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Inference of riverine nitrogen processing from longitudinal and diel variation in dual nitrate isotopes

机译:从双重硝酸盐同位素的纵向和双向变化推断河流氮处理

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摘要

Longitudinal and diel measurements of dual isotope composition (δN and δO) in nitrate (NO-N) were made in the Ichetucknee River, a large (∼8m s ), entirely spring-fed river in North Florida, to determine whether isotopic variation can deconvolve assimilatory and dissimilatory removal. Comparing nitrate concentrations and isotope composition during the day and night we predicted (1) daytime declines in total fractionation due to low assimilatory fractionation and (2) diurnal variation in dual isotope coupling between 1:1 (assimilation) and 2:1 (denitrification). Five daytime longitudinal transects comprising 10 sampling stations showed consistent NO-N removal (25-35% of inputs) and modest fractionation (ε between -2 and -6‰, enriching the residual nitrate pool). Lower fractionation (by ∼1‰) during two nighttime transects, suggests higher fractionation due to assimilation than denitrification. Total fractionation was significantly negatively associated with discharge, input [NO-N], N mass removal, and fractional water loss. Despite well-constrained mass balance estimates that denitrification dominated total N removal, isotope coupling was consistently 1:1, both for longitudinal and diel sampling. Hourly samples on two dates at the downstream location showed significant diel variation in concentration ([NO-N] amplitude = 60 to 90 μg N L) and isotope composition (δN amplitude = -0.7‰ to -1.6‰). Total fractionation differed between day and night only on one date but estimated assimilatory fractionation assuming constant denitrification was highly variable and implausibly large (for N, ε = -2 to -25‰), suggesting that fractionation and removal due to denitrification is not diurnally constant. Pronounced counterclockwise hysteresis in the relationship between [NO-N] and δN suggests diel variation in N isotope dynamics. Together, low fractionation, isotope versus concentration hysteresis, and consistent 1:1 isotope coupling suggests that denitrification is controlled by NO diffusion into the benthic sediments, the length of which is mediated by riverine oxygen dynamics. While using dual isotope behavior to deconvolve removal pathways was not possible, isotope measurements did yield valuable information about riverine N cycling and transformations. Copyright © 2012 by the American Geophysical Union.
机译:在北佛罗里达州的一条春季大河(约8m s),完全由春季补给的Ichetucknee河中,对硝酸盐(NO-N)中的双同位素组成(δN和δO)进行了纵向和狄尔测量,以确定同位素变化是否可以解卷积同化和异化去除。比较白天和晚上的硝酸盐浓度和同位素组成,我们预测(1)由于同化率低而导致总分馏率白天下降,以及(2)1:1(同化)和2:1(脱氮)之间的双同位素耦合的昼夜变化。五个由10个采样站组成的日间纵向样线显示出始终如一的NO-N去除率(输入量的25-35%)和适度的分馏率(ε在-2和-6‰之间,从而丰富了残留的硝酸盐池)。在两个夜间样带中较低的分馏率(约1‰)表明,由于同化作用,其分馏率要高于反硝化作用。总分馏与出水量,输入[NO-N],氮去除量和分数水分损失显着负相关。尽管对质量平衡的估计受到严格限制,但反硝化作用在总氮去除量中占优势,但对于纵向采样和Diel采样,同位素耦合始终为1:1。下游位置的两个日期的每小时样本显示浓度([NO-N]幅度= 60至90μgN L)和同位素组成(δN幅度= -0.7‰--1.6‰)有明显的狄尔变化。总分馏仅在一个日期的白天和晚上之间有所不同,但假设恒定反硝化作用高度可变且难以置信地大(对于N,ε= -2至-25‰),估计的同化分馏作用就表明,反硝化作用引起的分馏和去除不是昼夜恒定的。 [NO-N]与δN之间关系的明显逆时针磁滞表明N同位素动力学的diel变化。低分馏,同位素与浓度滞后以及一致的1:1同位素耦合共同表明,反硝化作用是由NO扩散到底栖沉积物中来控制的,底栖沉积物的长度由河流氧动力学介导。虽然不可能使用双重同位素行为对去除途径进行解卷积,但同位素测量确实能提供有关河流氮循环和转化的有价值的信息。版权所有©2012,美国地球物理联盟。

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