Phosphorus has long been recognized by agriculturists as being one of the elements essential for plant growth. Although the total phosphorus content of a soil may be high, the amount of phosphate actually available for plant growth is often low. Many agencies such as inherent low solubilities of phosphate compounds, adsorption on Ca C03, adsorption in the diffuse double layer of clay micelles, and chemical precipitation of phosphate which refers to the removal of phosphate ions from solution and their chemical bonding to the solid phase have been studied to explain the lack of phosphate availability.

TOTP is a prevalent industrial and environmental contaminant which has been shown to be a neurotoxic agent. This study was undertaken to investigate the effects of this compound on the immune system. Several techniques were employed to test the humoral as well as cellular effects. Male Swiss Webster mice were administered by gastric gavage with three doses of TOTP (5, 50, and 500 mg/kg) and one dose TMTP (50 mg/kg) in corn oil once a week for 13 weeks. Control animals were given corn oil alone. Lymphocyte transformation was determined on cultures of splenic cells obtained from animals sacrificed at 1, 4, 8, and 13 weeks. Relative Proliferation Index (RPI) and Stimulation Index (SI) was calculated for phytohemagglutinin (PHA), pokeweed (PWM), and lipopolysaccharide (LPS) mitogen treated cultures. Proliferation was measured by uptake of radioisotope labeled thymidine. Plaque formation as well as delayed hypersensitivity was evaluated at all dose levels after 4 weeks of treatment. Humoral effects were determined utilizing quantitative (Rocket) immunoelectropheresis. Serum was compared with control serum for IgA, IgG, and IgM fractions. TOTP was found to cause slight suppression in proliferation of splenic lymphocytes at 8 and 13 weeks although this suppression was non-specific and not dose related. No effects were seen on body and organ weights. Plaque forming cells and delayed hypersensitivity were not affected either by dose or time of treatment. Immunoglobulin fractions tested were similarly not affected by time or dosage. These findings suggest that neither TOTP nor TMTP exhibit immunotoxic effects at levels used.

Excessive microvascular permeability is a serious complication involved in traumatic injury and inflammatory diseases. Alcohol intoxication can exacerbate the physiological derangements produced by microvascular endothelial barrier dysfunction in such disease conditions. Sphingosine-1-phosphate (S1P) has known endothelial barrier-protective properties, and has been shown to ameliorate microvascular leakage in a model of combined alcohol intoxication and hemorrhagic shock and resuscitation (HSR). However, whether the barrier-protective properties of S1P extend to endothelial cells of the blood-brain barrier (BBB) is unclear. The mechanisms of S1P-induced barrier protection during alcohol intoxication or HSR are also unknown. In the current study, we tested the hypothesis that S1P could enhance endothelial barrier during alcohol intoxication or hemorrhagic shock by preserving the integrity of junction proteins and the endothelial glycocalyx, and protecting mitochondrial function. Cultured primary human brain microvascular endothelial cell (HBMEC) monolayers were used to characterize endothelial-specific mechanisms of S1P protection of the BBB during alcohol treatment. Transendothelial electrical resistance (TER) and apparent permeability coefficients for albumin, dextran-4 kDa, and sodium fluorescein were used as indices of barrier function. Junctional localization was determined by immunofluorescence confocal microscopy. We also used an established in vivo rat model of conscious HSR and assessed microvascular leakage, endothelial glycocalyx integrity, and mitochondrial function by intravital microscopy. Cultured rat intestinal microvascular endothelial cell (RIMEC) monolayers were used to test the ability of S1P to protect against glycocalyx shedding and endothelial barrier dysfunction caused by direct disruption of mitochondrial integrity due to inhibition of mitochondrial complex III. The results show that alcohol significantly impaired HBMEC TER and increased solute permeability, which was reversed with application of S1P after alcohol treatment. Alcohol caused the formation of gaps between cells. Treatment with S1P (after alcohol) increased junctional localization. Our in vivo results show that S1P protects against HSR-induced hyperpermeability, preserves the expression of adherens junctional proteins, and protects against glycocalyx degradation. S1P treatment during HSR also protects against mitochondrial membrane depolarization. Besides that, S1P protects RIMECs against mitochondrial dysfunction-induced endothelial barrier dysfunction and glycocalyx degradation by acting through mitochondrial complex III. Our results indicate that S1P may be useful for restoring BBB function during alcohol intoxication. Moreover, S1P protects against HSR-induced mitochondrial dysfunction in endothelial cells, which in turn improves the structure of the endothelial glycocalyx after HSR and allows for better junctional integrity to prevention of excess microvascular permeability.

Soils are critical to ecosystem function as they provide essential nutrients for primary producers, habitat and organic energy for decomposers, and storage of organic matter. Irrigation with reclaimed water is an increasingly popular water conservation strategy; yet its high salinity and nutrient content potentially affect soil properties. In this study, set in a residential neighborhood of Tampa (U.S.). I tested whether there are distinct lawn system management strategies characterized by systematic differences in reclaimed water usage and irrigation and fertilization practices. I then investigated whether soil biogeochemistry responds to lawn system management strategy. My results indicated that amendment strategy, which includes water source type, frequency of fertilization, and frequency of irrigation varies among residents of comparable neighborhoods. In this case, these three categories of management behaviors tend to co-occur. Analysis of irrigation water samples collected in this study showed significant differences between potable and reclaimed water. Mainly, reclaimed water had higher conductivity and phosphate content than potable water. When looking at the soil biogeochemical characteristics of the study area I found that there were significant differences in soil nutrients and microbial biomass across amendment strategy. Soils with a high amendment strategy (frequently irrigation with nutrient-rich reclaimed water, plus frequent fertilizer addition) showed higher conductivity and a higher microbial biomass than soils on lawns with a low amendment strategy (infrequent irrigation with dilute potable water, plus infrequent fertilizer addition). A positive correlation between soil conductivity and microbial biomass was observed. These findings suggest that high amendment strategy increases the input flux of some nutrients to the soils and acts as a nutrient resource for soil microorganisms. The differences between soil and microbial biomass amendment strategy support the idea that decisions made by individuals about which management intensity strategy to use do affect the spatial variability of the ecosystem. These results contribute to the hypothesis of urban ecological urbanization by looking at the vertical social interactions between municipalities and individual homeowners. These interactions might explain the observed spatial variability of ecological characteristics. The results of this research affect the way information about the advantages of using reclaim water is advertised, in particular to homeowners.

Le Phosphate Diphosphate de Thorium (β-PDT) est considéré comme une matrice<br />céramique potentielle en vue de l'immobilisation des actinides en formation géologique<br />profonde. Il s'est avéré donc impératif d'étudier les effets de l'irradiation sur la structure de<br />cette céramique et les conséquences sur sa durabilité chimique.<br />Des échantillons de β-PDT et des solutions solides associées de β-PDTU ont été irradiés<br />puis altérés en solution aqueuse. Selon la valeur du TEL électronique, le β-PDT peut<br />s'amorphiser totalement ou partiellement. Par ailleurs, la capacité de recristallisation du<br />matériau amorphe par recuit thermique a été démontrée. Les tests de lixiviation menés sur ces<br />échantillons irradiés ont montré une influence significative de la fraction amorphe sur la<br />vitesse de dissolution normalisée qui augmente d'environ un facteur 10 entre le matériau non<br />irradié et le matériau amorphe. Corrélativement, la fraction amorphe modifie le temps requis<br />pour atteindre les conditions de saturation associées aux équilibres thermodynamiques. En<br />revanche, elle ne présente aucune influence ni sur d'autres paramètres cinétiques, tels que<br />l'énergie d'activation du processus de dissolution ou l'ordre partiel par rapport aux protons, ni<br />la nature de la phase néoformée identifiée comme le Phosphate HydrogénoPhosphate de<br />Thorium Hydraté (PHPTH).<br />Des échantillons de β-PDTU ont aussi été irradiés sous rayonnements γ et α pendant les<br />tests de lixiviation afin d'étudier les effets de la radiolyse du milieu lixiviant sur la vitesse de<br />dissolution du matériau. Il est apparu que les espèces radiolytiques intervenant dans le<br />mécanisme de dissolution étaient peu stables, disparaissant rapidement dès la fin de<br />l'irradiation. Leur caractère fortement oxydant vis-à-vis de l'uranium tétravalent permet d'expliquer la différence de comportement entre les cations métalliques (U et Th)

Cette thèse est le résultat de travaux analytiques du Maestrichtien phosphaté et a pour but de - reconstituer la paléogéographie du bassin des Ouled Abdoun - de tenter d'établir une corrélation lithographique entre les faciès présentés par cet étage dans les différentes régions - de donner un cliché pétrographique du faisceau maestrichtien phosphaté rencontré lors des différents points étudiés.

Die arbuskuläre Mykorrhiza ist die wahrscheinlich älteste Form der Wurzelsymbiosen zwischen Pflanzen und Pilzen und hat sich vor 420 Millionen Jahren entwickelt. In dieser Symbiose, die zwischen nahezu allen Landpflanzen und Pilzen des Reiches Glomeromycota ausgebildet wird, versorgt der Pilz die Pflanze mit Nährstoffen, wobei die verbesserte Versorgung mit Phosphat für die Pflanze sicher den größten Vorteil darstellt. Im Gegenzug erhält der Pilz Zucker, welche die Pflanze aus der Photosynthese bereitstellt. Zu hohe Phosphatkonzentrationen im Boden oder Dünger führen allerdings zu einer Verringerung in der Ausprägung der arbuskulären Mykorrhiza. Diese Unterdrückung der Symbiose wird nicht durch eine lokale Reaktion der Wurzeln ausgelöst, sondern in erster Linie durch einen hohen Phosphatgehalt im Pflanzenspross. Somit handelt es sich also um eine systemische, also dem Gesamtsystem „Pflanze“ betreffende Antwort. Die molekularen Mechanismen dieser Anpassung sind noch wenig bekannt und sind vor allem für die Agrarwirtschaft von besonderem Interesse. Eine Mikro-RNA (miRNA) des bereits bekannten Phosphathomöostasesignalwegs (PHR1-miRNA399-PHO2 Signalweg) akkumuliert verstärkt in mykorrhizierten Wurzeln. Das deutet daraufhin, dass dieser Signalweg und diese miRNA eine wichtige Rolle in der Regulation der arbuskulären Mykorrhiza spielen. Ziel dieser Studie war es neue Einblicke in die molekularen Mechanismen, die zur Unterdrückung der arbuskulären Mykorrhiza bei hohen Phosphatkonzentrationen führen, zu gewinnen. Dabei sollte der Einfluss von PHO2, sowie von miRNAs in dieser Symbiose genauer untersucht werden. Ein funktionelles Ortholog von PHO2, MtPho2, wurde in der Pflanze Medicago truncatula identifiziert. MtPho2-Mutanten, welche nicht mehr in der Lage waren ein funktionales PHO2 Protein zu exprimieren, zeigten schnellere Kolonisierung durch den AM-Pilz. Jedoch wurde auch in den mtpho2-Mutanten die Symbiose durch hohe Phosphatkonzentrationen unterdrückt. Dies bedeutet, dass PHO2 und somit der PHR1-miRNA399-PHO2 Signalweg eine wichtige Funktion während der fortschreitenden Kolonisierung der Wurzel durch den Pilz hat, aber und weitere Mechanismen in der Unterdückung der Symbiose bei hohen Phosphatkonzentrationen beteiligt sein müssen. Die Analyse von Transkriptionsprofilen von Spross- und Wurzeln mittels Microarrays zeigte, dass die Unterdrückung der AM Symbiose durch hohe Phosphatkonzentrationen möglicherweise auf eine Unterdrückung der Expression einer Reihe symbiosespezifischer Gene im Spross der Pflanze beruht. Um die Rolle weiterer miRNA in der AM Symbiose zu untersuchen, wurden mittels einer Hochdurchsatz-Sequenzierung 243 neue und 181 aus anderen Pflanzen bekannte miRNAs in M. truncatula entdeckt. Zwei dieser miRNAs, miR5229 und miR160f*, sind ausschließlich während der arbuskulären Mykorrhiza zu finden und weitere miRNAs werden während dieser Symbiose verstärkt gebildet. Interessanterweise führen einige dieser miRNAs zum Abbau von Transkripten, die eine wichtige Funktion in der arbuskulären Mykorrhiza und Wurzelknöllchensymbiose besitzen. Die Ergebnisse dieser Studie liefern eine neue Grundlage für die Untersuchung von regulatorischen Netzwerken, die zur zellulären Umprogrammierung während der Interaktion zwischen Pflanzen und arbuskulären Mykorrhiza-Pilzen bei verschiedenen Phosphatbedingungen führen. / AM symbiosis has a positive influence on plant P-nutrition and growth, but little is known about the molecular mechanism of the symbiosis adaptation to different phosphate conditions. The recently described induction of several pri-miR399 transcripts in mycorrhizal shoots and subsequent accumulation of mature miR399 in mycorrhizal roots indicates that local PHO2 expression must be controlled during symbiosis, presumably in order to sustain AM symbiosis development, in spite of locally increased Pi-concentration. A reverse genetic approach used in this study demonstrated that PHO2 and thus the PHR1-miR399-PHO2 signaling pathway, is involved in certain stages of progressive root colonization. In addition, a transcriptomic approach using a split-root system provided a comprehensive insight into the systemic transcriptional changes in mycorrhizal roots and shoots of M. truncatula in response to high phosphate conditions. With regard to the transcriptional responses of the root system, the results indicate that, although the colonization is drastically reduced, AM symbiosis is still functional at high Pi concentrations and might still be beneficial to the plant. Additionally, the data suggest that a specific root-borne mycorrhizal signal systemically induces protein synthesis, amino acid metabolism and photosynthesis at low Pi conditions, which is abolished at high Pi conditions. MiRNAs, such as miR399, are involved in long-distance signaling and are therefore potential systemic signals involved in AM symbiosis. A deep-sequencing approach identified 243 novel miRNAs in the root tissue of M. truncatula. Read-count analysis, qRT-PCR measurements and in situ hybridizations clearly indicated a regulation of miR5229a/b, miR5204, miR160f*, miR160c, miR169 and miR169d*/l*/m*/e.2* during arbuscular mycorrhizal symbiosis. Moreover, miR5204* represses a GRAS TF, which is specifically transcribed in mycorrhizal roots. Since miR5204* is induced by high Pi it might represent a further Pi status-mediating signal beside miR399. This study provides additional evidence that MtNsp2, a key regulator of symbiosis-signaling, is regulated and presumably spatially restricted by miR171h cleavage. In summary, a repression of mycorrhizal root colonization at high phosphate status is most likely due to a repression of the phosphate starvation responses and the loss of beneficial responses in mycorrhizal shoots. These findings provide a new basis for investigating the regulatory network leading to cellular reprogramming during interaction between plants, arbuscular mycorrhizal fungi and different phosphate conditions.

Glucose-6-phosphate (G6P) plays an important role in carbohydrate metabolism of all living organisms. Compared to the conventional analytical methods available for estimation of G6P, the biosensors having relative simplicity, specificity, low-cost and fast response time are a promising alternative. We have reported a G6P biosensor based on screen-printed electrode utilizing Prussian Blue (PB) nanoparticles and enzymes, glucose-6-phosphate dehydrogenase and glutathione reductase. The PB nanoparticles acted as a mediator and thereby enhanced the rate of electron transfer in a bi-enzymatic reaction. The Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy study confirmed the formation of PB, whereas, the atomic forced microscopy revealed that PB nanoparticles were about 25-30 nm in diameter. Various optimization studies, such as pH, enzyme and cofactor loading, etc. were conducted to obtain maximum amperometric responses for G6P measurement. The developed G6P biosensor showed a broad linear response in the range of 0.01-1.25 mM with a detection limit of 2.3 mM and sensitivity of ­63.3 mA/mM at a signal-to-noise ratio of 3 within 15 s at an applied working potential of -100 mV. The proposed G6P biosensor also exhibited good stability, excellent anti-interference ability and worked well for serum samples.

Osteocytes have been proposed as the mechanosensory cells during the process of bone adaption. In this thesis, a microfluidics chamber system (MCS) device was designed, fabricated and tested as a means to maximally simulate the in vivo osteocytic ultrastructure and reproduce the in vivo shear stress experienced by osteocyte, providing an ideal platform for in vitro study on osteocyte mechanotransduction. By employing a micropipette aspiration technique, single osteocyte adhesion and osteocytic process formation were achieved on PDMS with MCS structure. In this study, the involvement of sphingosine-1-phosphate (S1P) signaling pathway in osteocytes responding to oscillatory fluid flow (OFF) was also examined. Firstly, MLO-Y4 osteocytes like cells were demonstrated to express integrated and functional S1P cascade. By modulating S1P cascade components and testing a series of cellular outcomes, it was indicated that exogenous S1P, endogenous S1P and S1P receptor S1P2 were involved in the regulation of loading induced osteocytic responses.

Phosphate is one of the essential minerals for all living organisms. It has to be supplied to the soil in order for plant growth. In Turkey, most of the soils lack phosphate mineral. Although this can be overcome by the use of phosphate fertilizers, in Turkey there are no phosphate mines being utilized / and this brings about the need to import phosphate rock and phosphate fertilizers. The estimated phosphate rock reserve of Turkey is around 300 million tons, but it cannot be utilized since no economical method of upgrading has been proved to work yet. The aim of this study has been two-fold / to determine the effects of several parameters on the cell flotation of Mardin-Mazidagi phosphate rock and to increase the grade of the product above 30% P2O5 content with a reasonable recovery rate, so that it could be used commercially. Phosphate rock upgrading was made by using flotation in a cell. There are many factors affecting the recovery and grade of the product such as, particle size, pulp pH, collector volume, acid and collector conditioning times and temperature. Phosphate rock samples used contained 14% P2O5, 43% CaCO3 and 1% SiO2 with a CaO/P2O5 ratio of 3.1. Due to the low silica content, one-stage flotation was made. In the experiments, effects of the important parameters were tested at constant pulp density (10% solids by weight). Particle sizes were between 53 m and 150 m, while the pH values were kept between 5,0 - 6,5 using amounts of acid within the range of 6 - 19 kg H3PO4/ton of rock. The collector (mixture of kerosene and oleic acid in 1:3 volumetric ratio) was used in the range of 0,6 ml (0,96 kg collector/ton rock) and 5,4 ml (8,64 kg collector/ton rock). Acid and collector conditioning times were changed between 10-110 s and 10-80 s, respectively. The temperature range was between 15-35 &deg / C. At the end of the parametric studies a grade of 36% P2O5 with a recovery of 93% could be obtained.