Tesi sul tema "Effect of salt on"
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Cropper, Paul Edward. "A kinetic template effect in arylphosphonium salt formation". Thesis, Sheffield Hallam University, 1988. http://shura.shu.ac.uk/19513/.
Testo completoSteward, Scott D. "The Effect of Salt Splash on Nylon 6,6". Thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/35635.
Testo completoMaster of Science
Andrade, Maria Isabel. "PHYSIOLOGY OF SALT TOLERANCE IN GUAR, CYAMOPSIS TETRAGONOLOBA (L.) TAUB". Thesis, The University of Arizona, 1985. http://hdl.handle.net/10150/275416.
Testo completoMorita, Tateo 1958. "Effect of inbreeding on germination salt tolerance in alfalfa". Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/276644.
Testo completoKalifa, Ali. "Salt stress, and phosphorus absorption by potato plants cv. 'Russet Burbank'". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq29727.pdf.
Testo completoAlm, David Michael. "Comparison and interaction of heat and salt stress in cultured tobacco cells". Virtual Press, 1986. http://liblink.bsu.edu/uhtbin/catkey/445616.
Testo completoMcKimmie, Timothy Irving 1948. "CHARACTERIZATION OF SALT TOLERANCE IN ALFALFA (MEDICAGO SATIVA L.)". Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/276348.
Testo completoAtkinson, Janelle. "A salt on the land: The osmolyte production and physiological responses of selected Myrtaceae species exposed to salt and water stress". Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2005. https://ro.ecu.edu.au/theses/135.
Testo completoAttumi, Al-Arbe. "Effect of salt stress on phosphorus and sodium absorptions by soybean plants". Thesis, McGill University, 1997. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=20242.
Testo completoKhrais, Tala. "Evaluation of salt tolerance in potato (Solanum spp.)". Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23901.
Testo completoWoodward, Andrew J. "The use of proline to determine salt tolerance in eucalyptus species and clones". Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2004. https://ro.ecu.edu.au/theses/841.
Testo completoCrystal, Susan. "Effect of early pregnancy vomiting on offspring salt taste preference /". Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/9014.
Testo completoZhou, Maoqian 1961. "Nitrogen fixation by alfalfa as affected by salt stress and nitrogen levels". Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277231.
Testo completoGuo, Kunmei. "Functional assessment of the role of cyclic nucleotide-gates channel (CNGC10) and salt overly sensitive (SOS1) antiporter in salinity tolerance in Arabidopsis". University of Western Australia. Faculty of Natural and Agricultural Sciences, 2009. http://theses.library.uwa.edu.au/adt-WU2009.0063.
Testo completoRobinson, David Lowell 1955. "RECURRENT SELECTION FOR GERMINATION SALT TOLERANCE IN ALFALFA (SALINITY, FORAGES, BREEDING)". Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/277015.
Testo completoMarvar, Paul J. "Effect of high salt intake on arteriolar responses to metabolic stimuli". Morgantown, W. Va. : [West Virginia University Libraries], 2006. https://eidr.wvu.edu/etd/documentdata.eTD?documentid=4696.
Testo completoTitle from document title page. Document formatted into pages; contains xiv, 197 p. : ill. Vita. Includes abstract. Includes bibliographical references.
Drake, Arly Marie. "EFFECT OF PLANT GROWTH REGULATORS ON CREEPING BENTGRASS GROWTH AND HEALTH DURING HEAT, SALT, AND COMBINED HEAT AND SALT STRESS". The Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1546450732510932.
Testo completoBadenhorst, Petrus Cornelius. "Identification of molecular markers for Thinopyrum distichum chromosomes contributing to salt tolerance". Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51794.
Testo completoENGLISH ABSTRACT: The detrimental effect of soil salinity on crop production is a growmg problem worldwide (Tanji, 1990b). The degree to which plants can tolerate high concentrations of salt in their rooting medium is under genetic control with different genetic and physiological mechanisms contributing to salt tolerance at different developmental stages (Epstein & Rains, 1987). Only limited variation exists for salt tolerance in the cultivated cereals. This has prompted attempts to select tolerant progeny following hybridisation of cultivated species and wild, salt-tolerant species. Thinopyrum distichum, an indigenous wheatgrass that is naturally adapted to saline environments (McGuire & Dvorak, 1981), was crossed with triticale (x Triticosecale) in an attempt to transfer its salt tolerance and other hardiness characteristics (Marais & Marais, 1998). The aims of this study were to (i) identify Thinopyrum chromosomes carrying genes for salt tolerance and to identify molecular markers for these chromosomes, (ii) identify a number of diverse monosomic and disomie addition plants. Bulked segregant analysis (BSA), in combination with AFLP, RAPD and DAF marker analysis was implemented to screen for polymorphisms associated with salt tolerance. Five putative AFLP markers and two RAPD markers were detected using bulks composed of salt tolerant plants and bulks composed of salt sensitive plants. The distribution of the markers in these bulks suggests that more than one Thinopyrum chromosome carry genes for salt tolerance. Salt tolerant monosomic and disomie addition plants were characterised for AFLP, RAPD and DAF polymorphisms in an attempt to find markers associated with the chromosome(s) conditioning salt tolerance. One salt tolerant monosomic and one disomie addition plant was identified. One AFLP and two RAPD markers were identified for the Thinopyrum chromosome( s) present in the monosomic addition plant, while three AFLP and three RAPD markers were identified for the disomie addition plant. An attempt was also made to identify diverse chromosome addition plants having complete or near complete triticale genomes plus an additional random Thinopyrum chromosome. Plants with 2n = 43 /44 were identified and characterised for molecular markers (AFLP and RAPD). Cluster analysis was used to group the putative monosomic or disomie addition plants according to the specific Thinopyrum chromosomes they retained. Seventeen AFLP and RAPD markers could be used to group the 24 putative addition plants into six broadly similar groups with different additional Thinopyrum chromosomes. While the members of each group are likely to carry the same additional Thinopyrum chromosomes, this may not necessarily be the case as the interpretation of the marker results is complicated by heterogeneity among plants with regard to the triticale background chromosomes they possess. It is also likely that chromosome translocations occurred during backerossing which may further complicate data. Nonetheless, it is now possible to select disomie addition plants from each group that are likely to represent different Thinopyrum chromosomes. The data will also be useful in future attempts to find further addition plants carrying the remaining Thinopyrum chromosomes.
AFRIKAANSE OPSOMMING: Die skadelike effek van grond versouting op gewasproduksie neem wêreldwyd toe (Tanji, 1990b). Die mate waartoe plante hoë konsentrasies sout in die wortelstelsel kan hanteer is onder genetiese beheer en verskillende genetiese en fisiologiese meganismes dra by tot die soutverdraagsaamheid tydens verskillende ontwikkelingstadia (Epstein & Rains, 1987). Slegs beperkte variasie bestaan vir soutverdraagsaamheid in verboude grane. Dit het aanleiding gegee tot pogings om soutverdraagsame nageslag te selekteer na hibridisasie van verboude spesies en wilde, soutverdraagsame spesies. Thinopyrum distichum, 'n inheemse koringgras, wat aangepas is by brak omgewings (McGuire & Dvorak, 1981), is met korog (x Triticosecale) gekruis in 'n poging om die gene vir soutverdraagsaamheid en ander gehardheidseienskappe oor te dra (Marais & Marais, 1998). Die oogmerke van hierdie studie was om (i) Thinopyrum chromosome te identifiseer wat gene bevat vir soutverdraagsaamheid en molekulêre merkers te vind vir hierdie chromosome, (ii) 'n aantal diverse monosomiese en disomiese addisieplante te identifiseer. Bulksegregaatanalise (BSA), gekombineer met AFLP-, RAPD- en DAF-merkeranalise, is gebruik om polimorfismes geassosieerd met soutverdraagsaamheid op te spoor. Vyf moontlike AFLPmerkers en twee RAPD-merkers is geïdentifiseer met gebruik van bulks bestaande uit soutverdraagsame plante en bulks bestaande uit soutgevoelige plante. Die verspreiding van die merkers in soutverdraagsame bulks dui daarop dat meer as een Thinopyrum chromosoom bydra tot soutverdraagsaamheid. Soutverdraagsame, monosomiese en disomiese addisieplante is gekarakteriseer vir AFLP- en RAPD-polimorfismes in 'n verdere poging om merkers te vind vir chromosome betrokke by soutverdraagsaamheid. Een soutverdraagsame monosomiese en een disomiese addisieplant is geïdentifiseer. Een AFLP- en twee RAPD-merkers is geïdentifiseer vir die Thinopyrum chromosoom(e) teenwoordig in die monosomiese addisieplant, terwyl drie AFLP- en drie RAPDmerkers geïdentifiseer is vir die disomiese addisieplant. 'n Poging is ook gemaak om diverse addisieplante te identifiseer met 'n volledige koroggenoom plus 'n addisionele Thinopyrum chromosoom. Plante met 2n = 43 / 44 is geïdentifiseer en gekarakteriseer met molekulêre merkers (AFLP en RAPD). Tros-analise is gebruik om die vermoedelik monosomiese of disomiese addisieplante te groepeer volgens die spesifieke Thinopyrum chromosome wat hulle behou het. Sewentien AFLP- en RAPD-merkers is gebruik om die 24 vermoedelike addisieplante in 6 groepe met verskillende Thinopyrum chromosome te groepeer. Alhoewel dit voorkom of die verskillende plante in 'n groep dieselfde addisionele Thinopyrum chromosoom het, is dit nie noodwendig die geval nie aangesien die interpretasie van die merkers bemoeilik word deur die heterogeniteit tussen die plante wat betref die agtergrond korogchromosome wat hulle besit. Dit is ook moontlik dat chromosoom herrangskikkings plaasgevind het gedurende die terugkruisings, wat die data verder kan bemoeilik. Nietemin, dit is nou moontlik om disomiese addisies te selekteer uit elke groep wat moontlik verskillende Thinopyrum chromosome bevat. Die data kan ook gebruik word om in die toekoms verdere addisieplante te identifiseer wat die oorblywende Thinopyrum chromosome bevat.
Al-Hagdow, Moftah Moh. "Interactions between sodium and potassium in micropropagated potato cultivars differing in salinity tolerance". Thesis, McGill University, 1998. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=20554.
Testo completoThe salt resistance of S is associated not only with a superior capacity to accumulate high Na+ in the roots for osmotic adjustment, but also with resistance to Na movement to the shoot.
The effect of [K] on plant growth showed two main characteristics. In non-saline media, increasing [K] enhanced growth of S, while RB showed optimum growth when the normal (20 mM) level was present in the MS medium. In saline media, elevating [K] alleviated the growth reduction of RB at low salinity, and S at both low and high salinity. This ameliorative effect of K may be attributed to the suppression of both Na+ uptake, and Na + translocation in the plant.
LEDBETTER, CRAIG ALLEN. "HERITABILITY OF SALT TOLERANCE DURING GERMINATION AND EMERGENCE IN SHORT STAPLE COTTON (GOSSYPIUM HIRSUTUM L.)". Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/183961.
Testo completoSlail, Nabeel Younis 1963. "INFLUENCE OF SODIUM-CHLORIDE ON TRANSPIRATION AND PLANT GROWTH OF TWO TOMATO CULTIVARS". Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/276516.
Testo completoLund, Lars. "Effekt av salt på telehiv". Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for bygg, anlegg og transport, 2012. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-18529.
Testo completoEl-Sheikh, Medhat. "Studies on the cellular and molecular basis of salt resistance in a halotolerant Arabidopsis thaliana cell line". Thesis, University of Glasgow, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274256.
Testo completoNjenga, H. N. "Low pressure and salt effect on the ethanol-water vapour-liquid equilibrium". Thesis, Swansea University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.638334.
Testo completoPEREZ, HERNAN EDUARDO EISENHARDT. "SALT CREEP EFFECT ON THE ANNULAR PRESSURE BUILD UP IN SUBSALT WELLS". PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO, 2015. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=25705@1.
Testo completoEste trabalho apresenta o crescimento de pressão no anular causado pela fluência do sal e relaciona com o cálculo deste fenômeno quanto ao efeito térmico, que é normalmente conhecido por APB (annular pressure build-up). Este fenômeno não é modelado em softwares comerciais e deve ser considerado em poços de pré-sal. O cálculo de APB considera três mecanismos geradores de pressão no anular: expansão térmica do fluido do anular, expansão do tubing e influxo e efluxo do fluido confinado no anular. Mudanças no volume do anular, causados pela fluência do sal, podem ser tratadas como um quarto mecanismo, equivalente ao influxo de fluido no cálculo do APB. O cálculo deste fenômeno pode ser incorporado a um modelo de cálculo acoplado ( multistring casing design ) através da programação do APB causado pelo efeito de expansão térmica dos fluidos confinados e o APB causado pela fluência do sal. Para isso é necessário adotar um modelo constitutivo para descrever o comportamento de fluência desta rocha em função do estado de tensão, perfil de temperatura, tipo de sal, tempo decorrido, energia de ativação e outros fatores. Os efeitos de APB devido à fluência do sal podem ser mais pronunciados quando a sapata do revestimento é assentada em um intervalo de sal com elevado gradiente de sobrecarga e elevado gradiente geotérmico. Não considerar o efeito da fluência do sal no crescimento de pressão do anular (APB) pode causar um dimensionamento inadequado de revestimento ou packoff e levar a perda da integridade do poço.
This paper presents the annular pressure build-up caused by salt creep and link to current calculation of this phenomenon due to thermal effect, which is commonly known as APB. This phenomenon is not currently modeled on commercial software and should be considered in subsalt wells. The calculation of APB considers three generator mechanisms: thermal expansion of annular fluid, influx or efflux and tubing buckling. Changes in the annular volume, caused by salt creep, may be treated as a fourth mechanism, equivalent to the influx in current calculation of APB. The calculation of this phenomenon can be incorporated into a multistring casing design model by programming the thermal expansion effect and the APB caused by salt creep. This requires adopting a constitutive model to describe the creep behavior of rock for differential stress, temperature profile, salt type, salt thermal activation and other factors. When the casing shoe is seated in deep salt sections with high overburden gradient and high temperature from the produced hydrocarbons, effects of APB due to salt creep and thermal effects may be more pronounced. Not considering the salt creep effect in the annular pressure build-up (APB) can lead to inadequate casing design and possible loss of well integrity.
Bristow, Gwendolyn. "The effect of tidal forcing on iron cycling in intertidal salt marsh sediments". Thesis, Available online, Georgia Institute of Technology, 2006, 2006. http://etd.gatech.edu/theses/available/etd-07102006-112540/.
Testo completoDr. Emanuele Di Lorenzo, Committee Member ; Dr. Ellery Ingall, Committee Member ; Dr. Martial Taillefert, Committee Chair.
Zhang, Yanling 1955. "Development of in vitro bioassays for determination of salinity tolerance in potato (Solanum spp.)". Thesis, McGill University, 1998. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=35659.
Testo completoLoubser, Dalene. "Molecular tagging of Thinopyrum distichum chromosomes involved in salt tolerance". Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/53754.
Testo completoENGLISH ABSTRACT: Much has been written about the effects of soil salinity on plant growth. Its devastating effects have already been reported 2000 years BC. In the 21· century an alarming 80 million hectares of cultivated land area are affected by salt (Munns, 2002a) and represent a growing threat to agriculture. Salt tolerance is a complex trait moderately expressed in only a few plant genotypes (Ruiz, 2001). An attempt to transfer salt tolerance genes from the wild grass, Thinopyrum distichum, to triticale and éommon wheat was initiated by Marais and Marais (2003). A study of Th. distichum x rye hybrids enabled the authors to identify chromosomes 2Jld , 3Jld , 4Jld and SJld as being involved in the determination of salt tolerance. Indirect (yet unconfirmed) evidence suggested that 7Jld might also have a role. A programme aiming to transfer regions of the critical chromosomes to homoeologous triticale chromosomes, which relies heavily on the use of molecular markers, was launched. While an RFLP marker is available for each of the Thinopyrum chromosomes, these are not suited for the screening of large numbers of segregates. This study therefore represents an attempt to convert the RFLP markers into less time consuming and cost-effective SCAR markers. The published DNA sequences of the RFLP probes in question were used as templates to design PCR primers. The PCR reactions were optimised using DNA of Th. distichum, rye and their FI hybrid. When Thinopyrum specific amplification products were obtained, the primers were also tested on a panel of genotypes with and without the target chromosomes. Seemingly polymorphic bands were confirmed by Southern blotting and hybridisation with the corresponding RFLP probes. The primers were also tested on a panel of genotypes that included 'Rex' triticale to ensure that they would also detect a difference in a triticale genetic background during transfer. Polymorphic bands were then isolated and sequenced to further refine the markers. In certain eases, sequences of the same fragment amplified in triticale ('Rex') and Thinopyrum were aligned in an attempt to design more specific markers. Using this approach, it was possible to develop chromosome specific SCARs for Thinopyrum chromosomes 3Jld and 7J2 d . Three and one set(s) of PCR markers, respectively, have been developed and can be used to unequivocally detect the Thinopyrum chromosomes involved in salt tolerance against a triticale background. A SCAR marker was also found for chromosome 6J. Thus, an attempt was made to convert thirteen RFLP probes to SCAR markers. Only three were successfully converted. The main reason for the low success rate is the syntenic relationships between the genomes of the different cereals that made it an arduous- task to find discriminating primer sets. Based on the results obtained, an adapted procedure is suggested for future attempts to develop chromosome specific markers utilizing published sequence information that was obtained for a different species.
AFRIKAANSE OPSOMMING: Baie is al geskryf oor die uitwerking van grond versouting op plantproduksie. Die vernietigende gevolge van versouting is alreeds 2000 jaar VC gerapporteer. In die 21* eeu is 'n geraamde 80 miljoen hektaar (Munns, 2002a) bewerkte land-area sout-geaffekteerd. Die ontstellende verwikkelinge verteenwoordig 'n groeiende bedreiging vir die landbou. Soutverdraagsaamheid is 'n komplekse kenmerk en slegs enkele plantgenotipes met matige verdraagsaamheid kon nog ontwikkel word (Ruiz, 2001). 'n Poging om soutverdraagsaamheidsgene vanaf die wilde gras, Thinopyrum distichum, na triticale en gewone koring oor te dra, is deur Marais en Marais (2003) geïnisieer. 'n Studie van Th. distichum x rog hibriede het die skrywers in staat gestelom chromosome (2Jld, 3Jld, 4Jld en SJld) wat bydra to soutverdraagsaamheid te identifiseer. Indirekte (maar onbevestigde) aanduidings is gevind dat 7J1dook' n rol mag speel. 'n Program is daarna geloods om segmente van chromosome na homoeoloë triticale chromosome oor te dra, 'n onderneming wat swaar steun op die gebruik van molekulêre merkers. Alhoewel daar'n RFLP merker beskikbaar is vir elk van die Thinopyrum chromosome, is hierdie merkers nie geskik vir die sifting van groot getalle segregate nie. Hierdie studie verteenwoordig 'n poging om die RFLP merkers om te skakel na 'n minder tydrowende en meer koste-effektiewe SCAR merkers. Die gepubliseerde DNS-volgordes van die betrokke RFLP peilers is as templaat gebruik om PKR inleiers te ontwerp. Die PKR reaksies is geoptimiseer deur gebruik te maak van DNS van Th. distichum. rog en hulle FI hibried. In gevalle waar Thinopyrum spesifieke amplifikasie produkte verkry is, is die inleiers ook getoets op 'n paneel van genotipes met en sonder die teikenchromosoom. Skynbare polimorfiese bande is bevestig deur 'n 'Southern' klad te maak en te hibridiseer met die tersaaklike RFLP peiler. Die inleiers is ook getoets op 'n paneel van genotipes waarby 'Rex' triticale ingesluit was om te verseker dat dit ook verskille in 'n triticale genetiese agtergrond opspoor (nodig tydens oordrag). Polimorfiese bande is verder verfyn. Dit is geïsoleer en die DNS-volgorde daarvan is bepaal. Tn sekere gevalle is ooreenstemmende fragmente geamplifiseer in triticale ('Rex') en Thinopyrum. Die volgordes is dan bepaal en met mekaar vergelyk in 'n poging om meer spesifieke merkers te ontwerp. Met die gebruik van hierdie benadering was dit moontlik om chromosoom-spesifieke SCAR-merkers vir die Thinopyrum chromosome 3Jld en 7J2d te ontwikkel. Drie en een stel(le) PKR merkers is onderskeidelik ontwikkel en kan gebruik word om ondubbelsinnig te bepaal of die betrokke Thinopyrum chromosoom segregeer in 'n triticale kruising. 'n SCAR merker is ook gevind vir chromosoom 6J. Dus, daar is probeer om dertien RFLP peilers na SCAR merkers om te skakel. Slegs drie van die pogings was suksesvol. Die hoofrede vir die lae sukseskoers is die hoë graad van sintenie tussen die genome van die verskillende grane wat dit 'n moeilike taak gemaak het om diskriminerende inleierstelle te ontwerp. Op grond van die resultate word 'n ietwat gewysigde prosedure vir die toekomstige pogings om chromosoom-spesifieke merkers te ontwerp met gebruik van gepubliseerde volgorde inligting vanaf' n ander spesie, voorgestel.
Suckling, Rebecca Jo. "Salt-potential mechanisms and its effects". Thesis, St George's, University of London, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546784.
Testo completoAl-Bahrany, Abdulaziz Maatook 1960. "Physiological and biochemical responses of short staple cotton (Gossypium hirsutum L.) to salt stress". Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184634.
Testo completoCollins, R. P. "The role of calcium and potassium in salinity tolerance in Brassica rapa L. cv. RCBr seed". Thesis, Coventry University, 2012. http://curve.coventry.ac.uk/open/items/e0d653ff-7d6b-4827-9467-dc8bcb6ff621/1.
Testo completoPosselt, Julia Rebekka. "Influence of giant sea salt aerosols on global precipitation and aerosol indirect effect /". Zürich : ETH, 2007. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=17467.
Testo completoLawson, L. J. "Vasopressin production in the salt loaded rat". Thesis, University of Bristol, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384031.
Testo completoMbanya, J.-C. N. "Atrial natriuretic peptide, sodium and erythrocyte membrane transport in hypertension associated with diabetes mellitus". Thesis, University of Newcastle Upon Tyne, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233334.
Testo completoAl-Rawahy, Salim Ali. "Nitrogen uptake, growth rate and yield of tomatoes under saline conditions". Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184894.
Testo completoKeyster, Marshall. "Nitric oxide-mediated signaling in legumes and its role in maize responses to salt stress". Thesis, Stellenbosch : University of Stellenbosch, 2011. http://hdl.handle.net/10019.1/6565.
Testo completoPilic, Leta. "Salt sensitivity : genetic and physiological markers and its effects on salt taste perception and intake". Thesis, St Mary's University, Twickenham, 2018. http://research.stmarys.ac.uk/2934/.
Testo completoBurke, R. M. "The effect of sodium chloride on the growth of Debaryomyces hansenii". Thesis, University of Liverpool, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380075.
Testo completoZheng, Liansheng 1955. "Gene expression in two different genotypes of alfalfa under salt stressed and unstressed conditions". Thesis, The University of Arizona, 1988. http://hdl.handle.net/10150/276936.
Testo completoAmin, Md Shahrier. "Epithelial Sodium Channels in the Brain: Effect of High Salt Diet on Their Expression". Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20074.
Testo completoHernandez, Adrian V., Erin E. Emonds, Brett A. Chen, Alfredo J. Zavala-Loayza, Priyaleela Thota, Vinay Pasupuleti, Yuani M. Roman, Antonio Bernabe-Ortiz e J. Jaime Miranda. "Effect of low-sodium salt substitutes on blood pressure, detected hypertension, stroke and mortality". BMJ Publishing Group, 2019. http://hdl.handle.net/10757/652462.
Testo completoWellcome Trust
Revisión por pares
Weeks, Jon Randall 1949. "The growth and water relations of a coastal halophyte, Salicornia bigelovii". Diss., The University of Arizona, 1986. http://hdl.handle.net/10150/191114.
Testo completo"Identification of salt stress responsive genes using salt tolerant and salt sensitive soybean germplasms". 2009. http://library.cuhk.edu.hk/record=b5893874.
Testo completoThesis (M.Phil.)--Chinese University of Hong Kong, 2009.
Includes bibliographical references (leaves 164-183).
Abstracts in English and Chinese.
Thesis Committee --- p.i
Statement --- p.ii
Abstract --- p.iii
摘要 --- p.v
Acknowledgements --- p.vi
General Abbreviations --- p.viii
Abbreviations of Chemicals --- p.xi
List of Figures --- p.xv
List of Tables --- p.xvii
Table of Contents --- p.xix
Chapter Chapter 1 --- Introduction --- p.1
Chapter 1.1 --- Salt stress in plants --- p.1
Chapter 1.2 --- Overview of the molecular basis of salt tolerance in plants --- p.2
Chapter 1.2.1 --- Stress perception --- p.3
Chapter 1.2.2 --- Signal transduction --- p.3
Chapter 1.2.2.1 --- Protein phosphatases --- p.4
Chapter 1.2.2.2 --- The SOS pathway for ion homeostasis --- p.4
Chapter 1.2.3 --- DNA and RNA helicases in post-transcriptional control --- p.6
Chapter 1.2.4 --- ROS scavengers --- p.7
Chapter 1.2.5 --- Proteases and proteinase inhibitors --- p.8
Chapter 1.2.6 --- Heat shock proteins (Hsps) --- p.9
Chapter 1.2.7 --- Highlights on DnaJ/Hsp40 --- p.9
Chapter 1.3 --- Review on functional genomics of salt stress responses in plants --- p.11
Chapter 1.3.1 --- Genomics on model organisms --- p.12
Chapter 1.3.2 --- Transcriptomics for identifying salt stress responsive genes --- p.12
Chapter 1.3.2.1 --- Multiple stress transcriptome analysis --- p.13
Chapter 1.3.2.2 --- Genome-wide transcriptome analysis on molecular crosstalk --- p.14
Chapter 1.3.2.3 --- Tissue specific transcriptome analysis --- p.16
Chapter 1.3.2.4 --- Comparative transcriptome analysis --- p.17
Chapter 1.3.2.5 --- Transcriptome analysis of soybean --- p.24
Chapter 1.3.3 --- Proteomics in plant salt stress studies --- p.26
Chapter 1.3.4 --- Beyond the transcriptome and proteome --- p.27
Chapter 1.4 --- Significance of using soybean germplasms for identifying salt stress responsive genes --- p.28
Chapter 1.5 --- Objectives --- p.29
Chapter Chapter 2 --- Materials and Methods --- p.30
Chapter 2.1 --- Materials --- p.30
Chapter 2.1.1 --- "Plants, bacterial strains,and vectors" --- p.30
Chapter 2.1.2 --- Enzymes and major chemicals --- p.33
Chapter 2.1.3 --- Primers --- p.34
Chapter 2.1.4 --- Commercial kits --- p.34
Chapter 2.1.5 --- Equipment and facilities --- p.34
Chapter 2.1.6 --- "Buffer, solution, gel and medium" --- p.34
Chapter 2.2 --- Methods --- p.35
Chapter 2.2.1 --- cDNA microarray analysis --- p.35
Chapter 2.2.1.1 --- Construction of cDNA subtraction libraries --- p.35
Chapter 2.2.1.2 --- Assembly of cDNA microarray --- p.36
Chapter 2.2.1.3 --- External control RNA synthesis --- p.39
Chapter 2.2.1.4 --- Probe labelling and hybridization --- p.40
Chapter 2.2.1.5 --- Hybridization signal collection --- p.41
Chapter 2.2.1.6 --- Image analysis --- p.41
Chapter 2.2.1.7 --- Data analysis --- p.42
Chapter 2.2.1.8 --- Selection of salt responsive genes using fold difference in expression --- p.45
Chapter 2.2.1.9 --- DNA sequencing --- p.46
Chapter 2.2.1.10 --- Real-time PCR analysis --- p.47
Chapter 2.2.2 --- Growth conditions and treatments of plants --- p.48
Chapter 2.2.2.1 --- Soybean for microarray hybridization and real-time PCR --- p.48
Chapter 2.2.2.2 --- Soybean for the study of GmDNJ1 expression under ABA treatment --- p.48
Chapter 2.2.2.3 --- Wild-type and transgenic Arabidopsis for functional analysis --- p.49
Chapter 2.2.2.4 --- Wild-type and transgenic rice for functional analysis --- p.49
Chapter 2.2.3 --- "DNA, RNA, and protein extraction" --- p.50
Chapter 2.2.3.1 --- Plasmid DNA extraction from E. coli cells --- p.50
Chapter 2.2.3.2 --- RNA extraction from plant tissues --- p.51
Chapter 2.2.3.3 --- Soluble protein extraction from plant tissues --- p.51
Chapter 2.2.4 --- Blot analysis --- p.51
Chapter 2.2.4.1 --- Northern blot analysis --- p.52
Chapter 2.2.4.2 --- Western blot analysis --- p.53
Chapter 2.2.5 --- Subcloning of GmDNJ1 into pGEX-4T-1 --- p.53
Chapter 2.2.5.1 --- "Restriction digestion, DNA purification and ligation" --- p.53
Chapter 2.2.5.2 --- Transformation of competent Escherichia coli (DH5a and BL21) --- p.54
Chapter 2.2.6 --- Luciferase refolding assay --- p.54
Chapter 2.2.6.1 --- Culture of E. coli strain BL21 (DE3) --- p.54
Chapter 2.2.6.2 --- Cell lysis --- p.55
Chapter 2.2.6.3 --- Purification of the GST-GmDNJ1 fusion protein --- p.55
Chapter 2.2.6.4 --- Quantitation of protein --- p.55
Chapter 2.2.6.5 --- Luciferase refolding assay --- p.56
Chapter Chapter 3 --- Results --- p.57
Chapter 3.1 --- Overview of cDNA microarray analysis --- p.57
Chapter 3.2 --- Identification of salt responsive genes in subtraction libraries concerning two contrasting soybean germplasms --- p.61
Chapter 3.3 --- Data processing before selection of salt stress responsive genes --- p.75
Chapter 3.3.1 --- M-A plots --- p.75
Chapter 3.3.2 --- Boxplots --- p.76
Chapter 3.3.3 --- Scatterplots --- p.76
Chapter 3.4 --- Selection of salt responsive genes using fold difference in expression --- p.77
Chapter 3.4.1 --- Selection of genes with differential expression between tolerant and sensitive germplasms --- p.77
Chapter 3.4.2 --- Selection of genes with differential expression between cultivated and wild germplasms --- p.89
Chapter 3.4.3 --- Data validation by real-time PCR analysis --- p.91
Chapter 3.5 --- Selection of salt responsive genes using statistical tools --- p.95
Chapter 3.5.1 --- Quantitative trait analysis for salt responsive genes --- p.95
Chapter 3.5.2 --- Identification of salt stress correlation genes --- p.100
Chapter 3.5.3 --- Cluster analyses --- p.104
Chapter 3.5.3.1 --- Clustering genes --- p.104
Chapter 3.5.3.2 --- Clustering samples --- p.108
Chapter 3.5.4 --- Data validation by real-time PCR analysis --- p.111
Chapter 3.6 --- Summary of cDNA microarray analysis --- p.112
Chapter 3.7 --- Studies on GmDNJ1 --- p.120
Chapter 3.7.1 --- Sequence analysis of GmDNJ1 --- p.120
Chapter 3.7.2 --- GmDNJ1 was induced by salt stress and ABA treatment in soybean (Glycine max) --- p.127
Chapter 3.7.3 --- Expressing GmDNJ1 in transgenic Arabidopsis (Arabidopsis thaliana) enhances the tolerance to salt stress and dehydration stress --- p.129
Chapter 3.7.4 --- Expressing GmDNJ1 in transgenic rice (Oryza sativa) enhances the tolerance to salt stress and dehydration stress --- p.135
Chapter 3.7.5 --- The GmDNJ1 protein can replace DnaJ in the in vitro luciferase refolding assay --- p.141
Chapter Chapter 4 --- Discussion --- p.145
Chapter 4.1 --- Overview of expression profiling of the 20 soybean germplasms --- p.145
Chapter 4.2 --- Identification of salt responsive genes from subtraction libraries --- p.146
Chapter 4.3 --- Normalization of data from microarray experiments --- p.148
Chapter 4.4 --- The fold difference analysis --- p.149
Chapter 4.4.1 --- Response to stress --- p.149
Chapter 4.4.2 --- Gene expression --- p.150
Chapter 4.4.3 --- Molecular function --- p.150
Chapter 4.4.4 --- Metabolic activity --- p.151
Chapter 4.4.5 --- Cellular component --- p.152
Chapter 4.4.6 --- Genes with 2.5-fold difference in expression between cultivated and wild germplasms --- p.153
Chapter 4.5 --- Selection of salt responsive genes using statistical tools --- p.153
Chapter 4.5.1 --- Quantitative trait analysis --- p.153
Chapter 4.5.2 --- Cluster analyses --- p.154
Chapter 4.6 --- Studies on GmDNJ1 --- p.157
Chapter 4.6.1 --- GmDNJ1 is a good candidate for gene studies --- p.157
Chapter 4.6.2 --- Sequence analysis of GmDNJ1 suggested it to be a DnaJ/Hsp40 homologue in soybean --- p.158
Chapter 4.6.3 --- GmDNJ1 was induced by salt stress and ABA treatment --- p.158
Chapter 4.6.4 --- GmDNJ1 has a higher expression in salt tolerant soybean germplasms over sensitive ones --- p.159
Chapter 4.6.5 --- Ectopic expression of GmDNJ1 enhanced the tolerance to salt stress and dehydration stress in transgenic Arabidopsis --- p.159
Chapter 4.6.6 --- Ectopic expression of GmDNJ1 enhanced the tolerance to salt stress and dehydration stress in transgenic rice --- p.160
Chapter 4.6.7 --- Luciferase activity assay showed that GmDNJ 1 functioned as a DnaJ/Hsp40 in vitro --- p.161
Chapter Chapter 5 --- Conclusion --- p.162
References --- p.164
Appendix I - Enzymes and major chemicals --- p.184
Appendix II - Primers --- p.188
Appendix III - Major commercial kits --- p.192
Appendix IV - Major equipment and facilities --- p.193
"Appendix V - Formulation of buffer, solution, gel, and medium" --- p.194
Appendix VI - Plots in microarray experiments --- p.198
Appendix VII - Clones with differential expression (>2.5-fold or >1.8-fold) between germplasms --- p.208
Appendix VIII - Salt responsive genes revealed by quantitative trait analysis --- p.216
Appendix IX - Supplementary data in real-time PCR analysis --- p.221
Appendix X - Supplementary data in functional analyses --- p.233
Gouda, Swati Rekha. "Effect of salt on the micellisation of bile salts in aqueous medium". Thesis, 2011. http://ethesis.nitrkl.ac.in/2109/1/M.Sc._Dissertation_Swati_Dspace.pdf.
Testo completoEn-Song, Ming, e 宋明恩. "Effect of multivalent salt on polyelectrolyte solution". Thesis, 2006. http://ndltd.ncl.edu.tw/handle/rw2dmn.
Testo completo國立中央大學
化學工程與材料工程研究所
94
Abstract The phenomenon of counterion condensation around a linear polyelectrolyte chain with N monomers is investigated by Monte Carlo simulation in terms of a degree of ionization α, which is proportional to the effective charge. It is define as the ratio of observed to intrinsic counterion concentration, α=co/ci..In order to know the effect of salt addition, we add different valent salts in the system. Fixing polyelectrolyte in the center of the Wigner-Seitz cell, we calculate the degree of ionization, radius of gyration and persistence length. We observe that multivalent salt make radius of gyration, persistence length and degree of ionization decrease rapidly. The driven mechanism of counterion condensation is primarily the electrostatic internal energy, manifested by the effect of dielectric constant, while the counterion entropy influences the degree of ionization as well. In the last of the thesis, we compare the difference with Ewald summation and Cell model. We set different valent charged particles in two systems and calculate the degree of ionization. As low valent and low concentration, the results of cell model and Ewald summation are the same.
Hou, Ching-Wen, e 侯景文. "Effect of Salt on the Activated Sludge". Thesis, 2015. http://ndltd.ncl.edu.tw/handle/22419215687276635291.
Testo completo國立高雄第一科技大學
環境與安全衛生工程研究所
103
Chloride/conductivity is a well-known inhibitor/factor on the microbial activity. However, what level might intrinsically affect the activity of activated sludge still is a question need to answer. For this purpose, the activated sludge obtained from the real field was cultured with various levels of sodium chloride of 10, 20, 25, 30 and 35 g/L and pH of 5.0, 6.0, and 9.0 according to experimental design. In this study, the specific oxygen uptake rate (SOUR) was represented for the activity of the activated sludge. Subsequently, the kinetic simulation was applied to estimate the limit of chloride level affecting on the activity sludge. The experimental results reveal that chloride level affected proportionally on the sludge activity, but no obvious difference of activity was obtained while simultaneously changing pH and conductivity values. However, acid environment would have a more effect than that of alkaline on the bioactivity while chloride level was lower than 25 g/L. Kinetic estimations indicate that SOUR of the sludge would decrease 10 and 50% while the chloride levels were 9.3 and 31 g/L, respectively. Not surprisingly, no SOUR was obtained while the chloride level was greater than 3.5 g/L.
Gao, Yuan Ph D. "Changes of tomato fruit composition in response to salinity". 1991. http://web4.library.adelaide.edu.au/theses/09A/09ag211.pdf.
Testo completoGao, Yuan. "Changes of tomato fruit composition in response to salinity". Thesis, 1991. http://hdl.handle.net/2440/110190.
Testo completoChen, Jun-Jay, e 陳俊傑. "Influences of Organic Salts in Salt Effect on n-Butyl acetate―n-Butanol― Water". Thesis, 2006. http://ndltd.ncl.edu.tw/handle/dn3jt6.
Testo completo國立臺北科技大學
化學工程所
94
The salt effect on ternary system of n-butyl acetate / n-butanol / water mixture was investigated. The molecular or ionic interaction in the water phase has been changed when the Liquid-Liquid Equilibria (LLE) has been achieved under the condition of which containing saturate Acetylcholine chloride or Acetylcholine bromide at 298.15K. The solvation of Acetylcholine chloride in water is better than Acetylcholine bromide. The simulation using TTK-Wilson activity coefficient model also presented. The mole fraction of each component in different phase of Liquid-Liquid Equilibria (LLE) experiments were in good agreement as the result of simulation using TTK-Wilson activity coefficient model.
Suntornvongsagul, Kallaya. "Effect of heavy metals on salt march biota". Thesis, 2005. http://library1.njit.edu/etd/fromwebvoyage.cfm?id=njit-etd2005-136.
Testo completo