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 Treguer 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.

Microbial life in the ocean contains immense taxonomic and physiological diversity, yet its collective activity yields global cycles of the major biolimiting elements N and P that are tightly linked. Moreover, the availability of N and P in seawater is closely matched to the metabolic demands of "average" plankton, as if plankton composition and the oceanic nutrient reservoirs were mutually influenced. These simple observations have broad implications for the function of nutrient cycles within the Earth system, which can operate either as a biological homeostat that buffers ocean fertility against large changes or as an amplifier of climate perturbations, by alleviating or exacerbating the nutrient limitation of biological productivity and ocean C storage. A mechanistic understanding of these observations and dynamics must draw upon diverse fields, from physiology and evolution to physical oceanography and paleoceanography, and must account for processes spanning a wide range of spatial and temporal scales. Here we summarize this understanding from the perspective of the nutrient distributions themselves and their changes over time. We offer a synthesis view in which ocean circulation communicates the resource constraints of stoichiometrically distinct planktonic biomes across large spatial scales, allowing geochemical constancy to emerge from rich biological diversity.

Previous studies have shown that various microorganisms can enhance the dissolution of silicate minerals at low (<5)or high (>8)pH. However, it was not known if they can have an effect at near-neutral pH. Almost half of 17 isolates examined in this study stimulated bytownite dissolution at near-neutral pH while in a resting state in buffered glucose. Most of the isolates found to stimulate dissolution also oxidized glucose to gluconic acid. More detailed analysis with one of these isolates suggested that this partial oxidation was the predominant, if not sole, mechanism of enhanced dissolution. Enhanced dissolution did not require direct contact between the dissolving mineral and the bacteria. Gluconate-promoted dissolution was also observed with other silicate minerals such as albite, quartz, and kaolinite.