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679 results for “intraspecific variation”
FIGURE 3 in INTRASPECIFIC VARIATION IN ACOUSTIC TRAITS AND BODY SIZE, AND NEW DISTRIBUTIONAL RECORDS FOR PSEUDOPALUDICOLA GIARETTAI CARVALHO, 2012 (ANURA, LEPTODACTYLIDAE, LEIUPERINAE): IMPLICATIONS FOR ITS CONGENERIC DIAGNOSIS
FIGURE 3: Advertisement call of P. giarettai from the type locality (Curvelo, Minas Gerais). From top to bottom: oscillogram section (ca. 1.6 s) depicting calling pattern, waveform, spectrogram, and power spectrum of the second advertisement from oscillogram section. Sound energy with relative amplitude below 40 dB was clipped to zero dB to remove background noise from power spectrum.
FIGURE 2 in INTRASPECIFIC VARIATION IN ACOUSTIC TRAITS AND BODY SIZE, AND NEW DISTRIBUTIONAL RECORDS FOR PSEUDOPALUDICOLA GIARETTAI CARVALHO, 2012 (ANURA, LEPTODACTYLIDAE, LEIUPERINAE): IMPLICATIONS FOR ITS CONGENERIC DIAGNOSIS
FIGURE 2: Adult specimens of P. giarettai in life from: Above – Parque Nacional Grande Sertão Veredas, Chapada Gaúcha, Minas Gerais (voucher male AAG-UFU 1920: CRC = 14.6 mm); Below – Coromandel (female AAG-UFU 3566: CRC 18.8 mm).
FIGURE 4 in INTRASPECIFIC VARIATION IN ACOUSTIC TRAITS AND BODY SIZE, AND NEW DISTRIBUTIONAL RECORDS FOR PSEUDOPALUDICOLA GIARETTAI CARVALHO, 2012 (ANURA, LEPTODACTYLIDAE, LEIUPERINAE): IMPLICATIONS FOR ITS CONGENERIC DIAGNOSIS
FIGURE 4: Advertisement call of P. giarettai from the Parque Nacional Grande Sertão Veredas (Chapada Gaúcha, Minas Gerais). From top to bottom: oscillogram section (ca. 1.6 s) depicting calling pattern, waveform, spectrogram, and power spectrum of the second advertisement from oscillogram section. Sound energy with relative amplitude below 40 dB was clipped to zero dB to remove background noise from power spectrum.
FIGURE 6 in INTRASPECIFIC VARIATION IN ACOUSTIC TRAITS AND BODY SIZE, AND NEW DISTRIBUTIONAL RECORDS FOR PSEUDOPALUDICOLA GIARETTAI CARVALHO, 2012 (ANURA, LEPTODACTYLIDAE, LEIUPERINAE): IMPLICATIONS FOR ITS CONGENERIC DIAGNOSIS
FIGURE 6: Typical breeding habitat of P. giarettai: a permanent pond associated with a Buriti palm grove marsh at the Parque Nacional Grande Sertão Veredas (Municipality of Chapada Gaúcha), northwestern Minas Gerais, southeastern Brazil.
FIGURE 1 in INTRASPECIFIC VARIATION IN ACOUSTIC TRAITS AND BODY SIZE, AND NEW DISTRIBUTIONAL RECORDS FOR PSEUDOPALUDICOLA GIARETTAI CARVALHO, 2012 (ANURA, LEPTODACTYLIDAE, LEIUPERINAE): IMPLICATIONS FOR ITS CONGENERIC DIAGNOSIS
FIGURE 1: Distribution map of Pseudopaludicola giarettai. Star (Type locality: Curvelo, MG); Circles (localities in Minas Gerais): 1 (Buritis), 2 (Chapada Gaúcha), 3 (Unaí), 4 (Buritizeiro), 5 (Coromandel), 6 (Conceição do Mato Dentro; Pimenta et al., 2014), 7 (Muriaé; Santana et al., 2009); Triangle (Flores de Goiás, GO). MG = Minas Gerais; GO = Goiás.
Figure 1 in Redescription of the ocellus-bearing cuskeel Neobythites kenyaensis (Ophidiidae), with new Southeast African records and remarks on intraspecific morphological and colour variation
Figure 1. – Map with sampling localities for Neobythites kenyaensis. Number of specimens indicated for localities with multiple occurrences.
Figure 4 in Redescription of the ocellus-bearing cuskeel Neobythites kenyaensis (Ophidiidae), with new Southeast African records and remarks on intraspecific morphological and colour variation
Figure 4. – Radiograph of Neobythites kenyaensis, SAIAB 98890, 102 mm SL (M. Lisher). Inverted colour version on bottom.
Figure 1 in Intraspecific C-value variation and the outcomes in Psidium cattleyanum Sabine essential oil
Figure 1. Relative area (%) of terpenic classes in relation to accessions of Psidium cattleyanum (CAT1, CAT2, CAT3, CAT4, CAT5, CAT6 and CAT8). Hydrogenated monoterpenes (HM), oxygenated monoterpenes (OM), hydrogenated sesquiterpenes (HS) and oxygenated sesquiterpenes (OS).
Database of Pines from the Forests paper: "Intraspecific Variation in Pines from the Trans-Mexican Volcanic Belt Grown Under Two Watering Regimes: Implications for Management of Genetic Resources"
<p>Raw data from the Forests paper: "Intraspecific Variation in Pines from the Trans-Mexican Volcanic Belt Grown under Two Watering Regimes: Implications for Management of Genetic Resources" Forests <strong>2018</strong> <em>9</em>(2), 71. doi:<a href="http://dx.doi.org/10.3390/f9020071">10.3390/f9020071. </a></p> <p>The database correspond to seedlings of four Mexican pines: <em>P. oocarpa, P. patula</em> and <em>P. pseudostrobus</em>, that were submitted to two watering treatments: Field Capacity (FC) and Drought-Stress (DS), during 90 days. Growth and biomass, survival and ontogenetic score were measured.</p>
Data from: Hydrology induces intraspecific variation in freshwater fish morphology under contemporary and future climate scenarios
<p>Datasets for manuscript "Andres, K. J., Chien, H., and Knouft, J. H. Hydrology induces intraspecific variation in freshwater fish morphology under contemporary and future climate scenarios. Science of the Total Environment. <a href="https://doi.org/10.1016/j.scitotenv.2019.03.292">https://doi.org/10.1016/j.scitotenv.2019.03.292</a>"</p> <p>landmarks.zip: landmarks digitized on images of 1081 specimens using TpsDig2 software.</p> <p>streamflow_estimates.csv: Contemporary (1980-2009) and future (2070-2099) streamflow estimates [avg: average annual streamflow discharge (m3 s-1); cv: coefficient of variation of annual discharge] in sub-basins containing populations of 6 minnow species in IL, USA</p>
Datasets for "Intraspecific interactions in the annual legume Medicago minima are shaped by both genetic variation for competitive ability and reduced competition among kin"
<p>Datasets for “Intraspecific interactions in the annual legume <em>Medicago minima</em> are shaped by both genetic variation for competitive ability and reduced competition among kin”</p> <p>Two datasets are provided.</p> <p>root_behavior_experiment_for_ms.csv: provides data relative to a root behaviour experiment where <em>Medicago minima</em> genotypes grew either with a kin or a non kin. Direction of root growth, root length and biomass were measured.</p> <p>Medicago_minima_biomass_dataMerge.csv: provides data relative to a minicommunity experiment where <em>Medicago minima </em>genotypes were grown surrounded by three kin genotypes, or three non-kin genotypes (i.e. stranger to the central plant but identical to each other) or three stranger genotypes (stranger to the central plant and to each other). For this second experiment above-ground growth and biomass were monitored.</p> <p>Detailed information on the dataset variables are provided in the metadata file.</p> <p>Code for data wrangling and analyses is included in the manuscript as an appendix.</p>
Figure 2 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey
Figure 2. Location of 17 two-dimensional landmarks on the dorsal (A) and ventral (B) skull side of a common toad. A. Dorsal side: 1. Snout tip, 2. Anterior end of suture between premaxilla and maxilla, 3. Anterior end of nasal, 4. Lateralmost point of nasal, 5. Mostanterior point of frontoparietal, 6. Lateralmost point of nasal (posterior), 7. Middle point of the median edge of frontoparietal, 8. Mostposterior median point of frontoparietal, 9. Posterior end of suture between frontoparietal and prootic, 10. Anterior end of suture between frontoparietal and prootic, 11. Middle point of the lateral edge of frontoparietal, 12. Mostanterior point of squamosal, 13. Posterior end of squamosal in contact with prootic, 14. Mostposterior point of prootic, 15. Mostposterior point of maxilla, 16. Posterior end of quadrate, 17. Medial tip of occipital. B. Ventral side: 1. Anteriormost point of premaxilla, 2. Anteriolateral end of premaxilla, 3. Mostposterior median end of premaxilla, 4. Posteriolateral end of premaxilla, 5. Lateralmost point of vomer, 6. Mostposterior end of vomer, 7. Most median point of palatine, 8. Anteriolateral end of palatine, 9. Posteriolateral end of palatine (anterior end of suture between palatine and pterygoid or anterior end of pterygoid), 10. Posteriomedian end of pterygoid, 11. Posteriolateral end of pterygoid, 12. Lateralmost end of parasphenoid, 13. Mostanterior median end of parasphenoid, 14. Mostposterior median end of parasphenoid, 15. Posterior end of maxilla in contact with quadratojugal, 16. Posterior end of quadratojugal, 17. Mostposterior end of occipital condyl.
Figure 1 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey
Figure 1. Distribution map of Bufo bufo (blue) and Bufo verrucosIssImus (yellow) in Turkey according to IUCN Red List and Özdemir et al. (2020), and geographical positions of analysed populations.
Figure 3 in Interspecific and intraspecific size and shape variation in skull of two closely related species Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) from Turkey
Figure 3. The positions of the specimens in morphospaces defined by the first two principal axes derived from covariance matrices of skull shape variables. Blue dots; B. bufo, yellow dots; B. verrucosissimus. DC: dorsal cranium, VC: ventral cranium.
FIGURE 1 in Intraspecific variation in fossil vertebrate populations: Fossil killifishes (Actinopterygii: Cyprinodontiformes) from the Oligocene of Central Europe
FIGURE 1. Photograph of a plate with Paralebias cephalotes (P.36131, NHM, collected from Aix-en-Provence, France). Scale bar equals 6 cm.
FIGURE 3 in Intraspecific variation in fossil vertebrate populations: Fossil killifishes (Actinopterygii: Cyprinodontiformes) from the Oligocene of Central Europe
FIGURE 3. Bar charts showing frequency distribution of meristic characters for the three fossil Killifish species Prolebias rhenanus (yellow), Pr. stenoura (green) and Paralebias cephalotes (blue). 1, number of vertebrae; 2, number of precaudal vertebrae; 3, number of caudal vertebrae; 4, number of dorsal pterygiophores; 5, number of anal pterygiophores.
FIGURE 2 in Intraspecific variation in fossil vertebrate populations: Fossil killifishes (Actinopterygii: Cyprinodontiformes) from the Oligocene of Central Europe
FIGURE 2. Photographs of fossil killifish species examined in this study. 1, Prolebias rhenanus (Ru 99, Naturhistorisches Museum Basel); 2, Pr. stenoura (28491 n, NHM); 3, Paralebias cephalotes (P.1831a, NHM). Scale bars equal 1 cm.
FIGURE 4 in Intraspecific variation in fossil vertebrate populations: Fossil killifishes (Actinopterygii: Cyprinodontiformes) from the Oligocene of Central Europe
FIGURE 4. Bar charts showing frequency distribution of morphometric data (in mm) for the three fossil Killifish species Prolebias rhenanus (yellow), Pr. stenoura (green) and Paralebias cephalotes (blue). 1, standard length; 2, precaudal length of vertebral column; 3, caudal length of vertebral column; 4, length of dorsal fin base; 5, length of anal fin base.
Linked collectors and determiners for: Revision of the whitefly genus, Asterochiton Maskell (Hemiptera: Aleyrodidae) from New Zealand, a study of intraspecific variation.
Natural history specimen data linked to collectors and determiners held within, "Revision of the whitefly genus, Asterochiton Maskell (Hemiptera: Aleyrodidae) from New Zealand, a study of intraspecific variation". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4fa02c9b-92c6-4c41-bc6c-265a30ffda5f">https://bionomia.net/dataset/4fa02c9b-92c6-4c41-bc6c-265a30ffda5f</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4fa02c9b-92c6-4c41-bc6c-265a30ffda5f">https://gbif.org/dataset/4fa02c9b-92c6-4c41-bc6c-265a30ffda5f</a>. Formatted as a Frictionless Data package.
Figure 11 in Intraspecific clinal variation in Plagiodontes patagonicus (Gastropoda: Orthalicidae, Odontostominae), an endemic species from Argentina
Figure 11. Relative frequencies of shells showing a rudimentary or developed transverse lamella as a function of shell length.
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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.