Electricity generation from defective tomatoes.

The United States faces a significant burden in treating 0.61billionkg of defective tomatoes (culls) every year. We present a proof-of-concept for generating electricity from culled tomatoes in microbial-electrochemical systems (MESs). This study delineates impedance behavior of the culled tomatoes in MESs and compares its impedance spectra with that of soluble substrates (dextrose, acetate, and wastewater). A series of AC and DC diagnostic tests have revealed the superior performance of the culled tomatoes compared to the pure substrates. Cyclic voltammetry results have indicated the active role of indigenous, diffusible redox-active pigments in the culled tomatoes on overall electricity production. Electrochemical impedance spectroscopy results have elucidated the role of peel and seed on the oxidation behavior of the culled tomatoes.

Impacts of viability and purification on the specific gravity of Cryptosporidium oocysts.

The specific gravity of unpurified and purified Cryptosporidium oocysts was measured using an isopycnic gradient centrifugation technique. Specific gravity varied depending on the viability of the oocysts, as defined by permeabilty to 4',6-diamidino-2-phenylindole (DAPI) and propidium iodide (PI), the presence or absence of internal structures, and whether or not oocysts were purified. The modal range of densities for a population of 1.4-week-old unpurified oocysts, was 1070-1073 kg/m3. This range was higher than that determined for 14-week-old purified oocysts, 1067-1070 kg/m3. Eleven- and 12-week-old unpurified populations exhibited a bimodal distribution of densities, with densities most frequently in the 1005-1041 and in the 1077-1108 kg/m3 range. In these populations, a high percentage of the oocysts having densities greater than 1077 kg/m3 were viable, while oocysts in the 1005-1024 kg/m3 range were predominately nonintact, and oocysts in the 1024-1041 kg/m3 range were intact, but permeable to DAPI and PI (nonviable). This work demonstrates the importance of controlling factors that may impact the viability of oocysts when conducting studies that examine the transport of these microorganisms in the environment and through water treatment processes.

Settling behavior of unpurified Cryptosporidium oocysts in laboratory settling columns.

The settling behavior of fresh and aged unpurified oocysts was examined in settling column suspensions with varied ionic strengths and concentrations of calcium and magnesium. Independent measurements of the size and density of unpurified oocysts were performed to determine a theoretical settling velocity for the test populations. Viability of the oocysts was assessed using a dye permeability assay. Latex microspheres were included to provide a standard by which to assess the settling conditions in the columns. Mean settling velocities for viable oocysts measured in this work were faster than predicted and faster than measured for purified oocysts in other work: 1.31 (+/-0.21) microm/s for viable oocysts from populations having a low percentage of viable oocysts and 1.05 (+/-0.20) microm/s for viable oocysts from populations with a high percentage of viable oocysts. Results were attributed to the higher than previously reported densities measured for oocysts in this study and the presence of fecal material, which allowed opportunity for particle agglomeration. Settling velocity of oocysts was significantly related to the viability of the population, particle concentration, ionic strength, and presence of calcium and magnesium in the suspending medium. Behavior of the latex microspheres was not entirely predictive of the behavior of the oocysts under the test conditions. Viable oocysts may have a greater probability of settling than previously assumed; however, nonviable, and especially nonintact, oocysts have the potential to be significantly transported in water. This work underscores the importance of assessing the viability of oocysts to predict their response to environmental and experimental conditions.

Regulatory role of n-propanol in propylene glycol biomethanization under overload.

This work examines the transient response of an anaerobic fluidized bed bioreactor to an overload of propylene glycol (PG), the primary component in aircraft de-icing waste. Under favorable operating conditions, PG was converted to n-propanol (n-PrOH) and propionate (HPr), and subsequently n-PrOH was completely converted into HPr. HPr was then fully degraded to methane and carbon dioxide via acetate. Under an overload condition, n-PrOH conversion to propionate was completely blocked but propionate degradation continued, contrary to free-energy computations in which n-PrOH should rapidly degrade and HPr should accumulate. When the imposed overload condition was relieved, the accumulated n-PrOH was rapidly converted into propionate. n-PrOH, then, could act as a temporal sink for reducing equivalents (XH(2)) and could regulate the overall PG methanazation process. n-PrOH should be monitored along with typical VFAs such as HPr to avoid sudden VFA accumulation and thus to optimize process performance for PG methanization.