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13,397 results for “sp. nov.”
Fig. 35 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Fig. 35: View from about 2100 m a. s. l. to Corn dal Solcun. Dichotrachelus sondereggeri sp. nov. was found in a single exemplar collected by C. Besuchet at this lower altitude. Foto: C. Germann.
Figs 33–34 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 33–34. Biotope of Dichotrachelus sondereggeri sp. nov. on Corn dal Solcun (2480 m a.s.l.): 33) side peak in loose rocks providing a cold and humid microclimate where moss cushions with larvae were found; 34) detailed view of those moss cushions. Fotos: C. Germann.
Figs 29–32 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 29–32: Different stages of Dichotrachelus sondereggeri sp. nov.: 29) last instar larva just before pupation; 30) pupa ventral view; 31) pupa dorsal view; 32) freshly hatched imago. Fotos: C. Germann.
Fig. 27 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Fig. 27: Map showing sites of Dichotrachelus alpestris species group. Black circles: D. alpestris; black square: D. sondereggeri sp. nov.; white squares: D. augusti species complex.
Figs 8–10 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 8–10: Dorsal and lateral views: 8) Dichotrachelus alpestris from Monte Viso, male; 9) Ditto from Anzeindaz, female; 10) Ditto male.
Figs 11–16 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 11–16: Overview of the variability of the tip of the aedeagus of Dichotrachelus alpestris: 11) Waadt, Anzeindaz; 12) Ticino, Monte Gene-Generoso; 13) Valle Aosta, Colle Arietta; 14) Valle Aosta, Champorcher; 15) Piemonte, Colle della Lombarda; 16) Piemonte, Portette Valdieri.
Figs 2–4 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 2–4: Dorsal and lateral views: 2) Dichotrachelus sondereggeri sp. nov. from Corn dal Solcun, male; 3) Ditto female; 4) Ditto male.
Figs 5–7 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)
Figs 5–7. Dorsal and lateral views: 5) Dichotrachelus augusti (form II from Val Ferret), male; 6) Ditto female; 7) Ditto male.
FIGURE 3. Secondary structures for the D1–D1 in New cyanobacterium Aliterella vladivostokensis sp. nov. (Aliterellaceae, Chroococcidiopsidales), isolated from temperate monsoon climate zone (Vladivostok, Russia)
FIGURE 3. Secondary structures for the D1–D1′ helices in the ITS regions for five Aliterella species and putative genus member Synechocystis sp. PCC 7509. Conservative nucleotides are grey colored.The unique marker mutations for the new species A. vladivostokensis are black colored. Arrowheads show compensatory (CBCs) and hemi-compensatory base changes (hCBCs). Homological base pairs among different species are indicated by dotted lines.
FIGURE 5 in Morphological and molecular characterization of two species of Gelidium (Gelidiales, Rhodophyta) from Mexico: G. nayaritense sp. nov. and the new record of G. sanyaense
FIGURE 5. Vegetative features of Gelidium sanyaense from Mexico. A–B. Thallus (FCME 10892). Scale = 0.2 mm. C. Apical cell (AP). Scale = 50 µm. D. Transvers section of erect branch with internal rhizoidal filaments (RHI). Scale = 40 µm. E. Enlargement of Fig. 5D. Scale = 25 µm.
FIGURE 4 in Morphological and molecular characterization of two species of Gelidium (Gelidiales, Rhodophyta) from Mexico: G. nayaritense sp. nov. and the new record of G. sanyaense
FIGURE 4. Reproductive features of Gelidium nayaritense sp. nov. A. Tetrasporangial branch with tetrasporangial sorus (TS). Scale = 400 µm. B. Tetrasporangial sorus with steril margin (EM) Scale = 100µm. C. Tetrasporangial sorus with tetrasporangia (TE). Scale = 100 µm. D. Cruciately divided tetrasporangia (TE). Scale = 40 µm.
FIGURE 1 in Morphological and molecular characterization of two species of Gelidium (Gelidiales, Rhodophyta) from Mexico: G. nayaritense sp. nov. and the new record of G. sanyaense
FIGURE 1. Maximum-likelihood tree inferred from rbcL sequences of Gelidium. ML bootstrap and Bayesian posterior probabilities values are shown at branches. Bold letters indicate newly generated sequences in this study. * indicates the holotype.
FIGURE 3 in Morphological and molecular characterization of two species of Gelidium (Gelidiales, Rhodophyta) from Mexico: G. nayaritense sp. nov. and the new record of G. sanyaense
FIGURE 3. Vegetative features of Gelidium nayaritense sp.nov. A. Holotype (FCME 10875). Scale =0.2 mm. B. Paratype (FCME 10889). Scale = 0.2 mm. C. Stolon (ST), haptera (H). Scale = 100 µm. D. Stolon (ST), haptera (H) and rhizoids (RI). Scale = 50 µm. E. Apical cell. Scale = 100 µm. F. Enlargement of Fig. 3E. Scale = 50 µm. G. Transvers section of erect branch. Scale = 40 µm. H. Enlargement of Fig. 3G, with internal rhizoidal filaments (RHI). Scale = 25 µm.
FIGURE 2 in Morphological and molecular characterization of two species of Gelidium (Gelidiales, Rhodophyta) from Mexico: G. nayaritense sp. nov. and the new record of G. sanyaense
FIGURE 2. Maximum-likelihood tree inferred from COI-5P sequences of Gelidium. ML bootstrap and Bayesian posterior probabilities values are shown at branches. Bold letters indicate newly generated sequences in this study. * indicates the holotype.
FIGURE 2 in Stagonosporopsis rhizophilae sp. nov. (Didymellaceae, Pleosporales), a new rhizospheric soil fungus associated with Populus deltoides Marsh
FIGURE 2. Stagonosporopsis rhizophilae sp. nov. (CGMCC3.19852). A–D. Colonies on PDA, MEA, CA, and OA, respectively (front and reverse); E. Pycnidia forming on OA. F. Section of pycnidium. G. Section of pycnidial wall. H. Conidiogenous cells. I. Conidia. Scale bars: 800 μm (E), 20 μm (F), 10 μm (G–I). PDA: potato dextrose agar, MEA: malt extract agar, CA: cherry-decoction agar, and OA: oatmeal agar.
FIGURE 5 in True branching and phenotypic plasticity in the planktonic cyanobacterium Dolichospermum brachiatum sp. nov. (Nostocales, Aphanizomenonaceae), from south-eastern Australia
FIGURE 5. Phylogenetic tree based on partial 16S ribosomal RNA gene sequence (1518 base pairs) of 128 OTUs showing the phylogenetic position of Dolichospermum brachiatum. Numbers indicate bootstrap values (> 50%) from 1000 replicates of ML and NJ analyses respectively. GenBank accession numbers are shown in parentheses. Scale bar = 0.01 nucleotide substitutions per site.
FIGURE 2 in True branching and phenotypic plasticity in the planktonic cyanobacterium Dolichospermum brachiatum sp. nov. (Nostocales, Aphanizomenonaceae), from south-eastern Australia
FIGURE 2. Sequence of development of T-type true branching of Dolichospermum brachiatum from Waranga Basin. Scale bars = 20 μm.
FIGURE 7 in True branching and phenotypic plasticity in the planktonic cyanobacterium Dolichospermum brachiatum sp. nov. (Nostocales, Aphanizomenonaceae), from south-eastern Australia
FIGURE 7. Secondary structure of the ITS sequence in D. brachiatum and allied species. Circles and oblongs highlight the differences in the structures; (A–D) D1-D1′ helix (A) D. brachiatum strains WB20619.B1, WB20619.B3, WB20619.C1 and WB20619.C2, (B) D. planctonicum strains 1-3; 19-1; 23-10; NRERC-101; D. ucrainicum CHAB623, (C) D. affinis CHAB28, (D) D. lemmermanni BC Ana 0032. (E–H) Box B helix (E) D. brachiatum strains WB20619.B1, WB20619.B3, WB20619.C1 and WB20619.C2, (F) D. planctonicum strains 1-3; 19-1; 23-10; NRERC-101; D. ucrainicum CHAB623, (G) D. affinis CHAB28 and CHAB964; D. flos-aquae CHAB1652 and NIES 1669, (H) D. lemmermannii BC Ana 0032. (I–M) V3 helix (I) D. brachiatum strains WB20619.B1, WB20619.B3, WB20619.C1 and WB20619.C2, (J) D. planctonicum strain 1-3; 1-9; 19-1; 23-10; NRERC-101, (K) D. affinis CHAB28; D. flos-aquae CHAB1652 and NIES 1669, (L) D. ucrainicum CHAB623, (M) D. lemmermannii BC Ana 0032.
FIGURE 6 in True branching and phenotypic plasticity in the planktonic cyanobacterium Dolichospermum brachiatum sp. nov. (Nostocales, Aphanizomenonaceae), from south-eastern Australia
FIGURE 6. Phylogenetic tree based on the ITS sequence of the 16S–23S rRNA operon of 25 OTUs showing the phylogenetic position of Dolichospermum brachiatum. Numbers indicate bootstrap values> 50% from 1000 replicates of ML and NJ analyses respectively. GenBank accession numbers shown in parentheses. Scale bar = 0.05 nucleotide substitutions per site. Strains isolated and sequenced in this study shown in bold.
FIGURE 2 in Bioluminescent fungus Roridomyces viridiluminus sp. nov. and the first Chinese record of the genus Roridomyces, from Southwestern China
FIGURE 2. Roridomyces viridiluminus (HKAS109712, holotype). a fruiting bodies on substrate in the field. b–c Cheilocystidia. d–f Basidia. g Stipitipellis cells. h Pileipellis cells. i Mature basidiospores. j Young basidiospores with sterigmata. k–l Basidiospores. Scale Bars: 10 µm (b–c); 5 µm (d–f); 40 µm (g–h); 1 µm (i–l).
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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
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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.
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.