Comparative Effectiveness of Three Release Rates for a Pteromalid Parasitoid (Hymenoptera) of House Flies (Diptera) in Beef Cattle Feedlots

1995 ◽  
Vol 5 (4) ◽  
pp. 561-565 ◽  
Author(s):  
J.J. Petersen ◽  
D.W. Watson ◽  
J.K. Cawthra
2003 ◽  
Vol 96 (3) ◽  
pp. 1016-1020 ◽  
Author(s):  
Paula C.R.G. Marçon ◽  
Gustave D. Thomas ◽  
Blair D. Siegfried ◽  
John B. Campbell ◽  
Steven R. Skoda

2003 ◽  
Vol 96 (3) ◽  
pp. 1016-1020 ◽  
Author(s):  
Paula C.R.G. Marçon ◽  
Gustave D. Thomas ◽  
Blair D. Siegfried ◽  
John B. Campbell ◽  
Steven R. Skoda

2010 ◽  
Author(s):  
Robert E DeOtte ◽  
B A Stewart ◽  
Anthony J Megel ◽  
Murali Darapuneni ◽  
Clay A Robinson ◽  
...  

2001 ◽  
Vol 44 (3) ◽  
Author(s):  
Y. Shi ◽  
D. B. Parker ◽  
N. A. Cole ◽  
B. W. Auvermann ◽  
J. E. Mehlhorn

2018 ◽  
Vol 637-638 ◽  
pp. 657-664 ◽  
Author(s):  
Lisa Tymensen ◽  
Rahat Zaheer ◽  
Shaun R. Cook ◽  
Kingsley K. Amoako ◽  
Noriko Goji ◽  
...  

2014 ◽  
Vol 7 ◽  
pp. ASWR.S12841 ◽  
Author(s):  
Orlando A. Aguilar ◽  
Ronaldo Maghirang ◽  
Charles W. Rice ◽  
Steven L. Trabue ◽  
Larry E. Erickson

Emission of greenhouse gases, including nitrous oxide (N2O), from open beef cattle feedlots is becoming an environmental concern; however, research measuring emission rates of N2O from open beef cattle feedlots has been limited. This study was conducted to quantify N2O emission fluxes as affected by pen surface conditions, in a commercial beef cattle feedlot in the state of Kansas, USA, from July 2010 through September 2011. The measurement period represented typical feedlot conditions, with air temperatures ranging from -24 to 39°C. Static flux chambers were used to collect gas samples from pen surfaces at 0, 15, and 30 minutes. Gas samples were analyzed with a gas chromatograph and from the measured concentrations, fluxes were calculated. Median emission flux from the moist/muddy surface condition was 2.03 mg m−2 hour−1, which was about 20 times larger than the N2O fluxes from the other pen surface conditions. In addition, N2O peaks from the moist/muddy pen surface condition were six times larger than emission peaks previously reported for agricultural soils.


2019 ◽  
Vol 48 (5) ◽  
pp. 1454-1461 ◽  
Author(s):  
S. M. McGinn ◽  
T. K. Flesch ◽  
K. A. Beauchemin ◽  
A. Shreck ◽  
M. Kindermann

1975 ◽  
Vol 18 (2) ◽  
pp. 0327-0330 ◽  
Author(s):  
C. B. Gilbertson ◽  
J. R. Ellis ◽  
J. A. Nienaber ◽  
T. M. McCalla ◽  
T. J. Klopfenstein
Keyword(s):  

1970 ◽  
Vol 46 (4) ◽  
pp. 173-177 ◽  
Author(s):  
W. J. Pryor
Keyword(s):  

2015 ◽  
Vol 78 (3) ◽  
pp. 567-572 ◽  
Author(s):  
ANURADHA GHOSH ◽  
LUDEK ZUREK

House flies are a common pest at food animal facilities, including cattle feedlots. Previously, house flies were shown to play an important role in the ecology of Escherichia coli O157:H7; house flies in cattle feedlots carried this zoonotic pathogen and were able to contaminate cattle through direct contact and/or by contamination of drinking water and feed. Because house flies aggregate in large numbers on fresh (≤6 h) steam-flaked corn (FSFC) used in cattle feed, the aim of this study was to assess FSFC in a cattle feedlot as a potentially important site of fecal coliform contamination by house flies. House flies and FSFC samples were collected, homogenized, and processed for culturing of fecal coliforms on membrane fecal coliform agar. Selected isolates were identified by 16S rRNA gene sequencing, and representative isolates from each phylogenetic group were genotyped by pulsed-field gel electrophoresis. Fecal coliforms were undetectable in FSFC shortly (0 h) after flaking; however, in summer, after 4 to 6 h, the concentrations of fecal coliforms ranged from 1.9 × 103 to 3.7 × 104 CFU/g FSFC (mean, 1.1 ± 3.0 × 104 CFU/g). House flies from FSFC carried between 7.6 × 102 and 4.1 × 106 CFU of fecal coliforms per fly (mean, 6.0 ± 2.3 × 105 CFU per fly). Fecal coliforms were represented by E. coli (85.1%), Klebsiella spp. (10.6%), and Citrobacter spp. (4.3%). Pulsed-field gel electrophoresis demonstrated clonal matches of E. coli and Klebsiella spp. between house flies and FSFC. In contrast, in winter and in the absence of house flies, the contamination of corn by fecal coliforms was significantly (~10-fold) lower. These results indicate that FSFC is an important site for bacterial contamination by flies and possible exchange of E. coli and other bacteria among house flies. Further research is needed to evaluate the potential use of screens or blowers to limit the access of house flies to FSFC and therefore their effectiveness in preventing bacterial contamination.


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