2008
DOI: 10.5474/geologija.2008.018
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Isotopic composition of precipitation in Ljubljana (Slovenia)

Abstract: The stable isotopic composition of hydrogen and oxygen (δ 2 H and δ 18 O) and tritium activity ( 3 H) are monitored in monthly precipitation at Ljubljana since 1981. Here we present complete set of numerical data and the statistical analysis for period

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Cited by 26 publications
(60 citation statements)
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“…This means that the source of the water of Sovra borehole is from higher altitudes or it originates from winter precipitation (Table ). Autumn to winter precipitation in the area usually has higher deuterium excess (Vreča et al ., ).…”
Section: Resultsmentioning
confidence: 99%
“…This means that the source of the water of Sovra borehole is from higher altitudes or it originates from winter precipitation (Table ). Autumn to winter precipitation in the area usually has higher deuterium excess (Vreča et al ., ).…”
Section: Resultsmentioning
confidence: 99%
“…The histogram in Figure 3 presents the distribution of tritium in groundwater with a mean value of 6.2 TU, and the arrow at 8.9 TU shows the mean value of tritium over the last few years (2002)(2003)(2004)(2005)(2006) in precipitation for Ljubljana. [45] Since the tritium values in the sampled groundwater are close to the values measured in the precipitation, it is expected that the sampled groundwater is quite young, not exceeding 10 years.…”
Section: Groundwater Dynamicsmentioning
confidence: 97%
“…The gas proportional counting technique (GPC) was used until 2009; since 2010, samples have been measured by the liquid scintillation counting technique (LSC) following electrolytic enrichment (EE), while during 2008 and 2009 both GPC and LSC-EE techniques were used, depending on the available sample quantity. The limit of detection (LOD) was 2.5 TU and 0.5 TU for GPC and LSC-EE techniques, respectively (for details see barešIć et al, 2010Krajcar bronIć et al, 2013;Vreča et al, 2014).…”
Section: Tritium Activitymentioning
confidence: 99%
“…However, most of the tritium present in the atmosphere and hydrosphere is of anthropogenic origin, i.e., tritium was released in atmospheric thermonuclear tests during 1960's, reaching in 1963 several orders of magnitudes higher tritium activity concentration in the atmosphere than the natural levels. After the test ban treaty in 1963, atmospheric tritium activity has been decreasing almost exponentially in the following decades, while during last 10-15 years the mean tritium activity has not been significantly changed (Krajcar BronIć et al, 2006;Vreča et al, 2014; Internet 2). Nowadays, tritium has reached in precipitation levels similar to those occurring before the thermonuclear tests, about 5 TU in central Europe (Internet 2).…”
Section: Introductionmentioning
confidence: 99%
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