Precursor island regions, lineages, transects, and ecotone on Martinique.
Geological boundaries between precursor islands are indicated by red lines. They are occupied by lineages labelled in red (NW = northwest, C = central, SW = southwest, S = south). The ecotone between xeric coastal and montane rainforest is indicated by a green, broken line, and the section of Transect III devastated by the 1902 pyroclastic surges that destroyed St Pierre [31] is indicated by grey shading. Transects and their sites are in blue and numbered with blue Roman numerals I to IX. The control transect (IX) within the central mesic zone, is without an ecotone or secondary contact. The photographs are of adult male anoles (locality on Martinique indicated by boxed numbers), 1 northeastern coastal, 2 littoral coastal form, 3 montane rainforest form, 4 widespread mesic/transitional form, and 5 xeric form occurring in the western rainshadow, St Anne Peninsular in the south and the eastern tip of the Caravelle peninsular in east where annual rainfall is circa 1500mm a year or less [50].

Precursor island regions, lineages, transects, and ecotone on Martinique. Geological boundaries between precursor islands are indicated by red lines. They are occupied by lineages labelled in red (NW = northwest, C = central, SW = southwest, S = south). The ecotone between xeric coastal and montane rainforest is indicated by a green, broken line, and the section of Transect III devastated by the 1902 pyroclastic surges that destroyed St Pierre [31] is indicated by grey shading. Transects and their sites are in blue and numbered with blue Roman numerals I to IX. The control transect (IX) within the central mesic zone, is without an ecotone or secondary contact. The photographs are of adult male anoles (locality on Martinique indicated by boxed numbers), 1 northeastern coastal, 2 littoral coastal form, 3 montane rainforest form, 4 widespread mesic/transitional form, and 5 xeric form occurring in the western rainshadow, St Anne Peninsular in the south and the eastern tip of the Caravelle peninsular in east where annual rainfall is circa 1500mm a year or less [50].

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Background: Island systems offer excellent opportunities for studying the evolutionary histories of species by virtue of their restricted size and easily identifiable barriers to gene flow. However, most studies investigating evolutionary patterns and processes shaping biotic diversification have focused on more recent (emergent) rather than ancient oceanic archipelagos. Here, we focus on the granitic islands of the Seychelles, which are unusual among island systems because they have been isolated for a long time and are home to a monophyletic radiation of caecilian amphibians that has been separated from its extant sister lineage for ca. 65-62 Ma. We selected the most widespread Seychelles caecilian species, Hypogeophis rostratus, to investigate intraspecific morphological and genetic (mitochondrial and nuclear) variation across the archipelago (782 samples from nine islands) to identify patterns and test processes that shaped their evolutionary history within the Seychelles. Results: Overall a signal of strong geographic structuring with distinct northern- and southern-island clusters were identified across all datasets. We suggest that these distinct groups have been isolated for ca. 1.26 Ma years without subsequent migration between them. Populations from the somewhat geographically isolated island of Frégate showed contrasting relationships to other islands based on genetic and morphological data, clustering alternatively with northern-island (genetic) and southern-island (morphological) populations. Conclusions: Although variation in H. rostratus across the Seychelles is explained more by isolation-by-distance than by adaptation, the genetic-morphological incongruence for affinities of Frégate H. rostratus might be caused by local adaptation over-riding the signal from their vicariant history. Our findings highlight the need of integrative approaches to investigate fine-scale geographic structuring to uncover underlying diversity and to better understand evolutionary processes on ancient, continental islands.
... This was accomplished using resistance surfaces parameterized as the inverse of predicted habitat suitability (McRae & Beier 2007;Wang et al. 2008;Storfer et al. 2010;Wang et al. 2012;MacDonald et al. 2020). This approach assumes that organisms are more likely to disperse within suitable habitat and experience high resistance when moving through unsuitable habitat; large stretches of unsuitable habitat thereby pose significant barriers to dispersal (Coyne & Orr 2004;Crispo et al. 2006;McRae 2006;McRae & Beier 2007;Thorpe et al. 2008Thorpe et al. , 2010Sánchez-Ramírez et al. 2018). We averaged resistance surfaces of the northern and southern S. hesperis lineages to generate a single resistance surface reflecting the probability that dispersing individuals of the two lineages will come into contact that could result in reciprocal gene flow. ...
... Such periods of geographic isolation are 693 unlikely to be unique to these species complexes that are predominantly maintained by 694 behavioral isolation. Recent demographic modeling studies of emblematic adaptive radiations 695 also maintained by divergent natural selection, such as the radiation of cichlid fishes (Meier, 696 Sousa, et al., 2017) or of Caribbean anoles (Thorpe, Surget-Groba, & Johansson, 2010), 697 confirm that geographic isolation favors adaptive processes that can lead to speciation. Yet, in 698 contrast with those well studied cases of ecological radiations, our study in Chorthippus 699 suggests that sexual selection can lead to radiations in the absence of strong divergent natural 700 selection, resulting in cryptic species that are genetically, morphologically and ecologically 701 similar but that otherwise generally behave as good biological species. ...
... Patterns of morphological diversity do not always represent phylogeny because factors such as local ecological adaptation or phenotypic plasticity can play a role in shaping phenotypic variation (e.g. 66), including at the intraspecific level (66)(67)(68). To understand evolutionary patterns and processes it can therefore be beneficial to analyze both genetic and morphological data. ...
... Patterns of morphological diversity do not always represent phylogeny because factors such as local ecological adaptation or phenotypic plasticity can play a role in shaping phenotypic variation (e.g. 66), including at the intraspecific level (66)(67)(68). To understand evolutionary patterns and processes it can therefore be beneficial to analyze both genetic and morphological data. ...
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Full-text available
Background: Island systems offer excellent opportunities for studying the evolutionary histories of species by virtue of their restricted size and easily identifiable barriers to gene flow. However, most studies investigating evolutionary patterns and processes shaping biotic diversification have focused on more recent (emergent) rather than ancient oceanic archipelagos. Here, we focus on the granitic islands of the Seychelles, which are unusual among island systems because they have been isolated for a long time and are home to a radiation of caecilian amphibians that have been separated from their extant sister lineage for ca. 65 Ma. We selected the most widespread Seychelles caecilian species, Hypogeophis rostratus , to investigate morphological and genetic (mitochondrial and nuclear) variation across the archipelago (782 samples from nine islands) to identify patterns and test processes that shaped their evolutionary history within the Seychelles. Results: Overall a signal of strong geographic structuring with distinct northern- and southern-island clusters were identified across all datasets. We suggest that these distinct groups have been isolated for ca. 1.2 Ma years without subsequent migration between them. Populations from the somewhat geographically isolated island of Frégate showed contrasting relationships to other islands based on genetic and morphological data, clustering alternatively with northern-island (genetic) and southern-island (morphological) populations. Conclusions: Although variation in H. rostratus across the Seychelles is explained more by isolation-by-distance than by adaptation, the genetic-morphological incongruence for affinities of Frégate H. rostratus might be caused by local ecological adaptation over-riding the signal from their vicariant history. Our findings highlight the need to investigate fine-scale geographic structuring to uncover underlying diversity and to better understand evolutionary processes on ancient, continental islands.
... Patterns of morphological diversity do not always represent phylogeny because factors such as local ecological adaptation and phenotypic plasticity can play a role in shaping phenotypic variation [e.g. 66], including at the intraspeci c level [67][68][69]. To understand evolutionary patterns and processes it can therefore be bene cial to analyze both genetic and morphological data. ...
Preprint
Full-text available
Background: Island systems offer excellent opportunities for studying the evolutionary histories of species by virtue of their restricted size and easily identifiable barriers to gene flow. However, most studies investigating evolutionary patterns and processes shaping biotic diversification have focused on more recent (emergent) rather than ancient oceanic archipelagos. Here, we focus on the granitic islands of the Seychelles, which are unusual among island systems because they have been isolated for a long time and are home to a monophyletic radiation of caecilian amphibians that has been separated from its extant sister lineage for ca. 65 – 62 Ma. We selected the most widespread Seychelles caecilian species, Hypogeophis rostratus, to investigate intraspecific morphological and genetic (mitochondrial and nuclear) variation across the archipelago (782 samples from nine islands) to identify patterns and test processes that shaped their evolutionary history within the Seychelles. Results: Overall a signal of strong geographic structuring with distinct northern- and southern-island clusters were identified across all datasets. We suggest that these distinct groups have been isolated for ca. 1.26 Ma years without subsequent migration between them. Populations from the somewhat geographically isolated island of Frégate showed contrasting relationships to other islands based on genetic and morphological data, clustering alternatively with northern-island (genetic) and southern-island (morphological) populations. Conclusions: Although variation in H. rostratus across the Seychelles is explained more by isolation-by-distance than by adaptation, the genetic-morphological incongruence for affinities of Frégate H. rostratus might be caused by local adaptation over-riding the signal from their vicariant history. Our findings highlight the need of integrative approaches to investigate fine-scale geographic structuring to uncover underlying diversity and to better understand evolutionary processes on ancient, continental islands.
... Patterns of morphological diversity do not always represent phylogeny because factors such as local ecological adaptation and phenotypic plasticity can play a role in shaping phenotypic variation [e.g. 66], including at the intraspeci c level [67][68][69]. To understand evolutionary patterns and processes it can therefore be bene cial to analyze both genetic and morphological data. ...
Preprint
Full-text available
Background: Island systems offer excellent opportunities for studying the evolutionary histories of species by virtue of their restricted size and easily identifiable barriers to gene flow. However, most studies investigating evolutionary patterns and processes shaping biotic diversification have focused on more recent (emergent) rather than ancient oceanic archipelagos. Here, we focus on the granitic islands of the Seychelles, which are unusual among island systems because they have been isolated for a long time and are home to a monophyletic radiation of caecilian amphibians that has been separated from its extant sister lineage for ca. 65 – 62 Ma. We selected the most widespread Seychelles caecilian species, Hypogeophis rostratus, to investigate intraspecific morphological and genetic (mitochondrial and nuclear) variation across the archipelago (782 samples from nine islands) to identify patterns and test processes that shaped their evolutionary history within the Seychelles. Results: Overall a signal of strong geographic structuring with distinct northern- and southern-island clusters were identified across all datasets. We suggest that these distinct groups have been isolated for ca. 1.26 Ma years without subsequent migration between them. Populations from the somewhat geographically isolated island of Frégate showed contrasting relationships to other islands based on genetic and morphological data, clustering alternatively with northern-island (genetic) and southern-island (morphological) populations. Conclusions: Although variation in H. rostratus across the Seychelles is explained more by isolation-by-distance than by adaptation, the genetic-morphological incongruence for affinities of Frégate H. rostratus might be caused by local adaptation over-riding the signal from their vicariant history. Our findings highlight the need of integrative approaches to investigate fine-scale geographic structuring to uncover underlying diversity and to better understand evolutionary processes on ancient, continental islands.