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) en Environmental variables, habitat discontinuity and life history shaping the genetic structure of Pomatoschistus marmoratus
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| 93 | wide fluctuations of environmental conditions and showing habitat | 103 | wide fluctuations of environmental conditions and showing habitat | ||
| 94 | fragmentation. These features may play an important role in separating | 104 | fragmentation. These features may play an important role in separating | ||
| 95 | species into different populations, even at small spatial scales. In | 105 | species into different populations, even at small spatial scales. In | ||
| 96 | this study, we evaluate the concordance between mitochondrial | 106 | this study, we evaluate the concordance between mitochondrial | ||
| 97 | (previous published data) and nuclear data analyzing the genetic | 107 | (previous published data) and nuclear data analyzing the genetic | ||
| 98 | variability of Pomatoschistus marmoratus in five localities, inside | 108 | variability of Pomatoschistus marmoratus in five localities, inside | ||
| 99 | and outside the Mar Menor coastal lagoon (SE Spain) using eight | 109 | and outside the Mar Menor coastal lagoon (SE Spain) using eight | ||
| 100 | microsatellites. High genetic diversity and similar levels of allele | 110 | microsatellites. High genetic diversity and similar levels of allele | ||
| 101 | richness were observed across all loci and localities, although | 111 | richness were observed across all loci and localities, although | ||
| 102 | significant genic and genotypic differentiation was found between | 112 | significant genic and genotypic differentiation was found between | ||
| 103 | populations inside and outside the lagoon. In contrast to the F (ST) | 113 | populations inside and outside the lagoon. In contrast to the F (ST) | ||
| 104 | values obtained from previous mitochondrial DNA analyses (control | 114 | values obtained from previous mitochondrial DNA analyses (control | ||
| 105 | region), the microsatellite data exhibited significant differentiation | 115 | region), the microsatellite data exhibited significant differentiation | ||
| 106 | among samples inside the Mar Menor and between lagoonal and marine | 116 | among samples inside the Mar Menor and between lagoonal and marine | ||
| 107 | samples. This pattern was corroborated using Cavalli-Sforza genetic | 117 | samples. This pattern was corroborated using Cavalli-Sforza genetic | ||
| 108 | distances. The habitat fragmentation inside the coastal lagoon and | 118 | distances. The habitat fragmentation inside the coastal lagoon and | ||
| 109 | among lagoon and marine localities could be acting as a barrier to | 119 | among lagoon and marine localities could be acting as a barrier to | ||
| 110 | gene flow and contributing to the observed genetic structure. Our | 120 | gene flow and contributing to the observed genetic structure. Our | ||
| 111 | results from generalized additive models point a significant link | 121 | results from generalized additive models point a significant link | ||
| 112 | between extreme lagoonal environmental conditions (mainly maximum | 122 | between extreme lagoonal environmental conditions (mainly maximum | ||
| 113 | salinity) and P. marmoratus genetic composition. Thereby, these | 123 | salinity) and P. marmoratus genetic composition. Thereby, these | ||
| 114 | environmental features could be also acting on genetic structure of | 124 | environmental features could be also acting on genetic structure of | ||
| 115 | coastal lagoon populations of P. marmoratus favoring their genetic | 125 | coastal lagoon populations of P. marmoratus favoring their genetic | ||
| 116 | divergence. The mating strategy of P. marmoratus could be also | 126 | divergence. The mating strategy of P. marmoratus could be also | ||
| 117 | influencing our results obtained from mitochondrial and nuclear DNA. | 127 | influencing our results obtained from mitochondrial and nuclear DNA. | ||
| 118 | Therefore, a special consideration must be done in the selection of | 128 | Therefore, a special consideration must be done in the selection of | ||
| 119 | the DNA markers depending on the reproductive strategy of the | 129 | the DNA markers depending on the reproductive strategy of the | ||
| 120 | species.", | 130 | species.", | ||
| 121 | "notes_translated": { | 131 | "notes_translated": { | ||
| 122 | "es": "Coastal lagoons are semi-isolated ecosystems exposed to | 132 | "es": "Coastal lagoons are semi-isolated ecosystems exposed to | ||
| 123 | wide fluctuations of environmental conditions and showing habitat | 133 | wide fluctuations of environmental conditions and showing habitat | ||
| 124 | fragmentation. These features may play an important role in separating | 134 | fragmentation. These features may play an important role in separating | ||
| 125 | species into different populations, even at small spatial scales. In | 135 | species into different populations, even at small spatial scales. In | ||
| 126 | this study, we evaluate the concordance between mitochondrial | 136 | this study, we evaluate the concordance between mitochondrial | ||
| 127 | (previous published data) and nuclear data analyzing the genetic | 137 | (previous published data) and nuclear data analyzing the genetic | ||
| 128 | variability of Pomatoschistus marmoratus in five localities, inside | 138 | variability of Pomatoschistus marmoratus in five localities, inside | ||
| 129 | and outside the Mar Menor coastal lagoon (SE Spain) using eight | 139 | and outside the Mar Menor coastal lagoon (SE Spain) using eight | ||
| 130 | microsatellites. High genetic diversity and similar levels of allele | 140 | microsatellites. High genetic diversity and similar levels of allele | ||
| 131 | richness were observed across all loci and localities, although | 141 | richness were observed across all loci and localities, although | ||
| 132 | significant genic and genotypic differentiation was found between | 142 | significant genic and genotypic differentiation was found between | ||
| 133 | populations inside and outside the lagoon. In contrast to the F (ST) | 143 | populations inside and outside the lagoon. In contrast to the F (ST) | ||
| 134 | values obtained from previous mitochondrial DNA analyses (control | 144 | values obtained from previous mitochondrial DNA analyses (control | ||
| 135 | region), the microsatellite data exhibited significant differentiation | 145 | region), the microsatellite data exhibited significant differentiation | ||
| 136 | among samples inside the Mar Menor and between lagoonal and marine | 146 | among samples inside the Mar Menor and between lagoonal and marine | ||
| 137 | samples. This pattern was corroborated using Cavalli-Sforza genetic | 147 | samples. This pattern was corroborated using Cavalli-Sforza genetic | ||
| 138 | distances. The habitat fragmentation inside the coastal lagoon and | 148 | distances. The habitat fragmentation inside the coastal lagoon and | ||
| 139 | among lagoon and marine localities could be acting as a barrier to | 149 | among lagoon and marine localities could be acting as a barrier to | ||
| 140 | gene flow and contributing to the observed genetic structure. Our | 150 | gene flow and contributing to the observed genetic structure. Our | ||
| 141 | results from generalized additive models point a significant link | 151 | results from generalized additive models point a significant link | ||
| 142 | between extreme lagoonal environmental conditions (mainly maximum | 152 | between extreme lagoonal environmental conditions (mainly maximum | ||
| 143 | salinity) and P. marmoratus genetic composition. Thereby, these | 153 | salinity) and P. marmoratus genetic composition. Thereby, these | ||
| 144 | environmental features could be also acting on genetic structure of | 154 | environmental features could be also acting on genetic structure of | ||
| 145 | coastal lagoon populations of P. marmoratus favoring their genetic | 155 | coastal lagoon populations of P. marmoratus favoring their genetic | ||
| 146 | divergence. The mating strategy of P. marmoratus could be also | 156 | divergence. The mating strategy of P. marmoratus could be also | ||
| 147 | influencing our results obtained from mitochondrial and nuclear DNA. | 157 | influencing our results obtained from mitochondrial and nuclear DNA. | ||
| 148 | Therefore, a special consideration must be done in the selection of | 158 | Therefore, a special consideration must be done in the selection of | ||
| 149 | the DNA markers depending on the reproductive strategy of the | 159 | the DNA markers depending on the reproductive strategy of the | ||
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| 318 | ], | 328 | ], | ||
| 319 | "title": "Environmental variables, habitat discontinuity and life | 329 | "title": "Environmental variables, habitat discontinuity and life | ||
| 320 | history shaping the genetic structure of Pomatoschistus marmoratus", | 330 | history shaping the genetic structure of Pomatoschistus marmoratus", | ||
| 321 | "title_translated": { | 331 | "title_translated": { | ||
| 322 | "es": "Environmental variables, habitat discontinuity and life | 332 | "es": "Environmental variables, habitat discontinuity and life | ||
| 323 | history shaping the genetic structure of Pomatoschistus marmoratus" | 333 | history shaping the genetic structure of Pomatoschistus marmoratus" | ||
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