Raw Materials and Pottery Production at the Late Bronze and Iron Age Site of Puig de Sa Morisca,Mallorca, Spain

This paper presents an analytical study of LateBronze andIronAge ceramics and natural clay deposits from the archaeological site ofPuig deSa Morisca in southwestMallorca,Spain. In our study, we combine petrographic, micropaleontological, mineralogical (X‐ray powder diffraction) and textural (laser particle size) analyses of sherds and local clays that may have been used as raw material in ceramic production. This approach allowed us to compare the ceramics’ formal characteristics with those observed in nearby plastic clays and assess raw clay procurement and paste preparation. The results indicate the use of local (<500 m distance) calcareous clays throughout theLateBronze andIron ages. This raw material was mixed with other coarser clays or crushed calcite, as well as other calcareous tempers, such as breccias or calcarenites, located close to the site. The results demonstrate that the same clay deposit was used to make ceramic vessels following different technological choices and recipes. Thus, local communities established a strong connection with the same raw materials through time that were located within the potters’ preferential range of exploitation.     

Clay Minerals in an Active Hydrothermal Field at Iheya‐North‐Knoll,Okinawa Trough

Iheya‐North‐Knoll is one of the small knolls covered with thick sediments in the Okinawa Trough back‐arc basin. At the east slope of Iheya‐North‐Knoll, nine hydrothermal vents with sulfide mounds are present. The Integrated Ocean Drilling Program (IODP) Expedition 331 studied Iheya‐North‐Knoll in September 2010. The expedition provided us with the opportunity to study clay minerals in deep sediments in Iheya‐North‐Knoll. To reveal characteristics of clay minerals in the deep sediments, samples from the drilling cores at three sites close to the most active hydrothermal vent were analyzed by X‐ray diffraction, scanning electron microscope and transmission electron microscope. The sediments are classified into Layer 0 (shallow), Layer 1 (deep), Layer 2 (deeper) and Layer 3 (deepest) on the basis of the assemblage of clay minerals. Layer 0 contains no clay minerals. Layer 1 contains smectite, kaolinite and illite/smectite mixed‐layer mineral. Layer 2 contains chlorite, corrensite and chlorite/smectite mixed‐layer mineral. Layer 3 is grouped into three sub‐layers, 3A, 3B and 3C; Sub‐layer 3A contains chlorite and illite/smectite mixed‐layer mineral, sub‐layer 3B contains chlorite/smectite and illite/smectite mixed‐layer minerals, and sub‐layer 3C contains chlorite and illite. Large amounts of di‐octahedral clay minerals such as smectite, kaolinite, illite and illite/smectite mixed‐layer mineral are found in Iheya‐North‐Knoll, which is rarely observed in hydrothermal fields in mid‐ocean ridges. Tri‐octahedral clay minerals such as chlorite, corrensite and chlorite/smectite mixed‐layer mineral in Iheya‐North‐Knoll have low Fe/(Fe + Mg) ratios compared with those in mid‐ocean ridges. In conclusion, the characteristics of clay minerals in Iheya‐North‐Knoll differ from those in mid‐ocean ridges; di‐octahedral clay minerals and Fe‐poor tri‐octahedral clay minerals occur in Iheya‐North‐Knoll but not in mid‐ocean ridges.     

An exploration of potential raw materials for prehistoric pottery production in the Tao River Valley,Gansu Province,China

Northwest China is known for its Majiayao-style Neolithic painted pottery which has received much praise for its high level of craftsmanship, yet its chain of production, in particular the step of raw material selection, is still poorly understood. To fill this lacuna, the present study explores the raw materials used in producing these wares from a geological and technological perspective. At its core stands the first geoarchaeological survey conducted around the eponymous site of Majiayao which collected 47 samples of raw materials suitable for ceramic production including clay, loess and rocks, which were all analysed macroscopically. A selection was analysed using thin-section petrography, and a subset of the clay and loess samples were subjected to firing experiments. Additionally, three clay samples were analysed by scanning electron microscope with energy-dispersive X-ray spectrometer to understand their composition and behaviour in ceramic production. These were then compared to archaeological ceramics, thus providing insights into raw-material availability and selection that will be of importance not only for research on Majiayao-style pottery but also for later-period ceramics produced in the area. This research shows how an archaeologically informed geological survey can contribute insights into human–environment interaction in early pottery production, especially the interplay between raw-material availability, technological know-how and potters' choices.     

Characteristics and distribution of clay minerals and their effects on reservoir quality: Huagang Formation in the Xihu Sag,East China Sea Basin

Abstract

The characteristics and distribution of clay minerals and their effects on reservoir quality in the Huagang sandstones in the Xihu Sag, East China Sea Basin were studied by using X-ray diffraction, casting thin-sections, scanning electron microscopy, electron microprobe analysis, fluid inclusion analysis, constant-rate mercury injection and nuclear magnetic resonance. Clay minerals consist of kaolinite, chlorite, illite and illite–smectite mixed layer (I/S); kaolinite forms from dissolved feldspars, chlorite occurs as clay coatings that are transformed from clay precursors owing to the flocculation of suspended detrital clays or the crystallisation of pore fluids, and illite forms from the illitisation of detrital smectite, authigenic kaolinite and K-feldspars. Clay distribution is controlled by sedimentary environments, burial history and lithologies. Typical reservoirs in the western sub-sag are thin and developed in braided river facies at relatively shallow burial depths with clays dominated by kaolinite. However, typical reservoirs in the central inversion tectonic zone are thicker and developed in a braided delta front facies at deeper burial depths with clays mainly consisting of chlorite, illite and I/S. High-quality reservoirs are characterised by coarse granularity, high quartz content and low clay content with widespread development of chlorite coatings that inhibit quartz cements at low temperatures. At higher temperatures, the high-quality reservoirs develop more pores providing growth space for quartz cements and result in the coexistence of chlorite coatings and quartz cements. The high-quality reservoirs are controlled by their lithological characteristics rather than chlorite coatings. Illite and I/S clays create severe damage to reservoirs by reducing the size and connectivity of pore-throats.     

Clay petrology of the Upper Triassic/Lower Jurassic terrestrial strata of the Newark Supergroup,Connecticut Valley,U.S.A.

The clay mineralogy of the Newark Supergroup (Upper Triassic/Lower Jurassic) in the Connecticut Valley was studied by X-ray diffraction analysis. Clay minerals identified in 126 samples are illite, chlorite, smectite, kaolinite, vermiculite, expandable chlorite, mixed-layer illite/smectite, mixed-layer chlorite/smectite, and mixed-layer chlorite/vermiculite. In general, the rocks are illitic with subordinate amounts of chlorite. However, the various lithofacies in the Newark Supergroup are characterized by distinct clay-mineral assemblages. Red beds of floodplain origin contain clays mainly of detrital nature with 2M illite most abundant. Subordinate amounts of chlorite, smectite, vermiculite, kaolinite and mixed-layer illite/smectite are also present. An interstratified chlorite/vermiculite occurs in red mudstone underlying basalt flows. Lacustrine gray beds are generally characterized by the clay-mineral assemblage 1Md illite + chlorite with minor amounts of smectite ane expandable chlorite. An interstratified chlorite/smectite predominates in gray mudstone associated with perennial lake cycles in the East Berlin Formation. Black shales of deeper lacustrine origin contain the assemblage 1Md ifillite + trioctahedral smectite and traces of chlorite. Illite and smectite also occur as mixed-layer phases.In many respects, the distribution of clay minerals in the Connecticut Valley can be likened to the general scheme proposed for the Permo-Triassic basins of Europe and Africa. These display both vertical and horizontal variations in clay-mineral assemblages that reflect the chemical and spatiotemporal evolution of intrabasin depositional and diagenetic environments. Chemical data indicate that magnesium, especially, was concentrated in the black muds of large perennial lakes that intermittently occupied the Connecticut rift valley. Pore waters derived from these sediments played an important role in the development of Mg-rich 2 : 1 and interstratified clay minerals during early diagenesis.     

Contribution of long-term hydrothermal experiments for understanding the smectite-to-chlorite conversion in geological environments

The smectite-to-chlorite conversion is investigated through long-duration experiments (up to 9 years) conducted at 300 °C. The starting products were the Wyoming bentonite MX80 (79 % smectite), metallic iron and magnetite in contact with a Na–Ca chloride solution. The predominant minerals in the run products were an iron-rich chlorite (chamosite like) and interstratified clays interpreted to be chlorite/smectite and/or corrensite/smectite, accompanied by euhedral crystals of quartz, albite and zeolite. The formation of pure corrensite was not observed in the long-duration experiments. The conversion of smectite into chlorite over time appears to take place in several steps and through several successive mechanisms: a solid-state transformation, significant dissolution of the smectite and direct precipitation from the solution, which is over-saturated with respect to chlorite, allowing the formation of a chamosite-like mineral. The reaction mechanisms are confirmed by X-ray patterns and data obtained on the experimental solutions (pH, contents of Si, Mg, Na and Ca). Because of the availability of some nutrients in the solution, total dissolution of the starting smectite does not lead to 100 % crystallization of chlorite but to a mixture of two dominant clays: chamosite and interstratified chlorite/smectite and/or corrensite/smectite poor in smectite. The role of Fe/(Fe + Mg) in the experimental medium is highlighted by chemical data obtained on newly formed clay particles alongside previously published data. The newly formed iron-rich chlorite has the same composition as that predicted by the geothermometer for diagenetic to low-grade metamorphic conditions, and the quartz + Fe-chlorite + albite experimental assemblage in the 9-year experiment is close to that fixed by water–rock equilibrium.     

Clay record of climate change since the mid‐Pleistocene in Jiujiang,south China

To obtain a better understanding of climate change in south China in the Quaternary, a clay mineralogical study was undertaken on the red earth profile at Jiujiang, using X‐ray diffraction (XRD) and particle‐size distribution analysis methods. The XRD results showed that the clay minerals of the Jiujiang red earth were mainly mixed‐layer illite–smectite (I/S), illite, kaolinite and vermiculite, with trace amounts of mixed‐layer kaolinite–smectite (K/S). Changes in clay mineral composition displayed a trend of three‐stage evolution. The higher mixed‐layer I/S clays and kaolinite contents in the lower portion suggest extremely warm and humid climates over the period c. 700 to c. 350 ka ago. A gradual decrease in I/S clays and kaolinite reveals a gradual climate change from warm/humid to cool/dry during the period c. 350 to c. 130 ka ago. The higher illite and vermiculite contents indicate a relatively cool and dry climate during the period since c. 130 ka ago. The particle‐size distribution pattern of the upper section was similar to that of the Xiashu loess, while that of the middle to lower section was similar to those of fluvially reworked red earth. A rapid increase in the abundance of large grain‐size components at 2.6 m depth indicates an intensification of the winter monsoon and a cool and dry climate during the period, in good agreement with results from the clay mineral composition and homogeneous structure. The red earth sequences in south China could probably be used to test the response of tropical to subtropical regions to global climate changes.     

Ceramic production during the Middle Horizon: Wari and Tiwanaku clay procurement in the Moquegua Valley,Peru

As the only place simultaneously occupied by the Middle Horizon (A.D. 600–1000) Andean states, the Tiwanaku and the Wari, the Moquegua Valley in southern Peru is of critical importance to understanding relations between the two states. Visual studies of Tiwanaku and Wari ceramics in the valley have elucidated differences in form and decoration. The procurement of raw clays was central to the production of these ceramics, and understanding where people procured their clay may provide insight into the social and economic interactions between these two states. Survey of the Moquegua Valley indicates the extensive availability of raw clays. Results of laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) analyses of clays indicate that there is heterogeneity in the chemical signature of the valley's clays and that at least five different clay groups can be distinguished. Comparison of these clays with LA‐ICP‐MS analysis of ceramics from a Tiwanaku site and a Wari site demonstrates that although Tiwanaku and Wari colonists in Moquegua used locally available clays during the Middle Horizon, the clay sources exploited by potters from each state were different and derived from areas located within their respective middle and upper valley territories. This information provides a basis for future chemical analysis of ceramics from the Moquegua Valley and improved understanding of past social and economic interactions. © 2009 Wiley Periodicals, Inc.     

Climatic and sea‐level control of Jurassic (Pliensbachian) clay mineral sedimentation in the Cardigan Bay Basin,Llanbedr (Mochras Farm) borehole,Wales

Early Jurassic climate is characterized by alternating cold and warm periods highlighted by studies based notably on oxygen isotopes measured on belemnite guards and other marine invertebrate shells. These climatic changes include changes in the hydrological cycle, and consequently weathering and runoff conditions. In order to clarify the erosion and weathering conditions during the Pliensbachian, this study determined the mineralogical composition of the clay fraction of 132 samples taken from the entire stage drilled in the Llanbedr (Mochras Farm) borehole (Cardigan Bay Basin). The clay mineral assemblages are composed of various proportions of chlorite, illite, illite/smectite mixed‐layers (R1 I–S), smectite and kaolinite, with possibly occasional traces of berthierine. The occurrence of abundant smectite indicates that the maximum burial temperature never exceeded 70°C. Consequently, clay minerals are considered mainly detrital, and their fluctuations likely reflect environmental changes. The variations in the proportions of smectite and kaolinite are opposite to each other. Kaolinite is particularly abundant at the base of the jamesoni Zone, in part coinciding with the δ¹³C negative excursion corresponding to the Sinemurian/Pliensbachian Boundary Event, and through the davoei Zone, whilst smectite is abundant in the upper part of jamesoni and base of ibex zones and through the subnodosus/gibbosus subzones of the margaritatus Zone. The kaolinite‐rich intervals reflect an intensification of hydrolysis and an acceleration of the hydrological cycle, while the smectite‐rich intervals indicate a more arid climate. The spinatum Zone is characterized by a distinct clay assemblage with abundant primary minerals, R1 I–S, kaolinite reworked from previously deposited sediments or from Palaeozoic rocks, and probably berthierine originating from contemporaneous ironstone‐generating environments of shallower waters. This mineralogical change by the end of the Pliensbachian likely reflects a transition from a dominant chemical weathering to a deeper physical erosion of the continent, probably related to a significant sea‐level fall consistent with a glacio‐eustatic origin.     

Pliocene clays from Aegina (Greece): Reference material for chemical provenance studies on bronze age pottery from the Island

Normally, the use of clays as reference materials in chemical provenance studies of ancient ceramics is complicated due to the original clay paste processing. The primary mixing and/or refining of raw materials during pottery production makes a straightforward comparison of archaeological ceramics with extant geological materials difficult if not impossible in many cases. However, in the case of Pliocene clays from Aegina (Greece), which were examined chemically and mineralogically and compared with Bronze Age pottery produced on the island, a successful exception can be presented. The chemical composition of a large group of Aeginetan pottery resembles the chemical composition of clays from a deposit in close vicinity to the main Bronze Age settlement of the island. Clays from specific outcrops exhibit considerable chemical and mineralogical homogeneity, and the suitability of those clays for pottery production apparently made substantial clay paste processing unnecessary. © 2004 Wiley Periodicals, Inc.     

Provenance of Clay Minerals in the Amami Sankaku Basin and Their Paleoclimate Implications Since Late Pleistocene

We analyzed the clay mineral assemblages, content and mineralogical characteristics of Hole U1438A sediment recovered from Amami Sankaku Basin during International Ocean Discovery Program (IODP) expedition 351. The results show that the clay minerals are mainly composed of illite (average 57%), smectite (average 26%), chlorite (average 14%) and minor kaolinite(average 3%). The crystallinity of illite in all samples are good (<0.4 Δ° 2θ), and the chemical indexes of illite in all samples are low (<0.4). Both indicate that illite in Hole U1438A formed in cold and dry climate. By comparing clay mineral assemblages of hole U1438A and the potential sediment sources, we suggest that smectite be mainly derived from the volcanic materials around Amami Sankaku Basin. Illite, chlorite and kaolinite are mainly derived from the Asian dust. The ratios of (illite+chlorite)/smectite show a phased increase over the last 350 ka, which is consistent with the cold and drying trend of the Asian continent since late Pleistocene. The high ratios of (illite+chlorite)/smectite and (illite+chlorite)/kaolinite during glacial period indicate that much more Asian dust was input into the Amami Sankaku Basin, which are responded to the aridity of Asian continent and strengthened east Asian Monsoon during glacial period.     

Mineralogy and chemical composition of the clay fraction of Neogene shales from the Surma Group in the Bengal basin,Bangladesh

Mineralogical and chemical investigations (<2μm clay separates) of shale samples from the Neogene-age Surma Group obtained from four wells (Habiganj-11, Shahbazpur-1, Titas-11, Titas-15) in the Bengal basin, Bangladesh, were carried out in order to reveal the clay mineral composition as reservoir exploration and exploitation requires a good understanding of the clay minerals. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-Ray fluorescence spectrometry (XRF). Mineralogically, the sub-surface Surma Group shales comprise predominantly quartz, plagioclase, illite, chlorite, kaolinite, with lesser amounts of K-feldspar, dolomite and smectite, and minor to trace amounts of calcite, siderite and pyrite. The chemical composition of the <2 μm clay separates also suggests an illite and chlorite-rich composition. With increasing burial depth, the Surma Group shales are enriched in illite. The gradual decreasing of the smectite clays with depth and ultimate disappearance at greater depths (≥ 3000 m) may have been responsible for the presence of the diagenetic illite. Based on the mineralogical composition it is most likely that the illite-chlorite associations together with quartz and feldspar were predominantly detrital in origin and thus reflect the presence of a rapidly-rising source terrain not subjected to intense weathering.     

Clay mineralogy of the ocean sediments from the Wilkes Land margin,east Antarctica: implications on the paleoclimate,provenance and sediment dispersal pattern

Core U1359 collected from the continental rise off Wilkes Land, east Antarctica, is analyzed for the clay mineralogy and carbon content. The temporal variation of the clay mineralogical data shows a dominance of illite with chlorite, smectite and kaolinite in decreasing concentration. Clay mineral illite is negatively correlated with smectite which shows enrichment during 6.2–6.8, 5.5–5.8, 4.5 and 2.5 Ma. The mineralogical analyses on the silt size fraction (2–53 μm) of some selected samples were also carried out. The combined result of both the size fractions shows the presence of chlorite and illite in both size fractions, smectite and kaolinite only in clay size fraction (<2 μm) and similarity in the crystallinity and chemistry of illite in both fractions. Similar nature of illite in both fractions suggests negligible role of sorting probably due to the deposition from the waxing ice sheet. During times of ice growth, nearby cratonic east Antarctica shield provided biotite-rich sediments to the depositional site. On the other hand, the presence of smectite, only in the clay size fraction, suggests the effective role of sorting probably due to the deposition from distal source in ice retreat condition. During times of ice retreat, smectite-rich sediment derived from Ross Orogen is transported to the core site through surface or bottom water currents. Poor crystallinity of illite due to degradation further corroborates the ice retreat condition. The ice sheet proximal sediments of U1359 show that in the eastern part of Wilkes Land, the ‘warming’ was initiated during late Miocene.     

Mineralogy and physico-chemical properties of Wadi Badaa clays (Cairo-Suez district,Egypt): a prospective resource for the ceramics industry

The Wadi Badaa (WB) Upper Miocene clays, Cairo-Suez district, Egypt, represent materials for the ceramic production. The clay raw materials are composed mainly of smectite and kaolinite with minor quartz, calcite, and rare feldspar. The plasticity indices vary between 24 and 30%, suggesting that these clays are plastic raw materials. IR bands of the investigated clays were observed at 3695, 3619, 1032, 916, 794, 690, 534, 466, and 423 cm^?1 for kaolinite; at 3436, 1635, 916, and 466 cm^?1 for smectite; and at 1179, 1104, 794, 690, and 466 cm^?1 for quartz. The <2 μm particle sizes of samples are relatively abundant in clays (～33%), which is adequate for uses of the ceramic products because of containing fine particle sizes. The studied WB clays contain 7.95 and 12.35% moisture water and interlayer water, respectively, with a maximum drying shrinkage of 7.87% at room temperature; therefore, the WB clays could be used in the ceramic manufacture.     

A plains ceramic clay source characterization by comparative geochemical and petrographic analyses: Results from the Calhan Paint Mines,Colorado, U.S.A.

The Calhan Paint Mines District, 5EP3258, Colorado, presents exposures of an exceptional clay source. When the area also produced prehistoric Ceramic stage sites, it provided the opportunity for both pottery and potential clay source analysis by optical petrography, X‐ray diffraction, and neutron activation. Although the main purpose of this study is the characterization of the ceramics and outcrop clays, results from a limited number of samples suggest that the colorful clays, the figurative “paints,” of the Calhan Paint Mines were purposely used in prehistoric times as clay source materials for ceramic production. The Calhan Paint Mines are quite possibly the only prehistoric Plains Ceramic stage clay source currently confirmed within the state of Colorado. © 2002 Wiley Periodicals, Inc.     

A comparative electron microprobe study of “Aeginetan” wares with potential raw material sources from Aegina,Methana, and Poros,Greece

Qualitative stylistic evidence from ceramic vessels and limited petrographic analysis suggested that a distinctive group of ceramics with visible inclusions of biotite (Gold Mica Fabric) was produced on the island of Aegina, Greece, during the Middle Helladic and Late Helladic I periods. To quantitatively evaluate this provenance, we sampled all potential source rocks on Aegina, Methana, and Poros. Electron microprobe analysis of amphibole in these samples revealed that each of these volcanic centers has its own unique mineralogical signature. Comparative analyses of amphibole in Zerner's original stylistic “Gold Mica Fabric” type sample with the reference samples reveal that two sherds are Aeginetan. Three additional sherds from this sample may have a non‐Aeginetan provenance, probably from a back‐arc setting outside the Saronic Gulf. These results suggest that the hypothesis of a single source production site for Aeginetan Ware should be reexamined. © 2002 Wiley Periodicals, Inc.     

上新世以来伊豆-小笠原海脊黏土矿物的来源与古气候意义

对伊豆-小笠原海脊(ODP 782A孔)上新世以来沉积物中黏土矿物的组成、含量及矿物学特征进行了分析,结果表明:黏土矿物以伊利石(42%)和蒙皂石(42%)为主,绿泥石的平均含量为14%,高岭石的含量最低,平均仅为2%。伊利石的结晶度较好,平均为0.25°Δ2θ;化学指数较低,平均为0.31;表明伊利石主要形成于干冷的气候环境。通过将ODP 782A孔黏土矿物组合特征和含量与周边可能源区对比,并结合伊利石和蒙皂石的矿物学参数特征,我们认为蒙皂石主要来源于伊豆-小笠原海脊周边岛弧火山物质;伊利石、绿泥石和高岭石主要来自亚洲大陆风尘。上新世以来(伊利石+绿泥石)/蒙皂石比值总体上呈增加的趋势,并且在5.3~3.6、3.6~1.6、1.6~0 Ma的三个阶段表现出不同的变化特征,该比值与全球深海δ¹⁸O值所记录的全球变冷、北太平洋ODP 885/886孔风尘通量和灵台黄土沉积速率,以及日本海U1430站伊利石/蒙皂石比值所指示的亚洲内陆干旱变化的总体变化趋势和阶段性变化的时间点大致同步,表明该比值敏感地响应了全球变冷和亚洲内陆的干旱。上新世以来(伊利石+绿泥石)/高岭石比值表现为高/低交替变化,分别与中国灵台黄土磁化率高/低变化相对应,由于黄土磁化率记录了亚洲内陆干/湿变化,因此该黏土矿物比值敏感地响应了亚洲内陆的古气候变化,因而可以作为可靠的亚洲大陆干/湿变化示踪指标。     

Patterns of rare earth and other trace elements in Paleogene and Miocene clayey sediments from the Mondego platform (Central Portugal)

In the present study the origin of clay deposits occurring in an inland platform, in central Portugal, was investigated by their mineralogical and chemical composition. The clay deposits, exploited for ceramic industry are composed of silt-clay facies, the Monteira Member and the Arroça Member, which are assigned to the Coja Formation (Paleogene) and the Campelo Formation (Miocene), respectively. These clayey facies show almost compositional homogeneity, especially concerning texture. The mineralogical composition of the Monteira Member displays slightly higher content in smectite and interstratified clay minerals, which is supported by the chemical composition of samples analyzed. Both members present similar REE patterns, displaying an intense weathering record and little variation in the source area composition. Minor element geochemistry suggests low content in heavy minerals and transition metals. REE patterns and ratios of geochemical parameters support the dominant metasedimentary provenance, with a granite source contribution and also mature recycled sediments of continental origin. The study results’ suggest that the clays of these two members have the same source in terms of lithology and recycled sediments from the Hesperian massif. During the deposition of the Arroça Member, a major remobilization of the Monteira Member is suggested, explaining the geochemical similarity of both facies.     

Clay mineralogy of Triassic sediments in southern Israel and Sinai

The clay mineral composition of Triassic sediments in the Negev and Sinai depends upon the environment of deposition. Kaolinite predominates in continental and epicontinental sediments. The mineralogical composition of the marine clays resembles that of corresponding samples from North Africa and Europe, which comprise various mixtures and interstratifications of illite, montmorillonite, vermiculite and chlorite. Evaporitic sediments are poor in clay minerals and those present are largely detrital. The results presented suggest that chlorite was formed diagenetically by prolonged percolation of seawater through pervious layers overlying impervious ones (hard beds).     

Quantitative analysis of the clay minerals in the Shurijeh Reservoir Formation using combined X-ray analytical techniques

The Shurijeh Reservoir Formation of Neocomian age is represented by a sandstone sequence, occasionally interbedded with shale, in the Gonbadli gas field, Kopet-Dagh Basin, Northeastern Iran. In this study X-ray diffraction (XRD) and X-ray fluorescence (XRF) techniques were used together to characterize the Shuirjeh clay minerals in 76 core samples collected from two deep Gonbadli wells. The results of XRF analysis showed high percentages of silicon and moderate to low percentages of aluminum, sulfur, calcium, potassium, sodium, magnesium, and iron in both wells. The XRD analysis indicated that the above elements were concentrated in the form of quartz, anhydrite, dolomite, calcite, plagioclase, K-feldspar, hematite, and clay minerals. Further XRD examination of the clay fraction revealed that illite, chlorite, and kaolinite were the major types of clay minerals. Unlike, glauconite, smectite, and a mixed layer clays of both the illite–smectite and chlorite–smectite types were observed only in very few samples. The percentages of individual clay minerals were determined using external standard calibration curves and successfully validated by a system of simultaneous linear equations acquired from detailed elemental information based on the XRF analysis. The error reached ± 5% for the main mineral constituent and ± 15% for minor minerals. A local regression relationship was also derived, based on the XRF elemental information, which can be used to estimate the clay contents of other Shurijeh drilled wells with data of pulsed-neutron spectroscopy tools. According to the proposed quantitative approach, the amount of illite varied considerably, reaching 18.3%. In contrast, the amounts of kaolinite and chlorite were generally small, i.e., less than 8.4%. The amount of total clay minerals changed greatly from a minimum of 5% to a maximum of 32.5%. An increase in illite with increasing burial depth and temperature was an obvious indication of deep burial diagenesis in this formation.