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The package PbIso is a free and open R toolbox for commonly used calculations and plots of Pb–Pb isotope data and for generating Pb evolution models. In this paper, we review Pb isotope systematics and the calculations that are commonly used, such as model age, model source μ (238U/204Pb), time-integrated κ (232Th/238U), and initial Pb isotope ratios. These equations are implemented into R functions in the package PbIso. In addition, functions are provided for generating Pb evolution models, paleoisochrons, and isochrons. This allows users to apply calculations to their data in a straightforward way while providing transparency and flexibility of the calculations used. We have implemented some basic features of the PbIso package into an online shiny R application (see https://shereearmistead.github.io/software/pbiso), which makes it easy for users without any R experience to use these calculations with their own data and to generate plots. We have provided a case study from the Superior Province in Canada, showing how different Pb evolution models can be generated in PbIso and compared to Pb isotope data. [ABSTRACT FROM AUTHOR]

We report the activity measured in rainwater samples collected in the Greater Sudbury area of eastern Canada on 3, 16, 20, and 26 April 2011. The samples were γ-ray counted in a germanium detector and the isotopes 131I and 137Cs, produced by the fission of 235U, and 134Cs, produced by neutron capture on 133Cs, were observed at elevated levels compared to a reference sample of ice water. These elevated activities are ascribed to the accident at the Fukushima Dai-ichi nuclear reactor complex in Japan that followed the 11 March 2011, earthquake and tsunami. The activity levels observed at no time presented health concerns. [ABSTRACT FROM AUTHOR]

Restoration and rehabilitation of native species in the Laurentian Great Lakes is a priority for fisheries management agencies. Restoration efforts are increasingly incorporating a perspective that considers species within a broader food web context. We used stable isotope analysis and museum-preserved specimens to describe and quantify 100 years of food web changes in the Lake Superior fish community. We validated stable isotope analysis of museum specimens by showing a positive correlation between isotope- and diet-based estimates of trophic position. While introductions have created a more trophically diverse food web than historically found in Lake Superior, two separate metrics revealed little community-wide change in the food web. Our species-specific analysis revealed trophic niche differences between shortjaw (Coregonus zenithicus) and shortnose (Coregonus reighardi) ciscoes, two species previously argued to be indistinguishable based on morphological characteristics. By providing a historical context, our findings show the ability of the Lake Superior food web to accommodate non-native species introductions over the last century while still supporting native species populations. This long-term information about food web structure can help guide management and restoration goals in Lake Superior. Furthermore, Lake Superior can serve as a basis for comparing food web changes in other, more highly altered Great Lakes. [ABSTRACT FROM AUTHOR]

Carbon stable isotope analyses have been widely used to estimate terrestrial carbon contribution to lake secondary production. In such approaches, phytoplankton is tacitly assumed as a single, isotopically homogenous source. Such assumption might be valid if (i) zooplankton do not feed selectively on specific algal taxa within bulk phytoplankton, or (ii) although zooplankton do feed selectively, the variability in the δ13C values amongst the different algal taxa is small compared with the variability between the δ13C values of bulk phytoplankton and terrestrial end-members. In a summer field study of six coastal lakes of British Columbia, Canada, we tested these assumptions using gut pigments and stable isotope measures on zooplankton and particulate organic matter. Results revealed that filter-feeding cladocerans positively selected cryptophytes, shown to be substantially 13C-enriched compared with bulk phytoplankton and even with the terrestrial end-member. Comparing a classical two-source mixing model and a model that accounted for algal isotopic heterogeneity, we showed that the use of a classical two-source model can result in an overestimation of terrestrial contribution to zooplankton secondary production. [ABSTRACT FROM AUTHOR]

Moonmilk, which is often seen coating walls in temperate caves, is a porous secondary calcite deposit composed of an aggregate of microcrystalline calcite and water. This study, based on moonmilk deposits found in Caverne de l'Ours, Ottawa Valley region, proposes a model for its formation based on the calcite and water isotope chemistry and evaluates its use as a climatic proxy. In Caverne de l'Ours, non-calcitic mineral inclusions protrude from the bedrock (Grenville marble) into the moonmilk, while others are entirely enclosed within the moonmilk. This observation suggests a mechanism of bedrock dissolution and reprecipitation for the formation of moonmilk, which is controlled by the changing seasonal climate in the cave. The δ18O of the moonmilk interstial water indicates that the condensation of water vapour occurs mostly in winter and spring. The condensation of water vapour on the surface of the walls allows for the dissolution of the Grenville marble and releases ions necessary for the precipitation of moonmilk. The δ18O and δ13C of calcite and δ18O of the moonmilk interstitial water indicate that precipitation of moonmilk occurs during summer and fall. During these seasons, the relative humidity in the cave decreases resulting in moonmilk growth through the slow evaporation of calcite-saturated water. A comparison of the δ18O record of moonmilk from caves in Gaspésie (Canada) and from Aven d'Orgnac (France) shows that this material retains temperature information valuable for paleoclimatic reconstructions. [ABSTRACT FROM AUTHOR]

The South Mountain Batholith (SMB) of southwestern Nova Scotia is a large, highly differentiated, peraluminous, granitic batholith in which the average A/CNK (mol Al2O3/mol(CaO + Na2O + K2O)) increases from 1.16 to 1.23 with chemical evolution. We use vector analysis of variations solely in Al2O3–(CaO + Na2O + K2O) space to assess the fractionation, assimilation, fluid, and source controls on the peraluminosity of the SMB. With increasing chemical evolution, Al2O3 decreases, CaO decreases sharply, Na2O is approximately constant, and K2O increases in the early and middle stages but decreases in the most evolved stage. Initial 87Sr/86Sr and 143Nd/144Nd isotopic ratios for granites and average Meguma Supergroup country rocks suggest an upper limit of ~33% of wall-rock contamination for the most evolved rocks, if the most primitive rocks are uncontaminated. The trend of chemical evolution of the SMB through Al2O3–(CaO + Na2O + K2O) space is the resultant of all input vectors (processes). In the early stages, those processes are fractional crystallization of plagioclase ± K-feldspar ± cordierite ± biotite and contamination by country rocks. In the later stages, those processes are fractionation of plagioclase ± K-feldspar ± andalusite ± muscovite, further contamination by country rocks, and selective partitioning of Ca–Na–K into aqueous fluid phases. Clear geochemical evidence for variation in the source composition is lacking. [ABSTRACT FROM AUTHOR]

Presents a study that examined neodymium isotope geochemistry of felsic volcanic and intrusive rocks from the Yukon-Tanana terrane (YTT) in the Finlayson Lake region, Yukon, Canada. Geological setting of the YTT in the Finlayson Lake region; Geochemical attributes of the intrusive rocks; Systematics of the neodymium isotopes.