Dissertations / Theses on the topic 'MITIGATION OF SALT STRESS'
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SINGH, SHATRUPA. "AUGMENTATIVE ROLE OF PLANT GROWTH PROMOTING BACTERIA (PGPB) IN MODULATING RESPONSES AGAINST MITIGATION OF SALT STRESS IN TRIGONELLA FOENUM-GRAECUM." Thesis, DELHI TECHNOLOGICAL UNIVERSITY, 2021. http://dspace.dtu.ac.in:8080/jspui/handle/repository/18463.
Full textHamzaoui, Soufiane. "Heat stress responses in dairy goats and effects of some nutritional strategies for mitigation." Doctoral thesis, Universitat Autònoma de Barcelona, 2014. http://hdl.handle.net/10803/285552.
Full textIn the current thesis 4 experiments were carried out using dairy goats under heat stress (HS) to measure responses to HS (Exp. 1 & 2) and to evaluate soybean oil and propylene glycol as feed supplements (Exp. 3 & 4). In Exp. 1 & 2, 8 Murciano-Granadina dairy goats in late (Exp. 1) and mid (Exp. 2) lactation were exposed to different ambient conditions, using metabolic cages in a climatic chamber. Experimental design was a crossover (2 periods of 28-35 d and 4 goats each), and conditions were: 1) thermal neutral (TN, 15 to 20°C day-night), and 2) heat stress (HS, 12-h day at 37°C and 12-h night at 30°C). Humidity was maintained at 40% and light-dark was constant (12-12 h). Rectal temperature and respiratory rate (0800, 1200 and 1700 h) and milk yield were recorded daily, whereas milk composition and blood parameters were evaluated weekly. Digestibility coefficients and N balance were determined and behavior was recorded by video cameras. Moreover, challenges with insulin (4.6 µg/kg BW), epinephrine (2 µg/kg BW) and glucose (0.25 g/kg BW) were done and blood samples were collected for the analysis insulin, NEFA and glucose concentrations. Compared to TN goats, HS goats experienced greater rectal temperature, respiratory rate, water intake, and water evaporation. Intake of HS goats decreased by 21 and 29 in Exp. 1 and 2, respectively. Milk of HS goats contained lower fat, protein and lactose. Panting reduced concentration and pressure of CO2 in blood of HS goats, but they were able to maintain their blood pH similar to TN group by lowering HCO3– in blood. The TN and HS goats had similar blood NEFA after insulin injection, but NEFA values were greater (P < 0.05) in TN than HS goats after epinephrine administration. The HS goats secreted lower (P < 0.05) amounts of insulin than TN goats in response to the glucose tolerance test. Furthermore, TN and HS goats had similar eating bouts, but the duration of each bout was lower in HS than in TN. On the other hand, HS had greater number of drinking bouts with no change in drinking bout durations. In Exp. 3 & 4, 8 multiparous Murciano-Granadina dairy goats at mid lactation were used in a replicated 4 × 4 Latin square design with 4 periods; 21 d each (14 d adaptation, 5 d for measurements and 2 d transition between periods). Goats were allocated to one of 4 treatments in a 2 x 2 factorial arrangement. Factors were supplementation or not with soybean oil (Exp. 3) or propylene glycol (Exp.4, and TN or HS conditions similar to Exp. 1 & 2. Feed intake, milk yield, milk composition, and blood metabolites were evaluated. From the point of view of human health, HS improved milk fatty acid profile by decreasing saturated fatty acids and increasing monounsaturated fatty acids with no effect on milk fat content. The soybean oil increased (P < 0.05) on average blood NEFA by 50%, milk fat by 30%, and conjugated linoleic acid by 360%. The response to soybean oil was with the same magnitude in thermo-neutral and heat stress conditions. On the other hand, the supplementation with propylene glycol increased blood glucose (P < 0.05) and tended to increase (P < 0.10) blood insulin, but dry matter intake and milk fat decreased (P < 0.10). Furthermore, blood NEFA and β-hydroxybutyrate acid decreased (P < 0.05) by propylene glycol. In conclusion, heat stress decreased milk yield by 3 to 10% with a marked reduction in milk protein. Lipid tissue of heat-stressed dairy goats became insensitive to lipolytic hormones and their pancreas secreted lower insulin when glucose was injected. Heat stress had no effect on eating bouts, but the time of each eating bout was shorter. The supplementation with soybean oil increased milk fat, trans-vaccenic acid and conjugated linoleic acid similarly in thermo-neutral as well as in heat stress conditions. Although propylene glycol increased blood glucose and insulin, no change in milk protein was observed.
Mian, Afaq Ahmad. "Improving salt stress resistance in cereals." Thesis, University of York, 2010. http://etheses.whiterose.ac.uk/1191/.
Full textCrowley, Cara Leilani. "Bile salt induced stress response pathways." Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/289231.
Full textUnruh, Ellen M. "Heat stress detection and mitigation in feedlot cattle." Thesis, Kansas State University, 2017. http://hdl.handle.net/2097/38179.
Full textDepartment of Clinical Sciences
Robert L. Larson
Bradley J. White
Feedlot cattle frequently endure high environmental temperature-humidity index conditions in the summer months within cattle feeding regions of North America. Heat stress develops when the total heat gain (combined effects of environmental and metabolic factors) exceeds an animal’s heat loss capabilities. The objective of my research was evaluating heat mitigation strategies and developing a practical method to identify animals that are of greatest risk of heat stress; thus improving animal welfare and performance. A number of heat abatement strategies have been utilized in US feedlots including shade, sprinklers, nutritional modifications, and misters. A literature review was performed using published journal articles demonstrated significant benefits of providing shade to feedlot cattle. Sprinkling the pen surface may be just as beneficial as sprinkling or misting cattle. Sprinkling the ground not only cooled the ground which increased the thermal gradient between lying cattle and the ground, but also provided increased thermal conductivity and better heat flow down that gradient. A study was performed to develop a noninvasive, remotely applied, practical method to identify animals at risk for heat stress. Infrared thermography images were obtained during the morning hours and pant scores obtained in the afternoon hours. Data mining techniques were employed to evaluate accuracy of potential classification methods to identify heat stress events in the afternoon based on the known morning data. Using infrared technology as a diagnostic test was not accurate for predicting heat stress events in the study presented. Finally a retrospective study of Kansas feedlot performance, medical and weather data was performed. Findings indicate that diagnostic counts of bovine respiratory disease are associated with elevated ambient temperature two days prior. In conclusion, heat stress in beef feedlot animals is an important area of research. Heat mitigation methods such as shade have been proven to be effective at reducing heat stress in beef feeder cattle. Further research is needed to evaluate the use of infrared technology to predict heat stress events in the feedlot setting.
Verbruggen, Nathalie. "Proline accumulation after salt-stress in arabidopsis thaliana." Doctoral thesis, Universite Libre de Bruxelles, 1992. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212895.
Full textMoser, Chase. "Experimental evolution of «Chlamydomonas reinhardtii » under salt stress." Thesis, McGill University, 2010. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=94916.
Full textRésumé Notre environnement change maintenant beaucoup plus rapidement que dans le passé géologique récent, précipitant l'extinction de plus en plus d'espèces. Des chercheurs ont démontré que, grâce à l'adaptation par la sélection naturelle, des espèces peuvent éviter l'extinction, un processus nommé sauvetage évolutif. J'ai d'abord étudié la capacité de Chlamydomonas à croitre dans des environnements dont la salinité augmente. J'ai trouvé que 5 g/L de sel diminue la croissance de moitié tandis que 8 g/L est suffisant pour empêcher toute croissance. Ici, la corrélation génétique entre environnement augmente avec la similarité des environnements comparés. J'ai ensuite soumis des populations contenant différentes quantités de diversité génétique initiale à une salinité de 5 g/L. La diversité génétique initiale ne semble pas influencer la capacité d'adaptation. Cependant, les populations semblent plutôt s'adapter en utilisant de nouvelles mutations dont l'effet est bénéfique. Ces résultats suggèrent que les populations s'adapteront plus facilement à des environnements similaires aux conditions présentes. De plus, ce processus sera dominé par la fixation de nouvelles mutations, même dans des populations contenant de la diversité génétique.
Shafiq-ur-Rehman. "Physiological responses of acacia seeds to salt stress." Thesis, Coventry University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363856.
Full textCrane, Andrew John. "The spectral detection of salt stress in cotton." Thesis, University of Portsmouth, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292358.
Full textStergiopoulos, Konstantinos. "Functional genomics of salt stress in 'Drosophila melanogaster'." Thesis, University of Glasgow, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433614.
Full textFancy, Nurun Nahar. "Role of S-nitrosylation in plant salt stress." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/29509.
Full textPessarakli, Mohammed, K. B. Marcum, and David M. Kopec. "Growth Responses of Desert Saltgrass under Salt Stress." College of Agriculture and Life Sciences, University of Arizona (Tucson, AZ), 2001. http://hdl.handle.net/10150/216374.
Full textMorales, Arturo Jason. "Physiological Assessment of Chenopodium quinoa to Salt Stress." BYU ScholarsArchive, 2009. https://scholarsarchive.byu.edu/etd/2205.
Full textDrake, 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.
Full textLima, Leonardo Warzea. "Selenium and sulfur : mitigation in plant stresses /." Jaboticabal, 2016. http://hdl.handle.net/11449/138897.
Full textCoorientador: André Rodrigues dos Reis
Banca: Tiago Tezotto
Banca: Tiago Santana Balbuena
Abstract: Plants do not have specific defense mechanisms to counteract the diverse range of abiotic stresses and pollutants into the environment, and its survival depends on the flexibility and adaptability of its own natural defense mechanisms. Furthermore, the maintenance of cellular homeostasis depends on several interlinked and complex mechanisms, while the cellular defense system does not follow a specific pattern of action and may differ due to various factors such as plant species, exposure time to the stress, plant developmental stage, different organs and tissues analyzed. In the light of these considerations, this dissertation aimed to highlight and investigate the role of Sulfur and Selenium against different plant stresses, through the enzymatic and non-enzymatic plant responses and other related defense mechanisms. In the first chapter the author characterize the general biochemical mechanisms of the antioxidant cell defense, specifically the reactive oxygen species (EROs) formation and its chemical singularities and the induced oxidative stress, the enzymatic antioxidant defense system, specifically the superoxide dismutase (SOD) and Catalase (CAT) enzymes, the non-enzymatic mechanisms against the stress, including the Ascorbate-Glutathione cycle, the GSH (reduced glutathione), the phytochelatins and also proline formation. The plant nutritional status during the stress is crucial in order to maintain a proper defense response. In view of this, the chapter two is a publis... (Complete abstract click electronic access below)
Resumo: As plantas não possuem mecanismos de defesa específicos para combater a diversidade de estresses abióticos e poluentes do ambiente, e sua sobrevivência depende da flexibilidade e adaptação dos seus próprios mecanismos de defesa naturais. Além disso, a manutenção da homeostase celular depende de vários mecanismos interligados e complexos, enquanto o sistema de defesa celular não segue um padrão específico de ação e pode ainda variar devido a vários fatores tais como a espécie do vegetal, o tempo de exposição ao estresse, o estágio de desenvolvimento da planta e também nos diferentes órgãos e tecidos analisados. Com base nessas considerações, esta dissertação teve como objetivo destacar e investigar o papel do Enxofre (S) e do Selênio (Se) contra diferentes estresses nas plantas, através das respostas enzimáticas, não enzimáticas e também outros mecanismos de defesa relacionados. No primeiro capítulo, o autor caracteriza os mecanismos bioquímicos gerais da defesa celular antioxidante, especificamente a formação das espécies reativas de oxigênio (EROs) e suas singularidades químicas e o estresse oxidativo induzido, o sistema de defesa antioxidante enzimático, especificamente as enzimas Superóxido Dismutase (SOD) e a Catalase (CAT), os mecanismos não-enzimáticas contra o estresse, incluindo o ciclo Aascorbato-Glutationa, a GSH (glutationa reduzida), as fitoquelatinas e também a formação de prolina. O estado nutricional da planta durante o estresse é crucial a fim de manter uma re... (Resumo completo, clicar acesso eletrônico abaixo)
Mestre
Lima, Leonardo Warzea [UNESP]. "Selenium and sulfur: mitigation in plant stresses." Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/138897.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
As plantas não possuem mecanismos de defesa específicos para combater a diversidade de estresses abióticos e poluentes do ambiente, e sua sobrevivência depende da flexibilidade e adaptação dos seus próprios mecanismos de defesa naturais. Além disso, a manutenção da homeostase celular depende de vários mecanismos interligados e complexos, enquanto o sistema de defesa celular não segue um padrão específico de ação e pode ainda variar devido a vários fatores tais como a espécie do vegetal, o tempo de exposição ao estresse, o estágio de desenvolvimento da planta e também nos diferentes órgãos e tecidos analisados. Com base nessas considerações, esta dissertação teve como objetivo destacar e investigar o papel do Enxofre (S) e do Selênio (Se) contra diferentes estresses nas plantas, através das respostas enzimáticas, não enzimáticas e também outros mecanismos de defesa relacionados. No primeiro capítulo, o autor caracteriza os mecanismos bioquímicos gerais da defesa celular antioxidante, especificamente a formação das espécies reativas de oxigênio (EROs) e suas singularidades químicas e o estresse oxidativo induzido, o sistema de defesa antioxidante enzimático, especificamente as enzimas Superóxido Dismutase (SOD) e a Catalase (CAT), os mecanismos não-enzimáticas contra o estresse, incluindo o ciclo Aascorbato-Glutationa, a GSH (glutationa reduzida), as fitoquelatinas e também a formação de prolina. O estado nutricional da planta durante o estresse é crucial a fim de manter uma resposta de defesa adequada. Em vista disso, o capítulo dois apresenta uma revisão sobre a participação de Enxofre (S) na defesa contra o estresse. Este nutriente tem um papel importante em processos fundamentais, tais como o transporte de elétrons, estrutura, regulação, produção de oxigênio fotossintético, resistência a estresses abióticos e bióticos e no metabolismo secundário. Além disso, alguns elementos químicos são considerados benéficos para as plantas, no qual o Selênio (Se) é o mais relevante. No capítulo três, o autor descreve o papel do Se na amenização do estresse induzido pela contaminação por metais pesados, suas poderosas características antioxidantes, a melhoria da atividade de enzimas antioxidantes e também dos mecanismos globais de defesa. O capítulo quatro consiste em um projeto científico conduzido pelo autor. O objetivo deste estudo foi investigar se o Selênio, sob a forma de selenito (Na2SeO3), é capaz de evitar a absorção, translocação e concentração de cádmio (CdCl2), em diferentes tecidos no tomate, indicando os possíveis mecanismos para amenizar o estresse, bem como também analisar o estado geral dos frutos através das análises nutricionais, peso seco, pigmentos e concentração de Prolina livre. Os resultados demonstram que efeito atenuante do Se em tomateiro submetido ao Cd poderia estar relacionado com a restrição da absorção e translocação de Cd2+, aumentando a concentração de micronutrientes nos frutos e, finalmente, aumentando a concentração de prolina livre nos frutos.
Plants do not have specific defense mechanisms to counteract the diverse range of abiotic stresses and pollutants into the environment, and its survival depends on the flexibility and adaptability of its own natural defense mechanisms. Furthermore, the maintenance of cellular homeostasis depends on several interlinked and complex mechanisms, while the cellular defense system does not follow a specific pattern of action and may differ due to various factors such as plant species, exposure time to the stress, plant developmental stage, different organs and tissues analyzed. In the light of these considerations, this dissertation aimed to highlight and investigate the role of Sulfur and Selenium against different plant stresses, through the enzymatic and non-enzymatic plant responses and other related defense mechanisms. In the first chapter the author characterize the general biochemical mechanisms of the antioxidant cell defense, specifically the reactive oxygen species (EROs) formation and its chemical singularities and the induced oxidative stress, the enzymatic antioxidant defense system, specifically the superoxide dismutase (SOD) and Catalase (CAT) enzymes, the non-enzymatic mechanisms against the stress, including the Ascorbate-Glutathione cycle, the GSH (reduced glutathione), the phytochelatins and also proline formation. The plant nutritional status during the stress is crucial in order to maintain a proper defense response. In view of this, the chapter two is a published review about the participation of Sulfur (S) on the stress defense. This nutrient has a role in fundamental processes such as electron transport, structure, regulation and it is also associated with photosynthetic oxygen production, abiotic and biotic stress resistance and secondary metabolism. Moreover, few chemical elements are considered benefic to plants, while Selenium (Se) is the most relevant. In the chapter three the author describes the role of Se to detoxify the stress induced by heavy metal contamination, its powerful antioxidant characteristics and the improvement of the antioxidant enzymes activity and overall defense mechanisms. The chapter four consists of a scientific project conducted by the author. The aim of this study was to investigate whether Selenium, under the form of selenite (Na2SeO3), may avoid the uptake, translocation and concentration of Cadmium (CdCl2), in different tomato tissues, indicating possible mechanisms to counteract the stress, as well as to analyze the fruits overall status through the nutritional analyses, dry weight, pigments and proline concentration. The results demonstrate that alleviating effect of Se in tomato under Cd contamination could be related to restriction of Cd2+ uptake and translocation, enhancing micronutrient concentration in fruits and, finally, enhancing fruit proline concentration.
CAPES: 445978/2014-7
Krell, Andreas. "Salt stress tolerance in the psychrophilic diatom Fragilariopsis cylindrus." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980889235.
Full textOROZCO, SERGIO OROZCO. "WELLBORE STABILITY IN SALT ZONES: USING STRESS TRANSFER TECHNIQUES." PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO, 2013. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=22966@1.
Full textCOORDENAÇÃO DE APERFEIÇOAMENTO DO PESSOAL DE ENSINO SUPERIOR
FUNDAÇÃO DE APOIO À PESQUISA DO ESTADO DO RIO DE JANEIRO
PROGRAMA DE EXCELENCIA ACADEMICA
BOLSA NOTA 10
A estabilidade de poços através de zonas de sal é um aspecto relevante em ambientes de perfuração offshore no Brasil. O fluxo convencional no planejamento de um poço de petróleo não reconhece a natureza complexa do estado de tensões in-situ em torno destes corpos de sal. Portanto, é necessária uma avaliação fiável das tensões in-situ considerando tanto a escala de campo (global) quanto as principais estruturas presentes no overburden. Neste trabalho, a análise de estabilidade de poços é realizada em três etapas. Primeiro, é realizada uma análise numérica a escala global para avaliar as tensões in-situ considerando a geometria de um corpo de sal. A seguir, são introduzidas as tensões in-situ em um modelo local, chamado subestrutura, através de duas técnicas de transferência de tensões propostas, denominadas as técnicas do Inverso Ponderado da Distância (IPD) e do Gradiente de Tensões (GT). O termo subestrutura é definido como uma linha curva no espaço composta por um conjunto de pontos, se assemelhando a uma seção ou trajetória completa de um poço. Finalmente, a janela operacional do poço é calculada acoplando os resultados de tensões da modelagem numérica com equações elásticas. Neste trabalho as técnicas IPD e GT são também utilizadas para transferir tensões em submodelos localizados dentro de um modelo global, visando realizar futuros estudos de submodelagem de estabilidade de poços. O termo submodelo consiste em uma malha de elementos finitos de um tamanho menor e um refinamento maior em relação ao modelo global.
Wellbore Stability drilling through salt zones is an important current endeavor in many areas offshore of Brazil. The conventional well design workflow does not recognize the complex nature of the stress field near these salt bodies. Therefore, a reliable assessment of the in-situ stresses must be carried out considering a field (global) scale of the problem and the presence of major structures in the overburden. The proposed stability analysis is carried out in three stages. Firstly, a global finite element analysis is employed to evaluate the in-situ stresses at a global scale considering the geometry of a salt body. Secondly, the global scale in-situ stresses are introduced in a local model, that we call substructure, by using two proposed stress transfer techniques called the Inverse Distance Weighted Technique (IDWT) and the Stress Gradient Technique (SGT). We define Substructure as a set of points forming a section or a complete trajectory of an oil well. Finally, optimal mud weights are calculated combining numerical stress results with analytical elastic equations. These two stress transfer techniques are also proposed to be used to transfer stresses to submodels inside a global model domain for submodeling wellbore stability purposes. The term submodel is defined as a finite element mesh with a smaller size relative to the size of the global model.
Roosens, Nancy. "Proline biosynthesis related to salt stress in higher plants." Doctoral thesis, Universite Libre de Bruxelles, 1999. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/211926.
Full textBrígido, Clarisse Cordeiro. "Tolerance of chickpea mesorhizobia to acid and salt stress." Doctoral thesis, Universidade de Évora, 2012. http://hdl.handle.net/10174/14546.
Full textKang, Ren. "Appliance-level demand side management for power network stress mitigation." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:1daf3825-1836-4bdb-89cb-763ecccca010.
Full textWibowo, Anjar Tri. "Epigenetic response and adaptation to salt stress in Arabidopsis thaliana." Thesis, University of Warwick, 2016. http://wrap.warwick.ac.uk/78172/.
Full textKader, Md Abdul. "Salt stress in rice : adaptive mechanisms for cytosolic sodium homeostasis /." Ultuna : Dept. of Plant Biology and Forest Genetics, Swedish University of Agricultural Sciences, 2006. http://epsilon.slu.se/200657.pdf.
Full textDadkhah, Ali Reza. "Ecophysiology of sugar beet (Beta vulgaris L.) under salt stress." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246614.
Full textLauer, Nathan T. "Physiological and Biochemical Responses of Bald Cypress to Salt Stress." UNF Digital Commons, 2013. http://digitalcommons.unf.edu/etd/454.
Full textPessarakli, Mohammad, David M. Kopec, and Jeff J. Gilbert. "Growth Responses of Selected Warm-Season Turfgrasses under Salt Stress." College of Agriculture and Life Sciences, University of Arizona (Tucson, AZ), 2008. http://hdl.handle.net/10150/216638.
Full textPessarakli, Mohammed, David M. Kopec, and Jeff J. Gilbert. "Growth Responses of Selected Warm-Season Turfgrasses under Salt Stress." College of Agriculture and Life Sciences, University of Arizona (Tucson, AZ), 2009. http://hdl.handle.net/10150/216660.
Full textWu, Xiao. "Design of a Tritium Mitigation and Control System for Fluoride-salt-cooled High-temperature Reactor Systems." The Ohio State University, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=osu1452249907.
Full textPeng, Licheng. "Mitigation of Oxygen Stress and Contamination-free Cultivation in Microalga Cultures." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34189.
Full textTsiantis, Miltiades S. "Regulation of V-ATPase gene expression by ionic stress in higher plants." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337540.
Full textWei, Wenxue. "Physiological and molecular mechanisms of salt tolerance in barley (Hordeum vulgare L.)." Thesis, University of Wolverhampton, 2002. http://hdl.handle.net/2436/93525.
Full textKalifa, 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.
Full textFerreira, Thalita Montoril. "Biochemical and physiological responses of sorghum plants submitted to salt stress." Universidade Federal do CearÃ, 2012. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17086.
Full textThe plants are frequently exposed to environmental stresses, which cause imbalances in physiological and biochemical metabolism. This work aimed to study the physiological and biochemical changes of plant forage sorghum (Sorghum bicolor) genotype CSF18, depending on the time of salt stress. The seeds were sown in vermiculite moistened with distilled water, in a greenhouse conditions, and after seven days, the seedlings were transferred to trays with Hoagland solution diluted 1:2. After seven days, treatment was established stress saline (75 mM NaCl), one group of plants kept in nutrient solution in the absence of salt (control). Samples were collected at 0, 5, 10 and 15 days after the initiation of stress. We evaluated the growth, gas exchange, contents and chlorophyll fluorescence, the concentration of organic solutes (proline, N-amino solutes, soluble carbohydrates, soluble proteins and polyamines free) and inorganic (Na+, Cl- and K+), as well as the activity of ribonuclease (RNase). We also determined the activities of catalase (CAT), superoxide dismutase (SOD), ascorbate peroxidase (APX) and guaicol peroxidase (GPX), as well as the levels of H2O2, ascorbate and glutathione in leaves and roots. Salinity reduced plant growth, being observed reductions in leaf area, and fresh and dry weights of shoots and roots. This was related to a reduction in net photosynthesis rate, even with the transpiration rate and stomatal conductance is not affected. The salinity increased contents of Na+ and Cl- in plant tissues, but the K+ decreased. The levels of organic solutes in leaves and roots increased, particularly at five and ten days of stress. The polyamines putrescine and spermidine were found at very low levels in both leaves and roots, while spermine was not detected in any analyzed portion of the plant. Although putrescine increased in salt stress, some must have contributed to the osmotic adjustment, however, their participation in oxidative protection was suggested. The salinity increased the activity of SOD, APX and GPX and the redox state of ascorbate, especially in the leaves, and this is related to the maintenance of H2O2 levels and increased protection against oxidative damage. The CAT showed the main enzyme remover H2O2 in the leaves while the roots that role was played by GPX. The RNase activity in leaves, stems and roots of sorghum increased in stress conditions, but their role in protection against the deleterious effects of salinity is not yet fully understood. In general, the data show that the antioxidative system (enzymatic and non-enzymatic) can play a key role in the acclimation of sorghum plants to salt stress, and that the reduction of plant growth was probably due to inhibition of biochemical phase of photosynthesis, caused by accumulation of toxic ions, Na+ and Cl-, reducing the relation K+/Na+ at levels harmful to the metabolism
As plantas estÃo freqÃentemente expostas a estresses ambientais, os quais causam desequilÃbrios no metabolismo fisiolÃgico e bioquÃmico. Este trabalho teve por objetivo estudar as alteraÃÃes fisiolÃgicas e bioquÃmicas de plantas de sorgo forrageiro [Sorghum bicolor (L.) Moench], genÃtipo CSF 18, em funÃÃo do tempo de exposiÃÃo ao estresse salino. As sementes foram semeadas em vermiculita umedecida com Ãgua destilada, em casa de vegetaÃÃo e, apÃs sete dias, as plÃntulas foram transferidas para bandejas com soluÃÃo nutritiva de Hoagland diluÃda 1:2. ApÃs sete dias, foi estabelecido o tratamento de estresse salino (NaCl a 75 mM), sendo um grupo de plantas mantido em soluÃÃo nutritiva na ausÃncia de sal (controle). As coletas foram realizadas aos 0, 5, 10 e 15 dias apÃs o inÃcio do estresse. Avaliou-se o crescimento, as trocas gasosas, os teores e a fluorescÃncia da clorofila, os teores de solutos orgÃnicos (prolina, N-aminossolÃveis, carboidratos solÃveis, proteÃnas solÃveis e poliaminas livres) e inorgÃnicos (Na+, Cl- e K+), bem como a atividade da ribonuclease (RNase). TambÃm foram determinadas as atividades das enzimas catalase (CAT), dismutase do superÃxido (SOD), peroxidase do ascorbato (APX) e peroxidase do guaicol (GPX), bem como os teores de H2O2, glutationa e ascorbato em folhas e raÃzes. O estresse salino reduziu o crescimento das plantas, sendo observadas reduÃÃes na Ãrea foliar, e nas matÃrias fresca e seca da parte aÃrea e das raÃzes. Isto foi relacionado com a reduÃÃo na taxa de fotossÃntese lÃquida, mesmo com a taxa de transpiraÃÃo e a condutÃncia estomÃtica nÃo sendo afetadas. A salinidade aumentou os teores de Na+ e Cl nos tecidos das plantas, porÃm, diminuiu os de K+. Os teores de solutos orgÃnicos em folhas e raÃzes aumentaram, principalmente aos cinco e dez dias de estresse. As poliaminas putrescina e espermidina foram encontradas em nÃveis muito baixos tanto em folhas como raÃzes, enquanto a espermina nÃo foi detectada em qualquer dos tecidos analisados. Embora a putrescina tenha aumentado em condiÃÃes de estresse salino, pouco deve ter contribuÃdo para o ajustamento osmÃtico, contudo, foi sugerida sua participaÃÃo na proteÃÃo oxidativa. A salinidade aumentou a atividade das enzimas SOD, APX e GPX e o estado redox do ascorbato, especialmente nas folhas, sendo isto relacionado com a manutenÃÃo dos nÃveis de H2O2 e com o aumento da proteÃÃo contra os danos oxidativos. A CAT mostrou-se a principal enzima removedora de H2O2 nas folhas, enquanto nas raÃzes esse papel foi desempenhado pela GPX. A atividade da RNase, em folhas, colmos e raÃzes de sorgo aumentou em condiÃÃes de estresse, porÃm seu papel na proteÃÃo contra os efeitos deletÃrios da salinidade ainda nÃo està totalmente esclarecido. Em geral, os dados mostram que o sistema antioxidativo (enzimÃtico e nÃo-enzimÃtico) pode desempenhar papel fundamental na aclimataÃÃo das plantas de sorgo ao estresse salino e que os efeitos deletÃrios da salinidade no crescimento das plantas, devem-se, provavelmente, à inibiÃÃo da fase bioquÃmica da fotossÃntese, causada pelo acÃmulo de Ãons tÃxicos, Na+ e Cl-, reduzindo a relaÃÃo K+/Na+ a nÃveis prejudiciais ao metabolismo.
Serra, Sara <1979>. "Salt stress responses in pear and quince: physiological and molecular aspects." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2009. http://amsdottorato.unibo.it/1620/1/Serra_Sara_Tesi_.pdf.
Full textSerra, Sara <1979>. "Salt stress responses in pear and quince: physiological and molecular aspects." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2009. http://amsdottorato.unibo.it/1620/.
Full textAttumi, Al-Arbe. "Effects of salt stress on phosphorus and sodium absorptions by soybean plants." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape11/PQDD_0001/MQ44119.pdf.
Full textElias, Demetra. "Characterization of ES147, a salt stress regulated protein kinase from Lophopyrum elongatum." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ59271.pdf.
Full textAbdelkader, Amal Fadl. "Salt stress in wheat (Triticum aestivum) and its impact on plastid development /." Göteborg : Göteborg University, 2007. http://www.loc.gov/catdir/toc/fy0714/2007423862.html.
Full textAttumi, 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.
Full textAlm, David Michael. "Comparison and interaction of heat and salt stress in cultured tobacco cells." Virtual Press, 1986. http://liblink.bsu.edu/uhtbin/catkey/445616.
Full textChevrot, Thierry. "Pressure effects on the hot-salt stress-corrosion cracking of titanium alloys." Thesis, Cranfield University, 1994. http://dspace.lib.cranfield.ac.uk/handle/1826/7745.
Full textSeebaruth, Khemnandanee. "A microstructural study of hot salt stress corrosion cracking in titanium alloys." Thesis, University of Cambridge, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308326.
Full textStory, Geraint-Wyn. "Development of a non-invasive screen for salt stress in Arabidopsis thaliana." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612986.
Full textFoust, Christy Marie. "Seeking Generalities in Salt Stress Effects on Herbivores: A Multi-Species Approach." UNF Digital Commons, 2010. http://digitalcommons.unf.edu/etd/377.
Full textZhou, 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.
Full textAl-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.
Full textBenothmane, Faycal. "Mycorrhizal Colonization and Growth Characteristics of Salt Stressed Solanum Lycopersicum L." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19908.
Full textWang, Lijun. "Physiological response of Kentucky bluegrass under salinity stress." DigitalCommons@USU, 2013. https://digitalcommons.usu.edu/etd/1492.
Full textSudiro, Cristina. "Unveiling salt-tolerance mechanisms in Italian rice varieties." Doctoral thesis, Università degli studi di Padova, 2017. http://hdl.handle.net/11577/3425725.
Full textLa tolleranza delle piante allo stress salino è un sistema complesso di tratti fisiologici, vie metaboliche, e reti molecolari e geniche (Gupta e Huang, 2014, Int J Genomics). Nelle piante, lo stress salino causa due tipi di stress: uno stress osmotico e uno stress ionico. Un’alta salinità provoca anche una eccessiva produzione di dannose specie reattive dell'ossigeno (Munns e Tester, 2008, Annu Rev impianto Biol). La percezione e il signalling dello stress sono necessari per l’attivazione di una risposta adeguata. I componenti chiave delle vie di signalling indotte da stress salino sono Ca2+ (Cavaliere et al., 1997, pianta J), NO e H2O2. I cereali sono generalmente considerati sensibile al sale e, tra questi, il riso è il più sensibile. Due varietà di riso italiano, Vialone Nano (VN) e Baldo (B), sono state selezionate per la loro contrastante sensibilità al sale: VN è risultato essere il più sensibile mentre B il più tollerante. Le analisi delle risposte allo stress salino in queste due varietà sono state effettuate sia in pianta che in colture cellulari generate a partire da semi. A livello dell’intera pianta, analisi morfologiche, fisiologiche e molecolari hanno dimostrato che B è in grado di rispondere rapidamente allo stress, mettendo in atto un programma di adattamento che permette di riprendere la crescita. I componenti della via di trasduzione del segnale indotto da stress sono stati studiati in colture cellulari in sospensione. Il ruolo di H2O2 e NO, come molecole segnale in risposta allo stress salino, è stato studiato in dettaglio. In particolare, un diverso andamento nella produzione di H2O2 sembra essere importante per determinare il destino delle cellule: acclimatazione in B contro morte cellulare programmata in VN. Inoltre, sono state ottenute piante esprimenti sensori per il calcio per entrambe le varietà di riso italiano. Queste piante saranno uno strumento utile per studiare il signalling del calcio indotto da stress salino.
Mattern, Heather R. "Laser peening for mitigation of stress corrosion cracking at welds in marine aluminum." Thesis, Monterey, California. Naval Postgraduate School, 2011. http://hdl.handle.net/10945/5710.
Full textThis work examines the use of laser peening (LP) for mitigation of stress corrosion cracking (SCC) in marine grade aluminum alloys (Al-Mg). These alloys can be sensitized during welding and will develop a tensile residual stress in the heat affected zone that may promote SCC in a salt water environment. Metal inert gas welded aluminum alloy 5083 (4.8wt% Mg) plate was laser peened using a variety of laser intensities to create compressive stresses. Mechanical tests were performed to investigate the SCC of the material including slow strain rate testing and potentiostatically driven, salt-water exposure. Microstructural and micromechanical tests were performed to characterize the effects of LP on the microstructure of the material. The slow strain rate testing showed a systematic decrease in ductility with increasing LP intensity. The fracture surfaces on all welded samples were indicative of ductile fracture but with a pre-crack length that scaled inversely with LP intensity. The hardness of the material increased with LP intensity. This work suggests that welded aluminum alloy 5083 does not readily stress corrosion crack. LP does affect the mechanical behavior of the material, but its full effect on stress corrosion behavior requires further study.