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) en In two waters: contemporary evolution of lagoonal and marine white seabream (Diplodus sargus) populations
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| 90 | "notes": "Brackish water ecosystems are often exposed to wide | 100 | "notes": "Brackish water ecosystems are often exposed to wide | ||
| 91 | variations in environmental variables, including temperature and | 101 | variations in environmental variables, including temperature and | ||
| 92 | salinity, which may cause strong selective pressures on organisms | 102 | salinity, which may cause strong selective pressures on organisms | ||
| 93 | modifying the genetic patterns of species. The aim of this work was to | 103 | modifying the genetic patterns of species. The aim of this work was to | ||
| 94 | test whether there is a divergence-with-gene flow in coastal lagoon | 104 | test whether there is a divergence-with-gene flow in coastal lagoon | ||
| 95 | populations of white seabream (Diplodus sargus) (Ria Formosa, S | 105 | populations of white seabream (Diplodus sargus) (Ria Formosa, S | ||
| 96 | Portugal and Mar Menor, SE Spain) respect to four marine populations, | 106 | Portugal and Mar Menor, SE Spain) respect to four marine populations, | ||
| 97 | by using partial sequences of cyt b mitochondrial gene and information | 107 | by using partial sequences of cyt b mitochondrial gene and information | ||
| 98 | from nine microsatellite loci. Genetic diversity was highest in both | 108 | from nine microsatellite loci. Genetic diversity was highest in both | ||
| 99 | coastal lagoons (Mar Menor and Ria Formosa) considering mitochondrial | 109 | coastal lagoons (Mar Menor and Ria Formosa) considering mitochondrial | ||
| 100 | and nuclear markers. Although some of FST population pairwise | 110 | and nuclear markers. Although some of FST population pairwise | ||
| 101 | comparisons were not significant, analyses of molecular variance | 111 | comparisons were not significant, analyses of molecular variance | ||
| 102 | (AMOVAs) detected differences between groups (coastal lagoon and | 112 | (AMOVAs) detected differences between groups (coastal lagoon and | ||
| 103 | marine) close to significance. Also, only two haplotypes (Cytb-17 and | 113 | marine) close to significance. Also, only two haplotypes (Cytb-17 and | ||
| 104 | Cytb-18) were detected in both coastal lagoon sampling sites and these | 114 | Cytb-18) were detected in both coastal lagoon sampling sites and these | ||
| 105 | localities (Mar Menor and Ria Formosa) showed the highest number of | 115 | localities (Mar Menor and Ria Formosa) showed the highest number of | ||
| 106 | singletons, some of them with a high number of mutations, as has been | 116 | singletons, some of them with a high number of mutations, as has been | ||
| 107 | already described for other Mar Menor populations (Pomatochistus | 117 | already described for other Mar Menor populations (Pomatochistus | ||
| 108 | marmoratus and Holothuria polii). Also, several tests detected | 118 | marmoratus and Holothuria polii). Also, several tests detected | ||
| 109 | significant positive and balancing selection considering mtDNA and | 119 | significant positive and balancing selection considering mtDNA and | ||
| 110 | microsatellite data. These data support the hypothesis of selection as | 120 | microsatellite data. These data support the hypothesis of selection as | ||
| 111 | one of the drivers of the genetic differences found between coastal | 121 | one of the drivers of the genetic differences found between coastal | ||
| 112 | lagoon and marine populations. The life strategy adopted by Diplodus | 122 | lagoon and marine populations. The life strategy adopted by Diplodus | ||
| 113 | sargus in coastal lagoons allows it to decrease its mortality rate and | 123 | sargus in coastal lagoons allows it to decrease its mortality rate and | ||
| 114 | improve the heritability of its genes. Also, the increase time spent | 124 | improve the heritability of its genes. Also, the increase time spent | ||
| 115 | in coastal lagoons with different temperatures and salinities favours | 125 | in coastal lagoons with different temperatures and salinities favours | ||
| 116 | the fitness selection and the maintenance of exclusive haplotypes and | 126 | the fitness selection and the maintenance of exclusive haplotypes and | ||
| 117 | genotypes in coastal lagoon inhabitants favouring the | 127 | genotypes in coastal lagoon inhabitants favouring the | ||
| 118 | divergence-with-gene-flow.", | 128 | divergence-with-gene-flow.", | ||
| 119 | "notes_translated": { | 129 | "notes_translated": { | ||
| 120 | "es": "Brackish water ecosystems are often exposed to wide | 130 | "es": "Brackish water ecosystems are often exposed to wide | ||
| 121 | variations in environmental variables, including temperature and | 131 | variations in environmental variables, including temperature and | ||
| 122 | salinity, which may cause strong selective pressures on organisms | 132 | salinity, which may cause strong selective pressures on organisms | ||
| 123 | modifying the genetic patterns of species. The aim of this work was to | 133 | modifying the genetic patterns of species. The aim of this work was to | ||
| 124 | test whether there is a divergence-with-gene flow in coastal lagoon | 134 | test whether there is a divergence-with-gene flow in coastal lagoon | ||
| 125 | populations of white seabream (Diplodus sargus) (Ria Formosa, S | 135 | populations of white seabream (Diplodus sargus) (Ria Formosa, S | ||
| 126 | Portugal and Mar Menor, SE Spain) respect to four marine populations, | 136 | Portugal and Mar Menor, SE Spain) respect to four marine populations, | ||
| 127 | by using partial sequences of cyt b mitochondrial gene and information | 137 | by using partial sequences of cyt b mitochondrial gene and information | ||
| 128 | from nine microsatellite loci. Genetic diversity was highest in both | 138 | from nine microsatellite loci. Genetic diversity was highest in both | ||
| 129 | coastal lagoons (Mar Menor and Ria Formosa) considering mitochondrial | 139 | coastal lagoons (Mar Menor and Ria Formosa) considering mitochondrial | ||
| 130 | and nuclear markers. Although some of FST population pairwise | 140 | and nuclear markers. Although some of FST population pairwise | ||
| 131 | comparisons were not significant, analyses of molecular variance | 141 | comparisons were not significant, analyses of molecular variance | ||
| 132 | (AMOVAs) detected differences between groups (coastal lagoon and | 142 | (AMOVAs) detected differences between groups (coastal lagoon and | ||
| 133 | marine) close to significance. Also, only two haplotypes (Cytb-17 and | 143 | marine) close to significance. Also, only two haplotypes (Cytb-17 and | ||
| 134 | Cytb-18) were detected in both coastal lagoon sampling sites and these | 144 | Cytb-18) were detected in both coastal lagoon sampling sites and these | ||
| 135 | localities (Mar Menor and Ria Formosa) showed the highest number of | 145 | localities (Mar Menor and Ria Formosa) showed the highest number of | ||
| 136 | singletons, some of them with a high number of mutations, as has been | 146 | singletons, some of them with a high number of mutations, as has been | ||
| 137 | already described for other Mar Menor populations (Pomatochistus | 147 | already described for other Mar Menor populations (Pomatochistus | ||
| 138 | marmoratus and Holothuria polii). Also, several tests detected | 148 | marmoratus and Holothuria polii). Also, several tests detected | ||
| 139 | significant positive and balancing selection considering mtDNA and | 149 | significant positive and balancing selection considering mtDNA and | ||
| 140 | microsatellite data. These data support the hypothesis of selection as | 150 | microsatellite data. These data support the hypothesis of selection as | ||
| 141 | one of the drivers of the genetic differences found between coastal | 151 | one of the drivers of the genetic differences found between coastal | ||
| 142 | lagoon and marine populations. The life strategy adopted by Diplodus | 152 | lagoon and marine populations. The life strategy adopted by Diplodus | ||
| 143 | sargus in coastal lagoons allows it to decrease its mortality rate and | 153 | sargus in coastal lagoons allows it to decrease its mortality rate and | ||
| 144 | improve the heritability of its genes. Also, the increase time spent | 154 | improve the heritability of its genes. Also, the increase time spent | ||
| 145 | in coastal lagoons with different temperatures and salinities favours | 155 | in coastal lagoons with different temperatures and salinities favours | ||
| 146 | the fitness selection and the maintenance of exclusive haplotypes and | 156 | the fitness selection and the maintenance of exclusive haplotypes and | ||
| 147 | genotypes in coastal lagoon inhabitants favouring the | 157 | genotypes in coastal lagoon inhabitants favouring the | ||
| 148 | divergence-with-gene-flow." | 158 | divergence-with-gene-flow." | ||
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