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153 results for “Ecological biogeography”
Supplementary material 1 from: Levanets A, Janse van Vuuren S (2023) Morphology, taxonomy, biogeography and ecology of Micrasterias foliacea Bailey ex Ralfs (Desmidiales, Zygnematophyceae). PhytoKeys 226: 33-51. https://doi.org/10.3897/phytokeys.226.103500
Geographical distribution of M. foliacea var. foliacea throughout the world.
Supplementary material 4 from: Levanets A, Janse van Vuuren S (2023) Morphology, taxonomy, biogeography and ecology of Micrasterias foliacea Bailey ex Ralfs (Desmidiales, Zygnematophyceae). PhytoKeys 226: 33-51. https://doi.org/10.3897/phytokeys.226.103500
Supplementary references
Figure 1 from: Printzen C, Domaschke S, Fernández-Mendoza F, Pérez-Ortega S (2013) Biogeography and ecology of Cetraria aculeata, a widely distributed lichen with a bipolar distribution. MycoKeys 6: 33-53. https://doi.org/10.3897/mycokeys.6.3185
Figure 1 - Cetraria aculeata, habit.
Figure 13 in Is mimicry a diversification-driver in ants? Biogeography, ecology, ethology, genetics and morphology define a second West-Palaearctic Colobopsis species (Hymenoptera: Formicidae)
Figure 13. Above Cr. scutellaris and species showing a similar chromatic pattern that were collected near Cr. scutellaris trails in Sicily (Italy): A, Co. imitans (worker from Mondello); B, Ca. lateralis (worker from Monte Pellegrino); C, Gelis sp. (Hymenoptera: Braconidae) from Monte Petroso; D, Cr. scutellaris from Levanzo island; E, Phrurolithus sp. (Araneae: Phrurolitidae) from Mondello; F, Ca. ruber (worker from Monte Pellegrino); G, Leptorchestes sp. (Araneae: Salticidae) from Monte Petroso. Below, D. quadripunctatus and species with a similar chromatic pattern collected near its trails or in the same trees in mainland Italy: H, Co. truncata (specimen from Bulgaria, AntWeb code CASENT0280000, photographer Michele Esposito); I, D. quadripunctatus (specimen from Czech Republic, AntWeb code CASENT0179916, photographer Michele Esposito); J, Formicomus pedestris (Rossi, 1790) (Coleoptera: Anthicidae) from Parma (Italy).
Fig. 7 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)
Fig. 7 Factor analysis by species calculated as principal component analysis with varimax rotation based on Jaccard similarity coefficients for 95 geographic regions. a–c All species, d–f broad-leaved feeders and g–i conifer feeders
Fig. 6 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)
Fig. 6 Factor analysis by regions calculated as principal components analysis with varimax rotation based on Jaccard similarity coefficients for 95 geographic regions. a, b All species, c, d broad-leaved feeders and e, f conifer feeders
Fig. 2 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)
Fig. 2 Species and genera richness of Cerambycoidea in 95 geographic regions of the western Palaearctic: a all species, b all genera, c Cerambycinae, d Lepturinae, e Spondylidinae, and f Lamiinae
Fig. 3 in Ecological patterns strongly impact the biogeography of western Palaearctic longhorn beetles (Coleoptera: Cerambycoidea)
Fig. 3 Percentages of the Cerambycoidea species in 95 geographic regions of the western Palaearctic a having an area <500,000 km2, b having wingless females or being wingless species, and c being winged species
Fig. 1 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species
Fig. 1 Habitat selection and altitudinal distribution of five Eurycorypha species on Kilimanjaro in relation to climatic parameters. Line a: linear regression of mean annual temperature scaled with 1°C:25 mm precipitation; Line b: linear regression of mean annual temperature scaled with 1°C:50 mm precipitation; Line c: linear regression of mean
Fig. 6 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species
Fig. 6 Stridulatory files of Eurycorypha species (photos of replicas). p: E. punctipennis, v: E. varia, r: E. resonans, m: E. meruensis
Fig. 10 in Biogeography, ecology, acoustics and chromosomes of East African Eurycorypha Stål species (Orthoptera, Phaneropterinae) with the description of new species
Fig. 10 Detailed images of Eurycorypha species. a–c Eurycorypha punctipennis Chopard. a, b Male abdominal apex. c Male subgenital plate. d–f Eurycorypha resonans n. sp. d Lateral view on male abdominal apex. e Dorsal view on male abdominal apex. f Male subgenital plate. g–i Eurycorypha combretoides n. sp. g Lateral view on male abdominal apex. h Rear view on male abdominal apex. i Male subgenital plate. j– l Eurycorypha conclusa n. sp. j, k Lateral view on male abdominal apex. l Male subgenital plate
Figure 2 in REVIEW Diplura in caves: diversity, ecology, evolution and biogeography
Figure 2. Conceptual model of the major compartments of the subterranean habitats and corresponding dipluran habitus. Soil horizons: O is mainly formed by leaf litter, whereas the A and B horizons have gradual increase in mineral fraction and decrease in voids' size, the C horizon is formed by unconsolidated, mid-size clasts with large voids; this horizon has the mesovoid shallow substratum (MSS).
The Lignicolous Genus Entonaema: Its Phylogenetic– Taxonomic Position within Hypoxylaceae (Xylariales, Fungi) and an Overview of its Species, Biogeography, and Ecology
<p>Abstract: The lignicolous saprotrophic genus <em>Entonaem</em>a contains six formally accepted species: <em>E. liquescens</em> (type species), <em>E. cinnabarinum</em>, <em>E. globosum</em>, <em>E. dengii</em>, <em>E. moluccanum</em>, and <em>E. siamensis</em>. Its stromatic ascomata develop on the surface of dead wood remnants; they are rather large, globose to irregularly shaped, and vividly coloured. The fresh stroma interior is filled with a liquid matter. In early studies, the genus was considered to have a preference for tropical habitats, while in more recent field research, numerous collections have been added from warm, temperate areas of Europe, North America, and Asia. Our taxonomic and phylogenetic studies were based on freshly collected <em>E. cinnabarinum</em> from Croatia and <em>E. liquescens</em> from the USA. A phylogenetic study of the sequence alignment of four concatenated gene regions (ITS, LSU, <em>rpb2</em>, and <em>β-tub</em>) revealed the true taxonomic position of <em>Entonaema</em> within <em>Hypoxylaceae</em> (<em>Xylariales</em>), a sister to <em>Hypoxylon carneum</em>. Detailed macroscopic and microscopic descriptions of <em>E. cinnabarinum</em> are accompanied by drawings and colour photographs, while the study of <em>E. liquescens</em> is focused on stromatal microchemical reaction. With new information, the worldwide identification key to the putative species of <em>Entonaema</em> is proposed. Ecological data and biogeographical patterns were studied using all available and reliable sources of recorded data. Climatic preferences of the two most widespread <em>Entonaema</em> species, <em>E. liquescens</em> and <em>E. cinnabarinum</em>, are discussed in detail. </p>
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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