Adoption Barriers in a High-Risk Agricultural Environment

Author(s):  
Shari R. Veil

To lessen the threat of an intentional or naturally occurring livestock disease, the Animal Plant Health Inspection Service of the United States Department of Agriculture introduced the National Animal Identification System (NAIS), encouraging the use of innovative tools such as radio frequency identification (RFID) tags to track cattle across the country. In this study, the author examines the barriers to adoption of NAIS and RFID technology as risk-reduction tools. Diffusion of innovation literature is used to analyze a case study of a state livestock association advocating the rejection of NAIS and RFID technology. Implications for the diffusion of risk reduction tools are provided.

2010 ◽  
Vol 6 (2) ◽  
pp. 30-46
Author(s):  
Shari R. Veil

To lessen the threat of an intentional or naturally occurring livestock disease, the Animal Plant Health Inspection Service of the United States Department of Agriculture introduced the National Animal Identification System (NAIS), encouraging the use of innovative tools such as radio frequency identification (RFID) tags to track cattle across the country. In this study, the author examines the barriers to adoption of NAIS and RFID technology as risk-reduction tools. Diffusion of innovation literature is used to analyze a case study of a state livestock association advocating the rejection of NAIS and RFID technology. Implications for the diffusion of risk reduction tools are provided.


2010 ◽  
Vol 6 (1) ◽  
pp. 69-85
Author(s):  
Shari R. Veil

To lessen the threat of an intentional or naturally occurring livestock disease, the Animal Plant Health Inspection Service of the United States Department of Agriculture introduced the National Animal Identification System (NAIS) encouraging the use of innovative tools such as radio frequency identification (RFID) tags to track cattle across the country. This study examines the barriers to adoption of NAIS and RFID technology as risk-reduction tools. Diffusion of innovation literature is used to analyze a case study of a state livestock association advocating the rejection of NAIS and RFID technology. Implications for the diffusion of risk reduction tools are provided.


2007 ◽  
Vol 8 (1) ◽  
pp. 20 ◽  
Author(s):  
Norman L. Dart ◽  
Gary A. Chastagner

The number and retail value of plants destroyed in Washington State nurseries due to Phytophthora ramorum quarantine efforts was estimated using Emergency Action Notification forms (EANs) issued by the United States Department of Agriculture Animal and Plant Health Inspection Service between 2004 and 2005. Data collected from EANs indicate that during this period 17,266 containerized nursery plants were destroyed at 32 nurseries, worth an estimated $423,043. The mean loss per nursery was estimated at $11,188 in 2004, $11,798 in 2005, and at $13,220 per nursery over the 2-year period. Accepted for publication 26 January 2007. Published 8 May 2007.


2020 ◽  
Vol 4 (2) ◽  
pp. 1216-1223
Author(s):  
Jerad R Jaborek ◽  
Alejandro E Relling ◽  
Francis L Fluharty ◽  
Steven J Moeller ◽  
Henry N Zerby

Abstract The U.S. Department of Agriculture (USDA) yield grade (YG) equation is used to predict the retail yield of beef carcasses, which facilitates a more accurate payment for cattle when they are sold on a grid pricing system that considers carcass composition instead of body weight alone. The current USDA YG equation was developed over 50 yr ago. Arguably, the population of cattle used to develop the YG equation is different than the current diverse U.S. beef cattle supply today. The objectives of this manuscript are to promote the adoption and use of precision agriculture technologies (i.e., camera grading and electronic animal identification) throughout the U.S. beef supply chain as a means to enhance the ability of the USDA YG equation to more accurately predict the retail yield across the population of cattle that contributes to the current U.S. beef supply. Camera grading has improved the accuracy of determining beef carcass retail yield; however, the use of electronic animal identification would allow for additional information to be passed back and forth between the packer, cattle feeder, and producer. Information, such as sex, genetics, medical treatment history, diets consumed, and growth promotant administration, as well as other information could be used to create additional variables for a new augmented USDA YG equation. Herein, fabrication yields demonstrated a 5.6 USDA YG and 12.8% boneless closely trimmed retail cut difference between actual cutout measurements and calculated values from the USDA YG equation for Jersey-influenced cattle. Evidence of such disparities between calculated and actual values warrants a reevaluation of the USDA YG system and consideration for implementing advancements in precision agriculture to improve the prediction of beef carcass retail yield to more accurately account for the large amount of variation in beef carcass retail yield from the cattle in the United States.


1997 ◽  
Vol 9 (4) ◽  
pp. 363-367 ◽  
Author(s):  
S. C. Olsen ◽  
M. G. Stevens ◽  
N. F. Cheville ◽  
G. Schurig

Brucella abortus strain RB51 was recently approved as an official brucellosis calfhood vaccine for cattle by the Animal and Plant Health Inspection Service branch of the United States Department of Agriculture. Currently available serologic surveillance tests for B. abortus do not detect seroconversion following SRB51 vaccination. The purpose of this study was to evaluate a dot-blot assay using γ-irradiated strain RB51 bacteria for its specificity and sensitivity to detect antibody responses of cattle vaccinated with strain RB51. Dot-blot titers of sera at a recommended dosage (1010 colony-forming units) were similar to those of sera from cattle vaccinated with similar numbers of B. abortus strain 19 and greater ( P < 0.05) than titers of nonvaccinated cattle. In the first 12 weeks after vaccination with 1010 colony-forming units of strain RB51, the RB51 dot-blot assay had 100% specificity for titers of 80 or less and a 53% sensitivity for titers of 160 or greater. Sensitivity of the RB51 dot-blot assay peaked at 4 weeks after vaccination with 1010 colony-forming units of strain RB51. Dot-blot responses of sera from cattle vaccinated with a reduced dosage of strain RB51 (109 colony-forming units) did not differ ( P > 0.05) from titers of sera from nonvaccinated cattle. Following intraconjunctival challenge with B. abortus strain 2308, titers on the RB51 dot-blot assay did not differ ( P > 0.05) between nonvaccinated cattle and cattle vaccinated at calfhood with strain 19 or strain RB51.


2008 ◽  
Vol 14 (5) ◽  
pp. 447-453
Author(s):  
H. Chen ◽  
M. Perchonok

Improving the quality, value, and safety of national food supplies is the common mission of several Federal agencies. Under different authorities, these agencies conduct basic and applied research, develop curriculum at higher educational institutions, and disseminate new scientific knowledge about food processing, formulation, and preservation to a broad range of stakeholders. Emerging food processing technologies, including various thermal and nonthermal processes, as well as chemical processes, have received increased attention and investment in recent years. Some agencies dealing with Emerging Technologies include the Cooperative State Research, Education, and Extension Service (CSREES), Agricultural Research Service (ARS), and Food Safety Inspection Service (FSIS), and all of the United States Department of Agriculture (USDA). The U.S. Army Natick Research Center of Department of Defense (DOD), National Aeronautics and Space Administration (NASA), and Food and Drug Administration (FDA) of Department of Human Health Service (DHHS) also are involved in this research area. These agencies have their vision, mission, strategic goals, and current programs and activities related to emerging food processing technologies. The synergy of effective collaboration and cooperation among all stakeholders is the key to generating an impact greater than the simple sum of all.


2015 ◽  
Vol 7 (1) ◽  
Author(s):  
Yandace K. Brown ◽  
Tyann Blessington

The United States Department of Agriculture (USDA) Animal and Plant Inspection Service (APHIS) announced the first diagnosed case of PEDV in U.S. swine on May 17, 2013. NBIC has been monitoring this epidemic primarily due to economic concerns. Without a formal response protocol by a single coordinating agency, PEDV spread rapidly between states. Though APHIS have been actively involved from the beginning of emergence, the Federal Order announced on June 5, 2014 marks more formalized and coordination response, which NBIC predicts will exert greater control over the epidemic despite the predicted viral surge in the colder months.


1994 ◽  
Vol 57 (8) ◽  
pp. 703-709 ◽  
Author(s):  
GERALDINE M. RANSOM ◽  
DAVID W. DREESEN ◽  
BONNIE E. ROSE ◽  
CHARLES P. LATTUADA

Three commercially available nucleic acid hybridization systems were evaluated in combination with the United States Department of Agriculture-Food Safety and Inspection Service (USDA/FSIS) cultural protocol for the detection of Campylobacter spp. from a variety of poultry products. Samples were enriched for 24 h in Hunt broth and then plated onto modified charcoal Campylobacter differential agar. Suspensions of growth from the selective agar plates were then analyzed by the probe assays. The GENE-TRAK® Campylobacter Assay (revised format) and the GEN-PROBE® ACCUPROBE™ Campylobacter Culture Confirmation Test showed sensitivities and specificities of 100% upon testing of 30 raw chicken rinses. The original format GENE-TRAK® test had a sensitivity of 93% and a specificity of 100% when these samples were tested. Ninety percent of the raw chicken rinses were found to contain Campylobacter spp. By either of the two more sensitive probes or by the USDA/FSIS cultural method. Eighty-three percent of the rinses registered Campylobacter-positive by the original format GENE-TRAK® probe. When inoculated ready-to-eat poultry samples were examined, the revised format GENE- TRAK® test and the ACCUPROBE™ assay had sensitivities of 83% and specificities of 100%. The original format GENE-TRAK® test showed a 75% sensitivity and a 100% specificity with these samples. The USDA/FSIS cultural method had a sensitivity of 79% and a specificity of 100% with the inoculated samples. The detection limit of the revised format GENE-TRAK® and the ACCUPROBE™ assays upon testing pooled cell suspensions of four Campylobacter jejuni poultry isolates was approximately 106 CPU/ml.


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