Impact of highly basic solutions on sorption of Cs to subsurface sediments from the Hanford site, USA

The effect of caustic NaNO₃ solutions on the sorption of ¹³⁷Cs to a Hanford site micaceous subsurface sediment was investigated as a function of base exposure time (up to 168 d), temperature (10°C or 50°C), and NaOH concentration (0.1 mol/L to 3 mol/L). At 10°C and 0.1 M NaOH, the slow evolution of [Al]_aq was in stark contrast to the rapid increase and subsequent loss of [Al]_aq observed at 50°C (regardless of base concentration). Exposure to 0.1 M NaOH at 10°C for up to 168 d exhibited little if any measurable effect on sediment mineralogy, Cs⁺ sorption, or Cs⁺ selectivity; sorption was well described with a two-site ion exchange model modified to include enthalpy effects. At 50°C, dissolution of phyllosilicate minerals increased with [OH]. A zeolite (tetranatrolite; Na₂Al₂Si₃O₁₀·2H₂O) precipitated in 0.1 M NaOH after about 7 days, while an unnamed mineral phase (Na₁₄Al₁₂Si₁₃O₅₁·6H₂O) precipitated after 4 and 2 days of exposure to 1 M and 3 M NaOH solutions, respectively. Short-term (16 h) Cs⁺ sorption isotherms (10⁻⁹-10⁻² mol/L) were measured on sediment after exposure to 0.1 M NaOH for 56, 112, and 168 days at 50°C. There was a trend toward slightly lower conditional equilibrium exchange constants (Δlog _Na^CsK_c ∼ 0.25) over the entire range of surface coverage, and a slight loss of high affinity sites (15%) after 168 days of pretreatment with 0.1 M base solution. Cs⁺ sorption to sediment over longer times was also measured at 50°C in the presence of NaOH (0.1 M, 1 M, and 3 M NaOH) at Cs⁺ concentrations selected to probe a range of adsorption densities. Model simulations of Cs⁺ sorption to the sediment in the presence of 0.1 M NaOH for 112 days slightly under-predicted sorption at the lower Cs⁺ adsorption densities. At the higher adsorption densities, model simulations under-predicted sorption by 57%. This under-prediction was surmised to be the result of tetranatrolite precipitation, and subsequent slow Na → Cs exchange. At higher OH concentrations, Cs⁺ sorption in the presence of base for 112 days was unexpectedly equal to, or greater than that expected for pristine sediment. The precipitation of secondary phases, coupled with the fairly unique mica distribution and quantity across all size-fractions in the Hanford sediment, appears to mitigate the impact of base dissolution on Cs⁺ sorption.     

Desorption kinetics of radiocesium from subsurface sediments at Hanford Site, USA

The desorption of ¹³⁷Cs⁺ was investigated on sediments from the United States Hanford site. Pristine sediments and ones that were contaminated by the accidental release of alkaline ¹³⁷Cs⁺-containing high level nuclear wastes (HLW, 2 × 10⁶ to 6 × 10⁷ pCi ¹³⁷Cs⁺/g) were studied. The desorption of ¹³⁷Cs⁺ was measured in Na⁺, K⁺, Rb⁺, and NH₄⁺electrolytes of variable concentration and pH, and in presence of a strong Cs⁺-specific sorbent (self-assembled monolayer on a mesoporous support, SAMMS). ¹³⁷Cs⁺ desorption from the HLW-contaminated Hanford sediments exhibited two distinct phases: an initial instantaneous release followed by a slow kinetic process. The extent of ¹³⁷Cs⁺ desorption increased with increasing electrolyte concentration and followed a trend of Rb⁺ ≥ K⁺ > Na⁺ at circumneutral pH. This trend followed the respective selectivities of these cations for the sediment. The extent and rate of ¹³⁷Cs⁺ desorption was influenced by surface armoring, intraparticle diffusion, and the collapse of edge-interlayer sites in solutions containing K⁺, Rb⁺, or NH₄⁺. Scanning electron microscopic analysis revealed HLW-induced precipitation of secondary aluminosilicates on the edges and basal planes of micaceous minerals that were primary Cs⁺ sorbents. The removal of these precipitates by acidified ammonium oxalate extraction significantly increased the long-term desorption rate and extent. X-ray microprobe analyses of Cs⁺-sorbed micas showed that the ¹³⁷Cs⁺ distributed not only on mica edges, but also within internal channels parallel to the basal plane, implying intraparticle diffusive migration of ¹³⁷Cs⁺. Controlled desorption experiments using Cs⁺-spiked pristine sediment indicated that the ¹³⁷Cs⁺ diffusion rate was fast in Na⁺-electrolyte, but much slower in the presence of K⁺ or Rb⁺, suggesting an effect of edge-interlayer collapse. An intraparticle diffusion model coupled with a two-site cation exchange model was used to interpret the experimental results. Model simulations suggested that about 40% of total sorbed ¹³⁷Cs⁺ was exchangeable, including equilibrium and kinetic desorbable pools. At pH 3, this ratio increased to 60-80%. The remainder of the sorbed ¹³⁷Cs⁺ was fixed or desorbed at much slower rate than our experiments could detect.     

Dissolution of uranyl microprecipitates in subsurface sediments at Hanford Site, USA

The dissolution of uranium was investigated from contaminated sediments obtained at the US. Department of Energy (U.S. DOE) Hanford site. The uranium existed in the sediments as uranyl silicate microprecipitates in fractures, cleavages, and cavities within sediment grains. Uranium dissolution was studied in Na, Na-Ca, and NH₄ electrolytes with pH ranging from 7.0 to 9.5 under ambient CO₂ pressure. The rate and extent of uranium dissolution was influenced by uranyl mineral solubility, carbonate concentration, and mass transfer rate from intraparticle regions. Dissolved uranium concentration reached constant values within a month in electrolytes below pH 8.2, whereas concentrations continued to rise for over 200 d at pH 9.0 and above. The steady-state concentrations were consistent with the solubility of Na-boltwoodite and/or uranophane, which exhibit similar solubility under the experimental conditions. The uranium dissolution rate increased with increasing carbonate concentration, and was initially fast. It decreased with time as solubility equilibrium was attained, or dissolution kinetics or mass transfer rate from intraparticle regions became rate-limiting. Microscopic observations indicated that uranium precipitates were distributed in intragrain microfractures with variable sizes and connectivity to particle surfaces. Laser-induced fluorescence spectroscopic change of the uranyl microprecipitates was negligible during the long-term equilibration, indicating that uranyl speciation was not changed by dissolution. A kinetic model that incorporated mineral dissolution kinetics and grain-scale, fracture-matrix diffusion was developed to describe uranium release rate from the sediment. Model calculations indicated that 50-95% of the precipitated uranium was associated with fractures that were in close contact with the aqueous phase. The remainder of the uranium was deeply imbedded in particle interiors and exhibited effective diffusivities that were over three orders of magnitude lower than those in the fractures.     

Cation exchange reactions controlling desorption of Sr from coarse-grained contaminated sediments at the Hanford site, Washington

Nuclear waste that bore ⁹⁰Sr²⁺ was accidentally leaked into the vadose zone at the Hanford site, and was immobilized at relatively shallow depths in sediments containing little apparent clay or silt-sized components. Sr²⁺, ⁹⁰Sr²⁺, Mg²⁺, and Ca²⁺ was desorbed and total inorganic carbon concentration was monitored during the equilibration of this sediment with varying concentrations of Na⁺, Ca²⁺. A cation exchange model previously developed for similar sediments was applied to these results as a predictor of final solution compositions. The model included binary exchange reactions for the four operant cations and an equilibrium dissolution/precipitation reaction for calcite. The model successfully predicted the desorption data. The contaminated sediment was also examined using digital autoradiography, a sensitive tool for imaging the distribution of radioactivity. The exchanger phase containing ⁹⁰Sr was found to consist of smectite formed from weathering of mesostasis glass in basaltic lithic fragments. These clasts are a significant component of Hanford formation sands. The relatively small but significant cation exchange capacity of these sediments was thus a consequence of reaction with physically sequestered clays in sediment that contained essentially no fine-grained material. The nature of this exchange component explained the relatively slow (scale of days) evolution of desorption solutions. The experimental and model results indicated that there is little risk of migration of ⁹⁰Sr²⁺ to the water table.     

Characterizing vertical contaminant distribution in a thick unconfined aquifer,Hanford site,Washington, USA

Drilling-intensive aquifer characterization techniques have been used to obtain depth-discrete water samples from a thick, hydrogeologically continuous unconfined aquifer system; groundwater results indicate that carbon tetrachloride contamination is widespread and extends deeper and at concentrations much higher than detected in monitoring networks at the water table. Carbon tetrachloride, a legacy waste, was used in the plutonium extraction process at the Hanford site in south-central Washington State. Vertical, depth-discrete groundwater samples were collected during well drilling throughout a 28-km² region to determine the concentration of carbon tetrachloride present as a dissolved phase in the aquifer. Results indicate that high concentrations of carbon tetrachloride, three orders of magnitude above the allowable regulatory limit, are present at depths greater than 25 m beneath the water table. In support of future efforts to remediate the carbon tetrachloride contamination, it is imperative to locate the remaining chemical inventory, determine the vertical as well as the lateral distribution of this contaminant and its physical form. Depth-discrete aquifer characterization throughout the uppermost-unconfined aquifer system is providing this information and improving the understanding of the contaminant distribution and the hydrogeologic framework through which it moves.

Sorption and precipitation of Co(II) in Hanford sediments and alkaline aluminate solutions

Sorption and precipitation of Co(II) in simplified model systems related to the Hanford site high-level nuclear waste tank leakage were investigated through solution studies, geochemical modeling, and X-ray absorption fine structure (XAFS) spectroscopy. Studies of Co(II) sorption to pristine Hanford sediments (ERDF and Sub), which consist predominantly of quartz, plagioclase, and alkali feldspar, show an adsorption edge centered at pH ≈ 8.0 for both sediments studied, with sorption >99% above pH ≈ 9.0. Aqueous SiO₂ resulting from dissolution of the sediments increased in concentration with increasing pH, though the systems remained undersaturated with respect to quartz. XAFS studies of Co(II) sorption to both sediment samples reveal the oxidation of Co(II) to Co(III), likely by dissolved O₂, although this oxidation was incomplete in the Sub sediment samples. The authors propose that Fe(II) species, either in aqueous solution or at mineral surfaces, partially inhibited Co(II) oxidation in the Sub sediment samples, as these sediments contain significantly higher quantities of Fe(II)-bearing minerals which likely partially dissolved under the high-pH solution conditions. In alkaline solutions, Al precipitated as bayerite, gibbsite, or a mixture of the two at pH > 7; an amorphous gel formed at pH values less than 7. Aqueous Co concentrations were well below the solubility of known Co-bearing phases at low pH, suggesting that Co was removed from solution through an adsorption mechanism. At higher pH values, Co concentrations closely matched the solubility of a Co-bearing hydrotalcite-like solid. XAFS spectra of Co(II) sorbed to Al-hydroxide precipitates are similar to previously reported spectra for such hydrotalcite-like phases. The precipitation processes observed in this study can significantly reduce the environmental hazard posed by ⁶⁰Co in the environment.     

Environmental change recorded in sediments from the Marmes rockshelter archaeological site, southeastern Washington state, USA

The Marmes Rockshelter archaeological site in southeastern Washington state contains a > 11 kyr stratigraphic record that was excavated in the 1960s but only recently analyzed in detail. We present the results of physical, chemical, and isotopic analyses of archived Marmes sediments from rockshelter, hillslope, and floodplain locations. Multiple lines of evidence including éboulis production, soil chemistry, and δ¹³C and δ¹⁸O signatures in soil organic matter and calcium carbonate suggest that relatively cool, moist conditions 10,600 to 9700 ¹⁴C yr BP were followed by relatively warm and dry conditions as early as 9000 ¹⁴C yr BP. Warm and dry conditions extended to the late Holocene, followed by a return to cooler and moister climate. The limited range of δ¹³C and δ¹⁸O values in Marmes paleosols suggests that the magnitude of moisture and temperature shifts was locally buffered in the lower Snake River Canyon but adequate to generate significant changes in sedimentation and soil formation, possibly due to nonlinear geological and pedological processes. These buffered canyon environments were well suited for establishing residential bases associated with foraging and logistical collecting strategies and may have minimized the influence of climate changes in food resource abundance.     

Single-grain OSL dating of sediments from the Southern High Plains,USA

Single-grain OSL dating is applied to sediments from different depositional settings on the Southern High Plains of western Texas and eastern New Mexico. Criteria of acceptance are used to screen equivalent doses from individual grains and resulting distributions are evaluated in terms of normality. Wide variation is found in proportion of acceptable grains and in the distributions. While some of the latter are normal, many show broadening that may be the result of mixing of different-aged grains and skewness that may result from variant depositional and post-depositional modes. Geological modeling will be required to understand better these distributions, although for most samples means produced ages that agree with independent evidence. The resolution possible with single grains is necessary for best estimates of equivalent dose for other samples. A few samples do not agree with independent evidence, even with a normal distribution of equivalent dose. Sand dunes seem the most difficult to date accurately, probably because of mixing.     

An investigation of the relationship between bulk composition, inferred reaction progress and fluid-flow parameters for layered micaceous carbonates from Maine, USA

Reaction progress exhibited by multivariant assemblages in micaceous limestones can provide an excellent record of metamorphic fluid flow. However, it is necessary to understand the sensitivity of these assemblages to bulk‐composition parameters. Here, analysis of bulk composition on different scales and pseudosection construction are used to draw conclusions on relationships between bulk composition, fluid flow and reaction progress. Issues addressed include the effects of bulk composition on the mineralogical evolution of micaceous carbonates, the sensitivity of bulk composition to bulk‐composition sampling methods, the magnitude of cross‐layer fluid‐composition gradients, the potential for metasomatism to drive reaction progress, and the relative timing of reaction in adjacent layers. Pseudosections successfully represent observed mineral assemblages, constrain the position of reactions in T–X(CO₂) space, and allow assessment of the sensitivity of reaction position, inferred reaction progress and calculated fluid fluxes to uncertainties in bulk composition. The scale of bulk‐composition sampling affects bulk compositions, calculated modes, predicted mineral assemblages and calculated fluid compositions. Larger samples record an average of different lithological subdomains, while point‐count‐derived bulk compositions are subject to uncertainties related to the small number of sample points. The optimum bulk composition for pseudosection purposes probably lies between measured bulk compositions. Results suggest that reaction progress in some extensively reacted layers was driven by infiltration of H₂O‐rich fluid which flowed or diffused parallel to layering, perpendicular to layering in response to fluid‐composition gradients, and out of veins. Small variations in fluid composition across layering (ΔX(CO₂) < 0.02) were maintained by internal buffering by the mineral assemblages. Internal buffering must also have driven samples up a sequence of narrow low‐variance fields in T–X(CO₂) space, and so reaction in adjacent layers must have close to simultaneous. Metasomatic effects on reaction progress are likely to have been small, so long as the porosity was low.     

青海共和盆地达连海湖积物137Cs示踪的初步结果

通过对青海省共和盆地达连海干湖盆中的＾１３７Ｃｓ和粒度样品的测定,结合区域调查结果及其他相关资料的分析,确定了两个＾１３７Ｃｓ蓄积峰和一个蓄积谷,由此建立了达连海湖相沉积物的＾１３７Ｃｓ时标,即１９６３年的＾１３７Ｃｓ最大蓄积峰值和２０世纪８０年代末至９０年代初大规模土地开垦引起的、与异常剧烈风沙沉积有关的＾１３７Ｃｓ最小蓄积谷,以及１９９４年的湖泊干涸事件形成的次一级＾１３７Ｃｓ蓄积峰,并估算出     

Sorption of radium-226 from oil-production brine by sediments and soils

The sorption of²²⁶Ra from oil-production brine by soils and sediments was investigated. Sorption was rapid, and the percentage sorbed increased with brine dilution. Greatest removals of²²⁶Ra from sediments in the laboratory occurred with alkaline DTPA, HCl, and BaCl₂, with lesser removals using CaCl₂ and NaCl solutions. Digestion of sediments with NaOCl indicates that most of the native and sorbed²²⁶Ra is associated with the mineral rather than organic fraction of the sediments. Correlation analysis based on 14 soils indicates that the retention of²²⁶Ra may involve precipitation reactions associated with sulfate-bearing minerals, as well as ion-exchange reactions with the clay mineral fractions of surficial earth materials. Oceanographer, Naval Ocean Research and Development Activity, Code 334; NSTL Station, Mississippi 39529 NORDA Contribution #83:334:01.     

Palynological dating and correlation of surface and subsurface sediments from Wardha valley coalfield,Maharashtra

42 genera of palynomorphs have been reported from the qualitative and quantitative analysis of the palynoflora from both open cast mine and bore holes viz., Ballarpur open cast mine, Durgapur open cast mine and Bore hole CMWNM-57 on barrier between Kawadi/Majri open cast and Hindustan Lalpeth Colliery from the Wardha valley coalfield of Wardha basin. Two palynoassemblages have been recorded i.e., an Upper Karharbari palynoassemblage comprising dominance of radial monosaccate genus Parasaccites and subdominance of nonstriate disaccate genus Scheuringipollenites and a Lower Barakar palynoassemblage consisting of dominance of Scheuringipollenites and subdominance of striate disaccates chiefly Faunipollenites, suggesting an Early Permian age (Late Sakmarian to Early Artinskian) to the sediments. It is further authenticated by the occurrence of palynotaxa viz., Crucisaccites, Caheniasaccites, Indotriradites and Tiwariasporis. Upper Karharbari Formation has been demarcated for the first time in lithologically designated Barakar Formations in Ballarpur, Durgapur, Majri and Hindustan Lalpeth Colliery while the sample 57/2 of bore hole CMWNM from Kawadi area may belong to the Kamthi Formation on the basis of pinkish yellowish coarse grained to medium grained sandstone. An attempt has been made to correlate these palynoassemblages with other Lower Gondwana basins of Early Permian affinity.     

Evidence of microbially mediated arsenic mobilization from sediments of the Aquia aquifer, Maryland, USA

Sediments from the Aquia aquifer in coastal Maryland were collected as part of a larger study of As in the Aquia groundwater flow system where As concentration are reported to reach levels as high as 1072 nmol kg⁻¹, (i.e., ∼80 μg/L). To test whether As release is microbially mediated by reductive dissolution of Fe(III) oxides/oxyhydroxides within the aquifer sediments, the Aquia aquifer sediment samples were employed in a series of microcosm experiments. The microcosm experiments consisted of sterilized serum bottles prepared with aquifer sediments and sterilized (i.e., autoclaved), artificial groundwater using four experimental conditions and one control condition. The four experimental conditions included the following scenarios: (1) aerobic; (2) anaerobic; (3) anaerobic + acetate; and (4) anaerobic + acetate + AQDS (anthraquinone-2,6-disulfonic acid). AQDS acts as an electron shuttle. The control condition contained sterilized aquifer sediments kept under anaerobic conditions with an addition of AQDS. Over the course of the 27 day microcosm experiments, dissolved As in the unamended (aerobic and anaerobic) microcosms remained constant at around ∼28 nmol kg⁻¹ (2 μg/L). With the addition of acetate, the amount of As released to the solution approximately doubled reaching ∼51 nmol kg⁻¹ (3.8 μg/L). For microcosm experiments amended with acetate and AQDS, the dissolved As concentrations exceeded 75 nmol kg⁻¹ (5.6 μg/L). The As concentrations in the acetate and acetate + AQDS amended microcosms are of similar orders of magnitude to As concentrations in groundwaters from the aquifer sediment sampling site (127-170 nmol kg⁻¹). Arsenic concentrations in the sterilized control experiments were generally less than 15 nmol kg⁻¹ (1.1 μg/L), which is interpreted to be the amount of As released from Aquia aquifer sediments owing to abiotic, surface exchange processes. Iron concentrations released to solution in each of the microcosm experiments were higher and more variable than the As concentrations, but generally exhibited similar trends to the As concentrations. Specifically, the acetate and acetate + AQDS amended microcosm typically exhibited the highest Fe concentrations (up to 1725 and 6566 nmol kg⁻¹, respectively). The increase in both As and Fe in the artificial groundwater solutions in these amended microcosm experiments strongly suggests that microbes within the Aquia aquifer sediments mobilize As from the sediment substrate to the groundwaters via Fe(III) reduction.     

Organic contaminants and characteristics of sediments from Oso Bay,south Texas,USA

The Oso Bay, Texas, sediments from nine sites were analyzed by GC-MS for organics to measure contamination in the bay. In most of the sites sediments contained tetrachloroethene (87–1433 g/kg), bis (2-ethylhexyl)phthalate (40–193 g/kg), and aliphatic hydrocarbons, C₈-C₁₃ (720–2491 g/kg). Sources of these contaminants include a landfill, military facilities, and municipal and industrial discharges. Size analysis of the sediments indicates they contain a high percentage of muddy sand (50–75 percent), which suggests that Oso Bay consists of common bay margin sediments.     

Palynodating of subsurface sediments,Raniganj Coalfield,Damodar Basin,West Bengal

The Gondwana sediments comprising fine-grained shales, carbonaceous shales, sandstones and the coal horizon in borecore RT-4 (approximately 547.00m thick) from Tamra block, Raniganj Coalfield, Damodar Basin, are analyzed palynologically. Based on the distribution pattern of marker palynotaxa, two assemblage zones are identified. In the Barren Measures Formation, dominance of enveloping monosaccate (Densipollenites) along with striate bisaccate (Striatopodocarpites, Faunipollenites) pollen taxa, and the FAD’s of Kamthisaccites and Arcuatipollenites observed at 30.75, have equated this strata (30.75–227.80 m thick) with the Raniganj Formation of Late Permian in age. Downwards in the Barakar Formation, between 423.80–577.70 m depths, an abundance of non-striate (Scheuringipollenites) and striate (Faunipollenites and Striatopodocarpites) bisaccate pollen taxa is observed, that dates late Early Permian in age.     

Characterization of uranium-contaminated sediments from beneath a nuclear waste storage tank from Hanford, Washington: Implications for contaminant transport and fate

The concentration and distribution of uranium (U) in sediment samples from three boreholes recovered near radioactive waste storage tanks at Hanford, Washington, USA, were determined in detail using bulk and micro-analytical techniques. The source of contamination was a plume that contained an estimated 7000 kg of dissolved U that seeped into the subsurface as a result of an accident that occurred during filling of tank BX-102. The desorption character and kinetics of U were also determined by experiment in order to assess the mobility of U in the vadose zone. Most samples contained too little moisture to obtain quantitative information on pore water compositions. Concentrations of U (and contaminant phosphate—P) in pore waters were therefore estimated by performing 1:1 sediment-to-water extractions and the data indicated concentrations of these elements were above that of uncontaminated “background” sediments. Further extraction of U by 8 N nitric acid indicated that a significant fraction of the total U is relatively immobile and may be sequestered in mobilization-resistant phases. Fine- and coarse-grained samples in sharp contact with one another were sub-sampled for further scrutiny and identification of U reservoirs. Segregation of the samples into their constituent size fractions coupled with microwave-assisted digestion of bulk samples showed that most of the U contamination was sequestered within the fine-grained fraction. Isotope exchange (²³³U) tests revealed that ∼51% to 63% of the U is labile, indicating that the remaining fund of U is locked up in mobilization-resistant phases. Analysis by Micro-X-ray Fluorescence and Micro-X-ray Absorption Near-Edge Spectroscopy (μ-XRF and μ-XANES) showed that U is primarily associated with Ca and is predominately U(VI). The spectra obtained on U-enriched “hot spots” using Time-Resolved Laser-Induced Fluorescence Spectroscopy (TRLIFS) provide strong evidence for uranophane-type [Ca(UO₂)₂(SiO₃OH)₂(H₂O)₅] and uranyl phosphate [Ca(UO₂)₂(PO₄)₂(H₂O)_10-12] phases. These data show that disseminated micro-precipitates can form in narrow pore spaces within the finer-grained matrix and that these objects are likely not restricted to lithic fragment environments. Uranium mobility may therefore be curtailed by precipitation of uranyl silicate and phosphate phases, with additional possible influence exerted by capillary barriers. Consequently, equilibrium-based desorption models that predict the concentrations and mobility of U in the subsurface matrix at Hanford are unnecessarily conservative.     

Chemical and physical responses to deformation in micaceous quartzites from the Tauern Window, Eastern Alps

Micaceous quartzites from a subvertical shear zone in the Tauern Window contain abundant quartz clasts derived from dismembered quartz‐tourmaline veins. Bulk plane strain deformation affected these rocks at amphibolite facies conditions. Shape changes suggest net shortening of the clasts by 11–64%, with a mean value of 35%. Quartz within the clasts accommodated this strain largely via dislocation creep processes. On the high‐stress flanks of the clasts, however, quartz was removed via solution mass transfer (pressure solution) processes; the resulting change in bulk composition allowed growth of porphyroblastic staurolite + chlorite ± kyanite on the clast flanks. Matrix SiO₂ contents decrease from c. 83 wt% away from the clasts to 49–58% in the selvages on the clast flanks. The chemical changes are consistent with c. 70% volume loss in the high‐stress zones. Calculated shortening values within the clast flanks are similar to the volume‐loss estimates, and are greatly in excess of the shortening values calculated from the clasts themselves. Flow laws for dislocation creep versus pressure solution imply large strain‐rate gradients and/or differential stress gradients between the matrix and the clast selvages. In a rock containing a large proportion of semirigid clasts, weakening within the clast flanks could dominate rock rheology. In our samples, however, weakening within the selvages was self limiting: (1) growth of strong staurolite porphyroblasts in the selvages protected remaining quartz from dissolution; and (2) overall flattening of the quartz clasts probably decreased the resolved shear stress on the flanks to values near those of the matrix, which would have reduced the driving force for solution‐transfer creep. Extreme chemical changes nonetheless occurred over short distances. The necessity of maintaining strain compatibility may lead to significant localized dissolution in rocks containing rheologic heterogeneities, and overall weakening of the rocks may result. Solution‐transfer creep may be a major process whereby weakening and strain localization occur during deep‐crustal metamorphism of polymineralic rocks.     

137Cs in sediments of deep lakes

Sedimentation rate of suspensions (0.3–18.2 mm/yr) was determined on the basis of layer-by-layer distribution of ¹³⁷Cs (global and Chernobyl) in the cores of bottom sediments (BS) from 16 lakes located in the high and moderate latitudes of the Northern Hemisphere. Profiles of ¹³⁷Cs concentration in the BS cores were analyzed. Sedimentation rates in the limnic zones of deep-water lakes were calculated using ¹³⁷Cs accumulated in the finely-dispersed component of mineral suspension.     

Mineralogy and petrology of cretaceous subsurface lamproite sills, southeastern Kansas, USA

Cores and cuttings of lamproite sills and host sedimentary country rocks in southeastern Kansas from up to 312 m depth were analyzed for major elements in whole rocks and minerals, certain trace elements in whole rocks (including the REE) and Sr isotopic composition of the whole rocks. The lamproites are ultrapotassic (K₂O/Na₂O = 2.0–19.9), alkalic [molecular (K₂O/Na₂O)/Al₂O₃ = 1.3-2.8], enriched in mantle-incompatible elements (light REE, Ba, Rb, Sr, Th, Hf, Ta) and have nearly homogeneous initial Sr isotopic compositions (0.707764-0.708114).

These lamproites could have formed by variable degrees of partial melting of harzburgite country rock and cross-cutting veins composed of phlogopite, K-Ti richterite, titanite, diopside, K-Ti silicates, or K-Ba-phosphate under high H₂O/CO₂ ratios and reducing conditions. Variability in melting of veins and wall rock and variable composition of the metasomatized veins could explain the significantly different composition of the Kansas lamproites.

Least squares fractionation models preclude the derivation of the Kansas lamproites by fractional crystallization from magmas similar in composition to higher silica phlogopite-sanidine lamproites some believe to be primary lamproite melts found elsewhere. In all but one case, least squares fractionation models also preclude the derivation of magmas similar in composition to any of the Kansas lamproites from one another. A magma similar in composition to the average composition of the higher SiO₂ Ecco Ranch lamproite (237.5–247.5 m depth) could, however, have marginally crystallized about 12% richterite, 12% sanidine, 7% diopside and 6% phlogopite to produce the average composition of the Guess lamproite (305–312 m depth).

Lamproite from the Ecco Ranch core is internally fractionated in K₂O, Al₂O₃, Ba, MgO, Fe₂O₃, Co and Cr most likely by crystal accumulation-removal of ferromagnesian minerals and sanidine. In contrast, the Guess core (305–312 m depth) has little fractionation throughout most of the sill except in several narrow zones. Lamproite in the Guess core has large enrichments in TiO₂, Ba, REE, Th, Ta and Sc and depletions in MgO, Cr, Co and Rb possibly concentrated in these narrow zones during the last dregs of crystallization of this magma.

The Ecco Ranch sill did not show any evidence of loss of volatiles or soluble elements into the country rock. This contrasts to the previously studied, shallow Silver City lamproite which did apparently lose H₂O-rich fluid to the country rock. Perhaps a greater confining pressure and lesser amount of H₂O-rich fluid prevented it from escaping.