Even with careful petrographic and mineralogic characterization of marine limestones, intertidally and subtidally lithified rocks are often difficult to differentiate, thus hindering an accurate delineation of the diagenetic environment. Limestones from water depths of 6 to 8 m off Kuwait vary in petrographic character from oosparite and biosparite (in which the cement is entirely aragonite) to oomicrite and biomicrite (in which at least some of the cement is microcrystalline magnesian calcite). Carbon‐14 dates suggest that the oosparite may have lithified at depths shallower than at present (possibly intertidally) during a lower stand of sea‐level. In contrast the biosparite, oomicrite and biomicrite appear to be contemporaneous and to have lithified subtidally. Copyright © 1987, Wiley Blackwell. All rights reserved

The large quantities of reduced carbon that are required to support the filter-feeding mytilid mussels (Mytilus sp.), vesi-comyid clams (Calyptogena sp.) and various other animals in the Galápagos hydrothermal vent systems are thought to be derived from either the in situ synthesis of particulate organic matter by chemoautotrophic, sulphide-oxidizing bacteria1,2 or by the advection of sedimentary organic carbon into the vent environment from surrounding areas3,4. In contrast, the dense populations of vestimentiferan tubeworms (Riftia pachyptila), which lack mouth organs and digestive tracts, apparently utilize organic carbon synthesized by symbiotic chemoautotrophs5. We present evidence here, based on 14C activities and 13C/12C ratios, that the principal source of dietary carbon for mussels and tubeworms is derived from the dissolved inorganic carbon (DIOC) in the vent effluent waters. © 1981 Nature Publishing Group.

ONE measure of transport rates and residence times of organic carbon within the various organic carbon pools in the ocean is to follow perturbations from the 1952-58 and 1961-62 atmospheric thermonuclear bomb tests on the natural 14C activities of living, detrital and dissolved organic matter. We report here our measurement of the 14C activity of the total sedimentary organic carbon (SOC) in an abyssal red clay, as no such data were available for this organic carbon pool. Ultimately, these sedimentary organic 14C activities may be compared with the 14C activity of the source organic material in the water column and estimates made of the magnitude of organic carbon consumption at the seawater-sediment interface. What was found, unexpectedly, was evidence for the penetration of recent organic carbon from the 4 cm mixed layer at the sediment-seawater interface down to at least 12 cm in the sedimentary column. This suggests a different and more rapid mechanism for the sedimentation of some fraction of the SOC other than direct association with clay minerals. © 1978 Nature Publishing Group.