BTX biodegradation rates, biochemical expression patterns and microbial ecology were studied under anoxic (denitrifying), anoxic/microaerobic/aerobic, and anoxic/microaerobic conditions in activated sludge sequencing batch reactors. The studies showed that toluene and m-xylene were denitrified via benzoyl-CoA reductase. Although benzene, o-, and p-xylene were recalcitrant under denitrifying conditions, they were biodegraded under microaerobic (< 0.2 mg/L dissolved oxygen) and nitrate or nitrite (NOx)-supplemented microaerobic conditions. The patterns of the specific enzymes associated with BTX biodegradation under microaerobic conditions indicated that the three compounds were metabolized by oxygen-dependent pathways. The expression levels of catechol 1, 2-dioxygenase and catechol 2, 3-dioxygenase under microaerobic conditions were induced to levels as high as under aerobic conditions (> 4 mg/L dissolved oxygen). Benzene, o-, and p-xylene biodegradation rates were twice as fast under NO_x-supplemented compared to NO_x-free microaerobic conditions, and the specific biodegradation rates under aerobic and NO_x-supplemented microaerobic conditions were comparable. 16S rRNA probes targeting representative toluene-degraders were used to investigate the microbial communities in the three sequencing batch reactors by using a dot blot hybridization technique. The hybridization results suggest that multiple redox environments fostered a more diverse microbial community and the activities of the target organisms in the reactors with multiple redox environments were higher than in the single redox reactor. Additionally, facultative toluene-degraders appeared to play a less significant role than the strict anoxic and aerobic toluene-degraders in all three SBRs. / Ph. D.

Plasmonic nanostructures can enhance light-matter interactions in the subwavelength domain, which is useful for photodetection, light emission, optical biosensing, and spectroscopy. However, conventional plasmonic devices are optimized to operate in a single wavelength band, which is not efficient for wavelength-multiplexed operations and quantum optical applications involving multi-photon nonlinear processes at multiple wavelength bands. Overcoming the limitations of single-resonant plasmonics requires development of plasmonic devices that can enhance the optical interactions at the same locations but at different resonance wavelengths. This dissertation comprehensively studies the theory, design, and applications of such devices, called "multiresonant plasmonic systems with spatial mode overlap". We start by a literature review to elucidate the importance of this topic as well as its current and potential applications. Then, we briefly discuss the fundamentals of plasmonic resonances and mode hybridization to thoroughly explore, classify, and compare the different architectures of the multiresonant plasmonic systems with spatial mode overlap. Also, we establish the black-box coupled mode theory to quantify the coupling of optical modes and analyze the complicated dynamics of optical interactions in multiresonant plasmonic systems. Next, we introduce the nanolaminate plasmonic crystals (NPCs), wafer-scale metamaterials structures that support many (>10) highly-excitable plasmonic modes with spatial overlap across the visible and near-infrared optical bands. The enabling factors behind the NPC's superior performance as multiresonant systems are also theoretically and experimentally investigated. After that, we experimentally demonstrate the NPCs application in simultaneous second harmonic generation and anti-Stokes photoluminescence (ASPL) with controllable nonlinear emission properties. By designing specific non-linear optical experiments and developing advanced ASPL models, this work addresses some important but previously unresolved questions on the ASPL mechanism as well. Finally, we conclude the dissertation by discussing the potential applications of out-of-plane plasmonic systems with spatial mode overlap in wavelength-multiplexed devices and presenting some preliminary results. / Doctor of Philosophy / Emergence of electronic devices such as cellphones and computers has revolutionized our lifestyles over the past century. By manipulating the flow/storage of electrons at the nanometer scale, electronic components can be very compact, but their speed and energy performance is ultimately limited due to ohmic losses and finite velocity of the electrons. In parallel, photonic devices and circuits have been proposed that by molding the flow of light can overcome the mentioned limitations but are not as integrable as their electronic counterparts. Plasmonics is an emerging research field that combines electronics and photonics using nanostructures that can couple the light waves to the free electrons in metals. By confining the light at deep subwavelength scales, plasmonic devices can highly enhance the light-matter interactions, with applications in ultrafast optical communications, energy-harvesting, optical sensing, and biodetection. Conventionally, plasmonic devices are optimized to operate with a single light color, which limits their performance in wavelength-multiplexed operations and ultrafast non-linear optics. For such applications, it is far more efficient to use the more advanced "multiresonant plasmonic systems with spatial mode overlap" that can enhance the optical interactions at the same locations but for multiple light colors. This dissertation comprehensively studies these systems in terms of the fundamental concepts, design ideas, and applications. Our work advances the plasmonic field from both science and technology perspectives. In particular, we explore and classify the strategies of building multiresonant plasmonic systems with spatial mode overlap for the first time. Also, we establish the black-box coupled mode theory, a novel framework for analysis and design of complicated plasmonic structures with optimized performance. Furthermore, we introduce the "nanolaminate plasmonic crystals" (NPCs), large area and cost-effective devices that can enhance the optical processes for both visible and near-infrared lights. Finally, we demonstrate NPCs ability in simultaneous frequency-doubling and broadband emission of light and come up with advanced theoretical models that can explain the light generation and color conversion in plasmonic devices.

Rhizoctonia blight (sensu lato) is a common and serious disease of many turfgrass species. The most widespread causal agent R. solani consists of several genetically different anastomosis groups (AGs) and subgroups. Though anastomosis or hyphal fusion reactions have been used to group Rhizoctonia species, they are time consuming and sometimes difficult to interpret. Anastomosis reactions are incapable of identifying isolates belonging to different AG subgroups within an AG. This study evaluated molecular techniques in comparison with traditional anastomosis grouping (AG) to identify and group isolates of Rhizoctonia. More than 400 Rhizoctonia isolates were collected from diseased turfgrass leaves from eight geographic areas in Virginia and Maryland. A random sample of 86 isolates was selected and initially characterized by colony morphology, nuclei staining and anastomosis grouping. Molecular identification was performed by analysis of rDNA-ITS region and DNA fingerprinting techniques universally primed PCR (UP-PCR) and amplified fragment length polymorphism (AFLP). The cladistic analysis of ITS sequences and UP-PCR fragments supported seven clusters. Isolates of R. solani AG 1-IB (n=18), AG 2-2IIIB (n=30) and AG 5 (n=1) clustered separately. Waitea circinata var. zeae (n=11), and var. circinata (n=4) grouped separately. A cluster of six isolates (UWC) did not fall into any known Waitea group. Most of the binucleate Rhizoctonia-like fungi (BNR) (n=16) grouped separately. AFLP grouping also largely agreed with the above results. However, UWC isolates clustered into two groups. Molecular analyses corresponded well with traditional anastomosis grouping by clustering isolates within an AG or AG subgroup together. UP-PCR cross-hybridization could distinguish closely related Rhizoctonia isolates to their infraspecies level. Genetically related isolates belonging to the same AG subgroups cross-hybridized strongly, while isolates of different AGs did not cross-hybridize or did so weakly. Sequence-characterized amplified region (SCAR) markers were generated from UP-PCR products to identify isolates of major pathogenic groups AG 1-IB and AG 2-2IIIB. Specific primer pairs successfully distinguished isolates of AG 1-IB and AG 2-2IIIB from isolates of other AGs. Sensitivity of Rhizoctonia species and AGs was tested in vitro to commercial formulations of iprodione, triticonazole and pyraclostrobin. W. circinata isolates were moderately sensitive to iprodione while isolates of R. solani and BNR were extremely sensitive. Isolates of AG 2-2IIIB showed less sensitivity to triticonazole than other Rhizoctonia isolates. W. circinata var. zeae isolates were moderately sensitive to pyraclostrobin while most of the other isolates were extremely sensitive. / Ph. D.

Hybridization was evaluated among three Laricobius spp. involved in the biological control of hemlock woolly adelgid (Adelges tsugae Annand). Following lab mating studies, there was no evidence that Laricobius osakensis Montgomery and Yu could produce hybrid progeny with either Laricobius nigrinus Fender or Laricobius rubidus LeConte. Interaction between L. osakensis and L. nigrinus did not result in a lower production of progeny as a result of fitness costs associated with interspecific mating attempts. Laricobius nigrinus and L. rubidus hybrids were produced in the lab and collected in the field. Hybrid progeny showed very little evidence of decreased fitness. For example, there was no significant difference in the number of days it took for hybrids and pure parental species to develop from egg hatch to the prepupal stage, there was no difference among hybrids and pure parental species in the head capsule widths and larval lengths for the first through third instar, and there was evidence of an F2 generation from field collected specimens. Hybrids produced in the lab had intermediate shaped genital paramere angles compared with parental species, and had elytra coloration similar to that of L. rubidus. Hybrids showed no host preference in the lab, but a preference for Adelges tsugae in the field. Of 12 site factors examined, only the number of years that L. nigrinus was present at the site was found to be associated with percent hybrids. Contamination of the L. osakensis colony with Laricobius naganoensis Leschen resulted in the need to develop molecular methods to differentiate L. osakensis from L. naganoensis. Three restriction enzymes were found that correctly differentiated the two species. / Ph. D.

Dissertation submitted in fulfilment with the requirements for the Masters Degree: Biotechnology, Durban University of Technology, 2011. / Untreated vegetable oil effluents (VOEs) are known for creating shock-loading problems for the receiving wastewater treatment installations, resulting in poor quality final effluents being produced which do not satisfy municipal discharge standards. Onsite activated sludge treatment as an alternative has not been fully investigated. Hence, in this investigation biological treatment using the activated sludge process was chosen as the method for the treatment of VOE. The effect of VOE on measured process parameters was also determined. Novel molecular techniques such as fluorescent in situ hybridisation (FISH) and dot-blot hybridization have become powerful tools for the analysis of complex microbial communities that exist within activated sludge. The aim of this investigation was to evaluate biological treatment, optimize and apply FISH and dot-blot hybridization in order to analyze the microbial community implicated the biological treatment of VOE using probes EUBmix, ALF1b, BET42a, GAM42a and HGC69a. A laboratory-scale modified Ludzack-Ettinger (MLE) process setup and fed VOE with a COD (chemical oxygen demand) of ± 1000 mg/L. Daily monitoring of the process involved COD and TKN (total kjeldahl nitrogen) analysis of the influent and effluent as well as direct OUR (oxygen utilization rate) measurement and monitoring of the MLVSS (mixed liquor volatile suspended solids) concentration of the aerobic mixed liquor. The process exhibited overall COD and TKN removal capacities of 84% and 90% respectively. The aerobic mixed liquor had an OUR of 19 mgO/L.h and an average MLVSS concentration of 3000 mg/L. FISH results revealed that 72% of cells stained with 4‟, 6-diamidino-2-phenylindole (DAPI) within the aerobic mixed liquor bound to probe EUBmix, indicating a substantial Bacterial population within the laboratory-scale biological process. The alpha-Proteobacteria was identified as the dominant bacterial community comprising 31% of Bacterial cells, followed by the beta-Proteobacteria (17% of EUBmix), gamma-Proteobacteria (8% of EUBmix) and Actinobacteria (4% of EUBmix). Results of dot-blot hybridization were in agreement with FISH Adrian Phillip Degenaar| CHAPTER 1: General Introduction - v - results reiterating dominance of the alpha-Proteobacteria. This indicated that the class alpha-Proteobacteria could play a primary role in the biological degradation of VOE. This research will therefore aid in process design and retrofitting of biological processes treating VOE.

Thesis (MSc (Wine Biotechnology))--Stellenbosch University, 2008. / In the wine industry, the importance of selecting an appropriate yeast strain, generally of the species Saccharomyces cerevisiae, to ensure reliable fermentation and to achieve a desired level of quality has been well established. As a consequence, the demand for new starter cultures with improved or new oenological characteristics is increasing. Appropriately selected starter cultures can reduce the occurrence of stuck fermentations, impart specific aroma profiles and reduce the development of offflavours. Using standard breeding and selection procedures, several wine yeast strains that would be less likely than currently existing strains to experience stuck fermentation have previously been developed at the Institute for Wine Biotechnology. The target of these projects had been to develop strains with improved nitrogen efficiency [defined as the amount of fermented hexoses for a given amount of free amino nitrogen (FAN)], improved fructose utilization and ethanol tolerance. These three parameters are known contributors to stuck fermentation. Two of the strains that had been isolated in these projects, strain 116 for nitrogen efficiency and strain 38-1 for efficient fructose utilization, were chosen as parental strains for the current study. The aim was to further improve and possibly combine these traits in yeast strains by using hybridization followed by various enrichment and directed evolution procedures in a continuous fermentation setup. The strategy was to sequentially subject the population of mass-mated hybrids to a number of selective environments for a large number of generations. The yeasts were subjected to a high fructose/glucose ratio for 12 generations, followed by selection in an environment with a limited supply of nitrogen for 54 generations and finally to high ethanol stress. After each round of enrichment, individual strains were analysed to assess the results. For the hybrid strains selected after enrichment in a medium with a high fructose/glucose ratio, no general improvement could be discerned. However, one of the hybrids, hybrid strain 331, fermented fructose better than the parental strains and other hybrid strains. These results may suggest that the selection pressure was not applied for a sufficient number of generations and may not have been sufficiently strong. In addition, the parental strain may already performing at a rate that may render further improvement more difficult in this genetic background. The next aim of this study was to enhance fermentation performance of wine yeast hybrid strains in low nitrogen and high sugar conditions. Several hybrid strains 331, RR03 and 05R generated in this study showed improvement in efficiency of nitrogen utilization when compared to the parental strains, indicating a successful selection strategy. Several strains also showed higher ethanol tolerance, and some strains possessed] combinations of the traits to be improved. Future research will evaluate these hybrids regarding the production of aromatic compounds and of the sensory profile produced. Such strains would help the wine industry to control the occurrence of stuck fermentations and to produce quality wines.

Student Number : 0214677F - PhD thesis - School of Camputational and Applied Mathematics - Faculty of Science / Many real-life problems are formulated as global optimization problems with continuous variables. These problems are in most cases nonsmooth, nonconvex and often simulation based, making gradient based methods impossible to be used to solve them. Therefore, ef#2;cient, reliable and derivative-free global optimization methods for solving such problems are needed. In this thesis, we focus on improving the ef#2;ciency and reliability of some global optimization methods. In particular, we concentrate on improving some population set-based methods for unconstrained global optimization, mainly through hybridization. Hybridization has widely been recognized to be one of the most attractive areas of unconstrained global optimization. Experiments have shown that through hybridization, new methods that inherit the strength of the original elements but not their weakness can be formed. We suggest a number of new hybridized population set-based methods based on differential evolution (de), controlled random search (crs2) and real coded genetic algorithm (ga). We propose #2;ve new versions of de. In the #2;rst version, we introduce a localization, called random localization, in the mutation phase of de. In the second version, we propose a localization in the acceptance phase of de. In the third version, we form a de hybrid algorithm by probabilistically combining the point generation scheme of crs2 with that of de in the de algorithm. The fourth and #2;fth versions are also de hybrids. These versions hybridize the mutation of de with the point generation rule of the electromagnetism-like (em) algorithm. We also propose #2;ve new versions of crs2. The #2;rst version modi#2;es the point generation scheme of crs2 by introducing a local mutation technique. In the second and third modi#2;cations, we probabilistically combine the point generation scheme of crs2 with the linear interpolation scheme of a trust-region based method. The fourth version is a crs hybrid that probabilistically combines the quadratic interpolation scheme with the linear interpolation scheme in crs2. In the #2;fth version, we form a crs2 hybrid algorithm by probabilistically combining the point generation scheme of crs2 with that of de in the crs2 algorithm. Finally, we propose #2;ve new versions of the real coded genetic algorithm (ga) with arithmetic crossover. In the #2;rst version of ga, we introduce a local technique. We propose, in the second version, an integrated crossover rule that generates two children at a time using two different crossover rules. We introduce a local technique in the second version to obtain the third version. The fourth and #2;fth versions are based on the probabilistic adaptation of crossover rules. The ef#2;ciency and reliability of the new methods are evaluated through numerical experiments using a large test suite of both simple and dif#2;cult problems from the literature. Results indicate that the new hybrids are much better than their original counterparts both in reliability and ef#2;ciency. Therefore, the new hybrids proposed in this study offer an alternative to many currently available stochastic algorithms for solving global optimization problems in which the gradient information is not readily available.

Partant d’une part, du constat selon lequel tous les travaux sur le gouvernement des entreprises considèrent que la propriété de l’entreprise (actionnariale ou symbolique) est le fondement de la souveraineté et donc de la légitimité du dirigeant et d’autre part, du fait que trois définitions de la propriété coexistent au Sénégal, ce travail cherche à établir comment un dirigeant légitime-t-il ses pratiques en matière de gouvernement des entreprises dans le contexte sénégalais de multi-références à la notion de propriété. En effet, sa position de carrefour des civilisations du monde donne au Sénégal une pléthore de mécanismes de régulation des affaires et un large éventail de sources de droits de propriété. Compte tenu de ces multiples références à la propriété comment peut-on définir le gouvernement des entreprises au Sénégal? L’objectif est d’observer la rationalité qui est en œuvre dans les pratiques de gouvernement des entreprises sénégalaises en particulier et africaines en général. Pour ce faire, l’évolution des pratiques de gouvernement des hommes dans les entreprises africaines est questionnée et suivie pas à pas pour identifier, décrypter, décrire et analyser les référentiels sur lesquels les dirigeants des entreprises africaines s’appuient pour justifier leurs pratiques des entreprises. Nous avons privilégié l’analyse des représentations des dirigeants des entreprises sénégalaises. Les données du terrain ont montré que les pratiques au Sénégal sont le résultat de bricolages que les dirigeants des entreprises effectuent en puisant dans les différents modèles de gouvernance se référant à des formes de propriété différentes, les éléments qui les arrangent. Cet « arrangement » institutionnel définit des hybridations par emprunts sans aboutir à un modèle hybride unique. C’est un bricolage qui concilie l’efficacité économique et la solidarité communautaire ou clanique en formalisant les pratiques fondées sur la confiance et le contrôle (la première n’excluant pas le dernier). On est non pas en présence d’un nouveau modèle de gouvernement d’entreprises mais d’une matrice de pratiques de gouvernement d’entreprises qui se voit assigner un rôle paradoxal. D’une part, il en émerge un champ de pratiques inédites, d’autre part, cette matrice fait entrevoir le maintien de pratiques s’appliquant souvent de manière isolée selon les situations de gestion. / Based on the one hand, the observation that all work on corporate governance believe that ownership of the company (ownership or symbolic) is the basis of sovereignty and therefore the legitimacy of the leader and the other, that three definitions of ownership coexist in Senegal, this work seeks to establish how a legitimate leader, he practices in corporate governance in the context of Senegalese multi-references to the concept of ownership. Indeed, its position as a crossroads of civilizations in the world gives Senegal a plethora of mechanisms for regulating business and a wide range of sources of property rights. Given these multiple references to the property how can we define corporate governance in Senegal? The objective is to observe the rationality that is implemented in the practices of corporate governance in Senegal particularly and in Africa in general. To do this, the evolution of governance practices of men in African enterprises is questioned and followed step by step to identify, decipher, describe and analyze the benchmarks on which the leaders of African companies rely to justify their business practices. We have emphasized analysis of representations of leaders of Senegalese companies. The field data showed that the practices in Senegal are the result of tinkering that leaders of companies engaged in drawing the different governance models referring to different types of property, elements that settle. This "arrangement" defines institutional hybridizations by borrowing without producing a unique hybrid model. It is a craft that combines economic efficiency and community solidarity in clan or formalizing practices based on trust and control (excluding the first not the last). We are not in the presence of a new model of corporate governance but an array of practices of corporate governance which is assigned a paradoxical role. On the one hand, there emerges a field of new practices and on the other hand, that array hinted maintenance practices often applied in isolation by management situations.

La diapause embryonnaire se manifeste par un arrêt réversible du développement embryonnaire durant la période de préimplantation et induit un retard de l’implantation. Chez le vison américain, une diapause embryonnaire obligatoire caractérise chaque gestation. Si les mécanismes de contrôle de la diapause embryonnaire obligatoire chez cette espèce sont bien connus, le rôle utérin impliqué dans la réactivation de l’embryon demeure, quant à lui, encore inconnu. Le sujet de ce doctorat a consisté dans un premier temps à explorer l’environnement utérin à la sortie de la diapause embryonnaire afin de caractériser, dans un deuxième temps, les principaux acteurs utérins qui provoquent la réactivation de l’embryon. Nous avons effectué une analyse du transcriptome utérin à l’émergence de la diapause embryonnaire ce qui a permis de construire une librairie de 123 séquences d’ADNc utérines différentiellement exprimées à la réactivation de l’embryon et homologues à des séquences de gènes connues chez d’autres espèces. Ces gènes sont impliqués dans la régulation du métabolisme (25 %), de l’expression génique (21 %), de la transduction de signal (15 %), du cycle cellulaire (15 %), du transport (10 %) et de la structure cellulaire (9 %), reflétant ainsi d’importantes modifications utérines à la réactivation embryonnaire. Nous avons validé l’expression différentielle de dix gènes ainsi identifiés : GDF3 (growth and differentiation 3), ALCAM (activated leukocyte cell adhesion molecule), ADIPOR1 (adiponectin receptor 1), HMGN1 (high mobility group N1), TXNL1 (thioredoxin like 1), TGM2 (tissue transglutaminase 2), SPARC (secreted protein acidic rich in cystein), et trois gènes codant pour AZIN1 (antizyme inhibitor 1), ODC1 (ornithine decarboxylase 1) et SAT1 (spermidine/spermine N1-acetyltransferase), des enzymes impliquées dans la biosynthèse des polyamines. Le patron de l’expression spatio-temporel de SPARC et d’HMGN1 illustrent spécifiquement un remodelage tissulaire et de la chromatine au niveau utérin à la sortie de la diapause embryonnaire. Ayant mesuré une augmentation des concentrations utérines en polyamines à la reprise du développement embryonnaire, nous avons émis l’hypothèse que les polyamines seraient impliquées dans les événements menant à la sortie de la diapause. L’inhibition de la biosynthèse des polyamines par un traitement à l’ α-difluoromethylornithine (DFMO) a provoqué une diminution significative de la proliferation cellulaire dans les embryons à la réactivation, un retard du moment de l’implantation, mais n’a pas affecté le succès de la reproduction. De manière similaire, nous avons induit un état de dormance dans les cellules de trophoblaste de vison en présence DFMO dans le milieu de culture, et constaté que cet état était réversible. En conclusion, cette étude a non seulement ouvert de nouveaux horizons quant à la compréhension du rôle utérin dans les événements menant à la sortie de la diapause embryonnaire, mais a démontré pour la première fois, l’existence de facteurs utérins indispensables à la réactivation de l’embryon: les polyamines. / Embryonic diapause is characterized by a reversible arrest of blastocyst development prior to implantation and delay in implantation. In the American mink, embryonic diapause is a characteristic of each gestation. Although the mechanisms which control obligate embryonic diapause of this species are well known, the role of the uterus involved in blastocyst reactivation remains elusive. The subject of this doctoral research consisted first in exploring the uterine environment at the emergence of embryonic diapause in order to subsequently determine, the main factors in the uterus that provoke reactivation of the embryo. We have undertaken an analysis of the uterine transcriptome at the emergence of embryonic diapause which has enabled us to set up a library of 123 cDNA uterine sequences differentially expressed at blastocyst reactivation, and homologue gene sequences known in other species. Twenty-five percent of these genes are implicated in genetic expression, 15 % in cell signal transduction, 15 % in cell cycle, 10 % in transport and 9 % in cell structure. All of them reflect significant uterine modifications at blastocyst reactivation. We have validated differential expression of ten genes, identified as: GDF3 (growth and differentiation 3), ALCAM (activated leukocyte cell adhesion molecule), ADIPOR1 (adiponectin receptor 1), HMGN1 (high mobility group N1), TXNL1 (thioredoxine like 1), TGM2 (tissue transglutaminase 2), SPARC (secreted protein acidic rich in cystein), and three genes encoding for AZIN1 (antizyme inhibitor 1), ODC1 (ornithine decarboxylase 1) and SAT1 (spermidine/spermine N1-acetyltransferase), which are enzymes implicated in polyamine biosynthesis. The spatio-temporal expression patterns of SPARC and HMGN1 illustrate tissue and chromatin remodelling in the uterus at the termination of embryonic diapause. Having measured an increase in concentration of polyamines in the uterus at the resumption of blastocyst development, we have hypothetized that polyamines are implicated in the emergence of blastocysts from diapause. We inhibited polyamine biosynthesis in pregnant mink females during early blastocyst reactivation. The inhibition of polyamine biosynthesis through treatment with α-difluoromehtylornithine (DFMO) provoked a major reduction in cell proliferation in blastocysts at reactivation and a delay in the timing of implantation, but did not affect the success of reproduction. Similarly, we induced a reversible dormant state in cultured mink trophoblast cells traited with DFMO. To conclude, not only are results of this study a breakthrough in the understanding of the role of the uterus in stimulating at the emergence of blastocysts from embryonic diapause, but also, for the very first time, they indicate the existence of uterine factors, the polyamines, that are responsible for blastocysts reactivation.

This thesis will study the Italian literary phenomenon Gomorra, viaggi nell'impero economico e nel sogno di dominio della Camorra. First, the focus will be on the text's hybrid nature and implications and also on its literary and intellectual inspirations (such as Truman Capote, Pier Paolo Pasolini and Leonardo Sciascia). Secondly, we will take a closer look at the structure of the novel's narrative and its literary details, in order to reveal the different processes used by Roberto Saviano to convince the reader. Interwoven in this book's central plot, we will find a main obsession: the need to understand. Lastly, we will discuss the question of the great power treated in this novel, the one of a criminal organisation transformed by the revelations made throughout the story. These revelations will allow us to draw interesting comparisons between organized crime and merchant capitalism. For this part, we will refer to Guy Debord's La société du spectacle, and to Hannah Arendt's work on the question of totalitarianism. All of these elements will allow us to discuss the different perspectives within the narrative's framework, and more precisely, the figure of the narrator/author/character that gives Saviano's novel anthropological qualities, in the form of an ethnofiction (Augé). / Ce Mémoire cherchera a étudier le phénomène littéraire italien Gomorra, viaggio nell’impero economico e nel sogno di dominio della Camorra. Au fil de l’analyse il sera évoqué autant son caractère hybride et les implications que cela représente que les influences littéraires et intellectuelles, auquel un tel texte fait écho ( Truman Capote, Pier Paolo Pasolini, Leonardo Sciascia…). Par la suite nous nous attacherons aux structures narratives et aux particularités littéraires du roman, afin de faire ressortir les différents procédés utilisés par Roberto Saviano dans son intention de convaincre. Une obsession qui s’inscrit dans la dynamique centrale du livre, celle de comprendre. Enfin, il sera question de la grande force qui entoure ce roman, celle d’un crime organisé rendu différent de par les révélations faites au sein du roman. De cela nous tirerons une étude comparative entre le crime organisé et le capitalisme marchand, faisant appel autant à Guy Debord et son œuvre La société du spectacle, qu’à Hannah Arendt pour ses nombreux travaux entourant la problématique du totalitarisme. Tous ces éléments nous permettront de conclure sur la particularité des points de vue, notamment avec la figure du narrateur/auteur/personnage qui nous permettra de rapprocher le roman de Roberto Saviano au travail anthropologique, dans la dynamique d’une forme d’ethno- fiction (Augé)