Consistent regional variations in deformation are seen in the normal human heart. Displacement and maximum shortening strains are well characterized with two-dimensional magnetic resonance tagging; however, higher-resolution images will be required to study transmural variations.

Abstract. In this study, two following experiments were performed to improve post-thaw motility and viability of frozen-thawed ram spermatozoa. We examined i) the effects of different concentrations of bovine serum albumin (0, 0.3, 1, 5, 10 and 15% BSA) in semen diluents lacking egg yolk and ii) the effects of four semen diluents, fructose (F: control) and trehalose (T) in semen diluents containing egg yolk, 15% BSA in semen diluents without egg yolk (BSA), and modified phosphate buffered saline (m-PBS). Frozen-thawed spermatozoa were examined for progressive sperm motility, viability, morphological abnormality, sperm tail swelling test, and sperm acrosome integrity. In Experiment 1, the rates of sperm motility immediately after thawing (0 h) were significantly (P<0.05) higher in the 10 and 15% BSA groups (55.0 ± 2.9 and 58.3 ± 6.7%, respectively) than in the positive control (F) group (41.7 ± 4.4%). The rate of sperm viability in the negative control (0% BSA) group (80.2 ± 3.3%) was significantly (P<0.05) lower than in the positive control (F) group (89.8 ± 1.5%), but when compared with the F group, no significant differences were found among the 0.3, 1, 5, 10 and 15% BSA groups at 0 h. The rates of sperm morphological abnormality of the 10 and 15% BSA groups (6.5 ± 1.3 and 6.3 ± 1.1%, respectively) were significantly (P<0.05) lower at 0 h than that in the 1% BSA group (16.3 ± 5.2%). In Experiment 2, T addition improved (P<0.05) the post-thaw motility compared with the F and BSA groups. Furthermore, at 3 and 6 h, the post-thaw motility of the T group (36.3 ± 2.4 and 25.0 ± 2.0%, respectively) was significantly (P<0.05) higher than in the BSA (26.3 ± 2.4 and 18.8 ± 1.3%, respectively) and F (28.8 ± 3.8 and 18.8 ± 2.4%, respectively) groups. The post-thaw sperm motility and viability in the m-PBS group were significantly (P<0.05) lower than those of the control (F), T, and BSA groups throughout all observation points. These results indicate that 10 and 15% BSA can be substituted for egg-yolk for ram semen diluent and that the addition of trehalose enhances motility and viability of ram spermatozoa after freezing and thawing. Key words: Bovine serum albumin (BSA), Semen diluent, Sheep, Spermatozoa, Trehalose (J. Reprod. Dev. 52: [675][676][677][678][679][680][681][682][683] 2006) t has been reported that frozen-thawed spermatozoa are greatly damaged during the freezing and thawing processes [1][2][3][4][5]. This damage may decrease sperm motility and the fertilization rate after artificial insemination (AI). Several semen analysis methods have been developed to evaluate the functional parameters of spermatozoa more objectively. The hypo-osmotic swelling test (HOS-test) has been applied to various species, such as dogs [6,7], cattle [8,9], horses [10][11][12], rams [13], minke whales (Balaenoptera bonarensis) [13] and humans [14,15]. It has been recognized that the HOS-Test is a simple and useful method with good reliability and repeatability for examination of the sperm plasma membrane.

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Abstract. The Japanese Greenhouse gases Observing SATellite-2 (GOSAT-2), in orbit since 29 October 2018, follows up the GOSAT mission, itself in orbit since 23 January 2009. GOSAT-2 monitors carbon dioxide and methane in order to increase our understanding of the global carbon cycle. It simultaneously measures carbon monoxide emitted from fossil fuel combustion and biomass burning and permits identification of the amount of combustion-related carbon. To do this, the satellite utilizes the Thermal and Near Infrared Sensor for Carbon Observation Fourier-Transform Spectrometer-2 (TANSO-FTS-2). This spectrometer detects gas absorption spectra of solar radiation reflected from the Earth's surface in the shortwave-infrared (SWIR) region as well as the emitted thermal infrared radiation (TIR) from the ground and the atmosphere. TANSO-FTS-2 can measure the oxygen A band (0.76 µm), weak and strong CO2 bands (1.6 and 2.0 µm), weak and strong CH4 bands (1.6 and 2.3 µm), a weak CO band (2.3 µm), a mid-wave TIR band (5.5–8.4 µm), and a long-wave TIR band (8.4–14.3 µm) with 0.2 cm−1 spectral sampling intervals. TANSO-FTS-2 is equipped with a solar diffuser target, a monochromatic light source, and a blackbody for spectral radiance calibration. These calibration sources permit characterization of time-dependent instrument changes in orbit. The onboard-recalibrated instrumental parameters are considered in operational level-1 processing and released as TANSO-FTS-2 level-1 version 102102 products, which were officially released on 25 May 2020. This paper provides an overview of the TANSO-FTS-2 instrument, the level-1 processing, and the first-year in-orbit performance. To validate the spectral radiance calibration during the first year of operation, the spectral radiance of the version 102102 product is compared at temporally coincident and spatially collocated points from February 2019 to March 2020 with TANSO-FTS on GOSAT for SWIR and with AIRS on Aqua and IASI on METOP-B for TIR. The spectral radiances measured by TANSO-FTS and TANSO-FTS-2 agree within 2 % of the averaged bias and 0.5 % standard deviation for SWIR bands. The agreement of brightness temperature between TANSO-FTS-2 and AIRS–IASI is better than 1 K in the range from 220 to 320 K. GOSAT-2 not only provides seamless global CO2 and CH4 observation but also observes local emissions and uptake with an additional CO channel, fully customized sampling patterns, higher signal-to-noise ratios, and wider pointing angles than GOSAT.

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Monocarboxylate transporter-1 (MCT-1) is a transmembrane transporter for monocarboxylates including lactate and pyruvate. Silencing Mct1 by its small interfering RNA (siRNA) suppressed the expression of marker genes for osteoblast differentiation, namely, Tnap, Runx2, and Sp7, induced by BMP-2 in mouse myoblastic C2C12 cells. Mct1 siRNA also suppressed alkaline phosphatase activity, as well as expressions of Tnap and Bglap mRNAs in mouse primary osteoblasts. On the other hand, Mct1 siRNA did not have effects on the Smad1/5 or ERK/JNK pathways in BMP-2-stimulated C2C12 cells, while it up-regulated the mRNA expression of p53 (Trp53) as well as nuclear accumulation of p53 in C2C12 cells in a BMP-2-independent manner. Suppression of osteoblastic differentiation by Mct1 siRNA in C2C12 cells was abolished by co-transfection of Trp53 siRNA. Together, these results suggest that MCT-1 functions as a positive regulator of osteoblast differentiation via suppression of p53.

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