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Abstract The Pacific inflow to the Arctic traditionally brings heat in summer, melting sea ice; dense waters in winter, refreshing the Arctic’s cold halocline; and nutrients year‐round, supporting Arctic ecosystems. Bering Strait moorings from 1990 to 2019 find increasing (0.010 ± 0.006 Sv/yr) northward flow, reducing Chukchi residence times by ∼1.5 months over this period (record maximum/minimum ∼7.5 and ∼4.5 months). Annual mean temperatures warm significantly (0.05 ± 0.02°C/yr), with faster change (∼0.1°C/yr) in warming (June/July) and cooling (October/November) months, which are now 2°C to 4°C above climatology. Warm (≥0°C) water duration increased from 5.5 months (the 1990s) to over 7 months (2017), mostly due to earlier warming (1.3 ± 0.7 days/yr). Dramatic winter‐only (January–March) freshening (0.03 psu/yr) makes winter waters fresher than summer waters. The resultant winter density change, too large to be compensated by Chukchi sea‐ice processes, shoals the Pacific Winter Water (PWW) equilibrium depth in the Arctic from 100–150 to 50–100 m, implying PWW no longer ventilates the Arctic’s cold halocline at 33.1 psu.
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The Genomic Capabilities of Microbial Communities Track Seasonal Variation in Environmental Conditions of Arctic Lagoons
In contrast to temperate systems, Arctic lagoons that span the Alaska Beaufort Sea coast face extreme seasonality. Nine months of ice cover up to ∼1.7 m thick is followed by a spring thaw that introduces an enormous pulse of freshwater, nutrients, and organic matter into these lagoons over a relatively brief 2–3 week period. Prokaryotic communities link these subsidies to lagoon food webs through nutrient uptake, heterotrophic production, and other biogeochemical processes, but little is known about how the genomic capabilities of these communities respond to seasonal variability. Replicate water samples from two lagoons and one coastal site near Kaktovik, AK were collected in April (full ice cover), June (ice break up), and August (open water) to represent winter, spring, and summer, respectively. Samples were size fractionated to distinguish free-living and particle-attached microbial communities. Multivariate analysis of metagenomes indicated that seasonal variability in gene abundances was greater than variability between size fractions and sites, and that June differed significantly from the other months. Spring (June) gene abundances reflected the high input of watershed-sourced nutrients and organic matter via spring thaw, featuring indicator genes for denitrification possibly linked to greater organic carbon availability, and genes for processing phytoplankton-derived organic matter associated with spring blooms. Summer featured fewer indicator genes, but had increased abundances of anoxygenic photosynthesis genes, possibly associated with elevated light availability. Winter (April) gene abundances suggested low energy inputs and autotrophic bacterial metabolism, featuring indicator genes for chemoautotrophic carbon fixation, methane metabolism, and nitrification. Winter indicator genes for nitrification belonged to Thaumarchaeota and Nitrosomonadales, suggesting these organisms play an important role in oxidizing ammonium during the under-ice period. This study shows that high latitude estuarine microbial assemblages shift metabolic capabilities as they change phylogenetic composition between these extreme seasons, providing evidence that these communities may be resilient to large hydrological events in a rapidly changing Arctic.
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- Award ID(s):
- 1656026
- PAR ID:
- 10279491
- Date Published:
- Journal Name:
- Frontiers in Microbiology
- Volume:
- 12
- ISSN:
- 1664-302X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3389/fmicb.2021.601901
