Tectonic evolution of a Paleozoic thrust fault influences the hydrogeology of a fractured rock aquifer,northeastern Appalachian foreland

In polyorogenic regions, the superposition of structures during a protracted tectonic history produces complex fractured bedrock aquifers. Thrust‐faulted regions, in particular, have complicated permeability patterns that affect groundwater flow paths, quantity, and quality. In the Appalachian foreland of northwestern Vermont, numerous bedrock wells that are spatially related to the Paleozoic Hinesburg thrust have elevated naturally occurring radioactivity and/or low yields. The association of groundwater quality and quantity issues with this thrust was a unique opportunity to investigate its structural and hydrogeologic framework. The Hinesburg thrust juxtaposed metamorphic rocks of the hanging wall with sedimentary rocks of the footwall during the Ordovician. It was then deformed by two orthogonal Devonian fold sets and was fractured during the Cretaceous. Median well yields in the hanging wall aquifer are significantly lower than those of the footwall aquifer, consistent with the respective permeability contrast between metamorphic and carbonate rocks. For wells drilled through the Hinesburg thrust, those completed closest (vertically) to the thrust have the highest median yields, whereas others completed farther below have yields in the footwall range. The geochemical signature of the hanging wall and footwall aquifers correlates with their whole‐rock geochemistry. The hanging wall aquifer is enriched in alpha radiation, Na+K‐Cl, Ba, and Sr, whereas the footwall aquifer is enriched in Ca‐Mg‐HCO₃ and alkalinity. Wells that penetrated the Hinesburg thrust generally have hanging wall geochemical signatures. A simple hydrogeologic model for the permeability evolution of the Hinesburg thrust involves the ductile emplacement of a low‐K hanging wall onto a high‐K footwall, with subsequent modification by fractures.     

Indigenous African Furnace Types and Slag Composition—Is there a Correlation?

Within variation, three major iron smelting furnaces were used in the Iron Age of sub‐Saharan Africa, ranging from the natural draught driven tall shaft to the forced draught powered low shaft and bowl furnaces. These furnace types are, however, mostly known from the ethnographic context. Often, archaeologists are confronted with remnants from the smelting process, forcing them to speculate on the anatomy of the extant furnaces. The presence of multiple fused tuyeres has been used to identify natural draught furnaces in the archaeological record. However, working back from smelting remains such as slag to the furnace type using physical and chemical evidence has generally proved to be ‘undoable’. Thus, when randomly selected, the chances are high that one cannot separate bowl furnace slags from those that formed in their tall or low shaft counterparts. This observation is hardly unexpected; analogous thermodynamics and thermo‐chemical reactions governed bloomery smelting irrespective of furnace type. Rehren et al. (2007) have labelled this phenomenon the ‘tyranny of system driven constraints’. In this study, we argue that the hierarchical use of statistical methods may add another layer of evidence which, when coupled to archaeological indicators, may be useful in correlating slag chemistry to furnace types used in antiquity.     

The Early Bronze Age settlement of Fidvár,Vráble (Slovakia): reconstructing prehistoric settlement patterns using portable XRF

This paper presents first results of chemical analyses of sediment samples from the Early Bronze Age (EBA) settlement Fidvár near Vráble (Slovakia). Large-scale geomagnetic prospection revealed detailed architectural remains of a fortified settlement. Other structures such as an earthwork of the linear pottery culture and at least two Roman march camps were found too. An Auger programme provided sediment samples of different depths, A) from an EBA house and the outer fortification ditch, B) from a potential metal workshop area as indicated by surface finds, and C) from an area located in the settlement's centre. The samples were analysed by a portable X-ray fluorescence (pXRF) spectrometer in order to investigate the vertical and horizontal distribution of chemical signatures. The comparison of geophysical data and three-dimensional chemical patterns gives us the opportunity to determine the human impact and to reconstruct activity patterns. The potentials and limits in the application of pXRF in archaeological soil chemical surveys are evaluated by systematic comparisons with high resolution laboratory measurements, including atomic absorption spectrometry (AAS) and inductively coupled plasma optical emission spectrometry (ICP-OES). The pXRF analyses can be reproduced well and show a good accuracy. Whilst (p)XRF analyses reflect the total composition of archaeological soil samples, the results of the AAS and ICP-OES analyses are fundamentally influenced by the acid digestion or extraction methods used. The pXRF analyses of the Vráble soils showed typical patterns of human occupation. For example, there are strong positive correlations between phosphorous, strontium and calcium. Phosphorous shows an enrichment in pathways and the fortification ditch. It is less strongly enriched within the sediments of house structures. Similar results apply to calcium and strontium distribution. But compared to the respective concentrations in sediment samples from the ditch they show a considerably higher variation in samples associated with house structures; that is, individual samples of sediments from house structures contained high concentrations of both, calcium and strontium. The deposits of an area that according to surface finds was thought to represent a potential metal workshop did not show indicative chemical signatures. Targeted excavations confirmed the absence of such as workshop. Finally it was shown that the refill history of the innermost fortification ditch (sample area D) and the overall cultural occupation sequence at the site correlate strongly with the chemical signatures of the respective ditch profile. The systematic variation of key elements along the profile opens up an entirely new perspective for interpreting the site's history. Overall, the study shows the great potential of pXRF as valuable part of an archaeological survey toolkit.     

古食谱与微量元素分析

近年来 ,古食谱研究已成为考古学研究中一个重要的领域。人体骨骼中微量元素已经广泛地应用为重建古代食物结构、生存方法、经济生活变化的指示剂。加以合理的研究设计 ,微量元素的分析能为我们研究过去生活方式和社会制度提供重要的资料。     

Wissenstransfer durch Zentrenbildung. Physikalische Methoden in der Chemie und den Biowissenschaften

From the 1950s to 1970s, physical techniques replaced many classical methods in the chemical and biological sciences. In this development, a novel type of method‐oriented scientists emerged, relying on cooperation with instrument manufacturers and forging close links with science‐funding agencies. Their main engagement was the development of methods and the improvement of instruments, responding to the needs of the chemical and biomedical communities. In the United States, an important institutional locus of such method‐oriented scientists were instrument centers, providing service to regional and national groups of scientific users. This article analyzes the knowledge transfer involved in investigating the Biotechnology Resources Program of the National Institutes of Health, and presenting the example of one of these centers, the Stanford Magnetic Resonance Laboratory.     

Boerhaave's Furnace. Exploring Early Modern Chemistry through Working Models

This article discusses the (re)construction and use of an Early modern instrument, better known as Herman Boerhaave's (1668–1738) little furnace. We investigate the origins, history and materiality of this furnace, and examine the dynamic relationship between historical study and reconstructing and handling an object. We argue that combining textual analysis with performative methods allows us to gain a better understanding of both the role of lost material culture in historical chemical practice, pedagogy, and knowledge production, and provide a deeper understanding of the embodied experiences and knowledge of historical actors. Having made and used two versions of Boerhaave's furnace, we provide insight in what present-day working models can tell us about historical materials and practices approximately three centuries ago.     

在化学教学中体现学生的主体性

传统意义上的教学设计,主要是老师从主观愿望出发,以老师为中心,以教材为依据,凭借自己的教学经验,主观意志．进行安排和策划,其适用性和合理性都较差．教学效果常会事倍功半。     

Southern African glass beads: chemistry,glass sources and patterns of trade

Three-hundred-and-sixty glass beads from 19 archaeological sites in southern Africa dating between about the 8th and 16th centuries AD were analyzed using LA-ICP-MS, determining 47 chemical elements. The eight different bead series, previously defined on morphological characteristics, possess different glass chemistries. Some bead series were made from plant-ash glasses, others from soda-alumina glasses. Zhizo series beads of the late 1st millennium AD were probably made from Iranian glass. Later bead series were made of glass probably manufactured in South Asia, though there are changes through time in both South Asian glass recipes and bead morphologies.     

Three-dimensional (3D) visualisation: the application of terrestrial laser scanning in the investigation of historical Scottish farming townships

Recent developments in digital technologies are heralding significant changes in the way we acquire, visualise and analyse archaeological data. Terrestrial laser scanners can be used to create photo-realistic virtual copies of landscapes, and archaeological features, and offer the potential to improve our understanding of three-dimensional (3D) spatial relationships at study sites. Here we present a methodology for the integration of a high-resolution 3D site model with soil chemical data obtained from an abandoned settlement site located in the Central Highlands of Scotland. At this site, the multi-element concentration in soil, co-visualised within a topographic setting, has an important role to play in elucidating settlement layout and activity. The methods described here are also of significance in archiving sites of archaeological/historical importance where development activities and/or environmental processes may destroy remains, or where access to field sites is restricted.     

Secular variations in seawater chemistry as a control on the chemistry of basinal brines: test of the hypothesis

The hypothesis that basinal brines inherited their major ion chemistries and elevated salinities from evaporated paleoseawaters is tested by comparing the compositions of basinal brines in Silurian (Michigan basin, Illinois basin, Appalachian basin in eastern Ohio) and Jurassic/Cretaceous (Central Mississippi Salt Dome basin, Arkansas shelf, and south‐central Texas) host rocks, when the world oceans were ‘CaCl₂ seas’, with those from Permian and Pennsylvanian rocks (Palo Duro basin, Central Basin Platform, and Delaware basin, Texas and New Mexico) when the world oceans were ‘MgSO₄ seas’. Basinal brines examined are assumed to have originally formed from evaporation of the same seawaters that produced major evaporites. Sulfate, Mg and K levels in basinal brines are below the concentrations expected from evaporation of seawater of any type, which emphasizes the importance of diagenetic mineral–brine interactions in controlling basinal brine chemistry. There are no major differences in SO₄, Mg and K concentrations between basinal brines hosted by rocks originally formed during ages when the world oceans were MgSO₄ seas versus CaCl₂ seas. Basinal brines in Pennsylvanian–Permian rocks are compositionally distinct (relatively high Na and low Ca) from basinal brines in Silurian, Jurassic and Cretaceous host rocks, which may reflect original differences in seawater chemistry. Basinal brines enriched in Ca and depleted in Na relative to evaporated seawater of any type have traditionally been interpreted to form by albitization of plagioclase feldspar. A new explanation for Ca enrichment and Na depletion of basinal brines is the mixing of evaporated CaCl₂‐type seawater with more dilute water. Some basinal brines are similar in major ion composition to evaporated seawater of a particular age, for example basinal brines in the Cretaceous Edwards Group carbonates, Texas, where dolomitization is the only reaction required to convert evaporated Mesozoic CaCl₂ seawater into Edwards Group brine.