ALBERT

Description: The Multitracers Experiment studied a transect of water column, sediment trap, and sediment data taken across the California Current to develop quantitative methods for hindcasting paleoproductivity. The experiment used three sediment trap moorings located 120 km, 270 km, and 630 km from shore at the Oregon/California border in North America. We report here about the sedimentation and burial of particulate organic carbon (Corg) and CaCO3. In order to observe how the integrated CaCO3 and Corg burial across the transect has changed since the last glacial maximum, we have correlated core from the three sites using time scales constrained by both radiocarbon and oxygen isotopes. By comparing surface sediments to a two-and-a-half year sediment trap record, we have also defined the modern preservation rates for many of the labile sedimentary materials. Our analysis of the Corg data indicates that significant amounts (20–40%) of the total Corg being buried today in surface sediments is terrestrial. At the last glacial maximum, the terrestrial Corg fraction within 300 km of the coast was about twice as large. Such large fluxes of terrestrial Corg obscure the marine Corg record, which can be interpreted as productivity. When we corrected for the terrestrial organic matter, we found that the mass accumulation rate of marine Corg roughly doubled from the glacial maximum to the present. Because preservation rates of organic carbon are high in the high sedimentation rate cores, corrections for degradation are straightforward and we can be confident that organic carbon rain rate (new productivity) also doubled. As confirmation, the highest burial fluxes of other biogenic components (opal and Ba) also occur in the Holocene. Productivity off Oregon has thus increased dramatically since the last glacial maximum. CaCO3 fluxes also changed radically through the deglaciation; however, they are linked not to CaCO3 production but rather to changes in deepwater carbonate chemistry between 18 Ka and now.

Description: Large euhedral crystals of calcium carbonate hexahydrate were recovered from a shelf basin of the Bransfield Strait, Antarctic Peninsula, at a water depth of 1950 meters and sub-zero bottom water temperatures. The chemistry, mineralogy, and stable isotope composition of this hydrated calcium carbonate phase, its environment of formation, and its mode of precipitation confirm the properties variously attributed to hypothetical precursors of the glendonites and thereby greatly expand their use in paleoceanographic interpretation.

Description: The physical, chemical/biological processes that control the methane dynamics in the Weddell Sea are revealed by the distributions of methane (CH4), its stable carbon isotope ratio, δ13C-CH4, and the conservative transient tracer, chlorofluorocarbon-11 (CFC-11, CCl3F). In general, a nearly linear correlation between CH4 and CFC-11 concentrations was observed. Air-sea exchange is the major source of methane to this region, and the distribution of methane is controlled mainly by mixing between surface water and methane-poor Warm Deep Water. A significant influence of methane oxidation over the predominant two end-member mixing was only found in the Weddell Sea Bottom Water (WSBW) of the deep central Weddell Basin, where the turnover time of methane appears to be about 20 years. Mixing also controls most of the δ13C-CH4 distribution, but lighter than expected carbon isotopic ratios occur in the deep WSBW of the basin. From box model simulations, it appears that this “anomaly” is due to methane oxidation with a low kinetic isotope fractionation of about 1.004. The surface waters in the Weddell Sea and the Antarctic Circumpolar Current showed a general methane undersaturation of 6 to 25% with respect to the atmospheric mixing ratio. From this undersaturation and model-derived air-sea exchange rates, we estimate a net uptake of CH4 of roughly −0.5 μmol m−2 d−1 during austral autumn.

Description: The δ13C of dissolved inorganic carbon was measured on samples collected at 49°N in the northeast Atlantic in January 1994. Deeper than 2000 m, δ13C exhibits the same negative correlation versus dissolved phosphate that is observed elsewhere in the deep Atlantic. Upward from 2000 m to about 600 m, δ13C shifts to values more negative than expected from the correlation with nutrients at depth, which is likely due to penetration of anthropogenic CO2. From these data, the profile of the anthropogenic δ13C decrease is calculated by using either dissolved phosphate or apparent oxygen utilization as a proxy for the preanthropogenic δ13C distribution. The shape of the anthropogenic anomaly profile derived from phosphate is similar to that of the increase in dissolved inorganic carbon derived by others in the same area. The reconstruction from oxygen utilization results in a lower estimate of the anthropogenic δ13C decrease in the upper water column, and the vertical anomaly profile is less similar to that of the dissolved inorganic carbon increase. A 13C budget for the atmosphere, ocean, and terrestrial biosphere indicates that within the range of probable ocean CO2 uptake the ratio of δ13C to inorganic carbon change should be mostly influenced by the 13C inventory change of the biosphere. However, the uncertainty in the ratio we derive prevents a strong contraint on the size of the exchangeable biosphere.

Description: Measurements of CH4 concentrations in the bottom water during two discrete sampling periods in subsequent years above different cold seeps at the Pacific margin off Costa Rica indicate large-scale variations of CH4 release. CH4 is emitted from mud extrusions and a slide scar at 1000–2300 m water depth. Maximum CH4 concentrations were found to be lower above all investigated sites in autumn 2003 than in autumn 2002 although seep sites are up to 300 km apart. Tidal and current changes were observed but found to apply only to individual seep sites. Increased seismic activity connected to the moment magnitude (M W ) 6.4 earthquake offshore Costa Rica in June 2002 could have had an impact on all seep sites and thereby caused an increase in CH4 emission. This is supported by the largest variations of CH4 concentration found above mud extrusions located above faults likely more strongly affected by tectonic movements. Even though our data indicate a relation between seismicity and CH4 seepage, the relation is not proven, and future work is needed to comprehensively test this hypothesis.

Description: Methane in surface waters and marine air off Oregon (44°24′N–44°54′N, 124°36′W–125°24′W) was continuously surveyed in July 1999. During a high-resolution survey after a period of steady winds from the north, CH4 concentrations were high in the northeastern region, near the shelf edge. The highest CH4 concentrations were 2.5 times higher than equilibrium with the atmospheric partial pressure. In contrast, concentrations were near equilibrium in the western part of the survey area, the Hydrate Ridge. The increase in CH4 from southwest to northeast correlates with a drop in sea surface temperature (SST), from 16.5°C to 〈13.5°C, toward the shelf edge. The observed SST pattern was caused by summer upwelling off Oregon. The results suggest that CH4 derived from bottom sources near the shelf/slope break and methane found in connection with shallow (100–300 m) turbidity layers is transported to the surface by coastal upwelling, which causes an enhanced net flux of CH4 to the atmosphere. Vertical profiles of the methane distribution on the shelf in October demonstrate the accumulation of methane introduced by shelf sources. Surface concentrations at these stations in October (during nonupwelling conditions) were lower than in July (during upwelling) and were only slightly oversaturated with respect to the atmosphere. An acoustic Doppler current profiler survey indicates that the observed trend cannot be attributed to a surface flow reversal in the area. The low-salinity waters in the core of the Columbia River plume (S 〈 31) showed no enhanced CH4 concentrations. The trend of higher CH4 concentrations at lower temperatures existed over the whole 17-day survey, but large spatial and temporal variations existed. The presence of methane sources in regions of coastal upwelling worldwide, such as shallow seeps, gas hydrates, and intermediate nepheloid layers, suggests that the enhancement of CH4 fluxes to the atmosphere by coastal upwelling occurs on a global scale.

Description: We used sediment traps to define the particulate fluxes of barium and organic carbon and investigate the use of barium as a proxy for ocean fertility. Strong correlations between Corg and Ba fluxes indicate a link between upper ocean biological processes and barium flux to the seafloor. The ratio of organic carbon to barium decreases systematically with water depth. Data from 10 sites indicate that organic debris settling from the 200-m depth has a Corg /Ba ratio of approximately 200. The systematic decrease in this ratio with increasing water depth results from the simultaneous decay of organic matter and uptake of Ba in settling particles. This behavior provides additional evidence that the formation of barite in oceanic particles is a consequence of decomposition/uptake in microenvironments rather than the secretion of barite by specific organisms. The decrease of the Corg/Ba ratio with depth is greatest in the North Pacific followed by the equatorial Pacific and is lowest in the western Atlantic. Since this spatial pattern is consistent with the variations in the deep-ocean barium contents which increase along the path of bottom water flow from the Atlantic to the North Pacific, it suggests that the particulate barium uptake and flux is enhanced by higher barium contents in the intermediate and deep waters of the ocean. Consequently, we have combined our particle flux data with existing water column Ba data to define an algorithm relating new productivity, dissolved barium contents, water depth, and particulate barium flux. This relationship provides a basis of applying barium flux measurements in sediments to estimating new production. In order to use barium as an indicator of productivity, it will be necessary to evaluate inputs from hydrothermal and aluminosilicate sources and xenophyophors. The application of a sequential leach procedure to the trap material indicates that 50-70% of the Ba in settling particles is in the form of barite and the remaining is adsorbed or bound to carbonates. Normative analysis demonstrates that in nearshore areas the contribution of barium from aluminosilicate sources can dominate that from biogenic inputs. It appears that normative estimates of biogenic barium contents can be made with accuracy if less than 50% of the Ba is associated with aluminosilicates; i.e., is of terrigenous origin. Since diagenetic mobilization of Ba can occur in reduced and suboxic sediments, highly productive nearshore areas also are likely to be inappropriate sites to use Ba measurements as productivity indicators. Comparisons between the rain rates of particulate Ba to the seafloor and the burial rate indicate that approximately 30% of the Ba rain is preserved. Although the preservation factor does not appear to be constant, it may be possible to predict the extent of preservation from an empirical relationship with the mass accumulation rate. These observations indicate that measurement of Ba burial fluxes in sediments can provide quantitative information on the paleoproductivity of the oceans. Joining the relationship between barium rain and burial with the barium and organic carbon algorithm, we make estimates of the new production in the northern California Current during the last 18,000 years. This calculation suggests that new production was at least a factor of 2 lower at this site during the last glacial maximum.

Description: [1] A systematic search for methane-rich fluid seeps at the seafloor was conducted at the Pacific continental margin offshore southern Nicaragua and northern central Costa Rica, a convergent margin characterized by subduction erosion. More than 100 fluid seeps were discovered using a combination of multibeam bathymetry, side-scan sonar imagery, TV-sled observations, and sampling. This corresponds, on average, to a seep site every 4 km along the continental slope. In the northwestern part of the study area, subduction of oceanic crust formed at the East Pacific Rise is characterized by pervasive bending-induced faulting of the oceanic plate and a relatively uniform morphology of the overriding continental margin. Seepage at this part of the margin typically occurs at approximately cone-shaped mounds 50 - 100 m high and up to 1 km wide at the base. Over 60 such mounds were identified on the 240 km long margin segment. Some normal faults also host localized seepage. In contrast, in the southeast, the 220 km long margin segment overriding the oceanic crust formed at the Cocos-Nazca Spreading Centre has a comparatively more irregular morphology caused mainly by the subduction of ridges and seamounts sitting on the oceanic plate. Over 40 seeps were located on this part of the margin. This margin segment with irregular morphology exhibits diverse seep structures. Seeps are related to landslide scars, seamount-subduction related fractures, mounds, and faults. Several backscatter anomalies in side-scan images are without apparent relief and are probably related to carbonate precipitation. Detected fluid seeps are not evenly distributed across the margin but occur in a roughly margin parallel band centered 28 ± 7 km landward of the trench. This distribution suggests that seeps are possibly fed to fluids rising from the plate boundary along deep-penetrating faults through the upper plate.

Description: A spectrum of halogenated hydrocarbon compounds in marine air masses were surveyed over an area in the western Pacific between 43°N, 150°E and 4°N, 113°E in September 1994. The ship's track between northern Japan and Singapore traversed three climatic zones of the northern hemisphere. Recently polluted air, clean marine air derived from the central Pacific Ocean from different latitudes, and marine air from the Indonesian archipelago were collected. Tetrachloroethene and trichloroethene of anthropogenic origin, brominated halocarbons as tribromomethane, dibromochloromethane and bromodichloromethane of anthropogenic and natural sources, and other trace gases were measured in the air samples. Very sparse data on the distribution of these compounds exist for the western Pacific atmosphere. The distribution patterns of the compounds were related to synoptic-scale meteorology, spatial conditions, and origin of the air masses. Anthropogenic and natural sources for both chlorinated and brominated substances were identified. Tetrachloroethene and trichloroethene concentrations and their ratios identify anthropogenic sources. Their mixing ratios were quite low compared to previously published data. They are in agreement with expected low concentrations of photochemically active substances during autumn, with an overall decrease in concentrations toward lower latitudes, and with a decrease of emissions during recent years. Strong evidence for a natural source of trichloroethene was discovered in the tropical region. The concentrations of naturally released brominated species were high compared to other measurements over the Pacific. Gradients toward the coasts and elevated concentrations in air masses influenced by coastal emissions point to significant coastal sources of these compounds. The trace gas composition of anthropogenic and natural compounds clearly identified the air masses which were traversed during the cruise.

Description: Measurements of dissolved methane in the surface waters of the western Sea of Okhotsk are evaluated in terms of methane exchange rates and are used to assess the magnitude of seasonal variations of methane fluxes from the ocean to the atmosphere in this area. Methane concentrations northeast of Sakhalin were observed to range from 385 nmol L−1 under the ice cover in winter to 6 nmol L−1 in the icefree midsummer season. The magnitude of supersaturations indicates that this part of the Okhotsk Sea is a significant source for atmospheric methane. From the seasonal variation of the supersaturations in the surface waters it is evident that the air-sea exchange is interrupted during the winter and methane from sedimentary sources accumulates under the ice cover. According to our measurements an initial early summer methane pulse into the atmosphere of the order of 560 mol km−2 d−1 can be expected when the supersaturated surface waters are exposed by the retreating ice. The methane flux in July is approximately 150 mol km−2 d−1 which is of the order of the average annual flux in the survey area. The magnitude of the seasonal CH4 flux variation northeast of Sakhalin corresponds to an amount of 7.3 × 105 g km−2 whereby 74% or 5.4 × 105 g km−2 are supplied to the atmosphere between April and July. For the whole Sea of Okhotsk the annual methane flux is roughly 0.13 × 1012 g (terragrams), based on the assumption that 15% of the entire area emit methane. Variations of long-term data of atmospheric methane which are recorded at the same latitude adjacent to areas with seasonal ice cover show a regional methane pulse between April and July. The large-scale level of atmospheric methane in the northern hemisphere undergoes an amplitudinal variation of about 25 parts per billion by volume (ppbv) which translates into approximately 36 Tg. Thus the estimated 0.6 Tg of ice-induced methane dynamics in northern latitudes can hardly explain this seasonal signal. However, the effects of seasonal ice cover on pulsed release of methane appear strong enough to contribute, in concert with other seasonal sources, to characteristic short-term wobbles in the atmospheric methane budget which are observed between 50°N and 60°N.