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En el instante 23 de junio de 2026, 16:14:25 UTC,
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Modificado el valor del campo
spatial_coverage
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en Variability of growth rates and thermohaline niches of Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)
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| 91 | "notes": "In recent decades, an increase in the abundance and | 91 | "notes": "In recent decades, an increase in the abundance and | ||
| 92 | frequency of bloom events has been reported for the scyphozoan | 92 | frequency of bloom events has been reported for the scyphozoan | ||
| 93 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | 93 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | ||
| 94 | requires a thorough assessment of the species' population dynamics | 94 | requires a thorough assessment of the species' population dynamics | ||
| 95 | through environmental windows allowing species development. The | 95 | through environmental windows allowing species development. The | ||
| 96 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | 96 | 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 | 97 | 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 | 98 | for investigating the population dynamics of the species, and how its | ||
| 99 | growth rates and environmental niches vary over time. Three cohorts | 99 | growth rates and environmental niches vary over time. Three cohorts | ||
| 100 | starting in April, May and June 2019 were identified, while the | 100 | starting in April, May and June 2019 were identified, while the | ||
| 101 | overall population growth reached the maximum biomass (10.2 g m(-3)) | 101 | 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 | 102 | in July. Bell diameter and total length were identified as the best | ||
| 103 | morphological proxies of biomass estimation. The abundances of the two | 103 | morphological proxies of biomass estimation. The abundances of the two | ||
| 104 | most abundant copepods' species appear to drive R. pulmo's dynamics in | 104 | most abundant copepods' species appear to drive R. pulmo's dynamics in | ||
| 105 | the lagoon. Based on multinomial analysis and using the von | 105 | the lagoon. Based on multinomial analysis and using the von | ||
| 106 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | 106 | 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 | 107 | 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 | 108 | the first two cohorts. Thermohaline niches varied during ontogeny, but | ||
| 109 | also among populations in three coastal Mediterranean lagoons: Bages | 109 | also among populations in three coastal Mediterranean lagoons: Bages | ||
| 110 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | 110 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | ||
| 111 | light on the metapopulation dynamics of R. pulmo inhabiting the | 111 | light on the metapopulation dynamics of R. pulmo inhabiting the | ||
| 112 | Mediterranean Sea. The pressing need for understanding the dynamics of | 112 | Mediterranean Sea. The pressing need for understanding the dynamics of | ||
| 113 | jellyfish abundances and their impacts on ecosystems, calls for | 113 | jellyfish abundances and their impacts on ecosystems, calls for | ||
| 114 | increased efforts on monitoring these populations and their life | 114 | increased efforts on monitoring these populations and their life | ||
| 115 | history traits to parametrize and build reliable ecosystem models.", | 115 | history traits to parametrize and build reliable ecosystem models.", | ||
| 116 | "notes_translated": { | 116 | "notes_translated": { | ||
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| 118 | frequency of bloom events has been reported for the scyphozoan | 118 | frequency of bloom events has been reported for the scyphozoan | ||
| 119 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | 119 | Rhizostoma pulmo in the Mediterranean Sea. Understanding such events | ||
| 120 | requires a thorough assessment of the species' population dynamics | 120 | requires a thorough assessment of the species' population dynamics | ||
| 121 | through environmental windows allowing species development. The | 121 | through environmental windows allowing species development. The | ||
| 122 | semi-enclosed coastal lagoon of Bages Sigean, France (43 degrees 05 ' | 122 | 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 | 123 | 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 | 124 | for investigating the population dynamics of the species, and how its | ||
| 125 | growth rates and environmental niches vary over time. Three cohorts | 125 | growth rates and environmental niches vary over time. Three cohorts | ||
| 126 | starting in April, May and June 2019 were identified, while the | 126 | starting in April, May and June 2019 were identified, while the | ||
| 127 | overall population growth reached the maximum biomass (10.2 g m(-3)) | 127 | 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 | 128 | in July. Bell diameter and total length were identified as the best | ||
| 129 | morphological proxies of biomass estimation. The abundances of the two | 129 | morphological proxies of biomass estimation. The abundances of the two | ||
| 130 | most abundant copepods' species appear to drive R. pulmo's dynamics in | 130 | most abundant copepods' species appear to drive R. pulmo's dynamics in | ||
| 131 | the lagoon. Based on multinomial analysis and using the von | 131 | the lagoon. Based on multinomial analysis and using the von | ||
| 132 | Bertalanffy model, different growth rates for juveniles (4.7 and 2.4 | 132 | 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 | 133 | 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 | 134 | the first two cohorts. Thermohaline niches varied during ontogeny, but | ||
| 135 | also among populations in three coastal Mediterranean lagoons: Bages | 135 | also among populations in three coastal Mediterranean lagoons: Bages | ||
| 136 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | 136 | Sigean (France), Mar Menor (Spain) and Bizerte (Tunisia), shedding | ||
| 137 | light on the metapopulation dynamics of R. pulmo inhabiting the | 137 | light on the metapopulation dynamics of R. pulmo inhabiting the | ||
| 138 | Mediterranean Sea. The pressing need for understanding the dynamics of | 138 | Mediterranean Sea. The pressing need for understanding the dynamics of | ||
| 139 | jellyfish abundances and their impacts on ecosystems, calls for | 139 | jellyfish abundances and their impacts on ecosystems, calls for | ||
| 140 | increased efforts on monitoring these populations and their life | 140 | increased efforts on monitoring these populations and their life | ||
| 141 | history traits to parametrize and build reliable ecosystem models." | 141 | history traits to parametrize and build reliable ecosystem models." | ||
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| 275 | "uri": | 246 | "uri": | ||
| 276 | atos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia" | 247 | atos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia" | ||
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| 283 | "es": "" | 254 | "es": "" | ||
| 284 | }, | 255 | }, | ||
| 285 | "tag_uri": [ | 256 | "tag_uri": [ | ||
| 286 | 257 | ||||
| 287 | tp://inspire.ec.europa.eu/metadata-codelist/TopicCategory/environment" | 258 | tp://inspire.ec.europa.eu/metadata-codelist/TopicCategory/environment" | ||
| 288 | ], | 259 | ], | ||
| 289 | "tags": [ | 260 | "tags": [ | ||
| 290 | { | 261 | { | ||
| 291 | "display_name": "aguas_interiores", | 262 | "display_name": "aguas_interiores", | ||
| 292 | "id": "ddab08b5-a7e4-4187-9b0f-d4459c83a9ba", | 263 | "id": "ddab08b5-a7e4-4187-9b0f-d4459c83a9ba", | ||
| 293 | "name": "aguas_interiores", | 264 | "name": "aguas_interiores", | ||
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| 299 | "id": "beac51fe-4177-49b8-8c38-807c43f94d03", | 270 | "id": "beac51fe-4177-49b8-8c38-807c43f94d03", | ||
| 300 | "name": "ciclo_vegetativo", | 271 | "name": "ciclo_vegetativo", | ||
| 301 | "state": "active", | 272 | "state": "active", | ||
| 302 | "vocabulary_id": null | 273 | "vocabulary_id": null | ||
| 303 | }, | 274 | }, | ||
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| 305 | "display_name": "crecimiento", | 276 | "display_name": "crecimiento", | ||
| 306 | "id": "b283bd04-cbae-4946-8031-ffed0cb5613a", | 277 | "id": "b283bd04-cbae-4946-8031-ffed0cb5613a", | ||
| 307 | "name": "crecimiento", | 278 | "name": "crecimiento", | ||
| 308 | "state": "active", | 279 | "state": "active", | ||
| 309 | "vocabulary_id": null | 280 | "vocabulary_id": null | ||
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| 312 | "display_name": "gradiente_termico", | 283 | "display_name": "gradiente_termico", | ||
| 313 | "id": "6f6a93d2-3b9d-49ce-bd99-d38372f6b273", | 284 | "id": "6f6a93d2-3b9d-49ce-bd99-d38372f6b273", | ||
| 314 | "name": "gradiente_termico", | 285 | "name": "gradiente_termico", | ||
| 315 | "state": "active", | 286 | "state": "active", | ||
| 316 | "vocabulary_id": null | 287 | "vocabulary_id": null | ||
| 317 | }, | 288 | }, | ||
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| 320 | "id": "004084d1-68d8-46ca-842a-c10278540bc9", | 291 | "id": "004084d1-68d8-46ca-842a-c10278540bc9", | ||
| 321 | "name": "marino", | 292 | "name": "marino", | ||
| 322 | "state": "active", | 293 | "state": "active", | ||
| 323 | "vocabulary_id": null | 294 | "vocabulary_id": null | ||
| 324 | }, | 295 | }, | ||
| 325 | { | 296 | { | ||
| 326 | "display_name": "temperatura", | 297 | "display_name": "temperatura", | ||
| 327 | "id": "5b7e46a9-0277-4e63-a2a6-39c30d363836", | 298 | "id": "5b7e46a9-0277-4e63-a2a6-39c30d363836", | ||
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| 329 | "state": "active", | 300 | "state": "active", | ||
| 330 | "vocabulary_id": null | 301 | "vocabulary_id": null | ||
| 331 | } | 302 | } | ||
| 332 | ], | 303 | ], | ||
| 333 | "thematic_area": [ | 304 | "thematic_area": [ | ||
| 334 | "espacios_protegidos" | 305 | "espacios_protegidos" | ||
| 335 | ], | 306 | ], | ||
| 336 | "theme_es": [ | 307 | "theme_es": [ | ||
| 337 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | 308 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | ||
| 338 | ], | 309 | ], | ||
| 339 | "title": "Variability of growth rates and thermohaline niches of | 310 | "title": "Variability of growth rates and thermohaline niches of | ||
| 340 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)", | 311 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)", | ||
| 341 | "title_translated": { | 312 | "title_translated": { | ||
| 342 | "es": "Variability of growth rates and thermohaline niches of | 313 | "es": "Variability of growth rates and thermohaline niches of | ||
| 343 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)" | 314 | Rhizostoma pulmo's pelagic stages (Cnidaria: Scyphozoa)" | ||
| 344 | }, | 315 | }, | ||
| 345 | "topic": | 316 | "topic": | ||
| 346 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | 317 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | ||
| 347 | "type": "dataset", | 318 | "type": "dataset", | ||
| 348 | "url": | 319 | "url": | ||
| 349 | //iepnb.es:443/catalogo/dataset/03f548dd-0997-52ac-baac-04bf5121f230", | 320 | //iepnb.es:443/catalogo/dataset/03f548dd-0997-52ac-baac-04bf5121f230", | ||
| 350 | "version_notes": { | 321 | "version_notes": { | ||
| 351 | "es": "" | 322 | "es": "" | ||
| 352 | } | 323 | } | ||
| 353 | } | 324 | } |