Methane-induced early diagenesis of foraminiferal tests in the southwestern Greenland Sea

Planktic and epibenthic foraminiferal δ¹³C records at Site PS62/015-3 (southwestern Greenland Sea) reveal a series of transient events of extreme ¹³C depletion down to − 6‰ during the period 90–40 ka. Scanning electron microscope studies of the ultrastructures of foraminiferal tests suggest that ¹³C depleted specimens are affected by some 10–20% overgrowth by authigenic calcite contributing to the light δ¹³C signal. Incremental-leaching experiments and census counts of pristine versus overgrowth-affected specimens show that the ¹³C depleted foraminiferal tests incorporate a primary δ¹³C signature most likely ranging from + 1‰ to − 1.7‰ and a post-depositional δ¹³C signature around − 17‰ to − 19.5‰. Extremely low values of productivity and organic carbon in Late Quaternary sediments along the east Greenland margin preclude organic matter as potential source of the isotopically light carbon. In contrast, thermal instability of clathrates and subsequent aerobic oxidation of (highly ¹²C enriched) methane in pore and ocean water provide a compelling mechanism to account for the negative δ¹³C excursions of both primary and post-depositional carbonates. Here, pore water methane may have led to a supersaturation of ¹³C depleted bicarbonate and precipitation of isotopically light authigenic calcite on and in foraminiferal tests, a feature that may serve as a tracer to former sites of clathrate destabilization.     

Carbon isotopic composition in suspended organic matter and bottom sediments of the East Arctic seas

The samples of water and bottom sediments of the East Siberian and Chukchi Seas collected during the second Russian-American RUSALCA expedition were used to analyze patterns of the isotopic composition of carbon in the organic matter (OM) of suspended material (SOM) and bottom sediments (BOM). Similar to other marine environments, the SOM isotopic composition depended on the ratio between the terrigenous and planktonic OM, both in the water body as a whole and in its parts. Thus, in the East Siberian Sea the carbon of SOM was poorer in ¹³C (??¹³C = ?24.51??) than the open part of the more productive Chukchi Sea (??¹³C = ?22.16??). In the less productive coastal waters of the Chukchi Sea, the ratio of terrigenous OM increased, resulting in a ??¹³C shift to lower values (?23.40??). Due to the influx of reduced products of anaerobic diagenesis of the sediments, elevated total number of microorganisms and dark CO₂ fixation were found in the near-bottom water at the water-sediment biogeochemical barrier. The newly formed biomass of autotrophic microorganisms shifted the carbon isotopic composition of the near-bottom suspended material to more positive ??¹³C values, with the average values of ?23.39 and ?20.37?? for the East Siberian and Chukchi Sea, respectively. Changes in the carbon isotopic composition of OM resulting from microbial activity continued in the upper sediment layers. When the rate of biomass synthesis increased that of biomass consumption, the ¹³C content increased further. At higher rates of OM mineralization, ¹²C accumulated in its remaining part.     

Microbiological and biogeochemical processes in a pockmark of the Gdansk depression,Baltic Sea

Comprehensive microbiological and biogeochemical investigation of a pockmark within one of the sites of gas-saturated sediments in the Gdansk depression, Baltic Sea was carried out during the 87th voyage of the Professor Shtokman research vessel. Methane content in the near-bottom water and in the underlying sediments indicates stable methane flow from the sediment into the water. In the 10-m water layer above the pockmark, apart from methane anomalies, elevated numbers of microorganisms and enhanced rates of dark CO₂ fixation (up to 1.15 µmol C/(l day)) and methane oxidation (up to 2.14 nmol CH₄/(l day)) were revealed. Lightened isotopic composition of suspended organic matter also indicates high activity of the near-bottom microbial community. Compared to the background stations, methane content in pockmark sediments increased sharply from the surface to 40–60 ml/dm³ in the 20–30 cm horizon. High rates of bacterial sulfate reduction (SR) were detected throughout the core (0–40 cm); the maximum of 74 µmol S/(dm³ day) was located in subsurface horizons (15–20 cm). The highest rates of anaerobic methane oxidation (AMO), up to 80 µmol/dm³ day), were detected in the same horizon. Good coincidence of the AMO and SR profiles with stoichiometry close to 1: 1 is evidence in favor of a close relation between these processes performed by a consortium of methanotrophic archaea and sulfate-reducing bacteria. Methane isotopic composition in subsurface sediments of the pockmark (from ?53.0 to ?56.5‰) does not rule out the presence of methane other than the biogenic methane from the deep horizons of the sedimentary cover.     

Effect of phytoplankton and microorganisms on the isotopic composition of organic carbon in the Russian Arctic seas

Carbon isotope composition of suspended organic matter (CIC_SOM) and of organic carbon of the bottom sediments (CIC_BS) was studied in a series of expeditions (starting in 1993) to the White, Kara, Chukchi, and Barents seas in the Russian Arctic. For each sea, CIC_SOM and CIC_BS was found to depend primarily on the ratio of OM produced in the water and OM of terrigenous origin. While in the White Sea, where the primary production (PP) is 5.3 times higher than the yearly inflow of terrigenous OM, δ¹³C of SOM carbon is ?29.1‰, in the Chukchi Sea, where PP is more than 300 times higher than the inflow of terrigenous OM, δ¹³C of SOM carbon is ?21.8‰. In the Barents and Chukchi seas, a considerable effect of suspended material arriving with the currents from the neighboring seas on formation of the CIC_SOM was demonstrated. The difference between CIC OM of the bottom sediments form CIC_SOM, the main component of organic matter in the sediments of all shelf seas, was demonstrated for the first time for all the seas studied. This results from production of additional microbial OM due to CO₂ assimilation at the water-sediment redox boundary or in near-bottom water.     

Microbiological and isotopic geochemical investigation of Lake Kislo-Sladkoe,a meromictic water body at the Kandalaksha Bay shore (White Sea)

Microbiological, biogeochemical, and isotopic geochemical investigation of Lake Kislo-Sladkoe (Polusolenoe in early publications) at the Kandalaksha Bay shore (White Sea) was carried out in September 2010. Lake Kislo-Sladkoe was formed in the mid-1900s out of a sea gulf due to a coastal heave. At the time of investigation, the surface layer was saturated with oxygen, while near-bottom water contained sulfide (up to 32 mg/L). Total number of microorganisms was high (12.3 × 10⁶ cells/mL on average). Light CO₂ fixation exhibited two pronounced peaks. In the oxic zone, the highest rates of photosynthesis were detected at 1.0 and 2.0 m. The second, more pronounced peak of light CO₂ fixation was associated with activity of anoxygenic phototrophic bacteria in the anoxic layer at the depth of 2.9 m (413 μg C L^?1 day^?1). Green-colored green sulfur bacteria (GSB) predominated in the upper anoxic layer (2.7–2.9 m), their numbers being as high as 1.12 × 10⁴ cells/mL, while brown-colored GSB predominated in the lower horizons. The rates of both sulfate reduction and methanogenesis peaked in the 2.9 m horizon (1690 μg S L^?1 day^?1 and 2.9 μL CH₄ L^?1 day^-1). The isotopic composition of dissolved methane from the near-bottom water layer (δ¹³C (CH₄) = ?87.76‰) was significantly lighter than in the upper horizons (δ¹³C (CH₄) = ?77.95‰). The most isotopically heavy methane (δ¹³C (CH₄) = ?72.61‰) was retrieved from the depth of 2.9 m. The rate of methane oxidation peaked in the same horizon. As a result of these reactions, organic matter (OM) carbon of the 2.9 m horizon became lighter (?36.36‰), while carbonate carbon became heavier (?7.56‰). Thus, our results demonstrated that Lake Kislo-Sladkoe is a stratified meromictic lake with active microbial cycles of carbon and sulfur. Suspended matter in the water column was mostly of autochthonous origin. Anoxygenic photo-synthesis coupled to utilization of reduced sulfur compounds contributed significantly to OM production.     

Isotope alteration caused by changes in biochemical composition of sedimentary organic matter

Stable carbon (C) and nitrogen (N) isotope ratios of sedimentary organic matter (OM) can reflect the biogeochemical history of aquatic ecosystems. However, diagenetic processes in sediments may alter isotope records of OM via microbial activity and preferential degradation of isotopically distinct organic components. This study investigated the isotope alteration caused by preferential degradation in surface sediments sampled from a eutrophic reservoir in Germany. Sediments were treated sequentially with hot water extraction, hydrochloric acid hydrolysis, hydrogen peroxide oxidation and di-sodium peroxodisulfate oxidation to chemically simulate preferential degradation pathways of sedimentary OM. Residue and extracts from each extraction step were analyzed using elemental analyzer-isotope ratio mass spectrometry and solid-state ¹³C nuclear magnetic resonance spectroscopy. Our results show that stable C and N isotope ratios reacted differently to changes in the biochemical composition of sedimentary OM. Preferential degradation of proteins and carbohydrates resulted in a 1.2‰ depletion of ¹³C, while the isotope composition of ¹⁵N remained nearly the same. Sedimentary δ¹⁵N values were notably altered when lignins and lipids were oxidized from residual sediments. Throughout the sequential fractionation procedure, δ¹³C was linearly correlated with the C:N of residual sediments. This finding demonstrates that changes in biochemical composition caused by preferential degradation altered δ¹³C values of sedimentary OM, while this trend was not observed for δ¹⁵N values. Our study identifies the influence of preferential degradation on stable C isotope ratios and provide additional insight into the isotope alteration caused by post-depositional processes.

     

Horizontal distribution of carbon and nitrogen and their isotopic compositions in the surface sediment of Lake Biwa

The horizontal distribution of the abundance and isotopic composition of carbon and nitrogen was studied on surface sediment samples (0–15 cm) collected from the entire area of Lake Biwa, the largest freshwater lake in Japan. As water depth increased, a marked increase in organic matter content was observed at the sampling sites, especially in the western North Basin, characterized by a steep slope. In the northwestern North Basin, which has no major inflowing streams, the sediments contained large amounts of organic matter, suggesting the possibility of lateral transportation of sedimented matter from other places by lake currents. The total amounts of carbon and nitrogen in the top-2 cm of sediment of the entire area of Lake Biwa were estimated to be 9.2 × 10⁴ tC and 1.0 × 10⁴ tN. The δ¹⁵N values in the littoral sediment were low and close to those in the inflowing river sediment, suggesting selective sedimentation of allochthonous organic matter onto the littoral area. In the North Basin, vertical profiles of organic matter content and δ¹³C values of the sediments in the littoral area showed a smaller downward decrease than in the profundal area, whereas δ¹⁵N values decreased with sediment depth in both areas. It was suggested that the littoral sediments contained abundant amounts of allochthonous and relatively refractory organic matter. Further, it was suggested that the autochthonous organic matter originated from primary production deposited mainly on the profundal zone and was easily decomposed in early diagenesis after sedimentation. Received: July 30, 1999 / Accepted: December 10, 1999     

Carbon sources of Antarctic nematodes as revealed by natural carbon isotope ratios and a pulse-chase experiment

δ¹³C of nematode communities in 27 sites was analyzed, spanning a large depth range (from 130 to 2,021 m) in five Antarctic regions, and compared to isotopic signatures of sediment organic matter. Sediment organic matter δ¹³C ranged from −24.4 to −21.9‰ without significant differences between regions, substrate types or depths. Nematode δ¹³C showed a larger range, from −34.6 to −19.3‰, and was more depleted than sediment organic matter typically by 1‰ and by up to 3‰ in silty substrata. These, and the isotopically heavy meiofauna at some stations, suggest substantial selectivity of some meiofauna for specific components of the sedimenting plankton. However, ¹³C-depletion in lipids and a potential contribution of chemoautotrophic carbon in the diet of the abundant genus Sabatieria may confound this interpretation. Carbon sources for Antarctic nematodes were also explored by means of an experiment in which the fate of a fresh pulse of labile carbon to the benthos was followed. This organic carbon was remineralized at a rate (11–20 mg C m⁻² day⁻¹) comparable to mineralization rates in continental slope sediments. There was no lag between sedimentation and mineralization; uptake by nematodes, however, did show such a lag. Nematodes contributed negligibly to benthic carbon mineralization.     

Methanogenesis produces strong 13C enrichment in stromatolites of Lagoa Salgada,Brazil: a modern analogue for Palaeo‐/Neoproterozoic stromatolites?

Holocene stromatolites characterized by unusually positive inorganic δ¹³C_PDB values (i.e. up to +16‰) are present in Lagoa Salgada, a seasonally brackish to hypersaline lagoon near Rio de Janeiro (Brazil). Such positive values cannot be explained by phototrophic fixation of CO₂ alone, and they suggest that methanogenesis was a dominating process during the growth of the stromatolites. Indeed, up to 5 mm methane was measured in the porewater. The archaeal membrane lipid archaeol showing δ¹³C values between ?15 and 0‰ suggests that archaea are present and producing methane in the modern lagoon sediment. Moreover, ¹³C‐depleted hopanoids diplopterol and 3β‐methylated C₃₂ 17β(H),21β(H)‐hopanoic acid (both ?40‰) are preserved in lagoon sediments and are most likely derived from aerobic methanotrophic bacteria thriving in the methane‐enriched water column. Loss of isotopically light methane through the water column would explain the residual ¹³C‐enriched pool of dissolved inorganic carbon from where the carbonate constituting the stromatolites precipitated. The predominance of methanogenic archaea in the lagoon is most likely a result of sulphate limitation, suppressing the activity of sulphate‐reducing bacteria under brackish conditions in a seasonally humid tropical environment. Indeed, sulphate‐reduction activity is very low in the modern sediments. In absence of an efficient carbonate‐inducing metabolic process, we propose that stromatolite formation in Lagoa Salgada was abiotically induced, while the ¹³C‐enriched organic and inorganic carbon pools are due to methanogenesis. Unusually, ¹³C‐enriched stromatolitic deposits also appear in the geological record of prolonged periods in the Palaeo‐ and Neoproterozoic. Lagoa Salgada represents a possible modern analogue to conditions that may have been widespread in the Proterozoic, at times when low sulphate concentrations in sea water allowed methanogens to prevail over sulphate‐reducing bacteria.     

Underwater sinkhole sediments sequester Lake Huron’s carbon

Lake Huron’s submerged sinkhole habitats are impacted by high-conductivity groundwater that allows photosynthetic cyanobacterial mats to form over thick, carbon-rich sediments. To better understand nutrient cycling in these habitats, we measured the stable isotopic content of carbon and nitrogen in organic and inorganic carbon pools in Middle Island sinkhole, a ~23 m deep feature influenced by both groundwater and overlying lake water. Two distinct sources of dissolved CO₂ (DIC) were available to primary producers. Lake water DIC (δ ¹³C = ?0.1 ‰) differed by +5.9 ‰ from groundwater DIC (δ ¹³C = ?6.0 ‰). Organic carbon fixed by primary producers reflected the two DIC sources. Phytoplankton utilizing lake water DIC were more enriched in ¹³C (δ ¹³C = ?22.2 to ?23.2 ‰) than mat cyanobacteria utilizing groundwater DIC (δ ¹³C = ?26.3 to ?30.0 ‰). Sinkhole sediments displayed an isotopic signature (δ ¹³C = ?23.1 ‰) more similar to sedimenting phytoplankton than the cyanobacterial mat. Corroborated by sediment C/N ratios, these data suggest that the carbon deposited in sinkhole sediments originates primarily from planktonic rather than benthic sources. ²¹⁰Pb/¹³⁷Cs radiodating suggests rapid sediment accumulation and sub-bottom imaging indicated a massive deposit of organic carbon beneath the sediment surface. We conclude that submerged sinkholes may therefore act as nutrient sinks within the larger lake ecosystem.     

Late Cretaceous marine arthropods relied on terrestrial organic matter as a food source: Geochemical evidence from the Coon Creek Lagerstätte in the Mississippi Embayment

The Upper Cretaceous Coon Creek Lagerstätte of Tennessee, USA, is known for its extremely well‐preserved mollusks and decapod crustaceans. However, the depositional environment of this unit, particularly its distance to the shoreline, has long been equivocal. To better constrain the coastal proximity of the Coon Creek Formation, we carried out a multiproxy geochemical analysis of fossil decapod (crab, mud shrimp) cuticle and associated sediment from the type section. Elemental analysis and Raman spectroscopy confirmed the presence of kerogenized carbon in the crabs and mud shrimp; carbon isotope (δ¹³C) analysis of bulk decapod cuticle yielded similar mean δ¹³C values for both taxa (?25.1‰ and ?26‰, respectively). Sedimentary biomarkers were composed of n‐alkanes from C₁₆ to C₃₆, with the short‐chain n‐alkanes dominating, as well as other biomarkers (pristane, phytane, hopanes). Raman spectra and biomarker thermal maturity indices suggest that the Coon Creek Formation sediments are immature, which supports retention of unaltered, biogenic isotopic signals in the fossil organic carbon remains. Using our isotopic results and published calcium carbonate δ¹³C values, we modeled carbon isotope values of carbon sources in the Coon Creek Formation, including potential marine (phytoplankton) and terrestrial (plant) dietary sources. Coon Creek Formation decapod δ¹³C values fall closer to those estimated for terrigenous plants than marine phytoplankton, indicating that these organisms were feeding primarily on terrigenous organic matter. From this model, we infer that the Coon Creek Formation experienced significant terrigenous organic matter input via a freshwater source and thus was deposited in a shallow, nearshore marine environment proximal to the shoreline. This study helps refine the paleoecology of nearshore settings in the Mississippi Embayment during the global climatic shift in the late Campanian–early Maastrichtian and demonstrates for the first time that organic δ¹³C signatures in exceptionally preserved fossil marine arthropods are a viable proxy for use in paleoenvironmental reconstructions.     

Bacterial abundance and composition in marine sediments beneath the Ross Ice Shelf,Antarctica

Marine sediments of the Ross Sea, Antarctica, harbor microbial communities that play a significant role in the decomposition, mineralization, and recycling of organic carbon (OC). In this study, the cell densities within a 153‐cm sediment core from the Ross Sea were estimated based on microbial phospholipid fatty acid (PLFA) concentrations and acridine orange direct cell counts. The resulting densities were as high as 1.7 × 10⁷ cells mL^?1 in the top ten centimeters of sediments. These densities are lower than those calculated for most near‐shore sites but consistent with deep‐sea locations with comparable sedimentation rates. The δ¹³C measurements of PLFAs and sedimentary and dissolved carbon sources, in combination with ribosomal RNA (SSU rRNA) gene pyrosequencing, were used to infer microbial metabolic pathways. The δ¹³C values of dissolved inorganic carbon (DIC) in porewaters ranged downcore from ?2.5‰ to ?3.7‰, while δ¹³C values for the corresponding sedimentary particulate OC (POC) varied from ?26.2‰ to ?23.1‰. The δ¹³C values of PLFAs ranged between ?29‰ and ?35‰ throughout the sediment core, consistent with a microbial community dominated by heterotrophs. The SSU rRNA gene pyrosequencing revealed that members of this microbial community were dominated by β‐, δ‐, and γ‐Proteobacteria, Actinobacteria, Chloroflexi and Bacteroidetes. Among the sequenced organisms, many appear to be related to known heterotrophs that utilize OC sources such as amino acids, oligosaccharides, and lactose, consistent with our interpretation from δ¹³C_PLFA analysis. Integrating phospholipids analyses with porewater chemistry, δ¹³C_DIC and δ¹³C_POC values and SSU rRNA gene sequences provides a more comprehensive understanding of microbial communities and carbon cycling in marine sediments, including those of this unique ice shelf environment.     

Assessing nature and dynamics of POM in transitional environment (the Curonian Lagoon,SE Baltic Sea) using a stable isotope approach

The nature of the particulate organic matter (POM) as well as its temporal and spatial distribution and dynamics in the Curonian Lagoon (south-eastern part of the Baltic Sea) were investigated. The organic matter was characterized by the organic carbon and nitrogen content, δ¹³C and δ¹⁵N signatures as well as POC/Chl-a and C/N ratios. Additionally, data on hydrological, chemical and biological parameters were used for better understanding the POM distribution and dynamics. The sampling was performed at 13 stations in the Curonian Lagoon and its outflow in the Baltic Sea during the 2012–2013 period. Samples were also collected at the Nemunas River mouth in order to test the riverine impact. Obtained results showed that isotopic values of carbon and nitrogen ranged from −36.1‰ to −25.2‰ and from −0.9‰ to 15.5‰, respectively. The isotopic composition, together with the low C/N molar (∼7) and POC/Chl-a ratios (<100) of the POM, suggested the dominance of living phytoplankton in POM throughout the year with the higher input of detrital material (C/N >10, POC/Chl-a ratios >100) in late autumn − winter.The results of multivariate analysis evidenced a spatial distinction of POM distribution in the northern-transitional and central confined areas and allowed us to distinguish the main driving factors. The seasonal variation of the δ¹³C and δ¹⁵N values in POM (towards higher δ¹³C and lower δ¹⁵N values in the summer − early autumn period and lower δ¹³C and higher δ¹⁵N values in the late autumn − spring period) was determined by combination of factors such as availability of inorganic carbon and nitrogen, the riverine discharge, seasonal phytoplankton succession and by the short-term saline water intrusion to the northern-transitional part of the lagoon.     

Relationship between δ13C of chironomid remains and methane flux in Swedish lakes

1. Methanogenic carbon can be incorporated by methane‐oxidising bacteria, leading to a ¹³C‐depleted stable carbon isotopic composition (δ¹³C) of chironomids that feed on these microorganisms. This has been shown for the chironomid tribe Chironomini, but very little information is available about the δ¹³C of other abundant chironomid groups and the relationship between chironomid δ¹³C and methane production in lakes. 2. Methane flux was measured at the water surface of seven lakes in Sweden. Furthermore, fluxes from the sediments to the water column were measured in transects in two of the lakes. Methane fluxes were then compared with δ¹³C of chitinous chironomid remains isolated from the lake surface sediments. Several different chironomid groups were examined (Chironomini, Orthocladiinae, Tanypodinae and Tanytarsini). 3. Remains of Orthocladiinae in the seven study lakes had the highest δ¹³C values (?31.3 to ?27.0‰), most likely reflecting δ¹³C of algae and other plant‐derived organic matter. Remains of Chironomini and Tanypodinae had lower δ¹³C values (?33.2 to ?27.6‰ and ?33.6 to ?28.0‰, respectively). A significant negative correlation was observed between methane fluxes at the lake surface and δ¹³C of Chironomini (r = ?0.90, P = 0.006). Methane release from the sediments was also negatively correlated with δ¹³C of Chironomini (r = ?0.67, P = 0.025) in the transect samples obtained from two of the lakes. The remains of other chironomid taxa were only weakly or not correlated with methane fluxes measured in our study lakes (P > 0.05). 4. Selective incorporation of methane‐derived carbon can explain the observed correlations between methane fluxes and δ¹³C values of Chironomini. Remains of this group might therefore have the potential to provide information about past changes in methane availability in lakes using sediment records. However, differences in productivity, algal δ¹³C composition and the importance of allochthonous organic matter input between the studied lakes may also have influenced Chironomini δ¹³C. More detailed studies with a higher number of analysed samples and detailed measurement of δ¹³C of different ecosystem components (e.g. methane, dissolved inorganic carbon) will be necessary to further resolve the relative contribution of different carbon sources to δ¹³C of chironomid remains.     

Sources of organic carbon and depositional environment in the Bengal delta plain sediments during the Holocene period

This study investigated the sources of organic matter and sediment depositional environment within fluviatile sediments of the Ganges–Meghna (GM) delta plains. The very low contents of trace metals e.g., chromium (Cr), cobalt (Co), scandium (Sc), and vanadium (V), organic carbon content, and cerium (Ce)-anomaly data of sediments indicate the redox conditions that fall within the boundary of oxic–anoxic condition, with dominantly oxic conditions in the sediment deposition environment. The higher atomic carbon nitrogen (C/N)a ratios and depleted stable carbon isotope ratio (δ¹³C) values for sediments from three study areas indicated the terrestrial sources of organic matter derived from C₃ plant materials, whereas the contribution of organic materials from C₄ vegetation and riverine productivity is low. Some silty sand samples exhibited lower (C/N)a ratios and enriched δ¹³C values in Sonargaon and Faridpur areas that are attributed to the adsorption of ammonium ions on clay minerals and the contribution of organic matter from C₄ plants. Total sulfur over total organic carbon (TS/TOC) ratios in sediments of the Ganges delta reflect the nonmarine environments of sediment deposition. The lower ratios of syringyl to vanillyl phenols (S/V), cinnamyl to vanillyl phenols (C/V), and acid to aldehyde in vanillyl phenols (Ad/Al)v observed in Daudkandi indicate that the lignin in sediments derived from dominant woody gymnosperm sources and is very highly degraded. By contrast, the S/V ratio, C/V ratios, and [Ad/Al]v ratios in Faridpur suggest that the lignin in sediments derived from a mixture of woody and nonwoody angiosperm plant tissue contribution that underwent high degradation as well.     

Arctic sediments (Svalbard): pore water and solid phase distributions of C,N, P and Si

Pore water and solid phase distributions of C, N, P and Si in sediments of the Arctic Ocean (Svalbard area) have been investigated. Concentrations of organic carbon (C_org) in the solid phase of the sediment varied from 1.3 to 2.8% (mean 1.9%), with highest concentrations found at shallow stations south/southwest of Svalbard. Relatively low concentrations were obtained at the deeper stations north/northeast of Svalbard. Atomic carbon to nitrogen ratios in the surface sediment ranged from below 8 to above 10. For some stations, high C/N ratios together with high concentrations of C_org suggest that sedimentary organic matter is mainly of terrigenous origin and not from overall biological activity in the water column. Organic matter reactivity (defined as the total sediment oxygen consumption rate normalized to the organic carbon content of the surface sediment) correlated with water depth at all investigated stations. However, the stations could be divided into two separate groups with different reactivity characteristics, representing the two most dominant hydrographic regimes: the region west of Svalbard mainly influenced by the West Spitsbergen Current, and the area east of Svalbard where Arctic polar water set the environmental conditions. Decreasing sediment reactivity with water depth was confirmed by the partitioning between organic and inorganic carbon of the surface sediment. The ratio between organic and inorganic carbon at the sediment-water interface decreased exponentially with water depth: from indefinite values at shallow stations in the central Barents Sea, to approximately 1 at deep stations north of Svalbard. At stations east of Svalbard there was an inverse linear correlation between the organic matter reactivity (as defined above) and concentration of dissolved organic carbon (DOC) in the pore water. The more reactive the sediment, the less DOC existed in the pore water and the more total carbonate (C_t or ΣCO₂) was present. This observation suggests that DOC produced in reactive sediments is easily metabolizable to CO₂. Sediment accumulation rates of opaline silica ranged from 0.35 to 5.7 μmol SiO₂ m⁻²d⁻¹ (mean 1.3 μmol SiO₂ m⁻²d⁻¹), i.e. almost 300 times lower than rates previously reported for the Ross Sea, Antarctica. Concentrations of ammonium and nitrate in the pore water at the sediment-water interface were related to organic matter input and water depth. In shallow regions with highly reactive organic matter, a pool of ammonium was present in the pore water, while nitrate conoentrations were low. In areas where less reactive organic matter was deposited at the sediment surface, the deeper zone of nitrification caused a build-up of nitrate in the pore water while ammonium was almost depleted. Nitrate penetrated from 1.8 to ≥ 5.8 cm into the investigated sediments. Significantly higher concentrations of “total” dissolved nitrogen (defined as the sum of NO₃, NO₂, NH₄ and urea) in sediment pore water were found west compared to east of Svalbard. The differences in organic matter reactivity, as well as in pore water distribution patterns of “total” dissolved nitrogen between the two areas, probably reflect hydrographic factors (such as ice coverage and production/import of particulate organic material) related to the dominant water mass (Atlantic or Arctic Polar) in each of the two areas. The data presented were collected during the European “Polarstern” Study (Arctic EPOS) sponsored by the European Science Foundation     

Tracing estuarine organic matter sources into the southern North Sea using C and N isotopic signatures

Sources and distribution of particulate organic matter in surface waters of the Humber and Thames estuaries and in the East Anglian plume in the southern North Sea were investigated in winter 2006/2007. Carbon (C) and nitrogen (N) stable isotopes provided evidence for the presence of three particulate organic matter sources; riverine plankton (δ¹³C ?30 ‰ and δ¹⁵N 7.9 ‰) identified in the Thames estuary only, marine plankton (average δ¹³C ?21.4 ‰ and δ¹⁵N 4.5 ‰) and a third source with an enriched ¹³C signature (>?16.7 ‰) and elevated C:N ratio (>12.7). Particulate organic matter with enriched ¹³C values were observed throughout the Humber estuary and at the marine end-member of the Thames estuary. While bacterial cycling of organic carbon undoubtedly takes place within these estuaries, these processes on their own are unlikely to account for the isotopic signatures seen. The ¹³C enriched organic matter source is suggested to be due to particulate organic matter input from marsh plants and seagrasses such as Spartina spp. and Zostera on the adjacent salt marshes and mudflats and/or macroalgae along the banks of the estuaries. This ¹³C enriched signal was also identified approximately 50 km offshore within the southern North Sea, in the East Anglian plume, which transports UK riverine water off-shore in a discrete plume. This plume therefore provides a mechanism to transport this estuarine derived organic matter pool offshore out of the estuaries. These results indicate that estuarine derived organic matter from marsh plants, seagrasses and/or macroalgae contributes to the southern North Sea organic matter pool and is therefore likely to contribute to winter-time shelf sea carbon and nitrogen cycles.     

Identifying critical habitat of the endangered vaquita (Phocoena sinus) with regional δ13C and δ15N isoscapes of the Upper Gulf of California,Mexico

The vaquita (Phocoena sinus) is the world's most endangered cetacean and has experienced a 60% reduction in the size of its population in the past decade. Knowledge of its basic ecology is essential for developing successful management plans to protect and conserve this species. In this study, we identified vaquita foraging areas by creating an isoscape of the Upper Gulf of California (UGC) based on sediment and zooplankton carbon (δ¹³C) and nitrogen (δ¹⁵N) isotope values. Our results confirm that this species is confined to the western region of the UGC, which is characterized by relatively high δ¹⁵N values (sediments: 10.2‰ ± 2.0‰, zooplankton: 15.8‰ ± 1.3‰), higher sea surface temperatures (～16°C–25°C), higher concentrations of silt in sediments, and the highest turbidity. In contrast, the eastern region of the UGC had relatively low sediment (7.7‰ ± 2.4‰) and zooplankton (14.6‰ ± 1.0‰) δ¹⁵N values, and the highest concentrations of sand in sediments. Our approach is an effective use of marine isoscapes over a small spatial scale (<200 km) to identify the environmental characteristics that define the critical habitat for an extremely endangered marine mammal.     

Detection of organic pollution of streams in southern Sweden using benthic macroinvertebrates

A ²¹⁰Pb-dated sediment core from a small bay in the southern basin of Lake Petén Itzá, Guatemala documents recent cultural eutrophication. Increased sediment accumulation beginning ～1930 A.D. coincided with catchment population growth and was a consequence of watershed deforestation and increased surface run-off. At the same time, geochemical records from the Lake Petén Itzá sediment core indicate increased phosphorus loading and organic matter accumulation. High nutrient concentrations after 1965 A.D. coincided with lower sediment C/N ratios, suggesting an increase in the relative contribution of phytoplankton to the organic matter pool. This inference is confirmed by the dominance of eutrophic and hypereutrophic diatom species. Organic matter δ¹³C values decreased after 1965 A.D., seemingly contradicting other indicators of recent eutrophication in the southern basin of Lake Petén Itzá. Relatively depleted δ¹³C values in recent sediments, however, may reflect a contribution from ¹³C-depleted sewage effluent. Increased δ¹⁵N of organic matter after 1965 A.D. indicates changes in the dissolved inorganic nitrogen delivered to the lake. The relatively small increase in δ¹⁵N (～0.6‰ ) is less than might be expected with nitrate loading from sewage and soils, and might be offset by the presence of nitrogen-fixing cyanobacteria with low δ¹⁵N values.     

Carbon isotopes and lipid biomarkers from organic‐rich facies of the Shuram Formation,Sultanate of Oman

The largest recorded carbon isotopic excursion in Earth history is observed globally in carbonate rocks of middle Ediacaran age. Known from the Sultanate of Oman as the ‘Shuram excursion’, this event records a dramatic, systematic shift in δ¹³C_carbonate values to ca. ?12‰. Attempts to explain the nature, magnitude and origin of this excursion include (i) a primary signal resulting from the protracted oxidation of a large dissolved organic carbon reservoir in seawater, release of methane from sediment‐hosted clathrates, or water column stratification; and (ii) a secondary signal from diagenetic processes. The compositions and isotope ratios of organic carbon phases during the excursion are critical to evaluating these ideas; however, previous work has focused on localities that are low in organic carbon, hindering straightforward interpretation of the observed time‐series trends. We report carbon isotope data from bulk organic carbon, extracted bitumen and kerogen, in addition to lipid biomarker data, from a subsurface well drilled on the eastern flank of the South Oman Salt Basin, Sultanate of Oman. This section captures Nafun Group strata through the Ediacaran–Cambrian boundary in the Ara Group and includes an organic‐rich, deeper‐water facies of the Shuram Formation. Despite the high organic matter contents, the carbon isotopic compositions of carbonates – which record a negative δ¹³C isotope excursion similar in shape and magnitude to sections elsewhere in Oman – do not covary with those of organic phases (bulk TOC, bitumen and kerogen). Paired inorganic and organic δ¹³C data only display coupled behaviour during the latter part of the excursion's recovery. Furthermore, lipid biomarker data reveal that organic matter composition and source inputs varied stratigraphically, reflecting biological community shifts in non‐migrated, syngenetic organic matter deposited during this interval.