14:30 〜 14:45
[HTT21-10] 菌類による放射性セシウムの吸収 -安定同位体による土壌中菌糸の分布推定-
キーワード：放射性セシウム、菌糸、安定同位体
Many studies after the Chernobyl nuclear accident in 1986 have reported that fungal fruit bodies accumulated higher 137Cs concentration than other organic materials in forest ecosystem. Some of the studies pointed out soil hyphal distribution as one of the main factors determining 137Cs concentration in fungi, but the viewpoint has not yet been examined well. We therefore have attempted multi stable isotopes (13C, 15N and 34S) to examine the relationship between hyphal vertical distribution and 137Cs concentration in fruit bodies.
Study site was a broad-leaved forest dominated by konara oak, mixed with fir, located at 20 km southwest from the Fukushima Daiichi Nuclear Power Plant, in Kawauchi Village, Fukushima Prefecture. Fruit bodies and soil core samples (down to 30 cm below the soil surface) were collected. After oven-dried, the fruit bodies were ground into powder, and isotope ratio (d13C, d15N and d34S) and 137Cs concentrations of samples were measured. Each soil core was separated into 2-cm long, sieved after air-dried, and isotope ratio and 137Cs concentrations were measured. For 34S measurement, sulfur was extracted from samples with Parr bomb and collected as precipitation of BaSO4. Litter and humus layers were also collected, treated and analyzed as other samples.
137Cs concentration in saprophytic fungi was lower than that of ectomycorrhizal (ECM) fungi in average, but there was wide variation among genera and within genus in ECM fungi. Saprophytic fungi did not accumulate so much 137Cs despite the high 137Cs concentration in litter and humus layers. The vertical profiles of d13C, d15N and d34S had a common trend; d values decreased with the depth. Saprophytic fungi showed most negative delta values for N and S isotopes, but most positive for C isotopes in the fungus groups. Genus-specific d values were observed for N and S isotopes, which variation was comparable to those observed for soil vertical profiles (figure).
Results of isotopes analysis suggested hyphal distributions of saprophytic and ECM fungi were completely different and that there was considerable difference in ECM fungi. Saprophytic fungi had d13C and d15N values close to those in organic layers after being adjusted based on the suggestions from previous studies about isotope fractionation. d34S values in saprophytic fungi also were close to those in organic layers. The results of 3 isotopes indicated the hyphae of saprophytic fungi were restricted almost to soil organic layers. On the contrary, hyphal distribution of ECM had wide variations in mineral soil as indicated by genus-specific variations of d15N and d34S.
We did not observe significant relationships between hyphal distribution and 137Cs concentration in fruit bodies. Saprophytic fungi showed lower 137Cs concentration than ectomycorrhizal fungi regardless of shallow distribution of hyphae; and some genera of ECM fungi had similar values though they had different stable isotope ratios. These data are not consistent with the view that emphasized the relationship between hyphal distribution and 137Cs concentration in fruit bodies. The view of soil-depth dependent 137Cs accumulation by fungi needs to be re-examined.
Sulfur isotope seemed to be useful for estimating hyphal vertical distributions. Since the vertical profile of d34S was similar to those of d13C and d15N, multi isotope approach will provide an effective tool for investigating biological processes in soil ecosystems. For further application to fungi study, isotope fractionation of sulfur and d34S of available sulfur by fungi has to be studied.
Study site was a broad-leaved forest dominated by konara oak, mixed with fir, located at 20 km southwest from the Fukushima Daiichi Nuclear Power Plant, in Kawauchi Village, Fukushima Prefecture. Fruit bodies and soil core samples (down to 30 cm below the soil surface) were collected. After oven-dried, the fruit bodies were ground into powder, and isotope ratio (d13C, d15N and d34S) and 137Cs concentrations of samples were measured. Each soil core was separated into 2-cm long, sieved after air-dried, and isotope ratio and 137Cs concentrations were measured. For 34S measurement, sulfur was extracted from samples with Parr bomb and collected as precipitation of BaSO4. Litter and humus layers were also collected, treated and analyzed as other samples.
137Cs concentration in saprophytic fungi was lower than that of ectomycorrhizal (ECM) fungi in average, but there was wide variation among genera and within genus in ECM fungi. Saprophytic fungi did not accumulate so much 137Cs despite the high 137Cs concentration in litter and humus layers. The vertical profiles of d13C, d15N and d34S had a common trend; d values decreased with the depth. Saprophytic fungi showed most negative delta values for N and S isotopes, but most positive for C isotopes in the fungus groups. Genus-specific d values were observed for N and S isotopes, which variation was comparable to those observed for soil vertical profiles (figure).
Results of isotopes analysis suggested hyphal distributions of saprophytic and ECM fungi were completely different and that there was considerable difference in ECM fungi. Saprophytic fungi had d13C and d15N values close to those in organic layers after being adjusted based on the suggestions from previous studies about isotope fractionation. d34S values in saprophytic fungi also were close to those in organic layers. The results of 3 isotopes indicated the hyphae of saprophytic fungi were restricted almost to soil organic layers. On the contrary, hyphal distribution of ECM had wide variations in mineral soil as indicated by genus-specific variations of d15N and d34S.
We did not observe significant relationships between hyphal distribution and 137Cs concentration in fruit bodies. Saprophytic fungi showed lower 137Cs concentration than ectomycorrhizal fungi regardless of shallow distribution of hyphae; and some genera of ECM fungi had similar values though they had different stable isotope ratios. These data are not consistent with the view that emphasized the relationship between hyphal distribution and 137Cs concentration in fruit bodies. The view of soil-depth dependent 137Cs accumulation by fungi needs to be re-examined.
Sulfur isotope seemed to be useful for estimating hyphal vertical distributions. Since the vertical profile of d34S was similar to those of d13C and d15N, multi isotope approach will provide an effective tool for investigating biological processes in soil ecosystems. For further application to fungi study, isotope fractionation of sulfur and d34S of available sulfur by fungi has to be studied.