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Subspecies and Distribution. M. t. tristis Waterhouse, 1845 — the Philippines including Palawan I. M. 1. celebensis Peterson, 1981 — Sulawesi and nearby Sanana, Togian, and ButonIs. M. t. grandis Peterson, 1981 — W New Guinea E to Chimbu Province in C Papua New Guina, including Waigeo, Supiori, Biak, and Yapen Is, and Louisiade Archipelago. M. t. insularis Peterson, 1981 — Admiralty Is, Bismarck Archipelago, Solomon Is, and Vanuatu (Espirito Santo and Efate Is). M. t. propitristis Peterson, 1981 — E New Guinea.: in Miniopteridae
Subspecies and Distribution. M. t. tristis Waterhouse, 1845 — the Philippines including Palawan I. M. 1. celebensis Peterson, 1981 — Sulawesi and nearby Sanana, Togian, and ButonIs. M. t. grandis Peterson, 1981 — W New Guinea E to Chimbu Province in C Papua New Guina, including Waigeo, Supiori, Biak, and Yapen Is, and Louisiade Archipelago. M. t. insularis Peterson, 1981 — Admiralty Is, Bismarck Archipelago, Solomon Is, and Vanuatu (Espirito Santo and Efate Is). M. t. propitristis Peterson, 1981 — E New Guinea.:
FIGURE. Conlarium sichuanense (HKAS 113024, holotype) a–c Colonies on dead branches. d–k Conidiogenous cells and conidia. l Germinated conidium. m, n Colony on PDA from surface and reverse. Scale bars: d-k = 10 μm, l = 20 μm. in Conlarium sichuanense sp. nov., on Ficus virens from Sichuan Province, China
FIGURE. Conlarium sichuanense (HKAS 113024, holotype) a–c Colonies on dead branches. d–k Conidiogenous cells and conidia. l Germinated conidium. m, n Colony on PDA from surface and reverse. Scale bars: d-k = 10 μm, l = 20 μm.
FIGURE. Phylogenetic tree based on RAxML analyses of a combined LSU, ITS and SSU dataset. Bootstrap support values for ML and MP equal to or greater than 75% and PP value greater than 0.95 are in thickened. Ex-type isolates are in bold, and new taxa are indicated in red. The tree is rooted with Atractospora aquatica (S-1297) and A. aquatica (MFLU 18–2322). in Conlarium sichuanense sp. nov., on Ficus virens from Sichuan Province, China
FIGURE. Phylogenetic tree based on RAxML analyses of a combined LSU, ITS and SSU dataset. Bootstrap support values for ML and MP equal to or greater than 75% and PP value greater than 0.95 are in thickened. Ex-type isolates are in bold, and new taxa are indicated in red. The tree is rooted with Atractospora aquatica (S-1297) and A. aquatica (MFLU 18–2322).
FIGURE 3 in Taxonomic and phylogenic appraisal of a novel species and a new record of Stictidaceae from coffee in Yunnan Province, China
FIGURE 3. Ostropomyces pruinosellus (HKAS 113187). a, b. Pycnidia on coffee wood. c–e. Vertical section through pycnidia (arrow showing short ostiole). f. Pycnidial wall. g. Conidiophores and conidiogenous cells. h–j. Conidia (arrow showing septation). k. Germinating conidium. l. Colony on PDA medium. m. Conidia forming a large branch. Scale bars: d, e = 100 µm, f, h, i = 10 µm, g, k = 20 µm, j = 5 µm, m = 30 µm.
The Tai Meuy of Bolikhamxay Province (Laos) and their language
<p>“Tay Mươy” were first mentioned in 1941 by R. Robert in Thanh Hóa (Vietnam). A linguistic account by James R. Chamberlain in 1984 deals with Tai Meuay varieties of Khamkeuth District (Bolikhamxay Province, Laos). This talk introduces data elicited in Khamkeuth, Pakkading, and Viengthong, three districts of Bolikhamxay, and includes speakers’ perception of their group and their language. Although Tai Meuay varieties share some lexical items with the Tai dialects of Nghệ An (Vietnam) called Tai Muong, it has a deep linguistic/ethnolinguistic relationship with Tai Daeng.</p>
FIGURE 2. A in First record of Cnemidochroma phyllopus (Coleoptera: Cerambycidae) in the province of Corrientes, Argentina and potential distribution in the southern part of South America
FIGURE 2. A) Geographical distribution of C. phyllopus allocated to countries. Occurrence records are shown as white circles; white square is the new locality record. Countries are identified with different colors: Argentina (light blue), Brazil (green), Paraguay (yellow) and Uruguay (purple). B) Model calibration map (test data are shown as red circles- and training data as -blackcircles). Calibration area (M) marked in yellow around the records. Biogeographic provinces are indicated with different colors: Caatinga (red), Araucaria Forest (blue), Atlantic (green), Pampean (brown), Chacoan (light blue) and Parana Forest (lilac).
FIGURE 3. A in First record of Cnemidochroma phyllopus (Coleoptera: Cerambycidae) in the province of Corrientes, Argentina and potential distribution in the southern part of South America
FIGURE 3. A) Potential suitable areas throughout the historical distribution for C. phyllopus based on the best model. Warmer colors (e.g., red) indicate areas of higher climatic suitability, whereas cooler colors (e.g., green) represent areas with lower climatic suitability. B) Binary map showing habitat suitability for C. phyllopus. Biogeographic provinces, as they are shown in figure 2B, are delimited by lines. Occurrence records are shown as black circles; white square is the new locality record.
FIGURE 1 in First record of Cnemidochroma phyllopus (Coleoptera: Cerambycidae) in the province of Corrientes, Argentina and potential distribution in the southern part of South America
FIGURE 1. Cnemidochroma phyllopus, dorsal (A), ventral (B) and lateral (C) habitus of male, deposited in the Universidad Nacional del Nordeste (CARTROUNNE 9063). Corrientes, Argentina.
FIGURE 2. A in A new species of the Gekko japonicus group (Squamata: Gekkonidae) from Khammouane Province, central Laos
FIGURE 2. A) Dorsal view of the male holotype (VNUF R.2021.23); B) dorsolateral view of the female paratype VNUF R.2021.02); C) dorsolateral view of the female paratype (NUOL R.2021.22) of Gekko khunkhamensis sp. nov.
FIGURE 1 in A new species of the Gekko japonicus group (Squamata: Gekkonidae) from Khammouane Province, central Laos
FIGURE 1. Bayesian phylogram based on a fragment of the mitochondrial ND2 gene. Numbers above and below branches are MP bootstrap/ML ultrafast bootstrap values and Bayesian posterior probabilities (>50%), respectively. Asterisk denotes 100% value.
FIGURE 4 in A new species of the Gekko japonicus group (Squamata: Gekkonidae) from Khammouane Province, central Laos
FIGURE 4. Dorsal (A) and ventral (B) views of type series of Gekko khunkhamensis sp. nov. from the top to the bottom: the male holotype (VNUF R.2021.23); female paratype (VNUF R.2021.02); and female paratype (NUOL R.2021.22).
VCF for neutral data set in Harpagifer bispinis along the Magellan Province
<p>Quaternary glacial cycles shaped the current distribution of polar and cold-temperate biotas. In the Magellan province of South America, ice covering during the last glacial maximum radically altered the landscape/seascape, speciation rate, and the distribution of species. Here we studied nototheniid fishes <i>Harpagifer </i>spp. along the Magellan province reported as two nominal species: <i>H. bispinis</i> in Patagonia and <i>H. palliolatus</i>, endemic to the Falkland/Malvinas Islands. Previous molecular analyses in <i>Harpagifer</i> showed that the genus may have recently colonized southern South America ~ 1 million years ago. The extensive use in systematics of molecular markers to determine evolutionary units has been improved due to the advances in NGS. Combining traditional DNA sequences and non-targeted GBS-SNPs we evaluated both, the presence of effective evolutionary units and contemporary patterns of genetic structure across the Magellan province. DNA sequences consistently showed an absence of phylogeographic structure, with shared dominant haplotypes between nominal species, pointing towards the presence of a single evolutionary unit. In contrast, SNPs identified three groups in Patagonia, two located north and south of the Strait of Magellan, and a third well-differentiated one in the Falkland/Malvinas Islands. Connectivity analyses using SNPs suggest limited and asymmetric gene flow from Patagonia to the Falkland/Malvinas. Contrasting rough- and fine-scale genetic evolutionary patterns recorded in <i>Harpagifer</i> enhance the relevance in the use of combined methodologies for species delimitation analyses. Depending on the question to be addressed, we could discriminate among phylogeographic structure discarding incipient speciation, and contemporary spatial differentiation processes linked to drift-migration equilibrium models.</p>
FIGURES 37–41 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 37–41. Neanura persica sp. nov.: 37, head and Th dorsal chaetotaxy; 38, Abd III−VI dorsal chaetotaxy; 39−40, Ant III−IV in dorsal (39) and ventral view (40); 41, labrum. Scales: 0.2 mm (37−38), 0.05 mm (39−41).
FIGURES 42–48 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 42–48. Neanura persica sp. nov.: 42, ventral and lateral head chaetotaxy; 43, Abd ventral chaetotaxy; 44, dorsal cephalic tubercles; 45, Di tubercle on Th II; 46, De tubercle on Th II; 47, Di+Di tubercle on Abd V; 48, hind tibiotarsus and unguis. Scales: 0.2 mm (43), 0.1 mm (42), 0.05 mm (44−47), 0.025 (48).
FIGURES 28–36 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 28–36. Cryptonura sariensis sp. nov.: 28−29, Ant III−IV in dorsal (28) and ventral view (29); 30, labium; 31, tubercles Cl and Af on head; 32, De tubercle on Th II; 33, Di tubercle on Abd V; 34, medial ventral chaetotaxy of Abd III−V on a male; 35, maxilla; 36, mandible. Scales: 0.05 mm (28−34), 0.02 mm (35−36).
FIGURES 16–25 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 16–25. Cryptonura abmalensis sp. nov.: 16, head and Th dorsal chaetotaxy; 17, Abd III−VI dorsal chaetotaxy; 18, mandible; 19, maxilla; 20, Abd ventral chaetotaxy; 21−22, Ant III−IV in dorsal (21) and ventral view (22); 23, ventral and lateral head chaetotaxy; 24, Cl+Af tubercle on head; 25, De tubercle on Th II. Scales: 0.2 mm (16−17, 20, 23), 0.1 mm (21−22, 24−25), 0.02 mm (18−19).
FIGURES 7–15 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 7–15. Cryptonura dohezarensis sp. nov.: 7, Di tubercle on Th II; 8−9, Ant III−IV in dorsal (8) and ventral view (9); 10, ventral and lateral head chaetotaxy; 11, tubercles Oc, Dl and L+So on head; 12, tubercles Cl and Af on head; 13, De tubercle on Th II; 14, Di tubercle on Abd V; 15, apical portion of labrum. Scales: 0.1 mm (7, 10−14), 0.05 mm (8−9), 0.02 mm (15).
FIGURES 1–6 in New species and records of Neanurinae (Collembola: Neanuridae) from Mazandaran Province (Northeastern Iran), with a key to Iranian species of the subfamily
FIGURES 1–6. Cryptonura dohezarensis sp. nov.: 1, head and Th dorsal chaetotaxy; 2, Abd dorsal chaetotaxy; 3, Abd ventral chaetotaxy; 4, chaetae types: long macrochaetae, rounded or pointed apically (Ml), short macrochaeta (Mc), very short macrochaeta (Mcc), mesochaeta (me), microchaeta (mi), sensorial chaeta (S), microsensillum (ms); 5, labium and ventromedial head chaetae; 6, hind tibiotarsus and unguis. Scales: 0.2 mm (1−3), 0.02 mm (5−6).
FIGURE 4. Gonolobus caamalii Carnevali & R. Duno. A in Twice lost, twice found: A new species of Gonolobus (Apocynaceae: Asclepiadoideae) with a reappraisal of the genus in the Yucatan Peninsula Biotic Province
FIGURE 4. Gonolobus caamalii Carnevali & R. Duno. A. Frontal view of the flower in anthesis. B. Posterior view of the flower featuring the reflexed calyx. C. Close up of the center of the flower with the gynostemium. Note the dark rim of the gynostemium head, the dark wine color of the anther appendages and the margins of the bright yellow green corona. Also, note the line of trichomes along the right margin of each corolla lobe as well as the reddish-brown band around the corona at the base of the corolla lobes. D. ¾ view of the center of the flower featuring the corona lobes. E. Flowering plant at the type locality. All based upon the type collection (G. Carnevali, R. Duno & M.A. Caamal Dzul 8573, CICY, GH, MEXU, MO).
FIGURE 3 in Twice lost, twice found: A new species of Gonolobus (Apocynaceae: Asclepiadoideae) with a reappraisal of the genus in the Yucatan Peninsula Biotic Province
FIGURE 3. Gonolobus species of the YPBP. A. Gonolobus barbatus (based upon G. Carnevali 8584, CICY). B. G. cteniophorus (based upon G. Carnevali 7547, CICY). C. G. fraternus (based upon L. Ibarra-González s.n. (unvouchered)). D. Gonolobus leianthus (B.K. Holst s.n, SEL). E-F. Gonolobus stenanthus subsp. stenanthus (based upon L. Ibarra-González 603, CICY). G-I Gonolobus stenanthus subsp. yucatanensis (G based on Diana Beas s.n., unvouchered. H. based upon M.A. Caamal 01, CICY; I. (Based upon G. Carnevali et al. 8377, CICY, GH, MO). Photographs: A-B and I, G. Carnevali. C and E-F, León Ibarra González. D, Bruce K. Holst, downloaded from https:// www.naturalista.mx/observations/35867653) G, Diana Beas, downloaded from https://www.naturalista.mx/observations/54694745; H, Miguel Ángel Caamal.
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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.