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Different Islands (different + island)
Selected AbstractsSHARED AND UNIQUE FEATURES OF DIVERSIFICATION IN GREATER ANTILLEAN ANOLIS ECOMORPHSEVOLUTION, Issue 2 2006R. Brian Langerhans Abstract Examples of convergent evolution suggest that natural selection can often produce predictable evolutionary outcomes. However, unique histories among species can lead to divergent evolution regardless of their shared selective pressures,and some contend that such historical contingencies produce the dominant features of evolution. A classic example of convergent evolution is the set of Anolis lizard ecomorphs of the Greater Antilles. On each of four islands, anole species partition the structural habitat into at least four categories, exhibiting similar morphologies within each category. We assessed the relative importance of shared selection due to habitat similarity, unique island histories, and unique effects of similar habitats on different islands in the generation of morphological variation in anole ecomorphs. We found that shared features of diversification across habitats were of greatest importance, but island effects on morphology (reflecting either island effects per se or phylogenetic relationships) and unique aspects of habitat diversification on different islands were also important. There were three distinct cases of island-specific habitat diversification, and only one was confounded by phylogenetic relatedness. The other two unique aspects were not related to shared ancestry but might reflect as-yet-unmeasured environmental differences between islands in habitat characteristics. Quantifying the relative importance of shared and unique responses to similar selective regimes provides a more complete understanding of phenotypic diversification, even in this much-studied system [source] Zoogeography of the southern African ascidian faunaJOURNAL OF BIOGEOGRAPHY, Issue 12 2004Carmen Primo Abstract Aim, To describe the biogeography of the ascidian fauna of southern Africa, to compare the results obtained with those reported for other fauna and flora of the same region, and to speculate about the origin of ascidians in the region. Location, Southern Africa extending over 4000 km from Mossâmedes (15° S,12° E) to Inhaca Island (26°30, S,33° E), including Vema Seamount (31°40, S,8 °20, E), Amsterdam-Saint Paul Islands (38° S,77°30, E) and the Tristan-Gough Islands (38° S,12°20, W). Methods, We constructed a presence/absence matrix of 168 species for 26 biogeographical divisions, 21 classical biogeographical regions described by Briggs (Marine zoogeography, McGraw-Hill, New York, 1974) and five provinces within the southern African region. We considered the following limits and divisions into provinces for the southern African region: Namibia, Namaqua, Agulhas and Natal as proposed by Branch et al. (Two oceans. A guide to the marine life of southern Africa, David Philip Publishers, 1994), and the West Wind Drift Islands province (WWD) according to Briggs (Global biogeography, Elsevier Health Sciences, Amsterdam, 1995). To examine the biogeographical structure, species and divisions were classified using cluster analysis (based on UPGMA as the aggregation algorithm) with the Bray,Curtis index of similarity. This classification was combined with MDS ordination. Main conclusions, Four main groups were obtained from the analysis of affinities among species: (1) species present in the WWD, separated by a high percentage of endemisms and a low number of species with a southern African distribution. Moreover, in the light of the species distribution and the results of further analysis, which revealed that they are completely separated and not at all related to the southern African region, it appears that there are no close relationships among the different islands and seamounts of the West Wind Drift Island province. This province was therefore removed from the remaining analyses; (2) species with a wide distribution; (3) species of colder waters present in Namaqua and Agulhas provinces, a transitional temperate area in which gradual mixing and replacement of species negate previous hypotheses on the existence of a marked distributional break at Cape of Good Hope; (4) species of warmer waters related to Natal province. The classification into biogeographical components was dominated by the endemic (47%), Indo-Pacific (25%) and cosmopolitan (13%) components. The analysis of affinities among biogeographical areas separated Namibia from the rest of the southern African provinces and showed that it was related to some extent to the Antarctic region because of the cold-temperate character of the province and the low sampling effort; Namaqua, Agulhas and Natal were grouped together and found to be closely related to the Indo-West Pacific region. In general, our results were consistent with those obtained for other southern African marine invertebrates. The frequency distribution of solitary/colonial strategies among provinces confirmed the domination of colonial organisms in tropical regions and solitary organisms in colder regions. Finally, we speculate that the southern African ascidian fauna mainly comprises Indo-Pacific, Antarctic and eastern Atlantic ascidians. [source] Colonization history, ecological shifts and diversification in the evolution of endemic Galápagos weevilsMOLECULAR ECOLOGY, Issue 4 2008A. S. SEQUEIRA Abstract Mitochondrial DNA sequence data were obtained for eight species of flightless Galapaganus endemic weevils and one winged close relative in order to study their colonization history and modes of diversification in the Galápagos Archipelago. Contrary to most other insular radiations, the phylogeny estimates we recovered for Galapaganus do not follow the progression rule of island biogeography. The penalized likelihood age estimates of colonization of the archipelago exceed the age of the emerged islands and underscore the potential role of now sunken seamounts for the early evolution of Galapaganus. The phylogeny proposes one intra-island origin for Galapaganus endemics, but monophyly tests suggest a larger contribution of in-situ speciation on older islands. Generalist habitat preferences were reconstructed as ancestral while shifts to highland habitats were reconstructed as having evolved independently on different islands. Magnitudes and patterns of diversification rate were found to differ between older and younger islands. Our analyses reveal that the colonization sequence of islands and timing of colonization of Galapaganus could be linked with the geological and volcanic history of the islands in a rather complex scenario. Even though most islands appear to have been colonized soon after their emergence, there are notable deviations from the pattern of sequential colonization expected under the progression rule when considering only the extant emerged islands. Patterns of diversification rate variation on older and younger islands correspond to the volcanic activity or remnants of such activity, while the pattern of independent evolution of restricted habitat preferences in different islands suggests that habitat shifts could also have contributed to species diversity in Galapaganus. [source] Site-specific genetic divergence in parallel hybrid zones suggests nonallopatric evolution of reproductive barriersMOLECULAR ECOLOGY, Issue 13 2006M. PANOVA Abstract The evolution of reproductive isolation in the presence of gene flow is supported by theoretical models but rarely by data. Empirical support might be gained from studies of parallel hybrid zones between interbreeding taxa. We analysed gene flow over two hybrid zones separating ecotypes of Littorina saxatilis to test the expectation that neutral genetic markers will show site-specific differences if barriers have evolved in situ. Distinct ecotypes found in contrasting shore habitats are separated by divergent selection and poor dispersal, but hybrid zones appear between them. Swedish islands formed by postglacial uplift 5000 years ago provide opportunities to assess genetic structure in a recently evolved system. Each island houses a discrete population containing subpopulations of different ecotypes. Hybrid zones between ecotypes may be a product of ecological divergence occurring on each island or a consequence of secondary overlap of ecotypes of allopatric origin that have spread among the islands. We used six microsatellite loci to assess gene flow and genetic profiles of hybrid zones on two islands. We found reduced gene flow over both hybrid zones, indicating the presence of local reproductive barriers between ecotypes. Nevertheless, subpopulations of different ecotypes from the same island were genetically more similar to each other than were subpopulations of the same ecotype from different islands. Moreover, neutral genetic traits separating the two ecotypes across hybrid zones were site-specific. This supports a scenario of in situ origin of ecotypes by ecological divergence and nonallopatric evolution of reproductive barriers. [source] Evolution on oceanic islands: molecular phylogenetic approaches to understanding pattern and processMOLECULAR ECOLOGY, Issue 6 2002B. C. Emerson Abstract By their very nature oceanic island ecosystems offer great opportunities for the study of evolution and have for a long time been recognized as natural laboratories for studying evolution owing to their discrete geographical nature and diversity of species and habitats. The development of molecular genetic methods for phylogenetic reconstruction has been a significant advance for evolutionary biologists, providing a tool for answering questions about the diversity among the flora and fauna on such islands. These questions relate to both the origin and causes of species diversity both within an archipelago and on individual islands. Within a phylogenetic framework one can answer fundamental questions such as whether ecologically and/or morphologically similar species on different islands are the result of island colonization or convergent evolution. Testing hypotheses about ages of the individual species groups or entire community assemblages is also possible within a phylogenetic framework. Evolutionary biologists and ecologists are increasingly turning to molecular phylogenetics for studying oceanic island plant and animal communities and it is important to review what has been attempted and achieved so far, with some cautionary notes about interpreting phylogeographical pattern on oceanic islands. [source] The colonization history of Olea europaea L. in Macaronesia based on internal transcribed spacer 1 (ITS-1) sequences, randomly amplified polymorphic DNAs (RAPD), and intersimple sequence repeats (ISSR)MOLECULAR ECOLOGY, Issue 7 2000J. Hess Abstract Phylogenetic relationships in the Olea europaea complex and the phylogeography of 24 populations of the Macaronesian olive (O. europaea ssp. cerasiformis) were assessed by using three molecular markers: nuclear ribosomal internal transcribed spacer 1 (ITS-1) sequences, randomly amplified polymorphic DNAs (RAPD), and intersimple sequence repeats (ISSR). Parsimony analysis of the ITS-1 sequences and Neighbour-joining (NJ) analyses of RAPD and ISSR banding variation revealed four major lineages in the O. europaea complex: (1) ssp. cuspidata; (2) ssp. cerasiformis from Madeira; (3) ssp. laperrinei; and (4) ssp. cerasiformis from the Canary Islands plus ssp. europaea. These results provide unequivocal support for two independent dispersal events of Olea to the Madeira and Canary Islands. Molecular and morphological evidence led to recognition of two separate olive taxa in Macaronesia, to date included in ssp. cerasiformis. NJ analyses of the combined RAPD and ISSR data suggest that the colonization of the Canaries by O. europaea may have followed an east to west stepping-stone model. An interisland dispersal sequence can be recognized, starting from the continent to Fuerteventura, Gran Canaria, Tenerife, La Gomera, and finally La Palma. High dispersal activity of the lipid-rich Olea fruits by birds in the Mediterranean region is congruent with multiple dispersal of olives to Macaronesia and successive colonization of the archipelagos. The observation of strong genetic isolation between populations of different islands of the Canary Islands suggests, however, that subsequent interisland dispersal and establishment has been very rare or may not have occurred at all. [source] Macrogeographical variability in the great call of Hylobates agilis: assessing the applicability of vocal analysis in studies of fine-scale taxonomy of gibbonsAMERICAN JOURNAL OF PRIMATOLOGY, Issue 2 2010R. Heller Abstract Vocal characteristics have been used extensively to distinguish different taxonomic units of gibbons (family Hylobatidae). The agile gibbon (Hylobates agilis) has a disjunct distribution range in the Southeast Asian archipelago (remnants of the former Sunda landmass), and populations on different islands are currently recognized as distinct subspecies or even species. We recorded great calls from female agile gibbons from two populations on Sumatra and two populations on Borneo and examined the vocal variability on four levels: within-individuals, between-individuals, between-populations and between-islands. The primary objective was to evaluate the effect of geographical isolation on variability in song pattern and to test whether proposed island-specific song characteristics exist, reflecting evolutionary divergence between Sumatran and Bornean agile gibbons. One hundred great calls were recorded from 20 females and analyzed for 18 spectral and temporal acoustic parameters. Principal component analysis followed by a nested ANOVA on components revealed a complex pattern of song variability not likely to reflect taxonomic or evolutionary relationship. We found no evidence that Sumatran and Bornean agile gibbons have evolved different vocal characteristics, refuting a distinction between them based on vocal characteristics. A high level of plasticity was found in great calls from the same individual, and generally the inferred pattern of variability suggested that ecological or social factors may confound any genetically based island dialects. Am. J. Primatol. 72:142,151, 2010. © 2009 Wiley-Liss, Inc. [source] | ||||||||||