Composition of bentonite-, smectite-rich- and ash beds from DSDP Leg 19 holes

Late Cenozoic ash deposits cored in Deep Sea Drilling Project Leg 19 in the far northwest Pacific and in the Bering Sea have altered to bentonite beds. Some bentonite layers were subsequently replaced by carbonate beds. A significant part of the Neogene volcanic history of land areas adjacent to the far north Pacific is represented by these diagenetic deposits. Bentonite beds are composed of authigenic smectite and minor amounts of clinoptilolite. Authigenic smectite has fewer illite layers than detrital smectite. Opal-A and opal-CT, abundant in Bering Sea sediment, are not found in ash or bentonite layers. The percentage of smectite in the total clay-mineral assemblage of ash beds is greater than that for adjacent terrigenous sediment, but the total amount of clay minerals in ash sequences is less than in surrounding deposits. Morphology of the 17-Å peak of smectite found in ash may represent newly formed, poorly crystalline smectite. Smectite becomes better crystallized as bentonite layers form. The percentage of smectite of the total clay-mineral assemblage in bentonite beds is greater than that in surrounding sediment, and, in contrast to ash beds, the total amount of clay minerals (mostly smectite) in bentonite layers is greater than in adjacent terrigenous sediment. Apparently, silica is not mobilized when volcanic ash layers transform to bentonite beds. Saponite-nontronite varieties of smectite and high Fe/Al and Ti/Al ratios distinguish bentonite beds derived from basaltic parent material from those beds formed from more silicic volcanic ash. These silicic ash beds produce bentonite composed mostly of montmorillonite. The basal sediment section at site 192 is rich with bentonite beds. Smectite in the upper part of this section (Eocene) was formed by low-temperature diagenesis of volcanic debris of intermediate or more silicic composition derived from arc or Pacific volcanoes. In contrast, smectite from the lowest 10 to 20 m of the sedimentary section (Cretaceous) is formed from either low-temperature or hydrothermal alteration of the underlying basaltic basement and associated pyroclastic debris. This near-basement smectite contains Mg and K acquired from sea water and Si, Al, Fe, Ti, and Mn released from the volcanic material.

Seawater carbonate chemistry and biological processes during experiments with phytoplankton Emiliania huxleyi (CS369), 2009

Increasing atmospheric CO2 concentration affects calcification in most planktonic calcifiers. Both reduced or stimulated calcification under high CO2 have been reported in the widespread coccolithophore Emiliania huxleyi. This might affect the response of cells to photosynthetically active radiation (PAR; 400-700 nm) and ultraviolet radiation (UVR; 280-400 nm) by altering the thickness of the coccolith layer. Here we show that in the absence of UVR, the calcification rates in E. huxleyi decrease under lowered pH levels (pHNBS of 7.9 and 7.6; pCO2 of 81 and 178 Pa or 804 and 1759 ppmv, respectively) leading to thinned coccolith layers, whereas photosynthetic carbon fixation was slightly enhanced at pH 7.9 but remained unaffected at pH 7.6. Exposure to UVR (UV-A 19.5 W m**-2, UV-B 0.67 W m**-2) in addition to PAR (88.5 W m**-2), however, results in significant inhibition of both photosynthesis and calcification, and these rates are further inhibited with increasing acidification. The combined effects of UVR and seawater acidification resulted in the inhibition of calcification rates by 96% and 99% and that of photosynthesis by 6% and 15%, at pH 7.9 and 7.6, respectively. This differential inhibition of calcification and photosynthesis leads to significant reduction of the ratio of calcification to photosynthesis. Seawater acidification enhanced the transmission of harmful UVR by about 26% through a reduction of the coccolith layer of 31%. Our data indicate that the effect of a high-CO2 and low-pH ocean on E. huxleyi (because of reduced calcification associated with changes in the carbonate system) enhances the detrimental effects of UVR on the main pelagic calcifier.