Dissertations / Theses on the topic 'Environmental microbiology (Analysis; Identification)'
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Pacheco, Fábio Luiz Camacho. "Identificação bacteriana por derivação de ácidos graxos extraídos de células íntegras." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-28092009-143513/.
Full textClean rooms are largely employed in pharmaceutical companies whose purpose is to produce sterile drugs and devices. We employed Gram staining and gas chromatography of fatty acid methyl esters extracted from whole cells of environmental isolates to characterize and identify bacteria isolated in each of 50 different clean rooms designed for the manufacturing of sterile medicinal products and to provide a fatty acid profile of the most common species of isolated bacteria. Statistical analysis allowed us to corroborate previous studies and confirm that Gram-positive cocci are the most relevant group of microorganisms inside the studied clean rooms. The predominant species is Micrococcus luteus, isolated from Grade B zones and from personnel, followed by Staphylococcus cohnii in Grade C, Bacillus subtilis in Grade A and S. hominis in Grade D. Fatty acid profiles of these bacteria are, to a great extent, consistent with standard libraries. We also attempted to establish a correlation between season and level of contamination, although variance analysis showed that there is no significant difference on the level of contamination throughout seasons. Furthermore, repeated analysis with a gradual increase in cell mass allowed us to conclude that the optimal amount of cell material depends on the species of the bacteria studied. Finally, a comparative study with some bacteria incubated in different temperatures confirmed that fatty acid profile is highly influenced by temperature. Therefore, we believe that this work can contribute to identify and understand the bacterial community of some pharmaceutical clean rooms.
O'Rourke, Michele Jane. "Identification and analysis of differentiation components in Bacillus subtilis 168." Thesis, University of Sheffield, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312365.
Full textInal, Jameel. "Identification and analysis of plasmid-encoded antigenic proteins in Bacillus anthracis." Thesis, Open University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314744.
Full textJutras, Eileen Maura 1958. "Field-scale biofiltration: Performance evaluation and microbial analysis." Diss., The University of Arizona, 1997. http://hdl.handle.net/10150/282533.
Full textGriffith, Rosemary Elaine. "Identification of mixtures of edible oils by the analysis of steryl esters." Thesis, University of Reading, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329564.
Full textMalecha, Michael Markus. "Identification of lubricant contaminants in beverage cans using spectroscopic analysis and chemometrics." Thesis, Cranfield University, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269638.
Full textYang, Zhan. "Conidia of Aspergillus fumigatus : functional analysis of surface components and identification of receptors for A549 epithelial cells." Thesis, Edinburgh Napier University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391004.
Full textFarnsworth, Jacob S. "Hot Spot Identification and Analysis Methodology." BYU ScholarsArchive, 2013. https://scholarsarchive.byu.edu/etd/3878.
Full textHoosain, Nisreen. "Phenotypic and molecular analysis of Helicobacter spp. and related micro-organisms identified in clinical & environmental specimens." Master's thesis, University of Cape Town, 2006. http://hdl.handle.net/11427/2709.
Full textAbruquah, Harry H. "Identification of host-pathogen interacting molecules of Campylobacter jejuni using phage display technology and in silico sequence analysis." Thesis, University of Nottingham, 2009. http://eprints.nottingham.ac.uk/10813/.
Full textMukherjee, Maitreyee. "Identification, enumeration, and diversity of ammonia-oxidizing archaea in the Laurentian Great Lakes." Bowling Green State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1368022892.
Full textZimmer, Sarah Kathryn. "Identification of the Hmu PSTUV operon and its’ role in Heme Utilization in Rhizobia Leguminosarum ATCC 14479." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/honors/501.
Full textSoutherland, L. S., Phillip R. Scheuerman, and N. S. Nicholas. "Analysis of Lead, Aluminum and Calcium in Southern Appalachian American Beach." Digital Commons @ East Tennessee State University, 2000. https://dc.etsu.edu/etsu-works/2926.
Full textChurchill, Robert. "Identification of environmental determinants of behavior disorders through functional analysis of precursor behaviors." Thesis, University of North Texas, 2001. https://digital.library.unt.edu/ark:/67531/metadc2814/.
Full textKo, Han Il. "Noncoliform enumeration and identification in potable water, and their senstivity to commonly used disinfectants." Virtual Press, 1997. http://liblink.bsu.edu/uhtbin/catkey/1041914.
Full textDepartment of Biology
Gallagher, L. K., Brian G. Evanshen, Kurt J. Maier, and Phillip R. Scheuerman. "Bacterial Source Tracking in the Sinking Creek Watershed, using Antibiotic Resistance Analysis (ARA) and Ribotyping." Digital Commons @ East Tennessee State University, 2007. https://dc.etsu.edu/etsu-works/2946.
Full textFisher, Suzanne, N. S. Nicholas, and Phillip R. Scheuerman. "Dendrochemical Analysis of Lead and Calcium in Southern Appalachian American Beech." Digital Commons @ East Tennessee State University, 2002. https://dc.etsu.edu/etsu-works/2872.
Full textLeCoultre, T. D., and Phillip R. Scheuerman. "A Metal-Analysis and Risk Assessment of Heavy Metal Uptake in Common Garden Vegetables." Digital Commons @ East Tennessee State University, 2001. https://dc.etsu.edu/etsu-works/2927.
Full textBassett, David R. "Use of Roadway Attributes in Hot Spot Identification and Analysis." BYU ScholarsArchive, 2015. https://scholarsarchive.byu.edu/etd/5642.
Full textTau, Kimberly R. "Molecular and Cellular Analysis of Chlamydia Trachomatis: Persistence and Reactivation." Digital Commons @ East Tennessee State University, 1992. https://dc.etsu.edu/etd/2804.
Full textBester, Linka. "Detection and identification of wine spoilage microbes using PCR-based DGGE analysis." Thesis, Stellenbosch : University of Stellenbosch, 2009. http://hdl.handle.net/10019.1/1558.
Full textGrape juice is transformed into wine through the complex processes of alcoholic and malolactic fermentation that is performed by yeasts, lactic acid bacteria and acetic acid bacteria. However, the microbes involved in these processes do not only take part in ensuring the successful production of wine, but also cause spoilage of the wine if their growth is not controlled. Conventional, culture-dependent methods of microbiology have been used as the main technique in detecting and identifying these spoilage microbes. Cultureindependent techniques of molecular biology have recently become more popular in detecting possible spoilage microbes present in must and wine, since it allows the detection and identification of viable, but non-culturable microbes and are not as timeconsuming as conventional microbiological methods. The aim of this study was to investigate the sustainability of polymerase chain reaction (PCR)-based denaturing gradient gel electrophoresis (DGGE) analysis in detecting wine spoilage microbes inoculated into sterile saline solution (SSS) (0.85% (m/v) NaCl) and sterile white wine and red wine as single microbial species and as part of mixed microbial populations. Three methods of DNA isolation from SSS, sterile white wine and sterile red wine inoculated with reference microbial strains were compared in terms of DNA concentration and purity, as well as simplicity of the technique. These three DNA isolation methods were the TZ-method, the proteinase K-method and the phenol extraction method. DNA could not successfully be isolated from red wine using any of the three DNA isolation methods. The TZ-method was the method of choice for the isolation of DNA from inoculated SSS and sterile white wine as this technique gave the best results in terms of simplicity, DNA concentration and purity. PCR and DGGE conditions were optimised for the universal primer pair, HDA1-GC and HDA2, the wine-bacteria specific primer pair, WBAC1-GC and WBAC2, and the yeast specific primer pair, NL1-GC and LS2. DNA from Acetobacter pasteurianus, Lactobacillus plantarum, Pediococcus pentosaceus, Oenococcus oeni, Brettanomyces bruxellensis and Saccharomyces cerevisiae were amplified with the appropriate primers and successfully resolved with DGGE analysis. PCR and DGGE detection limits were successfully determined when 106 cfu.ml-1 of the reference microbes, A. pasteurianus, Lb. plantarum, Pd. pentosaceus and B. bruxellensis were separately inoculated into SSS and sterile white wine. It was possible to detect low concentrations (101 cfu.ml-1) with PCR for A. pasteurianus, Lb. plantarum, Grape juice is transformed into wine through the complex processes of alcoholic and malolactic fermentation that is performed by yeasts, lactic acid bacteria and acetic acid bacteria. However, the microbes involved in these processes do not only take part in ensuring the successful production of wine, but also cause spoilage of the wine if their growth is not controlled. Conventional, culture-dependent methods of microbiology have been used as the main technique in detecting and identifying these spoilage microbes. Cultureindependent techniques of molecular biology have recently become more popular in detecting possible spoilage microbes present in must and wine, since it allows the detection and identification of viable, but non-culturable microbes and are not as timeconsuming as conventional microbiological methods. The aim of this study was to investigate the sustainability of polymerase chain reaction (PCR)-based denaturing gradient gel electrophoresis (DGGE) analysis in detecting wine spoilage microbes inoculated into sterile saline solution (SSS) (0.85% (m/v) NaCl) and sterile white wine and red wine as single microbial species and as part of mixed microbial populations. Three methods of DNA isolation from SSS, sterile white wine and sterile red wine inoculated with reference microbial strains were compared in terms of DNA concentration and purity, as well as simplicity of the technique. These three DNA isolation methods were the TZ-method, the proteinase K-method and the phenol extraction method. DNA could not successfully be isolated from red wine using any of the three DNA isolation methods. The TZ-method was the method of choice for the isolation of DNA from inoculated SSS and sterile white wine as this technique gave the best results in terms of simplicity, DNA concentration and purity. PCR and DGGE conditions were optimised for the universal primer pair, HDA1-GC and HDA2, the wine-bacteria specific primer pair, WBAC1-GC and WBAC2, and the yeast specific primer pair, NL1-GC and LS2. DNA from Acetobacter pasteurianus, Lactobacillus plantarum, Pediococcus pentosaceus, Oenococcus oeni, Brettanomyces bruxellensis and Saccharomyces cerevisiae were amplified with the appropriate primers and successfully resolved with DGGE analysis. PCR and DGGE detection limits were successfully determined when 106 cfu.ml-1 of the reference microbes, A. pasteurianus, Lb. plantarum, Pd. pentosaceus and B. bruxellensis were separately inoculated into SSS and sterile white wine. It was possible to detect low concentrations (101 cfu.ml-1) with PCR for A. pasteurianus, Lb. plantarum, iv Pd. pentosaceus, and B. bruxellensis in SSS when amplified with the HDA1-GC and HDA2 primer pair. A PCR detection limit of 102 cfu.ml-1 was determined in sterile white wine for Pd. pentosaceus and 103 cfu.ml-1 for B. bruxellensis using this primer pair. The results obtained from the PCR amplification with the WBAC1-GC and WBAC2 primer pair compared well with the results of the HDA1-GC and HDA2 primer pair. The results from the DGGE detection limits indicated that it was possible to detect lower concentrations (101 – 102 cfu.ml-1) of A. pasteurianus, Lb. plantarum and Pd. pentosaceus with the HDA1-GC and HDA2 primer pair than the WBAC-GC and WBAC2 primer pair (102 – 104 cfu.ml-1). Lower detection limits were also determined for B. bruxellensis amplified with the HDA1-GC and HDA2 primer pair (103 – 104 cfu.ml-1) than with the NL1-GC and LS2 primer pair (105 cfu.ml-1). PCR and DGGE detection limits for the inoculation of A. pasteurianus, Lb. plantarum and B. bruxellensis at an inoculum of 108 cfu.ml-1 as part of mixed populations in SSS and sterile white wine compared well with the results obtained from the reference microbes inoculated as single microbial species. PCR detection limits of 101 cfu.ml-1 were determined for all three reference microbes inoculated as part of mixed populations when amplified with the HDA1-GC and HDA2 and the WBAC1-GC and WBAC2 primer pairs. It was observed that similar or higher DGGE detection limits were obtained for the reference microbes inoculated in sterile white wine (101 – 107 cfu.ml-1) than when inoculated into SSS (101 – 105 cfu.ml-1). PCR-based DGGE analysis proved to be a technique that could be used successfully with the universal, wine-bacteria and yeast specific primer pairs for the detection of A. pasteurianus, Lb. plantarum, Pd. pentosaceus and B. bruxellensis. The culture-independent technique makes the early detection of possible spoilage microbes at low concentrations in wine possible.
Patent, Keisha Marie. "National Animal Identification System: An Analysis of Willingness to Comply Among Ohio and Kentucky Beef Show Participants." The Ohio State University, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=osu1392980060.
Full textSkutas, Jorie L. "Microbial and Genomic Analysis of Environmental Samples in Search of Pathogenic Salmonella." NSUWorks, 2017. http://nsuworks.nova.edu/occ_stuetd/461.
Full textSamols, Mark Atienza. "Identification and Functional Analysis of Micro-RNAs Encoded by Kaposi’s Sarcoma-Associated Herpesvirus." Case Western Reserve University School of Graduate Studies / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=case1181143062.
Full textRomas, Lisa. "Functional identification of microorganisms that transform mercury in marine sediments." Wright State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=wright1278616625.
Full textTrexler, Ryan Vincent. "Lipid Analysis and Microbial Community Characterization of Subsurface Shale." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480679153855158.
Full textLang, Cassandra C., and University of Lethbridge Faculty of Arts and Science. "Identification and metabolic characterization of host-specific enterococci for use in source-tracking faecal contamination." Thesis, Lethbridge, Alta. : University of Lethbridge, Faculty of Arts and Science, 2005, 2005. http://hdl.handle.net/10133/265.
Full textxxiii, 264 leaves ; 29 cm.
Marinelli, Zachary A. "Identification of a putative metK selenite resistance gene in Stenotrophomonas maltophilia OR02." Youngstown State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1516345597337997.
Full textBeligala, Dilshan Harshajith. "Identification of Rhizobial Symbionts Associated with Lupinus SPP." Bowling Green State University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1435855654.
Full textRay, Anirban. "Identification, Enumeration and Diversity of Nitrifying Bacteria in the Laurentian Great Lakes." Bowling Green State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1351276518.
Full textBoling, Bryan Kenneth. "A framework and quantitative methodology for the identification of cost-effective environmental policy for civil aviation." Diss., Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/53459.
Full textIdrus, Amwazi. "Identification of physical-environmental characteristics of Ciliwung Watershed, West Java, Indonesia, using a geographic information system." Virtual Press, 1992. http://liblink.bsu.edu/uhtbin/catkey/834631.
Full textDepartment of Natural Resources
Rutherford, Alexander Fenner. "Abundance and Distribution of Major and Understudied Archaeal Lineages at Globally Distributed Deep-Sea Hydrothermal Vents." PDXScholar, 2014. https://pdxscholar.library.pdx.edu/open_access_etds/1555.
Full textVigren, David. "Identification of Environmental Plastic Samples from a Caribbean Beach Survey by Near-Infrared Spectroscopy with the MicroNIR and Chemometric Analysis." Thesis, Örebro universitet, Institutionen för naturvetenskap och teknik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-45772.
Full textHudson, Kyle D. "Vibration-based damage detection with new operational response and waveform analysis methodology." Thesis, University of Iowa, 2010. https://ir.uiowa.edu/etd/820.
Full textLang, Ruby A. "ANALYSIS AND OPTIMIZATION OF COLORIMETRIC NANOSENSORS FOR RAPID DETECTION OF MICROBES IN WATER." DigitalCommons@CalPoly, 2020. https://digitalcommons.calpoly.edu/theses/2186.
Full textUnger, Maria. "Identification of brominated organic compounds in aquatic biota and exploration of bromine isotope analysis for source apportionment." Doctoral thesis, Stockholms universitet, Institutionen för material- och miljökemi (MMK), 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-38871.
Full textAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4: Manuscript.
Tarus, Anita, and Elea Juell-Skielse. "Identification of Key Activities Contributing to Macro Plastic Waste Flows on the Shoreline of Koh Chang, Thailand : A Quantification of Macroplastic Waste Items." Thesis, KTH, Hållbar utveckling, miljövetenskap och teknik, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-254208.
Full textEn hållbar utveckling är central för att Thailand ska kunna fortsätta utvecklas på samma sätt som skett de senaste åren. Hållbar utveckling kan dock inte uppnås om mängden makroplaster som hamnar i haven inte minskar. För att underlätta framtida beslutsfattande ämnar denna rapport att identifiera de mänskliga aktiviteter som i störst utsträckning bidrar till de makroplastföremål som går att finna på thailändska kuststräckor. Denna identifiering utfördes genom en simplifierad materialflödesanalys som baserades på observationer och simpla beräkningar på ön Koh Chang i Ranong. En jämförande studie utfördes på den annorlunda ön Koh Larn i Pattaya för att eliminera felfaktorer som kan ha uppstått på grund av Koh Changs specifika förutsättningar. Studien visade att Livsmedelskonsumption, Fiske, och Restaurangbesök var de Nyckelaktiviteter som bidrog till det befintliga makroplastavfallet. Turism visade sig också vara en stor bidragare till makroplastavfall. Studien kunde inte visa på någon Ackumuleringsgrad på Koh Chang. Trots detta fanns alltid makroplastföremål närvarande i provtagningsområdena på Koh Chang, vilket antyder att dessa föremål skulle kunna innebära ett hot mot ekosystemen. Vidare efterforskningar krävs för att hitta en passande lösning på problemet.
Borglin, Matthew R. "Analysis of Biofilm Remediation Capacity For Octenyl Succinic Anhydride (OSA), A Bioactive Food Starch Modifier Compound." DigitalCommons@CalPoly, 2020. https://digitalcommons.calpoly.edu/theses/2168.
Full textCouto, Manuela Soares. "Molecular identification of clinical and strains environmental Burkholderia pseudomallei, from the State of CearÃ: based on analysis regions 16S and 16S-23S ribosomal DNA nuclear." Universidade Federal do CearÃ, 2009. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=10501.
Full textMelioidosis is a potentially fatal disease caused by the bacterium Burkholderia pseudomallei, considered emerging in Brazil since the first cases were reported in 2003, on State of CearÃ. This study aimed to perform the molecular identification of 31 isolates of B. pseudomallei (26 clinical and 5 environmental) maintained in the culture collection of CEMM (Specialized Center for Medical Mycology), based on sequences 16S and 16S-23S rRNA. The DNA of these samples was extracted with the kit Wizard  Genomic DNA Purification (Promega), quantified by spectrophotometry and stored at 4ÂC. The amplification of a fragment of 302 bp of 16S-23S rRNA specific to B. pseudomallei was performed by PCR reaction with primers Bp1 and Bp4. The sequencing of 16S and 16S-23S rRNA was performed by using of the kit DYEnamicTM ET terminators cycle sequencing (GE Healthcare). The phylogenetic tree of 16S rRNA and the sequence identity matrix and sequence difference count matrix based on the 16S-23S rRNA were generated by the program MEGA4, version 4.1. The results confirmed the identification of 15 strains of B. pseudomallei (5 clinical and 10 environmental), which represents 48.4% of the isolates analyzed in this study. The phylogenetic tree based on 16S rRNA shows that the clinical and environmental isolates of B. pseudomallei of State of Cearà are evolutionarily clustered with the strains B. pseudomallei MSHR346 (Australia), B. pseudomallei 1106a (Thailand), B. pseudomallei K96243 (Thailand), B. pseudomallei 1710b (Thailand) and B. pseudomallei 668 (Australia). Using the same extraction kit was possible to extract DNA from B. pseudomallei directly from clinical specimen (bronchoalveolar lavage), confirming a new case of melioidosis in Ubajara/CE. In this study, the use of PCR for amplification of a fragment of 302 bp of 16S-23S rRNA identified correctly B. pseudomallei, and to confirm the discrimination between B. pseudomallei and B. mallei, the sequencing of the 16S and 16S-23S rRNA genes was performed. The technique of PCR coupled with sequencing of 16S and 16S-23S rRNA resulted in a high sensitivity and specificity of detection of B. pseudomallei in this study.
A melioidose à uma doenÃa potencialmente fatal causada pela bactÃria Burkholderia pseudomallei, sendo considerada emergente no Brasil desde que os primeiros casos foram reportados em 2003, no Estado do CearÃ. Este estudo pretendeu realizar a identificaÃÃo molecular de 31 isolados de B. pseudomallei (cinco clÃnicos e 26 ambientais) mantidos na coleÃÃo de culturas do CEMM (Centro Especializado em Micologia MÃdica), com base nas sequÃncias 16S e 16S-23S DNAr. O DNA destas amostras foi extraÃdo com o kit Wizard Genomic DNA Purification (Promega), quantificado por espectrofotometria e armazenado a 4ÂC. A amplificaÃÃo de um fragmento de 302 pb da regiÃo espaÃadora 16S-23S DNAr especÃfico para B. pseudomallei foi realizada por meio de reaÃÃo de PCR com os primers Bp1 e Bp4. O sequenciamento das regiÃes 16S e 16S-23S DNAr foi realizado pelo mÃtodo da terminaÃÃo da cadeia pelo didesoxinucleotÃdeo, usando-se o kit DYEnamicTM ET terminators cycle sequencing (GE Healthcare). A Ãrvore filogenÃtica da regiÃo 16S DNAr e as matrizes sequÃncia identidade e contagem de diferenÃas baseadas na regiÃo 16S-23S DNAr foram geradas pelo programa MEGA4, versÃo 4.1. Os resultados confirmaram a identificaÃÃo de 15 cepas de B. pseudomallei (cinco clÃnicas e dez ambientais), o que corresponde a 48.4% dos isolados em estudo. A Ãrvore filogenÃtica baseada na regiÃo 16S DNAr demonstra que os isolados clÃnicos e ambientais de B. pseudomallei do Estado do Cearà sÃo evolutivamente agrupados com as cepas B. pseudomallei MSHR346 (AustrÃlia), B. pseudomallei 1106a (TailÃndia), B. pseudomallei K96243 (TailÃndia), B. pseudomallei 1710b (TailÃndia) e B. pseudomallei 668 (AustrÃlia). Com a utilizaÃÃo do mesmo kit de extraÃÃo tambÃm foi possÃvel extrair DNA de B. pseudomallei diretamente de espÃcime clÃnico (lavado brÃnquico), confirmando um novo caso de melioidose no MunicÃpio de Ubajara/CE. Em nosso estudo, o uso da PCR para a amplificaÃÃo de um fragmento de 302 pb da regiÃo 16S-23S DNAr identificou corretamente B. pseudomallei, sendo que para confirmar a discriminaÃÃo entre B. pseudomallei e B. mallei, o sequenciamento das regiÃes 16S e 16S-23S DNAr foi realizado. A tÃcnica de PCR aliada ao sequenciamento das regiÃes 16S e 16S-23S do DNA ribossÃmico nuclear resultaram em uma elevada sensibilidade e especificidade de detecÃÃo de B. pseudomallei neste estudo.
Chendra, Edwin. "Examination of regression modeling for estimating airbone [sic] fungal infiltration loss factor." Oklahoma City : [s.n.], 2005.
Find full textMaris, Elisabeth. "Éco-conception par une Approche Multicritère d’un Système Polymère/Traceurs/Détecteur pour le tri automatisé par spectrométrie de fluorescence UV-VIS en vue d’augmenter la recyclabilité des produits." Thesis, Paris, ENSAM, 2014. http://www.theses.fr/2014ENAM0022/document.
Full textThe recycling of materials from end of life products is a important issue to preserve our resources of raw materials which are more and more rare and the extraction of which is more and more impactant for the environment. Nevertheless certain materials are little recycled. It is the case of dark colored polymers.The originality of this work is to have integrated into the process of design two strategies of ecodesign: the limits of current sorting processes and the limits on the resources. This approach succeeded to design a material and its process of recycling. This system brings potentially an environmental bonus by allowing producing more recycled materials on the market, satisfying the consumers by bringing a traceability of these materials and a new technology validated by the development of a demonstrator coupled with an industrial conveyor
Janjua, Safia. "Genetic Analysis of Snow Leopard Population Employing Next Generation Sequencing For Its Improved Conservation And Management." Wright State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1598870693394148.
Full textAx, Erika. "Dietary Patterns : Identification and Health Implications in the Swedish Population." Doctoral thesis, Uppsala universitet, Klinisk nutrition och metabolism, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-250280.
Full textMeinert, Cornelia [Verfasser], W. G. [Akademischer Betreuer] Lorenz, and U. J. [Akademischer Betreuer] Meierhenrich. "Isolation and identification of environmental pollutants from complex mixtures using effect-directed analysis and preparative capillary gas chromatography / Cornelia Meinert. Betreuer: W. G. Lorenz ; U. J. Meierhenrich." Halle, Saale : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2011. http://d-nb.info/1025134710/34.
Full textIbáñez-Peral, Raquel. "Analysis of microbial diversity in an extreme environment: White Island, New Zealand." Australia : Macquarie University, 2009. http://hdl.handle.net/1959.14/44764.
Full textThesis (PhD)--Macquarie University, Division of Environmental & Life Sciences, Dept. of Chemistry & Biomolecular Sciences, 2009.
Bibliography: p. 227-259.
Literature review -- Materials and methods -- Sampling sites and sampling material -- Enrichment cultures and molecular analyses -- Optical and binding characterisation of the QDs -- Applications of the QDs -- Concluding remarks.
White island, the most active volcano in New Zealand, is a poorly studied environment that represents an ideal site for the investigation of acidophilic thermophiles. The microorganisms present on here are continually exposed to extreme environmental conditions as they are surrounded by steamy sulphurous fumaroles and acidic streams. The sediment temperature ranges from 38°C to 104°C whilst maintaining pH values below 3. A survey of the volcanic hydrothermal system of White Island was undertaken in order to gain insights onto the microbial diversity using culture-dependant techniques and molecular and phylogenetic analyses. A novel liquid medium based on "soil-extract" was designed which supported growth of bacterial and archaeal mixed cultures. Molecular analyses revealed that the dominant culturable bacterial species belong to the Bacteroidetes, Firmicutes and α-Proteobacteria groups. Several previously uncultured archaeal species were also present in the mixed cultures. The knowledge gained from these studies was intended to help in the development of a novel microbial detection technique suitable for community analysis. -- Conventional molecular techniques used to study microbial biodiversity in environmental samples are both time-consuming and expensive. A novel bead-based assay employing Quantum dots (QDs) was considered to have many advantages over standard molecular techniques. These include high detection speeds, sensitivity, specificity, flexibility and the capability for multiplexed analysis. QDs are inorganic semiconductor nanoparticles made up of crystals about the size of proteins. It has been claimed that the physical and chemical properties of the QDs have significant advantages compared to organic dyes, including brighter fluorescence and resistance to photo-bleaching. Their optical properties facilitate the simultaneous imaging of multiple colours due to their flexible excitation and narrow band emission. Functionalised QDs are able to bind to different biological targets such as DNA, allowing high-throughput analysis for rapid detection and quantification of genes and cells. -- The optical and physical characteristics of the QDs as well their interaction with biomolecules are shown to be suitable for the development of a novel bead-based technique able to target the key microbial species and identify them by flow cytometric measurements (FCM). The broad absorption and narrow emission spectra of the QDs, as well as their fluorescence intensity and specify to target biomolecules, was compared to other organic fluorophores. The potential advantages and limitations of QDs as a fluorophores for biological applications are discussed. -- The data acquired during this study provides a broad overview of the microbial diversity and ecology of the volcanically-active hydrothermal systems of White Island and constitutes the baseline for the development of a novel bead-based technique based on QDs.
Mode of access: World Wide Web.
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Karolski, Bruno. "Metagenômica comparativa e perfil metabólico in silico de solos no município de Cubatão, SP." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-05112013-111556/.
Full textCubatão is the largest industrial site in Latin America and was in the past one of the most polluted cities in the world. 30 years of intense industrial activity has pushed environmental limits with toxic substances and has severely affected the inhabitants\' health. Among the contaminants found in the region, the petroleum derivatives benzene, toluene, ethylbenzene and xylenes are the most important. Known collectively as BTEX, they are produced and used at a large scale and contamination frequently occurs. Because it is highly soluble in water, when in soil BTEX can spread long distances from the original contamination site, thus affecting large areas. Some microorganisms are known to live in contaminated environments and use contaminants such as BTEX as a unique carbon source for energy production. They catabolize contaminants into less dangerous products or even eliminate them from environment, a feature which has great commercial and environmental interest. We therefore compared the microbial communities in soils which were affected and un-affected by BTEX contamination. To this end, we used a metagenomics approach and developed a comparison method to identify microorganisms and degradation potential of soils studied. We found qualitative and quantitative differences in microbial structures from three different sites in Cubatão County, one of which is contaminated with BTEX. We constructed a metabolic overview identifying important genes, degradation potential and microorganisms related to BTEX degradation. The results presented here could contribute to understanding the in situ dynamics of a BTEX affected microbial community as well as improving our knowledge of the microbial community of Cubatão, a highly environmentally impacted place.
Pisarczyk, Elizabeth W. "The effect of garlic mustard (Alliaria petiolata) density on soil nutrient availability and microbial enzyme activity in Northwest Ohio : a gradient analysis /." Connect to full text in OhioLINK ETD Center, 2009. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=toledo1260236506.
Full textTypescript. "Submitted as partial fulfillment of the requirements for The Master of Science Degree in Biology (Ecology-track)." "A thesis entitled"--at head of title. Bibliography: leaves 28-32.
Damaso, Natalie. "Biogeographical Patterns of Soil Microbial Communities: Ecological, Structural, and Functional Diversity and their Application to Soil Provenance." FIU Digital Commons, 2016. http://digitalcommons.fiu.edu/etd/3006.
Full textHendricks, Luanne R. "Soil Bioavailability of Aminomethylphosphonic Acid: A Metabolite of Glyphosate." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1592583268434087.
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