Contributors | Affiliation | Role |
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Drazen, Jeffrey C. | University of Hawaiʻi at Mānoa (SOEST) | Principal Investigator |
Popp, Brian N. | University of Hawaiʻi at Mānoa (SOEST) | Co-Principal Investigator |
Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Macrofauna and megafauna were collected in May and October 2019 using the HOV Alvin and the ROV Doc Ricketts, respectively, at Station M; and in July 2019, January 2020, and July 2020 using ROV Lu'ukai at Station Aloha. Macrofauna at Station M were collected using HOV-operated Ekman cores (20x20 centimeters (cm)). Macrofauna at Station Aloha were collected using a Brenke epibenthic sled towed across the seafloor due to the considerably lower macrofaunal densities at this oligotrophic site. Megafauna were collected using the submersible vehicle's manipulator arm and/or slurp gun. Upon retrieval to the surface, samples were placed in a cool room (5 degrees Celsius (ºC)) for further processing. Specimens of megafauna were weighed and measured, then they were dissected using a scalpel. All tissue samples were placed in cryovials and frozen in liquid nitrogen, and subsequently stored at -80ºC. Sieved (300 micrometers (um)) macrofauna samples were preserved in 10% buffered formalin. In the laboratory, macrofauna were further sorted by taxon. Samples of megafauna body tissues or macrofauna were freeze dried and ground to a homogenous powder using mortar and pestle.
Sediment samples were taken with ROV-operated push cores and sliced into 1 cm sections. Frozen samples were freeze dried, acidified, and then used for isotopic analysis. Sediment traps were McLane Parflux traps using formalin fixed collection cups varying from 10 to 30 day sample integration. Swimmers were removed from the samples under a dissecting microscope prior to concentration, freeze drying, and acidification for isotopic analysis.
Compound specific isotopic analysis of amino acids followed the protocols outlined in Hannides et al 2013.
- Imported original file "Abyssal food web AACSIA.xlsx" into the BCO-DMO data system.
- Flagged "NA" as a missing data value. Missing data are empty/blank in the final CSV file.
- Converted date fields to YYYY-MM-DD format.
- Converted positive Longitude values to negative (to indicate the direction is west).
- Renamed fields to comply with BCO-DMO naming conventions.
- PI provided updated copy of file named as "922789_v1_compound_specific_isotope_dataV2.csv".
- Imported the new file, "922789_v1_compound_specific_isotope_dataV2.csv", into the BCO-DMO system; converted dates and renamed fields as described above.
- Saved the final file as "922789_v1_compound_specific_isotope_data.csv".
File |
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922789_v1_compound_specific_isotope_data.csv (Comma Separated Values (.csv), 41.84 KB) MD5:745f16b62536afe3e50bc5d209370c73 Primary data file for dataset ID 922789, version 1 |
Parameter | Description | Units |
Sample | Sample identification code | unitless |
Cruise | Cruise designation | unitless |
Date_initial | Sampling initial date (UTC) | unitless |
Date_final | Sampling final date (UTC) | unitless |
Site | Site designation: StM = Station M; StALOHA = Station ALOHA | unitless |
Latitude | Latitude; positive values = North | decimal degrees |
Longitude | Longitude; negative values = West | decimal degrees |
Type | Type of sample: | unitless |
Species | Species of animal | unitless |
Type_filter | Filter size | unitless |
Depth | Depth of sample collection | meters (m) |
d15N | Bulk nitrogen isotopic composition | ‰, vs AIR |
d13C | Bulk carbon isotopic composition | ‰, vs VPDB |
ALA_N | Mean d15N value of all injections for amino acid alanine (ALA) | ‰, vs AIR |
GLY_N | Mean d15N value of all injections for amino acid glycine (GLY) | ‰, vs AIR |
THR_N | Mean d15N value of all injections for amino acid threonine (THR) | ‰, vs AIR |
SER_N | Mean d15N value of all injections for amino acid serine (SER) | ‰, vs AIR |
VAL_N | Mean d15N value of all injections for amino acid valine (VAL) | ‰, vs AIR |
LEU_N | Mean d15N value of all injections for amino acid leucine (LEU) | ‰, vs AIR |
ILE_N | Mean d15N value of all injections for amino acid isoleucine (ILE) | ‰, vs AIR |
PRO_N | Mean d15N value of all injections for amino acid proline (PRO) | ‰, vs AIR |
ASX_N | Mean d15N value of all injections for amino acid aspartic Acid + asparagine | ‰, vs AIR |
GLX_N | Mean d15N value of all injections for amino acid glutamic acid + glutamine | ‰, vs AIR |
PHE_N | Mean d15N value of all injections for amino acid phenylalanine (PHE) | ‰, vs AIR |
TYR_N | Mean d15N value of all injections for amino acid tyrosine (TYR) | ‰, vs AIR |
LYS_N | Mean d15N value of all injections for amino acid lysine (LYS) | ‰, vs AIR |
ALA_N_SD | Standand deviation of d15N values from all injections for amino acid alanine (ALA) | ‰, vs AIR |
GLY_N_SD | Standand deviation of d15N values from all injections for amino acid glycine (GLY) | ‰, vs AIR |
THR_N_SD | Standand deviation of d15N values from all injections for amino acid threonine (THR) | ‰, vs AIR |
SER_N_SD | Standand deviation of d15N values from all injections for amino acid serine (SER) | ‰, vs AIR |
VAL_N_SD | Standand deviation of d15N values from all injections for amino acid valine (VAL) | ‰, vs AIR |
LEU_N_SD | Standand deviation of d15N values from all injections for amino acid leucine (LEU) | ‰, vs AIR |
ILE_N_SD | Standand deviation of d15N values from all injections for amino acid isoleucine (ILE) | ‰, vs AIR |
PRO_N_SD | Standand deviation of d15N values from all injections for amino acid proline (PRO) | ‰, vs AIR |
ASX_N_SD | Standand deviation of d15N values from all injections for amino acid aspartic acid + asparagine | ‰, vs AIR |
GLX_N_SD | Standand deviation of d15N values from all injections for amino acid glutamic acid + glutamine | ‰, vs AIR |
PHE_N_SD | Standand deviation of d15N values from all injections for amino acid phenylalanine (PHE) | ‰, vs AIR |
TYR_N_SD | Standand deviation of d15N values from all injections for amino acid tyrosine (TYR) | ‰, vs AIR |
LYS_N_SD | Standand deviation of d15N values from all injections for amino acid lysine (LYS) | ‰, vs AIR |
ALA_C | Mean d13C value of all injections for amino acid alanine (ALA) | ‰, vs VPDB |
GLY_C | Mean d13C value of all injections for amino acid glycine (GLY) | ‰, vs VPDB |
THR_C | Mean d13C value of all injections for amino acid threonine (THR) | ‰, vs VPDB |
SER_C | Mean d13C value of all injections for amino acid serine (SER) | ‰, vs VPDB |
VAL_C | Mean d13C value of all injections for amino acid valine (VAL) | ‰, vs VPDB |
LEU_C | Mean d13C value of all injections for amino acid leucine (LEU) | ‰, vs VPDB |
ILE_C | Mean d13C value of all injections for amino acid isoleucine (ILE) | ‰, vs VPDB |
PRO_C | Mean d13C value of all injections for amino acid proline (PRO) | ‰, vs VPDB |
ASX_C | Mean d13C value of all injections for amino acid aspartic acid + asparagine | ‰, vs VPDB |
GLX_C | Mean d13C value of all injections for amino acid glutamic acid + glutamine | ‰, vs VPDB |
PHE_C | Mean d13C value of all injections for amino acid phenylalanine (PHE) | ‰, vs VPDB |
TYR_C | Mean d13C value of all injections for amino acid tyrosine (TYR) | ‰, vs VPDB |
LYS_C | Mean d13C value of all injections for amino acid lysine (LYS) | ‰, vs VPDB |
ALA_C_SD | Standand deviation of d13C values from all injections for amino acid alanine (ALA) | ‰, vs VPDB |
GLY_C_SD | Standand deviation of d13C values from all injections for amino acid glycine (GLY) | ‰, vs VPDB |
THR_C_SD | Standand deviation of d13C values from all injections for amino acid threonine (THR) | ‰, vs VPDB |
SER_C_SD | Standand deviation of d13C values from all injections for amino acid serine (SER) | ‰, vs VPDB |
VAL_C_SD | Standand deviation of d13C values from all injections for amino acid valine (VAL) | ‰, vs VPDB |
LEU_C_SD | Standand deviation of d13C values from all injections for amino acid leucine (LEU) | ‰, vs VPDB |
ILE_C_SD | Standand deviation of d13C values from all injections for amino acid isoleucine (ILE) | ‰, vs VPDB |
PRO_C_SD | Standand deviation of d13C values from all injections for amino acid proline (PRO) | ‰, vs VPDB |
ASX_C_SD | Standand deviation of d13C values from all injections for amino acid aspartic acid + asparagine | ‰, vs VPDB |
GLX_C_SD | Standand deviation of d13C values from all injections for amino acid glutamic acid + glutamine | ‰, vs VPDB |
PHE_C_SD | Standand deviation of d13C values from all injections for amino acid phenylalanine (PHE) | ‰, vs VPDB |
TYR_C_SD | Standand deviation of d13C values from all injections for amino acid tyrosine (TYR) | ‰, vs VPDB |
LYS_C_SD | Standand deviation of d13C values from all injections for amino acid lysine (LYS) | ‰, vs VPDB |
Dataset-specific Instrument Name | Ekman cores |
Generic Instrument Name | Bottom Sediment Grab Samplers |
Generic Instrument Description | These samplers are designed to collect an accurate representative sample of the sediment bottom. The bite of the sampler should be deep enough so all depths are sampled equally. The closing mechanism is required to completely close and hold the sample as well as prevent wash-out during retrieval. Likewise, during descent the sampler should be designed to minimize disturbance of the topmost sediment by the pressure wave as it is lowered to the bottom. |
Dataset-specific Instrument Name | Brenke epibenthic sled |
Generic Instrument Name | Epibenthic Sled |
Generic Instrument Description | An epibenthic sled is a semi-quantitative bottom-sampling device designed to trawl just above the bottom at the sediment water interface (the epibenthic zone). The sled consists of a rectangular steel frame with a mesh net (often more than one) attached to it. Towed along the ocean floor, its weight scrapes into the benthos, collecting any organisms on the surface or in the first few centimeters of sediment. It also collects the organisms in the water column just above the benthos.
Descriptions from WHOI and Census of Marine Life. |
Dataset-specific Instrument Name | trace gas chromatograph (GC) |
Generic Instrument Name | Gas Chromatograph |
Dataset-specific Description | TFA derivatives of amino acids were analyzed for stable N isotopic composition using a Thermo Scientific Delta V Plus IRMS interfaced to a trace gas chromatograph (GC) fitted with a 60 m BPx5 forte capillary column (0.32 mm internal diameter with 1.0 mm film thickness) through a GC–C III combustion furnace (980 ºC), reduction furnace (680 ºC), and liquid nitrogen cold trap. |
Generic Instrument Description | Instrument separating gases, volatile substances, or substances dissolved in a volatile solvent by transporting an inert gas through a column packed with a sorbent to a detector for assay. (from SeaDataNet, BODC) |
Dataset-specific Instrument Name | mortar and pestle |
Generic Instrument Name | Homogenizer |
Generic Instrument Description | A homogenizer is a piece of laboratory equipment used for the homogenization of various types of material, such as tissue, plant, food, soil, and many others. |
Dataset-specific Instrument Name | HOV Alvin |
Generic Instrument Name | HOV Alvin |
Generic Instrument Description | Human Occupied Vehicle (HOV) Alvin is part of the National Deep Submergence Facility (NDSF). Alvin enables in-situ data collection and observation by two scientists to depths reaching 6,500 meters, during dives lasting up to ten hours.
Commissioned in 1964 as one of the world’s first deep-ocean submersibles, Alvin has remained state-of-the-art as a result of numerous overhauls and upgrades made over its lifetime. The most recent upgrades, begun in 2011 and completed in 2021, saw the installation of a new, larger personnel sphere with a more ergonomic interior; improved visibility and overlapping fields of view; longer bottoms times; new lighting and high-definition imaging systems; improved sensors, data acquisition and download speed. It also doubled the science basket payload, and improved the command-and-control system allowing greater speed, range and maneuverability.
With seven reversible thrusters, it can hover in the water, maneuver over rugged topography, or rest on the sea floor. It can collect data throughout the water column, produce a variety of maps and perform photographic surveys. Alvin also has two robotic arms that can manipulate instruments, obtain samples, and its basket can be reconfigured daily based on the needs of the upcoming dive.
Alvin's depth rating of 6,500m gives researchers in-person access to 99% of the ocean floor. Alvin is a proven and reliable platform capable of diving for up to 30 days in a row before requiring a single scheduled maintenance day. Recent collaborations with autonomous vehicles such as Sentry have proven extremely beneficial, allowing PIs to visit promising sites to collect samples and data in person within hours of their being discovered, and UNOLs driven technological advances have improved the ability for scientific outreach and collaboration via telepresence
Alvin is named for Allyn Vine, a WHOI engineer and geophysicist who helped pioneer deep submergence research and technology.
(from https://www.whoi.edu/what-we-do/explore/underwater-vehicles/hov-alvin/, accessed 2022-09-09) |
Dataset-specific Instrument Name | Thermo Scientific Delta V Plus IRMS |
Generic Instrument Name | Isotope-ratio Mass Spectrometer |
Dataset-specific Description | TFA derivatives of amino acids were analyzed for stable N isotopic composition using a Thermo Scientific Delta V Plus IRMS interfaced to a trace gas chromatograph (GC) fitted with a 60 m BPx5 forte capillary column (0.32 mm internal diameter with 1.0 mm film thickness) through a GC–C III combustion furnace (980 ºC), reduction furnace (680 ºC), and liquid nitrogen cold trap. |
Generic Instrument Description | The Isotope-ratio Mass Spectrometer is a particular type of mass spectrometer used to measure the relative abundance of isotopes in a given sample (e.g. VG Prism II Isotope Ratio Mass-Spectrometer). |
Dataset-specific Instrument Name | push cores |
Generic Instrument Name | Push Corer |
Generic Instrument Description | Capable of being performed in numerous environments, push coring is just as it sounds. Push coring is simply pushing the core barrel (often an aluminum or polycarbonate tube) into the sediment by hand. A push core is useful in that it causes very little disturbance to the more delicate upper layers of a sub-aqueous sediment.
Description obtained from: http://web.whoi.edu/coastal-group/about/how-we-work/field-methods/coring/ |
Dataset-specific Instrument Name | ROV Doc Ricketts |
Generic Instrument Name | ROV Doc Ricketts |
Generic Instrument Description | The remotely operated vehicle (ROV) Doc Ricketts is operated by the Monterey Bay Aquarium Research Institute (MBARI). ROV Doc Ricketts is capable of diving to 4000 meters (about 2.5 miles). The R/V Western Flyer is the support vessel for Doc Ricketts and was designed with a center well whose floor can be opened to allow Doc Ricketts to be launched from within the ship into the water below. For a complete description, see: https://www.mbari.org/at-sea/vehicles/remotely-operated-vehicles/rov-doc... |
Dataset-specific Instrument Name | ROV Lu'ukai |
Generic Instrument Name | ROV Lu'ukai |
Generic Instrument Description | The UH remotely operated vehicle (ROV) Lu'ukai is a small work-class ROV that can be operated from the R/V Kilo Moana to conduct investigations in waters up to 6,000 meters deep. After beginning operations in early 2018, the Lu'ukai has supported a study of deep-sea biodiversity and ecological processes in the western Clarion-Clipperton Zone, an area where numerous manganese nodule mining exploration claims are located; has maintained and upgraded sensors at the ALOHA Cabled Observatory, the world's deepest operating ocean observatory; and has recovered a failed telecommunications cable used to support acoustic research in local waters. |
Dataset-specific Instrument Name | scalpel |
Generic Instrument Name | scalpel |
Generic Instrument Description | A scalpel, or lancet, or bistoury, is a small and extremely sharp bladed instrument used for dissection and surgery. |
Dataset-specific Instrument Name | McLane Parflux traps |
Generic Instrument Name | Sediment Trap |
Generic Instrument Description | Sediment traps are specially designed containers deployed in the water column for periods of time to collect particles from the water column falling toward the sea floor. In general a sediment trap has a jar at the bottom to collect the sample and a broad funnel-shaped opening at the top with baffles to keep out very large objects and help prevent the funnel from clogging. This designation is used when the specific type of sediment trap was not specified by the contributing investigator. |
Website | |
Platform | R/V Atlantis |
Start Date | 2019-04-28 |
End Date | 2019-05-09 |
Description | Collaborative Research: Assessing the relative importance of small vs large particles as sources of nutrition to abyssal communities
AT42-10; Alvin Dive numbers: D5027-D5030 |
Website | |
Platform | R/V Western Flyer |
Start Date | 2019-10-16 |
End Date | 2019-10-25 |
Description | Collaborative Research: Assessing the relative importance of small vs large particles as sources of nutrition to abyssal communities
Dive numbers: D1196, D1197, D1201
|
Website | |
Platform | R/V Kilo Moana |
Start Date | 2019-07-18 |
End Date | 2019-07-28 |
Description | See additional cruise information from Rolling Deck to Repository (R2R): https://www.rvdata.us/search/cruise/KM1914 |
Website | |
Platform | R/V Kilo Moana |
Start Date | 2020-01-17 |
End Date | 2020-01-26 |
Description | See additional cruise information from Rolling Deck to Repository (R2R): https://www.rvdata.us/search/cruise/KM2002 |
Website | |
Platform | R/V Kilo Moana |
Start Date | 2020-07-24 |
End Date | 2020-08-03 |
Description | See additional cruise information from Rolling Deck to Repository (R2R): https://www.rvdata.us/search/cruise/KM2008 |
NSF Award Abstract:
The abyssal plains of the oceans cover roughly half of the earth's surface, host enormous reservoirs of biodiversity and mineral resources, and play important roles in nutrient recycling and carbon sequestration. The most important process controlling the structure and function of these ecosystems is the quantity and quality of food (mostly sinking organic particles) that reaches the deep-sea floor. However, we do not fully understand the processes provisioning this vast ecosystem. We propose to evaluate the relative importance of small and larger "marine snow" particles that sink to deep-sea benthic communities by using the stable isotope signature of amino acids within various food sources and trace their consumption by fauna on the seafloor. This project compares ecosystems from the productive waters off California with the nutrient poor central Pacific, north of Hawaii. This project provides novel insights into how surface ocean processes are coupled to food-webs at the deep ocean seafloor and how changes in food sources potentially impact deep-sea communities. This project also provides excellent training opportunities for graduate students, a postdoctoral researcher, and undergraduates at UH and USC, particularly underrepresented minorities who pursue majors in the geosciences. The project will sponsor an annual G6-12 teacher workshop to inform Hawaii educators about the deep sea and broadly disseminate knowledge to the community. All results are communicated broadly to inform the public as concerns regarding abyssal ecosystems are rising due to interests in deep-sea mining.
The most important process controlling the structure and function of abyssal ecosystems is the quantity and quality of organic material that ultimately reaches the deep-sea floor. Despite the strong relationship between euphotic zone export flux and benthic ecology, studies of abyssal ecosystems have observed a deficit between food supply and benthic community demand. Additional work is therefore needed, particularly with regards to understanding the sources of nutrition to the deep-sea benthos. Recent evidence suggests that small particles may be significant contributors to carbon export, increasing in relative importance with depth in the mesopelagic and reaching the abyssal seafloor. This project is to evaluate the relative importance of small and larger "marine snow" particles to deep-sea benthic communities using a combination of particle flux measurements and state of the art compound specific stable isotope analysis of amino acids (AA-CSIA) at two abyssal locations that contrast in overlying productivity, seasonality, and export magnitude. Time series measurements at these locations (Sta. M off California and Sta. Aloha off Hawaii) provide a rich context for the work. In the mesopelagic central North Pacific larger particles (>53 um) can be resolved from microbially reworked, smaller (0.7-53 um) particles using AA-CSIA. This project is characterizing the isotopic compositions of key individual compounds in a continuum of particle sizes (< 1.0 um suspended particles to large sinking particles >53 um) collected using in situ filtration near the seafloor and bottom-moored sediment traps, thereby defining source-specific isotopic signatures that can be traced into benthic fauna and sediments (that are collected by ROVs and epibenthic sleds). This research to understand pelagic-benthic coupling from particles to megafauna using isotopic measurements at the compound-level will yield novel insights into the importance of small microbially reworked particles to deep-sea benthic food webs. This will more precisely couple surface ocean processes to food-webs at the deep ocean seafloor with implications for understanding climate change effects and the efficiency of energy transfer to higher trophic levels. Furthermore, isotopic measurements can also be used to further parameterize ecosystem models by quantifying trophic position across size classes and thus estimate predator-prey mass ratios in relation to variation in body size spectra, functional type, and ultimately to carbon flux and remineralization. Finally, the results will help refine interpretations of deep-sea paleorecords of past nitrogen dynamics by calibrating potential changes in organic matter isotope values between the surface and seafloor archives.
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) |