Composition and origin of organic matter in surface sediments of Lake Sarbsko: A highly eutrophic and shallow coastal lake (northern Poland)

We present an organic geochemical study of surface sediments of Lake Sarbsko, a shallow coastal lake on the middle Polish Baltic coast. The aim was to provide evidence concerning the origin of the organic matter (OM) and its compositional diversity in surface deposits of this very productive, highly dynamic water body. The content and composition of the OM in the bottom sediments were investigated at 11 sampling stations throughout the lake basin. OM sources were assigned on the basis of bulk indicators [total organic carbon (TOC), total nitrogen (TN), δ¹³C_TOC and δ¹⁵N and extractable OM yield], biomarker composition of extractable OM and compound-specific C isotope signatures. The source characterization of autochthonous compounds was verified via phytoplankton analysis. The distribution of gaseous hydrocarbons in the sediments, as well as temporal changes in lake water pH, the concentration of DIC (dissolved inorganic carbon) and δ¹³C_DIC were used to trace OM decomposition.The sedimentary OM is composed mainly of well preserved phytoplankton compounds and shows minor spatial variability in composition. However, the presence of CH₄ and CO₂ in the bottom deposits provides evidence for microbial degradation of sedimentary OM. The transformation of organic compounds in surface, bottom and pore waters via oxidative processes influences carbonate equilibrium in the lake and seasonally favours precipitation or dissolution of CaCO₃.The data enhance our understanding of the relationships between the composition of sedimentary OM and environmental conditions within coastal ecosystems and shed light on the reliability of OM proxies for environmental reconstruction of coastal lakes.     

The Medieval Warm Period and the Little Ice Age from a sediment record of Lake Ebinur,northwest China

Ma, L., Wu, J., Yu, H., Zeng, H. & Abuduwaili, J. 2011: The Medieval Warm Period and the Little Ice Age from a sediment record of Lake Ebinur, northwest China. Boreas, Vol. 40, pp. 518–524. 10.1111/j.1502‐3885.2010.00200.x. ISSN 0300‐9483. Lake Ebinur, Xinjiang, northwest China, is a closed‐basin, shallow lake that responds rapidly to changes in the ratio of precipitation to evaporation (P/E). A sediment record spanning the last 1500 years was obtained from the lake. We used δ¹⁸O and δ¹³C in bulk carbonate, and δ¹³C of organic matter in the lake sediments to infer environmental changes in the Ebinur region during the Medieval Warm Period (MWP) and the Little Ice Age (LIA). Decreased δ¹⁸O values of carbonate largely reflect an enhanced P/E ratio within the basin and a higher lake level. Bulk carbonates with higher δ¹³C values are deposited during periods when lake‐water pH is high, while lower δ¹³C values reflect a lower pH in the water column. δ¹³C in organic matter is associated with the amount of precipitation. The results indicate that the Ebinur region experienced a dry MWP and a wet LIA, although the MWP and LIA were warm and cold periods, respectively, as expected. Furthermore, the MWP and LIA were hydrologically complex and cannot be characterized as uniformly wet or dry. Peak wet periods are recorded in the sediment core around AD 1000, 1400 and 1700, and a dry event also occurred in the period of temperature change within the LIA (cold to warm around AD 1500). A comparison of the Lake Ebinur data with proxy records for the strength of the Siberian High and climate proxy indicators suggests that precipitation in the Ebinur region was a consequence, in part, of an enhanced Siberian High during the LIA.     

Holocene paleoenvironmental reconstruction in the Eastern Amazonian Basin: Comprido Lake

Two sediment cores were studied from Comprido Lake, a black water floodplain lake located near Monte Alegre City, Eastern Amazonian Basin. The total organic carbon (TOC), nitrogen content (TN), δ¹³C_TOC, sedimentary chlorophyll, diatom record and mineralogical composition revealed different hydrological and climatic regimes during the Holocene. Between 10,300 and 7800 cal yr BP, a dry climate was suggested by low values of TOC and chlorophyll derivatives concentrations that are related to the development of a C₄ grasses on unflooded mud banks. A gap in sedimentation due to a complete dryness of the lake occurred between 7800 and 3000 cal years BP corresponding to the Middle Holocene dry phase. From 3000 cal years BP onwards a gradual increase of the TOC, chlorophyll derivatives and Aulacoseira sp. suggest an increase in the productivity and in water lake level due to the high water flow of the Amazon River and the catchment area as well. The Comprido Lake record indicates that the Late Holocene in this region was characterized by a wetter climate, as also observed in other records of the Amazonian Basin.     

18.5kaB. P.以来东北四海龙湾玛珥湖全岩有机碳同位素记录及其古气候环境意义

结合含水量、TOC含量和TOC/TN比值变化曲线,18·5kaB·P·以来的四海龙湾玛珥湖沉积物全岩有机碳同位素组成（^δ13C_TOC）记录可划分为3个阶段:1)末次冰期晚期（18·5～14·7kaB·P·）,^δ13C_TOC值偏正,变化范围为-29·50‰～-26·18‰,平均值约为-28·10‰;2)末次冰消期（14·7～11·7kaB·P·）,^δ13C_TOC值显著偏负,变化范围为-33·92‰～-28·40‰,平均值约为-31·75‰,在^δ13C_TOC值变化曲线上表现为一个低谷,但在类似YoungerDryas的冷干事件期间（12·7～11·7kaB·P·）,^δ13C_TOC值再次显著偏正,最高可达-28·4‰;3)全新世以来（11·7kaB·P.至今）,^δ13C_TOC值变化幅度不大（-30·85‰～-27·37‰）,基本上都在平均值-29·1‰左右。研究表明,大气CO₂浓度变化是影响18·5kaB·P·以来四海龙湾玛珥湖^δ13C_TOC值变化的主导因素。     

Biogeochemical characterization of a Mediterranean shallow lake using stable isotopes: Laguna del Cristo (NW Iberian Peninsula)

The present multi-isotopic study (δ¹⁸O–δD_water, δ³⁴S–δ¹⁸O_{dissolved-sulphate}, δ¹³C_{dissolved-inorganic-carbon}, δ¹³C–δ¹⁸O_{shells-modern-gastropods}, δ¹³C_plants, and δ¹³C_{sedimentary-organic-matter}) is aimed at assessing the hydrogeochemical changes and biogeochemical dynamics in a Mediterranean shallow lake fed by a Quaternary–Tertiary aquifer, the “Laguna del Cristo” (NW Iberian Peninsula), a system sensitive to climate fluctuations, between 2010 and 2011. Lake water is of the bicarbonate type, and there are no major pollutants. δ¹⁸O-δD_water values plot on a local evaporation line (δD=5.29δ¹⁸O–12.29) indicating that evaporative enrichment had a significant impact on lake water isotopic features. Periods of high water levels are characterized by lower δ³⁴S–δ¹⁸O_{dissolved-sulphate} and δ¹³C_{dissolved-inorganic-carbon} values and suggest sulphate derived from weathering of sulphides in the catchment area, delivered to the lake by surface run-off or via groundwater, and in situ decay of organic matter. During lower water levels, sulphate reduction and enhanced primary productivity lead to higher δ³⁴S_{dissolved-sulphate} and δ¹³C_{dissolved-inorganic-carbon} values. Evaporation induced enrichment in ¹⁸O_sulphate, ¹³C_{dissolved-inorganic-carbon} and ¹³C–¹⁸O_{shells-Galba-Gyraulus}. δ¹³C_plant confirms the C3 photosynthetic pathway. Enrichment in ¹³C submerged aquatic plants indicates that HCO₃^? is the main carbon source, except for ¹³C-depleted Potamogeton. The TOC, δ¹³C_org values, and TC/TN ratios in sediments all confirm the autochthonous character of organic matter contribution. This study provides a baseline for isotopic research into shallow, flow-through lakes fed by siliciclastic aquifers, and stresses the importance of evaporation and refilling (direct precipitation and groundwater discharge) in controlling the solute chemistry and stable isotopic composition in temperate regions with contrasting seasonal climates. The results also provide a snapshot of modern lake isotope variability that can be applied to paleoenvironmental reconstructions.     

Bulk organic δ13C and C/N ratios as palaeosalinity indicators within a Scottish isolation basin

Microfossils in isolation basin sediments are frequently used to reconstruct sea‐level change, but preservation problems and non‐analogue situations can limit their usefulness. Here we investigate the potential of stable carbon isotopes (δ¹³C) and C/N ratios from bulk organic matter, as an alternative proxy of salinity within isolation basin sediments from a basin in northwest Scotland. Within the Holocene sediment δ¹³C and C/N are determined largely by the mean weighted values of the predominant source of the organic material. Analysis of modern materials and comparison with the diatom record shows that the marine parts of the sequence are dominated by high δ¹³C and variable C/N. In the fresh water sequences the organic material is a mixture of both freshwater aquatic and terrestrial plant input that have relatively low δ¹³C and high C/N. The application of δ¹³C and C/N ratios in the studied basin in general follow the environmental change recorded by the diatoms and shows the potential of bulk organic matter in the investigation of salinity change in isolation basins. Copyright © 2005 John Wiley & Sons, Ltd.     

Dinosterol δD values in stratified tropical lakes (Cameroon) are affected by eutrophication

In freshwater settings, dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is produced primarily by dinoflagellates, which encompass various species including autotrophs, mixotrophs and heterotrophs. Due to its source specificity and occurrence in lake and marine sediments, its presence and hydrogen isotopic composition (δD) should be valuable proxies for paleohydrological reconstruction. However, because the purity required for hydrogen isotope measurements is difficult to achieve using standard wet chemical purification methods, their potential as a paleohydrological proxy is rarely exploited. In this study, we tested δD values of dinosterol in both particulate organic matter (POM) and sediments of stratified tropical freshwater lakes (from Cameroon) as a paleohydrological proxy, the lakes being characterized by variable degrees of eutrophication. In POM and sediment samples, the δD values of dinosterol correlated with lake water δD values, confirming a first order influence of source water δD values. However, we observed that sedimentary dinosterol was D enriched from ca. 19 to 54‰ compared with POM dinosterol. The enrichment correlated with lake water column conditions, mainly the redox potential at the oxic–anoxic interface (E_h OAI). The observations suggest that paleohydrologic reconstruction from δD values of dinosterol in the sediments of stratified tropical lakes ought to be sensitive to the depositional environment, in addition to lake water δD values, with more positive dinosterol δD values potentially reflecting increasing lake eutrophication. Furthermore, in lake sediments, the concentration of partially reduced vs. non-reduced C₃₄ botryococcenes, stanols vs. stenols, and bacterial (diploptene, diplopterol and ββ-bishomohopanol) vs. planktonic/terrestrial lipids (cholesterol, campesterol and dinosterol) correlated with E_h OAI. We suggest using such molecular proxies for lake redox conditions in combination with dinosterol δD values to evaluate the effect of lake trophic status on sedimentary dinosterol δD values, as a basis for accurately reconstructing tropical lake water δD values.     

Influence of the ratio of planktonic to benthic diatoms on lacustrine organic matter δ13C from Erlongwan maar lake,northeast China

Carbon isotope ratio (δ¹³C_org) values of organic matter in lake sediments are commonly used to reconstruct environmental change, but the factors which influence change are varied and complex. Here we report δ¹³C values for sediments from Erlongwan maar lake in northeast China. In this record, changes in δ¹³C cannot be explained by simple changes in aquatic productivity. Instead, values were likely influenced by differences in the ratio between planktonic and benthic algae, as indicated by the remains of diatoms. This is because the variation of δ¹³C_org in algae from different habitats is controlled by the thickness of the diffusive boundary layer, which is dependent on the turbulence of the water. Compared with benthic algae, which grow in relatively still water, pelagic algae are exposed to greater water movement. This is known to dramatically reduce the thickness of the boundary layer and was found to cause even more severe δ¹³C depletion. In Erlongwan maar lake, low values were linked to the dominance of planktonic diatoms during the period commonly known as the Medieval Warm Period. Values gradually increased with the onset of the Little Ice Age, which we interpret as being driven by an increase in the proportion of benthic taxa, due to effect of the colder climate. The increase in planktonic diatoms at the end of the Little Ice Age, linked to higher temperature and a reduction in ice cover, resulted in a further decline in δ¹³C_org.     

Strontium and carbon isotope stratigraphy of the Late Jurassic shallow marine limestone in western Palaeo-Pacific,northwest Borneo

Strontium and carbon isotope stratigraphy was applied to a 202 m-thick shallow marine carbonate section within the Late Jurassic Bau Limestone at the SSF quarry in northwest Borneo, Malaysia, which was deposited in the western Palaeo-Pacific. Strontium isotopic ratios of rudist specimens suggest that the SSF section was formed between the latest Oxfordian (155.95 Ma) and the Late Kimmeridgian (152.70 Ma), which is consistent with previous biostratigraphy. The δ¹³C_carb values of bulk carbonate range from −0.10 to +2.28‰ and generally show an increasing upward trend in the lower part of the section and a decreasing upward trend in the upper part of the section. A comparable pattern is preserved in the δ¹³C_org isotope record. Limestone samples of the SSF section mainly preserve the initial δ¹³C_carb values, except for the interval 84–92 m, where an apparent negative anomaly likely developed as a result of meteoric diagenesis. Comparing with the Tethyan δ¹³C_carb profile, a negative anomaly in the lower SSF section can be correlated with the lowered δ¹³C values around the Oxfordian/Kimmeridgian boundary. In addition, δ¹³C_carb values of the Bau Limestone are generally ∼1‰ lower than the Tethyan values, but comparable with the values reported from Scotland and Russia, located in Boreal realm during the Late Jurassic. This suggests that either the Tethyan record or the other records have been affected by the δ¹³C values of regionally variable dissolved inorganic carbon (DIC). The Late Jurassic δ¹³C_DIC values are thought to have been regionally variable as a result of their palaeoceanographic settings. This study shows that δ¹³C chemostratigraphy of the Palaeo-Pacific region contributes to an improved understanding of global carbon cycling and oceanography during this time period.     

Carbon isotope composition of long chain leaf wax n-alkanes in lake sediments: A dual indicator of paleoenvironment in the Qinghai-Tibet Plateau

The carbon isotope composition (δ¹³C values) of long chain n-alkanes in lake sediments has been considered a reliable means of tracking changes in the terrigenous contribution of plants with C₃ and C₄ photosynthetic pathways. A key premise is that long chain leaf wax components used for isotope analysis are derived primarily from terrigenous higher plants. The role of aquatic plants in affecting δ¹³C values of long chain n-alkanes in lacustrine sediments may, however, have long been underestimated. In this study, we found that a large portion of long chain n-alkanes (C₂₇ and C₂₉) in nearshore sediments of the Lake Qinghai catchment was contributed by submerged aquatic plants, which displayed a relatively positive carbon isotope composition (e.g. −26.7‰ to −15.7‰ for C₂₉) similar to that of terrestrial C₄ plants. Thus, the use of δ¹³C values of sedimentary C₂₇ and C₂₉ n-alkanes for tracing terrigenous vegetation composition may create a bias toward significant overestimation/underestimation of the proportion of terrestrial C₄ plants. For sedimentary C₃₁, however, the contribution from submerged plants was minor, so that the δ¹³C values for C₃₁ n-alkane in surface sediments were in accord with those of the modern terrestrial vegetation in the Lake Qinghai region. Moreover, we found that changes in the δ¹³C values of sedimentary C₂₇ and C₂₉ n-alkanes were closely related to water depth variation. Downcore analysis further demonstrated the significant influence of endogenous lipids in lake sediments for the interpretation of terrestrial C₄ vegetation and associated environment/climate reconstruction. In conclusion, our results suggest that the δ¹³C values of sedimentary long chain n-alkanes (C₂₇, C₂₉ and C₃₁) may carry different environmental signals. While the δ¹³C values of C₃₁ were a reliable proxy for C₄/C₃ terrestrial vegetation composition, the δ¹³C values of C₂₇ and C₂₉ n-alkanes may have recorded lake ecological conditions and sources of organic carbon, which might be affected by lake water depth.     

The radiocarbon age of organic carbon in marine surface sediments

Long-term carbon cycling and climate change are strongly dependent on organic carbon (OC) burial in marine sediments. Radiocarbon (¹⁴C) has been widely used to constrain the sources, sinks, and processing of sedimentary OC. To elucidate the dominant controls on the radiocarbon content of total organic carbon (¹⁴C_TOC) accumulating in surface sediments we construct a box model that predicts ¹⁴C_TOC in the sediment mixed layer (measured as fraction modern, Fm). Our model defines three distinct OC pools (“degradable,” “semi-labile,” and “refractory”) and assumes that ¹⁴C_TOC flux to sediments is exclusively derived from surface ocean primary productivity, and hence follows a “generic” surface ocean dissolved inorganic carbon (DIC) bomb curve. Model predictions are compared to a set of 75 surface sediment samples, which span a wide geographic range and reflect diverse water column and depositional conditions, and for which sedimentation rate and mixed-layer depth are well characterized. Our model overestimates the Fm value for a majority (65%) of these sites, especially at shallow water depths and for sites characterized by depleted δ¹³C_TOC values. The model is most sensitive to sedimentation rate and mixed-layer depth. Therefore, slight changes to these parameters can lead to a match between modeled and measured Fm values at many sites. Yet, in some cases, we find that measured Fm values cannot be simulated without large and unrealistic changes to sedimentation rate and mixed-layer depth. These results point to sources of pre-aged OC to surface sediments and implicate soil-derived terrestrial OC, reworked marine OC, and/or anthropogenic carbon as important components of the organic matter present in surface sediments. This approach provides a valuable framework within which to explore controls on sedimentary organic matter composition and carbon burial over a range of spatial and temporal scales.     

Shoreline tufa and tufaglomerate from Pleistocene Lake Bonneville,Utah, USA: stable isotopic and mineralogical records of lake conditions,processes, and climate

Shoreline carbonate deposits of Pleistocene Lake Bonneville record the conditions and processes within the lake, including the evaporative balance as well as vertical and lateral chemical and isotopic gradients. Tufas (swash‐zone) and tufaglomerates (cemented, subaqueous colluvium or beachrock) on multiple, well‐developed shorelines near the Silver Island Range, Utah, also present an opportunity to examine physicochemical lake processes through time. Three shorelines are represented by carbonate deposits, including the 23–20 ka Stansbury stage, 15–14.5 ka Bonneville stage, and 14.5–14 ka Provo stage. Mean δ¹⁸O_VSMOW values of all three shorelines are statistically indistinguishable ( ～ 27 ± 1‰), when a few Bonneville samples of unusual composition are neglected. However, differences in primary carbonate mineralogy indicate that the correspondence is an artefact of the different fractionation factors between calcite or aragonite and water. Second, in order to sustain a much smaller, shallower lake during the colder Stansbury stage, the climate must have also been relatively dry. Third, δ¹⁸O values in tufa are higher than tufaglomerate by ～ 0.5‰, consistent with greater evaporative enrichment of lake water in the swash zone. Fourth, mean δ¹³C values for the Provo, Stansbury and Bonneville shorelines (4.4, 5.0 and 5.2‰, respectively) show that carbon species were dominated by atmospheric exchange, with the variations produced by differences in the oxidation of organic matter. Comparisons of shoreline carbonates with deep‐lake marls of the same approximate age indicate that shoreline carbonate was much higher in δ¹³C and δ¹⁸O values (both ～ 2.5‰) during Bonneville time, whereas isotopic differences were minor (both ～ 1‰) in Stansbury time. In particular, the Bonneville stage may have sustained large vertical or lateral isotopic gradients due to evaporative enrichment effects on δ¹⁸O values. In contrast, the lake during the much shallower Stansbury stage may have been well mixed. Differences in the primary mineralogy (Stansbury and Bonneville, aragonite > calcite; Provo, calcite > aragonite) reflect profound differences in lake chemistry in terms of open versus closed‐basin lakes. The establishment of a continuous outlet during Provo time probably reduced the Mg²⁺/Ca²⁺ ratio of lake water. Curiously, regardless of primary mineralogy, tufaglomerate cements are enriched in Na⁺ and Cl^? and depleted in Mg²⁺ relative to capping tufa of the same age. This probably reflects vital or kinetic effects in the swash zone (tufa). We suspect that ‘abiotic’ effects may have been important in the dark pore space of developing tufaglomerate, where the absence of light suppressed photosynthesis. Copyright © 2005 John Wiley & Sons, Ltd.     

Seasonal water-column dynamics of dissolved inorganic carbon stable isotopic compositions (δCDIC) in small hardwater lakes in Minnesota and Montana

The carbon stable isotopic value of dissolved inorganic carbon (δ¹³C_DIC) was measured over several years at different depths in the water column in six carbonate-precipitating temperate lakes. δ¹³C_DIC behavior in three of these lakes departed from the conventional model wherein epilimnetic waters are seasonally enriched relative to all hypolimnetic waters, and in general δ¹³C_DIC values in the water column were not readily correlated to parameters such as lake stratification, algal productivity, hydraulic residence time, or water chemistry. Additionally, the processes implicated in generating the δ¹³C_DIC values of individual lakes differ between lakes with similar δ¹³C_DIC compositions. Each lake thus initially appears idiosyncratic, but when the effects of carbonate mineral equilibria, microbial activity, and lake residence time are viewed in terms of the magnitude of distinct DIC pools and fluxes in stratified lakes, generalizations can be made that allow lakes to be grouped by δ¹³C_DIC behavior. We recognize three modes in the relationship between δ¹³C_DIC values and DIC concentration ([DIC]) of individual lakes: (A) δ¹³C_DIC values decreasing with increasing [DIC]; (B) δ¹³C_DIC values increasing with increasing [DIC]; (C) δ¹³C_DIC values decreasing with increasing [DIC] but increasing again at the highest [DIC]. This approach is useful both in understanding δ¹³C_DIC dynamics in modern hardwater lakes and in reconstructing the environmental changes recorded by sedimentary δ¹³C components in the lacustrine paleorecord.     

Stable isotope geochemistry of magnesite from Holocene salt lake deposits,Taoudenni, Mali

Stable isotope data (δ¹⁸O, δ¹³C) were obtained for magnesite (MgCO₃) from Holocene salt lake deposits of the Taoudenni–Agorgott basin, Mali, in which it is the only carbonate mineral present. The deposits have a high glauberite content (Na₂Ca(SO₄)₂), representing a type of continental evaporite formation that is commonly magnesite‐bearing. Samples from seven different levels in a 5 m long sequence were analysed. δ¹⁸O_V‐PDB values are between +3.17 and +5.91‰, which is lower than might be expected for evaporitic environments, recording reduced ¹⁸O enrichment at high salinity. δ¹³C_V‐PDB values are between −1.32‰ and −4.79‰, showing an influence of carbon derived from the decomposition of organic matter rather than from exchange with atmospheric CO₂. Covariance between δ¹⁸O and δ¹³C is strong for the lower part of the sequence, recording coupled ¹⁸O and ¹³C enrichment as commonly observed for closed basins. Covariance is lacking for the upper part of the sequence, with only periodic massive magnesite deposition in a more shallow lake. Copyright © 2012 John Wiley & Sons, Ltd.     

Application of stable carbon isotopes for reconstructing salt‐marsh floral zones and relative sea level,New Jersey,USA

We investigated use of δ¹³C in bulk organic sediment to define the botanical origin of samples preserved in coastal sediment as a means to reconstruct relative sea level in New Jersey, USA. Modern transects at three sites demonstrated that low and high salt‐marsh floral zones dominated by C₄ species (Spartina alterniflora and Spartina patens) were associated with sediment δ¹³C values between ?18.9‰ and ?15.8‰ and occurred from mean tide level (MTL) to mean higher high water (MHHW). Brackish transitional settings vegetated by Phragmites australis with Iva fructescens and Typha sp. (C₃ species) and freshwater upland samples (C₃ species) were characterized by bulk sediment δ¹³C values of ?27.0‰ to ?22.0‰ and existed above MHHW. Parallel transects at one site suggested that intra‐site variability was not discernible. The utility of δ¹³C values for reconstructing relative sea level in New Jersey is limited by an inability to differentiate between brackish sediments related to sea level and freshwater upland samples. To facilitate this distinction in a 4.4 m core, we used a multi‐proxy approach (δ¹³C values with presence or absence of agglutinated foraminifera) to recognize indicative meanings for four sample types. Sediment with δ¹³C values greater than ?18.9‰ was derived from a vegetated salt‐marsh and formed between MTL and MHHW. Sediment with δ¹³C values less than ?22.0‰ and containing agglutinated foraminifera formed in a brackish transitional zone between MHHW and highest astronomical tide (HAT). This is the narrowest elevational range of the four sample types and most precise sea‐level indicator. Sediment with δ¹³C values less than ?22.0‰ and lacking foraminifera can only constrain the upper bound of former sea level. Samples with intermediate values (?22.0‰ to ?18.9‰) formed between MTL and HAT. Using these indicative meanings and radiocarbon dates, we suggest that a transition from brackish to salt‐marsh δ¹³C values recorded in the core took approximately 350 years (from 1800 to 1450 cal. a BP). Copyright © 2011 John Wiley & Sons, Ltd.     

Assessing Li and other leachable geochemical proxies for paleo-salinity in lake sediments from the Mono Basin, CA (USA)

Regional climate-driven hydrological changes are accompanied by salinity changes in closed basin lakes. We have investigated acid leachable Li, along with other leachable ions including Mg, Ca and Sr, as geochemical proxies of salinity in lake sediments in the Mono Basin, California. All the elements in the acid leachable suite show a strong correlation with paleo-lake level estimates based on physical and stratigraphic evidence. The CaCO₃ content of lake sediments, which has been shown to be a reliable proxy for lake level changes in the Mono basin and the adjoining Owens Lake basin, corresponds well with our acid-leachable proxy data.     

δ18O and δ13C in fossil shells of Radix sp. from the sediment succession of a dammed palaeo‐lake in the Yarlung Tsangpo valley,Tibet, China

A series of confirmed and suspected dammed palaeo‐lake sedimentary successions is scattered within the middle Yarlung Tsangpo valley in Tibet. However, the chronology, the genesis of the dam and its location, the water level of the dammed lake, the process of dam failure and the spatiotemporal relationships between the sedimentary successions remain controversial. Here, we focus on one sedimentary succession of the suspected dammed palaeo‐lake at Xigazê. We measured the grain‐size distribution, magnetic susceptibility, organic and inorganic carbon content, and δ¹³C_org and δ¹⁵N_total ratios of the sediments. In addition, we measured the δ¹⁸O_shell and δ¹³C_shell values of modern and fossil Radix sp. shells, and the δ¹⁸O_water and δ¹³C_DIC values of the ambient water with different hydrological regimes. The results indicate that the δ¹⁸O_shell values of modern Radix sp. and the δ¹⁸O_water of the ambient water body significantly depend on its hydrological status. In addition, a strong positive relationship was observed between δ¹⁸O_shell values of modern Radix sp. shells and the δ¹⁸O_water of the ambient water on the Tibetan Plateau. According to this correlation, the δ¹⁸O_water values of the palaeo‐water body are reconstructed using the δ¹⁸O_shell values of Radix sp. fossil shells in the Xigazê section. Further, based on the δ¹⁸O_shell values of fossil Radix sp., the reconstructed δ¹⁸O_water of the palaeo‐water body and the specific habitats of Radix sp., we infer that the sedimentary succession in the Xigazê broad valley was mainly formed within the backwater terminal zone of a dammed palaeo‐lake and that the elevation of the water level of the lake was approximately 3811 m a.s.l. AMS ¹⁴C dating indicates that the deposits of the dammed palaeo‐lake were formed at about 33–22 cal. ka BP. Finally, the presence of Radix sp. fossil shells within the Xigazê section suggests that Radix sp. survived the late Last Glacial Period on the Tibetan Plateau.     

Biogeochemical controls on reaction of sedimentary organic matter and aqueous sulfides in holocene sediments of Mud Lake, Florida

The distribution and quantity of organic sulfur and iron sulfur species were determined in the Holocene sediments from Mud Lake, Florida. The sediments of this shallow, sinkhole lake are characterized by high sulfur and organic carbon contents as well as active sulfate reduction. They record a shift from a basal peat (below 2 m) comprised of water lily-dominated organic matter to the present cyanobacterial/algal-dominated lake deposit (upper 1 m). This shift in depositional environment and subsequent organic matter source was accompanied by variation in the amount of reactive iron delivered to the sediments, which in turn influenced the type and extent of organic matter sulfurization. Extractable intramolecular organic sulfur is principally found as C₂₅ highly branched isoprenoid (HBI) thiolanes. Extractable polysulfide-linked lipids, determined by selective chemical cleavage with MeLi/MeI and analyzed as methylthioethers (MTE), are dominated by n-alkanes with sulfur attachments at position 1 and 2, as well as lower amounts of C₂₅ HBI-MTE. The δ¹³C values and carbon-chain length distribution of both series of n-alkylMTE indicate that they are derived from distinct biological precursors. Among the n-alkylMTE with sulfur attachment at position 1 there are three homologous series: one saturated and two with both cis and trans enethiol isomers. The identification of the enethiol in the sulfur-linked macromolecules indicates that n-alkylaldehydes are precursors lipids. The intervals of high concentration of bulk organic sulfur and sulfurized lipids coincide with the intervals of high mineral sulfur content (acid volatile sulfide and chromium reducible sulfur). We suggest that the main control on the enhanced addition of sulfur to the organic matter in Mud Lake was the increased formation of polysulfides during the reduction of iron hydroxides and the subsequent reaction of those polysulfides with mildly oxidized sedimentary organic matter.     

Effect of Atmosphere and Temperature Treatment on Leoanardite for Increasing Humic Acid Yield

In this review, the shifts in organic matter (OM) accumulation and C:N ratios in lake sediments to reconstruct paleoclimate and paleo-environmental changes since the early Holocene period are presented. The C:N proxy data of total OM reflect wet climatic conditions during early Holocene (10 to 8.2 kyrs BP) due to enhanced southwest monsoon. This was followed by intermittent arid conditions during the mid and late Holocene period (8.2 to 2.8 kyr BP). Enhanced values of C:N ratio during middle to late Holocene (7.8–2.3 kyrs B.P) indicate periods with lower lake levels and minimum precipitation, while decreased C:N ratio point to stronger SW monsoon and expansion of the lakes. Further, C:N and δ¹³C results from the lake sediments reveal a detailed and continuous paleo-environmental changes in the relative sources of OM (allochthonous vs autochthonous). Proxy records using such natural archives have also been utilized to reconstruct past extreme events and environmental changes around the lake systems, such as causes for lake desiccation, hydrographic changes, alternations between C₃ and C₄ vegetation and historical disturbances in the catchment area since the early-late Holocene period coupled with the Indian summer monsoon.     

Geochemical arguments for identifying second‐order sea‐level changes in hemipelagic carbonate ramp deposits

Second‐order transgressive–regressive (T–R) cycles, previously recognized using sedimentological criteria in Lower Jurassic hemipelagic deposits from northern Spain, are distinguishable based upon bulk‐rock organic geochemistry [total organic carbon (TOC) and hydrogen index (HI)] and the stable carbon isotope compositions from belemnite rostra. There is a coincidence between regressions and decreasing δ¹³C_bel, TOC and HI values, and between transgressions and increasing δ¹³C_bel, TOC and HI values. The δ¹⁸O and Mg/Ca records from the belemnite rostra are not always in phase with the T–R cycles. The δ¹⁸O_bel record reveals, however, a prominent excursion towards higher values within the spinatum Zone that correlates, according to our results, with a regression and with negative shifts in Mg/Ca, δ¹³C_bel and TOC. On the other hand, an excursion in the δ¹⁸O_bel towards lower values in the serpentinus Zone also correlates with a peak transgression and with positive shifts in Mg/Ca, δ¹³C_bel and TOC. These two excursions have been identified in other European regions as geochemical perturbations of the same characteristics. This suggests a link between second‐order relative sea‐level changes and variations in seawater geochemistry that may reflect local and regional palaeoceanographic perturbations in sea‐water temperature, salinity and water circulation during the Early Jurassic. Terra Nova, 18, 233–240, 2006