Mahsa Haei

Efficient aquatic bacterial metabolism of dissolved low-molecular-weight compounds from terrestrial sources.

Carboxylic acids (CAs), amino acids (AAs) and carbohydrates (CHs) in dissolved free forms can be readily assimilated by aquatic bacteria and metabolized at high growth efficiencies. Previous studies have shown that these low-molecular-weight (LMW) substrates are released by phytoplankton but also that unidentified LMW compounds of terrestrial origin is a subsidy for bacterial metabolism in unproductive freshwater systems. We tested the hypothesis that different terrestrially derived CA, AA and CH compounds can offer substantial support for aquatic bacterial metabolism in fresh waters that are dominated by allochthonous dissolved organic matter (DOM). Drainage water from three catchments of different characters in the Krycklan experimental area in Northern Sweden were studied at the rising and falling limb of the spring flood, using a 2-week bioassay approach. A variety of CA, AA and CH compounds were significantly assimilated by bacteria, meeting 15–100% of the bacterial carbon demand and explaining most of the observed variation in bacterial growth efficiency (BGE; R2=0.66). Of the 29 chemical species that was detected, acetate was the most important, representing 45% of the total bacterial consumption of all LMW compounds. We suggest that LMW organic compounds in boreal spring flood drainage could potentially support all in situ bacterial production in receiving lake waters during periods of weeks to months after the spring flood.

Cold winter soils enhance dissolved organic carbon concentrations in soil and stream water

Concentrations of dissolved organic carbon ([DOC]) have increased in lakes, streams and rivers across a large part of the northern hemisphere and raised an animated scientific debate about the unde ...

Temperature response of litter and soil organic matter decomposition is determined by chemical composition of organic material

The global soil carbon pool is approximately three times larger than the contemporary atmospheric pool, therefore even minor changes to its integrity may have major implications for atmospheric CO2 concentrations. While theory predicts that the chemical composition of organic matter should constitute a master control on the temperature response of its decomposition, this relationship has not yet been fully demonstrated. We used laboratory incubations of forest soil organic matter (SOM) and fresh litter material together with NMR spectroscopy to make this connection between organic chemical composition and temperature sensitivity of decomposition. Temperature response of decomposition in both fresh litter and SOM was directly related to the chemical composition of the constituent organic matter, explaining 90% and 70% of the variance in Q10 in litter and SOM, respectively. The Q10 of litter decreased with increasing proportions of aromatic and O-aromatic compounds, and increased with increased contents of alkyl- and O-alkyl carbons. In contrast, in SOM, decomposition was affected only by carbonyl compounds. To reveal why a certain group of organic chemical compounds affected the temperature sensitivity of organic matter decomposition in litter and SOM, a more detailed characterization of the (13) C aromatic region using Heteronuclear Single Quantum Coherence (HSQC) was conducted. The results revealed considerable differences in the aromatic region between litter and SOM. This suggests that the correlation between chemical composition of organic matter and the temperature response of decomposition differed between litter and SOM. The temperature response of soil decomposition processes can thus be described by the chemical composition of its constituent organic matter, this paves the way for improved ecosystem modeling of biosphere feedbacks under a changing climate.

Winter climate controls soil carbon dynamics during summer in boreal forests

Boreal forests, characterized by distinct winter seasons, store a large proportion of the global terrestrial carbon (C) pool. We studied summer soil C-dynamics in a boreal forest in northern Sweden using a seven-year experimental manipulation of soil frost. We found that winter soil climate conditions play a major role in controlling the dissolution/mineralization of soil organic-C in the following summer season. Intensified soil frost led to significantly higher concentrations of dissolved organic carbon (DOC). Intensified soil frost also led to higher rates of basal heterotrophic CO2 production in surface soil samples. However, frost-induced decline in the in situ soil CO2 concentrations in summer suggests a substantial decline in root and/or plant associated rhizosphere CO2 production, which overrides the effects of increased heterotrophic CO2 production. Thus, colder winter soils, as a result of reduced snow cover, can substantially alter C-dynamics in boreal forests by reducing summer soil CO2 efflux, and increasing DOC losses.

Microbial mineralization of cellulose in frozen soils

High-latitude soils store ~40% of the global soil carbon and experience winters of up to 6 months or more. The winter soil CO2 efflux importantly contributes to the annual CO2 budget. Microorganisms can metabolize short chain carbon compounds in frozen soils. However, soil organic matter (SOM) is dominated by biopolymers, requiring exoenzymatic hydrolysis prior to mineralization. For winter SOM decomposition to have a substantial influence on soil carbon balances it is crucial whether or not biopolymers can be metabolized in frozen soils. We added 13C-labeled cellulose to frozen (−4 °C) mesocosms of boreal forest soil and followed its decomposition. Here we show that cellulose biopolymers are hydrolyzed under frozen conditions sustaining both CO2 production and microbial growth contributing to slow, but persistent, SOM mineralization. Given the long periods with frozen soils at high latitudes these findings are essential for understanding the contribution from winter to the global carbon balance.High latitude soils can store around 40 % of the Earth’s soil carbon. Here, the authors add 13C-labeled cellulose to frozen mesocosms of boreal forest soils and find that cellulose biopolymers are hydrolysed under frozen conditions and therefore contribute to the slow degradation of soil organic matter.