Strontium Isotopes in the Investigation of Early Glass Production: Byzantine and Early Islamic Glass from the Near East*

⁸⁷Sr/⁸⁶Sr ratios have been determined for glasses from four production sites, dated to between the sixth and the 11th centuries, in the Eastern Mediterranean region. On the basis of elemental analyses, the glasses at each location are believed to have been melted from different raw materials. Two glass groups, from Bet Eli‘ezer and Bet She‘an, in Israel, are believed to have been based upon mixtures of Levantine coastal sands and natron, and have ⁸⁷Sr/⁸⁶Sr ratios close to 0.7090, plus high elemental strontium, confirming a high concentration of modern marine shell (⁸⁷Sr/⁸⁶Sr ~ 0.7092) in the raw materials. The isotopic compositions of these two groups of glasses differ slightly, however, probably reflecting a varying ratio of limestone to shell because the sands that were utilized were from different coastal locations. Natron‐based glasses from a workshop at Tel el Ashmunein, Middle Egypt, have ⁸⁷Sr/⁸⁶Sr values of 0.70794–0.70798, and low elemental strontium, consistent with the use of limestone or limestone‐rich sand in the batch. High‐magnesia glasses based on plant ash, from Banias, Israel, have ⁸⁷Sr/⁸⁶Sr values of 0.70772–0.70780, probably reflecting the isotopic composition of the soils that were parental to the plants that were ashed to make the glass. Strontium and its isotopes offer an approach to identifying both the raw materials and the origins of ancient glasses, and are a potentially powerful tool in their interpretation.     

A simulation of the hydrothermal response to the Chesapeake Bay bolide impact

Groundwater more saline than seawater has been discovered in the tsunami breccia of the Chesapeake Bay Impact Crater. One hypothesis for the origin of this brine is that it may be a liquid residual following steam separation in a hydrothermal system that evolved following the impact. Initial scoping calculations have demonstrated that it is feasible such a residual brine could have remained in the crater for the 35 million years since impact. Numerical simulations have been conducted using the code HYDROTHERM to test whether or not conditions were suitable in the millennia following the impact for the development of a steam phase in the hydrothermal system. Hydraulic and thermal parameters were estimated for the bedrock underlying the crater and the tsunami breccia that fills the crater. Simulations at three different breccia permeabilities suggest that the type of hydrothermal system that might have developed would have been very sensitive to the permeability. A relatively low breccia permeability (1 × 10^?16 m²) results in a system partitioned into a shallow water phase and a deeper superheated steam phase. A moderate breccia permeability (1 × 10^?15 m²) results in a system with regionally extensive multiphase conditions. A relatively high breccia permeability (1 × 10^?14 m²) results in a system dominated by warm‐water convection cells. The permeability of the crater breccia could have had any of these values at given depths and times during the hydrothermal system evolution as the sediments compacted. The simulations were not able to take into account transient permeability conditions, or equations of state that account for the salt content of seawater. Results suggest, however, that it is likely that steam conditions existed at some time in the system following impact, providing additional evidence that is consistent with a hydrothermal origin for the crater brine.     

E-region nitric oxide concentrations inferred from the 26 February 1979 eclipse expedition

Nitric oxide (NO) concentrations have been determined from the analysis of positive ion composition data obtained by AFGL for eclipse and post-eclipse conditions near Red Lake, Canada. Values of about 3 × 10⁸ cm⁻³ for 105–110 km and about 3 × 107 cm⁻³ for 90 km have been established. A residual ion-pair production rate of about 50 cm⁻³ s⁻¹ is estimated for eclipse totality at 110 km. A factor of two uncertainty is thought to be appropriate for all deduced values. The calculated NO concentrations appear to be within the range of typical variations for this season (late winter) and latitude (51°N).     

Fluid mixing induced by hydrothermal activity in the ordovician carbonates in Tarim Basin,China

Permian hydrothermal activity in the Tarim Basin may have been responsible for the invasion of hot brines into Ordovician carbonate reservoirs. Studies have been undertaken to explain the origin and geochemical characteristics of the diagenetic fluid present during this hydrothermal event although there is no consensus on it. We present a genetic model resulting from the study of δ¹³C, δ¹⁸O, δ³⁴S, and ⁸⁷Sr/⁸⁶Sr isotope values and fluid inclusions (FIs) from fracture‐ and vug‐filling calcite, saddle dolomite, fluorite, barite, quartz, and anhydrite from Ordovician outcrops in northwest (NW) Tarim Basin and subsurface cores in Central Tarim Basin. The presence of hydrothermal fluid was confirmed by minerals with fluid inclusion homogenization temperatures being >10°C higher than the paleo‐formation burial temperatures both in the NW Tarim and in the Central Tarim areas. The mixing of hot (>200°C), high‐salinity (>24 wt% NaCl), ⁸⁷Sr‐rich (up to 0.7104) hydrothermal fluid with cool (60–100°C), low‐salinity (0 to 3.5 wt% NaCl), also ⁸⁷Sr‐rich (up to 0.7010) meteoric water in the Ordovician unit was supported by the salinity of fluid inclusions, and δ¹³C, δ¹⁸O, and ⁸⁷Sr/⁸⁶Sr isotopic values of the diagenetic minerals. Up‐migrated hydrothermal fluids from the deeper Cambrian strata may have contributed to the hot brine with high sulfate concentrations which promoted thermochemical sulfate reduction (TSR) in the Ordovician, resulting in the formation of ¹²C‐rich (δ¹³C as low as ?13.8‰) calcite and ³⁴S‐rich (δ³⁴S values from 21.4‰ to 29.7‰) H₂S, pyrite, and elemental sulfur. Hydrothermal fluid mixing with fresh water in Ordovician strata in Tarim Basin was facilitated by deep‐seated faults and up‐reaching faults due to the pervasive Permian magmatic activity. Collectively, fluid mixing, hydrothermal dolomitization, TSR, and faulting may have locally dissolved the host carbonates and increased the reservoir porosity and permeability, which has significant implications for hydrocarbon exploration.     

Considerations on the provenance determination of plant ash glasses using strontium isotopes

Strontium isotopic analysis has been proposed as a suitable method to determine the primary production location of ancient plant ash glasses. The technique is based upon the assumption that Sr enters this glass type with the plant ash used as a flux material, and that the ⁸⁷Sr/⁸⁶Sr ratio of the resulting glass reflects the geological provenance of that flux. In such case, the bulk Sr isotopic composition of the bedrock should be inherited unchanged in the plants growing on that bedrock. Different types of plant ash glasses have been shown to have widely differing ⁸⁷Sr/⁸⁶Sr compositions. In this study, the ⁸⁷Sr/⁸⁶Sr composition of several plant species growing on different bedrock types is measured, and compared to the bulk Sr isotopic composition and petrology of that bedrock. The paper shows that the ⁸⁷Sr/⁸⁶Sr ratio of these plants is a function not only, or even mostly, of the local geology, but also of the Sr isotopic composition of the total water consumed by that plant. This is highly likely to be both plant species dependent and dependent on the small-scale hydrology of the area immediately surrounding the plant. In this way, no definite relation between the isotopic composition of a geological outcrop and the plants growing on this bedrock can be inferred. Hence, the isotopic composition of a plant ash made from such plants is uncertain and moreover species dependent. Though groups of plant ash glasses can certainly be compared in time and space using Sr isotopes, it may prove difficult to ascertain a plant ash glass type to a specific geographical-geological region.     

Stable isotopic analysis of human bones from Jiahu site,Henan, China: implications for the transition to agriculture

We have investigated change in subsistence during the transition to agriculture in the site of Jiahu, Henan Province, China, using stable isotopic analysis of collagen and apatite in human bones. Millet agriculture is well documented at drier high latitudes of the Yellow River Valley, while rice agriculture predominated at wetter lower latitudes of the Yangtze Valley region. The early Neolithic site of Jiahu lies near the boundary between the drier north and wetter south. Archaeobotanical evidence shows that rice was a significant component of diet at Jiahu, but its δ¹³C value is similar to that of other foods, and therefore cannot be conclusively identified by carbon isotope analysis. Foxtail and broomcorn millets are the only C₄ crops known for the Chinese Neolithic. Because of their high δ¹³C values, their consumption can be evaluated by stable carbon isotope analysis of human bone. Collagen reflects mainly the δ¹³C value of dietary protein, and apatite accurately records that of the whole diet. Isotopic analysis of 15 well-preserved samples from three periods shows that collagen δ¹³C values were very low for almost all individuals, suggesting C₃-based foods dominated their diets. However, apatite carbonate δ¹³C values and δ¹³C spacing between collagen and apatite (Δ¹³C_ap-co) indicate that millet may have been a minor component of the diet in this region. Individuals, who consumed the smallest amounts of animal protein, as indicated by low δ¹⁵N, generally had the highest apatite δ¹³C values. Archaeobotanical evidence for millet at Jiahu is needed to support this interpretation.     

Chloride ion concentrations during the compression of rocks to extract pore water

Pore water needs to be extracted from rocks with low permeabilities to allow the major ion concentrations in the pore water to be estimated. Compressing a rock is the most widely used method of extracting the pore water. However, ion concentrations have been found to change during compression in previous studies, and the mechanisms involved in such ion concentration changes have not yet been fully assessed. In this study, two natural rocks and four artificially prepared samples were compressed, and changes in the chloride ion (Cl^?) concentrations as the compression pressure increased were investigated. Mechanisms that could have caused the changes observed were then assessed. The Cl^? concentrations in squeezed water decreased as the pressure increased if the sample contained a significant amount of smectite. The strong dependence of Cl^? concentration on the amount of smectite indicated that smectite played an important role in decreasing the Cl^? concentration. The dilution of the pore water with interlayer water from the smectite appeared to be the dominant mechanism involved in the decrease in Cl^? concentration found in a Kunigel‐V1 sample, because dilution of the pore water with interlayer water quantitatively explained the decrease in the Cl^? concentration. The filter effect caused by the anion exclusion effect did not appear to be a dominant mechanisms in our case. However, Cl^? concentration decrease found in natural rocks could not be fully explained by dilution with interlayer water, so other mechanisms must be involved the phenomenon in natural rocks.     

Stabilization of the Tlaltecuhtli monolith pigments

A painted monolith, as important as the Aztec Calendar or the Coyolxauhqui, has been discovered in the ritual Aztec center of Mexico City. It represents Tlaltecuhtli, the bisexual manifestation of the Earth from whom all life comes. Still, pigments, which have lost their conglomerating resins, have to be retained. In this study, the consolidation of ochre pigment on original fragments from the Aztec sculpture is presented. Several compounds were tested as consolidants, on the one hand natural polysaccharides, Funori and Slobber of Nopal exudate, on the other derivatives of cellulose, Methocel^® and Klucel^®, and also commercial consolidants as KSE 300^® and Paraloid B72^®. To simulate the ageing of consolidated samples, they were treated in an Accelerated Weathering Tester. Then, both sets of samples, fresh and aged, were characterized structural, morphological and texturally by using X-ray diffraction, electronic microscopy and nitrogen adsorption, respectively. A leaching test was performed on consolidated samples to evaluate the consolidant efficiency.     

Assessing natural variation and the effects of charring,burial and pre-treatment on the stable carbon and nitrogen isotope values of archaeobotanical cereals and pulses

The aim of this study is to assess the potential of charred archaeobotanical cereal grain and pulse seed δ¹³C and δ¹⁵N values to provide evidence of crop growing conditions and as a potential component of palaeodietary studies. In order to reliably interpret archaeobotanical δ¹³C and δ¹⁵N values it is necessary to take into account the impact of charring, burial and laboratory pre-treatment procedures. We examine the effects of charring and burial on bulk δ¹³C, δ¹⁵N, %C, %N and C:N ratios in modern cereal and pulse material, and of cleaning by acid–base–acid (ABA) pre-treatment on modern and archaeobotanical charred material. Our study utilised bulk grain and seed samples to help account for within-ear/pod and between-plant variability in δ¹³C and δ¹⁵N values. Heating at relatively low temperatures and for prolonged times (230 °C for up to 24 h) is conducive to the formation of well preserved, undistorted charred cereal grain and pulse seed. Heating for 24 h has a systematic and predictable effect on δ¹⁵N values, with increases of around 1‰ on average in cereal grains and pulse seeds, and no consistent impact on δ¹³C values. Increases in δ¹⁵N are likely due to the loss of lighter ¹⁴N via N-containing volatiles. Burial (for up to 2 years) and ABA pre-treatment have no significant effects on δ¹³C or δ¹⁵N values. After pre-treatment, however, the %C and %N contents of the archaeobotanical material more closely resembles that of the modern charred grains and seeds, suggesting that archaeobotanical remains accumulate non-structural material during burial but retain their original carbon and nitrogen content. Therefore %C, %N contents and C:N ratios can provide useful criteria for assessing archaeobotanical preservation.     

Sedimentation rates in the Lake Qattinah using 210Pb and 137Cs as geochronometer

The constant rate of supply (CRS) of excess ²¹⁰Pb model was successfully applied to assess ²¹⁰Pb data of two sediment cores from the lake Qattinah, Syria. Gamma spectrometry was used to determine ¹³⁷Cs and ²¹⁰Pb activity concentrations. The bottom of the cores was ²¹⁰Pb-dated to years 1907 and 1893. The accumulation rates were determined using ²¹⁰Pb method and found to vary similarly in both cores from 0.10 ± 0.01 to 3.78 ± 0.57 kg m^?2 y^?1 during the past century. ¹³⁷Cs was used as an in-dependent chronometer. The two distinct peaks observed on the ¹³⁷Cs record of both cores, corresponding to 1965 and 1986, have allowed a successful validation of the CRS model.     

Identifying immigrants to Tikal,Guatemala: Defining local variability in strontium isotope ratios of human tooth enamel

Stable strontium isotopes have been used to identify the skeletons of migrants in several recent archaeological studies, in which local ⁸⁷Sr/⁸⁶Sr values have been inferred through statistical parameters of human ⁸⁷Sr/⁸⁶Sr data, or by reference to local fauna or other environmental samples. This paper compares these approaches using data from the ancient Maya city of Tikal, Guatemala. The skeletons of eight migrants from distant geological zones are readily apparent among the 83 Tikal skeletons sampled. Three additional non-local skeletons can be eliminated to obtain a normally distributed “local” Tikal sample. The mean of this sample is higher than the available data for local fauna and for lime that may have been used to treat maize at Tikal. It is possible that imported sea salt with a high ⁸⁷Sr/⁸⁶Sr ratio could account for this elevated mean for Tikal humans. Modeling demonstrates that dietary ⁸⁷Sr/⁸⁶Sr may be raised to the level found at Tikal by a daily intake of only 6 g of sea salt.     

Sporadic neutral metal layers in the mesosphere and lower thermosphere

Although the existence of thin ionized layers at heights around 100 km has been known for many years, it is only much more recently that thin neutral metal layers have been observed. Such layers, initially sodium and more recently calcium and iron, have been detected by lidar. The layers, with thicknesses between about 100m and several kilometres, and concentrations between about 10² and 10⁵ cm⁻³, occur most frequently between 90 and 100 km, and are normally superimposed on a background layer about 10 km thick. The occurrence of thin neutral layers appears to be latitude dependent, and is strongly linked to the appearance of Es on ionograms. Several causative mechanisms have been suggested, none of which appears to be capable of providing an altogether satisfactory explanation for the formation of the layers.     

Constraining groundwater flow in the glacial drift and saginaw aquifers in the Michigan Basin through helium concentrations and isotopic ratios

³He and ⁴He concentrations in excess of those in water in solubility equilibrium with the atmosphere by up to two and three orders of magnitude are observed in the shallow Glacial Drift and Saginaw aquifers in the Michigan Basin. A simplified He transport model shows that in situ production is negligible and that most He excesses have a source external to the aquifer. Simulated results show that ³He and ⁴He fluxes entering the bottom of the Saginaw aquifer are 7.5 × 10^?14 and 6.1 × 10^?7 cm³STPcm^?2 yr^?1, both of which are lower than fluxes entering the underlying Marshall aquifer, 1.0 × 10^?13 and 1.6 × 10^?6 cm³STPcm^?2 yr^?1 for ³He and ⁴He, respectively. In contrast, He fluxes entering the Saginaw aquifer are higher than fluxes entering the overlying Glacial Drift aquifer of 5.2 × 10^?14 and 1.5 × 10^?7 cm³STPcm^?2 yr^?1 for ³He and ⁴He, respectively. The unusually high He fluxes and their decreasing values from the lower Marshall to the upper Glacial Drift aquifer strongly suggest the presence of an upward cross‐formational flow, with increasing He dilution toward the surface by recharge water. These fluxes are either comparable to or far greater than He fluxes in deeper aquifers around the world. Model simulations also suggest an exponential decrease in the horizontal groundwater velocity with recharge distance. Horizontal velocities vary from 13 to 2 myr^?1 for the Saginaw aquifer and from 18 to 6 myr^?1 for the Marshall aquifer. The highly permeable Glacial Drift aquifer displays a greater velocity range, from 250 to 5 myr^?1. While Saginaw ⁴He ages estimated based on the simulated velocity field display an overall agreement with ¹⁴C ages, ¹⁴C and ⁴He ages in the Glacial Drift and Marshall aquifers deviate significantly, possibly due to simplifications introduced in the He transport model leading to calculation of first‐order approximation He ages and high uncertainties in Glacial Drift ¹⁴C ages.     

Isotopic evidence for Middle Horizon to 16th century camelid herding in the Osmore Valley,Peru

Archaeological and zooarchaeological data indicate that camelid pastoralism was a subsistence and economic mainstay of Middle Horizon and more recent cultures in the Osmore region of southern Peru. However, it is not known whether camelids were primarily herded in highland puna pastures or near lower elevation sites in the middle valley or along the coast. This research examines the elevation of archaeological camelid herding in the Osmore Valley using stable isotope analysis. Stable carbon (δ¹³C) and nitrogen (δ¹⁵N) isotope ratios were measured on 28 archaeological camelid bone samples from the Middle Horizon sites of Cerro Baúl and Cerro Mejía, the Late Intermediate site of Yaral and the late pre‐Hispanic to Colonial period site of Torata Alta. Twenty‐three archaeological camelids have δ¹³C and δ¹⁵N values similar to five modern camelids maintained in highland puna pastures. In contrast, three camelids from the high status Wari site of Cerro Baúl, and two from Yaral have unexpectedly high δ¹³C and/or δ¹⁵N values outside the expected range for camelids pastured in highland puna habitats. The results may be explained by differences in foddering practices, altitudinal herding range or climatic conditions. Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) were also assessed to infer pasture elevation using the camelid remains from Cerro Baúl (n = 11). One individual in this sub‐sample exhibits a non‐local ⁸⁷Sr/⁸⁶Sr value indicative of an origin in the highland puna region east or south of Lake Titicaca. It was not possible to further distinguish between camelids herded in lower to middle elevation habitats outside the Lake Titicaca basin using ⁸⁷Sr/⁸⁶Sr values. This study suggests that multiple isotope proxies may be used to identify animals primarily pastured in lowland coastal versus highland puna (> 4000 masl (meters above sea level)) habitats, but are less useful at distinguishing between animals pastured in lower to middle elevation settings. Copyright © 2010 John Wiley & Sons, Ltd.     

Oxygen and strontium isotopes as provenance indicators of fish at archaeological sites: the case study of Sagalassos,SW Turkey

In this paper, we investigate the potential use of oxygen and strontium isotope ratios (δ¹⁸O_p and ⁸⁷Sr/⁸⁶Sr) measured in archaeological fish enamel as provenance indicators. δ¹⁸O_p and ⁸⁷Sr/⁸⁶Sr were measured in a suite of archaeological carp remains recovered from the Anatolian townsite of Sagalassos dated to the Early Byzantine period (AD 450–650) and compared to that of modern fish, river and lake waters from the Anatolian region. We used sequential leaches in weak acetic acid to remove diagenetic Sr from fossil tooth enamel, monitoring the effectiveness of this approach by measuring the Sr/Ca ratios of the leachates via an isotope dilution thermal ionization mass spectrometry method (ID-TIMS). δ¹⁸O_p values mostly excluded a riverine origin. ⁸⁷Sr/⁸⁶Sr ratios of one fish overlapped with the ⁸⁷Sr/⁸⁶Sr signatures of two lakes in the Anatolian region, and at least one lake (Gölcük) could be removed as a candidate owing to a very distinctive ⁸⁷Sr/⁸⁶Sr signature not found in any of the fish remains. Most of the tooth samples analyzed could not be assigned a precise geographical origin since the ⁸⁷Sr/⁸⁶Sr ratios measured in enamel did not match that of any of the local lakes selected as potential origin. This result suggests that carp may have originated from lakes that have not yet been sampled, although this conclusion is not supported by other archaeological evidence. Alternatively, the lack of correspondence between lakes and fish Sr isotope ratios highlights several possible sources of uncertainties including spatial heterogeneity in ⁸⁷Sr/⁸⁶Sr ratio within a lake, the contribution of dietary strontium to the ⁸⁷Sr/⁸⁶Sr ratio of fish tooth enamel, and post-mortem alteration of the tooth Sr isotope signal during fossilization. In spite of the high precision of the strontium isotope analyses and the wide range of variation in the surface waters of the Anatolian lakes and rivers, this method may remain limited to distinguishing between lakes situated in regions of bedrock of very distinct age and geology until these sources of uncertainty are more fully investigated.     

Iron mineralization and dolomitization in the Paran Fault zone,Israel: implications for low‐temperature basinal fluid processes near the Dead Sea Transform

Petrography, Eh‐pH calculations and the stable isotope composition of oxygen are used to interpret geochemical processes that occurred during iron oxide mineralization and dolomitization along the Menuha Ridge segment of the Paran Fault, southern Israel, adjacent to the Dead Sea Transform (DST). Iron mineralization is strongly localized in the fault zone as ferruginous lenses, whereas Fe dolomitization spreads laterally into the Cenomanian‐Turonian carbonate host rock as stratabound beds. The average oxygen isotope fractionation between syngenetic quartz and iron oxides in the ferruginous lenses gives a temperature of 50 ± 10°C and δ¹⁸O SMOW water = ?3.5‰; consistent with an origin from metalliferous groundwater flow in the sedimentary basin. Ferroan dolomite initially formed under strongly reducing conditions, but this was followed by oxidation and pseudomorphic replacement of the dolomite by a mesh of fine‐grained iron oxides (simple zoned dolomites). This cycle of ferroan dolomite formation and replacement by iron oxides was repeated in complex zoned dolomites. Dolomite oxygen isotope compositions fall into two groups: a high δ¹⁸O group corresponding to the simple zoned dolomites and non‐ferroan dolomites and a low δ¹⁸O group corresponding to the complex zoned dolomites. Water‐rock calculations suggest that the epignetic dolomites formed under fluid‐buffered conditions: the high δ¹⁸O group are indicated to have formed at temperatures of ca. 25°C for waters with δ¹⁸O = ?4 to 0‰; the low δ¹⁸O complex zoned dolomites at 50–75°C for waters with the same isotopic composition. A kinetic calculation for a complex zoned dolomite‐bearing bed indicates that dolomitization must have occurred at high values of the dolomite saturation index. This requirement for high Mg supersaturation and the indication that epigenetic dolomitization is more protracted in stratigraphically deeper formations located closer to the DST is consistent with models proposing that Mg‐rich solutions originated in the Dead Sea Rift.     

Textural and isotopic evidence on the fluid source and transport mechanism of antitaxial fibrous microstructures from the Alps and the Appalachians

The source of fluid‐forming veins is of great importance in order to understand the hydraulic system acting in the earth's crust. The study of syntectonic antitaxial veins is one of the few methods by which the opening history can be deduced from rocks, and thus these veins are of primary importance in determining rock kinematics. Antitaxial veins were taken from black shales in two different tectonic settings in the Helvetic Alps, Switzerland, and the Taconic Appalachians, New York State. These syntectonic extension veins are regularly spaced and are oriented sub‐normal to bedding. The vein microstructure displays a symmetry around the median line in the centre of the vein, and a symmetry in cathodoluminescence banding parallel to the vein–wall interface, which suggests transport along bedding‐parallel dissolution planes from both vein‐walls. Antitaxial veins nucleated in transgranular fractures, but evidence for ongoing multiple crack‐seal increments is lacking; rather, veins grew continuously keeping close contact to the vein‐wall. Radiogenic ⁸⁷Sr/⁸⁶Sr ratios are higher in the surrounding matrix than in the vein, and higher than the corresponding seawater data in all samples. Variations are small and calcite in both the vein and the host rock were derived from the same source of fluid in the Helvetic samples. Mass balance of Sr suggests that the amount of calcite is too small in the surrounding host rock to be derived locally. Stable oxygen compositions are heavier in the host rock than in the veins, with overall low variation in both δ¹⁸O and δ¹³C values in the Mesozoic Helvetic samples. Data point to a rock‐buffered system, the precipitate most likely derived from an external source. The lower Palaeozoic Appalachian veins have lesser δ¹⁸O values than the host rock, similar to the Helvetic veins. Radiogenic ⁸⁷Sr/⁸⁶Sr data and a large heterogeneity in stable isotope values indicate an open system. Microstructural and isotopic evidence suggests that the antitaxial veins were formed by pervasive fluid flow, with the solute at least partly derived from an external source.     

Chicken and Egg: Testing the Carbon Isotopic Effects of Carnivory and Herbivory

In bone, the spacing between δ¹³C in collagen and bioapatite carbonate is greater in herbivores than carnivores, with implications for understanding animal dietary ecology from surviving hard tissues. Two explanations have been proposed: varying diet composition or differences in physiology between herbivores and carnivores. We measured the isotopic effects of carnivorous and herbivorous diets on a single species, to test the effect of diet composition alone. Protein δ¹³C and δ¹⁵N and carbonate δ¹³C were measured on egg and bone from hens on different diets. Herbivorous hens had a +14.3‰ spacing between egg albumen and shell δ¹³C, compared to +12.4‰ for omnivorous hens, and +11.5‰ for carnivorous hens. The bioapatite–collagen Δ¹³C spacing was measured as +6.2‰ for herbivorous hens, and calculated as +4.3‰ for omnivorous hens, and +3.4‰ for carnivorous hens—similar to observed mammalian herbivore and carnivore bioapatite–collagen Δ¹³C differences. We conclude that a shift in diet composition from herbivory to carnivory in a single species does alter the bioapatite–collagen carbon isotopic spacing. Our data strongly suggest that this results from differences in the Δ¹³C_{bioapatite–diet} spacing, and not that of Δ¹³C_{collagen–diet}.     

Taxonomic, anatomical, and spatio-temporal variations in the stable carbon and nitrogen isotopic compositions of plants from an African savanna

Stable carbon (δ¹³C) and nitrogen (δ¹⁵N) isotope ratios are commonly used to reconstruct palaeodiets and palaeoenvironments. The method is based on our knowledge of isotopic patterns in plants, which are subject to taxonomic and environmental variability. While previous researchers have addressed isotopic variability amongst plants, no studies have looked extensively at a broad suite of taxa over multiple temporal scales from within the savanna biome so as to provide baseline data for palaeodietary and palaeoenvironmental studies. Here we document variations in the isotopic compositions of plants collected over two years from the Kruger National Park, South Africa, with respect to species and anatomical differences, and the influences of geological substrate and spatio-temporal shifts in climate. Results show that environmentally-induced carbon isotopic variations in plants within this region are generally smaller than 2‰, which is lower than what has been previously reported for plants compared across multiple habitat-types. These data suggest that δ¹³C differences of 2‰ or more (or 1‰ if the diet is predominantly C₄) between animals from a given area reliably indicate real dietary differences. Plant δ¹⁵N values vary greatly between different microhabitats (by up to 4‰), responding to a range of environmental influences that may, in turn, significantly influence variation in animal δ¹⁵N values.