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) en Variability of growth rates and thermohaline niches of Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)
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| 92 | frequency of bloom events has been reported for the scyphozoan | 102 | frequency of bloom events has been reported for the scyphozoan | ||
| 93 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | 103 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | ||
| 94 | requires a thorough assessment of the species' population dynamics | 104 | requires a thorough assessment of the species' population dynamics | ||
| 95 | through environmental windows allowing species development. The | 105 | through environmental windows allowing species development. The | ||
| 96 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | 106 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | ||
| 97 | 12.72 '' N; 3 degrees 00 ' 35.3 '' E) offers an exceptional framework | 107 | 12.72 '' N; 3 degrees 00 ' 35.3 '' E) offers an exceptional framework | ||
| 98 | for investigating the population dynamics of the species, and how its | 108 | for investigating the population dynamics of the species, and how its | ||
| 99 | growth rates and environmental niches vary over time. Three cohorts | 109 | growth rates and environmental niches vary over time. Three cohorts | ||
| 100 | starting in April, May and June 2019 were identified, while the | 110 | starting in April, May and June 2019 were identified, while the | ||
| 101 | overall population growth reached the maximum biomass (10.2 g m(-3)) | 111 | overall population growth reached the maximum biomass (10.2 g m(-3)) | ||
| 102 | in July. Bell diameter and total length were identified as the best | 112 | in July. Bell diameter and total length were identified as the best | ||
| 103 | morphological proxies of biomass estimation. The abundances of the two | 113 | morphological proxies of biomass estimation. The abundances of the two | ||
| 104 | most abundant copepods' species appear to drive R. pulmo's dynamics in | 114 | most abundant copepods' species appear to drive R. pulmo's dynamics in | ||
| 105 | the lagoon. Based on multinomial analysis and using the von | 115 | the lagoon. Based on multinomial analysis and using the von | ||
| 106 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | 116 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | ||
| 107 | mm day(-1)) and adults (1.8 and 0.9 mm day(-1)) were determined for | 117 | mm day(-1)) and adults (1.8 and 0.9 mm day(-1)) were determined for | ||
| 108 | the first two cohorts. Thermohaline niches varied during ontogeny, but | 118 | the first two cohorts. Thermohaline niches varied during ontogeny, but | ||
| 109 | also among populations in three coastal Mediterranean lagoons: Bages | 119 | also among populations in three coastal Mediterranean lagoons: Bages | ||
| 110 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | 120 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | ||
| 111 | light on the metapopulation dynamics of R. pulmo inhabiting the | 121 | light on the metapopulation dynamics of R. pulmo inhabiting the | ||
| 112 | Mediterranean Sea. The pressing need for understanding the dynamics of | 122 | Mediterranean Sea. The pressing need for understanding the dynamics of | ||
| 113 | jellyfish abundances and their impacts on ecosystems, calls for | 123 | jellyfish abundances and their impacts on ecosystems, calls for | ||
| 114 | increased efforts on monitoring these populations and their life | 124 | increased efforts on monitoring these populations and their life | ||
| 115 | history traits to parametrize and build reliable ecosystem models.", | 125 | history traits to parametrize and build reliable ecosystem models.", | ||
| 116 | "notes_translated": { | 126 | "notes_translated": { | ||
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| 119 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | 129 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | ||
| 120 | requires a thorough assessment of the species' population dynamics | 130 | requires a thorough assessment of the species' population dynamics | ||
| 121 | through environmental windows allowing species development. The | 131 | through environmental windows allowing species development. The | ||
| 122 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | 132 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | ||
| 123 | 12.72 '' N; 3 degrees 00 ' 35.3 '' E) offers an exceptional framework | 133 | 12.72 '' N; 3 degrees 00 ' 35.3 '' E) offers an exceptional framework | ||
| 124 | for investigating the population dynamics of the species, and how its | 134 | for investigating the population dynamics of the species, and how its | ||
| 125 | growth rates and environmental niches vary over time. Three cohorts | 135 | growth rates and environmental niches vary over time. Three cohorts | ||
| 126 | starting in April, May and June 2019 were identified, while the | 136 | starting in April, May and June 2019 were identified, while the | ||
| 127 | overall population growth reached the maximum biomass (10.2 g m(-3)) | 137 | overall population growth reached the maximum biomass (10.2 g m(-3)) | ||
| 128 | in July. Bell diameter and total length were identified as the best | 138 | in July. Bell diameter and total length were identified as the best | ||
| 129 | morphological proxies of biomass estimation. The abundances of the two | 139 | morphological proxies of biomass estimation. The abundances of the two | ||
| 130 | most abundant copepods' species appear to drive R. pulmo's dynamics in | 140 | most abundant copepods' species appear to drive R. pulmo's dynamics in | ||
| 131 | the lagoon. Based on multinomial analysis and using the von | 141 | the lagoon. Based on multinomial analysis and using the von | ||
| 132 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | 142 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | ||
| 133 | mm day(-1)) and adults (1.8 and 0.9 mm day(-1)) were determined for | 143 | mm day(-1)) and adults (1.8 and 0.9 mm day(-1)) were determined for | ||
| 134 | the first two cohorts. Thermohaline niches varied during ontogeny, but | 144 | the first two cohorts. Thermohaline niches varied during ontogeny, but | ||
| 135 | also among populations in three coastal Mediterranean lagoons: Bages | 145 | also among populations in three coastal Mediterranean lagoons: Bages | ||
| 136 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | 146 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | ||
| 137 | light on the metapopulation dynamics of R. pulmo inhabiting the | 147 | light on the metapopulation dynamics of R. pulmo inhabiting the | ||
| 138 | Mediterranean Sea. The pressing need for understanding the dynamics of | 148 | Mediterranean Sea. The pressing need for understanding the dynamics of | ||
| 139 | jellyfish abundances and their impacts on ecosystems, calls for | 149 | jellyfish abundances and their impacts on ecosystems, calls for | ||
| 140 | increased efforts on monitoring these populations and their life | 150 | increased efforts on monitoring these populations and their life | ||
| 141 | history traits to parametrize and build reliable ecosystem models." | 151 | history traits to parametrize and build reliable ecosystem models." | ||
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| 256 | "tag_uri": [ | 266 | "tag_uri": [ | ||
| 257 | 267 | ||||
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| 259 | ], | 269 | ], | ||
| 260 | "tags": [ | 270 | "tags": [ | ||
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| 263 | "id": "ddab08b5-a7e4-4187-9b0f-d4459c83a9ba", | 273 | "id": "ddab08b5-a7e4-4187-9b0f-d4459c83a9ba", | ||
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| 267 | }, | 277 | }, | ||
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| 270 | "id": "beac51fe-4177-49b8-8c38-807c43f94d03", | 280 | "id": "beac51fe-4177-49b8-8c38-807c43f94d03", | ||
| 271 | "name": "ciclo_vegetativo", | 281 | "name": "ciclo_vegetativo", | ||
| 272 | "state": "active", | 282 | "state": "active", | ||
| 273 | "vocabulary_id": null | 283 | "vocabulary_id": null | ||
| 274 | }, | 284 | }, | ||
| 275 | { | 285 | { | ||
| 276 | "display_name": "crecimiento", | 286 | "display_name": "crecimiento", | ||
| 277 | "id": "b283bd04-cbae-4946-8031-ffed0cb5613a", | 287 | "id": "b283bd04-cbae-4946-8031-ffed0cb5613a", | ||
| 278 | "name": "crecimiento", | 288 | "name": "crecimiento", | ||
| 279 | "state": "active", | 289 | "state": "active", | ||
| 280 | "vocabulary_id": null | 290 | "vocabulary_id": null | ||
| 281 | }, | 291 | }, | ||
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| 284 | "id": "6f6a93d2-3b9d-49ce-bd99-d38372f6b273", | 294 | "id": "6f6a93d2-3b9d-49ce-bd99-d38372f6b273", | ||
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| 287 | "vocabulary_id": null | 297 | "vocabulary_id": null | ||
| 288 | }, | 298 | }, | ||
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| 294 | "vocabulary_id": null | 304 | "vocabulary_id": null | ||
| 295 | }, | 305 | }, | ||
| 296 | { | 306 | { | ||
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| 298 | "id": "5b7e46a9-0277-4e63-a2a6-39c30d363836", | 308 | "id": "5b7e46a9-0277-4e63-a2a6-39c30d363836", | ||
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| 302 | } | 312 | } | ||
| 303 | ], | 313 | ], | ||
| 304 | "thematic_area": [ | 314 | "thematic_area": [ | ||
| 305 | "espacios_protegidos" | 315 | "espacios_protegidos" | ||
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| 307 | "theme_es": [ | 317 | "theme_es": [ | ||
| 308 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | 318 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | ||
| 309 | ], | 319 | ], | ||
| 310 | "title": "Variability of growth rates and thermohaline niches of | 320 | "title": "Variability of growth rates and thermohaline niches of | ||
| 311 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)", | 321 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)", | ||
| 312 | "title_translated": { | 322 | "title_translated": { | ||
| 313 | "es": "Variability of growth rates and thermohaline niches of | 323 | "es": "Variability of growth rates and thermohaline niches of | ||
| 314 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)" | 324 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)" | ||
| 315 | }, | 325 | }, | ||
| 316 | "topic": | 326 | "topic": | ||
| 317 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | 327 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | ||
| 318 | "type": "dataset", | 328 | "type": "dataset", | ||
| 319 | "url": | 329 | "url": | ||
| 320 | //iepnb.es:443/catalogo/dataset/03f548dd-0997-52ac-baac-04bf5121f230", | 330 | //iepnb.es:443/catalogo/dataset/03f548dd-0997-52ac-baac-04bf5121f230", | ||
| 321 | "version_notes": { | 331 | "version_notes": { | ||
| 322 | "es": "" | 332 | "es": "" | ||
| 323 | } | 333 | } | ||
| 324 | } | 334 | } |