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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Does Foraging Performance Change with Age in Female Little Penguins (<italic>Eudyptula minor</italic>
)?</title>
<author><name sortKey="Zimmer, Ilka" sort="Zimmer, Ilka" uniqKey="Zimmer I" first="Ilka" last="Zimmer">Ilka Zimmer</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ropert Coudert, Yan" sort="Ropert Coudert, Yan" uniqKey="Ropert Coudert Y" first="Yan" last="Ropert-Coudert">Yan Ropert-Coudert</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Kato, Akiko" sort="Kato, Akiko" uniqKey="Kato A" first="Akiko" last="Kato">Akiko Kato</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3"><addr-line>National Institute of Polar Research, Tokyo, Japan</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ancel, Andre" sort="Ancel, Andre" uniqKey="Ancel A" first="Andre" last="Ancel">Andre Ancel</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Chiaradia, Andre" sort="Chiaradia, Andre" uniqKey="Chiaradia A" first="Andre" last="Chiaradia">Andre Chiaradia</name>
<affiliation><nlm:aff id="aff4"><addr-line>Research Department, Phillip Island Nature Park, Cowes, Victoria, Australia</addr-line>
</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">21283573</idno>
<idno type="pmc">3026794</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026794</idno>
<idno type="RBID">PMC:3026794</idno>
<idno type="doi">10.1371/journal.pone.0016098</idno>
<date when="2011">2011</date>
<idno type="wicri:Area/Pmc/Corpus">002B97</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">002B97</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Does Foraging Performance Change with Age in Female Little Penguins (<italic>Eudyptula minor</italic>
)?</title>
<author><name sortKey="Zimmer, Ilka" sort="Zimmer, Ilka" uniqKey="Zimmer I" first="Ilka" last="Zimmer">Ilka Zimmer</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ropert Coudert, Yan" sort="Ropert Coudert, Yan" uniqKey="Ropert Coudert Y" first="Yan" last="Ropert-Coudert">Yan Ropert-Coudert</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Kato, Akiko" sort="Kato, Akiko" uniqKey="Kato A" first="Akiko" last="Kato">Akiko Kato</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff3"><addr-line>National Institute of Polar Research, Tokyo, Japan</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ancel, Andre" sort="Ancel, Andre" uniqKey="Ancel A" first="Andre" last="Ancel">Andre Ancel</name>
<affiliation><nlm:aff id="aff1"><addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
<affiliation><nlm:aff id="aff2"><addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Chiaradia, Andre" sort="Chiaradia, Andre" uniqKey="Chiaradia A" first="Andre" last="Chiaradia">Andre Chiaradia</name>
<affiliation><nlm:aff id="aff4"><addr-line>Research Department, Phillip Island Nature Park, Cowes, Victoria, Australia</addr-line>
</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">PLoS ONE</title>
<idno type="eISSN">1932-6203</idno>
<imprint><date when="2011">2011</date>
</imprint>
</series>
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</sourceDesc>
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<profileDesc><textClass></textClass>
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</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Age-related changes in breeding performance are likely to be mediated through changes in parental foraging performance. We investigated the relationship of foraging performance with age in female little penguins at Phillip Island, Australia, during the guard phase of the 2005 breeding season. Foraging parameters were recorded with accelerometers for birds grouped into three age-classes: (1) young, (2) middle age and (3) old females. We found the diving behaviour of middle-aged birds differed from young and old birds. The dive duration of middle age females was shorter than that of young and old birds while their dive effort (measure for dive and post-dive duration relation) was lower than that of young ones, suggesting middle-aged birds were in better physical condition than other ones. There was no difference in prey pursuit frequency or duration between age classes, but in the hunting tactic. Females pursued more prey around and after reaching the maximum depth of dives the more experienced they were (old > middle age > young), an energy saving hunting tactic by probably taking advantage of up-thrust momentum. We suggest middle age penguins forage better than young or old ones because good physical condition and foraging experience could act simultaneously.</p>
</div>
</front>
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<author><name sortKey="Stahler, Dr" uniqKey="Stahler D">DR Stahler</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gurven, M" uniqKey="Gurven M">M Gurven</name>
</author>
<author><name sortKey="Kaplan, H" uniqKey="Kaplan H">H Kaplan</name>
</author>
<author><name sortKey="Gutierrez, M" uniqKey="Gutierrez M">M Gutierrez</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Nisbet, I" uniqKey="Nisbet I">I Nisbet</name>
</author>
<author><name sortKey="Apanius, V" uniqKey="Apanius V">V Apanius</name>
</author>
<author><name sortKey="Friar, Ms" uniqKey="Friar M">MS Friar</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Bunce, A" uniqKey="Bunce A">A Bunce</name>
</author>
<author><name sortKey="Ward, Si" uniqKey="Ward S">SI Ward</name>
</author>
<author><name sortKey="Norman, Fi" uniqKey="Norman F">FI Norman</name>
</author>
</analytic>
</biblStruct>
</listBibl>
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<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
  <front><journal-meta><journal-id journal-id-type="nlm-ta">PLoS One</journal-id>
<journal-id journal-id-type="publisher-id">plos</journal-id>
<journal-id journal-id-type="pmc">plosone</journal-id>
<journal-title-group><journal-title>PLoS ONE</journal-title>
</journal-title-group>
<issn pub-type="epub">1932-6203</issn>
<publisher><publisher-name>Public Library of Science</publisher-name>
<publisher-loc>San Francisco, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">21283573</article-id>
<article-id pub-id-type="pmc">3026794</article-id>
<article-id pub-id-type="publisher-id">PONE-D-10-05053</article-id>
<article-id pub-id-type="doi">10.1371/journal.pone.0016098</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2"><subject>Biology</subject>
<subj-group><subject>Ecology</subject>
<subj-group><subject>Behavioral Ecology</subject>
<subject>Coastal Ecology</subject>
<subject>Ecophysiology</subject>
<subject>Marine Ecology</subject>
</subj-group>
</subj-group>
<subj-group><subject>Evolutionary Biology</subject>
<subj-group><subject>Aging</subject>
<subject>Animal Behavior</subject>
<subject>Behavioral Ecology</subject>
</subj-group>
</subj-group>
<subj-group><subject>Marine Biology</subject>
<subj-group><subject>Coastal Ecology</subject>
<subject>Marine Ecology</subject>
</subj-group>
</subj-group>
<subj-group><subject>Zoology</subject>
<subj-group><subject>Animal Behavior</subject>
<subject>Ornithology</subject>
</subj-group>
</subj-group>
</subj-group>
</article-categories>
<title-group><article-title>Does Foraging Performance Change with Age in Female Little Penguins (<italic>Eudyptula minor</italic>
)?</article-title>
<alt-title alt-title-type="running-head">Age-Related Changes in Foraging Performance</alt-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Zimmer</surname>
<given-names>Ilka</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ropert-Coudert</surname>
<given-names>Yan</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
<xref ref-type="corresp" rid="cor1"><sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kato</surname>
<given-names>Akiko</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ancel</surname>
<given-names>Andre</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Chiaradia</surname>
<given-names>Andre</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup>
</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label>
<addr-line>Université de Strasbourg, IPHC, Strasbourg, France</addr-line>
</aff>
<aff id="aff2"><label>2</label>
<addr-line>CNRS, UMR7178, Strasbourg, France</addr-line>
</aff>
<aff id="aff3"><label>3</label>
<addr-line>National Institute of Polar Research, Tokyo, Japan</addr-line>
</aff>
<aff id="aff4"><label>4</label>
<addr-line>Research Department, Phillip Island Nature Park, Cowes, Victoria, Australia</addr-line>
</aff>
<contrib-group><contrib contrib-type="editor"><name><surname>Peter</surname>
<given-names>Hans-Ulrich</given-names>
</name>
<role>Editor</role>
<xref ref-type="aff" rid="edit1"></xref>
</contrib>
</contrib-group>
<aff id="edit1">Institute of Ecology, Germany</aff>
<author-notes><corresp id="cor1">* E-mail: <email>yan.ropert-coudert@c-strasbourg.fr</email>
</corresp>
<fn fn-type="con"><p>Conceived and designed the experiments: IZ YRC AK AC. Performed the experiments: YRC AK AC. Analyzed the data: IZ AK. Wrote the paper: IZ YRC AK AC AA.</p>
</fn>
</author-notes>
<pub-date pub-type="collection"><year>2011</year>
</pub-date>
<pub-date pub-type="epub"><day>25</day>
<month>1</month>
<year>2011</year>
</pub-date>
<volume>6</volume>
<issue>1</issue>
<elocation-id>e16098</elocation-id>
<history><date date-type="received"><day>17</day>
<month>11</month>
<year>2010</year>
</date>
<date date-type="accepted"><day>10</day>
<month>12</month>
<year>2010</year>
</date>
</history>
<permissions><copyright-statement>Zimmer et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</copyright-statement>
</permissions>
<abstract><p>Age-related changes in breeding performance are likely to be mediated through changes in parental foraging performance. We investigated the relationship of foraging performance with age in female little penguins at Phillip Island, Australia, during the guard phase of the 2005 breeding season. Foraging parameters were recorded with accelerometers for birds grouped into three age-classes: (1) young, (2) middle age and (3) old females. We found the diving behaviour of middle-aged birds differed from young and old birds. The dive duration of middle age females was shorter than that of young and old birds while their dive effort (measure for dive and post-dive duration relation) was lower than that of young ones, suggesting middle-aged birds were in better physical condition than other ones. There was no difference in prey pursuit frequency or duration between age classes, but in the hunting tactic. Females pursued more prey around and after reaching the maximum depth of dives the more experienced they were (old > middle age > young), an energy saving hunting tactic by probably taking advantage of up-thrust momentum. We suggest middle age penguins forage better than young or old ones because good physical condition and foraging experience could act simultaneously.</p>
</abstract>
<counts><page-count count="6"></page-count>
</counts>
</article-meta>
</front>
<body><sec id="s1"><title>Introduction</title>
<p>In vertebrates, survival and reproductive performance generally increase with age <xref ref-type="bibr" rid="pone.0016098-CluttonBrock1">[1]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Newton1">[2]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Forslund1">[3]</xref>
. However, for long-lived species, this increase is often followed by stabilization in survival and reproductive performance at middle age, then a decline in old age, e.g. <xref ref-type="bibr" rid="pone.0016098-CluttonBrock1">[1]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Forslund1">[3]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Weimerskirch1">[4]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Kirkwood1">[5]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Reid1">[6]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Nisbet1">[7]</xref>
. This decline, or senescence, involves a loss of physiological functions and is accompanied by decreasing fertility and increased risks of mortality with advancing age <xref ref-type="bibr" rid="pone.0016098-Kirkwood1">[5]</xref>
.</p>
<p>Age-related changes in breeding performance are known to be the result of experience accumulated over time in several aspects of breeding in birds i.e. laying date, nest site selection, foraging <xref ref-type="bibr" rid="pone.0016098-Prt1">[8]</xref>
. The improvement in breeding success is likely to be mediated through improvement in individual foraging ability, which would correspond to an enhanced capacity to provide for the offspring <xref ref-type="bibr" rid="pone.0016098-Stearns1">[9]</xref>
. Foraging involves a hierarchical process of decision-making <xref ref-type="bibr" rid="pone.0016098-Wunderle1">[10]</xref>
, including choosing appropriate habitat/patch; searching for or/and recognizing suitable prey; and capturing them. At each of these stages, young individuals may experience deficiencies, i.e. less or lower energetic food supply to their offspring. Improved foraging performance at older ages has been explained by an increase in foraging efficiency with experience in birds <xref ref-type="bibr" rid="pone.0016098-Daunt1">[11]</xref>
, related to improvements in foraging ability <xref ref-type="bibr" rid="pone.0016098-Daunt2">[12]</xref>
, diet choice <xref ref-type="bibr" rid="pone.0016098-Rutz1">[13]</xref>
 and access to better foraging territories <xref ref-type="bibr" rid="pone.0016098-Prt2">[14]</xref>
.</p>
<p>Seabirds usually have long life spans and slow aging rates in relation to their body size <xref ref-type="bibr" rid="pone.0016098-Holmes1">[15]</xref>
, which makes them optimal models for studying aging processes. Seabird studies of the influence of age on foraging performance are challenging because: 1) long-term demographic datasets are scarce <xref ref-type="bibr" rid="pone.0016098-Wooller1">[16]</xref>
 and, as in all age-related studies, it is difficult to have a various sample size in age up to old age and 2) at-sea behaviour can only be recorded by remote sensing technologies compared to studies on age-related breeding performance on land. Hence only few studies have yet investigated the influence of age on seabird foraging performance in the wild <xref ref-type="bibr" rid="pone.0016098-Daunt1">[11]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Limmer1">[17]</xref>
.</p>
<p>In the present study we used an avian long-lived marine top predator, the little penguin (<italic>Eudyptula minor</italic>
) as a model to examine age-related foraging behaviour since age-related differences in breeding performance are well documented <xref ref-type="bibr" rid="pone.0016098-Nisbet1">[7]</xref>
. We investigated whether age affects penguin foraging performance by examining diving and hunting behaviour in relation to age.</p>
</sec>
<sec sec-type="methods" id="s2"><title>Methods</title>
<sec id="s2a"><title>Ethics Statement</title>
<p>Field work protocol was approved by the ethics committee of the Phillip Island Nature Park with a research permit issued by the Department of Sustainability and Environment of Victoria, Australia.</p>
</sec>
<sec id="s2b"><title>Fieldwork</title>
<p>This study was conducted on the little penguin breeding colony situated at Phillip Island Nature Parks (38°31′S, 145°09′E), Victoria, Australia. In order to reduce the variability of other influencing factors which may confound the effect of age on foraging performance, we investigated only breeding females at guard phase during one single season. During guard phase, breeding little penguins make one-day foraging trips since they alternate daily to attend small chicks of up to three weeks old <xref ref-type="bibr" rid="pone.0016098-Chiaradia1">[18]</xref>
. Thus age-related differences in foraging performance would not be masked by foraging trip duration and sexual differences <xref ref-type="bibr" rid="pone.0016098-Bethge1">[19]</xref>
.</p>
<p>From November to December 2005 we equipped 19 breeding females with miniature accelerometers to monitor their foraging activity (M190-D2GT, Little Leonardo, Tokyo, Japan). The mean body weight of females was 1042±77 (SD) g. Depth was measured every second with an accuracy of ±1 m and a resolution of 0.05 m. Acceleration was measured along the longitudinal body axis and the dorso-ventral axis between 0 and ±30 m s<sup>−2</sup>
 at 32 Hz. This sensor measured both dynamic acceleration (i.e., vibration) and static acceleration (i.e., gravity). The accelerometers were cylindrically shaped four-channel data loggers with domed heads (15×53 mm, 17 g) that accounted to 3.4% of the penguins' frontal area <xref ref-type="bibr" rid="pone.0016098-RopertCoudert1">[20]</xref>
. In stream-lined marine animals such as penguins it is the size of this frontal area which may influence the foraging behaviour <xref ref-type="bibr" rid="pone.0016098-Bannasch1">[21]</xref>
, including little penguins <xref ref-type="bibr" rid="pone.0016098-RopertCoudert1">[20]</xref>
. Therefore, we followed recommendations to reduce possible logger influences in this study. Females were caught in their nest boxes and the accelerometer was attached on the lower back of the bird to reduce hydrodynamic drag <xref ref-type="bibr" rid="pone.0016098-Bannasch1">[21]</xref>
 using waterproof tape preserving the integrity of the plumage <xref ref-type="bibr" rid="pone.0016098-Wilson1">[22]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Wilson2">[23]</xref>
. This method further allowed us to minimize the handling time, attaching and retrieving the logger in less than 5 min before birds were returned to their nest-boxes. After a single foraging trip, birds were recaptured in their nest boxes and the logger and tape were removed before birds were released. The bird's breeding activities were then monitored until chicks fledged or died. Penguins were marked with electronic transponders (Allflex, Australia Pty Ltd, Capalaba, Queensland, Australia, <ext-link ext-link-type="uri" xlink:href="http://www.allflex.com.au">www.allflex.com.au</ext-link>
) either before fledging or at their first sighting in this study area of the Phillip Island breeding colony to monitor penguins' arrivals and departures through an automated penguin-monitoring system installed on their natural path <xref ref-type="bibr" rid="pone.0016098-Chiaradia2">[24]</xref>
. The transponders (23×3.8 mm), supplied in individually packed sterilized needles, were injected under the loose skin on the back of the penguin's neck and the wound was closed with surgical glue (Vetbond™, 3 M worldwide, <ext-link ext-link-type="uri" xlink:href="http://www.3m.com">www.3m.com</ext-link>
) to prevent infection and transponder loss. Animal contact was kept to a minimum; the transponder injection taking less than 1 min. At Phillip Island, transponders have been used since 1994 and no ill effects have been reported, i.e. no tissue damage or transponder migration from injection site <xref ref-type="bibr" rid="pone.0016098-Daniel1">[25]</xref>
. Field work protocol was approved by the Animal Experimentation Ethics Committee, Phillip Island Nature Park (PINP AEEC, number PINP AEEC 2.2004) with a research permit issued by the Department of Sustainability and Environment, Flora and Fauna (number 10003419) of Victoria, Australia. In accordance with recommendations by these committees, procedures were adopted to minimise the impact of sampling protocol. These include: i) only marked birds with known breeding status were targeted to avoid repeated sampling on the same individuals in the same breeding season. No individual bird were sampled more than once in a breeding season; ii) only females over 800 g; iii) Birds were sampled on the point of collection to reduce handling and retaining time; iv) Procedures were ceased immediately if serious signs of distress were detected which is indicated by abnormal breathing and over-dilated pupils during handling – we did not face with any such case in this study; v) Birds were released immediately after the logger was attached. Procedure took less than 5 minutes; vi) Information on each sampled bird were entered in a database to prevent re-sampling of the same bird.</p>
<p>All studied females were of known age. Their age ranged from three to fourteen years. Age could not be treated as continuous variable since the sample size per year was unequal and severely reduced in some years. We then treated age as categorical variable by grouping them in three age classes following <xref ref-type="bibr" rid="pone.0016098-Daniel1">[25]</xref>
: class 1 for young birds (3 and 4 years, n = 7), class 2 for middle-aged birds (5 to 10 years, n = 7) and class 3 for old birds (11 to 14 years, n = 5). These three age groups coincide with the curvilinear relationship between age and breeding success <xref ref-type="bibr" rid="pone.0016098-Nisbet1">[7]</xref>
. By grouping the data, we could try to detect non-linear relationships which we would not be possible with continuous analysis due the limitations of our dataset.</p>
</sec>
<sec id="s2c"><title>Dive analysis</title>
<p>The dive analysis was conducted on depth and acceleration data using IGOR Pro (Wavemetrics Inc., USA, 2008, Version 6.04). Data were corrected for surface drift and according to the resolution of the loggers only dives >1 m were considered for analysis. The software analyzed dives sequentially (dive by dive analysis), writing a number of parameters for each dive into an output file. These were: maximum dive depth (m), total dive and post-dive duration (s), descent, bottom and ascent duration (s), and the number and duration of dashes (s), as a proxy of the prey pursuit <xref ref-type="bibr" rid="pone.0016098-RopertCoudert2">[26]</xref>
, <xref ref-type="bibr" rid="pone.0016098-RopertCoudert3">[27]</xref>
.</p>
<p>A dive started and ended when birds dived from and returned to the water surface. The start and end of bottom phases were defined as the first and last time in a dive when the rate of change of depth became <0.25 m.s<sup>−1</sup>
 <xref ref-type="bibr" rid="pone.0016098-Kato1">[28]</xref>
. The post-dive duration, representing the recovery time between dives at the surface, was considered when ≤100 s <xref ref-type="bibr" rid="pone.0016098-Chiaradia3">[29]</xref>
. Flipper beats were apparent in the acceleration signals as an oscillating pattern being simultaneously present on both axes, with each propulsive stroke recorded on the heaving axis resulting in a forward acceleration recorded on the surging axis. The amplitude and frequency of each wing beat were analysed using the heaving acceleration signal (the most sensitive to undulation in the birds' body resulting from flipper beats). We found there was an upper amplitude threshold for regular diving wing beats per dive phase, being highest during descent and lowest during ascent (see <xref ref-type="fig" rid="pone-0016098-g001">Fig. 1</xref>
). Wing beat characteristics differed between individuals so that the threshold was adjusted for the descent, bottom and ascent phase of each bird. Dashes were considered when the wing beat amplitude became greater than this defined threshold for more than three consecutive wing beats (<xref ref-type="fig" rid="pone-0016098-g001">Fig. 1</xref>
). The first 8 m of descent phases were excluded from dash detection because birds stroke their wings hardly to overcome buoyancy in the beginning of a dive and do therefore not represent the regular wing beat pattern.</p>
<fig id="pone-0016098-g001" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0016098.g001</object-id>
<label>Figure 1</label>
<caption><title>Example of a little penguin foraging dive and the heaving acceleration used to analyse wing beat amplitude and frequency.</title>
<p>Upper thresholds were defined for the regular wing beat amplitude of the descent, bottom and ascent phase, being highest during descent and lowest during ascent. Prey pursuits (dashes) were considered when the wing beat amplitude was greater than the threshold of the respective dive phase for more than three consecutive wing beats as shown by the dash example.</p>
</caption>
<graphic xlink:href="pone.0016098.g001"></graphic>
</fig>
<p>As a physical index to represent dive effort (DE), which considers the relationship between dive duration and post-dive duration, we divided the dive duration by the dive cycle (dive duration/dive duration + post-dive duration). Moreover, the acceleration records in this study provided the dash duration and allowed us to derive an efficiency index to indicate the effort spent in pursuing prey, here labelled as hunting efficiency (HE = sum of dash duration/dive cycle duration). We note that, even though the dash event is not a direct and quantative measure of prey ingestion, it remains a qualitive measure for prey encounter and pursuit. Once appropriate prey is found the chances to catch it are expected be high <xref ref-type="bibr" rid="pone.0016098-Simeone1">[30]</xref>
 and hence the capacity to pursue prey would be more sensitive to age related changes than the catch itself. In penguins a quantitative measure for prey ingestion remains still challenging. DE and HE are expressed as non-dimensional units.</p>
<p>In order to investigate where prey pursuit occurred within dives we examined dash frequency at any given depth. We compared the dash frequency among three categories (A, B, C) of depth percentage from the maximum dive depth, to indicate where in a single dive most prey were pursued: either (A) at depths shallower than 80% of maximum depth before reaching the maximum dive depth, coinciding with descent (i.e. from 0% to 80%), (B) in the deepest part of a dive around the bottom (i.e. from 80% to −80%), or (C) at depths shallower than −80% of maximum dive depth after penguins had reached the maximum dive depth, coinciding with ascent (i.e. from −80% to 0%). To avoid the high influence of upthrust in the upper part of the water column <xref ref-type="bibr" rid="pone.0016098-Wilson3">[31]</xref>
 we only included dives >8 m.</p>
<p>We moreover investigated the dash orientation, i.e. if penguins swam predominantly downward or upward when pursuing prey. This was calculated by subtracting the end depth of each single dash with the start depth of the dash (depth values being positive), so that negative results indicated upward movement.</p>
<p>In addition to the above parameters, which are based on a dive-by-dive analysis, we investigated two foraging parameters which provide information on the whole foraging trip (foraging trip based). These were the total time spent underwater, calculated as the sum of dive durations, and the total dash number, calculated as the sum of dashes per foraging trip and per penguin.</p>
</sec>
<sec id="s2d"><title>Statistics</title>
<p>To compare the diving behaviour between the three age classes, we used General Linear Mixed Models to avoid pseudo replication <xref ref-type="bibr" rid="pone.0016098-Zuur1">[32]</xref>
. Individuals were considered as random factors while the age-class was a fixed factor. If data were not normally distributed they were log10 transformed. Since the maximum depth influences all other dive parameters <xref ref-type="bibr" rid="pone.0016098-Wilson4">[33]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Cherel1">[34]</xref>
, we included maximum depth as a covariate into the model and calculated least square means per bird so as to compare among age classes independent on depth. We provide the denominator degrees of freedom. The numerator degree of freedom is equal to two for all diving parameters. For the two foraging trip based parameters, total time spent underwater and total dash number, the effect of age classes have been tested by General Linear Models as the each individual has only one value. Generalized Linear Models (GLM) were used with binominal distribution and post-hoc Tukey's test to test the difference in the proportion of dashes which occurred in the different parts of the dive among age classes. To test the differences among age classes in orientation of the dashes, we used a paired t-test and post-hoc ANOVA.</p>
<p>Analyses were conducted using JMP 8 (SAS Institute Inc.) and R 2.10.1 (R Development Core Team). Results are expressed as means ± SE and significance level was set at α = 0.05.</p>
</sec>
</sec>
<sec id="s3"><title>Results</title>
<p>All 19 loggers were recovered and full datasets were downloaded successfully from all devices. The mean dive depth did not differ between age classes (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). Middle age penguins showed differences in their foraging performance compared to young and old birds. These differences were related to the dive duration parameters and the within-dive orientation of dashes.</p>
<table-wrap id="pone-0016098-t001" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0016098.t001</object-id>
<label>Table 1</label>
<caption><title>General Linear Mixed Model and Tukey's HSD test results for age class comparison of diving parameters.</title>
</caption>
<alternatives><graphic id="pone-0016098-t001-1" xlink:href="pone.0016098.t001"></graphic>
<table frame="hsides" rules="groups"><colgroup span="1"><col align="left" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
</colgroup>
<thead><tr><td align="left" rowspan="1" colspan="1"></td>
<td colspan="2" align="left" rowspan="1">Young (N = 7)</td>
<td colspan="2" align="left" rowspan="1">Middle (N = 7)</td>
<td colspan="2" align="left" rowspan="1">Old (N = 5)</td>
<td align="left" rowspan="1" colspan="1"><italic>F</italic>
</td>
<td align="left" rowspan="1" colspan="1"><italic>dfd</italic>
</td>
<td align="left" rowspan="1" colspan="1"><italic>P</italic>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1">mean</td>
<td align="left" rowspan="1" colspan="1">SE</td>
<td align="left" rowspan="1" colspan="1">mean</td>
<td align="left" rowspan="1" colspan="1">SE</td>
<td align="left" rowspan="1" colspan="1">mean</td>
<td align="left" rowspan="1" colspan="1">SE</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
</thead>
<tbody><tr><td align="left" rowspan="1" colspan="1">Mean dive depth (m)</td>
<td align="left" rowspan="1" colspan="1">7.72<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.46</td>
<td align="left" rowspan="1" colspan="1">8.45<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.46</td>
<td align="left" rowspan="1" colspan="1">10.57<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.73</td>
<td align="left" rowspan="1" colspan="1">0.83</td>
<td align="left" rowspan="1" colspan="1">15.8</td>
<td align="left" rowspan="1" colspan="1">0.456</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean dive duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">10.32<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.93</td>
<td align="left" rowspan="1" colspan="1">7.73<sub>b</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.03</td>
<td align="left" rowspan="1" colspan="1">10.83<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.90</td>
<td align="left" rowspan="1" colspan="1">10.66<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">16.1</td>
<td align="left" rowspan="1" colspan="1"><bold>0.001</bold>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean descent duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">3.08<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.57</td>
<td align="left" rowspan="1" colspan="1">2.41<sub>b</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.18</td>
<td align="left" rowspan="1" colspan="1">3.10<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.17</td>
<td align="left" rowspan="1" colspan="1">8.00<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">16.1</td>
<td align="left" rowspan="1" colspan="1"><bold>0.004</bold>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean bottom duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">5.19<sub>ab</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.05</td>
<td align="left" rowspan="1" colspan="1">4.46<sub>b</sub>
</td>
<td align="left" rowspan="1" colspan="1">1.06</td>
<td align="left" rowspan="1" colspan="1">5.96<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.60</td>
<td align="left" rowspan="1" colspan="1">3.45<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">15.8</td>
<td align="left" rowspan="1" colspan="1">0.057</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean ascent duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">3.07<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.40</td>
<td align="left" rowspan="1" colspan="1">2.43<sub>b</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.20</td>
<td align="left" rowspan="1" colspan="1">3.12<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.12</td>
<td align="left" rowspan="1" colspan="1">12.47<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">16.1</td>
<td align="left" rowspan="1" colspan="1"><bold>0.001</bold>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean post-dive duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">13.82<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">2.84</td>
<td align="left" rowspan="1" colspan="1">17.04<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">4.83</td>
<td align="left" rowspan="1" colspan="1">15.98<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">2.44</td>
<td align="left" rowspan="1" colspan="1">1.25<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">16.0</td>
<td align="left" rowspan="1" colspan="1">0.313</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Total time spent underwater (h)</td>
<td align="left" rowspan="1" colspan="1">5.07<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.50</td>
<td align="left" rowspan="1" colspan="1">4.78<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.50</td>
<td align="left" rowspan="1" colspan="1">6.53<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.59</td>
<td align="left" rowspan="1" colspan="1">2.83</td>
<td align="left" rowspan="1" colspan="1">16</td>
<td align="left" rowspan="1" colspan="1">0.089</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean dive effort<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">0.33<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.08</td>
<td align="left" rowspan="1" colspan="1">0.24<sub>b</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.07</td>
<td align="left" rowspan="1" colspan="1">0.32<sub>ab</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.05</td>
<td align="left" rowspan="1" colspan="1">3.98<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">16.0</td>
<td align="left" rowspan="1" colspan="1"><bold>0.040</bold>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean dash number</td>
<td align="left" rowspan="1" colspan="1">1.63<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.07</td>
<td align="left" rowspan="1" colspan="1">1.52<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.07</td>
<td align="left" rowspan="1" colspan="1">1.56<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.09</td>
<td align="left" rowspan="1" colspan="1">0.59</td>
<td align="left" rowspan="1" colspan="1">16.6</td>
<td align="left" rowspan="1" colspan="1">0.567</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Total dash number</td>
<td align="left" rowspan="1" colspan="1">322<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">62</td>
<td align="left" rowspan="1" colspan="1">281<underline><sub>a</sub>
</underline>
</td>
<td align="left" rowspan="1" colspan="1">62</td>
<td align="left" rowspan="1" colspan="1">185<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">73</td>
<td align="left" rowspan="1" colspan="1">1.05</td>
<td align="left" rowspan="1" colspan="1">16</td>
<td align="left" rowspan="1" colspan="1">0.373</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean dash sum duration (s)<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">2.23<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.72</td>
<td align="left" rowspan="1" colspan="1">2.07<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.56</td>
<td align="left" rowspan="1" colspan="1">2.71<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.74</td>
<td align="left" rowspan="1" colspan="1">1.24<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">15.9</td>
<td align="left" rowspan="1" colspan="1">0.316</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Mean hunting efficiency<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">0.06<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.02</td>
<td align="left" rowspan="1" colspan="1">0.05<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.01</td>
<td align="left" rowspan="1" colspan="1">0.07<sub>a</sub>
</td>
<td align="left" rowspan="1" colspan="1">0.02</td>
<td align="left" rowspan="1" colspan="1">1.13<xref ref-type="table-fn" rid="nt102">*</xref>
</td>
<td align="left" rowspan="1" colspan="1">15.4</td>
<td align="left" rowspan="1" colspan="1">0.349</td>
</tr>
</tbody>
</table>
</alternatives>
<table-wrap-foot><fn id="nt101"><label></label>
<p>Least-square means were used for comparison. Denominator degrees of freedom (dfd) are provided. Numerator degree of freedom equal 2 for all parameters. Significant results are in bold. The results of post-hoc Tukey's HSD test are shown by the subscript letters: same letter showed no significant differences.</p>
</fn>
<fn id="nt102"><label></label>
<p>*Data were log10 transformed for the statistical analysis.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>Middle age penguins made shorter dives than young or old penguins (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). This was mainly due to middle age penguins having shorter descent and ascent phases, while the bottom duration showed a similar trend but was not significantly different between the three classes (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). Post-dive duration was not significantly different between age classes (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). The total time spent underwater during a foraging trip did not differ among age classes (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
).</p>
<p>Middle age penguins showed lower dive effort (DE) than young birds (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). We compared mean dash number, total dash number and mean dash sum duration between age classes, but there were no significant differences (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
). In addition, hunting efficiency (HE) did not differ between age classes (<xref ref-type="table" rid="pone-0016098-t001">Table 1</xref>
).</p>
<p>The proportion of dashes, before (0–80%), around (80–80%) or after (80–0%) reaching the deepest point of dives, were different among age classes (0–80%, LRT = 51.5, P<0.001, 80–80%, LRT = 10.8, P<0.01, 80–0%, LRT = 14.0, P<0.001, df = 2, <xref ref-type="fig" rid="pone-0016098-g002">Fig. 2</xref>
). In 0–80% depth, young birds pursued prey more often than middle age (z = −4.7, P<0.001) and old birds (z = −6.7, P<0.001), and middle-aged birds pursued more than old birds (z = −2.8, P<0.05). In 80–80% depth, young birds pursued prey less often than middle-aged birds (z = 3.2, P<0.01) and there was no difference between young and old birds (z = 2.1, P = 0.08) or between middle age and old birds (z = −0.73, P = 0.74). In 80–0% depth, old birds pursued prey more often than young (z = 3.6, P<0.01) and middle-aged birds (z = 2.9, P<0.05); there was no difference between young and middle-aged birds (z = 0.94, P = 0.61).</p>
<fig id="pone-0016098-g002" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0016098.g002</object-id>
<label>Figure 2</label>
<caption><title>Prey pursuit (dash) frequency (%) in relation to the depth percentage of the max.</title>
<p>dive depth (%) in three categories (see <xref ref-type="sec" rid="s2">methods</xref>
): (A) 0–80%, (B) 80–80% and (C) 80–0% for young, middle age and old little penguins. The results of post-hoc Tukey's test are shown by the bold letters: same letter showed no significant differences between age classes.</p>
</caption>
<graphic xlink:href="pone.0016098.g002"></graphic>
</fig>
<p>We moreover found that all penguins performed more upward-orientated dashes than downward-oriented ones (paired t-test, <italic>t</italic>
<sub>18</sub>
 = 2.9, <italic>P</italic>
<0.01, <xref ref-type="table" rid="pone-0016098-t002">Table 2</xref>
), without differences between age-classes (post-hoc ANOVA, <italic>F</italic>
<sub>2, 16</sub>
 = 0.26, <italic>P</italic>
 = 0.77).</p>
<table-wrap id="pone-0016098-t002" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0016098.t002</object-id>
<label>Table 2</label>
<caption><title>Dash end depth frequency (%) in relation to the hunting direction: downward and upward orientation for young, middle age and old little penguins.</title>
</caption>
<alternatives><graphic id="pone-0016098-t002-2" xlink:href="pone.0016098.t002"></graphic>
<table frame="hsides" rules="groups"><colgroup span="1"><col align="left" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
</colgroup>
<thead><tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1">Downward</td>
<td align="left" rowspan="1" colspan="1">Upward</td>
</tr>
</thead>
<tbody><tr><td align="left" rowspan="1" colspan="1">Young (N = 7)</td>
<td align="left" rowspan="1" colspan="1">41.0</td>
<td align="left" rowspan="1" colspan="1">59.0</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Middle age (N = 7)</td>
<td align="left" rowspan="1" colspan="1">41.0</td>
<td align="left" rowspan="1" colspan="1">59.0</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Old (N = 5)</td>
<td align="left" rowspan="1" colspan="1">42.7</td>
<td align="left" rowspan="1" colspan="1">57.3</td>
</tr>
</tbody>
</table>
</alternatives>
<table-wrap-foot><fn id="nt103"><label></label>
<p>No siginificant differences were found between age classes.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s4"><title>Discussion</title>
<p>Our results highlighted differences in the foraging activity of little penguin females according to their age. In several key variables used to measure diving behaviour, middle-aged females have showed better foraging performance than young and old penguins. Middle-aged females made shorter duration dives, getting to the bottom of the dive faster while reaching similar depths with less effort than the other age groups. These trend in age performance coincided with the curvilinear trend observed for breeding performance and group behaviour differences related to age on little penguins <xref ref-type="bibr" rid="pone.0016098-Nisbet1">[7]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Daniel1">[25]</xref>
. Since breeding success is closely related to foraging efficiency <xref ref-type="bibr" rid="pone.0016098-Morrison1">[35]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Cockburn1">[36]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Pugesek1">[37]</xref>
, we suggest that middle age females could be better at bringing food to their chicks compared with other age classes.</p>
<p>We grouped our data in three age classes rather than continuous data in the analysis due to the limitations in our dataset. Nevertheless we could detect age-related change in the dive parameters among the groups. This is an advantage compared with most foraging studies which compare only two age classes, but see <xref ref-type="bibr" rid="pone.0016098-Rutz1">[13]</xref>
, like a recent study <xref ref-type="bibr" rid="pone.0016098-Limmer1">[17]</xref>
, which could therefore only detect the initial increase in foraging ability from young to adult common terns <italic>Sterna hirundo</italic>
 while a change with age in old birds might have been overlooked.</p>
<p>If young breeders are less proficient foragers than experienced ones, the age difference may be expressed in several ways. (1) Young birds may spend more time foraging, like experienced terns that cover their feeding areas more quickly than inexperienced ones <xref ref-type="bibr" rid="pone.0016098-Buckley1">[38]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Dunn1">[39]</xref>
. Although we did not find an age-related difference in the total time spent underwater, we found differences in the organisation of the different phases of the dives. While our guarding penguins were constrained to forage within only one-day period, we could still reveal a trend as young inexperienced and older females had longer dive durations than middle age ones. (2) Young birds might also use different feeding spots or simply feed on different sizes or types of food, smaller or of less energetic value <xref ref-type="bibr" rid="pone.0016098-Limmer1">[17]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Buckley1">[38]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Dunn1">[39]</xref>
. Several avian studies have reported an improvement in foraging efficiency in terms of rate of energy gain <xref ref-type="bibr" rid="pone.0016098-Daunt1">[11]</xref>
. We examined the relation of age and foraging performance by using high-resolution data, which allowed us to investigate if there were differences in prey pursuit patterns at a fine scale. Hence we expected young females to have lower hunting efficiency and prey pursuit frequency or duration because these are the most obvious parameters to indicate foraging efficiency, but we did not find any significant differences. Since we did not know the chick provisioning rate, this does not necessarily mean that middle age and old birds were more or less successful capturing prey <xref ref-type="bibr" rid="pone.0016098-Daunt1">[11]</xref>
. However, we found a marked difference in the tactic of prey pursuit in the hunting pattern within dives among the three age classes. Prey pursuit increases across the age so more experienced birds (old > middle age > young) could take advantage of up-thrust momentum, expanding air in respiratory system <xref ref-type="bibr" rid="pone.0016098-Wilson5">[40]</xref>
 which facilitates acceleration to pursue prey. This prey pursuit pattern suggests an energy saving hunting skill <xref ref-type="bibr" rid="pone.0016098-Wilson6">[41]</xref>
 probably learned through age and foraging experience <xref ref-type="bibr" rid="pone.0016098-Greig1">[42]</xref>
, <xref ref-type="bibr" rid="pone.0016098-Grmillet1">[43]</xref>
.</p>
<p>The similar response in dive durations of young and old females in our study can result from different factors. While young females may not have fully developed their foraging skills, old females are probably affected by senescence and their progressive decline in physical condition <xref ref-type="bibr" rid="pone.0016098-Rose1">[44]</xref>
. Thus, we can suspect that middle age females combine well-developed foraging skills with good physical condition since they did not rely on longer dive durations to search or pursuit prey while taking advantage of the same post-dive duration for recovery at the surface, shown by their lower dive effort. Other factors could affect dive-pause ratio of diving seabirds, i.e. when prey density or the probability of losing contact with ephemeral prey is high <xref ref-type="bibr" rid="pone.0016098-Elliott1">[45]</xref>
. But since old females dived longer with the same prey pursuit rate as other age classes (there was no difference in the number or duration of prey pursuit between age classes); we suggest that older females have lower prey pursuit ability despite their use of energy saving hunting tactics. Senescence is the ‘persistent decline in age-specific fitness components of an organism due to internal physiological deterioration’ <xref ref-type="bibr" rid="pone.0016098-Rose1">[44]</xref>
, which is genetically determined <xref ref-type="bibr" rid="pone.0016098-Finch1">[46]</xref>
. One hypothesis about responsible intrinsic factors for aging processes is the oxidative theory of aging <xref ref-type="bibr" rid="pone.0016098-Harman1">[47]</xref>
. Cumulative damage on cell constituents can progressively reduce resistance to oxidative stress, leading to a gradual aging process. In greater flamingos this theory has been supported by a curvilinear relationship with middle-aged birds showing a greater resistance to oxidative stress than young and old ones <xref ref-type="bibr" rid="pone.0016098-Devevey1">[48]</xref>
. Decline in hunting ability due to physiological deterioration at old age was found in wolves <xref ref-type="bibr" rid="pone.0016098-MacNulty1">[49]</xref>
 and aboriginal human hunters <xref ref-type="bibr" rid="pone.0016098-Gurven1">[50]</xref>
, also supporting a curvilinear relation with age. Physiological deterioration at old age may be, however, balanced by increasing foraging experience until a certain age limit, which may well be related to our birds in the transition stage between middle age and old birds. Since it is often difficult to study the oldest individuals <xref ref-type="bibr" rid="pone.0016098-Nisbet2">[51]</xref>
 in wild populations, the nature of such limits is not fully understood yet and remains a challenge to future studies.</p>
<p>Our 2005 study season was a highly productive season, as indicated by high penguin breeding success <xref ref-type="bibr" rid="pone.0016098-RopertCoudert2">[26]</xref>
, and we may expect age-related differences to be more distinct when environmental conditions are poorer, i.e. lower prey availability <xref ref-type="bibr" rid="pone.0016098-Bunce1">[52]</xref>
. Also, our cross-sectional foraging study should be regarded as a snapshot within one breeding season. In order to confirm our hypothesis future studies should investigate age-related foraging performances over the complete breeding season, as well as across years, and ideally at a longitudinal scale.</p>
<p>Behavioural studies which aim to extrapolate their findings on the population level require the consideration of individual age differences. The behaviour of a whole population is usually assumed to be the sum of individual behaviour, disregarding the age structure of the population. By investigating the foraging performance in relation to age, future studies could make more accurate predictions on population trends. In this case, a population with a high proportion of middle age individuals would be expected to be more successful in foraging, and therefore chick provisioning, than a population dominated by young and old individuals. Thus, a population dominated by middle age individuals would better contribute to the next generation. This contribution would be especially relevant in years of low resource availability and probably influence the response of a population to environmental changes, which should be considered in conservation and management of populations.</p>
</sec>
</body>
<back><ack><p>We thank P. Fallow for her help in the field.</p>
</ack>
<fn-group><fn fn-type="conflict"><p><bold>Competing Interests: </bold>
The authors received funding from BHP-Billiton in the form of donation to support their research. The company does not participate in orinterfere with the design, data collection and analysis and output of this research. The authors also comply with PloS One policies on sharing data. All data are available at the National Ecological Meta Database (Australia) <ext-link ext-link-type="uri" xlink:href="http://www.bom.gov.au/jsp/bmrc/NEMDSearch/NemdSearch?lookup_id=81&submit=Submit">http://www.bom.gov.au/jsp/bmrc/NEMDSearch/NemdSearch?lookup_id=81&submit=Submit</ext-link>
. YRC is one of approximately 1,000 academic editors for PLoS ONE and as such had no access to the peer review or acceptance process for this manuscript (which was conducted with no regard to his position on the board). PLoS ONE academic editors are volunteers and receive no compensation for their services.</p>
</fn>
<fn fn-type="financial-disclosure"><p><bold>Funding: </bold>
This work was supported by the BHP-Billiton, the Japan Science Society, the Australian Academy of Science, the University of Strasbourg, the Penguin Foundation and the Japan Society for the Promotion of Science. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Note that Phillip Island Nature Park is a not-for-profit organization dedicated to the protection and conservation of little penguins. The Park is controlled by a Board of Management appointed by the Minister for Environment of Victoria, Australia.</p>
</fn>
</fn-group>
<ref-list><title>References</title>
<ref id="pone.0016098-CluttonBrock1"><label>1</label>
<mixed-citation publication-type="book">             <person-group person-group-type="author"><name><surname>Clutton-Brock</surname>
<given-names>TH</given-names>
</name>
</person-group>
             <year>1988</year>
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