Over the past few decades, we have realized that the silica cycle is strongly intertwined with other major biogeochemical cycles, like those of carbon and nitrogen, and as such is intimately related to marine primary production, the efficiency of carbon export to the deep sea, and the inventory of carbon dioxide in the atmosphere. For nearly 20 years, the marine silica budget compiled by Tréguer et al. (1995) , with its exploration of reservoirs, processes, sources, and sinks in the silica cycle, has provided context and information fundamental to study of the silica cycle. Today, the budget needs revisiting to incorporate advances that have notably changed estimates of river and groundwater inputs to the ocean of dissolved silicon and easily dissolvable amorphous silica, inputs from the dissolution of terrestrial lithogenic silica in ocean margin sediments, reverse weathering removal fluxes, and outputs of biogenic silica (especially on ocean margins and in the form of nondiatomaceous biogenic silica). The resulting budget recognizes significantly higher input and output fluxes and notes that the recycling of silicon occurs mostly at the sediment-water interface and not during the sinking of silica particles through deep waters.

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[1] Chemical weathering is an integral part of both the rock and carbon cycles and is being affected by changes in land use, particularly as a result of agricultural practices such as tilling, mineral fertilization, or liming to adjust soil pH. These human activities have already altered the terrestrial chemical cycles and land-ocean flux of major elements, although the extent remains difficult to quantify. When deployed on a grand scale, Enhanced Weathering (a form of mineral fertilization), the application of finely ground minerals over the land surface, could be used to remove CO 2 from the atmosphere. The release of cations during the dissolution of such silicate minerals would convert dissolved CO 2 to bicarbonate, increasing the alkalinity and pH of natural waters. Some products of mineral dissolution would precipitate in soils or be taken up by ecosystems, but a significant portion would be transported to the coastal zone and the open ocean, where the increase in alkalinity would partially counteract "ocean acidification" associated with the current marked increase in atmospheric CO 2 . Other elements released during this mineral dissolution, like Si, P, or K, could stimulate biological productivity, further helping to remove CO 2 from the atmosphere. On land, the terrestrial carbon pool would likely increase in response to Enhanced Weathering in areas where ecosystem growth rates are currently limited by one of the nutrients that would be released during mineral dissolution. In the ocean, the biological carbon pumps (which export organic matter and CaCO 3 to the deep ocean) may be altered by the resulting influx of nutrients and alkalinity to the ocean. This review merges current interdisciplinary knowledge about Enhanced Weathering, the processes involved, and the applicability as well as some of the consequences and risks of applying the method.

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By altering the number, size, and density of particles in the ocean, the activities of different phytoplankton, zooplankton, and microbial species control the formation, degradation, fragmentation, and repackaging of rapidly sinking aggregates of particulate organic carbon (POC) and are responsible for much of the variation in the efficiency of the biological carbon pump. A more systematic understanding of these processes will allow the biological pump to be included in global models as more than an empirically-determined decline in POC concentrations with depth that may not adequately represent past or future conditions. Although progress has been made on this front, key areas needing work are the amount of POC flux associated with appendicularians, the mechanisms by which coccoliths and coccolithophorid POC reach depth, and the impact of polymers such as TEP on the porosity of aggregates. In addition, an understanding of the interaction between biological and physical aspects of the pump, such as aggregate loading with suspended mineral particles, is also important for understanding the transmission of biogenic materials through the meso-and bathypelagic realms. Data suggest that variable biogenic silica to POC production ratios in various ocean regions are responsible for the poor correlation observed between silica and POC in deep sediment traps, and that high concentrations of suspended coccoliths in deep waters may be responsible for the homogeneous calcium carbonate to POC ratios observed in these same traps. Sedimentation of foraminiferal calcite does not appear to be as tightly correlated to POC flux as coccolith sedimentation. Suspended calcium carbonate particles, scavenged by sinking organic aggregates, have been observed to both fragment and increase the density of these aggregates. Analysis of the data suggests that scavenging of minerals by aggregates decreases the porosity of the aggregates and may increase their sinking velocities by hundreds of times. r

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Inorganic carbon concentrating mechanisms (CCMs) catalyse the accumulation of CO 2 around rubisco in all cyanobacteria, most algae and aquatic plants and in C 4 and crassulacean acid metabolism (CAM) vascular plants. CCMs are polyphyletic (more than one evolutionary origin) and involve active transport of HCO K 3 , CO 2 and/or H C , or an energized biochemical mechanism as in C 4 and CAM plants. While the CCM in almost all C 4 plants and many CAM plants is constitutive, many CCMs show acclimatory responses to variations in the supply of not only CO 2 but also photosynthetically active radiation, nitrogen, phosphorus and iron. The evolution of CCMs is generally considered in the context of decreased CO 2 availability, with only a secondary role for increasing O 2 . However, the earliest CCMs may have evolved in oxygenic cyanobacteria before the atmosphere became oxygenated in stromatolites with diffusion barriers around the cells related to UV screening. This would decrease CO 2 availability to cells and increase the O 2 concentration within them, inhibiting rubisco and generating reactive oxygen species, including O 3 .