Raw Materials for Archaeological Pottery from the Campania Region of Italy: A Petrophysical Characterization

We performed petrophysical analyses on 34 clayey samples of different geological origin within the Campania region of Italy in order to determine possible sources of raw materials used to produce ancient pottery. Possible raw material sources can be grouped into high‐CaO clays (HCC) and low‐CaO clays (LCC). HCC are mainly represented by more recent (Miocene‐Pleistocene) basinal sediments whereas LCC tend to be associated with basinal, alluvial, and pyroclastic deposits. A chemical comparison between clayey raw materials, modern ceramic replicas, and Campanian archaeological ceramics of several typologies (common ware, cooking ware, fine tableware, amphorae, and bricks) from 8th century B.C. to the Middle Ages (a total of 350 ceramic samples) indicates that HCC were extensively used for common wares and that these were either mixed with temper or levigated. In contrast, most of the LCC were used for the production of cookware. We also analyzed the technological potential of the sampled raw materials, taking into consideration their actual and possible uses. We observed that most HCC deposits were well suited for tableware and amphorae, whereas LCC were better for cookware and some fine tableware.     

Using Lead Isotopes to Determine Pottery Provenance in Cyprus: Clay Source Signatures and Comparison with Late Bronze Age Cypriote Pottery

This paper presents the lead isotopic composition of potential clay sources for pottery production, collected in the four major geological zones of Cyprus (Troodos Ophiolite, Circum Troodos Sedimentary Succession, Mamonia Terrane, Kyrenia Terrane) and evaluates its usefulness in Cypriote pottery provenance studies. The clay isotopic signatures from the four zones are compared to each other and to the isotopic composition of various utilitarian pottery wares from three Late Bronze Age sites, respectively located in southern Cyprus (Alassa‐Pano Mandilaris), east Cyprus (Enkomi), and southeast Cyprus (Hala Sultan Tekke). It also explores the potential of this method to better discriminate between potential raw materials used for the production of Base‐ring ware, one of the most characteristic fine pottery of Late Bronze Age Cyprus, which was widely spread in the Eastern Mediterranean (Courtois, 1981; Vaughan, 1991, 1994). Results show that three main lead isotopic fields can be distinguished among the Cypriote clay sources and the comparison of Plain sherds with the clay sources allows discrimination between local products and imports. They also clearly indicate that all the Base‐ring sherds analyzed in this study were made of the clays from the Kathikas Formation that crops out in only limited parts of southwest Cyprus.     

Genesis of the post-caldera eastern Upper Basin Member rhyolites, Yellowstone, WY: from volcanic stratigraphy, geochemistry, and radiogenic isotope modeling

An array of samples from the eastern Upper Basin Member of the Plateau Rhyolite (EUBM) in the Yellowstone Plateau, Wyoming, were collected and analyzed to evaluate styles of deposition, geochemical variation, and plausible sources for low δ¹⁸O rhyolites. Similar depositional styles and geochemistry suggest that the Tuff of Sulphur Creek and Tuff of Uncle Tom’s Trail were both deposited from pyroclastic density currents and are most likely part of the same unit. The middle unit of the EUBM, the Canyon flow, may be composed of multiple flows based on a wide range of Pb isotopic ratios (e.g., ²⁰⁶Pb/²⁰⁴Pb ranges from 17.54 to 17.86). The youngest EUBM, the Dunraven Road flow, appears to be a ring fracture dome and contains isotopic ratios and sparse phenocrysts that are similar to extra-caldera rhyolites of the younger Roaring Mountain Member. Petrologic textures, more radiogenic ⁸⁷Sr/⁸⁶Sr in plagioclase phenocrysts (0.7134–0.7185) than groundmass and whole-rock ratios (0.7099–0.7161), and δ¹⁸O depletions on the order of 5‰ found in the Tuff of Sulphur Creek and Canyon flow indicate at least a two-stage petrogenesis involving an initial source rock formed by assimilation and fractional crystallization processes, which cooled and was hydrothermally altered. The source rock was then lowered to melting depth by caldera collapse and remelted and erupted. The presence of a low δ¹⁸O extra-caldera rhyolite indicates that country rock may have been hydrothermally altered at depth and then assimilated to form the Dunraven Road flow.     

Environmental isotopes (18O, 2H, and 87Sr/86Sr) as a tool in groundwater investigations in the Keta Basin, Ghana

Analyses of environmental isotopes (¹⁸O, ²H, and ⁸⁷Sr/⁸⁶Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The ⁸⁷Sr/⁸⁶Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of ¹⁸O and ²H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Electronic Publication     

Petrographic and Geochemical Constraints on the Provenance of Sanidine‐Bearing Temper in Ceramic Potsherds,Four Corners Region,Southwest USA

Previous researchers proposed that trachybasalt temper with “poikilitic” sanidine, found in pottery from the Mesa Verde region of the American Southwest, was procured along the eastern Chuska Mountains. This served as one line of evidence that Chaco Canyon was a regional trade center linked to the Chuska Mountains in the ninth to thirteenth centuries. Recent geologic studies, however, revealed other potential sources for the trachybasalt temper. A comparison of petrographic features and geochemical signatures of poikilitic sanidine in rock samples and potsherds shows no definitive correlation of temper materials and a specific geologic source. Several outcrops of trachybasalt are identified as less viable prospects, but the results do not support the idea that the sanidine‐rich temper was exclusively gathered in the Chuska Mountains. This conclusion opens up the possibility that raw materials were gathered from local sources that were more accessible, reducing the dependence on a regional trade center.     

The San Gregorio Magno lacustrine basin (Campania,southern Italy): improved characterization of the tephrostratigraphic markers based on trace elements and isotopic data

Central–southern Italy is one of the most suitable areas in the world for tephrostratigraphic studies, owing to the numerous volcanic sources with explosive activity during the Pleistocene. This work presents a systematic investigation of the chemical (trace elements) and isotopic (Sr and Nd) compositions of the main tephra markers within lacustrine sediments of the San Gregorio Magno Basin (Campania, southern Italy). This study: (i) provides full geochemical (trace elements and isotopes) characterization of eight significant Upper Pleistocene marker layers (X‐6, X‐5, C‐22, MEGT/Y‐7, CI/Y‐5, C‐10, Y‐3, NYT/C2) widely dispersed over the Mediterranean area; (ii) proposes a new tephra marker for Marine Isotope Stage 7, dated to 240 ka; and (iii) refines the correlations of tephra levels belonging to the investigated sequence. This study highlights that in most cases the Nd isotope composition of the glass and Sr isotope composition of the coexisting minerals are more reliable than ⁸⁷Sr/⁸⁶Sr of the glass, and hence is more helpful as a further tool for tephrostratigraphic correlations, as recently proposed in the literature. Moreover, this study is a first step towards the construction of a complete geochemical database for future tephra investigations in the Mediterranean area. Copyright © 2019 John Wiley & Sons, Ltd.     

松嫩沙地Sr?Nd同位素组成特征

作为亚洲风尘源区的中国北方干旱—半干旱地区的Sr?Nd同位素组成已得到很好的研究,但位于欧亚黄土带最东端的松嫩沙地尚是空白,这影响了对该地区风尘系统的深入理解。为此,系统采集了松嫩沙地19个区域90个河流沙和风成沙样品,并对这些样品进行了分粒级处理（<63 μm、63~30 μm、30~10 μm、<10 μm和<30 μm）。对116个分粒级子样的酸不溶物（硅酸盐组分）进行了Sr?Nd同位素组成的测定。研究结果表明,松嫩沙地可划分出两个大区（嫩江水系和松花江水系）和七个小区,嫩江水系沉积物的Nd同位素组成显著高于松花江水系,而Sr同位素组成明显偏低。松嫩沙地8个剖面纵向上的同位素特征显示,Sr?Nd同位素组成存在“时间效应”,即随时间发生了明显变化,表明了源区地球化学组成的不稳定性。分粒级组成表明,粒度对87Sr/86Sr比值的影响很小,但对Nd同位素组成有明显影响,且存在Nd同位素比值富集在粗颗粒组分中的趋势,这与以往的研究结果不同。无论是地质历史时期还是现在,嫩江水系沉积物（大庆、杜蒙、齐齐哈尔、泰来、白城）对哈尔滨粉尘的贡献都很小。哈尔滨黄土与现代尘暴粉尘有不同的物源,哈尔滨黄土是春季尘暴天气作用的产物,有一个混合源,松花江水系沉积物（扶余、德惠、榆树等地）是哈尔滨黄土的主要粉尘源区,内蒙古中东部的沙地也为哈尔滨黄土贡献了部分的细颗粒粉尘。     

High‐Precision Sr‐Nd‐Hf‐Pb Isotopic Composition of Chinese Geological Standard Glass Reference Materials CGSG‐1, CGSG‐2, CGSG‐4 and CGSG‐5 by MC‐ICP‐MS and TIMS

To assess the homogeneity of and provide the first Sr‐Nd‐Hf‐Pb isotopic reference values for the Chinese Geological Standard Glasses CGSG‐1, CGSG‐2, CGSG‐4 and CGSG‐5, we measured these isotopes in several measurement sessions over the course of nearly 3 years. The results were obtained by high‐precision MC‐ICP‐MS and TIMS. Our investigation indicates that these CGSG glass reference materials are homogenous with regard to Sr‐Nd‐Hf‐Pb isotopic distribution and are therefore suitable geochemical materials for Sr‐Nd‐Hf‐Pb isotope measurements. Clear differences in Sr‐Nd‐Hf‐Pb isotopic composition were observed between the glasses and the original powdered rock reference materials (CGSG‐2 and GSR‐7, and especially CGSG‐5 and GSR‐2) because of flux addition during preparation of the glasses. The new Sr‐Nd‐Hf‐Pb isotope data provided here might be useful to the geochemical community for in situ and bulk analysis.     

塔东地区古城4井上寒武统—中、上奥陶统流体地球化学示踪

通过对塔东地区古城4井上寒武统和中、上奥陶统碳酸盐岩围岩及充填物的碳、氧、锶同位素地球化学和流体包裹体成分的对比研究表明,充填于中、上奥陶统和上寒武统的流体分属于2个不同来源的流体体系。充填于中、上奥陶统灰岩裂缝中方解石脉的w(87Sr)/w(86Sr)介于0.7084~0.7088,它与早奥陶世海水的w(87Sr)/w(86Sr)相近;流体体系为CH4-H2O体系;充填物与围岩间具有明显的碳、氧同位素差异,表明上部流体体系中的流体来自于奥陶系地层本身。上寒武统白云岩裂缝中方解石脉的w(87Sr)/w(86Sr)为0.7138,明显地高于同时代海水的锶同位素值;流体体系为CO2-H2O体系;下部流体体系中的流体为外来富锶流体。上、下流体体系间互不连通暗示着上寒武统地层具有相对较好的保存条件。     

青海湖盆地史前狩猎采集人群的石料利用策略研究

史前人类向青藏高原扩散的过程和适应高海拔缺氧环境的机制是多学科关注的热点科学问题。青海湖盆地是青藏高原旧石器-中石器时代遗址分布最为丰富的区域,对这些遗址出土的石制品原料的分析有助于深入理解青藏高原史前狩猎采集人群的石料开发策略、人群迁徙和交流联系。青海湖盆地151遗址出土的928件石制品的石料研究分析显示,处于末次冰消期的下文化层的石制品以近源的石英和石英岩为主要原料,而处于全新世早中期的上文化层在同类型近源石料仍占主体地位的情况下,开始出现较高比例和多样化的优质硅质石料,并且主要用于生产细石器。野外调查和查阅地质资料均未发现青海湖盆地内有151遗址中出现的同类型优质硅质石料产出,推测其来自远距离搬运。青海湖盆地内其他8个末次冰消期至全新世中期遗址的3269件石制品石料分析结果显示,与151遗址同类型的远源优质硅质石料在全新世早期开始在盆地内的遗址中出现。这一结果表明青海湖盆地末次冰消期古人类活动强度和范围有限,全新世早中期古人类受到全新世大暖期气候变好和周边地区农业人群兴起挤压活动空间的双重影响,在高原上的活动范围和强度大大增加,伴随着开始有意识地开发优质石料,较频繁地进行远距离迁...     

Evidence of multiple evaporite recycling processes in a salt‐tectonic context,Sivas Basin,Turkey

The isotopic composition of evaporites can shed light on their environment of precipitation and their subsequent recycling processes. In this study, we performed Sr, O and S isotopic analyses on evaporitic sulphates in the halokinetic Sivas Basin. The main objectives were to decipher the age and origin of the evaporites responsible for the salt tectonics, and to test whether diapir dissolution acts as the source of younger evaporitic layers in continental mini‐basins. The Sr isotopes demonstrate that the first evaporites precipitated from seawater during the Middle–Late Eocene. The similar isotopic values measured in the halokinetic domain confirm that the Eocene evaporites triggered the salt tectonics and were continuously recycled in Oligo‐Miocene mini‐basins as lacustrine to sabkha evaporites. Modern halite precipitates suggest that the dissolution and recycling of diapiric halite is ongoing. This study demonstrates the efficiency of isotopic analyses in constraining evaporite recycling processes in continental halokinetic domains.     

Geoarchaeological investigations of the “potters' quarter” at Sagalassos,southwest Turkey

The potters' quarter of the ancient city of Sagalassos, southwest Turkey, was one of the largest and most enduring ceramic‐producing manufactories in the eastern Mediterranean. The objective of our study was to determine environmental circumstances that favored development of different clay resources in the territory of Sagalassos and to assess utilization of these resources in the local pottery manufactory. The potters' quarter was established where, owing to favorable geological circumstances, a large clay body had developed. The bedrock in the potters' quarter, a tectonized ophiolite sequence, has synclinal structure; hence, surface runoff and groundwater tend to accumulate in its center. The weathering of the basic rock formed a smectite‐rich clay with vertic properties. This clay was mined in antiquity, and mineralogical and chemical analyses indicate that it was used for the production of local ceramics from Hellenistic to Byzantine times. It is likely that colluvium on top of the ophiolitic clay at the potters' quarter is related to deforestation and slope processes after the potters' quarter was abandoned. In sum, environmental circumstances determined the location of the artisanal quarter of Sagalassos, with its clay quarrying operation and ceramic manufactory. However, for the local mass‐produced Sagalassos red slip ware, the results of our chemical and mineralogical analyses indicate that a different, more suitable clay was used: detrital lake sediments, rich in chlorite and chlorite/smectite mixed layers, located about 8 km from the original artisanal quarter. The choice for this clay was determined both by the presence of a suitable clay deposit, as well as socio‐economic circumstances such as land ownership. The site of Sagalassos yielded unique evidence of mining of clay at a ceramic production site, as well as import of nearby clays. The local and imported clays were used side‐by‐side, but one for the production of common wares and building ceramics, and the other for the manufacturing of luxury fine tablewares. © 2003 Wiley Periodicals, Inc.     

辽东五龙地区燕山期侵入岩类同源岩浆演化微量元素、同位素证据与金矿成矿

辽东五龙地区中生代燕山期侵入岩类在时空上与金矿关系密切。该类侵入岩具有接近的微量元素Th／U、Zr／Hf、Nb／Ta值。随着不同岩石类型中的SiO2、MgO的含量的变化，(^87Sr／^66Sr)i和(^143Nd／^144Nd)i值保持不变，说明岩浆在侵位过程中没有明显受到围岩物质混染，且该类侵入岩有着相同的岩浆源区。Sr、Nd同位素组成表明成岩物质以下地壳为主。三股流花岗岩和矿石有相似的Pb同位家组成，结合含金石英脉(矿体)切穿已固结三股流花岗岩的地质事实，暗示了三股流花岗岩不太可能是直接的矿质提供者，推测成矿物质与成岩物质主体来自深部的同一岩浆源区，金矿成矿是同一岩浆源区岩浆演化不同阶段的产物。     

A basement-interacted fluid in the N81 deposit, Pine Point Pb-Zn District, Canada: Sr isotopic analyses of single dolomite crystals

The Mississippi Valley-type Pb-Zn deposits of the Pine Point district (Northwest Territories, Canada) are located close to the eastern edge of the present day Western Canadian Sedimentary Basin. The deposits are thought to have formed as the result of basin-wide fluid flow in the Presqu’ile Barrier, the host to the ore deposits. A laser ablation multi-collector inductively coupled plasma mass spectrometric study of ⁸⁷Sr/⁸⁶Sr ratios of ore-related dolomites from the N81 deposit at Pine Point indicates that at least two sources of Sr were present in the mineralizing system. One fluid has a range in Sr isotopic values from 0.07073 to 0.71200 and is interpreted to be derived from Middle Devonian seawater that interacted with clastic units in the basin. The second fluid has higher Sr isotopic values (up to 0.71520), similar to those found in some Canadian Shield brines, and is interpreted to represent an evaporated seawater-derived brine which has interacted with crystalline basement rocks. Reactivation of old structures in the basement may have provided a pathway for cross-formation fluid flow to the site of mineralization. The data suggest that the stratigraphic location of the Pine Point District, near the interface between the Western Canadian Sedimentary Basin and its basement, may have exerted a fundamental control on the formation of these deposits.     

Tracking selenium in the Chalk aquifer of northern France: Sr isotope constraints

Groundwater at the southern and eastern edges of France’s Paris Basin has a selenium content that at times exceeds the European Framework Directive’s drinking-water limit value of 10 μg/L. To better understand the dynamics of the Chalk groundwater being tapped to supply the city of Lille and the Se origins, we used a combination of geochemical and isotopic tools. Strontium isotopes, coupled with Ca/Sr, Mg/Sr and Se/Sr ratios, were used to identify the main groundwater bodies and their mixings, with the Mg/Sr and Se/Sr ratios constraining a ternary system. Groundwater in the agricultural aquifer-recharge zone represents a first end-member and displays the youngest water ages of the catchment along with the highest Sr isotopic signature (0.70842) and low Se contents. Anaerobic groundwater constitutes a second major end-member affected by water-rock interactions over a long residence time, with the lowest Sr isotopic signature (0.70789) and the lowest Se content, its low SF6 content confirming the contribution of old water. Se-rich groundwater containing up to 30 μg/L of Se represents a third major end-member, with an intermediate Sr isotopic ratio (0.70826), and is mainly constrained by the clayey Se-rich formation overlying the Chalk aquifer. The spatial and temporal Se variability in the groundwater is clearly linked to the presence of this formation identified as Tertiary and also to the hydrological conditions; saturation of the Se-rich clays by oxygenated groundwater enhances Se mobility and also Sr adsorption onto the clays. This multi-tool study including Sr isotopes successfully identified the Se origins in the aquifer and has led to a better understanding of the regional mixing and processes affecting the Chalk groundwater.     

滇西南思茅盆地盐岩Sr同位素特征及其对区域成盐作用的启示

滇西南思茅盆地是中国西部重要的中—新生代含钾盐盆地，但其成盐物质来源一直存在争议。文章测定了滇西南思茅 盆地磨黑地区钻孔中盐岩样品的87Sr/86Sr同位素比值，同时结合区域其他含盐带已发表的Sr同位素数据，讨论成盐物质来源。 磨黑地区盐岩的87Sr/86Sr比值介于0.708598~0.709333之间，与思茅盆地其他含盐带盐岩的87Sr/86Sr比值（0.707504~0.711069）一 致，较接近于中新生代海水的87Sr/86Sr比值（0.7068~0.7092），但87Sr/86Sr比值略高于海水，显示有陆源水混合现象。结合Sr同位 素证据与盆地演化史，一些地球化学和矿物特征，作者推测思茅盆地盐岩成盐物质来源主要是海水，存在少量陆源水的混入。     

Sr、C同位素对苏皖北部上前寒武系时代的界定

对苏皖北部上前寒武系碳酸盐岩地层系统采集灰岩样品 ,采用弱酸处理方法测定清液部分的 Sr同位素组成 ,对全岩样品测定 C同位素组成。测定结果与 Shields(1999)发表的新元古代古海水 Sr、C同位素组成随时间的演化曲线对比表明 ,苏皖北部上前寒武系是跨越北方青白口系与南方震旦系之间的一段连续地层 ,其时代约从70 0 Ma到 85 0 Ma,该研究进一步印证了淮南生物群属于先伊迪卡拉期的学术观点。     

滇西南思茅盆地盐岩Sr同位素特征及其对区域成盐作用的启示

滇西南思茅盆地是中国西部重要的中—新生代含钾盐盆地,但其成盐物质来源一直存在争议。文章测定了滇西南思茅 盆地磨黑地区钻孔中盐岩样品的87Sr/86Sr同位素比值,同时结合区域其他含盐带已发表的Sr同位素数据,讨论成盐物质来源。 磨黑地区盐岩的87Sr/86Sr比值介于0.708598~0.709333之间,与思茅盆地其他含盐带盐岩的87Sr/86Sr比值（0.707504~0.711069）一 致,较接近于中新生代海水的87Sr/86Sr比值（0.7068~0.7092）,但87Sr/86Sr比值略高于海水,显示有陆源水混合现象。结合Sr同位 素证据与盆地演化史,一些地球化学和矿物特征,作者推测思茅盆地盐岩成盐物质来源主要是海水,存在少量陆源水的混入。     

四川邻水华蓥山大峡谷地质公园地质遗迹资源体系及地学意义

华蓥山大峡谷地质公园是以峡谷、构造和岩溶地貌为代表的风景地貌类地质公园。本文以华蓥山大峡谷地质公园地质遗迹景观资源为基础, 以川东褶皱带构造单元、川东平行岭谷地貌单元和上扬子地层分区的部分地层区域为研究视角, 构建华蓥山大峡谷地质公园地质遗迹资源体系——包括地质(体、层)剖面、古生物活动遗迹、地貌景观、水体景观以及环境地质遗迹5个大类、15个类共100多处地质遗迹景点; 通过对各类地质遗迹的特征进行分析, 对前人研究进行总结, 探讨了地质公园地质遗迹重要的地学意义。研究表明, 华蓥山大峡谷地质遗迹在地质构造、地层、岩溶学、水文地质学以及地貌学等领域具有重要的科学价值。     

Multi-isotopic (Li,B, Sr,Nd) approach for geothermal reservoir characterization in the Limagne Basin (Massif Central,France)

A multi-isotopic study of thermo-mineral waters from the Limagne Basin (French Massif Central) is reported. Lithium, B, Sr and Nd isotopic signatures in thermo-mineral waters and bedrocks were combined in order to determine the origin of these fluids from a reservoir point of view. Strontium and Nd isotopic systems showed that the thermo-mineral waters are mostly derived from a granitic reservoir type, with the exception of a few water samples having Sr and Nd isotopic signatures also reflecting a volcanic contribution (basalts). In a second step, Li and B isotopes were investigated, given that Li and B isotopic systematics are potentially affected by mass dependent fractionation during water/rock interaction and could provide some information on what takes place during this process. A great diversity of thermo-mineral waters within the Aigueperse area was clearly observed, which is directly related to the origin of these thermal waters in terms of reservoirs. These different geothermal reservoirs are characterized by different geological settings and intensity of water/rock interaction (i.e. depth and temperature).