V033-0011
Synchrotron imaging and spectroscopy of sulfur and other low Z elements at the National Synchrotron Light Source II (NSLS-II) X-ray Fluorescence Microprobe (XFM) with examples from marine biogeochemistry
Abstract:
Sulfur is an essential component of all living cells, usually as metal sulfides or organosulfur compounds. Plants roots take in S as sulfate, reduce it to sulphite, then to sulfide, and then incorporate it into cells as organosulfur compounds (eg. cysteine and methionine). Sulfur is a constituent of many rock-forming minerals in terrestrial and extra-terrestrial systems. Sulfate is a major anion of natural waters and can be a significant constituent of calcareous organisms. Chemically reduced sulfur species are a key component of primary productivity potential via chemosynthesis in hydrothermal vent fluids and plumes (Cron et al 2020).
The speed of the stage in the Low Z experimental chamber and of the flyscanning monochromotor allows XFM to take advantage of the high flux from NSLS-II while minimizing sample exposure to photodamage. The process of changing configuration of the instrument to move from measurements in the hard X-ray range to the tender X-ray range takes less than 10 minutes, and requires no change or movement of the mounted sample. This allows multielement spectroscopy at the same point on the sample in a short amount of time.
The figures show XRF images and spectroscopy collected at XFM on two marine samples, a hydrothermal sulfide chimney from Juan de Fuca ridge (Toner et al 2009), and a coldwater coral Lophelia collected at depth in the NE Atlantic via remotely operated vehicle from the Irish research vessell R/V Celtic Explorer.
Cron et al. 2020 ACS Earth and Space Chemistry 4(2) 168-182.
Toner et al 2009 Geochimica et Cosmochimica Acta 73 (2) 388-403.
We wish to acknowledge the R/V Celtic Explorer, Professor Louise Allcock, and Dr. Ryan Young of the National University of Ireland, Galway for the coral sample.