ALBERT

Description: Halocarbons, halogenated short-chained hydrocarbons, are produced naturally in the oceans by biological and chemical processes. They are emitted from surface seawater into the atmosphere, where they take part in numerous chemical processes such as ozone destruction and the oxidation of mercury and dimethyl sulfide. Here we present oceanic and atmospheric halocarbon data for the Peruvian upwelling obtained during the M91 cruise onboard the research vessel Meteor in December 2012. Surface waters during the cruise were characterized by moderate concentrations of bromoform (CHBr3) and dibromomethane (CH2Br2) correlating with diatom biomass derived from marker pigment concentrations, which suggests this phytoplankton group as likely source. Concentrations measured for the iodinated compounds methyl iodide (CH3I) of up to 35.4 pmol L-1, chloroiodomethane (CH2ClI) of up to 58.1 pmol L-1 and diiodomethane (CH2I2) of up to 32.4 pmol L-1 in water samples were much higher than previously reported for the tropical Atlantic upwelling systems. Iodocarbons also correlated with the diatom biomass and even more significantly with dissolved organic matter (DOM) components measured in the surface water. Our results suggest a biological source of these compounds as significant driving factor for the observed large iodocarbon concentrations. Elevated atmospheric mixing ratios of CH3I (up to 3.2 ppt), CH2ClI (up to 2.5 ppt) and CH2I2 (3.3 ppt) above the upwelling were correlated with seawater concentrations and high sea-to-air fluxes. The enhanced iodocarbon production in the Peruvian upwelling contributed significantly to tropospheric iodine levels.

Description: During the cruise POS432 on board the German R/V Poseidon, we collected water with a CTD SBE 11plus equipped with 14 Hydrobios free flow bottles of 10 L each in 15 stations (resulting in almost 100 samples) in the Madeira basin region, Northeast Atlantic. We aimed to study the physical and biogeochemical conditions of the water column along the 22°W meridian, north and south of the Azores Front, in May 2012. We measured concentrations of chlorophyll a, phaeopigments, suspended particulate material (SPM), and nutrients such as nitrate, nitrite, phosphate, and silicate.

Description: During two cruises wiht RV Sonne, SO234-2 from 8 to 19 July 2014 (Durban, South Africa to Port Louis, Mauritius) and SO235 from 23 July to 7 August 2014 (Port Louis, Mauritius to Malé, Maldives), within the SPACES (Science Partnerships for the Assessment of Complex Earth System Processes) and OASIS (Organic very short-lived Substances and their air sea exchange from the Indian Ocean to the Stratosphere) research projects, surface water samples were sampled from a continuous running pump in the hydrographic shaft of RV Sonne at a depth of 5 m. Deep water samples were taken from a Niskin-bottle rosette sampler. The samples were then analyzed for halogenated compounds using a purge and trap system onboard, which was attached to a gas chromatograph with an electron capture detector for surface water samples and a GC/MS Agilent 5975 for the deep water samples. An analytical reproducibility of 10% was determined from measuring duplicate water samples, detection limit was 0.2 pmol /L. Calibration was performed with several dilutions of a mixed-compound standard prepared in methanol.

Description: In 2005, the species composition and spatial distribution of the seaweed community were investigated in the frame of diving surveys along a sublittoral transect in the North of Helgoland that had been investigated ~40 years earlier by Lüning (1970). The cover of dominant brown seaweeds, Fucus serratus, Sargassum muticum, Laminaria digitata, L. hyperborea and Saccharina latissima, was semi-quantitatively assessed to define vegetation zones. Within each zone, all macroalgal species were estimated quantitatively in 3 to 6 random 1 m² quadrats. Additionally, a replicated biomass survey was performed at 6 depths (0.5, 2, 4, 6, 8 and 10 m below mean low water spring tide). The survey investigated the occurrence, cover and relative frequency of the algae community and information about fresh mass and dry mass were obtained. For kelps also stipe length, blade area, blade fresh mass, age and fresh mass of epiphytes was recorded.

Description: We conducted two isotope experiments (described in Gibbin et al. 2018) to determine how the presence of pathogens influences resource partitioning in the coral holobiont. Specifically, we quantified: 1) 13C-assimilation in Symbiodinium and the amount of 13C-labelled photosynthates that are assimilated by the host; 2) the metabolic turnover of 13C in Symbiodinium and in their host and 3) the incorporation of bacterial-derived N within the tissues of the coral holobiont. NanoSIMS images (either 40×40 or 50×50 µm in size) were obtained by rasterizing a 16 keV Cs+ primary ion beam, focused to a spot-size of 150 nm, across the sample surface. Settings (dwell time = 5 ms; number of pixels = 256×256, layers = 5) were kept constant between images. Data was extracted from drift-corrected images using L'IMAGE (Dr. Larry Nittler, Carnegie Institution of Washington). Regions of interest (ROIs) were drawn around individual symbiont cells and the host gastrodermis (excluding symbionts), using the contour lines on the 12C14N- image. These ROIs were then used to quantify the average enrichment of 13C and 15N in each partner. Our measured values are expressed as Atom Percent Excess (APE, in %).

Description: This dataset contains in a zipfile the shapefiles for the seabird breeding colonies at Stinker Point (Elephant Island, Maritime Antarctic Peninsula), the elevation of Stinker Point and the Elephant Island contour. All shapefiles are projected in WGS 1984 World Mercator projected coordinate system.

Description: Coral reefs are currently experiencing substantial ecological impoverishment as a result of anthropogenic stressors, and the majority of reefs are facing immediate risk. Increasing ocean surface temperatures induce frequent coral mass bleaching events-the breakdown of the nutritional photo-symbiosis with intracellular algae (genus: Symbiodinium). Here, we report that Stylophora pistillata from a highly diverse reef in the Gulf of Aqaba showed no signs of bleaching despite spending 1.5 months at 1-2°C above their long-term summer maximum (amounting to 11 degree heating weeks) and a seawater pH of 7.8. Instead, their symbiotic dinoflagellates exhibited improved photochemistry, higher pigmentation and a doubling in net oxygen production, leading to a 51% increase in primary productivity. Nanoscale secondary ion mass spectrometry imaging revealed subtle cellular-level shifts in carbon and nitrogen metabolism under elevated temperatures, but overall host and symbiont biomass proxies were not significantly affected. Now living well below their thermal threshold in the Gulf of Aqaba, these corals have been evolutionarily selected for heat tolerance during their migration through the warm Southern Red Sea after the last ice age. This may allow them to withstand future warming for a longer period of time, provided that successful environmental conservation measures are enacted across national boundaries in the region.

Description: Benthic d13C values (F. wuellerstorfi), kaolinite/chlorite ratios and sortable silt median grain sizes in sediments of a core from the abyssal Agulhas Basin record the varying impact of North Atlantic Deep Water (NADW) and Antarctic Bottom Water (AABW) during the last 200 ka. The data indicate that NADW influence decreased during glacials and increased during interglacials, in concert with the global climatic changes of the late Quaternary. In contrast, AABW displays a much more complex behaviour. Two independent modes of deep-water formation contributed to the AABW production in the Weddell Sea: 1) brine rejection during sea ice formation in polynyas and in the sea ice zone (Polynya Mode) and 2) super-cooling of Ice Shelf Water (ISW) beneath the Antarctic ice shelves (Ice Shelf Mode). Varying contributions of the two modes lead to a high millennial-scale variability of AABW production and export to the Agulhas Basin. Highest rates of AABW production occur during early glacials when increased sea ice formation and an active ISW production formed substantial amounts of deep water. Once full glacial conditions were reached and the Antarctic ice sheet grounded on the shelf, ISW production shut down and only brine rejection generated moderate amounts of deep water. AABW production rates dropped to an absolute minimum during Terminations I and II and the Marine Isotope Transition (MIS) 4/3 transition. Reduced sea ice formation concurrent with an enhanced fresh water influx from melting ice lowered the density of the surface water in the Weddell Sea, thus further reducing deep water formation via brine rejection, while the ISW formation was not yet operating again. During interglacials and the moderate interglacial MIS 3 both brine formation and ISW production were operating, contributing various amounts to AABW formation in the Weddell Sea.

Description: Clay mineral assemblages in a sediment core from the distal Nile discharge plume off Israel have been used to reconstruct the late Quaternary Nile sediment discharge into the Eastern Mediterranean Sea (EMS). The record spans the last ca. 140 ka. Smectite abundances indicate the influence of the Blue Nile and Atbara that have their headwaters in the volcanic rocks of the Ethiopian highlands. Kaolinite abundances indicate the influence of wadis, which contribute periodically to the suspension load of the Nile. Due to the geographical position, the climate and the sedimentary framework of the EMS is controlled by two climate systems. The long-term climate regime was governed by the African monsoon that caused major humid periods with enhanced sediment discharge at 132 to 〈126 ka (AHP5), 116 to 99 ka (AHP4), and 89 to 77 ka (AHP3). They lasted much longer than the formation of the related sapropel layers S5 (〉2 ka), S4 (3.5 ka) and S3 (5 ka). During the last glacial period (MIS 4-2) the long-term changes of the monsoonal system were superimposed by millennial-scale changes of an intensified mid-latitude glacial system. This climate regime caused short but pronounced drought periods in the Nile catchment, which are linked to Heinrich Events and alternate with more humid interstadials. The clay mineral record further implies that feedback mechanisms between vegetation cover and sediment discharge of the Nile are detectable but of minor importance for the sedimentary record in the southeastern Mediterranean Sea during the investigated African Humid Periods.

Description: Siberian Traps flood basalt magmatism coincided with the end-Permian mass extinction approximately 252 million years ago. Proposed links between magmatism and ecological catastrophe include global warming, global cooling, ozone depletion, and changes in ocean chemistry. However, the critical combinations of environmental changes responsible for global mass extinction are undetermined. In particular, the combined and competing climate effects of sulfur and carbon outgassing remain to be quantified. Here we present model outputs from global climate model simulations of flood basalt outgassing that account for sulfur chemistry and aerosol microphysics with coupled atmosphere and ocean circulation. We consider the effects of sulfur and carbon in isolation and in tandem. We find that coupling with the ocean strongly influences the climate response to flood basalt-scale outgassing. We suggest that sulfur and carbon emissions from the Siberian Traps combined to generate systemic swings in temperature, ocean circulation, and hydrology within a longer-term trend towards a greenhouse world in the early Triassic. Read README.PDF first for a description of the remaining files.

Description: During the DRIVE (Diurnal and Regional Variability of Halogen Emissions) ship campaign we investigated the variability of the halogenated very short-lived substances (VSLS) bromoform (CHBr3), dibromomethane (CH2Br2) and methyl iodide (CH3I) in the marine atmospheric boundary layer in the eastern tropical and subtropical North Atlantic Ocean during May/June 2010. The highest VSLS mixing ratios were found near the Mauritanian coast and close to Lisbon (Portugal). With backward trajectories we identified predominantly air masses from the open North Atlantic with some coastal influence in the Mauritanian upwelling area, due to the prevailing NW winds. The maximum VSLS mixing ratios above the Mauritanian upwelling were 8.92 ppt for bromoform, 3.14 ppt for dibromomethane and 3.29 ppt for methyl iodide, with an observed maximum range of the daily mean up to 50% for bromoform, 26% for dibromomethane and 56% for methyl iodide. The influence of various meteorological parameters - such as wind, surface air pressure, surface air and surface water temperature, humidity and marine atmospheric boundary layer (MABL) height - on VSLS concentrations and fluxes was investigated. The strongest relationship was found between the MABL height and bromoform, dibromomethane and methyl iodide abundances. Lowest MABL heights above the Mauritanian upwelling area coincide with highest VSLS mixing ratios and vice versa above the open ocean. Significant high anti-correlations confirm this relationship for the whole cruise. We conclude that especially above oceanic upwelling systems, in addition to sea-air fluxes, MABL height variations can influence atmospheric VSLS mixing ratios, occasionally leading to elevated atmospheric abundances. This may add to the postulated missing VSLS sources in the Mauritanian upwelling region (Quack et al., 2007).

Description: Methyl iodide (CH3I), bromoform (CHBr3) and dibromomethane (CH2Br2), which are produced naturally in the oceans, take part in ozone chemistry both in the troposphere and the stratosphere. The significance of oceanic upwelling regions for emissions of these trace gases in the global context is still uncertain although they have been identified as important source regions. To better quantify the role of upwelling areas in current and future climate, this paper analyzes major factors that influenced halocarbon emissions from the tropical North East Atlantic including the Mauritanian upwelling during the DRIVE expedition. Diel and regional variability of oceanic and atmospheric CH3I, CHBr3 and CH2Br2 was determined along with biological and meteorological parameters at six 24 h-stations. Low oceanic concentrations of CH3I from 0.1-5.4 pmol/L were equally distributed throughout the investigation area. CHBr3 of 1.0-42.4 pmol/L and CH2Br2 of 1.0-9.4 pmol/L were measured with maximum concentrations close to the Mauritanian coast. Atmospheric mixing rations of CH3I of up to 3.3, CHBr3 to 8.9 and CH2Br2 to 3.1 ppt above the upwelling and 1.8, 12.8, respectively 2.2 ppt at a Cape Verdean coast were detected during the campaign. While diel variability in CH3I emissions could be mainly ascribed to oceanic non-biological production, no main driver was identified for its emissions in the entire study region. In contrast, oceanic bromocarbons resulted from biogenic sources which were identified as regional drivers of their sea-to-air fluxes. The diel impact of wind speed on bromocarbon emissions increased with decreasing distance to the coast. The height of the marine atmospheric boundary layer (MABL) was determined as an additional factor influencing halocarbon emissions. Oceanic and atmospheric halocarbons correlated well in the study region and in combination with high oceanic CH3I, CHBr3 and CH2Br2 concentrations, local hot spots of atmospheric halocarbons could solely be explained by marine sources. This conclusion is in contrast with previous studies that hypothesized the occurrence of elevated atmospheric halocarbons over the eastern tropical Atlantic mainly originating from the West-African continent.