Over 170,000 metric tonnes of high-grade clinoptilolite tuff were extracted from the open-pit mine in Nižný Hrabovec (eastern Slovak Republic) in 2018, making it one of the world’s major natural clinoptilolite producers. The mine is hosted in a Miocene volcanogenic-sedimentary deposit in the East Slovak basin, with estimated 150 million tonnes of clinoptilolite tuff—the economically most important reserve in the European Union. The 100-m-thick tuff horizon is under- and overlain by SW-dipping shallow-marine Badenian sediments (16.30–15.03 Ma ≅ Langhian stage). The tuff is rhyolitic (74.3–77.6 wt % SiO2, 4.09–5.49 wt % Na2O + K2O) with a generally high-K calc-alkaline affinity (3.07–4.28 wt % K2O), comparable to volcanic rocks in the central segment of the Carpathian-Pannonian region of similar age. Although some parts of the tuff underwent slight geochemical changes during formation, this did not significantly change the whole-rock composition of the strikingly homogeneous raw material present in the mine. Rare earth elements (ΣREE = 117–141 ppm) show a uniform pattern, with enriched light REEs and negative Eu anomalies of 0.42 to 0.6 (when normalized to chondrite), comparable to the upper continental crust composition. Mean 87Sr/86Sr = 0.70880 and 143Nd/144Nd = 0.512463 indicate an enriched magmatic source, with a dominant crustal contribution. X-ray diffraction data and electron probe microanalyses show that clinoptilolite-Ca is the only zeolite phase present in the deposit. High-resolution electron probe microanalytical imaging and measurement techniques reveal that clinoptilolite is present as (1) coarse patches that either form pseudomorphs of volcanic glass shards or grew in voids and (2) ultrafine material making up the matrix of the tuff. Both textural types have Si/Al >4, and their evolution is connected to dissolution-(transport)-precipitation reactions from acidic volcanic ash under alkaline fluid influence and slightly elevated pressure-temperature (44°–84°C) conditions. Authigenic cristobalite, detected as ultrafine-grained matrix crystallites, formed during the zeolitization process from excess Si. The large-scale, remarkably homogeneous and monomineralic natural zeolite deposit formed from a well-equilibrated magmatic source, with no syn- to postsedimentary reworking and with essentially isochemical conditions during the zeolitization process.

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Our observations confirm that a microparticulate preparation of clinoptilolite is safe and effective in a murine model of inflammatory bowel disease and supports the hypothesis that the adsorptive capacity of clinoptilolite is of potential therapeutic relevance.

The potential of enriched Pb (204Pb) was assessed to monitor pathways of trace levels of Pb in the pg range within the human body via isotope pattern variation in situations where natural lead cannot be used as a tracer due to regulatory limitations. Isotope ratio measurements were accomplished by means of (multi-collector) inductively coupled plasma mass spectrometry including a comparison of single and multi-collector ICP-MS for low-level 204Pb assessment. Isotopic pattern results from a blend of a large quantity of the element with a natural isotopic composition and an enriched stable isotope at orders of magnitude lower levels pose a nontrivial analytical problem. Isotope pattern deconvolution was successfully applied as mathematical tool based on multiple linear regressions. The method allowed for deconvolving the isotope pattern from measured isotope ratios without knowing the quantities of different isotope sources incorporated and mixed into the sample at levels of < 1 pg 204Pb/g blood. The objective of this manuscript is to evaluate and summarize the analytical aspects for Pb isotope pattern deconvolution based on the results of a clinical trial, where a 204Pb-enriched isotope tracer was applied to investigate the bioavailability of orally applied Pb along with purified clinoptilolite tuff as potential supplement. This unique approach allows to reduce tracer amounts to harmless levels to human health, which are in accordance with the legal regulative to study enrichment levels of < 0.01% in human blood. Graphical abstract

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