ALBERT

Description: We estimated the isoprene and monoterpene source strengths of a pristine tropical forest north of Manaus in the central Amazon Basin using three different micrometeorological flux measurement approaches. During the early dry season campaign of the Cooperative LBA Airborne Regional Experiment (LBA-CLAIRE-2001), a tower-based surface layer gradient (SLG) technique was applied simultaneously with a relaxed eddy accumulation (REA) system. Airborne measurements of vertical profiles within and above the convective boundary layer (CBL) were used to estimate fluxes on a regional scale by application of the mixed layer gradient (MLG) technique. The mean daytime fluxes of organic carbon measured by REA were 2.1 mg C m−2 h−1 for isoprene, 0.20 mg C m−2 h−1 for α-pinene, and 0.39 mg C m−2 h−1 for the sum of monoterpenes. These values are in reasonable agreement with fluxes determined with the SLG approach, which exhibited a higher scatter, as expected for the complex terrain investigated. The observed VOC fluxes are in good agreement with simulations using a single-column chemistry and climate model (SCM). In contrast, the model-derived mixing ratios of VOCs were by far higher than observed, indicating that chemical processes may not be adequately represented in the model. The observed vertical gradients of isoprene and its primary degradation products methyl vinyl ketone (MVK) and methacrolein (MACR) suggest that the oxidation capacity in the tropical CBL is much higher than previously assumed. A simple chemical kinetics model was used to infer OH radical concentrations from the vertical gradients of (MVK+MACR)/isoprene. The estimated range of OH concentrations during the daytime was 3–8×106 molecules cm−3, i.e., an order of magnitude higher than is estimated for the tropical CBL by current state-of-the-art atmospheric chemistry and transport models. The remarkably high OH concentrations were also supported by results of a simple budget analysis, based on the flux-to-lifetime relationship of isoprene within the CBL. Furthermore, VOC fluxes determined with the airborne MLG approach were only in reasonable agreement with those of the tower-based REA and SLG approaches after correction for chemical decay by OH radicals, applying a best estimate OH concentration of 5.5×106 molecules cm−3. The SCM model calculations support relatively high OH concentration estimates after specifically being constrained by the mixing ratios of chemical constituents observed during the campaign. The relevance of the VOC fluxes for the local carbon budget of the tropical rainforest site during the measurements campaign was assessed by comparison with the concurrent CO2 fluxes, estimated by three different methods (eddy correlation, Lagrangian dispersion, and mass budget approach). Depending on the CO2 flux estimate, 1–6% or more of the carbon gained by net ecosystem productivity appeared to be re-emitted through VOC emissions.

Description: We estimated the isoprene and monoterpene source strengths of a pristine tropical forest north of Manaus in the central Amazon Basin using three different micrometeorological flux measurement approaches. During the early dry season campaign of the Cooperative LBA Airborne Regional Experiment (LBA-CLAIRE-2001), a tower-based surface layer gradient (SLG) technique was applied simultaneously with a relaxed eddy accumulation (REA) system. Airborne measurements of vertical profiles within and above the convective boundary layer (CBL) were used to estimate fluxes on a landscape scale by application of the mixed layer gradient (MLG) technique. The mean daytime fluxes of organic carbon measured by REA were 2.1 mg C m−2 h−1 for isoprene, 0.20 mg C m−2 h−1 for α-pinene, and 0.39 mg C m−2 h−1 for the sum of monoterpenes. These values are in reasonable agreement with fluxes determined with the SLG approach, which exhibited a higher scatter, as expected for the complex terrain investigated. The observed VOC fluxes are in good agreement with simulations using a single-column chemistry and climate model (SCM). In contrast, the model-derived mixing ratios of VOCs were by far higher than observed, indicating that chemical processes may not be adequately represented in the model. The observed vertical gradients of isoprene and its primary degradation products methyl vinyl ketone (MVK) and methacrolein (MACR) suggest that the oxidation capacity in the tropical CBL is much higher than previously assumed. A simple chemical kinetics model was used to infer OH radical concentrations from the vertical gradients of (MVK+MACR)/isoprene. The estimated range of OH concentrations during the daytime was 3–8×106 molecules cm−3, i.e., an order of magnitude higher than is estimated for the tropical CBL by current state-of-the-art atmospheric chemistry and transport models. The remarkably high OH concentrations were also supported by results of a simple budget analysis, based on the flux-to-lifetime relationship of isoprene within the CBL. Furthermore, VOC fluxes determined with the airborne MLG approach were only in reasonable agreement with those of the tower-based REA and SLG approaches after correction for chemical decay by OH radicals, applying a best estimate OH concentration of 5.5×106 molecules cm−3. The SCM model calculations support relatively high OH concentration estimates after specifically being constrained by the mixing ratios of chemical constituents observed during the campaign. The relevance of the VOC fluxes for the local carbon budget of the tropical rainforest site during the measurements campaign was assessed by comparison with the concurrent CO2 fluxes, estimated by three different methods (eddy correlation, Lagrangian dispersion, and mass budget approach). Depending on the CO2 flux estimate, 1–6% or more of the carbon gained by net ecosystem productivity appeared to be re-emitted through VOC emissions.

Description: In this study we apply a simple and reliable method to derive recent changes in glacier area and volume by taking advantage of high resolution LIDAR (light detection and ranging) DEMs (digital elevation models) from the year 2006. Together with two existing glacier inventories (1969 and 1997) the new dataset enables to quantify area and volume changes over the past 37 years at three dates. This has been done for 81 glaciers (116 km2) in the Ötztal Alps which accounts for almost one third of Austria's glacier extent. Glacier area and volume have reduced drastically with significant differences within the individual size classes. Between 1997 and 2006 an overall area loss of 10.5 km2 or 8.2% occurred. Volume has reduced by 1.0 km3 which accounts for a mean thickness change of −8.2 m. The availability of three comparable inventories allows a comprehensive analysis of glacier changes over all size classes but lacks a high temporal resolution. We therefore used glacier length as well as mass balance measurements from all available glaciers within the study area to analyse the potential temporal course of glacier changes in terms of area and volume which allows a rough estimation of mean annual area and volume changes and thus acceleration trends. Comparing the net retreating period between 1969 and 1997 with the period 1997 to 2006, the analysis reveals that mean annual absolute area losses have remained constant. Relative area losses have accelerated slightly whereas volume as well as mean thickness losses have accelerated significantly.

Description: In this study we apply a simple and reliable method to derive recent changes in glacier area and volume by taking advantage of high resolution LIDAR (light detection and ranging) DEMs (digital elevation models) from the year 2006. Together with two existing glacier inventories (1969 and 1997) the new dataset enables us to quantify area and volume changes over the past 37 years at three dates. This has been done for 81 glaciers (116 km2) in the Ötztal Alps which accounts for almost one third of Austria's glacier extent. Glacier area and volume have reduced drastically with significant differences within the individual size classes. Between 1997 and 2006 an overall area loss of 10.5 km2 or 8.2% occurred. Volume has reduced by 1.0 km3 which accounts for a mean thickness change of −8.2 m. The availability of three comparable inventories allows a comprehensive size and altitude dependent analysis of glacier changes but lacks a high temporal resolution. For the comparison of rates of changes between the two different periods (1969 to 1997 with 1997 to 2006) we propose two approaches in this study: a) to estimate mean overall rates of changes (including a period of advance) and b) to extract periods of net-retreat by using additional information (length change and mass balance measurements). Analysis of the resulting acceleration factors reveals that the retreat of volume and mean thickness changes has accelerated significantly more than that of area changes.

Description: Laminated sediments in the Shaban Deep, a brine-filled basin in the northern Red Sea, were analyzed with backscattered electron imagery. Here we present possible mechanisms involved in the formation of laminae of various types and homogenous intervals arising from the detailed investigation of multicore GeoB 7805-1 (26°13.9' N and 35°22.6' E; water depth 1447 m) and gravity core GeoB 5836-2 (26°12.61' N, 35°21.56' E; water depth 1475 m). Sediment makeup includes six types: a) a laminated structure with alternating light (mainly coccoliths) and dark (diatom frustules) layers, where the diatom component is indicative of the intra-annual variability between stratification and mixing events; b) a pocket-like structure attributed to the sinking of particles within fecal pellets and aggregates; c) a matrix of tightly packed diatoms that relates to extended stratification/mixing periods of the water column; d) homogenous intervals that result from turbidity deposition; e) silt accumulations which origin may lie in agglutinated foraminifers; and f) pyrite layers with pyrite formation initiated at the seawater-brine interface.

Description: Laminated sediments in the Shaban Deep, a brine-filled basin in the northern Red Sea, were analyzed with backscattered electron imagery. Here we present possible mechanisms involved in the formation of laminae of various types and homogenous intervals arising from the detailed investigation of multicore GeoB 7805-1 (26 13.9' N and 35 22.6' E; water depth 1447 m) and gravity core GeoB 5836-2 (26 12.61' N, 35 21.56' E; water depth 1475 m). Sediment makeup includes six types: a) a laminated structure with alternating light (mainly coccoliths) and dark (diatom frustules) layers, where the diatom component is indicative of the intra-annual variability between stratification and mixing events; b) a pocket-like structure attributed to the sinking of particles within fecal pellets and aggregates; c) a matrix of tightly packed diatoms that relates to extended stratification/mixing periods of the water column; d) homogenous intervals that result from turbidity deposition; e) silt accumulations which origin may lie in agglutinated foraminifers; and f) pyrite layers with pyrite formation initiated at the seawater-brine interface.

Description: The effect of root inundation on the leaf emissions of ethanol, acetaldehyde and acetic acid was investigated with 2–3 years old tree seedlings of four Amazonian floodplain species by applying dynamic cuvette systems under greenhouse conditions. Emissions were monitored over a period of several days of inundation using a combination of Proton Transfer Reaction Mass Spectrometry (PTR-MS) and conventional techniques (HPLC, ion chromatography). Under non-flooded conditions, none of the species exhibited significant emissions of any of the compounds. A slight deposition of acetaldehyde and acetic acid was mainly observed, instead. Tree species specific variations in deposition velocities were largely due to variations in stomatal conductance. Flooding of the roots resulted in leaf emissions of ethanol and acetaldehyde by all species, while emissions of acetic acid occurred only by the species exhibiting the highest ethanol and acetaldehyde emission rates. All three compounds showed a similar diurnal emission profile, each displaying an emission burst in the morning, followed by a decline in the evening. This concurrent behavior supports the conclusion, that all three compounds emitted by the leaves are derived from ethanol produced in the roots by alcoholic fermentation, transported to the leaves with the transpiration stream and finally partly converted to acetaldehyde and acetic acid by enzymatic processes. Co-emissions and peaking in the early morning confirmed that root ethanol, after transportation with the transpiration stream to the leaves and enzymatic oxidation to acetaldehyde and acetate, is the metabolic precursor for all compounds emitted. Emission rates substantially varied among tree species, with maxima differing by up to two orders of magnitude (3–200 nmol m−2 min−1 for ethanol and 5–500 nmol m−2 min−1 for acetaldehyde). Acetic acid emissions reached 12 nmol m−2 min−1. The observed differences in emission rates between the tree species are discussed with respect to their root adaptive strategies to tolerate long term flooding, providing an indirect line of evidence that the root ethanol production is a major factor determining the foliar emissions. Species which develop morphological root structures allowing for enhanced root aeration produced less ethanol and showed much lower emissions compared to species which lack gas transporting systems, and respond to flooding with substantially enhanced fermentation rates. The pronounced differences in the relative emissions of ethanol to acetaldehyde and acetic acid between the tree species indicate that not only the ethanol production in the roots but also the metabolic conversion in the leaf is an important factor determining the release of these compounds to the atmosphere.

Description: We obtained regional estimates of surface CO2 exchange rates using atmospheric boundary layer budgeting techniques above tropical forest near Manaus, Brazil. Comparisons were made with simultaneous measurements from two eddy covariance towers below. Although there was good agreement for daytime measurements, large differences emerged for integrating periods dominated by the night-time fluxes. These results suggest that a systematic underestimation of night time respiratory effluxes may be responsible for the high Amazonian carbon sink suggested by several previous eddy covariance studies. Large CO2 fluxes from riverine sources or high respiratory losses from recently disturbed forests do not need to be invoked in order to balance the carbon budget of the Amazon. Our results do not, however, discount some contribution of these processes to the overall Amazon carbon budget.

Description: Using a dynamic branch enclosure technique European beech (Fagus sylvatica L.) was characterised as a strong emitter of monoterpenes, with sabinene being the predominant compound released. Since monoterpene emission was demonstrated to be a function of light and temperature, application of light and temperature dependent algorithms resulted in reasonable agreement with the measured data. Furthermore, during high temperature periods the depression of net CO2 exchange during midday (midday depression) was accompanied by a depression of monoterpene emission on one occasion. The species dependent standard emission factor and the light and temperature regulated release of monoterpenes is of crucial importance for European VOC emissions. All measurements were performed within the framework of the ECHO project (Emission and CHemical transformation of biogenic volatile Organic compounds) during two intensive field campaigns in the summers of 2002 and 2003.

Description: We obtained regional estimates of surface CO2 exchange rates using atmospheric boundary layer budgeting techniques above tropical forest near Manaus, Brazil. Comparisons were made with simultaneous measurements from two eddy covariance towers below. Although there was good agreement for daytime measurements, large differences emerged for integrating periods dominated by the night-time fluxes. These results suggest that a systematic underestimation of night time respiratory effluxes may be responsible for the high Amazonian carbon sink suggested by several previous eddy covariance studies. Large CO2 fluxes from riverine sources or high respiratory losses from recently disturbed forests do not need to be invoked in order to balance the carbon budget of the Amazon. Our results do not, however, discount some contribution of these processes to the overall Amazon carbon budget.