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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">SCIENTIA MARINA</journal-id>
			<journal-title-group>
				<journal-title>Scientia Marina</journal-title>
				<abbrev-journal-title>Sci Mar</abbrev-journal-title>
			</journal-title-group>
			<issn pub-type="epub">0214-8358</issn>
			<publisher>
				<publisher-name>Consejo Superior de Investigaciones Científicas</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			 <article-id pub-id-type="publisher-id">sm4746</article-id>
			 <article-id pub-id-type="doi">10.3989/scimar.04746.10A</article-id>
			 
			
		<title-group>
			  <article-title>Discard-ban policies can help improve our understanding of the ecological role of food availability to seabirds</article-title>
		<trans-title-group xml:lang="es">
		<trans-title>Las políticas sobre prohibición de descartes pueden ayudar a mejorar la comprensión sobre el papel ecológico de la disponibilidad de alimento en aves marinas</trans-title>
		</trans-title-group>
		<alt-title alt-title-type="running-head">Main knowledge gaps on seabird-discard interactions</alt-title>
		</title-group>

		<contrib-group>
			<contrib contrib-type="issue-editor"> 
				<name>
				 <surname>Demestre</surname>
				 <given-names>Montserrat</given-names>
				</name>
				<role>Special Issue Editor</role>
				</contrib>
			<contrib contrib-type="issue-editor"> 
				<name>
				 <surname>Maynou</surname>
				 <given-names>Francesc</given-names>
				</name>
				<role>Special Issue Editor</role>
				</contrib>
		</contrib-group>

		<contrib-group>
		<contrib contrib-type="author" corresp="yes"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6190-6303</contrib-id>
			<name>
				 <surname>Real</surname>
				 <given-names>Enric</given-names>
			</name>
			<xref ref-type="aff" rid="U1"/>
			<ext-link ext-link-type="email" xlink:href="mailto:ereal@imedea.uib-csic.es">ereal@imedea.uib-csic.es</ext-link>
		</contrib>
		<contrib contrib-type="author" corresp="no"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5435-2691</contrib-id>
			<name>
				 <surname>Tavecchia</surname>
				 <given-names>Giacomo</given-names>
			</name>
			<xref ref-type="aff" rid="U1"/>
			<ext-link ext-link-type="email" xlink:href="mailto:g.tavecchia@uib.es">g.tavecchia@uib.es</ext-link>
		</contrib>
		<contrib contrib-type="author" corresp="no"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2919-1288</contrib-id>
			<name>
				 <surname>Genovart</surname>
				 <given-names>Meritxell</given-names>
			</name>
			<xref ref-type="aff" rid="U2"/>
			<xref ref-type="aff" rid="U3"/>
			<ext-link ext-link-type="email" xlink:href="mailto:m.genovart@csic.es">m.genovart@csic.es</ext-link>
		</contrib>
		<contrib contrib-type="author" corresp="no"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4177-9749</contrib-id>
			<name>
				 <surname>Sanz-Aguilar</surname>
				 <given-names>Ana</given-names>
			</name>
			<xref ref-type="aff" rid="U1"/>
			<ext-link ext-link-type="email" xlink:href="mailto:asanz@imedea.uib-csic.es">asanz@imedea.uib-csic.es</ext-link>
		</contrib>
		<contrib contrib-type="author" corresp="no"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5482-242X</contrib-id>
			<name>
				 <surname>Payo-Payo</surname>
				 <given-names>Ana</given-names>
			</name>
			<xref ref-type="aff" rid="U1"/>
			<ext-link ext-link-type="email" xlink:href="mailto:anapayopayo@gmail.com">anapayopayo@gmail.com</ext-link>
		</contrib>		
		<contrib contrib-type="author" corresp="no"> 
			<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4782-3007</contrib-id>
			<name>
				 <surname>Oro</surname>
				 <given-names>Daniel</given-names>
			</name>
			<xref ref-type="aff" rid="U2"/>
			<xref ref-type="aff" rid="U3"/>
			<ext-link ext-link-type="email" xlink:href="mailto:d.oro@csic.es">d.oro@csic.es</ext-link>
		</contrib>		
			  <aff id="U1">Grupo de Ecología y Demografía Animal, IMEDEA, CSIC-UIB, Miquel Marquès 21, 07190 Esporles, Spain.</aff>
			  <aff id="U2">IMEDEA, CSIC-UIB, Miquel Marquès 21, 07190 Esporles, Spain.</aff>
			  <aff id="U3">Centre d’Estudis Avançats de Blanes, CSIC, Accés Cala Sant Francesc 14, 17300 Blanes, Spain.</aff>
			 </contrib-group>
	 <contrib-group>
			<contrib contrib-type="editor">
				<name>
					<surname>Maynou</surname>
					<given-names>F.</given-names>
				</name>
				<role>Editor</role>
			</contrib>
		</contrib-group>	 		
<pub-date pub-type="epub">
		<day>31</day>
		<month>12</month>
		<year>2018</year>
		</pub-date>
		<pub-date pub-type="collection">
		<year>2018</year>
		</pub-date>
		
		<volume>82S1</volume>
		<issue>Suppl. 1</issue>
		<issue-title>
 Discards regulation vs Mediterranean fisheries sustainability</issue-title>
		<fpage>115</fpage>
		<lpage>120</lpage>
		
		<elocation-id content-type="doi">10.3989/scimar.04746.10A</elocation-id>

		 <history>
		  	<date date-type="received">
				<day>22</day>
				<month>12</month>
				<year>2017</year>
			</date>
			<date date-type="accepted">
				<day>21</day>
				<month>6</month>
				<year>2018</year>
			</date>
			<date date-type="published">
				<day>25</day>
				<month>7</month>
				<year>2018</year>
			</date>
		 </history>
		 
		<permissions>
		<copyright-statement>&#x00A9; 2018 CSIC</copyright-statement>
		<copyright-year>2018</copyright-year>
		<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
		<license-p> This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License</license-p>
		</license>
		</permissions>
		
		<abstract xml:lang="en">
		<title>SUMMARY</title>
		<p>Discards from fisheries are the most important predictable anthropogenic food subsidies (PAFS) that are being incorporated into marine ecosystems. Changes on their availability and predictability can help us to understand the role that food availability (i.e. an important indicator of the carrying capacity) plays at different ecological levels, from individual fitness to community dynamic and ecosystem functioning. For several reasons, seabirds are an excellent model for evaluating the ecological effects arising from a lack of discards: 1) they are one of the most important discard scavengers, 2) they are easy to monitor and 3) they are apical predators are globally distributed, which makes them suitable health indicators of ecosystems. Here we review the existing information on seabird-discard interactions to identify the main knowledge gaps and propose new challenges for improving our understanding of the general role of food availability. We conclude that the new policies on the ban of fishery discards that are being progressively implemented in the European Union, Norway, Chile and New Zealand offer a suitable experimental scenario for improving our understanding of how a large decrease in the carrying capacity may alter demographic parameters such as survival, dispersal and reproduction, the resilience of populations against perturbations and the role of individual specialization in the foraging process.</p>
		</abstract>
		<trans-abstract xml:lang="es">
		<title>RESUMEN</title>
		<p>Los descartes pesqueros constituyen el recurso antropogénico predecible (PAFS) más importante que está siendo incorporado en los ecosistemas marinos. Cambios en su disponibilidad y predictibilidad pueden ayudar a entender mejor el papel ecológico de la disponibilidad de alimento (i.e. un importante indicador de la capacidad de carga) a diferentes niveles, desde la eficacia biológica individual hasta la dinámica de poblaciones o el funcionamiento de los ecosistemas. Las aves marinas constituyen un modelo excelente para estudiar los efectos ecológicos derivados de la falta de descartes por diversas razones: las aves marinas: 1) se encuentran entre los principales carroñeros de descartes, 2) son fáciles de monitorear y 3) son depredadores apicales globalmente distribuidos, lo cual las convierte en buenas indicadoras de la salud del ecosistema. En el presente estudio revisamos la información existente sobre las interacciones ecológicas entre las aves marinas y los descartes de la pesca, con el fin de identificar los principales vacíos de conocimiento y plantear retos futuros de cara a mejorar nuestra comprensión sobre el papel ecológico que tiene la disponibilidad de alimento. Concluimos que las políticas actuales en materia de prohibición de descartes que están siendo implementadas en la Unión Europea, Noruega, Chile o Nueva Zelanda, ofrecen un escenario ideal para mejorar nuestra comprensión sobre cómo una reducción de la capacidad de carga puede alterar parámetros demográficos tales como la supervivencia, la dispersión y la reproducción, la resiliencia de las poblaciones frente a perturbaciones y el papel de la especialización individual en el proceso de forrajeo.</p>
		</trans-abstract>
		<kwd-group xml:lang="en">
			<title>KEYWORDS</title>
			<kwd>food availability</kwd>
			<kwd>fishery discards</kwd>
			<kwd>seabirds</kwd>
			<kwd>ecological interactions</kwd>
			<kwd>discard policies</kwd>
		</kwd-group>
		<kwd-group xml:lang="es">
			<title>PALABRAS CLAVE</title>
			<kwd>disponibilidad de alimento</kwd>
			<kwd>descartes pesqueros</kwd>
			<kwd>aves marinas</kwd>
			<kwd>interacciones ecológicas</kwd>
			<kwd>políticas de descartes</kwd>
		</kwd-group>
</article-meta>
</front>

<body>
<sec id="S1">
<title>INTRODUCTION</title>
			<p>The large amount of discards in the form of offal that are generated daily by industrial and artisanal fisheries and thrown into the sea constitutes one of the most important and predictable anthropogenic food subsidies (PAFS) that are being incorporated into marine ecosystems worldwide (<xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>). Global discards generation in recent years has been estimated to be <italic>ca</italic>. 10 million t/year, with a peak of 19 million t/year in the late 1950s (<xref ref-type="bibr" rid="CIT43">Zeller et al. 2017</xref>). As a result of the high abundance and predictability of this anthropogenic food resource, together with a decrease in the natural prey availability due to industrial fisheries, fishery discards have important ecological implications at a global level for marine scavengers, including seabirds (<xref ref-type="bibr" rid="CIT39">Votier et al. 2004</xref>, <xref ref-type="bibr" rid="CIT07">Cury et al. 2011</xref>, <xref ref-type="bibr" rid="CIT03">Bicknell et al. 2013</xref>, <xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>). <xref ref-type="bibr" rid="CIT11">Garthe et al. (1996)</xref>, for instance, estimated that 5.9 million seabirds were potentially supported by fishery discards in the North Sea. </p>
			<p>Changes in the availability and predictability of fishery discards as PAFS can help to understand the ecological role that food availability (i.e. carrying capacity) have at multiple ecological levels, including individual fitness, community dynamics and ecosystem functioning. </p>
			<p> Seabirds constitute an excellent model for evaluating the ecological effects arising from a lack of PAFS for several reasons: seabirds are 1) one of the most important discard scavengers at a global level, 2) easy to monitor (because they breed on land) and 3) apical predators with a global distribution, which makes them suitable bioindicators of ecosystem health. The link between seabirds and fishery discards has been reviewed in several studies (<xref ref-type="bibr" rid="CIT36">Tasker et al. 2000</xref>, <xref ref-type="bibr" rid="CIT02">Arcos et al. 2008</xref>, <xref ref-type="bibr" rid="CIT41">Wagner and Boersma 2011</xref>). However, the ecological and evolutionary implications that fishery discards have as PAFS at a global level (<xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>), as well as the current changes in fishery policies (see e.g. <xref ref-type="bibr" rid="CIT05">Borges et al. 2016</xref>), call for a new revision of the existing information and the identification of knowledge gaps. </p>
			<p>Here we review current knowledge on the global ecological interactions between seabirds and fishery discards in order to identify the main knowledge gaps and propose new challenges for improving our understanding of the ecological role that food availability has for populations, communities and ecosystems. </p>
			</sec>
<sec id="S2">
<title>METHODS</title>
			<p>We considered the information available in SCI journals (6 June 2017) on the Web of Science platform (WOS; Clarivate Analytics). We first selected articles with concomitant terms: [(<italic>Seabirds AND “Fishery Waste”</italic>) <italic>OR </italic>(<italic>Seabirds AND Discard</italic>)] in title, abstract or keywords (Search field = Topic) as a representative sample of research focusing on the effects of discards on seabirds’ ecology. A second search with concomitant terms: [(<italic>Seabirds AND Ecosystem AND Discard</italic>)<italic> OR </italic>(<italic>Seabirds AND Ecosystem AND “Fishery Waste</italic>”)] (Search field = Topic) was conducted to find studies focusing on the effects arising from seabird-discard interactions at the ecosystem level. Then, the selected studies were classified according to: 1) the species and families of seabirds interacting with fishery discards, 2) the fishing gear used and 3) the ecological parameter or effect investigated. Additionally, in order to identify the areas where ecological interactions between seabirds and fishery discards are more likely to occur (e.g. with high discard availability or high presence of scavenger seabirds) we calculated: 1) the average amount of discards (in metric tons) for each major FAO fishing area (<ext-link ext-link-type="uri" xlink:href="http://www.fao.org">www.fao.org</ext-link>) from 2004 to 2014 (raw data from <ext-link ext-link-type="uri" xlink:href="http://www.seaaroundus.org">www.seaaroundus.org</ext-link>) and 2) the main distribution areas of seabird species (identified as discard scavengers by reviewed studies)(data from <ext-link ext-link-type="uri" xlink:href="http://www.iucn.org">www.iucn.org</ext-link>). We considered that the level of confluence of these species within each major FAO fishing area may vary throughout the year due to the large-scale movements of migratory species.</p>
  </sec>
<sec id="S3">
<title>RESULTS</title>
			<p>A total of 166 studies addressing up to 15 different ecological effects arising from seabird-discard interactions were selected and subsequently reviewed (<xref ref-type="table" rid="T1">Table 1</xref>, Supplementary Material Table S1). A total of 111 seabird species (Table S1) belonging to 14 taxonomic families (<xref ref-type="table" rid="T1">Table 1</xref>) were identified as scavengers of fishery discards. Demersal trawlers were by far the main fishing gear involving seabird-discard interactions (98% of studies). According to their attendance at fishing vessels, the most common discard scavengers were Laridae, Procellaridae and Diomedeidae (<xref ref-type="table" rid="T1">Table 1</xref>). The major FAO fishing areas with the highest discard availability per scavenger seabird species were the Northwest Pacific, the Eastern Central Atlantic and the Mediterranean and Black seas (<xref ref-type="fig" rid="F1">Fig. 1</xref>). </p>
				<table-wrap id="T1">
			<label>Table 1</label>
		<caption>
			<title>Percentage of species (regarding the total number of species of each taxonomic family) for which different ecological effects arising from seabird-discard interactions were evaluated by reviewed studies (e.g. the effect of fishery discards on the diet was evaluated in 25% of species belonging to the taxonomic family Laridae). The total number of species belonging to each family was consulted in <ext-link ext-link-type="uri" xlink:href="https://www.itis.gov">https://www.itis.gov</ext-link>. The most common seabird families attending fishing vessels are shown in the upper part and less common ones in the lower part.</title>
		</caption>
		<table frame="hsides" rules="groups">
  <thead>
			      <tr>
			        <th>Family
		            </th>
			        <th> Diet
			          
		            </th>
			        <th> Foraging Ecology
			          
		            </th>
			        <th> Energy requirements
			          
		            </th>
			        <th> Bycatch
			          
		            </th>
			        <th> Competition
			          
		            </th>
			        <th> Reproduction
			          
		            </th>
			        <th> Population dynanmics
			          
		            </th>
			        <th> Body condition
			          
		            </th>
			        <th> Pollutants
			          
		            </th>
			        <th> Predatory interactions
			          
		            </th>
			        <th> Migration patterns
			          
		            </th>
			        <th> Parasitism
			          
		            </th>
			        <th> Survival
			          
		            </th>
			        <th> Ecosystem level
			          
		            </th>
			        <th> Resilience
			          
		            </th>
			        <th> Dispersal
			          
		            </th>
		          </tr>
		        </thead>
			    <tbody>
			      <tr>
			        <td> Laridae (102 spp.)
			          </td>
			        <td> 25
			          </td>
			        <td> 12
			          </td>
			        <td> 13
			          </td>
			        <td> 11
			          </td>
			        <td> 15
			          </td>
			        <td> 4
			          </td>
			        <td> 9
			          </td>
			        <td> 3
			          </td>
			        <td> 6
			          </td>
			        <td> 3
			          </td>
			        <td> 0
			          </td>
			        <td> 4
			          </td>
			        <td> 1
			          </td>
			        <td> 0
			          </td>
			        <td> 2
			          </td>
			        <td> 1
			          </td>
		          </tr>
			      <tr>
			        <td> Procellaridae (88 spp.)
			          </td>
			        <td> 11
			          </td>
			        <td> 6
			          </td>
			        <td> 3
			          </td>
			        <td> 14
			          </td>
			        <td> 1
			          </td>
			        <td> 1
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 2
			          </td>
			        <td> 1
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 1
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Diomedeidae (21 spp.)
			          </td>
			        <td> 19
			          </td>
			        <td> 19
			          </td>
			        <td> 5
			          </td>
			        <td> 38
			          </td>
			        <td> 5
			          </td>
			        <td> 5
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Sulidae (10 spp.)
			          </td>
			        <td> 50
			          </td>
			        <td> 20
			          </td>
			        <td> 20
			          </td>
			        <td> 20
			          </td>
			        <td> 20
			          </td>
			        <td> 10
			          </td>
			        <td> 20
			          </td>
			        <td> 20
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Stercorariidae (7 spp.)
			          </td>
			        <td> 29
			          </td>
			        <td> 29
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 0
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 14
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Phalacrocoracidae (37 spp.)
			          </td>
			        <td> 5
			          </td>
			        <td> 0
			          </td>
			        <td> 3
			          </td>
			        <td> 3
			          </td>
			        <td> 3
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 3
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Hydrobatidae (25 spp.)
			          </td>
			        <td> 8
			          </td>
			        <td> 4
			          </td>
			        <td> 4
			          </td>
			        <td> 12
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Fregatidae (5 spp.)
			          </td>
			        <td> 40
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 20
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Alcidae (24 spp.)
			          </td>
			        <td> 17
			          </td>
			        <td> 0
			          </td>
			        <td> 17
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 8
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Spheniscidae (19 spp.)
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 5
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Chionidae (2 spp.)
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 50
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Ardeidae (68 spp.)
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 3
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Cathartidae (7 spp.)
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 29
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
			      <tr>
			        <td> Pelecanidae (8 spp.)
			          </td>
			        <td> 13
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
			        <td> 0
			          </td>
		          </tr>
		        </tbody>
		      </table>
	  </table-wrap>
	  			<fig id="F1">
				<label>Fig. 1</label>
				<caption>
				<title>Global distribution of fishery discards availability for seabirds in different major FAO fishing areas considering amounts of discards available per unit area and number of scavenger seabird species converging in each area.</title>
				</caption>
				<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="../sm82s1-4746-web-resources/image/sm4746fig1.jpg"/>
			</fig>

    <p>Few studies quantified the effect of discards on seabirds’ ecology, and most (68%) focused on the amount/type of fishing discard in seabirds’ diet and on species attendance rate. In particular, we found that for the most important scavenger seabirds (<xref ref-type="table" rid="T1">Table 1</xref>) there was a lack of studies addressing potentially important ecological effects of discards in terms of food availability on: a) demographic parameters such as survival, dispersal and reproduction, b) resilience of populations against perturbations and c) individual foraging specialization (e.g. changes of predatory interactions, foraging and migratory patterns and the possible consequences of this heterogeneity for population dynamics). More specifically, the effect of discards on scavenging seabirds’ survival has only been studied in the family Laridae, and only 1% of species belonging to this family have been considered (<xref ref-type="table" rid="T1">Table 1</xref>). The effect that fishery discards have on seabirds’ breeding success has been hardly studied in the species belonging to the families Procellariidae (only 1% of species studied) and Diomedeidae (only 5% of species studied), which are two of the most important seabird families in terms of discard scavenger species (<xref ref-type="table" rid="T1">Table 1</xref>). We only found three studies in which individual differences in seabird foraging strategies were related to fishing practices (<xref ref-type="bibr" rid="CIT20">Matich et al. 2011</xref>, <xref ref-type="bibr" rid="CIT42">Wakefield et al. 2015</xref>, <xref ref-type="bibr" rid="CIT40">Votier et al. 2017</xref>). Finally, the role that fishery discards play in the resilience of populations remains unknown for 98% of seabirds identified as discards scavengers and for 99% of seabirds in general (<xref ref-type="table" rid="T1">Table 1</xref>).</p>
			</sec>
<sec id="S4">
<title>DISCUSSION</title>
<sec id="S4.1">
<title>Main knowledge gaps in seabird-discard interactions</title>
<sec id="S4.1.1">
<title>The effect of discards on demographic parameters and population resilience</title>
			<p>Fishery discards may have important ecological effects on demographic parameters and on the resilience of scavenger populations. However, these effects have never been evaluated for most of species scavenging on fishery discards. A few studies have shown that fishery discards, like other PAFS, can increase average individual survival and reproductive output in several scavenger species (<xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref> and references therein), but they can also reduce adult survival by increasing bycatch of scavenger seabirds. Bycatch mortality might change over time according to the composition of the fishing fleet. <xref ref-type="bibr" rid="CIT18">Laneri et al. (2010)</xref> and <xref ref-type="bibr" rid="CIT35">Soriano-Redondo et al. (2016)</xref> observed a substantial increase in seabird bycatch by longliners in the absence of discards, when trawling vessels were not operating. This suggests that a ban of fishery discards, which are mainly generated by trawling vessels, may increase the attendance of seabirds at longliners, increasing their likelihood of mortality (<xref ref-type="bibr" rid="CIT18">Laneri et al. 2010</xref>, <xref ref-type="bibr" rid="CIT03">Bicknell et al. 2013</xref>).</p>
			<p>The availability of fishery discards could have important effects on dispersal of several species among breeding colonies, with potential consequences for the structure of communities and ecosystems. However, these effects remain unstudied for most species directly and indirectly associated with fishery discards. <xref ref-type="bibr" rid="CIT28">Oro et al. (2004)</xref>, for example, showed that fishery discards such as PAFS can have a direct effect on the dispersal between breeding patches and the functioning of a spatially structured population in a long-lived seabird. Dispersal could also be indirectly affected by fishery discards through an increase on predatory interactions among sympatric species competing for food and breeding habitats when discards are not available (see <xref ref-type="bibr" rid="CIT14">González-Solís 2003</xref>). In addition, discards from fisheries and other PAFS (<xref ref-type="bibr" rid="CIT31">Real et al. 2017</xref>) could also be altering migration patterns of generalist species (<xref ref-type="bibr" rid="CIT13">Gilbert et al. 2016</xref>). <xref ref-type="bibr" rid="CIT10">Furness et al. (2006)</xref>, for example, suggested that fishery discards may be affecting migration patterns of the great skua (<italic>Catharacta skua</italic>).</p>
			<p>Fishery discards may improve average breeding success in scavenger seabirds such as Larids (<xref ref-type="bibr" rid="CIT25">Oro et al. 1995</xref>, <xref ref-type="bibr" rid="CIT23">Oro 1996a</xref>, <xref ref-type="bibr" rid="CIT26">Oro et al. 1996</xref>, <xref ref-type="bibr" rid="CIT27">1999</xref>), shearwaters (<xref ref-type="bibr" rid="CIT19">Louzao et al. 2006</xref>, <xref ref-type="bibr" rid="CIT12">Genovart et al. 2016</xref>) and albatrosses (<xref ref-type="bibr" rid="CIT33">Rolland et al. 2008</xref>). By contrast, <xref ref-type="bibr" rid="CIT30">Pichegru et al. (2007)</xref> and <xref ref-type="bibr" rid="CIT15">Grémillet et al. (2008)</xref> observed that during periods of natural prey shortage and high energy requirements, fishery discards did not compensate for the breeding needs in Cape gannets (<italic>Morus capensis</italic>). However, more studies are needed in order to obtain a global assessment of the role that fishery discards play on the reproductive output of scavenger seabirds and to predict the consequences of discard prohibitions. </p>
			<p>Food availability is known to increase population resilience after perturbations (see e.g. <xref ref-type="bibr" rid="CIT34">Scheffers et al. 2017</xref>). Similarly, fishery discards have been shown to buffer natural food shortages, reducing the long-term variability of population fluctuations, especially in generalist species (<xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>, <xref ref-type="bibr" rid="CIT09">Fondo et al. 2015</xref>). However, very little is known on the role that fishery discards play in the resilience of populations in most scavenger species. Nevertheless, it is plausible to expect larger fluctuations of seabird populations after discard reduction in those ecosystems that are more tightly linked to climate anomalies and extreme climate events (<xref ref-type="bibr" rid="CIT16">Hansen et al. 2012</xref>, <xref ref-type="bibr" rid="CIT21">National Academies of Sciences 2016</xref>).</p>
			</sec>
<sec id="S4.1.2">
<title>Individual foraging specialization: a recent topic</title>
			<p>Individual specialization in foraging strategies may have important ecological implications by altering the dynamics of populations and the structure of communities and ecosystems (<xref ref-type="bibr" rid="CIT04">Bolnick et al. 2003</xref>), especially in highly mobile marine top predators (<xref ref-type="bibr" rid="CIT20">Matich et al. 2011</xref>). Within scavenger seabird populations, only certain individuals are fishery-discard scavengers, but little is known about which individual features (e.g. age, sex, condition, behaviour traits) may influence this difference. It is likely that there is a large individual heterogeneity within populations in discard use, and this may influence variance in demographic parameters and population dynamics. <xref ref-type="bibr" rid="CIT22">Navarro et al. (2010)</xref> showed that inexperienced, younger adults of Audouin’s gulls (<italic>Ichthyaetus audouinii</italic>) consumed more discards and fewer small pelagics, the natural prey of the species. Differences in resource availability (e.g. due to a ban of discards) and intraspecific competition may increase individual specialization (<xref ref-type="bibr" rid="CIT20">Matich et al. 2011</xref>). For example, when food resources (including discards) become scarce, predatory (<xref ref-type="bibr" rid="CIT14">González-Solís 2003</xref>, <xref ref-type="bibr" rid="CIT32">Regehr and Montevecchi 1997</xref>, <xref ref-type="bibr" rid="CIT39">Votier et al. 2004</xref>) and kleptoparasite (<xref ref-type="bibr" rid="CIT24">Oro 1996b</xref>) interactions among individuals may increase. Specialization in certain foraging strategies such as bird predation may have important associated advantages for individuals (e.g. by improving individual survival or breeding success). This may in turn favour the learning of these strategies by other individuals sharing the same habitat (see e.g. <xref ref-type="bibr" rid="CIT01">Annett and Pierotti 1999</xref>), with potential consequences for the structure of communities. However, despite the potential ecological consequences that individual specialization may have for populations, communities and ecosystems, little information is as yet available (but see <xref ref-type="bibr" rid="CIT37">Tuck et al. 2015</xref>). </p>
			</sec>
<sec id="S4.1.3">
<title>Ecosystem level effects arising from scavenger-discard interactions</title>
			<p>A reduction in fishery discards is expected to cause a population decrease of marine scavenger organisms (including generalist seabirds), but they can also trigger cascading effects through a change in nutrients in the water column. The general lack of studies addressing the potential impacts of fishery discards at an ecosystem level makes it difficult to predict the real ecological consequences of a ban of discards. For example, a population decrease of scavenger seabirds would alter the soil composition and the structure of animal and plant communities in coastal regions (<xref ref-type="bibr" rid="CIT38">Vidal et al. 2000</xref>, <xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>, <xref ref-type="bibr" rid="CIT08">Ellis 2005</xref>). <xref ref-type="bibr" rid="CIT17">Hawke (2006)</xref> found a decrease in the median soil N:P molar ratio at a Westland petrel (<italic>Procellaria westlandica</italic>) breeding colony when the birds fed on fishery discards, and <xref ref-type="bibr" rid="CIT06">Calvino-Cancela (2011)</xref> showed that Larids, a group characterized by a large use of fishery discards, may act as important seed dispersers in many regions worldwide.</p>
			</sec></sec>
<sec id="S4.2">
<title>A chance for an experimental scenario for ecologists</title>
			<p>Several large areas of the world where interactions between discards from fisheries and marine scavengers could be potentially important have received little or no attention. Furthermore, most important ecological effects that fishery discards have on marine ecosystems have never or seldom been studied. Considering this, the new policies on the ban of fishery discards, which are being progressively implemented in the European Union, Norway, Chile and New Zealand, offer a suitable experimental scenario for improving our understanding of how food availability (e.g. carrying capacity) can alter the dynamics of populations and the structure of communities and ecosystems. The example given at the Ebro Delta (e.g. <xref ref-type="bibr" rid="CIT29">Oro et al. 2013</xref>), where a long-term trawling moratorium was established in the early 1990s during the breeding season of the seabird community breeding there, is illustrative of the potential that discard banning offers to ecologists in their understanding of how food availability influences ecological processes and patterns. For instance, we expect an increase in competition at intra- and inter-specific level, with larger impacts on population densities for more opportunistic species, a decrease in the variance of breeding performance within populations and a decrease in the resilience of populations against anthropogenic impacts.</p>
			</sec>
			</sec>
			</body>
			<back>
<ack>
<title>ACKNOWLEDGEMENTS</title>
			<p>Funds for this study were supplied by the Spanish Ministry of Economy and by the European Social Fund (grant ref.: CGL2013-42203-R). The study also received funding from the European Commission’s Horizon 2020 Research and Innovation Programme under Grant Agreement no. 634495 for the project Science, Technology, and Society Initiative to Minimize Unwanted Catches in European Fisheries (MINOUW). MG and ASA are supported by postdoctoral contracts co-funded by the Regional Government of the Balearic Islands and the European Social Fund. Two reviewers helped to improve the manuscript.</p>
			</ack>
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		<supplementary-material>
		<title>SUPPLEMENTARY MATERIAL</title>
<p>The following supplementary material is available through the online version of this article and at the following link: 
<ext-link ext-link-type="uri" xlink:href="http://scimar.icm.csic.es/scimar/supplm/sm04746esm.pdf">http://scimar.icm.csic.es/scimar/supplm/sm04746esm.pdf</ext-link></p>
<p>Table S1. – Seabird species identified as scavengers of fishery discards according to reviewed studies and number of studies considering each ecological effect derived from seabird-discard interactions.</p> 
</supplementary-material>

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