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FIGURE 20 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 20. Piribelba piriformis (Mihelčič, 1964), collection of Mihelčič. A–E (left side) —original slides with labels of author; A1–D5—adult specimens observed in slides, with measured total length, single specimen in slide B designated as lectotype (B1), only juvenile instar (deutonymph) placed near specimen D4 on slide D.
FIGURE 5 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 5. Piribelba rossica (Bulanova-Zachvatkina, 1957), adult from Khabarovsk Krai, SEM micrograph: A—ventral view; B—lateral view; C—gnathosoma, lateral view; D, E—cerotegument of notogaster; F—cerotegument of prodorsal region; G—femur, genua and tibia III, antiaxial view. Scale bars 200 μm (A, B), 50 μm (G), 20 μm (C, D), 5 μm (F), 2 μm (E).
FIGURE 24 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 24. Piribelba piriformis (Mihelčič, 1964), paralectotypes (syntypes of the author, specimens marked according to Fig 20). A—ventral side, anogenital area (specimen A1); B—leg IV and part of notogastral setae (C1); C—leg I (C1); D—seta le (C1); E—parts of leg I and II and distal part of bothridial seta (A1); F—leg IV (D2); G—detail of setae and cerotegument on proximal part of leg IV (D3); H—reticular cerotegument of notogaster (C1). Scale bars 200 μm (F), 50 μm (A–E, G, H).
FIGURE 21 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 21. Piribelba piriformis (Mihelčič, 1964), lectotype. A—lateral view of the body (total length 678 µm); B—view of notogaster from adverse side; C—detail of prodorsal setae le, ro and ex; D—detail of selected setae of the body (C and D scale is increased).
FIGURE 23 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 23. Piribelba piriformis (Mihelčič, 1964), lectotype. A—lateral view with indication of areas depicted in detail; B—detail of sejugal area; C—ventral side, detail of epimeres; D—ventral side, anogenital area; E—detail of lamellar and rostral seta; F—parts of legs II-III-IV. Scale bars 200 μm (A), 100 μm (C, D), 50 μm (E), 20 μm (B).
FIGURE 2 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 2. Piribelba rossica (Bulanova-Zachvatkina, 1957), adult from Kemerovo region: A, B—part of epimeral III-IV region, left (genital area painted over); С—bothridial setae; D—chelicera, left, antiaxial view; E—subcapitulum, ventral view; F—palp, left, antiaxial view; G—prodorsal setae; H—notogastral setae. Scale bar 100 μm.
FIGURE 3 in Taxonomy of European Damaeidae (Acari, Oribatida) XI. European species of the genus Piribelba Miko 2021: redescriptions of P. rossica (Bulanova-Zachvatkina 1957) and P. piriformis (Mihelčič, 1964) using morphology and DNA sequence data
FIGURE 3. Piribelba rossica (Bulanova-Zachvatkina, 1957), adult from Kemerovo region: A—leg I, left, antiaxial view; B—leg II, left, antiaxial view; C—trochanter III, left, antiaxial view; D—femur, genu, tibia and tarsus III, left, antiaxial view; E—trochanter IV, left, antiaxial view; F—femur, genu, tibia and tarsus IV, left, antiaxial view. Scale bar 100 μm.
Fig. 4 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 4. Scanning electron photomicrographs of pollen grains from the Iresine clade (= Iresinoids). A, Iresine cassiniiformis (Borsch & al. 3792); B, Iresine type XXXIV (Borsch & al. 5412); C, Iresine rzedowskii (Borsch & al. 3793); D, Iresine ajuscana (Borsch & al. 5404); E, Iresine orientalis (Borsch & al. 5404); F, Iresine discolor (Purpus 3453); G, Magnification of aperture with details of mesoporium of pollen from the same plant; H, Iresine hartmanii (Tenorino 1864); I, Iresine type XXXIV (Borsch & al. 5390). — Scale = 10 µm apart from G where it is 4 µm.
Fig. 7. Scanning electron photomicrographs from the alternantheroid and gomphrenoid clades. A in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 7. Scanning electron photomicrographs from the alternantheroid and gomphrenoid clades. A, Pedersenia cardenasii (Borsch & Ortuño 3504); B, Pedersenia sp. (Borsch & Ibisch 3532); C, Magnification of aperture and details of mesoporia of pollen from the same plant; D, Hebanthe occidentalis (Borsch & Ortuño 3512); E, Pfaffia dunaliana (Borsch & Ortuño 3756); F, Magnification of aperture and details of mesoporia of pollen from the same plant. — Scale = 10 µm apart from C where it is 4 µm.
Fig. 5. Scanning electron photomicrographs from the Iresine clade. A in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 5. Scanning electron photomicrographs from the Iresine clade. A, Iresine hebanthoides (Borsch & al. 5415); B, Magnification of aperture and details of mesoporia of pollen from the same plant; C, Iresine sousae (Mendez Ton 7192, isotype B); D, Iresine nitens (Borsch & al. 3770); E, Magnification of aperture and details of mesoporia of pollen from the same plant; F, Iresine latifolia (Borsch & al. 3790); G, Magnification of aperture and details of mesoporia of pollen from the same plant; H, Iresine diffusa (Borsch & al. 3676); I, Irenella cysotricha (Asplund 16555). — Scale = 10 µm apart from B, E and G where it is 4 µm and I where it is 2 µm.
Fig. 6. Scanning electron photomicrographs from the Iresine clade. A in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 6. Scanning electron photomicrographs from the Iresine clade. A, Iresine angustifolia (Zumaya & al. 81); B, Iresine nigra (Zumaya & al. 77); C, View from a different angle onto a pollen grain from the same plant; D, Iresine interrupta (Zumaya 62); E, Iresine borschii (Ventura 9443, paratype); F, Iresine arbuscula (Castillo s.n.). — Scale = 10 µm.
Fig. 1 in Pollen characters and DNA sequence data converge on a monophyletic genus Iresine (Amaranthaceae, Caryophyllales) and help to elucidate its species diversity
Fig. 1. Morphological diversity of Iresine. A, Synflorescence of I. interrupta (Borsch & al. 3789); B, Pistillate flowers at maturity and C, Staminate flowers of I. interrupta (Borsch & al. 3789); D, Upright woody stem of Iresine type XXXIV (Borsch & al. 5390); E, Inflorescence and F, Woody stem of I. nigra (S. Zumaya & al. 77); G, Part of synflorescence with staminate (Borsch & al. 5385) and H, Pistillate flowers of I. ajuscana (Borsch & al. 5367). — Photos: T. Borsch.
Supplementary material 2 from: Zhao Y, Liu X-z, Bai F-y (2019) Four new species of Tremella (Tremellales, Basidiomycota) based on morphology and DNA sequence data. MycoKeys 47: 75-95. https://doi.org/10.3897/mycokeys.47.29180
Supplementary material 2 from: Zhao Y, Liu X-z, Bai F-y (2019) Four new species of Tremella (Tremellales, Basidiomycota) based on morphology and DNA sequence data. MycoKeys 47: 75-95. https://doi.org/10.3897/mycokeys.47.29180
Supplementary material 1 from: Zhao Y, Liu X-z, Bai F-y (2019) Four new species of Tremella (Tremellales, Basidiomycota) based on morphology and DNA sequence data. MycoKeys 47: 75-95. https://doi.org/10.3897/mycokeys.47.29180
Supplementary material 1 from: Zhao Y, Liu X-z, Bai F-y (2019) Four new species of Tremella (Tremellales, Basidiomycota) based on morphology and DNA sequence data. MycoKeys 47: 75-95. https://doi.org/10.3897/mycokeys.47.29180
FIGURE 7. Sparsorythus multilabeculatus, 7a in Description of nymphs and female subimago of Sparsorythus multilabeculatus Sroka & Soldán, 2008 (Ephemeroptera: Tricorythidae) associated with male imago based on DNA sequence data
FIGURE 7. Sparsorythus multilabeculatus, 7a. foreleg; 7b. midleg; 7c. hindleg; 7d. female cerci and paracercus; 7e. segment of female cerci; 7f. male cerci and paracercus; 7g. segment of female cerci. Scale bars: 0.5 mm (7a–7c); 0.1 mm (7d, 7f); 0.02 mm (7e, 7g).
FIGURE 2 in Description of nymphs and female subimago of Sparsorythus multilabeculatus Sroka & Soldán, 2008 (Ephemeroptera: Tricorythidae) associated with male imago based on DNA sequence data
FIGURE 2. Wang Tao waterfall, Thap Lan National Park, Khon Buri District, Nakhon Ratchasima Province, Thailand, where the specimens of Sparsorythus multilabeculatus were collected.
FIGURE 2 in Is Ronnbergia (Bromeliaceae, Bromelioideae) a geographically disjunct genus? Evidence from morphology and chloroplast DNA sequence data
FIGURE 2. Majority rule consensus tree from the BI analysis of the "total evidence" dataset from morphological and molecular data. Black lines represent the branches that remained identical in the strict consensus tree of the MP analysis. Grey lines represent branches obtained only in the BI analysis. Numbers in the nodes correspond to posterior probabilities and bootstrap values (PP/BT); dashes (-) represent low (<50%) or no BT support.
FIGURE 1 in Is Ronnbergia (Bromeliaceae, Bromelioideae) a geographically disjunct genus? Evidence from morphology and chloroplast DNA sequence data
FIGURE 1. Comparison of the phylogenetic hypothesis provided by the independent morphological and molecular datasets. Species of Ronnbergia are highlighted in red. A. Strict consensus of the four most parsimonious trees from the MP analysis of morphological data. Numbers in the nodes correspond to bootstrap values. B. Majority rule consensus tree from the BI analysis of the molecular dataset. Numbers in the nodes correspond to posterior probabilities and bootstrap values (PP/BT); dashes (-) represent low (<50%) or no BT support.
FIGURE 3 in Is Ronnbergia (Bromeliaceae, Bromelioideae) a geographically disjunct genus? Evidence from morphology and chloroplast DNA sequence data
FIGURE 3. Geographic distribution of the three clades containing species of Ronnbergia. Data points were obtained from the Global Biodiversity Information Facility—GBIF (www.gbif.org).
FIGURES 9–15 in Sporolithon indopacificum sp. nov. (Sporolithales, Rhodophyta) from tropical western Indian and western Pacific oceans: First report, confirmed by DNA sequence data, of a widely distributed species of Sporolithon
FIGURES 9–15. Tetrasporangial anatomy of the holotype of Sporolithon indopacificum (L 3964509). 9. Scanning electron micrograph (SEM) showing two tetra/bisporangial sori in surface view (arrowheads) (scale bar = 200 μm). 10. SEM showing a magnified view of several tetra/bisporangial chambers in surface view. Note the open, unoccluded pores (P), intact pore plugs (p) and the rosette cells surrounding the pores (scale bar = 15 μm). 11. Transverse section through two contiguously fused protuberances showing an extensive sorus (arrowheads) (scale bar = 300 μm). 12. Vertical section through the edge of a raised sorus (S) showing tetra/bisporangial chambers with floors (black arrowhead) that are flush with the surrounding vegetative surface (white arrowhead) (scale bar = 50 μm). 13. Vertical section through the edge of a raised sorus (S) showing tetra/bisporangial chambers with floors (black arrowhead) that are sunken below the surrounding vegetative surface (white arrowhead) (scale bar = 50 μm). 14. Vertical section through a sorus showing several tightly abutting, longitudinally elliptical tetra/bisporangial chambers bearing mostly uncleaved sporangia (t) borne on a single stalk cell (black arrowheads). Note the sporangial chamber pore plugs (white arrowheads), a 'T'-shaped divided tetrasporangium (T) and the sterile paraphyses of elongate cells (arrow) between two adjacent tetra/bisporangial chambers (scale bar = 50 μm). 15. Magnified view through a sorus showing three tetra/bisporangial chambers, one of which bears a zonately arranged bisporangium (B). Note the sporangial chamber pore plugs (white arrowheads) and the layer of elongate cells at the base of the sporangial chambers (black arrowheads) (scale bar = 30 μm).
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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.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.