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Sediment flux modeling: Simulating nitrogen, phosphorus, and silica cycles

机译:泥沙通量建模:模拟氮,磷和二氧化硅的循环

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摘要

Sediment-water exchanges of nutrients and oxygen play an important role in the biogeochemistry of shallow coastal environments. Sediments process, store, and release particulate and dissolved forms of carbon and nutrients and sediment-water solute fluxes are significant components of nutrient, carbon, and oxygen cycles. Consequently, sediment biogeochemical models of varying complexity have been developed to understand the processes regulating porewater profiles and sediment-water exchanges. We have calibrated and validated a two-layer sediment biogeochemical model (aerobic and anaerobic) that is suitable for application as a stand-alone tool or coupled to water-column biogeochemical models. We calibrated and tested a stand-alone version of the model against observations of sediment-water flux, porewater concentrations, and process rates at 12 stations in Chesapeake Bay during a 4-17 year period. The model successfully reproduced sediment-water fluxes of ammonium (NH_4~+), nitrate (NO_3~-), phosphate (PO_4~(3-)), and dissolved silica (Si(OH)_4 or DSi) for diverse chemical and physical environments. A root mean square error (RMSE)-minimizing optimization routine was used to identify best-fit values for many kinetic parameters. The resulting simulations improved the performance of the model in Chesapeake Bay and revealed the need for an aerobic-layer denitrification formulation to account for NO_3~- reduction in this zone, regional variability in denitrification that depends on oxygen levels in the overlying water, a regionally-dependent solid-solute PO_4~(3-) partitioning that accounts for patterns in Fe availability, and a simplified model formulation for DSi, including limited sorption of DSi onto iron oxyhydroxides. This new calibration balances the need for a universal set of parameters that remain true to biogeochemical processes with site-specificity that represents differences in physical conditions. This standalone model can be rapidly executed on a personal computer and is well-suited to complement observational studies in a wide range of environments.
机译:营养物质和氧气的沉积物-水交换在浅海沿岸环境的生物地球化学中起着重要作用。沉积物处理,存储和释放碳和养分的颗粒状和溶解形式以及沉积物-水溶质通量是养分,碳和氧气循环的重要组成部分。因此,已开发出各种复杂程度的沉积物生物地球化学模型,以了解调节孔隙水分布和沉积物-水交换的过程。我们已经校准并验证了两层沉积物生物地球化学模型(好氧和厌氧),适合用作独立工具或与水柱生物地球化学模型耦合。我们针对切萨皮克湾4-17年内12个站点的沉积物水通量,孔隙水浓度和处理速率的观测值,对模型的独立版本进行了校准和测试。该模型成功地再现了铵(NH_4〜+),硝酸盐(NO_3〜-),磷酸盐(PO_4〜(3-))和溶解的二氧化硅(Si(OH)_4或DSi)的沉积物-水通量,用于多种化学和物理过程环境。最小均方根误差(RMSE)优化例程用于确定许多动力学参数的最佳拟合值。所得模拟结果改善了切萨皮克湾模型的性能,并揭示了需氧层反硝化配方以解决该区域NO_3〜-还原的问题,反硝化的区域性取决于上覆水中的氧气含量依赖的固溶质PO_4〜(3-)分区,这说明了铁的有效性模式,以及DSi的简化模型公式,包括DSi在羟基氧化铁上的有限吸附。这项新的校准方法平衡了对通用参数集的需求,这些参数对生物地球化学过程仍然适用,并具有代表物理条件差异的位点特异性。这种独立的模型可以在个人计算机上快速执行,非常适合在各种环境中补充观测研究。

著录项

  • 来源
    《Estuarine Coastal and Shelf Science》 |2013年第10期|245-263|共19页
  • 作者单位

    Horn Point Laboratory, University of Maryland Center for Environmental Science, 2020 Horns Point Rd., Cambridge, MD 21613, USA;

    School of Marine Sciences, University of Maine, 193 Clark Cove Road, Walpole, ME 04573, USA;

    Department of Civil and Environmental Engineering, University of Delaware, 356 DuPont Hall, Newark, DE 19716, USA;

    Chesapeake Biological Laboratory, University of Maryland Center for Environmental Science, P.O. Box 38, Solomons, MD 20688, USA;

    Horn Point Laboratory, University of Maryland Center for Environmental Science, 2020 Horns Point Rd., Cambridge, MD 21613, USA;

    Horn Point Laboratory, University of Maryland Center for Environmental Science, 2020 Horns Point Rd., Cambridge, MD 21613, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    sediment modeling; Chesapeake Bay; nitrogen; phosphorus; denitrification; silica;

    机译:泥沙模拟切萨皮克湾氮;磷;反硝化二氧化硅;

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