Estimation of groundwater residence time using the 36Cl bomb pulse

We propose a methodology for estimating the residence time of groundwater based on bomb-produced (36)Cl. Water samples were collected from 28 springs and 2 flowing wells located around Mt. Fuji, Central Japan. (36)Cl/Cl ratios in the water samples, determined by accelerator mass spectrometry (AMS), were between 43 × 10(-15) and 412 × 10(-15). A reference time series of the above-background (i.e., bomb-derived) (36)Cl concentration was constructed by linearly scaling the background-corrected Dye-3 data according to the estimated total bomb-produced (36)Cl fallout in the Mt. Fuji area. Assuming piston flow transport, estimates of residence time were obtained by comparing the measured bomb-derived (36)Cl concentrations in spring water with the reference curve. The distribution of (36)Cl-based residence times is basically consistent with that of tritium-based estimates calculated from data presented in previous studies, although the estimated residence times differ between the two tracers. This discrepancy may reflect chlorine recycling via vegetation or the relatively small change in fallout rate, approximately since 1975, which would give rise to large uncertainties in (36)Cl-based estimates of recharge for the period, approximately since 1975. Given the estimated ages for groundwater from flowing wells, dating based on a (36)Cl bomb pulse may be more reliable and sensitive for groundwater recharged before 1975, back as far as the mid-1950s.     

http://www.sciencedirect.com/science/article/pii/S167498711200062X

This paper focuses on the formation mechanism of fractures induced by excavation of a gallery in soft sedimentary rocks in the Horonobe area of Japan.Detailed fracture mapping of the gallery indicates that the fractures consist of both pre-existing shear fractures and excavation damaged zone(EDZ) fractures. EDZ fractures correspond to weak planes associated with bedding planes or transgranular cracks.The EDZ fractures terminate against pre-existing shear fractures.Therefore,even for excavations in soft sedimentary rocks,formation of the EDZ fractures are controlled by pre-existing fractures and earlier weak planes.     

Trace-element compositions of single fluid inclusions in the Kofu granite, Japan: Implications for compositions of granite-derived fluids

Fluid inclusions in quartz from miarolitic cavities, pegmatites, and quartz veins in Miocene biotite-granite plutons, Kofu, Japan, were analyzed by particle-induced X-ray emission to examine chemistries and behaviors of granite-derived fluids in island-arc granite. Most inclusions are aqueous two-phase inclusions, and halite-bearing polyphase inclusions are also observed in quartz veins in the upper part of the plutons. From element contents of fluid inclusions in the miarolitic cavities, the original fluid released from the granite plutons during solidification is inferred to have concentrations of Mn, Fe, Cu, Zn, Ge, Br, Rb, Pb, and Ba of several tens to hundreds of parts per million by weight (ppm) and a salinity of about 10 wt% NaCl equivalent. We estimated the formation conditions of the fluid to have been at about 1.3–1.9 kb and 530–600°C on the basis of the homogenization temperatures of the inclusions and the solidification conditions of the plutons. The polyphase inclusions probably originated from hypersaline fluid by boiling of part of the released fluid during its ascent in the plutons. The polyphase inclusions contain several hundreds to tens of thousands of ppm of Fe and Mn, and tens to several hundreds of ppm of Cu, Zn, Br, Rb, and Pb. The salinities are about 35 wt% NaCl equivalent. Compositional variations in two-phase inclusions from the miarolitic cavities and quartz veins are primarily explained by mineral precipitation with dilution by surface water exerting a secondary influence. Thus, chemistries and behaviors of the granite-derived fluids in the plutons can be explained by mineral precipitation, boiling, and dilution of the originally released fluid.     

Trace Element Analysis of Fused Whole-Rock Glasses by Laser Ablation-ICP-MS and PIXE

The concentrations of fifty trace elements, including relatively volatile elements and transition metal elements, in fused glasses of Geological Survey of Japan rock reference materials GSJ JR-2, JA-1, JA-2, JB-1a, JB-3, JGb-1 and JF-1 were determined by particle (proton) induced X-ray emission (PIXE) and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The fused glasses were prepared by rapid fusion and subsequent quenching in welded platinum capsules and were found to be homogeneous for major elements and for trace elements with concentrations of more than 1 μg g^-1 within the observed precision (± 10% mean) on a 70 μm sampling scale. The values obtained by PIXE and LA-ICP-MS for the transition elements (Cr, Mn, Fe, Ni and Cu), the relatively volatile elements (Zn, Ga, Rb and Pb) and the refractory elements (Y, Zr, Nb and Th) with concentrations greater than a few μg g^-1 showed good agreement (within 10 % relative difference). The values for almost all the elements detected at concentrations higher than 1 μg g^-1 as determined by LA-ICP-MS also agreed well with the reference values (mean relative difference < ± 10%), except for B and Cu. The good agreement confirmed the appropriateness of the NIST SRM 600 series glass calibration reference material for LA-ICP-MS analysis of glasses with variable major-element compositions for almost all elements. The concentrations of Cu in all the samples were lower than the reference values, which was attributed to adsorption of the transition metals onto the platinum capsule during preparation.