This work focuses on testing and application of Sr isotope signatures for the fast and reliable authentication and traceability of Asparagus officinalis originating from Marchfeld, Austria, using multicollector inductively coupled plasma mass spectrometry after optimised Rb/Sr separation. The major sample pool comprises freeze-dried and microwave-digested asparagus samples from Hungary and Slovakia which are compared with Austrian asparagus originating from the Marchfeld region, which is a protected geographical indication. Additional samples from Peru, The Netherlands and Germany were limited in number and allowed therefore only restricted statistical evaluation. Asparagus samples from Marchfeld were harvested within two subsequent years in order to investigate the annual variation. The results show that the Sr isotope ratio is consistent within these 2 years of investigation. Moreover, the Sr isotope ratio of total Sr in soil was found to be significantly higher than in an NH4NO3 extract, reflecting the mobile (bioavailable) phase. The isotope composition in the latter extract corresponds well to the range found in the asparagus samples in Marchfeld, even though the concentration of Sr in asparagus shows no direct correlation to the concentration of Sr in the mobile phase of the soil. The major question was whether the 'Marchfelder Spargel' can be distinguished from samples from the neighbouring countries of Hungary and Slovakia. According to our findings, they can be clearly (100%) singled out from the Hungarian samples and can be distinguished from the Slovakian asparagus samples with a probability of more than 80%.
Environmental context. There is a need for slightly invasive techniques capable of in-situ probing of target analytes in environmental compartments. Owing to its passive sampling mode and small probe dimensions, microdialysis-based dosimetry is an appealing tool for monitoring of solute concentrations in both water bodies and pore soil waters with minimum disturbance of natural equilibrium. The development of field applications is challenging but will provide novel insights as to the speciation and bioaccessibility of environmental pollutants, e.g. trace metals, at high spatial resolution.Abstract. In-situ sampling of soil pore water is still a challenge for environmental scientists. Here, microdialysis is explored for probing metal concentrations in soil pore water at soil moisture contents ranging from 50 to 115% of the maximal water holding capacity and is compared with traditional sampling by suction cups. Metal concentrations obtained by the suction cup technique were consistently larger than those measured in the dialysate. Good agreement was obtained for Pb and Cu at soil moistures close to saturation after accounting for diffusion resistances whereas corrected Ni and Cd concentrations in the dialysates exceeded those measured by the suction cup technique. These deviations reflect inherent differences in the sampling mode and effects of soil heterogeneity at the microscale. Microdialysis offers new opportunities to probe solute concentrations at high spatial resolution and minimal disturbance of soil conditions at environmental interfaces such as the plant rhizosphere or at the transition between forest floors and the mineral soil.
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