Recent increase in atmospheric deposition of mercury to California aquatic systems inferred from a 300-year geochronological assessment of lake sediments

Age-dated sediment cores from 4 remote lakes across California were analyzed for total Hg (Hg_T) concentration as a function of pre- and post-industrialization. Particle size, magnetic susceptibility and organic C and N, were measured to determine if the Hg concentration in sediment cores could be related to atmospheric deposition and/or watershed processes. Results indicate that (a) for each lake modern (1970–2004) Hg_T lake sediment concentrations have increased by an average factor of 5 times more than historic (pre-1850) Hg_T concentrations; (b) the ratio of modern to pre-industrial lake sediment Hg_T for these lakes are higher than estimated for other locations where atmospheric deposition is presumed to be the main source of Hg; (c) 2 of the 4 studied lakes demonstrated significant relationships between Hg_T concentrations and percentage organic material (r² = 0.68 and p < 0.01; r² = 0.67 and p < 0.01) whereas the other two indicated no significant relationship (r² = 0.05 and p = 0.51; r² = 0.12 and p = 0.36).     

Recent paleorecords document rising mercury contamination in Lake Tanganyika

Recent Lake Tanganyika Hg deposition records were derived using ¹⁴C and excess ²¹⁰Pb geochronometers in sediment cores collected from two contrasting depositional environments: the Kalya Platform, located mid-lake and more removed from watershed impacts, and the Nyasanga/Kahama River delta region, located close to the lake’s shoreline north of Kigoma. At the Kalya Platform area, pre-industrial Hg concentrations are 23 ± 0.2 ng/g, increasing to 74 ng/g in modern surface sediment, and the Hg accumulation rate has increased from 1.0 to 7.2 μg/m²/a from pre-industrial to present, which overall represents a 6-fold increase in Hg concentration and accumulation. At the Nyasanga/Kahama delta region, pre-industrial Hg concentrations are 20 ± 3 ng/g, increasing to 46 ng/g in surface sediment. Mercury accumulation rate has increased from 30 to 70 μg/m²/a at this site, representing a 2–3-fold increase in Hg concentration and accumulation. There is a lack of correlation between charcoal abundance and Hg accumulation rate in the sediment cores, demonstrating that local biomass burning has little relationship with the observed Hg concentration or Hg accumulation rates. Examined using a sediment focusing-corrected mass accumulation rate approach, the cores have similar anthropogenic atmospheric Hg deposition profiles, suggesting that after accounting for background sediment concentrations the source of accumulating Hg is predominantly atmospheric in origin. In summary, the data document an increase of Hg flux to the Lake Tanganyika ecosystem that is consistent with increasing watershed sediment delivery with background-level Hg contamination, and regional as well as global increases in atmospheric Hg deposition.     

Toward a geochemical mass balance of major elements in Lake Qinghai,NE Tibetan Plateau: A significant role of atmospheric deposition

Sediments in Lake Qinghai archive important information about past environmental changes. In order to faithfully interpret the sediment records and constrain the elemental cycles, it is critical to trace various sources of sediments in the lake. The results show that the elemental input–output budgets are imbalanced for most major elements between riverine fluxes and mass accumulation rate (MAR) of Lake Qinghai sediments. A realistic model must include contributions of dry/wet atmospheric deposition that allow the major element mass balance for the lake to be defined. The budget estimation is based on mass balances of Si and Al, which are relatively immobile and carried to the lake via particulate forms. Estimated annual budget of dry atmospheric deposition is ∼1.3 ± 0.3 × 10³ kt/a (accounting for ∼65% of the total inputs) to the lake sediments, assuming local loess within the catchment as a candidate for dry atmospheric deposition to the lake. The resultant flux of 300 ± 45 g/m²/a falls within the flux average of the desert area (400 g/m²/a) and the loess plateau (250 g/m²/a), consistent with the geographical setting of Lake Qinghai. The role of atmospheric deposition would be more significant if wet deposition via rainfall and snow were taken into account. This highlights the potential importance of dust as a significant source for sediment preservation flux for other catchments worldwide. The results also indicate that nearly all Ca input was preserved in the lake sediments under modern conditions, consistent with Ca²⁺ supersaturation of the lake water.     

Dissolved noble gases in the porewater of lacustrine sediments as palaeolimnological proxies

This paper presents results from the numerical modelling of the transport of atmospheric noble gases (He, Ne, Ar, Kr, Xe), tritiated water and ³He produced by radioactive decay of ³H, in unconsolidated lacustrine sediment. Two case studies are discussed: (1) the evolution of ³H and ³He concentrations in the sediment porewater of Lake Zug (Switzerland) from 1953 up to the present; and (2) the response of dissolved atmospheric noble gas concentrations in the sediment porewater of a subtropical lake to an abrupt climatic change that occurred some 10 kyr before the present. (1) Modelled ³H and ³He porewater concentrations are compared with recent data from Lake Zug. An estimate of the effective diffusion coefficients in the sediment porewater is derived using an original approach which is also applicable also to lakes for which the historical ³H and ³He concentrations in the water column are unknown. (2) The air/water partitioning of atmospheric noble gases is sensitive to water temperature and salinity, and thus provides a mechanism by which these environmental variables are recorded in the concentrations of atmospheric noble gases in lakes. We investigate the feasibility of using noble gas concentrations in the porewater of lacustrine sediments as a proxy for palaeoenvironmental conditions in lakes. Numerical modelling shows that heavy noble gases in sediment porewater, because of their comparatively small diffusion coefficients and the strong temperature sensitivity of their equilibrium concentrations, can preserve concentrations corresponding to past lake temperatures over times on the order of 10 kyr. Noble gas analysis of sediment porewaters therefore promises to yield valuable quantitative information on the past environmental states of lakes.     

Geochemical and anthropogenic enrichments of Mo in sediments from perennially oxic and seasonally anoxic lakes in Eastern Canada

We measured the vertical distributions of Mo, Fe, Mn, sulfide, sulfate, organic carbon, major ions, and pH in sediment porewater from one perennially oxic and three seasonally anoxic lacustrine basins in Eastern Canada, as well as those of Mo, acid volatile sulfide, Fe, Mn, Al, organic C, ²¹⁰Pb and ¹³⁷Cs in sediment cores from the same sites. The only input of anthropogenic Mo to these lakes comes from atmospheric deposition.The relatively monotonous distribution of Mo in the porewater of three seasonally anoxic basins suggests that Mo is not redistributed in the sedimentary column during periods of anoxia. In contrast, porewater Mo profiles obtained at three sampling dates in a perennially oxic basin display sharp Mo peaks below the sediment-water interface, indicating redistribution subsequent to deposition. Modeling of these latter porewater Mo profiles with a diagenetic reaction-transport equation coupled to comparisons among the various porewater and solid phase profiles reveal that Mo is released at 1-2 cm depth as a consequence of the reductive dissolution of Fe oxyhydroxides and scavenged both at the vicinity of the sediment-water interface, by re-adsorption onto authigenic Fe oxyhydroxides, and deeper in the sediments where dissolved sulfide concentrations are higher. The estimated rate constant for the adsorption of Mo onto Fe oxyhydroxides is 36 ± 45 cm³ mol⁻¹ s⁻¹.Diagenetic modeling indicates that authigenic Mo in sediments of the perennially oxic basin represents about one-third of the total solid phase Mo in the first cm below the sediment-water interface and only one tenth below this horizon. If we assume that no authigenic Mo is accumulated in the seasonally anoxic lake sediments we conclude that the sediment Mo concentrations, which are up to 3-16 times higher than the average lithogenic composition, depending on the lake, are mainly due to atmospheric deposition of anthropogenic Mo and not to the formation of authigenic Mo phases. Reconstructed historical records of the atmospheric Mo deposition indicate maximum values in the 1970s and 1980s and significant decreases since then. Emissions to the atmosphere associated with the smelting of non-ferrous ores and coal combustion appear to be the most important sources of anthropogenic Mo.     

Late Quaternary sequence stratigraphy of Lake Malawi (Nyasa), Africa

High resolution seismic data, multichannel seismic data and sediment cores were used to examine the Songwe Sequence, the uppermost of four depositional sequences identifiable on multichannel seismic data from Lake Malawi (Nyasa). The sequence has a maximum thickness of about 115 m in two areas of the lake, but is typically less than 70 m thick over most of the basin. The sequence is distributed along the entire length of the 560 km long lake, and is concentrated in three main depocentres. ¹⁴C age dates from sediment piston cores are extrapolated to provide an age estimate of about 78 000 yr bp for the oldest sediments within the Songwe Sequence. In the North and Central bathymetric basins of the lake, high resolution seismic data indicate a dynamic depositional environment, dominated by turbidity and mass flow deposits. Seismic data from the southern basin show acoustically transparent sediments with relatively low amplitude internal reflections, indicative of pelagic and hemipelagic sedimentation. In many areas the Songwe Sequence is underlain by a pronounced angular unconformity, suggestive of a significant, prolonged, low lake stage prior to deposition of the sequence. Seismic reflectors within the Songwe Sequence can be correlated to younger low lake stages identified from sediment core data. Major late Quaternary low lake level stages in Lake Malawi, interpreted from features identified in the seismic data and sediment core analyses, are tentatively interpreted at 6000 to 10 000 yr bp , 28 000 to >40 000 yr bp , and prior to 78 000 yr bp . Budget calculations indicate mean sediment concentrations from catchment runoff during the period of deposition of the Songwe Sequence to be about 190 mg 1⁻¹, comparable to estimates of modern rainy season discharges from the major river systems. Erosion rates within the drainage basin are estimated to be higher than the African average by a factor of three or more, probably due to the high relief within the Lake Malawi catchment.     

The distribution of total mercury and methyl mercury in a shallow hypereutrophic lake (Lake Taihu) in two seasons

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.     

The onset of anthropogenic activity recorded in lake sediments in the vicinity of the Horne smelter in Quebec,Canada: Sulfur isotope evidence

Contents and δ³⁴S values of several S compounds, enumerations of S-reducing bacteria (SRB) and Fe-reducing bacteria (IRB), and Fe, Pb and In concentrations were determined for ²¹⁰Pb-dated sediment cores from two lakes in Quebec, Canada. Both lakes are located approximately 70 km downwind of the Horne smelter and refinery in Rouyn-Noranda. Increases in Fe, Pb and In concentrations and a decrease in the δ³⁴S values of total S in both lake sediment cores coincide with the start-up of the smelter in 1927. The shift towards more negative δ³⁴S values was primarily caused by an increase in the extent of S isotope fractionation during bacterial (dissimilatory) SO₄ reduction due to SO₄ loading of the lakes after smelting began. Consequently, an enhanced accumulation of ³²S-enriched reduced inorganic S compounds is evident in the sediments. δ³⁴S values of organic S in the sediments decreased only slightly due to the smelter emissions between 1930 and 1980. Hence, due to the sulfide depositing mechanisms, S isotope ratios constitute a useful tracer recording the onset of S pollution in sediments of the two previously SO₄-limited lakes investigated. In contrast, total S concentrations alone are not reliable indicators for anthropogenic S loading in lake sediment records.     

Sequestration mechanisms and anthropogenic inputs of rhenium in sediments from Eastern Canada lakes

The concentrations of Re, as well as those of several other geochemical variables, were measured in dated sediment cores and in porewater samples from four lacustrine basins in Eastern Canada: one, perennially oxic, located 40 km from Québec City and three, seasonally anoxic, located within 25 km of non-ferrous metal smelters. The drainage basins of these lakes are uninhabited and have not been affected by human activity or wildfires. All of the depth profiles of dissolved Re indicate: higher Re concentrations in the water overlying the sediment than in the porewater; diffusion of Re across the sediment-water interface; a progressive decrease in porewater Re concentrations to reach minimum values of ∼0.5 pM within a 10-cm sediment depth interval. Modeling of these Re porewater profiles with a one-dimensional transport-reaction equation indicates that Re is removed from porewater within this depth interval. Based on thermodynamic predictions of Re speciation and of saturation states and on comparison of these predictions with sulfide porewater profiles, we infer that Re is removed from porewater by precipitation of rheniite (ReS_2(s)). The rate constant for the formation of ReS_2(s) in sediments is estimated from the modeling exercise to be 0.51 ± 0.64 × 10⁻²¹ mol cm⁻³ s⁻¹. Accumulation of sedimentary Re shows a strong authigenic component, as in anoxic marine sediments. Sharp increases in solid-phase Re during the last century are attributed to atmospheric deposition of anthropogenic Re deriving from coal burning and nearby smelter emissions.     

137Cs测年的东北兴凯湖现代沉积速率研究

对兴凯湖我国水域沉积物137Cs比活度及通量空间分布进行了研究,利用137Cs测年法建立年代框架,估算了兴凯湖的沉积速率,结合粒度C-M图分析了湖泊现代沉积环境。兴凯湖我国水域西岸白棱河河口区域137Cs剖面形态区别于典型的137Cs全球大气沉降模式,且137Cs沉积通量高、平均137Cs活度高,中部和东部区域137Cs沉积通量低、平均137Cs活度低;137Cs沉积通量的空间分布主要受流域输入、水动力条件以及沉积物粒径的影响。兴凯湖沉积环境多表现为静水沉积,受特殊的风浪条件和泄洪闸等人类活动的影响,1963—2019年平均沉积速率空间分布上呈现西部高,中、东部低的特点,XKH-1、XKH-2和XKH-3柱样1963—2019年的平均沉积速率分别为0.143 cm/a、0.080 cm/a和0.036 cm/a。     

Study on Nitrogen Dynamics at the Sediment–Water Interface of Dongting Lake,China

Eutrophication of lakes and reservoirs has become a worldwide environmental problem, and nitrogen (N) has been recognized as one of the key factors responsible for eutrophication. Nitrogen adsorbed on sediments may be released via chemical and biological processes under changing environmental conditions. Spatial distributions of concentrations of ammonia nitrogen (NH₄ ⁺–N), nitrate nitrogen (NO₃ ^?–N) and total nitrogen (TN) were investigated in sediments and overlying water of Dongting Lake, the second largest freshwater lake in China. The concentration of TN in the sediments exhibited strong spatial variation with relatively high values in the eastern part and relatively low values in the southern part of the lake. The TN concentration in the water of different regions of Dongting Lake was affected by the internal load of sediment N. The vertical distribution of TN in sediment cores showed a decreasing trend with an increase in depth. Concentrations of NH₄ ⁺–N in the sediment cores decreased with the depth increase until 6–8 cm and then increased slowly. However, concentrations of NO₃ ^?–N in the sediment cores showed an opposite trend from those of NH₄ ⁺–N. A kinetic release experiment of NH₄ ⁺–N showed that the maximum release rate occurred in the first 5 min and the amount of NH₄ ⁺–N release reached 77.93–86.34 % of the total amount in 0–10 min. The release of NH₄ ⁺–N in the surface sediments of Dongting Lake fits a first-order kinetics function.     

Postglacial sediment yield to Chilliwack Lake,British Columbia,Canada

Tunnicliffe, J., Church, M. & Enkin, R. J. 2012 (January): Postglacial sediment yield to Chilliwack Lake, British Columbia, Canada. Boreas, Vol. 41, pp. 84–101. 10.1111/j.1502‐3885.2011.00219.x. ISSN 0300‐9483. Seismic records and evidence from sediment cores at Chilliwack Lake provide the basis for a long‐term (postglacial) sediment budget for a 324‐km² Cordilleran catchment. Chilliwack Lake (11.8 km² surface area), situated in the North Cascade Mountains, near Chilliwack, British Columbia, was formed behind a valley‐wide recessional moraine in the final phase of post‐Fraser alpine glaciation. Seismic surveys highlight the postglacial lacustrine record, which is underlain by a thick layer of sediments related to deglacial sedimentation. Sediment cores provide details of grain‐size fining from the delta to the distal lake basin. The cores also show a record of intermittent fire and debris flows. Magnetic measurements of lake sediments provide information on grain size, as well as a dating framework. The total postglacial lake‐floor deposit volume is estimated to be 397 ± 27 × 10⁶ m³. Including estimates of fan and delta deposition, the specific postglacial yield to the lake is calculated to be ～86 ± 13 Mg km² a^?1. The sediment volume in the uppermost (Holocene) lacustrine layer is 128 ± 9 × 10⁶ m³, representing ～41 ± 4 Mg km² a^?1 in the Holocene. Compared with other Cordilleran lakes of similar size, particularly those with glacial cover in the watershed, Chilliwack Lake has experienced relatively modest rates of sediment accumulation. This study provides an important contribution to a growing database of long‐term (postglacial) sediment yield data for major Cordilleran lakes, essential for advancing our understanding of the pace of landscape evolution in formerly glaciated mountainous regions.     

The Chemical Nature of Phosphorus in Subtropical Lake Sediments

The phosphorus (P) composition of sediment profiles in three subtropical lakes of contrasting trophic state in Florida, USA, was determined by sequential fractionation and solution ³¹P NMR spectroscopy. Sediment from Lake Annie, an oligo-mesotrophic sinkhole with moderately acidic sediment (pH 5.4; loss on ignition 58 %), contained higher total P concentrations than sediment from eutrophic Lake Okeechobee (pH 7.7, loss on ignition 36 %) and hyper-eutrophic Lake Apopka (pH 7.5, loss on ignition 69 %). The chemical nature of sediment P varied markedly among the three lakes, suggesting the predominance of different diagenetic processes. Lake Okeechobee sediment was dominated by inorganic P, indicating the dominance of abiotic reactions; Lake Annie sediment contained abundant organic P throughout the sediment profile, indicating the importance of organic P stabilization at acidic pH; Lake Apopka contained almost half of its sediment P in microbial biomass, indicating the importance of biotic processes in regulating P dynamics. Solution ³¹P NMR spectroscopy of NaOH–EDTA extracts revealed that organic P occurred mainly as phosphomonoesters in all lakes. However, sediment from Lake Apopka also contained abundant phosphodiesters and was the only lake to contain detectable concentrations of polyphosphate, perhaps due to a combination of alternating redox conditions and high concentrations of inorganic phosphate and organic carbon. Organic P concentrations determined by sequential fractionation and solution ³¹P NMR spectroscopy were similar for all lakes when microbial P was included in values for sequential fractionation. We conclude that the chemical nature of sediment P varies markedly depending on trophic state and can provide important information on the dominant processes controlling P cycling in subtropical lakes.     

Assessing the natural recovery of a lake contaminated with Hg using estimated recovery rates determined by sediment chronologies

Deer Lake is an impoundment located near Ishpeming, Michigan, USA. Iron mining assay laboratories located in Ishpeming disposed of Hg salts to the city sewer whose outfall was located along an inlet to Deer Lake. An effort to remediate the system in the mid 1980s which consisted of drawing down water in the impoundment in order to volatize Hg from the sediments did not result in recovery of the system. Since the mid 1990s, the remediation strategy has been to allow the continual burial of the contaminated sediments, i.e., natural recovery. The goal of this study was to assess the effectiveness of this strategy. This was accomplished by investigating the state of the system in terms of its recovery and estimating the time frame for recovery. Sediment cores were collected in 2000 to determine historical trends in accumulation rates and concentrations of Hg and other metals. Sedimentation rates and sediment ages were estimated using ²¹⁰Pb. Event-based dating (e.g., peak of ¹³⁷Cs in 1963) was used to supplement ²¹⁰Pb data due to non-monotonic features in the ²¹⁰Pb profile and activities that were not at supported levels at the base of the core. Selected results are that: (1) drawdown significantly influenced sedimentation patterns causing slopes for ²¹⁰Pb profiles that reflected the influx of older sediment, (2) periods of Fe production correlate to Hg loading indicating the point source for contamination, a relationship not previously identified, (3) Hg:Al ratios indicate a recent change to a watershed pathway for Hg loading and (4) Hg concentrations had decreased from their peak, remain elevated, and were increasing after 1997. The cause of the recent Hg concentrations may be related to influx of contaminated watershed soils or sediments. Estimating the time frame for recovery is challenging in this system because the process of natural recovery seems to have been arrested and deeper, uncontaminated sediments, were not recovered as a basis for reference. However, a recovery to background conditions is likely not achievable since rates of Hg loading to nearby lakes and the current rate of atmospheric deposition are greater than an estimate of background conditions for Deer Lake. Assuming recovery continued after 2000, estimates of the time required for recovery varied based on the system state used to define it (e.g., recent rates of wet Hg deposition or Hg surface concentrations/fluxes from similar systems), but were less than 12 a. However, the recent increasing values of recovery indicators (e.g., Hg concentrations) suggests that these estimates are conservative and will be longer if recovery remains arrested, which may in part be due to the legacy of Hg contamination on the landscape. This study shows that estimates of recovery of highly disturbed lake systems can be made in the absence of within lake reference conditions by using comparisons to reference systems and challenges of estimating ages from atypical ²¹⁰Pb activity profiles can be overcome in part using event-based dating techniques.     

Holocene records of eolian dust deposition from high-elevation lakes in the Uinta Mountains,Utah, USA

Radiocarbon-dated sediment cores from subalpine lakes were used to investigate post-glacial dust deposition in the Uinta Mountains (Utah, USA). Lake sediments were geochemically characterized with ICP-OES, ICP-MS and XRF core scanning. Collections from passive samplers constrain the properties of modern dust, and samples of regolith constrain properties of the local material within the watershed. Ca and Eu are more abundant in dust, whereas Ti and Zr are more abundant in local regolith. As a result, the Ca/Ti and Eu/Zr ratios are indices for the dust content of lake sediment. In all records, the dust index rises in the early Holocene as watersheds became stabilized with vegetation, reducing the influx of local material. After this point, values remained above average through the middle Holocene, consistent with an increased dust content in the sediment. Dust index values drop in the late Holocene in most lakes, suggesting a decrease in dust abundance. Generally synchronous shifts in dust index values in cores from lakes in different parts of this mountain range are evidence of enhanced dust deposition in this region during the middle Holocene, and are consistent with a variety of records for increased aridity in the south-western USA at this time.     

Regional variations in atmospheric deposition and sources of anthropogenic lead in lake sediments across the Canadian Arctic

Stable Pb isotope profiles in dated lake sediment cores were used to gauge the relative amounts and possible sources of anthropogenic Pb deposited from the atmosphere in different regions of the Canadian Arctic. A distinct north-south difference was found. In four High Arctic lakes (i.e., north of 66°N) in this study, recent Pb isotopic shifts or concentration increases attributable to anthropogenic Pb were negligible. The maximum possible contribution from anthropogenic Pb was 0 to 19% of acid-leachable Pb in the 1980s or 1990s. In contrast, two lakes in the Hudson Bay region displayed significantly lower Pb isotope ratios and threefold to fivefold increases of Pb concentrations in modern sediments, corresponding to anthropogenic Pb inputs of at least 72 to 91% of leachable Pb. Eurasian urban and industrial Pb is known to dominate the High Arctic atmosphere. A possible explanation for its negligible influence on northern lake sediments is that atmospheric Pb deposition at northern latitudes is reduced compared with southern regions and is small compared to local geological inputs. ²¹⁰Pb deposition declines with increasing latitude, apparently because of declining precipitation rates; stable Pb deposition may be similarly affected. Meteorological considerations and variations in the post-1900 Pb isotopic trajectories indicated that the predominant anthropogenic Pb source region in NW Hudson Bay was Eurasia, while in SE Hudson Bay, it was Canada and the United States, with a minor Eurasian component.     

全新世中期相对稳定的长江水位造成约3000年的湖泊沉积缺失

长江中下游地区浅水湖泊密布,全新世该区湖泊沉积的模式还不清晰。本研究在长江中下游的南漪湖、升金湖和菜子湖这3个湖泊开展了多钻孔AMS^14C测年工作,测年结果显示这些湖泊沉积地层中广泛出现长时间尺度的沉积物缺失。南漪湖湖泊钻孔的沉积物14C年龄介于5668~7828cal.aB.P.,菜子湖湖泊钻孔的沉积物^14C年龄介于6221~7929cal.aB.P.,升金湖围垦区钻孔14C年龄介于6302~7049cal.aB.P.。结合该地区以往湖泊钻孔研究资料,发现全新世长江中下游两岸洼地湖泊存在较广泛的6~3ka的沉积间断。结合长江水位重建资料,笔者提出关于全新世湖泊沉积存有长期间断的新认识:即6~3ka,长江水位相对平稳,湖泊沉积物虽有堆积,但易于被侵蚀搬运造成沉积间断;与此对应的是,在约8~7ka,海面上升造成长江水位较快上升,由于顶托作用,湖泊沉积物持续堆积;在约3ka以来,由于人类活动的影响,以及长江水位的进一步上升,湖泊沉积物也易于堆积,但在一些湖区沉积物也会被侵蚀。在6~3ka之间湖泊沉积物易于被侵蚀的一个可能原因是该时段长江上游来沙来水减少,自然堤易被破坏,对两岸湖泊洼地的封堵作用减少,使得湖泊泥沙易被侵蚀入江。     

Seasonal changes in glycerol dialkyl glycerol tetraether concentrations and fluxes in a perialpine lake: Implications for the use of the TEX86 and BIT proxies

To determine where and when glycerol dialkyl glycerol tetraether (GDGT) membrane lipids in lakes are produced, we collected descending particles in Lake Lucerne (Switzerland) using two sediment traps (at 42 and 72 m water depth) with a monthly resolution from January 2008 to late March 2009. Suspended particulate matter (SPM) was monthly filtered from the water column at three different depths. The potential application of GDGTs in palaeoenvironmental and palaeoclimatic reconstructions was investigated by comparing core lipids and their relative GDGT distribution, with lake water temperatures throughout the year. Fluxes of GDGTs and their concentrations in the water column vary according to a seasonal pattern, showing a similar trend in the SPM and sediment traps. Fluxes and concentrations of isoprenoid GDGTs increase with depth, maximum values being observed in the deeper part of the water column, indicating production of isoprenoid GDGTs by Thaumarchaeota in the deep (∼50 m), aphotic zone of Lake Lucerne. The flux-weighted averages of the proxies TEX₈₆ (0.27) and BIT (0.03) based on the total extracted GDGTs are similar at both trap depths. A sediment core from the same location showed that in the first few centimetres of the core TEX₈₆ and BIT values of 0.29 and 0.07, respectively, are similar to those recorded for descending particles and SPM, indicating that the sedimentary TEX₈₆ records the annual mean temperature of deeper waters in Lake Lucerne. TEX₈₆ values are slightly higher below 20 cm in the core. This offset is interpreted to be caused by the present-day trophic state of the lake, which probably resulted in a deeper niche of the Thaumarchaeota. Branched GDGTs represent only a minor fraction of the total GDGTs in the lake and their origin remains unclear. Our data reveal that GDGTs in lakes have a large potential for palaeoclimatic studies but indicate that knowledge of the system is important for accurate interpretation.     

Lake sediment cores as indicators of historical metal(loid) accumulation – A case study in Mexico

To examine and compare historical accumulation of metal(loid)s in Mexican lakes and reservoirs, ²¹⁰Pb and ¹³⁷Cs dated sediment cores were evaluated: two from the remote Zempoala and Miramar Lagoons and three from Lake Pátzcuaro, and the Intermedia and Silva dams that are affected by human activities. Sediment ecotoxicology was assessed using consensus-based sediment quality guidelines for freshwater ecosystems. The +100 a sediment core from the remote Miramar Lagoon had the highest concentrations of Cr and Ni these being higher than the Probable Effect Levels (PELs). Zinc concentrations were also higher in the Miramar Lagoon compared to the other lakes and reservoirs, with concentrations higher than the Threshold Effect Level (TEL). Mercury concentrations from this lagoon were comparable to those for the Intermedia dam that receives water from urban, industrial and agricultural areas. The higher metal concentrations in the core from the Miramar Lagoon suggest that metal concentrations in the rocks of the watershed are high. Another explanation for the higher metal concentrations is the slow sediment accumulation that causes metals to be accumulated over longer time-periods at the sediment–water interface. A decrease in the concentration of As in the Intermedia dam was observed in sediments corresponding to the last decades. This may be due to an increase in sediment accumulation rate or to the reduction in sources of this metalloid in the watershed. In the Miramar Lagoon, an increase was observed in concentrations of As and Cr in more recent sediments, probably related to increased deforestation in the area or the eruption of El Chichonal volcano in 1982. Concentrations of Pb showed a decreasing tendency over the past decades in the Lake Pátzcuaro, Miramar and Zempoala Lagoons sediment cores while such behavior was not be observed for the Intermedia dam. This reduction in concentrations of Pb was attributed to the decrease in use of leaded gasoline.     

Heavy metals in bottom sediments of great slave lake (Canada): A reconnaissance

Near the shores of Great Slave Lake, natural sources of heavy metals include gold and base metal deposits, mineralized greenstone belts and sedimentary bedrock, and uraniferous granites. Potential anthropogenic sources of heavy metals (As, Zn, Pb) include large gold and base metal extraction -processing facilities on the shores of the lake. Six sediment cores were collected on a traverse of the lake. Heavy metal concentrations and distributions are related to the regional bedrock geochemistry in the drainage basin. Higher uranium concentrations in the northernmost core are attributed to extensive uraniferous areas north of the lake. More subtle variations of concentration are related to sedimentologic characteristics and processes in the lake. The west basin is a natural sink for most of the heavy metals determined. Two centrally located west basin cores had mean zinc concentrations of 145 ppm, whereas cores closer to the north and south shores had mean concentrations of 80–110 ppm. Mn, Ni, and Pb were enriched in some of the cores from the area of shallower water near the MacKenzie River outlet, rather than in the central west basin. The enrichment is related to Mn-, Ni-, and Pb-rich amorphous coatings on quartz grains. Elevated zinc or lead levels from anthropogenic activities were not detected but elevated levels are suspected for arsenic. In the two cores from the center of the west basin, surface sediment contains up to 12 ppm arsenic, not high in comparison with noncontaminated freshwater lakes elsewhere in Canada but considerably elevated relative to concentrations of 1 ppm found deeper in the same cores. Contribution from the National Water Research Institute, Western and Northern Region. Presented at the 10th International Sedimentological Congress, Jerusalem, Israel, 1978.