Ecotoxicity of diethylene glycol and risk assessment for marine environment.

Diethylene glycol (DEG) is a chemical compound used during offshore oil activities to prevent hydrate formation, and it may be released into the sea. A full ecotoxicological characterization is required according to European and Italian regulations for chemical substances. We have evaluated long-term toxic effects of DEG on indicator species of the marine environment as algae (Phaeodactylum tricornutum), crustaceans (Artemia franciscana), molluscs (Tapes philippinarum) and fish (Dicentrarchus labrax). A range of no observed effect concentrations (365-25,000 mg/L) has been identified. Based on the toxicity results and the ratio between predicted environmental concentration and predicted no-effect concentration, we have estimated the maximum allowable value of DEG in the marine environment.

LC-ESI-MS determination of diethylene glycol pollution in sea water samples collected around gas extraction platform plants.

Produced formation waters (PFWs) represent the largest aqueous wastes that are normally discharged into the marine environment during the offshore gas production processes. The chemical additive diethylene glycol (DEG) is widely used in the gas production line and therefore can be found in the PFW, becoming of environmental concern. In this study, a new method has been developed for trace determination of DEG in sea water samples collected around offshore gas platforms. The method is based on liquid chromatography coupled to electrospray ionization mass spectrometry (LC-ESI-MS). Prior to analysis, water samples were derivatized using the Schotten-Baumann method for the benzoylation of glycols. The derivatization procedure allowed us to maximize the ESI-MS response of DEG and minimize the influence of interfering compounds. The method was validated and allowed a quantification of DEG in sea water samples with a method LOD of 0.4 ng/mL. The applicability of the procedure was demonstrated by analyzing sea water samples collected around eight gas platforms located in the Adriatic Sea (Italy).

Near-field dispersion of produced formation water (PFW) in the Adriatic Sea: an integrated numerical-chemical approach.

Produced formation waters (PFWs), a by-product of both oil and gas extraction, are separated from hydrocarbons onboard oil platforms and then discharged into the sea through submarine outfalls. The dispersion of PFWs into the environment may have a potential impact on marine ecosystems. We reproduce the initial PFW-seawater mixing process by means of the UM3 model applied to offshore natural gas platforms currently active in the Northern Adriatic Sea (Mediterranean Sea). Chemical analyses lead to the identification of a chemical tracer (diethylene glycol) which enables us to follow the fate of PFWs into receiving waters. The numerical simulations are realized in different seasonal conditions using both measured oceanographic data and tracer concentrations. The numerical results show the spatial and temporal plume development in different stratification and ambient current conditions. The analytical approach measures concentrations of the diethylene glycol at a maximum sampling distance of 25 m. The results show a good agreement between field observations and model predictions in the near-field area. The integration of numerical results with chemical analyses also provides new insight to plan and optimize PFW monitoring and discharge.

Ozone quenching properties of isoprene and its antioxidant role in leaves.

Isoprene is formed in and emitted by plants and the reason for this apparent carbon waste is still unclear. It has been proposed that isoprene stabilizes cell and particularly chloroplast thylakoid membranes. We tested if membrane stabilization or isoprene reactivity with ozone induces protection against acute ozone exposures. The reduction of visible, physiological, anatomical, and ultrastructural (chloroplast) damage shows that clones of plants sensitive to ozone and unable to emit isoprene become resistant to acute and short exposure to ozone if they are fumigated with exogenous isoprene, and that isoprene-emitting plants that are sensitive to ozone do not suffer damage when exposed to ozone. Isoprene-induced ozone resistance is associated with the maintenance of photochemical efficiency and with a low energy dissipation, as indicated by fluorescence quenching. This suggests that isoprene effectively stabilizes thylakoid membranes. However, when isoprene reacts with ozone within the leaves or in a humid atmosphere, it quenches the ozone concentration to levels that are less or non-toxic for plants. Thus, protection from ozone in plants fumigated with isoprene may be due to a direct ozone quenching rather than to an induced resistance at membrane level. Irrespective of the mechanism, isoprene is one of the most effective antioxidants in plants.