Dissolved extracellular polymeric substances (dEPS) dynamics and bacterial growth during sea ice formation in an ice tank study

Title
Dissolved extracellular polymeric substances (dEPS) dynamics and bacterial growth during sea ice formation in an ice tank study

Publication Type
Journal Article

Year of Publication
2012

Authors

Aslam SN, Underwood GJC, Kaartokallio H, Norman L, Autio R, Fischer M, Kuosa H, Dieckmann GS, Thomas DN

Journal
Polar Biology

Volume
35

Pagination
661-676

ISBN Number

Keywords

Sea ice, Extracellular polymeric substances, Frost flowers, Bacteria, Dissolved carbohydrate, DOM, EPS, mesocosm, HSVA test basin, Hamburg, Germany, 1.2 m3

Abstract

Extracellular polymeric substances (EPS) areknown to help microorganisms to survive under extremeconditions in sea ice. High concentrations of EPS arereported in sea ice from both poles; however, productionand dynamics of EPS during sea ice formation have beenlittle studied to date. This investigation followed the productionand partitioning of existing and newly formed dissolvedorganic matter (DOM) including dissolvedcarbohydrates (dCHO), dissolved uronic acids (dUA) anddissolved EPS (dEPS), along with bacterial abundancesduring early stages of ice formation. Sea ice was formedfrom North Sea water with (A) ambient DOM (NSW) and(B) with additional algal-derived DOM (ADOM) in a 6dexperiment in replicated mesocosms. In ADOM seawater,total bacterial numbers (TBN) increased throughout theexperiment, whereas bacterial growth occurred for 5d onlyin the NSW seawater. TBN progressively decreased withindeveloping sea ice but with a 2-fold greater decline in NSWcompared to ADOM ice. There were signiWcant increasesin the concentrations of dCHO in ice. Percentage contributionof dEPS was highest (63%) in the colder, uppermostparts in ADOM ice suggesting the development of a coldadaptedcommunity, producing dEPS possibly for cryoprotectionand/or protection from high salinity brines. Weconclude that in the early stages of ice formation, allochthonousorganic matter was incorporated from parent seawaterinto sea ice and that once ice formation had established,there were signiWcant changes in the concentrations andcomposition of dissolved organic carbon pool, resultingmainly from the production of autochthonous DOM by thebacteria.

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Partition of planktonic respiratory carbon requirements during a phytoplankton spring bloom

Title
Partition of planktonic respiratory carbon requirements during a phytoplankton spring bloom

Publication Type
Journal Article

Year of Publication
2012

Authors

Amin RM, Balmstedt U, Nejstgaard JC, Capua DI

Journal
Marine Ecology Progress Series

Volume
451

Pagination
15-29

ISBN Number

Keywords

mesocosm, plankton community, Respiratory carbon requirement, Energy transfer, Skeletonema, mesozooplankton, Calanus, Bergen, Espegrend, Norway, 11 m3

Abstract

ABSTRACT: We studied the effect of variable phytoplankton biomass and dominance of thediatom Skeletonema marinoi on the planktonic community respiratory carbon requirement over aperiod of 14 d (14 to 28 April 2008) in 3 different mesocosms filled with natural water at Espegrendmarine biological field station in Raunefjord, Norway. The carbon requirement was measured onmesozooplankton (the calanoid copepod Calanus finmarchicus) and 3 other size fractions of plankton—50% of the primary production, while bacterioplanktonshowed an intermediate and variable contribution (ca.

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Warming induces shifts in microzooplankton phenology and reduces time-lags between phytoplankton and protozoan production

Title
Warming induces shifts in microzooplankton phenology and reduces time-lags between phytoplankton and protozoan production

Publication Type
Journal Article

Year of Publication
2012

Authors

Aberle N, Bauer B, Lewandowska A, Gaedke U, Sommer U

Journal
Marine Biology

Volume

Pagination

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Keywords

mesocosm, Kiel indoor, Kiel, Germany, 1.4 m3

Abstract

Indoor mesocosm experiments were conducted to test for potential climate change effects on the springsuccession of Baltic Sea plankton. Two different temperature (D0 C and D6 C) and three light scenarios (62, 57and 49 % of the natural surface light intensity on sunny days), mimicking increasing cloudiness as predicted forwarmer winters in the Baltic Sea region, were simulated. By combining experimental and modeling approaches, wewere able to test for a potential dietary mismatch between phytoplankton and zooplankton. Two general predator–prey models, one representing the community as a tri-trophic food chain and one as a 5-guild food web were appliedto test for the consequences of different temperature sensitivities of heterotrophic components of the plankton.During the experiments, we observed reduced time-lags between the peaks of phytoplankton and protozoan biomassin response to warming. Microzooplankton peak biomass was reached by 2.5 day C-1 earlier and occurred almostsynchronously with biomass peaks of phytoplankton in the warm mesocosms (D6 C). The peak magnitudes ofmicrozooplankton biomass remained unaffected by temperature, and growth rates of microzooplankton werehigher at D6 C (lD0 C = 0.12 day-1 and lD6 C = 0.25 day-1). Furthermore, warming induced a shift in microzooplankton phenology leading to a faster species turnover and a shorter window of microzooplankton occurrence. Moderate differences in the light levels had no significant effect on the time-lags between autotrophic and heterotrophic biomass and on the timing, biomass maxima and growth rate of microzooplankton biomass. Both modelspredicted reduced time-lags between the biomass peaks of phytoplankton and its predators (both microzooplanktonand copepods) with warming. The reduction of time-lags increased with increasing Q10 values of copepods andprotozoans in the tritrophic food chain. Indirect trophic effects modified this pattern in the 5-guild food web. Ourstudy shows that instead of a mismatch, warming might lead to a stronger match between protist grazers and theirprey altering in turn the transfer of matter and energy toward higher trophic levels.

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