Rapid methods to determine potentially mineralizable nitrogen in broiler litter

Although broiler (chicken, Gallus gallus domesticus) litter has long been used as a fertilizer, estimating the rate required to supply a desired amount of plant-available N is still hampered by the lack of rapid methods to estimate potentially mineralizable nitrogen (PMN). Previous research has suggested that near infrared reflectance spectroscopy (NIRS) and certain poultry litter characteristics, such as water-soluble organic nitrogen (WSON), may be useful for estimating PMN. The objectives of this study were to evaluate NIRS and WSON as tools to estimate PMN in broiler litter. Sixty sieved (2 mm) and freeze-dried broiler litter samples were mixed with Cowarts sandy loam soil (fine-loamy, kaolinitic, thermic Typic Kanhapludult) and incubated at 25 degrees C for 112 d. Cumulative net N mineralized with time was fitted to a single-pool exponential model to determine PMN for each broiler litter sample. The PMN values obtained were regressed against NIRS (780 to 2500 nm) and WSON measurements. We found strong relationships between measured- and NIRS-predicted PMN (R2 = 0.82), and between measured PMN and WSON (R2 = 0.87). These results demonstrate the feasibility of using either of these two methods to estimate PMN in broiler litter. Future work should further test both methods for their ability to estimate mineralizable N in whole, moist broiler litter under field conditions.     

Aluminum effect on dissolution and precipitation under hyperalkaline conditions: II. Solid phase transformations

The high-level radioactive, Al-rich, concentrated alkaline and saline waste fluids stored in underground tanks have accidentally leaked into the vadose zone at the Hanford Site in Washington State. In addition to dissolution, precipitation is likely to occur when these waste fluids contact the sediments. The objective of this study was to investigate the solid phase transformations caused by dissolution and precipitation in the sediments treated with solutions similar to the waste fluids. Batch experiments at 323 K were conducted in metal- and glass-free systems under CO2 and O2 free conditions. Results from X-ray diffraction (XRD), quantitative X-ray diffraction (QXRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and energy dispersive X-ray fluorescence spectroscopy (EDXRF) indicated that significant solid phase transformations occurred in the sediments contacted with Al-rich, hyperalkaline, and saline solutions. The XRD and QXRD analyses confirmed that smectite and most likely biotite underwent dissolution. The SEM and the qualitative EDS analyses confirmed the formation of alumino-silicates in the groups of cancrinite and probably sodalite. The morphology of the alumino-silicates secondary phases changed in response to changes in the Si/Al aqueous molar ratio. The transformations in the sediments triggered by dissolution (weathering of soil minerals) and precipitation (formation of secondary phases with high specific surface area and probably high sorption capacities) may play a significant role in the immobilization and ultimate fate of radionuclides and contaminants such as Cs, Sr, and U in the Hanford vadose zone.     

Aluminum effect on dissolution and precipitation under hyperalkaline conditions: I. Liquid phase transformations

Substantial amounts of self-boiling, Al-rich, hyperalkaline, and saline high-level waste fluids (HLWF) were deposited to the vadose zone at the Hanford Site, in Washington State. The objective of this study was to investigate the effects of similar fluids on the extent of dissolution and precipitation in the sediments. Metal- and glass-free systems were used to conduct batch experiments at 323 K under CO2 and O2 free conditions. Base-induced dissolution of the soil minerals was rapid in the first 48 h as indicated by immediate releases of Si and Fe into the soil solution. Potassium release lagged behind and dissolution of K-bearing minerals (mica and K-feldspar) proceeded faster only after 2 to 3 d of the experiment. Silicon and Fe release exhibited high dependence on aqueous [Al] (rate orders <-1), because Al decreased free OH concentration in the contact solution and probably inhibited soil mineral dissolution. Initial K release exhibited low dependence on [Al] (fractional rate orders). Initial dissolution rates calculated based on Si release varied with aqueous [Al] from 29.47 to 4.35 x 10(-12) mol m(-2) s(-1). Aluminum participated in the formation of the secondary phases (precipitation rates of 10(-8) mol s(-1)) but the overall precipitation rate of alumino-silicate secondary phases was probably controlled by aqueous [Si] (rates of 10(-9), and rate constants between 0.0054 and 0.0084 h(-1)). The changes in the soil solution chemistry (release of K, Si, Fe, and other elements) may play a significant role in the fate of radionuclides and contaminants like Cs, Sr, Cr, and U in the Hanford sediments.