Loading…

Anthropogenic and naturally-produced organobrominated compounds in bluefin tuna from the Mediterranean Sea

Anthropogenic compounds, such as polybrominated diphenyl ethers (PBDEs), together with naturally-produced organobromines, such as methoxylated PBDEs (MeO-PBDEs), polybrominated hexahydroxanthene derivatives (PBHDs), 2,4,6-tribromoanisole (TBA) and a mixed halogenated monoterpene (MHC-1), were measur...

Full description

Saved in:
Bibliographic Details
Published in:Chemosphere (Oxford) 2009-09, Vol.76 (11), p.1477-1482
Main Authors: Pena-Abaurrea, Miren, Weijs, Liesbeth, Ramos, Lourdes, Borghesi, Nicoletta, Corsolini, Simonetta, Neels, Hugo, Blust, Ronny, Covaci, Adrian
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Anthropogenic compounds, such as polybrominated diphenyl ethers (PBDEs), together with naturally-produced organobromines, such as methoxylated PBDEs (MeO-PBDEs), polybrominated hexahydroxanthene derivatives (PBHDs), 2,4,6-tribromoanisole (TBA) and a mixed halogenated monoterpene (MHC-1), were measured in muscle from 26 farmed and wild bluefin tuna ( Thunnus thynnus) caught in the Mediterranean Sea. This species is ecological attractive because of the changes of geographic habitat throughout its long lifespan which affect its feeding. PBDE concentrations were similar between tuna samples of different groups (17–149 ng g −1 lipid weight – lw in farmed tuna, 25–219 ng g −1 lw in longline fished tuna and 26–126 ng g −1 lw in net-fished tuna). However, higher concentrations of naturally-produced MeO-PBDEs and PBHDs were observed in the two types of wild tuna (longline fished and net-fished) compared to farmed tuna suggesting that wild tunas come easily in contact with sources of these compounds. In all cases PBHDs presented the highest contribution to the sum of organobromines (50% in farmed tuna and >90% in wild tuna). TBA was detected at low concentrations (
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2009.07.004