Abstract:We report the seasonal and vertical variations of dimethylsulfide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) in fast ice at Cape Evans, McMurdo Sound (Antarctica) during the springsummer transition in 2011 and winter-spring transition in 2012. We compare the variations of DMS,P observed to the seasonal evolution of the ice algal biomass and of the physical properties of the ice cover, with emphasis on the ice texture and brine dynamics. Isolated DMS and DMSP maxima were found during both seasona… Show more
“…Historically, studies on Antarctic fast ice algal communities have focused primarily on the taxonomy and physiology of algae inhabiting high‐biomass microhabitats (Arrigo et al, ; Grossi et al, ; McMinn, Pankowskii, et al, ; Stoecker et al, ; Whitaker & Richardson, ). Time series studies have been conducted in specific regions but overall remain sparse (Carnat et al, ; Delille et al, ; Fiala et al, ; Günther & Dieckmann, ; Watanabe et al, ). Here we compiled a comprehensive database of ice algal Chl a concentrations from Antarctic fast‐ice cores collected from different regions around the continent.…”
Historical sea ice core chlorophyll‐a (Chla) data are used to describe the seasonal, regional, and vertical distribution of ice algal biomass in Antarctic landfast sea ice. The analyses are based on the Antarctic Fast Ice Algae Chlorophyll‐a data set, a compilation of currently available sea ice Chla data from landfast sea ice cores collected at circum‐Antarctic nearshore locations between 1970 and 2015. Ice cores were typically sampled from thermodynamically grown first‐year ice and have thin snow depths (mean = 0.052 ± 0.097 m). The data set comprises 888 ice cores, including 404 full vertical profile cores. Integrated ice algal Chla biomass (range: <0.1–219.9 mg/m2, median = 4.4 mg/m2, interquartile range = 9.9 mg/m2) peaks in late spring and shows elevated levels in autumn. The seasonal Chla development is consistent with the current understanding of physical drivers of ice algal biomass, including the seasonal cycle of irradiance and surface temperatures driving landfast sea ice growth and melt. Landfast ice regions with reported platelet ice formation show maximum ice algal biomass. Ice algal communities in the lowermost third of the ice cores dominate integrated Chla concentrations during most of the year, but internal and surface communities are important, particularly in winter. Through comparison of biomass estimates based on different sea ice sampling strategies, that is, analysis of full cores versus bottom‐ice section sampling, we identify biases in common sampling approaches and provide recommendations for future survey programs: for example, the need to sample fast ice over its entire thickness and to measure auxiliary physicochemical parameters.
“…Historically, studies on Antarctic fast ice algal communities have focused primarily on the taxonomy and physiology of algae inhabiting high‐biomass microhabitats (Arrigo et al, ; Grossi et al, ; McMinn, Pankowskii, et al, ; Stoecker et al, ; Whitaker & Richardson, ). Time series studies have been conducted in specific regions but overall remain sparse (Carnat et al, ; Delille et al, ; Fiala et al, ; Günther & Dieckmann, ; Watanabe et al, ). Here we compiled a comprehensive database of ice algal Chl a concentrations from Antarctic fast‐ice cores collected from different regions around the continent.…”
Historical sea ice core chlorophyll‐a (Chla) data are used to describe the seasonal, regional, and vertical distribution of ice algal biomass in Antarctic landfast sea ice. The analyses are based on the Antarctic Fast Ice Algae Chlorophyll‐a data set, a compilation of currently available sea ice Chla data from landfast sea ice cores collected at circum‐Antarctic nearshore locations between 1970 and 2015. Ice cores were typically sampled from thermodynamically grown first‐year ice and have thin snow depths (mean = 0.052 ± 0.097 m). The data set comprises 888 ice cores, including 404 full vertical profile cores. Integrated ice algal Chla biomass (range: <0.1–219.9 mg/m2, median = 4.4 mg/m2, interquartile range = 9.9 mg/m2) peaks in late spring and shows elevated levels in autumn. The seasonal Chla development is consistent with the current understanding of physical drivers of ice algal biomass, including the seasonal cycle of irradiance and surface temperatures driving landfast sea ice growth and melt. Landfast ice regions with reported platelet ice formation show maximum ice algal biomass. Ice algal communities in the lowermost third of the ice cores dominate integrated Chla concentrations during most of the year, but internal and surface communities are important, particularly in winter. Through comparison of biomass estimates based on different sea ice sampling strategies, that is, analysis of full cores versus bottom‐ice section sampling, we identify biases in common sampling approaches and provide recommendations for future survey programs: for example, the need to sample fast ice over its entire thickness and to measure auxiliary physicochemical parameters.
“…Keller et al, 1989;Stefels, 2000), environmental forcing are known to control DMSP, DMSO, and DMS concentrations. In ice-associated environments, brine volume fraction might also be key in explaining DMS cycling variability via the control of ice permeability (Carnat et al, 2014). Structural changes within sea ice during the melt season, namely increases in brine volume fraction and ice desalination, result in increased connectivity and permeability in the warming sea ice (Willis et al, 2016;Polashenski et al, 2012) and influence DMSP and DMS cycling Carnat et al, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…In ice-associated environments, brine volume fraction might also be key in explaining DMS cycling variability via the control of ice permeability (Carnat et al, 2014). Structural changes within sea ice during the melt season, namely increases in brine volume fraction and ice desalination, result in increased connectivity and permeability in the warming sea ice (Willis et al, 2016;Polashenski et al, 2012) and influence DMSP and DMS cycling Carnat et al, 2014). Also, phytoplankton blooms developing under the ice during the melting period have been shown to produce large quantities of DMSP p , potentially leading to a build-up of DMS concentrations (Levasseur et al, 1994).…”
Abstract. Melt pond formation is a seasonal pan-Arctic process. During the thawing season, melt ponds may cover up to 90 % of the Arctic first-year sea ice (FYI) and 15 to 25 % of the multi-year sea ice (MYI). These pools of water lying at the surface of the sea ice cover are habitats for microorganisms and represent a potential source of the biogenic gas dimethyl sulfide (DMS) for the atmosphere. Here we report on the concentrations and dynamics of DMS in nine melt ponds sampled in July 2014 in the Canadian Arctic Archipelago. DMS concentrations were under the detection limit (< 0.01 nmol L −1 ) in freshwater melt ponds and increased linearly with salinity (r s = 0.84, p ≤ 0.05) from ∼ 3 up to ∼ 6 nmol L −1 (avg. 3.7 ± 1.6 nmol L −1 ) in brackish melt ponds. This relationship suggests that the intrusion of seawater in melt ponds is a key physical mechanism responsible for the presence of DMS. Experiments were conducted with water from three melt ponds incubated for 24 h with and without the addition of two stable isotope-labelled precursors of DMS (dimethylsulfoniopropionate), (D6-DMSP) and dimethylsulfoxide ( 13 C-DMSO). Results show that de novo biological production of DMS can take place within brackish melt ponds through bacterial DMSP uptake and cleavage. Our data suggest that FYI melt ponds could represent a reservoir of DMS available for potential flux to the atmosphere. The importance of this ice-related source of DMS for the Arctic atmosphere is expected to increase as a response to the thinning of sea ice and the areal and temporal expansion of melt ponds on Arctic FYI.
“…The lower 50 mm of each, plus attached platelets, was cut off using a stainless steel hacksaw, and transferred to a shore laboratory in a dark, insulated box for processing within 2 h. Previous studies have shown that this length of the cut section of the core contains the majority of the chla biomass (>99% authors' unpublished data; see also Ryan et al, 2006, Carnat et al, 2014. Cores were imaged and characteristics of the ice core, specifically the presence or absence of embedded 25 platelets, whether algae were primarily interstitial within the congelation ice or associated with platelets, and whether the core itself appeared to have been recovered with or without some degree of damage to the ice undersurface, was recorded.…”
Abstract. Identifying spatial heterogeneity of sea ice algae communities is critical to predicting ecosystem response under future climate scenarios. Using an autonomous robotic sampling platform beneath sea ice in McMurdo Sound, Antarctica, we measured irradiance in spectral bands expected to describe the spatial heterogeneity. Derived estimates of ice algae biomass identified patchiness at length scales varying from 50-70 m under first-year sea ice. These results demonstrate that a 15 step-change in how these communities can be assessed and monitored. The developed methodologies could be subsequently refined to further categorize different ice algae communities and their associated productivity in both Arctic and Antarctic waters.
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