Contributors | Affiliation | Role |
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Karl, David M. | University of Hawaiʻi at Mānoa (SOEST) | Principal Investigator |
Segura-Noguera, Mariona | University of Hawaiʻi at Mānoa (SOEST) | Contact |
Curless, Susan E. | University of Hawaiʻi at Mānoa | Technician |
Nahorniak, Jasmine | Oregon State University (OSU-CEOAS) | Data Manager |
Gegg, Stephen R. | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Merchant, Lynne M. | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Urea data from HOE-DYLAN casts.
In the summer of 2012, C-MORE conducted a "continuous" long-term field experiment at Station ALOHA to observe and interpret temporal variability in microbial processes, and the consequences for ecological dynamics and biogeochemical cycling. Special focus was given to time-space coupling because proper scale sampling of the marine environment is an imperative, but generally neglected aspect of marine microbiology.
Hawaii Ocean Experiment - Dynamics of Light and Nutrients (HOE-DYLAN)
Seawater samples were collected from Niskin bottles with acid-washed syringes to avoid ammonium contamination with air and ship fumes. Samples were kept frozen (-20 ºC) until analysis. Urea was measured at the nanomolar level with the diacetyl monoxime automated method (Aminot and Kérouel, 1982), using a flow-injection system coupled to a 2m Liquid Waveguide Capillary Cell for reading the color. Low nutrient seawater exposed to daylight for two weeks was used for working standards preparation, blanks and carrier. The absorbance-concentration relationship was linear up to at least 800 nM Urea, with a method detection limit of 4.4 nM, and an error of 4.7% at 100nM.
The date and time columns were combined to create an ISO datetime column named ISO_DateTime_UTC and of format YYYY-MM-DDThh:mmZ
File |
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HOE_DYLAN cruise Urea observations filename: 4055_v1_hoe_dylan_cruises_urea.csv (Comma Separated Values (.csv), 15.08 KB) MD5:dd33136207334bbc289e3a6daea7751f File processed with laminar pipeline "4055_v1_HOE_DYLAN_Urea" at path 4055/1/data/4055_v1_hoe_dylan_cruises_urea.csv |
Parameter | Description | Units |
cruise_id | Cruise ID | unitless |
ISO_DateTime_UTC | Date and time (UTC) formatted to ISO 8601 standard | unitless |
sta | station number | unitless |
cast | Cast number | unitless |
bot | Rosette bottle number | unitless |
lat | Station latitude; south is negative | decimal degrees |
lon | Station longitude; west is negative | decimal degrees |
press | Pressure from CTD | dbar |
temp | Temperature from CTD | degrees Celcius |
sal | Salinity from CTD | PSS-78 |
O2 | Dissolved Oxygen from CTD | micromoles/kilogram |
fluor_re | Rescaled fluorescence from CTD estimate Chlorophyll | mircorgrams/liter |
Urea | N-Urea | nanomoles/liter |
Urea_sd | Standard deviation of Urea | unitless |
Dataset-specific Instrument Name | CTD Sea-Bird SBE 911plus |
Generic Instrument Name | CTD Sea-Bird SBE 911plus |
Generic Instrument Description | The Sea-Bird SBE 911 plus is a type of CTD instrument package for continuous measurement of conductivity, temperature and pressure. The SBE 911 plus includes the SBE 9plus Underwater Unit and the SBE 11plus Deck Unit (for real-time readout using conductive wire) for deployment from a vessel. The combination of the SBE 9 plus and SBE 11 plus is called a SBE 911 plus. The SBE 9 plus uses Sea-Bird's standard modular temperature and conductivity sensors (SBE 3 plus and SBE 4). The SBE 9 plus CTD can be configured with up to eight auxiliary sensors to measure other parameters including dissolved oxygen, pH, turbidity, fluorescence, light (PAR), light transmission, etc.). more information from Sea-Bird Electronics |
Dataset-specific Instrument Name | Fluorometer |
Generic Instrument Name | Fluorometer |
Generic Instrument Description | A fluorometer or fluorimeter is a device used to measure parameters of fluorescence: its intensity and wavelength distribution of emission spectrum after excitation by a certain spectrum of light. The instrument is designed to measure the amount of stimulated electromagnetic radiation produced by pulses of electromagnetic radiation emitted into a water sample or in situ. |
Dataset-specific Instrument Name | Liquid Waveguide Capillary Cells |
Generic Instrument Name | Liquid Waveguide Capillary Cells |
Dataset-specific Description | These low level nutrient measurements were made with an LWCC (not the usual autoanalyzer). The methods were developed by Susan Curless and Mariona Segura-Noguera. |
Generic Instrument Description | Liquid Waveguide Capillary Cells (LWCC) are optical sample cells that combine an increased optical pathlength (2-500 cm) with small sample volumes. They can be connected via optical fibers to a spectrophotometer with fiber optic capabilities. Similar to optical fibers, light is confined within the (liquid) core of an LWCC by total internal reflection at the core/wall interface. Ultra-sensitive absorbance measurements can be performed in the ultraviolet (UV), visible (VIS) and near-infrared (NIR) to detect low sample concentrations in a laboratory or process control environment. According to Beer’s Law the absorbance signal is proportional to chemical concentration and light path length. |
Dataset-specific Instrument Name | Niskin bottle |
Generic Instrument Name | Niskin bottle |
Generic Instrument Description | A Niskin bottle (a next generation water sampler based on the Nansen bottle) is a cylindrical, non-metallic water collection device with stoppers at both ends. The bottles can be attached individually on a hydrowire or deployed in 12, 24, or 36 bottle Rosette systems mounted on a frame and combined with a CTD. Niskin bottles are used to collect discrete water samples for a range of measurements including pigments, nutrients, plankton, etc. |
Website | |
Platform | R/V Kilo Moana |
Start Date | 2012-07-08 |
End Date | 2012-07-28 |
Description | In the summer of 2012, C-MORE conducted a "continuous" long-term field experiment at Station ALOHA to observe and interpret temporal variability in microbial processes, and the consequences for ecological dynamics and biogeochemical cycling. Special focus was given to time-space coupling because proper scale sampling of the marine environment is an imperative, but generally neglected aspect of marine microbiology.
Hawaii Ocean Experiment - Dynamics of Light and Nutrients (HOE-DYLAN) |
Website | |
Platform | R/V Kilo Moana |
Start Date | 2012-08-05 |
End Date | 2012-08-14 |
Description | In the summer of 2012, C-MORE conducted a "continuous" long-term field experiment at Station ALOHA to observe and interpret temporal variability in microbial processes, and the consequences for ecological dynamics and biogeochemical cycling. Special focus was given to time-space coupling because proper scale sampling of the marine environment is an imperative, but generally neglected aspect of marine microbiology.
Hawaii Ocean Experiment - Dynamics of Light and Nutrients (HOE-DYLAN) |
Website | |
Platform | R/V Kilo Moana |
Start Date | 2012-08-22 |
End Date | 2012-09-11 |
Description | In the summer of 2012, C-MORE conducted a "continuous" long-term field experiment at Station ALOHA to observe and interpret temporal variability in microbial processes, and the consequences for ecological dynamics and biogeochemical cycling. Special focus was given to time-space coupling because proper scale sampling of the marine environment is an imperative, but generally neglected aspect of marine microbiology.
Hawaii Ocean Experiment - Dynamics of Light and Nutrients (HOE-DYLAN) |
The Center for Microbial Oceanography: Research and Education (C-MORE) is a recently established (August 2006; NSF award: EF-0424599) NSF-sponsored Science and Technology Center designed to facilitate a more comprehensive understanding of the diverse assemblages of microorganisms in the sea, ranging from the genetic basis of marine microbial biogeochemistry including the metabolic regulation and environmental controls of gene expression, to the processes that underpin the fluxes of carbon, related bioelements and energy in the marine environment. Stated holistically, C-MORE's primary mission is: Linking Genomes to Biomes.
We believe that the time is right to address several major, long-standing questions in microbial oceanography. Recent advances in the application of molecular techniques have provided an unprecedented view of the structure, diversity and possible function of sea microbes. By combining these and other novel approaches with more well-established techniques in microbiology, oceanography and ecology, it may be possible to develop a meaningful predictive understanding of the ocean with respect to energy transduction, carbon sequestration, bioelement cycling and the probable response of marine ecosystems to global environmental variability and climate change. The strength of C-MORE resides in the synergy created by bringing together experts who traditionally have not worked together and this, in turn, will facilitate the creation and dissemination of new knowledge on the role of marine microbes in global habitability.
The new Center will design and conduct novel research, broker partnerships, increase diversity of human resources, implement education and outreach programs, and utilize comprehensive information about microbial life in the sea. The Center will bring together teams of scientists, educators and community members who otherwise do not have an opportunity to communicate, collaborate or design creative solutions to long-term ecosystem scale problems. The Center's research will be organized around four interconnected themes:
Each theme will have a leader to help coordinate the research programs and to facilitate interactions among the other related themes. The education programs will focus on pre-college curriculum enhancements, in service teacher training and formal undergraduate/graduate and post-doctoral programs to prepare the next generation of microbial oceanographers. The Center will establish and maintain creative outreach programs to help diffuse the new knowledge gained into society at large including policymakers. The Center's activities will be dispersed among five partner institutions:
and will be coordinated at the University of Hawaii at Manoa.
Funding Source | Award |
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NSF Division of Biological Infrastructure (NSF DBI) |