ALBERT

Description: Ice melting in the Arctic Ocean exposes the surface water to more radiative energy with poorly understood effects on photo-biogeochemical processes and heat deposition in the upper ocean. In August 2009, we documented the vertical variability of light absorbing components at 37 stations located in the southeastern Beaufort Sea including both Mackenzie river-influenced waters and polar mixed layer waters. We found that melting multi-year ice released significant amount of non-algal particulates (NAP) near the sea surface relative to sub-surface waters. NAP absorption coefficients at 440 nm (aNAP(440)) immediately below the sea surface (0-) were on average 3-fold (up to 10-fold) higher compared to sub-surface values measured at 2–3 m depth. The impact of this unusual feature on the light transmission and remote sensing reflectance (Rrs) was further examined using a radiative transfer model. A 10-fold particle enrichment homogeneously distributed in the first meter of the water column slightly reduced photosynthetically available and usable radiation (PAR and PUR) by ~6% and ~8%, respectively, relative to a fully homogenous water column with low particles concentration. In terms of Rrs, the particle enrichment significantly flattered the spectrum by reducing the Rrs by up to 20% in the blue-green spectral region (400–550 nm). These results highlight the impact of melt water on the concentration of particles at sea surface, and the need for considering nonuniform vertical distribution of particles in such systems when interpreting remotely sensed ocean color. Spectral slope of aNAP spectra calculated in the UV domain decreased with depth suggesting that this parameter is sensitive to detritus composition and/or diagenesis state (e.g., POM photobleaching).

Description: The precipitation of ikaite (CaCO3 ⋅ 6H2O) 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 × 106 crystals kg−1) to values of 100–200 μmol kg−1 ice (1–7 × 106 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 pCO2 of

Description: The precipitation of ikaite (CaCO3·6H2O) 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 surfaceice values of 700–900 µmol kg−1 ice (~ 25 × 106 crystals kg−1) to bottom-layer values of 100–200 µmol kg−1 ice (1–7 × 106 kg−1), 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 bottom layers were twice as high. This depth-related discrepancy suggests interior ice processes where ikaite crystals form in surface sea ice layers and partly dissolved in bottom layers. From these findings and model calculations we relate sea ice formation and melt to observed pCO2 conditions in polar surface waters, and hence, the air-sea CO2 flux.

Description: 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. A direct consequence is an increase in Arctic river discharge with an expectation of increased delivery of organic carbon sequestered in high-latitute soils since the last glacial maximum. Monitoring the fluxes and fate of this terrigenous organic carbon is problematic in such sparsely populated regions unless remote sensing techniques can be developed to an operational stage. 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 validated 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 within which 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 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.

Description: 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.

Description: Ice melting in the Arctic Ocean exposes the surface water to more radiative energy with poorly understood effects on photo-biogeochemical processes and heat deposition in the upper ocean. In August 2009, we documented the vertical variability of light absorbing components at 37 stations located in the southeastern Beaufort Sea including both Mackenzie River-influenced waters and polar mixed layer waters. We found that melting multiyear ice released significant amount of non-algal particulates (NAP) near the sea surface relative to subsurface waters. NAP absorption coefficients at 440 nm (aNAP(440)) immediately below the sea surface were on average 3-fold (up to 10-fold) higher compared to subsurface values measured at 2–3 m depth. The impact of this unusual feature on the light transmission and remote sensing reflectance (Rrs) was further examined using a radiative transfer model. A 10-fold particle enrichment homogeneously distributed in the first meter of the water column slightly reduced photosynthetically available and usable radiation (PAR and PUR) by ∼6 and ∼8%, respectively, relative to a fully homogenous water column with low particle concentration. In terms of Rrs, the particle enrichment significantly flattered the spectrum by reducing the Rrs by up to 20% in the blue-green spectral region (400–550 nm). These results highlight the impact of meltwater on the concentration of particles at sea surface, and the need for considering non-uniform vertical distribution of particles in such systems when interpreting remotely sensed ocean color. Spectral slope of aNAP spectra calculated in the UV (ultraviolet) domain decreased with depth suggesting that this parameter is sensitive to detritus composition and/or diagenesis state (e.g., POM (particulate organic matter) photobleaching).