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FIGURE 4. Corynesporopsis quercicola. a, b. Conidiophores and conidia. c in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 4. Corynesporopsis quercicola. a, b. Conidiophores and conidia. c. Young conidium emerging from apical pore of the terminal conidiogenous cell. d, e. Catenate conidia. Scale bars = 20 μm.
FIGURE 1 in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 1. Maximum Likelihood tree showing estimated relationships of Corynesporopsis acaciae among Xylariales and some other orders of Sordariomycetes based on 5.8S-ITS and LSU rDNA sequences. Bootstrap values above 50% (1,000 replicates) are indicated at the nodes. The tree was rooted with the clade representing Hypocreales (Claviceps purpurea and Nectria cinnabarina).
FIGURE 3. Corynesporopsis acaciae, microscopic characteristics. a. Conidiophores and conidia from the holotype. b. Conidiophores from another, overmature specimen. c in Phylogenetic placement of a new species of Corynesporopsis from dead acacia wood indicates occurrence of tretic conidiogenesis within Xylariales
FIGURE 3. Corynesporopsis acaciae, microscopic characteristics. a. Conidiophores and conidia from the holotype. b. Conidiophores from another, overmature specimen. c. Conidiophores from the ex-type culture shown in 2b. Scale bars: c, d, e = 10 μm.
FIGURES 11–14. Thalassiosira catharinensis. SEM, internal views. Rimoportula indicated with a white arrow. 11. Internal view showing fultoportulae with three satellite pores. 12. Internal general view showing a in A new species of nanoplanktonic diatom: Thalassiosira catharinensis (Bacillariophyceae) from Southern of Brazil
FIGURES 11–14. Thalassiosira catharinensis. SEM, internal views. Rimoportula indicated with a white arrow. 11. Internal view showing fultoportulae with three satellite pores. 12. Internal general view showing a rimoportula located next to a fultoportula with three satellite pores. 13. Detail of the central fultoportula with three satellite pores. 14. Part of a valve showing in detail central and marginal fultoportulae with three satellite pores. A small and shallow rimopotula is located at the same level than the marginal fultoportula. Scale bars: Figs 11–12, 14 = 1 μm, Fig. 13 = 500nm. FIGURE 15. Thalassiosira minima. SEM, internal view showing two central fultopotulae with three satellite pores and marginal fultoportulae with four satellite pores. Note the internal rimportula opening (white arrow) not aligned with the marginal fultoportulae ring. Scale bar: 1 μm
FIGURE 2. Agave jimenoi. A. Stem showing the bifurcation scar, indicated with a yellow arrow, B. Habit, C. Infrutescence, D in Agave jimenoi (Polycephalae group, Asparagaceae) a new species from the Totonacapan region, Veracruz, Mexico
FIGURE 2. Agave jimenoi. A. Stem showing the bifurcation scar, indicated with a yellow arrow, B. Habit, C. Infrutescence, D. Seedlings growing in dry capsules, E. Inflorescence. Photographs by Gerardo Sánchez-Vigil (A, B and D), Alberto Badía (C), and H. David Jimeno-Sevilla (E).
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com] in Contributions of biogeographical functions to species accumulation may change over time in refugial regions
FIG UR E 3 (a) Dated phylogeny of the genus Theodoxus constructed in BEAST based on COI, 16S and ATPα. Node labels denote divergence times in millions of years ago (Ma); node bars indicate the 95% credibility interval around these dates. Small squares at nodes indicate significant support of divergence events found with BEAST and other phylogenetic analyses (see Figures S2.1 and S2.2), as explained through the key. Where MOTUs (A–R) show conspecifics among a number of morphospecies, species names are given in order of their year of description. Morphospecies, incorporated from GenBank, where determination was potentially dubious are highlighted by an asterisk. Clades (C) and subclades (SC) are demarcated by dashed lines between MOTUs. (b) LTT plots indicating the build‐up of lineages in Theodoxus over geological time. Dashed lines surrounding the solid LTT lines indicate the 95% confidence intervals. Where intra‐ and interspecific diversity diverge, interspecific diversity is highlighted in blue and intraspecific diversity in red. Transitions in geological ages are highlighted by narrow grey lines, while the grey bar marks the period of pronounced glacial cycles (last 900 kyr) [Colour figure can be viewed at wileyonlinelibrary.com]
FIGURES NJ27–NJ30. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ27, Scrobipalpa acuminatella; NJ28, Sophronia gelidella; NJ29, Anthophila fabriciana; NJ30, Phiaris bipunctana. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ27–NJ30. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ27, Scrobipalpa acuminatella; NJ28, Sophronia gelidella; NJ29, Anthophila fabriciana; NJ30, Phiaris bipunctana.
FIGURES NJ17–NJ19, NJ21. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ17, Agonopterix conterminella. NJ18, Depressaria depressana; NJ19, Coleophora atriplicis; NJ21, Coleophora granulatella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ17–NJ19, NJ21. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ17, Agonopterix conterminella. NJ18, Depressaria depressana; NJ19, Coleophora atriplicis; NJ21, Coleophora granulatella.
FIGURES NJ20, NJ22–NJ26. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ20, Coleophora glitzella; NJ22, Coleophora texanella; NJ23, Coleophora vitisella; NJ24, Scythris sinensis; NJ25, Altenia perspersella; NJ26, Gnorimoschema jalavai. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ20, NJ22–NJ26. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ20, Coleophora glitzella; NJ22, Coleophora texanella; NJ23, Coleophora vitisella; NJ24, Scythris sinensis; NJ25, Altenia perspersella; NJ26, Gnorimoschema jalavai.
FIGURES NJ7–NJ12. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ7, Parornix betulae; NJ8, Phyllonorycter maestingella; NJ9, Paraswammerdamia albicapitella; NJ10, Paraswammerdamia conspersella; NJ11, Plutella hyperboreella; NJ12, Lyonetia pulverulentella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ7–NJ12. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ7, Parornix betulae; NJ8, Phyllonorycter maestingella; NJ9, Paraswammerdamia albicapitella; NJ10, Paraswammerdamia conspersella; NJ11, Plutella hyperboreella; NJ12, Lyonetia pulverulentella.
FIGURES NJ1–NJ6. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ1, Scardia amurensis; NJ2, Triaxomera parasitella; NJ3, Nemapogon cloacella; NJ4, Elabotia montelliella; NJ5, Tinea svenssoni; NJ6, Caloptilia suberinella. in Shared but overlooked: 30 species of Holarctic Microlepidoptera revealed by DNA barcodes and morphology
FIGURES NJ1–NJ6. Neighbor-joining trees. Scale bar = 1%. Blue circles indicate Nearctic specimens, red circles Palearctic specimens, and mixed circles indicate a combination of the two; diamonds indicate outgroups. In parentheses are numbers of specimens per node. NJ1, Scardia amurensis; NJ2, Triaxomera parasitella; NJ3, Nemapogon cloacella; NJ4, Elabotia montelliella; NJ5, Tinea svenssoni; NJ6, Caloptilia suberinella.
Fig. 1. Maryland map indicating Assateague Island State and National Seashore. Assateague study location indicated with a in Species Diversity and Succession of Dung Beetles (Coleoptera: Geotrupidae and Scarabaeidae) Attracted to Horse Dung on Assateague Island
Fig. 1. Maryland map indicating Assateague Island State and National Seashore. Assateague study location indicated with a box in the inset; the two mainland horse farms are indicated with black squares: Holly Ridge Equestrian Center = HR; Autumn Grove Stables = AG.
Figure 18 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 18. Sabellomma cupoculata sp. nov., colour micrographs. A–D, live specimens. A, anterior end, ventral view. B, specimen missing posterior abdominal chaetigers, lateral view. C, radiolar crown and anterior thoracic chaetigers, lateral view. D, same, dorsal view. E–M, preserved specimens. E–G, detail of radiolar eyes along radiolar lateral margins. H, base of crown, ventral view, with crown opened showing ventral lips, dorsal lips with long radiolar appendages, and anterior thoracic chaetigers with ventral shields in contact with neuropodial tori and a dark pigment spot in between. I, J, half of radiolar crown showing dorsal lips with long radiolar appendages and pinnular appendages (arrow); dyed with methylene blue. K, thoracic chaetigers, holotype, lateral view, lacking inter-ramal eyes. L, thoracic chaetigers and collar. M, posterior thoracic and anterior abdominal chaetigers, lacking conspicuous inter-ramal eyes. A–D, AM W.37060; E–H, AM W.37060; I, J: AM W.37029; K, AM W.47193 (holotype); L, M, AM W.47189.
Figure 17 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 17. Parasabella sp. cf. Parasabella rugosa, scanning electron microscope photographs. A, anterior thoracic chaetigers and base of radiolar crown, dorsal view, showing large collar dorsal margins. B, midthoracic parapodium with elongate, narrowly hooded (arrow) superior chaetae and broadly hooded (type B) in inferior group. C, detail of inferior thoracic broadly hooded chaetae of type B. D, thoracic uncini. E, companion chaetae, lateral view. F, companion chaetae, frontal view. G, midabdominal neurochaetae narrowly hooded. H, abdominal uncini. I, posterior abdominal chaetigers and (damaged) pygidium. A–I, AM W.36431.
Figure 15 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 15. Parasabella sp. cf. Parasabella japonica, scanning electron microscope photographs. A, anterior thoracic chaetigers and base of radiolar crown, ventral view, showing ventral shields separated from neuropodial tori, and ventral lappets. B, anterior chaetigers, lateral view. C, same, dorsal view. D, midthoracic parapodium, elongate, narrowly hooded superi- or chaetae and broadly hooded type B chaetae in inferior group. E, detail of inferior, broadly hooded type B chaeta. F, thoracic uncini and companion chaetae. G, thoracic uncini, detail. H, companion chaetae showing the laterally compressed hood. I, midabdominal narrowly hooded neurochaetae. J, abdominal uncini. A–J, AM W.36450.
Figure 16 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 16. Parasabella sp. cf. Parasabella rugosa, colour micrographs of preserved specimens. A, anterior thoracic chaetigers, ventral view, showing posterior peristomial ring collar, and ventral shields in contact with neuropodial tori. B, complete thorax, lateral view. C, same, dorsal view. D, posterior abdominal chaetigers and pygidium, ventral view. A, NMV F.108844; B–D, AM W.36431.
Figure 12 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 12. Parasabella crassichaetae sp. nov. complex, colour micrographs of preserved specimens. A, whole specimen, lateral view. B, anterior chaetigers, showing the base of crown and the collar margins. C, specimens with detached crown showing the peristomial eyes (arrows) near the insertion site of the radiolar lobes. A–B, AM W.31103; C, AM W.37028.
Figure 10 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 10. Parasabella bioculata sp. nov. colour micrographs. A–C, live specimen. A, radiolar crown and anterior thoracic chaetigers, lateral view. B, same, dorsal view. C, whole specimens with opened radiolar crown. D–I, preserved specimens. D, anterior thoracic chaetigers and base of radiolar crown, lateral view. E, same, ventrolateral view. F, specimen with detached crown, dorsal view. G, tip of lateral radioles showing the subdistal radiolar eyes. H, arrangement of radiolar eyes on lateral radiole. I, magnified detail showing cup-shaped radiolar eye. A–C, AM W.37053; D, E, G, H, AM W.46997; F, I, AM W.37056.
Figure 9 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 9. Parasabella sp. cf. Parasabella aulaconota scanning electron microscope photographs. A, anterior thoracic chaetigers and base of radiolar crown, ventral view, with ventral shields in contact with neuropodial tori. B, same, showing the collar, lateral view. C, collar dorsal margins, lateral view. D, anterior thoracic chaetigers and base of radiolar crown, showing collar dorsal margins, dorsal view. E, collar chaetae, elongate, narrowly hooded. F, thoracic elongate, narrowly hooded superior notochaetae and inferior, broadly hooded (type B) chaetae. G, detail of inferior thoracic chaetae. H, I, thoracic uncini from specimens collected in temperate and tropical sites, respectively. J, companion chaetae. K, complete row of uncini in abdominal notopodia, showing the range in size from dorsal- to ventral-most uncini. L, midabdominal narrowly hooded neurochaetae. M, abdominal uncini. B, C, F, H, K–M, AM W.22017; A, D, E, G, I, J, AM W.22480.
Figure 11 in Integrative taxonomy of Parasabella and Sabellomma (Sabellidae: Annelida) from Australia: description of new species, indication of cryptic diversity, and translocation of some species out of their natural distribution range
Figure 11. Parasabella bioculata sp. nov. scanning electron microscope photographs. A, anterior thoracic chaetigers and base of radiolar crown, ventral view, showing ventral shields separated from neuropodial tori. B, same, lateral view. C, same, dorsal view. D, inside of radiolar crown, frontal view, showing dorsal lips and long radiolar appendages. E, elongate, narrowly hooded collar chaetae. F, midthoracic chaetiger, elongate, narrowly hooded superior thoracic chaetae, and inferior, broadly hooded type B chaetae. G, thoracic uncini. H, companion chaetae. I, midabdominal, narrowly hooded neurochaetae. J, abdominal uncini. A–J, AM W.36449.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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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.
OpenNeuro
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