The analysis and control of volatile hydrocarbon concentrations (e. g. benzene) during oil bioassays

It is well known that volatile hydrocarbons such as benzene, toluene, and xylene, which are abundant in many refined oils, affect phytoplankton growth. However, experiments to determine these effects in many cases have been improperly designed resulting in questionable conclusions. Experiments presented in this paper indicate that ambient benzene concentrations reported in the published literature may be lower than stated by an order of 10 to 100. By continuous monitoring the benzene concentration decrease was observed and it was possible to determine whether the loss was due to degassing because of loose closures or biological uptake. Unless tight closures are used benzene is quickly lost to the atmosphere (exponential decay rate ≌ 1.2d ^-1). Experiments demonstrated that benzene is quickly lost from cotton stoppered bioassay flasks that are typically used. Rubber stoppered flasks with little gaseous headspace showed minimum benzene loss. Biological uptake of benzene can be demonstrated when closures are secure and the effect of certain concentrations on growth can be correctly interpreted. Benzene concentrations above 10 to 20 ppm significantly reduce the growth rate of Skeletonema sp. The benzene concentration decreased quickly in 10 to 20 ppm benzene solutions implying metabolic uptake. These experiments indicate that proper closures and analysis of the volatile pollutant concentration during bioassay experiments increase the likelihood of correct interpretation and may yield additional insights into the causation factors.