Matches in SemOpenAlex for { <https://semopenalex.org/work/W16946199> ?p ?o ?g. }
Showing items 1 to 56 of
56
with 100 items per page.
- W16946199 endingPage "4876" @default.
- W16946199 startingPage "4873" @default.
- W16946199 abstract "In a North Sea oil, the carotenoid derivatives -carotene, -isorenieratane, and isorenieratane were identified, together with a series of aryl isoprenoids with a 2,3,6-trimethyl substitution pattern for the aromatic ring. The 13C values of -carotene and -isorenieratane are similar, whereas isorenieratane is ca. 15% heavier. This suggests that -isorenieratane is not derived from -isorenieratane biosynthesised by Chlorobiaceae, but from aromatisation of -carotene. This was confirmed by laboratory aromatisation of partially hydrogenated -carotene, which yielded -isorenieratane as the main product. The aryl isoprenoids, which can be formed by C---C bond cleavage of both isorenieratane and -isorenieratane, have a mixed isotopic signature in the oil. These results indicate that mere identification of aryl isoprenoids, without determination of their 13C values, cannot be used to assess the presence of Chlorobiaceae, and, thus, photic zone anoxia in the depositional environment." @default.
- W16946199 created "2016-06-24" @default.
- W16946199 creator A5011673657 @default.
- W16946199 creator A5018073562 @default.
- W16946199 creator A5034816300 @default.
- W16946199 creator A5067673605 @default.
- W16946199 date "1996-01-01" @default.
- W16946199 modified "2023-09-26" @default.
- W16946199 title "Restricted utility of aryl isoprenoids as indicators of photic zone anoxia" @default.
- W16946199 hasPublicationYear "1996" @default.
- W16946199 type Work @default.
- W16946199 sameAs 16946199 @default.
- W16946199 citedByCount "1" @default.
- W16946199 crossrefType "journal-article" @default.
- W16946199 hasAuthorship W16946199A5011673657 @default.
- W16946199 hasAuthorship W16946199A5018073562 @default.
- W16946199 hasAuthorship W16946199A5034816300 @default.
- W16946199 hasAuthorship W16946199A5067673605 @default.
- W16946199 hasConcept C142796444 @default.
- W16946199 hasConcept C178790620 @default.
- W16946199 hasConcept C185592680 @default.
- W16946199 hasConcept C206103511 @default.
- W16946199 hasConcept C2780263894 @default.
- W16946199 hasConcept C2780892065 @default.
- W16946199 hasConcept C2781076698 @default.
- W16946199 hasConcept C71240020 @default.
- W16946199 hasConcept C86839594 @default.
- W16946199 hasConceptScore W16946199C142796444 @default.
- W16946199 hasConceptScore W16946199C178790620 @default.
- W16946199 hasConceptScore W16946199C185592680 @default.
- W16946199 hasConceptScore W16946199C206103511 @default.
- W16946199 hasConceptScore W16946199C2780263894 @default.
- W16946199 hasConceptScore W16946199C2780892065 @default.
- W16946199 hasConceptScore W16946199C2781076698 @default.
- W16946199 hasConceptScore W16946199C71240020 @default.
- W16946199 hasConceptScore W16946199C86839594 @default.
- W16946199 hasIssue "23" @default.
- W16946199 hasLocation W169461991 @default.
- W16946199 hasOpenAccess W16946199 @default.
- W16946199 hasPrimaryLocation W169461991 @default.
- W16946199 hasRelatedWork W2005029962 @default.
- W16946199 hasRelatedWork W2013293921 @default.
- W16946199 hasRelatedWork W2023621444 @default.
- W16946199 hasRelatedWork W2037451857 @default.
- W16946199 hasRelatedWork W2039965897 @default.
- W16946199 hasRelatedWork W2086766760 @default.
- W16946199 hasRelatedWork W2140264363 @default.
- W16946199 hasRelatedWork W2169515843 @default.
- W16946199 hasRelatedWork W2287094880 @default.
- W16946199 hasVolume "60" @default.
- W16946199 isParatext "false" @default.
- W16946199 isRetracted "false" @default.
- W16946199 magId "16946199" @default.
- W16946199 workType "article" @default.