Application of Bayesian statistics to estimate nitrous oxide emission factors of three nitrogen fertilisers on UK grasslands.

Trapezoidal integration by linear interpolation of data points is by far the most commonly used method of cumulative flux calculations of nitrous oxide (N2O) in studies that use flux chambers; however, this method is incapable of providing accurate uncertainty estimates. A Bayesian approach was used to calculate N2O emission factors (EFs) and their associated uncertainties from flux chamber measurements made after the application of nitrogen fertilisers, in the form of ammonium nitrate (AN), urea (Ur) and urea treated with Agrotain® urease inhibitor (UI) at four grassland sites in the UK. The comparison between the cumulative fluxes estimated using the Bayesian and linear interpolation methods were broadly similar (R2 = 0.79); however, the Bayesian method was capable of providing realistic uncertainties when a limited number of data points is available. The study reports mean EF values (and 95% confidence intervals) of 0.60 ±â€¯0.63, 0.29 ±â€¯0.22 and 0.26 ±â€¯0.17% of applied N emitted as N2O for the AN, Ur and UI treatments, respectively. There was no significant difference between N2O emissions from the Ur and UI treatments. In the case of the automatic chamber data collected at one site in this study, the data did not fit the log-normal model, implying that more complex models may be needed, particularly for measurement data with high temporal resolution.

The fate of photosynthetically-fixed carbon in Lolium perenne grassland as modified by elevated CO2 and sward management.

Prediction of the impact of climate change requires the response of carbon (C) flow in plant-soil systems to increased CO(2) to be understood. A mechanism by which grassland C sequestration might be altered was investigated by pulse-labelling Lolium perenne swards, which had been subject to CO(2) enrichment and two levels of nitrogen (N) fertilization for 10 yr, with (14)CO(2). Over a 6-d period 40-80% of the (14)C pulse was exported from mature leaves, 1-2% remained in roots, 2-7% was lost as below-ground respiration, 0.1% was recovered in soil solution, and 0.2-1.5% in soil. Swards under elevated CO(2) with the lower N supply fixed more (14)C than swards grown in ambient CO(2), exported more fixed (14)C below ground and respired less than their high-N counterparts. Sward cutting reduced root (14)C, but plants in elevated CO(2) still retained 80% more (14)C below ground than those in ambient CO(2). The potential for below-ground C sequestration in grasslands is enhanced under elevated CO(2), but any increase is likely to be small and dependent upon grassland management.

Leaf age-related differences in apoplastic NH(4)(+) concentration, pH and the NH(3) compensation point for a wild perennial.

Extracts of the foliar apoplast of leaves of different ages of Luzula sylvatica (Huds.) Gaud. were prepared by vacuum infiltration and centrifugation. Measurements of pH and concentration were performed on extracts. From these bioassay measurements the relative magnitude of NH(3) compensation points for leaves of different ages were inferred. Young leaves were found to have much higher apoplast pH than old leaves, leading to the calculation of 4-10-fold higher NH(3) compensation points. Such age-related differences in the NH(3) compensation point are considerably larger than those previously reported. Apoplast pH and concentration were found to increase during leaf expansion before declining prior to senescence. Bulk foliar tissue pH, and total N concentrations were also found to be generally higher in young leaves than in old leaves. Where a significant correlation was found, total foliar N, bulk tissue foliar and the calculated NH(3) compensation point were all found to increase with N supplied to roots, whilst apoplast and bulk tissue H(+) concentrations were found to decline. The potential of bulk foliar tissue measurements to act as simple predictors of the NH(3) compensation point is discussed.

Comparison of gas exchange and bioassay determinations of the ammonia compensation point in Luzula sylvatica (Huds.) Gaud.

Determinations of the NH(3) compensation point for the understory plant of semi-natural woodlands Luzula sylvatica (Huds.) Gaud. were carried out by measurements of gas exchange and by calculation from the NH(4)(+) concentration and pH of extracts of the foliar apoplast. Compensation points determined by gas exchange measurements were among the lowest yet reported (0.51-1.10 microg NH(3) m(-3)) and those calculated from apoplast extracts were lower than any yet reported (0.017-0.54 microg NH(3) m(-3)). Those determined by gas exchange were consistently found to be between 2 and 30 times higher than those determined from apoplast extracts. Consideration of possible causes of this discrepancy, which is not confined to this investigation, showed that all likely errors would result in an increase in the discrepancy, or were insufficient to account for observed differences. It is suggested that spatial variability of pH and NH(4)(+) concentration within the foliar apoplast represents the most promising line for further investigation. It is also shown that the foliar apoplast of L. sylvatica is sufficiently buffered to eliminate the need for correction of H(+) concentration for dilution during extraction, but that it is necessary to correct the NH(4)(+) concentration of apoplast extracts for dilution.

Bioenergetics and end-product regulation of Clostridium thermosaccharolyticum in response to nutrient limitation.

Fermentation of xylose by Clostridium thermosaccharolyticum was studied in batch and continuous culture in which the limiting nutrient was either xylose, phosphate, or ammonia. Transient results obtained in continuous cultures with batch grown inoculum and progressively higher feed substrate concentrations exhibited ethanol selectivities (moles ethanol/moles other products) in excess of 11. The hypothesis that this high ethanol selectivity was a general response to mineral nutrient limitation was tested but could not be supported. Growth and substrate consumption were related by the equation q(s)(1 - Y(x) (c))G(ATP) = (mu/Y(ATP) (max)) + m, with q(s) the specific rate of xylose consumption (moles xylose/hour . g cells), Y(x) (c) the carbon based cell yield (g cell carbon/g substrate carbon), G(ATP) the ATP gain (moles ATP produces/mol substrate catabolized), micro the specific growth rate (1/h), Y(ATP) (max) the ATP-based cell yield (g cells/mol ATP), and m the maintenance coefficient (moles ATP/hour . g cells). Y(ATP) (max) was found to be 11.6 g cells/mol ATP, and m 9.3 mol ATP/hour . g cells for growth on defined medium. Different responses to nutrient limitation were observed depending on the mode of cultivation. Batch and immobilized cell continuous cultures decreased G(ATP) by initiating production of the secondary metabolites, propanediol, and in some cases, D-lactate; in addition, batch cultures increased the fractional allocation of ATP to maintenance and/or wastage. Nitrogen-limited continuous free-cell cultures maintained a constant cell yield, whereas phosphate-limited continuous free-cell cultures did not. In the case of phosphate limitation, the decreased ATP demand associated with the lowered cell yield was accompanied by an increased rate of ATP consumption for maintenance and/or wastage. Neither nitrogen or phosphorus-limited continuous free-cell cultures exhibited an altered G(ATP) in response to mineral nutrient limitation, and neither produced secondary metabolites.

Evaluation of a commercial radioisotopic kit for folate assays.

A commercial kit for the radioisotopic assay of folate in serum, the Bio-Rad 'Quanta Count' folate kit, produced lower results than the Lactobacillus casei microbiological assay method. Its normal range was 2-0-13-0 microng/l and the reproducibility was similar to that of the microbiological assay method. The kit was also satisfactory for whole bood folate assays. The cost requires careful consideration before the kit is used for routine purposes.