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On October 22, 2024, 5:49:27 PM UTC,
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Added resource breeding_range.dbf to Data from: Global temperature homogenization can obliterate temporal isolation in migratory animals with potential loss of population structure
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| 2 | "author": null, | 2 | "author": null, | ||
| 3 | "author_email": null, | 3 | "author_email": null, | ||
| 4 | "code": "7b.b.dg", | 4 | "code": "7b.b.dg", | ||
| 5 | "contributor": "NIOZ Royal Netherlands Institute for Sea Research", | 5 | "contributor": "NIOZ Royal Netherlands Institute for Sea Research", | ||
| 6 | "creator_user_id": "c2e18181-f81f-48a1-9592-9348c107fe56", | 6 | "creator_user_id": "c2e18181-f81f-48a1-9592-9348c107fe56", | ||
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| 8 | me\":\"Bom\",\"orcid\":\"0000-0001-8180-1958\",\"affiliation\":\"Royal | 8 | me\":\"Bom\",\"orcid\":\"0000-0001-8180-1958\",\"affiliation\":\"Royal | ||
| 9 | Netherlands Institute for Sea | 9 | Netherlands Institute for Sea | ||
| 10 | dingauthor\":true,\"contactemailaddress\":\"roeland.bom@nioz.com\"}]", | 10 | dingauthor\":true,\"contactemailaddress\":\"roeland.bom@nioz.com\"}]", | ||
| 11 | "dataset_persistent_id": "DOI:10.25850/nioz/7b.b.dg", | 11 | "dataset_persistent_id": "DOI:10.25850/nioz/7b.b.dg", | ||
| 12 | "deposit_date": "2023-11-03", | 12 | "deposit_date": "2023-11-03", | ||
| 13 | "depositor": "Roeland Bom", | 13 | "depositor": "Roeland Bom", | ||
| 14 | "distribution_date": "2023-11-03", | 14 | "distribution_date": "2023-11-03", | ||
| 15 | "distributor": "Research Data Management(NIOZ Royal Netherlands | 15 | "distributor": "Research Data Management(NIOZ Royal Netherlands | ||
| 16 | Institute for Sea Research)", | 16 | Institute for Sea Research)", | ||
| 17 | "doi_date_published": "2023-11-03", | 17 | "doi_date_published": "2023-11-03", | ||
| 18 | "funding_references": | 18 | "funding_references": | ||
| 19 | "[{\"name\":\"MAVA\",\"awardnumber\":null,\"awardtitle\":\"Waders of | 19 | "[{\"name\":\"MAVA\",\"awardnumber\":null,\"awardtitle\":\"Waders of | ||
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| 22 | Premium 2014 \",\"formatted\":\"NWO - - Spinoza Premium 2014 | 22 | Premium 2014 \",\"formatted\":\"NWO - - Spinoza Premium 2014 | ||
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| 28 | "geographic_coverage": | 28 | "geographic_coverage": | ||
| 29 | longitude_1\":\"10\",\"longitude_2\":\"-20\",\"latitude_1\":\"80\"}]", | 29 | longitude_1\":\"10\",\"longitude_2\":\"-20\",\"latitude_1\":\"80\"}]", | ||
| 30 | "groups": [], | 30 | "groups": [], | ||
| 31 | "id": "19aed6d5-c569-4e0f-b71e-44b88fb9134a", | 31 | "id": "19aed6d5-c569-4e0f-b71e-44b88fb9134a", | ||
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| 36 | "metadata_created": "2024-10-22T17:49:26.182978", | 36 | "metadata_created": "2024-10-22T17:49:26.182978", | ||
| n | 37 | "metadata_modified": "2024-10-22T17:49:26.182986", | n | 37 | "metadata_modified": "2024-10-22T17:49:26.955399", |
| 38 | "name": "7bbdg", | 38 | "name": "7bbdg", | ||
| 39 | "notes": "Climate change is expected to increase the spatial | 39 | "notes": "Climate change is expected to increase the spatial | ||
| 40 | autocorrelation of temperature, resulting in greater synchronization | 40 | autocorrelation of temperature, resulting in greater synchronization | ||
| 41 | of climate variables worldwide. Possibly such \u2018homogenization of | 41 | of climate variables worldwide. Possibly such \u2018homogenization of | ||
| 42 | the world\u2019 leads to elevated risks of extinction and loss of | 42 | the world\u2019 leads to elevated risks of extinction and loss of | ||
| 43 | biodiversity. In this study, we develop an empirical example on how | 43 | biodiversity. In this study, we develop an empirical example on how | ||
| 44 | increasing synchrony of global temperatures can affect population | 44 | increasing synchrony of global temperatures can affect population | ||
| 45 | structure in migratory animals. We studied two subspecies of | 45 | structure in migratory animals. We studied two subspecies of | ||
| 46 | Bar-tailed Godwits Limosa lapponica breeding in tundra regions in | 46 | Bar-tailed Godwits Limosa lapponica breeding in tundra regions in | ||
| 47 | Siberia: yamalensis in the west and taymyrensis further east and | 47 | Siberia: yamalensis in the west and taymyrensis further east and | ||
| 48 | north. These subspecies share pre- and post-breeding stopover areas, | 48 | north. These subspecies share pre- and post-breeding stopover areas, | ||
| 49 | thus being partially sympatric, but exhibiting temporal segregation. | 49 | thus being partially sympatric, but exhibiting temporal segregation. | ||
| 50 | The latter is believed to facilitate reproductive isolation. Using | 50 | The latter is believed to facilitate reproductive isolation. Using | ||
| 51 | satellite tracking data, we show that migration timing of both | 51 | satellite tracking data, we show that migration timing of both | ||
| 52 | subspecies is correlated with the date of snowmelt in their respective | 52 | subspecies is correlated with the date of snowmelt in their respective | ||
| 53 | breeding sites (later at the taymyrensis breeding range). Snow-cover | 53 | breeding sites (later at the taymyrensis breeding range). Snow-cover | ||
| 54 | satellite images demonstrate that the breeding ranges are on different | 54 | satellite images demonstrate that the breeding ranges are on different | ||
| 55 | climate trajectories and become more synchronized over time: between | 55 | climate trajectories and become more synchronized over time: between | ||
| 56 | 1997 and 2020, the date of snowmelt advanced on average by 0.5 | 56 | 1997 and 2020, the date of snowmelt advanced on average by 0.5 | ||
| 57 | days/year in the taymyrensis breeding range, while it remained stable | 57 | days/year in the taymyrensis breeding range, while it remained stable | ||
| 58 | in the yamalensis breeding range. Previous findings showed how | 58 | in the yamalensis breeding range. Previous findings showed how | ||
| 59 | taymyrensis responded to earlier snowmelt by advancing arrival and | 59 | taymyrensis responded to earlier snowmelt by advancing arrival and | ||
| 60 | clutch initiation. In the predicted absence of such advancements in | 60 | clutch initiation. In the predicted absence of such advancements in | ||
| 61 | yamalensis, we expect that the two populations will be synchronized by | 61 | yamalensis, we expect that the two populations will be synchronized by | ||
| 62 | 2036 \u2013 2040. Since Bar-tailed Godwits are social migrants, this | 62 | 2036 \u2013 2040. Since Bar-tailed Godwits are social migrants, this | ||
| 63 | raises the possibility of population exchange and prompts the question | 63 | raises the possibility of population exchange and prompts the question | ||
| 64 | whether the two subspecies can maintain their geographic and | 64 | whether the two subspecies can maintain their geographic and | ||
| 65 | morphological differences and population-specific migratory routines. | 65 | morphological differences and population-specific migratory routines. | ||
| 66 | The proposed scenario may apply to a wide range of (social) migrants | 66 | The proposed scenario may apply to a wide range of (social) migrants | ||
| 67 | as temporal segregation is crucial for promoting and maintaining | 67 | as temporal segregation is crucial for promoting and maintaining | ||
| 68 | reproductive isolation in many (partially sympatric) migratory | 68 | reproductive isolation in many (partially sympatric) migratory | ||
| 69 | populations. Homogenization of previously isolated populations could | 69 | populations. Homogenization of previously isolated populations could | ||
| 70 | be an important consequence of increasing synchronized environments | 70 | be an important consequence of increasing synchronized environments | ||
| 71 | and hence climate change.", | 71 | and hence climate change.", | ||
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| 84 | "title": "Royal Netherlands Institute for Sea Research", | 84 | "title": "Royal Netherlands Institute for Sea Research", | ||
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| 105 | "name": "breeding_range.dbf", | ||||
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| 93 | "state": "active", | 116 | "state": "active", | ||
| 94 | "subject": "Earth and Environmental Sciences", | 117 | "subject": "Earth and Environmental Sciences", | ||
| 95 | "tags": [ | 118 | "tags": [ | ||
| 96 | { | 119 | { | ||
| 97 | "display_name": "Climate change", | 120 | "display_name": "Climate change", | ||
| 98 | "id": "e2c5ff5f-6513-4a74-b1f6-ef0aa3d31fcc", | 121 | "id": "e2c5ff5f-6513-4a74-b1f6-ef0aa3d31fcc", | ||
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| 101 | "vocabulary_id": null | 124 | "vocabulary_id": null | ||
| 102 | }, | 125 | }, | ||
| 103 | { | 126 | { | ||
| 104 | "display_name": "Limosa lapponica taymyrensis", | 127 | "display_name": "Limosa lapponica taymyrensis", | ||
| 105 | "id": "5d7c1650-d114-4d68-9010-7727e5eb5329", | 128 | "id": "5d7c1650-d114-4d68-9010-7727e5eb5329", | ||
| 106 | "name": "Limosa lapponica taymyrensis", | 129 | "name": "Limosa lapponica taymyrensis", | ||
| 107 | "state": "active", | 130 | "state": "active", | ||
| 108 | "vocabulary_id": null | 131 | "vocabulary_id": null | ||
| 109 | }, | 132 | }, | ||
| 110 | { | 133 | { | ||
| 111 | "display_name": "Limosa lapponica yamalensis", | 134 | "display_name": "Limosa lapponica yamalensis", | ||
| 112 | "id": "4fd8246b-aac8-49ac-820c-4790c50e8902", | 135 | "id": "4fd8246b-aac8-49ac-820c-4790c50e8902", | ||
| 113 | "name": "Limosa lapponica yamalensis", | 136 | "name": "Limosa lapponica yamalensis", | ||
| 114 | "state": "active", | 137 | "state": "active", | ||
| 115 | "vocabulary_id": null | 138 | "vocabulary_id": null | ||
| 116 | }, | 139 | }, | ||
| 117 | { | 140 | { | ||
| 118 | "display_name": "long-distance migration", | 141 | "display_name": "long-distance migration", | ||
| 119 | "id": "ff542cf4-50c0-43a6-a3db-211fff478be2", | 142 | "id": "ff542cf4-50c0-43a6-a3db-211fff478be2", | ||
| 120 | "name": "long-distance migration", | 143 | "name": "long-distance migration", | ||
| 121 | "state": "active", | 144 | "state": "active", | ||
| 122 | "vocabulary_id": null | 145 | "vocabulary_id": null | ||
| 123 | }, | 146 | }, | ||
| 124 | { | 147 | { | ||
| 125 | "display_name": "snowmelt", | 148 | "display_name": "snowmelt", | ||
| 126 | "id": "a9251cbd-78dd-4c49-b35d-0311540c84f4", | 149 | "id": "a9251cbd-78dd-4c49-b35d-0311540c84f4", | ||
| 127 | "name": "snowmelt", | 150 | "name": "snowmelt", | ||
| 128 | "state": "active", | 151 | "state": "active", | ||
| 129 | "vocabulary_id": null | 152 | "vocabulary_id": null | ||
| 130 | }, | 153 | }, | ||
| 131 | { | 154 | { | ||
| 132 | "display_name": "temporal segregation", | 155 | "display_name": "temporal segregation", | ||
| 133 | "id": "4ee06872-0025-4b99-9e89-7bd54fcd9695", | 156 | "id": "4ee06872-0025-4b99-9e89-7bd54fcd9695", | ||
| 134 | "name": "temporal segregation", | 157 | "name": "temporal segregation", | ||
| 135 | "state": "active", | 158 | "state": "active", | ||
| 136 | "vocabulary_id": null | 159 | "vocabulary_id": null | ||
| 137 | } | 160 | } | ||
| 138 | ], | 161 | ], | ||
| 139 | "title": "Data from: Global temperature homogenization can | 162 | "title": "Data from: Global temperature homogenization can | ||
| 140 | obliterate temporal isolation in migratory animals with potential loss | 163 | obliterate temporal isolation in migratory animals with potential loss | ||
| 141 | of population structure", | 164 | of population structure", | ||
| 142 | "type": "dataset", | 165 | "type": "dataset", | ||
| 143 | "url": "https://dataportal.nioz.nl/doi/10.25850/nioz/7b.b.dg", | 166 | "url": "https://dataportal.nioz.nl/doi/10.25850/nioz/7b.b.dg", | ||
| 144 | "version": "1" | 167 | "version": "1" | ||
| 145 | } | 168 | } |