Silburn B, Kröger S, Parker E R, Sivyer D B, Hicks N, Powell C F, Johnson M, Greenwood N
1Centre for Environment Fisheries and Aquaculture Science, Pakefield Road, Lowestoft, Suffolk NR33 0HT UK.
Scottish Marine Institute, Oban, Argyll PA37 1QA UK.
Biogeochemistry. 2017;135(1):69-88. doi: 10.1007/s10533-017-0323-z. Epub 2017 Mar 31.
This study used microelectrodes to record pH profiles in fresh shelf sea sediment cores collected across a range of different sediment types within the Celtic Sea. Spatial and temporal variability was captured during repeated measurements in 2014 and 2015. Concurrently recorded oxygen microelectrode profiles and other sedimentary parameters provide a detailed context for interpretation of the pH data. Clear differences in profiles were observed between sediment type, location and season. Notably, very steep pH gradients exist within the surface sediments (10-20 mm), where decreases greater than 0.5 pH units were observed. Steep gradients were particularly apparent in fine cohesive sediments, less so in permeable sandier matrices. We hypothesise that the gradients are likely caused by aerobic organic matter respiration close to the sediment-water interface or oxidation of reduced species at the base of the oxic zone (NH , Mn, Fe, S). Statistical analysis suggests the variability in the depth of the pH minima is controlled spatially by the oxygen penetration depth, and seasonally by the input and remineralisation of deposited organic phytodetritus. Below the pH minima the observed pH remained consistently low to maximum electrode penetration (ca. 60 mm), indicating an absence of sub-oxic processes generating H or balanced removal processes within this layer. Thus, a climatology of sediment surface porewater pH is provided against which to examine biogeochemical processes. This enhances our understanding of benthic pH processes, particularly in the context of human impacts, seabed integrity, and future climate changes, providing vital information for modelling benthic response under future climate scenarios.
本研究使用微电极记录了在凯尔特海采集的一系列不同类型新鲜陆架海沉积物岩芯中的pH值分布。在2014年和2015年的多次测量中捕捉到了空间和时间变异性。同时记录的氧微电极分布和其他沉积参数为解释pH值数据提供了详细背景。在沉积物类型、位置和季节之间观察到了分布的明显差异。值得注意的是,在表层沉积物(10 - 20毫米)内存在非常陡峭的pH值梯度,其中观察到pH值下降超过0.5个单位。陡峭的梯度在细粒粘性沉积物中尤为明显,在渗透性更强的砂质基质中则不太明显。我们推测这些梯度可能是由靠近沉积物 - 水界面的好氧有机物呼吸作用或在氧化层底部(NH、Mn、Fe、S)还原物种的氧化作用引起的。统计分析表明,pH最小值深度的变异性在空间上受氧渗透深度控制,在季节上受沉积有机植物碎屑的输入和再矿化作用控制。在pH最小值以下,观察到的pH值在电极最大穿透深度(约60毫米)范围内一直保持较低水平,表明该层不存在产生H的亚氧化过程或平衡的去除过程。因此,提供了沉积物表面孔隙水pH值的气候学数据,可据此研究生物地球化学过程。这增强了我们对底栖pH值过程的理解,特别是在人类影响、海床完整性和未来气候变化的背景下,为模拟未来气候情景下的底栖响应提供了重要信息。