Evaluation of denitrification from three biogeochemical models using laboratory measurements of N2, N2O and CO2

B. Grosz, R. Well, R. Dechow, J. Köster, M. Khalil, S. Merl, A. Rode, B. Ziehmer, A. Matson, Hongxing He
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Abstract

Abstract. Biogeochemical models are useful for the prediction of nitrogen (N) cycling processes, but accurate description of the denitrification and decomposition sub-modules is critical. Current models were developed before suitable soil N2 flux data were available; new measurement techniques have enabled the collection of improved N2 data. We use measured data from two laboratory incubations to test the denitrification sub-modules of existing biogeochemical models. Two arable soils – a silt-loam and a sand – were incubated for 34 and 58 days, respectively. Fluxes of N2, N2O and CO2 were quantified using gas chromatography and isotope-ratio mass spectrometry (IRMS). For the loamy soil, seven moisture and three NO3− contents were included, with temperature changing during the incubation. The sandy soil was incubated with and without incorporation of litter (ryegrass), with temperature, water content and NO3− content changing during the incubation. Three common biogeochemical models (Coup, DNDC and DeNi) were tested using the data. No systematic calibration of the model parameters was conducted since our intention was to evaluate the general model structure or “default” model runs. As compared with measured fluxes, the average N2+N2O fluxes of the default runs for loamy soil were approximately 3 times higher for Deni, 105 times smaller for DNDC and 22 times smaller for Coup. For the sandy soils, default runs were 3 times higher for DeNi, 7 times smaller for DNDC and 12 times smaller for Coup. While measured fluxes were overestimated by DeNi and underestimated by DNDC and Coup, the temporal patterns of the measured and the modeled emissions were similar for the different treatments. None of the models was able to determine litter-induced decomposition correctly. The reason for the differences between the measured and modeled values can be traced back to model structure uncertainty and/or parameter uncertainty. Given the aim of our work – to assess existing model processes for further development and/or to identify missing processes within the models – these results provide valuable insights into avenues for future research. We conclude that the predicting power of the models could be improved through future experiments that collect data on denitrification activity with a concurrent focus on control parameter determination.
利用实验室测量N2、N2O和CO2,评价三种生物地球化学模型的反硝化作用
摘要生物地球化学模型可用于预测氮循环过程,但准确描述脱氮和分解子模块至关重要。目前的模型是在获得合适的土壤N2通量数据之前开发的;新的测量技术使得能够收集改进的N2数据。我们使用两个实验室培养的测量数据来测试现有生物地球化学模型的反硝化子模块。两种可耕种的土壤——一种粉壤土和一种沙子——分别培育34天和58天。使用气相色谱法和同位素比质谱法(IRMS)对N2、N2O和CO2的通量进行定量。对于壤土,随着培养过程中温度的变化,包括7种水分和3种NO3−含量。在沙质土壤中加入和不加入凋落物(黑麦草),培养过程中温度、含水量和NO3−含量发生变化。使用这些数据测试了三种常见的生物地球化学模型(Coup、DNDC和DeNi)。由于我们的目的是评估一般模型结构或“默认”模型运行,因此没有对模型参数进行系统校准。与测得的通量相比,泥质土壤默认运行的平均N2+N2O通量Deni约高出3倍,DNDC约低105倍,Coup约低22倍。对于沙质土壤,DeNi的默认运行量高出3倍,DNDC的默认运行数低出7倍,Coup的默认运行率低出12倍。虽然DeNi高估了测量的通量,而DNDC和Coup低估了测量的流量,但不同处理的测量排放和模拟排放的时间模式相似。没有一个模型能够正确地确定枯枝落叶引起的分解。测量值和建模值之间存在差异的原因可以追溯到模型结构的不确定性和/或参数的不确定性。鉴于我们工作的目的——评估现有的模型过程以供进一步开发和/或识别模型中缺失的过程——这些结果为未来的研究提供了宝贵的见解。我们得出的结论是,通过未来收集反硝化活性数据的实验,同时关注控制参数的确定,可以提高模型的预测能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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