Laguna Potrok Aike, Argentina
This subsaline maar lake is located in a volcanic field in the southernmost tip of Patagonia, east of the Andes cordillera at 51°58′S and 70°22′W (Fig. 3). The lake has been the target of multidisciplinary investigations through continental drilling (Project PASADO: Potrok Aike Lake Sediment Archive Drilling Project; Zolitschka et al. 2013 and references therein) and more than 500 m of sedimentary cores were retrieved. One of the novelties in lacustrine deep drilling was that for the first time in the history of ICDP, a retrieved core was fully dedicated to a detailed geomicrobiological study. A one-meter-long gravity core and a 93-meter-long hydraulic piston core—PTA-5022-1D—were recovered at 100 m water depth and sampled following a newly established sampling strategy under aseptic conditions (Vuillemin et al. 2010). Its application has shown that despite the logistical constraints inherent to each project (e.g., absence of appropriate laboratory facilities on board), it is still possible to sample cores aseptically. Using aseptic techniques to sample cores is a key issue for the credibility of the findings for each of the studies reviewed herein.
In contrast to IODP operations, the size and configuration of lake drilling platforms prevent the establishment of a sampling laboratory with minimal conditions of asepsis right at the drilling site. As a result, an ad hoc laboratory was installed in a container on the campsite by the lakeshore and the retrieved cores were transported every 90 min from the platform to the laboratory. A complete in situ sampling procedure allowed recovering aseptic samples as well as determining the presence of active microbes. Once in the laboratory, the exterior surfaces of the core liners were first disinfected with isopropylic alcohol and sprayed with fungicide. Sampling windows were cut in the liner every 1 or 1 m and at higher resolution for the upper 15 m using a portable circular saw. Conversely, windows were cut every 5 cm in the empty liner of a gravity core and sealed with strong adhesive tape prior to coring. The latter allowed a faster sampling at a higher resolution at the uppermost part of the sedimentary column that encompasses the largest concentration of microbes. The interior surfaces of the core liners were not disinfected prior to coring. However, it is assumed that a contamination by preexisting microbes can be discarded because any potential microbes would have been washed out while descending the drilling tools throughout the water column.
A quick activity test was used to test microbial activity in the sediments immediately after coring. In situ adenosine 5′-triphosphate (ATP) measurements were taken as indication of living organisms within the sediments. The presence of ATP is a marker molecule for living cells since it is not known to form abiotically. ATP can be easily detected with high sensitivity and high specificity using an enzymatic assay because light is emitted as a result of the reaction. The further application of this test to water samples can aid in the evaluation of the degree of contamination of the drilling water, which percolated along the inside of the core liner.
Three and five milliliters of sediment were extracted from freshly opened windows using previously sterilized syringes that had an open-end cutoff in order to use them as minicores. Once the window was cut, the first extracted sample was for methane analyses to prevent it to escape due to volume expansion when exposed to ambient pressure. Hence, 3 ml of sediment was chemically stabilized and sealed in vials for headspace analysis. The sediments were further sampled for different techniques using 5-ml syringes and portioned out as follows: the first 1-ml portion of sample was placed in an Eppendorf tube and kept frozen for further DNA extraction; a second 1-ml portion was chemically fixed for DAPI (4′,6-diamidino-2-phenylindole) cell count; a third 1-ml portion of the sediment was mixed with 1 ml of deionized water in an Eppendorf tube and centrifuged for 5 min. Commercially available water testers (Biotrace International) were carefully submerged in the supernatant of the Eppendorf tube, and its ATP content measured with the Uni-Lite® NG luminometer from Biotrace International as an index of in situ microbial activity. The remnant sediment in the syringe was coated with plastic foil, sealed into hermetic aluminum foil bags and flushed with nitrogen prior to be sealed with a heating device in order to prevent oxidation. These samples can be further used for microbial culture experiments when back at the home laboratory. Once the sampling was accomplished, the windows were sealed with strong adhesive tape. This sampling procedure was carried out nonstop by both day and night shift teams. A more detailed description of the procedures as well as the different methods used can be found in Vuillemin et al. (2010).
The set of cores retrieved in Laguna Potrok Aike covers more than 50,000 years of environmental history of this remote area of the Southern Hemisphere. The multiproxy approach implemented in this research combined with radiocarbon and luminescence dating as well as stratigraphic techniques (tephrochronology and paleomagnetics) provided the opportunity to reconstruct the hydrological history of the region within a well-constrained chronological framework. Lake level was high from 51,000 cal. years BP until the early Holocene when a pronounced negative water balance triggered a lake level decrease of more than 50 m. Lake level started rising gradually two millennia later, reaching a maximum during the Little Ice Age (LIA). These contrasting climatically driven hydrological situations triggered changes in the influx of terrestrial organic matter, sedimentation type, trophic level and productivity. As a result, Vuillemin et al. (2013b) proposed that the structure and sustainability of microbial communities develop in the sediments reflecting the initial depositional conditions (Fig. 4). A detailed geomicrobiological study shows that the shift from an unproductive glacial environment to the more productive Holocene period initiated major and persistent changes in the associated microbial assemblages within sediments (Vuillemin et al. 2014a). Moreover, living microbes have been identified for the first time in sediments from the Holocene (uppermost 10 m) and Last Glacial Maximum (LGM; as low as 40 m depth) periods, providing evidence that environmental DNA can be used to trace paleoclimatic conditions. The comparison of these data with past climate reconstructions indicates that the microbial colonization of the sediment was systematically higher during warmer intervals (Holocene) when the hydrological system was very active (Fig. 4). The concomitant development of high productivity led to enhanced nutrient availability in the sediments, thus sustaining microbial development through organotrophy (Vuillemin et al. 2014b). Conversely, cold intervals, such as glacial times, are characterized by increasing occurrence of mass wasting events preventing the settlement of the same type of microbes but triggering the development of different communities instead. As a result, active microbes were identified at 30,000 cal. years BP in organic poor silts at ~40 m sediment depth. Despite the low population density, phylogenetic data indicate the presence of lithotrophic communities that have caused the formation of authigenic minerals (Vuillemin et al. 2013a). Moreover, these phylogenetic analyses of DNA extracts along with SEM and TEM investigations of selected samples allowed establishing the sequence of formation of framboidal magnetic iron sulfides (mackinawite and gregite) as well as pyrite (Fig. 5a, b). Similarly, the identified microbes can be related to the observed alteration of clays (Fig. 5c) and the presence of EPS remnants at different levels confirming the lithotrophic character of the microbes involved in these processes (Fig. 5d; Vuillemin et al. 2013a).
One of the general outcomes of these pioneer investigations in Laguna Potrok Aike is data to support the hypothesis that microbes react to climatically driven environmental changes that have a direct impact on their subsurface distribution and diversity. This is clear at conspicuous levels associated with well-known climatic periods such as the Medieval Climatic Anomaly (MCA) or the Little Ice Age (LIA). The discrepancy between the in situ microbial activity (ATP) measurements and the total cell counting by DAPI (4′,6-diamidino-2-phenylindole) at these levels is reflecting the accumulation of dead microbial cells. This is interpreted as the result of the initial colonization of the substrate by microbes (Vuillemin et al. 2013a, b). It also shows that microbes resolve the scarcity of both nutrients and energy, becoming dominantly lithotrophs or organotrophs in the last glacial and Holocene sediments, respectively. These results are critical to understanding the limits of life in the subsurface of lakes under contrasting physicochemical conditions. On a practical side, this study shows that in the search of biosignatures in the sediments such as diagenetic concretions, it is crucial to use a wide range of high-resolution geochemical and imagery techniques that can be further blended with microbiological results. Only through a careful examination of these two—apparently independent—datasets, it is possible to disentangle the actual role of different microbial metabolisms during early diagenesis.
Lake Van
Located in the east Anatolian high plateau at 1,648 m above sea level (a.s.l.) in southeast Turkey (38°38′N and 42°54′E; Fig. 3), Lake Van is the fourth largest terminal lake in the world with a salinity of 2.14 % and pH 9.81. The lake stands in a tectonically active area and is surrounded by active volcanoes. These volcanoes provide an excellent means to date the sediments, and the lake sediments themselves contain a unique geological archive of paleoclimate and paleoenvironment covering several glacial–interglacial cycles. The 445-m-deep lake was drilled in summer 2010 as part of the ICDP deep lake drilling project PaleoVan (Litt et al. 2009, 2011; Stockhecke et al. 2014). As previously stated, geomicrobiological studies on deep and large lakes are quite rare, most often due to technical and logistic limitations. However, during this drilling campaign, samples for immediate processing were taken from the core catcher (catching device at the end of each drilling pipe as shown in Fig. 6) for pore water sulfate concentration and microbial turnover rate determination (Glombitza et al. 2013; Kallmeyer et al. this issue). Core catchers were only sampled if the sediments appeared to be clearly undisturbed whole round pieces, which was the case for the majority of the core-catcher material (Glombitza et al. 2013). Shorter gravity cores (less than a meter long) were also retrieved at the drilled sites to recover undisturbed sediment/water interface. Cores were immediately sampled after retrieval for sedimentary OM characterization, pore water analyses and sulfate reduction rate measurements by radiotracer incubations. Biochemical investigations were carried out in high resolution in the uppermost part of the cores, whereas a ~3-m sampling resolution was acquired down to 130 m below lake floor. On-site analyses were carried out at the mobile laboratory container BugLab of the Helmholtz Center Potsdam, German Research Center for Geosciences (GFZ). This laboratory is ideal to carry out microbial and geochemical analyses under aseptic conditions. One of the main conclusions of this work is that organotrophs are the dominant microbes at the different drilled sites. It is true as well that the quality of the OM plays a fundamental role for the development of microbial activity and not just the total OM content (Glombitza et al. 2013). As a result, biochemical processes in the sediments of this type of lake basin appear to be very reactive to small variations in geological, physical or chemical parameters even at relatively short lateral distances (Glombitza et al. 2013). This dataset also shows that salinity and alkalinity are not the limiting factors for microbial development. All of these results have substantial implications for the study of early diagenesis in older lacustrine sediments, highlighting the importance of geomicrobiological studies to understand the physiological abilities and biogeochemical impact of subsurface life within the sedimentary column. More results about the subsurface biosphere studies of the long cores retrieved through the ICDP drilling can be found in Kallmeyer et al. (this issue).
Dead Sea
The present Dead Sea is located at ~425 m below sea level (b.s.l.) in the Levantine Basin, at the border between Israel, Jordan and the Palestinian Authority. At 31.4°N, 35.4°E, the lake lies along the Dead Sea Transform fault system (DST), turning it into a prime target for paleoseismic studies. The site is also ideal to study the impact of climate in the hydrology of the region, to extend the already long record of earthquakes for the area, and to investigate the presence of active microbes that could survive under extreme conditions of salinity (Dead Sea present salinity of 348 g L−1). ICDP drilling operations started in winter 2010, having retrieved 720 m of sediment from two different coring sites. Multidisciplinary investigations are currently ongoing, with a strong focus on paleoclimate and paleoseismicity reconstructions (Project DSDDP: Dead Sea Deep Drilling Project; Stein et al. 2011a, b). Based on the correlation of the main lithological units observed in the cores with numerous outcrop studies, down-hole logging and first 14C and U-Th dating, the composite core from the deepest area of the basin is interpreted to encompass the last two glacial–interglacial cycles (Neugebauer et al. 2014).
Within this framework, core catchers from the longest core were prioritized for the geomicrobiology study since, in contrast to Laguna Potrok Aike, no special hole was drilled for subsurface biosphere investigations. In the modern Dead Sea, the microbial content in the water column is very limited, preventing possible contamination of the sampled sediments with water column populations. Additionally, as in the previously described sites, we sampled the center of the individual core catchers (Fig. 6), disregarding their outermost part to minimize the possibility of contamination with drilling water. After each 12-h drilling shift, core catchers were brought onshore to a specially tailored facility for sampling under sterile conditions. Due to its unique salinity characteristics among all other aquatic environments (ten times higher than sea water), the Dead Sea drilling offers the opportunity to address life limits in a unique way. It also allows the assessment of the impact of microbial communities on the sedimentary record of extreme hypersaline environments.
While the chemistry of the Dead Sea sediments challenged the use of several routine methods for the assessment of microbial diversity and in situ activity, DNA extraction has revealed the existence of microbes down to 90 m below the lake floor (Thomas et al. 2014). Ongoing analyses further point toward their presence as deep as 200 m. The simultaneous analysis of sedimentary facies and microbial assemblages has allowed the identification of mutual patterns in the distribution of these subsurface communities adapted to extreme salinity conditions (348 g L−1). Halophilic species from the Bacteria and Archaea domains display differential distribution regarding the lithology from which they have been extracted. As in the case of Laguna Potrok Aike, these lithologies derive from the climatic conditions prevailing in the Dead Sea Basin at the time of sedimentation. Under humid conditions largely prevalent during glacial periods, the lake precipitated aragonite-forming varve-like sediments. This facies is named aragonite laminae alternating with detrital mud (aad facies). High freshwater inputs diluted the upper layer of the lake and subsequently formed a stratification of the water column. The nutrient-rich, diluted epilimnion was subjected to algal blooming events and subsequent aerobic degradation by microbial halophilic species (Fig. 7). Other transported—allochthonous—microbes potentially developed in these moderately saline conditions. In such settings, the Dead Sea hypersaline brine was restricted to the hypolimnion. This situation rapidly enabled anoxic hosting halophiles to degrade organic matter anaerobically. Resulting organic matter was buried and potentially degraded by fermenters, sulfate reducers and methanogens as revealed by metagenomes from the aragonitic sediment (Thomas et al. 2014). Under the more arid conditions prevailing during interglacials, the lake became monomictic and oxic conditions predominated in the entire water column. Evaporation exceeded precipitation, and the lake started to precipitate gypsum and, eventually, halite (as observed today). Hypersaline conditions only allow for Archaea of the Halobacteria class to survive in the water column (Bodaker et al. 2010). This very same class largely dominates in the corresponding sediment (Thomas et al. 2014). Consequently, this first dataset indicates that conditions existing in the water column at the time of sedimentation influence microbes preserved in the Dead Sea sediment. This is illustrated in the idealized sketch shown in Fig. 7.
These preliminary results indicate that the Dead Sea subsurface microbial community does not depend only on salinity. Although halophilic species are the dominant form obtained from sequencing techniques, Archaea of the Halobacteria class predominate within halite–gypsum sediments, while sequences related to hypersaline methanogens and fermenters are found in the shallowest aad facies. Thus, as in Laguna Potrok Aike, the sedimentary microbial communities in the Dead Sea seem to reflect the conditions in the water column at the time of sedimentation, linking their distribution to the prevailing climate. Additional investigations are necessary to better understand the microbial origin and evolution through time. Analogously, the traces of activity left by these microbes on the sediment are complex and not fully yet understood. However, Fe–S mineralization has been observed associated with EPS in some aragonitic-rich sediments, showing that even under extremely saline conditions, microbes can affect their environment (Thomas et al. 2014).
Lake Ohrid
This lake is located between Albania and Macedonia on the Balkan Peninsula (41.1° N and 20.8° E) at an altitude of 639 m above sea level (a.s.l.; Fig. 3). It is considered the oldest lake in continuous existence in Europe containing more than 200 endemic species (Wagner et al. 2014 and references herein; Wilke et al. 2010), which makes it a particularly interesting place to investigate the subsurface biosphere. It was successfully drilled in spring 2013. Although there were neither a planned geomicrobiological study nor cores specially retrieved for this purpose, a core-catcher sampling was implemented in the deepest site following the precautions mentioned for previous drilling projects. Samples were immediately frozen for subsequent studies. While this sampling is not ideal for in situ microbial activity investigation or incubation studies, immediately frozen samples are perfect for certain biogeochemistry and geomicrobiological investigations, such as biomarker analyses, DNA extraction and subsequent microbial ecology techniques (PCR and sequencing) studies. Ongoing analyses have allowed the extraction of DNA down to 134 m sediment depth. Hence, they may deliver a first view of the subsurface microbial activity and its genetic continuity in this unique site characterized by a large number of endemic eukaryote species.