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En el instante 23 de junio de 2026, 16:04:32 UTC,
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Modificado el valor del campo
spatial_coverage
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en Spatio-temporal Variation of Shallow Microhabitats and Associated Juvenile Fish Assemblages in a Mediterranean Lagoon
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| 93 | "notes": "Coastal lagoons are known to host numerous resident and | 93 | "notes": "Coastal lagoons are known to host numerous resident and | ||
| 94 | migrant fish species. Spatio-temporal variation in abiotic and biotic | 94 | migrant fish species. Spatio-temporal variation in abiotic and biotic | ||
| 95 | conditions in these ecosystems results, however, in a mosaic of | 95 | conditions in these ecosystems results, however, in a mosaic of | ||
| 96 | microhabitats that could differently affect juvenile growth\n and | 96 | microhabitats that could differently affect juvenile growth\n and | ||
| 97 | survival. To deepen our understanding of juvenile fish habitat | 97 | survival. To deepen our understanding of juvenile fish habitat | ||
| 98 | requirements and their spatio-temporal use of lagoons, microhabitat | 98 | requirements and their spatio-temporal use of lagoons, microhabitat | ||
| 99 | characteristics and fish assemblages were monitored jointly in a small | 99 | characteristics and fish assemblages were monitored jointly in a small | ||
| 100 | temperate lagoon (the Pr\u00e9vost lagoon),\n from March to October | 100 | temperate lagoon (the Pr\u00e9vost lagoon),\n from March to October | ||
| 101 | 2019. A total of 2206 juvenile fishes belonging to 22 species were | 101 | 2019. A total of 2206 juvenile fishes belonging to 22 species were | ||
| 102 | collected. Resident lagoon species, especially Atherina boyeri, | 102 | collected. Resident lagoon species, especially Atherina boyeri, | ||
| 103 | dominated the assemblage (74%), while, among migrant species, Sparus | 103 | dominated the assemblage (74%), while, among migrant species, Sparus | ||
| 104 | aurata (8%) and Liza\n aurata (5%) were the most represented. Changes | 104 | aurata (8%) and Liza\n aurata (5%) were the most represented. Changes | ||
| 105 | in overall juvenile abundance were mainly temporal, following the | 105 | in overall juvenile abundance were mainly temporal, following the | ||
| 106 | seasonal shifts in water temperature, salinity, and chlorophyll a | 106 | seasonal shifts in water temperature, salinity, and chlorophyll a | ||
| 107 | concentration (44.9% of the co-inertia). However, our results | 107 | concentration (44.9% of the co-inertia). However, our results | ||
| 108 | revealed\n that distinct types of microhabitats exist in small lagoons | 108 | revealed\n that distinct types of microhabitats exist in small lagoons | ||
| 109 | and that juvenile fish distribution among them is non-random. Indeed, | 109 | and that juvenile fish distribution among them is non-random. Indeed, | ||
| 110 | fish species richness mainly differed among sampling sites in relation | 110 | fish species richness mainly differed among sampling sites in relation | ||
| 111 | to their distance from the inlet and the complexity\n of the | 111 | to their distance from the inlet and the complexity\n of the | ||
| 112 | three-dimensional habitat structure (36.5% of the co-inertia). | 112 | three-dimensional habitat structure (36.5% of the co-inertia). | ||
| 113 | Juveniles preferentially selected microhabitats with medium to high | 113 | Juveniles preferentially selected microhabitats with medium to high | ||
| 114 | structural complexity, which were essentially created by macroalgae. | 114 | structural complexity, which were essentially created by macroalgae. | ||
| 115 | However, microhabitat preferences\n were both species and ontogenetic | 115 | However, microhabitat preferences\n were both species and ontogenetic | ||
| 116 | stage dependent, with more contrasting microhabitat requirements in | 116 | stage dependent, with more contrasting microhabitat requirements in | ||
| 117 | young juveniles. These results underline the need for conservation | 117 | young juveniles. These results underline the need for conservation | ||
| 118 | measures to consider each lagoon as a dynamic mosaic of microhabitats | 118 | measures to consider each lagoon as a dynamic mosaic of microhabitats | ||
| 119 | with radically different importance for the juveniles of the various | 119 | with radically different importance for the juveniles of the various | ||
| 120 | fish species that colonize them.", | 120 | fish species that colonize them.", | ||
| 121 | "notes_translated": { | 121 | "notes_translated": { | ||
| 122 | "es": "Coastal lagoons are known to host numerous resident and | 122 | "es": "Coastal lagoons are known to host numerous resident and | ||
| 123 | migrant fish species. Spatio-temporal variation in abiotic and biotic | 123 | migrant fish species. Spatio-temporal variation in abiotic and biotic | ||
| 124 | conditions in these ecosystems results, however, in a mosaic of | 124 | conditions in these ecosystems results, however, in a mosaic of | ||
| 125 | microhabitats that could differently affect juvenile growth\n and | 125 | microhabitats that could differently affect juvenile growth\n and | ||
| 126 | survival. To deepen our understanding of juvenile fish habitat | 126 | survival. To deepen our understanding of juvenile fish habitat | ||
| 127 | requirements and their spatio-temporal use of lagoons, microhabitat | 127 | requirements and their spatio-temporal use of lagoons, microhabitat | ||
| 128 | characteristics and fish assemblages were monitored jointly in a small | 128 | characteristics and fish assemblages were monitored jointly in a small | ||
| 129 | temperate lagoon (the Pr\u00e9vost lagoon),\n from March to October | 129 | temperate lagoon (the Pr\u00e9vost lagoon),\n from March to October | ||
| 130 | 2019. A total of 2206 juvenile fishes belonging to 22 species were | 130 | 2019. A total of 2206 juvenile fishes belonging to 22 species were | ||
| 131 | collected. Resident lagoon species, especially Atherina boyeri, | 131 | collected. Resident lagoon species, especially Atherina boyeri, | ||
| 132 | dominated the assemblage (74%), while, among migrant species, Sparus | 132 | dominated the assemblage (74%), while, among migrant species, Sparus | ||
| 133 | aurata (8%) and Liza\n aurata (5%) were the most represented. Changes | 133 | aurata (8%) and Liza\n aurata (5%) were the most represented. Changes | ||
| 134 | in overall juvenile abundance were mainly temporal, following the | 134 | in overall juvenile abundance were mainly temporal, following the | ||
| 135 | seasonal shifts in water temperature, salinity, and chlorophyll a | 135 | seasonal shifts in water temperature, salinity, and chlorophyll a | ||
| 136 | concentration (44.9% of the co-inertia). However, our results | 136 | concentration (44.9% of the co-inertia). However, our results | ||
| 137 | revealed\n that distinct types of microhabitats exist in small lagoons | 137 | revealed\n that distinct types of microhabitats exist in small lagoons | ||
| 138 | and that juvenile fish distribution among them is non-random. Indeed, | 138 | and that juvenile fish distribution among them is non-random. Indeed, | ||
| 139 | fish species richness mainly differed among sampling sites in relation | 139 | fish species richness mainly differed among sampling sites in relation | ||
| 140 | to their distance from the inlet and the complexity\n of the | 140 | to their distance from the inlet and the complexity\n of the | ||
| 141 | three-dimensional habitat structure (36.5% of the co-inertia). | 141 | three-dimensional habitat structure (36.5% of the co-inertia). | ||
| 142 | Juveniles preferentially selected microhabitats with medium to high | 142 | Juveniles preferentially selected microhabitats with medium to high | ||
| 143 | structural complexity, which were essentially created by macroalgae. | 143 | structural complexity, which were essentially created by macroalgae. | ||
| 144 | However, microhabitat preferences\n were both species and ontogenetic | 144 | However, microhabitat preferences\n were both species and ontogenetic | ||
| 145 | stage dependent, with more contrasting microhabitat requirements in | 145 | stage dependent, with more contrasting microhabitat requirements in | ||
| 146 | young juveniles. These results underline the need for conservation | 146 | young juveniles. These results underline the need for conservation | ||
| 147 | measures to consider each lagoon as a dynamic mosaic of microhabitats | 147 | measures to consider each lagoon as a dynamic mosaic of microhabitats | ||
| 148 | with radically different importance for the juveniles of the various | 148 | with radically different importance for the juveniles of the various | ||
| 149 | fish species that colonize them." | 149 | fish species that colonize them." | ||
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