Production of dissolved organic carbon and low-molecular weight organic acids in soil solution driven by recent tree photosynthate

2007 ◽  
Vol 84 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Reiner Giesler ◽  
Mona N. Högberg ◽  
Bjarne W. Strobel ◽  
Andreas Richter ◽  
Anders Nordgren ◽  
...  
1998 ◽  
Vol 17 (6) ◽  
pp. 975-981 ◽  
Author(s):  
Cathleen J. Hapeman ◽  
Susanna Bilboulian ◽  
Brent G. Anderson ◽  
Alba Torrents

2013 ◽  
Vol 93 (3) ◽  
pp. 295-304 ◽  
Author(s):  
Kazumichi Fujii ◽  
Kokoro Morioka ◽  
Ryan Hangs ◽  
Shinya Funakawa ◽  
Takashi Kosaki ◽  
...  

Fujii, K., Morioka, K., Hangs, R., Funakawa, S., Kosaki, and Anderson, D. W. 2013. Rapid turnover of organic acids in a Dystric Brunisol under a spruce–lichen forest in northern Saskatchewan, Canada. Can. J. Soil Sci. 93: 295–304. Organic acids released by lichen play an important role in mineral weathering and podzolization in the Boreal–Tundra transition zone of Canada; however, importance of low-molecular-weight organic acids in the soil carbon (C) cycle in the black spruce–lichen forests remains unclear. We examined soil solution composition and mineralization kinetics of 14C-radiolabelled oxalate and citrate to quantify the C fluxes from organic acid mineralization in a Dystric Brunisol under a spruce–lichen forest in northern Saskatchewan. Oxalate concentration in soil solution was greatest in the lichen layer, while the high levels of citrate were observed in the lichen and organic (O) layers to the Ae horizon with the lowest sorption capacity. Oxalate and citrate were rapidly mineralized within the lichen and O layers and had short mean residence times (0.5 to 2.7 h). Substantial C fluxes due to citrate mineralization were observed both within the lichen and O layers, but oxalate mineralization led to C flux in the lichen layer only. The contribution of citrate and oxalate to microbial respiration was large (up to 57%) in the surface soil layers. Citrate was the dominant substrate for microbial respiration of the surface soil; however, it appears that oxalate could also be an important microbial substrate within the lichen layer, at least in summer months. We conclude that the exudation of low-molecular-weight organic acids by lichenous fungi, followed by their rapid mineralization, could play an important role in the C cycles of the sandy soils under spruce–lichen forest.


Talanta ◽  
1999 ◽  
Vol 48 (1) ◽  
pp. 173-179 ◽  
Author(s):  
P VANHEES ◽  
J DAHLEN ◽  
U LUNDSTROM ◽  
H BOREN ◽  
B ALLARD

2011 ◽  
Vol 77 (8) ◽  
pp. 2791-2795 ◽  
Author(s):  
Johannes Rousk ◽  
Philip C. Brookes ◽  
Helen C. Glanville ◽  
David L. Jones

ABSTRACTWe studied how soil pH (pHs 4 to 8) influenced the mineralization of low-molecular-weight (LMW)-dissolved organic carbon (DOC) compounds, and how this compared with differences in microbial community structure. The mineralization of LMW-DOC compounds was not systematically connected to differences in soil pH, consistent with soil respiration. In contrast, the microbial community compositions differed dramatically. This suggests that microbial community composition data will be of limited use in improving the predictive power of soil C models.


2016 ◽  
Vol 13 (12) ◽  
pp. 3833-3846 ◽  
Author(s):  
Emily C. O'Donnell ◽  
Jemma L. Wadham ◽  
Grzegorz P. Lis ◽  
Martyn Tranter ◽  
Amy E. Pickard ◽  
...  

Abstract. Determining the concentration and composition of dissolved organic carbon (DOC) in glacial ecosystems is important for assessments of in situ microbial activity and contributions to wider biogeochemical cycles. Nonetheless, there is limited knowledge of the abundance and character of DOC in basal ice and the subglacial environment and a lack of quantitative data on low-molecular-weight (LMW) DOC components, which are believed to be highly bioavailable to microorganisms. We investigated the abundance and composition of DOC in basal ice via a molecular-level DOC analysis. Spectrofluorometry and a novel ion chromatographic method, which has been little utilized in glacial science for LMW-DOC determinations, were employed to identify and quantify the major LMW fractions (free amino acids, carbohydrates, and carboxylic acids) in basal ice from four glaciers, each with a different type of overridden material (i.e. the pre-entrainment sedimentary type such as lacustrine material or palaeosols). Basal ice from Joyce Glacier (Antarctica) was unique in that 98 % of the LMW-DOC was derived from the extremely diverse free amino acid (FAA) pool, comprising 14 FAAs. LMW-DOC concentrations in basal ice were dependent on the bioavailability of the overridden organic carbon (OC), which in turn was influenced by the type of overridden material. Mean LMW-DOC concentrations in basal ice from Russell Glacier (Greenland), Finsterwalderbreen (Svalbard), and Engabreen (Norway) were low (0–417 nM C), attributed to the relatively refractory nature of the OC in the overridden palaeosols and bedrock. In contrast, mean LMW-DOC concentrations were an order of magnitude higher (4430 nM C) in basal ice from Joyce Glacier, a reflection of the high bioavailability of the overridden lacustrine material (> 17 % of the sediment OC comprised extractable carbohydrates, a proxy for bioavailable OC). We find that the overridden material may act as a direct (via abiotic leaching) and indirect (via microbial cycling) source of DOC to the subglacial environment and provides a range of LMW-DOC compounds that may stimulate microbial activity in wet subglacial sediments.


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