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FIGURE 4 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 4. Germainiella sinica, sp. nov. LM. Figs 24–29 and 31–37, Valve views. Fig. 30 girdle view. All specimens from the holotype slide. Scale bars = 10 μm.
FIGURE 3 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 3. Germainiella maolaniana, sp. nov. SEM, external views. Fig. 20. Valve view, showing raphe slit and two openings of the conopeum extending the length of the valve. Fig. 21. Central area showing slightly dilated proximal raphe ends. No struts are evident. Small openings on the conopeum organized into rows of varying lengths, present on both sides of the longitudinal openings. The openings of the conopeum reveal the valve beneath it. Fig. 22. Break in the conopeum reveals struts oriented perpendicular to the raphe and situated beneath the raphe. Striae are single openings with hymenate occlusions. Fig. 23. Valve terminus showing raphe hook-shaped and extending onto the mantle.
FIGURE 6 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 6. Germainiella sinica, sp. nov. Figs 44, 45. Valve exterior showing view into valve between conopeum and margin. Siliceous granulaes are on the external valve face. Fig. 46. External girdle view, showing numerous girdle bands of the open type. Figs 47–50. Broken valves. Fig. 47. Valve view showing conopeum with short slits near the raphe, and then below it the external valve face with siliceous granules evident. Figs 48, 49. Girdle (side) views, showing presence of small siliceous struts, and the space (without any 'tubules') between the conopeum above and the external valve (with numerous granules) below. Fig. 50. Valve view showing the external valve face with numerous granules and internal valve face with hymenate occlusions over the areolae comprising the striae.
FIGURE 5 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 5. Germainiella sinica, sp. nov. SEM. Figs 38–41, valve exterior. Fig. 38. Whole valve with raphe slit and longitudinal openings between the conopeum and margins. Fig. 39. Valve apex showing narrow slits in conopeum bordering raphe. Distal raphe end is deflected onto the valve mantle. Fig. 40. Valve with undeveloped conopeum, with view to valve exterior beneath the conopeum. Fig. 41. Central portion of the valve with proximal raphe ends deflected slightly in the same direction. Small, narrow slits extending across the center of the conopeum beyond the proximal raphe ends. Figs. 42, 43, valve interior. Fig. 42. Terminus of the valve showing striae comprised of uniseriate rows of rounded areolae that are occluded internally. Raphe terminates as a helictoglossa. Fig. 43. Central area of the valve with narrow raphe and proximal raphe ends curved slightly in the same direction.
FIGURE 2. Germainiella spp. SEM. Figs 14–17. Germainiella enigmatica, external views. Fig. 14 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 2. Germainiella spp. SEM. Figs 14–17. Germainiella enigmatica, external views. Fig. 14. Entire valve showing large conopeum with raphe slit evident. Small struts oriented perpendicular to the raphe slit are evident. Raphe curves onto the valve mantle. Fig. 15. View showing struts under raphe slit. Figs 16, 17. Broken valve, showing conopeum laying overtop the valve. Internal valve face is evident. Figs 18, 19. Germainiella guizhouiana, sp. nov, external views. Fig. 18. Entire valve with large conopeum covering the face, with openings evident at the apices. Raphe slit with distal raphe ends deflected onto the mantle. Fig. 19. View of apex showing struts beneath conopeum oriented perpendicular to the raphe. Openings of the conopeum are evident. Raphe is hooked onto the mantle.
FIGURE 1. Germainiella spp. Light microscopy. Figs 1–7. Germainiella engimatica. Valve views. Figs 8–10 in First Report and New Freshwater Species of Germainiella (Bacillariophyta) from the Maolan Nature Reserve, Guizhou Province, China
FIGURE 1. Germainiella spp. Light microscopy. Figs 1–7. Germainiella engimatica. Valve views. Figs 8–10. Germainiella maolaniana, sp. nov. Valve views. All specimens from the holotype slide. Figs 11–13. Germainiella guizhouiana, sp. nov. Valve views. All specimens from the holotype slide. Scale bars = 10 μm.
FIGURE 1. Sadiria yingjiangensis. A in Sadiria yingjiangensis (Myrsinoideae, Primulaceae), a new species reported from West Yunnan, China
FIGURE 1. Sadiria yingjiangensis. A. plants; B. three new apical leaves; C. flowering branches with inflorescences; D. pyramid-paniculate inflorescences; E. young green fruit; F. flower; G. part of sepals; H. corolla and anthers; I. pistil. Photographed by Ze H.Wang.
FIGURE 2. Comparison between Sadiria yingjiangensis and S. longistyla. A. S in Sadiria yingjiangensis (Myrsinoideae, Primulaceae), a new species reported from West Yunnan, China
FIGURE 2. Comparison between Sadiria yingjiangensis and S. longistyla. A. S. yingjiangensis: A1. holotype, KUN!; B. S. longistyla: B1. holotype, KUN1342914!. Shown below are their inflorescences (A2 & B2), sepals (A3 & B3), corollas and anthers (A4 (the 4-merous flower) and B4).
FIGURE 1 in First report of Limacella from Bangladesh, with a new species description
FIGURE 1. Macro-and microscopic features of Limacella bangladeshana (HKAS 75316, holotype; PHI-4, isotype). a. Basidiomata and its caespitose habit, cottony white elements at the pileal margin (arrows). b. Showing fee lamellae, pileus surface and rudimentary elements on the stipe surface (arrow). c. Basidia at different stages of development. d. Basidiospores. Bars: a–c = 20 mm, d, e = 10 μm.
FIGURE 2 in First report of Limacella from Bangladesh, with a new species description
FIGURE 2. Phylogenetic relationship and placement of Limacella bangladeshana within Amanitaceae inferred from nrLSU sequences using RAxML. Bootstrap support values (ML BS ≥50% and PP ≥0.95) are shown above/beneath the branches at nodes. Limacella bangladeshana is in bold on the tree. GenBank accession number and location are provided after the species name. Amanita cinereovelata is rooted as the outgroup.
FIGURES 33–38. Spongoclonium caribaeum. 33 in A taxonomic account of species in the tribe Spongoclonieae (Ceramiaceae, Ceramiales, Rhodophyta) reported from Atlantic and Pacific Mexico
FIGURES 33–38. Spongoclonium caribaeum. 33) Sporophyte with numerous polysporangia. Scale bar: 450 μm. 34) Sessile mature polysporangia. Scale bar: 90 μm. 35) Sessile spermatangial cluster (arrow). Scale bar 70 μm. 36) Procarp four-celled stage (arrows). Scale bar: 75 μm. 37) Procarp at five-cell stage (arrow). Scale bar: 110 μm. 38) Young procarp with carpogonium initiating the trichogyne (arrow). Scale bar: 150 μm.
FIGURES 17–24 in A taxonomic account of species in the tribe Spongoclonieae (Ceramiaceae, Ceramiales, Rhodophyta) reported from Atlantic and Pacific Mexico
FIGURES 17–24. Species of Pleonosporium: Pleonosporium mexicanum, 17) Apical portion of a sporophyte with incurved branchlets. Scale bar: 600 μm. 18) Sessile mature polysporangium (arrows), and an immature polysporangium (arrowhead). Scale bar: 65 μm. 19) Sessile spermatangial cluster (arrow). Scale bar: 40 μm. 20) Young procarp (arrow); note that the trichogyne has not developed. Scale bar: 50 μm. 21) Mature carposporophyte (key), note the carposporangia (arrow) and mature carposporophyte (arrowheads). Scale bar: 130 μm. Pleonosporium pygmaeum, Punta Morro, Baja California (ENCB 9570). 22) Habit of sporophyte. Scale bar: 8 mm. 23) Basal portion of thallus showing strong rhizoidal cortication (arrow). Scale bar: 160 μm. 24) Branch tip of sporophyte with straight branchlets. Scale bar: 120 μm.
FIGURES 9–16 in A taxonomic account of species in the tribe Spongoclonieae (Ceramiaceae, Ceramiales, Rhodophyta) reported from Atlantic and Pacific Mexico
FIGURES 9–16. Species of Pleonosporium: Pleonosporium globuliferum, Salina Cruz, Oaxaca (ENCB 14958). 9) Habit, female gametophyte. Scale bar: 9 mm. 10) Ecorticate axis with determinate lateral branches. Scale bar: 150 μm. 11) Detail of upper portions showing strongly curved ultimate branchlets. Scale bar: 150 μm. 12) Branch of sporophyte with polysporangia (arrows) sessile. Scale bar: 75 μm. 13) Spermatangial cluster (arrow). Scale bar: 45 μm. 14) Mature carposporophyte (bracket) with carposporangia (arrows). Scale bar: 230 μm. Pleonosporium mexicanum, Santa Elena Cozoaltepec, Oaxaca (ENCB 14964). 15) Habit of male gametophyte. Scale bar: 9 mm. 16) Basal portion of thallus showing rhizoidal attachment. Scale bar: 450 μm.
FIGURES 1–8 in A taxonomic account of species in the tribe Spongoclonieae (Ceramiaceae, Ceramiales, Rhodophyta) reported from Atlantic and Pacific Mexico
FIGURES 1–8. Species of Pleonosporium. 1–4: Pleonosporium boergesenii, Playa El Pulpo, Barra de Cazones, Veracruz (ENCB 21801). 1) An entire, mature sporophyte. Scale bar: 7 mm. 2) Ecorticate branching axis and determinate lateral branch. Scale bar: 250 μm. 3) Branch tip of sporophyte showing incurving branchlets. Scale bar: 20 μm. 4) Branch of sporophyte showing sessile polysporangia (arrow). Scale bar: 60 μm. 5–8: Pleonosporium borreri, Playa El Pulpo, Barra de Cazones, Veracruz (ENCB 21896). 5) Habit of mature sporophyte. Scale bar: 8 mm. 6) Basal portion of thallus showing rhizoidal attachment. Scale bar: 150 μm. 7) Branch tip of sporophyte showing incurving and curved branchlets. Scale bar: 125 μm. 8) Branch of sporophyte with sessile polysporangia (arrows). Scale bar: 50 μm.
FIGURES 25–32 in A taxonomic account of species in the tribe Spongoclonieae (Ceramiaceae, Ceramiales, Rhodophyta) reported from Atlantic and Pacific Mexico
FIGURES 25–32. Species of Pleonosporium: Pleonosporium pygmaeum, 25) Branch of sporophyte showing sessile polysporangia (arrow). Scale bar: 90 μm. Pleonosporium rhizoideum, Puerto Peñasco, Sonora (ENCB 16338). 26) Habit of sporophyte. Scale bar: 5 mm. 27) Basal portion of the thallus; note the attachment structure (arrow). Scale bar: 280 μm. 28) Branch tip of a sporophyte with curved branchlets. Scale bar: 100 μm. 29) Group of spermatangial clusters (arrow) borne on a single branch. Scale bar: 80 μm. 30) Group of mature carposporophytes (key), with carposporangia (arrow). Scale bar: 200 μm. Species of Spongoclonium: Spongoclonium caribaeum, Escolleras Tuxpan, Veracruz (ENCB VER-2017/A). 31) Branch tips from sporophyte showing branching axis and determinate lateral branchlets. Scale bar: 600 μm. 32) Ecorticate axis and determinate lateral branches. Scale bar: 300 μm.
FIGURE 5 in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 5. Weekly capture in 2023 of Anisandrus maiche and Xylosandrus germanus in ethanol-baited traps along the woody edge of apple orchards.
FIGURE 1 in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 1. Adult beetle found in gallery, identified to Anisandrus maiche using morphological characteristics (Rabaglia et al., 2009). including A) median tuft of long setae at posterior margin of pronotum; B) impressed 2nd declivital interstriae and striae, and the raised 3rd declivital interstriae with numerous distinct granules; C) Procoxae contiguous; and D) Elytral declivity without a dorsal semi-circular carina.
FIGURE 2. A in First Report Of Anisandrus Maiche (Coleoptera: Curculionidae: Scolytinae) Infesting Apple Trees
FIGURE 2. A. Slides made from sections of gallery wall, with possible Ambrosiella ascospores (arrows) and clesitothecia debris (circles). B. Ambrosiella ascospores. Scale bars: 100µm.
Measurement report: The variation properties of aerosol hygroscopic growth related to chemical composition during new particle formation days in a coastal city of southeast China
<p>The aerosol scattering hygroscopic growth factor (f(RH)), along with conventional air pollutants and meteorological parameters were simultaneously observed from February to April 2022 in Xiamen, a coastal city of southeast China.</p>
Supplement information : Figures of the IAMM Project Report
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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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.