Meiobenthos at the Arctic Håkon Mosby Mud Volcano

Håkon Mosby Mud Volcano (HMMV, SW Barents Sea slope, 1280 m) is one of the numerous cold methane-venting seeps existing along the continental margins. Analyses of video-guided core samples revealed extreme differences in the diversity and density of the metazoan meiobenthic communities associated with the different sub-habitats (centre, microbial mats, Pogonophora field, outer rim) of this mud volcano. Diversity was lowest in the sulphidic, microbial mat sediments that supported the highest standing stock, with unusually high densities (11000 ind./10 cm**2) of 1 nematode species related to Geomonhystera disjuncta. Stable carbon isotope analyses revealed that this nematode species was thriving on chemosynthetically derived food sources in these sediments. Ovoviviparous reproduction has been identified as an important adaptation of parents securing the survival and development of their brood in this toxic environment. The proliferation of this single species in exclusive association with free-living, sulphide-oxidising bacteria (Beggiatoa) indicates that its dominance is strongly related to trophic specialisation, evidently uncommon among the meiofauna. This chemoautotrophic association was replaced by copepods in the bare, sulphide-free sediments of the volcano's centre, dominated by aerobic methane oxidation as the chemosynthetic process. Copepods and nauplii reached maximum densities and dominance in the volcano's centre (500 ind./10 cm**2). Their strongly depleted carbon isotope signatures indicated a trophic link with methane-derived carbon. This proliferation of only selected meiobenthic species supported by chemosynthetically derived carbon suggests that, in addition to the sediment geochemistry, the associated reduced meiobenthic diversity may equally be related to the trophic resource specificity in HMMV sub-habitats.

Organic geochemistry of Late Cretaceous to Paleogene sediments from MITI Sanriku-oki borehole

Perylene is present in high concentration in Paleogene sediments from the Sanriku-oki borehole of the Ministry of International Trade and Industry (MITI), northeastern Japan. The borehole penetrates a thick sequence of Late Cretaceous to Neogene sediments deposited under a range of conditions, including fluvial-deltaic and shallow marine. Organic petrological and geochemical data show the sediments to be rich in organic matter (OM) derived from higher plants. Biomarker analysis of aliphatic and aromatic hydrocarbons confirms a significant input from higher plants, with extracts dominated by numerous gymnosperm- and angiosperm-derived biomarkers such as diterpanes, oleanenes, des-A-triterpanes and their aromatized counterparts. The highest concentration of perylene occurs in Middle Eocene sediments deposited in a relatively reducing environment. Stable carbon isotope compositions show 13C enrichment in perylene compared to gymnosperm and angiosperm biomarkers, consistent with a fungal origin. This elevated abundance of sedimentary perylene could relate to a Paleogene continental climate where fungi probably flourished.

Seawater carbonate chemistry and processes during experiments with Emiliania huxleyi (PML B92/11), 2000

We have measured the stable carbon isotopic composition of bulk organic matter (POC), alkenones, sterols, fatty acids, and phytol in the coccolithophorid Emiliania huxleyi grown in dilute batch cultures over a wide range of CO2 concentrations (1.1-53.5 micromol L-1). The carbon isotope fractionation of POC (POC) varied by ca. 7 per mil and was positively correlated with aqueous CO2 concentration [CO2aq]. While this result confirms general trends observed for the same alga grown in nitrogen-limited chemostat cultures, considerable differences were obtained in absolute values of POC and in the slope of the relationship of POC with growth rate and [CO2aq]. Also, a significantly greater offset was obtained between the delta13C of alkenones and bulk organic matter in this study compared with previous work (5.4, cf. 3.8 per mil). This suggests that the magnitude of the isotope offset may depend on growth conditions. Relative to POC, individual fatty acids were depleted in 13C by 2.3 per mil to 4.1 per mil, phytol was depleted in 13C by 1.9 per mil, and the major sterol 24-methylcholesta-5,22E-dien-3beta-ol was depleted in 13C by 8.5 per mil. This large spread of delta13C values for different lipid classes in the same alga indicates the need for caution in organic geochemical studies when assigning different sources to lipids that might have delta13C values differing by just a few per mil. Increases in [CO2aq] led to dramatic increases in the alkenone contents per cell and as a proportion of organic carbon, but there was no systematic effect on values of U37k- used for reconstructions of paleo sea surface temperature.

Biogeochemical processes in anoxic sediment from Lake Plußsee, Germany

In anoxic environments, volatile methylated sulfides like methanethiol (MT) and dimethyl sulfide (DMS) link the pools of inorganic and organic carbon with the sulfur cycle. However, direct formation of methylated sulfides from reduction of dissolved inorganic carbon has previously not been demonstrated. When studying the effect of temperature on hydrogenotrophic microbial activity, we observed formation of DMS in anoxic sediment of Lake Plußsee at 55 °C. Subsequent experiments strongly suggested that the formation of DMS involves fixation of bicarbonate via a reductive pathway in analogy to methanogenesis and engages methylation of MT. DMS formation was enhanced by addition of bicarbonate and further increased when both bicarbonate and H2 were supplemented. Inhibition of DMS formation by 2-bromoethanesulfonate points to the involvement of methanogens. Compared to the accumulation of DMS, MT showed the opposite trend but there was no apparent 1:1 stoichiometric ratio between both compounds. Both DMS and MT had negative d13C values of -62 per mil and -55 per mil, respectively. Labeling with NaH**13CO3 showed more rapid incorporation of bicarbonate into DMS than into MT. The stable carbon isotopic evidence implies that bicarbonate was fixed via a reductive pathway of methanogenesis, and the generated methyl coenzyme M became the methyl donor for MT methylation. Neither DMS nor MT accumulation were stimulated by addition of the methyl-group donors methanol and syringic acid or by the methyl-group acceptor hydrogen sulphide. The source of MT was further investigated in a H2**35S labeling experiment, which demonstrated a microbially-mediated process of hydrogen sulfide methylation to MT that accounted for only <10% of the accumulation rates of DMS. Therefore, the major source of the 13C-depleted MT was neither bicarbonate nor methoxylated aromatic compounds. Other possibilities for isotopically depleted MT, such as other organic precursors like methionine, are discussed. This DMS-forming pathway may be relevant for anoxic environments such as hydrothermally influenced sediments and fluids and sulfate-methane transition zones in marine sediments.

Active methane seepage in the Southern Ocean, off the sub-Antarctic island of South Georgia

An extensive submarine cold-seep area was discovered on the northern shelf of South Georgia during R/V Polarstern cruise ANT-XXIX/4 in spring 2013. Hydroacoustic surveys documented the presence of 133 gas bubble emissions, which were restricted to glacially-formed fjords and troughs. Video-based sea floor observations confirmed the sea floor origin of the gas emissions and spatially related microbial mats. Effective methane transport from these emissions into the hydrosphere was proven by relative enrichments of dissolved methane in near-bottom waters. Stable carbon isotopic signatures pointed to a predominant microbial methane formation, presumably based on high organic matter sedimentation in this region. Although known from many continental margins in the world's oceans, this is the first report of an active area of methane seepage in the Southern Ocean. Our finding of substantial methane emission related to a trough and fjord system, a topographical setting that exists commonly in glacially-affected areas, opens up the possibility that methane seepage is a more widespread phenomenon in polar and sub-polar regions than previously thought.

Sedimentological, biogeomcial and geochronological data of thermokarst lake sediment core PG1967

Ice-rich permafrost landscapes are sensitive to climate and environmental change due to the melt-out of ground ice during thermokarst development. Thermokarst processes in the northern Yukon Territory are currently not well-documented. Lake sediments from Herschel Island (69°36'N; 139°04'W) in the western Canadian Arctic provide a record of thermokarst lake development since the early Holocene. A 727 cm long lake sediment core was analyzed for radiographic images, magnetic susceptibility, granulometry, and biogeochemical parameters (organic carbon, nitrogen, and stable carbon isotopes). Based on eight calibrated AMS radiocarbon dates, the sediment record covers the last ~ 11,500 years and was divided into four lithostratigraphic units (A to D) reflecting different thermokarst stages. Thermokarst initiation at the study area began ~ 11.5 cal ka BP. From ~ 11.5 to 10.0 cal ka BP, lake sediments of unit A started to accumulate in an initial lake basin created by melt-out of massive ground ice and thaw subsidence. Between 10.0 and 7.0 cal ka BP (unit B) the lake basin expanded in size and depth, attributed to talik formation during the Holocene thermal maximum. Higher-than-modern summer air temperatures led to increased lake productivity and widespread terrain disturbances in the lake's catchment. Thermokarst lake development between 7.0 and 1.8 cal ka BP (unit C) was characterized by a dynamic equilibrium, where lake basin and talik steadily expanded into ambient ice-rich terrain through shoreline erosion. Once lakes become deeper than the maximum winter lake ice thickness, thermokarst lake sediments show a great preservation potential. However, site-specific geomorphic factors such as episodic bank-shore erosion or sudden drainage through thermo-erosional valleys or coastal erosion breaching lake basins can disrupt continuous deposition. A hiatus in the record from 1.8 to 0.9 cal ka BP in Lake Herschel likely resulted from lake drainage or allochthonous slumping due to collapsing shore lines before continuous sedimentation of unit D recommenced during the last 900 years.

Abrupt vegetation change after the Late Quaternary megafaunal extinction in southeastern Australia

A substantial extinction of megafauna occurred in Australia between 50 and 45 kyr ago, a period that coincides with human colonization of Australia. Large shifts in vegetation also occurred around this time, but it is unclear whether the vegetation changes were driven by the human use of fire-and thus contributed to the extinction event-or were a consequence of the loss of megafaunal grazers. Here we reconstruct past vegetation changes in southeastern Australia using the stable carbon isotopic composition of higher plant wax n-alkanes and levels of biomass burning from the accumulation rates of the biomarker levoglucosan from a well-dated sediment core offshore from the Murray-Darling Basin. We find that from 58 to 44 kyr ago, the abundance of plants with the C-4 carbon fixation pathway was generally high-between 60 and 70%. By 43 kyr ago, the abundance of C-4 plants dropped to 30% and biomass burning increased. This transient shift lasted for about 3,000 years and came after the period of human arrival and directly followed megafauna extinction at 48.9-43.6 kyr ago. We conclude that the vegetation shift was not the cause of the megafaunal extinction in this region. Instead, our data are consistent with the hypothesis that vegetation change was the consequence of the extinction of large browsers and led to the build-up of fire-prone vegetation in the Australian landscape.

Results from ikaite investigations in the Kara Sea

The authigenic carbonate mineral ikaite is specific of low-temperature high latitude environments. The depletion of ikaite carbon in 13C isotopes in most cases implies a causal relation of ikaite generation with methane geochemistry. In this paper we present new data on ikaite minerals in Holocene sediments sampled along the Yenisei channel at the southern (74°N) and northern (77°N) ends. Stable carbon isotopes of the ikaite crystals were studied in conjunction with the hydrochemistry and isotope geochemistry of the sediments. Pore water and natural gas samples were separated from sediments to describe the methane carbon isotope distribution pattern throughout two sedimentary sequences embedding the ikaite crystals of different isotope composition (-24 per mil and -42 per mil). The biogenic nature of the methane is indicated by 51 C values being as low as -104.4 per mil. In the case of the moderately depleted sample (-24 per mil) from the southern location the small-scale ikaite formation fits best into the concept of a 'closed» sediment system, with a limited diagenetic carbon dioxide source being present. In the second case, formation of highly abundant and isotopically depleted ikaite crystals (-42 per mil) were caused by upwards flux of biogenic methane from below. Contribution of two main carbon sources to the ikaite crystals was estimated by using a isotope-mass balance equation. Organic-derived CO2 constitutes the principal source in both samples, amounting to 50 % of the total carbon of the strongly depleted ikaite crystals (-42 per mil) sampled at the northern end and 83 % for the moderately (-24 per mil) depleted crystals from the southern end. Methane-derived CO2 comes to 42 % for the isotopically light ikaite crystals and to 9% for the isotopically heavy crystals. The importance of sediment lithology and diffusive transport for ikaite formation is emphazied.