ALBERT

Description: The morphology and structure of the submarine flanks of the Canary Islands were mapped using the GLORIA long-range side-scan sonar system, bathymetric multibeam systems, and sediment echosounders. Twelve young (〈2 Ma) giant landslides have been identified on the submarine flanks of the Canary Islands up to now. Older landslide events are long buried under a thick sediment cover due to high sedimentation rates around the Canary Islands. Most slides were found on the flanks of the youngest and most active islands of La Palma, El Hierro, and Tenerife, but young giant landslides were also identified on the flanks of the older (15–20 Ma) but still active eastern islands. Large-scale mass wasting is an important process during all periods of major magmatic activity. The long-lived volcanic constructive history of the islands of the Canary Archipelago is balanced by a correspondingly long history of destruction, resulting in a higher landslide frequency for the Canary Islands compared to the Hawaiian Islands, where giant landslides only occur late in the period of active shield growth. The lower stability of the flanks of the Canaries is probably due to the much steeper slopes of the islands, a result of the abundance of highly evolved intrusive and extrusive rocks. Another reason for the enhanced slope instability is the abundance of pyroclastic deposits on Canary Islands resulting from frequent explosive eruptions due to the elevated volatile contents in the highly alkalic magmas. Dike-induced rifting is most likely the main trigger mechanism for destabilization of the flanks. Flank collapses are a major geological hazard for the Canary Islands due to the sector collapses themselves as well as triggering of tsunamis. In at least one case, a giant lateral blast occurred when an active magmatic or hydrothermal system became unroofed during flank collapse.

Description: The supply of limiting nutrients to the low latitude ocean is controlled by physical processes linked to climate variations, but methods for reconstructing past nutrient concentrations in the surface ocean are few and indirect. Here, we present laser ablation mass spectrometry results that reveal annual cycles of P/Ca in a 4-year record from the scleractinian coral Pavona gigantea (mean P/Ca = 118 μmol mol−1). The P/Ca cycles track variations in past seawater phosphate concentration synchronously with skeletal Sr/Ca-derived temperature variations associated with seasonal upwelling in the Gulf of Panamá. Skeletal P/Ca varies seasonally by 2–3 fold, reflecting the timing and magnitude of dissolved phosphate variations. Solution cleaning experiments on drilled coral powders show that over 60% of skeletal P occurs in intracrystalline organic phases. Coral skeleton P/Ca holds promise as a proxy record of nutrient availability on time scales of decades to millennia.

Description: [1] While recent studies have confirmed the ecological importance of vitamin B12, it is unclear whether the production of this vitamin could be limited by dissolved Co, a trace metal required for B12 biosynthesis, but found at only subnanomolar concentrations in the open ocean. Herein, we demonstrate that the spatial distribution of dissolved B12 (range: 0.13–5 pmol L−1) in the North Atlantic Ocean follows the abundance of total dissolved Co (range: 15–81 pmol L−1). Similar patterns were observed for bacterial productivity (range: 20–103 pmol 3H leucine L−1 hr−1) and algal biomass (range: 0.4–3.9 μg L−1). In contrast, vitamin B1 concentrations (range: 0.7–30 pM) were decoupled from both Co and B12 concentrations. Cobalt amendment experiments carried out in low-dissolved Co waters (∼20 pmol L−1) enhanced B12 production two-fold over unamended controls. This study provides evidence that B12 synthesis could be limited by the availability of Co in some regions of the world ocean.

Description: We present the first comprehensive investigation of the concentrations, fluxes and sources of aerosol trace elements over the Gulf of Aqaba. We found that the mean atmospheric concentrations of crustally derived elements such as Al, Fe and Mn (1081, 683, and 16.7 ng m�3) are about 2–3 times higher than those reported for the neighboring Mediterranean area. This is indicative of the dominance of the mineral dust component in aerosols over the Gulf. Anthropogenic impact was lower in comparison to the more heavily populated areas of the Mediterranean. During the majority of time (69%) the air masses over the Gulf originated from Europe or Mediterranean Sea areas delivering anthropogenic components such as Cu, Cd, Ni, Zn, and P. Airflows derived from North Africa in contrast contained the highest concentrations of Al, Fe, and Sr but generally lower Cu, Cd, Ni, Zn, and P. Relatively high Pb, Ni, and V were found in the local and Arabian airflows suggesting a greater influence of local emission of fuel burning. We used the data and the measured trace metal seawater concentrations to calculate residence times of dissolved trace elements in the upper 50 m surface water of the Gulf (with respect to atmospheric input) and found that the residence times for most elements are in the range of 5–37 years while Cd and V residence times are longer.

Description: Methane (CH4) concentration and stable isotope (δ2H-CH4 and δ13C-CH4) depth distributions show large differences in the water columns of the Earth's largest CH4-containing anoxic basins, the Black Sea and Cariaco Basin. In the deep basins, the between-basin stable isotope differences are large, 83‰ for δ2H-CH4 and 9‰ for δ13C-CH4, and the distributions are mirror images of one another. The major sink in both basins, anaerobic oxidation of CH4, results in such extensive isotope fractionation that little direct information can be obtained regarding sources. Recent measurements of natural 14C-CH4 show that the CH4 geochemistry in both basins is dominated (∼64 to 98%) by inputs of fossil (radiocarbon-free) CH4 from seafloor seeps. We derive open-system kinetic isotope effect equations and use a one-dimensional (vertical) stable isotope box model that, along with isotope budgets developed using radiocarbon, permits a quantitative treatment of the stable isotope differences. We show that two main factors control the CH4 concentration and stable isotope differences: (1) the depth distributions of the input of CH4 from seafloor seeps and (2) anaerobic oxidation of CH4 under open-system steady state conditions in the Black Sea and open-system non-steady-state conditions in the Cariaco Basin.

Description: Lake Superior has exhibited a continuous, century-long increase in nitrate whereas phosphate remains at very low levels. Increasing nitrate and low phosphate has led to a present-day severe stoichiometric imbalance; Lake Superior's deepwater NO3−:PO43− molar ratio is 10,000, more than 600 times the mean requirement ratio for primary producers. We examine the rate of [NO3−] increase relative to budgets for NO3− and fixed N. Nitrate in Lake Superior has continued to rise since 1980, though possibly at a reduced rate. We constructed whole-lake NO3− and N budgets and found that NO3− must be generated in the lake at significant rates. Stable O isotope results indicate that most NO3− in the lake originated by in-lake oxidation. Nitrate in the lake is responding not just to NO3− loading but also to oxidation of reduced forms of nitrogen delivered to the lake. The increasing [NO3−]:[PO43−] stoichiometric imbalance in this large lake is largely determined by these in-situ processes.

Description: Methane clathrate hydrate (structure I) is found to be very strong, based on laboratory triaxial deformation experiments we have carried out on samples of synthetic, high‐purity, polycrystalline material. Samples were deformed in compressional creep tests (i.e., constant applied stress, σ), at conditions of confining pressure P = 50 and 100 MPa, strain rate 4.5 × 10−8 ≤ equation image ≤ 4.3 × 10−4 s−1, temperature 260 ≤ T ≤ 287 K, and internal methane pressure 10 ≤ PCH4 ≤ 15 MPa. At steady state, typically reached in a few percent strain, methane hydrate exhibited strength that was far higher than expected on the basis of published work. In terms of the standard high‐temperature creep law, equation image = Aσne−(E*+PV*)/RT the rheology is described by the constants A = 108.55 MPa−n s−1, n = 2.2, E* = 90,000 J mol−1, and V* = 19 cm3 mol−1. For comparison, at temperatures just below the ice point, methane hydrate at a given strain rate is over 20 times stronger than ice, and the contrast increases at lower temperatures. The possible occurrence of syntectonic dissociation of methane hydrate to methane plus free water in these experiments suggests that the high strength measured here may be only a lower bound. On Earth, high strength in hydrate‐bearing formations implies higher energy release upon decomposition and subsequent failure. In the outer solar system, if Titan has a 100‐km‐thick near‐surface layer of high‐strength, low‐thermal conductivity methane hydrate as has been suggested, its interior is likely to be considerably warmer than previously expected.

Description: Most Central American volcanoes occur in an impressive volcanic front that trends parallel to the strike of the subducting Cocos Plate. The volcanic front is a chain, made of right-stepping, linear segments, 100 to 300 Km in length. Volcanoes cluster into centers, whose spacing is random but averages about 27 Km. These closely spaced, easily accessible volcanic centers allow mapping of geochemical variations along the volcanic front. Abundant back-arc volcanoes in southeast Guatemala and central Honduras allow two cross-arc transects. Several element and isotope ratios (e.g. BalLa, Uffh, B/La, IOBe/9Be, 87Sr/86Sr) that are thought to signal subducted marine sediments or altered MORB consistently define a chevron pattern along the arc, with its maximum in Nicaragua. BalLa, a particularly sensitive signal, is 130 at the maximum in Nicaragua but decreases out on the limbs to 40 in Guatemala and 20 in Costa Rica, which is just above the nominal mantle value of 15. This high amplitude regional variation, roughly symmetrical about Nicaragua, contrasts with the near constancy, or small gradient, in several plate tectonic parameters such as convergence rate, age of the subducting Cocos Plate, and thickness and type of subducted sediment. The large geochemical changes over relatively short distances make Central America an important margin for seeking the tectonic causes of geochemical variations; the regional variation has both a high amplitude and structure, including flat areas and gradients. The geochemical database continues to improve and is already adequate to compare to tectonic models with length scales of 100 Km or longer.

Description: A new version of SODA, which covers the time period 1958–2005, is used to analyze decadal variability of the Pacific Subtropical Cell (STC) circulation. The analysis is based on transport time series across 9°S and 9°N. At the interannual time scale, STC convergence anomalies decrease during El Niños and increase during La Niñas through Sverdrup transport convergence changes. At decadal time scales, the assimilation shows a reduction of interior STC convergence of about 8 Sv from the 1960s to the 1990s and a subsequent rebound into the early 2000s by a similar amount, in agreement with the STC tendencies reported earlier from geostrophic section analysis, and associated with the occurrence and intensity of ENSO events among the decades analyzed. The results are compared with, and differ significantly from, those obtained by the German ECCO (GECCO) assimilation.

Description: Laboratory experiments were carried out in a seawater mesocosm tank to investigate the influence of marine phytoplankton growth on air bubble residence time (BRT). Air bubbles of 10–1000 μm in diameter were injected by flushing a water jet into the top of the tank and BRT was determined acoustically. The tank was filled with seawater containing a natural phytoplankton population and growth stimulated by irradiating with artificial fluorescent light. A second experiment was conducted using a monoculture of the diatom Cylindrotheca closterium. BRT and several phytoplankton growth-related parameters (chlorophyll concentration, dissolved inorganic nutrients, dissolved organic carbon (DOC), oxygen saturation and bacteria numbers) as well as the water viscosity were monitored over periods of up to 24 days. BRT showed a statistically significant covariation with oxygen saturation (r = 0.69, α = 0.01 for natural phytoplankton; r = 0.93, α = 0.01 for the Cylindrotheca closterium) and chlorophyll concentration (r = 0.69, α = 0.05 natural phytoplankton; r = 0.76, α = 0.01 Cylindrotheca closterium) during phytoplankton growth periods. Increases in BRT of a factor 〉2 were found during the chlorophyll maximum, when the water was sufficiently supersaturated with oxygen (~〉110%). No clear relationship was evident between BRT and measurements of DOC or water viscosity. Model experiments with highly oxygen-supersaturated water and artificial polysaccharide compounds indicated that oxygen supersaturation alone is not the main factor causing increased BRT during phytoplankton growth, but it is most likely a combination of the degree of gas saturation and the composition of the organic exudates derived from the microalgal population.