ALBERT

Description: Eocene to Holocene sediments from Ocean Drilling Program (ODP) Site 647 (Leg 105) in the southern Labrador Sea, approximately 200 km south of the Gloria Drift deposits, were investigated for their biogenic silica composition. Three sections of different diagenetic alteration products of primary siliceous components could be distinguished: (1) opal-A was recorded in the Miocene and the early Oligocene time intervals with strongly corroded siliceous skeletons in the Miocene and mostly well preserved biogenic opal in the early Oligocene; (2) opal-CT precipitation occurs between 250-440 meters below seafloor (mbsf) (earliest Oligocene to late Eocene); (3) between 620-650 mbsf (early/middle Eocene), biogenic opal was transformed to clay minerals by authigenesis of smectites. Using accumulation rates of biogenic opal, paleoproductivity was estimated for the early Oligocene to late Eocene interval. A maximum productivity of biogenic silica probably occurred between 35.5 and 34.5 Ma (early Oligocene). No evidence for opal sedimentation during most of middle Eocene was found. However, at the early/middle Eocene boundary (around 52 Ma), increased opal fluxes were documented by diagenetic alteration products of siliceous skeletons.

Description: Hole 642E is located near the outer margin of the Voring Plateau in the Norwegian Sea. The thick pile of basaltic lavas penetrated during drilling are variably altered with extensive development of calcite, which fills vesicles and fractures along with saponite and celadonite. delta13C results, determined by mass spectrometry, show that most carbonates above about 1040 m have values between -2.5 and -5.5 per mil (PDB), but a few samples at approximately 1090 m have depleted delta13C values down to -26.3 per mil. Below 1100 m the delta13C values decrease from -6.0 per mil to -12 per mil. The delta 18O values range between -1.9 and -13.7 per mil (PDB), and generally decrease with depth. The results are interpreted as indicating that the calcites were precipitated from cool seawater percolating through the basalt pile at waterrrock of less than 10:1, during seawater incursion at about 54 Ma. The progressive depletion with depth may result from subsequent reequilibration at temperatures below those of formation, and the geothermal gradient on the Wring Plateau appears to have decreased with time. The very depleted values of delta13C for carbonates around the 1090-m level are probably related to organic matter from an underlying volcaniclastic unit.

Description: Subaerially erupted tholeiites at Hole 642E were never exposed to the high-temperature seawater circulation and alteration conditions that are found at subaqueous ridges. Alteration of Site 642 rocks is therefore the product of the interaction of rocks and fluids at low temperatures. The alteration mineralogy can thus be used to provide information on the geochemical effects of low temperature circulation of seawater. Rubidium-strontium systematics of leached and unleached tholeiites and underlying, continentally-derived dacites reflect interactions with seawater in fractures and vesicular flow tops. The secondary mineral assemblage in the tholeiites consists mainly of smectite, accompanied in a few flows by the assemblage celadonite + calcite (+/- native Cu). Textural relationships suggest that smectites formed early and that celadonite + calcite, which are at least in part cogenetic, formed later than and partially at the expense of smectite. Smectite precipitation occurred under variable, but generally low, water/rock conditions. The smectites contain much lower concentrations of alkali elements than has been reported in seafloor basalts, and sequentially leached fractions of smectite contain Sr that has not achieved isotopic equilibrium. 87Sr/86Sr results of the leaching experiments suggest that Sr was mostly derived from seawater during early periods of smectite precipitation. The basalt-like 87Sr/86Sr of the most readily exchangeable fraction seems to suggest a late period of exposure to very low water /rock. Smectite formation may have primarily occurred in the interval between the nearly 58-Ma age given by the lower series dacites and the 54.5 +/- 0.2 Ma model age given by a celadonite from the top of the tholeiitic section. The 54.5 +/- 0.2 Ma Rb-Sr model age may be recording the timing of foundering of the Voring Plateau. Celadonites precipitated in flows below the top of the tholeiitic section define a Rb-Sr isochron with a slope corresponding to an age of 24.3 +/- 0.4 Ma. This isochron may be reflecting mixing effects due to long-term chemical interaction between seawater and basalts, in which case the age provides only a minimum for the timing of late alteration. Alternatively, inferrential arguments can be made that the 24.3 +/- 0.4 isochron age reflects the timing of the late Oligocene-early Miocene erosional event that affected the Norwegian-Greenland Sea. Correlation of 87Sr/86Sr and 1/Sr in calcites results in a two-component mixing model for late alteration products. One end-member of the mixing trend is Eocene or younger seawater. Strontium from the nonradiogenic endmember can not, however, have been derived directly from the basalts. Rather, the data suggest that Sr in the calcites is a mixture of Sr derived from seawater and from pre-existing smectites. For Site 642, the reaction involved can be generalized as smectite + seawater ++ celadonite + calcite. The geochemical effects of this reaction include net gains of K and CO2 by the secondary mineral assemblage. The gross similarity of the reactions involved in late, low-temperature alteration at Site 642 to those observed in other sea floor basalts suggests that the transfer of K and C02 to the crust during low-temperature seawater-ocean crust interactions may be significant in calculations of global fluxes.

Description: During Ocean Drilling Program Leg 105, 11 holes were drilled in the Labrador Sea and Baffin Bay. Site 645 in Baffin Bay was drilled to a depth of 1147 meters below seafloor (mbsf); planktonic foraminifers were recovered in the upper 110.3 m and in a short interval between 283.8 and 293.5 mbsf. Low species diversity and the lack of species with short stratigraphic ranges inhibited establishment of a planktonic foraminifer biostratigraphic framework at Site 645. Holes 646B and 647A in the Labrador Sea were drilled to depths of 766.7 and 716.6 mbsf, respectively. Although the observed assemblages in the Labrador Sea holes were of low diversity, the first and last occurrences of several age-diagnostic species, when integrated with paleomagnetic stratigraphy, allowed the establishment of a high-latitude Miocene to Holocene planktonic foraminifer biochronology. To determine the relative timing of planktonic foraminifer datum events in the eastern North Atlantic and the Labrador Sea, this biochronology is compared with the temperate-subpolar biozonation of Weaver and Clement (1986, doi:10.1016/0377-8398(86)90033-2). The late Miocene dextral-to-sinistral coiling change in Neogloboquadrina atlantica was observed -1.6 m.y. earlier at Site 646 than at any other site in the Atlantic. The first appearance datums (FAD) of Globorotalia margaritae, Globorotalia puncticulata, Globorotalia inflata, and the last appearance datum (LAD) of N. atlantica are isochronous with their reported ages in the eastern North Atlantic, but the FADs of Globorotalia truncatulinoides and the modern, encrusted form of Neogloboquadrina pachyderma are diachronous.

Description: Authigenic carbonates were recovered in lower to middle Eocene claystones at Ocean Drilling Program Site 647 in the Labrador Sea. Detailed chemical, petrographic, and X-ray investigations reveal that these diagenetic carbonates have a complex mineralogical composition. At least five different carbonate phases are identified: calcium-rich rhodochrosite, rhodochrosite, manganosiderite, siderite, and calcite. Manganese carbonates are the dominant carbonate phases formed throughout the section. Textural analyses show two major generations of carbonate formation. Early cementation of micritic carbonate in burrow structures was followed by carbonate cementation forming microsparry to sparry crystals. At approximately 620 meters below seafloor (mbsf), three concretions of iron carbonates occur, which indicates a special pore-water chemistry. Thin section analyses from this level show (1) several generations of diagenetic carbonates, (2) widespread secondary cavity formation in burrow structures, and (3) various cement precipitations in voids. We suggest that this level represents a hiatus or highly condensed sequence, as indicated by (1) the low carbonate content in host sediments, (2) carbonate dissolution reflected by the high ratio of benthic to planktonic foraminifers, and (3) complex diagenetic alteration in the carbonate concretions. Iron and manganese enrichments observed in lithologic Unit IV may have been derived from a hydrothermal source at the adjacent, then active, Labrador Sea mid-ocean ridge. Authigenic smectites forming numerous pseudomorphs of siliceous microfossils are precipitated in burrow structures. We propose that diagenetic smectite formation from biogenic opal and iron oxyhydroxide (analogous to smectite formation in surface sediments of the East Pacific area) occurred in the Labrador Sea during the early and middle Eocene.

Description: During Ocean Drilling Program Leg 104 a 900-m-thick sequence of volcanic rocks was drilled at Hole 642E on the Vøring Plateau, Norwegian Sea. This sequence erupted in two series (upper and lower series) upon continental basement. The upper series corresponds to the seaward-dipping seismic reflectors and comprises a succession of about 122 flows of transitional oceanic tholeiite composition. They have been subdivided into several formations consisting of flows related to each other by crystal fractionation processes, magma mixing, or both. Major- and trace-element chemistry indicates affinities to Tertiary plateau lavas of northeast Greenland and to Holocene lavas from shallow transitional segments of the Mid-Atlantic Ridge, such as Reykjanes Ridge. The tholeiitic magmas have been derived from a slightly LREE-depleted mantle source. Two tholeiitic dikes that intruded the lower series derive from an extremely depleted mantle source. Interlayered volcaniclastic sediments are dominantly ferrobasaltic and more differentiated. They appear to come from a LREE-enriched mantle source, and may have been erupted in close vicinity of the Vøring Plateau during hydroclastic eruptions. The two tholeiitic dikes that intruded the lower series as well as some flows at the base of the upper series show evidence of assimilation of continental upper crustal material.

Description: Geochemical analyses of the middle Eocene through lower Oligocene lithologic Unit IIIC (260-518 meters below seafloor [mbsf]) indicate a relatively constant geochemical composition of the detrital fraction throughout this depositional interval at Ocean Drilling Program (ODP) Site 647 in the southern Labrador Sea. The main variability occurs in redox-sensitive elements (e.g., iron, manganese, and phosphorus), which may be related to early diagenetic mobility in anaerobic pore waters during bacterial decomposition of organic matter. Initial preservation of organic matter was mediated by high sedimentation rates (36 m/m.y.). High iron (Fe) and manganese (Mn) contents are associated with carbonate concretions of siderite, manganosiderite, and rhodochrosite. These concretions probably formed in response to elevated pore-water alkalinity and total dissolved carbon dioxide (CO2) concentrations resulting from bacterial sulfate reduction, as indicated by nodule stable-isotope compositions and pore-water geochemistry. These nodules differ from those found in upper Cenozoic hemipelagic sequences in that they are not associated with methanogenesis. Phosphate minerals (carbonate-fluorapatite) precipitated in some intervals, probably as the result of desorption of phosphorus from iron and manganese during reduction. The bulk chemical composition of the sediments differs little from that of North Atlantic Quaternary abyssal red clays, but may contain a minor hydrothermal component. The silicon/ aluminum (Si/Al) ratio, however, is high and variable and probably reflects original variations in biogenic opal, much of which is now altered to smectite and/or opal CT. An increase in the sodium/potassium (Na/K) ratio in the upper Eocene corresponds to the beginning of coarsergrained feldspar flux to the site, possibly marking the onset of more vigorous deep currents. Although the Site 647 cores provide a nearly complete high-resolution, high-latitude Eocene-Oligocene record, the high sedimentation rate and somewhat unusual diagenetic conditions have led to variable alteration of benthic foraminifers and fine-fraction carbonate and have overprinted the original stable-isotope records. Planktonic foraminifers are less altered, but on the whole, there is little chance of sorting out the nature and timing of environmental change on the basis of our stable-isotope analyses.

Description: Between 1086.6 and 1229.4 m below seafloor at Site 642 on the Outer Vøring Plateau, a series of intermediate volcanic extrusive flow units and volcaniclastic sediments was sampled. A mixed sequence of dacitic subaerial flows, andesitic basalts, intermediate volcaniclastics, subordinate mid-ocean ridge basalt, (MORB) lithologies, and intrusives was recovered, in sharp contrast to the more uniform tholeiitic T-type MORB units of the overlying upper series. This lower series of volcanics is composed of three chemically distinct groups, (B, A2, A1), rather than the two previously identified. Flows of the dacitic group (B) have trace-element and initial Sr isotope signatures which indicate that their source magma derived from the partial melting of a component of continental material in a magma chamber at a relatively high level in the crust. The relative proportions of crustal components in this complex melt are not known precisely. The most basic group (A2) probably represents a mixture of this material with MORB-type tholeiitic melt. A third group (A1), of which there was only one representative flow recovered, is chemically intermediate between the two groups above, and may suggest a repetition of, or a transition phase in, the mixing processes.