Molecular identification of the diet of Sardina pilchardus larvae in the SW Mediterranean Sea
Molecular techniques provide new insights into the feeding strategies and diets of planktonic organisms such as the larvae of marine fish. We applied multiplex PCR to obtain the first estimates of the diets of larval European sardine Sardina pilchardus in the Alboran Sea (SW Mediterranean), where th...
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Veröffentlicht in: | Marine ecology. Progress series (Halstenbek) 2019-05, Vol.617/618, p.41-52 |
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container_title | Marine ecology. Progress series (Halstenbek) |
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creator | Yebra, Lidia de Rojas, Alma Hernández Valcárcel-Pérez, Nerea Castro, M. Carmen García-Gómez, Candela Cortés, Dolores Mercado, Jesús M. Laiz-Carrión, Raúl García, Alberto Gómez-Jakobsen, Francisco Uriarte, Amaya Rodríguez, José M. Quintanilla, José-María |
description | Molecular techniques provide new insights into the feeding strategies and diets of planktonic organisms such as the larvae of marine fish. We applied multiplex PCR to obtain the first estimates of the diets of larval European sardine Sardina pilchardus in the Alboran Sea (SW Mediterranean), where this species represents an important fishery resource. The feasibility of this technique was tested in a 26 h continuous survey of a shoal of larvae (10.80 ± 0.73 mm standard length, mean ± SD). Multiplex PCR was designed to detect the presence of 5 copepod species, a microplanktonic dinoflagellate (Gymnodinium) and the picoeukaryote algae family Prasinophyceae in larval guts. We simultaneously sampled sardine larvae and their potential prey (pico- to mesoplankton) and compared diel variability of the prey field and ingested items. Microplankton was dominated by flagellates, and copepods represented the most abundant mesozooplankton, reaching peak abundance at night. Prey DNA was detected throughout the entire diel cycle, despite no visible prey in the guts of larvae collected at night. Sardine larvae preyed on early life stages of the most abundant copepod species (Oncaea waldemari, Paracalanus indicus and Temora stylifera), suggesting an opportunistic foraging behaviour. The use of multiplex PCR allowed species-level identification of ingested nauplii and protists, which otherwise would remain unidentified. |
doi_str_mv | 10.3354/meps12833 |
format | Article |
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Carmen ; García-Gómez, Candela ; Cortés, Dolores ; Mercado, Jesús M. ; Laiz-Carrión, Raúl ; García, Alberto ; Gómez-Jakobsen, Francisco ; Uriarte, Amaya ; Rodríguez, José M. ; Quintanilla, José-María</creator><creatorcontrib>Yebra, Lidia ; de Rojas, Alma Hernández ; Valcárcel-Pérez, Nerea ; Castro, M. Carmen ; García-Gómez, Candela ; Cortés, Dolores ; Mercado, Jesús M. ; Laiz-Carrión, Raúl ; García, Alberto ; Gómez-Jakobsen, Francisco ; Uriarte, Amaya ; Rodríguez, José M. ; Quintanilla, José-María</creatorcontrib><description>Molecular techniques provide new insights into the feeding strategies and diets of planktonic organisms such as the larvae of marine fish. We applied multiplex PCR to obtain the first estimates of the diets of larval European sardine Sardina pilchardus in the Alboran Sea (SW Mediterranean), where this species represents an important fishery resource. The feasibility of this technique was tested in a 26 h continuous survey of a shoal of larvae (10.80 ± 0.73 mm standard length, mean ± SD). Multiplex PCR was designed to detect the presence of 5 copepod species, a microplanktonic dinoflagellate (Gymnodinium) and the picoeukaryote algae family Prasinophyceae in larval guts. We simultaneously sampled sardine larvae and their potential prey (pico- to mesoplankton) and compared diel variability of the prey field and ingested items. Microplankton was dominated by flagellates, and copepods represented the most abundant mesozooplankton, reaching peak abundance at night. Prey DNA was detected throughout the entire diel cycle, despite no visible prey in the guts of larvae collected at night. Sardine larvae preyed on early life stages of the most abundant copepod species (Oncaea waldemari, Paracalanus indicus and Temora stylifera), suggesting an opportunistic foraging behaviour. The use of multiplex PCR allowed species-level identification of ingested nauplii and protists, which otherwise would remain unidentified.</description><identifier>ISSN: 0171-8630</identifier><identifier>EISSN: 1616-1599</identifier><identifier>DOI: 10.3354/meps12833</identifier><language>eng</language><publisher>Oldendorf: Inter-Research Science Center</publisher><subject>Algae ; Animal morphology ; Aquatic crustaceans ; Biometry ; Clupeoid fisheries ; Diet ; DNA ; Feasibility studies ; Fish ; Fisheries ; Fishery resources ; Flagellates ; Foraging ; Foraging behavior ; Identification ; Larvae ; Length ; Marine fish ; Marine fishes ; Multiplexing ; Nauplii ; Night ; Nucleotide sequence ; PCR ; Plankton ; Polymerase chain reaction ; Prey ; Protists ; Sardina pilchardus ; Shoals ; Species ; Surveying ; Zooplankton</subject><ispartof>Marine ecology. 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Carmen</creatorcontrib><creatorcontrib>García-Gómez, Candela</creatorcontrib><creatorcontrib>Cortés, Dolores</creatorcontrib><creatorcontrib>Mercado, Jesús M.</creatorcontrib><creatorcontrib>Laiz-Carrión, Raúl</creatorcontrib><creatorcontrib>García, Alberto</creatorcontrib><creatorcontrib>Gómez-Jakobsen, Francisco</creatorcontrib><creatorcontrib>Uriarte, Amaya</creatorcontrib><creatorcontrib>Rodríguez, José M.</creatorcontrib><creatorcontrib>Quintanilla, José-María</creatorcontrib><title>Molecular identification of the diet of Sardina pilchardus larvae in the SW Mediterranean Sea</title><title>Marine ecology. Progress series (Halstenbek)</title><description>Molecular techniques provide new insights into the feeding strategies and diets of planktonic organisms such as the larvae of marine fish. We applied multiplex PCR to obtain the first estimates of the diets of larval European sardine Sardina pilchardus in the Alboran Sea (SW Mediterranean), where this species represents an important fishery resource. The feasibility of this technique was tested in a 26 h continuous survey of a shoal of larvae (10.80 ± 0.73 mm standard length, mean ± SD). Multiplex PCR was designed to detect the presence of 5 copepod species, a microplanktonic dinoflagellate (Gymnodinium) and the picoeukaryote algae family Prasinophyceae in larval guts. We simultaneously sampled sardine larvae and their potential prey (pico- to mesoplankton) and compared diel variability of the prey field and ingested items. Microplankton was dominated by flagellates, and copepods represented the most abundant mesozooplankton, reaching peak abundance at night. Prey DNA was detected throughout the entire diel cycle, despite no visible prey in the guts of larvae collected at night. Sardine larvae preyed on early life stages of the most abundant copepod species (Oncaea waldemari, Paracalanus indicus and Temora stylifera), suggesting an opportunistic foraging behaviour. The use of multiplex PCR allowed species-level identification of ingested nauplii and protists, which otherwise would remain unidentified.</description><subject>Algae</subject><subject>Animal morphology</subject><subject>Aquatic crustaceans</subject><subject>Biometry</subject><subject>Clupeoid fisheries</subject><subject>Diet</subject><subject>DNA</subject><subject>Feasibility studies</subject><subject>Fish</subject><subject>Fisheries</subject><subject>Fishery resources</subject><subject>Flagellates</subject><subject>Foraging</subject><subject>Foraging behavior</subject><subject>Identification</subject><subject>Larvae</subject><subject>Length</subject><subject>Marine fish</subject><subject>Marine fishes</subject><subject>Multiplexing</subject><subject>Nauplii</subject><subject>Night</subject><subject>Nucleotide sequence</subject><subject>PCR</subject><subject>Plankton</subject><subject>Polymerase chain reaction</subject><subject>Prey</subject><subject>Protists</subject><subject>Sardina pilchardus</subject><subject>Shoals</subject><subject>Species</subject><subject>Surveying</subject><subject>Zooplankton</subject><issn>0171-8630</issn><issn>1616-1599</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNo90MtKAzEUBuAgCtbqwgcQAq5cjOY2mclSilWhxUUVVzLE5AxNmWbGJCP49qZWujr_4jsXDkKXlNxyXoq7LQyRsprzIzShksqClkodowmhFS1qyckpOotxQwiVopIT9LHsOzBjpwN2FnxyrTM6ud7jvsVpDdg6SLu80sE6r_HgOrPOeYw4N31rwM7_wdU7XoJ1CULQHrTHK9Dn6KTVXYSL_zpFb_OH19lTsXh5fJ7dLwrDqUiFUoxVJTEMjBCmlEbKT5vvY7oFK5RpQRGmaq0ULzlwWxnFBYABU4I1bc2n6Ho_dwj91wgxNZt-DD6vbBjjpOa1JDSrm70yoY8xQNsMwW11-GkoaXbfaw7fy_Zqbzcx9eEAmaxqVWXwC32WbMo</recordid><startdate>20190516</startdate><enddate>20190516</enddate><creator>Yebra, Lidia</creator><creator>de Rojas, Alma Hernández</creator><creator>Valcárcel-Pérez, Nerea</creator><creator>Castro, M. 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Carmen ; García-Gómez, Candela ; Cortés, Dolores ; Mercado, Jesús M. ; Laiz-Carrión, Raúl ; García, Alberto ; Gómez-Jakobsen, Francisco ; Uriarte, Amaya ; Rodríguez, José M. ; Quintanilla, José-María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-9922750c2ec44c56c66bd6472afed49cfe90298a99353e3d7c934eecec5edcf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Algae</topic><topic>Animal morphology</topic><topic>Aquatic crustaceans</topic><topic>Biometry</topic><topic>Clupeoid fisheries</topic><topic>Diet</topic><topic>DNA</topic><topic>Feasibility studies</topic><topic>Fish</topic><topic>Fisheries</topic><topic>Fishery resources</topic><topic>Flagellates</topic><topic>Foraging</topic><topic>Foraging behavior</topic><topic>Identification</topic><topic>Larvae</topic><topic>Length</topic><topic>Marine fish</topic><topic>Marine fishes</topic><topic>Multiplexing</topic><topic>Nauplii</topic><topic>Night</topic><topic>Nucleotide sequence</topic><topic>PCR</topic><topic>Plankton</topic><topic>Polymerase chain reaction</topic><topic>Prey</topic><topic>Protists</topic><topic>Sardina pilchardus</topic><topic>Shoals</topic><topic>Species</topic><topic>Surveying</topic><topic>Zooplankton</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yebra, Lidia</creatorcontrib><creatorcontrib>de Rojas, Alma Hernández</creatorcontrib><creatorcontrib>Valcárcel-Pérez, Nerea</creatorcontrib><creatorcontrib>Castro, M. 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Progress series (Halstenbek)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yebra, Lidia</au><au>de Rojas, Alma Hernández</au><au>Valcárcel-Pérez, Nerea</au><au>Castro, M. Carmen</au><au>García-Gómez, Candela</au><au>Cortés, Dolores</au><au>Mercado, Jesús M.</au><au>Laiz-Carrión, Raúl</au><au>García, Alberto</au><au>Gómez-Jakobsen, Francisco</au><au>Uriarte, Amaya</au><au>Rodríguez, José M.</au><au>Quintanilla, José-María</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular identification of the diet of Sardina pilchardus larvae in the SW Mediterranean Sea</atitle><jtitle>Marine ecology. 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We simultaneously sampled sardine larvae and their potential prey (pico- to mesoplankton) and compared diel variability of the prey field and ingested items. Microplankton was dominated by flagellates, and copepods represented the most abundant mesozooplankton, reaching peak abundance at night. Prey DNA was detected throughout the entire diel cycle, despite no visible prey in the guts of larvae collected at night. Sardine larvae preyed on early life stages of the most abundant copepod species (Oncaea waldemari, Paracalanus indicus and Temora stylifera), suggesting an opportunistic foraging behaviour. The use of multiplex PCR allowed species-level identification of ingested nauplii and protists, which otherwise would remain unidentified.</abstract><cop>Oldendorf</cop><pub>Inter-Research Science Center</pub><doi>10.3354/meps12833</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | Jstor Complete Legacy; Alma/SFX Local Collection |
subjects | Algae Animal morphology Aquatic crustaceans Biometry Clupeoid fisheries Diet DNA Feasibility studies Fish Fisheries Fishery resources Flagellates Foraging Foraging behavior Identification Larvae Length Marine fish Marine fishes Multiplexing Nauplii Night Nucleotide sequence PCR Plankton Polymerase chain reaction Prey Protists Sardina pilchardus Shoals Species Surveying Zooplankton |
title | Molecular identification of the diet of Sardina pilchardus larvae in the SW Mediterranean Sea |
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