CTD data from R/V Hugh R. Sharp cruise HRS2110 in the Chesapeake Bay during August 2021

Website: https://www.bco-dmo.org/dataset/868879
Data Type: Cruise Results
Version: 1
Version Date: 2022-01-26

Project
» Nitrite Oxidation in Oxygen Minimum Zones (NO2Ox_OMZs)
ContributorsAffiliationRole
Ward, Bess B.Princeton UniversityPrincipal Investigator
Newman, SawyerWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
This dataset includes CTD data from R/V Hugh R. Sharp cruise HRS2110 in the Chesapeake Bay during August 2021. These data are associated with the "Nitrate Oxidation in Oxygen Minimum Zones" project.


Coverage

Spatial Extent: N:39.1405 E:-76.0922 S:35.0061 W:-76.4395
Temporal Extent: 2021-08-04 - 2021-08-10

Methods & Sampling

Water samples were collected using a 12 x 10-liter Niskin bottle rosette sampler equipped with a conductivity, temperature, and pressure instrument package (SBE9, Sea-Bird Electronics, Bellevue, Washington, U.S.A.), a sensor for dissolved oxygen (SBE43, Sea-Bird), and a sensor for chlorophyll fluorescence (FluoroWetlabECO, AFL FL Sensor).


Data Processing Description

CTD data were processed with Seasave V 7.26.0.7.

BCO-DMO Processing Notes:
- Standardized UTC time formatting;
- Added a UTC datetime field in ISO 8601 format;
- Renamed fields to remove all special characters except underscores.


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Data Files

File
cb_2021_compiledctdfiles-1.csv
(Comma Separated Values (.csv), 90.12 KB)
MD5:84db1a8541471dc87cb5aec3cc3fd161
Primary data file for dataset ID 868879

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Parameters

ParameterDescriptionUnits
Cast

cast number

unitless
Station

station name

unitless
ISO_DateTime_UTC

Datetime of cast; YYYYY-MM-DDTHH:MM:SSZ

unitless
Date

Date of cast; YYYY-MM-DD

unitless
time_UTC

Time of deployent, UTC; HH:MM:SS

unitless
timeS

Time, Elapsed

seconds
depSM

Depth [salt water]

m
prDM

Pressure, Digiquartz

decibars
t090C

Temperature

oC
t190C

Temperature, 2

oC
c0S_per_m

Conductivity

S/m
c1S_per_m

Conductivity, 2

S/m
sal00_1

Salinity, Practical

PSU
sal11_1

Salinity, Practical, 2

PSU
timeQ

Time, NMEA

seconds
timeY

Time, System

seconds
latitude

Latitude

decimal degrees
longitude

Longitude

decimal degrees
svCM_1

Sound Velocity

m/s
flECO_AFL

Fluorescence, WET Labs ECO-AFL/FL

mg/m3
sbeox0ML_per_L

Oxygen, SBE 43

ml/l
sbox0Mm_per_Kg

Oxygen, SBE 43

µmol/kg
sbeox0Mg_per_L

Oxygen, SBE 43

mg/l
sigma_E00

Density [sigma-theta]

kg/m3
sigma_E11

Density, 2 [sigma-theta]

kgk/m3
potemp090C

Potential Temperature

oC
potemp190C

Potential Temperature, 2

oC
svCM_2

Sound Velocity [Chen-Millero]

m/s
sal00_2

Salinity, Practical

PSU
sal11_2

Salinity, Practical, 2

PSU
flag

flag

unitless


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Instruments

Dataset-specific Instrument Name
CTD Sea-Bird 9
Generic Instrument Name
CTD Sea-Bird 9
Dataset-specific Description
A conductivity, temperature, and pressure instrument package (SBE9, Sea-Bird Electronics, Bellevue, Washington, U.S.A) attached to the Niskin bottle rosette used for sample collection. 
Generic Instrument Description
The Sea-Bird SBE 9 is a type of CTD instrument package. The SBE 9 is the Underwater Unit and is most often combined with the SBE 11 Deck Unit (for real-time readout using conductive wire) when deployed from a research vessel. The combination of the SBE 9 and SBE 11 is called a SBE 911. The SBE 9 uses Sea-Bird's standard modular temperature and conductivity sensors (SBE 3 and SBE 4). The SBE 9 CTD can be configured with auxiliary sensors to measure other parameters including dissolved oxygen, pH, turbidity, fluorometer, altimeter, etc.). Note that in most cases, it is more accurate to specify SBE 911 than SBE 9 since it is likely a SBE 11 deck unit was used. more information from Sea-Bird Electronics

Dataset-specific Instrument Name
Niskin bottle rosette sampler
Generic Instrument Name
Niskin bottle
Dataset-specific Description
Water samples were collected using a 12 x 10 L Niskin bottle rosette sampler, which was equipped with CTD Sea-Bird 9, Sea-Bird SBE 43 Dissolved Oxygen, and Wet Labs ECO-AFL/FL Fluorometer sensors.
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.

Dataset-specific Instrument Name
SBE43, Sea-Bird
Generic Instrument Name
Sea-Bird SBE 43 Dissolved Oxygen Sensor
Dataset-specific Description
A dissolved oxygen sensor attached to the Niskin bottle rosette used for sample collection. 
Generic Instrument Description
The Sea-Bird SBE 43 dissolved oxygen sensor is a redesign of the Clark polarographic membrane type of dissolved oxygen sensors. more information from Sea-Bird Electronics

Dataset-specific Instrument Name
FluoroWetlabECO, AFL FL Sensor
Generic Instrument Name
Wet Labs ECO-AFL/FL Fluorometer
Dataset-specific Description
A sensor for chlorophyll fluorescence attached to the Niskin bottle rosette used for sample collection. 
Generic Instrument Description
The Environmental Characterization Optics (ECO) series of single channel fluorometers delivers both high resolution and wide ranges across the entire line of parameters using 14 bit digital processing. The ECO series excels in biological monitoring and dye trace studies. The potted optics block results in long term stability of the instrument and the optional anti-biofouling technology delivers truly long term field measurements. more information from Wet Labs


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Deployments

HRS2110

Website
Platform
R/V Hugh R. Sharp
Start Date
2021-08-03
End Date
2021-08-21
Description
See more information about this cruise in Rolling Deck to Repository (R2R): https://www.rvdata.us/search/cruise/HRS2110


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Project Information

Nitrite Oxidation in Oxygen Minimum Zones (NO2Ox_OMZs)

Coverage: Eastern Tropical South Pacific and Chesapeake Bay


NSF Award Abstract:
This research is grounded in the fundamental role of nitrogen in limiting production in the ocean. Nitrite is a pivotal compound in the nitrogen cycle: it can be oxidized to nitrate, and thus retained as an available nutrient, or it can be reduced to dinitrogen gas, and thus lost from the bioavailable nitrogen pool. Oxidation of nitrite by nitrite oxidizing bacteria (NOB) is the only biological pathway by which nitrate is produced, and all known NOB require oxygen for life. The reduction pathway is also carried out by microbes, in this case, bacteria that thrive only in the absence of oxygen. In previous experiments, however, both oxidation and reduction of nitrite were detected in the same samples from ocean waters in the absence of oxygen. We will investigate three explanations for the apparent oxidation of nitrite in the absence of oxygen on a research cruise to the low oxygen waters off the coast of Peru: 1) The presence of unknown kinds of NOB that do not require oxygen; 2) a new reaction called dismutation, which is possible but never detected in nature; 3) an artifact associated with oxygen stress in NOB. This research could lead to discovery of novel mechanisms and or novel organisms that determine the fate of nitrite and the availability of nitrogen to support primary production in the long run. This project will advance discovery and understanding while promoting teaching, training and learning by providing opportunities for Princeton students to get involved in and have hands on experience in research in the lab and potentially at sea. Both undergraduate and graduate students will participate in the research through internships and field experiences. We will also integrate our work at sea into teaching in the classroom via videos and assignments based on data collected during the cruise.

Nitrite oxidation is the only known biological process that produces nitrate, which comprises the largest fixed nitrogen reservoir in the ocean. Nitrite oxidation is carried out by nitrite oxidizing bacteria (NOB), and all known species are obligate aerobes. Nitrite reduction to N2 occurs in multiple microbial pathways, generally under anoxic conditions. Despite their apparent incompatibility regarding oxygen, both processes are detected in the low oxygen or anoxic waters of oxygen minimum zones (OMZs). Thus, the fate of nitrite in OMZs has implications for the global fixed N budget. Nitrite oxidation is detected at high rates in essentially zero oxygen water in the most oxygen depleted depth intervals in OMZ regions, which suggests that some nitrite oxidizers might possess anaerobic metabolic capabilities. Nitrite disproportionation (or dismutation), in which nitrite is simultaneously oxidized to nitrate and reduced to N2, is a thermodynamically favorable reaction, which would link the two processes in one organism – but it has never been observed in nature. The research proposed here will address two big questions about nitrite in the ocean: 1) How does anaerobic nitrite oxidation work? 2) What determines the fate of nitrite? The experimental approach will investigate three possible explanations for anaerobic nitrite oxidation: 1) Nitrite is oxidized to nitrate by different clades of NOB, which exhibit different tolerances/requirements for oxygen; 2) Nitrite dismutation, also performed by NOB, partially explains the cooccurrence of oxidation and reduction of nitrite; 3) Apparently anaerobic nitrite oxidation is indeed biologically mediated but does not always represent net production of nitrate from nitrite; rather it results from isotopic equilibration during enzyme-catalyzed interconversion of nitrite and nitrate. These questions will be addressed by performing a suite of 15N-tracer incubations at stations located within and outside of one of the major OMZs in the ocean, the Eastern Tropical South Pacific. The dependence of the rate processes on oxygen concentrations will be determined, and the composition of the microbial assemblages will be assessed in order to determine whether different microbial components are involved under different environmental conditions. The expression of genes involved in oxidation/reduction/ respiratory metabolisms at low oxygen concentrations will be measured across oxygen gradients and in oxygen manipulations to identify their potential role in supporting “anaerobic” nitrite oxidation. The possibility that the apparently anaerobic nitrite oxidation is due to an enzyme level interconversion between nitrite and nitrate, which does not lead to net nitrate production and is not linked to growth of nitrite oxidizing bacteria, will also be investigated.

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.



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Funding

Funding SourceAward
NSF Division of Ocean Sciences (NSF OCE)

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