Cleaning of lake sediment samples for diatom oxygen isotope analysis   总被引：1，自引：0，他引：1  

David W. Morley  Melanie J. Leng  Anson W. Mackay  Hilary J. Sloane  Patrick Rioual  Richard W. Battarbee 《Journal of Paleolimnology》2004,31(3):391-401

Detrital grain contamination in a diatom sample can considerably influence the δ¹⁸O_diatom signal. In order to obtain a meaningful signal, pure samples must be used. This can be achieved via a series of cleaning stages including organic and carbonate material removal, sieving, differential settling and heavy liquid separation. The method described here works best for sediments with >20% diatom content. Based on testing various clean-up methods, we propose a sequence of four clean-up stages to produce pure diatom samples from a range of lake sediments types starting with a few grams of sediment. The diatom content and the oxygen isotope composition of the samples at each stage were measured in order to assess the effect of differential amounts of contamination. Results show that a four stage clean-up is necessary to produce clean diatom samples and that contamination by silt and clay causes lower δ¹⁸O values.  相似文献   

Geochemical and biological consequences of groundwater augmentation in lakes of west-central Florida (USA)     

Mark Brenner  Thomas J. Whitmore  Melanie A. Riedinger-Whitmore  Brandy DeArmond  Douglas A. Leeper  William F. Kenney  Jason H. Curtis  Byron Shumate 《Journal of Paleolimnology》2006,36(4):371-383

We studied sediment cores from four Florida (USA) lakes that have received groundwater hydrologic supplements (augmentation) for >30 years to maintain lake stage. Top samples (0–4 cm) from sediment cores taken in Lakes Charles, Saddleback, Little Hobbs, and Crystal had ²²⁶Ra activities of 44.9, 17.5, 7.6, and 8.5 dpm g⁻¹, respectively, about an order of magnitude greater than values in deeper, older deposits. The surface sample from Lake Charles yielded the highest ²²⁶Ra activity yet reported from a Florida lake core. Several lines of evidence suggest that groundwater augmentation is responsible for the high ²²⁶Ra activities in recent sediments: (1) ²²⁶Ra activity in cores increased recently, (2) the Charles, Crystal, and Saddleback cores display ²²⁶Ra/²¹⁰Pb disequilibrium at several shallow depths, suggesting ²²⁶Ra entered the lakes in dissolved form, (3) cores show recent increases in Ca, which, like ²²⁶Ra, is abundant in augmentation groundwater, and (4) greater Sr concentrations are associated with higher ²²⁶Ra activities in recent Charles and Saddleback sediments. Sr concentrations in Eocene limestones of the deep Floridan Aquifer are high relative to Sr concentrations in surficial quartz sands around the lakes. Historical water quality inferences for the lakes were based on diatom assemblages in sediments. Recent alkalization in Lakes Charles, Saddleback, Little Hobbs, and Crystal was inferred from weighted-averaging calibration (WACALIB). The lakes also show recent trophic state increases based on WACALIB-derived estimates for limnetic total P. Although residential and agricultural sources might contribute to increased P loading, P in augmentation waters probably has had significant influence on eutrophication. Dystrophic diatoms were abundant in the early history of Lakes Saddleback, Little Hobbs, and Crystal, which suggests that these lakes contained more tannic waters during the past than at present, perhaps as a consequence of greater inflows from surrounding wetlands. Ionic content of lake waters increased, as indicated by diatom autecological analysis. Recent geochemical and biological changes detected in cores from these lakes probably are a result of deliberate groundwater augmentation, although inputs of groundwater pumped for agricultural and residential development in the watersheds also might have contributed to limnological changes.  相似文献   

Limnology of Two Antarctic Epishelf Lakes and their Potential to Record Periods of Ice Shelf Loss   总被引：1，自引：0，他引：1  

James A. Smith  Dominic A. Hodgson  Michael J. Bentley  Elie Verleyen  Melanie J. Leng  Steven J. Roberts 《Journal of Paleolimnology》2006,35(2):373-394

George VI Ice Shelf is the largest ice shelf on the western side of the Antarctic Peninsula and its northern margin marks the southern most latitudinal limit of recent ice shelf retreat. As part of a project to reconstruct the long-term (Holocene) history of George VI Ice Shelf we studied two epishelf lakes impounded by the ice shelf at Ablation Point, on the east coast of Alexander Island. These lakes, Moutonnée and Ablation, are stratified water bodies with a lower marine layer and an upper freshwater layer. To determine if their sediment records could be used to detect past changes in the presence or absence of the ice shelf it was necessary to describe their present-day limnology and sedimentology. We measured water column chemistry and sampled the water column and sediments of the lakes along vertical and horizontal transects. We analysed these samples for diatoms, stable isotopes (δ¹⁸O, δ²H, δ¹³C_DIC, δ¹³C_org), geochemistry (TOC, TN, C/N ratios) and physical sedimentology (grain-size). This was supplemented by chemical and biological reference data from the catchments. Results showed that the water columns of both lakes are nutrient limited and deficient in phytoplankton. Benthic productivity is low and decreases with depth. Comparison of water column chemistry with an earlier survey shows a net increase in the thickness of the freshwater layer in Moutonnée Lake between 1973 and 2001, which could indicate that George VI Ice Shelf has thinned during this period. However, a similar trend was not observed in Ablation Lake (5 km to the north) and an alternative explanation is that the changes are a seasonal phenomena. Data from the surface sediment transects identified a number of proxies that respond to the present day stratification of the water column including diatom species composition, stable isotopes and geochemistry, particularly in Moutonnée Lake. Collectively these data have been used to develop a conceptual model for determining past ice shelf configuration in epishelf lakes. Specifically, periods of past ice shelf loss, and the removal of the ice dam, would see the present stratified epishelf lake replaced by a marine embayment. It is suggested that this change would leave a clear signature in the lake sediment record, notably the deposition of an exclusively marine biological assemblage, increased ice rafted debris and δ¹³C_org values that are indicative of marine derived organic matter. These authors contributed equally to this work  相似文献   

Book reviews     

Michael Ed. Hohn  Melanie A. Wetzel  James R. Carr  W. E. Sharp  C. John Mann 《Mathematical Geosciences》1995,27(2):301-313

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Exploring former subglacial Hodgson Lake,Antarctica Paper I: site description,geomorphology and limnology     

Dominic A. Hodgson  Stephen J. Roberts  Michael J. Bentley  James A. Smith  Joanne S. Johnson  Elie Verleyen  Wim Vyverman  Andy J. Hodson  Melanie J. Leng  Andreas Cziferszky  Adrian J. Fox  David C.W. Sanderson 《Quaternary Science Reviews》2009,28(23-24):2295-2309

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Volatiles in a peralkaline system: Abiogenic hydrocarbons and F–Cl–Br systematics in the naujaite of the Ilímaussaq intrusion, South Greenland     

Thomas V. Krumrei  Ernst Pernicka  Melanie Kaliwoda  Gregor Markl 《Lithos》2007,95(3-4):298-314

Agpaitic rocks comprise most of the exposed part of the 1.16 Ga old, 8 × 17 km large and about 1700 m thick Ilímaussaq intrusion in South Greenland. Within these, more than 600 m thick sequence of sodalite-rich “naujaites” (mainly sodalite + arfvedsonite + alkali feldspar + nepheline + eudialyte + aenigmatite) are interpreted as a sodalite flotation cumulate. Sodalites show two to three different zones in cathodoluminescence (CL) and at least two zones in thin sections. The CL zones can be related to chemical differences detectable by electron microprobe, whereas relations with optical zonations are less obvious. Compositional trends in sodalite reflect trends in the evolution of volatile contents in the melt. The sodalite at Ilímaussaq is almost free of Ca and closely corresponds to the pure Na–Cl sodalite endmember with about 7 wt.% of Cl; S contents reach up to 0.9 wt.%. Cl/Br ratios range from 500 to 1700. Raman spectroscopy shows that S is present as [SO₄]²⁻ in sodalite, although sphalerite (ZnS) is a stable phase in naujaites. Peralkalinity and fO₂ conditions allow S²⁻ and [SO₄]²⁻ to be present contemporaneously.

The whole naujaite sequence is divided into two parts, an upper part with low, homogeneous S contents and Cl/Br ratios in the sodalite cores, and a lower part with strongly variable and higher S contents and with Cl/Br ratios, which are decreasing downwards. The details of the S content and the Cl/Br ratio evolution show that sodalite strongly influences the halogen contents of the melt by scavenging Cl and Br.

The naujaites were formed from a highly reduced, halogen-rich magma in equilibrium with magmatic methane at about 800 °C, which, upon ascent, cooling and fractionation, exsolved an aqueous fluid phase. Both fluids were trapped in separate inclusions indicating their immiscibility.

Micrometer-sized aegirine crystals and primary hydrocarbon-bearing inclusions are abundant in the crystal cores. The inclusions were trapped at pressures up to 4 kbar, although the emplacement pressure of the intrusion is about 1 kbar. This indicates growth of the sodalite during melt ascent and a very effective mechanism of trace element scavenging during sodalite growth. Sodalite rims are devoid of aegirine or primary hydrocarbon inclusions and probably reflect the emplacement stage.  相似文献   

Non-conservative behaviour of molybdenum in coastal waters: Coupling geochemical, biological, and sedimentological processes     

Olaf Dellwig  Melanie Beck  Mirko Lunau  Kerstin Kolditz  Hans-Jürgen Brumsack 《Geochimica et cosmochimica acta》2007,71(11):2745-2761

Non-conservative behaviour of dissolved Mo was observed during specific time periods in the water column of the Wadden Sea of NW Germany. In July 2005 dissolved Mo declined within 36 h from a level only slightly below seawater (82 nM) to a minimum value of 30 nM, whereas in August 2002 dissolved Mo revealed a tidal cyclicity with maximum values up to 158 nM at low tide. In contrast, cruises in August 2003 and 2004 displayed an almost conservative behaviour of Mo. The decrease in dissolved Mo during July 2005 and elevated values in August 2002 were accompanied by Mo enrichments on aggregates in the water column of the Wadden Sea. Along with Mo, dissolved Mn showed unusual concentration patterns in July 2005, with values distinctly below the common summer level (by a factor of five). A direct relation between the loss of Mo and scavenging by freshly formed MnO_x phases could not be inferred from our data because both metals revealed inverse patterns. Parallel to decreasing dissolved Mo concentrations dissolved Mn showed an increasing trend while particulate Mn decreased. Such finding is compatible with the formation of oxygen-depleted zones in aggregates, which provide suitable conditions for the rapid fixation of Mo and parallel release of Mn by chemically and/or microbially mediated processes. Our assumption is supported by biological (e.g. number of aggregate-associated bacteria) and sedimentological (e.g. aggregate abundance and size) parameters. The production of organic components (e.g. TEP) during breakdown of an algae bloom in July 2005 led to the formation of larger Mo-enriched aggregates, thus depleting the water column in dissolved Mo. After deposition on and incorporation into sandy tidal flats these aggregates are rapidly decomposed by microbial activity. Pore water profiles document that during microbial decomposition of these aggregates, substantial amounts of Mo are released and may replenish and even enrich Mo in the open water column. We postulate a conceptual model for the observed non-conservative behaviour of Mo in coastal waters, which is based on the tight coupling of geochemical, biological, and sedimentological processes.  相似文献   

Photochemistry of Cu complexed with chromophoric dissolved organic matter: implications for Cu speciation in rainwater     

Melanie Louise Inez Witt  Stephen Skrabal  Robert Kieber  Joan Willey 《Journal of Atmospheric Chemistry》2007,58(2):89-109

Significant quenching of fluorescence by Cu in rainwater samples from southeastern North Carolina demonstrates that chromophoric dissolved organic matter (CDOM) is an effective ligand for Cu in rainwater. A strong inverse correlation between the decrease in fluorescence upon Cu addition and CDOM abundance suggests the presence of excess binding sites for Cu in high CDOM samples. Electroanalytical studies indicate that CDOM extracted from C₁₈ cartridges formed Cu complexes with concentrations and conditional stability constants similar to ligands found in ambient rainwater. When authentic rainwater samples were photolyzed with simulated sunlight both photoproduction and photodestruction of ligands were observed, suggesting the photochemical response of Cu-complexing ligands in rainwater is the result of two competing reactions. The rate of CDOM photobleaching was directly related to changes in strong ligands (K_CuL ∼ 10¹⁵) whereas weaker ligands (K_CuL < 10¹³) were not correlated, suggesting the photolabile CDOM resides in the strong ligand class. A photolysis study comparing filtered and unfiltered rainwater samples indicated that Cu-complexing ligands adsorbed onto or otherwise associated with particles are photodegraded much more rapidly than dissolved ligands. Photolysis with UV radiation appears to be most effective at engendering changes in Cu ligands, however a significant photochemical response was also observed when samples were exposed to photosynthetically active radiation with wavelengths greater than 400 nm. Results from this study demonstrate that complexation of Cu by CDOM has important ramifications for controlling both the speciation of the metal and the reactivity of CDOM in rainwater.  相似文献   

An assessment of the water budget for contrasting vegetation covers associated with waste management     

Isa A. M. Yunusa  Melanie J. B. Zeppel  Sigfredo Fuentes    Catriona M. O. Macinnis‐Ng  Anthony R. Palmer  Derek Eamus 《水文研究》2010,24(9):1149-1158

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Rates of trace metal and nutrient diagenesis in an intertidal creek bank     

Thomas Riedel  Karsten Lettmann  Melanie Beck 《Geochimica et cosmochimica acta》2011,75(1):134-6555

Carbon mineralization in marine sediments is a key process involved in the cycling of carbon, nutrients and trace metals. However, as marine sediments are usually diffusion dominated, the pace of element and nutrient cycling is slow, because consumption of oxidants and/or nutrients in the pore waters via microbial activity often outpaces resupply. Adding an advective flow component to such a system should change the biogeochemical dynamics considerably. Numerical simulations show that shallow coastal aquifers affected by tidal forces can establish ground water velocities of up to 7 cm h⁻¹, driving a circulation of sea water through the sediments with subsequent discharge. Although known to enhance solute exchange, the impact of advection on early diagenesis has not received much attention.To address this issue we mapped the interstitial water chemistry down to 2.5 m sediment depth along a transect on an intertidal creek bank that is subject to a periodic advective flow. Additionally a recently developed hydrogeological simulation of the creek bank was applied to calculate ages of the sampled pore waters. Sample ages obtained were used to quantify (flow path integrated) production or depletion rates for trace metals, nutrients, and sulphate.We find young sea water percolating relatively fast through sediments close to the creek showing strong signs of alteration, whereas pore waters from diffusion dominated regions are less altered. The increase in inorganic nutrients and some trace elements along the flow path requires high rates of turnover. Sulphate, molybdenum, and uranium are almost completely depleted after 200 days, while dissolved inorganic carbon (DIC), ammonia, and manganese increase. Averaged production rates for DIC appear to be three times higher when advection dominated the subsurface flow regime. Our results demonstrate that sites dominated by advection generally show signs of faster rates of diagenetic reactions.  相似文献