Plant-minerals-water interactions: An investigation on Juncus acutus exposed to different Zn sources.

Juncus acutus has been proposed as a suitable species for the design of phytoremediation plans. This research aimed to investigate the role played by rhizosphere minerals and water composition on Zn transformations and dynamics in the rhizosphere-plant system of J. acutus exposed to different Zn sources. Rhizobox experiments were conducted using three different growing substrates (Zn from 137 to 20,400 mg/kg), and two irrigation lines (Zn 0.05 and 180 mg/l). The plant growth was affected by the substrate type, whereas the Zn content in the water did not significantly influence the plant height for a specific substrate. J. acutus accumulated Zn mainly in roots (up to 10,000 mg/kg dw); the metal supply by the water led to variable increases in the total Zn concentration in the vegetal organs, and different Zn distributions both controlled by the rhizosphere mineral composition. Different Zn complexation mechanisms were observed, mainly driven by cysteine and citrate compounds, whose amount increased linearly with Zn content in water, but differently for each of the investigated systems. Our study contributes to gain a more complete picture of the Zn pathway in the rhizosphere-plant system of J. acutus. We demonstrated that this vegetal species is not only capable of developing site-specific tolerance mechanisms, but it is also capable to differently modulate Zn transformation when Zn is additionally supplied by watering. These findings are necessary for predicting the fate of Zn during phytoremediation of sites characterized by specific mineralogical properties and subject to water chemical variations.

Trace-element XAFS sensitivity: a stress test for a new XRF multi-detector.

X-ray absorption fine-structure (XAFS) spectroscopy can assess the chemical speciation of the elements providing their coordination and oxidation state, information generally hidden to other techniques. In the case of trace elements, achieving a good quality XAFS signal poses several challenges, as it requires high photon flux, counting statistics and detector linearity. Here, a new multi-element X-ray fluorescence detector is presented, specifically designed to probe the chemical speciation of trace 3d elements down to the p.p.m. range. The potentialities of the detector are presented through a case study: the speciation of ultra-diluted elements (Fe, Mn and Cr) in geological rocks from a calcareous formation related to the dispersal processes from Ontong (Java) volcanism (mid-Cretaceous). Trace-elements speciation is crucial in evaluating the impact of geogenic and anthropogenic harmful metals on the environment, and to evaluate the risks to human health and ecosystems. These results show that the new detector is suitable for collecting spectra of 3d elements in trace amounts in a calcareous matrix. The data quality is high enough that quantitative data analysis could be performed to determine their chemical speciation.

Surface reactivity of Etna volcanic ash and evaluation of health risks.

This work is a part of a research project conducted in order to characterize the volcanic ash from Mount Etna, focusing in particular on the surface reactivity of ashes and possible consequence for human health. In this framework, a sampling campaign began on 16 March 2013, taking advantage of the intense volcanic activity on Etna. The interaction between volcanic ash and human organism was simulated treating two classes of representative Etnean particles with ultrapure water (grainsize of 850 um) and Gamble's solution mimic lug fluids (grainsize <38 µm) with the aim to evaluate the risk due to gastric and respiratory exposure to volcanic particles. The leachates were analysed by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES), Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and Ionic Chromatography (CI) in order to highlight possible dangerous elements released in water solutions according to USGS protocol. Analyses of Gamble's solution highlighted a release of elements smaller than in watery solutions and always below the thresholds established by the Italian law. On the contrary, analyses of watery solutions evidenced, for some elements (B, Cd, Ni and As), levels higher than permitted by Italian law. Considering the effects of these elements on human health, further investigations are necessary and currently carried out in order to better constrain the release process and the specific effects on human organism.

A two-step pH control method to remove divalent metals from near-neutral mining and metallurgical waste drainages by inducing the formation of layered double hydroxide.

A neutral M2+-rich and M3+-poor (M = metal) metallurgical waste drainage was used to test a metal removal method based on the precipitation of layered double hydroxide (LDH). The LDH precipitation was induced by adding a salt of Al3+ (trivalent metal missing in the drainage) and maintaining or restoring the pH to a circum-neutral value. The precipitates were characterized by chemical analysis, XRD, ESEM, HRTEM and XAS. The main parameter controlling the removal of metals and the type of precipitate appeared to be the pH. As a function of pH variation during the experiments, analyses of precipitates and solutions showed either the formation of poor crystalline LDH combined with very high removal of Zn, Ni and Pb (92-100%), more variable removal of Mn (46-98%) and less Cd (33-40%), or the formation of more crystalline LDH combined with lower removal of Zn (62%), Mn (43%), Ni (88%), Pb (64%) and especially Cd (1%). The different metal removal efficiency in the two cases is only indirectly due to the different LDH crystallinity, and it is clearly affected by the following factors: 1) the two pH steps of the method; 2) the direction of pH variation within each step. In particular, the highest removal of metals is obtained when the first pH step goes towards acidic conditions, as a consequence of Al salt addition, and precipitation of a quasi-amorphous hydrated hydroxysulfate of Al (probably a precursor of felsÓ§bányaite Al4(SO4)(OH)10 · 4H2O) occurs. This first acidic pH step removes little or no metals (just 0-3%) but it is essential so that the second pH step towards slightly alkaline conditions, as a consequence of NaOH addition, can be highly efficient in removing divalent metals as the quasi-amorphous hydrated hydroxysulfate of Al gradually turns into an LDH incorporating Zn, Mg and other metals. On the contrary, when both pH steps remain in the neutral-alkaline range, only LDH precipitation occurs and a lower metal removal is observed. These results encourage further investigations on the removal of metals by inducing LDH precipitation as a simple and effective method for the treatment of circum-neutral polluted drainages.

Chemical data on environmental matrices from an abandoned mining site.

This article contains analytical data on chemical composition of waters and solid samples (mining wastes and biominerals) collected in an abandoned mining area, and they are related with the research article "Geochemistry of rare earth elements in water and solid materials at abandoned mines in SW Sardinia (Italy)" (Medas et al., 2013). Specifically, we present physicochemical data (temperature, electrical conductivity, pH, and redox potential), major components and the main contaminants (Zn, Mn, Cd, Ni, Cu, Pb) detected in stream waters and drainages from mine wastes. Waters were monitored from 2009 to 2011 during different seasonal conditions to give an insight into metal dispersion under different hydrological conditions.

Geochemical and mineralogical datasets on waters and stream precipitates from an abandoned mining site: Montevecchio-Ingurtosu district, Rio Irvi (SW Sardinia).

Geochemical modelling data and Powder X-Ray Diffraction data on samples collected along Rio Irvi (Montevecchio-Ingurtosu mining district, SW Sardinia, Italy) are reported in this paper. The data show the results of data processing to calculate water chemical speciation of ions and saturation indices of relevant mineral phases. These data are related with the research article: De Giudici G. et al (2018), Application of hydrologic-tracer techniques to the Casargiu adit and Rio Irvi (SW-Sardinia, Italy): Using enhanced natural attenuation to reduce extreme metal loads, Applied Geochemistry, vol.96, 42-54. The comparison of the calculated saturation indices of relevant Fe-bearing phases with the PXRD data of samples collected along the stream confirm the quality of the SI dataset and the good correlation between the calculations and the observed data. The comparison of this dataset with others can help to deeper understand and quantify the impact of past and current mining activity on water bodies, contributing to implement the scientific background for the application of remediation actions.

Data on rare earth elements in mining environments under non-acidic conditions.

This article contains analytical data on Rare Earth Elements (REE) concentration in waters and solid samples (mining wastes and biominerals) collected in an abandoned mining site characterized by near-neutral conditions, and they are related with the research article "Geochemistry of rare earth elements in water and solid materials at abandoned mines in SW Sardinia (Italy)" (Medas et al., 2013). REE can show specific signatures due to fractionation processes, giving an insight to the understanding of the natural processes ruling the water-rock interactions and the geo-bio-interactions. Most researches on REE behavior were performed in acidic environments, while only few data on REE are available for neutral waters. Elaboration of this dataset can be useful to evaluate the reactions controlling the geochemical behavior of REE under near-neutral to slightly alkaline conditions, driving the scientific community toward an efficient management of monitoring actions and remediation technologies.

Binding of bis-(2-ethylhexyl) phthalate at the surface of hydrozincite nanocrystals: An example of organic molecules absorption onto nanocrystalline minerals.

As a contribution to understand the interactions between mineral surfaces and organic molecules, this study reports an accurate characterization of the bis-(2-ethylhexyl) phthalate (DEHP)-Hydrozincite (DEHP-HY), that has been conduced combining the following techniques: FTIR, NMR, XAS spectroscopies and XRD. XRD patterns indicate that the HY is made of nanocrystals whose size is not influenced by the presence of DEHP. The (1)H NMR analysis of DEHP-HY samples points out the presence of interactions of DEHP with HY. CPMAS NMR analysis suggests that the interaction is operated by ester carbonyl groups while the aliphatic chain, as expected, is not involved. MAS and CPMAS NMR measurements, performed on (13)C ester carbonyl enriched DEHP, allow to demonstrate that there are two ester carbonyl linkage sites interacting at the HY surface: an acid site with a strong link and a second one with weak chemical interactions. Zn K-edge XAS spectroscopy demonstrates that the local atomic structure around Zn in DEHP-HY sample remains essentially unchanged with respect to that of HY. Such a weak structural effect suggests that HY interaction with DEHP is limited to the nanoparticle surface.

Self-preservation strategies during bacterial biomineralization with reference to hydrozincite and implications for fossilization of bacteria.

The induction of mineralization by microbes has been widely demonstrated but whether induced biomineralization leads to distinct morphologies indicative of microbial involvement remains an open question. For calcium carbonate, evidence suggests that microbial induction enhances sphere formation, but the mechanisms involved and the role of microbial surfaces are unknown. Here, we describe hydrozincite biominerals from Sardinia, Italy, which apparently start life as smooth globules on cyanobacterial filaments, and evolve to spheroidal aggregates consisting of nanoplates. Complementary laboratory experiments suggest that organic compounds are critical to produce this morphology, possibly by inducing aggregation of nanoscopic crystals or nucleation within organic globules produced by metabolizing cells. These observations suggest that production of extracellular polymeric substances by microbes may constitute an effective mechanism to enhance formation of porous spheroids that minimize cell entombment while also maintaining metabolite exchange. However, the high porosity arising from aggregation-based crystal growth probably facilitates rapid oxidation of entombed cells, reducing their potential to be fossilized.

Stream water chemistry in the arsenic-contaminated Baccu Locci mine watershed (Sardinia, Italy) after remediation.

The abandoned Pb-As Baccu Locci mine represents the first and only case of mine site remediation in Sardinia, Italy. Arsenic is the most relevant environmental concern in the Baccu Locci stream watershed, with concentrations in surface waters up to and sometimes over 1 mg/L. The main remediation action consisted in creation of a "storage site", for the collection of contaminated materials from different waste-rock dumps and most of tailings piles occurring along the Baccu Locci stream. This paper reports preliminary results on the level of contamination in the Baccu Locci stream after the completion of remediation measures. Post-remediation stream water chemistry has not substantially changed compared to the pre-remediation situation. In particular, dissolved As maintains an increasing trend along the Baccu Locci stream, with a concentration of about 400 µg/L measured at a distance of 7 km from the storage site. Future monitoring will provide fundamental information on the effectiveness of remediation actions conducted and their applicability to other mine sites in Sardinia. At the stage of mine site characterisation of future remediation plans, it is recommended to pay more attention to the understanding of mineralogical and geochemical processes responsible for pollution. Moreover, mixing of materials with different composition and reactivity in a storage site should require careful consideration and long-term leaching tests.

Uptake of Pb by hydrozincite, Zn5(CO3)2(OH)6--implications for remediation.

Hydrozincite, Zn(5)(CO(3))(2)(OH)(6), periodically precipitates from heavy metal contaminated waters of the Rio Naracauli stream, Sardinia, in association with a biological photosynthetic community. The precipitation removes not only zinc from the waters, but also other toxic "heavy metals", such as Cd, Cu, Pb. The phenomenon is therefore of potential interest for "soft" remediation of contaminated waters. Previous cation exchange experiments suggested that binding of Pb to hydrozincite is fairly strong. This suggestion is in agreement with new release tests in deionized water and X-ray absorption spectroscopy (XAS) spectra collected at the Pb L(III) edge for natural hydrozincites from Naracauli, and synthetic Pb-doped hydrozincites. The results suggest that, up to bulk concentration of 1.5 wt.% Pb, uptake of this metal occurs in two distinct ways: (1) as a substitution for Zn in the tetrahedral site of the hydrozincite structure, possibly via formation of a surface mononuclear tridentate inner sphere complex; (2) as an ill-defined, presumably amorphous, phase with a local atomic structure similar to cerussite. These data support the concept that Pb binding to hydrozincite is strong enough to make this mineral a potential sink for the metal.

The kidney from prenatal to adult life: perinatal programming and reduction of number of nephrons during development.

Modified embryonic-fetal development resulting in low birth weight may lead to a reduced nephron endowment, hypertension and renal diseases in adulthood. Regarding the involvement of genetic factors, several environmental conditions may also contribute towards reducing the number of nephrons in the fetus and infant, subsequently constituting a health burden in later life. To date no methods of investigation for the early detection of a reduced nephron reserve are available. However, more structured studies should be implemented to investigate the role of angiotensin-converting enzyme inhibitors in managing proteinurias and glomerulosclerosis in children with renal conditions characterized by reduce nephron number and glomerular hypertrophic changes. In view of the current lack of specific methods of investigation and management, close monitoring of children and young adults at risk of reduced renal reserve should be carried out to enhance the early detection of potential changes in renal function.