• Asian-Australasian Journal of Animal Sciences
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• v.25 no.1
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• pp.33-36
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• 2012

A total of 423 blood samples were collected (during 2009 and 2010) from all the ram holdings at three major Jordanian governmental Awassi breeding stations (Al-Khanasry, Al- Mushairfa and Al-Fjaje) and two private flocks. All blood samples were screened for the presence of mutations at the CNGA3 gene (responsible for day blindness in Awassi sheep) using RFLP-PCR. The day blindness mutation was detected in all studied flocks. The overall allele and genotype frequencies of all studied flocks of the day blindness mutation were 0.088 and 17.49%, respectively. The genotype and allele frequencies were higher in station flocks than the farmer flocks (0.121, 24.15 and 0.012, 2.32, respectively). Al-Mushairfa and Al-Khanasry stations have the highest genotype and allele frequencies for the day blindness mutation that were 27.77, 30.00% and 0.14, 0.171, respectively. The investigated farmer flocks have low percentages (0.03, 5.88% at Al-Shoubak and 0.005 and 1.05%, at Al-Karak, respectively for genotype and allele frequencies) compared with the breeding stations. Ram culling strategy was applied throughout the genotyping period in order to gradually eradicate this newly identified day blindness mutation from Jordanian Breeding station, since they annually distribute a high percentage of improved rams to farmer's flocks.

• Journal of the Korean Mathematical Society
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• v.47 no.2
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• pp.235-246
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• 2010

A Banach space operator A $\in$ B(X) is polaroid if the isolated points of the spectrum of A are poles of the resolvent of A; A is hereditarily polaroid, A $\in$ ($\mathcal{H}\mathcal{P}$), if every part of A is polaroid. Let $X^n\;=\;\oplus^n_{t=i}X_i$, where $X_i$ are Banach spaces, and let A denote the class of upper triangular operators A = $(A_{ij})_{1{\leq}i,j{\leq}n$, $A_{ij}\;{\in}\;B(X_j,X_i)$ and $A_{ij}$ = 0 for i > j. We prove that operators A $\in$ A such that $A_{ii}$ for all $1{\leq}i{\leq}n$, and $A^*$ have the single-valued extension property have spectral properties remarkably close to those of Jordan operators of order n and n-normal operators. Operators A $\in$ A such that $A_{ii}$ $\in$ ($\mathcal{H}\mathcal{P}$) for all $1{\leq}i{\leq}n$ are polaroid and have SVEP; hence they satisfy Weyl's theorem. Furthermore, A+R satisfies Browder's theorem for all upper triangular operators R, such that $\oplus^n_{i=1}R_{ii}$ is a Riesz operator, which commutes with A.

• Journal of the Chungcheong Mathematical Society
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• v.31 no.4
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• pp.487-509
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• 2018

The Truncated Moment Problem (TMP) entails finding a positive Borel measure to represent all moments in a finite sequence as an integral; once the sequence admits one or more such measures, it is known that at least one of the measures must be finitely atomic with positive densities (equivalently, a linear combination of Dirac point masses with positive coefficients). On the contrary, there are more general moment problems for which we aim to find a "signed" measure to represent a sequence; that is, the measure may have some negative densities. This type of problem is referred to as the General Truncated Moment Problem (GTMP). The Jordan Decomposition Theorem states that any (signed) measure can be written as a difference of two positive measures, and hence, in the view of this theorem, we are able to apply results for TMP to study GTMP. In this note we observe differences between TMP and GTMP; for example, we cannot have an analogous to the Flat Extension Theorem for GTMP. We then present concrete solutions to lower-degree problems.

• Korean Journal of Ichthyology
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• v.11 no.1
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• pp.23-28
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• 1999

Two species of the unrecorded congrid eel, Ariosoma major (Asano, 1958) and Rhynchoconger ectenurus (Jordan and Richardson, 1909) were collected for the first time from the Southern and Western Sea of Korea. A. major closely resembled A. shiroanago, but differed from the latter in having lesser number of lateral line pores before vent and vertebrae. R. ectenurus was very similar to R. brachuata, but differed from the latter in having slender tail and a great number of vertebrae. A key to the genera and species of the family Congridae from Korea was given. New Korean name "Kunhuin-bungchangeo" was proposed for the A. major, and "Gomunkkori-bungchangeo", R. ectenurus, respectively.

• Korean Journal of Fisheries and Aquatic Sciences
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• v.9 no.2
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• pp.129-142
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• 1976

Optimum doses The optimum dose that may be defined as the dose below the maximum permissible dose, yet would bring about a significant storage life extension at refrigerated temperatures, varied with species of fish as well as with the postirradiation storage temperatures. Thus the dose of 0. 1 Mrad was considered to be optimum for the croaker and yellow corvenia at $0^{\circ}C$, while at $5^{\circ}C$ the dose of 0.2 Mrad would be suitable for both species. The roundnose flounder was more radiosensitive and even at the dose of 0.1 Mrad a slight irradiation odor was detected immediately after the radiation treatment. Such degree of irradiation odor disappeared upon storage, therefore, the dose of 0.1 Mrad was considered to be optimum for the roundnose flounder at both $0^{\circ}\;and\;5^{\circ}C$. Storage life extension The croaker meats irradiated at 0.1 Mrad could be held at $0^{\circ}C$ as long as 5 weeks in good acceptable conditions, while the unirradiated control became unacceptable within 2 weeks-3-4 for extension of storage life at $0^{\circ}C$. At the storage temperature of $5^{\circ}C$, the storage life of 0.2 Mrad irradiated samples was extended from less than one week to 4 weeks--4-5 fold extension. The storage life extension of 0.1 Mrad irradiated yellow corvenia at $0^{\circ}C$ was from less than 2 weeks for the unirradiated to 4 weeks-approximately a-s folds and that of 0.2 Mrad irradiated samples stored at $5^{\circ}C$ was from 5 days to 3 weeks 4-5 folds. The roundnose flounder meats irradiated at 0.1 Mrad could held at $0^{\circ}C$ for 3-4 weeks as compared to less than 1 week for the unirradiated and at $5^{\circ}C$ the storage life could be extended from less than 3 days to up to 3 weeks. Thus the storage life extension by 4-5 folds and by 6-7 folds was possible at $0^{\circ}C\;and\;5^{\circ}C$ storage, respectively. Postirradiation storage microbiology and biochemistry In general 10 fold reduction of initial microflora was realized as a result of irradiating fish samples at 0.1 Mrad. The extent of microflora reduction increased with increasing doses applied, but not proportionately dependent. The microbial growth in the irradiated was severely retarded during the subsequent storage period, lagging far behind that of the irradiated control samples except in the late storage phase, when the levels of microflora of the irradiated either approached to or rose above the levels of the unirradiated. The microbiological changes caused by irradiation was reflected in the pronounced suppression of TVB and TMA accumulation during the storage period. This suggests that irradiation treatment brought about both quantitative and qualitative changes in microflora initially present and it is reasonable to suggest that the microflora removed by irradiation in fact represent most of the flora capable of producing TVB and TMA in normal fish spoilage process.