Effects of natural and human-induced hypoxia on coastal benthos

Coastal hypoxia (defined here as <1.42 ml L−1; 62.5 μM; 2 mg L−1, approx. 30% oxygen saturation) develops seasonally in many estuaries, fjords, and along open coasts as a result of natural upwelling or from anthropogenic eutrophication induced by riverine nutrient inputs. Permanent hypoxia occurs...

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Published in:Biogeosciences
Main Authors: L.A. Levin, W. Ekau, A.J. Gooday, F. Jorissen, J.J. Middelburg, S.W.A. Naqvi, C. Neira, N.N. Rabalais, J. Zhang
Format: Article in Journal/Newspaper
Language:English
Published: European Geosciences Union 2009
Subjects:
Online Access:http://okina.univ-angers.fr/publications/ua3864
https://doi.org/10.5194/bg-6-2063-2009
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spelling ftunivangokina:oai:okina.univ-angers.fr:3864 2023-05-15T17:37:19+02:00 Effects of natural and human-induced hypoxia on coastal benthos L.A. Levin W. Ekau A.J. Gooday F. Jorissen J.J. Middelburg S.W.A. Naqvi C. Neira N.N. Rabalais J. Zhang 2009 http://okina.univ-angers.fr/publications/ua3864 https://doi.org/10.5194/bg-6-2063-2009 eng eng European Geosciences Union Biogeosciences Article scientifique dans une revue à comité de lecture 2009 ftunivangokina https://doi.org/10.5194/bg-6-2063-2009 2017-04-13T17:49:00Z Coastal hypoxia (defined here as <1.42 ml L−1; 62.5 μM; 2 mg L−1, approx. 30% oxygen saturation) develops seasonally in many estuaries, fjords, and along open coasts as a result of natural upwelling or from anthropogenic eutrophication induced by riverine nutrient inputs. Permanent hypoxia occurs naturally in some isolated seas and marine basins as well as in open slope oxygen minimum zones. Responses of benthos to hypoxia depend on the duration, predictability, and intensity of oxygen depletion and on whether H2S is formed. Under suboxic conditions, large mats of filamentous sulfide oxidizing bacteria cover the seabed and consume sulfide. They are hypothesized to provide a detoxified microhabitat for eukaryotic benthic communities. Calcareous foraminiferans and nematodes are particularly tolerant of low oxygen concentrations and may attain high densities and dominance, often in association with microbial mats. When oxygen is sufficient to support metazoans, small, soft-bodied invertebrates (typically annelids), often with short generation times and elaborate branchial structures, predominate. Large taxa are more sensitive than small taxa to hypoxia. Crustaceans and echinoderms are typically more sensitive to hypoxia, with lower oxygen thresholds, than annelids, sipunculans, molluscs and cnidarians. Mobile fish and shellfish will migrate away from low-oxygen areas. Within a species, early life stages may be more subject to oxygen stress than older life stages. Hypoxia alters both the structure and function of benthic communities, but effects may differ with regional hypoxia history. Human-caused hypoxia is generally linked to eutrophication, and occurs adjacent to watersheds with large populations or agricultural activities. Many occurrences are seasonal, within estuaries, fjords or enclosed seas of the North Atlantic and the NW Pacific Oceans. Benthic faunal responses, elicited at oxygen levels below 2 ml L−1, typically involve avoidance or mortality of large species and elevated abundances of enrichment opportunists, sometimes prior to population crashes. Areas of low oxygen persist seasonally or continuously beneath upwelling regions, associated with the upper parts of oxygen minimum zones (SE Pacific, W Africa, N Indian Ocean). These have a distribution largely distinct from eutrophic areas and support a resident fauna that is adapted to survive and reproduce at oxygen concentrations <0.5 ml L−1. Under both natural and eutrophication-caused hypoxia there is loss of diversity, through attrition of intolerant species and elevated dominance, as well as reductions in body size. These shifts in species composition and diversity yield altered trophic structure, energy flow pathways, and corresponding ecosystem services such as production, organic matter cycling and organic C burial. Increasingly the influences of nature and humans interact to generate or exacerbate hypoxia. A warmer ocean is more stratified, holds less oxygen, and may experience greater advection of oxygen-poor source waters, making new regions subject to hypoxia. Future understanding of benthic responses to hypoxia must be established in the context of global climate change and other human influences such as overfishing, pollution, disease, habitat loss, and species invasions. Article in Journal/Newspaper North Atlantic Université Angers: Okina (Open Knowledge, INformation, Access) Indian Pacific Biogeosciences 6 10 2063 2098
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collection Université Angers: Okina (Open Knowledge, INformation, Access)
op_collection_id ftunivangokina
language English
description Coastal hypoxia (defined here as <1.42 ml L−1; 62.5 μM; 2 mg L−1, approx. 30% oxygen saturation) develops seasonally in many estuaries, fjords, and along open coasts as a result of natural upwelling or from anthropogenic eutrophication induced by riverine nutrient inputs. Permanent hypoxia occurs naturally in some isolated seas and marine basins as well as in open slope oxygen minimum zones. Responses of benthos to hypoxia depend on the duration, predictability, and intensity of oxygen depletion and on whether H2S is formed. Under suboxic conditions, large mats of filamentous sulfide oxidizing bacteria cover the seabed and consume sulfide. They are hypothesized to provide a detoxified microhabitat for eukaryotic benthic communities. Calcareous foraminiferans and nematodes are particularly tolerant of low oxygen concentrations and may attain high densities and dominance, often in association with microbial mats. When oxygen is sufficient to support metazoans, small, soft-bodied invertebrates (typically annelids), often with short generation times and elaborate branchial structures, predominate. Large taxa are more sensitive than small taxa to hypoxia. Crustaceans and echinoderms are typically more sensitive to hypoxia, with lower oxygen thresholds, than annelids, sipunculans, molluscs and cnidarians. Mobile fish and shellfish will migrate away from low-oxygen areas. Within a species, early life stages may be more subject to oxygen stress than older life stages. Hypoxia alters both the structure and function of benthic communities, but effects may differ with regional hypoxia history. Human-caused hypoxia is generally linked to eutrophication, and occurs adjacent to watersheds with large populations or agricultural activities. Many occurrences are seasonal, within estuaries, fjords or enclosed seas of the North Atlantic and the NW Pacific Oceans. Benthic faunal responses, elicited at oxygen levels below 2 ml L−1, typically involve avoidance or mortality of large species and elevated abundances of enrichment opportunists, sometimes prior to population crashes. Areas of low oxygen persist seasonally or continuously beneath upwelling regions, associated with the upper parts of oxygen minimum zones (SE Pacific, W Africa, N Indian Ocean). These have a distribution largely distinct from eutrophic areas and support a resident fauna that is adapted to survive and reproduce at oxygen concentrations <0.5 ml L−1. Under both natural and eutrophication-caused hypoxia there is loss of diversity, through attrition of intolerant species and elevated dominance, as well as reductions in body size. These shifts in species composition and diversity yield altered trophic structure, energy flow pathways, and corresponding ecosystem services such as production, organic matter cycling and organic C burial. Increasingly the influences of nature and humans interact to generate or exacerbate hypoxia. A warmer ocean is more stratified, holds less oxygen, and may experience greater advection of oxygen-poor source waters, making new regions subject to hypoxia. Future understanding of benthic responses to hypoxia must be established in the context of global climate change and other human influences such as overfishing, pollution, disease, habitat loss, and species invasions.
format Article in Journal/Newspaper
author L.A. Levin
W. Ekau
A.J. Gooday
F. Jorissen
J.J. Middelburg
S.W.A. Naqvi
C. Neira
N.N. Rabalais
J. Zhang
spellingShingle L.A. Levin
W. Ekau
A.J. Gooday
F. Jorissen
J.J. Middelburg
S.W.A. Naqvi
C. Neira
N.N. Rabalais
J. Zhang
Effects of natural and human-induced hypoxia on coastal benthos
author_facet L.A. Levin
W. Ekau
A.J. Gooday
F. Jorissen
J.J. Middelburg
S.W.A. Naqvi
C. Neira
N.N. Rabalais
J. Zhang
author_sort L.A. Levin
title Effects of natural and human-induced hypoxia on coastal benthos
title_short Effects of natural and human-induced hypoxia on coastal benthos
title_full Effects of natural and human-induced hypoxia on coastal benthos
title_fullStr Effects of natural and human-induced hypoxia on coastal benthos
title_full_unstemmed Effects of natural and human-induced hypoxia on coastal benthos
title_sort effects of natural and human-induced hypoxia on coastal benthos
publisher European Geosciences Union
publishDate 2009
url http://okina.univ-angers.fr/publications/ua3864
https://doi.org/10.5194/bg-6-2063-2009
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op_source Biogeosciences
op_doi https://doi.org/10.5194/bg-6-2063-2009
container_title Biogeosciences
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container_issue 10
container_start_page 2063
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