Changes of dissolved organic matter compositions in artifical and natural seawater during Pseudovibrio growth experiment

To study the consumption of dissolved organic matter (DOM) by bacteria living in untra-oligotrophic artificial or natural seawater, we analyzed the composition of DOM before (timepoint t0, directly after inoculation) and after (timepoint t2, 3 weeks of incubation) growth of the bacteria using Fourier transform ion cyclotron mass spectrometry (ESI FT-ICR-MS). The oligotrophic natural seawater used originates from the South Pacific Gyre. Our data show that the bacteria were able to utilize a variety of different organic compounds. These compounds belong to different chemical compound groups and likely fuel the bacterial energy, carbon and nitrogen requirements under the ultra-oligotrophic conditions.

(Table 2) Organic residue at DSDP Hole 76-534A

The kind, sedimentation rate, and diagenesis of organic particles delivered to the North Atlantic seafloor during the Middle Jurassic-Early Cretaceous were responsible for the presence of carbonaceous sediments in Hole 534A. Organic-rich black clays formed from the rapid supply of organic matter; this organic matter was composed of either abundant, well-preserved, and poorly sorted particles of land plants deposited in clays and silty clays within terrigenous turbiditic sequences (tracheal facies) or abundant amorphous debris (xenomorphic facies) generated through the digestive tracts of marine zooplankton and sedimented as fecal pellets. Evidence for the fecal-pellet origin of xenomorphic debris is illustrated. Black clays were also produced in sediments containing less organic matter as a result of the black color of carbonized particles composing all or most of the residues (micrinitic facies). Slowly sedimented hematitic Aptian clays contain very little carbonized, organic debris that survived diagenetic oxidation. In the red calcareous clay sequence of the Late Jurassic, larger amounts of this oxidized debris turned several clay layers black or blackish red. Carbonized debris also dominates the residues recovered in interbedded black and green Albian clays. Carbonization of organic matter in these sediments either turned them black or provided the diagenetic environment for reduced iron. Carbonized debris is also appreciable in burrow-mottled black-green Kimmeridgian clay. The study of Hole 534A organic matter indicates that during the middle Callovian there was a rapid supply of terrigenous organic matter, followed by a late Callovian episode of rapidly supplied xenomorphic debris deposited as fecal pellets. The Late Jurassic-Berriasian was a time of slower sedimentation of organic matter, primarily of a marine dinoflagellate flora in a poorly preserved xenomorphic facies variously affected by diagenetic oxidation. Several intervals of carbonized tracheal tissue in the Oxfordian and Kimmeridgian suggest episodes of oxidized terrigenous matter. The same sequence of Callovian organic events is evident in much of the Early Cretaceous

(Appendix A) Organic facies at DSDP Hole 93-603B

The Palynology of two sections recovered during Leg 93 drilling by the Deep Sea Drilling Project in the continental rise along the western margin of the North Atlantic is reported. In Hole 603B at Site 603, the dinoflagellate stratigraphy indicates that the interval from Cores 603B-82 to 603B-26 ranges in age from late Berriasian to Santonian. The BlakeBahama Formation ranges from late Berriasian to Aptian. The Hatteras Formation ranges from Aptian to Cenomanian, although the uppermost part may be Turonian. Dinoflagellate evidence from the middle part of the Plantagenet Formation indicates an age from late Coniacian or early Santonian to Santonian within the interval of Cores 603B-28 to 603B-26. Magnetic polarity evidence of the stratigraphy of the Early Cretaceous for the western North Atlantic indicates a reliable correlation with the dinoflagellate zonation. The stratigraphic sequence of palynologically defined organic facies in carbonaceous claystone lithologies in Hole 603B shows that organic stratigraphic units consisting predominantly of fecal-pellet-derived, pelagic organic matter (xenomorphic facies) alternate with units consisting predominantly of terrigenous organic matter (tracheal and exinitic facies), corresponding to that described from other sites in the North Atlantic. A terrigenous organic facies is identified for the first time from the Plantagenet Formation. The claystone organic facies and major lithofacies are closely correlated. The tracheal and exinitic facies occur in carbonaceous terrigenous claystones and claystone turbidites associated with sandstone/siltstone terrigenous turbidites. The xenomorphic facies occurs in claystones within pelagic limestones lacking any turbidites, and in blackish, noncalcareous claystones which correlate in age with the marine-carbon-rich sapropels which are widespread in the North Atlantic Cenomanian. This facies also occurs with an admixture of terrigenous organic particles in the Blake-Bahama Formation, but the mixture is consistent with the submarine fan setting of this interval. The concentration of refractory organic matter (carbonized particles) in the micrinitic and carbonized tracheal facies is considered to be the result, at least in part, of the oxidation of sediment buried below a surface slowly accumulating pelagic clays below the carbonate compensation depth. The progressive increase in number of dinoflagellate species per stage through the Early Cretaceous (except for the late Barremian-Aptian) may have resulted indirectly from the generally progressive rise in global sea level during this time. At Site 605, the dinoflagellate stratigraphy across the Cretaceous/Tertiary boundary is remarkably close to that published from the Maestrichtian and Danian of Denmark. The Maestrichtian/Danian boundary is placed precisely within Section 605-66-1 by dinoflagellate evidence, agreeing with that predicted by other microfossils. The new dinoflagellate-cyst-based genus, Pierceites and its new species P. schizocystis, and the new combination P. ( = Trithyrodinium) pentagonum (May) are proposed. Diacanthum hollisteri Habib, type species of Diacanthum, is emended to accommodat e cysts with the archeopyle formulas P3'', 2P2''-3'', 2P3''-4'', and 3P2''-3''-4''.