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8,119 results for “species distribution”
Figs. 17–24. Mouthparts. 17–20 in Three new species of Pelidnota MacLeay (Coleoptera, Scarabaeidae, Rutelinae) and new distributional records from northeast Brazil
Figs. 17–24. Mouthparts. 17–20, labrum in frontal view; 17, P. beckeri sp. nov.; 18, P. unicolor (Drury); 19, P. nordestina sp. nov.; 20, P. pernambucana sp. nov.; 21–24, left mandible in dorsolateral view; 21, Pelidnota beckeri sp. nov.; 22, P. unicolor (Drury); 23, P. nordestina sp. nov.; 24, P. pernambucana sp. nov. Scale bars: Figs. 17–24 = 2.0 mm.
Figs. 1–10. Pelidnota. 1–8 in Three new species of Pelidnota MacLeay (Coleoptera, Scarabaeidae, Rutelinae) and new distributional records from northeast Brazil
Figs. 1–10. Pelidnota. 1–8, Pelidnota beckeri sp. nov.; 1–3, male holotype (dorsal, ventral, lateral); 4–6, female paratype (dorsal, ventral, lateral); 7–8, clypeus in dorsal view (male, female); 9–10, P. unicolor (Drury, 1778) (dorsal, lateral). Scale bars: Figs. 1–6 = 9.0 mm, Figs. 7–8 = 2.5 mm, Figs. 9–10 = 8.2 mm.
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.
Fig. 1 in Prevalence and distribution of Babesia and Theileria species in roe deer from Spain
Fig. 1. Map of Spain (modified from Morrondo et al., 2017) showing the four ecological areas. Dots represent the presence of Babesia spp. and/or Theileria spp. in each region.
Figure 5 in Distribution and diversity of intertidal marine faunal species along with Maharashtra and Goa coast, India
Figure 5. Relative proportion of species composition in the major phyla of intertidal marine faunal diversity.
Figure 2 in Distribution and diversity of intertidal marine faunal species along with Maharashtra and Goa coast, India
Figure 2. Shannon – Wiener (H') diversity indices of intertidal marine faunal communities from different stations of Maharashtra and Goa.
Fig. 1 in Species composition and distribution of ground beetles (Coleoptera, Carabidae) in the forests of the Kamanos State Strict Reserve (Lithuania)
Fig. 1. Similarity (Ics) between the forest types of the Kamanos State Strict Reserve with respect to species composition of ground beetles according to quantitative data (species similarity) (1 - oxalidosum spruce stand, 2 - myrtillosum pine stand, 3 - myrtillo - oxalidosum spruce stand, 4 - oxalidosum broadleaved birch stand, 5 - calamagrostics birch stand, 6 - caricosum birch stand, 7 - caricoso - ledosum pine stand, 8 - sphagno - ledosum pine stand).
Figure 4 in Distribution of two pine processionary moth species in Turkey evidences a contact zone
Figure 4. Distribution of pure T. wilkinsoni (black) and T. pityocampa (white), introgressed individuals (gray with Ia and Ib), dispersal routes and barriers, and the contact zone. Color and sign codes are given in the map legend.
Figure 3 in Distribution of two pine processionary moth species in Turkey evidences a contact zone
Figure 3. Consensus haplotype trees for COI, ITS-1, and photolyase. Three clades of wilkinsoni haplotypes are shown in shaded rectangles. All branches have bootstrap support values> 60%.
Figure 1 in Distribution of two pine processionary moth species in Turkey evidences a contact zone
Figure 1. Map of sampling locations and coniferous forests in Turkey and Cyprus (forest data is from EC-JRC Forest Map, 2006).
Figure 2 in Distribution of two pine processionary moth species in Turkey evidences a contact zone
Figure 2. Distribution maps of a) COI, b) ITS-1, and c) photolyase haplotypes. Haplotypes are colored and numbered in accordance with the network. Color and sign codes are given in the legends on the maps. d) Haplotype networks for COI, ITS-1, and photolyase. Numbers on the dashed lines indicate how many mutations separate two relevant haplotypes.
Figure 3 in A new species of voles, Microtus elbeyli sp. nov., from Turkey with taxonomic overview of social voles distributed in southeastern Anatolia
Figure 3. Dentition of M. elbeyli sp. nov. A) Upper tooth row, B) lower tooth row. M1: First upper molars, M2: second upper molars, M3: third upper molars. M1: First lower molars, M2: second lower molars, M3: third lower molars. La.: Labial side, Li.: lingual side. Type specimen, No: 2919, ♂, collected 10 km east of Kilis.
Figure 4 in A new species of voles, Microtus elbeyli sp. nov., from Turkey with taxonomic overview of social voles distributed in southeastern Anatolia
Figure 4. The metaphase plate (A) and karyotype (B) of the type specimen of M. elbeyli sp. nov. 2n = 46, NF = 50, NFa = 46.
Figure 1 in A new species of voles, Microtus elbeyli sp. nov., from Turkey with taxonomic overview of social voles distributed in southeastern Anatolia
Figure 1. Record locations of the specimens evaluated: M. elbeyli (●10 km east of Kilis and ⦿ Elbeyli), M. cfr. irani (▲ Ermenek, ✸ Nusaybin), M. guentheri (■ Türkoğlu and △ Nemrut), M. socialis (□ Muş), M. irani (★ Shiraz/Iran).
Figure 2 in A new species of voles, Microtus elbeyli sp. nov., from Turkey with taxonomic overview of social voles distributed in southeastern Anatolia
Figure 2. Skulls (dorsal and lateral views) and mandible (labial views) of species: A) M. elbeyli, B) M. cfr. irani, C) M. guentheri.
Figure 3 in Spatiotemporal distribution, abundance, and species-environment relationships of Scyphozoa (Cnidaria) species in Hisarönü, Marmaris, and Fethiye bays (Muğla, Turkey
Figure 3. RDA ordination plot for Scyphozoa species, environmental parameters, sampling months, and stations. Sampling stations in RDA plot indicated with □: Hisarönü 1; ■: Hisarönü 2; O: Marmaris 1; ●: Marmaris 2; ◇: Marmaris 3; ◆: Marmaris 4; ×: Marmaris 5; ∆: Fethiye 1; △: Fethiye 2; ▲: Fethiye 3. Scyphozoa species indicated by the following abbreviations: Aa: Aurelia aurita; Ct: Cotylorhiza tuberculata; Ca: Cassiopea andromeda. Sampling months in RDA plot indicated with: 1: September 2011; 2: October 2011; 3: November 2011; 4: December 2011; 5: January 2012; 6: February 2012; 7: March 2012; 8: April 2012; 9: May 2012; 10: June 2012; 11: July 2012; 12: August 2012; 13: September 2012; 14: October 2012. See Table 4 for abbreviations of environmental variables.
Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman). in Taxonomic status of Neomys species (Mammalia: Soricomorpha) and their distribution in Turkey
Figure. Distribution of Neomys teres and Neomys anomalus species in Turkey (square = Neomys anomalus, triangle = Neomys teres). 1: Ulubey (Ordu), 2: Meryemana (Trabzon), 3: Kutul (Artvin), 4: Yalnızçam (Kars), 5: Bendimahi Canyon (Muradiye, Van), 6: Seyfe (Amasya), 7: Safranbolu (Karabük), 8: Topçam (Ordu), 9: Tamdere (Giresun), 10: Çamlık (Rize), 11: Ovid Mountain (Rize), 12: Lake Abant (Bolu), 13: Kayseri, 14: Erzurum, 15: Samsun, 16: Belgrad Forest (İstanbul), 17: Lake Abant (Bolu), 18: İrve creek (İstanbul), 19: Erçek Mountain (Van), 20: Paşaalandere (Tekirdağ), 21: Lake Terkos (İstanbul), 22: Yeşiloba (Adana), 23: Yenice, Çayır (Zonguldak), 24: Abant (Bolu), 25: Hanyatak village (Sakarya), 26: Longoz forest, Dupnisa cave, Demirköy (Kırklareli), 27: Lake Eber (Afyon), 28: Çırpılar (Çanakkale), 29: Uludağ (Bursa), 30: Balkusan (Karaman).
Figure 2. Distribution map for N in Neobisium (N.) tothi sp. nov., a new species from Hungary and Romania, and first records of Neobisium (N.) noricum Beier, 1939 from Hungary (Pseudoscorpiones: Neobisiidae)
Figure 2. Distribution map for N. (N.) tothi sp. nov. (squares) and N. (N.) noricum Beier, 1939 (empty circles: earlier data; filled circles: new data).
Figure 3 in Human activity mediates reciprocal distribution and niche separation of two sympatric mongoose species on the Pothwar Plateau, Pakistan
Figure 3. Photomicrographs of whole mounts of hair structure of three rodent species (recovered from fecal samples and reference hairs) consumed by the small Indian mongoose on the Pothwar Plateau. A) Whole mount of recovered hair of Rattus rattus, B) Whole mount of reference hair of Rattus rattus, C) Whole mount of recovered hair of Nesokia indica, D) Whole mount of reference hair of Nesokia indica, E) Whole mount of recovered hair of Mus musculus, F) Whole mount of reference hair of Mus musculus.
Figure 2 in Human activity mediates reciprocal distribution and niche separation of two sympatric mongoose species on the Pothwar Plateau, Pakistan
Figure 2. Average length (cm), mass (g), and diameter (cm) of SIM and GM fecal samples collected from study sites on the Pothwar Plateau.
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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.