<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en"><id>http://publicationslist.org/data/sarah.pryke/atom.xml</id><title>Sarah Pryke's Publications List</title>
<link rel="self" type="application/atom+xml" href="http://publicationslist.org/data/sarah.pryke/atom.xml"/><link rel="alternate" type="text/html" href="http://publicationslist.org/sarah.pryke"/><author><name>Sarah Pryke</name><uri>http://publicationslist.org/sarah.pryke</uri></author><icon>$basepathfavicon.ico</icon><subtitle>Recent additions to Sarah Pryke's PublicationsList.org page</subtitle><logo>http://publicationslist.org/publications.png</logo><updated>2010-11-22T22:42:43Z</updated>

<entry>
<id>http://publicationslist.org/sarah.pryke/refid14</id>
<updated>2010-11-22T22:42:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid14'/>
<title type='html'>Sex chromosome linkage of mate preferences and color signal maintains assortative mating between interbreeding finch morphs</title>
<summary type='html'>Assortative mating is a key aspect in the speciation process because it is important for both initial divergence and maintenance of distinct species. However, it remains a challenge to explain how assortative mating evolves when diverging populations are undergoing gene flow (e g., during hybridization) Here I experimentally test how assortative mating is maintained with frequent gene flow between...&lt;br/&gt;&lt;br/&gt;S R Pryke (2010)  &lt;i&gt;EVOLUTION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 64: 5 1301-1310&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid13</id>
<updated>2010-11-22T22:28:47Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid13'/>
<title type='html'>Nest-site utilisation and niche overlap in two sympatric, cavity-nesting finches</title>
<summary type='html'>Determining the relative access of a species to critical limiting resources requires knowledge of the spectrum of their resource utilisation ( niche space) and that of potential competitors, and the frequency distribution of resources in the environment. We used this theoretical framework to assess the relative access to nesting sites and the potential for interspecific competition between two sym...&lt;br/&gt;&lt;br/&gt;J Brazill-Boast, S R Pryke, S C Griffith (2010)  &lt;i&gt;EMU&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 110: 2 170-177&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid12</id>
<updated>2010-11-22T22:40:47Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid12'/>
<title type='html'>Pronounced within-individual plasticity in sperm morphometry across social environments</title>
<summary type='html'>Sperm morphometry (i.e., size and shape) and function are important determinants of male reproductive success and are thought to be under stabilizing selection. However, recent studies suggest that sperm morphometry can be a phenotypically plastic trait, which can be adjusted to varying conditions. We tested whether different behavioral strategies in aggression between aggressive red and nonaggres...&lt;br/&gt;&lt;br/&gt;S Immler, S R Pryke, T R Birkhead, S C Griffith (2010)  &lt;i&gt;EVOLUTION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 64: 6 1634-1643&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid11</id>
<updated>2010-11-22T22:37:38Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid11'/>
<title type='html'>Females use multiple mating and genetically loaded sperm competition to target compatible genes</title>
<summary type='html'>Individuals in socially monogamous species may participate in copulations outside of the pair bond, resulting in extra-pair offspring. Although males benefit from such extra-pair behavior if they produce more offspring, the adaptive function of infidelity to females remains elusive. Here we show that female participation in extra-pair copulations, combined with a genetically loaded process of sper...&lt;br/&gt;&lt;br/&gt;S R Pryke, L A Rollins, S C Griffith (2010)  &lt;i&gt;SCIENCE&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 329: 5994 964-967&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid16</id>
<updated>2010-11-22T22:34:44Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid16'/>
<title type='html'>Low level of extrapair parentage in wild zebra finches</title>
<summary type='html'>The captive zebra finch, Taeniopygia guttata, has become one of the key vertebrate model systems for studying a range of behavioural, physiological and neurological phenomena. In particular, this species has played a key role in developing our understanding of sexual selection and sperm competition. In contrast with the large number of studies using domesticated zebra finches, relatively few studi...&lt;br/&gt;&lt;br/&gt;S C Griffith, C E Holleley, M M Mariette, S R Pryke, N Svedin (2010)  &lt;i&gt;ANIMAL BEHAVIOUR&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 79: 2 261-264&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid15</id>
<updated>2010-11-22T22:34:32Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid15'/>
<title type='html'>Maternal adjustment of parental effort in relation to mate compatibility affects offspring development</title>
<summary type='html'>Theory predicts that parents should adjust reproductive investment in a current breeding attempt by considering the relative fitness benefits of current and future reproductive attempts. Empirical tests, however, have proved problematic because of the difficulties in isolating variables that yield clear and predictable fitness returns to individuals and because partner compensation in socially mon...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2010)  &lt;i&gt;BEHAVIORAL ECOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 21: 2 226-232&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid17</id>
<updated>2010-11-22T22:35:44Z</updated>
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<title type='html'>Socially mediated trade-offs between aggression and parental effort in competing color morphs</title>
<summary type='html'>Individuals often face trade-offs between investment in parental care and alternative investments of time, energy, and resources into other life-history components, such as dominance, attractiveness, and health. Selection is thought to promote the optimal balance between the costs and the benefits of these conflicting activities by favoring individuals that adopt different tactics to maximize thei...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2009)  &lt;i&gt;AMERICAN NATURALIST&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 174: 4 455-464&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid18</id>
<updated>2010-11-22T22:28:47Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid18'/>
<title type='html'>The historical frequency of head-colour morphs in the Gouldian Finch (Erythrura gouldiae)</title>
<summary type='html'>The endangered Gouldian Finch (Erythura gouldiae) possesses a genetic colour polymorphism in the form of three genetically determined head-colours (yellow, black and red) that coexist in the same population. The spatial and temporal pattern of morph ratios within this species provides insight into the selective pressures acting on and maintaining the different forms. To investigate spatial and tem...&lt;br/&gt;&lt;br/&gt;A J Gilby, S R Pryke, S C Griffith (2009)  &lt;i&gt;EMU&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 109: 3 222-229&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid20</id>
<updated>2010-11-22T22:35:59Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid20'/>
<title type='html'>Is red an innate or learned signal of aggression and intimidation?</title>
<summary type='html'>Red coloration has been associated with dominance and aggression in a number of animals. However, it is unclear whether the increased aggression of red individuals or the avoidance of red opponents is an intrinsic or learnt response. By experimentally controlling for genetic and environmental effects, I tested for innate competitive differences and red-enhanced contest success in sexually immature...&lt;br/&gt;&lt;br/&gt;S R Pryke (2009)  &lt;i&gt;ANIMAL BEHAVIOUR&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 78: 2 393-398&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid21</id>
<updated>2010-11-22T22:37:08Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid21'/>
<title type='html'>Genetic incompatibility drives sex allocation and maternal investment in a polymorphic finch</title>
<summary type='html'>Genetic compatibility may drive individual mate choice decisions because of predictable fitness effects associated with breeding with incompatible partners. In Gouldian finches (Erythrura gouldiae), females paired with genetically incompatible males of alternative color morphs overproduce sons, presumably to reduce investment in inviable daughters. We also observed a reduced overall investment in ...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2009)  &lt;i&gt;SCIENCE&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 323: 5921 1605-1607&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid22</id>
<updated>2010-11-22T22:40:32Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid22'/>
<title type='html'>Postzygotic genetic incompatibility between sympatric color morphs</title>
<summary type='html'>Alternative genetically determined color morphs within a population or species are believed to successfully interbreed within a population. However, the occurrence of prezygotic or ecological selection in a number of polymorphic systems may lead to nonrandom mating and prevent genetic morphs from fully interbreeding. Here we show that postzygotic incompatibility significantly limits gene flow betw...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2009)  &lt;i&gt;EVOLUTION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 63: 3 793-798&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid23</id>
<updated>2010-11-22T22:29:09Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid23'/>
<title type='html'>Use of nest-boxes by the Zebra Finch (Taeniopygia guttata) : implications for reproductive success and research</title>
<summary type='html'>Nest-boxes have been used widely and for many decades in Europe and North America to increase avian reproductive success in species management and conservation programs and to increase the amenability and efficiency with which a species can be studied. Here we describe the establishment of a breeding population of Zebra Finches using nest-boxes in semi-arid, far-western New South Wales, over three...&lt;br/&gt;&lt;br/&gt;S C Griffith, S R Pryke, M Mariette (2008)  &lt;i&gt;EMU&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 108: 4 311-319&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid24</id>
<updated>2010-11-22T22:35:01Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid24'/>
<title type='html'>Female preferences for long tails constrained by species recognition in short-tailed red bishops</title>
<summary type='html'>Sexual selection and species recognition both play important roles in mate choice. Typically, females use the relative expression of male sexual traits to select high-quality or attractive mates (sexual selection) of the same species (species recognition). However, when the variation in male trait expression of both conspecifics and heterospecifics overlaps, females potentially face a conflict bet...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson (2008)  &lt;i&gt;BEHAVIORAL ECOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 19: 6 1116-1121&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid26</id>
<updated>2010-11-22T22:36:25Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid26'/>
<title type='html'>The relative role of male vs. female mate choice in maintaining assortative pairing among discrete colour morphs</title>
<summary type='html'>Mate choice has important evolutionary consequences because it influences assortative mating and the level of genetic variation maintained within populations. In species with genetically determined polymorphisms, nonrandom mate choice may affect the evolutionary stability and maintenance (or loss) of alternative phenotypes. We examined the mating pattern in the colour polymorphic Gouldian finch (E...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2007)  &lt;i&gt;JOURNAL OF EVOLUTIONARY BIOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 20: 4 1512-1521&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid27</id>
<updated>2010-11-22T22:36:37Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid27'/>
<title type='html'>Fiery red heads : female dominance among head color morphs in the Gouldian finch</title>
<summary type='html'>Although the evolution of genetic color polymorphisms has received much theoretical interest, few empirical studies have investigated the adaptive function of alternative color morphs. Furthermore, most studies have focused almost exclusively on the evolution and adaptive expression of male coloration, leaving the role of conspicuous female coloration largely unknown. Using the color polymorphic G...&lt;br/&gt;&lt;br/&gt;S R Pryke (2007)  &lt;i&gt;BEHAVIORAL ECOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 18: 3 621-627&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid25</id>
<updated>2010-11-22T22:36:12Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid25'/>
<title type='html'>Frequency-dependent physiological trade-offs between competing colour morphs</title>
<summary type='html'>Evolutionary theory suggests that alternative colour morphs (i. e. genetically controlled phenotypes) may derive similar fitness under frequency-dependent selection. Here we experimentally demonstrate opposing effects of frequency-dependent social environments on plasma hormone levels ( testosterone and corticosterone) and immune function between red-and black-headed male morphs of the Gouldian fi...&lt;br/&gt;&lt;br/&gt;S R Pryke, L B Astheimer, W A Buttemer, S C Griffith (2007)  &lt;i&gt;BIOLOGY LETTERS&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 3: 5 494-497&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid28</id>
<updated>2010-11-22T22:37:59Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid28'/>
<title type='html'>Red dominates black : agonistic signalling among head morphs in the colour polymorphic Gouldian finch</title>
<summary type='html'>Recent sexual selection studies on the evolution of bird colouration have mainly focused on signals with a high level of condition-dependent variation, with much less attention given to colour traits whose expression is genetically controlled. Here, we experimentally tested the relative importance of a genetic colour polymorphism in determining male dominance in the Gouldian finch (Erythrura gould...&lt;br/&gt;&lt;br/&gt;S R Pryke, S C Griffith (2006)  &lt;i&gt;PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 273: 1589 949-957&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid29</id>
<updated>2010-11-22T22:38:10Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid29'/>
<title type='html'>Experimental evidence for female choice and energetic costs of male tail elongation in red-collared widowbirds</title>
<summary type='html'>The black nuptial plumage of the highly polygynous male red-collared widowbird (Euplectes ardens) comprises a red carotenoid-based collar patch and a long graduated tail (c. 22 em). Tail length was the strongest predictor of male mating success in a previous selection analysis, motivating this experimental test of the relative importance of tail plumes in male contest competition and female choice...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson (2005)  &lt;i&gt;BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 86: 1 35-43&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid1</id>
<updated>2010-11-22T22:38:23Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid1'/>
<title type='html'>Female nest dispersion and breeding biology of polygynous Red-collared Widowbirds (Euplectes ardens)</title>
<summary type='html'>We explored characteristics and patterns of nest distribution, and their putative costs and benefits to breeding females, in polygynous Red-collared Widowbirds (Euplectes ardens). Red-collared Widowbirds differ from most other Euplectes species, in that male nest-building is reduced to simple nest-rings used in courtship; females alone position and build nests in the territories. Females used only...&lt;br/&gt;&lt;br/&gt;S R Pryke, M J Lawes (2004)  &lt;i&gt;AUK&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 121: 4 1226-1237&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid4</id>
<updated>2010-11-22T22:25:30Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid4'/>
<title type='html'>Carotenoid-based status signalling in red-shouldered widowbirds (Euplectes axillaris) : epaulet size and redness affect captive and territorial competition</title>
<summary type='html'>In breeding plumage, the African male red-shouldered widowbirds (Euplectes axillaris) are black except for red carotenoid-based epaulets ('shoulder patches'), similar to the well-studied American red-winged blackbirds (Agelailis phoeniceus). To experimentally test the signal function of the red epaulets in male red-shouldered widowbirds, we manipulated epaulet colour and size (within natural varia...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson (2003)  &lt;i&gt;BEHAVIORAL ECOLOGY AND SOCIOBIOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 53: 6 393-401&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid3</id>
<updated>2010-11-22T22:38:53Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid3'/>
<title type='html'>Quality of remnant indigenous grassland linkages for adult butterflies (Lepidoptera) in an afforested African landscape</title>
<summary type='html'>Retention of interconnected, remnant grassland linkages is proposed here to reduce the adverse effects of alien pine afforestation in Afromontane grasslands. Adult butterflies were sampled at 38 grassland sites, representing increasing levels of disturbance both within the afforested area and outside it. Butterfly species richness and abundance in the lesser disturbed grassland remnants within the...&lt;br/&gt;&lt;br/&gt;S R Pryke, M J Samways (2003)  &lt;i&gt;BIODIVERSITY AND CONSERVATION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 12: 10 1985-2004&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid2</id>
<updated>2010-11-22T22:38:36Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid2'/>
<title type='html'>Carotenoid-based epaulettes reveal male competitive ability : experiments with resident and floater red-shouldered widowbirds</title>
<summary type='html'>Many birds display carotenoid-based ornaments, which are typically considered to be honest indicators of individual health and condition. Experimental work on male red-shouldered widowbirds, Euplectes axillaris, has demonstrated a function of the carotenoid-based epaulettes in male contests and territory acquisition. Using two experiments, we investigated whether the natural variation in this colo...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson (2003)  &lt;i&gt;ANIMAL BEHAVIOUR&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 66:  217-224&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid5</id>
<updated>2010-11-22T22:39:06Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid5'/>
<title type='html'>Multiple receivers, multiple ornaments, and a trade-off between agonistic and epigamic signaling in a widowbird</title>
<summary type='html'>Sexual displays often involve several different ornamental traits. Yet most indicator models of sexual selection based on a single receiver (usually a choosy female) find that multiple handicap signals should be unstable. Here we study reasons for this contradiction, analyzing signal function, signal content, and trade-offs between signals in the polygynous red-collared widowbird Euplectes ardens....&lt;br/&gt;&lt;br/&gt;S Andersson, S R Pryke, J Ornborg, M J Lawes, M Andersson (2002)  &lt;i&gt;AMERICAN NATURALIST&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 160: 5 683-691&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid7</id>
<updated>2010-11-22T22:39:37Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid7'/>
<title type='html'>Carotenoid status signaling in captive and wild red-collared widowbirds : independent effects of badge size and color</title>
<summary type='html'>Carotenoid-based plumage ornaments are typically considered to be sexually selected traits, functioning as honest condition-dependent signals of phenotypic quality, but few studies have addressed the function of carotenoid color variation in male contest competition. Using two experiments, we investigated the status signaling function of the variable (ranging from yellow to red) carotenoid throat ...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson, M J Lawes, S E Piper (2002)  &lt;i&gt;BEHAVIORAL ECOLOGY&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 13: 5 622-631&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid6</id>
<updated>2010-11-22T22:39:18Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid6'/>
<title type='html'>A generalized female bias for long tails in a short-tailed widowbird</title>
<summary type='html'>Tail elongation in the polygynous widowbirds (Euplectes spp.) has evoked both adaptive and non-adaptive explanations. Female choice has been shown in the three longest tailed species (20-50 cm), whereas an agonistic function was proposed for a medium-tailed (10 cm) widowbird. To test the generality and directionality of sexual selection on tail length in widowbirds, we experimentally investigated ...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson (2002)  &lt;i&gt;PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 269: 1505 2141-2146&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid10</id>
<updated>2010-11-22T22:40:11Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid10'/>
<title type='html'>Width of grassland linkages for the conservation of butterflies in South African afforested areas</title>
<summary type='html'>Flight behaviours of 23 butterfly species were mapped to establish the effect of both pine afforestation and different-sized grassland linkages on localised butterfly movements. Blocks of pine trees caused most butterflies to change direction and move away from the pine edge. Only four species crossed the grassland/pine edge, and of these, only two flew farther than 20 m into the pine forest. The ...&lt;br/&gt;&lt;br/&gt;S R Pryke, M J Samways (2001)  &lt;i&gt;BIOLOGICAL CONSERVATION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 101: 1 85-96&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid8</id>
<updated>2010-11-22T22:39:48Z</updated>
<link rel='alternate' type='text/html' href='http://publicationslist.org/sarah.pryke#refid8'/>
<title type='html'>Agonistic carotenoid signalling in male red-collared widowbirds : aggression related to the colour signal of both the territory owner and model intruder</title>
<summary type='html'>Carotenoid colour displays are widely assumed to be honest indicators of individual health or quality, primarily in mate attraction. Here we show that sexually dimorphic carotenoid ornamentation functions as an agonistic signal in male red-collared widowbirds, Euplectes ardens. Mounted mate models differing (within natural limits) in the intensity of carotenoid signalling were presented to wild re...&lt;br/&gt;&lt;br/&gt;S R Pryke, M J Lawes, S Andersson (2001)  &lt;i&gt;ANIMAL BEHAVIOUR&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 62:  695-704&lt;br/&gt;</summary>
</entry>
<entry>
<id>http://publicationslist.org/sarah.pryke/refid9</id>
<updated>2010-11-22T22:40:00Z</updated>
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<title type='html'>Sexual selection of multiple handicaps in the red-collared widowbird : Female choice of tail length but not carotenoid display</title>
<summary type='html'>Although sexual selection through female choice explains exaggerated male ornaments in many species, the evolution of the multicomponent nature of most sexual displays remains poorly understood. Theoretical models suggest that handicap signaling should converge on a single most informative quality indicator, whereas additional signals are more likely to be arbitrary Fisherian traits, amplifiers, o...&lt;br/&gt;&lt;br/&gt;S R Pryke, S Andersson, M J Lawes (2001)  &lt;i&gt;EVOLUTION&lt;/i&gt; &lt;i&gt;&lt;/i&gt; &lt;i&gt;&lt;/i&gt; 55: 7 1452-1463&lt;br/&gt;</summary>
</entry>
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