Unraveling the groundwater transit time control of permafrost derived dissolved organic carbon processing in a hillslope headwater watershed of Qinghai-Tibetan Plateau

Author(s):  
Yuqin Sun ◽  
Kale Clauson ◽  
Min Zhou ◽  
Ziyong Sun ◽  
Chunmiao Zheng ◽  
...  

<p>Climate warming leads to massive thaws of the northern permafrost that has increased the release of soil organic carbon (SOC) to streams and rivers partly as dissolved organic carbon (DOC). The transport pathways of SOC releasing into porewater and entering into stream are undergoing profound hydrological changes triggered by permafrost thawing, yet the role that the groundwater plays in processing the permafrost derived DOC is ambiguous. Unravelling how subsurface flow affects permafrost sourced DOC processing is important especially in alpine watersheds of high-altitude permafrost region with extensive surface – groundwater interaction. Here, eight types of water were sampled from a small (25 km<sup>2</sup>), alpine (elevation 2960 to 4820 m a.s.l) watershed named Hulugou watershed (HLGW) with variably degraded permafrost in the Qinghai-Tibetan Plateau (QTP) in July and September of 2012, 2013 and 2018. The three end-members (glacier-snow meltwater, precipitation, and frozen soil meltwater) analysis suggested contribution of frozen soil meltwater to all types of water with variable DOC levels (0.4 to 22.6 mg L<sup>-1</sup>, n = 113), as constrained by <em>δ</em><sup>18</sup>O and electrical conductivity (EC). Spatial patterns of DOC quantity and quality between stream and subsurface waters (groundwater, spring, and seepage-II) point to differences in surface – groundwater exchanges in the upper-, mid- and lower stretch of the watershed. To evaluate the extent of DOC loss (ΔDOC), ΔDOC is calculated using an initial DOC (DOC<sub>0</sub>) estimated from mixing of three endmembers, minus the measured DOC concentration. The significant correlations between ΔDOC with proportion of protein-like fluorophores (<em>r</em> = -0.69, <em>p</em> < 0.01) and relatively aromatic C levels (<em>r</em> = -0.62, <em>p</em> = 0.02) indicate ΔDOC corresponding to the extent of microbial utilization of DOC in subsurface environment. Using previously established DOC biodegradation kinetics of 0.25 d<sup>-1</sup> in headwaters of QTP, the mean transit time of groundwater is estimated to be 6 and 20 days based on changes in subsurface ΔDOC of 32% and 74% from the outlet of HLGW for July and September, respectively. The more rapid groundwater transit time corresponds to the higher concentration and more boilable DOC in July (3.5 mg L<sup>-1</sup>, protein-like: 98%) than in September (1.0 mg L<sup>-1</sup>, protein-like: 53±26%). Together with the mass balance of DOC input and export fluxes showing half loss of C in HLGW, our results indicate that rapid groundwater transit time is associated with permafrost derived DOC processing in alpine hillslope subject to warming.</p>

PLoS ONE ◽  
2017 ◽  
Vol 12 (7) ◽  
pp. e0181295 ◽  
Author(s):  
Bin Qu ◽  
Mika Sillanpää ◽  
Chaoliu Li ◽  
Shichang Kang ◽  
Aron Stubbins ◽  
...  

2015 ◽  
Vol 12 (23) ◽  
pp. 6915-6930 ◽  
Author(s):  
J. E. Vonk ◽  
S. E. Tank ◽  
P. J. Mann ◽  
R. G. M. Spencer ◽  
C. C. Treat ◽  
...  

Abstract. As Arctic regions warm and frozen soils thaw, the large organic carbon pool stored in permafrost becomes increasingly vulnerable to decomposition or transport. The transfer of newly mobilized carbon to the atmosphere and its potential influence upon climate change will largely depend on the degradability of carbon delivered to aquatic ecosystems. Dissolved organic carbon (DOC) is a key regulator of aquatic metabolism, yet knowledge of the mechanistic controls on DOC biodegradability is currently poor due to a scarcity of long-term data sets, limited spatial coverage of available data, and methodological diversity. Here, we performed parallel biodegradable DOC (BDOC) experiments at six Arctic sites (16 experiments) using a standardized incubation protocol to examine the effect of methodological differences commonly used in the literature. We also synthesized results from 14 aquatic and soil leachate BDOC studies from across the circum-arctic permafrost region to examine pan-arctic trends in BDOC. An increasing extent of permafrost across the landscape resulted in higher DOC losses in both soil and aquatic systems. We hypothesize that the unique composition of (yedoma) permafrost-derived DOC combined with limited prior microbial processing due to low soil temperature and relatively short flow path lengths and transport times, contributed to a higher overall terrestrial and freshwater DOC loss. Additionally, we found that the fraction of BDOC decreased moving down the fluvial network in continuous permafrost regions, i.e. from streams to large rivers, suggesting that highly biodegradable DOC is lost in headwater streams. We also observed a seasonal (January–December) decrease in BDOC in large streams and rivers, but saw no apparent change in smaller streams or soil leachates. We attribute this seasonal change to a combination of factors including shifts in carbon source, changing DOC residence time related to increasing thaw-depth, increasing water temperatures later in the summer, as well as decreasing hydrologic connectivity between soils and surface water as the thaw season progresses. Our results suggest that future climate warming-induced shifts of continuous permafrost into discontinuous permafrost regions could affect the degradation potential of thaw-released DOC, the amount of BDOC, as well as its variability throughout the Arctic summer. We lastly recommend a standardized BDOC protocol to facilitate the comparison of future work and improve our knowledge of processing and transport of DOC in a changing Arctic.


1981 ◽  
Vol 38 (1) ◽  
pp. 68-76 ◽  
Author(s):  
Clifford N. Dahm

Removal of dissolved organic carbon (DOC) from water resulting from adsorption and microbial uptake was examined to determine the importance of biotic and abiotic pathways. Physical–chemical adsorption to components of the stream sediment or water and biotic assimilation associated with the microbial population was determined in recirculating chambers utilizing leachate from alder (Alnus rubra). Adsorptive mechanisms were further separated into interactions involving (1) specific clay minerals, (2) amorphous solid phases of hydrous aluminum and iron oxides, and (3) fine particulate organic matter. Physical–chemical adsorptive mechanisms for alder leachate removal exhibited rapid kinetic equilibration between the DOC and solid phases, but only a specific fraction of the DOC, likely containing certain chemical functional groups, was adsorbed. The amorphous aluminum and iron oxides possessed a much higher potential capacity than the clay minerals or fine particulate organics for DOC adsorption. Microbial uptake of DOC from the alder leachate was kinetically slower than adsorptive uptake. However, microbial activity was overall much more effective in the removal and degradation of the total DOC pool leached from alder leaves. Over a 48-h period, 97% of added 14C labeled leachate was removed from solution by adsorption (~ 20%) and microbial utilization (~ 77%). The rate of microbial uptake was 45 μg C/g sediment C∙h−1 or 14 mg C∙m−2∙h−1.


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