2019
DOI: 10.1016/j.scitotenv.2019.134037
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Occurrence and trophic transfer of aliphatic hydrocarbons in fish species from Yellow River Estuary and Laizhou Bay, China

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Cited by 10 publications
(6 citation statements)
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“…The total n-alkane concentrations in the fish tissues ranged from 7.27 µg/g Dwt in C. idella (herbivorous) to 23.14 µg/g Dwt in the P. abu (filter feeder). They were similar to the concentration ranges reported in fish tissues and muscles from different rivers and lakes (Colombo et al, 2007;Olaji et al, 2014;Al-Imarah et al, 2016;Wang et al, 2019) The predominance of nC 24 in the fish tissues may be due to the fish feeding on algae and detritus because the major source of nC 24 is likely from the algae, phytoplankton, and bacteria (Gomes and Azevedo, 2003;Shahbazi, 2009). The distribution of n-alkanes and the high level of nC 29 (0.393 µg/g ) in the fish tissue of C. carpio may be attributed to their feeding on a freshwater higher, mainly emergent, plants because usually nC 27 nC 29 and nC 31 are the major n-alkanes in plant waxes of these plants (Eglinton and Hamilton, 1967;Simoneit, 1978;Ficken et al, 2000;Duan and Xu, 2012).…”
Section: Aliphatic Hydrocarbon Distribution Levels and Similaritysupporting
confidence: 84%
“…The total n-alkane concentrations in the fish tissues ranged from 7.27 µg/g Dwt in C. idella (herbivorous) to 23.14 µg/g Dwt in the P. abu (filter feeder). They were similar to the concentration ranges reported in fish tissues and muscles from different rivers and lakes (Colombo et al, 2007;Olaji et al, 2014;Al-Imarah et al, 2016;Wang et al, 2019) The predominance of nC 24 in the fish tissues may be due to the fish feeding on algae and detritus because the major source of nC 24 is likely from the algae, phytoplankton, and bacteria (Gomes and Azevedo, 2003;Shahbazi, 2009). The distribution of n-alkanes and the high level of nC 29 (0.393 µg/g ) in the fish tissue of C. carpio may be attributed to their feeding on a freshwater higher, mainly emergent, plants because usually nC 27 nC 29 and nC 31 are the major n-alkanes in plant waxes of these plants (Eglinton and Hamilton, 1967;Simoneit, 1978;Ficken et al, 2000;Duan and Xu, 2012).…”
Section: Aliphatic Hydrocarbon Distribution Levels and Similaritysupporting
confidence: 84%
“…The mean BSAFs for the total of the eight MLPs in mollusks and crustaceans were 15.5 and 2.03, respectively. There are no MLP BSAFs available for comparison, but studies of other organic pollutants have revealed that the differences in the BSAF are a consequence of bioavailability, uptake-elimination, and biotransformation. , …”
Section: Resultsmentioning
confidence: 99%
“…The octanol–water partition coefficient ( K ow ) is an important factor affecting the bioaccumulation and biomagnification potential of nonionized organic compounds, while the octanol–water distribution coefficient ( D ow ) is an alternative for studying ionized analytes. , Our studied MLPs are soluble in lipids and are suggested to have high log K ow values. In addition, a previous study predicted the log K ow values for acidic MLPs, including AZA1 (4.06 ± 2.20), AZA2 (4.32 ± 2.33), OA (4.45 ± 2.60), DTX1 (4.79 ± 2.67), and DTX2 (4.46 ± 2.55) .…”
Section: Resultsmentioning
confidence: 99%
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“…Bioaccumulation occurs from sediment to biota when BSAF are close to, or greater than 1 (Yang et al, 2019). The BSAF values of aliphatic hydrocarbons dramatically varied from 0.829 in Cyprinus carpio to 17.3 in Silurus asotus (Wang et al, 2019), due to the differences in selective excretion abilities and elimination mechanisms among different species (Wang et al, 2018).…”
Section: Biota-sediment Accumulation Factormentioning
confidence: 99%