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The role of microzooplankton under future ocean acidification and warming scenarios

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Henriette Horn, Nicole Aberle, Martin Löder & Maarten Boersma

Leibniz Institute for Baltic Sea Research www.io-warnemuende.de BIOACID Phase II Meeting Warnemünde 1 - 2 Oct. 2013

The role of microzooplankton under future ocean acidification and warming scenarios

Consortium 2: Pelagic ecosystems under ocean acidification: Ecological, biogeochemical and evolutionary responses

WP 1.6. Microzooplankton

The autumn experiment started with very low densities of about 70 ciliates/L and reached up to 5,400 ciliates/L after 22 days (fig.1) with similar growth rates in all

treatments (fig.2). The MZP community was dominated by small strobilids (< 30 mm), with Mesodinium pulex

(cyclotrichids) being second most abundant (fig.3).

Variation within treatments was generally high and no large ciliates were present throughout the experiment.

In the summer experiment 2013, first results from the grazing experiments showed higher phytoplankton

growth rates and MZP grazing rates at 1500 ppm than at 3000 ppm (tab.1). While rates were lower for 1500 ppm at 22.5˚C compared to 16.5˚C, the high CO₂

treatments showed the opposite trend.

At the interface between microbial loop and higher trophic levels, micro-zooplankton (MZP) can be both buffer against low quality food for larger mesozooplankton as well as a competitor for food. Given the expected decrease in algal food quality with ocean acidification, the former trait may gain in importance. The MZP community was

analyzed during the BIOACID summer and autumn experiments in Kiel 2012/2013.

Contact: henriette.horn@awi.de

Alfred Wegener Institute for Polar and Marine Research, Biologische Anstalt Helgoland

For the indoor mesocosms, CO₂ concentrations of 840 and 2400 ppm with 3

replicates were used in the autumn experiment and a CO₂ gradient ranging from 500 to 3000 ppm was established during the summer experiment. These

concentrations were crossed with two temperatures: ambient water temperature and ambient water temperature +3˚C. MZP samples were taken three times a

week (Lugol fixation).

Grazing experiments with a 4-step dilution series, mesozooplankton treatment

and addition of nutrients were conducted twice in each experiment. Bottles were incubated at ambient conditions using a plankton wheel. Chlorophyll a was

measured at start and end point to calculate MZP grazing rates.

Experimental design

First results

Fig.1: Ciliate abundances on day 1 and day 22 of the BIOACID

autumn experiment showed the peak values after the phyto-

plankton bloom.

0,1 0,12 0,14 0,16 0,18 0,2 0,22 0,24

9° low 9° high 15° low 15° high

ciliate growth rate [d¯¹]

temperature and CO₂ treatment

Fig.2: Ciliate growth rates in the BIOACID autumn experiment

showed no significant CO or temperature effect.

Fig.3: Ciliate species composition in the BIOACID autumn experiment 2012 on day 1 and 22

(bloom phase). While contributing about half of the ciliate population at the start, small strobolids became the most abundant species during the experiment.

treatment MZP grazing rate

d⁻¹ phytoplankton growth rate d⁻¹

22.5°C/500 ppm -1,57 3,15

22.5°C/1500 ppm -3,48 4,57

22.5°C/3000 ppm -0,98 1,34

16.5°C/1500 ppm -4,69 5,70

16.5°C/3000 ppm -0,73 0,80

Tab.1: Preliminary MZP grazing rates from the

BIOACID summer experiment 2013, calculated using

linear regressions of apparent phytoplankton growth. To account for higher rates than natural due to nutrient

addition, a control without nutrients was included.

0 1000 2000 3000 4000 5000 6000 7000

day 1 day 22

ciliates / L

time

9° low CO₂ 9° high CO₂ 15° low CO₂ 15° high CO₂

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