Isotopic composition of strontium in planktonic foraminiferas from sediments of the DSDP Holes 90-588 and 94-607

Measurements of 87Sr/86Sr on samples of planktonic foraminifers were used to reconstruct changes in the Sr isotopic composition of seawater for the past 8 Ma. The late Neogene was marked by a general, but not regular, increase in 87S/86Sr with two breaks in slope at 5.5 and 2.5 Ma. These times mark the beginning of two periods of steep increase in 87Sr/86Sr values, relative to preceding periods characterized by essentially constant values. During the last 2.5 Ma, 87Sr/86Sr values increased at an average rate of 0.000054/Ma. This steep increase suggests that the modem ocean is not in Sr isotopic equilibrium relative to its major input fluxes. A non-equilibrium model for the modern Sr budget suggests that the residence time of Sr is ~2.5 Ma, which is significantly less than previously accepted estimates of 4-5 Ma. Modelling results suggest that the increase in 87Sr/86Sr over the past 8 Ma could have resulted from a 25% increase in the riverine flux of Sr or an increase in the average 87Sr/86Sr of this flux by 0.0006. The dominant cause of increasing 87Sr/86Sr values of seawater during the late Neogene is believed to be increased rates of uplift and chemical weathering of mountainous regions. Calculations suggest that uplift and weathering of the Himalayan-Tibetan region alone can account for the majority of the observed 87Sr/86Sr increase since the early Late Miocene. Exhumation of Precambrian shield areas by continental ice-sheets may have contributed secondarily to accelerated mechanical and chemical weathering of old crustal silicates with high 87Sr/86Sr values. In fact, the upturn in 87Sr/86Sr at 2.5 Ma coincides with increased glacial activity in the Northern Hemisphere. A variety of geochemical (87Sr/86Sr, Ge/Si, d13C, CCD, etc.) and sedimentologic data (accumulation rates) from the marine sedimentary record are compatible with a progressive increase in the chemical weathering rate of continents and dissolved riverine fluxes during the late Cenozoic. We hypothesize that chemical weathering of the continents and dissolved riverine fluxes to the oceans reached a maximum during the late Pleistocene because of repeated glaciations, increased continental exposure by lowered sea level, and increased continental relief resulting from high rates of tectonism.

(Table 1) Helium concentration and flux in DSDP Hole 94-607 samples

Most of the helium-3 in oceanic sediments conies from interplanetary dust particles (IDPs), and can therefore be used to infer the accretion rate of dust to the Earth through time (Ozima et al., 1984, doi:10.1038/311448a0; Takayanagi and Ozima, 1987, doi:10.1029/JB092iB12p12531; Farley, 1995, doi:10.1038/376153a0). 3He records from slowly accumulating pelagic clays indicate that the accretion rate varies considerably over millions of years, probably owing to cometary and asteroidal break-up events3. Muller and MacDonald have proposed (Muller and MacDonald, 1995, doi:10.1038/377107b0) that periodic changes in this accretion rate due to a previously unrecognized 100-kyr periodicity in the Earth's orbital inclination might account for the prominence of this frequency in climate records of the past million years (Imbrie et al., 1993, doi:10.1029/93PA02751). Here we report variations in the 3He flux to the sea floor that support this idea. We find that the flux recorded in rapidly accumulating Quaternary sediments from the Mid-Atlantic Ridge oscillates with a period of about 100 kyr. We cannot yet say, however, whether the 100-kyr climate cycle is a consequence of, a cause of, or an effect independent of these periodic changes in the rate of delivery of interplanetary dust to the sea floor.