Planktic foraminiferal populations and test flux in the eastern North Atlantic Ocean

Planktic foraminiferal assemblages vary in response to seasonal fluctuations of hydrographic properties, between water masses, and after periodical changes and episodic events (e.g. reproduction, storms). Distinct annual variability of the planktic foraminiferal flux is also known from sediment trap data. In this paper we discuss the short-term impacts on interannual flux rates based on data from opening-closing net hauls obtained between the ocean surface and 500 m water depth. Data were recorded during April, May, June, and August at around 47°N, 20°W (BIOTRANS) in 1988, 1989, 1990, 1992, 1993, and during May 1989 and 1992 at 57°N, 20-22°W. Species assemblages closely resemble each other when comparing the mixed layer fauna with the fauna of the upper 100 m and the upper 500 m of the water column. In addition, species assemblages >100 µm are almost indistinguishable from assemblages that are >125 µm in test size. The standing stock of planktic foraminifers at BIOTRANS can vary by more than one order of magnitude over different years; however, species assemblages may be similar when comparing corresponding seasons. Early summer assemblages (June) are distinctly different from late summer assemblages (August). Significant variations in the species composition during spring (April/May) are independent of the mixed layer depth. Spring assemblages are characterized by high numbers of Globigerinita glutinata. In particular, day-to-day variations of the number of specimens and in species composition may have the same order of magnitude as interannual variations. This appears to be independent of the reproduction cycle. Species assemblages at 47°N and 57°N are similar during spring, although surface water temperatures and salinities differ by up to 10°C and 0.7 (PSU). We suggest that the main factors controlling the planktic foraminiferal fauna are the trophic properties in the upper ocean productive layer. Planktic foraminiferal carbonate flux as calculated from assemblages reveals large seasonal variations, a quasi-annual periodicity in flux levels, and substantial differences in timing and magnitude of peak fluxes. At the BIOTRANS station, the average annual planktic foraminiferal CaCO3 fluxes at 100 and 500 m depth are estimated to be 22.4 and 10.0 g/m**2/yr, respectively.

Organic carbon flux through the benthic community in the temperate abyssal Northeast Atlantic

In order to assess the carbon flux through the deep-sea benthic boundary layer, sediment community oxygen consumption (SCOC) was measured in different months and years at the BIOTRANS area in the abyssal northeastern Atlantic. SCOC varied seasonally with a maximum in July/August. Evidence is given for a direct coupling between a substantial sedimentation of phytodetritus and the seasonal increase in SCOC. Rapid colonization, growth and decomposition rates indicate that the deep-sea benthic microbial and protozoan biota can react quickly to substantial falls of particulate organic matter. They seem to be the most important groups to generate seasonal changes in deep-sea benthic carbon flux rates.

Planktonic foraminifera in the Arabian Sea

Variations in primary productivity (PP) have been reconstructed in eutrophic, mesotrophic and oligotrophic parts of the Arabian Sea over the past 135 000 years applying principal component analysis and transfer function to planktic foraminiferal assemblages. Temporal variation in paleoproductivity is most pronounced in the mesotrophic northern (NAST site) and oligotrophic eastern (EAST site) Arabian Sea, and comparatively weak in the western eutrophic GeoB 3011-1 site in the upwelling area off Oman. Higher PP during interglacials (250-320 g C/m**2 year) than during cold stages (210-270 g C/m**2 year) at GeoB 3011-1 could have been caused by a strengthened upwelling during intensified summer monsoons and increased wind velocities. At NAST, during interglacials, PP is estimated to exceed g C/m**2 year 1, and during glacials to be as low as 140-180 g C/m**2 year. These fluctuations may result from a (1) varying impact of filaments that are associated to the Oman coastal upwelling, and (2) from open-ocean upwelling associated to the Findlater Jet. At EAST, highest productivity of about 380 g C/m**2 year is documented for the transition from isotope stage 5 to 4. We suggest that during isotope stages 2, 4, 5.2, the transition 5/4, and the end of stage 6, deep mixing of surface waters was caused by moderate to strong winter monsoons, and induced an injection of nutrients into the euphotic layer leading to enhanced primary production. The deepening of the mixed layer during these intervals is confirmed by an increased concentration of deep-dwelling planktic foraminiferal species. A high-productivity event in stage 3, displayed by estimated PP values, and by planktic foraminifera and radiolaria flux and accumulation rate, likely resulted from a combination of intensified SW monsoons with moderate to strong NE monsoons. Differential response of Globigerina bulloides, Globigerinita glutinata and mixed layer species to the availability of food is suited to subdivide productivity regimes on a temporal and spatial scale.

Geochemistry of sediments cores in the Mediterranean Sea

We investigated five time-equivalent core sections (180-110 kyr BP) from the Balearic Sea (Menorca Rise), the easternmost Levantine Basin and southwest, south, and southeast of Crete to reconstruct spatial patterns of productivity during deposition of sapropels S5 and S6 in the Mediterranean Sea. Our indicators are Ba, total organic carbon and carbonate contents. We found no indications of Ba remobilization within the investigated core intervals, and used the accumulation rate of biogenic Ba to compute paleoproductivity. Maximum surface water productivity (up to 350 g C/m2/yr) was found during deposition of S5 (isotope stage 5e) but pronounced spatial variability is evident. Coeval sediment intervals in the Balearic Sea show very little productivity change, suggesting that chemical and biological environments in the eastern and western Mediterranean basins were decoupled in this interval. We interpret the spatial variability as the result of two different modes of nutrient delivery to the photic zone: riverderived nutrient input and shoaling of the pycnocline/nutricline to the photic zone. The productivity increase during the formation of S6 was moderate compared to S5 and had a less marked spatial variability within the study area of the eastern Mediterranean Sea. Given that S6 formed during a glacial interval, glacial boundary conditions such as high wind stress and/or cooler surface water temperatures apparently favored lateral and vertical mixing and prevented the development of the spatial gradients within the Eastern Mediterranean Sea (EMS) observed for S5. A non-sapropel sediment interval with elevated Ba content and depleted 18O/16O ratios in planktonic foraminifer calcite was detected between S6 and S5 that corresponds to the weak northern hemisphere insolation maximum at 150 kyr. At this time, productivity apparently increased up to five times over surrounding intervals, but abundant benthic fauna show that the deep water remained oxic. Following our interpretation, the interval denotes a failed sapropel, when a weaker monsoon did not force the EMS into permanent stratification. The comparison of interglacial and glacial sapropels illustrates the relevance of climatic boundary conditions in the northern catchment in determining the facies and spatial variability of sapropels within the EMS.

Geochemistry and accumulation rates of the early Paleogene in the Weddel Sea, Maud Rise and Kerguelen Plateau

Marine biological productivity has been invoked as a possible climate driver during the early Paleogene through its potential influence on atmospheric carbon dioxide concentrations. However, the relationship of export productivity (the flux of organic carbon (C) from the surface ocean to the deep ocean) to organic C burial flux (the flux of organic C from the deep ocean that is buried in marine sediments) is not well understood. We examine the various components involved with atmosphere-to-ocean C transfer by reconstructing early Paleogene carbonate and silica production (using carbonate and silica mass accumulation rates (MARs)); export productivity (using biogenic barium (bio-Ba) MARs); organic C burial flux (using reactive phosphorus (P) MARs); redox conditions (using uranium and manganese contents); and the fraction of organic C buried relative to export productivity (using reactive P to bio-Ba ratios). Our investigations concentrate on Paleocene/Eocene sections of Sites 689/690 from Maud Rise and Site 738 from Kerguelen Plateau. In both regions, export productivity, organic C burial flux, and the fraction of organic C buried relative to export productivity decreased from the Paleocene/early Eocene to the middle Eocene. A shift is indicated from an early Paleogene two-gyre circulation in which nutrients were not efficiently recycled to the surface via upwelling in these regions, to a circulation more like the present day with efficient recycling of nutrients to the surface ocean. Export productivity was enhanced for Kerguelen Plateau relative to Maud Rise throughout the early Paleogene, possibly due to internal waves generated by the plateau regardless of gyre circulation.

(Table 1) Ice flux, polynya area and sea-ice drift speed in the Kara Sea during winter (Jan-Apr) 1997-2001

The Shelf Seas of the Arctic are known for their large sea-ice production. This paper presents a comprehensive view of the Kara Sea sea-ice cover from high-resolution numerical modeling and space-borne microwave radiometry. As given by the latter the average polynya area in the Kara Sea takes a value of 21.2 × 10**3 km**2 ± 9.1 × 10**3 km**2 for winters (Jan.-Apr.) 1996/97 to 2000/01, being as high as 32.0 × 10**3 km**2 in 1999/2000 and below 12 × 10**3 km**2 in 1998/99. Day-to-day variations of the Kara Sea polynya area can be as high as 50 × 10**3 km**2. For the seasons 1996/97 to 2000/01 the modeled cumulative winter ice-volume flux out of the Kara Sea varied between 100 km**3/a and 350 km**3/a. Modeled high (low) ice export coincides with a high (low) average and cumulative polynya area, and with a low (high) sea-ice compactness in the Kara Sea from remote sensing data, and with a high (low) sea-ice drift speed across its northern boundary derived from independent model data for the winters 1996/97 to 2000/01.

Biogeochemical measurements of sediments collected at station MSM15/1_492-PUC2 (reference site 1) in the Black Sea during the MSM15/1 cruise in 2010

Biogeochemical measurements in sediment cores collected with the submersible JAGO (pusch cores) and a TV-MUC in the Black Sea during MSM15/1, Northwest Crimea (HYPOX Project), at water depths between 152-156 m. A series of microbial mats were sampled on the hypoxic region of the Crimean Shelf. Concentrations of organic carbon (Corg) and nitrogen (N) were measured on finely powdered, freeze-dried subsamples of sediment using a using a Fisons NA-1500 elemental analyzer. For organic carbon determination samples were pre-treated with 12.5% HCl to remove carbonates. Chlorophyll a (chl a), phaeopigments (PHAEO) and chloroplastic pigment equivalents (CPE) was measured according to Schubert et al., (2005) and total hydrolyzable amino acids (THAA) and single amino acid: ASP, GLU, SER, HIS, GLY, THR, ARG, ALA, TYR, MET, VAL, PHE, ILE, LEU, LYS following Dauwe et al., 1998.

Biogeochemical measurements of sediments collected at station MSM15/1_377-1 (microbial mat 4) in the Black Sea during the MSM15/1 cruise in 2010

Biogeochemical measurements in sediment cores collected with the submersible JAGO (pusch cores) and a TV-MUC in the Black Sea during MSM15/1, Northwest Crimea (HYPOX Project), at water depths between 152-156 m. A series of microbial mats were sampled on the hypoxic region of the Crimean Shelf. Concentrations of organic carbon (Corg) and nitrogen (N) were measured on finely powdered, freeze-dried subsamples of sediment using a using a Fisons NA-1500 elemental analyzer. For organic carbon determination samples were pre-treated with 12.5% HCl to remove carbonates. Chlorophyll a (chl a), phaeopigments (PHAEO) and chloroplastic pigment equivalents (CPE) was measured according to Schubert et al., (2005) and total hydrolyzable amino acids (THAA) and single amino acid: ASP, GLU, SER, HIS, GLY, THR, ARG, ALA, TYR, MET, VAL, PHE, ILE, LEU, LYS following Dauwe et al., 1998.

Biogeochemical measurements of sediments collected at station MSM15/1_492-PUC3 (microbial mat 2) in the Black Sea during the MSM15/1 cruise in 2010

Biogeochemical measurements in sediment cores collected with the submersible JAGO (pusch cores) and a TV-MUC in the Black Sea during MSM15/1, Northwest Crimea (HYPOX Project), at water depths between 152-156 m. A series of microbial mats were sampled on the hypoxic region of the Crimean Shelf. Concentrations of organic carbon (Corg) and nitrogen (N) were measured on finely powdered, freeze-dried subsamples of sediment using a using a Fisons NA-1500 elemental analyzer. For organic carbon determination samples were pre-treated with 12.5% HCl to remove carbonates. Chlorophyll a (chl a), phaeopigments (PHAEO) and chloroplastic pigment equivalents (CPE) was measured according to Schubert et al., (2005) and total hydrolyzable amino acids (THAA) and single amino acid: ASP, GLU, SER, HIS, GLY, THR, ARG, ALA, TYR, MET, VAL, PHE, ILE, LEU, LYS following Dauwe et al., 1998.

Biogeochemical measurements of sediments collected at station MSM15/1_492-PUC5 (reference site 2) in the Black Sea during the MSM15/1 cruise in 2010

Biogeochemical measurements in sediment cores collected with the submersible JAGO (pusch cores) and a TV-MUC in the Black Sea during MSM15/1, Northwest Crimea (HYPOX Project), at water depths between 152-156 m. A series of microbial mats were sampled on the hypoxic region of the Crimean Shelf. Concentrations of organic carbon (Corg) and nitrogen (N) were measured on finely powdered, freeze-dried subsamples of sediment using a using a Fisons NA-1500 elemental analyzer. For organic carbon determination samples were pre-treated with 12.5% HCl to remove carbonates. Chlorophyll a (chl a), phaeopigments (PHAEO) and chloroplastic pigment equivalents (CPE) was measured according to Schubert et al., (2005) and total hydrolyzable amino acids (THAA) and single amino acid: ASP, GLU, SER, HIS, GLY, THR, ARG, ALA, TYR, MET, VAL, PHE, ILE, LEU, LYS following Dauwe et al., 1998.