Octave-wide phase-matched four-wave mixing in dispersion engineered crystalline microresonators: erratum.

This erratum presents the corrections to the Letter published in Opt. Lett.44, 3146 (2019)OPLEDP0146-959210.1364/OL.44.003146.

Octave-wide phase-matched four-wave mixing in dispersion-engineered crystalline microresonators.

In this Letter, we report phase-matched four-wave mixing separated by over one octave in a dispersion-engineered crystalline microresonator. Experimental and numerical results presented here confirm that primary sidebands were generated with a frequency shift up to 140 THz, and that secondary sidebands formed a localized comb structure, known as a clustered comb in the vicinity of the primary sidebands. A theoretical analysis of the phase-matching condition validated our experimental observations, and our results agree well with numerical simulations. These results offer the potential to realize a frequency-tunable comb cluster generator operating from 1 µm to mid-infrared wavelengths with a single and compact device.

Method for rapid screening analysis of Sr-90 in edible plant samples collected near Fukushima, Japan.

A screening method for measuring (90)Sr in edible plant samples by focusing on (90)Y in equilibrium with (90)Sr is reported. (90)Y was extracted from samples with acid, co-precipitated with iron hydroxide, and precipitated with oxalic acid. The dissolved oxalate precipitate was loaded on an extraction chromatography resin, and the (90)Y-enriched eluate was analyzed by Cherenkov counting with a TDCR liquid scintillation counter. (90)Sr ((90)Y) concentration was determined in plant samples collected near the damaged Fukushima Daiichi Nuclear Power Plants with this method.

An updated and more accurate drip infusion solution monitoring system - biomed 2013.

We have developed a drip infusion solution monitoring system for hospital and care facility use that is much more accurate than our previous reported system. The system consists of two electrodes and an acceleration sensor. The electrodes, which are wrapped around the infusion supply polyvinyl chloride (PVC) tube from the solution bag and the drip chamber, measure the growth and fall of each drop of infusion solution. The drip rate is detected from the fall of each drop. In addition, the acceleration sensor is attached to the outside of the drip chamber and detects the tilt angle of that chamber. The injected infusion solution amount is calculated by the infusion solution quantity per one drop and the drip rate. However, the quantity changes depend on the tilt angle of the drip chamber. The quantity of each drop is then corrected by the tilt angle of the drip chamber.

A drip infusion warning system.

We have developed a drip infusion warning system for hospital and care facility use. In general, two kinds of infusion sets are used, which have drop factors of either 20 or 60. (A drop factor is the number of drops to deliver 1 ml of infusion solution.) When an infusion set having a 20 drop factor is used, the number of drops per drip is adjusted to 20. If an infusion set has a drop factor of 60, then the infusion volume rate becomes three times as much. This may result in legal consequences if the patient is injured. In this study, a drip infusion warning system detects whether the infusion is a 20 or a 60 drop factor. The system consists of two electrodes, one wrapped around the infusion supply polyvinyl-chloride tube, and another one around the drip chamber. The electrical impedance between two electrodes is changed by the growth and fall of each drop of fluid. The drop growth length especially changes, depending on the type of infusion set used. Therefore, the two types of infusion sets can be identified by monitoring the drop length. Our warning system detects whether the infusion set used corresponds to a 20 or 60 drop factor, so the system can reduce human errors.

A remote drip infusion monitoring system employing Bluetooth.

We have developed a remote drip infusion monitoring system for use in hospitals. The system consists of several infusion monitoring devices and a central monitor. The infusion monitoring device employing a Bluetooth module can detect the drip infusion rate and an empty infusion solution bag, and then these data are sent to the central monitor placed at the nurses' station via the Bluetooth. The central monitor receives the data from several infusion monitoring devices and then displays graphically them. Therefore, the developed system can monitor intensively the drip infusion situation of the several patients at the nurses' station.

Radiation measurements in the Chiba Metropolitan Area and radiological aspects of fallout from the Fukushima Dai-ichi Nuclear Power Plants accident.

Large amounts of radioactive substances were released into the environment from the Fukushima Dai-ichi Nuclear Power Plants in eastern Japan as a consequence of the great earthquake (M 9.0) and tsunami of 11 March 2011. Radioactive substances discharged into the atmosphere first reached the Chiba Metropolitan Area on 15 March. We collected daily samples of air, fallout deposition, and tap water starting directly after the incident and measured their radioactivity. During the first two months maximum daily concentrations of airborne radionuclides observed at the Japan Chemical Analysis Center in the Chiba Metropolitan Area were as follows: 4.7 × 10(1) Bq m(-3) of (131)I, 7.5 Bq m(-3) of (137)Cs, and 6.1 Bq m(-3) of (134)Cs. The ratio of gaseous iodine to total iodine ranged from 5.2 × 10(-1) to 7.1 × 10(-1). Observed deposition rate maxima were as follows: 1.7 × 10(4) Bq m(-2) d(-1) of (131)I, 2.9 × 10(3) Bq m(-2) d(-1) of (137)Cs, and 2.9 × 10(3) Bq m(-2) d(-1) of (134)Cs. The deposition velocities (ratio of deposition rate to concentration) of cesium radionuclides and (131)I were detectably different. Radioactivity in tap water caused by the accident was detected several days after detection of radioactivity in fallout in the area. Radiation doses were estimated from external radiation and internal radiation by inhalation and ingestion of tap water for people living outdoor in the Chiba Metropolitan Area following the Fukushima accident.

Relationship between frequency and impedance change in an infusion rate measurement system employing a capacitance sensor - biomed 2011.

We have been searching for a suitable frequency range for an electrical impedance measurement infusion solution drip monitoring system, which we have previously reported. This electrical impedance, which is formed between two electrodes wrapped around the infusion supply polyvinyl-chloride tube and around the drip chamber, is changed by the growth and fall of each drop of fluid. Thus, the drip rate can be detected by measuring this impedance. However, many different kinds of infusion solutions such as glucose, amino acid, soya oil, and lactated Ringer’s solution are used in hospitals and care facilities. Therefore, it was necessary to find a suitable frequency for driving the capacitance-change sensor with a wide range of infusion solutions. In this study, the sensor electrical impedance change of 16 infusion solutions was measured from 1 kHz up to 1 MHz. The drip impedance produced by 5% glucose solution, 10% glucose solution and soya oil indicated the maximum sensor output change at 10 kHz, 20 kHz, and 70 kHz, respectively. The other 13 infusion solutions increased up to 10 kHz, and were constant from 10 kHz to 1 MHz. However, the growth, fall, and drip rate of the drops of all the infusion solutions were monitored by measuring the impedance change from 10 kHz to 30 kHz. Our experimental results indicated that most suitable excitation range for the infusion monitoring system is from 10 kHz to 30 kHz. Thus, we can now “fine-tune” the system for optimal sensing.

A new drip infusion solution monitoring system with a free-flow detection function.

A new drip infusion solution monitoring system has been developed for hospital and care facility use. The system detects the fall of each drip chamber drop of fluid and also a free-flow situation. Three non-contacting copper foil electrodes are used. The electrodes are wrapped around the infusion supply polyvinyl chloride (PVC) tube from the solution bag, the drip chamber, and the infusion PVC tube from the drip chamber. Drip infusion fluids have electrical conductivity, so a capacitor is formed between the infusion fluid and each electrode. A thirty kHz sine wave is applied to the electrode wrapped around the infusion supply PVC tube from the solution bag. The capacity-coupled signal on the drip chamber electrode is the transducer output. When an infusion fluid drop is forming, its length and diameter, and therefore the drip chamber capacitance, are increasing, causing change in the output signal. The drip chamber electrode can detect the fall of each drip chamber drop of fluid. When the infusion solution becomes free-flow, an infusion fluid drop is not forming and the infusion fluid flows continuously. Therefore, the capacitance of the electrode around drip chamber does not change the output signal. On the other hand, the electrode wrapped around the infusion supply polyvinyl chloride tube under the drip chamber detects the thirty kHz sine wave conducted by the infusion fluid. The drip chamber electrodes and the infusion supply PVC tube under the drip chamber detect each drop of fluid and free-flow, respectively.

Tracing the sources of gaseous components (222Rn, CO2 and its carbon isotopes) in soil air under a cool-deciduous stand in Sapporo, Japan.

Radon ((222)Rn) and carbon dioxide were monitored simultaneously in soil air under a cool-temperate deciduous stand on the campus of Hokkaido University, Sapporo, Japan. Both (222)Rn and CO(2) concentrations in soil air varied with atmospheric (soil) temperature in three seasons, except for winter when the temperature in soil air remained constant at 2-3 degrees C at depth of 80 cm. In winter, the gaseous components were influenced by low-pressure region passing through the observation site when the ground surface was covered with snow of ~1 m thickness. Carbon isotopic analyses of CO(2) suggested that CO(2) in soil air may result from mixing of atmospheric air and soil components of different origins, i.e. CO(2) from contemporary soil organic matter and old carbon from deeper source, to varying degrees, depending on seasonal meteorological and thus biological conditions.

Iodine-129 measurements in soil samples from Dolon village near the Semipalatinsk nuclear test site.

Dolon village, located about 60 km from the border of the Semipalatinsk nuclear test site, is known to be heavily contaminated by the first USSR atomic bomb test in August 1949. Soil samples around Dolon were taken in October 2005 in an attempt to evaluate internal thyroid dose arising from incorporation of radioiodine isotopes (mainly (131)I). Iodine-129 in soil was measured by using the technique of accelerator mass spectrometry. The (129)I/(127)I atom ratios measured were in the range from 3.3 x 10(-9) to 3.3 x 10(-7). These values were within the range of the current background level ( approximately 10(-9) to 10(-7)) in the environment, including contributions from the global fallout of atmospheric nuclear tests and local fallout of nuclear facilities. The (129)I atom accumulated level in soil ranged from 1.28 x 10(13) to 1.59 x 10(14) atoms m(-2), the average (8.0 x 10(13)) of which was higher than the background level of (2-5) x 10(13). From the relationship between (129)I and( 137)Cs (corrected for background and decay from 1949 to 2005) accumulated levels, the background level of (129)I and the (129)I/(137)Cs ratio around Dolon were estimated to be (6.4 +/- 0.4) x 10(13) atoms m(-2) and 0.25 +/- 0.16, respectively. This (129)I/(137)Cs ratio is almost similar to the fission yield ratio for (239)Pu fast fission (0.24).

Characteristics of humic substances in the Kuji River waters as determined by high-performance size exclusion chromatography with fluorescence detection.

Direct measurement by high-performance size exclusion chromatography with fluorescence detection was applied to the characterization of humic substances in river waters from the Kuji River system, which runs through forest hills and an agricultural plain in Japan. The monitoring wavelength of excitation 320 nm and emission 430 nm corresponds to the fluorescence maxima for aquatic fulvic acid. Chromatograms of the river waters showed four peaks; each peak position was in good agreement among these samples. Peak height ratios for the samples from the upstream Kuji River and its tributaries were different from those of the midstream and downstream sections of the Kuji River, which may reflect differences in the characteristics of humic substances and other organic materials supplied from soil to river.

Formation and retention of organically bound deuterium in rice in deuterium water release experiment.

As a substitute of tritium, deuterated water (D2O) vapor release experiments were performed in a greenhouse to estimate the different formation and subsequent retention of organically bound deuterium in rice plants between daytime and nighttime exposure. Potted rice plants were exposed to D2O vapor in the greenhouse for 8 h, under day or night conditions. Deuterium concentrations in free water and organic matter in rice leaves and ears were investigated until harvest time. The formation of organically bound deuterium in the daytime was higher than during the nighttime by the factors of 2.4 for the ear and 2.9 for the leaf. The decrease of the organically bound deuterium concentration in the ear after the nighttime exposure was faster than that after the daytime exposure. Data analysis was carried out using a compartment model in which different generating processes of organic matter were considered. The calculated organically bound deuterium retention in rice agreed with the measured value.

Estimation of 14CO2 flux at soil-atmosphere interface and distribution of 14C in forest ecosystem.

To realize the dynamical behavior of 14C among exchangeable carbon reservoirs in terrestrial environment, a method for in situ determination of 14CO2 flux at soil-atmosphere interface and a high flow rate CO2 sampler were developed. This method allowed us to collect integrated quantity of CO2 for determining 14C activity over an extended time period under environmental conditions with minimal site disturbance. The 14CO2 flux from ground surface was estimated to be 1.59 x 10(-5) Bq m (-2) S (-1) in a forest floor with the method. The specific activities of 14C in environmental materials such as some biological and air samples were also determined in the vicinity of the place, where the flux measurement was made, to discuss the behavior of 14C in the forest ecosystem. The results indicated that fresh pine needles had a similar 14C specific activity to the atmospheric CO2 at the same height due to its fairly rapid equilibrium, 14C specific activity in the atmospheric CO2 has a concentration gradient near the ground surface and, at least in this site, CO2 with high 14C specific activity was generated by decomposition of soil organic matter which may be accumulated in soil as a result of former nuclear weapons tests.

Accumulation and potential dissolution of Chernobyl-derived radionuclides in river bottom sediment.

Areas contaminated with radionuclides from the Chernobyl nuclear accident have been identified in Pripyat River near the Chernobyl Nuclear Power Plant. The river bottom sediment cores contained 137Cs (10(5)-10(6) Bq/m2) within 0-30 cm depth, whose concentration is comparable to that in the ground soil in the vicinity of the nuclear power plant (the Exclusion Zone). The sediment cores also accumulated 90Sr (10(5) Bq/m2), (239,240)Pu (10(4) Bq/m2) and 241Am (10(4)Bq/m2) derived from the accident. Several nuclear fuel particles have been preserved at 20-25 cm depth that is the peak area of the concentrations of the radionuclides. These inventories in the bottom sediments were compared with those of the released radionuclides during the accident. An analysis using a selective sequential extraction technique was applied for the radionuclides in the sediments. Results suggest that the possibility of release of 137Cs and (293,240)Pu from the bottom sediment was low compared with 90Sr. The potential dissolution and subsequent transport of 90Sr from the river bottom sediment should be taken into account with respect to the long-term radiological influence on the aquatic environment.