Clay Minerals In Sediments Research Articles

Clay Minerals in Sediments from the Central Part of the Guaymas Basin, the Gulf of California, Hole 478

The clay minerals in the Upper Pleistocene sediments from DSDP Hole 478 (a drilled depth of 464 m) located in the central area of the Guaymas Basin, Gulf of California, are studied. The composition of the clay minerals and their quantitative proportions in natural mixtures are determined by modeling of X-ray diffraction patterns for oriented specimens of finely dispersed particles. The terrigenous clay minerals are mainly dioctahedral (mixed-layer smectite–illite is dominant, the amount of illite is smaller) with admixtures of chlorite and kaolinite. They are distributed throughout the entire sedimentary section, except for thermally altered sediments from the contact zones with the top of the sills, where terrigenous dioctahedral clay minerals disappear, except for illite, and are substituted by trioctahedral mixed-layer chlorite–smectite and corrensite–chlorite; trioctahedral smectite also appears. Terrigenous illite is missing in the sediments at the base of the sedimentary cover exposed by the hole, on the top of the sill complex with a thickness of no less than 125 m.

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

AbstractEarly 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.

Clay minerals in sediments from contact zones with basalt sills

Clay minerals (fraction <0.001 mm) of Upper Pleistocene clayey-sandy-silty sediments recovered by DSDP Holes 481 and 481A in the Northern Trough, Guaymas Basin, Gulf of California, were studied by X-ray based on the modeling of diffraction patterns and their comparison with experimental diffractograms. Terrigenous clay minerals are represented mainly by dioctahedral micaceous varieties (mixed-layer disordered illite-smectites, illite) with the chlorite admixture and by kaolinite in the upper section of unaltered sediments. Intrusion of hot basalt sills (total thickness of the complex is about 27 m) provoked alterations in the phase composition of clay minerals in sediments (7.5 m thick) overlying the sill complex. These sediments include newly formed triooctahedral layered silicates (mixed-layer chlorite-smectites, smectite). Sediments inside the sill complex include trioctahedral mixed-layer mica-smtctite-vermiculite or trioctahedral smectite. The trioctahedral mixed-layer chlorite-smectite coexisting with smectite was found in a single sample of the same complex.

Clay Minerals in Sediments from Contact Zones with Basalt Sills

Clay minerals (fraction <0.001 mm) of Upper Pleistocene clayey–sandy–silty sediments recovered by DSDP Holes 481 and 481A in the Northern Trough, Guaymas Basin, Gulf of California, were studied by X-ray methods based on the modeling of diffraction patterns and their comparison with experimental diffractograms. Terrigenous clay minerals are represented mainly by dioctahedral micaceous varieties (mixed-layer disordered illite–smectites, illite) with the chlorite admixture and by kaolinite in the upper section of unaltered sediments. Intrusion of hot basalt sills (total thickness of the complex is about 27 m) provoked alterations in the phase composition of clay minerals in sediments (7.5 m thick) overlying the sill complex. These sediments include newly formed trioctahedral layered silicates (mixed-layer chlorite–smectites, smectite). Sediments inside the sill complex include trioctahedral mixed-layer mica–smectite–vermiculite or trioctahedral smectite. The trioctahedral mixed-layer chlorite–smectite coexisting with smectite was found in a single sample of the same complex.

The boron isotope geochemistry of smectites from sodium, magnesium and calcium bentonite deposits

The mineralogical, chemical and isotopic analyses of smectites, with variable interlayer cation occupancies, from bentonite deposits in various depositional environments, reveal new insights into the boron sources and the fluids involved in bentonitization in marine and non-marine environments.Smectites from bentonites have non-exchangeable, structural boron concentrations of 0.2 to 196 μg/g B. Smectites from sodium bentonites have higher boron concentrations (>30 μg/g) than those from magnesium or calcium bentonites. Most smectites have a small, interstratified illitic component that has a major influence on boron concentrations, requiring the use of modified fluid-mineral boron partitioning coefficients, which indicate that bentonites formed from fluids of highly variable boron concentrations of <0.1 mg/L B to >100 mg/L B, and a chlorine content of 76.4 mg/L to 59,076 mg/L. The sodium bentonites formed from boron-rich saline fluids or brines whereas the fluids involved in calcium and magnesium bentonite formation have a more variable boron composition and salinity.The δ11B values of the structural boron in tetrahedral sites of smectites range from −30.1‰ to +12.2‰. The smectites from terrestrial depositional settings have δ11B values of −30.1‰ to about 0‰, whereas smectites from marine depositional settings have negative as well as positive δ11B values. The boron isotope values indicate that all examined bentonites from terrestrial depositional settings as well as many bentonites from marine depositional settings formed from basinal fluids or brines.The boron isotope geochemistry of smectites is demonstrated to be a tool for elucidating the fluids involved in the formation of clay mineral deposits. It also has great potential for tracing fluids in other settings involving authigenic clay minerals such as sedimentary basins and surficial crystalline rocks, as well as man-made applications such as in disposal sites for highly active nuclear waste.

Characteristics of clay minerals in sediments of Hemudu area, Zhejiang, China in Holocene and their environmental significance

ABSTRACT The Ningshao Plain experienced sea-level fluctuation and climate change in the Holocene and gave birth to a Neolithic Civilization, the Hemudu Culture (about 5000 BC). Using XRD method, this paper studied the clay mineralogy of sediments in core HMD-1301 from Hemudu Site area in Ningshao Plain. Results show that the clay mineral assemblages in all samples are quite consistent. They are dominated by illite (about 57%) and smectite (about 26%), and a small amount of kaolinite (about 6%) and chlorite (about 9%). In addition, illite, chlorite, and kaolinite are originated mainly from eolian loesses. Smectite is resulted mainly from chemical weathering of local volcanic rocks outcropped. Illite crystallinity indicates the climatic characteristics of the source region, and illite chemistry index reflects the climate nature of the sedimentary area. It is our understanding that water medium properties in a sedimentary environment affect clay mineral assemblage and the distribution, based on which were cognized the Holocene transgression-regression events in the Hemudu Site area. These mineral indices are well comparable with geochemical indicators in identifying the transgression-regression events. We believe that these events affected the ancient civilization of the ancient residential communities at the time. ©2019 China Geology Editorial Office.

REE patterns and trustworthiness of stable carbon isotopes of Salitre Formation, Irecê Basin (Neoproterozoic), São Francisco Craton

Neoproterozoic limestones have been subject to variations in their original isotopic ratios, which has led to studies to verify the reliability of isotopic data obtained in these rocks. A Brazilian example of Neoproterozoic carbonate succession is found in Irecê Basin (BA) (Salitre Formation, São Francisco Supergroup). The present research aims to evaluate the reliability of the δ13C, mainly through REE patterns of samples gathered in Upper Nova America Unit. This unit represents an intermediate section included in a thick carbonate cover that represents the Salitre Formation. X-Ray fluorescence and inductive plasma mass spectrometry (ICP-MS) techniques were used to obtain elemental geochemistry. X-ray diffraction, including the fraction < 4 μm, and microscope with coupled fluorescence were used to verify the presence of carbonate, organic matter, siliciclastic phases and their proportions. Samples are mainly calcitic and have REE patterns with enrichment of light REEs, strong positive La anomalies, slightly positive Ce anomalies, variety of Gd anomalies, absence of strong Y anomaly and Y/Ho ratio of 31.5 ± 1.5. These anomalies indicate a mixture of oceanic and fresh waters during precipitation. Ce positive anomalies indicate anoxic states of early digenetic conditions of the environment. δ13C values have little contrast around 0‰. As a result, calcareous from Nova América Unit precipitated under shallow depths on carbonate platform. High concentration of Zr and SiO2 suggests high rates of weathering on marginal belts of São Francisco craton through high energy input of detrital material by freshwater. On the other hand, low concentration of Al2O3 indicates deposition of clay minerals occurred in a mild area of the plataform. The Mn/Sr and Fe/Sr ratios did not indicate the presence of significant diagenetic or metamorphic alterations. From the petrographic point of view, the samples do not present preserved organic matter, but they are recrystallized instead, sometimes dolomitized and dissolution features are present. The results indicate that Nova América limestones were precipitated on shallow carbonate restricted platform close to the coastline prone to fresh water and detrital input, therefore, δ13C does not correspond to the isotopic composition of the global ocean.

Classification of gravity-flow deposits and their significance for unconventional petroleum exploration, with a case study from the Triassic Yanchang Formation (southern Ordos Basin, China)

The ongoing exploration for shale oil and gas has focused sedimentological research on the transport and deposition mechanisms of fine-grained sediments, and more specifically on fine-grained mass-flow deposits. It appears, however, that no easily applicable classification scheme for gravity-flow deposits exists, and that such classifications almost exclusively deal with sandy and coarser sediments. Since the lack of a good classification system for fine-grained gravity flow deposits hampers scientific communication and understanding, we propose a classification scheme on the basis of the mud content in combination with the presumed transport mechanism. This results in twelve types of gravity-flow deposits. In order to show the practical applicability of this classification system, we apply it to the Triassic lacustrine Yanchang Formation in the southern Ordos Basin (China), which contains numerous slumps, debris–flows deposits, turbidites and hyperpycnites. The slumps and debrites occur mostly close to a delta front, and the turbidites and hyperpycnites extend over large areas from the delta slopes into the basin plain.The case study shows that (1) mud cannot only be transported but also deposited under active hydrodynamic conditions; (2) fine-grained gravity-flow constitute a significant part of the lacustrine mudstones and shales; (3) muddy gravity flows are important for the transport and deposition of clastic particles, clay minerals and organic matter, and thus are important mechanisms involved in the generation of hydrocarbons, also largely determining the reservoir capability for unconventional petroleum.

Continental weathering as a driver of Late Cretaceous cooling: new insights from clay mineralogy of Campanian sediments from the southern Tethyan margin to the Boreal realm

Abstract New clay mineralogical analyses have been performed on Campanian sediments from the Tethyan and Boreal realms along a palaeolatitudinal transect from 45° to 20°N (Danish Basin, North Sea, Paris Basin, Mons Basin, Aquitaine Basin, Umbria-Marche Basin and Tunisian Atlas). Significant terrigenous inputs are evidenced by increasing proportions of detrital clay minerals such as illite, kaolinite and chlorite at various levels in the mid- to upper Campanian, while smectitic minerals predominate and represented the background of the Late Cretaceous clay sedimentation. Our new results highlight a distinct latitudinal distribution of clay minerals, with the occurrence of kaolinite in southern sections and an almost total absence of this mineral in northern areas. This latitudinal trend points to an at least partial climatic control on clay mineral sedimentation, with a humid zone developed between 20° and 35°N. The association and co-evolution of illite, chlorite and kaolinite in most sections suggest a reworking of these minerals from basement rocks weathered by hydrolysis, which we link to the formation of relief around the Tethys due to compression associated with incipient Tethyan closure. Diachronism in the occurrence of detrital minerals between sections, with detrital input starting earlier during the Santonian in the south than in the north, highlights the northward progression of the deformation related to the anticlockwise rotation of Africa. Increasing continental weathering and erosion, evidenced by our clay mineralogical data through the Campanian, may have resulted in enhanced CO2 consumption by silicate weathering, thereby contributing to Late Cretaceous climatic cooling.

Risk assessment and driving factors for artificial topography on element heterogeneity: Case study at Jiangsu, China.

The rapid expansion of construction related to coastal development evokes great concern about environmental risks. Recent attention has been focused mainly on factors related to the effects of waterlogging, but there is urgent need to address the potential hazard caused by artificial topography: derived changes in the elemental composition of the sediments. To reveal possible mechanisms and to assess the environmental risks of artificial topography on transition of elemental composition in the sediment at adjoining zones, a nest-random effects-combined investigation was carried out around a semi-open seawall. The results implied great changes induced by artificial topography. Not only did artificial topography alter the sediment elemental composition at sites under the effect of artificial topography, but also caused a coupling pattern transition of elements S and Cd. The biogeochemical processes associated with S were also important, as suggested by cluster analysis. The geo-accumulation index shows that artificial topography triggered the accumulation of C, N, S, Cu, Fe, Mn, Zn, Ni, Cr, Pb, As and Cd, and increased the pollution risk of C, N, S, Cu, As and Cd. Enrichment factors reveal that artificial topography is a new type of human-activity-derived Cu contamination. The heavy metal Cu was notably promoted on both the geo-accumulation index and the enrichment factor under the influence of artificial topography. Further analysis showed that the Cu content in the sediment could be fitted using equations for Al and organic carbon, which represented clay mineral sedimentation and organic matter accumulation, respectively. Copper could be a reliable indicator of environmental degradation caused by artificial topography.

Mineral resources of Novokuznetsk administrative district of Kemerovo region (metallic and non-metallic minerals)

The article summarizes data on metallic and non-metallic minerals of Novokuznetsk district of Kemerovo region. Consistently reviewed are iron deposits (Tersinskaya group of deposits), gold deposits (placer accumulations and vein gold deposits), mineral water deposits (Tersinskoe deposit), deposit of refractory clay (Barkinskoe) and wide spread mineral deposits such as brick clay, keramzite materials, sand and gravel, building stones, ornamental stones, facing stones, peat, materials for lime production. It is indicated that resource base of metallic and nonmetallic minerals is inferior to that of mineral coal. At the same time it can be of considerable interest to small and medium-size businesses as objects with quick return of investment (facing and ornamental stones). For a number of wide spread mineral resources (brick clay, keramzite materials, sand and gravel) it is an important component of local industry.

Clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin (Gulf of California)

The results of the study of clay mineral alterations in Upper Pleistocene sediments of the southern trough in the Guaymas Basin (Gulf of California) due to the influence of hydrothermal solutions and heat produced by sill intrusions are discussed. Core samples from DSDP Holes 477 and 477A were taken for the analysis of clay minerals. Application of the method of modeling X-ray diffraction patterns of oriented specimens of the finely dispersed particles made it possible to establish the phase composition of clay minerals, determine their structural parameters, and obtain reliable quantitative estimates of their contents in natural mixtures. The modeling data allowed us to characterize reliably the transformation of clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin. In Upper Pleistocene sandy–clayey sediments of the southern trough, changes in the composition of clay minerals occurred under the influence of a long-living hydrothermal system. Its lower part (interval 170.0–257.5 m) with maximum temperatures (~300°C) was marked by the formation of chlorite. Terrigenous clay minerals are not preserved here. Saponite appears at a depth of 248 m in the chlorite formation zone. Higher in the sedimentary section, the interval 146–170 m is also barren of terrigenous clay minerals. Sediments of this interval yielded two newly formed clay minerals (chlorite and illite), which were formed at lower temperatures (above 180°C and below 300°C, approximately up to ~250°C), while the relatively low-temperature upper part (110–146 m) of the hydrothermal system (from ~140°C to ~180°C) includes the mixture of terrigenous and newly formed clay minerals. Terrigenous illite is preserved here. Illitization of the mixed-layer illite–smectite was subjected to illitization. The terrigenous montmorillonite disappeared, and chlorite–smectite with 5–10% of smectite layers were formed. In the upper interval (down to approximately 110 mbsf), the composition of terrigenous clay minerals remains unchanged. They are composed of the predominant mixed-layer illite–smectite and montmorillonite, the subordinate illite, mixed-layer chlorite–smectite with 5% of smectite layers, mixed-layer kaolinite–smectite with 30% of smectite layers, and kaolinite. This composition of clay minerals changed under the influence of sill intrusions into the sedimentary cover at 58–105 m in the section of Hole 477. The most significant changes are noted in the 8-m-thick member above the sill at 50–58 m. The upper part of this interval is barren of the terrigenous mixed-layer illite–smectite, which is replaced by the newly formed trioctahedral smectite (saponite). At the same time, the terrigenous dioctahedral smectite (montmorillonite) is preserved. The composition of terrigenous clay minerals remains unchanged at the top of the unit underlying the sill base.

Relationship between heavy metal contents and clay mineral properties in surface sediments: Implications for metal pollution assessment

Clay minerals in surface sediments can affect the adsorption of heavy metals. However, few historical studies have focused on the influence of fine clay mineral characteristics on metal sorption. Since the reactions between heavy metals and fine clay minerals in sediments remain obscure, this study investigates the influence of fine clay mineral characteristics on metal sorption in a typical urbanizing small watershed. Clay minerals, including nanoparticles with various size fractions ranging from 1000 to 2000 (clay), 450–1000 (fine clay), and 220–450 (very fine clay)nm were used to demonstrate their transformation from well crystalline to poorly crystalline. The nanoparticles were collected and evaluated by determination of their surface area, X-ray diffraction, scanning electron microscopy (SEM) and chemical analyses. The relationship between metal content and properties of the surface sediments was also revealed by canonical correlation analysis. With smaller particle sizes, nanoparticles (very fine clay) were observed to be poorly crystalline, possibly indicating few repetitions of unit cells as a result of preferential structural disruption of other crystal planes caused by pressure-induced phase transition in the fine-size fractions. The first canonical matrix (M) variables of metal contents can be predicted by both surface area and pore volume, followed by kaolinite and illite contents. On the other hand, the category of metal, i.e., Cu, Cr, Zn, or Pb, was significantly correlated with the first ‘M’ canonical variables. The data obtained in the present study are of fundamental significance in advancing our understanding of the reactions between heavy metals and fine clay minerals in the terrestrial ecosystem.

Characterizing clay mineralogy in Lake Towuti, Indonesia, with reflectance spectroscopy

We tested the use of visible to near-infrared (VNIR) reflectance spectroscopy to characterize the relative abundances of clay minerals in sediments from Lake Towuti, a large tectonic lake in Sulawesi, Indonesia. We measured VNIR spectra of lake and river sediments from Lake Towuti and its catchment to identify clay minerals, fit major VNIR absorption features with a modified Gaussian model to estimate relative abundances of these minerals, and compared these absorptions to the samples’ chemistry to test the utility of VNIR spectroscopy to characterize sediment compositional variations. We found that major absorptions are caused by vibrations of Al–OH in kaolinite (2.21 μm), Fe–OH in nontronite (2.29 μm), Mg–OH in saponite and serpentine (2.31 μm), and Mg–OH in serpentine (2.34 μm). This was confirmed with X-ray diffraction data. The correlations between absorption band areas for Fe–OH, Al–OH, and Mg–OH vibrations and Fe, Al and Mg concentrations, respectively, are statistically significant, varying between r = 0.51 and r = 0.90, and spatial variations in inferred clay mineralogy within the lake are consistent with variations in the geology of the catchment. We conclude that VNIR spectroscopy is an effective way to characterize the clay mineralogy of lake sediments, and can be used to investigate changes in mineral inputs to lake deposits.

Spatial and temporal distributions of clay minerals in mud deposits on the inner shelf of the East China Sea: Implications for paleoenvironmental changes in the Holocene

We present a paleoclimatic reconstruction for the Holocene by clay mineral analyses of sediments from core MZ02 retrieved from the mud area of the inner continental shelf of the East China Sea (ECS). The clay minerals mainly consist of illite (66%–79%) and chlorite (12%–19%), with minor kaolinite (7%–13%) and smectite (0–6%). Provenance analysis suggests that the illite-dominated clay minerals were derived mainly from the detrital outputs of the Changjiang, Minjiang, and small rivers from Taiwan Island. Our study indicates that the sea level rise since the last glacial, the strength of the Taiwan Warm Current (TWC) and Chinese Coastal Current (CCC) have controlled the dispersal and deposition of clay minerals on the ECS, that in turn determined the clay mineral compositions in the core sediments. During 13,000–9500 BP, due to the lower sea level and shorter distance between these three estuaries and core MZ02, fine sediments on the inner shelf of the ECS were primarily supplied by mixed provenances from the Changjiang, Taiwanese, and Minjiang rivers. During the early Holocene (9500–6200 BP), stronger sediment reworking and erosion at the shelf edge was responsible for the increased lateral transport of fine sediments in the ECS, which lead to a dominance of the sediment source from the Changjiang, while the Taiwanese and Minjiang rivers only provided minor components of detrital sediment to the shelf. Increased strength of TWC might have played an important role in the sediment dispersal and deposition on the inner shelf of the ECS during 6200–2400 BP, with a dominance of more than 60% sediments transported from Taiwanese rivers. Furthermore, our study implies that the Asian monsoon and the weakening of TWC were linked to the abrupt increase of Changjiang and Minjiang derived terrigenous detritus materials since 2400 BP.

Mineralogical and physico-chemical characterizations of clay from Keur Saër (Senegal)

AbstractThere is interest in exploiting and developing natural resources, particularly deposits of natural clays. Senegal has several clay mineral deposits for which chemical and mineralogical compositions have been little studied. Some of these natural materials are nowadays used in pottery and ceramics. To extend applications, a better basic knowledge is required and, for this objective, the raw clay and separated &lt;2 μm clay fraction from Keur Saër (Senegal) were subjected to chemical and mineralogical studies. Several techniques including X-ray diffraction (XRD), thermal analysis (TG-DTA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), N2 adsorption-desorption isotherms, cation exchange capacity (CEC) measurements and solid state nuclear magnetic resonance (NMR) have been used to characterize the material. It was found that the raw clay and the separated clay fraction consist of a mineral mixture in which kaolinite is the main component. 29Si and 27Al MAS-NMR spectra show the presence of silicon atoms linked to three other silicon atoms via an oxygen atom and six coordinated Al atoms. Significant increases in the specific surface area and cation exchange capacity were observed on purification, reaching a maximum of about 73.2 m2g–1 and 9.5 meq/100 g for the separated fine clay fraction while the values for the raw material were around 28.9 m2g–1 and 7.3 meq/100 g.

Geochemical Consequences of Widespread Clay Mineral Formation in Mars’ Ancient Crust

Clays form on Earth by near-surface weathering, precipitation in water bodies within basins, hydrothermal alteration (volcanic- or impact-induced), diagenesis, metamorphism, and magmatic precipitation. Diverse clay minerals have been detected from orbital investigation of terrains on Mars and are globally distributed, indicating geographically widespread aqueous alteration. Clay assemblages within deep stratigraphic units in the Martian crust include Fe/Mg smectites, chlorites and higher temperature hydrated silicates. Sedimentary clay mineral assemblages include Fe/Mg smectites, kaolinite, and sulfate, carbonate, and chloride salts. Stratigraphic sequences with multiple clay-bearing units have an upper unit with Al-clays and a lower unit with Fe/Mg-clays. The typical restriction of clay minerals to the oldest, Noachian terrains indicates a distinctive set of processes involving water-rock interaction that was prevalent early in Mars history and may have profoundly influenced the evolution of Martian geochemical systems. Current analyses of orbital data have led to the proposition of multiple clay-formation mechanisms, varying in space and time in their relative importance. These include near-surface weathering, formation in ice-dominated near-surface groundwaters, and formation by subsurface hydrothermal fluids. Near-surface, open system formation of clays would lead to fractionation of Mars’ crustal reservoir into an altered crustal reservoir and a sedimentary reservoir, potentially involving changes in the composition of Mars’ atmosphere. In contrast, formation of clays in the subsurface by either aqueous alteration or magmatic cooling would result in comparatively little geochemical fractionation or interaction of Mars’ atmospheric, crustal, and magmatic reservoirs, with the exception of long-term sequestration of water. Formation of clays within ice would have geochemical consequences intermediate between these endmembers. We outline the future analyses of orbital data, in situ measurements acquired within clay-bearing terrains, and analyses of Mars samples that are needed to more fully elucidate the mechanisms of martian clay formation and to determine the consequences for the geochemical evolution of the planet.

Sources and Sinks of Phosphorus for a Perturbed Stream and the Effects of Mineral Deposits1

Effler, Steven W., Anthony R. Prestigiacomo, David A. Matthews, and Feng Peng, 2012. Sources and Sinks of Phosphorus for a Perturbed Stream and the Effects of Mineral Deposits. Journal of the American Water Resources Association (JAWRA) 48(2): 321‐335. DOI: 10.1111/j.1752‐1688.2011.00617.xAbstract: Patterns of concentrations and loading rates of multiple forms of phosphorus (P) are resolved and analyzed along Ninemile Creek, New York, a stream perturbed by a domestic waste discharge and residual effects of a closed industry. This analysis is based on biweekly monitoring of total, dissolved, and soluble reactive P (SRP) for 19 months at four sites that bracket each of these effects, and 15 years of biweekly measurements at the two sites that bound industrial deposits. The minerogenic particle populations of the stream and the surficial sediments along the reach with extensive CaCO3 and clay mineral deposits are characterized with an individual particle analysis technique. Mass balance analyses depict: (1) increasing nonpoint inputs of particulate and dissolved organic P along the stream length; (2) input of P from a domestic waste facility, almost entirely in the form of SRP; and (3) a compensating downstream loss of SRP over the reach with the extensive industrial deposits of CaCO3. The downstream sink process for SRP is attributed to sorption processes with minerogenic deposits. The domestic waste‐based source and the compensating industrial waste‐based sink are noteworthy fluxes relative to other prevailing loads received by downstream Onondaga Lake, for which a major rehabilitation program targeting cultural eutrophication is underway. The P source/sink conditions of this stream are considered in the context of this rehabilitation program.

Relationship between sediment clay minerals and total mercury

A group of 262 sediment samples were collected from various lakes, rivers, reservoirs, and bayous of Louisiana. All samples were analyzed for total mercury. Twenty nine of the samples with total mercury content ranging from 11 to 401 ppb (μg/kg) were analyzed for clay minerals and other sediment physical and chemical properties. Clay content in sediments varied from 3 to 72%. Clay minerals were determined by X-ray diffraction (XRD) technique. Identification of clay minerals was determined by MacDiff software and quantification of clay minerals was obtained by Peak Height Percentage (PHP) calculation. The dominant clay mineral was Hydrated Interlayer Vermiculite (HIV), which represented 51–83% of the total clay mineral. Significant linear correlations were observed between Hg and total clay content (r= 0.538**). However Smectite was the only individual clay type correlated (r= 0.465**) with mercury in sediment. Cation exchange capacity (r= 0.404*), organic matter (r= 0.577**), and sulfur (r= 0.676**) were also correlated significantly with mercury level in sediment.

Analysis of major and trace elements by INAA to predict the thousands year old sediment deposition environment in the Meghna river delta

Major, trace and rare earth elements have been measured in sediments of different layers to determine the controls of constituent minerals on the distribution of elements and sediment deposition environment in the Meghna river delta. The geochemical composition of sediments was enriched in SiO2, Ca, Mg and Ba and depleted in Al, Fe, Ti, Mn, and Sr relative to PAAS (Post-Archaen Average Shale) value. The X-ray diffraction and elemental analyses demonstrate the dominant presence of quartz, micas, feldspar, chlorite, amphibole and clay minerals in sediments. The very low contents of trace elements suggest that the oxic condition was more prevalent during sediment deposition of Pleistocene-Holocene period and reflect the massive chemical weathering by biogeochemical reactions. The enrichment of light rare earth elements and La/Yb ratio reflect the intense silicate weathering of crustal materials and the high sediment depositional rate in the Meghna river delta.