• Proceedings of the Korean Powder Metallurgy Institute Conference
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• 2006.09b
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• pp.1095-1096
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• 2006

When $Y_2O_3$ was added to Ti-excess $BaTiO_3$ ((Ba+Y)/Ti =1), the area occupied by $Y^{3+}$ ion was confirmed by its microstructure development, electrical conductivity behavior and lattice constant. Grain growth inhibition was observed when the content of donor dopant exceeded a critical value ($x{\approx}.0.01$) in $BaTiO_3+x(0.5Y_2O_3+TiO_2)$ system. A donor-doped behavior was observed at various Y contents ($0.2\sim3.0$ mol% Y) when $Y_2O_3$ was added to $TiO_2$-excess $BaTiO_3$. As Y content was increased, (002) and (200) peaks shifted to higher angles and the lattice constant (a and c axis) decreased gradually.

• Kyungpook Mathematical Journal
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• v.53 no.2
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• pp.233-245
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• 2013

Let $\mathcal{A}$ be a Banach ternary algebra over a scalar field R or C and $\mathcal{X}$ be a ternary Banach $\mathcal{A}$-module. A quartic mapping $D\;:\;(\mathcal{A},[\;]_{\mathcal{A}}){\rightarrow}(\mathcal{X},[\;]_{\mathcal{X}})$ is called a $4^{th}$- order ternary derivation if $D([x,y,z])=[D(x),y^4,z^4]+[x^4,D(y),z^4]+[x^4,y^4,D(z)]$ for all $x,y,z{\in}\mathcal{A}$. In this paper, we prove Ulam stability generalizations of $4^{th}$- order ternary derivations associated to the following JMRassias quartic functional equation on fr$\acute{e}$che algebras: $$f(kx+y)+f(kx-y)=k^2[f(x+y)+f(x-y)]+2k^2(k^2-1)f(x)-2(k^2-1)f(y)$$.

• BMB Reports
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• v.35 no.5
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• pp.488-493
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• 2002

IgY was separated from a hen's egg yolk that was immunized with Helicobacter pyroli. The anti-H. pyroli IgY activity at acidic pH and the suppressive effect of polyol on acid-induced inactivation of IgY were investigated. Sorbitol and xylitol were used as polyols. IgY was quite stable at pH 5~7. Irreversible inactivation of IgY was observed at pH below 4, and proceeded rapidly at pH below 3. The acid stability of IgY was enhanced in the presence of 30% sorbitol or above. In a 50% aqueous sorbitol solution, an acid-induced inactivation was almost completely suppressed at pH 3. However, the improvement of IgY activity was not observed in the aqueous xylitol solution. IgY showed almost the same activity as native IgY when sucrose was substituted for sorbitol. On the other hand, the xylitol replacement with sucrose did not enhance the acid stability of IgY. The acid-induced inactivation of IgY was related to tryptophyl fluorescence. Fluorescence emission spectra suggested that structural changes near the tryptophan residues may occur under acidic conditions. An increase in sorbitol concentration induced a blue shift. The fluorescence emission of IgY in a 50% sorbitol solution had a peak at 330 nm, which was the same emission peak that was exhibited by native IgY. Sorbitol could, therefore, be used as a good stabilizer of IgY under acidic conditions.

• Asian-Australasian Journal of Animal Sciences
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• v.28 no.8
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• pp.1066-1074
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• 2015

In contrast to high genetic diversity of mitochondrial DNA (mtDNA), equine Y chromosome shows extremely low variability, implying limited patrilines in the domesticated horse. In this study, we applied direct sequencing and restriction fragment length polymorphism (RFLP) methods to investigate the polymorphisms of 33 Y chromosome specific loci in 304 Chinese indigenous horses from 13 breeds. Consequently, two Y-single nucleotide polymorphisms (SNPs) (Y-45701/997 and Y-50869) and one Y-indel (Y-45288) were identified. Of those, the Y-50869 (T>A) revealed the highest variation frequency (24.67%), whereas it was only 3.29% and 1.97% in Y-45288 (T/-) and Y-45701/997 (G>T) locus, respectively. These three mutations accounted for 27.96% of the total samples and identified five Y-SNP haplotypes, demonstrating genetic diversity of Y chromosome in Chinese horses. In addition, all the five YSNP haplotypes were shared by different breeds. Among 13 horse breeds analyzed, Balikun horse displayed the highest nucleotide diversity (${\pi}=5.6{\times}10^{-4}$) and haplotype diversity (h = 0.527), while Ningqiang horse showed the lowest nucleotide diversity (${\pi}=0.00000$) and haplotype diversity (h = 0.000). The results also revealed that Chinese horses had a different polymorphic pattern of Y chromosome from European and American horses. In conclusion, Chinese horses revealed genetic diversity of Y chromosome, however more efforts should be made to better understand the domestication and paternal origin of Chinese indigenous horses.

• Journal of the Korean Geotechnical Society
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• v.34 no.7
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• pp.51-58
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• 2018

In this study a series of centrifuge tests were carried out in dry sand to analyze the comparison of lateral pile behavior for static loading and dynamic loading condition. In case of static loading condition, the lateral displacement was applied up to 50% of pile diameter by deflection control method. And the input sine wave of 0.1 g~0.4 g amplitude and 1 Hz frequency was applied at the base of the soil box using shaking table for dynamic loading condition. From comparison of experimental static p-y curve obtained from static loading tests with API p-y curves, API p-y curves can predict well within 20% error the ultimate subgrade reaction force of static loading condition. The ultimate subgrade reaction force of experimental dynamic p-y curve is 5 times larger than that of API p-y curves and experimental static p-y curves. Therefore, pseudo-static analysis applied to existing p-y curve for seismic design could greatly underestimate the soil resistance at non-linear domain and cause overly conservative design.

• Journal of the Chungcheong Mathematical Society
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• v.9 no.1
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• pp.77-87
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• 1996

For any map $v:X{\rightarrow}Y$, the generalized Gottlieb set $G({\Sigma}A;X,v,Y)$ with respect to v is a subgroup of $[{\Sigma}A,Y]$. If $v:X{\rightarrow}Y$ has a left homotopy inverse $u:X{\rightarrow}Y$, then for any $f{\in}G({\Sigma}A;X,v,Y)$, $g{\in}G({\Sigma}A;X,u,Y)$, the function spaces $L({\Sigma}A,X;uf)$ and $L({\Sigma}A,X;g)$ have the same homotopy type.

• Korean Journal of Mathematics
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• v.20 no.1
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• pp.77-89
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• 2012

Using fixed point method, we prove the Hyers-Ulam stability of the orthogonally additive functional equation (0.1) $f(2x+y)=2f(x)+f(y)$ and of the orthogonally quadratic functional equation (0.2) $2f(\frac{x}{2}+y)+2f(\frac{x}{2}-y)=f(x)+4f(y)$ for all $x$, $y$ with $x{\perp}y$ in orthogonality spaces.

• Journal of Plant Biology
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• v.25 no.4
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• pp.175-180
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• 1982

This paper is proposed to describe three new species and four varieties from Cheju Island to central part of Korea in Southern Korea. The new plant taxa are as follows: clematis taeguensis Y. Lee, sp. nov.; Prunus linearipetalus Y. Lee, sp. nov.; Vicia linearifolia Y. Lee, sp. nov.; Clematis brachyura Maxim. var. hexasepala Y. Lee, var. nov.; Ranunculus quelpaertensis(Lev.) Nakai var. albiflorus Y. Lee, var. nov.; Aconitum napiforme Lev. et Vaniot var. albiflorum Y. Lee, var. nov.; Ajuga decumbens Thunb. var. rosa Y. Lee, var. nov.

• Communications of the Korean Mathematical Society
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• v.19 no.2
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• pp.253-266
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• 2004

In this note, by using the fixed point alternative, we investigate the modified Hyers-Ulam-Rassias stability for the following mixed type functional inequality which is either cubic or quadratic: $\parallel$8ｆ(x-3y) + 24f(x+y) + f(8y) -8〔f(x+3y) + 3f(x-y) + 2f(2y)〕$\parallel$$\leq$$\varphi$(x,y).

• Journal of the Chungcheong Mathematical Society
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• v.30 no.4
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• pp.467-476
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• 2017

In this paper, we obtain the stability of the additive-quadratic functional equation f(x+y, z+w)+f(x+y, z-w) = 2f(x, z)+2f(x, w)+2f(y, z)+2f(y, w) and the bi-Jensen functional equation $$4f(\frac{x+y}{2},\;\frac{z+w}{2})=f(x,\;z)+f(x,\;w)+f(y,\;z)+f(y,\;w)$$ in 2-Banach spaces.