Abstract

To invest in energetically demanding life history stages, individuals require a substantial amount of resources. Physiological traits, particularly those related to energetics, can be useful for examining variation in life history decisions and trade‐offs because they result from individual responses to environmental variation. Leptin is a protein hormone found in mammals that is proportional to the amount of endogenous fat stores within an individual. Recently, researchers have confirmed that a mammalian leptin analogue (MLA), based on the mammalian sequence of leptin, is present with associated receptors and proteins in avian species, with an inhibitory effect on foraging and body mass gain at high circulating levels. While MLA has been both quantified and manipulated in avian species, little is currently known regarding whether plasma MLA in wild‐living species and individuals is associated with key reproductive decisions. We quantified plasma MLA in wild, Arctic‐nesting female common eiders (Somateria mollissima) at arrival on the breeding grounds and followed them to determine subsequent breeding propensity, and reproductive phenology, investment, and success. Common eiders are capital‐income breeding birds that require the accumulation of substantial fat stores to initiate laying and successfully complete incubation. We found that females with lower plasma MLA initiated breeding earlier and in a shorter period of time. However, we found no links between plasma MLA levels and breeding propensity, clutch size, or reproductive success. Although little is still known about plasma MLA, based on these results and its role in influencing foraging behaviors and condition gain, plasma MLA appears to be closely linked to reproductive timing and is therefore likely to underlie trade‐offs surrounding life history decisions.

Highlights

  • Life history trade‐offs can be generated through the constraints of allocating limited resources to multiple competing life history traits and decisions (McNamara & Houston, 1996; Stearns, 1989)

  • Leptin receptors based on mammalian sequences have been identified in multiple tissue types in chicken (Gallus gal‐ lus; Taoius et al, 2001, Paczoska‐Eliasiewicz et al, 2006, Ohkubo, Nishio, Tsurudome, Ito, & Ito, 2007), leptin protein sequences have been identified in a number of avian species (Prokop et al, 2014), and leptin gene expression has been identified in avian adipose and liver tissues (Quillfeldt, Everaert, Buyse, Masello, & Dridi, 2009; Taouis et al, 1998)

  • Little is known about plasma mammalian leptin analogue (MLA) in avian species (Cerasale et al, 2011; Kordonowy et al, 2010; Quillfeldt et al, 2009), and to date, no studies have examined how variation in plasma MLA relates to reproductive decisions, invest‐ ment, or reproductive success in wild birds

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Summary

| INTRODUCTION

Life history trade‐offs can be generated through the constraints of allocating limited resources to multiple competing life history traits and decisions (McNamara & Houston, 1996; Stearns, 1989). Leptin receptors based on mammalian sequences have been identified in multiple tissue types in chicken (Gallus gal‐ lus; Taoius et al, 2001, Paczoska‐Eliasiewicz et al, 2006, Ohkubo, Nishio, Tsurudome, Ito, & Ito, 2007), leptin protein sequences have been identified in a number of avian species (Prokop et al, 2014), and leptin gene expression has been identified in avian adipose and liver tissues (Quillfeldt, Everaert, Buyse, Masello, & Dridi, 2009; Taouis et al, 1998) Given that this trait and its associated receptors have been identified based on mammalian leptin sequences, it has been suggested that these studies have instead quantified a mammalian leptin analogue (MLA) rather than true avian leptin (Seroussi et al, 2016). TA B L E 1 Statistical summary of variables included in analyses, split by year and breeding stage, of common eider females nesting at Mitivik Island

| MATERIALS AND METHODS
Findings
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