Accumulation and metal fluxes in the central Venice Lagoon during the last century

Samples from 18 short sediment cores were analyzed for major and trace metals (Al, Fe, Ca, K, Mg, Mn, Si, Ti, Pb, Zn, Cu, Ni, and Cr), ²¹⁰Pb, ¹³⁷Cs, total organic carbon, grain size, and mineralogical composition to find the record of major environmental changes, either natural or anthropogenic, and to establish their chronologies. Some sediments are characterized by nearly constant composition over time, but others clearly show signs of an increasing marine influence, as an increase of the carbonate contents, after the opening of the Malamocco-Marghera Canal in 1969. These changes sometimes obscure the real pattern of pollutants and tracers, which is revealed by normalization against Al. Zn is the most important contaminant, with concentration factors up to 9.3 times the background level, and the most contaminated sediments are those within a few kilometers from the industrial district of Porto Marghera. ²¹⁰Pb activity-depth profiles were used to calculate apparent accumulation rates that provide a basis for the assessment of metal fluxes. The sediments of several sites show a significant increase in anthropogenic metal contamination starting from the second decade of last century, with maximum inputs from 1930 to 1970. The decrease of heavy metal concentrations observed in surficial sediments of some sampling sites could be related to a recent reduction of pollutant inputs.     

A PRECIPITATION ESTIMATION TECHNIQUE FOR DEVELOPING ISOHYETS IN AN ARID AREA USING VEGETATION AND TOPOGRAPHIC PARAMETERS1

A technique is presented for developing an isohyet map for the Hualapai Valley, a closed hydrologic basin of about 315 square miles in the northwestern Great Basin in Nevada. In this basin there is practically no climatic data, and in the northwest Great Basin there are too few stations for determination of rainfall on a detailed basis. Using a vegetational typing to represent a range in elevation and precipitation, an initial mean annual rainfall is determined for selected points on a grid pattern. This rainfall is then modified by using topographic parameters of slope, orientation, exposure, and rainfall shadow effect. The resulting point determinations of mean annual rainfall are then smoothed using a trend surface analysis, and an isohyetal map is drawn from the smoothed points. The technique provides an estimated accuracy of one inch of mean annual precipitation and one mile of resolution on isohyets.     

Validation and global uncertainty of a gas chromatographic with mass spectrometry method for fenamidone analysis in grapes and wines

Fenamidone is an imidazolinone fungicide recently introduced in viticulture practices. This work reports the validation and assessment of global uncertainty of a gas chromatographic with mass spectrometry method to analyze fenamidone in grapes and wines. This method consists in a simple and fast liquid-liquid extraction step followed by chromatographic determination. Limits of detection for fenamidone in grapes and wines were, respectively, 0.05 mg/kg and 0.06 mg/L, precision was below 9.4% and average recovery was 89 ± 5%. In the concentration range from 0.05 to 1.00 mg/kg (or mg/L) of fenamidone, global uncertainty calculated following the EURACHEM/CITAC rules, and also by the Horwitz function, was below 25%. The EURACHEM/CITAC global uncertainty budget used gave lower estimates than those obtained from the Horwitz function.     

Spiked sample standards; Their uses and disadvantages in analytical quality control

Standard samples, that is matrices containing precisely known concentrations of various radionuclides, are necessary adjuncts to any analytical quality control program. In general, we prefer the use of “natural matrix standards,” samples into which the radionuclides have become incorporated under natural conditions, and over as long a time span as possible. Under some circumstances, however, real advantages are offered by “spiked sample standards” samples to which the isotope of interest has been added in a precisely known amount, at the time of preparing the standard. It is our purpose to discuss the advantages and disadvantages of spiked standards and to contrast them with those of natural matrix standards, as well as to discuss the preparation of the former class of standards and the evidence supporting our recommendation of caution in their use.In general, spiked standards offer advantages of low cost of preparation, of advance assurance that the amount and chemical form of the radioisotopes added are known, and of the possibility of preparation of unnatural matrices, or of nuclides that are to be expected but not yet to be found in nature. The most salient disadvantages of spiked standards derive from the usual uncertainty concerning the concentration of any radionuclides in the matrix before spiking and from the difficulty of insuring that there will be no difference in analytical behavior between the spike and the same isotope that has become incorporated in the matrix under natural conditions. Consideration of these advantages and disadvantages leads to identification of a list of special problems for which spiked standards may be advantageous and of a list of precautions indicated in the interpretation of the resulting data. The argument against the general applicability of spiked standards appear overwhelming.