Impact of bacterial and fungal processes on 14C-hexadecane mineralisation in weathered hydrocarbon contaminated soil.
Identifieur interne : 000433 ( Main/Exploration ); précédent : 000432; suivant : 000434Impact of bacterial and fungal processes on 14C-hexadecane mineralisation in weathered hydrocarbon contaminated soil.
Auteurs : Eric M. Adetutu [Australie] ; Andy S. Ball ; John Weber ; Samuel Aleer ; Catherine E. Dandie ; Albert L. JuhaszSource :
- The Science of the total environment [ 1879-1026 ] ; 2012.
Descripteurs français
- KwdFr :
- ARN ribosomique 16S (génétique), Alcanes (composition chimique), Analyse de regroupements (MeSH), Analyse de séquence d'ADN (MeSH), Analyse de variance (MeSH), Azote (MeSH), Azoture de sodium (MeSH), Bactéries (effets des médicaments et des substances chimiques), Bactéries (génétique), Bactéries (métabolisme), Dépollution biologique de l'environnement (MeSH), Nystatine (pharmacologie), Phanerochaete (croissance et développement), Phanerochaete (effets des médicaments et des substances chimiques), Phanerochaete (métabolisme), Phosphore (MeSH), Polluants du sol (analyse), Polysorbates (pharmacologie), Pétrole (analyse), Radio-isotopes du carbone (métabolisme), Réaction de polymérisation en chaîne (MeSH).
- MESH :
- analyse : Polluants du sol, Pétrole.
- composition chimique : Alcanes.
- croissance et développement : Phanerochaete.
- effets des médicaments et des substances chimiques : Bactéries, Phanerochaete.
- génétique : ARN ribosomique 16S, Bactéries.
- métabolisme : Bactéries, Phanerochaete, Radio-isotopes du carbone.
- pharmacologie : Nystatine, Polysorbates.
- Analyse de regroupements, Analyse de séquence d'ADN, Analyse de variance, Azote, Azoture de sodium, Dépollution biologique de l'environnement, Phosphore, Réaction de polymérisation en chaîne.
English descriptors
- KwdEn :
- Alkanes (chemistry), Analysis of Variance (MeSH), Bacteria (drug effects), Bacteria (genetics), Bacteria (metabolism), Biodegradation, Environmental (MeSH), Carbon Radioisotopes (metabolism), Cluster Analysis (MeSH), Nitrogen (MeSH), Nystatin (pharmacology), Petroleum (analysis), Phanerochaete (drug effects), Phanerochaete (growth & development), Phanerochaete (metabolism), Phosphorus (MeSH), Polymerase Chain Reaction (MeSH), Polysorbates (pharmacology), RNA, Ribosomal, 16S (genetics), Sequence Analysis, DNA (MeSH), Sodium Azide (MeSH), Soil Pollutants (analysis).
- MESH :
- chemical , analysis : Petroleum, Soil Pollutants.
- chemical , chemistry : Alkanes.
- drug effects : Bacteria, Phanerochaete.
- genetics : Bacteria, RNA, Ribosomal, 16S.
- growth & development : Phanerochaete.
- metabolism : Bacteria, Carbon Radioisotopes, Phanerochaete.
- chemical , pharmacology : Nystatin, Polysorbates.
- Analysis of Variance, Biodegradation, Environmental, Cluster Analysis, Nitrogen, Phosphorus, Polymerase Chain Reaction, Sequence Analysis, DNA, Sodium Azide.
Abstract
In this study, the impact of bacterial and fungal processes on (14)C-hexadecane mineralisation was investigated in weathered hydrocarbon contaminated soil. The extent of (14)C-hexadecane mineralisation varied depending on the bioremediation strategy employed. Under enhanced natural attenuation conditions, (14)C-hexadecane mineralisation after 98 days was 8.5 ± 3.7% compared to <1.2% without nitrogen and phosphorus additions. (14)C-hexadecane mineralisation was further enhanced through Tween 80 amendments (28.9 ± 2.4%) which also promoted the growth of a Phanerochaete chyrsosporium fungal mat. Although fungal growth in weathered hydrocarbon contaminated soil could be promoted through supplementing additional carbon sources (Tween 80, sawdust, compost, pea straw), fungal (14)C-hexadecane mineralisation was negligible when sodium azide was added to soil microcosms to inhibit bacterial activity. In contrast, when fungal activity was inhibited through nystatin additions, (14)C-hexadecane mineralisation ranged from 6.5 ± 0.2 to 35.8 ± 3.8% after 98 days depending on the supplied amendment. Bacteria inhibition with sodium azide resulted in a reduction in bacterial diversity (33-37%) compared to microcosms supplemented with nystatin or microcosms without inhibitory supplements. However, alkB bacterial groups were undetected in sodium azide supplemented microcosms, highlighting the important role of this bacterial group in (14)C-hexadecane mineralisation.
DOI: 10.1016/j.scitotenv.2011.11.044
PubMed: 22154183
Affiliations:
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Le document en format XML
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Ball</name></author><author><name sortKey="Weber, John" sort="Weber, John" uniqKey="Weber J" first="John" last="Weber">John Weber</name></author><author><name sortKey="Aleer, Samuel" sort="Aleer, Samuel" uniqKey="Aleer S" first="Samuel" last="Aleer">Samuel Aleer</name></author><author><name sortKey="Dandie, Catherine E" sort="Dandie, Catherine E" uniqKey="Dandie C" first="Catherine E" last="Dandie">Catherine E. Dandie</name></author><author><name sortKey="Juhasz, Albert L" sort="Juhasz, Albert L" uniqKey="Juhasz A" first="Albert L" last="Juhasz">Albert L. 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The extent of (14)C-hexadecane mineralisation varied depending on the bioremediation strategy employed. Under enhanced natural attenuation conditions, (14)C-hexadecane mineralisation after 98 days was 8.5 ± 3.7% compared to <1.2% without nitrogen and phosphorus additions. (14)C-hexadecane mineralisation was further enhanced through Tween 80 amendments (28.9 ± 2.4%) which also promoted the growth of a Phanerochaete chyrsosporium fungal mat. Although fungal growth in weathered hydrocarbon contaminated soil could be promoted through supplementing additional carbon sources (Tween 80, sawdust, compost, pea straw), fungal (14)C-hexadecane mineralisation was negligible when sodium azide was added to soil microcosms to inhibit bacterial activity. In contrast, when fungal activity was inhibited through nystatin additions, (14)C-hexadecane mineralisation ranged from 6.5 ± 0.2 to 35.8 ± 3.8% after 98 days depending on the supplied amendment. Bacteria inhibition with sodium azide resulted in a reduction in bacterial diversity (33-37%) compared to microcosms supplemented with nystatin or microcosms without inhibitory supplements. However, alkB bacterial groups were undetected in sodium azide supplemented microcosms, highlighting the important role of this bacterial group in (14)C-hexadecane mineralisation.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22154183</PMID><DateCompleted><Year>2012</Year><Month>05</Month><Day>07</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1879-1026</ISSN><JournalIssue CitedMedium="Internet"><Volume>414</Volume><PubDate><Year>2012</Year><Month>Jan</Month><Day>01</Day></PubDate></JournalIssue><Title>The Science of the total environment</Title><ISOAbbreviation>Sci Total Environ</ISOAbbreviation></Journal><ArticleTitle>Impact of bacterial and fungal processes on 14C-hexadecane mineralisation in weathered hydrocarbon contaminated soil.</ArticleTitle><Pagination><MedlinePgn>585-91</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.scitotenv.2011.11.044</ELocationID><Abstract><AbstractText>In this study, the impact of bacterial and fungal processes on (14)C-hexadecane mineralisation was investigated in weathered hydrocarbon contaminated soil. The extent of (14)C-hexadecane mineralisation varied depending on the bioremediation strategy employed. Under enhanced natural attenuation conditions, (14)C-hexadecane mineralisation after 98 days was 8.5 ± 3.7% compared to <1.2% without nitrogen and phosphorus additions. (14)C-hexadecane mineralisation was further enhanced through Tween 80 amendments (28.9 ± 2.4%) which also promoted the growth of a Phanerochaete chyrsosporium fungal mat. Although fungal growth in weathered hydrocarbon contaminated soil could be promoted through supplementing additional carbon sources (Tween 80, sawdust, compost, pea straw), fungal (14)C-hexadecane mineralisation was negligible when sodium azide was added to soil microcosms to inhibit bacterial activity. In contrast, when fungal activity was inhibited through nystatin additions, (14)C-hexadecane mineralisation ranged from 6.5 ± 0.2 to 35.8 ± 3.8% after 98 days depending on the supplied amendment. Bacteria inhibition with sodium azide resulted in a reduction in bacterial diversity (33-37%) compared to microcosms supplemented with nystatin or microcosms without inhibitory supplements. However, alkB bacterial groups were undetected in sodium azide supplemented microcosms, highlighting the important role of this bacterial group in (14)C-hexadecane mineralisation.</AbstractText><CopyrightInformation>Copyright © 2011 Elsevier B.V. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Adetutu</LastName><ForeName>Eric M</ForeName><Initials>EM</Initials><AffiliationInfo><Affiliation>School of Biological Sciences, Flinders University, Adelaide, South Australia 5001, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ball</LastName><ForeName>Andy S</ForeName><Initials>AS</Initials></Author><Author ValidYN="Y"><LastName>Weber</LastName><ForeName>John</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Aleer</LastName><ForeName>Samuel</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Dandie</LastName><ForeName>Catherine E</ForeName><Initials>CE</Initials></Author><Author ValidYN="Y"><LastName>Juhasz</LastName><ForeName>Albert L</ForeName><Initials>AL</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2011</Year><Month>12</Month><Day>07</Day></ArticleDate></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>Sci Total Environ</MedlineTA><NlmUniqueID>0330500</NlmUniqueID><ISSNLinking>0048-9697</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000473">Alkanes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D002250">Carbon Radioisotopes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010578">Petroleum</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011136">Polysorbates</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012336">RNA, Ribosomal, 16S</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012989">Soil Pollutants</NameOfSubstance></Chemical><Chemical><RegistryNumber>1400-61-9</RegistryNumber><NameOfSubstance UI="D009761">Nystatin</NameOfSubstance></Chemical><Chemical><RegistryNumber>27YLU75U4W</RegistryNumber><NameOfSubstance UI="D010758">Phosphorus</NameOfSubstance></Chemical><Chemical><RegistryNumber>968JJ8C9DV</RegistryNumber><NameOfSubstance UI="D019810">Sodium Azide</NameOfSubstance></Chemical><Chemical><RegistryNumber>F8Z00SHP6Q</RegistryNumber><NameOfSubstance UI="C007932">n-hexadecane</NameOfSubstance></Chemical><Chemical><RegistryNumber>N762921K75</RegistryNumber><NameOfSubstance UI="D009584">Nitrogen</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000473" MajorTopicYN="N">Alkanes</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000704" MajorTopicYN="N">Analysis of Variance</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001419" MajorTopicYN="N">Bacteria</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001673" MajorTopicYN="N">Biodegradation, Environmental</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002250" MajorTopicYN="N">Carbon Radioisotopes</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016000" MajorTopicYN="N">Cluster Analysis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009584" MajorTopicYN="N">Nitrogen</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009761" MajorTopicYN="N">Nystatin</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010578" MajorTopicYN="N">Petroleum</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010758" MajorTopicYN="N">Phosphorus</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016133" MajorTopicYN="N">Polymerase Chain Reaction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011136" MajorTopicYN="N">Polysorbates</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012336" MajorTopicYN="N">RNA, Ribosomal, 16S</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019810" MajorTopicYN="N">Sodium Azide</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012989" MajorTopicYN="N">Soil Pollutants</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year><Month>08</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2011</Year><Month>10</Month><Day>11</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2011</Year><Month>11</Month><Day>03</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2011</Year><Month>12</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2011</Year><Month>12</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>5</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">22154183</ArticleId><ArticleId IdType="pii">S0048-9697(11)01358-1</ArticleId><ArticleId IdType="doi">10.1016/j.scitotenv.2011.11.044</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Australie</li></country></list><tree><noCountry><name sortKey="Aleer, Samuel" sort="Aleer, Samuel" uniqKey="Aleer S" first="Samuel" last="Aleer">Samuel Aleer</name><name sortKey="Ball, Andy S" sort="Ball, Andy S" uniqKey="Ball A" first="Andy S" last="Ball">Andy S. Ball</name><name sortKey="Dandie, Catherine E" sort="Dandie, Catherine E" uniqKey="Dandie C" first="Catherine E" last="Dandie">Catherine E. Dandie</name><name sortKey="Juhasz, Albert L" sort="Juhasz, Albert L" uniqKey="Juhasz A" first="Albert L" last="Juhasz">Albert L. Juhasz</name><name sortKey="Weber, John" sort="Weber, John" uniqKey="Weber J" first="John" last="Weber">John Weber</name></noCountry><country name="Australie"><noRegion><name sortKey="Adetutu, Eric M" sort="Adetutu, Eric M" uniqKey="Adetutu E" first="Eric M" last="Adetutu">Eric M. Adetutu</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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