Bacterial abundance in the Strait of Magellan

Bacterial abundance, bacterial secondary production (BSP) and potential ectoproteolytic activity (PEA) were measured at 6 stations along the Strait of Magellan, South America, toward the end of summer 1995. Because of hydrological and climatic factors, 3 main areas could be identified in which the bacterial component displayed specific characteristics. In the Pacific Ocean side, subjected to freshwater inputs from rainfalls and melting of glaciers, the bacterial activities showed the highest values (BSP: 228.2 ng C/l h; PEA: 12.2 nmol/l h). The bacterial biomass was greater than the phytoplanktonic biomass, probably due to organic inputs from land stimulating the bacterial growth. The central part of the Strait demonstrated the lowest values (BSP: 32.6 ng C/l h, PEA: 4.6 nmol/l h), although the ratio of bacterial biomass to phytoplanktonic biomass was greater than 1. In the third area, the Atlantic Ocean opening, subjected to strong tidal currents, BSP and PEA displayed high values, 80 to 88.7 ng C/l h and 11.7 nmol/l h respectively. Nevertheless, the ratio of bacterial to phytoplanktonic biomass was less than 1, like in eutrophic areas. On the other hand, no impact of the tide was noted on bacterial parameters. Considering all samples measured in the 0 to 50 m layer, although BSP and PEA were positively correlated with bacterial abundance, the PEA to BSP ratio was negatively correlated with the bacterial biomass (r = -0.72, p < 0.001, n = 22). This ratio could be an indicator of trophic conditions in the 3 subsystems of the Strait.

Silicoflagellate abundance in ODP Holes 183-1138A and 183-1140A

The biostratigraphic distribution and abundance of lower Oligocene and Miocene to Pleistocene silicoflagellates are documented from Ocean Drilling Program Leg 183 Holes 1138A and 1140A, on the Kerguelen Plateau. The Distephanus speculum speculum forma pseudofibula plexus is found in the upper Miocene in Hole 1138A, but other important biostratigraphic markers are not available. Diversity and abundance of silicoflagellates vary considerably in Hole 1138A, with silicoflagellates more abundant in the Pliocene and Pleistocene and some intervals of the Miocene barren of silicoflagellates or containing only limited numbers of specimens. The silicoflagellates of Hole 1140A include a new skeletal morphology, described here as Distephanus speculum speculum forma cylindrus. Silicoflagellates were generally abundant throughout the lower and middle Miocene in Hole 1140A.

Diatom abundance in middle-to-late Pleistocene sediments of IODP Site 303-U1304

We examined diatom assemblages in a series of remarkable laminated diatomaceous ooze (LDO) horizons in the marine sediments from Integrated Ocean Drilling Program (IODP) Site U1304 to reconstruct the middle-to-late Pleistocene paleoceanographic evolution of the northern North Atlantic Ocean. Four confirmed diatom biohorizons combined with calcareous nannofossil and paleomagnetic stratigraphies established the chronological framework for the material. The planktonic, araphid, needle-like species Thalassiothrix longissima was the greatest contributor to the LDO facies. From the results of a principal component analysis using the percent abundances of 65 significant (p = 5%) diatom taxa, except for Tx. longissima, which was extremely dominant in almost all horizons observed, we identified two principal component (PC) axes. Taxa probably associated with the stratigraphic distribution of the major zonal marker Neodenticula seminae (ranging from 1.26 to 0.84 Ma in this ocean) loaded on PC1 with a high value. PC2 was related to the ocean surface temperature. The stratigraphic variability of the PC2 score indicated that switching between warm- and cold-water assemblages occurred concurrently with LDO deposition (or extreme Tx. longissima dominance) episodes in several horizons (particularly after 0.84 Ma), suggesting that the Subarctic Convergence (SAC) oceanic front passed over Site U1304 during Pleistocene glacial/interglacial cycles. Our floral evidence supports the model of nearly monospecific LDO formation caused by the enhanced physical accumulation of particular diatoms such as Tx. longissima. On the other hand, Nd. seminae, which probably contributes to spring phytoplankton blooms in the modern ocean, was present only between 1.26 and 0.84 Ma in this area. Thus, we infer that the main contributor of export flux in the regional annual primary production cycle would have shifted drastically from one of a spring phytoplankton bloom leader (Nd. seminae) to minor but mass dump assemblages (Tx. longissima etc.) in the mid-Pleistocene.