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111 results for “Global biogeography”

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zenodo28/100

Figure 2 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 2 Geographical distribution of Montagnula species with known ITS sequence data. a the map summarizes data from the GlobalFungi database (shown by circles). Each circle symbolizes a unique sample, with each color representing the specific biome from which it has been collected b the distribution of Montagnula sequences as a percentage of total abundance across different biomes c the distribution of Montagnula sequences as a percentage of total abundance across different continents. See Suppl. material 1 for primary data.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 4 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 4 The species richness of recorded Montagnula species across different plant families (Table 1).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 3 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 3 The distribution of Montagnula occurrences across oceans, continents and various substrates, as documented in the existing literature. On the x-axis, the logarithmic abundance of each record for different sources is displayed.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 1 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 1 Phylogenetic analysis of SSU, LSU, ITS, tef1-α, and rpb2 of the Montagnula. Species names given in bold are ex-type, ex-epitype and ex-paratype strains. Species names highlighted in blue are generated from this study. Branch support of nodes ≥75% ML BS and ≥0.95 PP is indicated above the branches. The genus Montagnula is depicted within a pale gray box, with new species highlighted in white, and the outgroup indicated by a blue box.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 8 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 8 Montagnula shangrilana (HKAS 126541, holotype) a ascomata on natural wood surface b vertical section through an ascoma c pseudoparaphyses d peridium cells e–h asci i–o ascospores (see verruculose feature of the ascospore in o). Scale bars: 100 μm (b); 10 μm (c, d, j–o); 20 μm (e–h).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 7 from: Wanasinghe DN, Nimalrathna TS, Qin Xian L, Faraj TK, Xu J, Mortimer PE (2024) Taxonomic novelties and global biogeography of Montagnula (Ascomycota, Didymosphaeriaceae). MycoKeys 101: 191-232. https://doi.org/10.3897/mycokeys.101.113259

Figure 7 Montagnula menglaensis (HKAS 130318, holotype) a–c ascomata on natural wood surface d, e vertical section through ascomata f, g pseudoparaphyses h peridium i–k asci l, m ascospores (see verruculose feature of the ascospore in n) o, p culture characters on PDA (o = above, p = reverse) q, r conidiomata s pycnidial wall t conidia. Scale bars: 100 μm (d, e); 10 μm (f–h, l–n, s, t); 20 μm (i–k).

opencc-by-4.0Jan 2024View details →
zenodo28/100

Climatic drivers of the global biogeography of simple- and compound-leaved woody species

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opencc-by-4.0Apr 2024View details →
dryad28/100

Data from: Global biogeography of scaly tree ferns (Cyatheaceae): evidence for Gondwanan vicariance and limited transoceanic dispersal

Aim: Scaly tree ferns, Cyatheaceae, are a well-supported group of mostly tree-forming ferns found throughout the tropics, the subtropics and the south-temperate zone. Fossil evidence shows that the lineage originated in the Late Jurassic period. We reconstructed large-scale historical biogeographical patterns of Cyatheaceae and tested the hypothesis that some of the observed distribution patterns are in fact compatible, in time and space, with a vicariance scenario related to the break-up of Gondwana. Location: Tropics, subtropics and south-temperate areas of the world. Methods: The historical biogeography of Cyatheaceae was analysed in a maximum likelihood framework using Lagrange. The 78 ingroup taxa are representative of the geographical distribution of the entire family. The phylogenies that served as a basis for the analyses were obtained by Bayesian inference analyses of mainly previously published DNA sequence data using MrBayes. Lineage divergence dates were estimated in a Bayesian Markov chain Monte Carlo framework using beast. Results: Cyatheaceae originated in the Late Jurassic in either South America or Australasia. Following a range expansion, the ancestral distribution of the marginate-scaled clade included both these areas, whereas Sphaeropteris is reconstructed as having its origin only in Australasia. Within the marginate-scaled clade, reconstructions of early divergences are hampered by the unresolved relationships among the Alsophila, Cyathea and Gymnosphaera lineages. Nevertheless, it is clear that the occurrence of the Cyathea and Sphaeropteris lineages in South America may be related to vicariance, whereas transoceanic dispersal needs to be inferred for the range shifts seen in Alsophila and Gymnosphaera. Main conclusions: The evolutionary history of Cyatheaceae involves both Gondwanan vicariance scenarios as well as long-distance dispersal events. The number of transoceanic dispersals reconstructed for the family is rather few when compared with other fern lineages. We suggest that a causal relationship between reproductive mode (outcrossing) and dispersal limitations is the most plausible explanation for the pattern observed.

opencc-zeroDec 2012View details →
dryad28/100

Data from: Global biogeography of scaly tree ferns (Cyatheaceae): evidence for Gondwanan vicariance and limited transoceanic dispersal

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publicOct 2014View details →
dryad28/100

Data from: Global biogeography of mating system variation in seed plants

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publicJan 2018View details →
dryad28/100

Data from: Pathogeography: leveraging the biogeography of human infectious diseases for global health management

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publicMar 2018View details →

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Allen Brain Atlas

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
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Last verified 2026-04-29Open record

OpenNeuro

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openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record