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  "code": "7b.b.dg",
            
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  "contributor": "NIOZ Royal Netherlands Institute for Sea Research",
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  "contributor": "NIOZ Royal Netherlands Institute for Sea Research",
            
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me\":\"Bom\",\"orcid\":\"0000-0001-8180-1958\",\"affiliation\":\"Royal 
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me\":\"Bom\",\"orcid\":\"0000-0001-8180-1958\",\"affiliation\":\"Royal 
            
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Netherlands Institute for Sea 
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Netherlands Institute for Sea 
            
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  "distribution_date": "2023-11-03",
            
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  "distributor": "Research Data Management(NIOZ Royal Netherlands 
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  "distributor": "Research Data Management(NIOZ Royal Netherlands 
            
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Institute for Sea Research)",
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Institute for Sea Research)",
            
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  "doi_date_published": "2023-11-03",
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  "name": "7bbdg",
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  "name": "7bbdg",
            
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  "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 
            
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and hence climate change.",
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and hence climate change.",
            
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