Extractability of 15N-labeled corn-shoot tissue in a sandy and a clay soil by 0.01 MCaCl2 method in laboratory incubation experiments

1996 ◽  
Vol 22 (1-2) ◽  
pp. 109-115 ◽  
Author(s):  
Diedrich Steffens ◽  
Roland Pfanschilling ◽  
Sala Feigenbaum
2011 ◽  
Vol 31 (5) ◽  
pp. 978-986 ◽  
Author(s):  
Tarek Abichou ◽  
Koenraad Mahieu ◽  
Jeff Chanton ◽  
Mehrez Romdhane ◽  
Imane Mansouri

1979 ◽  
Vol 19 (101) ◽  
pp. 739 ◽  
Author(s):  
RE Reid ◽  
SA Waring

Two laboratory incubation experiments were carried out to investigate the relation between soil water, Eh 7, nitrification and denitrification and to examine the relation between pH and nitrification. Samples were incubated for 16 days under aerobic and waterlogged conditions with 50 mg N kg-1 of added nitrate or ammonium. Apparent denitrification on waterlogging was rapid with 50% of nitrate disappearing in three days, but the presence of more than 7 mg N kg-1 as nitrate prevented Eh, falling below 270 mV. An initial wetting to 0.1 bar tension after drying and grinding caused apparent denitrification but a subsequent wetting to the same tension did not. If high nitrate levels occurred in the field, denitrification losses would be important. Net mineralization and nitrification were independent of soil water in the range 2 to 30% gravimetric. Samples of a pasture soil of initial pH about 4.2 were incubated aerobically with added ammonium and increasing amounts of K2CO3 to increase pH. Nitrate production increased with increasing pH and the relation between pH and nitrate production changed between pH 5.0 and 5.1. Denitrification losses from ammonium-containing fertilizers on waterlogging will be reduced if low pH has inhibited nitrification.


2020 ◽  
Author(s):  
Yang Ding ◽  
Maria Heiling ◽  
Mohammad Zaman ◽  
Christian Resch ◽  
Gerd Dercon ◽  
...  

<p>Accurate measurements of nitrous oxide (N<sub>2</sub>O) fluxes from soils are necessary to understand dynamic changes in soil nitrogen cycles. Laboratory incubation experiments provide a controlled condition to measure these N<sub>2</sub>O fluxes. Before incubation experiments, soils are often stored at certain conditions to minimize the microbial activities. However, the effect of soil storage on N<sub>2</sub>O emission has been poorly studied. A laboratory incubation experiment was conducted using disturbed soils to study the storage effect. The soil was sieved to 2mm and the following four treatments were tested: fresh undisturbed (FU), fresh sieved (FS), fridge stored at 4ºC (ST), and stored at room temperature after drying (PI). After soil samples were brought to 60% water-filled pore space (WFPS), <sup>15</sup>N labelled urea (1 At%) was applied at the rate of 50 mg N kg<sup>-1</sup> soil and the soil was incubated at room temperature (23 ºC). The N<sub>2</sub>O fluxes were measured for 7 weeks using off-axis integrated cavity output spectroscopy (OA-ICOS, Los Gatos Research, California, USA). Cumulative N<sub>2</sub>O fluxes and Keeling plot intercepts (δ<sup>15</sup>N source) were calculated. The results showed that soil storage has a significant effect on N<sub>2</sub>O emission. Over the 7-week period, ST produced the highest cumulative N<sub>2</sub>O emissions (2.70 µg N g<sup>-1</sup> soil) as well as the largest amount of N derived from fertiliser (Ndff) (1.4 µg N g<sup>-1</sup> soil). FU produced the lowest cumulative N<sub>2</sub>O emissions (1.0 µg N g<sup>-1</sup> soil) but the largest amount of N derived from soil (Ndfs) (0.6 µg N g<sup>-1</sup> soil). The daily N<sub>2</sub>O fluxes of FS and FU declined rapidly after the peak emissions, but the fluxes of PI and ST fluctuated after the peaks. These results indicate that soil storage affects microbial processes and therefore N<sub>2</sub>O emissions. Our results suggest using fresh soil to avoid storage effects. If this is not possible the effect of soil storage should be considered before the experiment.  </p>


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