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666 results for “type locality”
FIGURE 4 in Rediscovery of the enigmatic Andean frog Telmatobius halli Noble (Anura Telmatobiidae), re-description of the tadpole and comments on new adult's characters, type locality and conservation status
FIGURE 4. Morphological details of a female of Telmatobius halli (IZUA 3531). (A) Dorsal and (B) lateral anterior body. (C) Representation of the pectoral girdle. (D) Ventral palmar and (E) plantar surfaces.
FIGURE 3 in Rediscovery of the enigmatic Andean frog Telmatobius halli Noble (Anura Telmatobiidae), re-description of the tadpole and comments on new adult's characters, type locality and conservation status
FIGURE 3. Adult female (IZUA 3530) of Telmatobius halli. (A) Dorso-lateral and (B) ventral views (in life). Ventral colour patterns (in fixative) of the specimens (C) IZUA 007, and (D) IZUA 3531. (E) Dorsal and (F) ventral views of the holotype (AMNH 44753).
FIGURE 2 in Rediscovery of the enigmatic Andean frog Telmatobius halli Noble (Anura Telmatobiidae), re-description of the tadpole and comments on new adult's characters, type locality and conservation status
FIGURE 2. The tadpole of Telmatobius halli (IZUA 3529, stage 33). (A) Lateral, (B) dorsal and (C) ventral views. (D) oral disc. Lateral view of tadpoles: (E) live specimen from "Aguas Calientes", and (F) specimen (in fixative) stored in the AMNH (4479).
FIGURE 1 in Rediscovery of the enigmatic Andean frog Telmatobius halli Noble (Anura Telmatobiidae), re-description of the tadpole and comments on new adult's characters, type locality and conservation status
FIGURE 1. Type locality of Telmatobius halli, near Ollagüe, Chile. (A) "Aguas Calientes", a warm spring (red circle), where we collected the samples identified as T. halli. Type localities of T. fronteriensis (square) and T. philippii (triangle). (B) Panoramic view of Aguas Calientes spring feeding the Carcote salt pan. (C) Close up view of the warm spring. The white and yellow arrows in B and C indicate the origin of the stream and the constructed swimming pool, respectively. The up left inset represents a physic map of South America.
FIGURE 1 in Paratelmatobius mantiqueira Pombal & Haddad, 1999 (Anura: Leptodactylidae) New specimens and rectification of the type locality of a rare species from the Serra da Mantiqueira, southeastern Brazil
FIGURE 1. (A) Location records for Paratelmatobius mantiqueira: the original type locality in the state of São Paulo (SP) published by Pombal & Haddad (1999) (blue circle), the rectified type locality in the state of Minas Gerais (MG) (white star), the record from the municipality of Resende in the state of Rio de Janeiro (RJ) (red circle), and the presently reported locality in the state of São Paulo (yellow circle). (B) A sign found on the dirt road from Sapucaí-Mirim to São Francisco Xavier, in the border area between the states of Minas Gerais and São Paulo (C) Dorsolateral and (D) ventral views of an adult male of Paratelmatobius mantiqueira (ZUEC-AMP 24836; 16 mm SVL), recently found in the sub-district of São Francisco Xavier, municipality of São José dos Campos, state of São Paulo.
FIGURE 1 in The advertisement call of the rare casque-headed frog Nyctimantis galeata (Anura Hylidae) from its type locality, Morro do Chapéu, Bahia, Brazil
FIGURE 1. Advertisement call of Nyctimantis galeata from the municipality of Morro do Chapéu, state of Bahia, Brazil (air temperature 18–20ºC). A: Spectrogram and waveform of call (in the background noise calls of Proceratophrys redacta can be observed); B: Spectrogram, waveform and power spectrum of a note; C: Photograph of an adult N. galeata (MZUESC 21978, SVL = 4.43 cm).
Data from: Effects of experimental warming on biodiversity depend on ecosystem type and local species composition
Climatic warming is a primary driver of change in ecosystems worldwide. Here, we synthesize responses of species richness and evenness from 187 experimental warming studies in a quantitative meta-analysis. We asked 1) whether effects of warming on diversity were detectable and consistent across terrestrial, freshwater and marine ecosystems, 2) if effects on diversity correlated with intensity, duration, and experimental unit size of temperature change manipulations, and 3) whether these experimental effects on diversity interacted with ecosystem types. Using multilevel mixed linear models and model averaging, we also tested the relative importance of variables that described uncontrolled environmental variation and attributes of experimental units. Overall, experimental warming reduced richness across ecosystems (mean log-response ratio = –0.091, 95% bootstrapped CI: –0.13, –0.05) representing an 8.9% decline relative to ambient temperature treatments. Richness did not change in response to warming in freshwater systems, but was more strongly negative in terrestrial (–11.8%) and marine (–10.5%) experiments. In contrast, warming impacts on evenness were neutral overall and in aquatic systems, but weakly negative on land (7.6%). Intensity and duration of experimental warming did not explain variation in diversity responses, but negative effects on richness were stronger in smaller experimental units, particularly in marine systems. Model-averaged parameter estimation confirmed these main effects while accounting for variation in latitude, ambient temperature at the sites of manipulations, venue (field versus lab), community trophic type, and whether experiments were open or closed to colonization. These analyses synthesize extensive experimental evidence showing declines in local richness with increased temperature, particularly in terrestrial and marine communities. However, the more variable effects of warming on evenness were better explained by the random effect of site identity, suggesting that effects on species' relative abundances were contingent on local species composition.
Data from: Kicking Triturus arntzeni when it's down: large-scale nuclear genetic data confirm that newts from the type locality are genetically admixed
We collected nuclear DNA data (52 markers) with next-generation sequencing for nine Triturus newt specimens, including the holotype and two of the paratypes of T. arntzeni, from the type locality at Vrtovać in eastern Serbia. We compare these data to a reference set composed of the four crested newt species distributed in eastern Serbia namely T. cristatus, T. dobrogicus, T. ivanbureschi and T. macedonicus to determine to which of these species the newts from the type locality of T. arntzeni should be attributed. The majority of alleles in individuals from Vrtovać is derived from T. macedonicus, but a considerable number of T. ivanbureschi alleles is also present; alleles typical for T. cristatus and T. dobrogicus are found at low frequency. Accordingly, we interpret Vrtovać as a T. macedonicus – T. ivanbureschi hybrid population, albeit not composed of F1 hybrids but of genetically admixed individuals derived through multiple generations of backcrossing. The data support the notion that the name T. arntzeni should not be applied to a species newly distinguished in T. karelinii sensu lato (to which the name T. ivanbureschi has been given). We conclude that because of the hybrid nature of the individuals from Vrtovać, the name T. arntzeni should be placed not only in the synonymy of T. macedonicus but also in the synonymy of T. ivanbureschi. In this study we demonstrate that next-generation sequencing can provide high quality data for type material with degraded DNA and therefore can play an important role in taxonomy.
FIGURE 2 in Considerations on the type specimens and type locality of Pyrrhura roseifrons (Gray, 1859) (Psittacidae)
FIGURE 2. Ventral (above) and lateral views (below) of the three syntypes of Pyrrhura roseifrons (Gray, 1859), NHMUK 58.4.27.35 (A), NHMUK 58.1.11.3 (B), and NHMUK 58.1.11.2 (C).
FIGURE 1 in Considerations on the type specimens and type locality of Pyrrhura roseifrons (Gray, 1859) (Psittacidae)
FIGURE 1. Map depicting the major localities (Tefé and São Paulo de Olivença) visited by Henry W. Bates in the upper Amazon river, Western Amazonia, near the Brazil-Peru border. Shaded area represents the known range of Pyrrhura roseifrons, according to Forshaw (2010).
FIGURE 5 in A new locality and host for Pseudione minimocrenulata Nierstrasz & Brender à Brandis, 1931 (Crustacea: Isopoda: Bopyridae) in the Indian Ocean, with comments on the identity of the type specimens
FIGURE 5. Pseudione minimocrenulata, male: A, antennule (distal); B, antennular tip; C, antenna (distal); D, antennal tip; E, pereopod I; F, pereopod VII. Scale bars: B, D = 0.2 mm; A, C, E, F = 0.75 mm.
FIGURE 3. Pseudione minimocrenulata, 11.5 in A new locality and host for Pseudione minimocrenulata Nierstrasz & Brender à Brandis, 1931 (Crustacea: Isopoda: Bopyridae) in the Indian Ocean, with comments on the identity of the type specimens
FIGURE 3. Pseudione minimocrenulata, 11.5 mm female: A, antennule; B, tip of antennule; C, antenna; D, antennal tip; E, pereopod I; F, pereopod VII (right detail showing unidentified protist tests). Scale bars: B, D = 0.125 mm; A, C, E, F = 0.75 mm.
FIGURE 4. Pseudione minimocrenulata, 11.5 in A new locality and host for Pseudione minimocrenulata Nierstrasz & Brender à Brandis, 1931 (Crustacea: Isopoda: Bopyridae) in the Indian Ocean, with comments on the identity of the type specimens
FIGURE 4. Pseudione minimocrenulata, 11.5 mm female: A, oostegite I, internal view; B, maxilliped, outer view; C, maxilliped, inner view; D, left side of barbula. Scale bar = 0.5 mm.
FIGURE 2 in A new locality and host for Pseudione minimocrenulata Nierstrasz & Brender à Brandis, 1931 (Crustacea: Isopoda: Bopyridae) in the Indian Ocean, with comments on the identity of the type specimens
FIGURE 2. Pseudione minimocrenulata: A, 12 mm female, dorsal view; B, 12 mm female, ventral view; C, male, dorsal view; D, male, ventral view. Scale bars: A, B = 5 mm; C, D = 1.75 mm.
FIGURE 1 in A new locality and host for Pseudione minimocrenulata Nierstrasz & Brender à Brandis, 1931 (Crustacea: Isopoda: Bopyridae) in the Indian Ocean, with comments on the identity of the type specimens
FIGURE 1. Munida andamanica Alcock (13 mm CL, exclusive of rostrum) host showing double infestation of Pseudione minimocrenulata. Scale bar = 9 mm.
FIGURES 27–29. Type localities. 27 in Three new species of Inseliellum (Diptera: Simuliidae) from Polynesia
FIGURES 27–29. Type localities. 27. Simulium adelaideae. Above Lac Vaihiria on crossTahiti road. Larva collected in denselyshaded portion of stream in background. 28. S. sublonckei. Second cascade on road to Maroto River barrage, Vaitamanu Valley, Papenoo River catchment. 29. S. englundi. Unnamed stream, Mohotani Island, Hiva Oa, Marquesas Islands. Photograph courtesy of R. Englund.
FIGURES 11–12. Type locality, Hopkins Falls. 11 in Dinotoperla walkeri sp. nov. (Plecoptera: Gripopterygidae), a brachypterous stonefly from western Victoria, Australia
FIGURES 11–12. Type locality, Hopkins Falls. 11. View of site, specimens were collected from the base of the falls at the far right and from the foreground riffle. 12. Collecting area at base of falls.
FIGURE 1 in Type specimens and type localities of birds (Aves) collected by Eduard Eversmann and Christian Pander during the Negri Expedition to Bukhara in 1820 – 1821
FIGURE 1. Selected localities in Middle Asia visited by Eversmann and Pander in 1820–1821. Geographic coordinates and alternative names used by Lichtenstein (1822, 1823a), Eversmann (1823) and Meyendorff (1826) are given in parentheses. Numbering of localities approximates Eversmann's and Pander's itinerary on the way there.
FIGURE 3 in Type locality and identity of Acrossocheilus kreyenbergii (Regan, 1908), a senior synonym of Acrossocheilus cinctus (Lin, 1931) (Teleostei: Cyprinidae)
FIGURE 3. Lateral views of two syntype specimens of Gymnostoma kreyenbergii: (A) BMNH 1907.11.26.1–2 (1), male, 132.9 mm SL; (B) BMNH 1907.11.26.1–2 (2), female, 71.1 mm SL. Scale bar =10 mm.
FIGURE 2 in Type locality and identity of Acrossocheilus kreyenbergii (Regan, 1908), a senior synonym of Acrossocheilus cinctus (Lin, 1931) (Teleostei: Cyprinidae)
FIGURE 2. Lateral views of body in A. kreyenbergii. (A) IHB 75V2912, juvenile, 40.56 mm SL, Jinxiu, Guangxi Province; (B) IHB 0605415, subadult, female, 81.36 mm SL, Yiyang, Jiangxi Province; (C) IHB 0605427, subadult, male, 99.23 mm SL, Yiyang, Jiangxi Province; (D) IHB 20080500002, adult, female, 128.3 mm SL, Rongshui, Guangxi Province; (E) IHB 20080500001, adult, male, 124.1 mm SL, Rongshui, Guangxi Province. Scale bar =10 mm.
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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)
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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.