ALBERT

Description: An estimate of average river particulate matter (RPM) composition was bàsed on analyses of more than 40 elements in the Amazon, Congo, Ganges, Magdalena, Mekong, Parana and Orinoco rivers, to which were added literature data for 13 other major world rivers, covering the whole spectrum of morphoclimatic features. Geographic variations of major elements in RPM are mostly linked to weathering types and to the balance between weathering rate and river transport. As a result of chemical erosion, Al, Fe and Ti are enriched in RPM with respect to the average parent rock, while Na, Ca, Mg and Sr are strongly depleted. These figures are directly related to the relative importance of dissolved and particulate transport in rivers; this has been computed for each of 40 elements. In order to study weathering on a global scale, the total observed elemental fluxes (dissolved + particulate) have been computed and compared to theoretical ones. The latter were derived from the elemental content in the average parent rock and the total quantity of weathered material, computed from the Al ratio in RPM and in parent rock. Observed and theoretical fluxes are balanced for the less mobilized elements (rare earths, Co, Cr, Cs, Fe, Mn, Rb, Si, Th, Ti, U and V) for which no enrichment relative to Al is noted in RPM, and for B, Ba, Ca, K, Mg, Na, Sr which are relatively depleted in RPM due to their high dissolved transport. Additional fluxes have been found for Br, Sb, Pb, Cu, Mo, Zn and are possible also for Ni and P. This is reflected by marked enrichments in RPM relative to Al for the poorly or moderately dissolved transports (Pb, Cu, Zn). Several hypotheses involving either the natural origin (volcanic dust, marine aerosols, geochemical fractionation) or the artificial origin (worldwide pollution) are discussed to explain these discrepancies, assuming river transport and weathering either to be in a steady state on a global scale or not. However, none of them can fully account for these additional fluxes. It is most likely that these excesses have multiple origins, anthropogenic or natural or both. The comparison between RPM and deep-sea clay compositions emphasizes the prime influence of river input on oceanic sedimentation of Si, Al, Fe, Ti, lanthanides, Sc, Rb, V, etc. A few elements such as Zn, Sb, occur in excess in RPM as compared to deep-sea clays; in order to balance this excess, a remobilization of these elements out of the sediment can be considered. Finally, the enrichment of Co, Cu, Mn and Ni in deep-sea clays compared to RPM is discussed and attributed to several sources and processes.

Description: Several types of abyssal bedforms have been discovered during surveys with a deeply towed instrument package at water depths of 1.5–6 km in the Pacific and Atlantic Oceans. Cores and current-meter records obtained at the same sites provide data for interpreting their dynamics. Wave and current ripples are best portrayed in bottom photographs, but medium-scale bedforms, including sand waves, mud waves and erosional furrows, are described by interpreting high-resolution side-looking sonar records. The largest examples affect surface-ship echograms, though their shape and structure can seldom be resolved without near-bottom observations. Wave ripples are common on the slopes of seamounts and ridges, while current ripples and sand waves occur beneath some fast thermohaline currents whose beds are shallower than the foraminiferal compensation depth. Depositional and erosional bedforms in cohesive sediment have been found beneath the deepest thermohaline currents; they may be restricted to areas where the flow is unusually steady in direction.

Description: Two thousand and twenty well-characterized coral specimens from 17 localities have been analyzed for Sr. Seventy-three genera and subgenera, mostly hermatypic scleractinians, are represented. For some genera, specimens living in surface reef environments are compared with those from 18.3 m depths on the same reefs. Growth rates for some species have also been measured at these depths at one of the sampling sites. Skeletal strontium for a given genus decreases with increasing water temperature, a relationship which previously eluded detection. Aragonite deposited by corals living on the reef at a depth of 18.3 m contains more strontium than the skeletal aragonite of the same coral genera from shallow-water, surface environments. Quantitative treatment of the data for Acropora, one of the most abundant and widely distributed of the reef-building corals, suggests that the observed strontium variations may reflect variations in the rate of skeletal calcification, rather than direct dependence upon temperature or water depth. There is evidence for ‘species effects’, apparently unrelated to growth rate differences, in that certain coral genera are consistently enriched or depleted in skeletal strontium content relative to other genera living in the same reef environments under identical ambient conditions. Temperature, salinity, water depth, seawater composition, and/or other such parameters may in part determine the levels of trace element concentration in carbonates deposited by corals and other marine invertebrates, but it would appear that these variables more directly affect physiological processes which in turn control skeletal chemistry.

Description: When determining vertical velocity spectra from temperature time series and the mean vertical temperature gradient, restrictions may arise friom the existence of fine-structre. Phillips (1971) and Garrett and Munk (1971_ have shown that the fine-structure contamination of internal gravity wave spectra can be written as a function of some statistical properties of the internal wave field and the vertical wave number spectrum of the fine-structure. A consistent set of current and temperature data was obtained during an experiment at Site D to study this problem. The wave number spectrum of the vertical temperature fine-structure and the apparent frequently spectrum of internal waves are determined from these data. In contrast to the asasumptions in the above models, our fine-structure data imply a wave number spectrum proportional to (wave number)−3 in the range which is important here. Using the above set of data, a model is suggested to describe the effect of fine-structure on vertical velocity spectra computed with the mean vertical temperature gradient. It indicates a maximum fine-structure contamination of the true frequency spectrum of internal gravity waves in the middle of the internal wave band, with less contamination at low and high frequencies.

Description: A complete set of linearly independent relationships among the different cross spectral components obtained from pairs of moored instruments is derived which can be utilized to test whether or not the observed fluctuations within the internal wave frequency band represent a field of propagating internal waves. A further complete set of relationships is derived which enables to test whether or not the internal wave field is horizontally isotropic and (or) vertically symmetric. These relations are compared with corresponding relations for alternative models (standing internal wave modes, three-dimensional isotropic turbulence) and their capability to discriminate between the various models is investigated. The tests are applied to a set of data for which it is found that the observed fluctuations are consistent with both propagating and standing internal waves whereas isotropic turbulence must be rejected for the most part of the internal wave frequency band.

Description: This chapter discusses the carbon turnover, calcification, and growth in coral reefs. Carbon turnover within a total reef community is a function of two distinct, biochemically interacting cycles. The first is the metabolic cycle consisting of the photosynthetic fixation of CO2 and the release of CO2 by respiration and decomposition processes. Superimposed on this are the direct incorporation of organic compounds (dissolved or particulate; living or non-living) originating outside the reef systems (in the adjacent ocean waters), and the loss of organic compounds from the reef system into the out-flowing water. The second is the inorganic carbonate cycle involving the biological and non-biological precipitation and dissolution of carbonates. Superimposed on this is the loss of particulate carbonates in suspension in the out-flowing water. The main chemical component of a coral-reef system is calcium carbonate, which occurs either as high-Mg calcite, aragonite, or low-Mg calcite. The mean calcification values in various environments at One Tree Reef are presented in the chapter. These data may be converted to an implied vertical growth rate potential assuming that accrual is dominantly aragonite (density = 2.89 g cm–3) and that there is 50% porosity after normal compaction.