Evaporation effects as reflected in freshwaters and ostracod calcite from modern environments in Central and Northeast Yakutia (East Siberia,Russia)

Taxonomical and geochemical investigations on freshwater ostracods from 15 waters in Central and Northeast (NE) Yakutia have been undertaken in order to estimate their potential usefulness in palaeoenvironmental reconstructions based on regional fossil records. Higher variability in environmental factors such as pH, electrical conductivity, and ionic content was observed in thermokarst-affected lakes in Central Yakutia than in NE Yakutia lakes. Species diversity of freshwater ostracods reached up to eight taxa per lake, mostly dominated by Candona weltneri Hartwig 1899, in Central Yakutia, whereas in NE Yakutian waters the diversity was lower and Candona muelleri jakutica Pietrzeniuk 1977 or Fabaeformiscandona inaequivalvis (Sars 1898) had highest frequencies. Coupled analyses of stable isotopes (δ¹⁸O, δ¹³C) and element ratios (Sr/Ca, Mg/Ca) were performed on both host waters and ostracod calcite, aiming to estimate the modern relationships. Correlations between host waters and ostracod calcite of single species were found for δ¹⁸O, δ¹³C and Sr/Ca and Mg/Ca ratios. The relationships between δ¹⁸O, Mg/Ca and Sr/Ca ratios and electrical conductivity (salinity) as an expression of solute concentrations in the waters mainly controlled by evaporation are more complicated but evident, and may be useful in future interpretation of geochemical data from fossil Siberian ostracods. Handling editor: K. Martens     

Composition of the early Oligocene ocean from coral stable isotope and elemental chemistry

A sectioned and polished specimen of the coral Archohelia vicksburgensis from the early Oligocene Byram Formation (～30 Ma) near Vicksburg, Mississippi, reveals 12 prominent annual growth bands. Stable oxygen isotopic compositions of 77 growth‐band‐parallel microsamples of original aragonite exhibit well‐constrained fluctuations that range between ?2.0 and ?4.8. Variation in δ¹⁸O of coral carbonate reflects seasonal variation in temperature ranging from 12 to 24 °C about a mean of 18 °C. These values are consistent with those derived from a bivalve and a fish otolith from the same unit, each using independently derived palaeotemperature equations. Mg/Ca and Sr/Ca ratios were determined for 40 additional samples spanning five of the 12 annual bands. Palaeotemperatures calculated using elemental‐ratio thermometers calibrated on modern corals are consistently lower; mean temperature from Mg/Ca ratios are 12.5 ± 1 °C while those from Sr/Ca are 5.8 ± 2.2 °C. Assuming that δ¹⁸O‐derived temperatures are correct, relationships between temperature and elemental ratio for corals growing in today's ocean can be used to estimate Oligocene palaeoseawater Mg/Ca and Sr/Ca ratios. Calculations indicate that early Oligocene seawater Mg/Ca was ～81% (4.2 mol mol^?1) and Sr/Ca ～109% (9.9 mmol mol^?1) of modern values. Oligocene seawater with this degree of Mg depletion and Sr enrichment is in good agreement with that expected during the Palaeogene transition from ‘calcite’ to ‘aragonite’ seas. Lower Oligocene Mg/Ca probably reflects a decrease toward the present day in sea‐floor hydrothermal activity and concomitant decrease in scavenging of magnesium from seawater. Elevated Sr/Ca ratio may record lesser amounts of Oligocene aragonite precipitation and a correspondingly lower flux of strontium into the sedimentary carbonate reservoir than today.     

Magnesium and strontium in non-marine ostracod shells as indicators of palaeosalinity and palaeotemperature

Measurements of the Ca, Sr, and Mg contents of individual calcitic shells of non-marine ostracods and their host waters, both in lakes and controlled aquaria, permit the calculation of the distribution coefficients of Sr/Ca and Mg/Ca partitioning in ostracod shells. We report new K_D[Sr] for seven genera of non-marine ostracods and K_D[Mg] for Cyprideis at 25°C.Strontium partitioning is virtually temperature-independent, and is related to the Sr/Ca of the host water, and in Ca²⁺-saturated waters, to the salinity of the water. Magnesium partitioning is dependent on both temperature and Mg/Ca of the host water.For simple closed-basin lakes (crater lakes are ideal), the Sr content of ostracods is a sensitive indicator of salinity and thus evaporation/precipitation changes, which in turn, indicate variations in continental climate. A 10000-year continuous palaeosalinity record established by Sr and Mg contents of fossil ostracods for Lake Keilambete, southeastern Australia, is in close agreement with an independent palaeosalinity estimate based on sediment textures.We suggest rules that allow Sr and Mg analyses of suites of individual fossil ostracod shells from lacustrine sediments to be interpreted in terms of palaeosalinity and palaeotemperature variations.     

Some factors controlling the major ion chemistry of small lakes: Examples from the prairie parkland of Canada

The management of recreational lakes in the prairie region of Canada requires that their physical, chemical and biological setting be clearly defined. This study relates the major ion chemistry of two lakes to significant ion contributions from groundwater, surface runoff and snow. The major ion concentrations in addition are related to several important limnological processes.Lake Wabamun is a 84.6 km² lake with a basin set in Cretaceous bedrock. Groundwater studies in the watershed indicate that rather large quantities of groundwater enter the lake from fractured coal and bedrock units. Hastings Lake has a considerably smaller surface area and is formed in a shallow depression in glacial drift. Generally, smaller quantities of groundwater enter this lake because the glacial drift has a low permeability.Evaluation of the data indicates that relative quantity and quality of groundwater inflow is probably the most important factor controlling the major ion chemistry of the lakes. Other factors are mineral precipitation, freezing out and the timing of major water inflows.     

Saline systems of the Great Plains of western Canada: an overview of the limnogeology and paleolimnology

In much of the northern Great Plains, saline and hypersaline lacustrine brines are the only surface waters present. As a group, the lakes of this region are unique: there is no other area in the world that can match the concentration and diversity of saline lake environments exhibited in the prairie region of Canada and northern United States. The immense number of individual salt lakes and saline wetlands in this region of North America is staggering. Estimates vary from about one million to greater than 10 million, with densities in some areas being as high as 120 lakes/km². Despite over a century of scientific investigation of these salt lakes, we have only in the last twenty years advanced far enough to appreciate the wide spectrum of lake types, water chemistries, and limnological processes that are operating in the modern settings. Hydrochemical data are available for about 800 of the lake brines in the region. Composition, textural, and geochemical information on the modern bottom sediments has been collected for just over 150 of these lakes. Characterization of the biological and ecological features of these lakes is based on even fewer investigations, and the stratigraphic records of only twenty basins have been examined. The lake waters show a considerable range in ionic composition and concentration. Early investigators, concentrating on the most saline brines, emphasized a strong predominance of Na⁺ and SO₄ ^-2 in the lakes. It is now realized, however, that not only is there a complete spectrum of salinities from less than 1 ppt TDS to nearly 400 ppt, but also virtually every water chemistry type is represented in lakes of the region. With such a vast array of compositions, it is difficult to generalize. Nonetheless, the paucity of Cl-rich lakes makes the northern Great Plains basins somewhat unusual compared with salt lakes in many other areas of the world (e.g., Australia, western United States). Compilations of the lake water chemistries show distinct spatial trends and regional variations controlled by groundwater input, climate, and geomorphology. Short-term temporal variations in the brine composition, which can have significant effects on the composition of the modern sediments, have also been well documented in several individual basins. From a sedimentological and mineralogical perspective, the wide range of water chemistries exhibited by the lakes leads to an unusually large diversity of modern sediment composition. Over 40 species of endogenic precipitates and authigenic minerals have been identified in the lacustrine sediments. The most common non-detrital components of the modern sediments include: calcium and calcium-magnesium carbonates (magnesian calcite, aragonite, dolomite), and sodium, magnesium, and sodium-magnesium sulfates (mirabilite, thenardite, bloedite, epsomite). Many of the basins whose brines have very high Mg/Ca ratios also have hydromagnesite, magnesite, and nesquehonite. Unlike salt lakes in many other areas of the world, halite, gypsum, and calcite are relatively rare endogenic precipitates in the Great Plains lakes. The detrital fraction of the lacustrine sediments is normally dominated by clay minerals, carbonate minerals, quartz, and feldspars. Sediment accumulation in these salt lakes is controlled and modified by a wide variety of physical, chemical, and biological processes. Although the details of these modern sedimentary processes can be exceedingly complex and difficult to discuss in isolation, in broad terms, the processes operating in the salt lakes of the Great Plains are ultimately controlled by three basic factors or conditions of the basin: (a) basin morphology; (b) basin hydrology; and (c) water salinity and composition. Combinations of these parameters interact to control nearly all aspects of modern sedimentation in these salt lakes and give rise to four 'end member' types of modern saline lacustrine settings in the Great Plains: (a) clastics-dominated playas; (b) salt-dominated playas; (c) deep water, non-stratified lakes; and (d) deep water, "permanently" stratified lakes.     

6000 years of environmental changes recorded in Blue Lake, South Australia, based on ostracod ecology and valve chemistry

A 4 m long core taken from the freshwater Blue Lake crater near the township of Mount Gambier in southeastern South Australia provided a high-resolution palaeoclimatic record for the last six millennia. Accelerator Mass Spectrometry (AMS) radiocarbon (¹⁴C) dates were obtained from organic plant fibres and biogenic carbonates from the laminated sequence of the core and from a modern water sample. Large discrepancies between the radiocarbon ages determined from plant fibres and biogenic carbonates indicate the presence of a time-variable lacustrine reservoir, which is consistent with what is known of the lake's hydrology.Ostracod assemblages, associated with stable isotope (δ¹³C, δ¹⁸O) analyses and, in combination with Mg/Ca, Sr/Ca and Na/Ca analyses done on ostracod valves, infer salinity, temperature and water level changes in Blue Lake over the last 6 millenia. The influence of local aquifers through time has also been determined from the Na/Ca of ostracod valves. Approximately 900 year cycles are evident in the δ¹³C record from 5.4 ka to 1.8 ka.The history of Blue Lake records an initial period of high hydrological variability around 6 ka, becoming increasingly deeper as groundwater flowed into the basin. By 4 ka, the lake had reached steady state with the lake level fluctuating by as much as 9 m, although significant geochemical variations represent temperature fluctuations until European settlement near the lake in 1839.     

Reconstruction of limnology and microbialite formation conditions from carbonate clumped isotope thermometry

Quantitative tools for deciphering the environment of microbialite formation are relatively limited. For example, the oxygen isotope carbonate‐water geothermometer requires assumptions about the isotopic composition of the water of formation. We explored the utility of using ‘clumped’ isotope thermometry as a tool to study the temperatures of microbialite formation. We studied microbialites recovered from water depths of 10–55 m in Pavilion Lake, and 10–25 m in Kelly Lake, spanning the thermocline in both lakes. We determined the temperature of carbonate growth and the ¹⁸O/¹⁶O ratio of the waters that microbialites grew in. Results were then compared to current limnological data from the lakes to reconstruct the history of microbialite formation. Modern microbialites collected at shallow depths (11.7 m) in both lakes yield clumped isotope‐based temperatures of formation that are within error of summer water temperatures, suggesting that clumped isotope analyses may be used to reconstruct past climates and to probe the environments in which microbialites formed. The deepest microbialites (21.7–55 m) were recovered from below the present‐day thermoclines in both lakes and yield radioisotope ages indicating they primarily formed earlier in the Holocene. During this time, pollen data and our reconstructed water ¹⁸O/¹⁶O ratios indicate a period of aridity, with lower lake levels. At present, there is a close association between both photosynthetic and heterotrophic communities, and carbonate precipitation/microbialite formation, with biosignatures of photosynthetic influences on carbonate detected in microbialites from the photic zone and above the thermocline (i.e., depths of generally <20 m). Given the deeper microbialites are receiving <1% of photosynthetically active radiation (PAR), it is likely these microbialites primarily formed when lower lake levels resulted in microbialites being located higher in the photic zone, in warm surface waters.     

Geochemistry of recent marine sediments in the Bardawil lagoon,northern Sinai,Egypt

The concentrations of major (Al, Fe, Mg, Ti, K and Na) and minor (Ba, Sr, V, Cu, Mn, Cr, Ni, Zn, Pb and Mo) elements as well as carbonate, organic carbon and total nitrogen have been determined in surface sediments collected at 12 stations from the Bardawil lagoon. The aim of the study was to characterize the geochemistry of the sediments in three different environments, the lagoon, the salt pans and the inlet between the lagoon and the Mediterranean Sea. Higher CaCO₃ percentage (53.5–70.5%) were found in the salt pans where biogenic calcareous components and carbonate rock fragments were found in sufficient quantities in the sediment fractions. Based on high C/N ratios, the organic carbon fraction of the Bardawil lagoon surface sediments is clearly dominated by terrigenous material. The distribution of Al, Fe, Mg and Ti are essentially controlled by the mineralogy of the sediments. The ratios of Ba, Sr, Cu, Mn, Pb and Mo to Al are all high in the salt pans and reflect changes in mineralogy and sediment texture.     

Nitrogen mass balances and denitrification rates in central Ontario Lakes

Nitrogen mass balances for seven unproductive lakes and 20 forested catchments in central Ontario were measured between 1977 and 1989. Average annual lake denitrification rates calculated with the N/P ratio method were strongly correlated with summer anoxic factor (extent of surficial sediment anoxia) whereas denitrification rates calculated with a²¹⁰Pb sediment N accumulation method were poorly correlated with the anoxic factor suggesting that the N/P method is superior. Substantial denitrification occurred in all lakes — an average of 36% of TN inputs or 75% of the net gain. On a regional area-weighted basis, 67% of bulk atmospheric TN deposition was stored or denitrified terrestrially, 12% was denitrified in lakes, 4% was stored in lake sediments, and 17% was exported from lakes. N/P ratios were generally less in streams than in precipitation suggesting preferential N retention in catchments, whereas the N/P ratios in lake outputs were slightly higher than lake input ratios, suggesting preferential P retention in lakes. This is consistent with the notion that P-limited lakes can exist adjacent to N-limited forests.     

Magnesium and strontium compositions of Recent benthic foraminifera from the Coral Sea, Australia and Prydz Bay, Antarctica

Analyses of the Mg/Ca and Sr/Ca ratios of the modern benthic foraminifera, Cibicides wuellerstorfi (epifaunal) and Uvigerina species (infaunal) from the Coral Sea, and Cibicides refulgens (epifaunal) and Trifarina angulosa (infaunal) from Prydz Bay, Antarctica revealed relationships with temperature that have possible applications for reconstructions of bottom-water paleotemperatures. A positive relationship exists between the Mg/Ca and Sr/Ca ratios of Cibicides wuellerstorfi and Cibicides refulgens and ambient temperatures, at least within the range of 2 and 6°C. For the correlation between Mg/Ca compositions and temperature the r² values range from 0.78 (C. wuellerstorfi alone) to 0.88 (C. wuellerstorfi and C. refulgens together). At present, the Mg/Ca-temperature relationship must be regarded as tentative because of significant overlap of standard error values. The relationship between the Sr/Ca compositions of C. wuellerstorfi and bottom-water temperature yields an r² value of 0.95. These results indicate that Sr/Ca and possibly Mg/Ca ratios of Cibicides wuellerstorfi may provide useful information for the assessment of paleotemperature. Single-species data are presently insufficient to assess the influence of ambient temperature on trace-element compositions of Uvigerina species. Trifarina angulosa may have Mg/Ca compositions which are positively related to temperature, but Sr/Ca values seem unaffected by temperature. This may be due to pore-water influences on infaunal tests or to vital effects. Although more modern data are needed, our present results suggest that Sr/Ca ratios and possibly Mg/Ca ratios of some benthic foraminifera have the potential to be useful paleothermometers, at least within a temperature range of −2 to 6°C.     

Effect of salinity and seawater calcite saturation state on Mg and Sr incorporation in cultured planktonic foraminifera

Trace elements incorporated in planktonic foraminiferal test carbonate are commonly used as paleoproxies. For instance, Mg/Ca ratios are frequently used for reconstructing sea surface temperature and, together with the foraminiferal stable oxygen isotope ratios, are also used as paleosalinity proxy. Foraminiferal Sr/Ca ratios constitute another example of the application of trace elements in paleostudies since they may reflect the Sr/Ca values of seawater. However, over the past few decades it has been proven that the incorporation of trace elements in foraminiferal calcite is controlled by more than one environmental parameter. To quantify the effect of salinity on Mg and Sr incorporation planktonic foraminifera Globigerinoides sacculifer (sensu stricto) were grown in the laboratory under different environmental conditions. Laboratory experiments allowed us to separate a direct salinity effect from a possible independent impact through differences in the calcite saturation state of the seawater (Ω). Although the temperature effect is more important than the salinity effect, a change of 4 salinity units is equivalent to a 1 °C bias on Mg/Ca-based temperatures. This effect of salinity on Mg incorporation is minor. However, when using Mg/Ca-based temperatures in combination with foraminiferal δ¹⁸O to calculate salinity, it cannot be neglected. The present study shows salinity as the overriding control on Mg incorporation within the range of Ω studied (Ω between 5.25 and 6.50; [CO₃²⁻] between 218 and 270 μmol/kg) at a constant temperature of 26 °C. In contrast, Ω appears to be the main control on foraminiferal Sr incorporation (0.10 mmol/mol per 100 µmol/kg rise in [CO₃²⁻]), whereas salinity has a non significant influence on Sr/Ca.     

Paleolimnological reconstruction of the effects of atmospheric deposition of acids and heavy metals on the chemistry and biology of lakes in New England and Norway

Sediment cores from nine lakes in southern Norway (N) and six in northern New England (NE) were dated by ¹³⁷Cs, ²¹⁰Pb and in NE also by pollen, and were analyzed geochemically and for diatoms. Cores from two N and three NE lakes were analyzed for cladocerans. ¹³⁷Cs dating is unreliable in these lakes, probably due to mobility of Cs in the sediment. In Holmvatn sediment, an up-core increase in Fe, starting ca. 1900, correlates with geochemical indications of decreasing mechanical erosion of soils. Diatoms indicate a lake acidification starting in the 1920's. We propose that soil Fe was mobilized and runoff acidified by acidic precipitation and/or by soil acidification resulting from vegetational succession following reduced grazing. Even minor land use changes or disturbances in lake watersheds introduce ambiguity to the sedimentary evidence relating to atmospheric influences. Diatom counts from surface sediments in 36 N and 31 NE lakes were regressed against contemporary water pH to obtain coefficients for computing past pH from subsurface counts. Computed decreases of 0.3–0.8 pH units start between I890 and I930 in N lakes already acidic (pH 5.0–5.5) before the decrease. These and lesser decreases in other lakes start decades to over a century after the first sedimentary indications of atmospheric heavy metal pollution. It is proposed that the acidification of precipitation accompanied the metal pollution. The delays in lake acidification may be due to buffering by the lakes and watersheds. The magnitude of acidification and heavy metal loading of the lakes parallels air pollution gradients. Shift in cladoceran remains are contemporary with acidification, preceding elimination of fishes.     

Constraining carbon sources and growth rates of freshwater microbialites in Pavilion Lake using 14C analysis

This study determined the natural abundance isotopic compositions (¹³C, ¹⁴C) of the primary carbon pools and microbial communities associated with modern freshwater microbialites located in Pavilion Lake, British Columbia, Canada. The Δ¹⁴C of dissolved inorganic carbon (DIC) was constant throughout the water column and consistent with a primarily atmospheric source. Observed depletions in DIC ¹⁴C values compared with atmospheric CO₂ indicated effects due either to DIC residence time and/or inputs of ¹⁴C‐depleted groundwater. Mass balance comparisons of local and regional groundwater indicate that groundwater DIC could contribute a maximum of 9–13% of the DIC. ¹⁴C analysis of microbial phospholipid fatty acids from microbialite communities had Δ¹⁴C values comparable with lake water DIC, demonstrating that lake water DIC was their primary carbon source. Microbialite carbonate was also primarily derived from DIC. However, some depletion in microbialite carbonate ¹⁴C relative to lake water DIC occurred, due either to residence time or mixing with a ¹⁴C‐depleted carbon source. A detrital branch covered with microbialite growth was used to estimate a microbialite growth rate of 0.05 mm year^?1 for the past 1000 years, faster than previous estimates for this system. These results demonstrate that the microbialites are actively growing and that the primary carbon source for both microbial communities and recent carbonate is DIC originating from the atmosphere. While these data cannot conclusively differentiate between abiotic and biotic formation mechanisms, the evidence for minor inputs of groundwater‐derived DIC is consistent with the previously hypothesized biological origin of the Pavilion Lake microbialites.     

Stable Isotopic and Trace Elemental Compositions of Otoliths and the Stock Structure of Pacific Cod, Gadus macrocephalus

Synopsis We examined the stock composition and life history of Pacific cod, Gadus macrocephalus, in the northeast Pacific Ocean from sagittal otoliths collected from three marine fishing areas in Washington State, U.S.A. We analyzed both stable isotope ratios (δ¹⁸O and δ¹³C) and trace elemental concentrations (Sr, Mg, Na, Fe, Mn) for these otoliths. The combination of δ¹⁸O and δ¹³C, and correlation of δ¹⁸O vs. 1000Sr/Ca and 1000Mg/Ca showed clear separations between North Puget Sound and coastal cod, suggesting there might be two different spawning stocks in the region. The North Puget Sound cod might represent an ‘Estuary-type’ from the Strait of Georgia, whereas coastal cod might represent an ‘Ocean-type’ from the Pacific west coast. Isotopic variations from five representative otoliths also showed a two-stage life history for Pacific cod, and a critical transition period for cod in migration to the ocean or in age of sexual maturity. These chemical interpretations and conclusions appear in agreement with biological observations of Pacific cod, and are consistent with results of previous studies for other marine fish species in nearby areas.     

Responses of microbial phototrophs to late‐Holocene environmental forcing of lakes in south‐west Greenland

1. The biological structure of arctic lakes is changing rapidly, apparently in response to global change processes such as increasing air temperatures, although altered nutrient stoichiometry may also be an important driver. Equally important, however, are local factors (e.g. landscape setting, hydrological linkages and trophic interactions) that may mediate responses of individual lakes at the regional scale. Despite general acknowledgement of the importance of local factors, there has been little focus on among‐lake variability in the response to environmental change. 2. Sedimentary pigments, organic carbon and nitrogen, and biogenic silica (BSi) in ²¹⁰Pb and ¹⁴C‐dated sediment cores from three contrasting lakes in the Kangerlussuaq area (c. 67°N, 51°W) of south‐west Greenland were used to reconstruct algal and phototrophic bacterial ecological change during the late‐Holocene. Water chemistry for the individual lakes varies in terms of conductivity (range: 30–3000 μS cm^?1) and stratification regimes (cold monomictic, dimictic and meromictic), linked with their position along the regional climate gradient from the coast and to the present ice sheet margin. 3. Despite essentially similar regional climate forcing over the last c. 1000 years, marked differences among lake types were observed in the phototrophic communities and their temporal variability. Considerable short‐term variability occurred in an oligosaline, meromictic lake (SS1371), dominated by purple sulphur bacterial pigments, most likely due to a tight coupling between the position of the chemocline and the phototrophic community. Communities in a lake (SS86) located on a nunatak, just beyond the edge of the present ice sheet shifted in a nonlinear pattern, approximately 1000 cal. years BP, possibly due to lake‐level lowering and loss of outflow during the Medieval Climate Anomaly. This regime shift was marked by a substantial expansion of green sulphur bacteria. 4. A dilute, freshwater coastal lake (SS49) dominated by benthic algae was relatively stable until ca. 1900 AD when rates of community change began to increase. These changes in benthic algal pigments are correlated with substantial declines (1.3–0.44‰) in δ¹⁵N that are indicative of increased deposition of atmospheric inputs of industrially derived NOx into the atmosphere. 5. Climate control on lake ecosystem functioning has been assumed to be particularly important in the Arctic. This study, however, illustrates a complex spatial response to climate forcing at the regional scale and emphasises differences in the relative importance of changes in the mass (m, both precipitation and nutrients) and energy flux (E) to lakes for the phototrophic community structure of low‐arctic Greenland lakes.     

Distinguishing sources of base cations in irrigated and natural soils: evidence from strontium isotopes

Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) of soil solids, soil cation extracts, irrigation water and plant material are used to determine strontium and therefore cation sources and fluxes in irrigated and natural soil–plant systems. Strontium isotopes of soil solids from four soil profiles (two irrigated vineyard soils and two 'natural' profiles from nearby reserves) show large differences between soil horizons with depth. These differences are not reflected in ⁸⁷Sr/⁸⁶Sr ratios of soil labile cations, which show both little variation down-profile and much lower ratios than soil solids. In the undisturbed, natural soil profiles, labile cation ⁸⁷Sr/⁸⁶Sr ratios are close to the ratio of modern seawater, indicating that solutes of marine origin from precipitation are the primary input of strontium (and calcium) to the labile cation pool. In the irrigated soil profiles, ⁸⁷Sr/⁸⁶Sr ratios of labile cations are consistently shifted towards that of the irrigation water. Mass-balance calculations using ⁸⁷Sr/⁸⁶Sr ratios of the different inputs to the labile cation pool indicate more than 90% of labile strontium is derived from precipitation solutes in unirrigated soils, and up to 44% from irrigation water solutes as an additional source in irrigated soils. The ⁸⁷Sr/⁸⁶Sr ratios of grapes grown in irrigated soils match precisely with those of the labile soil cations, demonstrating that cation nutrients are drawn wholly from the labile cation pool and have the same mix of precipitation, irrigation, and soil solid sources. The ⁸⁷Sr/⁸⁶Sr ratios of grapes grown in the irrigated soils may therefore vary over time depending on (1) the changing mix of irrigation water and local precipitation and (2) potential change to irrigation water. These findings suggest limitations to the use of strontium isotopes in the tracing of grapes and wines to their soil of origin.     

Geochemical evidence for the formation of a large miocene “travertine” mound at a sublacustrine spring in a soda lake (Wallerstein castle rock, nördlinger ries, Germany)

Summary “Travertines” (tufa pinnacles) of the Miocene Riescrater basin have been investigated to test whether carbon, oxygen and strontium isotopes can be used for the recognition of fossil subaquatic spring deposits in high-alkalinity settings. The Ries basin “travertines” have so far been interpreted as a product of subaerial to sublacustrine artesian springs discharging calcareous groundwater into a freshwater or slightly saline lake. However, recent studies on microfacies and fabric development propose a formation at Ca²⁺-supplying sublacustrine springs of a soda lake. Geochemical analysis of “travertines” of the castle rock Wallerstein, including “sickle-cell” limestones, thrombolites, non-skeletal stromatolites, and speleothems, now support the latter interpretation. High Sr contents surpassing that of the contemporaneously formed dolomitic algal biocherms of the lake shore point to an aragonitic composition of primary precipitates. the δ¹³C values of diagenetically moderately to weakly altered “travertine” facies types are in the same range of the impact-brecciated Upper Jurassic limestones, thus, are inconsistent with a mixture of soil-derived CO₂ and CO₃ ²⁻ from the Jurassic limestones. In addition, the δ¹⁸O values are too high to support a significant contribution of CO₃ ²⁻ by meteoric waters seeping through marine Jurassic limestones. Instead the δ¹³C and δ¹⁸O values indicate an origin of the CO₃ ²⁻ from a lake water body characterized by evaporation. This is consistent with a sodium-rich lake water as indicated by high sodium contents of aragonitic algal bioherms of the lake shore. The⁸⁷Sr/⁸⁶Sr isotope ratio of the “travertine” mound carbonates are consistent with calculated mixing of spring waters discharging from the crystalline basement and lake water high in dissolved inorganic carbon. This points to an origin of the divalent cations from sublacustrine spring waters. In turn,⁸⁷Sr/⁸⁶Sr isotope ratios of green algal reef carbonates of the lake shore are closer to that of the Upper Jurassic carbonates, due to surface run-off from surrounding limestone uplands.     

Hydrochemistry from Sr and Mg contents of ostracodes in Pleistocene lacustrine deposits,Baza Basin (SE Spain)

A reconstruction of the early Pleistocene paleohydrochemistry based on the Mg, Sr and Ca content of the Cyprideis valves is presented for shallow lacustrine sequences of the Baza basin. A large number of environmental changes in this marginal area has been recorded by the recurrent alternation of two fossil assemblages which differ in their salinity requirements. Measurements of the Sr/Ca and Mg/Ca ratios of individual calcite shells of Cyprideis show that the water in the higher saline stages (with thalassic organisms indicating marine-like conditions) was of non-marine origin. The Sr/Ca values of Cyprideis valves from sands deposited during a saline water phase show lower values than those from an overlying carbonate sequence which was formed under lower salinity conditions. These unexpected values are assumed to be the result of major changes in the chemical composition of the water in shallow, littoral ponded areas of a hydrologically complex lake. In the sequences that originated in these areas, Sr/Ca values may be used only as salinity indicators within each portion of the sequence formed in a single, continuous evolution. In more open areas, the wide fluctuations of Sr/Ca and Mg/Ca recorded in ostracodes from individual layers of rippled ostracode-shell sands probably reflect the mixing of valves from changing short-term environmental conditions.     

Diatom preservation: experiments and observations on dissolution and breakage in modern and fossil material

Selected aspects of diatom preservation in both laboratory and field environments are examined with a view to improving techniques and to help understand why only some lake sediments have good diatom preservation.Laboratory measurements of biogenic silica following diatom dissolution by alkali digestion are questioned because results are shown to be dependant on initial sample size. Diatom breakage experiments identified drying carbonate rich sediment as a major cause of fragmentation of the large robust diatom Campylodiscus clypeus Ehrenb. Diatom dissolution experiments in carbonate media indicated that carbonate rich lakes should preserve diatoms better in order of the particular alkali metal type (Ca > Mg > Na). A preliminary assessment of the role of depth in diatom preservation is made for Lake Baikal where partly dissolved Cyclotella are more common in deep water surface sediments. The effect of time on diatom dissolution is examined in a saline lake sediment core and by comparing dissolution rates of recent and geologically old diatom samples in the laboratory. A simple link between diatom dissolution and sample age was not established. Factors thought to be important in controlling diatom preservation in lake sediments are discussed.     

Elemental chemistry of left and right sagittal otoliths in a marine fish Hippoglossus stenolepis displaying cranial asymmetry

The hypothesis was tested that the sagittae of age 2 year Pacific halibut Hippoglossus stenolepis are interchangeable, by analysing whole‐otolith preparations for element‐to‐calcium ratios of 10 trace metals (⁷Li, ²⁵Mg, ⁵⁵Mn, ⁵⁶Fe, ⁶⁰Ni, ⁶³Cu, ⁶⁶Zn, ⁸⁸Sr, ¹³⁸Ba and ²⁰⁸Pb) and carbon and oxygen stable isotope ratios (δ¹³C and δ¹⁸O). After detrending for significant (α= 0·05) relationships between elemental concentration and otolith mass, significant (paired t‐tests, P < 0·01) asymmetry was detected in δ¹³C and δ¹⁸O, and ⁸⁸Sr:⁴⁸Ca. Right (smaller) sagittae exhibited higher δ¹³C and δ¹⁸O, and lower ⁸⁸Sr:⁴⁸Ca, than left sagittae. Significant (α= 0·05) left–right differences were not detected in the remained trace metals. Given that sagittae are the same size at hatch and diverge as H. stenolepis age, the larger otolith is presumably biased towards later‐accreted carbonate. Estuarine‐reared flatfish probably exhibit more pronounced dissimilarities than observed here, given greater environmental variability in such habitats relative to coastal halibut nurseries, and the importance of salinity and temperature in regulating elemental uptake.