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13 results for “Liliales”
Linked collectors and determiners for: Colección de Laurales, Liliales, Lycopodiales, Magnoliales y Malpighiales del Museo Botánico CORD - IMBIV.
Natural history specimen data linked to collectors and determiners held within, "Colección de Laurales, Liliales, Lycopodiales, Magnoliales y Malpighiales del Museo Botánico CORD - IMBIV". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/6896d821-08cd-49e6-9fa0-559bd37d86a4">https://bionomia.net/dataset/6896d821-08cd-49e6-9fa0-559bd37d86a4</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/6896d821-08cd-49e6-9fa0-559bd37d86a4">https://gbif.org/dataset/6896d821-08cd-49e6-9fa0-559bd37d86a4</a>. Formatted as a Frictionless Data package.
Data from: The rapid radiation of <em>Bomarea</em> (Alstroemeriaceae: Liliales), driven by the rise of the Andes
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Unearthing modes of climatic adaptation in underground storage organs across Liliales
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FIGURE 5 in The fundamental karyotype and plastid DNA of Alstroemeria piperata (Liliales, Alstroemeriaceae), a species endemic to the Valparaíso Region, Chile
FIGURE 5. Phylogenetic relationships from analyses of three plastid markers (petA-psbJ, trnL-rpl32 and intron rpl16) of Alstroemeria piperata and other Chilean alstroemerias (Baeza et al. 2022). A. Network inferred with TCS. B. Maximum likelihood tree inferred from DNA sequences and indels. The branch lengths in B were modified for aesthetic reasons.
FIGURE 1 in Smilax jiankunii, a new synonym in Chinese Smilax (Liliales: Smilacaceae)
FIGURE 1. Potential distribution area of S. pottingeri with specimen occurrence of S. pottingeri and S. jiankunii.
The rapid radiation of Bomarea (Alstroemeriaceae: Liliales), driven by the rise of the Andes
<p>This dataset contains the data to fully reproduce analyses on the evolutionary history, diversification, and biogeography of <em>Bomarea</em> and outgroups in Alstroemeriaceae. These data include intermediate and processed molecular data (raw molecular data is on NCBI SRA as BioProject PRJNA881339), the results of phylogenetic analyses, biogeographic data on species' ranges, and the results of diversification and biogeographic analyses. </p> <p>All code is additionally available on GitHub at <a href="https://github.com/cmt2/bom_phy_analysis">https://github.com/cmt2/bom_phy_analysis</a></p>
FIGURE 1 in The fundamental karyotype and plastid DNA of Alstroemeria piperata (Liliales, Alstroemeriaceae), a species endemic to the Valparaíso Region, Chile
FIGURE 1. Flowers of Alstroemeria piperata.
FIGURE 4 in The fundamental karyotype and plastid DNA of Alstroemeria piperata (Liliales, Alstroemeriaceae), a species endemic to the Valparaíso Region, Chile
FIGURE 4. Metaphase of Alstroemeria piperata. Scale 10 µm.
FIGURE 3 in The fundamental karyotype and plastid DNA of Alstroemeria piperata (Liliales, Alstroemeriaceae), a species endemic to the Valparaíso Region, Chile
FIGURE 3. Storage roots of Alstroemeria piperata.
FIGURE 2 in The fundamental karyotype and plastid DNA of Alstroemeria piperata (Liliales, Alstroemeriaceae), a species endemic to the Valparaíso Region, Chile
FIGURE 2. Habitat of Alstroemeria piperata.
Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
We present the first phylogenomic analysis of relationships among all ten families of Liliales, based on 75 plastid genes from 35 species in 29 genera, and 97 additional plastomes stratified across angiosperm lineages. We used a supermatrix approach to extend our analysis to 58 of 64 genera of Liliales, and calibrated the resulting phylogeny against 17 fossil dates to produce a new timeline for monocot evolution. Liliales diverged from other monocots 124 Mya and began splitting into separate families 113 Mya. Our data support an Australian origin for Liliales, with close relationships between three pairs of lineages (Corsiaceae/Campynemataceae, Philesiaceae/Ripogonaceae, tribes Alstroemerieae/Luzuriageae) in South America and Australia or New Zealand reflecting teleconnections of these areas via Antarctica. Long-distance dispersal (LDD) across the Pacific and Tasman Sea led to re-invasion of New Zealand by two lineages (Luzuriaga, Ripogonum); LDD allowed Campynemanthe to colonize New Caledonia after its submergence until 37 Mya. LDD permitted Colchicaceae to invade East Asia and Africa from Australia, and re-invade Africa from Australia. Periodic desert greening permitted Gloriosa and Iphigenia to colonize Southeast Asia overland from Africa, and Androcymbium–Colchicum to invade the Mediterranean from South Africa. Melanthiaceae and Liliaceae crossed the Bering land-bridge several times from the Miocene to the Pleistocene.
Data from: Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
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Data from: Distribution and genetic diversity of the rare plant Veratrum woodii (Liliales: Melanthiaceae) in Georgia: a preliminary study with AFLP fingerprint data
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