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The biogeochemical cycles of trace elements and their isotopes (TEIs) constitute an active area of oceanographic research due to their role as essential nutrients for marine organisms and their use as tracers of oceanographic processes. Selected TEIs also provide diagnostic information about the physical, geological, and chemical processes that supply or remove solutes in the ocean. Many of these same TEIs provide information about ocean conditions in the past, as their imprint on marine sediments can be interpreted to reflect changes in ocean circulation, biological productivity, the ocean carbon cycle, and more. Other TEIs have been introduced as the result of human activities and are considered contaminants. The development and implementation of contamination-free methods for collecting and analyzing samples for TEIs revolutionized marine chemistry, revealing trace element distributions with oceanographically consistent features and new insights about the processes regulating them. Despite these advances, the volume and geographic coverage of high-quality TEI data by the end of the twentieth century were insufficient to constrain their global biogeochemical cycles. To accelerate progress in this field of research, marine geochemists developed a coordinated international effort to systematically study the marine biogeochemical cycles of TEIs—the GEOTRACES program. Following a decade of planning and implementation, GEOTRACES launched its main field effort in 2010. This review, roughly midway through the field program, summarizes the steps involved in designing the program, its management structure, and selected findings. 

Changes in bioavailable dust-borne iron (Fe) supply to the iron-limited Southern Ocean may influence climate by modulating phytoplankton growth and CO₂fixation into organic matter that is exported to the deep ocean. The chemical form (speciation) of Fe impacts its bioavailability, and glacial weathering produces highly labile and bioavailable Fe minerals in modern dust sources. However, the speciation of dust-borne Fe reaching the iron-limited Southern Ocean on glacial−interglacial timescales is unknown, and its impact on the bioavailable iron supply over geologic time has not been quantified. Here we use X-ray absorption spectroscopy on subantarctic South Atlantic and South Pacific marine sediments to reconstruct dust-borne Fe speciation over the last glacial cycle, and determine the impact of glacial activity and glaciogenic dust sources on bioavailable Fe supply. We show that the Fe(II) content, as a percentage of total dust-borne Fe, increases from ∼5 to 10% in interglacial periods to ∼25 to 45% in glacial periods. Consequently, the highly bioavailable Fe(II) flux increases by a factor of ∼15 to 20 in glacial periods compared with the current interglacial, whereas the total Fe flux increases only by a factor of ∼3 to 5. The change in Fe speciation is dominated by primary Fe(II) silicates characteristic of glaciogenic dust. Our results suggest that glacial physical weathering increases the proportion of highly bioavailable Fe(II) in dust that reaches the subantarctic Southern Ocean in glacial periods, which represents a positive feedback between glacial activity and cold glacial temperatures.

 

The deep ocean has long been recognized as the reservoir that stores the carbon dioxide (CO₂) removed from the atmosphere during Pleistocene glacial periods. The removal of glacial atmospheric CO₂into the ocean is likely modulated by an increase in the degree of utilization of macronutrients at the sea surface and enhanced storage of respired CO₂in the deep ocean, known as enhanced efficiency of the biological pump. Enhanced biological pump efficiency during glacial periods is most easily documented in the deep ocean using proxies for oxygen concentrations, which are directly linked to respiratory CO₂levels. We document the enhanced storage of respired CO₂during the Last Glacial Maximum (LGM) in the Pacific Southern Ocean and deepest Equatorial Pacific using records of deglacial authigenic manganese, which form as relict peaks during increases in bottom water oxygen (BWO) concentration. These peaks are found at depths and regions where other oxygenation histories have been ambiguous, due to diagenetic alteration of authigenic uranium, another proxy for BWO. Our results require that the entirety of the abyssal Pacific below approximately 1,000 m was enriched in respired CO₂and depleted in oxygen during the LGM. The presence of authigenic Mn enrichment in the deep Equatorial Pacific for each of the last five deglaciations suggests that the storage of respired CO₂in the deep ocean is a ubiquitous feature of late‐Pleistocene ice ages.

 

One of the primary sources of micronutrients to the sea surface in remote ocean regions is the deposition of atmospheric dust. Geographic patterns in biogeochemical processes such as primary production and nitrogen fixation that require micronutrients like iron (Fe) are modulated in part by the spatial distribution of dust supply. Global models of dust deposition rates are poorly calibrated in the open ocean, owing to the difficulty of determining dust fluxes in sparsely sampled regions. We present new estimates of dust and Fe input rates from measurements of dissolved and particulate thorium isotopes²³⁰Th and²³²Th on theFS SonneSO245 section (GEOTRACES process study GPpr09) in the South Pacific. We first discuss high‐resolution upper water column profiles of Th isotopes and the implications for the systematics of dust flux reconstructions from seawater Th measurements. We find dust fluxes in the center of the highly oligotrophic South Pacific Gyre that are the lowest of any mean annual dust input rates measured in the global oceans, but that are 1–2 orders of magnitude higher than those estimated by global dust models. We also determine dust‐borne Fe fluxes and reassess the importance of individual Fe sources to the surface South Pacific Gyre, finding that dust dissolution, not vertical or lateral diffusion, is the primary Fe source. Finally, we combine our estimates of Fe flux in dust with previously published cellular and enzymatic quotas to determine theoretical upper limits on annual average nitrogen fixation rates for a given Fe deposition rate.

 

The Southern Ocean hosts complex connections between ocean physics, chemistry, and biology. Changes in these connections are hypothesized to be responsible for significant alterations of ocean biogeochemistry and carbon storage both on glacial‐interglacial timescales and in the future due to anthropogenic forcing. Isotopes of thorium (²³⁰Th and²³²Th) and protactinium (²³¹Pa) have been widely applied as tools to study paleoceanographic conditions in the Southern Ocean. However, understanding of the chemical behavior of these isotopes in the modern Southern Ocean has been limited by a paucity of high‐resolution observations. In this study, we present measurements of dissolved²³⁰Th,²³¹Pa, and²³²Th on a meridional transect along 170°W from 67°S to 54°S in the Pacific sector of the Southern Ocean, with high vertical and meridional sampling resolution. We find Th/Pa fractionation factors below 1, highlighting the preferential removal of Pa relative to Th in a region with low lithogenic inputs where the particle flux is dominated by biogenic opal. We also find steep gradients in all three of these isotopes along neutral density surfaces from north to south, demonstrating the importance of isopycnal mixing in transporting these nuclides to the Southern Ocean. Our results suggest that²³¹Pa and²³⁰Th in the Southern Ocean are highly sensitive tracers of physical transport that may find use in studies of Southern Ocean biogeochemical‐physical connections in the past, present, and future.