Oxygen consumption in Arctic sediments

Total sediment oxygen consumption rates (TSOC or Jtot), measured during sediment-water incubations, and sediment oxygen microdistributions were studied at 16 stations in the Arctic Ocean (Svalbard area). The oxygen consumption rates ranged between 1.85 and 11.2 mmol m**-2 d**-1, and oxygen penetrated from 5.0 to >59 mm into the investigated sediments. Measured TSOC exceeded the calculated diffusive oxygen fluxes (Jdiff) by 1.1-4.8 times. Diffusive fluxes across the sediment-water interface were calculated using the whole measured microprofiles, rather than the linear oxygen gradient in the top sediment layer. The lack of a significant correlation between found abundances of bioirrigating meiofauna and high Jtot/Jdiff ratios as well as minor discrepancies in measured TSOC between replicate sediment cores, suggest molecular diffusion, not bioirrigation, to be the most important transport mechanism for oxygen across the sediment-water interface and within these sediments. The high ratios of Jtot/Jdiff obtained for some stations were therefore suggested to be caused by topographic factors, i.e. underestimation of the actual sediment surface area when one-dimensional diffusive fluxes were calculated, or sampling artifacts during core recovery from great water depths. Measured TSOC correlated to water depth raised to the -0.4 to -0.5 power (TSOC = water depth**-0.4 to -0.5) for all investigated stations, but they could be divided into two groups representing different geographical areas with different sediment oxygen consumption characteristics. The differences in TSOC between the two areas were suggested to reflect hydrographic factors (such as ice coverage and import/production of reactive particulate organic material) related to the dominating water mass (Atlantic or polar) in each of the two areas. The good correlation between TSOC and water depth**-0.4 to -0.5 rules out any of the stations investigated to be topographic depressions with pronounced enhanced sediment oxygen consumption.

Concentrations of As and other chemical elements in bottom sediments of the Baltic Sea

As is less toxic than Hg, Cd, Pb, Se, Zn, and Cu. The As clarke for clays and shales is 10 ppm. Our samples of bottom sediments from Kurshskii Bay were determined to contain from 15 to 26 ppm As and up to 34 ppm As in the vicinity of the Neman River mouth. Elevated As concentrations (50-114 ppm) were detected in four columns of subsurface bottom sediments (at depths of 10-65 cm) from the Vistula Lagoon. Elevated As concentrations (50-180 ppm) were also found in a few surface samples of sand from the Gdansk Deep near oil platform D-6. These sediments are either partly contaminated with anthropogenic As or contain Fe sulfides and glauconite, which can concentrate As and contain its elevated concentrations. The As concentration in columns of bottom sediments from the Gulf of Finland were at the natural background level (throughout the columns) typical of the area (9-34 ppm). We repeatedly detected very high As concentrations (up to 227 ppm As) in politic ooze from Bornholm Deep, in the vicinity of the sunken vessel with chemical weapons. The sources of elevated As concentrations in the Baltic Sea are the following: (1) chemical weapon (CW) material buried in the floor of the Baltic Sea; (2) As-bearing pesticides, agricultural mineral fertilizers, and burned coal and other fuels; (3) kerogen-bearing Ordovician rocks exposed on the bottom; and (4) As-rich Fe sulfides brought to the area together with construction sand and gravel. This mixture was used in paper production and for the construction of hydraulic engineering facilities in the Vistula Lagoon in the early 20th century and later caused the so-called lagoon disease.

Bolboforma in Paleogene sediments of the Subantarctic

Sediments from ODP Holes 699A, 700B, 702B, 703A, and 704B were studied in order to determine and to understand the distribution of Bolboforma. Ten Bolboforma taxa were detected in the 294 samples analyzed. Based on Bolboforma species, a zonation correlated to the paleomagnetic record is proposed for the late middle Eocene to early Oligocene. Four biozones can be defined: the Bolboforma indistincta Zone for the lower part of the upper middle Eocene sequence, the Bolboforma eocena Zone for the upper part of the upper middle Eocene to upper Eocene, the Bolboforma geomaris Zone for the upper Eocene, and the Bolboforma latdorfensis Zone for the lower Oligocene sequence.

Frequency distribution of graded turbidite cycles in DSDP sediments from the Coral Sea Basin and the Sea of Japan

At sites 390 and 392 (Deep Sea Drilling Project, Leg 44) on the Blake nose, thoroughly lithified Lower Cretaceous limestone more than 250 m thick is abruptly overlain by a condensed sequence of Barremian to Eocene pelagic carbonate ooze. The Lower Cretaceous sediments consist of three units: limestone with moldic porosity (base), oolitic limestone, and fenestral limestone. Subaerial diagenesis of the limestone section is recorded by (1) caverns with vertical dimensions of up to 10 m, (2) stalactitic intergranular cement, and (3) meniscus sediment (or cement). Compatible with these subaerial features are mud cracks, fenestral fabrics, intraclasts, and cryptalgal structures. Inasmuch as these shallow-water and tidal-flat deposits are now beneath 2,607 m of sea water (plus 99 m of younger sediments), they serve to dramatize the apparent degree of Barremian and later subsidence of this part of the Atlantic outer continental shelf. Porosity and permeability are high in vuggy samples, which are common in the skelmoldic limestone. Cementation has destroyed most of the extensive primary porosity of the two younger units.

Ba distribution in surface sediments of the Southern Ocean

We present excess Ba (Baxs) data (i.e., total Ba corrected for lithogenic Ba) for surface sediments from a north-south transect between the Polar Front Zone and the northern Weddell Gyre in the Atlantic sector and between the Polar Front Zone and the Antarctic continent in the Indian sector. Focus is on two different processes that affect excess Ba accumulation in the sediments: sediment redistribution and excess Ba dissolution. The effect of these processes needs to be corrected for in order to convert accumulation rate into vertical rain rate, the flux component that can be linked to export production. In the Southern Ocean a major process affecting Ba accumulation rate is sediment focusing, which is corrected for using excess 230Th. This correction, however, may not always be straightforward because of boundary scavenging effects. A further major process affecting excess Ba accumulation is barite dissolution during exposure at the sediment-water column interface. Export production estimates derived from excess 230Th and barite dissolution corrected Baxs accumulation rates (i.e., excess Ba vertical rain rates) are of the same magnitude but generally larger than export production estimates based on water column proxies (234Th-deficit in the upper water column; particulate excess Ba enrichment in the mesopelagic water column). We believe export production values based on excess Ba vertical rain rate might be overestimated due to inaccurate assessment of the Baxs preservation rate. Barite dissolution has, in general, been taken into account by relating it to exposure time before burial depending on the rate of sediment accumulation. However, the observed decrease of excess Ba content with increasing water column depth (or increasing hydrostatic pressure) illustrates the dependence of barite preservation on degree of saturation in the deep water column in accordance with available thermodynamic data. Therefore correction for barite dissolution would not be appropriate by considering only exposure time of the barite to some uniformly undersaturated deep water but requires also that regional differences in degree of undersatuation be taken into account.

CaCO3 size distribution in surface sediments

Lysocline reconstructions play an important role in scenarios purporting to explain the lowered atmospheric CO2 content of glacial time. These reconstructions are based on indicators such as the CaCO3 content, the percent of coarse fraction, the ratio of fragments to whole foraminifera shells, the ratio of solution-susceptible to solution-resistant species, and the ratio of coarse to fine CaCO3. All assume that changes with time in the composition of the input material do not bias the result. However, as the composition of the input material does depend on climate, none of these indicators provides an absolute measure of the extent of dissolution. In this paper we evaluate the reliability of the ratio of >63 µm CaCO3 to total CaCO3 as a dissolution indicator. We present here results that suggest that in today's tropics this ratio appears to be determined solely by CO3= ion concentration and water depth (i.e., the saturation state of bottom waters). This finding offers the possibility that the size fraction index can be used to reconstruct CO3= ion concentrations for the late Quaternary ocean to an accuracy of ±5 µmol/kg.

Phosphorus in bottom sediments and micronodules from Core VITYAZ7414, Central Indian Ocean

Study of phosphorus distribution in grain size fractions of eupelagic clays showed high (up to 3%) content of P in Fe-Mn micronodules that can contain up to 20-30% of total P. Mineral P associated with Fe in ocean sediments is an analog of manganese in ocean sedimentogenesis. Sharp decrease of P contents in ocean Fe-Mn nodules compared to ones from seas results from decrease of Fe contents and partial neutralization of Fe activity by Mn.

Chemical composition of organic matter in ocean sediments

Group composition of organic matter in recent ocean sediments with high Corg content has been studied in detail. It has been shown that organic matter in sediments with Corg content greater than 4% is present in the very earliest stages of transformation. Group composition of amino acids is practically similar to that of their main producer, namely phytoplankton. Organic matter of sediments with Corg content below 4% is, from this standpoint, more transformed and is close to organic matter in usual type sediments with similar Corg content.

Calcareous nannofossil abundances in Mesozoic sediments of ODP Leg 129 holes

Calcareous nannofossils were studied from Jurassic and Cretaceous sediments drilled in the western Pacific during Ocean Drilling Program Leg 129. Mesozoic sediments at Sites 800, 801, and 802 are dominated by volcaniclastic turbidites, claystones, porcellanites, and radiolarites. Pelagic limestones are limited to the middle Cretaceous, and a few calcareous claystones were recovered in the Upper Jurassic section at Site 801. We documented the distribution of nannofossils, their total abundance, preservation, and relative species abundance based on semiquantitative and qualitative studies. Preservation of the calcareous nannofloras is poor to moderate, and the total abundance fluctuates from rare to very abundant. Marker species proposed for the middle and Late Cretaceous were recognized, allowing the application of standard nannofossil biozonations. At Site 800 calcareous nannofloras are abundant and moderately preserved in the Aptian-Cenomanian, and nannofossil biostratigraphy constitutes the basic stratigraphic framework for this interval. Radiolarians are the most abundant and persistent group throughout the sequence drilled at Site 801. Long intervals are barren of nannofloras and assemblages are usually characterized by low abundance and poor preservation. Nannofossil biostratigraphy was applied to the upper Aptian-Cenomanian interval and a few marker species were recognized for the late Tithonian. At Site 802 Cretaceous biostratigraphy is mainly based on calcareous nannofossil biozones corroborated by radiolarian and palynomorph events in the late Aptian-Coniacian age interval. A hiatus was indicated between the Santonian and the late Campanian, and another is suspected in the interval between the Cenomanian and the Coniacian.

n-Alkanes and lignin in bottom sediments of the Norwegian Sea

Investigations of bottom sediments from the central and northern parts of the Norwegian Sea including study regions at the Storegga landslide, the Haakon Mosby mud volcano, and Knipovich Ridge were carried out. Concentration of n-alkanes in bottom sediments from these regions ranges from 0.53 to 22.1 µg/g of dry sediments that corresponds to 0.02-1.97% of Corg. Molecular composition of hydrocarbons indicates mixed allochtonous-authochtonous genesis of total organic matter (TOC) formed by hydrobiota and residuals of terrestrial plants. Terrigenous organic mater dominates in bottom sediments. Active redox, microbial and thermolytic processes of organic matter transformation take place in the sedimentary mass. Special character of chromatographic spectra of n-alkane distribution in both low and high-molecular ranges, as well as increased naphtene contents can be interpreted as a sign of oil hydrocarbon generation from maternal organic matter as a result of thermocatalytic reactions within sedimentary mass and their displacement into the upper sedimentary layers. Molecular compositions and concentrations of phenols and lignin were determined in core samples from the Norwegian Sea. Total concentration of phenols in the cores ranges from 8.1 to 101.8 (µg/g of dry sediments that corresponds to 0.15-1.15% of TOC. Lignin concentration was estimated at 21.0-459.0 µg/g of dry sediments (0.59-7.9% of ?org. Phenol compounds of p-hydroxybenzoic, vanillin, syringyl and cinnamyl families as basic components of lignin macromolecules were identified. It was found that sea currents and aerosols are the main contributors of lignin into the abyssal part of the Norwegian Sea.