(Table 2) Details of laminated intervals of ODP Leg 158 holes

Scanning electron microscope (SEM)-based analyses of the laminated diatom oozes encountered during Leg 138 reveal three major laminae types. The first lamina type is composed of multiple layers of ~20-?m-thick diatom mats, which form laminae dominated by assemblages of the pennate diatom, Thalassiothrix longissima. More than one variety/subspecies of T. longissima occurs within these laminae (referred to as the T. longissima Group). The second lamina type is composed of a mixed-assemblage of several species of diatoms (centric and pennate varieties), calcareous nannofossils, and subordinate quantities of radiolarians, silicoflagellates and foraminifers. The third lamina type is dominated by an assemblage of nannofossils and minor amounts of those fossil components mentioned above. This last form of lamination is compositionally similar to the background sediment type, foraminifernannofossil ooze (F-NO). Two lamina associations occur within the laminated intervals; the first comprises alternations of T. longissima Group and mixed-assemblage laminae (average thickness is ~6 mm) and the second is composed of T. longissima and nannofossil-rich laminae (average thickness is ~3.5 mm). The arrangement of laminae probably originates from the deposition of multiple layers of 20-?m-thick mats from one mat-flux episode. The much thinner nannofossil-rich laminae are interpreted to represent periods of more ônormalö deposition between mat-flux episodes. The occurrence of several varieties/subspecies of T. longissima within individual mat layers is consistent with observations of Rhizosolenia diatom mats in the modern world ocean.

Diatom abundances in sediment core CESAR_83-006

The modern Arctic Ocean is regarded as a barometer of global change and amplifier of global warming (Graversen et al., 2008, doi:10.1038/nature06502) and therefore records of past Arctic change are critical for palaeoclimate reconstruction. Little is known of the state of the Arctic Ocean in the greenhouse period of the Late Cretaceous epoch (65-99 million years ago), yet records from such times may yield important clues to Arctic Ocean behaviour in near-future warmer climates. Here we present a seasonally resolved Cretaceous sedimentary record from the Alpha ridge of the Arctic Ocean. This palaeo-sediment trap provides new insight into the workings of the Cretaceous marine biological carbon pump. Seasonal primary production was dominated by diatom algae but was not related to upwelling as was previously hypothesized (Kitchell and Clark, 1982, doi:10.1016/0031-0182(82)90087-6). Rather, production occurred within a stratified water column, involving specially adapted species in blooms resembling those of the modern North Pacific subtropical gyre (Dore et al., 2008, doi:10.1016/j.pocean.2007.10.002), or those indicated for the Mediterranean sapropels (Kemp et al., 1999, doi:10.1038/18001). With increased CO2 levels and warming currently driving increased stratification in the global ocean (Sarmiento et al., 1998, doi:10.1038/30455), this style of production that is adapted to stratification may become more widespread. Our evidence for seasonal diatom production and flux testify to an ice-free summer, but thin accumulations of terrigenous sediment within the diatom ooze are consistent with the presence of intermittent sea ice in the winter, supporting a wide body of evidence for low temperatures in the Late Cretaceous Arctic Ocean (Falcon-Lang et al., 2004, doi:10.1016/j.palaeo.2004.05.016; Amiot et al., 2004, doi:10.1016/j.epsl.2004.07.015; Otto-Bliesner et al., 2002, doi:10.1029/2001JD000821), rather than recent suggestions of a 15 °C mean annual temperature at this time (Jenkyns et al., 2004, doi:10.1038/nature03143).

Bacterial production in the eastern Mediteranean Sea in August and September 2008 during SES_GR2

The SES_GR2_MICROBIAL PARAMETERS dataset is based on samples collected in the framework of the project SESAME, in the Ionian, Libyan and Aegean Sea during August-September 2008. The objectives were to measure the standing stocks and calculate the production of the microbial compartment of the food web, describe the vertical distribution pattern and characterize its structure and function through the water column. Bacterial production was estimated by the 3H-leucine method (Kirchman et al. 1986, Kirchman 1993). At each depth, duplicate samples and a control were incubated with 20 nM L-[4,5 3H]-leucine. Samples were incubated in the dark, at in situ temperature.

Diatoms and laminae of Mediterranean sapropels

The origins of sapropels (sedimentary layers rich in organic carbon) are unclear, yet they may be a key to understanding the influence of climate on ocean eutrophication, the mechanisms of sustaining biological production in stratified waters and the genesis of petroleum source rocks (Rohling, 1994, doi:10.1016/0025-3227(94)90202-X; Castradori, 1993, doi:10.1029/93PA00756; Calvert et al., 1992, doi:10.1038/359223a0). Recent microfossil studies of foraminifera (Rohling, 1994, doi:10.1016/0025-3227(94)90202-X) and calcareous nannofossils (Castradori, 1993, doi:10.1029/93PA00756) have focused attention on a deep chlorophyll maximum as a locus for the high production inferred (Calvert et al., 1992, doi:10.1038/359223a0) for sapropel formation, but have not identified the agent responsible. Here we report the results of a high-resolution, electron-microscope-based study of a late Quaternary laminated sapropel in which the annual flux cycle has been preserved. We find that much of the production was by diatoms, both mat-forming and other colonial forms, adapted to exploit a deep nutrient supply trapped below surface waters in a stratified water column. Reconstructed organic-carbon and opal fluxes to the sediments are comparable to those at high-productivity sites in today's oceans, and calculations based on diatom Si/C ratios suggest that the high organic-carbon content of sapropels may be entirely accounted for by sedimenting diatoms. We propose that this style of production may have been common in ancient Palaeogene and Cretaceous seas, environments for which conventional appeals to upwelling-driven production to account for the occurrence of diatomites, and some organic-carbon-rich sediments, have never seemed wholly appropriate.

Grain-size and carbon/carbonate analyses at DSDP Site 61-462

Sand-silt-clay distribution was determined on 10-cm**3 sediment samples collected at the time the cores were split and described. The sediment classification used here is that of Shepard (1954), with the sand, silt, and clay boundaries based on the Wentworth (1922) scale. Thus, the sand, silt, and clay fractions are composed of particles whose diameters range from 2000 to 62.5 µm, 62.5 to 3.91 µm, and less than 3.91 µm, respectively. This classification is applied regardless of sediment type and origin; therefore, the sediment names used in this table may differ from those used elsewhere in this volume, e.g., a silt composed of nannofossils in this table may be called a nannofossil ooze in a site-summary chapter.

Bacterial production in the Aegean Sea in April 2008 during SES_GR1

The HCMR_SES_LAGRANGIAN_GR1_ MICROBIAL PARAMETERS dataset is based on samples collected in the framework of the project SESAME, in the North Aegean Sea during April 2008. The objectives were to measure the standing stocks and calculate the production of the microbial compartment of the food web, describe the vertical distribution pattern and characterize its structure and function through the water column as influenced by the BSW. Bacterial production was estimated by the 3H-leucine method (Kirchman et al. 1986, Kirchman 1993). At each depth, duplicate samples and a control were incubated with 20 nM L-[4,5 3H]-leucine. Samples were incubated in the dark, at in situ temperature.