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Coastal wetlands can serve as natural laboratories for assessing the future impacts of sea-level rise and the intricacies of the effect of sulfate (SO42-) on emissions of greenhouse gases, such as methane (CH4) and carbon dioxide. In the case of previously drained and freshened wetlands, we can observe how freshwater terrestrial microbial communities react and adapt to intrusion of SO42- rich saline waters. We conducted a 3-month anoxic incubation experiment with soil extracted from a peatland on the German Baltic coast which was rewetted with brackish water in late 2019 to examine how microbial communities at the site had adapted to the new conditions after two years. Soil slurries were incubated at a moderate temperature of 15 °C at two different salinities (reflecting surface water and average peat soil water salinity) and sampled at 8 timepoints. At each timepoint 5 replicates of each treatment were destructively harvested and sampled for concentrations of CH4, dissolved inorganic carbon (DIC), total aqueous organic carbon, SO42-, ammonium, and other major ions, pH values, qPCR analysis, and δ13DIC and δ13CH4 values.
This dataset is a continuously growing collection of lead isotope reference data. Lead isotopes are an established method to reconstruct the raw material provenance of archaeological objects. They are typically applied to artefacts made of copper, lead, silver, and their alloys. However, also the raw material provenance of other materials such as glass, pigments and pottery was already investigated using lead isotopes. To successfully reconstruct the origin of the raw material, lead isotope signatures from as many as possible suitable raw material occurrences must be known. In the past, large-scaled research projects were carried out to characterise ore deposits especially in the Mediterranean area and Western Europe. However, many of these data are dispersed in the literature and were published in scientific articles or monographs. Consequently, each researcher or at least each research group had to build their own up-to-date database of reference data from the literature. To overcome these restrictions, to facilitate work with lead isotope reference data and particularly to make the data FAIR, i.e., findable, accessible, interoperable and reusable (Wilkinson et al. 2016), these published data are compiled and transferred into a uniform layout. They are further enhanced with additional metadata to facilitate their use in raw material provenance studies. Currently, the database is restricted to ores and minerals as these are the most relevant materials for provenance studies of ancient metals. Future updates will include hitherto uncovered regions but also additional data from countries already present. Slag and other metallurgical (by-) products from ancient sites in close vicinity to ore deposits generally are a genuine representation of the ores utilised in historic times. As such, they are highly relevant for provenance studies and an extension to these materials is therefore planned. GlobaLID is a representation of the collective work of researchers on Pb isotope studies. As such, the database is seen as a community engagement project that invites scientists all over the world to become active contributors of GlobaLID. The initiators of the database dedicate their effort to the continuation and maintenance of the database but only the support of the whole community will allow a rapid and successful growth of GlobaLID.
The project from which the data derived aimed to establish the first systematic study of Cu isotope fractionation during the prehistoric smelting and refining process. For this reason, an experimental approach was used to smelt sulfide copper ore according to reconstructed prehistoric smelting models. The ore was collected by E. Hanning as part of her PhD thesis work from a Bronze Age mining site, the Mitterberg region, Austria (Hanning and Pils 2011) and was made available for the experiments.All starting materials for the experiments such as the natural ore, roasted ore, construction clay, flux, dung (used for the roasting), wood and charcoal (fuel) were natural materials. All firing conditions including the amount of fuel or charging material and the temperatures in the furnaces were recorded, and the experimental procedures were documented in the very detail. In total, 30 experiments were carried out in 4 experimental series. The smelting products, both intermediate products and final products were sampled during or after the respective experiment. Slag, matte and copper metal were the major smelting products. All other materials used in and produced by the experiments were sampled, too. Materials used and produced in the two most promising experimental series with regard to potential Cu isotope fractionation were analyzed. Based on the analytical results, the potential of Cu isotopes as a tool in archaeometallurgical research was systematically evaluated and consequences for the copper isotope application as a provenance tool in archaeometry were identified.The data include the documentation of the experiments, laboratory procedures and analytical methods. An experimental outline was previously published in Rose et al. (2019). Analytical methods applied were ICP-MS (elemental analysis, 80 samples), MC-ICP-MS (copper isotopes, 98 samples), and XRD (phase analysis, 25 samples). The experiments were carried out at the Römisch-Germanisches Zentralmuseum, Labor für Experimentelle Archäologie, Mayen, Germany. Laboratories used for the analytical part of the project were the research laboratories at the Deutsches Bergbau-Museum Bochum and FIERCE (Frankfurt Isotope and Element Research Center), Goethe-University Frankfurt, both Germany. Data were processed and plots created with R (R Core Team 2019) in RStudio®. Data are provided as data tables or text files, the R scripts used to create the time-temperature plots of the smelting experiments are also included.The full description of the data and methods is provided in the data description file.
This dataset is a continuously growing collection of lead isotope reference data. Lead isotopes are an established method to reconstruct the raw material provenance of archaeological objects. They are typically applied to artefacts made of copper, lead, silver, and their alloys. However, also the raw ma- terial provenance of other materials such as glass, pigments and pottery was already investigated us- ing lead isotopes. To successfully reconstruct the origin of the raw material, lead isotope signatures from as many as possible suitable raw material occurrences must be known. In the past, large-scaled research projects were carried out to characterise ore deposits especially in the Mediterranean area and Western Eu- rope. However, many of these data are dispersed in the literature and were published in scientific articles or monographs. Consequently, each researcher or at least each research group had to build their own up-to-date database of reference data from the literature. To overcome these restrictions, to facilitate work with lead isotope reference data and particularly to make the data FAIR, i.e., finda- ble, accessible, interoperable and reusable (Wilkinson et al. 2016), these published data are compiled and transferred into a uniform layout. They are further enhanced with additional metadata to facili- tate their use in raw material provenance studies. Currently, the database is restricted to ores and minerals as these are the most relevant materials for provenance studies of ancient metals. Future updates will include hitherto uncovered regions but also additional data from countries already present. Slag and other metallurgical (by-) products from ancient sites in close vicinity to ore deposits generally are a genuine representation of the ores uti- lised in historic times. As such, they are highly relevant for provenance studies and an extension to these materials is therefore planned. GlobaLID is a representation of the collective work of researchers on Pb isotope studies. As such, the database is seen as a community engagement project that invites scientists all over the world to be- come active contributors of GlobaLID. The initiators of the database dedicate their effort to the con- tinuation and maintenance of the database but only the support of the whole community will allow a rapid and successful growth of GlobaLID.
The data publication presented is concerned with the collection of geochemical results enhanced with metadata of archaeologic, stylistic, geographic and other crucial information. The publication covers analytical and metadata sets of analysed projectiles, both from own and published works. Starting point for the data collection was the PhD thesis Müller 2018 were projectiles from different find sites, dating into the Roman Republic, were analysed and published. The objects up to date included in the current database are from various find sites with varying archaeological background, which have been collected and evaluated by the authors for diachronic comparison within a supra-regional frame. Own unpublished data are also included. These data are of objects, which are too isolated in terms of a research question to be published in a journal. However, our intention is to make them accessible in the context compiled here for any further use. We hereby encourage other researchers to contribute to this database either with their published or even their unpublished data so that it can continuously develop for the specific objects presented here. The samples taken by the project group were analysed in the laboratories of FIERCE, the Frankfurt Isotope and Element Research Center of Goethe-University Frankfurt and the Research Laboratory of the Deutsches Bergbau-Museum Bochum, a central unit within its research department using Multicollector ICP mass spectrometry. We are initiating this database with the goal that it will grow through collective contributions from researchers working on this topic. It should therefore be seen as a project of collaborative engagement. The research team is dedicating its efforts to the continuation and maintenance of the database. Anyone who contributes data will be named as a contributor in subsequent versions of the database.
This dataset is a continuously growing collection of lead isotope reference data. Lead isotopes are an established method to reconstruct the raw material provenance of archaeological objects. They are typically applied to artefacts made of copper, lead, silver, and their alloys. However, also the raw material provenance of other materials such as glass, pigments and pottery was already reconstructed with lead isotopes. To successfully reconstruct the origin of the raw material, lead isotope signatures from as many as possible suitable raw material occurrences must be known. In the past, large-scaled research projects were carried out to characterise ore deposits especially in the Mediterranean area and Western Europe. However, many of these data are dispersed in the literature and were published in scientific articles or monographies. Consequently, each researcher or at least each research group had to build their own up-to-date data base of reference data from the literature. To overcome these restrictions, to facilitate work with lead isotope reference data and particularly to make the data FAIR, i.e. findable, accessible, interoperable and reusable (Wilkinson et al., 2016), these published data are compiled and transferred into a uniform layout. They are further enhanced with additional metadata to facilitate their use in raw material provenance studies. Currently, the database is restricted to ores and minerals as these are the most relevant materials for provenance studies of ancient metals. Future updates will include hitherto uncovered regions but also additional data from countries already present. Slag and other metallurgical (by-) products from ancient sites in close vicinity to ore deposits generally are a genuine representation of the ores utilised in historic times. As such, they are highly relevant for provenance studies and an extension to these materials is therefore planned. GlobaLID is a representation of the collective work of researchers on Pb isotope studies. As such, the database is seen as a community engagement project that invites scientists all over the world to become active contributors of GlobaLID. The initiators of the database dedicate their effort to the continuation and maintenance of the database but only the support of the whole community will allow a rapid and successful growth of GlobaLID.
The stable isotopic composition of pyrite (δ34Spyrite) and barite (δ34Sbarite, δ18Obarite) in marine sedimentary rocks provides a valuable archive for reconstructing the biogeochemical processes that link the sulfur, carbon, and iron cycles. Highly positive δ34Spyrite values that exceed coeval unmodified seawater sulfate (δ34Spyrite > δ34SSO4(SW)), have been recorded in both modern sediments and ancient sedimentary records and are interpreted to result from various biotic and abiotic processes under a range of environmental conditions. A host of processes, including basin restriction, euxinia, low seawater sulfate, dissimilatory microbial sulfate reduction, sulfide reoxidation, and sulfur disproportionation, have been suggested to account for the formation of highly positive δ34Spyrite values in marine environments. Significantly, determining which of these factors was responsible for the pyrite formation is impeded by a lack of constraints for coeval sulfate, with relatively few examples available where δ34Spyrite and proxies for δ34Ssulfate values (e.g., barite) have been paired at high resolution. In the Selwyn Basin, Canada, the Late Devonian sedimentary system is host to large, mudstone-hosted bedded barite units. These barite units have been interpreted in the past as distal expressions of SEDEX mineralization. However, recent studies on similar settings have highlighted how barite may have formed by diagenetic processes before being subsequently replaced during hydrothermal sulfide mineralization. Coincidentally, highly positive δ34Sbarite values have been recorded in such barite occurring coevally with pyrite in diagenetic redox front, where sulfate reduction is coupled to anaerobic oxidation of methane (SR-AOM) at the sulfate methane transition zone (SMTZ). The mechanisms of sulfur cycling and concurrent processes are, nevertheless, poorly constrained. Grema et al. (2021) integrate high-resolution scanning electron microscopy petrography of barite (+ associated barium phases) and pyrite, together with microscale isotopic microanalyses of δ34Spyrite, δ34Sbarite, and δ18Obarite of selected samples from the Late Devonian Canol Formation of the Selwyn Basin. Samples containing both barite and pyrite were targeted to develop paired isotopic constraints on the evolution of sulfur during diagenesis. We have focused on the precise mechanism by which highly positive δ34Spyrite values developed in the Canol Formation and discuss the implications for interpreting sulfur isotopes in similar settings. This data report comprises microscale secondary ion mass spectrometry (SIMS) analyses of the isotopic compositions of pyrite (δ34Spyrite; n= 200) and barite (δ34Sbarite; n= 485, δ18Obarite; n= 338) in nine stratigraphic sections of the Northwest Territories’ part of the Selwyn Basin. Microdrills of regions of interest (n= 54) were made on polished sections to obtain suitable subsamples, using a 4 mm diameter diamond core drill. Several representative subsamples were cast into 25 mm epoxy pucks, together with reference materials (RMs) of pyrite S0302A (δ34S V-CDT = 0.0 ± 0.2‰ (Liseroudi et al., 2021)) and barite S0327 (δ34SV-CDT = 11.0 ± 0.5 ‰; δ18OV-SMOW = 21.3 ± 0.2 ‰ (Magnall et al., 2016)). Microscale isotopic analyses were carried out using Cameca IMS1280 large-geometry secondary ion mass spectrometer (SIMS) operated in multi-collector mode at the NordSIMS laboratory, Stockholm, Sweden. External analytical reproducibility (1 σ) was typically ± 0.04‰ δ34S for pyrite, ± 0.15‰ δ34S, and ± 0.12‰ δ18O for barite. The sample identification, location, and depth are reported in the data files.
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