• Korean Journal of Mathematics
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• 제15권1호
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• pp.13-26
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• 2007

We prove that every strong null sequence in a Banach space X lies inside the range of a vector measure of bounded variation if and only if the condition $\mathcal{N}_1(X,{\ell}_1)={\Pi}_1(X,{\ell}_1)$ holds. We also prove that for $1{\leq}p<{\infty}$ every strong ${\ell}_p$ sequence in a Banach space X lies inside the range of an X-valued measure of bounded variation if and only if the identity operator of the dual Banach space $X^*$ is ($p^{\prime}$,1)-summing, where $p^{\prime}$ is the conjugate exponent of $p$. Finally we prove that a Banach space X has the property that any sequence lying in the range of an X-valued measure actually lies in the range of a vector measure of bounded variation if and only if the condition ${\Pi}_1(X,{\ell}_1)={\Pi}_2(X,{\ell}_1)$ holds.

• Korean Journal of Mathematics
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• 제12권1호
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• pp.55-65
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• 2004

Let $h_e(y)$, $h_o(y)$ denote the limits of the sequences {$^{2n}x$}, {$^{2n+1}x$}, respectively. From these two functions, we obtain a function $y=p(x)$ as an inverse function of them. Several differential properties of $y=p(x)$ are induced.

• 대한수학회지
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• 제51권2호
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• pp.239-250
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• 2014

Let R be a commutative Noetherian (not necessarily local) ring, I an ideal of R and M a finitely generated R-module. In this paper, by computing the local cohomology modules and Ext-modules via the injective resolution of M, we proved that, if for an integer t > 0, dim$_RH_I^i(M){\leq}k$ for ${\forall}i$ < t, then $$\displaystyle\bigcup_{i=0}^{j}(Ass_RH_I^i(M))_{{\geq}k}=\displaystyle\bigcup_{i=0}^{j}(Ass_RExt_R^i(R/I^n,M))_{{\geq}k}$$ for ${\forall}j{\leq}t$ and ${\forall}n$ >0. This shows that${\bigcup}_{n>0}(Ass_RExt_R^i(R/I^n,M))_{{\geq}k}$ is a finite set for ${\forall}i{\leq}t$. Also, we prove that $\displaystyle\bigcup_{i=1}^{r}(Ass_RM/(x_1^{n_1},x_2^{n_2},{\ldots},x_i^{n_i})M)_{{\geq}k}=\displaystyle\bigcup_{i=1}^{r}(Ass_RM/(x_1,x_2,{\ldots},x_i)M)_{{\geq}k}$ if $x_1,x_2,{\ldots},x_r$ is M-sequences in dimension > k and $n_1,n_2,{\ldots},n_r$ are some positive integers. Here, for a subset T of Spec(R), set $T_{{\geq}i}=\{{p{\in}T{\mid}dimR/p{\geq}i}\}$.

• Journal of applied mathematics & informatics
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• 제28권3_4호
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• pp.977-986
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• 2010

Let $X_1$, $X_2$, $\cdots$ be identically distributed negatively associated random variables with $EX_1\;=\;0$ and $E|X_1|^3$ < $\infty$. In this paper we prove $lim_{{\epsilon\downarrow}0}\;\frac{1}{-\log\;\epsilon}\sum\limits_{n=1}^\infty\frac{1}{n^2}ES_n^2I\{|S_n|\;{\geq}\;{\sigma\epsilon}n\}\;=\;2$ and $lim_{\epsilon\downarrow0}\;\epsilon^{2-p}\sum\limits_{n=1}^\infty\frac{1}{n^p}$ $E|S_n|^pI\{|S_n|\;{\geq}\;{\sigma\epsilon}n\}\;=\;\frac{2}{2-p}$ for 0 < p < 2, where $S_n\;=\;\sum\limits_{i=1}^{n}X_i$ and 0 < $\sigma^2\;=\;EX_1^2\;+\;\sum\limits_{i=2}^{\infty}Cov(X_1,\;X_i)$ < $\infty$. We consider some results of i.i.d. random variables obtained by Liu and Lin(2006) under negative association assumption.

• Journal of the Korean Society for Industrial and Applied Mathematics
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• 제11권1호
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• pp.41-56
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• 2007

A 3-partite 2-digraph is an orientation of a 3-partite multi-graph that is without loops and contains at most two edges between any pair of vertices from distinct parts. Let D(X, Y, Z) be a 3-partite 2-digraph with ${\mid}X{\mid}=l,\;{\mid}Y{\mid}=m,\;{\mid}Z{\mid}=n$. For any vertex v in D(X, Y, Z), let $d^+_{\nu}\;and\;d^-_{\nu}$ denote the outdegree and indegree respectively of v. Define $p_x=2(m+n)+d^+_x-d^-_x,\;q_y=2(l+n)+d^+_y-d^-_y\;and\;r_z=2(l+m)+d^+_z-d^-_z$ as the marks (or 2-scores) of x in X, y in Y and z in Z respectively. In this paper, we characterize the marks of 3-partite 2-digraphs and give a constructive and existence criterion for sequences of non-negative integers in non-decreasing order to be the mark sequences of some 3-partite 2-digraph.

• Journal of Microbiology
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• 제34권1호
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• pp.37-37
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• 1996

The internal regions of nuclear small subunit rRNA from 6 plaeurotus species and 5 Pleurotus ostreatus strains were amplified by PCR and sequenced. The DNA sequences of 8 Pleurotus strains (P. ostreatus NFFA2, NFFA4501, NFFA4001, KFFA4001, KFCC11635, P florida, P. florida, P. sajor-cuju, P. pulmonarius, and P. spodoleucus) were idential, but P. cornucopiae differed from them in two bases out of 605 bases. However, p[hylogenetic analysis of the sequences by DNA-distance matrix and UPGMA methods showed that P. ostreatus NFFA2m1 and NFFA2m2, known as mutants of P. ostreatus NFFA2, belonged to anther group of Basidiomycotina, which is close to the genus Auricularia. The difference of the SSU rDNA sequences of P. cornucopiae from other Pleurotus species tested corresponds to the difference of mitochondrial plasmid type present in Pleurotus species as observed by Kim et al. (1993, Korean J. Microbiol. 31, 141-147).ishement of silencing at the HMR/hsp82 locus can occur in G1-arrested cells. Cell cycle arrest at G1 phase was achieved by treatment of early log a cell cultures with .alpha.-factor mating pheromone, which induces G1 arrest. The result suggests that passage through S phase (and therefore DNA replication) is nor required for re-establishing silencer-mediated repression at the HMNRa/HSP82 locus. Finally, to test whether de nono protein synthesis is required for re-establishment of silencer-mediated repression, cells were pretreated with cycloheximide (500 /.mu.g/ml) 120 min. It was apparent that inhibiting protein synthesis delays, but does not prevent, re-establishment of silencer-mediated repression. Altogether, these results indicate that re-establishment of silencer-mediated repression is not dependent on the DNA replication and has no requirement for protein synthesis.

• The Plant Pathology Journal
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• 제32권1호
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• pp.33-46
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• 2016

In this study, the full-length nucleotide sequences of four Iranian PVY isolates belonging to $PVY^N$ strain were determined. The genome of Iranian PVY isolates were 9,703-9,707 nucleotides long encoding all potyviral cistrons including P1, HC-Pro, P3, 6K1, CI, 6K2, VPg, NIa-Pro, NIb and CP with coding regions of 825, 1,395, 1,095, 156, 1,902, 156, 564, 732, 1,557 and 801 nucleotides in length, respectively. The length of pipo, embedded in the P3 cistron, was 231 nucleotides. Phylogenetic analysis showed that the Iranian isolates clustered with European recombinant NTN isolates in the N lineage. Recombination analysis demonstrated that Iranian $PVY^N$ isolates had a typical European $PVY^{NTN}$ genome having three recombinant junctions while $PVY^N$ and $PVY^O$ were identified as the parents. We used dN/dS methods to detect candidate amino acid positions for positive selection in viral proteins. The mean ${\omega}$ ratio differed among different genes. Using model M0, ${\omega}$ values were 0.267 (P1), 0.085 (HC-Pro), 0.153 (P3), 0.050 (CI), 0.078 (VPg), 0.087 (NIa-pro), 0.079 (NIb) and 0.165 (CP). The analysis showed different sites within P1, P3 and CP were under positive selection pressure, however, the sites varied among PVY populations. To the best of our knowledge, our analysis provides the first demonstration of population structure of $PVY^N$ strain in mid-Eurasia Iran using complete genome sequences and highlights the importance of recombination and selection pressure in the evolution of PVY.

• 정보보호학회논문지
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• 제12권2호
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• pp.11-20
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• 2002

본 논문에서는 q는 p의 멱승이고, $F_{q^{n}}$이 원소의 개수가 $q^{n}$ 개인 유한체라 할 때, $F_{q^{n}}${0}으로부터의 $F_{q}$ 로의 차균형 성질을 갖는 d-동차함수로부터 (equation omitted) 순회상대차집합이 얻어질 수 있음을 보인다. 이에 따라 주기가 $q^{n}$ -1이고, 이상적인 자기상관성질을 갖는 p진 시퀀스 Helleseth-Gong 시퀀스 및, d-형 시퀀스로부터 (equation omitted)의 파라미터를 갖는 새로운 순회상대차집합을 생성시킨다.

• Journal of applied mathematics & informatics
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• 제7권1호
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• pp.195-203
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• 2000

In this paper, the concept of strongly p-Cesaro summability of sequences of fuzzy numbers is introduced. The relationship between statistical convergence and strongly p-Cesaro summability is discussed.

• Journal of Ginseng Research
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• 제40권2호
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• pp.176-184
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• 2016

Background: Wild ginseng, Panax ginseng Meyer, is an endangered species of medicinal plants. In the present study, we analyzed variations within the ribosomal DNA (rDNA) cluster to gain insight into the genetic diversity of the Oriental ginseng, P. ginseng, at artificial plant cultivation. Methods: The roots of wild P. ginseng plants were sampled from a nonprotected natural population of the Russian Far East. The slides were prepared from leaf tissues using the squash technique for cytogenetic analysis. The 18S rDNA sequences were cloned and sequenced. The distribution of nucleotide diversity, recombination events, and interspecific phylogenies for the total 18S rDNA sequence data set was also examined. Results: In mesophyll cells, mononucleolar nuclei were estimated to be dominant (75.7%), while the remaining nuclei contained two to four nucleoli. Among the analyzed 18S rDNA clones, 20% were identical to the 18S rDNA sequence of P. ginseng from Japan, and other clones differed in one to six substitutions. The nucleotide polymorphism was more expressed at the positions 440-640 bp, and distributed in variable regions, expansion segments, and conservative elements of core structure. The phylogenetic analysis confirmed conspecificity of ginseng plants cultivated in different regions, with two fixed mutations between P. ginseng and other species. Conclusion: This study identified the evidences of the intragenomic nucleotide polymorphism in the 18S rDNA sequences of P. ginseng. These data suggest that, in cultivated plants, the observed genome instability may influence the synthesis of biologically active compounds, which are widely used in traditional medicine.