| Contributors | Affiliation | Role |
|---|---|---|
| Gonsior, Michael | Chesapeake Biological Laboratory (CBL) | Principal Investigator |
| Powers, Leanne | Chesapeake Biological Laboratory (CBL) | Scientist |
Sample collection
Grab water samples (surface, ~0m) were collected dockside or by small boat in in 10-L low-density polyethylene cubitainers that had been pre-cleaned with 0.1 M NaOH for 24 h followed by several rinses of ultrapure Milli-Q water. Within 3 h of collection, samples for DOC and TDN analysis were 0.2-µm filtered through cellulose acetate filters into 40-mL combusted amber glass vials. Single samples for DOC/TDN were collected at each site, unless otherwise noted. The remaining samples were 0.7 µm-filtered through pre-combusted Whatman GF/F glass fiber filters into clean combusted 1-L bottles. SPE samples were collected in duplicate or triplicate. The 0.7 µm-filtered samples were then acidified to pH 2 using ultrapure concentrated HCl and underwent solid phase extraction (SPE). Sargassum exudates were generated by placing fragments of Sargassum in clear 500-mL Teflon bottles with seawater collected on the Atlantic shore with no visible Sargassum. Bottles were placed in a cooler with running water to maintain ambient temperature for 5 h. Seawater in bottles without Sargassum served as a control. After 5 h, exudates and the control were 0.7 µm-filtered as above and also underwent SPE.
Solid phase extraction (SPE)
We utilized 1 g Agilent Bond Elut PPL cartridges for SPE. Cartridges were activated with 10 mL ultrapure methanol and rinsed with 10 mL ultrapure 0.1% formic acid water prior to extraction. Samples were then loaded onto cartridges through clean Teflon tubing and extracted by gravity (final extraction volumes ranged from 0.4 to 1.2 L). After extraction, cartridges were rinsed with 30 mL 0.1% formic acid water and dried. Cartridges were then eluted in 10 mL ultrapure MeOH and these methanolic extracts were stored at -20 °C until ICP-MS and FT-ICR MS analysis.
ICP-MS
Dissolved organic compound (DOS, DOP, DOBr, DOI) analysis followed the methods described in Gonsior et al. (2024) (doi:10.1039/D3VA00361B) for DOS and DOP and in Powers et al. (2024) (doi: 10.1016/j.scitotenv.2023.169292) and Powers et al. (2026) (doi: 10.1029/2025GL119062) for dissolved organic bromine (DOBr) and dissolved organic iodine (DOI). Briefly, methanolic extract aliquots were dried under a gentle stream of nitrogen gas and redissolved in ultrapure water. Samples for DOBr and DOI analysis were also passed through silver cartridges prior to analysis to remove residual halides. DOS and DOP were analyzed by ICP-MS/MS using oxygen as the reaction gas and DOBr and DOI were analyzed by ICP-MS/MS with no gas in the Octopole Reaction System. Final concentrations were corrected for both extraction and dilution volumes. Reported values are the average and standard deviation of three replicate injections per sample.
Data processing details have not been detailed by the dataset author, please refer to the methods desription.
Curation Actions Performed on Data File:
- Loaded PuertoRico_Sargassum_DOP_DOS_DOBr_DOI.xlsx (XLSX, sheet 1, header row 1, formatting preserved); empty strings were treated as missing values. The table was named 1010606_v1_sargassum_inundation_event_dop_dos_dobr_and_doi_data.
- Set column types: DOP, DOS, sdev_DOP, sdev_DOS, lat_dec, and long_dec as numbers; depth and n as integers; Date as a date formatted %Y-%m-%d; and Sample_ID, Site, location, DOBr, DOI, sdev_DOBr, and sdev_DOI as strings.
- Updated metadata for all columns, including descriptions, BCO-DMO standard parameter IDs, and supplied units. Depth, lat_dec, and long_dec were flagged as primary parameters.
- Set supplied units: DOP and sdev_DOP as ug P/L; DOS and sdev_DOS as ug S/L; DOBr and sdev_DOBr as ug Br/L; DOI and sdev_DOI as ug I/L; depth as meters; lat_dec and long_dec as decimal degrees; - Date as yyyy-mm-dd; and n as count.
- Saved the final table as 1010606_v1_sargassum_inundation_event_dop_dos_dobr_and_doi_data.csv.
| Dataset-specific Instrument Name | Agilent 8900 ICP-QQQ triple-quadrupole inductively coupled plasma mass spectrometer |
| Generic Instrument Name | Mass Spectrometer |
| Dataset-specific Description | We utilized 1 g Agilent Bond Elut PPL cartridges for SPE. Cartridges were activated with 10 mL ultrapure methanol and rinsed with 10 mL ultrapure 0.1% formic acid water prior to extraction. Samples were then loaded onto cartridges through clean Teflon tubing and extracted by gravity (final extraction volumes ranged from 0.4 to 1.2 L). |
| Generic Instrument Description | General term for instruments used to measure the mass-to-charge ratio of ions; generally used to find the composition of a sample by generating a mass spectrum representing the masses of sample components. |
| Dataset-specific Instrument Name | Bruker Solarix 12 Tesla FT-ICR mass spectrometer |
| Generic Instrument Name | Mass Spectrometer |
| Dataset-specific Description | Mass spectrometric analyses were undertaken at the Helmholtz Zentrum, Munich, Germany using a Bruker Solarix 12 Tesla Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) using negative electrospray ionization at -3600 V. The flow rate was 120 µL/h, 500 spectra were averaged. Pre-calibration was performed with arginine clusters and spectra were post-calibrated in the Bruker Data Analysis software using known DOM m/z ions across the m/z range of 200-700, with signal-to-noise set to 10. |
| Generic Instrument Description | General term for instruments used to measure the mass-to-charge ratio of ions; generally used to find the composition of a sample by generating a mass spectrum representing the masses of sample components. |
| Dataset-specific Instrument Name | Shimadzu Total Carbon Analyzer (TOC-Vcph) |
| Generic Instrument Name | Total Organic Carbon Analyzer |
| Dataset-specific Description | DOC and TDN concentrations were measured using a Shimadzu TOC-V. |
| Generic Instrument Description | A unit that accurately determines the carbon concentrations of organic compounds typically by detecting and measuring its combustion product (CO2). See description document at: http://bcodata.whoi.edu/LaurentianGreatLakes_Chemistry/bs116.pdf |
NSF Award Abstract:
Chromophoric dissolved organic matter (CDOM), the sunlight absorbing components in filtered water, is important in the study of marine and freshwater ecosystems as it can be used to trace the mixing of surface waters, as a proxy for carbon cycles, and other biogeochemical processes. Although its importance in ocean studies has been firmly established over the last several decades, sources and structural composition of CDOM within the oceans remains unclear and continues to be a subject of debate. Sargassum, a brown alga, is widely distributed in temperate and subtropical marine waters and may be important source of CDOM to the Sargasso Sea and Gulf of Mexico where Sargassum is abundant. This project will investigate the contribution of macro brown algae-derived compounds to the marine CDOM pool. Results from this study will have implications for the marine carbon cycle and satellite remote sensing of ocean color to assess mixing of surface water masses and biogeochemical processes. The project will provide educational opportunities for a postdoctoral scholar, summertime undergraduate internships (through a local NSF-sponsored Research Experiences for Undergraduates (REU) program), and workshop and research opportunities for local high schools students.
Sources of marine CDOM remain debatable and a comprehensive understanding of its origins, distribution and fate have been difficult. Marine CDOM, and in particular the "humic-like" component, have been suggested to originate from terrestrial sources, primarily lignins. However, recent evidence indicates that the exudation of phlorotannins produced by macro brown algae may contribute significantly to the marine CDOM pool. Phlorotannins, a class of polyphenols that are only found in, and continuously exuded by macro brown algae such as Sargassum, strongly absorb ultraviolet light and may have been underestimated in their contribution to the marine CDOM pool within certain geographic locales. Upon partial oxidation, light absorption by these specific compounds extends into longer wavelengths in the visible creating an absorption spectrum similar to that of lignin. These phlorotannins and their transformation products absorb light that might explain in part the "humic-like" signatures observed in open ocean environments. This study aims to characterize the optical properties and molecular composition of Sargassum-derived CDOM including its aerobic oxidation and photochemical behavior, as well as quantify Sargassum-derived CDOM to better estimate its possible contribution to the CDOM pool in the Sargasso Sea and Gulf of Mexico.
| Funding Source | Award |
|---|---|
| NSF Division of Ocean Sciences (NSF OCE) | |
| NSF Division of Ocean Sciences (NSF OCE) |