Corrected index properties for ODP Leg 127 and 128 sites

During Legs 127 and 128, we found a systematic error in the index property measurements, in that the wet bulk density, grain density, and porosity did not satisfy well-established interrelationships. We have found that an almost constant difference exists between the weight of water lost during drying and the volume of water lost. This discrepancy is independent of volume or water content of the sample. The water losses should be equal because the density of water is close to 1.0 g/cm**3. The pycnometer wet volume measurement has been identified as the source of the systematic error. The wet volume on average is 0.2 cm**3 too low. For the rare cases when the water content is negligible, there is no offset. The source of the wet volume error results from the partial vapor pressure of water in the pycnometer cell. Newly corrected tables of index properties measured during Legs 127 and 128 are included. The corrected index properties are internally consistent. The data are in better agreement with theoretical models that relate the index properties to other physical properties, such as thermal conductivity and acoustic velocity. In future, a standard volume sampler should be used, or the wet volume should be calculated from the dry volume and the water loss by weight.

Miocene pollen of ODP Leg 127 sites

Pollen floras were obtained from Miocene sediments recovered at four sites drilled during Ocean Drilling Program Leg 127. The local pollen floras of each site were correlated to the standard pollen zones of northeast Japan by using the concept of the essential members for each pollen zone. At Site 797, the complete floral range was obtained for recognition of the NP2 zone and the pollen components of the NP1 zone were also clarified continuously. The ages of the boundaries between pollen zones NP4/NP3, NP3/NP2, and NP2/NP1 are estimated to be about 7 Ma, 13 Ma, and 17-18.5 Ma, respectively. Even in the same pollen zone, the ratios of major pollen taxa vary with the location. This variation is expressed on maps representing two different times during the Miocene.

Palynology of ODP Leg 127 sites

This initial survey of pollen from 192 samples from Hole 794A, supplemented by 189 samples from Hole 795 and 797B, suggests that marine pollen assemblages from the southwestern Sea of Japan provide a consistent Neogene pollen stratigraphy and a solid basis for regional paleoenvironmental reconstructions. Late Miocene vegetation inferred from these pollen data, a mix of conifer and broad-leaf elements with now-extinct Tertiary types well represented, appears similar to Aniai-type floras of Japan. During the late Miocene through early Pliocene, as Tertiary types declined, conifers (including the Sequoia/Cryptomeria group) became more prominent than broad-leaf elements, and herbs played an increasing role in the vegetation. Middle Pliocene pollen assemblages imply significant changes in forest composition. In a 500,000-yr interval centered at ~4 m.y., Tertiary and warm-temperate deciduous types re-expanded and were comparable to or greater than middle-late Miocene levels. Temperate and cold-temperate conifers {Picea, Abies, Tsuga) were minimal. Subsequently, Tertiary and deciduous forest components (including Quercus) decreased, Picea, Tsuga, and Abies were again prominent, and herbs formed an increasingly larger part of the vegetation. Between ~3 m.y. and -2.5 m.y., conifers, except for Cryptomeria types, were prominent, Quercus continued to decline, and other broad-leaf trees were minor. Over the last 2 Ma, the very large and frequent changes in forest composition inferred from pollen in the Sea of Japan correspond to forest dynamics inferred from changes in pollen and floral assemblages throughout Japan. Given present vegetation/climate relationships, broad trends in Neogene climate inferred from these preliminary pollen data include decreasing temperatures, increasing seasonality in temperatures and precipitation, and increasing amplitude and frequency of climatic change. Two significant events, centered at ~9 m.y. and ~4 m.y., punctuate the gradual deterioration of the equable warm, humid subtropical/warm temperate late Miocene and early Pliocene climates. The first indication of cold-temperate conditions comparable to those of Pleistocene glacial intervals occurs ~3 m.y. Subsequently, regional climates oscillated rapidly between temperate and cold-temperate regimes that supported conifer and mixed broad-leaf forests; however, climatic extremes were apparently never great enough to displace warm-temperate and temperate forests from Honshu nor to produce arctic climates on the west coast of Japan.

(Table S1) Diatom species richness from the Early Pleistocene to present

The extent to which the spatial distribution of marine planktonic microbes is controlled by local environmental selection or dispersal is poorly understood. Our ability to separate the effects of these two biogeographic controls is limited by the enormous environmental variability both in space and through time. To circumvent this limitation, we analyzed fossil diatom assemblages over the past ~1.5 million years from the world oceans and show that these eukaryotic microbes are not limited by dispersal. The lack of dispersal limitation in marine diatoms suggests that the biodiversity at the microbial level fundamentally differs from that of macroscopic animals and plants for which geographic isolation is a common component of speciation.