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Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina)

Authorized Users Only
2014
Authors
Grba, Nenad
Šajnović, Aleksandra
Stojanović, Ksenija
Simić, Vladimir
Jovančićević, Branimir
Roglić, Goran
Eric, Vladisav
Article (Published version)
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Abstract
Sedimentary rocks from the saline formation of the Lopare Basin were investigated. Sediments contain a moderate amount of immature to marginally mature algal organic matter deposited under slightly reducing to anoxic and slightly saline to hypersaline conditions. Almost all of the samples contain beta-carotane in a relatively high quantity, and in some, it represents the most abundant compound in the total distribution of hydrocarbons. The objective of the study was to determine the conditions that are favourable to precursors of beta-carotene and/or the preservation of the carotenoid hydrocarbon skeleton. Moreover, the dominant transformation pathways of beta-carotene under different redox and salinity conditions, which lead to the formation of aromatic carotenoids were defined. Based on the content of beta-carotane, the examined sedimentary rocks are divided into groups A, B and C. Group A does not contain or contains up to 1% of beta-carotane, group B contains between 1 and 5% of be...ta-carotane, while group C contains more than 5% of 13-carotane in the overall distribution of hydrocarbons. The organic matter (OM) of the sediments of group A is characterized by a higher contribution of prokaryotic precursor organisms, in comparison with the other samples. The OM was deposited in a slightly saline reductive environment, with an increased erosion activity. This environment was unfavourable for the precursors of beta-carotene and/or for preservation of its hydrocarbon skeleton. Evidence for the degradation of the poliene chain in beta-carotene is the domination of monoaromatic compounds in the aromatic carotenoids distribution. The OM of sediments of groups B and C is similar, predominantly of algal origin deposited in a reducing to anoxic calm carbonate environment with salinity changes from hypersaline to saline. Such reduced to anoxic saline, but not hypersaline environments are most appropriate for precursors of beta-carotene and for the preservation of carotenoid skeleton. Cyclization and aromatization of polyene isoprenoid chain, whereby terminal groups remain the main pattern, is the main pathway of beta-carotene aromatization in anoxic hypersaline environments, whereas aromatization of terminal 1,1,5-trimethylcyclohexen-5-enyl groups and expulsion of toluene and m-xylene are typical for the reduced to anoxic saline environments.

Keywords:
Lopare Basin / Saline/hypersaline depositional / environment / Geochemistry / beta-Carotane / Aromatic carotenoids
Source:
Chemie Der Erde-Geochemistry, 2014, 74, 1, 107-123
Publisher:
  • Elsevier Gmbh, Urban & Fischer Verlag, Jena
Funding / projects:
  • Geochemical investigations of sedimentary rocks - fossil fuels and environmental pollutants (RS-176006)
  • Magmatism and geodynamics of the Balkan Peninsula from Mesozoic to present day: significance for the formation of metallic and non-metallic mineral deposits (RS-176016)

DOI: 10.1016/j.chemer.2013.10.002

ISSN: 0009-2819

WoS: 000336116800007

Scopus: 2-s2.0-84898543552
[ Google Scholar ]
13
9
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/1578
Collections
  • Radovi istraživača / Researchers' publications
Institution/Community
IHTM
TY  - JOUR
AU  - Grba, Nenad
AU  - Šajnović, Aleksandra
AU  - Stojanović, Ksenija
AU  - Simić, Vladimir
AU  - Jovančićević, Branimir
AU  - Roglić, Goran
AU  - Eric, Vladisav
PY  - 2014
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1578
AB  - Sedimentary rocks from the saline formation of the Lopare Basin were investigated. Sediments contain a moderate amount of immature to marginally mature algal organic matter deposited under slightly reducing to anoxic and slightly saline to hypersaline conditions. Almost all of the samples contain beta-carotane in a relatively high quantity, and in some, it represents the most abundant compound in the total distribution of hydrocarbons. The objective of the study was to determine the conditions that are favourable to precursors of beta-carotene and/or the preservation of the carotenoid hydrocarbon skeleton. Moreover, the dominant transformation pathways of beta-carotene under different redox and salinity conditions, which lead to the formation of aromatic carotenoids were defined. Based on the content of beta-carotane, the examined sedimentary rocks are divided into groups A, B and C. Group A does not contain or contains up to 1% of beta-carotane, group B contains between 1 and 5% of beta-carotane, while group C contains more than 5% of 13-carotane in the overall distribution of hydrocarbons. The organic matter (OM) of the sediments of group A is characterized by a higher contribution of prokaryotic precursor organisms, in comparison with the other samples. The OM was deposited in a slightly saline reductive environment, with an increased erosion activity. This environment was unfavourable for the precursors of beta-carotene and/or for preservation of its hydrocarbon skeleton. Evidence for the degradation of the poliene chain in beta-carotene is the domination of monoaromatic compounds in the aromatic carotenoids distribution. The OM of sediments of groups B and C is similar, predominantly of algal origin deposited in a reducing to anoxic calm carbonate environment with salinity changes from hypersaline to saline. Such reduced to anoxic saline, but not hypersaline environments are most appropriate for precursors of beta-carotene and for the preservation of carotenoid skeleton. Cyclization and aromatization of polyene isoprenoid chain, whereby terminal groups remain the main pattern, is the main pathway of beta-carotene aromatization in anoxic hypersaline environments, whereas aromatization of terminal 1,1,5-trimethylcyclohexen-5-enyl groups and expulsion of toluene and m-xylene are typical for the reduced to anoxic saline environments.
PB  - Elsevier Gmbh, Urban & Fischer Verlag, Jena
T2  - Chemie Der Erde-Geochemistry
T1  - Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina)
VL  - 74
IS  - 1
SP  - 107
EP  - 123
DO  - 10.1016/j.chemer.2013.10.002
ER  - 
@article{
author = "Grba, Nenad and Šajnović, Aleksandra and Stojanović, Ksenija and Simić, Vladimir and Jovančićević, Branimir and Roglić, Goran and Eric, Vladisav",
year = "2014",
abstract = "Sedimentary rocks from the saline formation of the Lopare Basin were investigated. Sediments contain a moderate amount of immature to marginally mature algal organic matter deposited under slightly reducing to anoxic and slightly saline to hypersaline conditions. Almost all of the samples contain beta-carotane in a relatively high quantity, and in some, it represents the most abundant compound in the total distribution of hydrocarbons. The objective of the study was to determine the conditions that are favourable to precursors of beta-carotene and/or the preservation of the carotenoid hydrocarbon skeleton. Moreover, the dominant transformation pathways of beta-carotene under different redox and salinity conditions, which lead to the formation of aromatic carotenoids were defined. Based on the content of beta-carotane, the examined sedimentary rocks are divided into groups A, B and C. Group A does not contain or contains up to 1% of beta-carotane, group B contains between 1 and 5% of beta-carotane, while group C contains more than 5% of 13-carotane in the overall distribution of hydrocarbons. The organic matter (OM) of the sediments of group A is characterized by a higher contribution of prokaryotic precursor organisms, in comparison with the other samples. The OM was deposited in a slightly saline reductive environment, with an increased erosion activity. This environment was unfavourable for the precursors of beta-carotene and/or for preservation of its hydrocarbon skeleton. Evidence for the degradation of the poliene chain in beta-carotene is the domination of monoaromatic compounds in the aromatic carotenoids distribution. The OM of sediments of groups B and C is similar, predominantly of algal origin deposited in a reducing to anoxic calm carbonate environment with salinity changes from hypersaline to saline. Such reduced to anoxic saline, but not hypersaline environments are most appropriate for precursors of beta-carotene and for the preservation of carotenoid skeleton. Cyclization and aromatization of polyene isoprenoid chain, whereby terminal groups remain the main pattern, is the main pathway of beta-carotene aromatization in anoxic hypersaline environments, whereas aromatization of terminal 1,1,5-trimethylcyclohexen-5-enyl groups and expulsion of toluene and m-xylene are typical for the reduced to anoxic saline environments.",
publisher = "Elsevier Gmbh, Urban & Fischer Verlag, Jena",
journal = "Chemie Der Erde-Geochemistry",
title = "Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina)",
volume = "74",
number = "1",
pages = "107-123",
doi = "10.1016/j.chemer.2013.10.002"
}
Grba, N., Šajnović, A., Stojanović, K., Simić, V., Jovančićević, B., Roglić, G.,& Eric, V.. (2014). Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina). in Chemie Der Erde-Geochemistry
Elsevier Gmbh, Urban & Fischer Verlag, Jena., 74(1), 107-123.
https://doi.org/10.1016/j.chemer.2013.10.002
Grba N, Šajnović A, Stojanović K, Simić V, Jovančićević B, Roglić G, Eric V. Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina). in Chemie Der Erde-Geochemistry. 2014;74(1):107-123.
doi:10.1016/j.chemer.2013.10.002 .
Grba, Nenad, Šajnović, Aleksandra, Stojanović, Ksenija, Simić, Vladimir, Jovančićević, Branimir, Roglić, Goran, Eric, Vladisav, "Preservation of diagenetic products of beta-carotene in sedimentary rocks from the Lopare Basin (Bosnia and Herzegovina)" in Chemie Der Erde-Geochemistry, 74, no. 1 (2014):107-123,
https://doi.org/10.1016/j.chemer.2013.10.002 . .

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