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En el instante 23 de junio de 2026, 16:12:00 UTC,
-
Modificado el valor del campo
spatial_coverage
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en Morphology and molecular phylogeny of Hyalosynedra lanceolata sp nov and an extended description of Hyalosynedra (Bacillariophyta)
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| 95 | "notes": "The araphid diatom genus Hyalosynedra is a very common | 95 | "notes": "The araphid diatom genus Hyalosynedra is a very common | ||
| 96 | component of marine benthic communities, occurring as an epiphyte or | 96 | component of marine benthic communities, occurring as an epiphyte or | ||
| 97 | colonizing hard substrata, and has a worldwide distribution. The | 97 | colonizing hard substrata, and has a worldwide distribution. The | ||
| 98 | hyaline appearance of the valve and the high striation density, which | 98 | hyaline appearance of the valve and the high striation density, which | ||
| 99 | is indiscernible under a light microscope, makes the identification of | 99 | is indiscernible under a light microscope, makes the identification of | ||
| 100 | most species difficult and very few studies have investigated their | 100 | most species difficult and very few studies have investigated their | ||
| 101 | morphology, phylogeny or ecology in detail. In an extensive study of | 101 | morphology, phylogeny or ecology in detail. In an extensive study of | ||
| 102 | diatom communities from the hypersaline Mar Menor coastal lagoon (SE | 102 | diatom communities from the hypersaline Mar Menor coastal lagoon (SE | ||
| 103 | Spain), several new taxa were found. Herein we propose Hyalosynedra | 103 | Spain), several new taxa were found. Herein we propose Hyalosynedra | ||
| 104 | lanceolata sp. nov. based on morphological observations (light and | 104 | lanceolata sp. nov. based on morphological observations (light and | ||
| 105 | electron microscopy) and molecular data (phylogenetic and sequence | 105 | electron microscopy) and molecular data (phylogenetic and sequence | ||
| 106 | divergence analyses). The species has distinctive morphological | 106 | divergence analyses). The species has distinctive morphological | ||
| 107 | characters (radiate colony, biseriate striation, lanceolate sternum | 107 | characters (radiate colony, biseriate striation, lanceolate sternum | ||
| 108 | and two long laminar lobed chloroplasts) that are new for the genus | 108 | and two long laminar lobed chloroplasts) that are new for the genus | ||
| 109 | and have been included in a proposal to extend the genus description. | 109 | and have been included in a proposal to extend the genus description. | ||
| 110 | Our results also show that H. toxoneides does not belong to | 110 | Our results also show that H. toxoneides does not belong to | ||
| 111 | Hyalosynedra, but appears to be more closely related to Thalassionema | 111 | Hyalosynedra, but appears to be more closely related to Thalassionema | ||
| 112 | and Thalassiothrix. However, further molecular and morphological | 112 | and Thalassiothrix. However, further molecular and morphological | ||
| 113 | research is needed to clarify its taxonomic position.", | 113 | research is needed to clarify its taxonomic position.", | ||
| 114 | "notes_translated": { | 114 | "notes_translated": { | ||
| 115 | "es": "The araphid diatom genus Hyalosynedra is a very common | 115 | "es": "The araphid diatom genus Hyalosynedra is a very common | ||
| 116 | component of marine benthic communities, occurring as an epiphyte or | 116 | component of marine benthic communities, occurring as an epiphyte or | ||
| 117 | colonizing hard substrata, and has a worldwide distribution. The | 117 | colonizing hard substrata, and has a worldwide distribution. The | ||
| 118 | hyaline appearance of the valve and the high striation density, which | 118 | hyaline appearance of the valve and the high striation density, which | ||
| 119 | is indiscernible under a light microscope, makes the identification of | 119 | is indiscernible under a light microscope, makes the identification of | ||
| 120 | most species difficult and very few studies have investigated their | 120 | most species difficult and very few studies have investigated their | ||
| 121 | morphology, phylogeny or ecology in detail. In an extensive study of | 121 | morphology, phylogeny or ecology in detail. In an extensive study of | ||
| 122 | diatom communities from the hypersaline Mar Menor coastal lagoon (SE | 122 | diatom communities from the hypersaline Mar Menor coastal lagoon (SE | ||
| 123 | Spain), several new taxa were found. Herein we propose Hyalosynedra | 123 | Spain), several new taxa were found. Herein we propose Hyalosynedra | ||
| 124 | lanceolata sp. nov. based on morphological observations (light and | 124 | lanceolata sp. nov. based on morphological observations (light and | ||
| 125 | electron microscopy) and molecular data (phylogenetic and sequence | 125 | electron microscopy) and molecular data (phylogenetic and sequence | ||
| 126 | divergence analyses). The species has distinctive morphological | 126 | divergence analyses). The species has distinctive morphological | ||
| 127 | characters (radiate colony, biseriate striation, lanceolate sternum | 127 | characters (radiate colony, biseriate striation, lanceolate sternum | ||
| 128 | and two long laminar lobed chloroplasts) that are new for the genus | 128 | and two long laminar lobed chloroplasts) that are new for the genus | ||
| 129 | and have been included in a proposal to extend the genus description. | 129 | and have been included in a proposal to extend the genus description. | ||
| 130 | Our results also show that H. toxoneides does not belong to | 130 | Our results also show that H. toxoneides does not belong to | ||
| 131 | Hyalosynedra, but appears to be more closely related to Thalassionema | 131 | Hyalosynedra, but appears to be more closely related to Thalassionema | ||
| 132 | and Thalassiothrix. However, further molecular and morphological | 132 | and Thalassiothrix. However, further molecular and morphological | ||
| 133 | research is needed to clarify its taxonomic position." | 133 | research is needed to clarify its taxonomic position." | ||
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| 238 | ], | ||||
| 239 | [ | ||||
| 240 | -0.69, | ||||
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| 242 | ], | ||||
| 243 | [ | ||||
| 244 | -0.69, | ||||
| 245 | 38.76 | ||||
| 246 | ], | ||||
| 247 | [ | ||||
| 248 | -2.34, | ||||
| 249 | 38.76 | ||||
| 250 | ], | ||||
| 251 | [ | ||||
| 252 | -2.34, | ||||
| 253 | 37.38 | ||||
| 254 | ] | ||||
| 255 | ] | ||||
| 256 | ], | ||||
| 257 | "type": "Polygon" | ||||
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| 260 | "coordinates": [ | ||||
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| 263 | ], | ||||
| 264 | "type": "Point" | ||||
| 265 | }, | ||||
| 266 | "text": "Regi\u00f3n de Murcia", | 237 | "text": "Regi\u00f3n de Murcia", | ||
| 267 | "uri": | 238 | "uri": | ||
| 268 | atos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia" | 239 | atos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia" | ||
| 269 | } | 240 | } | ||
| 270 | ], | 241 | ], | ||
| 271 | "spatial_uri": | 242 | "spatial_uri": | ||
| 272 | tos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia", | 243 | tos.gob.es/recurso/sector-publico/territorio/Autonomia/Region-Murcia", | ||
| 273 | "state": "active", | 244 | "state": "active", | ||
| 274 | "study_variables": { | 245 | "study_variables": { | ||
| 275 | "es": "" | 246 | "es": "" | ||
| 276 | }, | 247 | }, | ||
| 277 | "tag_uri": [ | 248 | "tag_uri": [ | ||
| 278 | 249 | ||||
| 279 | tp://inspire.ec.europa.eu/metadata-codelist/TopicCategory/environment" | 250 | tp://inspire.ec.europa.eu/metadata-codelist/TopicCategory/environment" | ||
| 280 | ], | 251 | ], | ||
| 281 | "tags": [ | 252 | "tags": [ | ||
| 282 | { | 253 | { | ||
| 283 | "display_name": "aloctonas", | 254 | "display_name": "aloctonas", | ||
| 284 | "id": "806f953e-3e98-4d2c-ad99-507b520b101a", | 255 | "id": "806f953e-3e98-4d2c-ad99-507b520b101a", | ||
| 285 | "name": "aloctonas", | 256 | "name": "aloctonas", | ||
| 286 | "state": "active", | 257 | "state": "active", | ||
| 287 | "vocabulary_id": null | 258 | "vocabulary_id": null | ||
| 288 | }, | 259 | }, | ||
| 289 | { | 260 | { | ||
| 290 | "display_name": "bentos", | 261 | "display_name": "bentos", | ||
| 291 | "id": "b491284f-4e9e-4de3-926c-ae9ab3c06c34", | 262 | "id": "b491284f-4e9e-4de3-926c-ae9ab3c06c34", | ||
| 292 | "name": "bentos", | 263 | "name": "bentos", | ||
| 293 | "state": "active", | 264 | "state": "active", | ||
| 294 | "vocabulary_id": null | 265 | "vocabulary_id": null | ||
| 295 | }, | 266 | }, | ||
| 296 | { | 267 | { | ||
| 297 | "display_name": "distribucion", | 268 | "display_name": "distribucion", | ||
| 298 | "id": "00f1c689-883f-44f3-a6ba-7b7901acf822", | 269 | "id": "00f1c689-883f-44f3-a6ba-7b7901acf822", | ||
| 299 | "name": "distribucion", | 270 | "name": "distribucion", | ||
| 300 | "state": "active", | 271 | "state": "active", | ||
| 301 | "vocabulary_id": null | 272 | "vocabulary_id": null | ||
| 302 | }, | 273 | }, | ||
| 303 | { | 274 | { | ||
| 304 | "display_name": "diversidad_genetica", | 275 | "display_name": "diversidad_genetica", | ||
| 305 | "id": "36b1105b-eac3-4355-a30c-57c1a0a3e973", | 276 | "id": "36b1105b-eac3-4355-a30c-57c1a0a3e973", | ||
| 306 | "name": "diversidad_genetica", | 277 | "name": "diversidad_genetica", | ||
| 307 | "state": "active", | 278 | "state": "active", | ||
| 308 | "vocabulary_id": null | 279 | "vocabulary_id": null | ||
| 309 | }, | 280 | }, | ||
| 310 | { | 281 | { | ||
| 311 | "display_name": "marino", | 282 | "display_name": "marino", | ||
| 312 | "id": "004084d1-68d8-46ca-842a-c10278540bc9", | 283 | "id": "004084d1-68d8-46ca-842a-c10278540bc9", | ||
| 313 | "name": "marino", | 284 | "name": "marino", | ||
| 314 | "state": "active", | 285 | "state": "active", | ||
| 315 | "vocabulary_id": null | 286 | "vocabulary_id": null | ||
| 316 | }, | 287 | }, | ||
| 317 | { | 288 | { | ||
| 318 | "display_name": "morfologia", | 289 | "display_name": "morfologia", | ||
| 319 | "id": "d7dc0288-78e7-41dd-bab2-2758781d4541", | 290 | "id": "d7dc0288-78e7-41dd-bab2-2758781d4541", | ||
| 320 | "name": "morfologia", | 291 | "name": "morfologia", | ||
| 321 | "state": "active", | 292 | "state": "active", | ||
| 322 | "vocabulary_id": null | 293 | "vocabulary_id": null | ||
| 323 | } | 294 | } | ||
| 324 | ], | 295 | ], | ||
| 325 | "thematic_area": [ | 296 | "thematic_area": [ | ||
| 326 | "espacios_protegidos" | 297 | "espacios_protegidos" | ||
| 327 | ], | 298 | ], | ||
| 328 | "theme_es": [ | 299 | "theme_es": [ | ||
| 329 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | 300 | "http://datos.gob.es/kos/sector-publico/sector/medio-ambiente" | ||
| 330 | ], | 301 | ], | ||
| 331 | "title": "Morphology and molecular phylogeny of Hyalosynedra | 302 | "title": "Morphology and molecular phylogeny of Hyalosynedra | ||
| 332 | lanceolata sp nov and an extended description of Hyalosynedra | 303 | lanceolata sp nov and an extended description of Hyalosynedra | ||
| 333 | (Bacillariophyta)", | 304 | (Bacillariophyta)", | ||
| 334 | "title_translated": { | 305 | "title_translated": { | ||
| 335 | "es": "Morphology and molecular phylogeny of Hyalosynedra | 306 | "es": "Morphology and molecular phylogeny of Hyalosynedra | ||
| 336 | lanceolata sp nov and an extended description of Hyalosynedra | 307 | lanceolata sp nov and an extended description of Hyalosynedra | ||
| 337 | (Bacillariophyta)" | 308 | (Bacillariophyta)" | ||
| 338 | }, | 309 | }, | ||
| 339 | "topic": | 310 | "topic": | ||
| 340 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | 311 | "http://inspire.ec.europa.eu/metadata-codelist/TopicCategory/biota", | ||
| 341 | "type": "dataset", | 312 | "type": "dataset", | ||
| 342 | "url": | 313 | "url": | ||
| 343 | //iepnb.es:443/catalogo/dataset/24131dd3-adea-59f7-a74d-f12fb1326d9d", | 314 | //iepnb.es:443/catalogo/dataset/24131dd3-adea-59f7-a74d-f12fb1326d9d", | ||
| 344 | "version_notes": { | 315 | "version_notes": { | ||
| 345 | "es": "" | 316 | "es": "" | ||
| 346 | } | 317 | } | ||
| 347 | } | 318 | } |