Modification of the DC-III portable droplet measurement system, permitting its use under field conditions, is described. Under laboratory conditions, the system effectively sampled water droplets from aerosols produced by a dry ice/water generator and high-pressure syringe. Seven droplet sizes, totaling 71,053 droplets within 22 tests (dry ice method), consisted of 1-, 2-, 6-, 11-, 18-, 25-, and 34-microm droplets with individual (rounded) percentages of 45.25, 37.22, 13.85, 3.17, 0.45, 0.02, and 0.005, respectively, for each size. Cumulatively, 1-microm droplets accounted for ca. 45.25% of the droplets sampled; combined with 2-microm (ca. 82.48% together), 6-microm (ca. 96.33% together), and 11-microm droplets, yielded ca. 99.51% of the droplets sampled. The syringe produced 12 droplet sizes, with 4,121 droplets sampled, consisting of 1, 2, 6, 11, 18, 25, 34, 45, 56, 69, 83, and 99 microm with individual percentages of 15.43, 21.91, 24.58, 17.30, 10.62, 4.65, 2.93, 1.33, 0.63, 0.33, 0.16, 0.07, respectively, for each size. The 6-microm droplets contributed the highest individual percentage, and cumulatively, these droplets combined with 1- and 2-microm droplets, yielding 61.93%, whereas 11- to 45-microm droplets contributed 36.83%, for a total of 98.76%. Droplets measuring 56-99 microm accounted for ca. 1.24% of droplets sampled. Hand-fogger oil aerosols produced 12 droplet sizes (1-38 microm) at test distances of 7.6 and 15.2 m, with 1,979 and 268 droplets sampled, respectively, during 10 tests at each distance. With analysis of variance of transformed individual percentages for each size at both distances, no significant differences were observed for 7.6 and 15.2 m. Cumulatively, 1-, 2-, 3-, and 5-microm droplets contributed 82.87 and 80.97%, whereas 8-, 11-, 14-, and 18-microm droplets added 14.55% to totals at both 7.6 and 15.2 m, respectively. Droplets measuring 22, 27, 32, and 38 microm contributed 2.57% and 4.47% to samples obtained at 7.6 and 15.2 m. The average mass median diameter (MMD) of mineral oil aerosols obtained at 7.6 and 15.2 m were 19.55 +/- 1.62 and 15.49 +/- 1.35, respectively. Positioned at 15 m (50 ft) within a field cage test plot during 12 separate tests, the MMD values obtained downrange were less than calibration MMD values in 5 tests (10-93% of calibration values), but 1.1 to 4.4 times greater in 7 remaining tests. With exception of 2 tests, susceptible Sebring strain Culex quinquefasciatus mortality at the 31-m (100-ft) stake, 15 m (50 ft) behind the DC-III, was consistently 100%. The average MMD values for malathion, permethrin, and resmethrin (at 0.003 and 0.007 rates) at this distance were 13.24 +/- 6.08, 7.48 +/- 5.69, 16.64 +/- 5.54, and 15.48 +/- 2.89, respectively.
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http://dx.doi.org/10.2987/8756-971X(2006)22[707:EOADSB]2.0.CO;2 | DOI Listing |
Sci Rep
January 2025
College of Animal Science and Technology, Ningxia Key Laboratory of Ruminant Molecular and Cellular Breeding, Ningxia University, Yinchuan, 750021, China.
Currently, the identification of valuable candidate genes affecting milk fat synthesis in dairy cows is still limited, and the specific regulatory mechanism is still unknown. In this study, we used primary bovine mammary epithelial cells(BMECs)as a model and utilized overexpression and knockdown techniques for the PI4K2A gene to investigate the specific mechanisms by which it regulates lipid metabolism in BMECs. We studied whether PI4K2A regulates the inhibition of trans-10, cis-12 conjugated linoleic acid (t10,c12-CLA) on lipid synthesis in BMECs.
View Article and Find Full Text PDFAnal Chem
January 2025
Mechanical Engineering, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton SO17 1BJ, U.K.
Total free thiols are an important marker of the whole-body redox state, which has been shown to be associated with clinical outcome in health and disease. Recent investigations have suggested that increased insight may be gained by monitoring alterations of redox state in response to exercise and hypoxia and to monitor redox trajectories in disease settings. However, conducting such studies is challenging due to the requirement for repeated venous blood sampling and intensive lab work.
View Article and Find Full Text PDFVet Clin Pathol
January 2025
Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
MicroRNAs (miRNAs or miRs) are small, non-coding RNAs that play a crucial role in gene regulation, making them potential biomarkers for various diseases. In the field of veterinary medicine, there is a growing interest in exploring the diagnostic and therapeutic potential of miRNAs in kidney diseases affecting dogs and cats. This review focuses on the use of urinary miRNAs as biomarkers for chronic kidney disease (CKD) in these companion animals.
View Article and Find Full Text PDFClin Chim Acta
January 2025
Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China. Electronic address:
Invasive pulmonary aspergillosis (IPA), the most common fungal infection, is associated with high mortality of affected patients. Traditional diagnostic methods exhibit limited sensitivity and specificity, raising big challenges for precise management of the patients. There is thus an urgent need to find out a timely and accurate diagnostic method in clinical practice.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
High Complexity Center, Instituto Galzu, Campos dos Goytacazes 28110-000, RJ, Brazil.
In the year 2019, a highly virulent coronavirus named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged, precipitating the outbreak of the illness known as coronavirus disease 2019 (COVID-19). The commonly employed reverse transcription polymerase chain reaction (RT-qPCR) methodology serves to estimate the viral load in each patient's sample by employing a standard curve. However, it is imperative to recognize that this technique exhibits limitations with respect to clinical diagnosis and therapeutic applications, since an advancement of the conventional polymerase chain reaction methods, digital polymerase chain reaction (digital PCR or DDPCR), enables the direct quantification and clonal amplification of nucleic acid strands.
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