Abstract. Biogenic volatile organic compounds (BVOCs) play an important role in the chemistry of the troposphere, especially in the formation of tropospheric ozone (O3) and secondary organic aerosols (SOA). Ecosystems produce and emit a large number of BVOCs. It is estimated on a global scale that approximately 90 % of annual BVOC emissions are from terrestrial sources. In this study, measurements of BVOCs were conducted at the Welgegund measurement station (South Africa), which is considered to be a regionally representative background site situated in savannah grasslands. Very few BVOC measurements exist for savannah grasslands and results presented in this study are the most extensive for this type of landscape. Samples were collected twice a week for 2 h during the daytime and 2 h during the night-time through two long-term sampling campaigns from February 2011 to February 2012 and from December 2013 to February 2015, respectively. Individual BVOCs were identified and quantified using a thermal desorption instrument, which was connected to a gas chromatograph and a mass selective detector. The annual median concentrations of isoprene, 2-methyl-3-butene-2-ol (MBO), monoterpene and sesquiterpene (SQT) during the first campaign were 14, 7, 120 and 8 pptv, respectively, and 14, 4, 83 and 4 pptv, respectively, during the second campaign. The sum of the concentrations of the monoterpenes were at least an order of magnitude higher than the concentrations of other BVOC species during both sampling campaigns, with α-pinene being the most abundant species. The highest BVOC concentrations were observed during the wet season and elevated soil moisture was associated with increased BVOC concentrations. However, comparisons with measurements conducted at other landscapes in southern Africa and the rest of the world that have more woody vegetation indicated that BVOC concentrations were, in general, significantly lower for savannah grasslands. Furthermore, BVOC concentrations were an order of magnitude lower compared to total aromatic concentrations measured at Welgegund. An analysis of concentrations by wind direction indicated that isoprene concentrations were higher from the western sector that is considered to be a relatively clean regional background region with no large anthropogenic point sources, while wind direction did not indicate any significant differences in the concentrations of the other BVOC species. Statistical analysis indicated that soil moisture had the most significant impact on atmospheric levels of MBO, monoterpene and SQT concentrations, whereas temperature had the greatest influence on isoprene levels. The combined O3 formation potentials of all the BVOCs measured calculated with maximum incremental reactivity (MIR) coefficients during the first and second campaign were 1162 and 1022 pptv, respectively. α-Pinene and limonene had the highest reaction rates with O3, whereas isoprene exhibited relatively small contributions to O3 depletion. Limonene, α-pinene and terpinolene had the largest contributions to the OH reactivity of BVOCs measured at Welgegund for all of the months during both sampling campaigns.

Abstract. Tropical savannas and grasslands are estimated to contribute significantly to the total primary production of all terrestrial vegetation. Large parts of African savannas and grasslands are used for agriculture and cattle grazing, but the carbon flux data available from these areas are limited. This study explores carbon dioxide fluxes measured with the eddy covariance method for 3 years at a grazed savanna grassland in Welgegund, South Africa. The tree cover around the measurement site, grazed by cattle and sheep, was around 15 %. The night-time respiration was not significantly dependent on either soil moisture or soil temperature on a weekly temporal scale, whereas on an annual timescale higher respiration rates were observed when soil temperatures were higher. The carbon dioxide balances of the years 2010-2011, 2011-2012 and 2012-2013 were −85 ± 16, 67 ± 20 and 139 ± 13 gC m −2 yr −1 , respectively. The yearly variation was largely determined by the changes in the early wet season fluxes (September to November) and in the mid-growing season fluxes (December to January). Early rainfall enhanced the respiratory capacity of the ecosystem throughout the year, whereas during the mid-growing season high rainfall resulted in high carbon uptake.

Abstract. Field measurement data on greenhouse gas (GHG) emissions are still scarce for many land-use types in Africa, causing a high level of uncertainty in GHG budgets. To address this gap, we present in situ measurements of carbon dioxide (CO2), nitrous oxide (N2O), and methane (CH4) emissions from the lowlands of southern Kenya. We conducted eight chamber measurement campaigns on gas exchange from four dominant land-use types (LUTs) comprising (1) cropland, (2) bushland, (3) grazing land, and (4) conservation land between 29 November 2017 and 3 November 2018, accounting for regional seasonality (wet and dry seasons and transitions periods). Mean CO2 emissions for the whole observation period were the highest by a significant margin (p value < 0.05) in the conservation land (75±6 mg CO2-C m−2 h−1) compared to the three other sites, which ranged from 45±4 mg CO2-C m−2 h−1 (bushland) to 50±5 mg CO2-C m−2 h−1 (grazing land). Furthermore, CO2 emissions varied between seasons, with significantly higher emissions in the wet season than the dry season. Mean N2O emissions were highest in cropland (2.7±0.6 µg N2O-N m−2 h−1) and lowest in bushland (1.2±0.4  µg N2O-N m−2 h−1) but did not vary with season. In fact, N2O emissions were very low both in the wet and dry seasons, with slightly elevated values during the early days of the wet seasons in all LUTs. On the other hand, CH4 emissions did not show any significant differences across LUTs and seasons. Most CH4 fluxes were below the limit of detection (LOD, ±0.03 mg CH4-C m−2 h−1). We attributed the difference in soil CO2 emissions between the four sites to soil C content, which differed between the sites and was highest in the conservation land. In addition, CO2 and N2O emissions positively correlated with soil moisture, thus an increase in soil moisture led to an increase in emissions. Furthermore, vegetation cover explained the seasonal variation in soil CO2 emissions as depicted by a strong positive correlation between the normalized difference vegetation index (NDVI) and CO2 emissions, most likely because, with more green (active) vegetation cover, higher CO2 emissions occur due to enhanced root respiration compared to drier periods. Soil temperature did not show a clear correlation with either CO2 or N2O emissions, which is likely due to the low variability in soil temperature between seasons and sites. Based on our results, soil C, active vegetation cover, and soil moisture are key drivers of soil GHG emissions in all the tested LUTs in southern Kenya. Our results are within the range of previous GHG flux measurements from soils from various LUTs in other parts of Kenya and contribute to more accurate baseline GHG emission estimates from Africa, which are key to reducing uncertainties in global GHG budgets as well as for informing policymakers when discussing low-emission development strategies.

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