Biomedical subjects

N H Spliid

Publications and source records attributed to N H Spliid.

6 recordsLinked to original sources

PubMed2005

Drift of 10 herbicides after tractor spray application. 2. Primary drift (droplet drift).

In the present study the primary drift of 10 herbicides was investigated in five field experiments, and the amount deposited per surface area was quantified outside the application area using simple passive dosimeters. In addition, samples for measuring a possible background value were taken upwind of the sprayed field. Deposits of spray drift were common to all spray equipment and spray was detected up to 150 m off-target. There were deposits of 0.1-9% of the applied amount close to the sprayed field (up to 2 m). But 3m from the spraying zone deposits were reduced to 0.02-4%. The amounts decreased exponentially when moving away from the field. The differences in drift could be described mainly by the different drop sizes, the wind velocity, the formulation and the filtering effect of vegetation on the sampling area. The tendency of the active ingredients to evaporate could also have an, although less important, influence on the drift. This is a factor, which ought to be exposed to a further study. The findings supported that it is the physical properties of the spray and the conditions of application (i.e. equipment and meteorology) that are the primary determinants of primary drift rather than the chemical property of the pure active ingredients.

Aerosols↗

PubMed2005

Drift of 10 herbicides after tractor spray application. 1. Secondary drift (evaporation).

In the present study the evaporation of 10 herbicides was investigated during five field experiments, and the amount deposited per surface area was quantified inside the field using simple passive dosimeters consisting of microscope slides placed on plastic lids. On an average basis 90% of the applied amount reached the field. The accumulated evaporation from the microscope slides was largest during the first hours after application, and the losses in 24 h (from 0% for tribenuron-methyl, fluroxypyr-1-methylheptylester and phenmedipham to 80% for prosulfocarb) was similar to other studies of losses from plant surfaces. An indication of a diurnal difference in the evaporation was observed, probably caused by the differences in temperature or by global radiation. The evaporation did not generally correlate to the vapour pressure. The amounts collected at t=0 on the passive dosimeters were for all field experiments in the same range as the reported amounts applied to the field, and the passive-dosimeters method was found to be a good and reliable method for collection of sprayed pesticides. The advantage of this method was also that it was simple and cheap and easy to set up for screening of evaporation of pesticides from the field after spraying.

Air Pollutants↗

PubMed2000

Sorption and mobility of metronidazole, olaquindox, oxytetracycline and tylosin in soil.

Laboratory studies were conducted to characterise four different antibiotic compounds with regard to sorption and mobility in various soil types. Distribution coefficients (Kd values) determined by a batch equilibrium method varied between 0.5 and 0.7 for metronidazole, 0.7 and 1.7 for olaquindox and 8 and 128 for tylosin. Tylosin sorption seems to correlate positively with the soil clay content. No other significant interactions between soil characteristics and sorption were observed. Oxytetracycline was particularly strongly sorbed in all soils investigated, with Kd values between 417 in sand soil and 1026 in sandy loam, and no significant desorption was observed. Soil column leaching experiments indicated large differences in the mobility of the four antibiotic substances, corresponding to their respective sorption capabilities. For the weakly adsorbed substances metronidazole and olaquindox the total amounts added were recovered in the leachate of both sandy loam and sand soils. For the strongly adsorbed oxytetracyline and tylosin nothing was detected in the leachate of any of the soil types, indicating a much lower mobility. Results from defractionation and extraction of the columns (30 cm length) showed that 60-80% of the tylosin added had been leached to a depth of 5 cm in the sandy loam soil and 25 cm in the sand soil.

Adsorption↗

PubMed1998

Determination of acidic herbicides using liquid chromatography with pneumatically assisted electrospray ionization mass spectrometric and tandem mass spectrometric detection.

Liquid chromatography-pneumatically assisted electrospray mass spectrometry with negative ionization has been used for the determination of acidic herbicides in ground water. Eighteen pesticides or pesticide degradation products belonging to several different groups of acidic herbicides (phenoxy acids, sulfonylureas, phenols, etc.) were covered in the study. Optimization of electrospray inlet conditions is described as well as results from investigations of the linearity of the detector response. Conditions for tandem mass spectrometry (MS-MS) detection of characteristic daughter ions formed by collision-induced dissociation (CID) of the parent ion are described and a comparison of obtainable instrument detection limits by single MS and MS-MS was made. Detection limits using MS in the selected ion monitoring (SIM) mode were generally in the order of 1 microgram/l or below, whereas detection limits were three-four times higher using MS-MS detection. A principle of analysis is proposed based on single quadrupole MS as a method for quantitative determination followed by verification of positive findings by CID MS-MS. Application of the method for detecting acidic herbicides residues in a "real-world" ground water sample is demonstrated.

Calibration↗

PubMed1998

Occurrence of pesticides in Danish shallow ground water.

Shallow ground water from four different catchment areas, two sandy and two clayey locations, were investigated for content of pesticides and -degradation products. The samples were taken from screens in extraction wells placed from 1.5 to 5 meters below surface 46 different compounds were included in the study, and the analysis were performed with liquid chromatography mass spectrometry (LC-MS) with detection limits below 0.01 microgram/L. In total more than 300 samples were analysed and the most frequently found compounds being atrazine and its degradation products, bentazone, MCPA, metamitron, isoproturon and simazine. 23 out of the 46 compounds were detected in one or more samples. Four different sulfonylurea herbicides were included in the study as they to some extent have substituted phenoxyacid herbicides in agricultural practice and in much lower dosage. Sulfonylurea herbicides did not occur in any samples.

Agriculture↗

PubMed1996

Determination of polar pesticides in ground water using liquid chromatography-mass spectrometry with atmospheric pressure chemical ionization.

A method is described for determination of pesticides in ground water by liquid chromatography combined with mass spectrometry (LC-MS) using atmospheric pressure chemical ionization (APCI). The study demonstrates the sensitivity of the technique, with detection limits for water samples of about 0.001-0.005 microgram/l, corresponding to 50-300 pg injected. Performance data for the method such as recovery, precision and linearity are also reported. It is illustrated that the technique is applicable for many different types of pesticide structures, such as triazines, phenylurea herbicides, acetanilides, organophosphorus insecticides, etc. Twelve different pesticides and pesticide degradation products are included in the study. The optimization of inlet conditions with respect to sheath gas pressure, vaporizer temperature, capillary temperature and corona current is reported. Applicability of the method for analysis of "real-world" ground water samples is demonstrated.

Chromatography, High Pressure Liquid↗