Sulphur contents and partition of iron in ODP Leg 112 sediments

Porewaters in site 680 Peru Margin sediments contain dissolved sulfide over a depth of approximately 70 m which, at a sedimentation rate of 0.005 cm/yr, gives a sediment exposure time to dissolved sulfide of about 1.4 Myr. Reactions with dissolved sulfide cause the site 680 sediments to show a progressive decrease in a poorly-reactive silicate iron fraction, defined as the difference between iron extracted by dithionite (FeD) at room temperature and that extracted by boiling concentrated HCl (FeH), normalised to the total iron content (FeT). Straight line plots are obtained for ln[(FeH - FeD)/FeT] against time of burial, from which a first order rate constant of 0.29 1/Myr (equivalent to a half-life of 2.4 Myr) can be derived for the sulfidation of this silicate iron. Comparable half-lives are also found for the same poorly-reactive iron fraction in the nearby site 681 and 684 sediments. This silicate Fe fraction comprises 0.8-1.0% Fe, only 30-60% of which reacts even with 1.5-3 million years exposure to dissolved sulfide. Diagenetic models based on porewater concentrations of sulfate and sulfide, and solid phase iron contents, at site 680 are consistent in indicating that this poorly-reactive iron fraction is only sulfidized on a million year time scale. Silicate iron not extracted by HCl can be regarded as unreactive towards dissolved sulfide on the time scales encountered in marine sediments.

Chemistry of interstitial waters of ODP Leg 112 samples

Two distinct hydrogeochemical regimes currently dominate the Peruvian continental margin. One, in shallower water (150-450 m) shelf to upper-slope regions, is characterized by interstitial waters with strong positive chloride gradients with depth. The maximum measured value of 1043 mM chloride at Site 680 at ITS corresponds to a degree of seawater evaporation of ~2 times. Major ion chemistry and strontioum isotopic composition of the interstitial waters suggest that a subsurface brine that has a marine origin and is of pre-early Miocene "age," profoundly influences the chemistry and diagenesis of this shelf environment. Site 684 at ~9°S must be closest to the source of this brine, which becomes diluted with seawater and/or interstitial water as it flows southward toward Site 686 at ~13?S (and probably beyond) at a rate of approximately 3 to 4 cm/yr, since early Miocene time. The other regime, in deep water (3000-5000 m) middle to lower-slope regions, is characterized by interstitial waters with steep negative and nonsteady-state chloride gradients with depth. The minimum measured value of 454 mM chloride, at Site 683 at ITS, corresponds to ~20% dilution of seawater chloride The most probably sources of these low-chloride fluids are gas hydrate dissociation and mineral (particularly clay) dehydration reactions. Fluid advection is consistent with (1) the extent of dilution shown in the chloride profiles, (2) the striking nonsteady-state depth profiles of chlorides at Sites 683 and 688 and of 87Sr/86Sr ratios at Site 685, and (3) the temperatures resulting from an average geothermal gradient of 50°C/km and required for clay mineral dehydration reactions. Strontium isotope data reveal two separate fluid regimes in this slope region: a more northerly one at Sites 683 and 685 that is influenced by fluids with a radiogenic continental strontium signature, and a southerly one at Sites 682 and 688 that is influenced by fluids with a nonradiogenic oceanic signatures. Stratigraphically controlled fluid migration seems to prevail in this margin. Because of its special tectonic setting, Site 679 at ITS is geochemically distinct. The interstitial waters are characterized by seawater chloride concentrations to -200 mbsf and deeper by a significantly lower chloride concentration of about two-thirds of the value in seawater, suggesting mixing with a meteoric water source. Regardless of the hydrogeochemical regime, the chemistry and isotopic compositions of the interstitial waters at all sites are markedly modified by diagenesis, particularly by calcite and dolomite crystallization.

Carbon and Sulphur concentrations of sediments from Peru, Oman and Benguela upwelling environments

Abundances of organic carbon, sulfur, and reactive iron in sediments of three upwelling environments (Peru, Oman and Benguela) suggest that organic carbon/reduced sulfur ratios (C/S-ratios) in this category of marine sediments deviate considerably from previously established empirical ratios in normal marine sediments. To clarify the discrepancies, we investigated those components of the diagenetic system that limit the formation of pyrite: sulfate concentrations and reduction rates in pore waters, availability of reactive iron, and the quantity and quality of organic matter. All three limitations are evident in our sample pools. The results suggest that C/S-ratios in recent and fossil marine sediments rich in organic matter may be unsuitable as paleoenvironmental indicators.

Planktonic foraminifera in ODP Hole 112-688A (Table 1)

Species of Globorotalia are among the most dissolution-resistant planktonic foraminifers in sediments of the inner wall of the Middle America Trench; parts of their Phylogenetic history have been recognized in sediments of Leg 107 (Glacon and Bourgois, 1985). These species can be integrated into the biostratigraphic scheme on the basis of calcareous and siliceous nannoplankton and calibrated on the basis of paleomagnetism (Keller, 1980, 1981; Keller et al., 1982; Barron and Keller, 1982). Data compiled for this data report extend to the southern area of occurrence of Globorotalia species. About 250 sediment samples were collected on board JOIDES Resolution and examined as follows: 20-cm**3 samples were dried for 8 hr at 60°C, weighed, and then washed through sieves of 0.5, 0.2, 0.125, and 0.063 mm mesh size. The residues were dried and reweighed. The abundance of planktonic foraminifers counted is reported as numbers of specimens per weight of the original sample.

Tertiary and Quaternary calcareous nannoplankton biostratigraphy of ODP Leg 112 holes

Positions of all cores recovered during Ocean Drilling Program (ODP) Leg 112 off Peru are shown in the standard calcareous nannoplankton zonation. Stratigraphic and regional occurrences and preservation of calcareous nannoplankton are discussed for all sites, and fossil lists are presented for selected samples. Late Miocene to Holocene nannoplankton assemblages in the upwelling systems off Peru and scattered blooms, especially of Gephyrocapsa species and Helicosphaera carteri, are described. Scyphosphaera assemblages found in late Miocene Zone NN9 {Discoaster hamatus Zone) at Site 684 are compared with similar assemblages from Gabon on the west coast of Africa. Remarkable subsidence is indicated by early and middle Eocene nearshore and shallow-water nannoplankton assemblages for Sites 682, 683, and 688. Besides several local hiatuses, major regional hiatuses were noted at Site 682 (upper Eocene, uppermost middle Eocene, and part of the lower and middle Oligocene missing), Site 683 (uppermost middle Eocene to lower part of the middle Miocene missing), and Site 688 (part of the middle Eocene, uppermost middle Eocene to upper Oligocene, and parts of the lower and middle Miocene missing).

Costs - UCPR rr 681 and 684

In BHP Coal Pty Ltd v K Orenstein & Koppel AG (No 2) [2009] QSC 64 McMurdo J considered the circumstances in which the ordinary rule under r 681 of the Uniform Civil Procedure Rules 1999 (Qld) (UCPR) that costs should follow the event should be departed from in favour of a party who was unsuccessful overall, but who succeeded on particular questions. When the court is satisfied that a departure from the usual order under r 681 of the UCPR is justified, it appears increasingly willing to exercise the power in r 684(2) to declare what percentage of costs was applicable to a particular issue

Sapientia, 1974, Vol. XXIX, nº 112 (número completo)

Contenido: Le príncipe d’idetité chez Saint Thomas / R. Verneaux – Unidad de ser y analogía en Santo Tomás de Aquino / Cesáreo López Salgado – St. Thomas’ solution of the problema of faith and reason / A. G. M. Van Melsen – Necesidad de la directa confrontación de textos / Carlos A. Iturralde Colombres – Notas y comentarios -- Bibliografía