Contamination with retinoic acid receptor agonists in two rivers in the Kinki region of Japan.

This study was conducted to investigate the agonistic activity against human retinoic acid receptor (RAR) alpha in the Lake Biwa-Yodo River and the Ina River in the Kinki region of Japan. To accomplish this, a yeast two-hybrid assay was used to elucidate the spatial and temporal variations and potential sources of RARalpha agonist contamination in the river basins. RARalpha agonistic activity was commonly detected in the surface water samples collected along two rivers at different periods, with maximum all-trans retinoic acid (atRA) equivalents of 47.

Identification of retinoic acid receptor agonists in sewage treatment plants.

Retinoic acid receptor (RAR) agonists are speculated to be one possible cause for the widely observed frog deformities in North America, although little is known about the specific RAR agonists in aquatic environments. We identified the specific RAR egonists in sewage treatment plants (STPs) and receiving rivers using an RAR yeast two-hybrid bioassay. Water samples were extracted by solid-phase extract cartridges, which were successively eluted by hexane, ethyl acetate, and methanol for bioassay.

Evaluation of wastewater reclamation technologies based on in vitro and in vivo bioassays.

When municipal secondary effluent is used as the main supplementation water source for surface water bodies, its potential adverse ecological effects should not be neglected. The objective of this work was to investigate the effectiveness of several technologies, i.e.

Decomposition of two haloacetic acids in water using UV radiation, ozone and advanced oxidation processes.

The decomposition of two haloacetic acids (HAAs), dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA), from water was studied by means of single oxidants: ozone, UV radiation; and by the advanced oxidation processes (AOPs) constituted by combinations of O(3)/UV radiation, H(2)O(2)/UV radiation, O(3)/H(2)O(2), O(3)/H(2)O(2)/UV radiation. The concentrations of HAAs were analyzed at specified time intervals to elucidate the decomposition of HAAs. Single O(3) or UV did not result in perceptible decomposition of HAAs within the applied reaction time.