Airflow Resistance of Some Pelleted Feed

2013 ◽  
Author(s):  
S. J. Ray ◽  
L. O. Pordesimo ◽  
L. R. Wilhelm ◽  
M. J. Buschermohle
2004 ◽  
Vol 47 (2) ◽  
pp. 513-519 ◽  
Author(s):  
S. J. Ray ◽  
L. O. Pordesimo ◽  
L. R. Wilhelm

2021 ◽  
Vol 3 (2) ◽  
pp. 937-948
Author(s):  
Agasthiyaraj Lakshmanan ◽  
Deepak S. Gavali ◽  
Ranjit Thapa ◽  
Debabrata Sarkar

1988 ◽  
Vol 74 (s18) ◽  
pp. 61P-61P
Author(s):  
M Gugger ◽  
GA Gould ◽  
JC Molloy ◽  
NJ Douglas

2009 ◽  
Vol 30 (11) ◽  
pp. 1197-1209 ◽  
Author(s):  
T Seppänen ◽  
M Koskinen ◽  
T M Seppänen ◽  
O-P Alho

2020 ◽  
Vol 164 ◽  
pp. 107255
Author(s):  
Thamasha Samarasinghe ◽  
Carl Hopkins ◽  
Gary Seiffert ◽  
Jilly Knox

1984 ◽  
Vol 56 (1) ◽  
pp. 133-137 ◽  
Author(s):  
D. W. Hudgel ◽  
R. J. Martin ◽  
B. Johnson ◽  
P. Hill

The purposes of this investigation were to describe the changes in 1) dynamic compliance of the lungs, 2) airflow resistance, and 3) breathing pattern that occur during sleep in normal adult humans. Six subjects wore a tightly fitting face mask. Flow and volume were obtained from a pneumotachograph attached to the face mask. Transpulmonary pressure was calculated as the difference between esophageal pressure obtained with a balloon and mask pressure. At least 20 consecutive breaths were analyzed for dynamic compliance, airflow resistance, and breathing pattern during wakefulness, non-rapid-eye-movement stage 2 and rapid-eye-movement (REM) sleep. Dynamic compliance did not change significantly. Airflow resistance increased during sleep; resistance was 3.93 +/- 0.56 cmH2O X 1–1 X s during wakefulness, 7.96 +/- 0.95 in stage 2 sleep, and 8.66 +/- 1.43 in REM sleep (P less than 0.02). By placing a catheter in the retroepiglottic space and thus dividing the airway into upper and lower zones, we found the increase in resistance occurred almost entirely above the larynx. Decreases in tidal volume, minute ventilation, and mean inspiratory flow observed during sleep were not statistically significant.


2007 ◽  
Vol 70 (10) ◽  
pp. 2251-2258 ◽  
Author(s):  
O. BUCHER ◽  
R. A. HOLLEY ◽  
R. AHMED ◽  
H. TABOR ◽  
C. NADON ◽  
...  

Raw, frozen chicken nuggets and strips have been identified as a significant risk factor in contracting foodborne salmonellosis. Cases of salmonellosis as a result of consuming partly cooked chicken nuggets may be due in part to Salmonella strains originating in broiler feed. This study was undertaken to determine the occurrence and characterize the strains of Salmonella contaminating chicken nuggets, strips, and pelleted feeds, in an attempt to demonstrate whether the same Salmonella strains present in broiler feed could be isolated from raw, frozen chicken nuggets and strips available for human consumption. Salmonellae were recovered using the Health Canada MFHPB-20 method for the isolation and identification of Salmonella from foods. Strains were characterized by serotyping, phage typing, antimicrobial resistance typing (R-typing), and by pulsed-field gel electrophoresis (PFGE). Salmonellae were isolated from 25-g samples in 27% (n = 92) of nugget and strip samples, 95% (n = 20) of chicken nugget meat samples, and from 9% (n = 111) of pelleted feed samples. Salmonella Heidelberg, Salmonella Enteritidis, and Salmonella Orion were the most commonly isolated serovars from chicken nuggets and strips, nugget and strip meat, and pelleted broiler feeds, respectively. Salmonella Enteritidis phage type (PT) 13a with PFGE pattern SENXAI.0006 and R-type sensitive as well as Salmonella Enteritidis PT13a with PFGE pattern SENXAI.0068 and R-type sensitive were isolated from pelleted feed, and chicken nugget and strip meat in two separate instances. Data showed that Salmonella strains isolated from broiler feed were indistinguishable from strains isolated from packaged raw, frozen chicken nuggets and strips. However, results did not rule out the possibility that breeding stock or contamination during processing may have contributed to chicken meat contamination by Salmonella.


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