The role of isotopic techniques on the evaluation of the agronomic effectiveness of P fertilizers

Many isotopic techniques can be applied to determine the relative immediate and residual effectiveness of P fertilizers. Using isotopes as tracers, the percentage of utilization by plants of the P derived from a fertilizer can be determined. However this is only possible during the three or four months after the application. Therefore, the P fertilizers may be classified only according to their relative immediate effectiveness. To also evaluate residual effect, which can be observed when more P is applied than is removed with harvest, isotopes of phosphorus can be used. This residual effect is determined by comparing pool sizes of bioavailable soil P in soils with and without P fertilizer aged in soil. The bioavailable soil P pool may be analyzed according to three isotopic experimental procedures which give access to either the A value, or the E value or the L value. The aims, the similarities and the differences between these three procedures, are examined. Some of the theoretical and practical constraints of each method are described in this paper; they must be followed in order to obtain reliable information for agronomic purposes. A method involves measuring the rate of isotopic exchange of phosphate ions in soil-solution systems maintained in steady-state. It is now possible to predict the effectiveness of P fertilizers, whatever their chemical form when this method is applied on soil samples where P fertilizers were applied.This paper was originally submitted as part of the special issue on Evaluation of the Agronomic Effectiveness of Phosphate Fertilizers through the use of Nuclear Related Techniques edited by F. Zapata     

Enhancement by SO2 of initial activity for selective catalytic reduction of NO with CH3OH over \gamma-alumina

The effect of SO₂ on catalytic activity for NO reduction to N₂ by methanol in excess oxygen over $\gamma$ -alumina has been investigated. SCR activity increased initially upon exposure of a fresh $\gamma$ -alumina catalyst to SO₂ which is attributed to formation of Brønsted acid sites. Longer exposure to SO₂ leads to a decline in catalytic activity to a lower steady-state NO_x reduction activity which is independent of the SO₂ content in the feed gas.     

Mineral nutrition of slash pine in subtropical Australia. II. foliar nutrient response to fertilization

In the previous paper, we reported the stand growth of slash pine (Pinus elliottii) during the first 11.5 years of plantation in response to (1) initial fertilization at plantation establishment with P rates of 11, 22, 45 and 90 kg P ha^–1 which were either banded or broadcast in the presence or absence of basal fertilizers containing 50 kg N ha^–1, 50 kg K ha^–1 and 5 kg Cu ha^–1 and (2) application of additional 40 kg P ha^–1 at age 10 years. Here we present the responses in foliar nutrient concentrations of slash pine in the first 11.5 years to the initial fertilization and the additional P applied at age 10 years.Foliar N and K concentrations in the first 9.6 years of plantation decreased with the initial P rate. Application of the basal fertilizers improved foliar Cu concentration. Foliar Ca and Mg concentrations increased linearly with the initial P rate. The initial fertilization did not affect foliar Mn concentration in the first 9.6 years. Foliar P concentration increased quadratically with the initial P rate, which accounted for 77–86% of the variation in foliar P concentration. Most of the explained variation in foliar nutrient concentrations was attributable to the plantation age except for foliar P concentration. In the case of foliar P concentration, 53% was explained by the initial P rate, 31% by the plantation age and 2% by the positive interaction between the initial P rate and the plantation age. Foliar P concentration of slash pine at age 11.5 years increased quadratically with the initial P rate and linearly with the additional 40 kg P ha^–1 applied at age 10 years, accounting for 81% of the variation in the foliar P concentration. Foliar nutrient analysis indicated that P was the major limiting nutrient affecting the stand growth of slash pine in the first 11.5 years.     

化学镀Ni-Cu-P添加剂的研究

通过对化学镀Ni-Cu-P合金的稳定剂、表面活性剂、光亮剂对镀层性能及镀液稳定性的影响研究，得出最佳实验配方。     

Phosphorus seed coating increases phosphorus uptake,early growth and yield of pearl millet (Pennisetum glaucum (L.) R. Br.) grown on an acid sandy soil in Niger,West Africa

In pot and field experiments conducted in 1990 and 1991 on an acid sandy, phosphorus (P) deficient soil in Niger, West Africa, the effect of seed coating on seedling emergence, early growth and grain yield of pearl millet (Pennisetum glaucum (L.) R. Br.) was studied. Seeds of pearl millet were coated with different rates (0; 0.5; 1.0; 2.0; 5.0; 10.0 mg P seed^–1) and types of P fertilizers (single superphosphate, ammonium dihydrogen phosphate; monocalcium phosphate, sodium dihydrogen phosphate and sodium triphosphate). Seedling emergence was generally reduced at coating rates higher than 0.5 mg P seed^–1 and prevented with single superphosphate and sodium triphosphate at rates higher than 5 mg P seed^–1. No correlation was found between the pH and osmomolity of the coatings and final emergence of millet seedlings. The most favourable effect on plant growth and P content was achieved with ammonium dihydrogen phosphate (AHP) as seed coating. This was attributed to the enhancement effect of ammonium on P uptake. Compared to the untreated control dry matter production at 20 days after planting (DAP) was increased by 280%, P content per plant by 330%, total biomass at maturity by 30% and grain yield by 45%. Although seed coating with AHP may be harmful to seedlings emergence, it represents a suitable method to enhance early growth and increase yield of pearl millet.     

Peer-to-peer bichromatic reverse nearest neighbours in mobile ad-hoc networks

The increasing use of mobile communications has raised many issues of decision support and resource allocation. A crucial problem is how to solve queries of Reverse Nearest Neighbour (RNN). An RNN query returns all objects that consider the query object as their nearest neighbour. Existing methods mostly rely on a centralised base station. However, mobile P2P systems offer many benefits, including self-organisation, fault-tolerance and load-balancing. In this study, we propose and evaluate 3 distinct P2P algorithms focusing on bichromatic RNN queries, in which mobile query peers and static objects of interest are of two different categories, based on a time-out mechanism and a boundary polygon around the mobile query peers. The Brute-Force Search Algorithm provides a naive approach to exploit shared information among peers whereas two other Boundary Search Algorithms filter a number of peers involved in query processing. The algorithms are evaluated in the MiXiM simulation framework with both real and synthetic datasets. The results show the practical feasibility of the P2P approach for solving bichromatic RNN queries for mobile networks.     

Study of miscibility,crystallization, mechanical properties,and thermal stability of blends of poly(3‐hydroxybutyrate) and poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate)

Natural amorphous polymer poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) (P3HB4HB) containing 41 mol % of 4HB was blended with poly(3‐hydroxybutyrate) (PHB) with an aim to improve the properties of PHB. The influence of P3HB4HB contents on thermal and mechanical properties of the blends was evaluated with differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, stress–strain measurement and thermo gravimetric analyzer. Miscibility of PHB/P3HB4HB blends was mainly decided by the contents of P3HB4HB. When P3HB4HB exceeded 50 wt %, the two polymer phases separated and showed immiscibility. The addition of P3HB4HB did not alter the crystallinity of PHB, yet it diluted the PHB crystalline phase as revealed by DSC studies. DSC and FTIR results showed that the overall crystallinity of the blends decreased remarkably with increasing of P3HB4HB contents. Decreased glass transition temperature and crystallinity imparted desired flexibility for the blends. The ductility of the blends increased progressively with increasing of P3HB4HB content. Thus, the PHB mechanical properties can be modulated by changing the blend composition. P3HB4HB did not significantly improve the thermal stability of PHB, yet it is possible to melt process PHB without much molecular weights loss via blending it with suitable amounts of P3HB4HB. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Nucleation of isolated PO4 units on CeO2 driven by high temperatures and the effect on its oxygen storage and release properties

The chemical nature of P-containing species of varying concentration present in CeO₂ after impregnation with (NH₄)₂HPO₄ and calcination at 1273 K, and their effects on the oxygen storage and release (OSR) properties of ceria are reported for the first time. The samples were characterized by different techniques and the results were compared with those recently reported on the same samples but calcined at 873 K. When P-containing ceria solids were calcined at 1273 K, CePO₄ (monazite) was the predominant P-containing species on the surface of ceria, confirming previous studies that showed that monazite exists for those samples in which the surface P loading (P atoms per nm⁻²) is larger than 5.5. For lower surface P concentrations, isolated orthophosphate units are present at the surface and within the subsurface region of the solid. Severe sintering of CeO₂ after calcination at 1273 K resulted in P concentrations >5.5 P atoms·nm⁻² in all samples. Isolated PO₄ units that could initially be present in the samples calcined at 873 K nucleated and CePO₄ was formed when samples were calcined at 1273 K. OSR properties of CeO₂ deteriorated progressively when P loading increased due to the presence of larger crystals of the very stable Ce(III) phase of CePO₄ at the surface of the P-containing ceria solids.