Evidence for a single clay/temper source for the manufacture of Middle and Late Helladic Aeginetan pottery from Asine,Greece

In an effort to further characterize the Middle and Late Helladic pottery industry on Aegina, we have analyzed amphibole in 23 sherds imported to the coastal settlement of Asine. The sherds derive from vessels of different classes and shapes and range in age from MH I‐II to LH IIIB‐IIIC Early. All sherds come from vessels that carry manufacturing marks, and their amphiboles have compositions that are incompatible with those of Methana, Poros, and Melos. Twenty of the sherds have amphiboles that are identical in composition and overlap a narrow range of amphibole compositions found in specific lava flows on the northern portion of Aegina. Given that the dacites across Aegina contain amphiboles with a wide range in compositions, we suggest that the narrow range of amphibole compositions in the sherds indicates that they were derived from either a specific clay source on the island, located in a stream system southeast of the prehistoric settlement at Kolonna, or that the potters used a specific temper source along the same stream system. Multiple clay or temper sources would have produced sherds with a broader range of amphibole compositions reflecting the diversity of amphibole compositions found on Aegina. One sherd has amphibole compositions indicative of an additional Aeginetan component that is not found in the other sherds. Two sherds have amphiboles with compositions that do not match any known reference amphiboles for Aegina, Methana, Poros, or Melos. These may have been derived from still unsampled dacites on Aegina or have been manufactured from materials located outside the Saronic Gulf. © 2004 Wiley Periodicals, Inc.     

It all comes out in the wash: Actualistic petrofacies modeling of temper provenance,Tonto Basin,Arizona, USA

Prehistoric potters frequently tempered their pottery with sand, the provenance of which can be established petrographically. In the Tonto Basin of central Arizona, the bedrock geology is highly variable, giving rise to geographically unique sands. Zones of sands with similar compositions can be modeled at an archaeologically relevant scale. Here we use the actualistic petrofacies concept, the Gazzi–Dickinson point‐counting technique, and multivariate statistics to create a petrofacies model, then apply it to sand‐tempered utilitarian pottery recovered from three Tonto Basin project areas. Data analysis reveals strong temporal and spatial ceramic production and consumption patterns. Production of pottery for exchange was established in at least one petrofacies ca. A.D. 600–950, with increasing specialization through time. By ca. A.D. 1150, corrugated wares had been added, and specialized production by ware was established in two petrofacies. Provenance evidence suggests different regional affiliations for groups in different parts of the basin. © 2001 John Wiley & Sons, Inc.     

Optical and thermoluminescence dating of Middle Stone Age and Kintampo bearing sediments at Birimi,a multi-component archaeological site in Ghana

We report the first luminescence ages for the archeological and geological sediments forming the substrate of the Birimi archaeological site in the Northern Region of Ghana. The site's significance rests on the fact that it contains a rich collection of artifact assemblages representative of three distinct cultures, and that, on the basis of artifact typology, the earliest assemblage is diagnostic of the Middle Stone Age (MSA). In situ occurrences of MSA artifacts are found at over 1 m below today's surface. They are overlain by a ceramic-rich complex of a sedentary or semi-sendentary Later Stone Age culture known as the Kintampo. The western half of the site is dominated by the industrial remains of Iron Age smelting activity.Elemental, mineralogical, and sedimentological analysis of the cultural and sub-cultural sedimentary horizons at the site revealed at least three distinct lithostratigraphic units. The quartz sediments are derived from the sandstone of the Gambaga escarpment, mass wasted and accreted fluvially at a rate of 3.2 cm/ka, forming a wide terrace at Birimi. Silts and finer fractions derive from windblown dust, likely from White Volta River and granitic sources to the north. Soil forming processes and wide fluctuations in moisture have progressively reduced the sediments at depth to the resistant quartz and kaolinite, with rich iron oxide coatings, and created two ironstone horizons composed of goethite-cemented quartz nodules.Multiple aliquot green-light stimulated optical ages for 125–150 μm quartz grains yielded ages of 23.6±2.9 and 40.8±11.8 ka for the MSA-bearing sediments, and 58.4±15.3 ka for the base of the terrace. Radiocarbon ages on charcoal from Kintampo-bearing units are 3.36–3.83 ka cal BP, and are supported by thermoluminescence (TL) ages on pottery sherds and burnt house daub fragments of this cultural complex. A 0.4 ka age on sediment from the site's surface confirms that the quartz zeroes well when exposed to natural light. Sediments bearing the Kintampo artifacts, however, yielded ages of 7.8–16.9 ka. These ages were obtained on sediments from large pits, some over 50 cm deep, and they deviate only slightly from the ages expected for naturally aggraded sediments at these depths. We conclude, therefore, that extensive digging of pits by the Kintampo dwellers was followed by rapid refilling, and that the bulk mobilization of the matrix did not permit the sedimentary quartz grains to experience any appreciable zeroing at that time.     

Geochemistry of Palaeoproterozoic volcanic rocks of the Iricoumé Group,Pitinga Mining District,Amazonian craton,Brazil

The Iricoumé Group includes 1.88 Ga volcanic units of the Iricoumé–Mapuera volcano-plutonic association, part of the Uatumã magmatic series in the Guyana shield portion of the Amazonian craton. In the Pitinga Mining District, these rocks consist dominantly of felsic trachyte to rhyolite, associated with voluminous ignimbrite and minor ash-fall tuffs and surge deposits. Mafic rocks are present as basaltic clasts within volcanic breccias, and mostly as mafic microgranular enclaves in the associated Mapuera plutonic rocks. The felsic rocks have high contents of SiO₂, FeO_t, K₂O, Rb, and alkalis; low TiO₂, CaO, Sr, Ba, Nb, Ta, and Eu; and show metaluminous to weakly peraluminous bulk-rock compositions. They exhibit alkaline geochemical features, expressed by Na₂O?+?K₂O averages of 8.8 wt.%, FeO_t/(FeO_t?+?MgO) ≥ 0.8, and high Ga/Al ratios, compatible with A-type magmas. The studied samples plot in the field of within-plate or post-collisional rocks in a (Nb?+?Y) versus Rb diagram. Nb/Y ratios indicate that they are comparable to A2-type rocks which, allied with their high LREE/Nb ratios, suggest that they were produced from mantle sources modified by previous subduction in a post-collisional setting. Two compositional populations of Ca-amphibole, a Mg-rich (actinolite to Mg-hornblende) and a Fe-rich one (Fe-edenite to Fe-pargasite, Fe-hornblende and Fe-actinolite), characterize the Iricoumé Group volcanics. The Fe-rich amphiboles crystallized under lower fO₂ and higher pressure conditions compared with the Mg-rich amphiboles, indicating different levels of crystallization or re-equilibration during ascent of the magmas. Zircons from rhyolites show trace-element compositions typical of magmatic crystals with high Th/U ratios, and REE patterns compatible with zircon-melt partition coefficients for silicic magma compositions. Their relatively lower zircon/rock partition coefficients are due to early apatite crystallization. Fractional crystallization mainly of plagioclase-hornblende and biotite-alkali feldspar with minor amounts of apatite explains the geochemical trends observed in the felsic Iricoumé volcanic rocks.     

A geological study of clayey laterite and clayey hydromorphic material of the region of Yaoundé (Cameroon): a prerequisite for local material promotion

A geological survey carried out in the Yaoundé (Cameroon) region has revealed the presence of homogeneous clayey laterite in the upper part of a laterite cover on interfluves, thickest on hills (780–800 m altitude) where ferricrete is absent, and clayey heterogeneous hydromorphic material in valleys. We present in this paper the physical, mineralogical and geochemical properties of these occurrences and discuss their potential as raw material for pottery, manufacture of bricks and tiles. These clayey raw materials are mostly made up of fine particles (ranging from 55 to 60% clay + silt in the clayey laterite, more than 70% clay + silt in the clayey hydromorphic material). Their chemical composition is characterized by silica (<60% SiO₂), alumina (<35% Al₂O₃) and iron (ranging from 3 to 14% Fe₂O₃). Their main clay minerals are disorganized and poorly crystallized kaolinites. The average limits of liquidity (44.56% versus 91.58%) and limits of plasticity (22.4 versus 45.93) revealed that clayey hydromorphic material has the greatest plasticity. The studied raw materials are suitable for making pottery as well as the manufacture of bricks and tiles. However, the high iron content in the clayey laterite (between 11 and 12% Fe₂O₃) prevents their efficient use in the manufacture of ceramics.     

Re‐creation of the 1744 Heylyn and Frye ceramic patent wares using Cherokee clay: Implications for raw materials,kiln conditions,and the earliest English porcelain production

Porcelain wares have been produced following the directions contained in the Heylyn and Frye patent of 1744, using Cherokee clay and a lime‐alkali glass frit. The wares were fired to the bisque (˜ 950°C), glazed using a clay‐glass mixture, and then fired to a “heat‐work” level of Orton cone 9–90° deflection at 150°C per hour (1279°C). Modal mineralogy comprises Caplagioclase and two glass phases, one relict frit and the other a melt phase. The bulk chemistry of the body comprises 64.3 wt % SiO₂, 21.7 wt % Al₂O₃, and 5.6 wt % CaO. Molecular ratios are SiO₂:Al₂O₃ 5.0 and SiO₂:CaO 10.7. It is concluded that the patent, whose significance has been questioned over many years, was a practical working recipe, that close comparison may be made with porcelains of the “A”‐marked group, and that the patent represents a remarkable landmark in English ceramic history. © 2004 Wiley Periodicals, Inc.     

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.     

Provenance and microprobe assays of phyllite‐tempered ceramics from the uplands of central Arizona

The ceramics in use across a broad upland zone of central Arizona during the early Classic period (ca. A.D. 1100–1300) were characterized by a lack of mineralogical variability; nearly all of the clay containers were tempered with one rock type, phyllite. Consequently, nearly all of the upland pottery is assigned to a single pottery type, Wingfield Plain. This compositional uniformity has frustrated ceramic provenance studies, and, as a result, little has been learned previously about the organization of ceramic production and exchange in the upland territory. There are, however, considerable and interpretable chemical differences in the phyllite‐tempered wares, as shown with microanalyses of the temper fragments and pottery clay fractions with an electron microprobe. The chemical patterning is useful for investigating issues pertaining to the upland zone, including the organization of ceramic manufacture, community arrangements, and pottery transactions during a time of prevalent hostilities in central Arizona. © 2008 Wiley Periodicals, Inc.     

Geochemical dissociation of major and trace elements in bed and suspended sediment phases of the phosphate mines effluent water, Jordan

The bed and suspended (slime) sediment phases associated with effluent water that are produced from phosphate-ore-upgrading process at Al-Abyad mine in the southern part of Jordan were analyzed chemically and mineralogically. The results show that the effluent water is highly oxic and mildly alkaline in nature. The geochemical behavior of each phase was controlled by the effluent water physicochemical parameters, sediment particle size, mineralogical constituents of the studied phases, and the prevailing climatic nature of the area. Bed sediments have higher concentrations of many elements than slime. Accordingly, the bed sediments can be considered as a sink rather than a pool for many elements. The geochemical dissociation of major oxides and trace elements between bed and slime sediments was evident using t test, particularly between P₂O₅, SiO₂, CaO, K₂O, Mn, Sr, Y, and Co, and to lesser extent, V, U, Zn, and Cr. This might be attributed to effluent water characteristics, mineralogy, and the presence of fine-grained materials. The spatial distribution of major oxide and trace element concentrations along the stream drainage exhibited a slight increase with distance either in bed or slime sediment phases. However, they increased suddenly at the last three sampling sites, which might be due to the abundance of fine-grained materials that are mainly composed of clay minerals (montmorillonite) that would enhance the adsorption process. Moreover, the XRD results confirmed the existence of elemental geochemical dissociation as a function of mineral control.     

Some factors affecting TDS and pH values in groundwater of the Beihai coastal area in southern Guangxi,China

Groundwater of low total dissolved solids (TDS) of 10 mg/L and low pH ranging commonly from 4.0 to 7.0 occurs in the unconsolidated unconfined and confined aquifers in the coastal plain near Beihai, Guangxi, China. Minerals in the unconsolidated sediment of Quaternary are predominated by quartz (more than 50%) with small amount of clay minerals, such as kaolinite, illite and chlorite. SiO₂ accounts for most (more than 70%) of the chemical compositions of the sediments. The sediments contain low concentrations of soluble constituents (below 300 μg/g) and are predominated by SO₄. Abundant recharge from low-TDS precipitation and a long time’s dissolution of the unconsolidated sediments containing small amount of soluble compositions lead to low TDS of the groundwater in the area.     

Turbidity development and dissipation in paleoplacer gold deposits, southern New Zealand

Placer gold mining inevitably produces highly turbid processing waters. Five historic paleoplacer mining sites in Central Otago, New Zealand, provided 24 samples which were used in laboratory-based settling experiments. Turbidity was examined in the context of stratigraphy of paleoplacer deposits, their environments of formation, and the groundwater processes that affected the deposits as well as the underlying bedrock. Settling rates were characterised by measuring turbidity levels over time (up to 40 days) using turbidimeter and Coulter counter methods. High clay mineral (mostly kaolinite) contents of the materials were confirmed by X-ray diffraction. Grain size distributions of suspended materials were very comparable across all samples with majority of particles falling between <1.2 and 2.5 μm. The levels of turbidity produced by the auriferous sediments were partly controlled by the level of sorting and winnowing that the sediments were subjected to during transport and deposition. Debris flow material generated high turbidity [initial levels of 120–420 nephelometric turbidity units (NTU)] which settled slowly, as did eolian siltstone (1,600 NTU). Fluvial sediments generally generated lower turbidity which settled more rapidly, on the scale of hours to days. It was found that cementation of the sediment can reduce turbidity generation by limiting disaggregation of the clay minerals. On the other hand, the presence of altered lithic clasts within the sediments contributes to higher turbidity production. There was poor correlation between the level of bedrock alteration, as indicated by Chemical Index of Alteration, and the resulting turbidity. Settling rates were more rapid in experiments conducted in saline solution, as opposed to stream water, due to floc formation.     

Determination of Mercury in Thirty‐three International Stream Sediment and Soil Reference Samples by Direct Mercury Analyser

Mercury was determined in thirty‐three international stream sediment and soil reference samples (eleven Chinese soils, GSS‐1 to GSS‐11; twelve Chinese stream sediments, GSD‐1A to GSD‐12; four Canadian stream sediments STSD‐1 to STSD‐4; South African stream sediments, SARM‐42, SARM‐46 and SARM‐47; Japanese stream sediments, JSd‐1 to JSd‐3) by direct mercury analyser. Samples were taken in 500 μl quartz boats, placed in an auto sampler and processed (drying time 60 s at 300 °C; decomposition time 120 s at 850 °C; waiting time 45 s). The instrument was calibrated in the low (0‐50 ng) and high ranges (50‐500 ng) with two reference materials GSS‐5 and GXR‐2 (USGS). Using the calibration line, reference samples were analysed for Hg. The results of the determinations agreed with the recommended values of RMs in all cases except JSd‐1. The RSD calculated for the RMs was found to be within 20%. The detection limit was 1 ng g^?1.     

Status of sedimentation in King Talal Dam,case study from Jordan

This paper focuses on characterizing the current status of physical and chemical characteristics of King Talal Dam (KTD) sediments. The quality of sediments was investigated based on several international sediment quality guidelines. The volume of sediment and sedimentation rate in (KTD) was also estimated. Five types of granulometric textural facies were observed for the sediments of KTD reservoir bed, with an average grain size distribution of gravel (1.38%), sand (32.38%), silt (32.35%) and clay (32.38%). The fraction of <63 micron showed that the total mean size was 8.0 micron. Other sediment parameters in KTD were 7.0% for total organic matter (TOM), 7.3 for pH, 35.9% for CaCO₃ and 100.5 meq/100 g for cation exchange capacity, with dominant mineralogical constituents of quartz, calcite, dolomite, clay minerals and minor feldspar. The total concentrations of F, Cl, NO₂, NO₃, PO₄ and SO₄ in sediment samples were lower inward for KTD. The vast majority of trace metals in sediments were generally within the standard limits recommended for soils. TOM and grain size of sediment are major factors governing the trace metal concentrations. The calculated geoaccumulation index (I _geo) and enrichment factor of metals in bottom sediments showed that the metals were in the following order: Cd > Pb > Zn > Co > Cr > Ni > Fe > Cu > Sr > Mn and Cd > Zn > Pb > Co > Cr > Ni > Cu > Sr > Mn, respectively. Based on the sonic survey of KTD reservoir, the annual sedimentation rate was about 0.4061 MCM/year, in which about 18.66% of the reservoir initial storage capacity was lost to sediments and a projected lifespan of about 198 years.     

Clay minerals in SW Indian continental shelf sediment cores as indicators of provenance and palaeomonsoonal conditions: a statistical approach

Two sediment cores from the inner continental shelf of SW India, SK‐148/13 (4.66 m long; from 50 m water depth) and SK‐148/14 (5.37 m long; from 22 m water depth), were studied for provenance and palaeomonsoonal implications. Sediment layers at different depth intervals in these cores were estimated for clay minerals and organic matter content. Five surface sediment samples from the nearby Kali River estuary of the adjacent hinterland were also analysed for clay mineral contents. In both cores and Kali River sediments, smectite is the dominant clay followed by illite, and kaolinite or chlorite. Based on the similarities of the abundances of clay minerals and their relative wt‐% in the inner shelf sediment cores and in surface sediments of the estuary as demonstrated by significance tests, Al‐rich illite, and negligible contribution of clay from the deep‐sea and aeolian sources, it can be inferred that the sediments of the two inner continental shelf cores were derived from the adjacent hinterland. Application of statistical discordancy and significance tests on the down‐core variations in the crystallinity index (CI) of illite and organic matter content in the sediment cores indicates intense monsoonal (high rainfall) conditions at the adjacent hinterland during about 4300–6200 and 9300–10,400 years BP. These inferences are comparable to those from other well‐established palaeomonsoonal indicators such as sedimentation rates and mineral magnetic properties. The CI of illite, an easily determinable and climatically sensitive parameter, can thus be a reliable palaemonsoonal indicator for inner shelf sediment cores. The statistical methodology used in this work highlights the advantages of a quantitative interpretation of the data instead of the conventional qualitative visual examination.     

Distinctive Volcanic Material for the Production of Campana A Ware: The Workshop Area of Neapolis at the Duomo Metro Station in Naples,Italy

Recent transportation infrastructure works in Naples, Italy, provided important discoveries related to the production of pottery in the Hellenistic workshop area of Piazza Nicola Amore. A minero‐petrographic investigation was conducted on 35 samples belonging to the widespread Campana A ware and production indicators (clayey raw materials, unfired Graeco‐Italic amphorae, kiln wastes, workshop tools). Additional analysis was conducted on black‐glaze and common ware samples for comparison. The analyses reveal compositional and technological homogeneity of Campana A ware. Samples are characterized by low CaO content with evidence of both volcanic and sedimentary components, suggesting that different clay sources were properly mixed to prepare a standard recipe. Production indicators, black‐glaze and common wares, have a composition well consistent with the calcareous clays from the island of Ischia. Leucite‐ and garnet‐bearing temper from the Somma Volcano were used for the preparation of coarse‐grained pastes, unfired Graeco‐Italic amphorae, and clayey raw materials, thus suggesting that they represented the clay sources for amphorae production. Our results reveal new technological and socioeconomic aspects of Hellenistic pottery production in the Bay of Naples, in particular for the Campana A ware, now representing a new reference group: Neapolis.     

Early Cretaceous Ice Rafting and Climate Zonation in Australia

Lower Cretaceous (Valanginian to Albian) strata of the southwestern Eromanga and Carpentaria basins of central and northern Australia, respectively, provide evidence of strongly seasonal climates at high paleolatitudes. These include dispersed clasts (lonestones) in fine sediments and pseudomorphs of calcite after ikaite (glendonites), the latter being known to form only at temperatures below about 7° C.

Rafting is regarded as the transport mechanism for clasts up to boulder size (lonestones) enclosed within dark mudrocks; this interpretation rests on rare occurrences of penetration by clasts into substrate layers. Driftwood and large floating algae are eliminated as possible rafts because fossil wood is found mainly concentrated in nearshore areas of the basins and large algal masses have not been observed. Rafting by icebergs is considered unlikely in view of the global lack of tillites and related glacial deposits of this age. Our interpretation is that seasonal ice, formed in winter along stream courses and strandlines, incorporated clasts which, during the melt season, were dropped into muddy sediments in both basins. Eromanga fine-sediment and lonestone clasts in places were reworked subsequently by storm activity, producing lag concentrations of large clasts and associated sand lenses, both lying above local erosion surfaces. In the Carpentaria Basin, local dumping of sediment from raft surfaces resulted in accumulation of pods of small clasts.

Three zones can be identified for the Early Cretaceous climate of eastern Australia: (1) a very cold southern region, at latitudes above about 72 ° S, characterized by meteoric waters possibly originating as Antarctic glacial meltwaters; (2) a zone of strongly seasonal climates, with freezing winters and warm summers, between about 72° and 53° S. Lat.; and (3) a mid-latitude zone (below about 50° S. Lat.), where freezing temperatures were not common. However, owing to scant biostratigraphic control on the successions, the time span of specific climates in both the cold and the seasonal zones cannot be determined and probably existed only for short intervals.     

Effects of sediment texture on in-stream nitrogen uptake

A comparative experiment was conducted in two cross sections with sandy and sandy loam sediment textures along an agricultural drainage stream in eastern China to address the effects of sediment texture on in-stream nitrogen uptake efficiency. Using dimerous chambers for in situ incubations, NO₃-N and NH₄-N uptake metrics (i.e., areal uptake rate and uptake velocity) and associated hydrochemical variables in the enclosed sediment–water column system were measured for 8 days and two nights across April–July in 2011 and March–June in 2012. For the investigated sites, in-stream uptake accounted for 2–45 and 9–36 % of the initial NH₄-N and NO₃-N within the enclosed water column, respectively. Although similar daytime, diel and day-to-day (daytime) variation patterns of NO₃-N or NH₄-N uptake metrics were observed for the two sites, the sandy loam sediments had average net NO₃-N and NH₄-N uptake efficiency ~50 % higher and ~40 % lower than for the sandy sediments, respectively. As NO₃-N was the dominant nitrogen form in the studied water columns (typical of agricultural drainage rivers), the sandy loam sediment site had an average of about 47 % higher net uptake efficiency for dissolved inorganic nitrogen (i.e., NO₃-N + NH₄-N). This study demonstrates that sediment texture has a considerable effect on spatial variation of nitrogen uptake along the river system. Changing sediment texture due to anthropogenic modifications on catchment land use and stream channels has the potential to change stream nitrogen cycling as well as altering nitrogen inputs and forms to downstream aquatic ecosystems.     

Effects of grain size distribution on mineralogical and chemical compositions: a case study from size‐fractional sediments of the Huanghe (Yellow River) and Changjiang (Yangtze River)

The influence of hydrodynamics on the chemical composition of sediments is based on the uneven distribution of element abundances in different size fractions. In this study, 72 size‐fractional sediments from the Huanghe (Yellow River) and Changjiang (Yangtze River) riverbeds were measured with XRD, SEM, ICP‐AES and ICP‐MS. The analysis results show that the mineral and chemical characteristics change with grain size in the Huanghe and Changjiang sediments. According to the principal components analysis, three independent geochemical factors were found. The first factor elements, Zr, Hf, Th, U, Y, La and TiO₂ are influenced by the existence of heavy minerals. The second factor elements, Al₂O₃, alkalis, alkaline earth (excluding Ca and Sr) and most of the transitional metals are dominated by clay minerals. The third factor group includes Ca and Sr, which were controlled by calcium‐bearing mineral contents and chemical weathering intensities. The various grain size distributions greatly affect the mineralogical and chemical compositions of bulk sediments. Compared to other size fractions, the 5–6PHI size fractions of the Huanghe and Changjiang sediments have special mineralogical and chemical compositions, and intermediate volume percentages. Weight or volume percentage of each size fraction may be more suitable than mean grain‐size of the bulk sediment to elucidate the grain size effects. Chemical Index of Alteration (CIA) values increase steeply with decreasing grain size, while Weathering Index of Parker (WIP) values are relatively stable. Because of the big influence of the abundance of clay minerals on CIA values, it is questionable to use CIA as a proxy of weathering intensity. Considering the clay mineral effects, stability in values and heterogeneous material properties, WIP has the potential to indicate the chemical weathering intensity of sediments. Copyright © 2014 John Wiley & Sons, Ltd.     

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.