- Effects from climate change, adaptations and
greenhouse gas reduction at 2050

Abstract:

The sampling design in the all six Gi-FACE rings is standardised. Subplots 1-3 are used for weekly measurements of greenhouse gas fluxes and biannual biomass harvest. Subplots 4-25 are used for biannual biomass harvests and cover more or less the two species inventory subplots for biannual vegetations surveys. Subplots 24 and 25 have been used in 2013 for a 15N-13C Tracing study and in Subplot 25 the topsoil (7.5 cm) was used in 2014 for an incubation study and the soil was replaced by soil from outside the rings. Small circles within the ring area indicate Licor soil colomne for soil respiration measurements. The yellow rectangles mark the area where soil profiles have been opened in 2015 to install new soil moisture and temperature sensors. "Needles" and asterix mark positions where soil samples have been taken.

Abstract:

Overview of the model setup for the Giessen FACE grassland ecosystem, including preliminary simulation results for CO2 emissions and outlook.

Abstract:

Global warming is currently a much discussed topic with as yet largely unexplored consequences for agro-ecosystems. Little is known about the warming effect on the bacterial microbiota inhabiting the plant surface (phyllosphere), which can have a strong impact on plant growth and health, as well as on plant diseases and colonization by human pathogens. The aim of this study was to investigate the effect of moderate surface warming on the diversity and composition of the bacterial leaf microbiota of the herbaceous plant Galium album. Leaves were collected from four control and four surface warmed (+2°C) plots located at the field site of the Environmental Monitoring and Climate Impact Research Station Linden in Germany over a 6-year period. Warming had no effect on the concentration of total number of cells attached to the leaf surface as counted by Sybr Green I staining after detachment, but changes in the diversity and phylogenetic composition of the bacterial leaf microbiota analyzed by bacterial 16S rRNA gene Illumina amplicon sequencing were observed. The bacterial phyllosphere microbiota were dominated by Proteobacteria, Bacteroidetes, and Actinobacteria. Warming caused a significant higher relative abundance of members of the Gammaproteobacteria, Actinobacteria, and Firmicutes, and a lower relative abundance of members of the Alphaproteobacteria and Bacteroidetes. Plant beneficial bacteria like Sphingomonas spp. and Rhizobium spp. occurred in significantly lower relative abundance in leaf samples of warmed plots. In contrast, several members of the Enterobacteriaceae, especially Enterobacter and Erwinia, and other potential plant or human pathogenic genera such as Acinetobacter and insect-associated Buchnera and Wolbachia spp. occurred in higher relative abundances in the phyllosphere samples from warmed plots. This study showed for the first time the long-term impact of moderate (+2°C) surface warming on the phyllosphere microbiota on plants. A reduction of beneficial bacteria and an enhancement of potential pathogenic bacteria in the phyllosphere of plants may indicate that this aspect of the ecosystem which has been largely neglected up till now, can be a potential risk for pathogen transmission in agro-ecosystems in the near future.

Abstract:

Four yellow-pigmented, Gram-stain-negative, rod-shaped bacteria, strains PP-WC-4G-234T, PP-CE-2G-454T, PP-WC-1G-202 and PP-CC-3G-650, were isolated from the phyllosphere of Galium album. The strains shared 99.7–100?% 16S rRNA gene sequence similarity but could be differentiated by genomic fingerprinting using rep- and random amplification of polymorphic DNA PCRs. Phylogenetic analysis based on the 16S rRNA gene placed the strains within the family Aurantimonadaceae with highest 16S rRNA gene sequence similarity of 97.2–97.3?% to the type strain of Aureimonas phyllosphaerae. Sequence similarities to all other Aurantimonadaceae were below 97?%. The main cellular fatty acids of the strains were C18?:?1 ?7c as the predominant fatty acid followed by C16?:?0 and summed feature 3 (C16?:?1 ?7c/C16?:?1 ?8c). The polyamine patterns of strains PP-WC-4G-234T and PP-CE-2G-454T contained sym-homospermidine as a major compound, and the major respiratory quinone was ubiquinone Q-10. Predominant polar lipids were diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylmonomethylethanolamine, phosphatidylglycerol, phosphatidylcholine, sulfoquinovosyldiacylglycerol, three unidentified phospholipids and one unidentified lipid only detectable after total lipid staining. The DNA G+C content was 66.4, 68.9, 67.4 and 70.5 mol% for strains PP-WC-4G-234T, PP-CE-2G-454T, PP-WC-1G-202 and PP-CC-3G-650, respectively. Based on phylogenetic, chemotaxonomic and phenotypic analyses we propose two novel species of the genus Aureimonas, Aureimonas galii sp. nov. with PP-WC-4G-234T (=LMG 28655T=CIP 110892T) as the type strain and Aureimonas pseudogalii sp. nov. with PP-CE-2G-454T (=LMG 29411T=CCM 8665T) as the type strain and two further strains representing the same species, PP-WC-1G-202 and PP-CC-3G-650.

Abstract:

Rising atmospheric CO2 concentrations are expected to increase nitrous oxide (N2O) emissions from soils via changes in microbial nitrogen (N) transformations. Several studies have shown that N2O emission increases under elevated atmospheric CO2 (eCO2), but the underlying processes are not yet fully understood. Here, we present results showing changes in soil N transformation dynamics from the Giessen Free Air CO2 Enrichment (GiFACE): a permanent grassland that has been exposed to eCO2, +20% relative to ambient concentrations (aCO2), for 15 years. We applied in the field an ammonium-nitrate fertilizer solution, in which either ammonium (NHþ 4 ) or nitrate (NO 3 ) was labelled with 15N. The simultaneous gross N transformation rates were analysed with a 15N tracing model and a solver method. The results confirmed that after 15 years of eCO2 the N2O emissions under eCO2 were still more than twofold higher than under aCO2. The tracing model results indicated that plant uptake of NHþ 4 did not differ between treatments, but uptake of NO 3 was significantly reduced under eCO2. However, the NHþ 4 and NO 3 availability increased slightly under eCO2. The N2O isotopic signature indicated that under eCO2 the sources of the additional emissions, 8,407 lg N2O–N/m2 during the first 58 days after labelling, were associated with NO 3 reduction (+2.0%), NHþ 4 oxidation (+11.1%) and organic N oxidation (+86.9%). We presume that increased plant growth and root exudation under eCO2 provided an additional source of bioavailable supply of energy that triggered as a priming effect the stimulation of microbial soil organic matter (SOM) mineralization and fostered the activity of the bacterial nitrite reductase. The resulting increase in incomplete denitrification and therefore an increased N2O:N2 emission ratio, explains the doubling of N2O emissions. If this occurs over a wide area of grasslands in the future, this positive feedback reaction may significantly accelerate climate change.

Abstract:

Displays how field site data from the Giessen FACE are processed into simulations of soil moisture, biomass and greenhouse gas emissions (CO2 and N2O). Simulations are displayed in GLUE-like uncertainty analysis. Gives an outlook how the N-deficit of the field site may be connected to groundwater N supply.

Abstract:

Compares simulations of plant biomass and CO2 emissions of the Giessen FACE grassland with and without groundwater-borne nitrate.

Abstract:

Overview of the B3 working package of the FACE2FACE Programme. Includes methods and model setup, N balance of the field site, simulation results of biomass and CO2 emissions with and without groundwater, as well as an outlook for the phase-out period.

Abstract:

A pink-pigmented, Gram-stain-negative, rod-shaped, non-spore-forming bacterial strain, PP-F2F-G21T, was isolated from the phyllosphere of Galium album. Phylogenetic analysis of the nearly full-length 16S rRNA gene sequence of strain PP-F2F-G21T showed the closest relationship to type strains of the species Mucilaginibacter lutimaris (97.7?%), Mucilaginibacter soli (97.3?%) and Mucilaginibacter rigui (97.1?%). Sequence similarities to all other type strains were below 97?%. The predominant cellular fatty acids of strain PP-F2F-G21T are C16?:?1 ?7c/iso-C15?:?0 2-OH (measured as summed feature 3 fatty acids) and iso-C15?:?0 followed by iso-C17?:?0 3-OH, C16?:?1 ?5c and C16?:?0. The major compound in the polyamine pattern was sym-homospermidine and the diamino acid of the peptidoglycan was meso-diaminopimelic acid. The quinone system was exclusively composed of menaquinone MK-7. The polar lipid profile contained the major lipid phosphatidylethanolamine and in addition 18 unidentified lipids. Based on phylogenetic, chemotaxonomic and phenotypic analyses, we propose a novel species of the genus Mucilaginibacter named Mucilaginibacter phyllosphaerae sp. nov. The type strain is PP-F2F-G21T (=CCM 8625T=CIP 110921T=LMG 29118T).

Abstract:

Facing rising atmospheric CO2 concentrations, subsoils may play an important role in the global carbon (C) cycle due to the presence of unsaturated mineral surfaces. Further, macroaggregation is considered a crucial process influencing C sequestration. However, analyses on subsoil aggregation and C retention processes under long-term elevated CO2 (eCO2) are lacking. In this study we investigated the long-term effect of +20% above ambient CO2 concentration (corresponds to conditions reached 2035–2045) in a temperate grassland ecosystem at the Giessen Free Air CO2 Enrichment (Gi-FACE), Germany. A depth-dependent response of macroaggregation to eCO2 was observed: While in subsoil (15–45?cm depth) macroaggregation increased under eCO2, no CO2 induced change in macroaggregation was detected in topsoil (0–15?cm). Increased macroaggregation in subsoil coincided with higher SOC content of large macroaggregates (LM). Mean residence time (MRT) of SOC in aggregate-size classes were not different among each other under eCO2. However, macroaggregates and bulk soil differed in their MRT between soil depths. Despite increased macroaggregation and an estimated high SOC sequestration potential in subsoil we could not observe an increase in SOC content of bulk soil.

Abstract:

Rising atmospheric CO2 concentrations are expected to increase nitrous oxide (N2O) emissions from soils via changes in microbial nitrogen (N) transformations triggering a positive feedback reaction that could accelerate climate change. Several studies have shown N2O emission increases under elevated atmospheric CO2 (eCO2), but the underlying processes are not yet fully understood. Here we present results showing changes in soil N transformation dynamics from the Giessen Free Air CO2 Enrichment (GiFACE): a permanent grassland that has been exposed to eCO2, +20% relative to ambient concentrations (aCO2), for 15 years. We applied in the field an ammonium-nitrate fertilizer solution, in which either ammonium (NH4+) or nitrate (NO3-) was labelled with 15N. The simultaneous gross N transformation rates were analysed with a 15N tracing model and a solver method. The results confirmed that after 15 years of eCO2 the N2O emissions under eCO2 were still more than 2-fold higher than under aCO2. The tracing model results indicated that plant uptake of NH4+ did not differ between treatments, but uptake of NO3- was significantly reduced under eCO2. However, the ratio of gross production and consumption of NH4+ remained unchanged under eCO2, but decreased slightly for NO3-, which increased NO3- availability under eCO2. The N2O isotopic signature indicated that under eCO2 the sources of the additional emissions, 8407 µg N2O-N m-2 during the first 58 days after labelling, were associated with NO3- reduction (+2.0%), NH4+ oxidation (+11.1%) and organic N oxidation (+86.9%). We presume that increased root exudation under eCO2 provided an additional source of bioavailable supply of energy that triggered the stimulation of microbial soil organic matter (SOM) mineralization, as a priming effect, and an increased activity of bacterial nitrite reductase, which caused the shift in N2O:N2 emission ratio, via incomplete denitrification, explaining the positive feedback reaction of doubled N2O emissions.