scholarly journals Behaviour of dissolved organic matter and inorganic nutrients during experimental sea-ice formation

2001 ◽  
Vol 33 ◽  
pp. 317-321 ◽  
Author(s):  
Virginia Giannelli ◽  
David N. Thomas ◽  
Christian Haas ◽  
Gerhard Kattner ◽  
Hilary Kennedy ◽  
...  

AbstractIt is well established that during sea-ice formation, crystals aggregate into a solid matrix, and dissolved sea-water constituents, including inorganic nutrients, are rejected from the ice matrix. However, the behaviour of dissolved organic matter (DOM) during ice formation and growth has not been studied to date. DOM is the primary energetic substrate for microbial heterotrophic activity in sea water and sea ice, and therefore it is at the base of the trophic fluxes within the microbial food web. The aim of our study was to compare the behaviour of DOM and inorganic nutrients during formation and growth of sea ice. Experiments were conducted in a large indoor ice-tank facility (Hamburg Ship Model Basin, Germany) at −15°C. Three 1 m3 tanks, to which synthetic sea water, nutrients and dissolved organic compounds (diatom-extracted DOM) had been added, were sampled over a period of 5 days during sea-ice formation. Samples were collected throughout the experiment from water underlying the ice, and at the end from the ice as well. Brine was obtained from the ice by centrifuging ice cores. Inorganic nutrients (nitrate and phosphate) were substantially enriched in brine in comparison to water and ice phases, consistent with the processes of ice formation and brine rejection. Dissolved organic carbon (DOC) was also enriched in brine but was more variable and enriched in comparison to a dilution line. No difference in bacteria numbers was observed between water, ice and brine. No bacteria growth was measured, and this therefore had no influence on the measurable DOC levels. We conclude that the incorporation of dissolved organic compounds in newly forming ice is conservative. However, since the proportions of DOC in the brine were partially higher than those of the inorganic nutrients, concentrating effects of DOC in brine might be different compared to salts.

1997 ◽  
Vol 43 (143) ◽  
pp. 138-151 ◽  
Author(s):  
M. O. Jeffries ◽  
K. Morris ◽  
W.F. Weeks ◽  
A. P. Worby

AbstractSixty-three ice cores were collected in the Bellingshausen and Amundsen Seas in August and September 1993 during a cruise of the R.V. Nathaniel B. Palmer. The structure and stable-isotopic composition (18O/16O) of the cores were investigated in order to understand the growth conditions and to identify the key growth processes, particularly the contribution of snow to sea-ice formation. The structure and isotopic composition of a set of 12 cores that was collected for the same purpose in the Bellingshausen Sea in March 1992 are reassessed. Frazil ice and congelation ice contribute 44% and 26%, respectively, to the composition of both the winter and summer ice-core sets, evidence that the relatively calm conditions that favour congelation-ice formation are neither as common nor as prolonged as the more turbulent conditions that favour frazil-ice growth and pancake-ice formation. Both frazil- and congelation-ice layers have an av erage thickness of 0.12 m in winter, evidence that congelation ice and pancake ice thicken primarily by dynamic processes. The thermodynamic development of the ice cover relies heavily on the formation of snow ice at the surface of floes after sea water has flooded the snow cover. Snow-ice layers have a mean thickness of 0.20 and 0.28 m in the winter and summer cores, respectively, and the contribution of snow ice to the winter (24%) and summer (16%) core sets exceeds most quantities that have been reported previously in other Antarctic pack-ice zones. The thickness and quantity of snow ice may be due to a combination of high snow-accumulation rates and snow loads, environmental conditions that favour a warm ice cover in which brine convection between the bottom and top of the ice introduces sea water to the snow/ice interface, and bottom melting losses being compensated by snow-ice formation. Layers of superimposed ice at the top of each of the summer cores make up 4.6% of the ice that was examined and they increase by a factor of 3 the quantity of snow entrained in the ice. The accumulation of superimposed ice is evidence that melting in the snow cover on Antarctic sea-ice floes ran reach an advanced stage and contribute a significant amount of snow to the total ice mass.


2013 ◽  
Vol 155 ◽  
pp. 148-157 ◽  
Author(s):  
Susann Müller ◽  
Anssi V. Vähätalo ◽  
Colin A. Stedmon ◽  
Mats A. Granskog ◽  
Louiza Norman ◽  
...  

2015 ◽  
Vol 56 (69) ◽  
pp. 1-8 ◽  
Author(s):  
Mats A. Granskog ◽  
Daiki Nomura ◽  
Susann Müller ◽  
Andreas Krell ◽  
Takenobu Toyota ◽  
...  

AbstractAbsorption and fluorescence of chromophoric dissolved organic matter (CDOM) in sea ice and surface waters in the southern Sea of Okhotsk was examined. Sea-water CDOM had featureless absorption increasing exponentially with shorter wavelengths. Sea ice showed distinct absorption peaks in the ultraviolet, especially in younger ice. Older first-year sea ice had relatively flat absorption spectra in the ultraviolet range. Parallel factor analysis (PARAFAC) identified five fluorescent CDOM components, two humic-like and three protein-like. Sea water was largely governed by humic-like fluorescence. In sea ice, protein-like fluorescence was found in considerable excess relative to sea water. The accumulation of protein-like CDOM fluorescence in sea ice is likely a result of biological activity within the ice. Nevertheless, sea ice does not contribute excess CDOM during melt, but the material released will be of different composition than that present in the underlying waters. Thus, at least transiently, the CDOM introduced during sea-ice melt might provide a more labile source of fresher protein-like DOM to surface waters in the southern Sea of Okhotsk.


2001 ◽  
Vol 33 ◽  
pp. 297-303 ◽  
Author(s):  
David N. Thomas ◽  
Gerhard Kattner ◽  
Ralph Engbrodt ◽  
Virginia Giannelli ◽  
Hilary Kennedy ◽  
...  

AbstractIt has been hypothesized that there are significant dissolved organic matter (DOM) pools in sea-ice systems, although measurements of DOM in sea ice have only rarely been made. The significance of DOM for ice-based productivity and carbon turnover therefore remains highly speculative. DOM within sea ice from the Amundsen and Bellingshausen Seas, Antarctica, in 1994 and the Weddell Sea, Antarctica, in 1992 and 1997 was investigated. Measurements were made on melted sea-ice sections in 1994 and 1997 and in sea-ice brines in 1992. Dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) concentrations in melted ice cores were up to 1.8 and 0.78 mM, respectively, or 30 and 8 times higher than those in surface water concentrations, respectively. However, when concentrations within the brine channel/pore space were calculated from estimated brine volumes, actual concentrations of DOC in brines were up to 23.3 mM and DON up to 2.2 mM, although mean values were 1.8 and 0.15 mM, respectively. There were higher concentrations of DOM in warm, porous summer second-year sea ice compared with colder autumn first-year ice, consistent with the different biological activity supported within the various ice types. However, in general there was poor correlation between DOC and DON with algal biomass and numbers of bacteria within the ice. The mean DOC/DON ratio was 11, although again values were highly variable, ranging from 3 to highly carbon-enriched samples of 95. Measurements made on a limited dataset showed that carbohydrates constitute on average 35% of the DOC pool, with highly variable contributions of 1−99%.


2011 ◽  
Vol 52 (57) ◽  
pp. 233-241 ◽  
Author(s):  
Susann Müller ◽  
Anssi V. Vähätalo ◽  
Mats A. Granskog ◽  
Riitta Autio ◽  
Hermanni Kaartokallio

AbstractDuring sea-ice formation, the dissolved constituents of water are rejected from ice crystals. the initial fractionation of dissolved organic matter (DOM) in the Baltic Sea ice was studied through two freezing experiments and by sampling natural sea ice. DOM was characterized by the spectral absorption of chromophoric DOM (CDOM) and the parallel factor analysis of DOM fluorescence. Molecular weight measurements of DOM were applied to assess changes in the molecular size distribution of DOM in new sea ice relative to parent sea water. Both in the newly formed artificial and the natural sea ice, CDOM was enriched by 34–39% relative to salinity. the same three identified DOM fluorophores were present both in sea water and ice but enriched by 15–54% relative to salinity in ice. After the incorporation of DOM into ice, the ageing of ice decreased the spectral slope coefficient and the molecular weight of DOM. This study shows that physical processes during freezing of brackish water enrich chromo- and fluorophoric DOM relative to salts in sea ice.


2014 ◽  
Vol 15 (4) ◽  
pp. 790 ◽  
Author(s):  
G. PETIHAKIS ◽  
K. TSIARAS ◽  
G. TRIANTAFYLLOU ◽  
S. KALARONI ◽  
A. POLLANI

The effect of Black Sea Water (BSW) inputs on the North Aegean Sea productivity and food web dynamics was investigated, by means of sensitivity simulations, investigating the effect of the inflowing BSW, in terms of inorganic nutrients and dissolved organic matter. The model used has been successfully applied in the area in the past and extensively presented. Considering the importance of the microbial loop in the ecosystem functioning, the role of the dissolved organics and in order to achieve a more realistic representation of the Dissolved Organic Matter pool, the bacteria sub-model was appropriately revised. The importance of the microbial loop is highlighted by the carbon fluxes where almost 50% of carbon is channelled within it. The impact of dissolved organic matter (DOM) (in the inflowing to the Aegean Sea, BSW) appears to be stronger than the impact of dissolved inorganic nutrients, showing a more extended effect over the N Aegean. Bacterial production and biomass is more strongly affected in the simulations by modified DOM, unlike phytoplankton biomass and production, which are more dependent on the inflowing nutrients and particularly phosphorus (inorganic and dissolved organic). In the phytoplankton composition, the dinoflagellates appear to be mostly affected, being favoured by higher nutrient availability at the expense of all other groups, particularly picoplankton, indicating a shift to a more classical food chain.


1997 ◽  
Vol 43 (143) ◽  
pp. 138-151 ◽  
Author(s):  
M. O. Jeffries ◽  
K. Morris ◽  
W.F. Weeks ◽  
A. P. Worby

AbstractSixty-three ice cores were collected in the Bellingshausen and Amundsen Seas in August and September 1993 during a cruise of the R.V.Nathaniel B. Palmer. The structure and stable-isotopic composition (18O/16O) of the cores were investigated in order to understand the growth conditions and to identify the key growth processes, particularly the contribution of snow to sea-ice formation. The structure and isotopic composition of a set of 12 cores that was collected for the same purpose in the Bellingshausen Sea in March 1992 are reassessed. Frazil ice and congelation ice contribute 44% and 26%, respectively, to the composition of both the winter and summer ice-core sets, evidence that the relatively calm conditions that favour congelation-ice formation are neither as common nor as prolonged as the more turbulent conditions that favour frazil-ice growth and pancake-ice formation. Both frazil- and congelation-ice layers have an av erage thickness of 0.12 m in winter, evidence that congelation ice and pancake ice thicken primarily by dynamic processes. The thermodynamic development of the ice cover relies heavily on the formation of snow ice at the surface of floes after sea water has flooded the snow cover. Snow-ice layers have a mean thickness of 0.20 and 0.28 m in the winter and summer cores, respectively, and the contribution of snow ice to the winter (24%) and summer (16%) core sets exceeds most quantities that have been reported previously in other Antarctic pack-ice zones. The thickness and quantity of snow ice may be due to a combination of high snow-accumulation rates and snow loads, environmental conditions that favour a warm ice cover in which brine convection between the bottom and top of the ice introduces sea water to the snow/ice interface, and bottom melting losses being compensated by snow-ice formation. Layers of superimposed ice at the top of each of the summer cores make up 4.6% of the ice that was examined and they increase by a factor of 3 the quantity of snow entrained in the ice. The accumulation of superimposed ice is evidence that melting in the snow cover on Antarctic sea-ice floes ran reach an advanced stage and contribute a significant amount of snow to the total ice mass.


2001 ◽  
Vol 33 ◽  
pp. 311-316 ◽  
Author(s):  
M. A. Granskog ◽  
J. Virkanen

AbstractSea-ice and surface-water samples collected in January-April 1999 in coastal areas in the northern Baltic Sea were analyzed for particle, nutrient and trace-element concentrations and salinity. Stratigraphic analyses of ice cores were also carried out. Bulk nutrient and trace-element concentrations in sea ice fluctuated widely. Nutrient concentrations in sea ice normalized to sea-water salinities showed that sea ice had, almost without exception, an excess of nutrients compared to underlying waters. For phosphorus and phosphate this can be explained by particle incorporation and snow-ice formation, whereas for nitrogen and the sum of nitrite and nitrate snow-ice formation and other mechanisms are important. The levels of Al, Cu, Fe and Ni in the ice were similar to those observed in underlying waters. Pb was observed in detectable concentrations in the ice only. This indicates that sea ice contributes lead to underlying waters during melting, and in some degree also affects the other elements. Furthermore, the observations indicate that incorporation of lead into the ice cover is governed by different processes than for the other elements studied.


Author(s):  
G. S. Canterford ◽  
D. R. Canterford

The possibility of dissolved organic compounds acting as complexing or chelating agents in natural waters has received considerable attention in the last two to three decades. Stumm & Morgan (1970) have expressed doubts about the existence of humicmetal ion complexes in natural waters. Strickland (1972) has also stated that although the addition of chelating agents to sea water often improved the growth of phytoplankton, there was little evidence that the function of dissolved organic matter in oceans and lakes was to complex metals so as to increase or decrease their availability to phytoplankton. Strickland argued that even if all dissolved organic carbon were present as a compound of strong complexing ability it would not be able to compete for most metals with inorganic ligands such as chloride, sulphate and hydroxide. However, there is an increasing amount of data indicating that metals in natural waters may exist in chelated forms with dissolved organic matter (see, for example, Davey, Morgan & Erickson, 1973; Chau & Lum-Shue-Chan, 1974).


2014 ◽  
Vol 3 (1) ◽  
pp. 139-156 ◽  
Author(s):  
Eeva Eronen‐Rasimus ◽  
Hermanni Kaartokallio ◽  
Christina Lyra ◽  
Riitta Autio ◽  
Harri Kuosa ◽  
...  

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