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Introduction

The Joint Research Group on Deep-Sea Ecology and Technology was co-founded in December 2008, the by the Alfred-Wegener-Institute for Polar and Marine Research of the Helmholtz (HGF) Society and the Max-Planck-Institute for Marine Microbiology, with Antje Boetius as the group leader. This Joint Research Group comprises the expertise of the MPI in the area of marine microbial ecology and biogeochemistry, development of new molecular-biological and in situ analytical methods (former Microbial Habitat Group, 2003-2010) together with the capacity of AWI to conduct research in polar environments and to carry out long-term observation in the deep sea (former Deep-Sea Research group). The goal is to contribute significantly to the study of global change effects on deep-sea ecosystems and to the exploration of extreme and unknown deep-sea habitats.

The main themes for all researchers of the HGF-MPG deep-sea ecology group is to obtain 1) “true” quantitative insight to ecosystem structure, dynamics and biogeochemical fluxes based on in-situ measurements and 2) a better understanding of the related variations in microbial to macrobial biodiversity on relevant spatial and temporal scales. The development of novel instrumentation for in situ studies of submarine ecosystems, ranging from coastal sands to reefs, continental margins, ice-covered polar waters, cold seeps and hydrothermal vents enables this group in collaboration with the Microsensor group to improve the quantification of transport and reaction at the ocean floor. Furthermore, we link our in situ biogeochemistry and biodiversity studies closely to the investigation of microbial function in the respective habitats, in collaboration with the departments of Microbiology and Molecular Ecology. For more information on AWI related research see here.

Spatial and temporal patterns of microbial biodiversity

A. Ramette, C. Bienhold, A.Boetius, A. Gobet, S. Grünke, M. Jacob, M. Meiners, W. Rentzsch, D.Santillano, S. Schöttner, E. Weiz, L. Zinger

Despite significant progresses in molecular techniques to unravel microbial diversity, still little is known about the ecological factors that shape bacterial and archaeal communities at different spatial or temporal scales and along environmental gradients. Microbial biodiversity, i.e. species richness and community structure, is at the center of our group’s focus, as its changes may have dramatic consequences on global biogeochemical processes in the oceans. Reproducible high-throughput, high-resolution molecular methods are used to assess microbial biodiversity in its environmental context such as coastal sandy sediments, coral-associated surfaces, microbial mats, oligotrophic deep-sea sediments, or deep-sea sediments impacted by high hydrocarbon fluxes. Molecular techniques such as Terminal Restriction Fragment Length Polymorphism (T-RFLP), Automated Ribosomal Intergenic Spacer Analysis (ARISA) and Next Generation Sequencing (NGS) provide a thorough analysis of the source of community variation for large datasets, and when combined with contextual parameters, enable disentangling the respective effects of multiple factors acting on microbial community structure and functions. Ecological processes implicated in community assembly are thus investigated from local to global scales.

Main recent achievements include:

  • Quantification of the dynamics of rare and of resident bacterial populations in coastal sands (Gobet et al. 2012), also making use of specific software tools that were developed to assess the significance of rarity in large sequencing datasets (Gobet et al. 2010).
  • Modeling complex ecological scenarios involving cross-domain interactions in their natural context, including, e.g. cold-water corals (Schöttner et al. 2012) and tropical corals (Schöttner et al. 2011; Sawall et al. submitted).
  • First synthesis of bacterial biogeographic patterns at the global scale in seafloor and seawater ecosystems (Zinger et al. 2011), as well as diversity and biogeography analyses in specific ocean provinces, e.g. deep-sea sediments of the South Atlantic Ocean (Schauer et al. 2010) or in the Arctic Ocean (Bienhold et al. 2012).

Figure: Global beta-diversity patterns of marine bacterial communities according to realms and ecosystem types. NMDS ordination of the dissimilarity in bacterial community composition based on 454 massively parallel tag sequencing (Zinger et al. 2011).

Global change effects on microbial biodiversity and function

A. Boetius, M. Alisch, V. Asendorf, C. Bienhold, M. Jacob, G. Jessen, M. Fernandez, S. Grünke, A. Lichtschlag, M. Meiners, J. Neumann, A. Ramette, F. Raulf, G. Schüssler, R. Stiens, M. Viehweger, E. Weiz, F. Wenzhöfer

The ocean is affected by global change in multiple ways: Hypoxic conditions in aquatic ecosystems increase in number and duration and are accompanied by changes in biodiversity and ecosystem functions. In many aquatic ecosystems, warming, eutrophication, acidification, and deoxygenation co-occur. An increased resource exploitation of the ocean such as by littering, mining and mineral extraction, fisheries, introduction of alien invasive species shows a substantial impact even in the remote deep sea. It is obvious that any of these factors alone or in combination will alter ocean ecosystems, but it is not trivial to monitor consequent changes in ecosystem biodiversity or function (e.g. productivity, remineralization, bioturbation) due to missing baselines, and due to the technical and logistical challenges of long- term observation in the sea. Furthermore, the role of microbes in global change effects and feedback mechanisms are not known.

Main recent achievements and current tasks include:

  • Bacterial communities and warming in the Arctic Ocean: At the HAUSGARTEN long-term deep-sea observatory off Svalbard (Fram Strait) and at the formerly ice-covered Laptev Sea margin we are exploring the effect of ocean warming and changing particle fluxes on microbial community composition. A significant energy-diversity relationship was revealed for bacterial communities in Arctic deep-sea sediments. This strongly suggests that changes in primary production and subsequent export to the seafloor will have a significant impact on benthic diversity and activity (Bienhold et al. 2012). (POLMAR; GLOMAR).
  • Methane flux and warming: In the framework of the EU project ESONET we study the effect of seafloor warming on gas hydrate dissolution and methane emission using a long term observatory deployed at the Håkon Mosby Mud Volcano (ESONET LOOME, collaboration with microsensor group).
  • Increasing hypoxia in aquatic systems: We coordinate the EU project HYPOX and combine our expertise in the monitoring of oxygen dynamics with studying the effects of oxygen depletion on the biogeochemistry and biodiversity of a range of aquatic systems. Here, we also collaborate with the Biogeochemistry and Microsensor Groups.
  • Microbes and ocean acidification: Within the project BIOACID we use experimental flow-through sediment systems to study the effect of high pCO2 levels (750, 1500, 4000 ppm) within the IPCC scenarios, on community functions and diversity.
  • Impact of high CO2 / low pH on benthic life: At natural CO2 vents (e.g. Okinawa Trough, Panarea, Papua New Guinea), we study the effects of high CO2 on benthic communities, as an analogue to potential leaks from industrial subseafloor CO2 storage (BMBF SUMSUN, BMBF BIOACID, EU 7th FP ECO2).

Figure: Activities in the Arctic. Left: Analysis of the causal relationships between bacterial community structure, bacterial activity and food availability at the Laptev Sea continental slope. The availability of energy (pigments and protein as indicators for the presence of labile organic matter, and depth for other flux-related processes) was the strongest factor directly affecting changes in both bacterial community structure and activity (Bienhold et al. 2012). Right: Drilling samples for primary productivity studies in Arctic sea ice.

Extreme environments and geosphere-biosphere interactions

A. Boetius, C. Bienhold, J. Felden, M. Fernandez, S. Grünke, V. Krukenberg, A. Lichtschlag, S. Mau, J. P. Meyer, J. Neumann, A. Nordhausen, P. Pop Ristova, A. Ramette, W. Rentzsch, E. Ruff, D. Santillano, G. Schüssler, R. Stiens, N. Strackbein, M. Weber, G. Wegener, E. Weiz, F. Wenzhöfer

Extreme environments are defined by one or more environmental characteristics at which life operates close to its known limits. Often the greatest challenges to life are extreme temporal fluctuations or short-term impacts, which select for highly adapted organisms and alter community structure and function. In this regard, the main focus of our studies is to identify and quantify biogeochemical processes and their link to microbial diversity at different types of ecosystems with one or more extreme characteristics: cold seeps (EU 7th FP HERMIONE; Excellence Cluster MARUM), acidic vents (EU 7th FP ECO2), hydrothermal vents (Excellence Cluster MARUM), wood and whale falls (ESF EuroCores CHEMECO and MPG-CNRS GDRE DIWOOD), as well polar habitats (e.g. microbial-life in sea ice). To improve our knowledge of the functioning of these ecosystems we combine studies on the dynamics of fluxes and biogeochemical processes with biodiversity studies.

Main recent achievements and current tasks inlcude:

  • Budgeting of in situ benthic respiration, carbon degradation and fixation at different mud volcanoes (HMMV in the Barents Sea, Amon mud volcano, East Med.) (e.g. Felden et al. 2010).
  • Enrichment of methanotrophic microorganisms (ANME-1) and their sulfate-reducing partner from hydrothermal sediments of the Guaymas Basin. Current physiological and genomic studies of these new cultures aim at a better understanding of the ecology and physiology of methanotrophic communities (Holler et al. 2011).
  • Development of a novel stable isotope probing based approach for the quantification of microbial productivity under extreme environmental conditions (e.g. starvation); application of the method in coastal sediments (Wegener et al. in revision).

Figure: Micrograph of moderately thermophilic methanotrophic archaea (ANME-1; in red) and their partner bacteria (Seep-2 cluster; in green). Aggregates are retrieved from Guaymas Basin sediments via continuous cultivation with methane as sole energy source.
Copyright: V. Krukenberg/G. Wegener

Method developments: In situ technologies for microbial habitat studies

In situ technologies

F. Wenzhöfer, V. Asendorf, A. Boetius, D. Donis, J. Felden, J. Fischer, K. Koop-Jakobsen, A. Lichtschlag, J. P. Meyer, A. Nordhausen, M. Viehweger

The marine environment still hosts many unexplored ecosystems with unknown functions in biogeochemical cycles and global ocean biodiversity. Especially the deep-sea realm is largely unknown due to its inaccessibility because of high pressure, total darkness, low temperature as well as its remoteness and size. Over the last decade there has been a great achievement in developing and using various under water platform, like ROVs, AUVs, crawler and observatories, to advance the exploration and research of the deep sea. To fully understand the link between oceanic processes and the response of ecosystems and communities to environmental change, the need forin situ observationenabled by fixed point and mobile platforms equipped with sensors is critical. To investigate long-term variations at cold seeps a deep-sea observatory has been developed and deployed at the Håkon Mosby Mud Volcano (EU 6th FP ESONET). An array of instruments for the observation of oxygen depletion in suboxic and hypoxic aquatic environments (EU 7th FP HYPOX) was used in the Black Sea.
These projects are carried out in close collaboration with the microsensor group.

Main recent achievements and current tasks inlcude:

  • Miniaturized Microprofiler for targeted ROV operations at microbial habitats
  • Improving the power consumption of the in situ electronics for long-term measurements
  • Construction of an autonomous “Handheld Profiler” for environmental characterization of macrofauna habitats (e.g. bottom water above mussel beds, tubeworm communities)
  • Development, construction and deployment of a deep-sea observatory at cold seeps (EU 6th FP ESONET DM LOOME, collaboration with microsensor group). With the first 12-month monitoring at an active mud volcano (HMMV) we were able to document an eruption of fresh warm mud and to investigate its consequences for the biogeochemical processes
  • Design of multiscale probe arrays for high-resolution monitoring of oxygen depletion in sediments and bottom waters (EU 7th FP HYPOX and EU ITN-SenseNet). During an expedition to the Crimean shelf (Black Sea) high frequency temporal and spatial variations in the oxygen concentration directly above the seafloor could be detected
  • Developing a national and international strategy for long term autonomous and cabled observation of environmental variation related to global change in the Arctic

Figure: Developing methods for the study of Arctic ecosystems and biogeochemical processes. Left: 3D profiler on a lander to be deployed under ice. Right: SenseNet field campaign Baltic Sea (Hel, Poland).