Linear sedimentation rates and approximate mass accumulation rates at DSDP Site 61-462

A 560-meter-thick sequence of Cenomanian through Pleistocene sediments cored at DSDP Site 462 in the Nauru Basin overlies a 500-meter-thick complex unit of altered basalt flows, diabase sills, and thin intercalated volcaniclastic sediments. The Upper Cretaceous and Cenozoic sediments contain a high proportion of calcareous fossils, although the site has apparently been below the calcite compensation depth (CCD) from the late Mesozoic to the Pleistocene. This fact and the contemporaneous fluctuations of the calcite and opal accumulation rates suggest an irregular influx of displaced pelagic sediments from the shallow margins of the basin to its center, resulting in unusually high overall sedimentation rates for such a deep (5190 m) site. Shallow-water benthic fossils and planktonic foraminifers both occur as reworked materials, but usually are not found in the same intervals of the sediment section. We interpret this as recording separate erosional interludes in the shallow-water and intermediate-water regimes. Lower and upper Cenozoic hiatuses also are believed to have resulted from mid-water events. High accumulation rates of volcanogenic material during Santonian time suggest a corresponding significant volcanic episode. The coincidence of increased carbonate accumulation rates during the Campanian and displacement of shallow-water fossils during the late Campanian-early Maestrichtian with the volcanic event implies that this early event resulted in formation of the island chains around the Nauru Basin, which then served as platforms for initial carbonate deposition.

Abundance and biomass of macrobenthic infauna of the offshore northern North Sea

Between 1980 and 1985 ninety-seven stations were sampled by Smith-Mclntyre grab from the offshore northern section of the North Sea. Four hundred and nine infaunal species were identified from the 76 selected macrofaunal stations. The number of species per station varied from 25 to 80 with a maximum abundance of 9,600 individuals m**2. The biomass ranged from 0.13 to 18.86 g dry weight m**2. At most stations, however, biomass varied between 1 and 4 g dry weight m**2. Diversity and abundance were highest in the 120-140 m zone, characterised by fine sand containing variable amounts of silt. The highest biomasses were recorded in two areas; firstly where stronger currents predominate and the sediments are coarser (east of Shetland and west of the Norwegian Trough), and secondly in the fine sandy deposits of the centrally located area. In the silty sediments (Fladen Ground and smaller depressions) there was a predominantly subsurface deposit-feeding community, whereas in the coarser area east of the Shetlands carnivores predominated. Over the remaining area surface deposit feeders were dominant.

Chemical composition of bottom sediments along the Transpacific section

Distribution of Fe, Mn, Ti, Cu, Ni, Co, V, Cr, Mo, As in bottom sediments of a section from the Hawaiian Islands to the coast of Mexico. In the surface layer and isochronic layers of sediments from biogenic-terrigenous sediments of the Mexico coast to pelagic red clays of the Northeast Basin contents of all studied elements increase, and more sharply for mobile ones - Mn, Mo, Cu, Ni, Co, As. In near Hawaii sediments rich in coarsely fragmented volcanic-terrigenous and pyroclastic material of basalt composition enriched in Ti, Fe, Cr, V, P contents of these elements in surface sediments and in sediment mass increase and contents of Mn, Mo, Ni, Co, Cu, As (for the same reason) decrease compared to red clays. An area of hemipelagic and transition sediments is identified; these sediments have much higher contents of Mn, Fe, Cu, Ni, Mo, As, (Ba) than red clays and similar sediments of the Northwest Pacific Ocean. This is due to hydrothermal activity in the tectonically active zone at the northern extension of the East Pacific Rise. Similar character of distribution of the elements in the surface layer and in the isochrone layers of bottom sediments along the most part of the section is shown. Similarity between distribution of the elements in sediments of the western and the eastern parts of the Transpacific section is established.

Silicoflagellate abundances in sediments of ODP Leg 207 sites

The Ocean Drilling Program (ODP) drilled at five sites in the western Atlantic Ocean during Leg 207. The objective of the drilling was to recover samples from the shallow buried Cretaceous and Paleocene sediments on the Demerara Rise off Suriname, South America. These sediments are being studied for a number of paleoceanographic studies of the low-latitude Atlantic off the coast of Suriname (this volume). For this report two sites, Sites 1257 and 1258, were selected for silicoflagellate study because shipboard results suggested these two sites as the only ones with siliceous microfossils of Paleocene-Eocene age. The Demarara Rise is a predominant submarine plateau located off the coast of Suriname and French Guyana. This plateau stretches 380 km along the coast and is 220 km wide. The depth to seafloor along the depth transect drilled during ODP Leg 207 ranges from 1000 to 4500 m, but most of the remainder of the plateau lies in shallow water of 700 m. Much of this area is covered with 2-3 km of sediments. The Demerara Rise is built on rifted Precambrian continental crust. The plateau was one of the last places to be in contact with West Africa during the opening of the Atlantic Ocean (see Shipboard Scientific Party, 2004). Site 1257 (9°27'N, 54°20'W; water depth = 2951 m) is located on a terrace on the northwestern Demerara Rise ~400 km from Suriname. This is the second deepest water depth location drilled during Leg 207. Sediments from this area range in age from Miocene to Albian. This area is part of the transform fault that separated from Central America and western Africa. Three holes were drilled at Site 1257. Site 1258 (9°26'N, 54°43'W; water depth = 3192 m) is located on the western slope of the Demerara Rise ~380 km north of Suriname. This site is the distal and deepest site of the paleoceanographic depth transect drilled across Demerara Rise during Leg 207. The area is located on a ridge of Paleocene sediments cropping out on the seafloor. Three holes were drilled at Site 1258, but only one is studied.

Pelagic, turbiditic, and contouritic sequential deposits on the Cape Verde Plateau

On the Cape Verde Plateau, Neogene deposits are composed of major pelagic and hemipelagic sediments. These sediments show climatic sequences composed of two lithologic terms that differ in their siliciclastic and carbonate contents. Several turbiditic and contouritic sequences are interbedded in these deposits. Turbidite sequences are fine grained and thin bedded with a very low frequency (about 12 sequences during the Neogene). They are composed of quartz-rich siliciclastic or volcaniclastic sediments. Quartz-rich turbidites originated from the Senegalese margin. Their slightly higher frequency during the early Pliocene indicates that the stronger turbidity currents, and probably the most abundant continental inputs, occur at that period. Volcaniclastic turbidites are only present in the early Miocene (about 17 Ma) and the early Pleistocene (1 Ma). They have flown from adjacent Cape Verde Islands and reflect two episodes of high volcanic activity in this area. Contourite sequences, composed of biogenic sandy silts, represent less than 5% of the sediment pile and seem to have been mainly deposited during the late Pleistocene. These different sequences show clay mineral variations throughout Neogene time. Kaolinite is predominant in the Miocene and lower Pliocene deposits; this mineral decreases thereafter, with an increased trend of illite in the uppermost Pliocene and Pleistocene sediments, suggesting a change in sediment sources on the Saharan continent at about 2.6 Ma.

Geochemistry of Baltic Sea sediments

The Baltic Sea has experienced three major intervals of bottom water hypoxia following the intrusion of seawater ca. 8 kyrs ago. These intervals occurred during the Holocene Thermal Maximum (HTM), Medieval Climate Anomaly (MCA) and during recent decades. Here, we show that sequestration of both Fe and Mn in Baltic Sea sediments generally increases with water depth, and we attribute this to shelf-to-basin transfer ("shuttling") of Fe and Mn. Burial of Mn in slope and basin sediments was enhanced following the lake-brackish/marine transition at the beginning of the hypoxic interval during the HTM. During hypoxic intervals, shelf-to-basin transfer of Fe was generally enhanced but that of Mn was reduced. However, intensification of hypoxia within hypoxic intervals led to decreased burial of both Mn and Fe in deep basin sediments. This implies a non-linearity in shelf Fe release upon expanding hypoxia with initial enhanced Fe release relative to oxic conditions followed by increased retention in shelf sediments, likely in the form of iron sulfide minerals. For Mn, extended hypoxia leads to more limited sequestration as Mn carbonate in deep basin sediments, presumably because of more rapid reduction of Mn oxides formed after inflows and subsequent escape of dissolved Mn to the overlying water. Our Fe records suggest that modern Baltic Sea hypoxia is more widespread than in the past. Furthermore, hypoxia-driven variations in shelf-to-basin transfer of Fe may have impacted the dynamics of P and sulfide in the Baltic Sea thus providing potential feedbacks on the further development of hypoxia.

Bulk mineralogy of Cretaceous to Quaternary sediments from the Kerguelen Plateau

Carbonate-free portions of Upper Cretaceous to Holocene sediment samples from the Kerguelen Plateau in the southern Indian Ocean were investigated by X-ray diffraction. Downhole variations in the content of opal-A, opal-CT, quartz, feldspar, barite, and clinoptilolite were studied at Site 737 on the northern Kerguelen Plateau and at Sites 744 and 738 on the southern Kerguelen Plateau. The variation of these components reflects temporal changes in the depositional history of the Kerguelen Plateau as well as major differences in the sedimentary evolution between the northern plateau and the southern plateau. Carbonate is the dominant component in the pelagic sediments on the Kerguelen Plateau. In addition, biogenic opal sedimentation plays an important role throughout most of the sequence. A major increase in opal accumulation is documented at all sites in late Miocene time, which is in accordance with the well-known increase in silica productivity probably caused by a major cooling step. Because of its position near the Polar Frontal Zone, sediments from Site 737 show a more extensive opal deposition than at Sites 744 and 738. An earlier productivity pulse is documented at Site 744 on the southern plateau within the early Oligocene, following the initial phase of intense East Antarctic glaciation. This cooling event resulted in higher amounts of ice-rafted terrigenous quartz and, to a lesser extent, feldspar. With the exception of the Site 744 sediments, opal deposition in Paleogene and older sediments can be reconstructed only from the diagenetic transformation products of opal-CT and probably clinoptilolite. In contrast to the southern sequence, on the northern Kerguelen Plateau higher amounts of clinoptilolite and no opal-CT were found. These major differences in the diagenetic environments may be due to extensive volcanism in the northern area. The volcanic influence at Site 737 is well recorded by the higher feldspar content and higher amounts of volcanic glass shards.

(Table 1) Geochemistry of upper Paleocene and upper Eocene glass particles at DSDP Hole 80-549

Two ash horizons have been identified in Hole 549, one in the upper Paleocene (basal NP9), the other in the upper Eocene (NP18); both are mixed lithic crystal tuffs of rhyolitic composition. These tuffs are absent in Hole 550 owing to unconformities, but the basal Eocene (NP10) of Hole 550 includes a series of over 50 thin bentonite layers. Intermediate plagioclase associated with these bentonites indicates that the original ash was of basaltic to andesitic composition. The bentonites are absent in Hole 549, probably because of an unconformity, but they have been identified in Hole 401 (Leg 48, Bay of Biscay). Two of the pyroclastic phases can be matched with phases previously reported for the North Sea Basin. The bentonites of Site 550 are probably equivalent to the widespread "ash series" of northwestern Europe, which may therefore be regarded as being lower Eocene in terms of Martini's calcareous nannoplankton zonation.

Geochemistry of subducted volcaniclastic sediments from Mariana arc magmas

The phase relations of natural volcaniclastic sediments from the west Pacific Ocean were investigated experimentally at conditions of 3-6 GPa and 800-900 °C with 10 wt.% added H2O (in addition to ~ 10 wt.% structurally-bound H2O) to induce hydrous melting. Volcaniclastic sediments are shown to produce a sub-solidus assemblage of garnet, clinopyroxene, biotite, quartz/coesite and the accessory phases rutile ± Fe-Ti oxide ± apatite ± monazite ± zircon. Hydrous melt appears at temperatures exceeding 800-850 °C, irrespective of pressure. The melt-producing reaction consumes clinopyroxene, biotite and quartz/coesite and produces orthopyroxene. These phase relations differ from those of pelagic clays and K-bearing mid ocean ridge basalts (e.g. altered oceanic crust) that contain phengite, rather than biotite, as a sub-solidus phase. Despite their relatively high melt productivity, the wet solidus for volcaniclastic sediments is found to be higher (825-850 °C) than other marine sediments (700-750 °C) at 3 GPa. This trend is reversed at high-pressure conditions (6 GPa) where the biotite melting reaction occurs at lower temperatures (800-850 °C) than the phengite melting reaction (900-1000 °C). Trace element data was obtained from the 3 GPa run products, showing that partial melts are depleted in heavy rare earth elements (REE) and high field strength elements (HFSE), due to the presence of residual garnet and rutile, and are enriched in large ion lithophile elements (LILE), except for Sr and Ba. This is in contrast to previous experimental studies on pelagic sediments at sub-arc depths, where Sr and Ba are among the most enriched trace elements in glasses. This behavior can be partly attributed to the presence of residual apatite, which also host some light REE in our supra-solidus residues. Our new experimental results account for a wide range of trace element and U-series geochemical features of the sedimentary component of the Mariana arc magmas, including imparting a substantial Nb anomaly to melts from an anomaly-free protolith.

Annual 10Be concentrations from Lakes Tiefer See and Czechowskie AD1983-2009

Beryllium 10 concentrations (10Becon) were measured at annual resolution from varved sediment cores of Lakes Tiefer See (TSK) and Czechowskie (JC) for the period 1983-2009 (~solar cycles 22 and 23). Calibrating the 10Becon time-series against complementing proxy records from the same archive as well as local precipitation and neutron monitor data, reflecting solar forced changes in atmospheric radionuclide production, allowed (i) identifying the main depositional processes and (ii) evaluating the potential for solar activity reconstruction. 10Becon in TSK and JC sediments are significantly correlated to varying neutron monitor counts (TSK: r=0.5, p=0.05, n=16; JC: r=0.46, p=0.03, n=22). However, the further correlations with changes in organic carbon contents in TSK as well as varying organic carbon and detrital matter contents in JC point to catchment specific biases in the 10Becon time-series. In an attempt to correct for these biases multiple regression analysis was applied to extract an atmospheric 10Be production signal (10Be atmosphere). To increase the signal to noise ratio a 10Be composite record (10Be composite) was calculated from the TSK and JC 10Be atmosphere time-series. 10Becomposite is significantly correlated to variations in the neutron monitor record (r=0.49, p=0.01, n=27) and matches the expected amplitude changes in 10Be production between solar cycle minima and maxima. This calibration study on 10Be from two sites indicates the large potential but also, partly site-specific, limitations of 10Be in varved lake sediments for solar activity reconstruction.

Clay minerals at DSDP Sites 71-511 and 71-513

The distribution of clay minerals, determined by X-ray diffraction, is given for Jurassic to Holocene sediments recovered at DSDP Sites 511 and 513 in the Southwest Atlantic. These data, plus the lithologic and paleoenvironmental information gathered by the shipboard scientists, are used to subdivide the sedimentary sequence into genetic lithologic facies labeled series, seven for Site 511 and two for Site 513. Sediments of these series reflect the main historical and paleoenvironmental events which other means of study have determined to affect this region; particularly important was the opening of the South Atlantic during the Early Cretaceous.

(Table 1) Oxygen and carbon isotope compositions of altered carbonates from DSDP Hole 6-53 from the western Pacific Ocean

In the lower part of DSDP core 53.0, partly recrystallized carbonate sediments and well recrystallized limestone breccias of Oligo-Miocene age are associated with altered volcanic flows, lithified tuffs, and tuff breccias, suggesting that carbonate alteration was the result of thermal metamorphism. However, the oxygen isotope compositions of these carbonates (-3.4 to +0.6 per mil rel. PDB) are not compatible with recrystallization and isotope exchange with sea water at high temperatures. Evaluating the effects of the composition of the water which exchanged with the carbonates and of carbonate-water isotope exchange in closed systems yields the following approximate maximum temperature of recrystallization: limestone breccias, 100°C; calcite veins rimming breccia clasts, 30°C; and unconsolidated sediments overlying the breccias, 20°C. Therefore, the volcanics at site 53.0 must have been emplaced into the primary carbonate sediments at relatively low temperatures. Subsequent carbonate alteration was probably a consequence of chemical changes in ambient pore waters resulting from the submarine weathering of volcanic material.