TY - JOUR
T1 - Use of fecal glucocorticoid metabolite measures in conservation biology research
T2 - Considerations for application and interpretation
AU - Millspaugh, Joshua J.
AU - Washburn, Brian E.
N1 - Funding Information:
We thank the University of Missouri (MU) for financial and logistical support of our research over the past several years. Some of our work has been funded by a MU Research Board Grant, a MU Life Science Mission Enhancement Postdoctoral Fellowship, and the MU Department of Fisheries and Wildlife Sciences and Division of Biological Sciences. We thank the Missouri Department of Conservation for supporting much of our glucocorticoid work with mourning doves and white-tailed deer. Also, the South Dakota Department of Game, Fish, and Parks, Custer State Park, University of Washington, Woodland Park Zoo, and South Dakota State University have supported our prior research with elk. We thank J. Faaborg, R. Slotow, G. van Dyk, M. Milanick, S. Jones, J. Schadt, S. Chinnaduarai, S. Ganjum, D. Tempel, R. Gutiérrez, S. Wasser, K. Hunt, J. Schulz, L. Hansen, J. Beringer, and M. Leu for stimulating discussions regarding the use of FGM analyses. We thank T. Meyer, C. Rittenhouse, B. Woeck, J. Sumners, T. Mong, A. Knox, B. Hoenes, and T. Bonnot for their assistance in collecting fecal samples and sample processing in our laboratory. R. Gitzen, B. Kernohan, several anonymous reviewers, and R. Dores provided helpful comments on the manuscript.
PY - 2004/9/15
Y1 - 2004/9/15
N2 - Fecal glucocorticoid metabolite analyses are increasingly being used by a variety of scientists (e.g., conservation biologists, animal scientists) to examine glucocorticoid (i.e., stress hormone) secretion in domestic and wild vertebrates. Adrenocortical activity (i.e., stress response) is of interest to conservation biologists because stress can alter animal behavior, reduce resistance to disease, and affect population performance. The noninvasiveness of fecal-based assessments is attractive, particularly when studying endangered species, because samples can often be obtained without disturbing the animal. Despite such advantages, many confounding factors inhibit the utility of this technique in addressing conservation problems. In particular, interpretation of fecal glucocorticoid metabolite (FGM) measures may be confounded by the length of time animals are held in captivity, normal seasonal and daily rhythms, body condition, sample storage and treatment techniques, diet of the animal, assay selection, animal status (i.e., social ranking, reproductive status), sample age and condition, and sample mass. Further complicating interpretation and utility of these measures is the apparent species-specific response to these factors. The purpose of this paper is to discuss the factors that confound interpretation of FGM measures, summarize research that addresses these issues, and offer an agenda for future research and interpretation. We urge conservation biologists to carefully consider confounding factors and the relationship between FGM secretion and population performance and biological costs when investigating effects of environmental and human-induced disturbances on wildlife. The crisis nature of many decisions in conservation biology often requires decisions from limited data; however, confirmatory results should not be posited when data are incomplete or confounding factors are not understood. Building reliable databases, and research with surrogate species when possible, will aid future efforts and enhance the utility of FGM assays.
AB - Fecal glucocorticoid metabolite analyses are increasingly being used by a variety of scientists (e.g., conservation biologists, animal scientists) to examine glucocorticoid (i.e., stress hormone) secretion in domestic and wild vertebrates. Adrenocortical activity (i.e., stress response) is of interest to conservation biologists because stress can alter animal behavior, reduce resistance to disease, and affect population performance. The noninvasiveness of fecal-based assessments is attractive, particularly when studying endangered species, because samples can often be obtained without disturbing the animal. Despite such advantages, many confounding factors inhibit the utility of this technique in addressing conservation problems. In particular, interpretation of fecal glucocorticoid metabolite (FGM) measures may be confounded by the length of time animals are held in captivity, normal seasonal and daily rhythms, body condition, sample storage and treatment techniques, diet of the animal, assay selection, animal status (i.e., social ranking, reproductive status), sample age and condition, and sample mass. Further complicating interpretation and utility of these measures is the apparent species-specific response to these factors. The purpose of this paper is to discuss the factors that confound interpretation of FGM measures, summarize research that addresses these issues, and offer an agenda for future research and interpretation. We urge conservation biologists to carefully consider confounding factors and the relationship between FGM secretion and population performance and biological costs when investigating effects of environmental and human-induced disturbances on wildlife. The crisis nature of many decisions in conservation biology often requires decisions from limited data; however, confirmatory results should not be posited when data are incomplete or confounding factors are not understood. Building reliable databases, and research with surrogate species when possible, will aid future efforts and enhance the utility of FGM assays.
KW - ACTH challenge
KW - Conservation biology
KW - Corticosterone
KW - Cortisol
KW - Fecal glucocorticoids
KW - Feces
KW - Noninvasive
KW - Physiology
KW - Stress
KW - Stress response
KW - Wildlife
UR - http://www.scopus.com/inward/record.url?scp=4444346055&partnerID=8YFLogxK
U2 - 10.1016/j.ygcen.2004.07.002
DO - 10.1016/j.ygcen.2004.07.002
M3 - Review article
AN - SCOPUS:4444346055
SN - 0016-6480
VL - 138
SP - 189
EP - 199
JO - General and Comparative Endocrinology
JF - General and Comparative Endocrinology
IS - 3
ER -