Description: We examine the importance of dispersed volcanic ash as a critical component of the aluminosilicate sediment entering the Nankai Trough, located south of Japan’s island of Honshu, via the subducting Philippine Sea plate. Multivariate statistical analyses of an extensive major, trace, and rare earth element data set from bulk sediment and discrete ash layers at Integrated Ocean Drilling Program (IODP) Sites C0011 and C0012 quantitatively determine the abundance and accumulation of multiple aluminosilicate inputs to the Nankai subduction zone. We identify the eolian input of continental material to both sites, and we further find that there are an additional three ash sources from Kyushu and Honshu, Japan and other regions. Some of these ash sources may themselves represent mixtures of ash inputs, although the final compositions appear statistically distinct. The dispersed ash comprises 38 ± 7 weight percent (wt%) of the bulk sediment at Site C0011, and 34 ± 4 wt% at Site C0012. When considering the entire sediment thickness at Site C0011, the dispersed ash component supplies 38000 ± 7000 g/cm2 of material to the Nankai subduction system, whereas Site C0012 supplies 20000 ± 3000 g/cm2. These values are enormous compared to the ~2500 g/cm2 (C0011) and ~1200 g/cm2 (C0012) of ash in the discrete ash layers. Therefore, the mass of volcanic ash and chemically equivalent alteration products (e.g., smectite) that are dispersed throughout the stratigraphic succession of bulk sediment appears to be up to 15–17 times greater than the mass of discrete ash layers. The composition of the dispersed ash component at Site C0011 appears linked to that of the discrete layers, and the mass accumulation rate for dispersed ash correlates best with discrete ash layer thickness. In contrast, at Site C0012 the mass accumulation rate for dispersed ash correlates better with the number of ash layers. Together, the discrete ash layers, dispersed ash, and clay-mineral assemblages present a complete record of volcanism and erosion of volcanic sources; and indicate that mass balances and subduction factory budgets should include the mass of dispersed ash for a more accurate assessment of volcanic contributions to large-scale geochemical cycling.

Description: Volcanic ash has long been recognized in marine sediment, and given the prevalence of oceanic and continental arc volcanism around the globe in regard to widespread transport of ash, its presence is nearly ubiquitous. However, the presence/absence of very fine-grained ash material, and identification of its composition in particular, is challenging given its broad classification as an “aluminosilicate” component in sediment. Given this challenge, many studies of ash have focused on discrete layers (that is, layers of ash that are of millimeter-to-centimeter or greater thickness, and their respective glass shards) found in sequences at a variety of locations and timescales and how to link their presence with a number of Earth processes. The ash that has been mixed into the bulk sediment, known as dispersed ash, has been relatively unstudied, yet represents a large fraction of the total ash in a given sequence. The application of a combined geochemical and statistical technique has allowed identification of this dispersed ash as part of the original ash contribution to the sediment. In this paper, we summarize the development of these geochemical/statistical techniques and provide case studies from the quantification of dispersed ash in the Caribbean Sea, equatorial Pacific Ocean, and northwest Pacific Ocean. These geochemical studies (and their sedimentological precursors of smear slides) collectively demonstrate that local and regional arc-related ash can be an important component of sedimentary sequences throughout large regions of the ocean.

Description: Great subduction earthquakes are thought to rupture portions of the megathrust where interseismic coupling is high and velocity-weakening frictional behavior is dominant, releasing elastic deformation accrued over a seismic cycle. Conversely, post-seismic afterslip is assumed to occur primarily in regions of velocity-strengthening frictional characteristics that may correlate with lower interseismic coupling. However, it remains unclear if fixed frictional properties of the subduction interface, co-seismic or aftershock-induced stress redistribution, or other factors control the spatial distribution of afterslip. Here, we use InSAR and GPS observations to map the distribution of co-seismic slip of the 2015 M w 8.3 Illapel, Chile earthquake and afterslip within the first 38 days following the earthquake. We find that afterslip overlaps the co-seismic slip area and propagates along-strike into regions of both high and moderate interseismic coupling. The significance of these observations, however, is tempered by the limited resolution of geodetic inversions for both slip and coupling. Additional afterslip imaged deeper on the fault surface bounds a discrete region of deep co-seismic slip, and both contribute to net uplift of the Chilean Coastal Cordillera. A simple partitioning of the subduction interface into regions of fixed frictional properties cannot reconcile our geodetic observations. Instead, stress heterogeneities, either pre-existing or induced by the earthquake, likely provide the primary control on the afterslip distribution for this subduction zone earthquake. We also explore the occurrence of co- and post-seismic coastal uplift in this sequence and its implications for recent hypotheses concerning the source of permanent coastal uplift along subduction zones.

Description: Since Dymond et al. (1992, doi:10.1029/92PA00181) proposed the paleoproductivity algorithm based on “Bio-Ba”, which relies on a strong correlation between Ba and organic carbon fluxes in sediment traps, this proxy has been applied in many paleoproductivity studies. Barite, the main carrier of particulate barium in the water column and the phase associated with carbon export, has also been suggested as a reliable paleoproductivity proxy in some locations. We demonstrate that Ba(excess) (total barium minus the fraction associated with terrigenous material) frequently overestimates Ba(barite) (barium associated with the mineral barite), most likely due to the inclusion of barium from phases other than barite and terrigenous silicates (e.g., carbonate, organic matter, opal, Fe-Mn oxides, and hydroxides). A comparison between overlying oceanic carbon export and carbon export derived from Ba(excess) shows that the Dymond et al. (1992) algorithm frequently underestimates carbon export but is still a useful carbon export indicator if all caveats are considered before the algorithm is applied. Ba(barite) accumulation rates from a wide range of core top sediments from different oceanic settings are highly correlated to surface ocean 14C and Chlorophyll a measurements of primary production. This relationship varies by ocean basin, but with the application of the appropriate f ratio to 14C and Chlorophyll a primary production estimates, the plot of Ba(barite) accumulation and carbon export for the equatorial Pacific, Atlantic, and Southern Ocean converges to a global relationship that can be used to reconstruct paleo carbon export.

Description: In order to quantify changes in export production and carbonate dissolution over the past 1 Myr in the central equatorial Pacific Ocean we analyzed Ba, P, Al Ti, and Ca in 1106 samples from five piston cores gathered from 5°S to 4°N at 140°W. We focused on Ba/Ti, Al/Ti, and P/Ti ratios as export proxies and employed areally integrated time slice as well as time series strategies. Carbonate maxima from 0-560 kyr are characterized by 15-30% greater export than carbonate minima. The increases in export fall on glacial delta18O transitions rather than glacial maxima. From 560-800 kyr, overlapping with the mid-Pleistocene transition, there is a very large increase in total export yet no glacial-interglacial variability. The highest latitudes (5°S and 4°N) record minimal absolute export change from glacials to interglacials and yet record the most extreme minima in percent CaCO3, indicating that carbonate records there are dominated by dissolution, whereas near the equator they are more influenced by changes in export.