The foraminiferal genera Pararotalia, Neorotalia, and Calcarina: taxonomic revision

Scanning electron microscopy of the architecture of Rotalina inermis Terquem, 1882, the type-species of the genus Pararotalia Le Calvez, 1949, and of Rotalia mexicana Nuttall, 1928, the type-species of the genus Neorotalia Bermudez, 1952, reveals that both taxa have in common: 1) an umbilical bowl closed by either a single or a compound umbilical plug; 2) an interiomarginal extraumbilical aperture, restricted by a toothplate that protrudes with a free edge into the aperture and forms an umbilical spiral canal; and 3) a septal flap and intraseptal interlocular spaces. Rotalia mexicana, however, also possesses an enveloping canal-system, similar to that found in the Calcarinidae. For this reason Neorotalia must be regarded as a valid distinct genus, not synonymous with Pararotalia, as proposed by some authors. Calcarina calcar d'Orbigny, 1839, variously placed by authors in Rotalia Lamarck, 1804, in Pararotalia Le Calvez, 1949, and lately again in Calcarina d'Orbigny, 1826, is shown to possess the same basic architecture as Neorotalia and is placed, consequently, into this latter genus. Irregular supplementary apertures occurring in N. calcar are not considered of generic value and neither are they regarded as indicating a relationship with Nautilus spengleri Gmelin, 1788, the type-species of Calcarina. The latter, although characterized by a complex enveloping canal-system, possesses primary multiple interioareal main apertures, surrounded by thick rims, as well as a small umbilical plate, but lacks a toothplate with a free edge. For comparison, Pararotalia spinigera (Le Calvez, 1949) and Neorotalia viennoti (Greig, 1935) were also studied. The subfamily Pararotaliinae Reiss, 1963, is emended to include the canal-system as a characteristic feature. A glossary of selected terms is appende

The graphical presentation of lead isotope data for environmental source apportionment

Lead isotope ratios are widely used to identify original sources of Pb in the environment. Such source apportionment depends on the ability to distinguish potential sources on the basis of their isotopic composition. However, almost all terrestrial Pb is co-linear in some of the plots i.e. <sup>206</sup>Pb/<sup>208</sup>Pb versus <sup>206</sup>Pb/<sup>207</sup>Pb and <sup>206</sup>Pb/<sup>204</sup>Pb versus <sup>206</sup>Pb/<sup>207</sup>Pb commonly presented in the literature. These diagrams are unable to distinguish more than two sources of environmental Pb. Linear trends in such plots are an inevitable consequence of the co-linearity of terrestrial leads and should not be taken necessarily to indicate simple binary mixing of sources. A more reliable test for multiple source mixing can be obtained from plots involving <sup>206</sup>Pb/<sup>204</sup>Pb, <sup>207</sup>Pb/<sup>204</sup>Pb and <sup>208</sup>Pb/<sup>204</sup>Pb and therefore requires measurements of the minor <sup>204</sup>Pb isotope

Existence of long-lived isotopes of a superheavy element in natural Au

Evidence for the existence of long-lived isotopes with atomic mass numbers 261 and 265 and abundance of (1-10)x10$^{-10}$ relative to Au has been found in a study of natural Au using an inductively coupled plasma - sector field mass spectrometer. The measured masses fit the predictions made for the masses of $^{261}$Rg and $^{265}$Rg (Z=111) and for some isotopes of nearby elements. The possibility that these isotopes belong to the recently discovered class of long-lived high spin super- and hyperdeformed isomeric states is discussed.Comment: 4 pages, 3 figures, 2 table

Heavy metal distribution in some French forest soils: evidence for atmospheric contamination

This study is one of very few dealing with the distribution and the origin of heavy metals in French soils from a priori non-polluted forest areas. The abundance of heavy metals measured in these soils decreases as follows: Cr) Zn)Pb)Ni)Cu)Co4Cd. Total concentrations of Pb, Cr and Ni in some soils exceed the European thresholds for non-polluted soils and even the French association of normalization critical values for sludge spreading. The lowest heavy metal contents are observed in acid soils while the highest concentrations are in the calcaric cambisol and in the mollic andosol, which is rather scarce as compared with the other French forest soils. With the exception of the podzol, Cr and Ni concentrations increase with depth in all soil profiles. The distribution pattern of Co, Cu, Zn depends on the soil characteristics. In some acid soils, however, Cu and Zn decrease with depth. Pb and Cd are accumulated in the upper soil horizons. Heavy metals accumulate in deep soil horizons in relation to important clay content in the dystric planosol and stagnic luvisol. The concentration of each heavy metal is always controlled by different parameters (soil pH, iron and aluminum oxide content, clay content, organic matter and cation exchange capacity), which are heavy metal specific. This study highlights the metal-trapping character of andosol and calcaric soil, the weak heavy metal retention in acid soils, the leaching and trapping character in leached clayed soils, and the migration of heavy metals in the podzol. Pb and Cr concentrations indicate a significant enrichment in surface horizons from various soils in areas which receive significant acid atmospheric pollution. Particularly, the highest Pb content is observed in a soil located in the N-NE part of France. Lead isotope ratios measured in the cambic podzol and the calcaric cambisol, exhibit the importance of the anthropogenic sources and particularly the influence of global atmospheric inputs from leaded gasoline compared to regional and local industrial emissions. The anthropogenic Pb contribution is estimated to 83, 30 and 11%, respectively, for surface, intermediate and deep horizons of the cambic podzol located in the northern part of France, and to 68% in surface horizon of the calcaric cambisol located in the Alps

Online preconcentration ICP-MS analysis of rare earth elements in seawater

The rare earth elements (REEs) with their systematically varying properties are powerful tracers of continental inputs, particle scavenging intensity and the oxidation state of seawater. However, their generally low (∼pmol/kg) concentrations in seawater and fractionation potential during chemical treatment makes them difficult to measure. Here we report a technique using an automated preconcentration system, which efficiently separates seawater matrix elements and elutes the preconcentrated sample directly into the spray chamber of an ICP-MS instrument. The commercially available “seaFAST” system (Elemental Scientific Inc.) makes use of a resin with ethylenediaminetriacetic acid and iminodiacetic acid functional groups to preconcentrate REEs and other metals while anions and alkali and alkaline earth cations are washed out. Repeated measurements of seawater from 2000 m water depth in the Southern Ocean allows the external precision (2σ) of the technique to be estimated at <23% for all REEs and <15% for most. Comparison of Nd concentrations with isotope dilution measurements for 69 samples demonstrates that the two techniques generally agree within 15%. Accuracy was found to be good for all REEs by using a five point standard addition analysis of one sample and comparing measurements of mine water reference materials diluted with a NaCl matrix with recommended values in the literature. This makes the online preconcentration ICP-MS technique advantageous for the minimal sample preparation required and the relatively small sample volume consumed (7 mL) thus enabling large data sets for the REEs in seawater to be rapidly acquired

Strontium isotope fractionation of planktic foraminifera and inorganic calcite

We have investigated the strontium isotope fractionation (Δ88/86Srcarb–aq) between inorganic calcite and aqueous Sr2+ ions by precipitation experiments at a constant temperature of 25 °C and precipitation rates (R) ranging from 102.3 to 104.2 μmol/m2/h. Strontium isotope ratios were measured using the 87Sr–84Sr double spike technique. It was found that strontium isotope fractionation in these calcites is strongly dependent on the precipitation rate: View the MathML source The measured δ88/86Sr values are significantly correlated with previously measured δ44/40Ca and Sr/Ca values of the same calcite samples: Δ88/86Srcarb–aq=+0.18∗Δ44/40Cacarb–aq-0.01 View the MathML source The slope of 88Sr/86Sr versus 44Ca/40Ca fractionation is 0.18 ± 0.04 and compatible with a kinetic fractionation during dehydration of the strontium and calcium ions, but not with isotope fractionation in a diffusive boundary layer. Using published equilibrium Δ44/40Cacarb–aq and View the MathML source values we estimate the equilibrium isotope fractionation of strontium to be very close to zero (Δ88/86Sreq(carb–aq) = −0.01 ± 0.06‰). This estimate is confirmed by strontium isotope values of natural inorganic calcites that precipitated very slowly in basalts of the ocean crust. The results from the inorganic calcites are used to explain strontium isotope fractionation of planktic foraminifera. Specimens of two warm water species (Globigerinoides ruber and Globigerinoides sacculifer) were picked from the Holocene section of a Caribbean sediment core. We found no significant difference in δ88/86Sr between the two species. In addition, G. ruber specimens from Marine Isotope Stage 2 in the same core show δ88/86Sr values identical to the Holocene specimens. The strontium isotopes of both foraminifera species are strongly fractionated (Δ88/86Srcarb–aq = −0.248 ± 0.005‰) when compared to published data of other major marine calcifiers. Applying the results from the inorganic precipitation experiments we find that the strong foraminiferal strontium isotope fractionation can be explained by calcification in a largely open system at high precipitation rates, comparable in magnitude to rates known from scleractinian reef corals. This interpretation is in good agreement with the kinetic calcification model for planktic foraminifera by Kisakürek et al. (2011), which was based on calcium isotopes and elemental Sr/Ca ratios

Selected isotope ratio measurements of light metallic elements (Li, Mg, Ca, and Cu) by multiple collector ICP-MS

The unique capabilities of multiple collector inductively coupled mass spectrometry (MC-ICP-MS) for high precision isotope ratio measurements in light elements as Li, Mg, Ca, and Cu are reviewed in this paper. These elements have been intensively studied at the Geological Survey of Israel (GSI) and other laboratories over the past few years, and the methods used to obtain high precision isotope analyses are discussed in detail. The scientific study of isotopic fractionation of these elements is significant for achieving a better understanding of geochemical and biochemical processes in nature and the environment

Constraining calcium isotope fractionation (δ44/40Ca) in modern and fossil scleractinian coral skeleton

The present study investigates the influence of environmental (temperature, salinity) and biological (growth rate, inter-generic variations) parameters on calcium isotope fractionation (δ44/40Ca) in scleractinian coral skeleton to better constrain this record. Previous studies focused on the δ44/40Ca record in different marine organisms to reconstruct seawater composition or temperature, but only few studies investigated corals. This study presents measurements performed on modern corals from natural environments (from the Maldives for modern and from Tahiti for fossil corals) as well as from laboratory cultures (Centre Scientifique de Monaco). Measurements on Porites sp., Acropora sp., Montipora verrucosa and Stylophora pistillata allow constraining inter-generic variability. Our results show that the fractionation of δ44/40Ca ranges from 0.6 to 0.1‰, independent of the genus or the environmental conditions. No significant relationship between the rate of calcification and δ44/40Ca was found. The weak temperature dependence reported in earlier studies is most probably not the only parameter that is responsible for the fractionation. Indeed, sub-seasonal temperature variations reconstructed by δ18O and Sr/Ca ratio using a multi-proxy approach, are not mirrored in the coral's δ44/40Ca variations. The intergeneric variability and intrageneric variability among the studied samples are weak except for S. pistillata, which shows calcium isotopic values increasing with salinity. The variability between samples cultured at a salinity of 40 is higher than those cultured at a salinity of 36 for this species. The present study reveals a strong biological control of the skeletal calcium isotope composition by the polyp and a weak influence of environmental factors, specifically temperature and salinity (except for S. pistillata). Vital effects have to be investigated in situ to better constrain their influence on the calcium isotopic signal. If vital effects could be extracted from the isotopic signal, the calcium isotopic composition of coral skeletons could provide reliable information on the calcium composition and budget in ocean. Highlights ► Corals cultured in aquaria or from natural environment show the same Ca isotopic composition. ► δ44/40Ca of coral skeleton is independent of depositional setting environment. ► Strong influence of vital effects on coral skeleton δ44/40Ca composition and calcification mechanism