N and C mineralization in soil amended with the N immobilization inhibitor, methionine sulphoximine

1995 ◽  
Vol 27 (3) ◽  
pp. 377-379 ◽  
Author(s):  
D.W. Hopkins ◽  
L. Anderson ◽  
S.E. Scott
2014 ◽  
Vol 37 (11) ◽  
pp. 988-997 ◽  
Author(s):  
Li XU ◽  
Shu-Xia YU ◽  
Nian-Peng HE ◽  
Xue-Fa WEN ◽  
Pei-Li SHI ◽  
...  

Author(s):  
Amir Sadeghpour ◽  
Oladapo Adeyemi ◽  
Dane Hunter ◽  
Yuan Luo ◽  
Shalamar Armstrong

Abstract Growing winter cereal rye (Secale cereale) (WCR) has been identified as an effective in-field practice to reduce nitrate-N and phosphorus (P) losses to Upper Mississippi River Basin, USA. In the Midwestern USA, growers are reluctant to plant WCR especially prior to corn (Zea mays L.) due to N immobilization and establishment issues. Precision planting of WCR or ‘skipping the corn row’ (STCR) can minimize some issues associated with WCR ahead of corn while reducing cover crop seed costs. The objective of this study was to compare the effectiveness of ‘STCR’ vs normal planting of WCR at full seeding rate (NP) on WCR biomass, nutrient uptake and composition in three site-yrs (ARC2019, ARC2020, BRC2020). Our results indicated no differences in cover crop dry matter biomass production between the STCR (2.40 Mg ha−1) and NP (2.41 Mg ha−1) supported by similar normalized difference vegetative index and plant height for both treatments. Phosphorus, potassium (K), calcium (Ca) and magnesium (Mg) accumulation in aboveground biomass was only influenced by site-yr and both STCR and NP removed similar amount of P, K, Ca and Mg indicating STCR could be as effective as NP in accumulating nutrients. Aboveground carbon (C) content (1086.26 kg h−1 average over the two treatments) was similar between the two treatments and only influenced by site-yr differences. Lignin, lignin:N and C:N ratios were higher in STCR than NP in one out of three site-yrs (ARC2019) indicating greater chance of N immobilization when WCR was planted later than usual. Implementing STCR saved $8.4 ha−1 for growers and could incentivize growers to adopt this practice. Future research should evaluate corn response to STCR compared with NP and assess if soil quality declines by STCR practice over time.


Agronomy ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 128
Author(s):  
Ruihuan She ◽  
Yongxiang Yu ◽  
Chaorong Ge ◽  
Huaiying Yao

Soil salinization typically inhibits the ability of decomposer organisms to utilize soil organic matter, and an increase in soil clay content can mediate the negative effect of salinity on carbon (C) mineralization. However, the interactive effects of soil salt concentrations and properties on C mineralization remain uncertain. In this study, a laboratory experiment was performed to investigate the interactive effects of soil salt content (0.1%, 0.3%, 0.6% and 1.0%) and texture (sandy loam, sandy clay loam and silty clay soil with 6.0%, 23.9% and 40.6% clay content, respectively) on C mineralization and microbial community composition after cotton straw addition. With increasing soil salinity, carbon dioxide (CO2) emissions from the three soils decreased, but the effect of soil salinity on the decomposition of soil organic carbon varied with soil texture. Cumulative CO2 emissions in the coarse-textured (sandy loam and sandy clay loam) soils were more affected by salinity than those in the fine-textured (silty clay) soil. This difference was probably due to the differing responses of labile and resistant organic compounds to salinity across different soil texture. Increased salinity decreased the decomposition of the stable C pool in the coarse-textured soil, by reducing the proportion of fungi to bacteria, whereas it decreased the mineralization of the active C pool in the fine-textured soil through decreasing the Gram-positive bacterial population. Overall, our results suggest that soil texture controlled the negative effect of salinity on C mineralization through regulating the soil microbial community composition.


Author(s):  
Chen-Chi Tsai ◽  
Yu-Fang Chang

In Taiwan, farmers often apply excess compost to ensure adequate crop yield in highly frequent tillage, highly weathered, and lower fertility soils. The potential of biochar (BC) for diminishing soil C mineralization, and improving soil nutrient availability in compost over-fertilized soil is promising, but the study is still under-examined. To test the hypothesis, 434 days in vitro C mineralization kinetics of incubation experiment were conducted. Woody BC 0%, 0.5%, 1.0% and 2.0% (w/w) made of lead tree (Leucaena leucocephala (Lam.) de. Wit) were added to an Oxisols, and two Inceptisols of Taiwan. In each treatment, 5% swine manure compost (2 times recommended amount) was added and served as the over-fertilized soil. The results indicated that soil type strongly influenced the impact of BC addition on soil carbon mineralization potential. Respiration per unit of total organic carbon (total mineralization coefficient, TMC) of three studied soils significantly decreased with BC addition increased. Principal component analysis (PCA) suggested that for retaining more plant nutrients in addition to the effects of carbon sequestration, it is recommended that farmer could use locally produced biochars and composts in highly weathered and highly frequent tillage soil. Adding 0.5%-1% woody BC in soil should be reasonable and appropriate.


1990 ◽  
Vol 70 (4) ◽  
pp. 555-564 ◽  
Author(s):  
SUZANNE BEAUCHEMIN ◽  
MARC R. LAVERDIÈRE ◽  
ADRIEN N'DAYEGAMIYE

Intensive potato cropping has been reported as a major cause of degradation of sandy soils. Wood residues from tree clipping applied to soils can substitute for crop residues to maintain adequate organic matter levels and crop productivity. However, this ligneous material presents a C:N ratio varying from 50 to 175 and, when applied in large quantities, may induce N immobilization at the expense of the crop. The objectives of this study were to quantify the importance of this N immobilization following addition of residues and its effect on yield and quality of potato crops. Fresh or humified residues (50 t ha−1) were applied to the soil and incorporated. The third treatment received no residue. Each treatment was subdivided into subtreatments which received either 0, 150, 200 or 250 kg N ha−1. P, K, Mg and S were applied at the same rate on all treatments. Following the application of wood residues in 1987, 46 kg N ha−1 were immobilized in amended plots. N recovery from fertilizer was 51%. To obtain comparable yields of similar quality to those measured on unamended plots, an additional 1.9 kg N t−1 residues added or 100 kg N ha−1 were required. In 1988, N immobilization was considerably reduced; yield and quality of potato tubers in plots that received wood residues the previous year were comparable to those of the unamended plots with appropriate fertilization. Water retention was significantly improved in plots that received wood residues. Partial decomposition of the residues for 1 yr prior to application on the soil did not significantly improve plant growth compared to fresh residues. Key words: Wood residues, tree clippings, potato yield, dry matter content, nitrogen immobilization, soil water content


Author(s):  
Gwenaëlle Lashermes ◽  
Sylvie Recous ◽  
Gonzague Alavoine ◽  
Baldur Janz ◽  
Klaus Butterbach-Bahl ◽  
...  

2021 ◽  
Author(s):  
Meng Na ◽  
Mingyue Yuan ◽  
Lettice Hicks ◽  
Johannes Rousk

<p>Soil organic matter (SOM) stabilization plays an important role in the long-term storage of carbon (C). However, many ecosystems are undergoing climate change, which will change the soil C balance via altered plant communities and productivity that change C inputs, and altered C losses via changes in SOM decomposition. The ongoing change of aboveground plant communities in the Subarctic (“greening”) will increase rhizosphere inputs containing low molecular weight organic substances (LMWOS), which will likely affect C-starved microbial decomposers and their subsequent contribution to SOM mineralization (priming effect).In the present study, we simulated the effects of climate change with N fertilization (simulating warming enhanced nutrient cycling) and litter additions (simulating arctic greening) in Abisko, Sweden. The 6 sampled field-treatments included a full factorial combination of 3-years of chronic N addition and litter additions, as well as, a single year of extreme climate change (3x N fertilizer or litter additions in one growth season). We found that N treatments changed plant community composition and productivityand that the associated shift in belowground LMWOS induced shifts in the soil microbial community. In the chronic N fertilization treatments, plant productivity, and therefore belowground LMWOS input, increased. This coincided with a tendency for more bacterial dominated decomposition (lower fungi/bacterial growth ratio). However, N treatments had no effect on soil C mineralization, but increased gross N mineralization.</p><p>These responses in belowground communities and processes driven by rhizosphere input prompted the next question: how does simulated climate change affect the susceptibility of SOM to priming by LMWOS? To assess this question and determine the microbial mechanisms underpinning priming of SOM mineralization, we added a factorial set of additions including <sup>13</sup>C-glucose with and without mineral N, and <sup>13</sup>C-alanine semi-continuously (every 48 hours) to simulate the effect of rhizosphere LMWOS on SOM mineralization and microbial activity. We incubated these samples for 2 weeks and assessed the priming of soil C and gross N mineralization, bacterial and fungal growth rates, PLFAs, enzyme activities, and microbial C use efficiency (CUE). We found that alanine addition primed soil C mineralization by 34%, which was higher than soil C priming induced by glucose and glucose with N. Furthermore, glucose primed fungal growth, whereas the alanine primed bacterial growth, but microbial PLFAs did not respond to either treatment. The C enzyme acquisition activity was higher than N enzyme acquisition activity in all the treatments, while P enzyme acquisition activity was higher than C for all the treatments. Surprisingly, this suggested a chronic microbial limitation by P, which was unaffected by field and lab treatments. LMWOS additions generally reduced microbial CUE. Responses of microbial mineralization of N from SOM to LMWOS suggested a directed microbial effort towards targeting resources that limited bacterial or fungal growth, suggesting that microbial SOM-use shifted to N-rich components (selective microbial “N-mining”), in contrast with enzyme results. Surprisingly, alanine primed the highest N mineralization compared other additions indicating that there was strong N-mining even if N was sufficient.</p>


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