Journal of Japan Society on Water Environment
Online ISSN : 1881-3690
Print ISSN : 0916-8958
ISSN-L : 0916-8958
Volume 41, Issue 1
Displaying 1-2 of 2 articles from this issue
Research Paper
  • Shiho KOBAYASHI, Tateki FUJIWARA, Yukio KOMAI, Shuhei TANAKA, Yuji SUZ ...
    Article type: Research Paper
    2018 Volume 41 Issue 1 Pages 1-10
    Published: 2018
    Released on J-STAGE: January 10, 2018
    JOURNAL FREE ACCESS
    The method of estimating the source origin of the organic matter that consumes dissolved oxygen in an aquatic environment using carbon stable isotope (δ13C) of dissolved inorganic carbon (DIC) is effective because the method needs only a small portion of water and a brief duration. In an anoxic water mass in a low-lying depression in a port, δ13C-DIC decreases in accordance with the increase in the concentration of DIC (R2=0.93) ; and hence, δ13C of the organic matter that consumes dissolved oxygen can be estimated with considerable accuracy using the relationship between the concentration of DIC and δ13C-DIC. We demonstrated that the method of using in situ δ13C-DIC, which had been applied to lakes, performs effectively under the condition of continually decreasing pH in an anoxic water mass formed at the bottom of the sea. The contribution ratio of the phytoplankton-derived and land-derived organic matter was estimated using their δ13C values estimated in previous studies. As a result, 59-88% of organic matter that consumes oxygen was estimated to originate from phytoplankton. Low-lying depressions in coastal seas, where the water exchange rate is significantly small, is suitable for examining remineralization processes of organic matter in coastal seas.
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Survey Paper
  • Taro URASE, Hirofumi TSUTSUI, Kazuya NAKAMURA
    Article type: Survey Paper
    2018 Volume 41 Issue 1 Pages 11-17
    Published: 2018
    Released on J-STAGE: January 10, 2018
    JOURNAL FREE ACCESS
    Supplementary material
    A gas chromatography - olfactometry analysis was conducted for biologically treated wastewater samples from seven different plants to clarify the compounds responsible for the odor of biologically treated wastewater. The odor of 2,4,6-trichloroanisole was detected with the highest or second-highest odor intensity for the treated wastewater samples from large-scale plants whose biological reactors are covered with a roof. The treated wastewater from these large-scale plants contained 11.6–21.2 ng L-1 of 2,4,6-trichloroanisole, and this range of concentration was approximately 100 times as high as the olfactory threshold. Earthy and musty odors, probably caused by geosmin and 2-methylisoborneol, were also detected with high odor intensities in all samples. A large contribution of an unidentified compound with a sweet odor was also observed in the analysis of treated water samples. In addition to earthy and musty odors, sulfuric and septic odors were detected in the samples from small-scale plants.
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