ALBERT

Description: The availability of microwave instruments on satellite platforms allows the retrieval of essential water cycle components at high quality for improved understanding and evaluation of water processes in climate modelling. HOAPS-3, the latest version of the satellite climatology "Hamburg Ocean Atmosphere Parameters and Fluxes from Satellite Data" provides fields of turbulent heat fluxes, evaporation, precipitation, freshwater flux and related atmospheric variables over the global ice-free ocean. This paper describes the content, methodology and retrievals of the HOAPS climatology. A sophisticated processing chain, including all available Special Sensor Microwave Imager (SSM/I) instruments aboard the satellites of the Defense Meteorological Satellites Program (DMSP) and careful inter-sensor calibration, ensures a homogeneous time-series with dense data sampling and hence detailed information of the underlying weather situations. The completely reprocessed data set with a continuous time series from 1987 to 2005 contains neural network based algorithms for precipitation and wind speed and Advanced Very High Resolution Radiometer (AVHRR) based SST fields. Additionally, a new 85 GHz synthesis procedure for the defective SSM/I channels on DMSP F08 from 1989 on has been implemented. Freely available monthly and pentad means, twice daily composites and scan-based data make HOAPS-3 a versatile data set for studying ocean-atmosphere interaction on different temporal and spatial scales. HOAPS-3 data products are available via http://www.hoaps.org.

Description: The availability of microwave instruments on satellite platforms allows the retrieval of essential water cycle components at high quality for improved understanding and evaluation of water processes in climate modelling. HOAPS-3, the latest version of the satellite climatology "Hamburg Ocean Atmosphere Parameters and Fluxes from Satellite Data" provides fields of turbulent heat fluxes, evaporation, precipitation, freshwater flux and related atmospheric variables over the global ice-free ocean. This paper describes the content, methodology and retrievals of the HOAPS climatology. A sophisticated processing chain, including all available Special Sensor Microwave Imager (SSM/I) instruments aboard the satellites of the Defense Meteorological Satellites Program (DMSP) and careful inter-sensor calibration, ensures a homogeneous time-series with dense data sampling and hence detailed information of the underlying weather situations. The completely reprocessed data set with a continuous time series from 1987 to 2005 contains neural network based algorithms for precipitation and wind speed and Advanced Very High Resolution Radiometer (AVHRR) based SST fields. Additionally, a new 85 GHz synthesis procedure for the defective SSM/I channels on DMSP F08 from 1988 on has been implemented. Freely available monthly and pentad means, twice daily composites and scan-based data make HOAPS-3 a versatile data set for studying ocean-atmosphere interaction on different temporal and spatial scales. HOAPS-3 data products are available via http://www.hoaps.org.

Description: In recent years, ocean acidification has gained continuously increasing attention from scientists and a number of stakeholders and has raised serious concerns about its effects on marine organisms and ecosystems. With the increase in interest and the number of scientific investigations of this environmental problem, the number of opinions, often emotional, and misinterpretations of the issue have also increased. Regrettably, this is not necessarily helping to advance scientific understanding of the problem. In this article, we revisit a number of issues relevant to ocean acidification that we think require thoughtful consideration including: (1) surface seawater CO2 chemistry in shallow water coastal areas, (2) experimental manipulation of marine systems using CO2 gas or by acid addition, (3) net versus gross calcification and dissolution, and (4) CaCO3 mineral dissolution and seawater buffering.

Description: Climate warming in Northeastern Siberia may induce thaw-remobilization of the organic carbon (OC) now held in permafrost. This study investigated the composition of terrestrial OC exported to Arctic coastal waters to both obtain a natural integration of terrestrial permafrost OC release and to further understand the fate of remobilized carbon in the extensive Siberian Shelf Seas. Application of a variety of elemental, molecular and isotopic (δ13C and Δ14C) analyses of both surface water suspended particulate matter and underlying surface sediments along a 500 km transect from Kolyma River mouth to the mid-shelf of the East Siberian Sea yielded information on the sources, degradation status and transport processes of thaw-remobilized soil OC. A three end-member dual-carbon-isotopic mixing model was applied to deduce the relative contributions from riverine, coastal erosion and marine sources. The mixing model was solved numerically using Monte Carlo simulations to obtain a fair representation of the uncertainties of both end-member composition and the end results. Riverine OC contributions to sediment OC decrease with increasing distance offshore (35±15 to 13±9%), whereas coastal erosion OC exhibits a constantly high contribution (51±1 to 60±12%) and marine OC increases offshore ward (9±7 to 36±10%). We attribute the remarkably strong imprint of OC from coastal erosion, extending up to ~500 km from the coast, to efficient offshoreward transport in these shallow waters presumably through both the benthic boundary layer and ice-rafting. There are also indications of simultaneous selective preservation of erosion OC compared to riverine OC. Molecular degradation proxies and radiocarbon contents indicated a degraded but young (Δ14C ca. −60‰ or ca. 500 14C yr) terrestrial OC pool in surface water particulate matter, underlain by a less degraded but old (Δ14C ca. −500‰ or ca. 5500 14C yr) terrestrial OC pool in bottom sediments. We suggest that the terrestrial OC fraction in surface water particulate matter is mainly derived from surface soil and recent vegetation fluvially released as buoyant organic-rich aggregates (e.g., humics), which are subjected to extensive processing during coastal transport. In contrast, terrestrial OC in the underlying sediments is postulated to originate predominantly from erosion of mineral-rich Pleistocene coasts (i.e., yedoma) and inland mineral soils. Sorptive association of this organic matter with mineral particles protects the OC from remineralization and also promotes rapid settling (ballasting) of the OC. Our findings corroborate recent studies by indicating that different Arctic surface soil OC pools exhibit distinguishing susceptibilities to degradation in coastal waters. Consequently, the general postulation of a positive feedback to global warming from remineralization of permafrost carbon may be both attenuated (by reburial of one portion) and geographically displaced (degradation of released terrestrial permafrost OC far out over the Arctic shelf seas).

Description: The world's largest continental shelf, the East Siberian Shelf Sea, receives substantial input of terrestrial organic carbon (terr-OC) from both large rivers and erosion of its coastline. Degradation of organic matter from thawing permafrost in the Arctic is likely to increase, potentially creating a positive feedback mechanism to climate warming. This study focuses on the Buor-Khaya Bay (SE Laptev Sea), an area with strong terr-OC input from both coastal erosion and the Lena river. To better understand the fate of this terr-OC, molecular (acyl lipid biomarkers) and isotopic tools (stable carbon and radiocarbon isotopes) have been applied to both particulate organic carbon (POC) in surface water and sedimentary organic carbon (SOC) collected from the underlying surface sediments. Clear gradients in both extent of degradation and differences in source contributions were observed both between surface water POC and surface sediment SOC as well as over the 100 s km investigation scale (about 20 stations). Depleted δ13C-OC and high HMW/LMW n-alkane ratios signaled that terr-OC was dominating over marine/planktonic sources. Despite a shallow water column (10–40 m), the isotopic shift between SOC and POC varied systematically from +2 to +5 per mil for δ13C and from +300 to +450 for Δ14C from the Lena prodelta to the Buor-Khaya Cape. At the same time, the ratio of HMW n-alkanoic acids to HMW n-alkanes as well as HMW n-alkane CPI, both indicative of degradation, were 5–6 times greater in SOC than in POC. This suggests that terr-OC was substantially older yet less degraded in the surface sediment than in the surface waters. This unusual vertical degradation trend was only recently found also for the central East Siberian Sea. Numerical modeling (Monte Carlo simulations) with δ13C and Δ14C in both POC and SOC was applied to deduce the relative contribution of plankton OC, surface soil layer OC and yedoma/mineral soil OC. This three end-member dual-carbon-isotopic mixing model suggests quite different scenarios for the POC vs SOC. Surface soil is dominating (63 ± 10%) the suspended organic matter in the surface water of SE Laptev Sea. In contrast, the yedoma/mineral soil OC is accounting for 60 ± 9% of the SOC. We hypothesize that yedoma-OC, associated with mineral-rich matter from coastal erosion is ballasted and thus quickly settles to the bottom. The mineral association may also explain the greater resistance to degradation of this terr-OC component. In contrast, more amorphous humic-like and low-density terr-OC from surface soil and recent vegetation represents a younger but more bioavailable and thus degraded terr-OC component held buoyant in surface water. Hence,these two terr-OC components may represent different propensities to contribute to a positive feedback to climate warming by converting OC from coastal and inland permafrost into CO2.

Description: Ocean acidification is a threat to marine ecosystems globally. In shallow-water systems, however, ocean acidification can be masked by benthic carbon fluxes, depending on community composition, seawater residence time, and the magnitude and balance of net community production (pn) and calcification (gn). Here, we examine how six benthic groups from a coral reef environment on Heron Reef (Great Barrier Reef, Australia) contribute to changes in seawater aragonite saturation state (Ωa). Results of flume studies showed a hierarchy of responses across groups, depending on CO2 level, time of day and water flow. At low CO2 (350–450 μatm), macroalgae (Chnoospora implexa), turfs and sand elevated Ωa of the flume water by around 0.10 to 1.20 h−1 – normalised to contributions from 1 m2 of benthos to a 1 m deep water column. The rate of Ωa increase in these groups was doubled under acidification (560–700 μatm) and high flow (35 compared to 8 cm s−1). In contrast, branching corals (Acropora aspera) increased Ωa by 0.25 h−1 at ambient CO2 (350–450 μatm) during the day, but reduced Ωa under acidification and high flow. Nighttime changes in Ωa by corals were highly negative (0.6–0.8 h−1) and exacerbated by acidification. Calcifying macroalgae (Halimeda spp.) raised Ωa by day (by around 0.13 h−1), but lowered Ωa by a similar or higher amount at night. Analyses of carbon flux contributions from four different benthic compositions to the reef water carbon chemistry across Heron Reef flat and lagoon indicated that the net lowering of Ωa by coral-dominated areas can to some extent be countered by long water residence times in neighbouring areas dominated by turfs, macroalgae and potentially sand.

Description: High loadings of anthropogenic carbonaceous aerosols in Chinese air influence the air quality for over 1 billion people and impact the regional climate. A large fraction (17–80%) of this aerosol carbon is water soluble, promoting cloud formation and thus climate cooling. Recent findings, however, suggest that water-soluble carbonaceous aerosols also absorb sunlight, bringing additional direct and indirect climate warming effects, yet the extent and nature of light absorption by this water-soluble brown carbon (WS-BrC) and its relation to sources is poorly understood. Here, we combine source estimates constrained by dual-carbon-isotope with light absorption measurements of WS-BrC for a March 2011 campaign at the Korea Climate Observatory at Gosan (KCOG), a receptor station in SE Yellow Sea for the outflow from N. China. The mass absorption cross-section (MAC) of WS-BrC for air masses from N. China were in general higher (0.8–1.1 m2 g−1), than from other source regions (0.3–0.8 m2 g−1). We estimate that this effect corresponds to 13–49% of the radiative forcing caused by light absorption by black carbon. Radiocarbon constraints show that the WS-BrC in Chinese outflow had significantly higher amounts of fossil sources (30–50%) compared to previous findings in S. Asia, N. America and Europe. Stable carbon (δ13C) measurements indicated influence of aging during air mass transport. These results indicate the importance of incorporating WS-BrC in climate models and the need to constrain climate effects by emission source sector.

Description: A detailed analysis of optical and microphysical properties of aerosol particles during the dry winter monsoon season above the northern Indian Ocean is presented. The Cloud Aerosol Radiative Forcing Experiment (CARDEX), conducted in February and March 2012 at the Maldives Climate Observatory on Hanimaadhoo island (MCOH) in the Republic of the Maldives, used autonomous unmanned aerial vehicles (AUAV) to perform vertical in-situ measurements of particle number concentration, particle number size distribution as well as particle absorption. These measurements were used together with surface-based Mini Micro Pulse Lidar (MiniMPL) observations and aerosol in-situ and off-line measurements to investigate the vertical distribution of aerosol particles. Air masses were mainly advected over the Indian subcontinent and the Arabian Peninsula. Mean surface aerosol number concentration was 1717±604 cm−3 and the highest values were found in air masses from the Bay of Bengal and Indo–Gangetic Plain (2247±370 cm−3). Investigations of the free tropospheric air showed that elevated aerosol layers with up to 3 times higher aerosol number concentrations than at the surface occurred mainly during periods with air masses originating from the Bay of Bengal and the Indo–Gangetic Plain. Compared to the Indian Ocean Experiment (INDOEX) conducted in winter 1999, elevated aerosol layers with increased aerosol number concentration were observed more frequently in 2012. However, lower particle absorption at the surface (σabs(520 nm)=8.5±4.2 Wm−1) was found during CARDEX compared to INDOEX 1999. By combining vertical in-situ measured particle absorption with scattering calculated with Mie-theory, layers with single-scattering albedo (SSA) values of specific source regions were derived and utilized to calculate vertical particle absorption profiles from MiniMPL profiles. SSA surface values for dry conditions were found to be 0.94±0.02 and 0.91±0.02 for air masses from the Arabian Sea (and Middle East countries) and India (and Bay of Bengal), respectively. Lidar-derived particle absorption profiles showed both a similar magnitude and structure as the in-situ profiles measured with the AUAV. However, primarily due to insufficient accuracy in the SSA estimates, the lidar-derived absorption profiles have large uncertainties and are generally weakly correlated to vertically in-situ measured particle absorption. Furthermore, the mass absorption efficiency (MAE) for the northern Indian Ocean during the dry monsoon season was calculated to determine equivalent black carbon (EBC) concentrations from particle absorption measurements. A mean MAE of 11.6 and 6.9 m2 g−1 for 520 and 880 nm, respectively, was found, likely representing internally mixed BC containing particles. Lower MAE values for 880 nm were found for air masses originating from dust regions such as the Arabian Peninsula and western Asia (5.6 m2 g−1) or from closer source regions as southern India (4.3m2 g−1).

Description: Through absorption of sun light atmospheric black carbon (BC) is expected to influence regional/global climate by warming the atmosphere and dimming the surface. To evaluate the impact of these effects it is of interest to examine both the radiative properties of BC and the concentrations in air. Building on recent developments we present a novel application for combining these two aspects using the common thermal-optical (OC/EC) instrument. By correlating the OC/EC laser transmission with the FID-carbon detection non-carbon contributions to the light attenuation are detected. Such analysis allows the calculation of mass absorption cross-sections (MACs) for BC, corrected for certain in-organic components. This approach has been applied to data from two SS Asian and two SNS European sites, including a time series analysis for one of the SNS European sites. Taken together this study demonstrates broad applicability for this method while providing new insights into the optical properties of BC.

Description: The world's largest continental shelf, the East Siberian Shelf Sea, receives substantial input of terrestrial organic carbon (terr-OC) from both large rivers and erosion of its coastline. Degradation of organic matter from thawing permafrost in the Arctic is likely to increase, potentially creating a positive feedback mechanism to climate warming. This study focuses on the Buor-Khaya Bay (SE Laptev Sea), an area with strong terr-OC input from both coastal erosion and the Lena river. To better understand the fate of this terr-OC, molecular (acyl lipid biomarkers) and isotopic tools (stable carbon and radiocarbon isotopes) have been applied to both particulate organic carbon (POC) in surface water and sedimentary organic carbon (SOC) collected from the underlying surface sediments. Clear gradients in both extent of degradation and differences in source contributions were observed both between surface water POC and surface sediment SOC as well as over the 100 s km investigation scale (about 20 stations). Depleted δ13C-OC and high HMW/LMW n-alkane ratios signaled that terr-OC was dominating over marine/planktonic sources. Despite a shallow water column (10–40 m), the isotopic shift between SOC and POC varied systematically from +2 to +5 per mil for δ13C and from +300 to +450 for Δ14C from the Lena prodelta to the Buor-Khaya Cape. At the same time, the ratio of HMW n-alkanoic acids to HMW n-alkanes as well as HMW n-alkane CPI, both indicative of degradation, were 5–6 times greater in SOC than in POC. This suggests that terr-OC was substantially older yet less degraded in the surface sediment than in the surface waters. This unusual vertical degradation trend was only recently found also for the central East Siberian Sea. Numerical modeling (Monte Carlo simulations) with δ13C and Δ14C in both POC and SOC was applied to deduce the relative contribution of – plankton OC, surface soil layer OC and yedoma/mineral soil OC. This three end-member dual-carbon-isotopic mixing model suggests quite different scenarios for the POC vs SOC. Surface soil is dominating (63 ± 10 %) the suspended organic matter in the surface water of SE Laptev Sea. In contrast, the yedoma/mineral soil OC is accounting for 60 ± 9 % of the SOC. We hypothesize that yedoma-OC, associated with mineral-rich matter from coastal erosion is ballasted and thus quickly settles to the bottom. The mineral association may also explain the greater resistance to degradation of this terr-OC component. In contrast, more amorphous humic-like and low-density terr-OC from surface soil and recent vegetation represents a younger but more bioavailable and thus degraded terr-OC component held buoyant in surface water. Hence, these two terr-OC components may represent different propensities to contribute to a positive feedback to climate warming by converting OC from coastal and inland permafrost into CO2.