isotope studies
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Author(s):  
Azadeh Hosseini ◽  
Mohammad Hossein Saberi ◽  
Bahman ZareNezhad

AbstractHydrocarbon exploration has long been based on such costly and time-intensive methods as geophysical surveys, geological studies, and drilling. In recent years, however, researchers have started to consider such inexpensive alternatives as surface geochemistry for hydrocarbon exploration. Some 100 years ago, the leakage of hydrocarbons onto the surface in the form of micro- and macro-seepages motivated researchers toward drilling a well in the Khourian Desert in the south of Semnan Province, Iran. Upon drilling the well, researchers found evidences of non-released (free) hydrocarbons. These findings drove further study of the area using surface geochemistry while considering the nearby hydrocarbon accumulation in Qom Formation. Conventional and indirect surface geochemical methods provide an insight into the relationship between surface and subsurface hydrocarbons. In the present work, the results of the Rock–Eval pyrolysis showed total organic carbon (TOC) values in the range of 0.31–4.13 wt.% and S1 peaks between 0.07 and 27.35. Sulfur isotope analysis showed a sulfur isotopic value of −0.4. The study of hydrocarbon-oxidizing bacteria showed the presence of bacterial colonies in MSM at 1.22 × 106 cfu/g of soil sample. We further investigated surface changes due to the presence of free hydrocarbons and pH variations (4.9–8) resulted from the changes in the concentrations of calcium carbonate and iron. According to the results and given the presence of organic sulfur in the samples, the occurrence of Gach-i-turush and alike phenomena was proposed in this area. The results of geo-microbial prospecting method, surface secondary changes, and sulfur isotope studies were well in agreement with the characteristics of the existing hydrocarbon reserves in this area. Surface geochemical surveys can precede other geochemical and geophysical surveys to identify surface anomalies and hence focus on more probable locales of hydrocarbon accumulation in the Khourian Desert, central Iran.


2021 ◽  
Author(s):  
A. Sturbois ◽  
J. Cucherousset ◽  
M. De Cáceres ◽  
N. Desroy ◽  
P. Riera ◽  
...  

2021 ◽  
Vol 150 ◽  
pp. 23-47
Author(s):  
Kenneth Brophy ◽  
Dene Wright

Although the Neolithic period is defined by farming, physical evidence for processes associated with farming are rare, with agricultural practices usually indicated by environmental and biomolecular proxies for domesticates such as pollen evidence, ceramic residues and lipids, animal bones, plant remains and stable isotope studies. This paper will, we hope, invigorate discussion on the recognition, interpretation and significance of physical traces of farming in Scotland. The starting point will be the summary of two excavations, Wellhill and Cranberry, both Perth and Kinross, in 2014 and 2016 respectively, part of the Strathearn Environs and Royal Forteviot (SERF) project. These cropmark sites revealed evidence for possible Neolithic farming in the form of possible ard marks and field ditches. There follows a synthesis of physical evidence for Neolithic farming in Scotland, drawing together evidence for ard marks, field boundaries, cultivation ridges, cultivated middens, and soils. Recommendations are made for recognising and interpreting such features on excavations, and the potential benefits of giving a higher profile to the act of farming in our narratives about Neolithic lifeways in Scotland and beyond are briefly explored.


Author(s):  
М. А. Самородова

Анализ стабильных изотопов азота и углерода активно применяется в палеодиетических реконструкциях археологического материала. Однако на результаты изотопного исследования могут повлиять существующие отличия в соотношениях изотопов разных типов костей одного индивида, которые могут возникать из-за разницы в скорости ремоделирования (разрушение старой кости и образование новой) различных костей скелета. Данные отличия часто не учитываются при выборе образцов для проведения изотопного исследования. Таким образом, перед настоящей статьей ставятся следующие задачи. Во-первых, показать существование разницы в изотопных соотношениях костей скелета на основе материалов, представленных древнерусским сельским населением из могильника Шекшово 9 в Суздальском Ополье (X-XII вв.). И, во-вторых, предоставить основные рекомендации при отборе проб для изучения изотопного состава археологических материалов. В ходе исследования удалось установить, что при выборе образцов для проведения изотопного анализа следует отдавать предпочтения костям со схожей скоростью ремоделирования. The analysis of stable nitrogen and carbon isotopes is actively used in paleodiet reconstructions of archaeological materials. However, the results of the stable isotope study can be affected by differences in the isotope ratios of collagen in different types of bones of the same individual. This can arise due the different speed of remodeling (the process by which osteoclasts breakdown the tissue in bones and new bones form) of various bones in the skeleton. These differences are often disregarded when selecting samples for isotope studies. Therefore, this paper is intended to address the following tasks: (i) to show that there exists difference in the isotope ratios of the skeleton bones by analyzing human remnants of the Medieval Russia rural population from the Shekshovo-9 cemetery in Suzdal Opolye (10th-12th centuries); (ii) to provide basic recommendations for selecting samples for the studies of the stable isotope composition of archaeological materials. Our research evidences that. when selecting samples for the isotope analysis. preference should be given to the bones with similar remodeling speed.


Author(s):  
María del Pilar Alvarez ◽  
Eleonora Carol ◽  
Inés Eymard ◽  
Andrés Bilmes ◽  
Daniel Ariztegui

Ecosphere ◽  
2021 ◽  
Vol 12 (11) ◽  
Author(s):  
Marie R. G. Attard ◽  
Anna Lewis ◽  
Stephen Wroe ◽  
Channing Hughes ◽  
Tracey L. Rogers

2021 ◽  
Vol 929 (1) ◽  
pp. 012005
Author(s):  
B G Polyak ◽  
E A Bataleva ◽  
A K Rybin

Abstract The research shows new results of isotope-helium studies carried out in the Tien Shan - Naryn and Atbashi basins. Sampling of thermal mineral springs in the Eastern Tien Shan was carried out in order to identify traces of mantle emanations in fluids and to assess the degree of permeability of the Earth’s crust for the introduction of deep masses, which would make it possible to clarify the nature of the interaction of the crust and mantle in the zone of recent orogeny. Concentrations of helium isotopes were measured in gas and water samples from 6 thermal mineral springs in the Central Tien Shan. It was found that fluids from three sources contain an abnormally high amount of mantle helium. In the gases of the Narzan source, the ratio 3He/4He in the gas phase (597÷600) × 10−8 reaches the Central Asian maximum found earlier on the Fergana ridge in the Kyzyl-Beles source (510÷630) × 10−8. The obtained results support the ideas on the existence of two sublatitudinal positive helium isotope anomalies on the northern and southern flanks of the Eastern Tien Shan - in the zones of junction of the epiplatform neoorogene with more ancient tectonically stable structures.


Geosciences ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 402
Author(s):  
Christopher T. Halsted ◽  
Paul R. Bierman ◽  
Greg Balco

We assess if variations in the in situ cosmogenic 26Al/10Be production ratio expected from nuclear physics are consistent with empirical data, knowledge critical for two-isotope studies. We do this using 313 samples from glacially transported boulders or scoured bedrock with presumed simple exposure histories in the Informal Cosmogenic-nuclide Exposure-age Database (ICE-D) from latitudes between 53°S to 70°N and altitudes up to 5000 m above sea level. Although there were small systematic differences in Al/Be ratios measured in different laboratories, these were not significant and are in part explained by differences in elevation distribution of samples analyzed by each laboratory. We observe a negative correlation between the 26Al/10Be production ratio and elevation (p = 0.0005), consistent with predictions based on the measured energy dependence of nuclear reaction cross-sections and the spatial variability in cosmic-ray energy spectra. We detect an increase in the production ratio with increasing latitude, but this correlation is significant only in a single variate model, and we attribute at least some of the correlation to sample elevation bias because lower latitude samples are typically from higher elevations (and vice versa). Using 6.75 as the 26Al/10Be production ratio globally will bias two-isotope results at higher elevations and perhaps higher latitudes. Data reported here support using production rate scaling that incorporates such ratio changes, such as the LSDn scheme, to minimize such biases.


2021 ◽  
Vol 59 (5) ◽  
pp. 1111-1131
Author(s):  
Paul A. Polito ◽  
Thomas K. Kyser ◽  
April Vuletich ◽  
Yvonne Bone

ABSTRACT The Junction orogenic gold deposit in the St Ives district of Western Australia is characterized by a syn-gold mineral assemblage dominated by quartz-calcite-albite-biotite-chlorite-pyrrhotite. The deposit had a light hydrocarbon,CO2, and O2 soil-gas signature above known mineralization prior to mining and it has been proposed that the source of the light hydrocarbon gases in the soil was gas-rich fluid inclusions trapped in gold-related alteration minerals, particularly calcite, albite, quartz, and pyrrhotite. Linking the soil gases with those in the deposit is extremely difficult. However, establishing that the gases in the soil are indeed present within the deposit and that those gases are related to the syn-Au alteration minerals is achievable through stable-isotope studies. Carbon and O stable-isotope compositions of pre-gold, syn-gold, and post-gold quartz veins; syn-gold and post-gold calcite; and CO2 and CH4 in the fluid inclusions that each of these minerals host were investigated to establish if the various mineral and fluid-gas species in the deposit are in isotopic equilibrium with each other, an important first step to relate syn-ore minerals with the relevant gases. Pre-ore Mo-type quartz veins contain CO2 (δ13Cgas = –1‰) and CH4 (δ13Cgas = ca. –33‰) in fluid inclusions at a ratio of ca. 93:7. The paucity of Mo-type quartz veins in the deposit suggests that these veins were not the main source of the soil-gas signature. Syn-gold alteration post-dates the Mo-type quartz veins. Quartz and co-existing calcite in the Au-bearing Junction shear zone have δ18Omineral values around 12.0 and 10.5‰, respectively. Multiple co-existing quartz-calcite pairs indicate that gold deposition occurred at ∼400 °C. This temperature agrees with mineral equilibria temperature estimates, the entrapment temperatures of fluid inclusions, and temperature modelling of solid-solution mineral phases. The temperature dictates that the quartz and calcite are in isotopic equilibrium with each other. The calcite in the Junction shear zone has δ13Cmineral values from –7.4 to –2.5‰, indicating that the CO2-rich ore fluid had a δ13Cfluid value of –3.7 ± 0.9‰. CO2 and CH4 released from quartz-hosted fluid inclusions have δ13Cgas values from –4.3 to +3.5‰ (mean = –1.5 ± 1.9‰) and –50.5 to –35.2‰, respectively. The isotopic composition of the fluid inclusion CO2 is in disequilibrium with co-existing CH4 that was co-released from the same quartz vein and the calculated δ13Cfluid value from co-existing calcite. Isotopic mass balance calculations using the two co-released gases show that the CO2 was initially in equilibrium with the syn-ore calcite but has since re-equilibrated with CH4 at temperatures below 200 °C. The abundance of CH4 in some quartz veins suggests that the syn-gold vein assemblage could be the source for the soil-gas anomaly. Post-gold veins contain quartz and calcite that have δ18Omineral values of ca. 11.0 and 10.0‰, respectively. Individual mineral pairs indicate precipitation at ∼320 °C from a fluid with a δ18Ofluid value of 4.7 ± 0.9‰, distinct from that which formed the syn-gold quartz veins. The post-gold calcite has δ13Ccalcite values from –7.5 to –5.4‰, indicative of formation from a CO2-bearing fluid having a δ13Cfluid value of –4.6 ± 0.9‰. The δ13Cfluid values are indistinguishable from fluid inclusion CO2 values of –3.6 ± 0.9‰, indicating no post entrapment re-equilibration, which suggests that CH4 was at trace volumes or absent in the post-gold quartz veins. These data lead to the conclusion that post-entrapment reequilibration between fluid inclusion CO2 and CH4 has occurred, but that the two gases were likely in equilibrium at the time of entrapment. This has implications for the interpretation of C isotope studies that focus on fluid inclusion CO2 measured from other gold and base-metal deposits, especially when the isotopic value of that CO2 is assumed to represent a specific source for the ore-forming fluids. The data also lead to a model that proposes that the syn-gold alteration assemblage could have produced the soil-gas anomalies observed above the mineralization.


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