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FIGURES 56–61 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 56–61. Bionomics of Coptotriche turpinia Xu & Dai, sp. nov. 56, habitat, Jiangxi Province, China; 57–61, leaf mines on Turpinia arguta (Lindl.) Seem. (Staphyleaceae)

opennotspecifiedNov 2021View details →
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FIGURES 23–28 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 23–28. Male genitalia of Coptotriche turpinia Xu & Dai, sp. nov., Lao Cai Province, Vietnam, paratype, slide no. AD1056 (ZIN). 23, ventral view, focused on uncus and transtilla; 24, same, focused on valva; 25, same, multifocus; 26, same, focused on tegumen; 27, same, focused on vinculum; 28, same, focused on spines of phallus

opennotspecifiedNov 2021View details →
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FIGURES 12–18 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 12–18. Genitalia of Coptotriche camptotheca Xu & Dai, sp. nov. 12, 13, male genitalia, paratype, slide no. BX12094. 14, same, another paratype, slide no. Liu0117; 15, female genitalia, paratype, slide no. BH12093; 16, same, another paratype, slide no. Liu01160001; 17, male genitalia, phallus, paratype, slide no. BX12094; 18, same, another paratype, slide no. Liu0117 (GNU)

opennotspecifiedNov 2021View details →
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FIGURES 49–55 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 49–55. Bionomics of Coptotriche camptotheca Xu & Dai, sp. nov. 49, habitat, Guizhou Province, China; 50, host plant Camptotheca acuminata Decne. (Nyssaceae); 51–55, leaf mines

opennotspecifiedNov 2021View details →
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FIGURES 67–73 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 67–73. Leaf mines of Coptotriche asiana Diškus & Stonis, sp. nov. on Symplocos sumuntia Buch.-Ham. ex D. Don (Symplocaceae), sample no. 5191, Lao Cai Province, Vietnam

opennotspecifiedNov 2021View details →
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FIGURES 1–4 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 1–4. Adults of new Coptotriche species. 1, C. camptotheca Xu & Dai, sp. nov., female paratype, Jiangxi Province, China; 2, same, another female paratype (GNU); 3, 4, C. turpinia Xu & Dai, sp. nov., male holotype, Jiangxi Province, China (GNU)

opennotspecifiedNov 2021View details →
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FIGURES 43–48 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 43–48. Female genitalia of Coptotriche asiana Diškus & Stonis, sp. nov. 43, general view, paratype, slide no. AD1053 (GNU); 44, coils of ductus spermathecae, paratype, slide no. AD1041 (ZIN); 45–48, variously focused on ovipositor lobes, paratype, slide no. AD1053 (GNU)

opennotspecifiedNov 2021View details →
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FIGURES 62–66 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 62–66. Habitat and host plants of Coptotriche asiana Diškus & Stonis, sp. nov. 62, habitat 15 km NW of Sa Pa, Lao Cai Province, Vietnam, 22°20'N, 103°46'E, elevation ca. 1900 m; 63, Symplocos sumuntia Buch.-Ham. ex D. Don, sample no. 5191; 64, S. poilanei Guill., sample no. 5193; 65, 66, Symplocos glauca (Thunb.) Koidz., sample no. 5197

opennotspecifiedNov 2021View details →
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FIGURES 37–42 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 37–42. Male genitalia of Coptotriche asiana Diškus & Stonis, sp. nov. 37, 38, ventral view of capsule, paratype, slide no. AD1054 (NRC); 39, vinculum, paratype, slide no. AD1057 (GNU); 40, 41, lateral view of capsule with phallus removed, paratype, slide no. AD1043 (ZIN); 42, lateral view of valva, paratype, slide no. AD1057 (GNU)

opennotspecifiedNov 2021View details →
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FIGURES 29–36 in Discovery of the new Coptotriche species in China revealed two novel host-plant families and host-plant orders for Tischeriidae, a family of stenophagous, leafmining lepidopterans

FIGURES 29–36. Male genitalia of Coptotriche asiana Diškus & Stonis, sp. nov., Lao Cai Province, Vietnam. 29, general view, holotype, slide no. AD1044 (ZIN); 30–34, spines of phallus, paratype, slide no. AD1057 (GNU); 35, phallus, paratype, slide no. AD944 (NRC); 36, same, capsule, with phallus removed

opennotspecifiedNov 2021View details →
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FIGURE 5 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 5. Map of point localities of Turrana abnormis Distant (triangles) and T. ejuncida sp. nov. (circle). Localities of T. abnormis from Cassis & Gross (2002).

opennotspecifiedJan 2022View details →
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FIGURE 4 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 4. Turrana ejuncida sp. nov. Micro-CT images of female terminalia (WAME106180). A) dorsal, B) ventral, and C) lateral views of tip of abdomen. Scale bar = 100 µm.

opennotspecifiedJan 2022View details →
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FIGURE 3 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 3. Turrana ejuncida sp. nov. Micro-CT images of male genitalia (WAME106179). A) pygophore and semi-inflated aedeagus, lateral view; sclerotized portions of conjunctival processes coloured green. B) anterior of aedeagus. C) right paramere. Scale bars = 100 µm.

opennotspecifiedJan 2022View details →
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FIGURE 2 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 2. Scanning electron micrographs of Turrana ejuncida sp. nov. female (WAME106180). A) head, lateral; B) head, dorsal; C) head and thorax, ventral; D) pronotum, dorsal; E) hemelytra, detail; F) metathoracic scent gland. Anterior to left in all images.

opennotspecifiedJan 2022View details →
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FIGURE 1 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 1. Turrana ejuncida sp. nov. dorsal and lateral habitus images. A, B) holotype male (WAME106179); C, D) paratype female (WAME106180).

opennotspecifiedJan 2022View details →
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FIGURE 6 in Turrana ejuncida, a new species of Acanthocorini (Hemiptera: Heteroptera: Coreidae) from Cape Range, Western Australia, with discussion of its systematic position and host plant associations

FIGURE 6. Collecting sites of Turrana ejuncida sp. nov. in Cape Range National Park. A) flowering Ipomoea yardiensis (detail in inset) on remote rocky ridge adjacent to canyon. B) Triodia epactia (inset shows dry, brown underside of plant) at side of Charles Knife Canyon Road, on ridge.

opennotspecifiedJan 2022View details →
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FIGURE. Phylogenetic tree of specimens on Poaceae and related host plants constructed by MP method based on ITS+28S regions of rDNA. Bootstrap values of MP and ML are followed by the Bayesian posterior probabilities (Bpp) on the nodes in the topology. Asterisk (*) represents bootstrap values or Bpp less than 50% in the topology. Sample data are shown with voucher specimen number or GenBank accession number, and host plant. Sequence data determined in this study are shown in color. Teliospore shapes are shown in each clade detected, and new species are shown by asterisk (*) on clades. 0, I: Spermogonial and aecial host genus. Asterisk (*) on host plants: Spermogonial and aecial host plants. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China

FIGURE. Phylogenetic tree of specimens on Poaceae and related host plants constructed by MP method based on ITS+28S regions of rDNA. Bootstrap values of MP and ML are followed by the Bayesian posterior probabilities (Bpp) on the nodes in the topology. Asterisk (*) represents bootstrap values or Bpp less than 50% in the topology. Sample data are shown with voucher specimen number or GenBank accession number, and host plant. Sequence data determined in this study are shown in color. Teliospore shapes are shown in each clade detected, and new species are shown by asterisk (*) on clades. 0, I: Spermogonial and aecial host genus. Asterisk (*) on host plants: Spermogonial and aecial host plants.

opennotspecifiedFeb 2022View details →
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FIGURE. Phylogenetic relationships among species on Poaceae shown with synoptic phylogenetic tree constructed by MP method based on ITS+28S regions of rDNA. Same color branches show phylogenetic groups. 0, I: Spermogonial and aecial host genus. in Phylogenetic approach for identification and life cycles of Puccinia (Pucciniaceae) species on Poaceae from northeastern China

FIGURE. Phylogenetic relationships among species on Poaceae shown with synoptic phylogenetic tree constructed by MP method based on ITS+28S regions of rDNA. Same color branches show phylogenetic groups. 0, I: Spermogonial and aecial host genus.

opennotspecifiedFeb 2022View details →
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Fig. 2. A in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts

Fig. 2. A maximum-likelihood phylogenetic tree reconstructed using core genes (n=100) identified from whole-genome sequences, showing the evolutionary relationships among five novel Limosilactobacillus species, six L. reuteri subspecies and other recognized species in the genus Limosilactobacillus. GenBank or JGI accession numbers of these genomes are provided in parentheses. The tree was inferred based on the GTR+G model with 1000 bootstrap replicates and only bootstrap values above 60% are shown. Strains of five novel Limosilactobacillus species are labelled by different colours; labels of six L. reuteri subspecies are colour representing vertebrate host origin: green for rodents, red for pigs, blue for humans and orange for poultry. The tree was drawn with iTOL [54].

opennotspecifiedJan 2021View details →
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Fig. 1. A maximum-likelihood phylogenetic tree reconstructed using 16S in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts

Fig. 1. A maximum-likelihood phylogenetic tree reconstructed using 16S rRNA gene sequences. GenBank or JGI accession numbers of these genomes are provided in parentheses. The tree was inferred based on the GTR+G model with 1000 bootstrap replicates and only bootstrap values above 60% are shown. Strains of five novel Limosilactobacillus species are labelled by different colours; labels of six L. reuteri subspecies are colour representing vertebrate host origin: green for rodents, red for pigs, blue for humans and orange for poultry. The tree was drawn with iTOL [54].

opennotspecifiedJan 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record