{"id":{"repo_id":"soton","oai_identifier":"oai:eprints.soton.ac.uk:168945"},"canonical_url":"https://search.dev.ndltd.org/etd/soton/oai:eprints.soton.ac.uk:168945","repository":{"repo_id":"soton","name":"University of Southampton","base_url":"https://eprints.soton.ac.uk/cgi/oai2"},"display":{"title":"The role of microbial populations in the cycling of iron and manganese from marine aggregates","abstract":"Marine aggregates play an important role in the cycling of carbon, nutrients and trace<br/>metals. Within aggregates the oxygen depleted by aerobic microbial respiration may<br/>not be replaced rapidly, generating anoxic or suboxic microzones. Reduced<br/>compounds that are unstable in the oxygenated water column have been previously<br/>found associated with marine snow. Therefore, in the experiments described in this<br/>thesis, artificial aggregates were made in the laboratory from senescent phytoplankton<br/>material and incubated to investigate the role of the associated microbial populations<br/>to the biogeochemical redox cycling of iron and manganese and to the degradation of<br/>organic matter.<br/>The release of dissolved iron from artificial aggregates which did not contain any<br/>measurable (~10 ?m) anoxic microzones, was demonstrated under dark conditions.<br/>The rate of release was controlled by the amount of reducible Fe(III) available, and<br/>appears to be limited by the competing oxidation of Fe(II). Moreover highly significant<br/>releases in reduced Mn were detected from aggregates incubated under a constant<br/>velocity shear, although the same aggregates did not affect the dissolution of iron. A<br/>possible reason is likely associated with the higher stability of Mn(II), compared to<br/>Fe(II) in aerobic environments.<br/>Molecular (16S rRNA gene) analyses showed the bacterial community<br/>associated with artificial aggregates to be similar to that found in natural aggregates<br/>and dominated by (predominantly uncultured) ?- and ?-Proteobacteria, Bacteroidetes,<br/>Planctomycetes and Cyanobacteria. It was possible to culture NO3<br/>--, Fe(III)- and<br/>Mn(IV)-reducing bacteria from the artificial aggregates, and marine particles incubated<br/>with Fe(III) under anaerobic conditions contained a range of ?- and ?-Proteobacteria<br/>known to respire Fe(III) and in most cases Mn(IV). Moreover several microorganisms<br/>belonging to ?-Proteobacteria were isolated from marine aggregates and strains<br/>affiliated to the genera Amphritea, Marinobacterium and Marinobacter, were<br/>demonstrated to grow through the reduction of Fe(III), with Marinobacter also capable<br/>of respiring Mn(IV). Whilst the precise mechanism of reduction is not clear, it is evident<br/>that marine aggregates can be a source of Fe(II) and dissolved Mn, in coastal waters<br/>and most probably other natural water systems.<br/>Fatty acid analyses revealed the prevalence of saturated over unsaturated fatty<br/>acids indicating that aggregates were already partially degraded when incubation<br/>started. Nonetheless, the lipids in the artificial aggregates were rapidly degraded<br/>further as indicated by a depletion in short chain (&lt;20) saturated and<br/>monounsaturated fatty acids. In contrast, the concentrations of linear and branched,<br/>saturated long chain (&gt;20) fatty acids fluctuated, suggesting that some of these lipids<br/>could have been produced in situ by marine microorganisms rather than deriving from<br/>II<br/>higher plant debris. In addition, a bacterial branched monounsaturated fatty acid (11-<br/>methyl-octadecenoic acid), which has not previously been found in marine particles<br/>was present in artificial aggregates. Roseobacter litoralis found among the aggregateattached<br/>bacteria contains 11-methyl-octadecenoic acid, and other bacteria present in<br/>artificial aggregates have the potential to produce long-chain saturated and<br/>polyunsaturated fatty acids. Thus, the fatty acid assemblage appears to reflect both<br/>organic matter degradation, including selective preservation, but also changes in the<br/>microbial assemblage.<br/>A range of future studies are suggested to elucidate the mechanisms for Fe(III)<br/>and Mn(IV) reduction in aggregates. These include microscale analyses of dissolved<br/>species and evaluation of the presence of metal binding ligands associated with<br/>aggregates. Moreover it is important to assess the activity of the Fe(III)- and Mn(IV)-<br/>reducing bacteria present in aggregates in situ and the production of long chain fatty<br/>acids in degrading aggregates.","abstract_html":"Marine aggregates play an important role in the cycling of carbon, nutrients and trace&lt;br/&gt;metals. Within aggregates the oxygen depleted by aerobic microbial respiration may&lt;br/&gt;not be replaced rapidly, generating anoxic or suboxic microzones. Reduced&lt;br/&gt;compounds that are unstable in the oxygenated water column have been previously&lt;br/&gt;found associated with marine snow. Therefore, in the experiments described in this&lt;br/&gt;thesis, artificial aggregates were made in the laboratory from senescent phytoplankton&lt;br/&gt;material and incubated to investigate the role of the associated microbial populations&lt;br/&gt;to the biogeochemical redox cycling of iron and manganese and to the degradation of&lt;br/&gt;organic matter.&lt;br/&gt;The release of dissolved iron from artificial aggregates which did not contain any&lt;br/&gt;measurable (~10 ?m) anoxic microzones, was demonstrated under dark conditions.&lt;br/&gt;The rate of release was controlled by the amount of reducible Fe(III) available, and&lt;br/&gt;appears to be limited by the competing oxidation of Fe(II). Moreover highly significant&lt;br/&gt;releases in reduced Mn were detected from aggregates incubated under a constant&lt;br/&gt;velocity shear, although the same aggregates did not affect the dissolution of iron. A&lt;br/&gt;possible reason is likely associated with the higher stability of Mn(II), compared to&lt;br/&gt;Fe(II) in aerobic environments.&lt;br/&gt;Molecular (16S rRNA gene) analyses showed the bacterial community&lt;br/&gt;associated with artificial aggregates to be similar to that found in natural aggregates&lt;br/&gt;and dominated by (predominantly uncultured) ?- and ?-Proteobacteria, Bacteroidetes,&lt;br/&gt;Planctomycetes and Cyanobacteria. It was possible to culture NO3&lt;br/&gt;--, Fe(III)- and&lt;br/&gt;Mn(IV)-reducing bacteria from the artificial aggregates, and marine particles incubated&lt;br/&gt;with Fe(III) under anaerobic conditions contained a range of ?- and ?-Proteobacteria&lt;br/&gt;known to respire Fe(III) and in most cases Mn(IV). Moreover several microorganisms&lt;br/&gt;belonging to ?-Proteobacteria were isolated from marine aggregates and strains&lt;br/&gt;affiliated to the genera Amphritea, Marinobacterium and Marinobacter, were&lt;br/&gt;demonstrated to grow through the reduction of Fe(III), with Marinobacter also capable&lt;br/&gt;of respiring Mn(IV). Whilst the precise mechanism of reduction is not clear, it is evident&lt;br/&gt;that marine aggregates can be a source of Fe(II) and dissolved Mn, in coastal waters&lt;br/&gt;and most probably other natural water systems.&lt;br/&gt;Fatty acid analyses revealed the prevalence of saturated over unsaturated fatty&lt;br/&gt;acids indicating that aggregates were already partially degraded when incubation&lt;br/&gt;started. Nonetheless, the lipids in the artificial aggregates were rapidly degraded&lt;br/&gt;further as indicated by a depletion in short chain (&amp;lt;20) saturated and&lt;br/&gt;monounsaturated fatty acids. In contrast, the concentrations of linear and branched,&lt;br/&gt;saturated long chain (&amp;gt;20) fatty acids fluctuated, suggesting that some of these lipids&lt;br/&gt;could have been produced in situ by marine microorganisms rather than deriving from&lt;br/&gt;II&lt;br/&gt;higher plant debris. In addition, a bacterial branched monounsaturated fatty acid (11-&lt;br/&gt;methyl-octadecenoic acid), which has not previously been found in marine particles&lt;br/&gt;was present in artificial aggregates. Roseobacter litoralis found among the aggregateattached&lt;br/&gt;bacteria contains 11-methyl-octadecenoic acid, and other bacteria present in&lt;br/&gt;artificial aggregates have the potential to produce long-chain saturated and&lt;br/&gt;polyunsaturated fatty acids. Thus, the fatty acid assemblage appears to reflect both&lt;br/&gt;organic matter degradation, including selective preservation, but also changes in the&lt;br/&gt;microbial assemblage.&lt;br/&gt;A range of future studies are suggested to elucidate the mechanisms for Fe(III)&lt;br/&gt;and Mn(IV) reduction in aggregates. These include microscale analyses of dissolved&lt;br/&gt;species and evaluation of the presence of metal binding ligands associated with&lt;br/&gt;aggregates. Moreover it is important to assess the activity of the Fe(III)- and Mn(IV)-&lt;br/&gt;reducing bacteria present in aggregates in situ and the production of long chain fatty&lt;br/&gt;acids in degrading aggregates.","abstract_has_math":false,"creators":["Balzano, Sergio"],"institution":"University of Southampton","degree_name":"Ph.D.","degree_level":"doctoral","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2009,"date_issued":"2009-06","date_published":"2009-06","updated_at":"2026-07-24T04:36:17Z","subjects":[],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":null,"outbound_label":null,"outbound_source":null},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Balzano, Sergio"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2009-06"]},{"key":"dc:date.issued","label":"Date","values":["2009-06"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Ocean and Earth Science (pre 2011 reorg)","School of Ocean and Earth Science"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Southampton"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://eprints.soton.ac.uk/168945/"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Ph.D."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://eprints.soton.ac.uk/168945/1/Balzano_PhD_2010.pdf"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Marine aggregates play an important role in the cycling of carbon, nutrients and trace<br/>metals. Within aggregates the oxygen depleted by aerobic microbial respiration may<br/>not be replaced rapidly, generating anoxic or suboxic microzones. Reduced<br/>compounds that are unstable in the oxygenated water column have been previously<br/>found associated with marine snow. Therefore, in the experiments described in this<br/>thesis, artificial aggregates were made in the laboratory from senescent phytoplankton<br/>material and incubated to investigate the role of the associated microbial populations<br/>to the biogeochemical redox cycling of iron and manganese and to the degradation of<br/>organic matter.<br/>The release of dissolved iron from artificial aggregates which did not contain any<br/>measurable (~10 ?m) anoxic microzones, was demonstrated under dark conditions.<br/>The rate of release was controlled by the amount of reducible Fe(III) available, and<br/>appears to be limited by the competing oxidation of Fe(II). Moreover highly significant<br/>releases in reduced Mn were detected from aggregates incubated under a constant<br/>velocity shear, although the same aggregates did not affect the dissolution of iron. A<br/>possible reason is likely associated with the higher stability of Mn(II), compared to<br/>Fe(II) in aerobic environments.<br/>Molecular (16S rRNA gene) analyses showed the bacterial community<br/>associated with artificial aggregates to be similar to that found in natural aggregates<br/>and dominated by (predominantly uncultured) ?- and ?-Proteobacteria, Bacteroidetes,<br/>Planctomycetes and Cyanobacteria. It was possible to culture NO3<br/>--, Fe(III)- and<br/>Mn(IV)-reducing bacteria from the artificial aggregates, and marine particles incubated<br/>with Fe(III) under anaerobic conditions contained a range of ?- and ?-Proteobacteria<br/>known to respire Fe(III) and in most cases Mn(IV). Moreover several microorganisms<br/>belonging to ?-Proteobacteria were isolated from marine aggregates and strains<br/>affiliated to the genera Amphritea, Marinobacterium and Marinobacter, were<br/>demonstrated to grow through the reduction of Fe(III), with Marinobacter also capable<br/>of respiring Mn(IV). Whilst the precise mechanism of reduction is not clear, it is evident<br/>that marine aggregates can be a source of Fe(II) and dissolved Mn, in coastal waters<br/>and most probably other natural water systems.<br/>Fatty acid analyses revealed the prevalence of saturated over unsaturated fatty<br/>acids indicating that aggregates were already partially degraded when incubation<br/>started. Nonetheless, the lipids in the artificial aggregates were rapidly degraded<br/>further as indicated by a depletion in short chain (&lt;20) saturated and<br/>monounsaturated fatty acids. In contrast, the concentrations of linear and branched,<br/>saturated long chain (&gt;20) fatty acids fluctuated, suggesting that some of these lipids<br/>could have been produced in situ by marine microorganisms rather than deriving from<br/>II<br/>higher plant debris. In addition, a bacterial branched monounsaturated fatty acid (11-<br/>methyl-octadecenoic acid), which has not previously been found in marine particles<br/>was present in artificial aggregates. Roseobacter litoralis found among the aggregateattached<br/>bacteria contains 11-methyl-octadecenoic acid, and other bacteria present in<br/>artificial aggregates have the potential to produce long-chain saturated and<br/>polyunsaturated fatty acids. Thus, the fatty acid assemblage appears to reflect both<br/>organic matter degradation, including selective preservation, but also changes in the<br/>microbial assemblage.<br/>A range of future studies are suggested to elucidate the mechanisms for Fe(III)<br/>and Mn(IV) reduction in aggregates. These include microscale analyses of dissolved<br/>species and evaluation of the presence of metal binding ligands associated with<br/>aggregates. Moreover it is important to assess the activity of the Fe(III)- and Mn(IV)-<br/>reducing bacteria present in aggregates in situ and the production of long chain fatty<br/>acids in degrading aggregates."]},{"key":"dc:format","label":"Dc Format","values":["text"]},{"key":"dc:title","label":"Title","values":["The role of microbial populations in the cycling of iron and manganese from marine aggregates"]}]}],"canonical_facts":{"dc:creator":["Balzano, Sergio"],"dc:date":["2009-06"],"dc:date.issued":["2009-06"],"dc:description.abstract":["Marine aggregates play an important role in the cycling of carbon, nutrients and trace<br/>metals. Within aggregates the oxygen depleted by aerobic microbial respiration may<br/>not be replaced rapidly, generating anoxic or suboxic microzones. Reduced<br/>compounds that are unstable in the oxygenated water column have been previously<br/>found associated with marine snow. Therefore, in the experiments described in this<br/>thesis, artificial aggregates were made in the laboratory from senescent phytoplankton<br/>material and incubated to investigate the role of the associated microbial populations<br/>to the biogeochemical redox cycling of iron and manganese and to the degradation of<br/>organic matter.<br/>The release of dissolved iron from artificial aggregates which did not contain any<br/>measurable (~10 ?m) anoxic microzones, was demonstrated under dark conditions.<br/>The rate of release was controlled by the amount of reducible Fe(III) available, and<br/>appears to be limited by the competing oxidation of Fe(II). Moreover highly significant<br/>releases in reduced Mn were detected from aggregates incubated under a constant<br/>velocity shear, although the same aggregates did not affect the dissolution of iron. A<br/>possible reason is likely associated with the higher stability of Mn(II), compared to<br/>Fe(II) in aerobic environments.<br/>Molecular (16S rRNA gene) analyses showed the bacterial community<br/>associated with artificial aggregates to be similar to that found in natural aggregates<br/>and dominated by (predominantly uncultured) ?- and ?-Proteobacteria, Bacteroidetes,<br/>Planctomycetes and Cyanobacteria. It was possible to culture NO3<br/>--, Fe(III)- and<br/>Mn(IV)-reducing bacteria from the artificial aggregates, and marine particles incubated<br/>with Fe(III) under anaerobic conditions contained a range of ?- and ?-Proteobacteria<br/>known to respire Fe(III) and in most cases Mn(IV). Moreover several microorganisms<br/>belonging to ?-Proteobacteria were isolated from marine aggregates and strains<br/>affiliated to the genera Amphritea, Marinobacterium and Marinobacter, were<br/>demonstrated to grow through the reduction of Fe(III), with Marinobacter also capable<br/>of respiring Mn(IV). Whilst the precise mechanism of reduction is not clear, it is evident<br/>that marine aggregates can be a source of Fe(II) and dissolved Mn, in coastal waters<br/>and most probably other natural water systems.<br/>Fatty acid analyses revealed the prevalence of saturated over unsaturated fatty<br/>acids indicating that aggregates were already partially degraded when incubation<br/>started. Nonetheless, the lipids in the artificial aggregates were rapidly degraded<br/>further as indicated by a depletion in short chain (&lt;20) saturated and<br/>monounsaturated fatty acids. In contrast, the concentrations of linear and branched,<br/>saturated long chain (&gt;20) fatty acids fluctuated, suggesting that some of these lipids<br/>could have been produced in situ by marine microorganisms rather than deriving from<br/>II<br/>higher plant debris. In addition, a bacterial branched monounsaturated fatty acid (11-<br/>methyl-octadecenoic acid), which has not previously been found in marine particles<br/>was present in artificial aggregates. Roseobacter litoralis found among the aggregateattached<br/>bacteria contains 11-methyl-octadecenoic acid, and other bacteria present in<br/>artificial aggregates have the potential to produce long-chain saturated and<br/>polyunsaturated fatty acids. Thus, the fatty acid assemblage appears to reflect both<br/>organic matter degradation, including selective preservation, but also changes in the<br/>microbial assemblage.<br/>A range of future studies are suggested to elucidate the mechanisms for Fe(III)<br/>and Mn(IV) reduction in aggregates. These include microscale analyses of dissolved<br/>species and evaluation of the presence of metal binding ligands associated with<br/>aggregates. Moreover it is important to assess the activity of the Fe(III)- and Mn(IV)-<br/>reducing bacteria present in aggregates in situ and the production of long chain fatty<br/>acids in degrading aggregates."],"dc:format":["text"],"dc:identifier.uri":["https://eprints.soton.ac.uk/168945/1/Balzano_PhD_2010.pdf"],"dc:publisher.department":["Ocean and Earth Science (pre 2011 reorg)","School of Ocean and Earth Science"],"dc:publisher.institution":["University of Southampton"],"dc:relation.isreferencedby":["https://eprints.soton.ac.uk/168945/"],"dc:title":["The role of microbial populations in the cycling of iron and manganese from marine aggregates"],"dc:type":["Thesis"],"dc:type.qualificationlevel":["doctoral"],"dc:type.qualificationname":["Ph.D."]},"updated_at":"2026-07-24T04:36:17Z"}