Phytoplankton blooms over Arctic Ocean continental shelves are thought to be restricted to waters free of sea ice. Here, we document a massive phytoplankton bloom beneath fully consolidated pack ice far from the ice edge in the Chukchi Sea, where light transmission has increased in recent decades because of thinning ice cover and proliferation of melt ponds. The bloom was characterized by high diatom biomass and rates of growth and primary production. Evidence suggests that under-ice phytoplankton blooms may be more widespread over nutrient-rich Arctic continental shelves and that satellite-based estimates of annual primary production in these waters may be underestimated by up to 10-fold.
The Arctic icescape is rapidly transforming from a thicker multiyear ice cover to a thinner and largely seasonal first-year ice cover with significant consequences for Arctic primary production. One critical challenge is to understand how productivity will change within the next decades. Recent studies have reported extensive phytoplankton blooms beneath ponded sea ice during summer, indicating that satellite-based Arctic annual primary production estimates may be significantly underestimated. Here we present a unique time-series of a phytoplankton spring bloom observed beneath snow-covered Arctic pack ice. The bloom, dominated by the haptophyte algae Phaeocystis pouchetii, caused near depletion of the surface nitrate inventory and a decline in dissolved inorganic carbon by 16 ± 6 g C m−2. Ocean circulation characteristics in the area indicated that the bloom developed in situ despite the snow-covered sea ice. Leads in the dynamic ice cover provided added sunlight necessary to initiate and sustain the bloom. Phytoplankton blooms beneath snow-covered ice might become more common and widespread in the future Arctic Ocean with frequent lead formation due to thinner and more dynamic sea ice despite projected increases in high-Arctic snowfall. This could alter productivity, marine food webs and carbon sequestration in the Arctic Ocean.
[1] A winter time series of the inorganic carbon system above, within, and beneath the landfast sea ice of the southern Beaufort Sea confirmed that sea ice is an active participant in the carbon cycle of polar waters. Eddy covariance measurements above the ice identified significant vertical CO 2 fluxes, mostly upward away from the ice but with short periods of downward fluxes as well. A novel, in situ method revealed extremely high pCO 2 values within the ice that are not inconsistent with theory. The total carbon content of the ice increased slightly through the winter season, and increasing variability in the vertical profiles as spring began indicated that the inorganic carbon became mobile as the ice began to melt. During early winter, as the ice formed, inorganic carbon concentrations in the surface waters increased dramatically, along with salinity, partly because of rejection from the ice and partly from advective mixing. Brine drainage was apparently not sufficient to initiate convection, and the excess carbon remained in the surface waters into the summer.Citation: Miller, L. A., T.
The Canadian Beaufort Sea has been categorized as an oligotrophic system with the potential for enhanced production due to a nutrient‐rich intermediate layer of Pacific‐origin waters. Using under‐ice hydrographic data collected near the ice‐edge of a shallow Arctic bay, we documented an ice‐edge upwelling event that brought nutrient‐rich waters to the surface during June 2008. The event resulted in a 3‐week long phytoplankton bloom that produced an estimated 31 g C m−2 of new production. This value was approximately twice that of previous estimates for annual production in the region, demonstrating the importance of ice‐edge upwelling to the local marine ecosystem. Under‐ice primary production estimates of up to 0.31 g C m−2 d−1 showed that this production was not negligible, contributing up to 22% of the daily averaged production of the ice‐edge bloom. It is suggested that under‐ice blooms are a widespread yet under‐documented phenomenon in polar regions, which could increase in importance with the Arctic's thinning ice cover and subsequent increase in transmitted irradiance to the under‐ice environment.
[1] Extensive spatial and temporal observations of sea ice algae remain limited due in part to current destructive and time intensive sampling techniques. In this paper we examine the influence of snow cover and ice algal biomass on the spectral dependence of photosynthetically available radiation transmitted through the snow-ice matrix using a data set collected in Resolute Passage, Canada, from 3 to 21 May 2003. The relationships between a normalized difference index (NDI) of transmitted irradiance with ice algal biomass and with snow cover provided a means to examine and compare observational and modeled data. In contrast to the dominant scattering properties of snow, absorption largely controls the spectral diffuse attenuation coefficient of algae. Our results show that snow has little effect on the distribution of transmitted spectral irradiance at wavelengths between 400 and 550 nm, whereas algae have a strong absorption peak near 440 nm that dominates changes in spectral transmission across this wavelength range. Up to 89% of the total variation in algae biomass was accounted for with a single NDI wavelength combination. Therefore the blue wavelength peak in algal spectral absorption lends particularly well to the remote estimation of algae biomass using transmitted irradiance. Deviations between observed and modeled data highlight the need for improvements to model inputs and therefore more detailed observations of processes controlling snow, ice, and algae in situ optical properties.Citation: Mundy, C. J., J. K. Ehn, D. G. Barber, and C. Michel (2007), Influence of snow cover and algae on the spectral dependence of transmitted irradiance through Arctic landfast first-year sea ice,
Abstract. The precipitation of ikaite (CaCO 3 ·6H 2 O) in polar sea ice is critical to the efficiency of the sea ice-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the ice is poorly known. We report unique observations of ikaite in unmelted ice and vertical profiles of ikaite abundance and concentration in sea ice for the crucial season of winter. Ice was examined from two locations: a 1 m thick land-fast ice site and a 0.3 m thick polynya site, both in the Young Sound area (74 • N, 20 • W) of NE Greenland. Ikaite crystals, ranging in size from a few µm to 700 µm, were observed to concentrate in the interstices between the ice platelets in both granular and columnar sea ice. In vertical sea ice profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surface-ice values of 700-900 µmol kg −1 ice (∼25 × 10 6 crystals kg −1 ) to values of 100-200 µmol kg −1 ice (1-7 × 10 6 crystals kg −1 ) near the sea ice-water interface, all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration, whereas TA concentrations in the lower half of the sea ice were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolve in layers below. Melting of sea ice and dissolution of observed concentrations of ikaite would result in meltwater with a pCO 2 of <15 µatm. This value is far below atmospheric values of 390 µatm and surface water concentrations of 315 µatm. Hence, the meltwater increases the potential for seawater uptake of CO 2 .
Abstract. Climate change significantly impacts Arctic shelf regions in terms of air temperature, ultraviolet radiation, melting of sea ice, precipitation, thawing of permafrost and coastal erosion. Direct consequences have been observed on the increasing Arctic river flow and a large amount of organic carbon sequestered in soils at high latitudes since the last glacial maximum can be expected to be delivered to the Arctic Ocean during the coming decade. Monitoring the fluxes and fate of this terrigenous organic carbon is problematic in such sparsely populated regions unless remote sensing techniques can be developed and proved to be operational.The main objective of this study is to develop an ocean colour algorithm to operationally monitor dynamics of suspended particulate matter (SPM) on the Mackenzie River continental shelf (Canadian Arctic Ocean) using satellite imagery. The water optical properties are documented across the study area and related to concentrations of SPM and particulate organic carbon (POC). Robust SPM and POC : SPM proxies are identified, such as the light backscattering and attenuation coefficients, and relationships are established between these optical and biogeochemical parameters. Following a semi-analytical approach, a regional SPM quantification relationship is obtained for the inversion of the water reflectance signal into SPM concentration. This relationship is reproduced based on independent field optical measurements. It is successfully applied to a selection of MODIS satellite data which allow estimating fluxes at the river mouth and monitoring the extension and dynamics of the Mackenzie River surface plume in 2009, 2010 and 2011. Good agreement is obtained with field observations representative of the whole water column in the river delta zone where terrigenous SPM is mainly constrained (out of short periods of maximum river outflow). Most of the seaward export of SPM is observed to occur within the west side of the river mouth.Future work will require the validation of the developed SPM regional algorithm based on match-ups with field measurements, then the routine application to ocean colour satellite data in order to better estimate the fluxes and fate of SPM and POC delivered by the Mackenzie River to the Arctic Ocean.
The evolution of landfast sea ice melt pond coverage, surface topography, and mass balance was studied in the Canadian Arctic during May-June 2011 and 2012, using a terrestrial laser scanner, snow and sea ice sampling, and surface meteorological characterization. Initial melt pond formation was not limited to low-lying areas, rather ponds formed at almost all premelt elevations. The subsequent evolution of melt pond coverage varied considerably between the 2 years owing to four principle, temporally variable factors. First, the range in premelt topographic relief was 0.5 m greater in 2011 (rougher surface) than in 2012 (smoother surface), such that a seasonal maximum pond coverage of 60% and maximum hydraulic head of 204 mm were reached in 2011, versus 78% and 138 mm in 2012. A change in the meltwater balance (production minus drainage) caused the ponds to spread or recede over an area that was almost 90% larger in 2012 than in 2011. Second, modification of the premelt topography was observed during mid-June, due to preferential melting under certain drainage channels. Some of the lowest-lying premelt areas were subsequently elevated above these deepening channels and unexpectedly became drained later in the season. Third, ice interior temperatures remained 1-2 C colder later into June in 2012 than in 2011, even though the ice was 0.35 m thinner at melt onset, thereby delaying permeability increases in the ice that would allow vertical meltwater drainage to the ocean. Finally, surface melt was estimated to account for approximately 62% of the net radiative flux to the sea ice cover during the melt season.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.