Matching Items (106)
Description
Bioparticles comprise a diverse amount of materials ubiquitously present in nature. From proteins to aerosolized biological debris, bioparticles have important roles spanning from regulating cellular functions to possibly influencing global climate. Understanding their structures, functions, and properties provides the necessary tools to expand our fundamental knowledge of biological systems and exploit them for useful applications. In order to contribute to this efforts, the work presented in this dissertation focuses on the study of electrokinetic properties of liposomes and novel applications of bioaerosol analysis. Using immobilized lipid vesicles under the influence of modest (less than 100 V/cm) electric fields, a novel strategy for bionanotubule fabrication with superior throughput and simplicity was developed. Fluorescence and bright field microscopy was used to describe the formation of these bilayer-bound cylindrical structures, which have been previously identified in nature (playing crucial roles in intercellular communication) and made synthetically by direct mechanical manipulation of membranes. In the biological context, the results of this work suggest that mechanical electrostatic interaction may play a role in the shape and function of individual biological membranes and networks of membrane-bound structures. A second project involving liposomes focused on membrane potential measurements in vesicles containing trans-membrane pH gradients. These types of gradients consist of differential charge states in the lipid bilayer leaflets, which have been shown to greatly influence the efficacy of drug targeting and the treatment of diseases such as cancer. Here, these systems are qualitatively and quantitatively assessed by using voltage-sensitive membrane dyes and fluorescence spectroscopy. Bioaerosol studies involved exploring the feasibility of a fingerprinting technology based on current understanding of cellular debris in aerosols and arguments regarding sampling, sensitivity, separations and detection schemes of these debris. Aerosolized particles of cellular material and proteins emitted by humans, animals and plants can be considered information-rich packets that carry biochemical information specific to the living organisms present in the collection settings. These materials could potentially be exploited for identification purposes. Preliminary studies evaluated protein concentration trends in both indoor and outdoor locations. Results indicated that concentrations correlate to certain conditions of the collection environment (e.g. extent of human presence), supporting the idea that bioaerosol fingerprinting is possible.
ContributorsCastillo Gutiérrez, Josemar Andreina (Author) / Hayes, Mark A. (Thesis advisor) / Herckes, Pierre (Committee member) / Ghrilanda, Giovanna (Committee member) / Arizona State University (Publisher)
Created2011
Description
This study investigated the difference in biofilm growth between pristine polypropylene microplastics and aged polypropylene microplastics. The microplastics were added to Tempe Town Lake water for 4 weeks. Each week the microplastic biofilms were quantified. Comparing the total biofilm counts, the results showed that the aged microplastic biofilms were larger than the pristine each week. By week 3 the aged microplastic counts had almost doubled in size increasing from 324 to 626 Colony Forming Units per gram in just one week. There was a significant difference in the diversity found from week 1 to week 4. About 40% of the diversity for the pristine microplastic biofilm was seen as light-yellow dots and about 60% of these dots were seen on the aged microplastic biofilms in both weeks. As the microplastics were submerged in the lake water, new phenotypes emerged varying from week 1 to week 4 and from pristine to aged microplastic biofilms. Generally, it was found that as the microplastics stay in the environment there is more biofilm on the particles. The aged microplastics have a larger amount of biofouling, and the pristine microplastic biofilms were found to have more diversity of phenotypes.
ContributorsMushro, Noelle Sararose (Author) / Perreault, Francois (Thesis director) / Jay, Oswald (Committee member) / Civil, Environmental and Sustainable Eng Program (Contributor) / School of Sustainable Engineering & Built Envirnmt (Contributor) / Barrett, The Honors College (Contributor)
Created2021-05
Description
Atmospheric particulate matter has a substantial impact on global climate due to its ability to absorb/scatter solar radiation and act as cloud condensation nuclei (CCN). Yet, little is known about marine aerosol, in particular, the carbonaceous fraction. In the present work, particulate matter was collected, using High Volume (HiVol) samplers, onto quartz fiber substrates during a series of research cruises on the Atlantic Ocean. Samples were collected on board the R/V Endeavor on West–East (March–April, 2006) and East–West (June–July, 2006) transects in the North Atlantic, as well as on the R/V Polarstern during a North–South (October–November, 2005) transect along the western coast of Europe and Africa. The aerosol total carbon (TC) concentrations for the West–East (Narragansett, RI, USA to Nice, France) and East–West (Heraklion, Crete, Greece to Narragansett, RI, USA) transects were generally low over the open ocean (0.36±0.14 μg C/m3) and increased as the ship approached coastal areas (2.18±1.37 μg C/m3), due to increased terrestrial/anthropogenic aerosol inputs. The TC for the North–South transect samples decreased in the southern hemisphere with the exception of samples collected near the 15th parallel where calculations indicate the air mass back trajectories originated from the continent. Seasonal variation in organic carbon (OC) was seen in the northern hemisphere open ocean samples with average values of 0.45 μg/m3 and 0.26 μg/m3 for spring and summer, respectively. These low summer time values are consistent with SeaWiFS satellite images that show decreasing chlorophyll a concentration (a proxy for phytoplankton biomass) in the summer. There is also a statistically significant (p<0.05) decline in surface water fluorescence in the summer. Moreover, examination of water–soluble organic carbon (WSOC) shows that the summer aerosol samples appear to have a higher fraction of the lower molecular weight material, indicating that the samples may be more oxidized (aged). The seasonal variation in aerosol content seen during the two 2006 cruises is evidence that a primary biological marine source is a significant contributor to the carbonaceous particulate in the marine atmosphere and is consistent with previous studies of clean marine air masses.
ContributorsHill, Hansina Rae (Author) / Herckes, Pierre (Thesis advisor) / Westerhoff, Paul (Committee member) / Hartnett, Hilairy (Committee member) / Arizona State University (Publisher)
Created2011
Description
Titanium dioxide (TiO2) nanomaterial use is becoming more prevalent as is the likelihood of human exposure and environmental release. The goal of this thesis is to develop analytical techniques to quantify the level of TiO2 in complex matrices to support environmental, health, and safety research of TiO2 nanomaterials. A pharmacokinetic model showed that the inhalation of TiO2 nanomaterials caused the highest amount to be absorbed and distributed throughout the body. Smaller nanomaterials (< 5nm) accumulated in the kidneys before clearance. Nanoparticles of 25 nm diameter accumulated in the liver and spleen and were cleared from the body slower than smaller nanomaterials. A digestion method using nitric acid, hydrofluoric acid, and hydrogen peroxide was found to digest organic materials and TiO2 with a recovery of >80%. The samples were measured by inductively coupled plasma-mass spectrometry (ICP-MS) and the method detection limit was 600 ng of Ti. An intratracheal instillation study of TiO2 nanomaterials in rats found anatase TiO2 nanoparticles in the caudal lung lobe of rats 1 day post instillation at a concentration of 1.2 ug/mg dry tissue, the highest deposition rate of any TiO2 nanomaterial. For all TiO2 nanomaterial morphologies the concentrations in the caudal lobes were significantly higher than those in the cranial lobes. In a study of TiO2 concentration in food products, white colored foods or foods with a hard outer shell had higher concentrations of TiO2. Hostess Powdered Donettes were found to have the highest Ti mass per serving with 200 mg Ti. As much as 3.8% of the total TiO2 mass was able to pass through a 0.45 um indicating that some of the TiO2 is likely nanosized. In a study of TiO2 concentrations in personal care products and paints, the concentration of TiO2 was as high as 117 ug/mg in Benjamin Moore white paint and 70 ug/mg in a Neutrogena sunscreen. Greater than 6% of Ti in one sunscreen was able to pass through a 0.45 um filter. The nanosized TiO2 in food products and personal care products may release as much as 16 mg of nanosized TiO2 per individual per day to wastewater.
ContributorsWeir, Alex Alan (Author) / Westerhoff, Paul K (Thesis advisor) / Hristovski, Kiril (Committee member) / Herckes, Pierre (Committee member) / Arizona State University (Publisher)
Created2011
Description
Black carbon (BC) is the product of incomplete combustion of biomass and fossil fuels. It is found ubiquitously in nature and is relevant to studies in atmospheric science, soil science, oceanography, and anthropology. Black carbon is best described using a combustion continuum that sub-classifies BC into slightly charred biomass, char, charcoal and soot. These sub-classifications range in particle size, formation temperature, and relative reactivity. Interest in BC has increased because of its role in the long-term storage of organic matter and the biogeochemistry of urban areas. The global BC budget is unbalanced. Production of BC greatly outweighs decomposition of BC. This suggests that there are unknown or underestimated BC removal processes, and it is likely that some of these processes are occurring in soils. However, little is known about BC reactivity in soil and especially in desert soil. This work focuses on soot BC, which is formed at higher temperatures and has a lower relative reactivity than other forms of BC. Here, I assess the contribution of soot BC to central AZ soils and use the isotopic composition of soot BC to identify sources of soot BC. Soot BC is a significant (31%) fraction of the soil organic matter in central AZ and this work suggests that desert and urban soils may be a storage reservoir for soot BC. I further identify previously unknown removal processes of soot BC found naturally in soil and demonstrate that soil soot BC undergoes abiotic (photo-oxidation) and biotic reactions. Not only is soot BC degraded by these processes, but its chemical composition is altered, suggesting that soot BC contains some chemical moieties that are more reactive than others. Because soot BC demonstrates both refractory and reactive character, it is likely that the structure of soot BC; therefore, its interactions in the environment are complex and it is not simply a recalcitrant material.
ContributorsHamilton, George (Author) / Hartnett, Hilairy E (Thesis advisor) / Herckes, Pierre (Committee member) / Hall, Sharon (Committee member) / Arizona State University (Publisher)
Created2013
Description
Contaminants of emerging concern (CECs) present in wastewater effluent can threat its safe discharge or reuse. Additional barriers of protection can be provided using advanced or natural treatment processes. This dissertation evaluated ozonation and constructed wetlands to remove CECs from wastewater effluent. Organic CECs can be removed by hydroxyl radical formed during ozonation, however estimating the ozone demand of wastewater effluent is complicated due to the presence of reduced inorganic species. A method was developed to estimate ozone consumption only by dissolved organic compounds and predict trace organic oxidation across multiple wastewater sources. Organic and engineered nanomaterial (ENM) CEC removal in constructed wetlands was investigated using batch experiments and continuous-flow microcosms containing decaying wetland plants. CEC removal varied depending on their physico-chemical properties, hydraulic residence time (HRT) and relative quantities of plant materials in the microcosms. At comparable HRTs, ENM removal improved with higher quantity of plant materials due to enhanced sorption which was verified in batch-scale studies with plant materials. A fate-predictive model was developed to evaluate the role of design loading rates on organic CEC removal. Areal removal rates increased with hydraulic loading rates (HLRs) and carbon loading rates (CLRs) unless photolysis was the dominant removal mechanism (e.g. atrazine). To optimize CEC removal, wetlands with different CLRs can be used in combination without lowering the net HLR. Organic CEC removal in denitrifying conditions of constructed wetlands was investigated and selected CECs (e.g. estradiol) were found to biotransform while denitrification occurred. Although level of denitrification was affected by HRT, similar impact on estradiol was not observed due to a dominant effect from plant biomass quantity. Overall, both modeling and experimental findings suggest considering CLR as an equally important factor with HRT or HLR to design constructed wetlands for CEC removal. This dissertation provided directions to select design parameters for ozonation (ozone dose) and constructed wetlands (design loading rates) to meet organic CEC removal goals. Future research is needed to understand fate of ENMs during ozonation and quantify the contributions from different transformation mechanisms occurring in the wetlands to incorporate in a model and evaluate the effect of wetland design.
ContributorsSharif, Fariya (Author) / Westerhoff, Paul (Thesis advisor) / Halden, Rolf (Committee member) / Fox, Peter (Committee member) / Herckes, Pierre (Committee member) / Arizona State University (Publisher)
Created2013
Description
In recent years, products advertised to contain nanosilver have become increasingly popular; however, while companies often advertise for nanosilver products, little regulation occurs to verify that these products actually contain silver nanoparticles. Furthermore, there currently exists much dispute regarding the safety and toxicity of silver nanoparticles. As more and more products incorporate nanosilver, the resolution of this dispute proves progressively important. The present study addressed these issues, with goals to synthesize silver nanoparticles, determine the solubility of the synthesized silver nanoparticles, and to evaluate leaching of nanosilver from commercially produced food storage containers. The silver nanoparticles were synthesized by a procedure devised by Leopold and Lendl, and subsequently evaluated for size and distribution by ICP-MS (Inductively Coupled Plasma Mass Spectrometry), SEC (Size Exclusion Chromatography), and DLS (Dynamic Light Scattering). The results indicated an average particle size of approximately 85 nm and a relatively monodispersed solution with a polydispersity value of 0.1245. The solubility of the nanoparticles was then examined using a dialysis experiment; however, the results of the dialysis experiments were inconclusive due to an aggregation that occurred which prevented the silver from diffusing out of the dialysis tubing. Lastly, commercially produced food storage containers advertised to contain silver nanoparticles were examined. These containers were digested using microwave assisted digestion, and subsequently analyzed using ICP-MS. It was determined that the containers contained between 7 .5 and 27 ug of silver per gram of container, and that the silver was not distributed uniformly throughout the container. While ICP-MS indicated the presence of silver, SEM (Scanning Electron Microscopy) failed to unambiguously identify silver nanoparticles in the container. The food storage containers were also examined for silver leaching under various conditions; it was found that the containers leached most greatly following exposure to an acidic solution and leached the least due to exposure to UV light. However, additional trials of the leaching experiments must be performed to validate the results obtained in these experiments.
ContributorsWilson, Amanda (Author) / Herckes, Pierre (Thesis director) / Westerhoff, Paul (Committee member) / McAllister, Chad (Committee member) / Barrett, The Honors College (Contributor)
Created2012-05
Description
-Please adjust the format of the abstract. m-3 should be typed as "m to the minus 3" with the "minus 3" in superscript
-see the additional "abstract.pdf" document for formatting
In arid environments like Phoenix, many professional and residential outdoor spaces are cooled by the use of misting systems. These systems spray a fine mist of water droplets that cool down the surrounding air through the endothermic evaporation process. When the water droplets evaporate, they leave behind dissolved material that is present in the water, generating ambient particulate matter (PM). Thus, misting systems are a point source of PM. Currently there is no information on their impact on air quality in close proximity to these systems, or on the chemical composition of the particulate matter generated by the evaporating mist.
In this project, PM concentrations are found to increase on average by a factor of 8 from ambient levels in the vicinity of a residential misting system in controlled experiments. PM concentrations in public places that use misting systems are also investigated. The PM10 concentrations in public places ranged from 0.102 ± 0.010 mg m-3 to 1.47 ± 0.15 mg m-3, and PM2.5 ranged from 0.095 ± 0.010 mg m-3 to 0.99 ± 0.10 mg m-3. Air quality index (AQI) values based on these concentrations indicate that these levels of PM range from unhealthy to hazardous in most cases. PM concentrations tend to decrease after remaining relatively constant with increasing distance from misting systems. Chemical data reveal that chloride and magnesium ions may be used as tracers of aerosolized water from misting systems. The average chloride concentration was 71 µg m-3 in misting samples and below the detection limit for Cl- (< 8.2 µg m-3) in ambient samples. The average magnesium concentration was 11.7 µg m-3 in misting samples and 0.23 µg m-3 in ambient samples.
-see the additional "abstract.pdf" document for formatting
In arid environments like Phoenix, many professional and residential outdoor spaces are cooled by the use of misting systems. These systems spray a fine mist of water droplets that cool down the surrounding air through the endothermic evaporation process. When the water droplets evaporate, they leave behind dissolved material that is present in the water, generating ambient particulate matter (PM). Thus, misting systems are a point source of PM. Currently there is no information on their impact on air quality in close proximity to these systems, or on the chemical composition of the particulate matter generated by the evaporating mist.
In this project, PM concentrations are found to increase on average by a factor of 8 from ambient levels in the vicinity of a residential misting system in controlled experiments. PM concentrations in public places that use misting systems are also investigated. The PM10 concentrations in public places ranged from 0.102 ± 0.010 mg m-3 to 1.47 ± 0.15 mg m-3, and PM2.5 ranged from 0.095 ± 0.010 mg m-3 to 0.99 ± 0.10 mg m-3. Air quality index (AQI) values based on these concentrations indicate that these levels of PM range from unhealthy to hazardous in most cases. PM concentrations tend to decrease after remaining relatively constant with increasing distance from misting systems. Chemical data reveal that chloride and magnesium ions may be used as tracers of aerosolized water from misting systems. The average chloride concentration was 71 µg m-3 in misting samples and below the detection limit for Cl- (< 8.2 µg m-3) in ambient samples. The average magnesium concentration was 11.7 µg m-3 in misting samples and 0.23 µg m-3 in ambient samples.
ContributorsKnight, William Louis (Co-author) / Knight, William (Co-author) / Herckes, Pierre (Thesis director) / Fraser, Matthew (Committee member) / Hamilton, Kerry (Committee member) / School of Sustainability (Contributor) / School of Molecular Sciences (Contributor) / Barrett, The Honors College (Contributor)
Created2020-05
Description
Cerebral lateralization describes the asymmetries between the two halves of the brain which results in side-specialized processing of certain functions. This phenomenon provides a selective advantage by promoting enhanced cognitive abilities. However, due to the plastic nature of lateralization, an individual’s lateralization is highly subject to change by many external factors, such as pollution, throughout its life. Additionally, lateralized regions are dependent on different contexts, so lateralized elements do not all experience the same effects. A common pollutant found worldwide is bisphenol-A (BPA), a critical component of many plastics. BPA is a known endocrine disruptor that can agonize and antagonize the functions of sex steroids. Other studies have demonstrated the importance of sex steroids in regulating the development of cerebral lateralization; BPA may similarly affect lateralization. A popular research animal for studying toxicology is the zebrafish. Its advantages include a fully sequenced genome, many human orthologs, and more importantly, expresses lateralized behaviors that are indicative of the strength of its cerebral lateralization. This experiment analyzed the effects of BPA exposure on visual lateralization of zebrafish. Given the role that sex steroids play in moderating lateralization, it was hypothesized that exposing zebrafish to BPA would diminish the strength of lateralization in the brain which would translate into reduced behavioral lateralization. To test this, one group was exposed to 0.01 mg/L BPA for one week and compared against a control group in their eye preference when approaching a visual cue. Two settings, a foraging context and a social context, were utilized to examine the scope of impairment in lateralization. The control group in both settings displayed similar strengths in behavioral lateralization with a left eye preference. However, the lateralized response faded completely with BPA treatment. This experiment demonstrates that BPA induces loss of lateralization and possesses similar impacts on mechanisms controlling investigatory behavior in these two contexts. Wild populations may encounter higher concentrations of BPA, and although there is greater variability in these exposures, this experiment proves that exposure even beyond critical periods of development can impair lateralization. Additional research will have to be conducted to identify the effects of BPA on other lateralized behaviors and sensory modalities to pinpoint the exact mechanisms through which BPA influences lateralization.
ContributorsHuang, Alexander (Author) / Martins, Emilia (Thesis director) / Suriyampola, Piyumika (Committee member) / Conroy-Ben, Otakuye (Committee member) / School of Life Sciences (Contributor) / School of Molecular Sciences (Contributor) / Dean, W.P. Carey School of Business (Contributor) / Barrett, The Honors College (Contributor)
Created2020-05
Description
To successfully launch and maintain a long-term colony on Mars, Martian agricultural systems need to be capable of sustaining human life without requiring expensive deliveries from Earth. There is a need for more studies on this topic to make this a feasible mission. This thesis aims to study from a high level one such agricultural system, specifically examining the requirements and flow of Nitrogen, Phosphorus and Potassium required to sustain a given human colony size. We developed a Microsoft Excel based model that relates human nutritional needs to the amount available in food crops and in turn the amount of Martian soil required for agriculture. The model works by inputting the number of humans, and then utilizing the built-in calculations and datasets to determine how much of each nutrient is needed to meet all nutritional needs of the colony. Using that information, it calculates the amount of plants needed to supply the nutrition and then calculates the amount of nutrients that would be taken from the soil. It compares the Martian regolith to the nutrient uptake, accounting for inedible biomass from the plants and human waste that can be added to the regolith. Any deficiencies are used to determine if and how much fertilizer should be added to the system initially and over time. Using the total amount of plants and the number of harvests, the amount of Martian land required for sustaining the colony is computed. These results can be used as a building block to enable the successful design of an agricultural system on Mars.
ContributorsGarland, Michael (Co-author) / Zinke, Sarah (Co-author) / Muenich, Rebecca (Thesis director) / Perreault, Francois (Committee member) / Mechanical and Aerospace Engineering Program (Contributor) / Barrett, The Honors College (Contributor)
Created2020-05