Tawni L Crippen

Dr. Tawni L Crippen

United States Department of Agriculture, Agricultural Research Service, Southern Plains Agricultural Research Center, Food and Feed Safety Research Unit, College Station, TX 77845-4988, USA
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Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 June 2013 in Journal of Chemical Ecology
Verified
Journal Article
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TDThomas Seth Davis
Thomas Seth Davis
TCTawni L Crippen
Tawni L Crippen
RHRichard W. Hofstetter
Richard W. Hofstetter
JTJeffery K. Tomberlin
Jeffery K. Tomberlin

10 June 2013 in International journal of legal medicine
Verified
Journal Article
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JPJennifer Pechal
Jennifer Pechal
TCTawni L Crippen
Tawni L Crippen
MBMark Eric Benbow
Mark Eric Benbow
ATAaron M. Tarone
Aaron M. Tarone
SDScot Dowd
Scot Dowd
JTJeffrey Tomberlin
Jeffrey Tomberlin

12 November 2013 in PLOS ONE
Verified
Journal Article
Open access
PDF file
JPJennifer Pechal
Jennifer Pechal
TCTawni L Crippen
Tawni L Crippen
ATAaron M. Tarone
Aaron M. Tarone
ALAndrew J. Lewis
Andrew J. Lewis
JTJeffery K. Tomberlin
Jeffery K. Tomberlin
MBMark Eric Benbow
Mark Eric Benbow
Microorganisms play a critical role in the decomposition of organic matter, which contributes to energy and nutrient transformation in every ecosystem. Yet, little is known about the functional activity of epinecrotic microbial communities associated with carrion. The objective of this study was to provide a description of the carrion associated microbial community functional activity using differential carbon source use throughout decomposition over seasons, between years and when microbial communities were isolated from eukaryotic colonizers (e.g., necrophagous insects). Additionally, microbial communities were identified at the phyletic level using high throughput sequencing during a single study. We hypothesized that carrion microbial community functional profiles would change over the duration of decomposition, and that this change would depend on season, year and presence of necrophagous insect colonization. Biolog EcoPlates™ were used to measure the variation in epinecrotic microbial community function by the differential use of 29 carbon sources throughout vertebrate carrion decomposition. Pyrosequencing was used to describe the bacterial community composition in one experiment to identify key phyla associated with community functional changes. Overall, microbial functional activity increased throughout decomposition in spring, summer and winter while it decreased in autumn. Additionally, microbial functional activity was higher in 2011 when necrophagous arthropod colonizer effects were tested. There were inconsistent trends in the microbial function of communities isolated from remains colonized by necrophagous insects between 2010 and 2011, suggesting a greater need for a mechanistic understanding of the process. These data indicate that functional analyses can be implemented in carrion studies and will be important in understanding the influence of microbial communities on an essential ecosystem process, carrion decomposition.

12 January 2012 in The ISME Journal
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Journal Article
Closed access
QMQun Ma
Qun Ma
AFAlicia Fonseca
Alicia Fonseca
WLWenqi Liu
Wenqi Liu
AFAndrew T Fields
Andrew T Fields
MPMeaghan Pimsler
Meaghan Pimsler
Thomas WoodThomas Wood
Thomas Wood
Flies transport specific bacteria with their larvae that provide a wider range of nutrients for those bacteria. Our hypothesis was that this symbiotic interaction may depend on interkingdom signaling. We obtained Proteus mirabilis from the salivary glands of the blow fly Lucilia sericata; this strain swarmed significantly and produced a strong odor that attracts blow flies. To identify the putative interkingdom signals for the bacterium and flies, we reasoned that as swarming is used by this bacterium to cover the food resource and requires bacterial signaling, the same bacterial signals used for swarming may be used to communicate with blow flies. Using transposon mutagenesis, we identified six novel genes for swarming (ureR, fis, hybG, zapB, fadE and PROSTU_03490), then, confirming our hypothesis, we discovered that fly attractants, lactic acid, phenol, NaOH, KOH and ammonia, restore swarming for cells with the swarming mutations. Hence, compounds produced by the bacterium that attract flies also are utilized for swarming. In addition, bacteria with the swarming mutation rfaL attracted fewer blow flies and reduced the number of eggs laid by the flies. Therefore, we have identified several interkingdom signals between P. mirabilis and blow flies.

1 April 2018 in Waste Management
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Journal Article
Closed access
KBKelly V. Beskin
Kelly V. Beskin
CHChelsea D. Holcomb
Chelsea D. Holcomb
JCJonathan A. Cammack
Jonathan A. Cammack
TCTawni L Crippen
Tawni L Crippen
AKAnthony H. Knap
Anthony H. Knap
JTJeffery K. Tomberlin
Jeffery K. Tomberlin

1 May 2013 in Journal of Medical Entomology
Verified
Journal Article
Closed access
PDF file
LZLongyu Zheng
Longyu Zheng
TCTawni L Crippen
Tawni L Crippen
BSBaneshwar Singh
Baneshwar Singh
ATAaron M. Tarone
Aaron M. Tarone
SDScot Dowd
Scot Dowd
JTJeffrey Tomberlin
Jeffrey Tomberlin
Sustainable methods for managing waste associated with people and animals have been proposed in the past. Black soldier fly, Hermetia illucens (L.),