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214 results for “Species problem”
FIGURES 11–20. Barsine spp. adults. 11, B in Taxonomic problems surrounding Barsine orientalis bigamica Černý & Pinratana 2009 with description of a new species (Lepidoptera, Erebidae, Arctiinae Lithosiini)
FIGURES 11–20. Barsine spp. adults. 11, B. bigamica, paratype male, Thailand, Phetchabun, slide AV2349 (CKC); 12, B. bigamica, male, Vietnam, Da Nang (CAV); 13, B. tongi sp. nov., holotype male, China, Hainan (SCAU); 14, B. tongi sp. nov., paratype male, China, Hainan (SCAU); 15, B. tongi sp. nov., paratype female, China, Hainan (SCAU); 16, B. tongi sp. nov., paratype female, China, Hainan (SCAU); 17, B. orientalis, holotype male, spring form, China, Fujian (ZFMK); 18, B. orientalis, paratype female, spring form, China, Fujian (ZFMK); 19, B. orientalis, male, summer form, China, Fujian (ZFMK); 20, B. orientalis, female summer form,, China, Fujian (ZFMK). Scale=1 cm.
FIGURES 21–24 in Taxonomic problems surrounding Barsine orientalis bigamica Černý & Pinratana 2009 with description of a new species (Lepidoptera, Erebidae, Arctiinae Lithosiini)
FIGURES 21–24. Male genitalia of Barsine bigamica. 21, paratype, Thailand, Phetchabun, slide AV2349; 22, Thailand, Khao Yai National Park, paratype of B. kampoli, slide NHMUK010313301; 23, China, Yunnan, slide MWM37151; 24, China, Yunnan, slide ZSM Arct. 2020-086.
FIGURES 1–10. Barsine bigamica adults. 1 in Taxonomic problems surrounding Barsine orientalis bigamica Černý & Pinratana 2009 with description of a new species (Lepidoptera, Erebidae, Arctiinae Lithosiini)
FIGURES 1–10. Barsine bigamica adults. 1, holotype, male, Thailand, Phetchabun (©NHMUK); 2, male, China, Yunnan (MWM/ZSM); 3, male, China, Yunnan (MWM/ZSM); 4, male, China, Yunnan (MWM/ZSM); 5, male, Thailand, Nan (MWM/ ZSM); 6, male, holotype of Barsine kampoli, Thailand, Chiang Mai (©NHMUK); 7, male, China, Yunnan (MWM/ZSM); 8, male, paratype of Barsine kampoli, Thailand, Nakhon Ratchasima, Khao Yai (©NHMUK); 9, female, red form, Cambodia, Kampot (MWM/ZSM); 10, female, yellow form, Thailand, Chiang Mai (MWM/ZSM). Scale=1 cm.
FIGURES 33–38 in Taxonomic problems surrounding Barsine orientalis bigamica Černý & Pinratana 2009 with description of a new species (Lepidoptera, Erebidae, Arctiinae Lithosiini)
FIGURES 33–38. Female genitalia of Barsine spp. 33, B. bigamica, Thailand, Phetchabun, slide AV2350; 34, B. bigamica, Vietnam, Da Nang, slide AV2282; 35, B. bigamica, China, Yunnan, slide ZSM Arct. 2020-087; 36, B. tongi sp. nov. paratype, China, Hainan, prep. Huang, from the specimen in fig. 16; 37, B. orientalis paratype, China, Fujian, slide AV1833; 38, B. orientalis, China, Zhejiang, slide AV1984.
FIGURE 7 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 7. Scatter plot of Multivariate Principal Component Analysis (PCA) for male individuals using 13 morphometric characters marked as * Supplementary file Table 1 transformed to their ratio to SVL for Minervarya species A (M. species A) and Minervarya species B (M. species B)
FIGURE 3 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 3. Morphological characters of Minervarya species A and Minervarya species B. Minervarya species A (A) and Minervarya species B (B) in life. Note the longitudinal skin folds on dorsal side of Minervarya species A and granular blotches on Minervarya species B. Difference in the webbing pattern on the foot of Minervarya species A (C) and Minervarya species B (D).
FIGURE 10 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 10. Morphological variation in Minervarya syhadrensis frogs from different localities in the Western Ghats. (A and B) Coorg, (C) Goa, (D) Koyna, (E) Silvasa and (F) Calicut.
FIGURE 9 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 9. Dorsal view of M. syhadrensis (Minervarya species A collected for the present study, ZSI/WRC/A/2255) and M. caperata (type specimen BNHS4657). Note the presence of longitudinal skin folds on dorsal side. Scale bar = 1cm.
FIGURE 5 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 5. Advertisement call of Minervarya species B. Microtemporal structure (A) and spectrogram (B) of a call group. (C) Microtemporal structure of a call depicting its pulsatile nature.
FIGURE 2 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 2. Type specimen of Minervarya syhadrensis (ZSI 19764). Note the presence of longitudinal skin folds on dorsal side. Scale bar = 1cm.
FIGURE 1 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 1. Map showing type localities of Minervarya syhadrensis (▲), M. caperata (■) and collection localities (●) in the present study.
FIGURE 4 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 4. Advertisement call of Minervarya species A. Microtemporal structure (A) and spectrogram (B) of a call group. (C) Microtemporal structure of a single call. Note the pulsed nature of call.
FIGURE 6 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 6. Comparison of five call properties between Minervarya species A and Minervarya species B. Bar graphs represent mean±SE (P ˂ 0.05). CD = call duration, PRR = pulse repetition rate, FF = fundamental frequency, and DF = dominant frequency.
FIGURE 8 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
FIGURE 8. Maximum Likelihood tree based on 574 bp of mitochondrial (16S) gene for Minervarya clade having predominant distribution in Sri Lanka, India, Bangladesh and Nepal (Fig 2, Phuge et al. 2019). Locations marked as blue represents the localities from where samples were collected for the present study.
SUPPLEMENTARY TABLE 3 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
SUPPLEMENTARY TABLE 3. Call properties measurements of Minervarya species A and Minervarya species B in the present study.
SUPPLEMENTARY TABLE 2 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
SUPPLEMENTARY TABLE 2. Morphometric data (in mm) of type specimens of Minervarya caperata deposited at BNHS and described by Kuramoto et al. (2007).
SUPPLEMENTARY TABLE 1 in Importance of genetic data in resolving cryptic species: A century old problem of understanding the distribution of Minervarya syhadrensis Annandale 1919 (Anura: Dicroglossidae)
SUPPLEMENTARY TABLE 1. Morphometric data (in mm) of Minervarya species A (M. syhadrensis) and Minervarya species B (M. agricola / M. granosa) from Pune
Data from: Two new phragmotic ant species from Africa: morphology and next-generation sequencing solve a caste association problem in the genus Carebara Westwood
Phragmotic or "door head" ants have evolved independently in several ant genera across the world, but in Africa only one case has been documented until now. Carebara elmenteitae (Patrizi) is known from only a single phragmotic major worker collected from sifted leaf-litter near Lake Elmenteita in Kenya, but here the worker castes of two species collected from Kakamega Forest, a small rainforest in Western Kenya, are studied. Phragmotic major workers were previously identified as Carebara elmenteitae and non-phragmotic major and minor workers were assigned to C. thoracica (Weber). Using evidence of both morphological and next-generation sequencing analysis, it is shown that phragmotic and non-phragmotic workers of the two different species are actually the same and that neither name – C. elmenteitae or C. thoracica – correctly applies to them. Instead, this and another closely related species from Ivory Coast are both morphologically different from C. elmenteitae, and thus they are described as the new species Carebara phragmotica sp. n. and Carebara lilith sp. n.
FIGURE 2. Scolymia species from Brazil. A,B in The occurrence of Scolymia cubensis in Brazil: revising the problem of the Caribbean solitary mussids
FIGURE 2. Scolymia species from Brazil. A,B. New occurrence: specimen of Scolymia cubensis (UFBA 485-CNI) reported to Sergipe State. C. Detail of dentition: regular, not fused teeth. D,E. Scolymia wellsi (UFBA 486-CNI), specimen from Pernambuco State. F. Detail of dentition: irregular, often fused teeth (mesh-like arrangement).
FIGURE 3 in Two new species of Onthophagus (Coleoptera: Scarabaeidae) from Indochina, with a discussion of some problems with the classification of Serrophorus and similar subgenera
FIGURE 3. Elements of genitalia of Onthophagus nampatensis. a—lamella copulatrix; b—lamella copulatrix, AIS and ALS removed; c—aedeagus, lateral view; d—aedeagus, apical view.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.