Abstract

Glucocorticoids are often measured in wildlife to assess physiological responses to environmental or ecological stress. Hair, blood, saliva, or fecal samples are generally used depending on the timescale of the stress response being investigated and species‐specific considerations. Here, we report the first use of hair samples to measure long‐term corticosterone levels in the climate‐sensitive American pika (Ochotona princeps). We validated an immunoassay‐based measurement of corticosterone extracted from hair samples and compared corticosterone estimates obtained from plasma, hair, and fecal samples of nine pikas. To demonstrate an ecological application of this technique, we characterized physiological stress in 49 pikas sampled and released at eight sites along two elevational transects. Microclimate variation was measured at each site using both ambient and subsurface temperature sensors. We used an information theoretic approach to compare support for linear, mixed‐effects models relating corticosterone estimates to microclimate, body size, and sex. Corticosterone was measured accurately in pika hair samples after correcting for the influence of sample mass on corticosterone extraction efficiency. Hair‐ and plasma‐based estimates of corticosterone were weakly correlated. The best‐supported model suggested that corticosterone was lower in larger, male pikas, and at locations with higher ambient temperatures in summer. Our results are consistent with a general negative relationship between body mass and glucocorticoid concentration observed across mammalian species, attributed to the higher mass‐specific metabolic rates of smaller bodied animals. The higher corticosterone levels in female pikas likely reflected the physiological demands of reproduction, as observed in a wide array of mammalian species. Additionally, we establish the first direct physiological evidence for thermal stress in the American pika through nonlethal sampling of corticosterone. Interestingly, our data suggest evidence for cold stress likely induced during the summer molting period. This technique should provide a useful tool to researchers wishing to assess chronic stress in climate‐sensitive mammals.

Highlights

  • Rapid environmental change represents a potential stressor and selective force on wildlife populations (Reeder & Kramer, 2005; Wingfield, Romero, & Goodman, 2001)

  • While we agree with other authors regarding the power of biological validation of GC measurements (Sheriff et al, 2011; Touma & Palme, 2005), the limited feasibility of validation must be acknowledged for some species

  • Mastromonaco et al (2014) were only able to resample 12 of the original 23 eastern chipmunks used in a biological validation of hair samples (ACTH challenge), and only three of the five samples in their experimental group exhibited elevated glucocorticoid levels

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Summary

| INTRODUCTION

Rapid environmental change represents a potential stressor and selective force on wildlife populations (Reeder & Kramer, 2005; Wingfield, Romero, & Goodman, 2001). While the direct mechanism by which GC is incorporated into hair is still unknown (Gow, Thomson, Rieder, Van Uum, & Koren, 2010), this sample source offers the potential to measure relative levels of GC over the duration of time the hair was grown, which typically encompasses several weeks or months This longer-­term record makes hair analysis a powerful approach for assessing long-­term chronic stress (Russell, Koren, Rieder, & Van Uum, 2012). We demonstrate the sensitivity of the assay protocol through validation, and we compare estimates of GC from hair with estimates of plasma GC and fecal GCM from the same individuals We apply this method to investigate relationships between hair GC, microclimate, body size, and sex over two elevational gradients to assess whether hair samples can provide direct insights related to climate-­mediated stress responses

| MATERIALS AND METHODS
Findings
| DISCUSSION
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