CTD profiles collected with RV Connecticut on the Continental shelf and slope south of Montauk, NY on 14-15 June 2022.

Website: https://www.bco-dmo.org/dataset/879380
Data Type: Cruise Results
Version: 1
Version Date: 2022-09-16

Project
» Collaborative Research: Combining single-cell and community 'omics' to test hypotheses about diversity and function of planktonic ciliates (Ciliate Omics)
ContributorsAffiliationRole
McManus, GeorgeUniversity of Connecticut (UConn)Principal Investigator, Contact
Katz, Laura A.Smith CollegeCo-Principal Investigator
Santoferrara, LucianaHofstra UniversityCo-Principal Investigator
Soenen, KarenWoods Hole Oceanographic Institution (WHOI BCO-DMO)BCO-DMO Data Manager

Abstract
Seven stations on the shelf and slope south of Montauk, NY on 14-15 June 2022 were sampled. Basic hydrographic properties, including temperature, salinity, dissolved oxygen, and pH were measured and rosette samples were taken for chlorophyll, nutrients, and microplankton. Water was filtered for metagenomics and metatranscriptomics and picked individual microplankters for sequencing. Three to ten depths were sampled at each station. Our shallowest station was on the shelf at 38m and the deepest was at the slope edge at 2400m. Due to limitations of the CTD our deepest sampled depth was 1150m. At the two shallowest stations, we also deployed a Wetstar fluorometer for phytoplankton fluorescence. The CTD data were processed with SeaBird's Seasoft program and converted to spreadsheet format.


Coverage

Spatial Extent: N:40.994 E:-71.3587 S:39.3804 W:-71.7138
Temporal Extent: 2022-06-14 - 2022-06-15

Methods & Sampling

Seven stations on the shelf and slope south of Montauk, NY on 14-15 June 2022 were sampled.  Basic hydrographic properties, including temperature, salinity, dissolved oxygen, and pH were measured and rosette samples were taken for chlorophyll, nutrients, and microplankton.  Water was filtered for metagenomics and metatranscriptomics and picked individual microplankters for sequencing.  Three to ten depths were sampled at each station.  Our shallowest station was on the shelf at 38m and the deepest was at the slope edge at 2400m.  Due to limitations of the CTD our deepest sampled depth was 1150m. At the two shallowest stations, we also deployed a Wetstar fluorometer for phytoplankton fluorescence.


Data Processing Description

The CTD data were processed with SeaBird's Seasoft program and converted to spreadsheet format.


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Data Files

File
ctd_all.csv
(Comma Separated Values (.csv), 38.34 MB)
MD5:173c3f3bd7c58dbd9b178181a0ca5e3f
Primary data file for dataset ID 879380
CTD_files
filename: CTD_files.zip
(ZIP Archive (ZIP), 2.94 MB)
MD5:5587a53921ab10da5f12fdad02145331
Original CTD Seabird files for RV Connecticut Cruise June 2022. Files are divided up per station number.

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Parameters

ParameterDescriptionUnits
Station

Station number

unitless
latitude

Station latitude, south is negative

decimal degrees
longitude

Station longitude, west is negative

decimal degrees
Date

Date of CTD sampling

unitless
Time

Start time of CTD sampling

unitless
density

Density

kg/m^3
depth

Depth

meters (m)
Fluorescence

Fluorescence, arbitrary

mg/m^3
oxygen

dissolved oxygen

mg/L
pH

pH

unitless
salinity

Salinity

unitless
scan

sampling event number for station

unitless
Temperature

Temperature

Degrees Celsius (°C)
flag

Quality flag

untless
ISO_DateTime_Local

Sampling date and time (Eastern Daylight Time (GMT-4)) in ISO 8601 format yyyy-mm-ddTHH:MM:SS

units
ISO_DateTime_UTC

Sampling date and time (UTC) in ISO 8601 format yyyy-mm-ddTHH:MM:SSZ

units


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Instruments

Dataset-specific Instrument Name
Generic Instrument Name
CTD Sea-Bird 9
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
Wetstar fluorometer
Generic Instrument Name
WET Labs (Sea-Bird WETLabs) WETStar fluorometer
Dataset-specific Description
Wetstar fluorometer for phytoplankton fluorescence
Generic Instrument Description
Submersible fluorometer designed for through-flow or pumped CTD applications manufactured by WetLabs and which can be configured for various types of fluorescence. The probe has a temperature range of 0-30 degrees C and a depth rating of 600 meters.


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Project Information

Collaborative Research: Combining single-cell and community 'omics' to test hypotheses about diversity and function of planktonic ciliates (Ciliate Omics)


Coverage: New England continental shelf


NSF Award Abstract:
Planktonic ciliates are key members of marine food webs where they serve diverse roles, including as food chain links between smaller microbes and larger plankton. Due to their small size and difficulties in identifying and cultivating them, we know less about ciliate diversity and distributions in the ocean than we do about larger organisms such as fish and invertebrates. Previous work from this team measured ciliate diversity in coastal waters and found that distinct genetic variants were separated in time and space in a way that could be related to factors such as ocean temperature, salinity, and depth gradients. Many questions remained unanswered, and it is important to understand the environmental factors that control the diversity and distribution of plankton such as ciliates to predict how these organisms may respond to a changing enviroment in the coming decades. This project focuses on: 1) how ciliate species are delineated using single-cell genomics and transcriptomics; 2) DNA-based studies of all ciliates and other planktonic members of the SAR clade (Stramenopila, Alveolata, Rhizaria), which will provide ecological context; 3) in situ gene expression by single-cell and meta- transcriptomics; and 4) laboratory studies of gene expression in cultivated ciliate species. This project involves training of postdoctoral scholars, graduate students, and undergraduates. The researchers are committed to creating diverse and inclusive research labs; recruitment of participants will be done through partnership with appropriate groups on our campuses. The project integrates with summer Research Experiences for Undergraduates (REU) activities at both Smith College and UCONN (including the UCONN/Mystic Aquarium joint REU), which are especially focused on underrepresented students. This project also enhances efforts to broaden understanding of biodiversity in partnership with the UCONN Noyce Scholars Program, which facilitates career-changing STEM professionals to become teachers in underserved secondary schools.

This project will assess distributions of reproductively-isolated species, determined using a new method to characterize regions of the ciliate germline genome. Furthermore, it will use phylogenomic methods to identify clade-specific transcripts (e.g. those of spirotrich ciliates) within metatranscriptomes from the shelf environment and to expand knowledge of ciliate function with single-cell transcriptomics of field-collected cells. These approaches will be a substantial improvement over the culture-based methods that are potentially biased towards "weedy" species in the ocean. The combination of definitive species identification with assessment of function via single-cell and meta- transcriptomics promises to provide significant advances in marine plankton ecology. The research focuses on two broad questions: 1) does the observed high diversity in phylogenetically-informative genes reflect reproductive isolation and functional differentiation in planktonic ciliates? and 2) do different co-occurring species of planktonic ciliates show substantial functional differences that correspond to different niches in the ocean? The project assesses species boundaries (i.e. reproductive isolation) through analyses of patterns in the germline micronuclei of planktonic ciliate morphospecies; characterizes transitions of closely-related ciliates across ecological gradients in the ocean; and examines functional differences within and between species, and in communities, through analyses of transcriptomics.

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)
NSF Division of Ocean Sciences (NSF OCE)

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