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303 results for “habitat preference”
Fig. 1 in Assessments of environmental variables affecting the spatiotemporal distribution and habitat preferences of living Ostracoda (Crustacea) species in the Enez Lagoon Complex (Enez-Evros Delta, Turkey)
Fig. 1. Map of the eight studied coastal lagoons. Selected sampling sites at Tuzla Lake 1 (St-1), Tuzla Lake 2 (St-2), Tuzla Lake 3 (St-3), Taz (St-4), Işık (St-5), Dalyan (St-7, 8, and 9), Kuvalak (St-10), and Taşaltı (St-11 and 12) were used for comparisons of the lagoons. The sampling sites are indicated by red circles; the red arrows show the direction of water currents.
Figure 2 in Seasonal distribution and habitat use preference of Barking deer (Muntiacus vaginalis) in Murree-Kotli Sattian-Kahuta National Park, Punjab Pakistan
Figure 2. Vegetation composition of Barking deer habitat in Murree-Kotli Sattian-Kahuta National Park.
Fig. 4 in Ground beetles (Coleoptera: Carabidae) from the region of Cape Emine (Central Bulgarian Black sea coast). Part I. Taxonomic and zoogeographic structure, life forms, habitat and humidity preferences
Fig. 4. Proportions of the subclasses of life forms in the carabid complex (I – class Zoophaga, II – class Mixophytophaga).
Fig. 3 in Soil and habitat preferences of ground beetles (Coleoptera, Carabidae) in natural mountain landscape
Fig. 3. Biplot of redundancy analysis with forward selection of explanatory variables, indicating the distribution of particular species along significant environmental factors (abbreviations of species names as in table 2)
Figure 2 in Activity patterns and habitat preference of eastern Hermann's tortoise (Testudo hermanni boettgeri) in Serbia
Figure 2. Percent of occurrence of tortoises in specific habitat types in consecutive years. For description of habitat types, see Section 2.2.
Figure 1 in Activity patterns and habitat preference of eastern Hermann's tortoise (Testudo hermanni boettgeri) in Serbia
Figure 1. The study area. The map was constructed with Google Earth. The white line borders the area where monitoring was conducted. Triangles mark the position of open habitat or grassland. Squares mark the position of human-modified habitat. Surface without symbols represents forest.
Figure 3 in Iranian Branchiostoma species (Cephalochordata, Branchiostomatidae) inhabiting Chabahar Bay (Gulf of Oman), with remarks on habitat preferences
Figure 3. Anterior (A) and posterior (B) end of the Branchiostoma lanceolatum (INIOC-2-8S) of the present study. AN, Anus; AT, atriopore; BT, buccal tentacle; CF, caudal fin; DFC; dorsal fin chamber; M, metaplural fold; RS, rosterum; VFC, ventral fin chamber.
Figure 2 in Iranian Branchiostoma species (Cephalochordata, Branchiostomatidae) inhabiting Chabahar Bay (Gulf of Oman), with remarks on habitat preferences
Figure 2. Branchiostoma lanceolatum collected in this study: A (INIOC-2-7S); B (INIOC-2-6S). AT, Atriopore; AN, anus; BT, buccal tentacle; BC, buccal cavity; DF, dorsal fin; G, gonad; PH, pharynx; LM, left metaplural; MY, myotome; RM, right metaplural; RS, rosterum; VF; ventral fin.
Figure 1. Cryptocephalus surdus Rapilly, 1980. a in Redescription of a little-known species, Cryptocephalus surdus Rapilly, 1980 (Coleoptera: Chrysomelidae: Cryptocephalinae), with notes on new distribution localities and habitat preference in Türkiye
Figure 1. Cryptocephalus surdus Rapilly, 1980. a. Habitus (male) Scale bars = 1 mm; b. Aedeagus; dorsal and lateral view. Scale bars = 0.5 mm; c. Spermatheca.
Fig 2. Three dwarf spinner dolphins, Stenella l in Cetacean Diversity And Habitat Preferences In Tropical Waters Of East Kalimantan, Indonesia
Fig 2. Three dwarf spinner dolphins, Stenella l. roseiventris with obscure, lateral color pattern, photographed in the Berau Archipelago, October 2003. Photo: Budiono.
Fig 3 in Cetacean Diversity And Habitat Preferences In Tropical Waters Of East Kalimantan, Indonesia
Fig 3. Two Gray's (pantropical) spinner dolphins, Stenella longirostris with distinctive tripartite color pattern, photographed in the Berau Archipelago, October 2003. Photo: Budiono.
Linked collectors and determiners for: Faunal study of velvet ants (Hymenoptera: Mutillidae) and their activity patterns and habitat preference at Ash Meadows National Wildlife Refuge, Nye County, Nevada, USA.
Natural history specimen data linked to collectors and determiners held within, "Faunal study of velvet ants (Hymenoptera: Mutillidae) and their activity patterns and habitat preference at Ash Meadows National Wildlife Refuge, Nye County, Nevada, USA". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/20d58797-2815-434b-a9c5-5786e926af9d">https://bionomia.net/dataset/20d58797-2815-434b-a9c5-5786e926af9d</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/20d58797-2815-434b-a9c5-5786e926af9d">https://gbif.org/dataset/20d58797-2815-434b-a9c5-5786e926af9d</a>. Formatted as a Frictionless Data package.
FIG. 4 in Habitat preferences of Papilio alexanor Esper, [1800]: implications for habitat management in the Italian Maritime Alps
FIG. 4.— Pre-imaginal development of Papilio alexanor Esper, [1800] under laboratory conditions; box plots illustrate increases in larval length; vertical lines: median larval length; box: 25th-75th percentiles; whiskers: minimum and maximum observed values; outliers; dark grey band width represents the standard deviations of mean development intervals (days). Abbreviations: e, egg; I-IV, larval instars; p, pupa.
FIG. 2 in Habitat preferences of Papilio alexanor Esper, [1800]: implications for habitat management in the Italian Maritime Alps
FIG. 2.— Stable range of P. alexanor Esper, [1800] in Italy (Balletto et al. 2007), observations from S Italy are interpreted as being based on vagrant specimens from the Balkans, the arrow indicates the Valdieri study area.
FIG. 6 in Habitat preferences of Papilio alexanor Esper, [1800]: implications for habitat management in the Italian Maritime Alps
FIG. 6.— Comparison of mean values of larval survival rates calculated for the 21 (occupied) plots ranked by increasing total number of P. saxifraga (L.) Loret & Barrandon plants.
FIG. 5 in Habitat preferences of Papilio alexanor Esper, [1800]: implications for habitat management in the Italian Maritime Alps
FIG. 5.— Pre-imaginal development of P. alexanor Esper, [1800] in the field. Mean (± SE) number of eggs and larvae of P. alexanor collected during the four sampling events (2010).
Fig. 5 in The habitat preference of dung beetle species associated with elephant dung of the Malay Peninsula
Fig. 5. The Non-metric multidimensional scaling(NMDS) ordination of 25 species of dung beetle from 271 forest and forest edge sampling points. Filled squares represent species that prefer forest habitats, open squares represent species that prefer forest edge habitats, and crossed squares represent species that are evenly distributed among habitat types. Species codes: L.fem: Liatongus femoratus, On.tes: Oniticellus tessellatus, On.cinc: On. cinctus, Y.sar: Yvescambefortius sarawacus, O.babi: Onthophagus babirussa, O.rufi: O. rufiobscurior, O.vul: O. vulpes, O.ror: O. rorarius, O.prot: O. proletarius, O.pac: O. pacificus, O.rugi: O. rugicollis, O.ori: O. oreintalis, O.cras: O. crassicollis, O.lae: O. laevis, O.dayc: O. dayacus, O.kar: O. karenensis, O. lur: O. luridipennis, O.leu: O. leusermontis, O.viri: O. viridicervicapra, O.tsu: O. tsubakii, Cc.un: Caccobius unicornis, Ct.ren: Catharsius renaudpauliani, Cp.dor: Copris doriae, Cp.spi: Cp. spinator, M.brah: Megatelus brahminus.
Fig. 4 in The habitat preference of dung beetle species associated with elephant dung of the Malay Peninsula
Fig. 4. Unweighted Pair Group Method with Arithmetic Mean (UPGMA) hierarchical clustering with Bray-Curtis distances of the 25 dung beetle species. Two major clusters are indicated, dung beetles that prefer (A) forest sampling points and (B) forest edge sampling points.
Fig. 2 in The habitat preference of dung beetle species associated with elephant dung of the Malay Peninsula
Fig. 2. Boxplots of the dung beetle relative abundance, species richness, and Shannon diversity for forest (n = 131) and forest edge (n = 140) sampling points.
Fig. 3. A in The habitat preference of dung beetle species associated with elephant dung of the Malay Peninsula
Fig. 3. A, Species accumulation curves for dung beetle species in 271 sampling points; B, Rarefaction curves comparing forest and forest edge samples. The solid line represents forest sampling points while the dotted line represents forest edge sampling points.
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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)
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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.