2018
DOI: 10.1080/17550874.2018.1534289
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Patterns of phylogenetic community structure of sand dune plant communities in the Yucatan Peninsula: the role of deterministic and stochastic processes in community assembly

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Cited by 13 publications
(14 citation statements)
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“…Results showed no phylogenetic signal in temporal flowering overlap (λ = 0.06-0.48, p > 0.05; Appendix 2, Figure S1) and floral trait similarity (λ = 0.05-0.62, p > 0.05; Appendix 2, Figure S2) indicating that similarity in species' flowering phenology and floral traits are not determined by shared evolutionary history. This is not surprising since in our communities plant families are represented by one or very few species (Angulo et al, 2018). The lack of significant phylogenetic signal in temporal flowering overlap and floral trait similarity suggest that phylogenetic relatedness is likely not a main driver of the structure of these co-flowering communities.…”
Section: Co-flowering Networkmentioning
confidence: 75%
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“…Results showed no phylogenetic signal in temporal flowering overlap (λ = 0.06-0.48, p > 0.05; Appendix 2, Figure S1) and floral trait similarity (λ = 0.05-0.62, p > 0.05; Appendix 2, Figure S2) indicating that similarity in species' flowering phenology and floral traits are not determined by shared evolutionary history. This is not surprising since in our communities plant families are represented by one or very few species (Angulo et al, 2018). The lack of significant phylogenetic signal in temporal flowering overlap and floral trait similarity suggest that phylogenetic relatedness is likely not a main driver of the structure of these co-flowering communities.…”
Section: Co-flowering Networkmentioning
confidence: 75%
“…These communities are located in the east (20°58′37″N–90°21′18″W), centre (21°20′26″N–89°17′47″W) and west (21°33′42″N–87°50′17″W) of the Peninsula. The floras of these three communities have different biogeographic influences (Angulo, Tun‐Garrido, Arceo‐Gómez, Munguía‐Rosas, & Parra‐Tabla, 2018; Moreno‐Casasola & Espejel, 1986) and hence plant species diversity (6–46 species; Parra‐Tabla et al., 2018) and composition are significantly different (PERMANOVA: F 2,47 = 4.28, p < 0.001; C. Albor & V. Parra‐Tabla, unpubl. results).…”
Section: Methodsmentioning
confidence: 99%
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“…Castillo and Moreno-Casasola 1996; Angulo et al 2018) which, besides the low rainfall and high temperatures, are exposed to other adverse abiotic conditions (e.g., tropical storms, continuous salt spray, and low nutrient availability). The dune plant community is composed of annuals (Cakile edentula -Brassicaceae) and perennial herbs (Sesuvium portulacastrum -Aizoaceae, Licium carollinianum -Solanaceae, Ipomoea pes-caprae -Convolvulaceae), and shrubs such as Scaevola plumieri (Goodeniaceae) and Suriana maritima (Surianaceae) (Espejel 1987;Angulo et al 2018). In this ecosystem, shrubs play an essential role as dune builders and in helping contain soil erosion, which is very relevant for these communities dominated by substrate mobility (Miller et…”
Section: Study Sitementioning
confidence: 99%
“…A diferencia de algunos sistemas del golfo de México, se les considera un sistema de dunas fijas en las que la sedimentación está controlada por la vegetación (Eskuche, 1992;Rust e Illenberg, 1996;Torres et al, 2010). Las comunidades de dunas de esta región presentan una estructura diversa debido a las características hidrológicas, climáticas y edáficas en el litoral (Angulo et al, 2018;Espejel, 1987), lo cual se ve reflejado en los caracteres funcionales de las especies de plantas que les permiten soportar condiciones de alta temperatura, baja disponibilidad de agua y alta exposición a la sal (Martínez et al, 2014, Munguía-Rosas et al, 2019. Espejel (1984) clasificó la vegetación de dunas en 2 tipos, considerando su cercanía al mar.…”
Section: Materiales Y Métodosunclassified