<Papers><AcademicPaper><Titles><Title>DEVELOPMENT OF 2-ENERGY GROUP, ONE-DIMENSIONAL, FREQUENCY-DEPENDENT DETECTOR ADJOINT FUNCTIONS BASED ON THE NODAL METHOD</Title></Titles><Source>ANNALS OF NUCLEAR ENERGY</Source><PublicationDate>SEP</PublicationDate><YearPublished>1992</YearPublished><Volume>19</Volume><Issue>9</Issue><BeginningPage>495</BeginningPage><EndingPage>506</EndingPage><Authors><Author><AuthorShortName>DANOFSKY, RA</AuthorShortName></Author><Author><AuthorShortName>KHERICHA, ST</AuthorShortName><AuthorAddress>UNIV IOWA,DEPT NUCL MED,IOWA CITY,IA 52242</AuthorAddress></Author><Author><AuthorShortName>ROHACH, AF</AuthorShortName></Author></Authors><ReprintAddress>KHERICHA, ST, EG&amp;G IDAHO INC,IDAHO FALLS,ID 83402</ReprintAddress><ConceptCodes/><ChemicalBioChemicals/><Diseases/><MajorConcepts/><PartsStructuresSystems/><Keywords><IndexKeyword>CONTROL ROD VIBRATIONS</IndexKeyword><IndexKeyword>MODEL</IndexKeyword><IndexKeyword>NEUTRON NOISE DIAGNOSTICS</IndexKeyword></Keywords><SubjectCategories><SubjectCategory><SC>Nuclear Science &amp; Technology</SC></SubjectCategory></SubjectCategories><Abstract><Abstract>One-dimensional, two-energy group computer codes designed to calculate the response of a detector to a vibrating absorber in a reactor core were developed. This work incorporated a concept of local/global components based on the frequency-dependent detector adjoint function and a nodalization technique. The frequency-dependent detector adjoint functions presented by complex equations were expanded into real and imaginary parts. In the nodalization technique, the flux or detector adjoint function was expanded into polynomials about the center point of each node. The phase angles and the magnitudes of the two-energy group detector adjoint functions were calculated using a one-dimensional computer code. The calculations were made for a neutron detector located in the middle of the south core tank of the UTR-10 reactor. The reactor is located at Iowa State University. Results were compared with the exact analytical solution and were found to be within 2% of the values.</Abstract></Abstract><CitedReferences><CitedReference>ALAMMAR M, 1981, T AM NUCL SOC, V39, P955</CitedReference><CitedReference>ALAMMAR M, 1981, THESIS IOWA STATE U</CitedReference><CitedReference>ANALYTIS GT, 1980, ANN NUCL ENERGY, V7, P351</CitedReference><CitedReference>BENGHANAM M, 1983, THESIS IOWA STATE U</CitedReference><CitedReference>BORELAND RJ, 1982, THESIS IOWA STATE U</CitedReference><CitedReference>BURDEN RL, 1981, NUMERICAL ANAL</CitedReference><CitedReference>FEIZ M, 1983, THESIS IOWA STATE U</CitedReference><CitedReference>FOWLER TB, 1967, ORNLTM4078 REP</CitedReference><CitedReference>HENNESSY WJ, 1983, THESIS IOWA STATE U</CitedReference><CitedReference>HUANG LR, 1980, T AM NUCL SOC, V34, P831</CitedReference><CitedReference>KHERICHA ST, 1987, THESIS IOWA STATE U</CitedReference><CitedReference>KOSALY G, 1971, ATOMKERNENERG/KERNT, V18, P203</CitedReference><CitedReference>LEE SJ, 1981, T AM NUCL SOC, V39, P953</CitedReference><CitedReference>LEE SJ, 1983, NUCL SCI ENG, V83, P427</CitedReference><CitedReference>LUCIA A, 1973, ATOMKERNENERG/KERNT, V22, P1</CitedReference><CitedReference>PAZSIT I, 1977, ATOMKERNENERG/KERNT, V30, P29</CitedReference><CitedReference>PAZSIT I, 1978, ANN NUCL ENERGY, V5, P185</CitedReference><CitedReference>PAZSIT I, 1980, ANN NUCL ENERGY, V7, P171</CitedReference><CitedReference>PAZSIT I, 1983, NUCL SCI ENG, V85, P167</CitedReference><CitedReference>PAZSIT I, 1984, NUCL SCI ENG, V88, P77</CitedReference><CitedReference>ROBINSON JC, 1967, ORNL4149 REP</CitedReference><CitedReference>ROHACH AF, 1986, ANN NUCL ENERGY, V13, P549</CitedReference><CitedReference>ROHACH AF, 1986, ANN NUCL ENERGY, V13, P57</CitedReference><CitedReference>SANKOORIKAL JT, 1986, THESIS IOWA STATE U</CitedReference><CitedReference>STEPHENSON SE, 1966, ORNLTM1401 REP</CitedReference><CitedReference>VANDAM H, 1976, ATOMKERNENERG/KERNT, V27, P8</CitedReference><CitedReference>WEINBERG AM, 1948, PHYS REV, V74, P851</CitedReference></CitedReferences><CitedReferenceCount>27</CitedReferenceCount><TimesCited>3</TimesCited><LanguageOriginal>English</LanguageOriginal><DocumentTypes><DocumentType>Article</DocumentType></DocumentTypes><PubType>J</PubType><PublisherNameAddress>PERGAMON-ELSEVIER SCIENCE LTD</PublisherNameAddress><PublisherCity>OXFORD</PublisherCity><PublisherAddress>THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD, ENGLAND OX5 1GB</PublisherAddress><MeetingSponsors/><CharacterSourceAbbreviation>ANN NUCL ENERG</CharacterSourceAbbreviation><ISOSourceAbbreviation>Ann. Nucl. Energy</ISOSourceAbbreviation><PageCount>12</PageCount><ThomsonDocumentDeliverNumber>JK212</ThomsonDocumentDeliverNumber><ThomsonUniqueArticleID>ISI:A1992JK21200002</ThomsonUniqueArticleID><ArticleIdentifiers/><ISSN>0306-4549</ISSN><SourcePath>G:\x\isis\nuclear terms</SourcePath><SourceFile>reactor25.txt</SourceFile><SourceType>ISI</SourceType><Classification>UNCLASSIFIED</Classification></AcademicPaper><AcademicPaper><Titles><Title>Aspergillus species isolated from pistachio and determination of their aflatoxin production</Title></Titles><Source>Rostaniha</Source><PublicationDate>2007</PublicationDate><YearPublished>2007</YearPublished><Volume>8</Volume><Issue>1</Issue><BeginningPage>8</BeginningPage><PageSpan>8-10</PageSpan><Authors><Author><AuthorFullName>Bahar, M.</AuthorFullName><AuthorNameBiomed>Bahar, M.</AuthorNameBiomed></Author><Author><AuthorFullName>Rahimi, P.</AuthorFullName><AuthorNameBiomed>Rahimi, P.</AuthorNameBiomed><AuthorAddress>Rahimi, P.</AuthorAddress></Author><Author><AuthorFullName>Sharifnabi, B.</AuthorFullName><AuthorNameBiomed>Sharifnabi, B.</AuthorNameBiomed><AuthorAddress>Isfahan Univ Technol, Coll Agr, Esfahan, Iran</AuthorAddress></Author></Authors><ConceptCodes><ConceptCode>00504, General biology - Taxonomy, nomenclature and terminology</ConceptCode><ConceptCode>10060, Biochemistry studies - General</ConceptCode><ConceptCode>13502, Food technology - General and methods</ConceptCode><ConceptCode>13504, Food technology - Fruits, nuts and vegetables</ConceptCode><ConceptCode>50506, Botany: general and systematic - Fungi</ConceptCode><ConceptCode>50528, Botany: general and systematic - Floristics and distribution</ConceptCode></ConceptCodes><ChemicalBioChemicals><ChemicalBioChemical>(toxin)</ChemicalBioChemical><ChemicalBioChemical>aflatoxin</ChemicalBioChemical></ChemicalBioChemicals><Diseases/><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus alliaceus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus candidus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus niger</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus ochraceus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus parasiticus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus terreus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(contaminant)] [Aspergillus unguis</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(new record</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(new record</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(new record</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>(new record</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>[Aspergillus flavus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>contaminant)]</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>contaminant)] [Aspergillus niveus</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>contaminant)] [Aspergillus tamari</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>contaminant)] [Aspergillus wentii</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi Imperfecti or Deuteromycetes [15500-New]</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi, Microorganisms, Nonvascular Plants, Plants</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi, Plantae</Taxonomic></TaxonomicData><MajorConcepts><MajorConcept>Foods</MajorConcept><MajorConcept>Systematics and Taxonomy</MajorConcept></MajorConcepts><PartsStructuresSystems/><Keywords/><SubjectCategories/><Abstract><Abstract>Aflatoxins are the most serious problem in production and export of pistachio of Iran. They are amongst the most toxic mycotoxins and are produced predominantly by Aspergillus flavus and A. parasiticus. Pistachio is susceptible to invasion by aflatoxigenic Aspergillus species and subsequent production of aflatoxins, during preharvesting, processing, transportation or storage. Various methods have been used to detect toxin in pistachio such as chromatography (TLC and HPLC), ELISA and PCR base methods. Some of these methods e.g. chromatography, are time consuming, labor-intensive and expensive. In this study, nuts sample of pistachio were collected from pistachio orchards in Kerman, Rafsanjan and Isfahan. Culture media AFPA and PDA, were used to isolate Aspergillus species. Two hundred and fifty isolates were obtained and based on microscopic and macroscopic studies, the isolates belonged to the genera, Aspergillus, Fusarium, Rhizopus, Alternaria and Cladosporium. Comparing morphological characters of Aspergillus species grown on CYA, CY20S and MEA after one week, 10 following, Aspergillus species were identified:A. alliaceus, A. candidus, A. flavus, A. niger, A. niveus, A. ochraceus, A. parasiticus, A. tamari, A. terreus, A. unguis and A. wentii, that A. afflaceus, A. candidus, A. niveus, A. unguis and A. wentii, were reported for first time from pistachio in Iran. There was not a direct relationship between sclerotium and aflatoxin production in this study. Application of methylated B-cyclodextrin in culture media showed that it can be used for rapid detection of aflatoxigenic aspergilli.</Abstract></Abstract><CitedReferences/><LanguageOriginal>English</LanguageOriginal><DocumentTypes><DocumentType>Article</DocumentType></DocumentTypes><PubType>J</PubType><MeetingSponsors/><BiosisArticleNumber>PREV200800106869</BiosisArticleNumber><ArticleIdentifiers/><ISSN>1608-4306</ISSN><SourcePath>Q:\ISIS\1BOLOGICAL WARFARE\BIOSIS\BIOSIS_MISC</SourcePath><SourceFile>1.txt</SourceFile><SourceType>BIOSIS</SourceType><Classification>UNCLASSIFIED</Classification></AcademicPaper><AcademicPaper><Titles><Title>Evaluation of mutagenic potential of mold extracts isolated from buildings using the mouse lymphoma thymidine kinase gene mutation assay (MLA)</Title></Titles><Source>Polish Journal of Environmental Studies</Source><PublicationDate>2007</PublicationDate><YearPublished>2007</YearPublished><Volume>16</Volume><Issue>6</Issue><BeginningPage>807</BeginningPage><PageSpan>807-815</PageSpan><Authors><Author><AuthorFullName>Arkusz, J.</AuthorFullName><AuthorNameBiomed>Arkusz, J.</AuthorNameBiomed><AuthorAddress>Stepnik, M.</AuthorAddress></Author><Author><AuthorFullName>Gutarowska, B.</AuthorFullName><AuthorNameBiomed>Gutarowska, B.</AuthorNameBiomed></Author><Author><AuthorFullName>Lewinska, D.</AuthorFullName><AuthorNameBiomed>Lewinska, D.</AuthorNameBiomed></Author><Author><AuthorFullName>Piotrowska, M.</AuthorFullName><AuthorNameBiomed>Piotrowska, M.</AuthorNameBiomed></Author><Author><AuthorFullName>Stanczyk, M.</AuthorFullName><AuthorNameBiomed>Stanczyk, M.</AuthorNameBiomed></Author><Author><AuthorFullName>Stepnik, M.</AuthorFullName><AuthorNameBiomed>Stepnik, M. (mstep@imp.lodz.pl)</AuthorNameBiomed><AuthorAddress>Nofer Inst Occupat Med, Dept Toxicol and Carcinogenesis, Sw Teresy 8, PL-91348 Lodz, Poland</AuthorAddress><AuthorEmail>mstep@imp.lodz.pl</AuthorEmail></Author></Authors><ConceptCodes><ConceptCode>02506, Cytology - Animal</ConceptCode><ConceptCode>03502, Genetics - General</ConceptCode><ConceptCode>03504, Genetics - Plant</ConceptCode><ConceptCode>03506, Genetics - Animal</ConceptCode><ConceptCode>10802, Enzymes - General and comparative studies: coenzymes</ConceptCode><ConceptCode>22501, Toxicology - General and methods</ConceptCode><ConceptCode>51518, Plant physiology - Enzymes</ConceptCode></ConceptCodes><ChemicalBioChemicals><ChemicalBioChemical>(toxin, mutagen)</ChemicalBioChemical><ChemicalBioChemical>(toxin, mycotoxin)/mold extract</ChemicalBioChemical><ChemicalBioChemical>(toxin, mycotoxin)/sterigmatocystin</ChemicalBioChemical><ChemicalBioChemical>10048-13-2</ChemicalBioChemical><ChemicalBioChemical>303-47-9</ChemicalBioChemical><ChemicalBioChemical>ochratoxin A</ChemicalBioChemical></ChemicalBioChemicals><Diseases/><MethodsEquipment><MethodEquipment>laboratory techniques, bioassay techniques</MethodEquipment></MethodsEquipment><MethodsEquipment><MethodEquipment>mouse lymphoma assay</MethodEquipment></MethodsEquipment><GeneNameData><GeneName>mouse LTK gene [Muridae]</GeneName></GeneNameData><GeneNameData><GeneName>mouse lymphoma thymidine kinase gene</GeneName></GeneNameData><GeneNameData><GeneName>mutation</GeneName></GeneNameData><TaxonomicData><Taxonomic>(mouse lymphoma cells)]</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>[mouse] [L5178Y cell line</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>[Penicillium chrysogenum] [Aspergillus niger] [Penicillium expansum] [Alternaria alternata] [Aspergillus versicolor] [Cladosporium cladosporioides]/Rodentia, Mammalia, Vertebrata, Chordata, Animalia</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Animals, Chordates, Mammals, Nonhuman Vertebrates, Nonhuman Mammals, Rodents, Vertebrates</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi Imperfecti or Deuteromycetes [15500]</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi, Microorganisms, Nonvascular Plants, Plants</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Fungi, Plantae</Taxonomic></TaxonomicData><TaxonomicData><Taxonomic>Muridae [86375]</Taxonomic></TaxonomicData><MajorConcepts><MajorConcept>Enzymology (Biochemistry and Molecular Biophysics)</MajorConcept><MajorConcept>Methods and Techniques</MajorConcept><MajorConcept>Molecular Genetics (Biochemistry and Molecular Biophysics)</MajorConcept><MajorConcept>Toxicology</MajorConcept></MajorConcepts><PartsStructuresSystems/><Keywords/><SubjectCategories/><Abstract><Abstract>In recent years interest in mycotoxin-producing fungi growing in indoor environments has increased. Evidence of mutagenic potential of some molds or their mycotoxins is still equivocal. Much more information is available for single mycotoxins or their metabolites than for complex mixtures composed of different fungi products.The aim of this study was to identify the mutagenic potential of extracts isolated from mold-attacked buildings using the mouse lymphoma assay (MLA).Although a thin-layer chromatography analysis of extracts isolated from test buildings showed the presence of well known mycotoxins (ochratoxin A and sterigmatocystin), the test extracts aswell as control extracts did not reveal mutagenic potential after 3-hr exposure without or with metabolic activation as tested with MLA. Negative results were also obtained after 24-hr treatment with every test sample in the absence of S9 fraction. The data indicates that extracts prepared from control and test buildings under experimental conditions did not induce mutations affecting the expression of the thymidine kinase gene in the cultured L5178Y TK+/- cells.</Abstract></Abstract><CitedReferences/><LanguageOriginal>English</LanguageOriginal><DocumentTypes><DocumentType>Article</DocumentType></DocumentTypes><PubType>J</PubType><MeetingSponsors/><BiosisArticleNumber>PREV200800106124</BiosisArticleNumber><ArticleIdentifiers/><ISSN>1230-1485</ISSN><SourcePath>Q:\ISIS\1BOLOGICAL WARFARE\BIOSIS\BIOSIS_MISC</SourcePath><SourceFile>1.txt</SourceFile><SourceType>BIOSIS</SourceType><Classification>UNCLASSIFIED</Classification></AcademicPaper></Papers>