Summary of Study ST002539

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001635. The data can be accessed directly via it's Project DOI: 10.21228/M8C42F This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002539
Study TitleMicrobial metabolomic responses to changes in temperature and salinity along the western Antarctic Peninsula.
Study TypeStudy of particulate metabolites in phytoplankton and sea-ice algae along the Western Antarctic Peninsula
Study SummarySeasonal cycles within the marginal ice zones in polar regions include large shifts in temperature and salinity that strongly influence microbial abundance and physiology. However, the combined effects of concurrent temperature and salinity change on microbial community structure and biochemical composition during transitions between seawater and sea ice are not well understood. Coastal marine communities along the western Antarctic Peninsula were sampled and surface seawater was incubated at combinations of temperature and salinity mimicking the formation (cold, salty) and melting (warm, fresh) of sea ice to evaluate how these factors may shape community composition and particulate metabolite pools during seasonal transitions. Bacterial and algal community structures were tightly coupled to each other and distinct across sea-ice, seawater, and sea-ice-meltwater field samples, with unique metabolite profiles in each habitat. During short-term (approximately 10-day) incubations of seawater microbial communities under different temperature and salinity conditions, community compositions changed minimally while metabolite pools shifted greatly, strongly accumulating compatible solutes like proline and glycine betaine under cold and salty conditions. Lower salinities reduced total metabolite concentrations in particulate matter, which may indicate a release of metabolites into the labile dissolved organic matter pool. Low salinity also increased acylcarnitine concentrations in particulate matter, suggesting a potential for fatty acid degradation and reduced nutritional value at the base of the food web during freshening. Our findings have consequences for food web dynamics, microbial interactions, and carbon cycling as polar regions undergo rapid climate change.
Institute
University of Washington, School of Oceanography
DepartmentSchool of Oceanography
LaboratoryYoung Lab
Last NameDawson
First NameHannah
Address1501 NE Boat St, Seattle, WA, 98195, USA
Emailhmdawson@uw.edu
Phone5404547754
Submit Date2023-03-27
Raw Data AvailableYes
Raw Data File Type(s)mzXML
Analysis Type DetailLC-MS
Release Date2023-05-25
Release Version1
Hannah Dawson Hannah Dawson
https://dx.doi.org/10.21228/M8C42F
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN004181 AN004182 AN004183 AN004184
Analysis type MS MS MS MS
Chromatography type HILIC HILIC Reversed phase Reversed phase
Chromatography system Waters Acquity I-Class Waters Acquity I-Class Waters Acquity I-Class Waters Acquity I-Class
Column SeQuant ZIC- pHILIC (150 x 2.1mm,5um) SeQuant ZIC- pHILIC (150 x 2.1mm,5um) Waters ACQUITY UPLC CSH C18 (150 x 2.1mm,1.7um) Waters ACQUITY UPLC HSS CN (100 x 2.1mm,1.8um)
MS Type ESI ESI ESI ESI
MS instrument type Orbitrap Orbitrap Orbitrap Orbitrap
MS instrument name Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap
Ion Mode POSITIVE NEGATIVE POSITIVE NEGATIVE
Units Estimated metabolite carbon concentration (nmol C per L) Estimated metabolite carbon concentration (nmol C per L) Estimated metabolite carbon concentration per particulate carbon (nmol C per umol C) Estimated metabolite carbon concentration (nmol C per L)

Chromatography:

Chromatography ID:CH003098
Chromatography Summary:See attached summary.
Instrument Name:Waters Acquity I-Class
Column Name:SeQuant ZIC- pHILIC (150 x 2.1mm,5um)
Column Temperature:30
Flow Gradient:100% B for 2 minutes, ramped to 64% A over 18 minutes, ramped up to 100% A over 1 minute, held at 100% A for 7 minutes, and equilibrated at 100% B for 22 minutes (total time is 50 minutes)
Flow Rate:0.15 mL/min
Solvent A:10mM ammonium carbonate;85% water/15% acetonitrile
Solvent B:10mM ammonium carbonate;85% acetonitrile/15% water
Chromatography Type:HILIC
  
Chromatography ID:CH003099
Chromatography Summary:See attached summary.
Instrument Name:Waters Acquity I-Class
Column Name:Waters ACQUITY UPLC CSH C18 (150 x 2.1mm,1.7um)
Column Temperature:65
Flow Gradient:Initial conditions were 90% A and 10% B. The column was ramped to 80% B over 33 minutes, ramped up to 90% B over 12 minutes, held at 90% B for 1 minute, and equilibrated to 90%A and 10% B for 6 minutes (total time is 52 minutes).
Flow Rate:0.45 mL/min
Solvent A:10mM ammonium formate; 60% acetonitrile/40% water; 0.1% formic acid
Solvent B:10mM ammonium formate; 90% isopropyl alcohol/10% acetonitrile; 0.1% formic acid
Chromatography Type:Reversed phase
  
Chromatography ID:CH003100
Chromatography Summary:See attached summary.
Instrument Name:Waters Acquity I-Class
Column Name:Waters ACQUITY UPLC HSS CN (100 x 2.1mm,1.8um)
Column Temperature:35
Flow Gradient:The column was held at 5% B for 2 minutes, ramped to 100% B over 18 minutes, held at 100% B for 2 minutes, and equilibrated at 5% B for 5 minutes (total run time is 25 minutes)
Flow Rate:0.4 mL/min
Solvent A:0.1% formic acid in water
Solvent B:0.1% formic acid in acetonitrile
Chromatography Type:Reversed phase
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