Here I report the confirmation of a long-term modulation of a period of 92 + 21 − 13 years with the "time-delay correlation" method on the sunspot data compiled over the last a total of 289 years. This periodicity better specifies the cycle which falls pretty well within Gleissberg cycle, and clearly contrasts with the 55 year grand cycle which Yoshimura (1979) claimed. It is argued that the period-amplitude diagram method. which Yoshimura used, ana lysed peak amplitudes only so that a large number of data were disregarded, and thus was more susceptible to a bias. The planetary tidal force on Sun as for the possible cause to the solar activity was investigated and its possibility was ruled out in view of no period correlation between them.

In the presence of synchrotron losses, diffusion of an ensembel of relativistic particles in an intraculster medium is investigated. The diffusion coefficient in the medium is found to be constrained by 28.8 ± 0.4 ≤ L o g D ≤ 30.5 ± 0.4 c m 2 s − 1 with the energy dependency of D 0 ε μ of μ = 0.4 ± 0.2 as the previous observations suggested. As an important implication of the result, the brightest head-tail radio source NGC 4869, whose radio tail structure is indicative for its orbit within the cluster core, is considered to be the major contributor of particles for the formation of the Coma radio halo.

Offspring have been produced from somatic cells in a number of species. This biotechnology introduced a new phenomenon in reprogramming and differentiation of somatic cell, namely totipotency. However, birth of oversized calves and perinatal abnormalities such as increased gestation length, lack of spontaneous parturition, higher incidence of dystocia, and reduced perinatal viability of offspring are frequently observed in pregnancies of cloned bovine fetuses. Disturbance of feto-placenta has been proposed as likely causes for abnomal growth. However. Little is known the mechanism responsible for the perinatal problems. Therefore, we focused on gestation length in somatic cell nuclear recipient cows. To solve this issues, placental tissues of control and cloned bovine were obtained by a cesarean section (C-section) before 5 days of paturition. Total RNA from control and cloned bovine placenta was extractd by TRIzol reagent. GeneFishing DEG kits (Seegene) were used to identify differentially expression genes. Total RNA (3 ug) were synthesized by M-MLV reverse transcriptase (200 u/ul) with 10 uM dT-annealing control primer (ACP1) at 42C for 90 min. Then, first-strand cDNA (50 ng) was amplified using the 5 uM arbitary ACP (1-20) and 10 uM dT-ACP2 primers. Some specific expression genes were amplified, Now, we are cloning and sequencing. These finding strongly can be support to solve the problems for parturition delay in nuclear transfer cows, suggest that placenta specific proteins are key indicators for the aberration of gestation and placental function in cows.