| 1. |
- Kutscher, Liselott, 1976-
(författare)
-
Export and sources of organic carbon in the Lena River basin, Northeastern Siberia
- 2016
-
Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Permafrost areas are considered to be one of the largest terrestrial storages of carbon. In a warming climate these areas are expected to experience changes in carbon transport to rivers and the oceans due to permafrost thawing, which could enhance erosion, change water flow pathways and increase greenhouse gas emissions. Large amounts of the carbon transported from the terrestrial environment to rivers are in the form of natural organic matter (NOM). The Lena River basin in northeastern Siberia, which is mainly underlain by continuous permafrost, is the largest contributor of NOM to the Arctic Ocean. In this study we present a spatial data set of NOM, including concentrations and stable carbon isotope values (δ13C) of dissolved (DOC) and particulate organic carbon (POC) as well as carbon and nitrogen ratios (C/N) from 77 sample stations in the Lena River and its tributaries. The samples were collected during two field seasons in July 2012 and June 2013.The results from this study showed large spatial variations in concentrations, annual export and fluxes of organic carbon. These variations were primarily due to variations in discharge and topography. The δ13C and C/N indicated that terrestrial sources such as plants and soil organic matter (SOM), were the main sources of the dissolved organic matter (DOM), while particulate organic matter (POM) was mainly derived from aquatic produced material or SOM. There were clear differences in δ13C and C/N of DOM between sampling years, indicating more surficial flow pathways in samples collected earlier in the summer compared to samples collected later in the summer. The δ13C of POM was correlated with water temperatures and topography, showing that tributaries with origin in mountainous areas in general had soil derived POM and lower water temperatures, while tributaries from lowland areas had higher water temperatures and more influence of aquatic sources. We suggest that this pattern is probably due to differences in water flow pathways. Shifts in export of NOM from drainage areas underlain by permafrost will likely be dependent of spatial changes in hydroclimate and the depth of the active layer in a warming climate.
|
|
| 2. |
- Kokic, Jovana, 1987-
(författare)
-
Gas Exchange over Aquatic Interfaces and its Importance for Greenhouse Gas Emission
- 2017
-
Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Aquatic ecosystems play a substantial role in global cycling of carbon (C), despite covering only about 4% of the earth surface. They emit large amounts of greenhouse gases (GHG) to the atmosphere, comparable to the amount of C stored annually in terrestrial ecosystems. In addition, C can be buried in lake sediments. Headwater systems are located at the interface of the terrestrial and aquatic environment, and are first in line to process terrestrial C and throughout its journey through the aquatic continuum. The uncertainties in global estimates of aquatic GHG emissions are largely related to these headwater systems, as they are highly variable in time and space, and underrepresented in global assessments. The overall aim of this thesis was therefore to study GHG exchange between sediment, water and air in headwater systems, from both an ecosystem perspective and at the small scale of physical drivers of gas exchange.This thesis demonstrates that carbon dioxide (CO2) emission from headwater systems, especially streams, was the main pathway of C loss from surface waters from a lake catchment. Of the total aquatic CO2-emission of the catchment, 65% originated from stream systems that covered only 0.1% of the total catchment area. The gas transfer velocity (k) was the main driver of stream CO2-emission, but there was a high variability in k on small spatial scales (meters). This variability may have implications for upscaling GHG emissions, especially when using scaled k estimates. Lake sediments only contributed 16% to total lake C emission, but in reality, sediment C emission is probably even lower because experimentally determined sediment C flux returns high estimates that are biased since artificially induced turbulence enhances C flux rates beyond in-situ conditions. When sediment C flux is estimated in-situ, in natural bottom water turbulence conditions, flux rates were lower than those estimated experimentally.Conclusively, this thesis shows that GHG emissions from small aquatic ecosystems are dominant over other aquatic C fluxes and that our current knowledge regarding the physical processes controlling gas exchange from different small aquatic systems is limited, implying an inherent uncertainty of GHG emission estimates from small aquatic ecosystems.
|
|
