Contributors | Affiliation | Role |
---|---|---|
Gutierrez Rodriguez, Andres | New Zealand National Institute of Water and Atmospheric Research (NIWA) | Principal Investigator |
Stukel, Michael | Florida State University (FSU) | Co-Principal Investigator |
Yingling, Natalia | Florida State University (FSU) | Co-Principal Investigator |
Newman, Sawyer | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Field Collection
Data was collected in the Chatham Rise section of the Southern Ocean, located east of Aotearoa New Zealand, as part of the SALPOOP (‘Salp Particle expOrt and Ocean Production’) voyage during October to November 2018. ). We conducted five Lagrangian experiments (hereafter referred to as “cycles”) that lasted four to eight days (Décima et al., 2023). There were three cycles that were sampled in SA waters (1, 2 and 5) and two cycles in ST waters (3 and 4) while salps were only present in three cycles (1, 2 and 4). Six depths were chosen to span the euphotic zone (based on chlorophyll fluorescence measured during the conductivity-temperature-depth (CTD) downcast profiles).
Size Fractionated Chlorophyll a Measurements
Samples for size fractionated chlorophyll a (SF Chla) were analyzed by first gravity filtering a sample (250 mL) through a 20 µm 47-mm polycarbonate filter, then with low vacuum pressure, filtering sequentially through a 2 µm and a 0.2 µm filter. Filters were then folded, placed in 1.5 mL cryovials and frozen (-80 °C) until analysis (Gutiérrez‐Rodríguez et al., 2020). Chla and acidified phaeopigment-a concentrations were measured (within 3 months) using ice-cold 90% acetone extraction by spectrofluorometric methods (APHA 10200 H) on a Varian Cary Eclipse fluorescence spectrophotometer (Rice et al., 2012).
Chl and acidified phaeopigment-a concentrations were measured in the lab (within 3 months) using an ice-cold 90% acetone extraction by spectrofluorometric methods (APHA 10200 H) on a Varian Cary Eclipse fluorescence spectrophotometer (Rice et al., 2012).
Removed units from column headers.
Percent sign (%) replaced by "_percent" in column headers to remove special characters. Periods removed from float numeric values in column names; see parameter details for full information.
Dates converted from %m/%d/%y format to %Y-%m-%d format.
Latitude and longitude coordinates rounded to 6 decimal places.
Parameter | Description | Units |
Cycle | Lagrangian experiment number | unitless |
Cast | CTD deployment number | unitless |
Depth | Depth the sample originated in meters | meters |
Lat | Latitude in decimal degrees; a positive value indicates an Eastern coordinate | decimal degrees |
Lon | Longitude in decimal degrees; a negative value indicates a Northern coordinate | decimal degrees |
Date | Date in New Zealand Standard time | unitless |
Chl_a_02 | Chlorophyll concentration for the 0.2 µm filter | mg/m^3 |
Chl_a_2 | Chlorophyll concentration for the 2 µm filter | mg/m^3 |
Chl_a_20 | Chlorophyll concentration for the 20 µm filter | mg/m^3 |
Summed_SF_Chl | Total or summed chlorophyll concentration for the 0.2, 2 and 20 µm filter | mg/m^3 |
Chl_a_02_percentage | Percentage of total summed chlorophyll represented by 0.2 µm cells | unitless |
Chl_a_2_percentage | Percentage of total summed chlorophyll represented by 2 µm cells | unitless |
Chl_a_20_percentage | Percentage of total summed chlorophyll represented by 20 µm cells | unitless |
Dataset-specific Instrument Name | Varian Cary Eclipse fluorescence spectrophotometer |
Generic Instrument Name | Spectrophotometer |
Dataset-specific Description | Chl and acidified phaeopigment-a concentrations were measured in the lab (within 3 months) using an ice-cold 90% acetone extraction by spectrofluorometric methods (APHA 10200 H) on a Varian Cary Eclipse fluorescence spectrophotometer (Rice et al., 2012). |
Generic Instrument Description | An instrument used to measure the relative absorption of electromagnetic radiation of different wavelengths in the near infra-red, visible and ultraviolet wavebands by samples. |
Website | |
Platform | R/V Tangaroa |
Start Date | 2018-10-23 |
End Date | 2018-11-21 |
NSF Award Abstract:
Salps are unique open-ocean animals that range in size from a few millimeters to greater than twenty centimeters, have a gelatinous (jelly-like) body, and can form long chains of many connected individuals. These oceanic organisms act as oceanic vacuum cleaners, having incredibly high feeding rates on phytoplankton and, unusual for consumers of their size, smaller bacteria-sized prey. This rapid feeding and the salps' tendency to form dense blooms, allows them move substantial amounts of prey carbon from the surface into the deep ocean, leading to carbon dioxide removal from the atmosphere. However, salps are often considered a trophic dead-end, rather than a link, in the food web due to the assumption that they themselves are not consumed, since their gelatinous bodies are less nutritious than co-occurring crustacean prey. Along with this, salp populations are hypothesized to be increasing due to climate change. This proposal addresses these questions: 1) Do salps compete primarily with crustaceans (as in the prevailing paradigm) or are they competitors of single-celled protists, which are the dominant grazers of small phytoplankton? 2) Do salp blooms increase the efficiency of food-web pathways from tiny phytoplankton to fisheries production in nutrient-poor ocean regions?
This project will support the interdisciplinary education of a graduate student who will learn modeling and laboratory techniques in the fields of biological and chemical oceanography and stimulate international collaborations between scientists in the United States and New Zealand. Additionally, several Education and Outreach initiatives are planned, including development of a week-long immersive high school class in biological oceanography, and education modules that will serve the "scientists-in-the schools" program in Tallahassee, FL.
It is commonly assumed that salps are a trophic sink. However, this idea was developed before the discovery that protists (rather than crustaceans) are the dominant grazers in the open ocean and was biased by the difficulty of recognizing gelatinous salps in fish guts. More recent studies show that salps are found in guts of a diverse group of fish and seabirds and are a readily available prey source when crustacean abundance is low. This proposal seeks to quantify food web flows through contrasting salp-dominated and salp-absent water parcels near the Chatham Rise off western New Zealand where salp blooms are a predictable phenomenon. The proposal will leverage previously obtained data on salp abundance, bulk grazing impact, and biogeochemical significance during Lagrangian experiments conducted by New Zealand-based collaborators. The proposal will determine 1) taxon- and size-specific phytoplankton growth rate measurements, 2) taxon- and size-specific protozoan and salp grazing rate measurements, 3) compound specific isotopic analysis of the amino acids of mesozooplankton to quantify the trophic position of salps, hyperiid amphipods, and other crustaceans, 4) sediment traps to quantify zooplankton carcass sinking rates, and 5) linear inverse ecosystem modeling syntheses. Secondary production and trophic flows from this well-constrained ecosystem model will be compared to crustacean-dominated and microbial loop-dominated ecosystems in similarly characterized regions (California Current, Costa Rica Dome, and Gulf of Mexico).
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
Funding Source | Award |
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NSF Division of Ocean Sciences (NSF OCE) | |
NSF Division of Ocean Sciences (NSF OCE) |