Linking the contents of hydrophobic PAHs with the canopy water storage capacity of coniferous trees.

The canopy water storage capacity (S) is an important parameter for the hydrological cycle in forests. One factor which influences the S is leaf texture, which in turn is thought to be affected by the contents of polycyclic aromatic hydrocarbons (PAHs). In order to improve our understanding of S we simulated rainfall and measured the S of coniferous species growing under various conditions. The contents of 18 PAHs were measured in the needles. The species chosen were: Scots pine (Pinus sylvestris L), Norway spruce (Picea abies (L.) H. Karst) and silver fir (Abies Alba Mill.). Sample branches were collected in 3 locations: A - forest; B - housing estate; C - city center. We found that PAHs have a significant impact on the S of tree crowns. The increase in the total content of all of polycyclic aromatic hydrocarbons (SUM.PAH) translates into an increase of S for all species. The S is the highest for the P. abies species, followed by P. sylvestris and A. alba at all locations. Within the same species, an increase in the value of S is associated with an increase in the PAH content in needles measured by gas chromatography. For A.alba, the average S increased from 11.54% of the total amount of simulated rain (ml g-1) at location A, to 17.10% at location B, and 21.02% at location C. Similarly for P. abies the S was 21.78%, 29.06% and 34.36% at locations A, B and C respectively. The study extends the knowledge of the mechanisms of plant surface adhesion and the anthropogenic factors that may modify this process as well as foliage properties.

[Determination of thyreostats in bovine urine using ultra-high performance liquid chromatography-tandem mass spectrometry].

Five thyreostats (TSs), namely tapazole, thiouracil, methylthiouracil, propylthiouracil, and phenylthiouracil, were determined in bovine urine using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) in positive electrospray ionization mode. Extraction and clean-up were achieved using a ChemElut cartridge with tert-butyl methyl ether, without a derivatization step. Separation was achieved on an Acquity UPLC SS T3 column. The mobile phase was acetonitrile and water containing 0.2% (v/v) formic acid. The mass spectrometer was operated in multiple reaction monitoring mode. Urine samples were spiked with TS solution at levels corresponding to 5, 10, 15, and 20 µg/L. The accuracy (internal standard corrected) ranged from 92% to 107%, with a repeatability precision (relative standard deviation, RSD) less than 15% for all five analytes. The RSDs within-laboratory reproducibility was less than 26%. The decision limits (CCα) and detection capabilities (CCß) were obtained from a calibration curve and were in the ranges of 3.1-6.1 µg/L and 4.0-7.4 µg/L, respectively. The CCα and CCß values were below the recommended concentration, which was set at 10 µg/L. The results show that the described method is suitable for the direct detection of TSs in bovine urine. This method can also be used to determine TSs in porcine urine.