Yasunori Hamajima

Radar-Enabled Recovery of the Sutter’s Mill Meteorite, a Carbonaceous Chondrite Regolith Breccia

The Meteor That Fell to Earth In April 2012, a meteor was witnessed over the Sierra Nevada Mountains in California. Jenniskens et al. (p. 1583) used a combination of photographic and video images of the fireball coupled with Doppler weather radar images to facilitate the rapid recovery of meteorite fragments. A comprehensive analysis of some of these fragments shows that the Sutters Mill meteorite represents a new type of carbonaceous chondrite, a rare and primitive class of meteorites that contain clues to the origin and evolution of primitive materials in the solar system. The unexpected and complex nature of the fragments suggests that the surfaces of C-class asteroids, the presumed parent bodies of carbonaceous chondrites, are more complex than previously assumed. Analysis of this rare meteorite implies that the surfaces of C-class asteroids can be more complex than previously assumed. Doppler weather radar imaging enabled the rapid recovery of the Sutter’s Mill meteorite after a rare 4-kiloton of TNT–equivalent asteroid impact over the foothills of the Sierra Nevada in northern California. The recovered meteorites survived a record high-speed entry of 28.6 kilometers per second from an orbit close to that of Jupiter-family comets (Tisserand’s parameter = 2.8 ± 0.3). Sutter’s Mill is a regolith breccia composed of CM (Mighei)–type carbonaceous chondrite and highly reduced xenolithic materials. It exhibits considerable diversity of mineralogy, petrography, and isotope and organic chemistry, resulting from a complex formation history of the parent body surface. That diversity is quickly masked by alteration once in the terrestrial environment but will need to be considered when samples returned by missions to C-class asteroids are interpreted.

Distribution of cesium-137 in Japanese forest soils: correlation with the contents of organic carbon

The spatial and vertical distributions of 137Cs in surface soils were surveyed and analyzed then correlated with the contents of organic carbon in the hinoki (Chamaecyparis obtusa Sieb. et Zucc.) plantation forest and secondary forest dominated by red pine (Pinus densiflora Sieb. et Zucc.) in Japan. The spatial variation of 137Cs activity was observed in the surface soil around the red pine. The average activity of 16 samples around the tree is 42.4 Bq/kg and the standard deviation is 25.9 Bq/kg. This finding indicates the importance in the selection of a sampling site and the number of samples from the surface soils especially around a tree. For the vertical distribution of 137Cs activity, it was found that the concentration in the surface soil is highest, 149 Bq/kg in the hinoki stand and 101 Bq/kg in the red pine stand, and decreases with depth. The relationship between 137Cs activity and carbon content in the forest soil was investigated in two undisturbed forest stands. The relations were more precisely expressed using an exponential equation than by a linear equation. From the same forest, similar regression equations were obtained. This indicates that the distribution of 137Cs could be characterized by the organic carbon content in an undisturbed forest. It is also suggested that the coefficient values in the regression equation help to define the movement of 137Cs accompanying the decomposition of organic matter.

Southward spreading of the Fukushima-derived radiocesium across the Kuroshio Extension in the North Pacific

The accident of the Fukushima Dai-ichi nuclear power plant in March 2011 released a large amount of radiocesium into the North Pacific Ocean. Vertical distributions of Fukushima-derived radiocesium were measured at stations along the 149°E meridian in the western North Pacific during the winter of 2012. In the subtropical region, to the south of the Kuroshio Extension, we found a subsurface radiocesium maximum at a depth of about 300 m. It is concluded that atmospheric-deposited radiocesium south of the Kuroshio Extension just after the accident had been transported not only eastward along with surface currents but also southward due to formation/subduction of subtropical mode waters within about 10 months after the accident. The total amount of decay-corrected 134Cs in the mode water was an estimated about 6 PBq corresponding to 10–60% of the total inventory of Fukushima-derived 134Cs in the North Pacific Ocean.

134Cs and 137Cs activities in coastal seawater along Northern Sanriku and Tsugaru Strait, northeastern Japan, after Fukushima Dai-ichi Nuclear Power Plant accident

A total of 37 seawater samples were collected at 10 sites along the coastline of the Northern Sanriku and Tsugaru Strait, 250-450 km north of the Fukushima Dai-ichi Nuclear Power Plant in April-December 2009 and May-June 2011, and analyzed for (134)Cs and (137)Cs activities using low-background γ-spectrometry. The (134)Cs and (137)Cs activities measured in these samples in May 2011 were found to be 2-3 mBq/L and 2.5-4 mBq/L, respectively. By June, these values had decreased by 25-45%/month and 5-30%/month, respectively. These results can be plausibly explained by surface infusion of these isotopes into the sea by atmospheric transport from Fukushima and their subsequent reduction by water migration to off-shore and deeper regions.

Neutron Activation Analysis of a Particle Returned from Asteroid Itokawa

Laboratory analysis of samples returned from an asteroid establishes a direct link between asteroids and meteorites and provides clues to the complex history of the asteroid and its surface. A single grain (~3 micrograms) returned by the Hayabusa spacecraft was analyzed by neutron activation analysis. This grain is mainly composed of olivine with minor amounts of plagioclase, troilite, and metal. Our results establish that the Itokawa sample has similar chemical characteristics (iron/scandium and nickel/cobalt ratios) to chondrites, confirming that this grain is extraterrestrial in origin and has primitive chemical compositions. Estimated iridium/nickel and iridium/cobalt ratios for metal in the Itokawa samples are about five times lower than CI carbonaceous chondrite values. A similar depletion of iridium was observed in chondrule metals of ordinary chondrites. These metals must have condensed from the nebular where refractory siderophile elements already condensed and were segregated.

Lateral variation of 134Cs and 137Cs concentrations in surface seawater in and around the Japan Sea after the Fukushima Dai-ichi Nuclear Power Plant accident.

A total of 82 surface seawater samples was collected in the Japan Sea and the southwestern Okhotsk Sea before and after the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident. Analysis of (134)Cs and (137)Cs concentrations using low-background γ-spectrometry revealed that the (137)Cs concentration of the samples collected in June 2011 was 1.5-2.8mBq/L, which is approximately 1-2 times higher than the pre-accident (137)Cs level, while the (134)Cs concentration was less than detectable to 1mBq/L. In addition to (134)Cs being clearly detected (∼1mBq/L), (137)Cs concentration in water samples from the northeastern Japan Sea (2-2.8mBq/L) was also higher than that from the coast in the southwestern Japan Sea (∼1.5mBq/L). These higher concentrations in the northeastern Japan Sea could be ascribed to the atmospheric transport of nuclides from the FDNPP as aerosols and subsequent transport and dilution after delivery to the sea surface.

Impact of Fukushima-derived radiocesium in the western North Pacific Ocean about ten months after the Fukushima Dai-ichi nuclear power plant accident.

We measured vertical distributions of radiocesium ((134)Cs and (137)Cs) at stations along the 149°E meridian in the western North Pacific during winter 2012, about ten months after the Fukushima Dai-ichi Nuclear Power Plant (FNPP1) accident. The Fukushima-derived (134)Cs activity concentration and water-column inventory were largest in the transition region between 35 and 40°N approximately due to the directed discharge of the contaminated water from the FNPP1. The bomb-derived (137)Cs activity concentration just before the FNPP1 accident was derived from the excess (137)Cs activity concentration relative to the (134)Cs activity concentration. The water-column inventory of the bomb-derived (137)Cs was largest in the subtropical region south of 35°N, which implies that the Fukushima-derived (134)Cs will also be transported from the transition region to the subtropical region in the coming decades. Mean values of the water-column inventories decay-corrected for the Fukushima-derived (134)Cs and the bomb-derived (137)Cs were estimated to be 1020 ± 80 and 820 ± 120 Bq m(-2), respectively, suggesting that in winter 2012 the impact of the FNPP1 accident in the western North Pacific Ocean was nearly the same as that of nuclear weapons testing. Relationship between the water-column inventory and the activity concentration in surface water for the radiocesium is essential information for future evaluation of the total amount of Fukushima-derived radiocesium released into the North Pacific Ocean.

A convenient method for discriminating between natural and depleted uranium by γ-ray spectrometry

A convenient method for discriminating between natural and depleted uranium reagent was developed by measuring and analyzing the gamma-ray spectra of some reagents with no standard source. The counting rates (R) of photoelectric peaks of gamma-rays from nuclides with the same radioactivity divided by their emission probability (B) are expressed as a function of gamma-ray energy. The radioactivities of 234Th and 234mPa and 21.72 times that of 235U are equal to the radioactivity of 235U in natural uranium. Therefore, the plot of 21.72-fold R/B for 235U should be on a curve fitted to the points for 234Th and 234mPa in natural uranium. Depleted uranium with a 235U isotopic composition of less than 0.68% could be discriminated from natural uranium in the case of a reagent containing 4.0 g of uranium.

Spatial variations of low levels of 134Cs and 137Cs in seawaters within the Sea of Japan after the Fukushima Dai-ichi Nuclear Power Plant accident

Our method based on low background γ-spectrometry enabled the measurement of low radiocesium concentrations in only 20 L of seawater. In May 2011 after deposition of radiocesium, (134)Cs concentration in surface water within the Sea of Japan was confirmed to be significantly small (<0.1-1 mBq/L) by the method. The concentration was not detected (<0.1 mBq/L) below 50 m depth. The Fukushima-derived radiocesium migrated from the surface water of the Sea of Japan without advection to below the thermocline.

Meridional distribution of Fukushima-derived radiocesium in surface seawater along a trans-Pacific line from the Arctic to Antarctic Oceans in summer 2012

In summer 2012, we measured activity concentration of radiocesium in surface seawater collected in the Arctic Ocean, Bering Sea, western Pacific Ocean, and Antarctic Ocean. The radiocesium derived from the Fukushima Dai-ichi Nuclear Power Plant accident in March 2011 was found in the Bering Sea and western North Pacific between 25°N and 63°N, which agrees with model simulation results of atmospheric deposition. A semi-synoptic view suggests that a main body of radiocesium discharged directly had been transported eastward to 170°W, northward to 50°N, and southward to 30°N by summer 2012, about one and half years after the accident.