |
author_facet | Bagshaw, Elizabeth A. Wadham, Jemma L. Tranter, Martyn Perkins, Rupert Morgan, Alistair Williamson, Christopher J. Fountain, Andrew G. Fitzsimons, Sean Dubnick, Ashley |
author_sort | Bagshaw, Elizabeth A. |
collection | PubMed |
description | Microbial communities on polar glacier surfaces are found dispersed on the ice surface, or concentrated in cryoconite holes and cryolakes, which are accumulations of debris covered by a layer of ice for some or all of the year. The ice lid limits the penetration of photosynthetically available radiation (PAR) to the sediment layer, since the ice attenuates up to 99% of incoming radiation. This suite of field and laboratory experiments demonstrates that PAR is an important control on primary production in cryoconite and cryolake ecosystems. Increased light intensity increased efficiency of primary production in controlled laboratory incubations of debris from the surface of Joyce Glacier, McMurdo Dry Valleys, Antarctica. However, when light intensity was increased to levels near that received on the ice surface, without the protection of an ice lid, efficiency decreased and measurements of photophysiology showed that the communities suffered light stress. The communities are therefore well adapted to low light levels. Comparison with Arctic cryoconite communities, which are typically not covered by an ice lid for the majority of the ablation season, showed that these organisms were also stressed by high light, so they must employ strategies to protect against photodamage. |
format | Online Article Text |
id | pubmed-4864406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48644062016-05-13 Response of Antarctic cryoconite microbial communities to light Bagshaw, Elizabeth A. Wadham, Jemma L. Tranter, Martyn Perkins, Rupert Morgan, Alistair Williamson, Christopher J. Fountain, Andrew G. Fitzsimons, Sean Dubnick, Ashley FEMS Microbiol Ecol Research Article Microbial communities on polar glacier surfaces are found dispersed on the ice surface, or concentrated in cryoconite holes and cryolakes, which are accumulations of debris covered by a layer of ice for some or all of the year. The ice lid limits the penetration of photosynthetically available radiation (PAR) to the sediment layer, since the ice attenuates up to 99% of incoming radiation. This suite of field and laboratory experiments demonstrates that PAR is an important control on primary production in cryoconite and cryolake ecosystems. Increased light intensity increased efficiency of primary production in controlled laboratory incubations of debris from the surface of Joyce Glacier, McMurdo Dry Valleys, Antarctica. However, when light intensity was increased to levels near that received on the ice surface, without the protection of an ice lid, efficiency decreased and measurements of photophysiology showed that the communities suffered light stress. The communities are therefore well adapted to low light levels. Comparison with Arctic cryoconite communities, which are typically not covered by an ice lid for the majority of the ablation season, showed that these organisms were also stressed by high light, so they must employ strategies to protect against photodamage. Oxford University Press 2016-04-18 2016-06-01 /pmc/articles/PMC4864406/ /pubmed/27095815 http://dx.doi.org/10.1093/femsec/fiw076 Text en © FEMS 2016. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bagshaw, Elizabeth A. Wadham, Jemma L. Tranter, Martyn Perkins, Rupert Morgan, Alistair Williamson, Christopher J. Fountain, Andrew G. Fitzsimons, Sean Dubnick, Ashley Response of Antarctic cryoconite microbial communities to light |
title | Response of Antarctic cryoconite microbial communities to light |
title_full | Response of Antarctic cryoconite microbial communities to light |
title_fullStr | Response of Antarctic cryoconite microbial communities to light |
title_full_unstemmed | Response of Antarctic cryoconite microbial communities to light |
title_short | Response of Antarctic cryoconite microbial communities to light |
title_sort | response of antarctic cryoconite microbial communities to light |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4864406/ https://www.ncbi.nlm.nih.gov/pubmed/27095815 http://dx.doi.org/10.1093/femsec/fiw076 |
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