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Niko Finke - Academia.edu

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class="suggested-user-card__user-info__subheader ds2-5-body-xs">Universidad de La Sabana</p></div></div><div class="suggested-user-card"><div class="suggested-user-card__avatar social-profile-avatar-container"><a href="https://independent.academia.edu/LarsHolmkvist"><img class="profile-avatar u-positionAbsolute" border="0" alt="" src="//a.academia-assets.com/images/s200_no_pic.png" /></a></div><div class="suggested-user-card__user-info"><a class="suggested-user-card__user-info__header ds2-5-body-sm-bold ds2-5-body-link" href="https://independent.academia.edu/LarsHolmkvist">Lars Holmkvist</a></div></div><div class="suggested-user-card"><div class="suggested-user-card__avatar social-profile-avatar-container"><a href="https://independent.academia.edu/MarcMussmann"><img class="profile-avatar u-positionAbsolute" border="0" alt="" src="//a.academia-assets.com/images/s200_no_pic.png" /></a></div><div class="suggested-user-card__user-info"><a class="suggested-user-card__user-info__header 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id="Pill-react-component-63539517-9fc2-403d-b241-667fd14cbdbf"></div> </a></div></div></div></div><div class="right-panel-container"><div class="user-content-wrapper"><div class="uploads-container" id="social-redesign-work-container"><div class="upload-header"><h2 class="ds2-5-heading-sans-serif-xs">Uploads</h2></div><div class="documents-container backbone-social-profile-documents" style="width: 100%;"><div class="u-taCenter"></div><div class="profile--tab_content_container js-tab-pane tab-pane active" id="all"><div class="profile--tab_heading_container js-section-heading" data-section="Papers" id="Papers"><h3 class="profile--tab_heading_container">Papers by Niko Finke</h3></div><div class="js-work-strip profile--work_container" data-work-id="18458465"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach"><img alt="Research paper thumbnail of Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach" class="work-thumbnail" src="https://attachments.academia-assets.com/40074573/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach">Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://io-warnemuende.academia.edu/MichaelEB%C3%B6ttcher">Michael E. Böttcher</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/NikoFinke">Niko Finke</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/MK%C3%B6nneke">M. Könneke</a></span></div><div class="wp-workCard_item"><span>Aquatic Microbial Ecology</span><span>, 2002</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the Germa...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the German Wadden Sea (Site Dangast, Jade Bay) was studied and related to sedimentary biogeochemical gradients and processes. Below the penetration depths of oxygen (~3 mm) and nitrate (~4 mm), the presence of dissolved iron and manganese and the absence of dissolved sulfide indicated suboxic conditions within the top 10 cm of the sediment. Moderate to high bacterial sulfate reduction rates were measured with radiotracers throughout the sediment, and dissimilatory sulfate reduction was also demonstrated by the presence of acid-volatile sulfides (AVS, essentially iron monosulfide). Stable sulfur isotope discrimination between dissolved sulfate and AVS was dominated by sulfate reduction. The diversity of SRB was studied using denaturant gradient gel electrophoresis of 16S rDNA, phospholipid fatty acid analysis and counting viable cells with the most probable number technique. Phylogenetic groups of SRB identified with these techniques were almost evenly distributed throughout the top 20 cm of the sediment. Application of fluorescence in situ hybridization, however, demonstrated a maximum of active members of the Desulfovibrio and Desulfosarcina-Desulfococcus-Desulfofrigus groups between 2 and 3 cm depth. These 2 groups encompass acetate and lactate utilizing SRB. The coincidence of this SRB maximum with a local maximum of sulfate reduction rates and the depletion of acetate and lactate reflects the microbiological processes related to sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2be6220db56716fd48580dc3f1c9cb3a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:40074573,&quot;asset_id&quot;:18458465,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/40074573/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="18458465"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="18458465"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 18458465; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=18458465]").text(description); $(".js-view-count[data-work-id=18458465]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 18458465; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='18458465']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "2be6220db56716fd48580dc3f1c9cb3a" } } $('.js-work-strip[data-work-id=18458465]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":18458465,"title":"Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach","internal_url":"https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach","owner_id":38469597,"coauthors_can_edit":true,"owner":{"id":38469597,"first_name":"Michael E.","middle_initials":null,"last_name":"Böttcher","page_name":"MichaelEBöttcher","domain_name":"io-warnemuende","created_at":"2015-11-16T11:09:57.767-08:00","display_name":"Michael E. 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For low-molecular-weight metabolites, δ 13 C values are routinely acquired for methane and used to examine details of its production and consumption. On the other hand, systematic information about the isotopic compositions of volatile fatty acids (VFAs) and other water-soluble metabolites in natural environments is very rare. The isotopic composition of acetate, a ubiquitous intermediate in anaerobic metabolism, is affected by biological processes that produce and/or consume it . Therefore, δ 13 C values of acetate extracted from natural systems are potentially powerful probes to decipher the dominant carbon-transforming processes in situ.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="83132c8867074720523f3361db0b8d9e" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:38053282,&quot;asset_id&quot;:13454107,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/38053282/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454107"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454107"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454107; 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W h e n you r a bst r a ct w ill n ot be a cce pt e d for or a l pr e se n t a t ion , you r a bst r a ct w ill be con side r e d for t h e post e r pr ogr a m . • You n g Scie n t ist a u t h or s of a n a bst r a ct su bm it t e d t o t h e sym posiu m m a y a pply for a n I SM E t r a ve l gr a n t . Ple a se se e t h e I SM E 1 3 w e bsit e for fu r t h e r de t a ils.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="fd0db65fefe808c4e7c87944143d63f3" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:38053283,&quot;asset_id&quot;:13454105,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/38053283/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454105"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454105"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454105; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454104"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454104/Pathways_of_carbon_oxidation_in_an_Arctic_fjord_sediment_Svalbard_and_isolation_of_psychrophilic_and_psychrotolerant_Fe_III_reducing_bacteria"><img alt="Research paper thumbnail of Pathways of carbon oxidation in an Arctic fjord sediment (Svalbard) and isolation of psychrophilic and psychrotolerant Fe(III)-reducing bacteria" class="work-thumbnail" src="https://attachments.academia-assets.com/45330584/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454104/Pathways_of_carbon_oxidation_in_an_Arctic_fjord_sediment_Svalbard_and_isolation_of_psychrophilic_and_psychrotolerant_Fe_III_reducing_bacteria">Pathways of carbon oxidation in an Arctic fjord sediment (Svalbard) and isolation of psychrophilic and psychrotolerant Fe(III)-reducing bacteria</a></div><div class="wp-workCard_item"><span>Marine Ecology-progress Series</span><span>, 2006</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The main mineralization pathways were determined in permanently cold fjord sediment on the west c...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The main mineralization pathways were determined in permanently cold fjord sediment on the west coast of Svalbard. In whole core incubations, the total oxygen uptake rate was 4.2 ± 0.4 mmol m -2 d -1 and the sulfate reduction rate 2.6 ± 0.6 mmol m -2 d -1 at 0 to 20 cm depth. Sulfate reduction was the most important anaerobic mineralization process, accounting for 57% of anaerobic organic carbon oxidation in anoxic bag incubations of the top 5 cm of the sediment. The remaining 43% oxidation was attributed to microbial Fe(III) reduction. Both processes occurred concurrently in the uppermost 2 cm, and the Fe-reducing community appeared to be limited mainly by the availability of Fe(III). Below 2 cm, sulfate reduction was the dominant electron-accepting process. Calculations for the uppermost 10 cm of the sediment yielded the following contribution of the different respiratory pathways to total carbon oxidation: aerobic respiration 53%, sulfate reduction 34%, Fe(III) reduction 13%. In situ, the importance of Fe(III) reduction may vary through competition for substrate with oxygen-and nitrate-reducing bacteria in the surface sediment. Fe(III)-reducing bacteria belonging to the genera Desulfuromonas, Desulfuromusa, Shewanella and Desulfovibrio were isolated from enrichment cultures of 2 fjord sediments from Svalbard. Strains related to Desulfovibrio reduced Fe(III) without energy generation for growth. All isolates were psychrophilic or psychrotolerant and grew at -2°C, the freezing point of sea water, indicating adaptation to permanently cold temperatures. Besides Fe(III), the strains reduced other electron acceptors such as oxygen, manganese, elemental sulfur and sulfate.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2414972e912d0961a8efad6627426059" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330584,&quot;asset_id&quot;:13454104,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330584/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454104"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454104"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454104; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13167724"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria"><img alt="Research paper thumbnail of Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria" class="work-thumbnail" src="https://attachments.academia-assets.com/45619196/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria">Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://univie.academia.edu/AlexanderLoy">Alexander Loy</a> and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/NikoFinke">Niko Finke</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Dissimilatory manganese reduction dominates anaerobic carbon oxidation in marine sediments with h...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Dissimilatory manganese reduction dominates anaerobic carbon oxidation in marine sediments with high manganese oxide concentrations, but the microorganisms responsible for this process are largely unknown. In this study, the acetate-utilizing manganese-reducing microbiota in geographically well-separated, manganese oxide-rich sediments from Gullmar Fjord (Sweden), Skagerrak (Norway) and Ulleung Basin (Korea) were analyzed by 16S rRNA-stable isotope probing (SIP). Manganese reduction was the prevailing terminal electron-accepting process in anoxic incubations of surface sediments, and even the addition of acetate stimulated neither iron nor sulfate reduction. The three geographically distinct sediments harbored surprisingly similar communities of acetateutilizing manganese-reducing bacteria: 16S rRNA of members of the genera Colwellia and Arcobacter and of novel genera within the Oceanospirillaceae and Alteromonadales were detected in heavy RNA-SIP fractions from these three sediments. Most probable number (MPN) analysis yielded up to 10 6 acetate-utilizing manganese-reducing cells cm À 3 in Gullmar Fjord sediment. A 16S rRNA gene clone library that was established from the highest MPN dilutions was dominated by sequences of Colwellia and Arcobacter species and members of the Oceanospirillaceae, supporting the obtained RNA-SIP results. In conclusion, these findings strongly suggest that (i) acetatedependent manganese reduction in manganese oxide-rich sediments is catalyzed by members of taxa (Arcobacter, Colwellia and Oceanospirillaceae) previously not known to possess this physiological function, (ii) similar acetate-utilizing manganese reducers thrive in geographically distinct regions and (iii) the identified manganese reducers differ greatly from the extensively explored iron reducers in marine sediments.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b1d29991de797fa63ce21c552fde35bf" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45619196,&quot;asset_id&quot;:13167724,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45619196/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13167724"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13167724"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13167724; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "b1d29991de797fa63ce21c552fde35bf" } } $('.js-work-strip[data-work-id=13167724]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13167724,"title":"Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria","internal_url":"https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria","owner_id":32422511,"coauthors_can_edit":true,"owner":{"id":32422511,"first_name":"Alexander","middle_initials":null,"last_name":"Loy","page_name":"AlexanderLoy","domain_name":"univie","created_at":"2015-06-22T02:28:18.637-07:00","display_name":"Alexander Loy","url":"https://univie.academia.edu/AlexanderLoy","email":"Mmg3cXVDbkRoNHNJbEJsVSsvSTJ2ZjJZc2JUVXdLWlNHU21RQU43THh3ckJaSFdzYUpGNy9nNWdzVmx6SHQxUC0tRmw0NGdJSXdLVTQxalVERm9uZVd2dz09--861ab9a2caa8dacf4ac6c9a1ec6553f89b45aee6"},"attachments":[{"id":45619196,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45619196/thumbnails/1.jpg","file_name":"Three_manganese_oxide-rich_marine_sedime20160514-23012-5kr5ar.pdf","download_url":"https://www.academia.edu/attachments/45619196/download_file","bulk_download_file_name":"Three_manganese_oxide_rich_marine_sedime.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45619196/Three_manganese_oxide-rich_marine_sedime20160514-23012-5kr5ar-libre.pdf?1463228653=\u0026response-content-disposition=attachment%3B+filename%3DThree_manganese_oxide_rich_marine_sedime.pdf\u0026Expires=1741264439\u0026Signature=QQNI-jT9U-SPT-J-ExKOc-p1-GRikc5fw9x3xaObo--YKy0lxDhEF-eMf3T3jjGS-NfOM7fInoDuq~qqwZPg6VlFJomRdu4M5OKGp1lK~zMkgDj5HCs19ggAUZCi6ffm5-8UO1mGGQsovoSEBUdmiuLA8pp18-0CypZR-z6m~lNNcP23zykX-rpThVV39d2lRh~wuvrYNhmDDCClaBNK6AgT4ThSzn7chRPW0EzakJudLnrJVXXopMjdR1g~psj2W2U2avj2GGzN7QRXXWIeLCXYExE39TCTglSwX9bbBOkAEYJ5L~hsj0APlu5Y9ytLOb-miObBVVsLdLKWQSPdZA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454103"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454103/Response_of_fermentation_and_sulfate_reduction_to_experimental_temperature_changes_in_temperate_and_Arctic_marine_sediments"><img alt="Research paper thumbnail of Response of fermentation and sulfate reduction to experimental temperature changes in temperate and Arctic marine sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330598/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454103/Response_of_fermentation_and_sulfate_reduction_to_experimental_temperature_changes_in_temperate_and_Arctic_marine_sediments">Response of fermentation and sulfate reduction to experimental temperature changes in temperate and Arctic marine sediments</a></div><div class="wp-workCard_item"><span>The ISME Journal</span><span>, 2008</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Anaerobic degradation of organic material generally proceeds through a sequence of steps, includi...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Anaerobic degradation of organic material generally proceeds through a sequence of steps, including polymer hydrolysis, fermentation and respiration or methanogenesis. The intermediates, such as volatile fatty acids (VFA) or H 2 , are generally maintained at low concentration, showing a close coupling of the terminal oxidation to fermentation. We exposed marine sediments to extreme temperature perturbations to study the nature and robustness of this coupling. Bacterial sulfate reduction and its dependence on fermentation were studied experimentally over a broad temperature range of À0.3 to 40 1C in sediments from temperate and permanently cold environments. In an Arctic sediment from Svalbard, the apparent optimum temperature for sulfate reduction decreased with prolonged incubation, whereas sulfate reduction rates increased. In a temperate sediment from the North Sea, the apparent optimum temperature was higher and did not change with incubation time. Up to a critical temperature, the concentrations of VFA remained low, o3 lM for acetate and o1 lM for the other VFA, the H 2 concentration showed thermodynamic control by sulfate-reducing bacteria, revealing a close coupling of fermentation and sulfate reduction. Above the critical temperature, the concentrations of VFA and H 2 increased transiently by 100-1000fold. According to the different in situ temperatures of the samples, the critical temperature was lower for sediments from the Arctic than from the North Sea. The H 2 concentrations decreased again upon prolonged incubation to values typical for sulfate-depleted methanogenic sediments. This suggests that fermentative bacteria and methanogenic archaea in both sediments tolerated higher temperatures than the sulfate-reducing community.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6609b9e7a09dd050715df89fe4feaf64" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330598,&quot;asset_id&quot;:13454103,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330598/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454103"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454103"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454103; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=13454103]").text(description); $(".js-view-count[data-work-id=13454103]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 13454103; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='13454103']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454102"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454102/Acetate_lactate_propionate_and_isobutyrate_as_electron_donors_for_iron_and_sulfate_reduction_in_Arctic_marine_sediments_Svalbard"><img alt="Research paper thumbnail of Acetate, lactate, propionate, and isobutyrate as electron donors for iron and sulfate reduction in Arctic marine sediments, Svalbard" class="work-thumbnail" src="https://attachments.academia-assets.com/45330592/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454102/Acetate_lactate_propionate_and_isobutyrate_as_electron_donors_for_iron_and_sulfate_reduction_in_Arctic_marine_sediments_Svalbard">Acetate, lactate, propionate, and isobutyrate as electron donors for iron and sulfate reduction in Arctic marine sediments, Svalbard</a></div><div class="wp-workCard_item"><span>FEMS Microbiology Ecology</span><span>, 2000</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The contribution of volatile fatty acids (VFA) as e --donors for anaerobic terminal oxidation of ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The contribution of volatile fatty acids (VFA) as e --donors for anaerobic terminal oxidation of organic carbon through iron and sulfate reduction was studied in Arctic fjord sediment. Dissolved inorganic carbon, Fe 21 , VFA concentrations, and sulfate reduction were monitored in slurries from the oxidized (0-2 cm) and the reduced (5-9 cm) zone. In the 0-2 cm layer, 2/3 of the mineralization could be attributed to sulfate reduction and 1/3 to iron reduction. In the 5-9 cm layer, sulfate reduction was the sole mineralization process. Acetate and lactate turnover rates were measured by radiotracer. Inhibition of sulfate reduction with selenate resulted in the accumulation of acetate, propionate, and isobutyrate. The acetate turnover rates determined by radiotracer and accumulation after inhibition were similar. VFA turnover accounted for 21% and 52% of the mineralization through sulfate reduction in the 0-2 and 5-9 cm layer, respectively. Acetate and lactate turnover in the inhibited 0-2 cm slurry was attributed to iron reduction and accounted for 10% and 2% of the iron reduction. Therefore, 88% and 79% of the iron and sulfate reduction in the 0-2 cm layer, respectively, must be fueled by alternative e --donors. The accumulation of VFA in the selenate-inhibited 0-2 cm slurry did not enhance iron reduction, indicating that iron reducers were not limited by VFA availability.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5adc4cb58a14b2789a8cb3d597c2d251" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330592,&quot;asset_id&quot;:13454102,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330592/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454102"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454102"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454102; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "5adc4cb58a14b2789a8cb3d597c2d251" } } $('.js-work-strip[data-work-id=13454102]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454102,"title":"Acetate, lactate, propionate, and isobutyrate as electron donors for iron and sulfate reduction in Arctic marine sediments, Svalbard","internal_url":"https://www.academia.edu/13454102/Acetate_lactate_propionate_and_isobutyrate_as_electron_donors_for_iron_and_sulfate_reduction_in_Arctic_marine_sediments_Svalbard","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke"},"attachments":[{"id":45330592,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330592/thumbnails/1.jpg","file_name":"Finke_N_Vandieken_V_Jrgensen_BB.._Acetat20160503-19951-n2m6b3.pdf","download_url":"https://www.academia.edu/attachments/45330592/download_file","bulk_download_file_name":"Acetate_lactate_propionate_and_isobutyra.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330592/Finke_N_Vandieken_V_Jrgensen_BB.._Acetat20160503-19951-n2m6b3-libre.pdf?1462326765=\u0026response-content-disposition=attachment%3B+filename%3DAcetate_lactate_propionate_and_isobutyra.pdf\u0026Expires=1741320351\u0026Signature=fpUXZACNKc2xKo5MBpQO974TK8XEitZWsPJ~fdA-PxmBQDtpAEizvrPCz9rSaXu0D3E~eDaDnXH9e~ybelgFACfUlzzoMeIIrnIRBze4cH02vLdddQrGlc0qUiIU5UKQt2dWCZbWut6c-eu2v2M6TbC8SwJcEBH4S-C-39XBjjeJMU~7uNxr~WSietzcgxziMDC5Cj5U9JuEekS6d8TxHMsCGU884Mn~xdUd-g~OjCKDcum287OjMnz0snGYUSNHzTPrmZ3mW73HQzC35QOM4Loll25NMhKB5oNow-t3GTePZNsM3hEYifOcN6xqw~OaveifmyOGJ~9rik6jamk4zg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454101"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454101/Structural_and_functional_analysis_of_a_microbial_mat_ecosystem_from_a_unique_permanent_hypersaline_inland_lake_%C3%A2_La_Salada_de_Chiprana%C3%A2_NE_Spain_"><img alt="Research paper thumbnail of Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’ (NE Spain)" class="work-thumbnail" src="https://attachments.academia-assets.com/45330596/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454101/Structural_and_functional_analysis_of_a_microbial_mat_ecosystem_from_a_unique_permanent_hypersaline_inland_lake_%C3%A2_La_Salada_de_Chiprana%C3%A2_NE_Spain_">Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’ (NE Spain)</a></div><div class="wp-workCard_item"><span>FEMS Microbiology Ecology</span><span>, 2000</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The benthic microbial mat community of the only permanent hypersaline natural inland lake of West...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The benthic microbial mat community of the only permanent hypersaline natural inland lake of Western Europe, &#39;La Salada de Chiprana&#39;, northeastern Spain, was structurally and functionally analyzed. The ionic composition of the lake water is characterized by high concentrations of magnesium and sulfate, which were respectively 0.35 and 0.5 M at the time of sampling while the total salinity was 78 g l 31 . Community composition was analyzed by microscopy, high-performance liquid chromatography (HPLC) pigment analyses and by studying culturable bacteria from different functional groups. Therefore, denaturing gradient gel electrophoresis (DGGE) was applied on most probable number (MPN) dilution cultures. Microscopy revealed that a thin layer of Chloroflexus-like bacteria overlaid various cyanobacteria-dominated layers each characterized by different morphotypes. DGGE analysis of MPN dilution cultures from distinct mat layers showed that various phylotypes of anoxygenic phototrophic, aerobic heterotrophic, colorless sulfur-, and sulfate-reducing bacteria were present. The mats were furthermore functionally studied and attention was focussed on the relationship between oxygenic primary production and the flow of carbon through the microbial community. Microsensor techniques, porewater and sediment photopigment analysis were applied in order to estimate oxygenic photosynthetic rates, daily dynamics of (in)organic carbon porewater concentration and migration behavior of phototrophs. Chiprana microbial mats produced dissolved organic carbon (DOC) both during the day and night. It was estimated that 14% of the mats gross photosynthetic production and 49% of the mats net photosynthetic production diffused out of the mat in the form of low molecular mass fatty acids, although these compounds made up only 2% of the total DOC pool. The high flux of dissolved fatty acids from the microbial mat to the water column may explain why in this system Chloroflexus-like bacteria proliferate on top of the cyanobacterial layers since these photoheterotrophic bacteria grow preferably on organic phototrophic exudates. Furthermore it may also explain why high numbers of viable sulfate-reducing bacteria were found in the fully oxygenated sediment surface layers. These organisms apparently do not have to compete with aerobic heterotrophic community members due to the ample availability of organic substrates. Moreover, the high production of DOC strongly indicates that the mat community was nutrient limited in its growth. Photopigment analysis revealed furthermore that chlorophyll a (Chla) and three of its allomeres had a complementary depth distribution what suggests that the Chla allomeres are functional adaptations to differences in light quality and/or quantity and may be species specific.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="ad4ac26364a9025e9081bd0668838445" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330596,&quot;asset_id&quot;:13454101,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330596/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454101"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454101"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454101; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "ad4ac26364a9025e9081bd0668838445" } } $('.js-work-strip[data-work-id=13454101]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454101,"title":"Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’ (NE Spain)","internal_url":"https://www.academia.edu/13454101/Structural_and_functional_analysis_of_a_microbial_mat_ecosystem_from_a_unique_permanent_hypersaline_inland_lake_%C3%A2_La_Salada_de_Chiprana%C3%A2_NE_Spain_","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke","email":"OWsrOU5YSXRTZXhzUU5wdTNhOHVRbmxnbWZENFhWUVoweTdIMWptNWM5dz0tLTVpSHc4UXgyejRRYW1HRFh5aE5GMnc9PQ==--1edfa45a419d1ca9c842ab5fa6e94d1501a16c26"},"attachments":[{"id":45330596,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330596/thumbnails/1.jpg","file_name":"Jonkers_HM_Ludwig_R_De_Wit_R_Pringault_O20160503-17400-8cfgk6.pdf","download_url":"https://www.academia.edu/attachments/45330596/download_file","bulk_download_file_name":"Structural_and_functional_analysis_of_a.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330596/Jonkers_HM_Ludwig_R_De_Wit_R_Pringault_O20160503-17400-8cfgk6-libre.pdf?1462326765=\u0026response-content-disposition=attachment%3B+filename%3DStructural_and_functional_analysis_of_a.pdf\u0026Expires=1741264439\u0026Signature=Fim6hcWIUP0J1dK0egvpf~VMHKT37ReoC-n2oXImfwAhmqFLawqn0kHwg0lkkKg3PgmliPsfOxmDKuuH7mwsFIlIJFb0Zf1gSm0zneLjK2f7H0P93vyyiZQPn0ZhV6wtGNoN3jpngxDJ3IzYGb1UrcJWJzRCCVgGo7dMiaYZKrhtlA0g9699ckX4qn4UUNxpCf2YSd6r9OXx~aDI29OmL3zZ~WZuZeFmcN~PEu7GQOX76bHoP4Huj1hTpmTiXJKe7Z5tr8Y7toc9PZ06ECmHdUHZtUNaIiw8oWygtH7b~Gp2VIrdT5PAkoRxl7~bdVPgi~Ujv0Eb-W9XLazqGy2Mkg__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454100"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454100/Competition_for_inorganic_carbon_between_oxygenic_and_anoxygenic_phototrophs_in_a_hypersaline_microbial_mat_Guerrero_Negro_Mexico"><img alt="Research paper thumbnail of Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico" class="work-thumbnail" src="https://attachments.academia-assets.com/45330605/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454100/Competition_for_inorganic_carbon_between_oxygenic_and_anoxygenic_phototrophs_in_a_hypersaline_microbial_mat_Guerrero_Negro_Mexico">Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico</a></div><div class="wp-workCard_item"><span>Environmental Microbiology</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">While most oxygenic phototrophs harvest light only in the visible range (400-700 nm, VIS), anoxyg...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">While most oxygenic phototrophs harvest light only in the visible range (400-700 nm, VIS), anoxygenic phototrophs can harvest near infrared light (&gt; 700 nm, NIR). To study interactions between the photosynthetic guilds we used microsensors to measure oxygen and gross oxygenic photosynthesis (gOP) in a hypersaline microbial mat under full (VIS + NIR) and VIS illumination. Under normal dissolved inorganic carbon (DIC) concentrations (2 mM), volumetric rates of gOP were reduced up to 65% and areal rates by 16-31% at full compared with VIS illumination. This effect was enhanced (reduction up to 100% in volumetric, 50% in areal rates of gOP) when DIC was lowered to 1 mM, but diminished at 10 mM DIC or lowered pH. In conclusion, under full-light illumination anoxygenic phototrophs are able to reduce the activity of oxygenic phototrophs by efficiently competing for inorganic carbon within the highly oxygenated layer. Anoxygenic photosynthesis, calculated from the difference in gOP under full and VIS illumination, represented between 10% and 40% of the C-fixation. The DIC depletion in the euphotic zone as well as the significant C-fixation by anoxygenic phototrophs in the oxic layer influences the carbon isotopic composition of the mat, which needs to be taken into account when interpreting isotopic biosignals in geological records.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="0b634c9e2222e55b37e06e1c4810577f" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330605,&quot;asset_id&quot;:13454100,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330605/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454100"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454100"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454100; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454099"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments"><img alt="Research paper thumbnail of Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330590/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments">Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments</a></div><div class="wp-workCard_item"><span>Environmental Microbiology</span><span>, 2007</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The effect of variations in H2 concentrations on methanogenesis from the non-competitive substrat...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The effect of variations in H2 concentrations on methanogenesis from the non-competitive substrates methanol and methylamine (used by methanogens but not by sulfate reducers) was investigated in methanogenic marine sediments. Imposed variations in sulfate concentration and temperature were used to drive systematic variations in pore water H2 concentrations. Specifically, increasing sulfate concentrations and decreasing temperatures both resulted in decreasing H2 concentrations. The ratio of CO2 and CH4 produced from 14 C-labelled methylamine and methanol showed a direct correlation with the H2 concentration, independent of the treatment, with lower H2 concentrations resulting in a shift towards CO2. We conclude that this correlation is driven by production of H2 by methylotrophic methanogens, followed by loss to the environment with a magnitude dependent on the extracellular H2 concentrations maintained by hydrogenotrophic methanogens (in the case of the temperature experiment) or sulfate reducers (in the case of the sulfate experiment). Under sulfate-free conditions, the loss of reducing power as H2 flux out of the cell represents a loss of energy for the methylotrophic methanogens while, in the presence of sulfate, it results in a favourable free energy yield. Thus, hydrogen leakage might conceivably be beneficial for methanogens in marine sediments dominated by sulfate reduction. In low-sulfate systems such as methanogenic marine or freshwater sediments it is clearly detrimental -an adverse consequence of possessing a hydrogenase that is subject to externally imposed control by pore water H 2 concentrations. H2 leakage in methanogens may explain the apparent exclusion of acetoclastic methanogenesis in sediments dominated by sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="593b8c8c6f1f9a45f2a4c32afb4d846a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330590,&quot;asset_id&quot;:13454099,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330590/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454099"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454099"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454099; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=13454099]").text(description); $(".js-view-count[data-work-id=13454099]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 13454099; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='13454099']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "593b8c8c6f1f9a45f2a4c32afb4d846a" } } $('.js-work-strip[data-work-id=13454099]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454099,"title":"Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments","internal_url":"https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke","email":"cEVWdDM0dkZIRU1HVkVrV0FIcUN1RENYN2V4aTh1SmxBZnFGTUljVXMwWT0tLTJwUlNVQmdQRTBGK1NpYVBQM3MvT3c9PQ==--b18407dae975137745504f1f75f62a07774da52b"},"attachments":[{"id":45330590,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330590/thumbnails/1.jpg","file_name":"Finke_N_Hoehler_TM_Jorgensen_BB.._Hydrog20160503-2509-1po8i08.pdf","download_url":"https://www.academia.edu/attachments/45330590/download_file","bulk_download_file_name":"Hydrogen_leakage_during_methanogenesis_f.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330590/Finke_N_Hoehler_TM_Jorgensen_BB.._Hydrog20160503-2509-1po8i08-libre.pdf?1462326764=\u0026response-content-disposition=attachment%3B+filename%3DHydrogen_leakage_during_methanogenesis_f.pdf\u0026Expires=1741264439\u0026Signature=ROX9C8OHc3W0x5ofxAjAIFAunqAeLH99r9M5qmJw0jidXb3EqIIOI-st2h3-gx8qc-ooy18E4ODnqdrgQ~2QGxMtzfwG8kiRHh79TaUy4MMHZoLEfNp0bX99nmtiWZCBUhsEpjprv~V2ADx9YYQt2~fNpTevS3mUKCthb7P3wBfl2SV7V84uMwdcLdyb96ezDxmibTzLHB2GgTfHMQQgbPYpsES2s-G385Uu9OW60jeQ~QfCpMtxqe4QVeG0zbZO6iauWssBhP3kXEKdS8YHnxz9bn7-ittP6ARDDgN7O1QJrXzTG2UWkyRfoTk4VeLH7Oq8jNsPZz46QIJ9joHzdw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454098"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454098/Effects_of_Deposition_of_Heavy_Metal_Polluted_Harbor_Mud_on_Microbial_Diversity_and_Metal_Resistance_in_Sandy_Marine_Sediments"><img alt="Research paper thumbnail of Effects of Deposition of Heavy-Metal-Polluted Harbor Mud on Microbial Diversity and Metal Resistance in Sandy Marine Sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330577/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454098/Effects_of_Deposition_of_Heavy_Metal_Polluted_Harbor_Mud_on_Microbial_Diversity_and_Metal_Resistance_in_Sandy_Marine_Sediments">Effects of Deposition of Heavy-Metal-Polluted Harbor Mud on Microbial Diversity and Metal Resistance in Sandy Marine Sediments</a></div><div class="wp-workCard_item"><span>Archives of Environmental Contamination and Toxicology</span><span>, 2008</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Deposition of dredged harbor sediments in relatively undisturbed ecosystems is often considered a...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Deposition of dredged harbor sediments in relatively undisturbed ecosystems is often considered a viable option for confinement of pollutants and possible natural attenuation. This study investigated the effects of deposition of heavy-metal-polluted sludge on the microbial diversity of sandy sediments during 12 months of mesocosm incubation. Geochemical analyses showed an initial increase in pore-water metal concentrations, which subsided after 3 months of incubation. No influence of the deposited sediment was observed in denaturing gradient gel electrophoresis (DGGE) profiles of bacterial 16S rRNA genes, whereas a minor, transient impact on the archaeal community was revealed. Phylogenetic analyses of bacterial 16S rRNA clone libraries showed an abundance of members of the Flavobacteriaceae, the aand c-Proteobacteria, in both the muddy and the sandy sediments. Despite the finding that some groups of clones were shared between the metal-impacted sandy sediment and the harbor control, comparative analyses showed that the two sediments were significantly different in community composition. Consequences of redeposition of metalpolluted sediment were primarily underlined with cultivation-dependent techniques. Toxicity tests showed that the percentage of Cd-and Cu-tolerant aerobic heterotrophs was highest among isolates from the sandy sediment with metal-polluted mud on top.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="48cb82036e2c18aab863dd20e3f92a78" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330577,&quot;asset_id&quot;:13454098,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330577/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454098"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454098"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454098; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=13454098]").text(description); $(".js-view-count[data-work-id=13454098]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 13454098; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='13454098']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "48cb82036e2c18aab863dd20e3f92a78" } } $('.js-work-strip[data-work-id=13454098]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454098,"title":"Effects of Deposition of Heavy-Metal-Polluted Harbor Mud on Microbial Diversity and Metal Resistance in Sandy Marine Sediments","internal_url":"https://www.academia.edu/13454098/Effects_of_Deposition_of_Heavy_Metal_Polluted_Harbor_Mud_on_Microbial_Diversity_and_Metal_Resistance_in_Sandy_Marine_Sediments","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke"},"attachments":[{"id":45330577,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330577/thumbnails/1.jpg","file_name":"toes_2008.pdf","download_url":"https://www.academia.edu/attachments/45330577/download_file","bulk_download_file_name":"Effects_of_Deposition_of_Heavy_Metal_Pol.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330577/toes_2008-libre.pdf?1462326764=\u0026response-content-disposition=attachment%3B+filename%3DEffects_of_Deposition_of_Heavy_Metal_Pol.pdf\u0026Expires=1741320351\u0026Signature=dnaA9fBLp-1sjFm1KNoGjmQCwI79JYwJM7AvzHr8UvbQZFzKqeyK-sZ~-G7aMitwWSszdlOxQMGevkeElUL9M87z5mFsFimc4qxcX1CrhG6Okx6mK0LezvMUGMe2O72Q7vKNX4hnZLa0LXvUr-rtkrSn9V679wwjR75m1rNByRueexhfS1OF-JPpcx57Z2rNrAZl~-hlKmryN3ywyWURuIFxO88xvxYzEjU-Lui7~RWZM5~pAHZegJNM~oz-KA7R-L8Xqy2LifhkQhPdzuO5dGGgpX7BbSde0KuI-q53EESPxG1pTn~mCFM5~Ea9zRneh-3473nbcuXJVhE8Wa5GnQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454097"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454097/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach"><img alt="Research paper thumbnail of Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach" class="work-thumbnail" src="https://attachments.academia-assets.com/45330599/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454097/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach">Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach</a></div><div class="wp-workCard_item"><span>Aquatic Microbial Ecology</span><span>, 2002</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the Germa...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the German Wadden Sea (Site Dangast, Jade Bay) was studied and related to sedimentary biogeochemical gradients and processes. Below the penetration depths of oxygen (~3 mm) and nitrate (~4 mm), the presence of dissolved iron and manganese and the absence of dissolved sulfide indicated suboxic conditions within the top 10 cm of the sediment. Moderate to high bacterial sulfate reduction rates were measured with radiotracers throughout the sediment, and dissimilatory sulfate reduction was also demonstrated by the presence of acid-volatile sulfides (AVS, essentially iron monosulfide). Stable sulfur isotope discrimination between dissolved sulfate and AVS was dominated by sulfate reduction. The diversity of SRB was studied using denaturant gradient gel electrophoresis of 16S rDNA, phospholipid fatty acid analysis and counting viable cells with the most probable number technique. Phylogenetic groups of SRB identified with these techniques were almost evenly distributed throughout the top 20 cm of the sediment. Application of fluorescence in situ hybridization, however, demonstrated a maximum of active members of the Desulfovibrio and Desulfosarcina-Desulfococcus-Desulfofrigus groups between 2 and 3 cm depth. These 2 groups encompass acetate and lactate utilizing SRB. The coincidence of this SRB maximum with a local maximum of sulfate reduction rates and the depletion of acetate and lactate reflects the microbiological processes related to sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="bb752a052e8a1334349fa81754187dd7" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330599,&quot;asset_id&quot;:13454097,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330599/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454097"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454097"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454097; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="3124994" id="papers"><div class="js-work-strip profile--work_container" data-work-id="18458465"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach"><img alt="Research paper thumbnail of Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach" class="work-thumbnail" src="https://attachments.academia-assets.com/40074573/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach">Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://io-warnemuende.academia.edu/MichaelEB%C3%B6ttcher">Michael E. Böttcher</a>, <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/NikoFinke">Niko Finke</a>, and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/MK%C3%B6nneke">M. Könneke</a></span></div><div class="wp-workCard_item"><span>Aquatic Microbial Ecology</span><span>, 2002</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the Germa...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the German Wadden Sea (Site Dangast, Jade Bay) was studied and related to sedimentary biogeochemical gradients and processes. Below the penetration depths of oxygen (~3 mm) and nitrate (~4 mm), the presence of dissolved iron and manganese and the absence of dissolved sulfide indicated suboxic conditions within the top 10 cm of the sediment. Moderate to high bacterial sulfate reduction rates were measured with radiotracers throughout the sediment, and dissimilatory sulfate reduction was also demonstrated by the presence of acid-volatile sulfides (AVS, essentially iron monosulfide). Stable sulfur isotope discrimination between dissolved sulfate and AVS was dominated by sulfate reduction. The diversity of SRB was studied using denaturant gradient gel electrophoresis of 16S rDNA, phospholipid fatty acid analysis and counting viable cells with the most probable number technique. Phylogenetic groups of SRB identified with these techniques were almost evenly distributed throughout the top 20 cm of the sediment. Application of fluorescence in situ hybridization, however, demonstrated a maximum of active members of the Desulfovibrio and Desulfosarcina-Desulfococcus-Desulfofrigus groups between 2 and 3 cm depth. These 2 groups encompass acetate and lactate utilizing SRB. The coincidence of this SRB maximum with a local maximum of sulfate reduction rates and the depletion of acetate and lactate reflects the microbiological processes related to sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2be6220db56716fd48580dc3f1c9cb3a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:40074573,&quot;asset_id&quot;:18458465,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/40074573/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="18458465"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="18458465"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 18458465; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=18458465]").text(description); $(".js-view-count[data-work-id=18458465]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 18458465; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='18458465']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "2be6220db56716fd48580dc3f1c9cb3a" } } $('.js-work-strip[data-work-id=18458465]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":18458465,"title":"Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach","internal_url":"https://www.academia.edu/18458465/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach","owner_id":38469597,"coauthors_can_edit":true,"owner":{"id":38469597,"first_name":"Michael E.","middle_initials":null,"last_name":"Böttcher","page_name":"MichaelEBöttcher","domain_name":"io-warnemuende","created_at":"2015-11-16T11:09:57.767-08:00","display_name":"Michael E. 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For low-molecular-weight metabolites, δ 13 C values are routinely acquired for methane and used to examine details of its production and consumption. On the other hand, systematic information about the isotopic compositions of volatile fatty acids (VFAs) and other water-soluble metabolites in natural environments is very rare. The isotopic composition of acetate, a ubiquitous intermediate in anaerobic metabolism, is affected by biological processes that produce and/or consume it . 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454104"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454104/Pathways_of_carbon_oxidation_in_an_Arctic_fjord_sediment_Svalbard_and_isolation_of_psychrophilic_and_psychrotolerant_Fe_III_reducing_bacteria"><img alt="Research paper thumbnail of Pathways of carbon oxidation in an Arctic fjord sediment (Svalbard) and isolation of psychrophilic and psychrotolerant Fe(III)-reducing bacteria" class="work-thumbnail" src="https://attachments.academia-assets.com/45330584/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454104/Pathways_of_carbon_oxidation_in_an_Arctic_fjord_sediment_Svalbard_and_isolation_of_psychrophilic_and_psychrotolerant_Fe_III_reducing_bacteria">Pathways of carbon oxidation in an Arctic fjord sediment (Svalbard) and isolation of psychrophilic and psychrotolerant Fe(III)-reducing bacteria</a></div><div class="wp-workCard_item"><span>Marine Ecology-progress Series</span><span>, 2006</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The main mineralization pathways were determined in permanently cold fjord sediment on the west c...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The main mineralization pathways were determined in permanently cold fjord sediment on the west coast of Svalbard. In whole core incubations, the total oxygen uptake rate was 4.2 ± 0.4 mmol m -2 d -1 and the sulfate reduction rate 2.6 ± 0.6 mmol m -2 d -1 at 0 to 20 cm depth. Sulfate reduction was the most important anaerobic mineralization process, accounting for 57% of anaerobic organic carbon oxidation in anoxic bag incubations of the top 5 cm of the sediment. The remaining 43% oxidation was attributed to microbial Fe(III) reduction. Both processes occurred concurrently in the uppermost 2 cm, and the Fe-reducing community appeared to be limited mainly by the availability of Fe(III). Below 2 cm, sulfate reduction was the dominant electron-accepting process. Calculations for the uppermost 10 cm of the sediment yielded the following contribution of the different respiratory pathways to total carbon oxidation: aerobic respiration 53%, sulfate reduction 34%, Fe(III) reduction 13%. In situ, the importance of Fe(III) reduction may vary through competition for substrate with oxygen-and nitrate-reducing bacteria in the surface sediment. Fe(III)-reducing bacteria belonging to the genera Desulfuromonas, Desulfuromusa, Shewanella and Desulfovibrio were isolated from enrichment cultures of 2 fjord sediments from Svalbard. Strains related to Desulfovibrio reduced Fe(III) without energy generation for growth. All isolates were psychrophilic or psychrotolerant and grew at -2°C, the freezing point of sea water, indicating adaptation to permanently cold temperatures. Besides Fe(III), the strains reduced other electron acceptors such as oxygen, manganese, elemental sulfur and sulfate.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="2414972e912d0961a8efad6627426059" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330584,&quot;asset_id&quot;:13454104,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330584/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454104"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454104"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454104; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "2414972e912d0961a8efad6627426059" } } $('.js-work-strip[data-work-id=13454104]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454104,"title":"Pathways of carbon oxidation in an Arctic fjord sediment (Svalbard) and isolation of psychrophilic and psychrotolerant Fe(III)-reducing bacteria","internal_url":"https://www.academia.edu/13454104/Pathways_of_carbon_oxidation_in_an_Arctic_fjord_sediment_Svalbard_and_isolation_of_psychrophilic_and_psychrotolerant_Fe_III_reducing_bacteria","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke","email":"K2R0MVRRRUp2REdnRzA0TTNtWnZlUmVkYno0NU5md0tPUzVsWmwycDV2Zz0tLXp3WVRnWUdia0l1TG9WQk11UmR1TFE9PQ==--92f56f5b27068766a8f7e52f62f025243d64e980"},"attachments":[{"id":45330584,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330584/thumbnails/1.jpg","file_name":"Pathways_of_carbon_oxidation_in_an_Arcti20160503-19951-pqoqw9.pdf","download_url":"https://www.academia.edu/attachments/45330584/download_file","bulk_download_file_name":"Pathways_of_carbon_oxidation_in_an_Arcti.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330584/Pathways_of_carbon_oxidation_in_an_Arcti20160503-19951-pqoqw9-libre.pdf?1462326765=\u0026response-content-disposition=attachment%3B+filename%3DPathways_of_carbon_oxidation_in_an_Arcti.pdf\u0026Expires=1741264439\u0026Signature=O6vL5MXfqNsrRWLxQyS2UYgJ2e8lfmN4eP3Y7FipvCgG1AtqFbIa6aw5HC~hD~lTpj8OzPnjwDcRfrcJzE70g4V4JLOshjZDRbPZ6FClzzycDpTvVfLZC6OYDWad9P0tzTL7ndYHci1d8vT0qtWo3xAkoQG8Av-ALtrQQaJ5C2FMjHZluRBDfl9NvhXjKbvsik3knYtxfCwBJFeXsJzto565X4idRCdfkTrAuaua0SF~re~~Jaa5eNQ0bC3CMk2KTdrl1auzRTJ-xzrsg9VLV-~puF12z5m4cdJgRyLW1-usRbYH9RpF4gM2ndeiPH5KS-5g8q~-ckgvUZh31D43cw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13167724"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria"><img alt="Research paper thumbnail of Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria" class="work-thumbnail" src="https://attachments.academia-assets.com/45619196/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria">Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://univie.academia.edu/AlexanderLoy">Alexander Loy</a> and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/NikoFinke">Niko Finke</a></span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Dissimilatory manganese reduction dominates anaerobic carbon oxidation in marine sediments with h...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Dissimilatory manganese reduction dominates anaerobic carbon oxidation in marine sediments with high manganese oxide concentrations, but the microorganisms responsible for this process are largely unknown. In this study, the acetate-utilizing manganese-reducing microbiota in geographically well-separated, manganese oxide-rich sediments from Gullmar Fjord (Sweden), Skagerrak (Norway) and Ulleung Basin (Korea) were analyzed by 16S rRNA-stable isotope probing (SIP). Manganese reduction was the prevailing terminal electron-accepting process in anoxic incubations of surface sediments, and even the addition of acetate stimulated neither iron nor sulfate reduction. The three geographically distinct sediments harbored surprisingly similar communities of acetateutilizing manganese-reducing bacteria: 16S rRNA of members of the genera Colwellia and Arcobacter and of novel genera within the Oceanospirillaceae and Alteromonadales were detected in heavy RNA-SIP fractions from these three sediments. Most probable number (MPN) analysis yielded up to 10 6 acetate-utilizing manganese-reducing cells cm À 3 in Gullmar Fjord sediment. A 16S rRNA gene clone library that was established from the highest MPN dilutions was dominated by sequences of Colwellia and Arcobacter species and members of the Oceanospirillaceae, supporting the obtained RNA-SIP results. In conclusion, these findings strongly suggest that (i) acetatedependent manganese reduction in manganese oxide-rich sediments is catalyzed by members of taxa (Arcobacter, Colwellia and Oceanospirillaceae) previously not known to possess this physiological function, (ii) similar acetate-utilizing manganese reducers thrive in geographically distinct regions and (iii) the identified manganese reducers differ greatly from the extensively explored iron reducers in marine sediments.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b1d29991de797fa63ce21c552fde35bf" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45619196,&quot;asset_id&quot;:13167724,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45619196/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13167724"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13167724"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13167724; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "b1d29991de797fa63ce21c552fde35bf" } } $('.js-work-strip[data-work-id=13167724]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13167724,"title":"Three manganese oxide-rich marine sediments harbor similar communities of acetate-oxidizing manganese-reducing bacteria","internal_url":"https://www.academia.edu/13167724/Three_manganese_oxide_rich_marine_sediments_harbor_similar_communities_of_acetate_oxidizing_manganese_reducing_bacteria","owner_id":32422511,"coauthors_can_edit":true,"owner":{"id":32422511,"first_name":"Alexander","middle_initials":null,"last_name":"Loy","page_name":"AlexanderLoy","domain_name":"univie","created_at":"2015-06-22T02:28:18.637-07:00","display_name":"Alexander Loy","url":"https://univie.academia.edu/AlexanderLoy","email":"Mmg3cXVDbkRoNHNJbEJsVSsvSTJ2ZjJZc2JUVXdLWlNHU21RQU43THh3ckJaSFdzYUpGNy9nNWdzVmx6SHQxUC0tRmw0NGdJSXdLVTQxalVERm9uZVd2dz09--861ab9a2caa8dacf4ac6c9a1ec6553f89b45aee6"},"attachments":[{"id":45619196,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45619196/thumbnails/1.jpg","file_name":"Three_manganese_oxide-rich_marine_sedime20160514-23012-5kr5ar.pdf","download_url":"https://www.academia.edu/attachments/45619196/download_file","bulk_download_file_name":"Three_manganese_oxide_rich_marine_sedime.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45619196/Three_manganese_oxide-rich_marine_sedime20160514-23012-5kr5ar-libre.pdf?1463228653=\u0026response-content-disposition=attachment%3B+filename%3DThree_manganese_oxide_rich_marine_sedime.pdf\u0026Expires=1741264439\u0026Signature=QQNI-jT9U-SPT-J-ExKOc-p1-GRikc5fw9x3xaObo--YKy0lxDhEF-eMf3T3jjGS-NfOM7fInoDuq~qqwZPg6VlFJomRdu4M5OKGp1lK~zMkgDj5HCs19ggAUZCi6ffm5-8UO1mGGQsovoSEBUdmiuLA8pp18-0CypZR-z6m~lNNcP23zykX-rpThVV39d2lRh~wuvrYNhmDDCClaBNK6AgT4ThSzn7chRPW0EzakJudLnrJVXXopMjdR1g~psj2W2U2avj2GGzN7QRXXWIeLCXYExE39TCTglSwX9bbBOkAEYJ5L~hsj0APlu5Y9ytLOb-miObBVVsLdLKWQSPdZA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454103"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454103/Response_of_fermentation_and_sulfate_reduction_to_experimental_temperature_changes_in_temperate_and_Arctic_marine_sediments"><img alt="Research paper thumbnail of Response of fermentation and sulfate reduction to experimental temperature changes in temperate and Arctic marine sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330598/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454103/Response_of_fermentation_and_sulfate_reduction_to_experimental_temperature_changes_in_temperate_and_Arctic_marine_sediments">Response of fermentation and sulfate reduction to experimental temperature changes in temperate and Arctic marine sediments</a></div><div class="wp-workCard_item"><span>The ISME Journal</span><span>, 2008</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Anaerobic degradation of organic material generally proceeds through a sequence of steps, includi...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Anaerobic degradation of organic material generally proceeds through a sequence of steps, including polymer hydrolysis, fermentation and respiration or methanogenesis. The intermediates, such as volatile fatty acids (VFA) or H 2 , are generally maintained at low concentration, showing a close coupling of the terminal oxidation to fermentation. We exposed marine sediments to extreme temperature perturbations to study the nature and robustness of this coupling. Bacterial sulfate reduction and its dependence on fermentation were studied experimentally over a broad temperature range of À0.3 to 40 1C in sediments from temperate and permanently cold environments. In an Arctic sediment from Svalbard, the apparent optimum temperature for sulfate reduction decreased with prolonged incubation, whereas sulfate reduction rates increased. In a temperate sediment from the North Sea, the apparent optimum temperature was higher and did not change with incubation time. Up to a critical temperature, the concentrations of VFA remained low, o3 lM for acetate and o1 lM for the other VFA, the H 2 concentration showed thermodynamic control by sulfate-reducing bacteria, revealing a close coupling of fermentation and sulfate reduction. Above the critical temperature, the concentrations of VFA and H 2 increased transiently by 100-1000fold. According to the different in situ temperatures of the samples, the critical temperature was lower for sediments from the Arctic than from the North Sea. The H 2 concentrations decreased again upon prolonged incubation to values typical for sulfate-depleted methanogenic sediments. This suggests that fermentative bacteria and methanogenic archaea in both sediments tolerated higher temperatures than the sulfate-reducing community.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="6609b9e7a09dd050715df89fe4feaf64" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330598,&quot;asset_id&quot;:13454103,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330598/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454103"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454103"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454103; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454102"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454102/Acetate_lactate_propionate_and_isobutyrate_as_electron_donors_for_iron_and_sulfate_reduction_in_Arctic_marine_sediments_Svalbard"><img alt="Research paper thumbnail of Acetate, lactate, propionate, and isobutyrate as electron donors for iron and sulfate reduction in Arctic marine sediments, Svalbard" class="work-thumbnail" src="https://attachments.academia-assets.com/45330592/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454102/Acetate_lactate_propionate_and_isobutyrate_as_electron_donors_for_iron_and_sulfate_reduction_in_Arctic_marine_sediments_Svalbard">Acetate, lactate, propionate, and isobutyrate as electron donors for iron and sulfate reduction in Arctic marine sediments, Svalbard</a></div><div class="wp-workCard_item"><span>FEMS Microbiology Ecology</span><span>, 2000</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The contribution of volatile fatty acids (VFA) as e --donors for anaerobic terminal oxidation of ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The contribution of volatile fatty acids (VFA) as e --donors for anaerobic terminal oxidation of organic carbon through iron and sulfate reduction was studied in Arctic fjord sediment. Dissolved inorganic carbon, Fe 21 , VFA concentrations, and sulfate reduction were monitored in slurries from the oxidized (0-2 cm) and the reduced (5-9 cm) zone. In the 0-2 cm layer, 2/3 of the mineralization could be attributed to sulfate reduction and 1/3 to iron reduction. In the 5-9 cm layer, sulfate reduction was the sole mineralization process. Acetate and lactate turnover rates were measured by radiotracer. Inhibition of sulfate reduction with selenate resulted in the accumulation of acetate, propionate, and isobutyrate. The acetate turnover rates determined by radiotracer and accumulation after inhibition were similar. VFA turnover accounted for 21% and 52% of the mineralization through sulfate reduction in the 0-2 and 5-9 cm layer, respectively. Acetate and lactate turnover in the inhibited 0-2 cm slurry was attributed to iron reduction and accounted for 10% and 2% of the iron reduction. Therefore, 88% and 79% of the iron and sulfate reduction in the 0-2 cm layer, respectively, must be fueled by alternative e --donors. The accumulation of VFA in the selenate-inhibited 0-2 cm slurry did not enhance iron reduction, indicating that iron reducers were not limited by VFA availability.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="5adc4cb58a14b2789a8cb3d597c2d251" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330592,&quot;asset_id&quot;:13454102,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330592/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454102"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454102"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454102; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454101"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454101/Structural_and_functional_analysis_of_a_microbial_mat_ecosystem_from_a_unique_permanent_hypersaline_inland_lake_%C3%A2_La_Salada_de_Chiprana%C3%A2_NE_Spain_"><img alt="Research paper thumbnail of Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’ (NE Spain)" class="work-thumbnail" src="https://attachments.academia-assets.com/45330596/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454101/Structural_and_functional_analysis_of_a_microbial_mat_ecosystem_from_a_unique_permanent_hypersaline_inland_lake_%C3%A2_La_Salada_de_Chiprana%C3%A2_NE_Spain_">Structural and functional analysis of a microbial mat ecosystem from a unique permanent hypersaline inland lake: ‘La Salada de Chiprana’ (NE Spain)</a></div><div class="wp-workCard_item"><span>FEMS Microbiology Ecology</span><span>, 2000</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The benthic microbial mat community of the only permanent hypersaline natural inland lake of West...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The benthic microbial mat community of the only permanent hypersaline natural inland lake of Western Europe, &#39;La Salada de Chiprana&#39;, northeastern Spain, was structurally and functionally analyzed. The ionic composition of the lake water is characterized by high concentrations of magnesium and sulfate, which were respectively 0.35 and 0.5 M at the time of sampling while the total salinity was 78 g l 31 . Community composition was analyzed by microscopy, high-performance liquid chromatography (HPLC) pigment analyses and by studying culturable bacteria from different functional groups. Therefore, denaturing gradient gel electrophoresis (DGGE) was applied on most probable number (MPN) dilution cultures. Microscopy revealed that a thin layer of Chloroflexus-like bacteria overlaid various cyanobacteria-dominated layers each characterized by different morphotypes. DGGE analysis of MPN dilution cultures from distinct mat layers showed that various phylotypes of anoxygenic phototrophic, aerobic heterotrophic, colorless sulfur-, and sulfate-reducing bacteria were present. The mats were furthermore functionally studied and attention was focussed on the relationship between oxygenic primary production and the flow of carbon through the microbial community. Microsensor techniques, porewater and sediment photopigment analysis were applied in order to estimate oxygenic photosynthetic rates, daily dynamics of (in)organic carbon porewater concentration and migration behavior of phototrophs. Chiprana microbial mats produced dissolved organic carbon (DOC) both during the day and night. It was estimated that 14% of the mats gross photosynthetic production and 49% of the mats net photosynthetic production diffused out of the mat in the form of low molecular mass fatty acids, although these compounds made up only 2% of the total DOC pool. The high flux of dissolved fatty acids from the microbial mat to the water column may explain why in this system Chloroflexus-like bacteria proliferate on top of the cyanobacterial layers since these photoheterotrophic bacteria grow preferably on organic phototrophic exudates. Furthermore it may also explain why high numbers of viable sulfate-reducing bacteria were found in the fully oxygenated sediment surface layers. These organisms apparently do not have to compete with aerobic heterotrophic community members due to the ample availability of organic substrates. Moreover, the high production of DOC strongly indicates that the mat community was nutrient limited in its growth. Photopigment analysis revealed furthermore that chlorophyll a (Chla) and three of its allomeres had a complementary depth distribution what suggests that the Chla allomeres are functional adaptations to differences in light quality and/or quantity and may be species specific.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="ad4ac26364a9025e9081bd0668838445" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330596,&quot;asset_id&quot;:13454101,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330596/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454101"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454101"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454101; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454100"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454100/Competition_for_inorganic_carbon_between_oxygenic_and_anoxygenic_phototrophs_in_a_hypersaline_microbial_mat_Guerrero_Negro_Mexico"><img alt="Research paper thumbnail of Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico" class="work-thumbnail" src="https://attachments.academia-assets.com/45330605/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454100/Competition_for_inorganic_carbon_between_oxygenic_and_anoxygenic_phototrophs_in_a_hypersaline_microbial_mat_Guerrero_Negro_Mexico">Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico</a></div><div class="wp-workCard_item"><span>Environmental Microbiology</span><span>, 2013</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">While most oxygenic phototrophs harvest light only in the visible range (400-700 nm, VIS), anoxyg...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">While most oxygenic phototrophs harvest light only in the visible range (400-700 nm, VIS), anoxygenic phototrophs can harvest near infrared light (&gt; 700 nm, NIR). To study interactions between the photosynthetic guilds we used microsensors to measure oxygen and gross oxygenic photosynthesis (gOP) in a hypersaline microbial mat under full (VIS + NIR) and VIS illumination. Under normal dissolved inorganic carbon (DIC) concentrations (2 mM), volumetric rates of gOP were reduced up to 65% and areal rates by 16-31% at full compared with VIS illumination. This effect was enhanced (reduction up to 100% in volumetric, 50% in areal rates of gOP) when DIC was lowered to 1 mM, but diminished at 10 mM DIC or lowered pH. In conclusion, under full-light illumination anoxygenic phototrophs are able to reduce the activity of oxygenic phototrophs by efficiently competing for inorganic carbon within the highly oxygenated layer. Anoxygenic photosynthesis, calculated from the difference in gOP under full and VIS illumination, represented between 10% and 40% of the C-fixation. The DIC depletion in the euphotic zone as well as the significant C-fixation by anoxygenic phototrophs in the oxic layer influences the carbon isotopic composition of the mat, which needs to be taken into account when interpreting isotopic biosignals in geological records.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="0b634c9e2222e55b37e06e1c4810577f" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330605,&quot;asset_id&quot;:13454100,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330605/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454100"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454100"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454100; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=13454100]").text(description); $(".js-view-count[data-work-id=13454100]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 13454100; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='13454100']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "0b634c9e2222e55b37e06e1c4810577f" } } $('.js-work-strip[data-work-id=13454100]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454100,"title":"Competition for inorganic carbon between oxygenic and anoxygenic phototrophs in a hypersaline microbial mat, Guerrero Negro, Mexico","internal_url":"https://www.academia.edu/13454100/Competition_for_inorganic_carbon_between_oxygenic_and_anoxygenic_phototrophs_in_a_hypersaline_microbial_mat_Guerrero_Negro_Mexico","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke"},"attachments":[{"id":45330605,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330605/thumbnails/1.jpg","file_name":"Competition_for_inorganic_carbon_between20160503-17400-1du1eng.pdf","download_url":"https://www.academia.edu/attachments/45330605/download_file","bulk_download_file_name":"Competition_for_inorganic_carbon_between.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330605/Competition_for_inorganic_carbon_between20160503-17400-1du1eng-libre.pdf?1462326764=\u0026response-content-disposition=attachment%3B+filename%3DCompetition_for_inorganic_carbon_between.pdf\u0026Expires=1741320351\u0026Signature=IMX7Sw0dx2vLMWN5YEZnLbhLWxt8JhUCQbq6K0VvfP3fmAPVBLF5nDtuhaos1R0fQdS9yhWm9TqkUUWlTauTLFT5mg4O6~mnrk~H48dNJvL8TgL7S~i1~XyPtLP5JRJ1hY45NOv1JokIjyne6-3k3ca70z-Py~6KnVoHjFyl9y8hPjEHUeuuzsaNzjBEBdnCns1Ab3OajczWQCl14QvLpiZ6C3LENH2GEg7VyPZPKiNK9B4ZIFjvd6FcV5Ndmgz~tOISQtXRN~WNgYtzoKP0hY6IW~-bdFW-pT6SPXCDrW6nuLoHoBO9y2W6HhklxSpwZAhiNSUSXn9o9gMmbOctSQ__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454099"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments"><img alt="Research paper thumbnail of Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330590/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments">Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments</a></div><div class="wp-workCard_item"><span>Environmental Microbiology</span><span>, 2007</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The effect of variations in H2 concentrations on methanogenesis from the non-competitive substrat...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The effect of variations in H2 concentrations on methanogenesis from the non-competitive substrates methanol and methylamine (used by methanogens but not by sulfate reducers) was investigated in methanogenic marine sediments. Imposed variations in sulfate concentration and temperature were used to drive systematic variations in pore water H2 concentrations. Specifically, increasing sulfate concentrations and decreasing temperatures both resulted in decreasing H2 concentrations. The ratio of CO2 and CH4 produced from 14 C-labelled methylamine and methanol showed a direct correlation with the H2 concentration, independent of the treatment, with lower H2 concentrations resulting in a shift towards CO2. We conclude that this correlation is driven by production of H2 by methylotrophic methanogens, followed by loss to the environment with a magnitude dependent on the extracellular H2 concentrations maintained by hydrogenotrophic methanogens (in the case of the temperature experiment) or sulfate reducers (in the case of the sulfate experiment). Under sulfate-free conditions, the loss of reducing power as H2 flux out of the cell represents a loss of energy for the methylotrophic methanogens while, in the presence of sulfate, it results in a favourable free energy yield. Thus, hydrogen leakage might conceivably be beneficial for methanogens in marine sediments dominated by sulfate reduction. In low-sulfate systems such as methanogenic marine or freshwater sediments it is clearly detrimental -an adverse consequence of possessing a hydrogenase that is subject to externally imposed control by pore water H 2 concentrations. H2 leakage in methanogens may explain the apparent exclusion of acetoclastic methanogenesis in sediments dominated by sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="593b8c8c6f1f9a45f2a4c32afb4d846a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330590,&quot;asset_id&quot;:13454099,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330590/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454099"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454099"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454099; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=13454099]").text(description); $(".js-view-count[data-work-id=13454099]").attr('title', description).tooltip(); }); });</script></span></span><span><span class="percentile-widget hidden"><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 13454099; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-work-strip[data-work-id='13454099']"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></span></div><div id="work-strip-premium-row-container"></div></div></div><script> require.config({ waitSeconds: 90 })(["https://a.academia-assets.com/assets/wow_profile-a9bf3a2bc8c89fa2a77156577594264ee8a0f214d74241bc0fcd3f69f8d107ac.js","https://a.academia-assets.com/assets/work_edit-ad038b8c047c1a8d4fa01b402d530ff93c45fee2137a149a4a5398bc8ad67560.js"], function() { // from javascript_helper.rb var dispatcherData = {} if (true){ window.WowProfile.dispatcher = window.WowProfile.dispatcher || _.clone(Backbone.Events); dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "593b8c8c6f1f9a45f2a4c32afb4d846a" } } $('.js-work-strip[data-work-id=13454099]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":13454099,"title":"Hydrogen ?leakage? during methanogenesis from methanol and methylamine: implications for anaerobic carbon degradation pathways in aquatic sediments","internal_url":"https://www.academia.edu/13454099/Hydrogen_leakage_during_methanogenesis_from_methanol_and_methylamine_implications_for_anaerobic_carbon_degradation_pathways_in_aquatic_sediments","owner_id":32681744,"coauthors_can_edit":true,"owner":{"id":32681744,"first_name":"Niko","middle_initials":null,"last_name":"Finke","page_name":"NikoFinke","domain_name":"independent","created_at":"2015-06-30T17:31:19.237-07:00","display_name":"Niko Finke","url":"https://independent.academia.edu/NikoFinke","email":"cEVWdDM0dkZIRU1HVkVrV0FIcUN1RENYN2V4aTh1SmxBZnFGTUljVXMwWT0tLTJwUlNVQmdQRTBGK1NpYVBQM3MvT3c9PQ==--b18407dae975137745504f1f75f62a07774da52b"},"attachments":[{"id":45330590,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/45330590/thumbnails/1.jpg","file_name":"Finke_N_Hoehler_TM_Jorgensen_BB.._Hydrog20160503-2509-1po8i08.pdf","download_url":"https://www.academia.edu/attachments/45330590/download_file","bulk_download_file_name":"Hydrogen_leakage_during_methanogenesis_f.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/45330590/Finke_N_Hoehler_TM_Jorgensen_BB.._Hydrog20160503-2509-1po8i08-libre.pdf?1462326764=\u0026response-content-disposition=attachment%3B+filename%3DHydrogen_leakage_during_methanogenesis_f.pdf\u0026Expires=1741264439\u0026Signature=ROX9C8OHc3W0x5ofxAjAIFAunqAeLH99r9M5qmJw0jidXb3EqIIOI-st2h3-gx8qc-ooy18E4ODnqdrgQ~2QGxMtzfwG8kiRHh79TaUy4MMHZoLEfNp0bX99nmtiWZCBUhsEpjprv~V2ADx9YYQt2~fNpTevS3mUKCthb7P3wBfl2SV7V84uMwdcLdyb96ezDxmibTzLHB2GgTfHMQQgbPYpsES2s-G385Uu9OW60jeQ~QfCpMtxqe4QVeG0zbZO6iauWssBhP3kXEKdS8YHnxz9bn7-ittP6ARDDgN7O1QJrXzTG2UWkyRfoTk4VeLH7Oq8jNsPZz46QIJ9joHzdw__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454098"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454098/Effects_of_Deposition_of_Heavy_Metal_Polluted_Harbor_Mud_on_Microbial_Diversity_and_Metal_Resistance_in_Sandy_Marine_Sediments"><img alt="Research paper thumbnail of Effects of Deposition of Heavy-Metal-Polluted Harbor Mud on Microbial Diversity and Metal Resistance in Sandy Marine Sediments" class="work-thumbnail" src="https://attachments.academia-assets.com/45330577/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454098/Effects_of_Deposition_of_Heavy_Metal_Polluted_Harbor_Mud_on_Microbial_Diversity_and_Metal_Resistance_in_Sandy_Marine_Sediments">Effects of Deposition of Heavy-Metal-Polluted Harbor Mud on Microbial Diversity and Metal Resistance in Sandy Marine Sediments</a></div><div class="wp-workCard_item"><span>Archives of Environmental Contamination and Toxicology</span><span>, 2008</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Deposition of dredged harbor sediments in relatively undisturbed ecosystems is often considered a...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Deposition of dredged harbor sediments in relatively undisturbed ecosystems is often considered a viable option for confinement of pollutants and possible natural attenuation. This study investigated the effects of deposition of heavy-metal-polluted sludge on the microbial diversity of sandy sediments during 12 months of mesocosm incubation. Geochemical analyses showed an initial increase in pore-water metal concentrations, which subsided after 3 months of incubation. No influence of the deposited sediment was observed in denaturing gradient gel electrophoresis (DGGE) profiles of bacterial 16S rRNA genes, whereas a minor, transient impact on the archaeal community was revealed. Phylogenetic analyses of bacterial 16S rRNA clone libraries showed an abundance of members of the Flavobacteriaceae, the aand c-Proteobacteria, in both the muddy and the sandy sediments. Despite the finding that some groups of clones were shared between the metal-impacted sandy sediment and the harbor control, comparative analyses showed that the two sediments were significantly different in community composition. Consequences of redeposition of metalpolluted sediment were primarily underlined with cultivation-dependent techniques. Toxicity tests showed that the percentage of Cd-and Cu-tolerant aerobic heterotrophs was highest among isolates from the sandy sediment with metal-polluted mud on top.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="48cb82036e2c18aab863dd20e3f92a78" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330577,&quot;asset_id&quot;:13454098,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330577/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454098"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454098"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454098; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13454097"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13454097/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach"><img alt="Research paper thumbnail of Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach" class="work-thumbnail" src="https://attachments.academia-assets.com/45330599/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13454097/Community_structure_and_activity_of_sulfate_reducing_bacteria_in_an_intertidal_surface_sediment_a_multi_method_approach">Community structure and activity of sulfate-reducing bacteria in an intertidal surface sediment: a multi-method approach</a></div><div class="wp-workCard_item"><span>Aquatic Microbial Ecology</span><span>, 2002</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the Germa...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">The community structure of sulfate-reducing bacteria (SRB) in an intertidal mud flat of the German Wadden Sea (Site Dangast, Jade Bay) was studied and related to sedimentary biogeochemical gradients and processes. Below the penetration depths of oxygen (~3 mm) and nitrate (~4 mm), the presence of dissolved iron and manganese and the absence of dissolved sulfide indicated suboxic conditions within the top 10 cm of the sediment. Moderate to high bacterial sulfate reduction rates were measured with radiotracers throughout the sediment, and dissimilatory sulfate reduction was also demonstrated by the presence of acid-volatile sulfides (AVS, essentially iron monosulfide). Stable sulfur isotope discrimination between dissolved sulfate and AVS was dominated by sulfate reduction. The diversity of SRB was studied using denaturant gradient gel electrophoresis of 16S rDNA, phospholipid fatty acid analysis and counting viable cells with the most probable number technique. Phylogenetic groups of SRB identified with these techniques were almost evenly distributed throughout the top 20 cm of the sediment. Application of fluorescence in situ hybridization, however, demonstrated a maximum of active members of the Desulfovibrio and Desulfosarcina-Desulfococcus-Desulfofrigus groups between 2 and 3 cm depth. These 2 groups encompass acetate and lactate utilizing SRB. The coincidence of this SRB maximum with a local maximum of sulfate reduction rates and the depletion of acetate and lactate reflects the microbiological processes related to sulfate reduction.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="bb752a052e8a1334349fa81754187dd7" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45330599,&quot;asset_id&quot;:13454097,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45330599/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13454097"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13454097"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13454097; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="13167779"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/13167779/Vandieken_etal_12IMSE_J_supp"><img alt="Research paper thumbnail of Vandieken etal 12IMSE J-supp" class="work-thumbnail" src="https://attachments.academia-assets.com/45619174/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/13167779/Vandieken_etal_12IMSE_J_supp">Vandieken etal 12IMSE J-supp</a></div><div class="wp-workCard_item wp-workCard--coauthors"><span>by </span><span><a class="" data-click-track="profile-work-strip-authors" href="https://univie.academia.edu/AlexanderLoy">Alexander Loy</a> and <a class="" data-click-track="profile-work-strip-authors" href="https://independent.academia.edu/NikoFinke">Niko Finke</a></span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="de799c8b16bb66957c6a4a3a2f18101f" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{&quot;attachment_id&quot;:45619174,&quot;asset_id&quot;:13167779,&quot;asset_type&quot;:&quot;Work&quot;,&quot;button_location&quot;:&quot;profile&quot;}" href="https://www.academia.edu/attachments/45619174/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="13167779"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="13167779"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 13167779; 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