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. 2020 Apr 22;15(4):e0231178.
doi: 10.1371/journal.pone.0231178. eCollection 2020.

Seasonal and latitudinal variations in sea ice algae deposition in the Northern Bering and Chukchi Seas determined by algal biomarkers

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Free PMC article

Seasonal and latitudinal variations in sea ice algae deposition in the Northern Bering and Chukchi Seas determined by algal biomarkers

Chelsea Wegner Koch et al. PLoS One. .
Free PMC article

Abstract

An assessment of the production, distribution and fate of highly branched isoprenoid (HBI) biomarkers produced by sea ice and pelagic diatoms is necessary to interpret their detection and proportions in the northern Bering and Chukchi Seas. HBIs measured in surface sediments collected from 2012 to 2017 were used to determine the distribution and seasonality of the biomarkers relative to sea ice patterns. A northward gradient of increasing ice algae deposition was observed with localized occurrences of elevated IP25 (sympagic HBI) concentrations from 68-70°N and consistently strong sympagic signatures from 71-72.5°N. A declining sympagic signature was observed from 2012 to 2017 in the northeast Chukchi Sea, coincident with declining sea ice concentrations. HBI fluxes were investigated on the northeast Chukchi shelf with a moored sediment trap deployed from August 2015 to July 2016. Fluxes of sea ice exclusive diatoms (Nitzschia frigida and Melosira arctica) and HBI-producing taxa (Pleurosigma, Haslea and Rhizosolenia spp.) were measured to confirm HBI sources and ice associations. IP25 was detected year-round, increasing in March 2016 (10 ng m-2 d-1) and reaching a maximum in July 2016 (1331 ng m-2 d-1). Snowmelt triggered the release of sea ice algae into the water column in May 2016, while under-ice pelagic production contributed to the diatom export in June and July 2016. Sea ice diatom fluxes were strongly correlated with the IP25 flux, however associations between pelagic diatoms and HBI fluxes were inconclusive. Bioturbation likely facilitates sustained burial of sympagic organic matter on the shelf despite the occurrence of pelagic diatom blooms. These results suggest that sympagic diatoms may sustain the food web through winter on the northeast Chukchi shelf. The reduced relative proportions of sympagic HBIs in the northern Bering Sea are likely driven by sea ice persistence in the region.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Biomarker compounds and chromatograms.
The highly branched isoprenoid molecular structures for IP25, HBI II, HBI III and the internal standard, 9-OHD. The compounds correspond with an example chromatogram from the surface sediment samples, showing the retention times and relative abundances.
Fig 2
Fig 2. Study site in the Pacific Arctic region.
A) The surface sediment sampling locations in the northern Bering and Chukchi Seas occurred within the framework of the Distributed Biological Observatory (DBO) regions (black boxes). The DBO regions in this study from south to north include: The St. Lawrence Island polynya (SLIP), Chirikov Basin (CHIR), southeast Chukchi Sea (SECS), northeast Chukchi Sea (NECS) and Barrow Canyon (BARC). B) The northeast Chukchi Sea region with the locations of the Chukchi Ecosystem Observatory (CEO) moored sediment trap and Haps core locations. Reprinted from Ocean Data View under a CC BY license, with permission from R. Schlitzer, original copyright 2020.
Fig 3
Fig 3. Sea ice concentration, snow depth, and annual fluxes of diatoms and biomarkers at the Chukchi Ecosystem Observatory 2015–2016.
The parameters measured from the CEO sediment trap from August 2015 –August 2016 included: A) sea ice concentration (%) and snow depth (cm). The blue-dashed line indicates the 15% sea ice concentration threshold defining open water, B) chlorophyll a fluxes (mg m-2d-1) and POC fluxes (g C m-2 d-1). POC and chl a data from Lalande et al. 2020 [49] C) Nitzschia frigida and Melosira arctica fluxes (sea ice exclusive diatoms), D) Gyrosigma/Haslea/Pleurosigma fluxes (group containing HBI-producing species), E) Rhizosolenia spp. fluxes (group containing HBI III-producing species), F) IP25 fluxes (ng m-2d-1), and G) HBI III fluxes (ng m-2d-1). All panels indicate the ice-covered period within the blue shaded boxes and the onset of snow melt is depicted by the red-dashed line.
Fig 4
Fig 4. IP25 and HBI III biomarker distributions.
Spatial distribution of the relative abundances of IP25 and HBI III concentrations (μg g-1 TOC) in surface sediments from 2012–2017. The white and grey bounding boxes indicate the DBO regions from south to north (SLIP, CHIR, SECS, NECS and BARC). Not all sampling stations and DBO regions were able to be occupied every year due to sea ice or weather, indicated by grey boxes (no data collected). IP25 and HBI III values were used as sympagic and pelagic diatom proxies, respectively, for the H-Print analysis. Reprinted from Ocean Data View under a CC BY license, with permission from R. Schlitzer, original copyright 2020.
Fig 5
Fig 5. H-Print index and satellite-derived sea ice concentration.
The spatial distribution of H-Print (%) in surface sediments from 2012–2017 and the spring sea ice concentration (SpSIC%) derived from April–June mean sea ice concentrations collected from SSMIS passive microwave data (NSIDC). The white and grey bounding boxes indicate the DBO regions from south to north (SLIP, CHIR, SECS, NECS and BARC). Not all sampling stations and DBO regions were able to be occupied every year due to sea ice or weather, indicated by grey boxes (no data collected). H-print ranges from 0–100%, where low values indicate elevated sea ice algae contributions while high values indicate higher contributions of pelagic diatoms. Reprinted from Ocean Data View under a CC BY license, with permission from R. Schlitzer, original copyright 2020.
Fig 6
Fig 6. Latitudinal variation and correlation of the H-Print index with sea ice.
The 2012–2017 H-Print values were compared with two different metrics for sea ice to determine the influence on the biomarkers. A) Linear regression of H-Print and the mean Spring Sea Ice Concentration (SpSIC) derived from April-June monthly sea ice concentration values. B) Linear regression of H-Print and the ice free period determined by the sea ice break-up date relative to sample collection date. Both relationships are shown with respect to latitude.
Fig 7
Fig 7. H-Print index by DBO region.
Statistical analysis of the H-Print values from surface sediments in relation to the location A) boxplot of H-Print variability by DBO region and latitude B) Multivariate separation of surface sediments visualized by principal components analysis (PCA) of individual HBIs (IP25, HBI II isomers, and HBI III) grouped by DBO region.
Fig 8
Fig 8
Annual Trends in H-Print and Spring Sea Ice Concentration (A) the northern Chukchi DBO regions (NECS and BARC) for 2012–2017 and (B) the Bering-southeast Chukchi DBO regions (SLIP, CHIR and SECS) for 2014–2017. The bold dashed line shows the only significant trend (p<0.01).
Fig 9
Fig 9. H-Print and radiocesium profiles in sediment cores.
H-Print profiles for a core collected on the Chukchi slope, NNE-14 (blue), and a bioturbated core collected on the shallower Chukchi shelf at DBO 4.6 (red). 137Cs profiles for NNE-14 and UTX13-23, a core collected in close proximity to DBO 4.6, depict the consistent sedimentation or bioturbation of deposited material.
Fig 10
Fig 10. Conceptual diagram for the production, flux and fate of HBIs in the Pacific Arctic.
Sea ice persistence increases from the northern Bering Sea to the northeast Chukchi Sea. There is a brief opportunity for sympagic production (yellow shading) in the Bering Sea due to the timing of sea ice retreat and return of sunlight, followed by extensive ice-edge and open water phytoplankton blooms (green shading) in the spring and fall. Sympagic production can occur over a longer period in the Chukchi Sea. Sympagic IP25 production (yellow circles) occurs in much lower proportions to pelagic HBI III (green circles) owing to the extensive open water period in the northern Bering Sea. In the Chukchi Sea, there is a greater proportion of IP25 to HBI III. This relative proportionality is observed in the surface sediments when sampled in the summer (pie chart). There is rapid burial of the sympagic HBIs (yellow spiral) owing to aggregation and rapid sedimentation in both regions, with a greater proportion available on the Chukchi shelf. Resuspension (upward arrows) plays a larger role in the Chukchi Sea, sustaining the suspension of IP25 and in the water column. Advection (horizontal arrows) is also likely to be a more prominent contribution to the HBI signal in the Chukchi than the northern Bering Sea. Symbols courtesy of the Integration and Application Network, University of Maryland Center for Environmental Science (ian.umces.edu/symbols/) and reprinted under a CC BY license, permission from B. Walsh, original copyright 2020.

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Grants and funding

Financial support was provided by grants from the NSF Arctic Observing Network program (1204082,1702456 and 1917469 to J. Grebmeier and L. Cooper; 1204044,1702137 and 1917434 to K. Frey, https://www.nsf.gov/funding/pgm_summ.jsp?pims_id=503222) and NOAA Arctic Research Program (CINAR 22309.07_UMCES_Grebmeier, https://arctic.noaa.gov/) to J. Grebmeier and L. Cooper. Research cruises in 2012 and 2013 were part of the Hanna Shoal Ecosystem Study for the COMIDA project funded by the U.S. Department of the Interior, Bureau of Ocean Energy Management (BOEM), Alaska Outer Continental Shelf Region, Anchorage, Alaska (https://www.boem.gov/regions/alaska-ocs-region/alaska-ocs-region) under BOEM Cooperative Agreement No. M11AC00007 with The University of Texas at Austin as part of the Chukchi Sea Offshore Monitoring in Drilling Area (COMIDA) and the BOEM Alaska Environmental Studies Program (https://www.boem.gov/about-boem/alaska-environmental-studies), to PIs J. Grebmeier and L. Cooper. Additional funding support was provided to C. Wegner (Koch) by the North Pacific Research Board Graduate Research Award (https://www.nprb.org/), the Cove Point Natural Heritage Trust (http://www.covepoint-trust.org/) and the Chesapeake Biological Laboratory Graduate Education Committee (https://www.umces.edu/cbl). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.