Peat as an archive of atmospheric pollution and environmental change : A case study of lead in Europe

Inorganic geochemistry in peat deposits provides unique and valuable indications of human activities and consequent environmental changes

Mineral Chemistry Of The Llaima Pumice, Southern Chile : Evidence For Magma Mixing

This paper details the mineralogy and the chemistry of the Llaima pumice deposit from in southern Chile. This andesitic to dacitic pumice was erupted from Llaima Volcano. This eruption took place in the early Holocene through at least two pulses that are well recorded in deposits around the Icalma-Galletué area. In 2001, the Llaima pumice was sampled from six outcrops. The mineralogy has been studied under polarizing microscope and electron microprobe (EPMA).The Llaima pumice contains phenocrystals of orthopyroxene, clinopyroxene, olivine and titano–magnetite. The olivine is characterized by two chemically distinguishable populations (i.e. Fo32 to Fo35 and Fo76 to Fo82). The respective chemical compositions of these two distinct olivines emphazise that the eruption was triggered by magma mixing

Coring and sub-sampling of peatlands for palaeoenvironmental research

Every palaeoenvironmental, palaeoecological and palaeogeochemical study of a peatland begins with coring or section sampling and sub-sampling. This first step in a peat-based palaeoenvironmental study is the most crucial, as a high-quality investigation can be achieved only from a foundation of high-quality stratigraphic sampling and sub-sampling. Various techniques for coring, sampling and sub-sampling are described, aiming to: (a) provide the reader with an overview of existing approaches and techniques; (b) offer guidance on good practice for achieving high-quality results efficiently; and (c) standardise the methodology in order to achieve comparable sequences and samples for future multiproxy, multi-site and multi-core projects

Emissions from pre-Hispanic metallurgy in the South American atmosphere

Peer reviewedPublisher PD

Quantitative WD-XRF calibration for small ceramic samples and their source material

A wavelength-dispersive X-ray fluorescence (WD-XRF) calibration is developed for small powdered samples (300mg) with the purpose of analyzing ceramic artifacts that might be available only in limited quantity. This is compared to a conventional calibration using a larger sample mass (2g). The comparison of elemental intensities obtained in both calibrations shows that the decrease in analyzed sample mass results in a linear decrease in measured intensity for the analyzed elements. This indicates that the small- and large-sample calibrations are comparable. Moreover, the elemental contents of four ceramic sherds and two potential clay sources fall well within the range of the certified reference materials that are the basis of the calibration curves. The advantage with the analytical method presented here is that it is rapid and requires only a small amount of sample that can easily be re-used for further analyses. This method has great potential in ceramic provenance studies

Comment on “The biosphere: A homogeniser of Pb-isotope signals” by C. Reimann, B. Flem, A. Arnoldussen, P. Englmaier, T.E. Finne, F. Koller and Ø. Nordgulen

Reimann et al. (2008) recently published a study on Pb-isotope signature along a 120 km long transect cutting the city of Oslo. Based on concentration but also isotope data, they misinterpret Pb concentration of the biosphere in rural places and explain these large enrichments of Pb as being due to natural processes. The study ignores numerous previous studies either on local, regional or global scales (see reviews by Shotyk and Le Roux, 2005 and Callender, 2003, and references therein), which clearly demonstrate that anthropogenic Pb emitted in the atmosphere from different sources (leaded gasoline, coal burning, metallurgy, etc.) was and is dispersed worldwide. The study also ignores work on Norway by the Steinnes and colleagues group (Harmens et al., 2008, Steinnes et al., 2005a, Steinnes et al., 2005b and Åberg et al., 2004), and measurements and modelling by the EMEP network (www.emep.int/, EMEP, 2005). The study also neglects numerous works on preanthropogenic Pb deposition rate and isotopic signature using continental archives of atmospheric deposition like peat bogs (Shotyk et al., 1998, Klaminder et al., 2003, Kylander et al., 2005 and Le Roux et al., 2005). These studies have shown that preanthropogenic Pb atmospheric deposition rate and its Pb isotopic signature is regionally defined, but also that those signals are negligible compared to past 2 ka and recent Pb atmospheric fluxes (Table 1)

Assessment of the spatial distributions of total- and methyl-mercury and their relationship to sediment geochemistry from a whole-lake perspective

The aim of this study was to determine the spatial variability for total- and methylmercury in surface sediments (0–2 cm) across a single whole-lake basin, and to relate this variability to the sediment’s geochemical composition. 83 surface sediment samples from Stor-Strömsjön – a lake with multiple sub-basins located in northern Sweden – were analyzed for geochemical composition as well as total-mercury (total-Hg) and methylmercury (methyl-Hg; 35 samples) concentrations. Our results indicate that variations in fine-grained mineral matter (36%) and organic matter (34%) explain an equal amount of the total-Hg variation, but that their relative importance varies between different parts of the lake. Total-Hg concentrations were similar in locations controlled by organic matter or fine-grained mineral matter (average 109 ng g␣1); however, total-Hg inventories (mass per unit area) were significantly higher in the latter (35 and 53 mg m␣2, respectively). Methyl-Hg concentrations are largely (55% of variance) controlled by water depth and sulfur concentration, which supports the importance of within lake methylation reported from other studies. Both for concentrations and inventories the spatial distribution for methyl-Hg in surface sediments is patchy, and interestingly the highest methyl-Hg inventory (1.4 mg m␣2) was found in a shallow location with coarse-grained minerogenic sediment (very low organic matter). A large spatial variability, even within a single lake, is something that needs to be recognized, e.g., when studying processes affecting mercury cycling, mercury loadings and when using lake sediments to reconstruct historic mercury deposition

Variation in methanotroph-related proxies in peat deposits from Misten Bog, Hautes-Fagnes, Belgium

Methane emissions from peat bogs are strongly reduced by aerobic methane oxidising bacteria (methanotrophs) living in association with Sphagnum spp. Field studies and laboratory experiments have revealed that, with increasing water level and temperature, methanotrophic activity increases. To gain a better understanding of how longer term changes in methanotrophic activity are reflected in methanotroph biomarkers, a peat record (0–100 cm) from the Hautes-Fagnes (Belgium) encompassing the past 1500 years, was analysed for methanotroph-specific intact bacteriohopanepolyols (BHPs) and the carbon isotopic composition of diploptene. A predominance of aminobacteriohopanetetrol (aminotetrol) over aminobacteriohopanepentol (aminopentol) indicated the prevalence of type II methanotrophs. Relatively high methanotrophic activity was indicated by all methanotroph markers between 20 and 45 cm depth, around the present oxic–anoxic boundary, most likely representing the currently active methanotrophic community. Comparing methanotrophic markers in the deeper part of the peat profile with environmental variables afforded, however, no clear correlation between change in water level and methanotrophic activity. This is potentially caused by a predominance of type II methanotrophs, a combination of sources for methanotrophic biomarkers or insufficient variation in climatic changes. A proposed way forward would include a study of a core covering a longer timescale, thereby involving greater variability

Selected papers from the 29th SEGH Conference on Environmental Geochemistry and Health

The 29th Conference on Environmental Geochemistry and Health took place in Toulouse (France) from 8 to 12 July 2013