Influence of seawater Sr content on coral Sr/Ca and Sr thermometry

The Ca content of a Porites coral from Xisha, South China Sea is quite uniform along its 18-year growth axis. A comparison with previously published data shows that the Ca content of corals from different sites varies by only 0.4%. This is much smaller than the variation of Ca in seawater (2.2%), indicating that Ca variations in seawater do not significantly affect the Ca compositions of coral skeletons. The variation in skeletal Ca contents results in only ±0.6°C of uncertainty in SST calculations, which is much smaller than the large disparities observed for previously established coral Sr/Ca thermometers. In contrast, Sr in tropical seawater varies spatially by as much as 2.4%, corresponding to ~4°C offset for coral Sr/Ca calibrations. The effect of seawater Sr variations on coral Sr/Ca thermometers is evaluated and we demonstrate that the content of seawater Sr is the major factor responsible for disparities in these coral Sr/Ca thermometers. The disparities can be significantly reduced when seawater Sr contents are included in the Sr/Ca thermometers.     

Changes in Sr/Ca, Ba/Ca and 87Sr/86Sr ratios between trophic levels in two forest ecosystems in the northeastern U.S.A.

The variability and biologicalfractionation of Sr/Ca, Ba/Ca and ⁸⁷Sr/⁸⁶Srratios were studied in a soil–plant–invertebrate–bird food chain in two forested ecosystems withcontrasting calcium availability in the northeasternU.S.A. Chemical measurements were made of the soilexchange pool, leaves, caterpillars, snails, and boththe femurs and eggshells of breeding insectivorousmigratory songbirds. ⁸⁷Sr/⁸⁶Sr values weretransferred up the food chain from the soil exchangepool to leaves, caterpillars, snails and eggshellswithout modification. Adult birds were the oneexception; their ⁸⁷Sr/⁸⁶Sr values generallyreflected those of lower trophic levels at each site,but were lower and more variable, probably becausetheir strontium was derived in part from foods intropical winter habitats where lower⁸⁷Sr/⁸⁶Sr ratios are likely to predominate. Sr/Ca and Ba/Ca ratios decreased at each successive trophiclevel, supporting previous suggestions that Sr/Ca andBa/Ca ratios can be used to identify the trophic levelat which an organism is primarily feeding. The changesin Sr/Ca and Ba/Ca ratios we measured for vegetationand insects were comparable to similar measurementsmade previously (but based on single samples of eachorganism) in an alpine ecosystem. Changes in Sr/Ca andBa/Ca ratios between birds and their food have notpreviously been measured, but the values we obtainedwere similar to those for herbivorous and carnivorousmammals at similar trophic levels. Our results provideevidence that supports the use of Sr/Ca ratios in thedetermination of human paleodiets and suggests thatSr/Ca ratios may also provide a useful tool in studiesof modern food webs. Furthermore, our findings suggestthat ⁹⁰Sr from nuclear fallout will notbioaccumulate in forests and that changes in Sr/Caratios between trophic levels will need to beconsidered in some cases when using⁸⁷Sr/⁸⁶Sr as a tracer of calciumbiogeochemistry.     

A comparison between Ca and Sr cycling in forest ecosystems

In favourable conditions, the ⁸⁷Sr/⁸⁶Sr isotope ratios of the Sr delivered by rain and soil mineral weathering differ. Assuming that Ca and Sr behave similarly in forest ecosystems, several authors have used the ⁸⁷Sr/⁸⁶Sr variation in forest compartments to calculate the contribution of rain and mineral weathering to Ca fluxes and pools. However, there are a number of experimental reports showing that Ca and Sr may behave differently in the soil and in the plant. We have tested this Ca–Sr analogy in the field by measuring the variation of Sr and Ca concentrations, fluxes and pools in spruce, beech and maple stands on granite, sandstone and limestone. Results show that (1) variations of Ca and Sr concentrations are generally correlated at each level of the ecosystems. (2) In spruce on acid soils, a preferential uptake of Ca over Sr occurs (Aubure spruce Sr/Ca = 0.8×10⁻³; soil exchangeable Sr/Ca between 2 and 6×10⁻³). On calcareous soils, a preferential uptake of Sr over Ca by spruce may occur. (3) In spruce and beech on acid and calcareous soils, a preferential translocation of Ca over Sr from roots to leaves occurs ((Sr/Ca) in leaves was between 10 and 90% of that in roots). (4) The biological cycling of Ca and Sr leads to an enrichment of the upper soil layers in Ca and Sr. Compared to Sr, Ca accumulates in the upper layer of acid soils because Ca cycling through litterfall is favoured over Sr cycling, and possibly because of the selectivity of acid organic exchangers for Ca. This revised version was published online in June 2006 with corrections to the Cover Date.     

Use of foliar Ca/Sr discrimination and <Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr ratios to determine soil Ca sources to sugar maple foliage in a northern hardwood forest

Calcium/strontium and ⁸⁷Sr/⁸⁶Sr ratios in foliage can be used to determine the relative importance of different soil sources of Ca to vegetation, if the discrimination of Ca/Sr by the plant between nutrient sources and foliage is known. We compared these tracers in the foliage of sugar maple (Acer saccharum) to the exchange fraction and acid leaches of soil horizons at six study sites in the White Mountains of New Hampshire, USA. In a previous study, sugar maple was shown to discriminate for Ca compared to Sr in foliage formation by a factor of 1.14 ± 0.12. After accounting for the predicted 14% shift in Ca/Sr, foliar Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios closely match the values in the Oie horizon at each study site across a 3.6-fold variation in foliar Ca/Sr ratios. Newly weathered cations, for which the Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios are estimated from acid leaches of soils, can be ruled out as a major Ca source to current foliage. Within sites, the ⁸⁷Sr/⁸⁶Sr ratio of the soil exchange pool in the Oa horizon and in the 0–10 cm and 10–20 cm increments of the mineral soil are similar to the Oie horizon and sugar maple foliar values, suggesting a common source of Sr in all of the actively cycling pools, but providing no help in distinguishing among them as sources to foliage. The Ca/Sr ratio in the soil exchange pool, however, decreases significantly with depth, and based on this variation, the exchange pool below the forest floor can be excluded as a major Ca source to the current sugar maple foliage. This study confirms that internal recycling of Ca between litter, organic soil horizons and vegetation dominate annual uptake of Ca in northern hardwood ecosystems. Refinement of our understanding of Ca and Sr uptake and allocation in trees allows improvement in the use of Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios to trace Ca sources to plants.     

Sr/Ca and early hominin diets revisited: new data from modern and fossil tooth enamel

A previous study of strontium/calcium (Sr/Ca) ratios in Paranthropus suggested that it consumed more animal foods than was previously believed. However, that study looked at Sr/Ca in fossil bone, which is known to be highly susceptible to diagenesis. Enamel, in contrast, is resistant to post-mortem alteration making it a more appropriate material for Sr/Ca analysis of Plio-Pleistocene fossils. Yet, we know virtually nothing about Sr/Ca in the enamel of modern African mammals, much less fossil taxa. To address this gap, we studied Sr/Ca in tooth enamel from modern mammals in the greater Kruger National Park, South Africa, as well as fossil fauna from the Sterkfontein Valley. Grazing herbivores have the highest Sr/Ca, followed by browsers and carnivores in both modern and fossil fauna. This similarity in ecological Sr/Ca patterning between modern and fossil fauna shows that diagenesis has not obscured the primary dietary signals. Australopithecus has significantly higher Sr/Ca than Paranthropus, and higher Sr/Ca than fossil papionins, browsers, and carnivores. Paranthropus has lower Sr/Ca than grazers, but its Sr/Ca is higher or equal to that of fossil papionins, browsers, and carnivores. Thus, Sr/Ca for both hominins is relatively high, and provides no direct evidence for omnivory in either taxon. The consumption of underground resources or insects are among the possible explanations for the highly elevated Sr/Ca in Australopithecus.     

The relative uptake of Ca and Sr into tree foliage using a whole-watershed calcium addition

The use of strontium isotopes and ratios of alkaline earth elements (i.e., ⁸⁷Sr/⁸⁶Sr and Ca/Sr) to trace Ca sources to plants has become common in ecosystem studies. Here we examine the relative uptake of Ca and Sr in trees and subsequent accumulation in foliage. Using a whole-watershed Ca addition experiment at the Hubbard Brook Experimental Forest in N.H., we measured the uptake of Ca relative to Sr in foliage and roots of sugar maple (Acer saccharum), yellow birch (Betula alleghaniensis), American beech (Fagus grandifolia), and red spruce (Picea rubens). Vegetation was analyzed for Ca and Sr concentrations and the ⁸⁷Sr/⁸⁶Sr ratio. A comparison of the Ca/Sr ratio in the vegetation and the Ca/Sr ratio of the applied mineral allows for the calculation of a discrimination factor, which defines whether Ca and Sr are incorporated and allocated in the same ratio as that which is available. A discrimination factor greater than unity indicates preferential uptake of Ca over Sr; a factor less than unity reflects preferential uptake of Sr over Ca. We demonstrate that sugar maple (SM) and yellow birch (YB) have similar and small discrimination factors (1.14 ± 0.12,1σ and 1.16 ± 0.09,1σ) in foliage formation and discrimination factors of less than 1 in root formation (0.55–0.70). Uptake into beech suggests a larger discrimination factor (1.9 ± 1.2) in foliage but a similar root discrimination factor to SM and YB (0.66 ± 0.06,1σ). Incorporation into spruce foliage occurs at a much slower rate than in these other tree species and precludes evaluation of Ca and Sr discrimination in spruce foliage at this time. Understanding the degree to which Ca is fractionated from Sr in different species allows for refinement in the use of ⁸⁷Sr/⁸⁶Sr and Ca/Sr ratios to trace Ca sources to foliage. Methods from this study can be applied to natural environments in which various soil cation pools have different ⁸⁷Sr/⁸⁶Sr and Ca/Sr ratios. The results reported herein have implications for re-evaluating Ca sources and fluxes in forest ecosystems.     

Factors influencing Sr/Ca ratios in otoliths of Girella elevata: an experimental investigation

The utility of Sr/Ca ratios in otoliths as indicators of thermal history in fish was investigated for juvenile Girella elevata . There was no direct relationship between ratios of Sr/Ca and temperature of the water, as has been assumed in many previous studies. Sr/Ca ratios did not decrease when water temperature was elevated from 19 to 28° C. Elevation of ambient Sr levels in the sea water caused a significant increase in Sr/Ca ratios in otoliths, and there was a detectable increase in Sr/Ca ratios in otoliths of some individuals fed an Sr-enriched diet. Multiple factors may influence natural Sr/Ca ratios in otoliths of juvenile G. elevata and their interactions make it difficult to interpret the chronology of conditions experienced by an individual fish during early life in the pelagic or benthic environment.     

Ontogenetic variations in Sr/Ca and Ba/Ca ratios of dental bioapatites from Bos taurus and Odocoileus virginianus

Sr/Ca and Ba/Ca ratios of bone are commonly used as biochemical indicators of trophic level in modern and fossil mammals. Concerns over the effects of diagenesis on Sr/Ca and Ba/Ca ratios of bone led archaeologists and paleontologists to favor tooth enamel, which is less prone to alteration. Sr/Ca and Ba/Ca ratios of bone, enamel, and dentin from three farm-raised steers (Bos taurus) and five wild white-tailed deer (Odocoileus virginianus) from central Missouri were compared. Our results show that changes in diet, discrimination, and growth rate during ontogeny can lead to significant differences in Sr/Ca and Ba/Ca ratios of different bioapatite types as well as significant differences within the same bioapatite forming at different times. Early- and late-forming tooth enamel can have significant differences in Sr/Ca and Ba/Ca ratios equivalent to almost one full trophic step. Although differences between early- and late-forming dentin are typically not significant, dentin Sr/Ca and Ba/Ca ratios are significantly greater than enamel values. This difference in Sr/Ca or Ba/Ca ratios between enamel and dentin from the same tooth can be greater than one full trophic step. These results have profound implications for the use of dental bioapatites in trophic level reconstructions. They highlight the importance of consistency in bioapatite selection, tooth selection, and relative location of sampling within the enamel cap. Furthermore, this expected difference in Sr/Ca and Ba/Ca ratios could be used as another means of checking for diagenetic alteration in ancient samples.     

Coccolith Sr/Ca ratios in the eastern Mediterranean: Production versus export processes

Samples collected by two sediment traps located southwest of Crete in the eastern Mediterranean (EMED) [48A (1953 m) and 48B (950 m)] from June 2005 to May 2006 were used to study fluxes of organic carbon, carbonate and coccolithophores in combination with the variations of Sr/Ca ratios in different individually picked coccolith species. Considering the complexity of the EMED, we validate the use of Sr/Ca ratios as productivity proxy and unravel the varied processes which may influence it. We examined the relationship between the seasonal peaks in export fluxes and the Sr/Ca ratio in coccoliths of three upper photic zone coccolithophores species collected in the traps, Calcidiscus leptoporus, Helicosphaera carteri and Emiliania huxleyi. We aimed at testing whether high export fluxes are correlated with high Sr/Ca ratios, suggestive of higher nutrient-stimulated production, or Sr/Ca ratios are unchanged during high export periods, suggestive of increased export efficiency or scavenging. Periods of enhanced trap fluxes in March and June result from surface water blooms recognized in satellite imagery. An additional peak flux was found in January, but this peak represents re-suspended or recycled material in the water column.The amplitude of seasonal variations in the Sr/Ca ratios of the three investigated species is small in both traps. In the shallow trap, a decrease in the Sr/Ca ratio of C. leptoporus occurred synchronously with minimal fluxes. The other two species were not measured for this period. In the deep trap, no such decrease in Sr/Ca was observed during minimal fluxes, in either C. leptoporus or H. carteri, probably due to a long residence of coccoliths in the water column, recycling and low export efficiency. Absolute Sr/Ca ratios for all species are lower than in other more productive environments like the Bay of Bengal, Arabian Sea, or Sargasso Sea. We conclude that Sr/Ca ratios in coccoliths of surface sediments in the EMED reflect mainly spring–summer bloom conditions averaged over hundreds to thousands of years.In addition, the origin of varying calcite thickness in H. carteri was investigated. The similarity of average Sr/Ca ratios in differently-calcified specimens confirms that coccolith thickness variations in this species result from primary biomineralization processes and not from variable overgrowth by (low Sr) abiogenic calcite in the water column or the sediments.     

Test of soil extractants for their suitability in predicting Ca/Sr ratios in leaves and stems of sugar maple seedlings

Differential uptake and translocation of Ca and Sr in organisms have been reported, calling into question the use of Sr to track Ca cycling in the environment. We investigated the relationship between Ca/Sr ratios in soil extracts of various strengths (H₂O, NH₄Cl, and NH₄EDTA) and seedlings of sugar maple (Acer saccharum Marsh.) grown from natural regeneration on 37 sites. Our objectives were to determine if Ca/Sr ratios in soil extracts are correlated with those in sugar maple tissues, and what soil extractant best duplicate plant tissue Ca/Sr ratios. Leaves had higher Ca/Sr ratios than stems and the extractants did not produce equal Ca/Sr ratios: H₂O had the lowest Ca/Sr, and NH₄EDTA the highest. The relationships between soil extract Ca/Sr ratios and leaf and stem Ca/Sr ratios were significant and linear, but the slopes differed among extractants. The lowest slope (0.45) was observed for the water extract/leaves and the highest (2.15) for the NH₄EDTA extract/stem with discrimination factors ranging from 0.22 with NH₄EDTA to 1.59 for water. Leaf extracts were more strongly correlated with soil Ca/Sr than stem extracts (R ² of 0.57–0.7 vs. R ² of 0.45–0.6, respectively). These findings support the use of Ca/Sr ratios in plants to track their source of soil Ca, but they highlight the need to calibrate the relationships for the plant tissue and soil extractant used.     

Determination of foliar Ca/Sr discrimination factors for six tree species and implications for Ca sources in northern hardwood forests

Plant and Soil - Discrimination during foliar uptake between the alkaline earth elements Ca and Sr must be understood to fully utilize Ca/Sr and 87Sr/86Sr ratios as a monitor of Ca sources to...     

Shoot Sr concentrations in relation to shoot Ca concentrations and to soil properties

This work was aimed to investigate whether shoot Sr concentrations of plant species are related to respective Ca concentrations and to soil properties and to compare the Sr-Ca observed ratios (OR), defined as the quotient of the ratios Sr/Ca in shoots and in the soil solution or in the extractable form, among species and soils. Ten pasture plant species were grown in pots (1-L volume) filled with eight soils differing in the various physicochemical characteristics. Each pot received 50 mg Sr except those of the soil with the highest cation exchange capacity (C.E.C.) that received 100 mg Sr per pot. For each soil, shoot Sr concentrations of species were linearly and positively related with the respective Ca concentrations. C.E.C, organic matter content and Ca in the soil solution or in the extractable form were the only soil properties that were related, all negatively, with shoot Sr concentrations. The ratio of extractable Sr and Ca was positively and linearly related with the ratio of Sr and Ca. in the soil solution. OR was affected by both species and soils. Most of OR values of all species in all soils ranged between 0.8 and 1.5, except for the grass Agrostis capillaris which had the highest values for most of soils. This indicates that Agrostis capillaris compared to other species, takes up proportionally more Sr than Ca.     

Localisation of mineral uptake by roots using Sr isotopes

To assess the contribution of deep soil horizons to the mineral supply of trees, we investigated the natural variation in the⁸⁷ Sr/⁸⁶Sr isotopic ratio of plant-available strontium with soil depth. In three sites of North-western Spain, this ratio increased with soil depth. The comparison of isotopic ratios of tree leaves and roots at different depths showed that most of the Sr accumulation in Eucalyptus globulus and Pinus pinaster growing on shallow and poor soils in this rainy climate originated from the upper soil layers. As Ca and Sr behave similarly in the soil-plant system, this conclusion can be applied to Ca. This superficial uptake is attributed to the low availability of Sr and Ca in the soil as well as to the shortness of the drought period as compared to the length of the growth period. This technique appears to offer a promising way of studying relative root distributions in soils and plant competition for nutrients.     

Allometric constraints on Sr/Ca and Ba/Ca partitioning in terrestrial mammalian trophic chains

In biological systems, strontium (Sr) and barium (Ba) are two non-essential elements, in comparison to calcium (Ca) which is essential. The Sr/Ca and Ba/Ca ratios tend to decrease in biochemical pathways which include Ca as an essential element, and these processes are termed biopurification of Ca. The quantitative pathway of the biopurification of Ca in relation to Sr and Ba between two biological reservoirs (R _n and R_{n -1}) is measured with an observed ratio (OR) expressed by the (Sr/Ca) _Rn /(Sr/Ca) _Rn-1 and (Ba/Ca) _Rn /(Ba/Ca) _Rn-1 ratios. For a mammalian organism, during the whole biopurification of Ca starting with the diet to the ultimate reservoir of Ca which is the bone, the mean values for OR_Sr and OR_Ba are 0.25 and 0.2, respectively. In this study, published Sr/Ca and Ba/Ca ratios are used for three sets of soils, plants, and bones of herbivorous and carnivorous mammals, each comprising a trophic chain, to illustrate the biopurification of Ca at the level of trophic chains. Calculated OR_Sr and OR_Ba of herbivore bones in relation to plants and of bones of carnivores in relation to bones of herbivores give OR_Sr=0.30±0.08 and OR_Ba=0.16±0.08, thus suggesting that trophic chains reflect the Sr/Ca and Ba/Ca fluxes that are prevalent at the level of a mammalian organism. The slopes of the three regression equations of log(Sr/Ca) vs. log(Ba/Ca) are similar, indicating that the process of biopurification of Ca with respect to Sr and Ba is due to biological processes and is independent of the geological settings. Modifications of the logarithmic expression of the Sr/Ca and Ba/Ca relationship allow a new formula of the biopurification process to be deduced, leading to the general equation OR_Ba=OR_Sr^1.79±0.33,where the allometric coefficient is the mean of the slopes of the three regression equations. Some recent examples are used to illustrate this new analysis of predator-prey relations between mammals. This opens up new possibilities for the utilization of Ba/Ca and Sr/Ca in addition to stable isotope ratios (¹³C and ¹⁵N) for the determination of the relative contribution of different food sources to an animals diet.     

Identifying migratory contingents of fish by combining otolith Sr:Ca with temporal collections of ambient Sr:Ca concentrations

Ambient strontium:calcium (Sr:Ca) concentrations were determined at the temporal scales of months, weeks and days, in summer and winter at two estuarine sites, and experimentally derived correlations between ambient and otolith Sr:Ca were used to estimate the otolith Sr:Ca concentrations of 'resident' black bream Acanthopagrus butcheri . Wild black bream were collected in summer and winter at the end of the temporal water sampling, and their otolith Sr:Ca concentrations were examined. Wild fish were classified as 'resident' if their otolith Sr:Ca matched the predicted concentrations of resident fish, and 'migrant' if this did not occur. In winter, all fish were classified as resident. In summer, all fish were classified as migrants, with fish spending an average of only 16·8% (estuary 1) and 61·1% (estuary 2) of their time at each estuarine location.     

Variations of bioavailable Sr concentration and 87Sr/86Sr ratio in boreal forest ecosystems

The mean depth of Sr and water uptake in mixed Norway spruce (Picea abies) and Scots pine (Pinus sylvestris) stands was investigated, using natural variations of ⁸⁷Sr/⁸⁶Sr and ¹⁸O/¹⁶O in soils in relation to depth. Three spruce-pine pairs were studied on a podzol and a peat site in Northern Sweden. Tree leaf and wood, as well as soils, soil solutions and roots below each tree were analysed for Sr and Ca concentrations and ⁸⁷Sr/⁸⁶Sr ratio. The ¹⁸O/¹⁶O ratio was also determined in xylem sap and soil solutions in relation to depth. Soil solution ¹⁸O/¹⁶O decreased in relation to depth. Comparing with xylem sap ¹⁸O/¹⁶O data indicated a deeper uptake of soil water by pine than spruce on the podzol site and a superficial uptake by both species on the peat. The ⁸⁷Sr/⁸⁶Sr ratio of bioavailable Sr generally increased in soils in relation to depth. Contrastingly, the ⁸⁷Sr/⁸⁶Sr ratio in spruce wood was generally higher than in pine wood suggesting a deeper uptake of Sr by spruce. But the ⁸⁷Sr/⁸⁶Sr ratio and concentrations of bioavailable Sr were systematically higher below spruce than below pine. In order to explain these unexpected results, we built a simple flux model to investigate the possible effects of interspecific variations in Sr cycling, soil mineral weathering and depth of Sr uptake on soil and tree ⁸⁷Sr/⁸⁶Sr ratio. At the study sites, spruce cycled in litterfall up to 12 times more strontium than pine. The use of the model showed that this difference in Sr cycling could alone explain higher isotopic signatures of trees and topsoils below spruce. Besides, high isotopic signatures of roots in the A/E horizons below spruce led us to hypothesise a species-specific weathering process. Finally, the comparison between the ⁸⁷Sr/⁸⁶Sr ratios in wood and root or soil solutions below each species suggested that the average depth of Sr and water uptake were close, but irregular variations of the Sr isotopic ratio with depth reduce the accuracy of the results. Tree species strongly influence Sr isotopic ratios in boreal forest soils through differences in Sr cycling, and possibly through specific mineral weathering.     

Transfer factors for Sr as influenced by species Ca uptake and soil Ca availability

Strontium (Sr) and calcium (Ca) concentrations were studied in different plant species grown in five soil treatments. For either shoots or roots, a positive linear relationship was found between Sr and Ca concentrations in different plant species grown in the same soil treatment. Strontium and calcium concentrations of different species were related to the soil selectivity coefficient for Sr and Ca, defined as the ratio of CH₃COONH₄-extractable Sr and Ca to the ratio of Sr and Ca in the soil solution. For the species used in all soils, transfer factors (TF) for Sr, defined as the ratios of the Sr amount per g of dry plant material and the Sr amount per g of dry soil, were negatively correlated with extractable Ca of the soil. Transfer factors for Sr varied greatly among species or between roots and shoots. This variation of transfer factor was reduced when transfer factor values were divided by the shoot or root Ca concentration of each species. The proposed index TF for Sr per Ca concentration could be used to compare various soils according to their ability to supply plants with Sr when different plant species are grown in these soils.     

A possible explanation for effects of Sr2+ on contraction-relaxation cycle in canine stomach

Effects of Sr2+ on smooth muscle activity and Ca2+ movement by plasma membrane (PM) were examined in preparations isolated from canine stomach to determine how Sr2+ modulates the contraction-relaxation cycle in smooth muscle. Sr2+ caused contraction in Ca2+-free solution. In the presence of Sr2+, KCl caused a response similar to that in normal Ringer's solution, this contraction was inhibited by both nitroprusside and verapamil. Sr2+ inhibited Ca2+ uptake by PM in the presence and absence of ATP. Release of Ca2+ from loaded PM vesicles was accelerated by Sr2+. Results suggest that Sr2+ could replace Ca2+ in Ca2+ binding sites in the cell.     

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.     

Étude de la discrimination strontium-calcium chez le Haricot en fonction du rapport et des teneurs respectives en Sr et Ca de la solution nutritive

The discrimination between strontium and calcium is not only conditioned by the Sr/Ca ratio of the nutrient solution but also by the total dose (Ca + Sr) of the medium. The variation of the observed ratio in relation to the total dose is closely related with the Sr/Ca ratio of the solution. Sr is preferentially fixed by the roots when the Sr/Ca ratio of the solution is low; such a result is observed in the shoots for higher ratios. For all the treatments, the OR of the leaves is lower than unity (discrimination against strontium). When the stable strontium concentration of the solution is not detectable, an increase in the calcium concentration reduces the radiostrontium retention by the roots.