Behavior of PAHs during cold storage of historically contaminated soil samples

The stability of historically polycyclic aromatic hydrocarbon (PAH)-contaminated soils during cold storage was investigated. Samples from two former manufactured gas plants exhibited quantitative recoveries of PAHs over the whole period of sample holding at 4 °C in the dark (8–10 months), whereas significant losses of PAHs were observed for soils received from a former railroad sleeper preservation plant with low molecular weight compounds being notably more affected compared to heavier PAHs. Already after 2 weeks of holding time, 3-ring PAHs in one of theses samples were down to 29–73% of the initial concentration and significant losses were observed for up to 5-ring compounds. Dissipation of PAHs was found to be predominantly due to aerobic microbial metabolism since sodium azide poisoned samples showed quantitative recoveries for all PAHs over the entire storage time of 3 months. A similar stabilizing effect was observed for freezing at −20 °C as means of preservation. Except for acenaphthene, no significant loss for any of the PAHs was observed over 6 weeks of holding time. Eventually, selected chemical, physical, and biological parameters of two soils were investigated and identified as potential indicators for the stability of PAH-contaminated soil samples.     

Production of reactive oxygen species and 8-hydroxy-2'deoxyguanosine in KB cells co-exposed to benzo[a]pyrene and UV-A radiation

Previous studies have shown that ultraviolet (UV) A light and the polycyclic aromatic hydrocarbon benzo[a]pyrene (BaP) can synergistically enhance the formation of 8-hydroxy-2'deoxyguanosine (8-OHdG) in living cells. It has been postulated that the underlying mechanism is production of reactive oxygen species (ROS) via photosensitization, but direct evidence supporting this hypothesis has been lacking. This study examined intracellular ROS production in living cells co-exposed to UV-A and BaP as well as the relationship between intracellular production of ROS and formation of 8-OHdG. KB cells were exposed to BaP for 24 h, followed by exposure to UV-A (365 nm) or UV-B (312 nm). The levels of intracellular ROS were directly measured by use of the fluorescent probe dihydrorhodamine 123 (DHR-123) in flow cytometry. Levels of 8-OHdG were measured by high performance liquid chromatography coupled with electrochemical detection (HPLC-ECD). The results demonstrated that UV-B itself induced a much greater level of intracellular ROS than did UV-A alone under the same dose of energy (0.10 mW/cm(2), 20 min). The presence of BaP (13.3 microM) substantially increased ROS production in UV-A-treated cells (2.9-fold), but only slightly enhanced ROS production in UV-B-treated cells (1.3-fold). These results show that BaP acts mainly as a photosensitizer of UV-A, but not UV-B. Furthermore, greater intracellular ROS production was proportional to both BaP concentration and UV-A dosage. There was a linear relationship between ROS production and 8-OHdG formation in cells co-exposed to BaP and UV-A. Results of this study suggest that UV-A and BaP act synergistically to enhance ROS production and formation of 8-OHdG, resulting in increased DNA damage.     

Nutzung der induzierbaren Genexpression des NematodenCaenorhabditis elegans als Biomonitor

The soil nematodeCaenorhabditis elegans is one of the simplest animals having the status of a laboratory model. Its already completely sequenced genome contains the remarkable number of 80 cytochrome P450 genes (CYP) and many further genes coding for enzymes involved in biotransformation. In order to study xenobiotically induced gene expression inC. elegans, liquid cultures were exposed to different, well-known xenobiotic inducers. The mRNA expression was detected by two different types of DNA arrays and semi-quantitative RT-PCR. β-naphthoflavone, PCB52 and lansoprazol were the most active and, in particular, induced almost all CYP35 isoforms strongly. In conclusion, the xenobiotic dependent gene expression ofC. elegans is a useful tool to reveal defense mechanisms against potential damaging substances as well as for developing a biomonitoring system.     

Managing the offspring environment: brood care in the bromeliad crab,Metopaulias depressus

Summary Maternal modification of the larval environment was studied in the bromeliad crab, Metopaulias depressus (Decapoda, Grapsidae). The bromeliad crab breeds in rain water stored in the leaf axils of large Jamaican bromeliads. The physico-chemical water conditions are highly unfavorable for the development of the larvae. Water in nursery axils contained no leaf litter and up to 14 empty snail shells, whereas other axils were partly or completely covered with leaf litter and rarely held snail shells. Mother crabs removed leaf litter from nursery axils, and occasionally from neighboring axils. Nursery axils contained twice as much dissolved oxygen (DO₂) at night when DO₂ is at a minimum, and less dissolved carbon dioxide (DCO₂) than axils unattended by a crab. The higher DO₂ content in nurseries meets the respiratory needs of an average sized brood, but the lower concentration in axils with litter may not. It is suggested that the higher DO₂ and lower DCO₂ concentrations in the nursery axils result from a water circulation produced by the mother and her leaf litter cleaning behavior. The low pH and the Ca²⁺ content in the water of unattended bromeliad axils are unfavorable for development of larvae and young. Mother crabs significantly increased pH and Ca²⁺ by adding empty snail shells to the nursery-axil water. In experiments where the brood was transferred to other axils, mothers switched from the nursery axil to the new axil containing the brood, and there continued caring for their offspring.