ALBERT

Description: A submersible study has been conducted in February - March 1978 at the axis of the East Pacific Rise near 21°N. The expedition CYAMEX, the first submersible program to be conducted on the East Pacific Rise, is part of the French-American-Mexican project RITA (Rivera - Tamayo), a 3-year study devoted to detailed geological and geophysical investigations of the East Pacific Rise Crest. On the basis of the 15 dives made by CYANA in the axial area of the Rise, a morphological and tectonic zonation can be established for this moderately-fast spreading center. A narrow, 0.6 to 1.2 km wide zone of extrusion (zone 1), dominated by young lava flows, is flanked by a highly fissured and faulted zone of extension (zone 2) with a width of 1 to 2 km. Further out, zone 3 is dominated by outward tilted blocks bounded by inward-facing fault scarps. Active or recent faults extend up to 12 km from the axis of extrusion of the East Pacific Rise. This represents the first determination from direct field evidence of the width of active tectonism associated with an accreting plate boundary. Massive sulfide deposits, made principally of zinc, copper and iron, were found close to the axis of the Rise. Other signs of the intense hydrothermal activity included the discovery of benthic fauna of giant size similar to that found at the axis of the Galapagos Rift. We emphasize the cyclic character of the volcanicity. The main characteristics of the geology of this segment of the East Pacific Rise can be explained by the thermal structure at depth below this moderately-fast spreading center. The geological observations are compatible with the existence of a shallow magma reservoir centered at the axis of the Rise with a half-width of the order of 10 km.

Description: Nitrate concentration and isotopic (δ15NNO3) data, ice density, and surface mass balance estimates from the ABN1314-103 ice core. This 103 m long core was drilled beginning on 07 January 2014 as one of three ice cores at Aurora Basin North, Antarctica (-71.17, 111.37, 2679 m.a.s.l), in the 2013-2014 field season. The age-depth model for ABN1314-103 was matched through ion profiles from an annually-resolved model (ALC01112018) originally developed for one of the other ABN cores through seasonal ion and water isotope cycles and constrained by volcanic horizons. Each 1 m segment of the core was weighed and measured for ice density calculations, and then sampled for nitrate at 0.33 m resolution. Nitrate concentrations were taken on melted ice aliquots with ion chromatography, while isotopic analysis was achieved through bacterial denitrification and MAT 253 mass spectrometry after concentrating with anionic resin. Using the density data and the age-depth model's dates for the top and bottom of each 1 m core segment, we reconstructed a history of surface mass balance changes as recorded in ABN1314-103. Additionally, we also estimated the effect of upstream topographic changes on the ice core's surface mass balance record through a ground penetrating radar transect that extended 11.5 km against the direction of glacial ice flow. The modern SMB changes along this upstream transect were linked to ABN1314-103 core depths by through the local horizontal ice flow rate (16.2 m a-1) and the core's age-depth model, and included here for comparative analysis. See Akers et al., 2022 for more analytical details.

Description: This study presents data collected from International Ocean Discovery Program (IODP) Expedition 355 Arabian Sea Monsoon to investigate changes in sediment provenance as well as the effect of sediment transport processes on deep-sea sediment samples. From Site U1457, 83 sediment samples were analyzed, complemented by 44 samples from Site U1456. Samples were analyzed for bulk grain-size using a Malvern Mastersizer 2000. The clay fraction was separated, digested, and analyzed for K/Al ratios using inductively couple plasma optical emission spectroscopy (ICP-OES). Radiogenic strontium (87Sr/86Sr) was measured using a Neptune Plus multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS) and a Triton Plus multicollector thermal ionization mass spectrometer (TIMS). A subset of 38 samples were analyzed for radiogenic neodymium composition (143Nd/144Nd) using TIMS.

Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. The volatility and hygroscopicity of nascent SSA was determined with a volatility and hygroscopicity tandem differential mobility analyser (VH-TDMA) (Johnson et al., 2004: doi:10.1016/j.jaerosci.2003.10.008, 2008: doi:10.1016/j.jaerosci.2008.05.005). A diffusion drier was used to dry the sample flow to 20 ± 5 % RH prior to characterisation by the VH-TDMA. The VH-TDMA used two TSI 3010 condensation particle counters. The aerosol sample flow rate for each scanning mobility particle sizer was 1 L/min, resulting in a total inlet flow of 2 L/min, the sheath flow for the pre-DMA, V-DMA and H-DMA were 11, 6 and 6 L/min, respectively. The dependence of HGF on RH at ambient temperature was measured for one water sample (workboat 9) to provide the deliquescence relative humidity (DRH). All VH-TDMA data were inverted using the TDMAinv algorithm (Gysel et al., 2009: doi:10.1016/j.jaerosci.2008.07.013). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).

Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. Filters were collected for compositional analysis using transmission Fourier Transform Infra Red (FTIR) and Ion Beam analysis (IBA). The nascent SSA was sampled through a 1 μm sharp cut cyclone (SCC 2.229PM1, BGI Inc., Waltham, Massachusetts) and collected on Teflon filters, with the sample confined to deposit on a 10 mm circular area. Back filter blanks were used to characterise the contamination during handling, and before analysis samples were dehydrated to remove all water, including SSA hydrates, as described in (Frossard and Russell, 2012: doi:10.1021/es3032083). Filter samples underwent simultaneous particle induced X-ray emission (PIXE) and gamma ray emission (PIGE) analysis (Cohen et al., 2004: doi:10.1016/j.nimb.2004.01.043). Si was the only compound with blank measurements above the IBA detection limit. The measured S mass was used to calculate the SO4 mass, all S was assumed to be in the form of SO4. The filter exposed area (0.785 cm2) was used to convert inorganic areal concentrations into total mass. The inorganic mass (IM) was computed as the sum of Na, Mg, SO4, Cl, K, Ca, Zn, Br and Sr. The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).