Contributors | Affiliation | Role |
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Hurst, Matthew P. | California Polytechnic State University Humboldt (Cal Poly Humboldt) | Principal Investigator |
Marchetti, Adrian | University of North Carolina at Chapel Hill (UNC-Chapel Hill) | Principal Investigator |
Till, Claire P. | California Polytechnic State University Humboldt (Cal Poly Humboldt) | Principal Investigator |
York, Amber D. | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
See the "Related Datasets" section for other datasets from this experiment.
Sampling:
Seawater for the incubation was collected from ~15m at 35°55.4’N, 121°32.4’W using acid-cleaned HDPE tubing taped directly to the amsteel blue line. A lead weight coated with fiberglass and epoxy paint was at the bottom of the line. The pump was a teflon Wilden air-operated double-diaphragm pump. The tubing was run into a trace metal clean positive pressure bubble, where it was homogenized in acid-cleaned 50 gallon plastic barrels. From there, 4L cubitainers for the different treatments were rinsed and filled with the homogenized seawater, and then spiked appropriately based on treatment. These cubitainers had been pre-cleaned using the methods of Crawford et al. 2003.
The incubation setup:
We had five different treatments, with three replicates each:
control: no addition
+Fe: 5 nmol/kg added dissolved Fe
+Sc: 5 nmol/kg added dissolved Sc
+Fe and +Sc: 5 nmol/kg each of dissolved Sc and Fe added
filtered +Fe and + Sc: the seawater was filtered with 0.2 micrometer pre-cleaned supor Acropak filter before rinsing and filling the cubitainer, and then spiking with 5 nmol/kg each of dissolved Sc and Fe.
The cubitainers were incubated in an on-deck plexiglass incubator that was surface-seawater chilled and covered with a screening to achieve 30% of the incident irradiance. After 24 hours, the incubation was ended and each treatment was harvested.
Sample analysis:
Samples for labile particulates were sampled and analyzed by the Hurst lab. The cubitainers were sampled into 2 L polycarbonate bottles with three rinses before filling. They were filtered immediately through pre-cleaned 0.2 mm pore-size polycarbonate track-etched (PCTE) membrane filters (47 mm dia., Nuclepore, Whatman) mounted in Teflon filter sandwiches (Millipore). Filters were stored in the freezer before digestion with a Berger et al. (2008) leach (acetic acid and hydroxylamine), used to extract the labile particulates. Extracts were analyzed for Fe and Sc on the Thermo Fisher Element 2 extended range ICP-MS at UC Santa Cruz.
* Sheet 1 of submitted file "May 2019 Sc incubation particulates for BCO-DMO.xlsx" was imported into the BCO-DMO data system for this dataset.
** In the BCO-DMO data system missing data identifiers are displayed according to the format of data you access. For example, in csv files it will be blank (null) values. In Matlab .mat files it will be NaN values. When viewing data online at BCO-DMO, the missing value will be shown as blank (null) values.
* Column names adjusted to conform to BCO-DMO naming conventions designed to support broad re-use by a variety of research tools and scripting languages. [Only numbers, letters, and underscores. Can not start with a number]
File |
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940088_v1_ scandium-inc-exp-p-metals.csv (Comma Separated Values (.csv), 1.13 KB) MD5:2f54c0326be8980b916b23c36d9c0f3f Primary data file for dataset ID 940088, version 1 |
Parameter | Description | Units |
Label | The name of each sample | unitless |
Timepoint | Timepoint (hours). how long the particular sample incubated for (24 hours in most cases; 0 hours for measurements of the initial conditions before the incubation) | hours |
Treatment | Description of the treatment for the particular sample | unitless |
Replicate | There were three replicates for each treatment. This parameter serves to disambiguate them. | unitless |
leachable_particulate_Fe | Concentration of iron in particles greater than 0.2 micrometers that were leachable with the weak acid leach | nanomoles per kilogram (nmol/kg) |
leachable_particulate_Sc | Concentration of scandium in particles greater than 0.2 micrometers that were leachable with the weak acid leach | picomoles per kilogram (pmol/kg) |
Dataset-specific Instrument Name | Thermo Element XR |
Generic Instrument Name | Inductively Coupled Plasma Mass Spectrometer |
Dataset-specific Description | Trace metal extracts were analyzed with a Thermo Element XR magnetic sector inductively coupled plasma mass spectrometer (ICP-MS) |
Generic Instrument Description | An ICP Mass Spec is an instrument that passes nebulized samples into an inductively-coupled gas plasma (8-10000 K) where they are atomized and ionized. Ions of specific mass-to-charge ratios are quantified in a quadrupole mass spectrometer. |
Website | |
Platform | R/V Oceanus |
Start Date | 2019-05-24 |
End Date | 2019-06-06 |
NSF Award Abstract:
Upwelling zones are hotspots of photosynthesis that are very dynamic in space and time. Microsocopic algae, known as phytoplankton, bloom when deep, nutrient-rich waters are upwelled into sunlit surface layers of the ocean, providing nourishment that supports productive food webs and draws down carbon dioxide (CO2) from the atmosphere to the deep ocean. Photosynthetic microbes in these regions must constantly adapt to changes in their chemical and physical environments. For example, subsurface populations respond to changes in light as they approach the surface. When upwelled waters move offshore, cells sink out of the illuminated zone, establishing seed populations that remain inactive until the next upwelling event. This process is called the upwelling conveyor belt cycle (UCBC). How phytoplankton respond to these changes in environmental conditions and how they may influence their nutrient requirements remains unknown. With future ocean changes predicted to alter seawater chemistry, including ocean acidification and decreased iron availability, some phytoplankton groups may be more vulnerable than others. Accompanying educational activities provide learning experiences to enhance understanding and awareness of marine microbes. The development of a research hub at UNC aims to provide infrastructure and support for scientists and students conducting research on environmental genomics. A laboratory component for an upper-level undergraduate course focused on marine phytoplankton is being developed. Educational outreach activities to broader communities include creation of a lesson plan on phytoplankton in upwelling zones and a virtual research cruise experience for middle-school students, as well as a hands-on lab activity for a local museum focused on marine phytoplankton and the important roles they play in shaping our planet.
The project examines how phytoplankton respond at the molecular and physiological level to the different UCBC stages, which seed populations (i.e., surface versus subsurface) contribute most to phytoplankton blooms during upwelling events of varying intensity, how phytoplankton elemental compositions are altered throughout UCBC stages, and how future predicted ocean conditions will affect the phytoplankton responses to UCBC conditions. This project contains both laboratory and fieldwork. In the laboratory, phytoplankton isolates recently obtained from upwelling regions are exposed to simulated UCBC conditions to examine changes in gene expression, growth and photosynthetic characteristics and elemental composition. Cultures are subjected to both current and future ocean conditions, including reduced iron availability and higher CO2. In the field, research cruises within upwelling regions study the dynamics of natural phytoplankton communities (both surface and subsurface) experiencing upwelling and relaxation and within simulated upwelling incubation experiments. Knowledge of how phytoplankton are affected by UCBC conditions at an integrated molecular, physiological and elemental level under both current and future scenarios is imperative for the proper conservation and management of these critically important ecosystems.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) |