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1.
Modeling the bulk sediment XRD patterns allows insight into the environmental and depositional histories of two neighboring rift lake basins within the Baikal watershed. Parallel 14C-dated LGM-Holocene records in Lakes Baikal and Hovsgol are used to discuss the mineralogical signatures of regional climate change. In both basins, it is possible to distinguish ‘glacial’ and ‘interglacial’ mineral associations. Clay minerals comprise in excess of 50% of layered silicates in bulk sediment.The abundance of smectite (expandable) layers in mixed-layer illite–smectites and the total illite abundance are the main paleoclimatic indices in the clay mineral assemblage. Both indices exhibit coherent responses to the Bølling–Allerød and the Younger Dryas. The smectite layer index is not equivalent to the abundance of illite–smectite, because illite–smectite tends to transform into illite. Repeated wetting–drying cycles in soils and high abundance of expandable layers in illite–smectites (>42%) favor the process of illitization. This relationship is clearly shown in both Baikal and Hovsgol records for the first time. The opposite late Holocene trends in illite abundance in Lake Baikal and Lake Hovsgol records suggest that a sensitive optimal regime may exist for illite formation in the Baikal watershed with regard to warmth and effective moisture.The Lake Hovsgol sediments of the last glacial contain carbonates, suggesting a positive trend in the lake's water budget. A progressive change towards lower Mg content in carbonates indicates lowering mineralization of lake waters. This trend is consistent with the lithologic evidence for lake-level rise in the Hovsgol basin.The pattern of mineralogical changes during the past 20 ka is used to interpret bulk sediment and carbonate mineralogy of the long 81-m Lake Hovsgol drill core (HDP-04) with a basal age of 1 Ma. The interglacial-type silicate mineral associations are confined to several thin intervals; most of the sediment record is calcareous. Carbonates are represented by six main mineral phases: calcite, low-Mg calcite, intermediate/high-Mg calcite, dolomite, excess-Ca dolomite and metastable monohydrocalcite. These mineral phases tend to form stratigraphic successions indicative of progressive changes in lake water chemistry. Five sediment layers with abundant Mg-calcites in the HDP-04 section suggest deposition in a low standing lake with high mineralization (salinity) and high Mg/Ca ratios of lake waters. Lake Hovsgol sediments contain the oldest known monohydrocalcite, found tens of meters below lake bottom in sediments as old as 800 ka. This unusual find is likely due to the conditions favorable to preservation of this metastable carbonate.  相似文献   

2.
Lake sediment composition as an indicator of mineralization within the catchment area has found widespread application in recent years, particularly in Canada. Results have indicated, however, the existence of varying relationships between lake sediment composition and mineralization resulting from local features of the limnological environment. Accordingly it was considered appropriate to examine the nature of metal transport in the lake and stream environment, the partitioning of metal between the stream waters and stream sediments and between lake waters and lake sediments to obtain some understanding of the factors that affect the lake sediment-mineralization relationship. This investigation was carried out over an area containing Pb-Zn occurrences of supposed “Mississippi-Valley type” in Grenville and Paleozoic bedrock in southeastern Ontario.The headwater drainage systems comprise active streams, swamps, beaver ponds and small lake-bog systems giving way downstream to open lakes. The beaver swamps and seasonal swamps act as drainage sinks for metals, restricting the extent of geochemical dispersion in drainage systems adjacent to mineralization. Selective extraction analysis of bog, stream and lake sediments indicates that metals are preferentially concentrated with amorphous iron oxides, which readily adsorb and complex lead and zinc and are stable in the alkaline environment common in swamps adjacent to carbonate-hosted lead-zinc mineralization. The accumulation of lead and zinc with amorphous iron oxides combined with the adsorbing and chelating action of organic matter on lead and zinc makes organic-rich sediments from these small swampy areas an excellent sample medium for reflecting local mineralization. Down drainage anomalies of these elements can be accentuated by selective analysis for the amorphous iron oxide-held metal, involving selective extraction techniques.In contrast, within larger lake systems, the analysis of water samples indicates that geochemical dispersion in surface waters in the high pH environment (pH = 8.0) associated with the carbonate-hosted lead-zinc deposits is extremely restricted. In this environment, anomalous metal contents in lake water were not evident in lakes adjacent to mineralization, while anomalous lake sediment compositions exist only in lakes immediately adjacent to Pb-Zn mineralization and do not extend down the drainage system. The restricted dispersion necessitates basing geochemical reconnaissance surveys on collection and analysis of samples from the headwater organic-rich swamps at a higher sample density and resulting higher cost than in areas where a lower sample density is acceptable due to a wider dispersion.  相似文献   

3.
R. W. RENAUT 《Sedimentology》1993,40(2):271-301
Late Quaternary fluviolacustrine siltstones, mudstones and claystones (Loboi Silts) on the northern margins of the saline, alkaline Lake Bogoria in the Kenya Rift Valley contain up to c. 40% authigenic analcime and minor natrolite. The zeolitic sediments are reddish brown and up to 1 m thick. The amount of analcime increases upward in the profile, but decreases with distance from the lake. The altered sediments show many pedogenic features including zeolitic root mats, rootmarks, concretions and carbonate rhizoliths. Residual patches of calcrete locally cap the zeolitic rocks. The profile is interpreted as an exhumed palaeosol and land surface on the former margins of the lake. The analcime occurs as submicroscopic (0–5–2–5 μ.m) subhedral and euhedral crystals, which have an average Si/A 1 ratio of 2–33 (as determined by X-ray microanalysis) or 2–18 (d-value of 639 analcime peak). The analcime formed in lake marginal sediments (soils) by reaction of silicate detritus with Na2CO3 rich pore waters concentrated close to the land surface by evaporative pumping and evapotranspiration. Poorly ordered clay minerals were probably the main reactants. Authigenic illite may have been a by-product of the reactions. Chemical analyses suggest that pore waters supplied some of Na+, and possibly K+ and SiO2. The associated calcrete and rhizoliths were formed during or shortly after the main period of zeolitic alteration. The Ca2+ may have originated from infiltrating dilute runoff and groundwater. Authigenic smectite was precipitated in open porosity following analcime formation. The zeolitic alteration at Lake Bogoria provides a relatively recent analogue for lake marginal zeolites found in many ancient saline, alkaline lake sediments.  相似文献   

4.
To understand the geochemical cycle of Hg in hypereutrophic freshwater lake, two sampling campaigns were conducted in Lake Taihu in China during May and September of 2009. The concentrations of unfiltered total Hg (unfTHg) were in the range of 6.8–83 ng L−1 (28 ± 18 ng L−1) in the lake water and total Hg in the sediment was 12–470 ng g−1, both of which are higher than in other background lakes. The concentration of unfTHg in ∼11% of the lake water samples exceeded the second class of the Chinese environmental standards for surface water of 50 ng L−1 (GB 3838-2002), indicating that a high ecological risk is posed by the Hg in Lake Taihu. However, the concentrations of unfiltered total MeHg (unfMeHg) were relatively low in the lake water (0.14 ± 0.05 ng L−1, excluding two samples with 0.81 and 1.0 ng L−1). Lake sediment MeHg varied from 0.2–0.96 ng g−1, with generally low ratios of MeHg/THg of <1%. The low concentrations of TMeHg in the lake water may have resulted from a strong uptake by the high primary productivity and the demethylation of MeHg in oxic conditions. In addition, contrary to the results of previous research conducted in deep-water lakes and reservoirs, the low concentrations of MeHg and low ratio of MeHg/THg in the lake sediment indicates that the net methylation of Hg was not accelerated by the elevated organic matter load created by the eutrophication of Lake Taihu. The results also showed that sediments were a source of THg and MeHg in the water. Higher diffusion fluxes of THg and MeHg may be partly responsible for the higher concentrations of THg in the lake water in May, 2009.  相似文献   

5.
Long-chain alkenones in lacustrine settings are potentially excellent biomarkers for the reconstruction of past terrestrial environmental conditions, and have been found in many different types of lakes around the globe. A wider range of factors influence the occurrence and distribution of alkenones in lake sediments and waters when compared to marine systems. Lake environmental conditions, such as temperature (in particular) and salinity, are among the key factors controlling alkenone distributions in lacustrine settings. Here we investigated alkenone distribution patterns in lakes of the northern Qinghai-Tibetan Plateau, China, and their possible relationship with environmental conditions, by analyzing paired samples of suspended particulate matter in surface waters and surface sediments. Salinity of investigated lake waters ranges from almost 0 to ∼100 g/L, while temperature variation among the lakes is minimal, effectively eliminating temperature effects on the alkenone distribution patterns observed here. We show that (1) alkenone concentrations vary substantially between the lakes, yet controlling mechanisms remain elusive; (2) C37/C38 ratios are substantially lower in the lakes of the Qaidam Basin than in the Lake Qinghai region, probably indicating different alkenone producers in the two regions; and (3) large variations in %C37:4 (the percentage of the C37:4 alkenone), determined from both surface waters and sediments, are negatively correlated with salinity. We suggest that the %C37:4 index could be used as a salinity indicator at least on a regional scale, with careful considerations of other potentially complicating factors. However, potential reasons for why salinity could significantly affect %C37:4 values need further investigation.  相似文献   

6.
The sediments in Lake Huguang Maar in coastal South China were previously thought to originate mainly from wind-blown dust transported from North China, such that the lake sediments recorded the varying strength of the Asian winter monsoon. An alternative explanation was that the local pyroclastic rocks supplied the lake sediments, but the actual contributions from the different sources remained unclear. Geochemical analyses including 87Sr/86Sr and 143Nd/144Nd and trace elements support the local pyroclastic rock as the dominant source: < 22% of the total Sr in the lake sediments and  17% of the Nd arises from the distant source. Nb/Ta and Zr/Hf for the lake sediments are identical to those for the local rock but differ from the ratios for the wind-blown dust, and chondrite-normalized rare earth element patterns for the lake sediments are similar to those for the local rock and soil, but differ from those for the distant source. The sediments in Lake Huguang Maar are probably input into the lake through runoff and thus controlled by the hydrology of the lake. Wind-blown dust transported by the Asian winter monsoon from arid North China is only a minor contribution to the sediments.  相似文献   

7.
The carbonates, clays and major chemical compositions of lacustrine sediments in Nam Co (Lake) were examined by X-ray diffraction, scanning electron microscopy and chemical analysis. Carbonates include monohydrocalcite (MHC, first report from China and in a high-altitude lake), low-Mg calcite and traces of dolomite. MHC in Nam Co is developed in water (1.8 g/L) with high Mg/Ca molar ratios (10.03–15.03), high pH (8.04–9.72) and the presence of bacteria, algae, diatom and ostracoda. Illite and Mg-chlorite provide a strong evidence for physical weathering in the Holocene. Most Ca and Sr in sediments originate from carbonates as the molar ratios of Ca and CO32− are all less than 1 and the curve of Sr is very similar to that of Ca. However, most of the Mg, Fe and Rb are from clays. The lake water shifted from a fresh water environment to an evaporative, alkaline environment by 2.06 cal. ka BP. There was a depositional event that the depositional rate changed from 0.134 to 1.639 mm/a at about 2 cal. ka BP.  相似文献   

8.
Capillary gas chromatography-mass spectrometry (C-GC-MS) and Iatroscan thin layer chromatography-flame ionisation detection (TLC-FID) were used to study hydrocarbon distributions in a sediment core from Ace Lake, a saline, meromictic lake in the Vestfold Hills of Antarctica. Hydrocarbons were abundant in most core sections (up to 125/μg/g dry wt), particularly in near-surface samples, and the distributions were very complex. Major constituents were identified as phytane, 2,6,10,15,19-pentamethyleicosane, tetrahydrosqualene, a mixture of phytenes, cholesta-3,5-diene and fern-7-ene. Smaller amounts of sterenes and hopenes were also present. The predominance of the first 3 acyclic isoprenoids in sediments buried less than 30 cm is consistent with high populations of methanogenic bacteria known to be present.Phytenes were abundant in all core sections, and there was no relationship between their abundance and that of phytane which suggests that they were not derived from methanogenic bacteria. Phytadienes were minor constituents at all depths studied. An unusual feature of some distributions was the high concentrations of fern-7-ene which was the major hydrocarbon in the 20–25 cm core section. This alkene was only abundant in sediments which contained high concentrations of methanogen markers suggesting that it may also be indicative of anoxic depositional environments. A possible source might be from purple non-sulphur bacteria. High concentrations of straight-chain C29 and C34 alkenes were also found in these sediments but their origin has not been determined. Major changes in the hydrocarbon distributions with depth indicate that the depositional environment in the lake has altered dramatically since the lake was formed less than 8000 years ago. The present condition of permanent anoxic bottom waters probably developed only in the last 1000 years.  相似文献   

9.
《Applied Geochemistry》2006,21(10):1799-1817
Release of acid drainage from mine-waste disposal areas is a problem of international scale. Contaminated surface water, derived from mine wastes, orginates both as direct surface runoff and, indirectly, as subsurface groundwater flow. At Camp Lake, a small Canadian Shield lake that is in northern Manitoba and is ice-covered 6 months of the year, direct and indirect release of drainage from an adjacent sulfide-rich tailings impoundment has severely affected the quality of the lake water. Concentrations of the products from sulfide oxidation are extremely high in the pore waters of the tailings impoundment. Groundwater and surface water derived from the impoundment discharge into a semi-isolated shallow bay in Camp Lake. The incorporation of this aqueous effluent has altered the composition of the lake water, which in turn has modified the physical limnology of the lake. Geochemical profiles of the water column indicate that, despite its shallow depth (6 m), the bay is stratified throughout the year. The greatest accumulation of dissolved metals and SO4 is in the lower portion of the water column, with concentrations up to 8500 mg L−1 Fe, 20,000 mg L−1 SO4, 30 mg L−1 Zn, 100 mg L−1 Al, and elevated concentrations of Cu, Cd, Pb and Ni. Meromictic conditions and very high solute concentrations are limited to the bay. Outside the bay, solute concentrations are lower and some stratification of the water column exists. Identification of locations and composition of groundwater discharge relative to lake bathymetry is a fundamental aspect of understanding chemical evolution and physical stability of mine-impacted lakes.  相似文献   

10.
The wide boron isotopic variations occurring in natural waters mainly are derived from the 20‰ fractionation between dissolved boric acid and borate anions, associated with the preferential removal from the system of 11B depleted borate ions by adsorption and/or minerals formation. Typical adsorbants of boron dissolved in groundwater are clay minerals of the aquifer matrix. Boron (and strontium) isotopes were used in investigating two alluvial aquifers in Tuscany, where boron concentration is often above 1 mg L− 1 and may attain 8 mg L− 1. The isotopic results indicate that, in the first case (Cecina River basin), the boron contamination is anthropogenic and derives from past discharge into streams of boron-rich industrial wastes. In the second case (Cornia Plain), the dissolved boron is released by boron-rich clayey sediments of the aquifer matrix and has, therefore, a natural origin.  相似文献   

11.
As one of the lakes on the Yunnan-Guizhou plateau, Lake Chenghai, which is a typical closed lake with the precipitation accounting for one-third or more of the annual water input, has a high total salinity (almost like a saline lake). The inorganic C, O isotopic composition of lake sediments bears much sensitive information about environmental change in the catchment, while their correlations revealed the hydrological conditions under which the lake was closed. Their compositional variations are controlled by temperature, precipitation, photosynthesis, dissolving equilibrium of the carbonate system and hydrological condition. According to our research on inorganic C, O isotopic composition of Lake Chenghai sediments, we investigated the environmental change of this catchment several decades ago. The results showed that Lake Chenghai has kept good hydrological closing conditions in the past several decades, as indicated by the good correlation of inorganic C, O isotopic composition of sediments; and that the environmental change in this catchment shows a tendency of periodical evolution on a 10−11-years scale, although the signal noise is relatively high at the bottom of the sediment core. And we also can extend C, O isotopes, a sensitive environmental indicator, to nearly saline lake environments with a high degree of mineralization.  相似文献   

12.
Concentrations of Au, Ag, As, Cd and Sb in aquatic bryophytes collected from the Dolgellau Mineral Belt, North Wales, U.K. are reported. One aquatic liverwort, Scapania undulata (L) Dum. and two mosses, Fontinalis squamosa Hedw. and Racomitrium aciculare (Hedw.) Brid. were collected from sites upstream and downstream of the recently reopened Gwynfyndd Au mine. There was little inter-species variation in metal contents for these three bryophytes, but Scapania undulata appeared the most sensitive to changes in water concentrations of Ag, As and Sb. Gold concentrations varied little between the contaminated and control sites. Concentrations in the range < 4–18 ng Aug g−1 D.W. were typical background levels, while bryophytes collected immediately below the mine contained 6–45 ng Au g−1. Silver and Sb both showed more pronounced ( 5–10 fold) elevations above control concentrations in samples collected downstream of the mine. Background concentrations for these elements were 5–85 ng Ag g−1 and 0.15–1.3 μg Sb g−1.Arsenic concentrations downstream of the mine (160–1080 μg g−1) greatly exceeded the background range of 9–32 μg g−1. It is suggested, therefore, that As may be an ideal ‘pathfinder’ element when prospecting for auriferous deposits using aquatic bryophytes.  相似文献   

13.
Lacustrine sediments, submerged tailings, and their pore waters have been collected at several sites in Yellowknife Bay, Great Slave Lake, Canada, in order to investigate the biogeochemical controls on the remobilization of As from mining-impacted materials under different depositional conditions. Radiometric dating confirms that a mid-core enrichment of Pb, Zn, Cu and Sb corresponds to the opening of a large Au mine 60 a ago. This was evident even in a relatively remote site. Arsenic was enriched at mid-core, coincident with mining activity, but clearly exhibited post-depositional mobility, migrating upwards towards the sediment water interface (SWI) as well as down-core. Deep-water (15 m) Yellowknife Bay sediments that contain buried mine waste are suboxic, relatively organic-rich and abundant in microbes with As in pore waters and sediments reaching 585 μg/L and 1310 mg/kg, respectively. Late summer pore waters show equal proportions of As(III) and As(V) (16–415 μg/L) whereas late winter pore waters are dominated by As(III) (284–947 μg/L). This can be explained by As(III) desorption mechanisms associated with the conversion of FeS to FeS2 and the reduction of As(V) to As(III) through the oxidation of dissolved sulfide, both microbially-mediated processes. Processes affecting As cycling involve the attenuating efficiency of the oxic zone at the SWI, sediment redox heterogeneity and the reductive dissolution of Fe(hydr)oxides by labile organic matter, temporarily and spatially variable.  相似文献   

14.
A strategy to neutralize acidic pit lakes was tested in an upscaling process using field mesocosms of 26 to ca. 4500 m3 volume in the acidic pit Mining Lake 111 in Germany. After addition of the substrates Carbokalk and straw a neutral sediment layer formed, in which microbial sulfate and iron reduction as well as sulfide precipitation occurred. The net rate of neutralization was limited by the precipitation of iron sulfides rather than by microbial reactions. Oxidation of H2S by ferric iron in the anoxic sediment lowered the net sulfate reduction rate. Seasonal fluctuations of iron sulfides in the sediment showed that the reaction products were not necessarily stable. The long-term success of the approach depends on the net partition of the precipitated iron-(mono-/di-) sulfide that is permanently buried in the anoxic sediment. It could be shown by field experiments that the long-term success of the neutralization depends on the spatial scale and duration of the experiments. Volumes from 26 to 4500 m3, exposition times from 4 months to 5 years, and increasingly thick coverings of the sediments with straw, from zero to 40 cm, were used. Net neutralization rates decreased from 41 meq m− 2 d− 1 in laboratory microcosms to a mean rate of 2.3 meq m− 2 d− 1 in the 4500 m3 field experiment. The results show that the success of the microbial treatment of acid pit lakes lastly depends on the limnological conditions in the lake that cannot be simulated by upscaling of simple laboratory experiments.  相似文献   

15.
Waters from abandoned Sb-Au mining areas have higher Sb (up to 2138 μg L−1), As (up to 1252 μg L−1) and lower Al, Zn, Li, Ni and Co concentrations than those of waters from the As-Au mining area of Banjas, which only contain up to 64 μg L−1 As. In general, Sb occurs mainly as SbO3− and As H2AsO4−. In general, waters from old Sb-Au mining areas are contaminated in Sb, As, Al, Fe, Cd, Mn, Ni and NO2−, whereas those from the abandoned As-Au mining area are contaminated in Al, Fe, Mn, Ni, Cd and rarely in NO2−. Waters from the latter area, immediately downstream of mine dumps are also contaminated in As. In stream sediments from Sb-Au and As-Au mining areas, Sb (up to 5488 mg kg−1) and As (up to 235 mg kg−1) show a similar behaviour and are mainly associated with the residual fraction. In most stream sediments, the As and Sb are not associated with the oxidizable fraction, while Fe is associated with organic matter, indicating that sulphides (mainly arsenopyrite and pyrite) and sulphosalts containing those metalloids and metal are weathered. Arsenic and Sb are mainly associated with clay minerals (chlorite and mica; vermiculite in stream sediments from old Sb-Au mining areas) and probably also with insoluble Sb phases of stream sediments. In the most contaminated stream sediments, metalloids are also associated with Fe phases (hematite and goethite, and also lepidocrocite in stream sediments from Banjas). Moreover, the most contaminated stream sediments correspond to the most contaminated waters, reflecting the limited capacity of stream sediments to retain metals and metalloids.  相似文献   

16.
《Applied Geochemistry》1994,9(5):597-608
In Pacheta Lake, a high-elevation alkaline lake proximal to the smelting region of southern Arizona-New Mexico, concentrations of transition metal ions in pore waters and co-existing sediments were compared. Copper, Fe, Mn and Zn have been partitioned among operationally defined sediment solid phases (exchangeable sites, organic complexes, amorphous oxides, crystalline oxides, sulfides and residual silicates) and their concentrations in interstitial waters were measured. Concentrations are reported as a function of depth in the sediment column. The diagenetic environment is described and cycling mechanisms postulated for the above metals.Selective, sequential extraction of metals from lake sediments showed different binding mechanisms for Cu and Zn, the former most strongly associated with organic complexes, and the latter with iron oxyhydroxides. This difference has strong implications for selective metal remobilization under variable environmental conditions, both naturally and anthropogenically induced. Copper and zinc in porewaters were estimated to diffuse to overlying waters at 12.8 and 21.9 μg/cm2/a, respectively. These fluxes are large enough to account for observed concentrations of Cu and Zn in overlying waters. No sediment metal contamination was directly attributable to smelting activity. However, this study does document a flux from sediments, which have accumulated Cu and Zn, to overlying waters no longer receiving trace metal deposition from now inactive smelters.  相似文献   

17.
Lake Shala, the deepest lake in the internal Galla lakes basin of the Ethiopian Rift, fills a depression in Pleistocene volcanic rocks. Its sodium-bicarbonate (-chloride) water (salinity 16 g/l) is remarkably low in earth alkalines and sulphate. Stratification is indicated by different ion concentrations in the surface and bottom waters and by a thermocline in a water depth of 50–70 m. Hot soda springs emerging on the shores of Lakes Shala and Langano are believed to be derived from a hot saline underground reservoir recharged by meteoric waters. The ion composition of the hot spring waters is uniform and matches that in the Galla Lakes except for total salinities. Anomalous heavy metal concentrations are lacking in lake and hot spring waters. Sediments of Lake Shala belong to an extremely fine-grained group of deposits. They are poorly sorted and the lateral distribution of the grain sizes does not follow the normal scheme for aquatic depositional environments. A belt, 50–100 m below lake level containing the finest-grained sediments, separates the shallow periphery of the lake bottom from the deep center, both characterized by coarser-grained deposits. The sediments consist of a large portion of glassy components. A poorly cristallized smectite is most abundant in the clay mineral group. The components of the sand fraction are quartz, feldspar, glass particles and occasionally calcite. Nickel, cobalt and lead are depleted in the Lake Shala sediments compared with the averages of shales. Iron, manganese and zinc are relatively high. Silver, cadmium and some of the rare earth elements are enriched by factors of > 5.  相似文献   

18.
Multiproxy analyses of sediment cores from Lago Taypi Chaka Kkota (LTCK) Cordillera Real, Bolivia, provide a record of drier conditions following late Pleistocene deglaciation culminating in pronounced aridity between 6.2 and 2.3 ka B.P. Today LTCK is a glacial-fed lake that is relatively insensitive to changes in P–E because it is largely buffered from dry season draw-down through the year-round supply of glacial meltwater. This was not the case during the middle to late Holocene when glaciers were absent from the watershed. Lake-water δ18O values inferred from δ18O analysis of sediment cellulose range from −12.9 to −5.3‰ and average −8.7‰ between 6.2 and 2.3 ka B.P. Modern lake-water δ18O from LTCK averages −14.8‰ which is compatible with the δ18Olw value of −14.3‰ for the surface sediment cellulose. Analyses of δ18O from modern surface waters in 23 lakes that span the range from glacial-fed to closed basin vary from −16.6 to −2.5‰. This approximates the magnitude of the down-core shift in δ18Olw values in LTCK during the middle to late Holocene from −12.9 to −5.3‰. Strong paleohydrologic change during the middle Holocene is also evident in diatom assemblages that consist of shallow-water, non-glacial periphytic taxa and bulk organic δ13C and δ15N that show increases likely resulting from degradation of lacustrine organic matter periodically exposed to subaerial conditions. Neoglaciation began after 2.3 ka B.P. as indicated by changes in the composition of the sediments, lower δ18O values, and a return to diatom assemblages characteristic of the glacial sediments that formed during the Late Pleistocene. Collectively, these data indicate that the past 2.3 ka B.P. have been the wettest interval during the Holocene. Millennial-scale shifts in the paleohydrologic record of LTCK during the early to middle Holocene conform to other regional paleoclimatic time-series, including Lake Titicaca and Nevado Sajama, and may be driven by insolation and resultant changes in atmospheric circulation and moisture supply. In contrast, an apparent 1200-year lag in the onset of wetter conditions at LTCK (2.3 ka B.P.) compared to Lake Titicaca (3.5 ka B.P.) provides evidence for variable sub-regional hydrologic response to climate change during the middle to late Holocene.  相似文献   

19.
Age estimates of NaCl and NaHCO3 in the sediments at Searles Lake, California have been obtained using electron spin resonance (ESR). ESR signals are identified as H+Ca2+---CO33− or H+---CO2− electron type and hole CO3− type centres, stabilized by impurities in NaHCO3 and in NaCl. The total dose of natural radiation (TD) and the tentative ESR ages were determined using these signals based on U, Th and K analyses assuming uranium series disequilibrium for a simple infinite medium. Although ESR ages are concordant with the stratigraphy, radiation assessment considering the loss and incorporation of radioactive elements must be made to get reliable absolute ages.  相似文献   

20.
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), δ13CTOC 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 δ13CDIC 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.  相似文献   

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