Geochemistry of Great Salt Lake,Utah I: Hydrochemistry since 1850

The hydrochemistry of Great Salt Lake, Utah, has been defined for the historic period, 1850 through 1982, from published data combined with new observations. The water balance depends largely on river inflow, atmospheric precipitation onto the lake surface and evaporation. Input of the major solutes can best be accounted for by mixing dilute calcium-bicarbonate type river waters with NaCl-dominated hydrothermal springs.Prior to 1930, lake concentrations fluctuated inversely with lake volume in response to small climatic variations. Since then, salt precipitation and dissolution have significantly modified lake brine compositions and have led to density stratification and the formation of brine pockets of differing composition. Brine mixing has become an important component of brine evolution. We have used calculated evaporation curves with mineral precipitation and dissolution to clarify these processes.Pore fluids represent important storage for solutes. Solute profiles can be modeled by simple one-dimensional diffusion calculations. Short-term historic variations in lake composition affect shallow pore fluids in the upper 2 metres of sediment.     

Geochemical Evolution of Great Salt Lake, Utah, USA

The Great Salt Lake (GSL) of Utah, USA, is the largest saline lake in North America, and its brines are some of the most concentrated anywhere in the world. The lake occupies a closed basin system whose chemistry reflects solute inputs from the weathering of a diverse suite of rocks in its drainage basin. GSL is the remnant of a much larger lacustrine body, Lake Bonneville, and it has a long history of carbonate deposition. Inflow to the lake is from three major rivers that drain mountain ranges to the east and empty into the southern arm of the lake, from precipitation directly on the lake, and from minor groundwater inflow. Outflow is by evaporation. The greatest solute inputs are from calcium bicarbonate river waters mixed with sodium chloride-type springs and groundwaters. Prior to 1930 the lake concentration inversely tracked lake volume, which reflected climatic variation in the drainage, but since then salt precipitation and re-solution, primarily halite and mirabilite, have periodically modified lake-brine chemistry through density stratification and compositional differentiation. In addition, construction of a railway causeway has restricted circulation, nearly isolating the northern from the southern part of the lake, leading to halite precipitation in the north. These and other conditions have created brine differentiation, mixing, and fractional precipitation of salts as major factors in solute evolution. Pore fluids and diagenetic reactions have been identified as important sources and especially sinks for CaCO₃, Mg, and K in the lake, depending on the concentration gradient and clays.     

Genetic Analysis of Invertebrates From Great Salt Lake,Utah

正Great Salt Lake(GSL),in northern Utah,is one of the largest lakes in the United States,with a total surface area of 4400 square kilometers.Arthropods constitute the most conspicuous and abundant animals inhabiting the waters     

Great Salt Lake,and precursors,Utah: The last 30,000 years

Sediment cores up to 6.5 m in length from the South Arm of Great Salt Lake, Utah, have been correlated. Radiocarbon ages and volcanic tephra layers indicate a record of greater than 30,000 years. A variety of approaches have been employed to collect data used in stratigraphic correlation and lake elevation interpretation; these include acoustic stratigraphy, sedimentologic analyses, mineralogy, geochemistry (major element, C, O and S isotopes, and organics), paleontology and pollen.The results indicate that prior to 32,000 year B.P. an ephemeral saline lake-playa system was present in the basin. The perennial lake, which has occupied the basin since this time, rose in a series of three major steps; the freshest water conditions and presumably highest altitude was reached at about 17,000 year B.P. The lake remained fresh for a brief period, followed by a rapid increase in salinity and sharp lowering in elevation to levels below that of the present Great Salt Lake. The lake remained at low elevations, and divided at times into a north and south Basin, until about 8,000 year B.P. Since that time, with the exception of two short rises to about 1290 m, the lake level has remained near the present elevation of 1280 m.     

Estimating selenium removal by sedimentation from the Great Salt Lake,Utah

The mass of Se deposited annually to sediment in the Great Salt Lake (GSL) was estimated to determine the significance of sedimentation as a permanent Se removal mechanism. Lake sediment cores were used to qualitatively delineate sedimentation regions (very high to very low), estimate mass accumulation rates (MARs) and determine sediment Se concentrations. Sedimentation regions were defined by comparison of isopach contours of Holocene sediment thicknesses to linear sedimentation rates determined via analysis of ²¹⁰Pb, ²²⁶Ra, ⁷Be and ¹³⁷Cs activity in 20 short cores (<5 cm), yielding quantifiable results in 13 cores. MARs were developed via analysis of the same radioisotopes in eight long cores (>10 cm). These MARs in the upper 1–2 cm of each long core ranged from 0.019 to 0.105 g_sed/cm²/a. Surface sediment Se concentrations in the upper 1 or 2 cm of each long core ranged from 0.79 to 2.47 mg/kg. Representative MARs and Se concentrations were used to develop mean annual Se removal by sedimentation in the corresponding sedimentation region. The spatially integrated Se sedimentation rate was estimated to be 624 kg/a within a range of uncertainty between 285 and 960 kg/a. Comparison to annual Se loading and other potential removal processes suggests burial by sedimentation is not the primary removal process for Se from the GSL.     

The lacustrine microbial carbonate factory of the successive Lake Bonneville and Great Salt Lake,Utah, USA

The Bonneville Basin is a continental lacustrine system accommodating extensive microbial carbonate deposits corresponding to two distinct phases: the deep Lake Bonneville (30 000 to 11 500 ¹⁴C bp ) and the shallow Great Salt Lake (since 11 500 ¹⁴C bp ). A characterization of these microbial deposits and their associated sediments provides insights into their spatio‐temporal distribution patterns. The Bonneville phase preferentially displays vertical distribution of the microbial deposits resulting from high‐amplitude lake level variations. Due to the basin physiography, the microbial deposits were restricted to a narrow shoreline belt following Bonneville lake level variations. Carbonate production was more efficient during intervals of relative lake level stability as recorded by the formation of successive terraces. In contrast, the Great Salt Lake microbial deposits showed a great lateral distribution, linked to the modern flat bottom configuration. A low vertical distribution of the microbial deposits was the result of the shallow water depth combined with a low amplitude of lake level fluctuations. These younger microbial deposits display a higher diversity of fabrics and sizes. They are distributed along an extensive ‘shore to lake’ transect on a flat platform in relation to local and progressive accommodation space changes. Microbial deposits are temporally discontinuous throughout the lake history showing longer hiatuses during the Bonneville phase. The main parameters controlling the rate of carbonate production are related to the interaction between physical (kinetics of the mineral precipitation, lake water temperature and runoff), chemical (Ca²⁺, Mg²⁺ and HCO₃^? concentrations, Mg/Ca ratio, dilution and depletion) and/or biological (trophic) factors. The contrast in evolution of Lake Bonneville and Great Salt Lake microbial deposits during their lacustrine history leads to discussions on major chemical and climatic changes during this interval as well as the role of physiography. Furthermore, it provides novel insights into the composition, structure and formation of microbialite‐rich carbonate deposits under freshwater and hypersaline conditions.     

An Equation of State for Hypersaline Water in Great Salt Lake,Utah, USA

Great Salt Lake (GSL) is one of the largest and most saline lakes in the world. In order to accurately model limnological processes in GSL, hydrodynamic calculations require the precise estimation of water density (ρ) under a variety of environmental conditions. An equation of state was developed with water samples collected from GSL to estimate density as a function of salinity and water temperature. The ρ of water samples from the south arm of GSL was measured as a function of temperature ranging from 278 to 323 degrees Kelvin (^oK) and conductivity salinities ranging from 23 to 182 g L⁻¹ using an Anton Paar density meter. These results have been used to develop the following equation of state for GSL (σ = ± 0.32 kg m⁻³):

Density-Stratified Flow Events in Great Salt Lake,Utah, USA: Implications for Mercury and Salinity Cycling

Density stratification in saline and hypersaline water bodies from throughout the world can have large impacts on the internal cycling and loading of salinity, nutrients, and trace elements. High temporal resolution hydroacoustic and physical/chemical data were collected at two sites in Great Salt Lake (GSL), a saline lake in the western USA, to understand how density stratification may influence salinity and mercury (Hg) distributions. The first study site was in a causeway breach where saline water from GSL exchanges with less saline water from a flow restricted bay. Near-surface-specific conductance values measured in water at the breach displayed a good relationship with both flow and wind direction. No diurnal variations in the concentration of dissolved (<0.45 μm) methylmercury (MeHg) were observed during the 24-h sampling period; however, the highest proportion of particulate Hg_total and MeHg loadings was observed during periods of elevated salinity. The second study site was located on the bottom of GSL where movement of a high-salinity water layer, referred to as the deep brine layer (DBL), is restricted to a naturally occurring 1.5-km-wide “spillway” structure. During selected time periods in April/May, 2012, wind-induced flow reversals in a railroad causeway breach, separating Gunnison and Gilbert Bays, were coupled with high-velocity flow pulses (up to 55 cm/s) in the DBL at the spillway site. These flow pulses were likely driven by a pressure response of highly saline water from Gunnison Bay flowing into the north basin of Gilbert Bay. Short-term flow reversal events measured at the railroad causeway breach have the ability to move measurable amounts of salt and Hg from Gunnison Bay into the DBL. Future disturbance to the steady state conditions currently imposed by the railroad causeway infrastructure could result in changes to the existing chemical balance between Gunnison and Gilbert Bays. Monitoring instruments were installed at six additional sites in the DBL during October 2012 to assess impacts from any future modifications to the railroad causeway.     

青海察尔汗盐湖碳酸盐的硼同位素地球化学特征

盐湖蒸发岩的硼(B)同位素组成(δ~(11)B)对卤水古盐度变化具有一定的指示意义,但关于盐湖体系碳酸盐沉积的B同位素组成研究较少。本文对察尔汗盐湖百米钻(ISL1A)岩芯碳酸盐进行了B含量及B同位素组成的精确测定。结果表明,所测样品的B含量在10.88×10~(-6)~265.66×10~(-6)之间,δ~(11)B值的变化范围为-1.28‰~+9.94‰,B含量和δ~(11)B值呈现较明显的正相关关系。分析表明,随着盐湖卤水盐度的增大,卤水的B同位素组成也逐渐增大,这导致盐类沉积物的B同位素组成也相应增大。在天然盐湖中,不充分的沉积分异作用使得蒸发岩析出时依然可能存在碳酸盐沉积,碳酸盐的析出可能贯穿盐湖演化的各个阶段,因此可以尝试利用碳酸盐的B同位素组成分析盐湖在整个演化过程中卤水的盐度变化情况。ISL1A钻孔碳酸盐B同位素组成的变化较好地反映了察尔汗盐湖在41.8ka以来古卤水盐度的变化及其在析盐过程中经历的气候干湿波动。     

Diel variation of selenium and arsenic in a wetland of the Great Salt Lake, Utah

Diel (24-h) changes in Se and As concentrations in a freshwater wetland pond bordering the Great Salt Lake (GSL) were examined. Selenium concentrations (filtered and unfiltered) changed on a diel basis, i.e., were depleted during early morning and enriched during daytime over August 17-18. During the May 24-25, 2006 and September 29-30 diel studies, no significant 24-h trends were observed in Se concentrations compared to August, which showed daily maximums up to 59% greater than the daily minimum. Both filtered and unfiltered As concentrations also varied on a diel cycle, with increased concentrations during early morning and decreased concentrations during daytime. Filtered As concentrations increased 110% during the May 24-25, 2006 diel study. Selenium varied in phase with pH, dissolved O₂ (DO), and water temperature (T_w) whereas As varied opposite to Se, pH, DO and T_w. Changes in pH, DO and T_w showed a direct linear correlation (r = 0.74, 0.75, and 0.55, respectively) to filtered Se. Also pH, DO and T_w were inversely correlated to filtered As concentration (r = −0.88, −0.87, and −0.84, respectively). Equilibrium geochemical speciation and sorption models were used to examine the potential oxidation state changes in Se and As, and sorption and desorption reactions corresponding to the observed 24-h variations in pe and pH. In this wetland it was postulated that diel Se variation was driven by sorption and desorption due to photosynthesis-induced changes in pH and redox conditions. Diel variations of As were hypothesized to be linked to pH-driven sorption and desorption as well as co-precipitation and co-dissolution with mineral phases of Mn.     

Paleomagnetic Investigation of the Bonneville Alloformation, Lake Bonneville, Utah

Paleomagnetic secular variation in a portion of the Bonneville Alloformation is compared with secular variation in lacustrine sediments in the Mono Basin, California, and with secular variation in Lake Lahontan sediments in the northwestern Great Basin. The comparison places an age of about 18,000 yr B.P., and a span of 1000 to 3000 yr, on part of a transgressive stage of Lake Bonneville near Delta, Utah, that is coeval with a wet period in the Lahontan Basin.     

Mineralogy and Geochemistry of Major,Trace and Rare Earth Elements in Sediments of the Hypersaline Urmia Salt Lake,Iran

Urmia Salt Lake(USL) is a hypersaline lake located at the NW corner of the Iran platform. The lake area is estimated to have been over 5000 km~2 at one point, but has now decreased to 1000 km~2 in the last two decades. It contains 4.6×10~9 tons of halite and other detrital and evaporative minerals such as calcite, aragonite, dolomite, quartz, feldspars, augite and sylvite. This study examined the mineralogy and geochemistry of bed sediments along the mid-east toward NE bank sediments collected from 1.5 meters depth and nearby augite placer. Due to the diverse lithology of the surrounding geology, bed sediments vary from felsic in the mid-east to mafic in the northeast. Weathering of tephrite and adakite rocks of the Islamic Island at the immediate boundary has produced a large volume of augite placer over a 40 km length, parallel to the shoreline. Based on the study result, weathering increases from south to north and the geochemistry of the sediments shows enrichment of Mg O, Ca O, Sr and Ba associated with Sr deployment in all samples. Rare earth elements(REE) patterns normalized to the upper continental crust(UCC) indicated LREEs enrichment compared to HREEs with an elevated anomaly of Eu, possibly due to surface absorbance of Mn and Fe minerals, associated with Sr elevation originating from adakites in the lake basin vicinity.     

Geochemistry of hydrothermal alteration at the Roosevelt hot springs thermal area,Utah

Hot spring deposits in the Roosevelt thermal area consist of opaline sinter and sintercemented alluvium. Alluvium, plutonic rocks, and amphibolite-facies gneiss have been altered by acidsulfate water to alunite and opal at the surface, and alunite, kaolinite, montmorillonite, and muscovite to a depth of 70 m. Marcasite, pyrite, chlorite, and calcite occur below the water table at about 30 m.The thermal water is dilute (ionic strength 0.1–0.2) sodium-chloride brine. The spring water now contains 10 times as much Ca, 100 times as much Mg, and up to 2.5 times as much SO₄ as the deep water. Although the present day spring temperature is 25°C, the temperature was 85°C in 1950.A model for development of the observed alteration is supported by observation and irreversible mass transfer calculations. Hydrothermal fluid convectively rises along major fractures. Water cools by conduction and steam separation, and the pH rises due to carbon dioxide escape. At the surface, hydrogen and sulfate ions are produced by oxidation of H₂S. The low pH water percolates downward and reacts with feldspar in the rocks to produce alunite, kaolinite, montmorillonite, and muscovite as hydrogen ion is consumed.     

Kiglapait Geochemistry II: Petrography

The mode of the Kiglapait intrusion carries 73 per cent feldspar,but average rocks near the base of the Upper Zone contain aslittle as 48 per cent feldspar. Olivine remained stable throughoutthe crystallization, but was locally suppressed by abundantcrystallization of augite and titano-magnetite. Red biotiteoccurs as rims on Fe–Ti oxide minerals and is probablyfluorine oxybiotite; its frequently similar occurrence in troctoliticrocks may, perversely, indicate dry magmas rather than dampones. Excluded modal components follow Rayleigh fractionation behaviour;their presence in trace amount permits estimation of residualporosity in the Lower Zone. This porosity diminishes directlywith accumulation rate from 0.14 to 0.03 over the first 80 percent of crystallization history. The saturation ratio of excludedmodal components is a well-behaved function of fraction solidified,and implies that the decrease in porosity continues above the80 per cent solidified level. The saturation ratio links withbulk composition, porosity, and F_L, allowing one of these parametersto be estimated from the others. The cumulus arrival of apatite is abrupt, but the earlier arrivalsof augite, oxide minerals, and sulfide each occur over an interval,followed by an interval of overproduction. This behaviour isattributed to feedback on concentration gradients generatedby a long history of plagioclase + olivine extraction, in theabsence of perfect stirring. Diffusion plays a role in the differentiationof large, slowly cooled magma systems because radial mixingby convection is inefficient. Inherited potential supersaturationis the inevitable result. This leads to modal irregularities,and to crystallization effectively on metastable extensionsof field boundaries. The track of the liquid in the Lower Zone is closely parallelto that in the system Fo–Di–An, but offset fromit by the combined effects of Ab and P (toward plagioclase)and Fa (away from plagioclase). The latter effect is important,with the result that the shedding of plagioclase by an ascendingmagma will be much less marked than predicted from iron-freeexperimental systems.     

The Geochemistry of Scapolite: Part II. Trace Elements, Petrology, and General Geochemistry

Fifty scapolites have been analysed spectrographically for numerouselements. Average concentrations (p.p.m.) were as follows: B25, Be 9–3, Ga 33, Ti 82, Li 56, Cu 4–4, Zr 59,Mn 57, Sr 1,800, Pb 45, Ba 120, Rb 20. The following were seldomor never detected: Cr, Ni, Co, Mo, Sn, V, Sc, Ag, Y, La. Themajor elements Ca, Na, K were also determined. The distributionof the trace elements can be explained by isomorphous substitution,but no detailed correlation of trace elements with each otheror with major elements was found. Refractive indices were determined and the relation betweenaverage index and per cent Me was examined: correlation waspoor, which may in part be attributed to analytical error. Examination of scapolite parageneses shows that scapolite characteristicallyoccurs in the upper amphibolite facies or the pyroxene hornfelsfacies: it is not restricted to these and may occur in any faciesfrom zeolitic to granulitic and in any hornfels facies. Theelements generally concentrated in scapolite include Ca, Na,C, Cl, S, H, B, Be, Li, Sr, Pb. The presence of C, Cl, S, Htestify to genesis in the presence of high partial pressureof CO₂, Cl₂, SO₃, H₂O (or related compounds), that is in pneumatolytic,pegmatitic, or hydrothermal environments. The concentrationof B, Be, Li can also be attributed to these conditions. The source of the elements concentrated in scapolite must inpart be common rocks. In a limited contact zone, the nearbymagma supplied some elements, but where regional scapolitizationhas taken place the presence of magma is less clear. Many commonrocks or rock series contain all the necessary constituents,but some particular conjunction of conditions is necessary forscapolite to form, or it would be more common.     

Geochemistry of sediments from Lake Grand,Northeast Russia

Major and trace element distribution in the bottom sediments from Hole 13 drilled in Lake Grand, Magadan district, was studied using the method of principal components. It was established that geochemical characteristics are correlated with environmental changes. The sediments of cold MIS2 and MIS4 are characterized by the enriched TiO₂, MgO, Al₂O₃, Fe₂O₃, and Cr and low Na₂O, K₂O contents, which is related to the grain-size composition of sediments. Sediments of warm stages show an opposite tendency. High concentration peaks of iron, phosphorus, and manganese correspond to the accumulation levels of vivianite and ferromanganese rocks. Silica is represented by biogenic and abiogenic varieties. Maximum SiO₂ contents were found in the Late Holocene sediments and mark the high biological productivity of the basin. Revealed variations of some elements are correlated with the Heinrich events.     

The Geochemistry of Lake Joyce, McMurdo Dry Valleys, Antarctica

Lake Joyce is one of the least studied lakes of the McMurdo Dry Valleys. Similar to other lakes in this region, Lake Joyce is a closed-basin, permanently ice-covered, meromictic lake. We present here a detailed investigation of major ions, nutrients, and dissolved trace elements for Lake Joyce. Specifically, we investigate the role of iron and manganese oxides and hydrous oxides in trace metal cycling.Lake Joyce is characterized by fresh, oxic waters overlying an anoxic brine, primarily Na–Cl. Surface waters have a maximum nitrate concentration of 26M with a molar dissolved inorganic nitrogen to phosphorus ratio of 477. The supply of nitrogen is attributed to atmospheric deposition, possibly from polar stratospheric clouds. Dissolved phosphorus is scavenged by hydrous iron oxides. The pH is highest (10.15) just beneath the 7-m thick ice cover and decreases to a minimum of 7.29 in the redox transition zone. Dissolved Al exceeds 8M in surface waters, and appears to be controlled by equilibrium with gibbsite. In contrast, concentrations of other trace elements in surface waters are quite low (e.g., 5.4nM Cu, 0.19nM Co, <20pM La). Dissolved Fe, Mn, Ni and Cd were below our detection limits of 13 nM, 1. 8 nM, 4.7 nM and 15pM (respectively) in surface waters. There was a 6-m vertical separation in the onset of Mn and Fe reduction, with dissolved Mn appearing higher in the water column than Fe. Based on thermodynamic calculations, dissolved Mn appears to be controlled by equilibrium with hausmannite (Mn3O4). Co tracks the Mn profile closely, suggesting Co(III) is bound in the lattice of Mn oxides, whereas the Ce profile is similar, yet the Ce anomaly suggests oxidative scavenging of Ce. Release of Cu, Ni, Cd and trivalent REE appears to be controlled by pH-induced desorption from Fe and Mn oxides, although Cu (and perhaps Ni) may be scavenged by organic matter in surface waters.