Time series measurements of dissolved nitrous oxide, nutrients, and chlorophyll at stations in the South Shetland Islands

The data set comprises concentrations of dissolved nitrous oxide (N2O), an important green house gas, d nutrients and chlorophyll-a from surface ocean. Seawater samples collected in a time series stations located in Greenwich Island within the South Shetland Islands, an area n of the western Antarct...

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Bibliographic Details
Main Authors: Farias, Laura, Alcaman Arias, María Estrella
Format: Dataset
Language:English
Published: PANGAEA 2024
Subjects:
CTD
MON
Online Access:https://doi.pangaea.de/10.1594/PANGAEA.969584
https://doi.org/10.1594/PANGAEA.969584
Description
Summary:The data set comprises concentrations of dissolved nitrous oxide (N2O), an important green house gas, d nutrients and chlorophyll-a from surface ocean. Seawater samples collected in a time series stations located in Greenwich Island within the South Shetland Islands, an area n of the western Antarctic Peninsula influenced by the circumpolar current system and adjacent to Bellinghausen. Two specific marine sampling points (Station P1: -62,489S; -59,683W and station P3: -62,461; -59,677 W) were monitored over four late summer periods (February and early March) in the years 2017, 2018, 2019, and 2020. Physical variables were measured with a Conductivity Temperature Depth profiler (CTD; SeaBird19 plus). Seawater samples for biological and biogeochemical variables were superficially collected at a depth of 2, 5 or 10 meters using a handheld pump or Niskin bottles (5 and 10 m depth) aboard a Zodiac boat for nitrous oxide, nutrient, and chlorophyll analysis. Simultaneously, a CTD instrument was deployed to obtain temperature (°C) and salinity profiles. For chlorophyll a (Chl-a) measurements, triplicate 1-L samples of seawater from both 2 and 30 m depth were prefiltered with a 150-µm net to exclude large organisms, and then the remaining biomass was collected by subsequent filtration with 0.7-µm GF/F glass fiber filters. Each filter was frozen until processing, using acetone extraction protocols, after which extracts were analyzed by fluorometric (measured with a 10-AU Turner fluorometer (Turner, USA). ([Holm-Hansen & Riemann, 1978] techniques, respectively. Samples for the determination of inorganic nutrients (nitrite (NO2−), nitrate (NO3−) and phosphate (PO43−)) were also taken in triplicate stored in 15 mL polyethylene tubes and frozen at −20 °C in the dark until analysis. NO2−, NO3− and PO4−3 concentrations were measured with a Seal AutoAnalyzer 3 (AA3, SEAL Analytical, Mequon, WI, USA) [Grashoff et al., 2009]. N2O samples were taken in triplicate in 20 mL vials and carefully sealed to avoid air bubbles. They ...