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BREMERHAVEN Am Handelshafen 12 27570 Bremerhaven Telefon 0471 4831 www.awi.de

Objective 1:

Characterize bio-physical sea ice properties Objective 3:

Quantify the contribution of sea ice algae derived carbon in polar foodwebs

Figure 1: Generalized

rendition of the SUIT (vertical cross-section) sensor array setup.

Figure 3: Sea ice thickness distributions comparing SUIT haul 285 and an EM- 31 survey of a nearby ice floe.

Methods: Conducted Surface and Under-Ice Trawls (SUIT) with a mounted sensor array (Fig. 1) consisting of: i) CTD with an upward-looking altimeter for ice draft/thickness and fluorometer for chl a; ii) ADCP for tilt, roll, and water inflow and; iii) Two spectroradiometers for light transmission and ice algae biomass. Fig. 2 shows a SUIT profile of the sensor array data.

Spectral-derived ice algae biomass estimates will be determined by relating ice core algae biomass (HPLC) with coincident ROV and L-arm spectral measurements (Fig. 4; e.g. Mundy et al., 2007) which will then be up-scaled to the larger scale ROV and SUIT measurements (Nicolaus et al., 2013).

Figure 2: SUIT sensor array profiles, station 223 (summer 2012, Arctic Ocean), of light transmission, draft, freeboard, depth of SUIT, Temperature, Salinity and chl a (uncalibrated).

Results from a summer expedition to the Central Arctic Ocean in 2012 (PS80 “IceArc”)

SUIT Sensor Array Profile

Sea Ice Thickness Distributions (SUIT and EM-31)

Correlation Surfaces for Ice Algae Biomass with NDIs

Figure 4: Correlation surfaces for ice algae with NDIs. Spectral measurements

conducted under melt ponds only (left) and under white ice only (right). Dashed lines highlight the absorption peaks of chl a at 440 and 670 nm.

Methods: Different taxonomic groups of microalgae can be distinguished by the composition of Fatty Acid Trophic Markers (FATM). Investigation of solvent-extracted (Dichloromethane/Methanol 2:1) lipids is carried out via gas chromatography after derivatization into Fatty Acid Methyl Esters (FAME).

Results & Conclusions :

• There are FATM exclusively produced by diatoms, representing the main part of the ice algae community, as well as FATM only

biosynthesized by dinoflagellates, the main taxonomic group of pelagic phytoplankton (Fig. 7). That allows a qualitative determination of

consumer diets.

• Regarding to the fatty acid pattern, Calanus glacialis fed on both, ice algae and phytoplankton (Fig. 8).

• For determining the relative contribution of ice-algae produced carbon, combination with STABLE ISOTOPE ANALYSIS is essential.

Figure 8 : Fatty Acid Signature of the Arctic copepod Calanus glacialis (n= 10). The fatty acid composition shows high amounts of both diatom and dinoflagellate FATM.

Results & Conclusions:

• SUIT sensor array data are good quality and are ideal for relating to under-ice communities (see Objective 2).

• Spectral-derived algae biomass models (NDIs) show good correlations for melt ponds in 2 spectral regions of highest chl a absorption: 400-

550 nm (Fig. 4 circle) and 600-690 nm (Fig.4 square).

No clear correlation for white ice but this could be due to variable ice properties (e.g. thickness, snow, scattering layer). Further analysis and model development will be conducted to improve accuracy of the

model(s) before up-scaling to ROV and SUIT spectral measurements.

A

B C

Figure 4: SUIT net system A) being

winched out of water after deployment; B) on deck of the Polarstern laying on its side, with Carmen David and crew members, and; C) in the water just before being hauled in; D) birdeye sketch of SUIT shearing behind vessel.

D

Introduction

Polar sea ice habitats are undergoing rapid change. Because Polar sea ice ecosystems thrive significantly on carbon produced by ice-associated microalgae, these changes have a significant impact on ecosystem functioning. Species dwelling at the ice-water interface (e.g. Antarctic krill Euphausia superba and Polar cod Boreogadus saida) play a key role in transferring carbon from sea ice into pelagic food webs. Understanding the association of under-ice fauna with sea ice habitat properties is therefore essential to understanding future changes of sea ice ecosystems. Until now, the dependency of Polar food webs on carbon produced by ice algae is barely understood in quantitative terms. Recent progress in biomarker analysis makes it possible to quantify the significance of ice algal production along food chains. On this poster we present the progress of our group in linking biological and physical sea ice data, and first results from trophic biomarker studies from the Arctic Ocean.

Under-ice sampling in the Arctic Ocean

Results & Conclusions:

• The first basin-wide trawl survey of under-ice fauna in the Arctic Ocean provided a unique dataset.

• Principal Component Analysis (PCA) of physical parameters revealed two different

environmental regimes, which were broadly consistent with the two basins (Fig. 6A).

Sea ice properties and

nutrient concentrations were the major factors separating the two regimes.

• This environmental seperation was mirrored in the community

structure (Fig. 6B).

• In open water, ice amphipods and Polar cod were replaced by pelagic amphipods, causing a pronounced difference with the under-ice

community.

Under-ice fauna was sampled with a Surface and Under-Ice Trawl (SUIT3). The SUIT consits of a sideward-shearing steel frame equipped with floaters enabling the net to glide along the underside of sea ice (Fig. 4). An environmental sensor array was mounted in the SUIT frame, consisting of an Acoustic Doppler Current Profiler (ADCP), a CTD probe with built-in fluorometer and altimeter, two spectral radiometers, and a GoPro underwater camera. The 12 SUIT stations were distributed over the Nansen and Amundsen Basins of the central Arctic Ocean (Fig. 5).

Objective 2:

Relate environmental properties to under- ice communities

Figure 5: Stations map during RV Polarstern Expedition PS80 “IceArc”.

Figure 6: Visualisations of (A) PCA using environmental properties of sea ice and underlying water column, and (B) NMDS ordination of sampling

locations based on differences in species composition and abundance.

References

1. Mundy, C.J., et al. 2007, J Geophys Res.,112, C03007, doi:10.1029/2006JC003683.

2. Nicolaus, M. et al. 2013, Geoph. Res. Let., 39, L24501, doi:10.1029/2012GL053738

3. Van Franeker et al. 2009, The Surface and Under-Ice Trawl. In: Flores, H.: Frozen Desert Alive. The role of sea ice for macrofauna and its predators: implications for the Antarctic pack-ice food web.

PhD thesis, University of Groningen.

Iceflux: Ice-Ecosystem Carbon Flux in Polar Oceans

Benjamin A. Lange

1,2

, D. Kohlbach

1,2

, C.L. David

1,2

, *H. Flores

1,2

, I. Peeken

1

, M. Nicolaus

1

, C. Katlein

1

, T. Krumpen

1

, S. Hendricks

1

1

Alfred Wegener Institut Helmholtz-Zentrum für Polar- und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany

2

Zoological Museum Hamburg, University of Hamburg, Martin-Luther-King-Platz 1, 20146 Hamburg, Germany

Results

-1.5 -1.0 -0.5 0.0 0.5 1.0 1.5

-2-1012

PCA 1 (36.63%)

PCA 2 (26.94)

Cov.

Temperature Chla.srf.

Salinity Thickness

SD_thickness

Relative.light MLD

Chla.max.

Si

NOx

NMDS 1

NMDS 2

Apherusa glacialis

Onisimus nanseni Themisto libellula Boreogadus saida Calanus glacialis

owice Nansen

Amundsen

A B

Polar cod Boreogadus saida

SUITcam view as SUIT approaches pressure ridge stained with ice algae

Sea Ice Algae

Pelagic Phyto- plankton

similar taxonomic composition

FATTY ACID ANALYSIS

a= 14:0 j= 18:2(n-6)

b= 16:0 k= 18:3(n-3)

c= 16:1(n-9) l= 18:4(n-3) d= 16:1(n-7) m= 18:5(n-3) e= 16:2(n-4) n= 20:5(n-3) f= 16:4(n-1) o= 22:1(n-11)

g=18:0 p= 22:5(n-3)

h= 18:1(n-9) q= 22:6(n-3) i= 18:1(n-7)

SEA ICE ALGAE green= diatom FATM

blue= dinoflagellate FATM

%

PELAGIC PHYTOPLANKTON

gg g ggg

Fatty Acids

%

Figure 7 : Fatty Acid Signatures (“fingerprints”) of sea ice algae (n=10) and pelagic phytoplankton samples (n=10) taken in August /September 2012 in the Arctic Ocean (PS80 IceArc“). Green bars FATMs originated mostly from diatoms, blue bars FATMs produced by dinoflagellates.

CALANUS GLACIALIS

a= 14:0 k= 20:1(n-9)

b= 16:0 l= 20:1(n-7)

c= 16:1(n-7) m= 20:4(n-3) d= 16:4(n-1) n= 20:5(n-3)

e= 18:0 o= 22:1(n-11)

f= 18:1(n-9) p= 22:1(n-9) g= 18:1(n-7) q= 22:5(n-3) h= 18:1(n-5) r= 22:6(n-3) i= 18:2(n-6) s= 24:1(n-9) j= 18:4(n-3)

f f

green= diatom FATM

blue= dinoflagellate FATM yellow= copepod FATM

Fatty Acids

%

d

diatom dominated dinoflagellate dominated

Melt Ponds White Ice

Iceflux

*Presenting author:

hauke.flores@awi.de

+49 471 4831 1444

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