Influence of humic acid on the sorption of pentachlorophenol by aged sediment amended with rice-straw biochar

Black carbon (BC), especially biochar, is a potential material for the remediation of hydrophobic organic compounds (HOCs) pollution in soils and sediments. Recent studies have reported that the adsorption capability of BC in sediment was reduced as time increased. It was hypothesised that this behaviour was caused by the presence of natural organic matter (NOM), but few systematic studies have examined the influence of NOM on the sorption ability of BC in sediment (S). The results of this study revealed that a humic acid (HA) coating changed the surface properties, blocked the micropores, and decreased the sorption capacity of rice-straw biochar (RBC) towards pentachlorophenol. With increasing aging time, the reductions in the sorption capacity of the S + RBC and S + HA + RBC systems occurred more rapidly than in the S + HA/RBC (HA-coated RBC) system, and the sorption curves became closer to that of the S + HA/RBC system, indicating that HA may play a primary role in reducing the sorption capacity of RBC in the sediment. With higher HA contents, the sorption capacity of the complex sediments was lower and decreased more rapidly.     

Isolation and compound specific radiocarbon dating of terrigenous branched glycerol dialkyl glycerol tetraethers (brGDGTs)

The relative abundances and distributions of branched glycerol dialkyl glycerol tetraethers (brGDGTs) in marine and lacustrine sediments have been recently used as paleo-environmental proxies for the input of soil organic matter and past continental temperatures, respectively. The putative main source of brGDGTs is soil bacteria. Therefore, these biomarkers are also part of the soil organic matter stock that accumulates in the terrigenous environment. Here we present a method for isolating and purifying these compounds from lake sediments, soils and peat for radiocarbon (¹⁴C) measurement using a combination of normal and reversed phase high performance liquid chromatography, allowing complete separation of co-eluting compounds. Radiocarbon analysis was performed on an accelerator mass spectrometer system equipped with a gas ion source. We assessed the accuracy and the necessary corrections with modern and radiocarbon-dead procedural blanks. Blank assessment revealed that the reverse phase step introduced significant amounts of extraneous carbon, while the normal phase step did not. We show that with our method and instrumentation it is possible to obtain accurate and precise ¹⁴C analyses of brGDGTs with sample amounts as small as 10 μg C. Finally we demonstrate the application of the measurement of ¹⁴C concentrations of several brGDGTs isolated from lake sediments and peat soils.     

Properties of fluorescent dissolved organic matter in the Gironde Estuary

The isolation, characterization and study of the properties of aquatic dissolved organic matter (DOM) still represent a challenge because of the heterogeneity, complexity and low concentration of organic material in natural waters. Based on its ability to interact with contaminants and thus to modify their transport and bioavailability, DOM is of interest for environmental purposes. The objective of this work was to better characterize DOM in the Gironde Estuary (southwestern France). The estuary represents an exchange zone between the continent and the Atlantic Ocean and conditions the transfer of organic and inorganic substances from the continental to the oceanic environment. Several samples were collected along the estuary during three cruises in 2002 and 2006. They were analysed using excitation–emission matrix (EEM) spectroscopy, a sensitive technique that allows direct analysis of water samples. Fluorescent DOM and dissolved organic carbon (DOC) did not behave conservatively in this estuarine system, i.e. the organic material did not undergo simple dilution from the upstream to the downstream part of the estuary. A seasonal variability in DOC content was pointed out, whereas few seasonal variations in DOM fluorescence were observed. DOM sources and processing in the estuary were further evaluated by determining two fluorescence indices – the humification index (HIX) and the index of recent autochthonous contribution (BIX). By applying these indices, the relative degree of humification (HIX) and autotrophic productivity (BIX) could be assessed. Based on the fluorescence and DOC results, the estuary was divided into three zones depending on salinity (S) and characterized by specific DOM: (i) A turbid zone of low salinity (S < 5) and high suspended particulate matter concentration with increase in the intensities of the α′ and α fluorophores, characteristic of humic-like compounds. (ii) A mid-estuarine zone (5 < S < 25) characterized by low autotrophic productivity and containing strongly degraded organic material, as shown by the low values of BIX and high values of HIX. (iii) A higher salinity area (S > 25) characterized by increased autotrophic productivity and a marked marine influence, and associated with high and low values of BIX and HIX, respectively. The HIX and BIX indices were shown as useful tools for readily defining and classifying DOM characteristics in estuarine waters.     

Sources of polycyclic aromatic hydrocarbons (PAHs) to northwestern Saskatchewan lakes east of the Athabasca oil sands

The past several decades have witnessed a significant expansion of mining activities in the Athabasca oil sands region, raising concerns about their impact on the surrounding boreal forest ecosystem. To better understand the extent to which distal sites are impacted by oil sands-derived airborne contaminants, we examine sources of polycyclic aromatic hydrocarbons (PAHs) in surface sediments and dated sediment cores from Saskatchewan lakes situated ∼100–220 km east–northeast of the main area of bitumen mining activities. The concentrations and fluxes of both parent and alkylated PAHs are low and show considerable variability over the past 70–100 years. Small yet discernible increases in PAH concentrations and fluxes occurred over the past 30 years, a trend which coincides with the rapid growth in bitumen production. However, several lines of evidence point to wildfires as the principal source of PAHs to these lakes: (1) the significant co-variations in most cores between retene (1-methyl-7-isopropyl phenanthrene) and other groups of parent and alkylated PAHs, (2) the similarity in compound specific δ¹³C signatures of the parent PAHs phenanthrene and pyrene in recently deposited surficial sediments and those corresponding to time intervals considerably pre-dating the large scale development of the oil sands and (3) the discernible up-core increases in the proportion of refractory carbon (i.e., char) in Rock-Eval 6 data. The collective evidence points to softwood combustion from boreal forest fires as the principal source of retene in sediments and the general increase in forest fire activity in this region over the past several decades as the source of refractory carbon. Mining activities associated with the Athabasca oil sands are thus not considered a major source of PAHs to these lakes.     

Holocene hydro-climatic change and effects on carbon accumulation inferred from a peat bog in the Attawapiskat River watershed,Hudson Bay Lowlands,Canada

Multiple proxies from a 319-cm peat core collected from the Hudson Bay Lowlands, northern Ontario, Canada were analyzed to determine how carbon accumulation has varied as a function of paleohydrology and paleoclimate. Testate amoeba assemblages, analysis of peat composition and humification, and a pollen record from a nearby lake suggest that isostatic rebound and climate may have influenced peatland growth and carbon dynamics over the past 6700 cal yr BP. Long-term apparent rates of carbon accumulation ranged between 8.1 and 36.7 g C m^? 2 yr^? 1 (average = 18.9 g C m^? 2 yr^? 1). The highest carbon accumulation estimates were recorded prior to 5400 cal yr BP when a fen existed at this site, however following the fen-to-bog transition carbon accumulation stabilized. Carbon accumulation remained relatively constant through the Neoglacial period after 2400 cal yr BP when pollen-based paleoclimate reconstructions from a nearby lake (McAndrews et al., 1982) and reconstructions of the depth to the water table derived from testate amoeba data suggest a wetter climate. More carbon accumulated per unit time between 1000 and 600 cal yr BP, coinciding in part with the Medieval Climate Anomaly.     

Late Pleistocene desiccation of Lake Tana,source of the Blue Nile

High-resolution seismic data from Lake Tana, the source of the Blue Nile in northern Ethiopia, reveal a deep sedimentary sequence divided by four strong reflectors. Data from nearshore cores show that the uppermost strong reflector represents a stiff silt unit, interpreted as a desiccation surface. Channel cuts in this surface, bordered by levee-like structures, are apparent in the seismic data from near the lake margin, suggesting fluvial downcutting and over-bank deposition during seasonal flood events. Periphytic diatoms and peat at the base of a core from the deepest part of the lake overlie compacted sediments, indicating that desiccation was followed by development of shallow-water environments and papyrus swamp in the central basin between 16,700 and 15,100 cal BP. As the lake level rose, open-water evaporation from the closed lake caused it to become slightly saline, as indicated by halophytic diatoms. An abrupt return to freshwater conditions occurred at 14,750 cal BP, when the lake overflowed into the Blue Nile. Further reflection surfaces with downcut structures are identifiable in seismic images of the overlying sediments, suggesting at least two lesser lake-level falls, tentatively dated to about 12,000 and 8000 cal BP. Since Lake Victoria, the source of the White Nile, was also dry until 15,000 cal BP, and did not reach overflow until 14,500 cal BP, the entire Nile system must have been reduced to intermittent seasonal flow until about 14,500 cal BP, when baseflow was re-established with almost simultaneous overflow of the headwater lakes of both the White and Blue Nile rivers. Desiccation of the Nile sources coincides with Heinrich event 1, when cessation of northward heat transport from the tropical Atlantic disrupted the Atlantic monsoon, causing drought in north tropical Africa. The strong reflectors at deeper levels in the seismic sequence of Lake Tana may represent earlier desiccation events, possibly contemporaneous with previous Late Pleistocene Heinrich events.     

Modern carbon burial in Lake Qinghai,China

The quantification of carbon burial in lake sediments, and carbon fluxes derived from different origins are crucial to understand modern lacustrine carbon budgets, and to assess the role of lakes in the global carbon cycle. In this study, we estimated carbon burial in the sediment of Lake Qinghai, the largest inland lake in China, and the carbon fluxes derived from different origins. We find that: (1) The organic carbon burial rate in lake sediment is approximately 7.23 g m⁻² a⁻¹, which is comparable to rates documented in many large lakes worldwide. We determined that the flux of riverine particulate organic carbon (POC) is approximately 10 times higher than that of dissolved organic carbon (DOC). Organic matter in lake sediments is primarily derived from POC in lake water, of which approximately 80% is of terrestrial origin. (2) The inorganic carbon burial rate in lake sediment is slightly higher than that of organic carbon. The flux of riverine dissolved inorganic carbon (DIC) is approximately 20 times that of DOC, and more than 70% of the riverine DIC is drawn directly and/or indirectly from atmospheric CO₂. (3) Both DIC and DOC are concentrated in lake water, suggesting that the lake serves as a sink for both organic and inorganic carbon over long term timescales. (4) Our analysis suggests that the carbon burial rates in Lake Qinghai would be much higher in warmer climatic periods than in cold ones, implying a growing role in the global carbon cycle under a continued global warming scenario.     

Sorption of monoaromatic compounds to heated and unheated coals,humic acid,and biochar: Implication for using combustion method to quantify sorption contribution of carbonaceous geosorbents in soil

Batch sorption isotherms of two nonpolar compounds (1,3-dichlorobenzene and 1,3,5-trichlorobenzene) and two polar compounds (1,3-dinitrobenzene and 1,3,5-trinitrobenzene) to heated (at 375 °C for 24 h) and unheated coals (lignite and anthracite) were compared with those to a soil humic acid and a maize stalk derived biochar. For all test compounds, unheated lignite and anthracite exhibited much stronger sorption than humic substances (the organic carbon-normalized distribution coefficient was up to 2–3 orders of magnitude larger), but lower sorption than biochar. This sorption trend is consistent with the degree of sorbent condensation (biochar > coal > humic acid). The results indicate that sorption of the test sorbates (regardless of the difference in polarity) to soils would be dominated by carbonaceous geosorbents. Notably, the organic carbon contents of the coals were pronouncedly lowered by the heat treatment, from 47.4% to 7.3% for lignite, and from 80.1% to 58.1% for anthracite. Moreover, the heat treatment markedly decreased organic carbon-normalized distribution coefficient to coals (up to one order of magnitude), attributable to the decreased hydrophobicity of sorbents due to increased O-containing groups from oxidation. An important implication is that heat treatment, which is commonly used to quantify the content of carbonaceous geosorbents in soil and sediment, may cause significant underestimation of sorption contribution of carbonaceous geosorbents due to the combined effect of reduced organic carbon content and decreased hydrophobicity of less graphitized carbonaceous geosorbents (coals). This was illustrated using a widely adopted dual-component model that combines linear partition to humic substances (represented by humic acid) and nonlinear adsorption on condensed geosorbents (represented by biochar and coal).     

Isotope geochemistry of Swan Lake Basin in the Nebraska Sandhills,USA: Large 13C enrichment in sediment-calcite records

This study presents isotope geochemical analyses conducted on water column samples and core sediments collected from the Swan Lake Basin. Water analyses include the dissolved methane (CH₄) content and the ratio of carbon-13 to carbon-12 (δ¹³C) in dissolved inorganic carbon (DIC). The core sediments – sandy muds containing inorganic calcite, organic matter, and opal phases ± ostracods – were examined by X-ray diffraction, dated by radiocarbon (¹⁴C), analyzed for wt% organic carbon, wt% organic nitrogen, wt% organic matter, wt% calcite, δ¹³C of bulk-sediment insoluble organic matter (kerogen), ¹⁸O:¹⁶O ratio (δ¹⁸O) and δ¹³C of bulk and ostracod calcite. Of particular significance is the large enrichment in carbon-13 (δ¹³C = +4.5 to +20.4‰ V-PDB) in the calcite of these sediments. The ¹³C-enriched calcite is primarily formed from DIC in the water column of the lake as a result of the following combined processes: (i) the incorporation of ¹³C enriched residual carbon dioxide (CO₂) after partial reduction to CH₄ in the sediments and its migration into the water column-DIC pool; (ii) the preferential assimilation of ¹²C by phytoplankton during photosynthesis; (iii) the removal of ¹³C-depleted CH₄ by ebullition and of organic matter by sedimentation and burial. The ¹³C enrichment was low between 3624 and 2470 yr BP; high between 2470 and 1299 yr BP; and moderate since 1299 yr BP. Low ¹³C enrichment was formed under low water-column carbon levels while higher ones were formed under elevated rates of biomass and calcite deposition. These associations seem to imply that biological productivity is the main reason for carbon-13 enrichments.     

Historical lead pollution in the central region of Guizhou province,China: A record of lead stable isotopes of lake sediments

Economic reform in China since 1978 has accelerated economic development nationwide hugely, but has also brought about some environmental pollution. In order to identify the primary Pb source to the atmosphere in the central Guizhou region, Pb isotopic ratios in the acid soluble fraction of sediment from Hongfeng Lake were investigated. Lead isotopes in the lake sediments record the history of regional atmospheric Pb pollution. Before the economic reform in 1978, the ²⁰⁸Pb/²⁰⁶Pb and ²⁰⁶Pb/²⁰⁷Pb ratios in the leachates of lake sediments were constant, with a range of 2.0060 to 2.0117 and of 1.2314 to 1.2355, respectively. In the early period of economic reform (1978 to 1988), with the rapid industrial growth in Guizhou province, the acid soluble Pb isotope ratios in the lake sediments changed sharply: the ²⁰⁸Pb/²⁰⁶Pb ratios increased from 2.0212 to about 2.05, while the ²⁰⁶Pb/²⁰⁷Pb ratios decreased from 1.2251 to 1.2060. Emissions from Pb-ore-related industries are suggested to be the major pollution source of Pb in this period. Due to output from a local power plant since 1988, the isotope ratios of the acid soluble Pb in sediments in 1990s are characterized by a little higher radiogenic Pb (²⁰⁸Pb/²⁰⁶Pb = 2.0340–2.0400; ²⁰⁶Pb/²⁰⁷Pb = 1.2122–1.2158) than for the 1980s.     

Exploring former subglacial Hodgson Lake,Antarctica. Paper II: palaeolimnology

Direct exploration of subglacial lakes buried deep under the Antarctic Ice Sheet has yet to be achieved. However, at retreating margins of the ice sheet, there are a number of locations where former subglacial lakes are emerging from under the ice but remain perennially ice covered. One of these lakes, Hodgson Lake (72°00.549′S, 068°27.708′W) has emerged from under more than 297–465 m of glacial ice during the last few thousand years. This paper presents data from a multidisciplinary investigation of the palaeolimnology of this lake through a study of a 3.8 m sediment core extracted at a depth of 93.4 m below the ice surface. The core was dated using a combination of radiocarbon, optically stimulated luminescence, and relative palaeomagnetic intensity dating incorporated into a chronological model. Stratigraphic analyses included magnetic susceptibility, clast provenance, organic content, carbonate composition, siliceous microfossils, isotope and biogeochemical markers. Based on the chronological model we provisionally assign a well-defined magnetic polarity reversal event at ca 165 cm in the lake sediments to the Mono Lake excursion (ca 30–34 ka), whilst OSL measurements suggest that material incorporated into the basal sediments might date to 93 ± 9 ka. Four stratigraphic zones (A–D) were identified in the sedimentological data. The chronological model suggests that zones A–C were deposited between Marine Isotope Stages 5–2 and zone A during Stage 1, the Holocene. The palaeolimnological record tracks changes in the subglacial depositional environment linked principally to changing glacier dynamics and mass transport and indirectly to climate change. The sediment composition in zones A–C consists of fine-grained sediments together with sands, gravels and small clasts. There is no evidence of overriding glaciers being in contact with the bed reworking the stratigraphy or removing this sediment. This suggests that the lake existed in a subglacial cavity beneath overriding LGM ice. In zone D there is a transition to finer grained sediments characteristic of lower energy delivery coupled with a minor increase in the organic content attributed either to increases in allochthonous organic material being delivered from the deglaciating catchment, a minor increase in within-lake production or to an analytical artefact associated with an increase in the clay fraction. Evidence of biological activity is sparse. Total organic carbon varies from 0.2 to 0.6%, and cannot be unequivocally linked to in situ biological activity as comparisons of δ¹³C and C/N values with local reference data suggest that much of it is derived from the incorporation of carbon in catchment soils and gravels and possibly old CO₂ in meteoric ice. We use the data from this study to provide guidelines for the study of deep continental subglacial lakes including establishing sediment geochronologies, determining the extent to which subglacial sediments might provide a record of glaciological and environmental change and a brief review of methods to use in the search for life.     

Holocene lake stages and thermokarst dynamics in a discontinuous permafrost affected region,north-eastern Tibetan Plateau

Sediments of a thermokarst system on the north-eastern Tibetan Plateau were studied to infer changes in the lacustrine depositional environment related to climatic changes since the early Holocene. The thermokarst pond with a length of 360 m is situated in a 14.5 × 6 km tectonically unaffected intermontane basin, which is underlain by discontinuous permafrost.A lake sediment core and bankside lacustrine onshore deposits were analysed. Additionally, fossil lake sediments were investigated, which document a former lake-level high stand. The sediments are mainly composed of marls with variable amounts of silt carbonate micrite, and organic matter.On the basis of sedimentological (grain size data), geochemical (XRF), mineralogical (XRD) and micropaleontological data (ostracods and chironomide assemblages) a reconstruction of a paleolake environment was achieved.Lacustrine sediments with endogenic carbonate precipitation suggest a lacustrine environment since at least 19.0 cal ka BP. However, because of relocation and reworking processes in the lake, the sediments did not provide distinct information about the ultimate formation of the lake. The high amount of endogenic carbonate suggests prolonged still-water conditions at about 9.3 cal ka BP. Ostracod shells and chironomid head capsules in fossil lake sediments indicate at least one former lake-level high stand, which were developed between the early and middle Holocene. From the late Holocene the area was possibly characterized by a lake-level decline, documented by a hiatus between lacustrine sediments and a reworked loess or loess-like horizon. After the lake-level decline and the following warming period, the area was affected by thermally-induced subsidence and a re-flooding of the basin because of thawing permafrost.     

Ancient landslide-dam events in the Jishi Gorge,upper Yellow River valley,China

Some scholars have argued that the formation and outburst of an ancient dammed lake in the Jishi Gorge at ca. 3700 cal yr BP resulted in the destruction of Lajia, the site of a famous prehistoric disaster in the Guanting Basin, upper Yellow River valley, China. However, the cause of the dammed lake and the exact age of the dam breaching are still debated. We investigated ancient landslides and evidence for the dammed lake in the Jishi Gorge, including dating of soil from the shear zone of an ancient landslide, sediments of the ancient dammed lake, and loess above lacustrine sediments using radiocarbon and optically stimulated luminescence (OSL) dating methods. Six radiocarbon dates and two OSL dates suggested that the ancient landslides and dammed lake events in the Jishi Gorge probably occurred around 8100 cal yr BP, and the ancient dammed lake was breached between 6780 cal yr BP and 5750 cal yr BP. Hence, the outburst of the ancient dammed lake in the Jishi Gorge was unrelated to the ruin of the Lajia site, but likely resulted in flood disasters in the Guanting Basin around 6500 cal yr BP.     

Holocene variability of the Southern Hemisphere westerlies in Argentinean Patagonia (52°S)

High-resolution analyses of allochthonous pollen input into crater lake sediments of Laguna Potrok Aike in the semi-arid Patagonian steppe reflect the variability of zonal wind intensities during the Holocene at 52° southern latitude. These indicators for Southern Hemisphere westerlies (SHW) strength vary on centennial timescales in concert with carbon/nitrogen (C/N) ratios and titanium (Ti) contents, interpreted as differential organic matter sources and minerogenic input to the sediment, respectively. The correlations underline a linkage between hydrological variability and west wind variability in Extra-Andean Patagonia. A shift to generally more intense SHW suggests intensification towards modern wind conditions at that latitude since 9.2 ka cal BP.     

The distribution and abundance of chironomids in high-latitude Eurasian lakes with respect to temperature and continentality: development and application of new chironomid-based climate-inference models in northern Russia

The large landmass of northern Russia has the potential to influence global climate through amplification of climate change. Reconstructing climate in this region over millennial timescales is crucial for understanding the processes that affect the global climate system. Chironomids, preserved in lake sediments, have the potential to produce high resolution, low error, quantitative summer air temperature reconstructions. Canonical correspondence analysis of modern surface sediments from high-latitude lakes, located in northern European Russia and central Siberia, suggests that mean July air temperature is the most significant variable explaining chironomid distribution and abundance. This strong relationship enabled the development of a chironomid-based mean July air temperature-inference model based on 81 lakes and 89 taxa which has a r_jack² = 0.92 and RMSEP = 0.89 °C. Comparison of taxon responses to July temperature between this Russian and existing Norwegian data-sets shows that the temperature optima of individual taxa were between 1 and 3 °C higher in the Russian data regardless of modelling technique. Reconstructions based on fossil assemblages from a Russian tundra lake core (VORK5) using a Norwegian chironomid-based inference model provide mean July air temperature estimates that are 1.0–2.7 °C colder than from the 81-lake Russian model and are also lower than the instrumental record from a nearby meteorological station. The Norwegian model also did not reconstruct decadal-scale fluctuations in temperature seen in the instrumental record. These observations suggest that chironomid-based inference models should only be applied to sediment cores which have similar climate regimes to the geographic area of the training set. In addition a 149 lake, 120 taxa chironomid-based continentality inference model was also developed from the modern Norwegian and Russian training sets. A 2-component WA-PLS model was the minimal adequate model with r_jack² = 0.73 and RMSEP = 9.9 using the Gorczynski continentality index. Comparison of reconstructed continentality indices from the tundra lake, VORK5, show close agreement with local instrumental records over the past 70 years and suggest that the model is reliable. Recent warming in the Arctic has been spatially and seasonally heterogeneous; in many areas warming is more pronounced in the spring and autumn leading to a lengthening of the summer, while summer temperatures have remained relatively stable. A continentality inference model has the potential to detect these seasonal changes in climate.     

Sustainability of humic acids in the presence of magnesium oxide

The Waste Isolation Pilot Plant (WIPP) is a U.S. Department of Energy (DOE) repository for the disposal of transuranic waste generated from the U.S. defense program. Humic acids (HA), known to strongly bind to actinides and which may be generated by the degradation of organic materials present in the waste, may influence the performance of the WIPP. This work presents experimental results on the effect of WIPP brines, ERDA-6 and GWB, and of the WIPP engineered barrier, Premier Chemicals magnesium oxide, on the solubility of HA. In the absence of MgO, a portion of HA initially precipitates, but a constant concentration of HA remains in solution: over a 60 day period of time, at least 290 ± 10 mg/L HA can remain soluble in de-ionized (DI) water, 30 ± 4 mg/L in 95% ERDA-6, and 31 ± 4 mg/L in 95% GWB. For solutions initially containing from 0 to 400 mg/L HA, the ratio of the initial HA concentration and the soluble HA concentration is 1.3 in DI water, 13 in 95% ERDA-6, and 11 in 95% GWB. In the presence of MgO, all HA precipitate within 60 days in systems with a high liquid-to-solid ratio (10.0 g/g) or a low ratio (2.4 g/g). This phenomenon is due to HA precipitation and/or sorption on the surface of MgO.     

The varve-related ice-dammed lake events in Glen Roy and vicinity: a new interpretation

This paper presents a new interpretation of the sequence of events in Glen Roy and vicinity during the Loch Lomond Stadial that can be inferred from a detailed varve record constructed by Palmer et al. (2010). 300 years of Younger Dryas glacier advance in the Scottish Highlands are recorded by very thin varves formed in an ice-dammed lake up to 35 km long. At a varve site now occupied by Loch Laggan the lake stood permanently at 260 m, but in Glen Roy varves were also laid down in a lake at 325 m and, later, 350 m caused by glacier advance. Initial ice retreat recorded by a gradual increase in varve thickness was soon followed by much thicker varves. The varve sequences are interrupted by a sand bed caused by sudden drainage of the 350 m lake. The major varves of the Glen Roy sequence show that storminess was still increasing in intensity at least 160 years after glacier retreat had begun. At the Loch Laggan site 15 cm of deformed sediments register an earthquake that produced 3 m faulted uplift of all three Glen Roy shorelines, a response to the abrupt removal of 5 km³ of water when the 260 m lake was catastrophically drained by jökulhlaup. The deformed sediments are immediately followed by varves deposited in a local lake, ice-dammed lake sedimentation now having ceased, having lasted more than 460 years.     

Hydrothermal petroleum of Lake Chapala,Citala Rift,western Mexico: Bitumen compositions from source sediments and application of hydrous pyrolysis

Hydrothermal simulation experiments were performed with contemporary sediments from Lake Chapala to assess the source of the lake tars. The precursor-product relationships of the organic compounds were determined for the source sediments and their hydrous pyrolysis products. The pyrolysis products contained major unresolved complex mixtures of branched and cyclic hydrocarbons, low amounts of n-alkanes, dinosterane, gammacerane, and immature and mature hopane biomarkers derived from lacustrine biomass sources. The results support the proposal that the tar manifestations in the lake are not biodegraded petroleum, but were hydrothermally generated from lacustrine organic matter at temperatures not exceeding about 250 °C over brief geological times.     

Thermal degradation of rye and maize straw: Lipid pattern changes as a function of temperature

Future climatic conditions may coincide with an increased potential for wildfires in grassland and forest ecosystems, whereby charred biomass would be incorporated into soils. Molecular changes in biomass upon charring have been frequently analysed with a focus on black carbon. Aliphatic and aromatic hydrocarbons, known to be liberated during incomplete combustion of biomass have been preferentially analysed in soot particles, whereas determinations of these compounds in charred biomass residues are scarce. We discuss the influence of increasing charring temperature on the aliphatic and aromatic hydrocarbon composition of crop grass combustion residues. Straw from rye, representing C₃ grasses and maize, representing C₄ grasses, was charred in the presence of limited oxygen at 300, 400 and 500 °C. Typical n-alkane distribution patterns with a strong predominance of long chain odd-numbered n-alkanes maximising at C₃₁ were observed in raw straw. Upon combustion at 300 °C aliphatic hydrocarbons in char were dominated by sterenes, whereas at 400 °C sterenes disappeared and medium chain length n-alkanes, maximising around n-C₂₀, with a balanced odd/even distribution were present. At a charring temperature of 500 °C n-alkane chain length shifted to short chain homologues, maximising at C₁₈ with a pronounced predominance of even homologues. Even numbered, short chain n-alkanes in soils may thus serve as a marker for residues of charred biomass. Aromatic hydrocarbons indicate an onset of aromatization of biomass already at 300 °C, followed by severe aromatization upon incomplete combustion at 400–500 °C. The diagnostic composition of aliphatic and aromatic hydrocarbons from charred biomass affords potential for identifying residues from burned vegetation in recent and fossil soils and sediments.     

Carbon chain length distribution in n-alkyl lipids: A process for evaluating source inputs to Lake Qinghai

Lake sediments generally contain a mixture of terrestrial and aquatic source inputs, and determining the major inputs is important for understanding geological records in paleoenvironment and paleoclimate research. In this study we describe the distribution of n-alkanes and n-fatty acids (FAs) in representative modern plants from around Lake Qinghai. We found a significant difference in the average length of n-FA carbon chains (ACL Fa_16–32) in terrestrial (23.3) and aquatic plants (18.6). The results reveal that ACL Fa_16–32 may essentially serve as a proxy for evaluating the major source inputs to lake sediments. Assessment of surface sediments from the lake showed that the FAs originated from a mixture of inputs, with the aquatic source input predominant at most sites. Additionally, the δD values of sediment mid-chain n-acids (C₂₂) showed a relationship with the ACL Fa_16–32 proxy: an increased Fa ACL corresponded to more negative hydrogen isotope ratio values. We suggest that different sources should be considered and ACL Fa_16–32 could be a potential calibration proxy before using δD values to extract reliable isotopic information from lake water. More attention should be paid to source inputs and their relationship to other geochemical proxies in future studies of lake sediments.