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303 results for “habitat preference”
FIGURE 23 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURE 23. Type locality of Sympycnus septentrionalis sp. nov. (Sweden, Södermanland, Trosa, Hunga Södergård nr 1, behind stable, N58°55.244' E17°31.274'; photo: SMTP).
FIGURES 16–19 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 16–19. Sympycnus cinerellus (Chrysotus). 16, lectotype; 17, paralectotype; 18, lectotype label; 19, paralectotype label (photos: M. Pollet).
FIGURES 20–22. Sympycnus desoutteri. 20 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 20–22. Sympycnus desoutteri. 20, lectotype; 21, paralectotype; 22, lectotype (left) and paralectotype labels (right) (photos: M. Pollet).
FIGURES 13–15 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 13–15. Sympycnus annulipes (Porphyrops). 13, lectotype; 14, paralectotype; 15, lectotype (left) and paralectotype labels (right) (photos: M. Pollet).
FIGURES 6–7. Hind tarsus. 6 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 6–7. Hind tarsus. 6, Sympycnus pulicarius; 7, Sympycnus septentrionalis sp. nov. (photos: M. Persson).
FIGURES 11–12 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 11–12. Sympycnus pulicarius (Dolichopus). 11, lectotype; 12, paralectotype (photos: Y. Brodin, NRM).
FIGURES 2–5. Sympycnus pulicarius. 2 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 2–5. Sympycnus pulicarius. 2, habitus; 3, head; Sympycnus septentrionalis sp. nov. 4, habitus; 5, head (photos: M. Persson).
FIGURE 10 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURE 10. Sympycnus pulicarius, hypopygium (central parts), pgo: postgonites, pgo bva: basoventral appendages of postgonites. Scale: 0.1 mm.
FIGURES 8–9. Hypopygium. 8 in A long-lasting taxonomic problem in European Sympycnus resolved, with the description of a new species and data on habitat preferences
FIGURES 8–9. Hypopygium. 8, Sympycnus pulicarius; 9, Sympycnus septentrionalis sp. nov.; apv lobe: apicoventral epandrial lobe, cer: cercus, hyp: hypandrium, pha: phallus, pgo: postgonites, pgo bva: basoventral appendages of postgonites. Scale: 0.1 mm.
Effects of natal habitat preference induction on juvenile loon movements
<p>NHPI develops in natural systems. Here, we tested for NHPI in juvenile common loons (<i>Gavia immer</i>) that foraged on lakes in the vicinity of their natal lake after fledging. Juveniles visited lakes similar in pH to their natal lakes, and this significant effect persisted after controlling for spatial autocorrelation. On the other hand, juveniles showed no preference for foraging lakes of similar size to their natal one. When lakes were assigned to discrete classes based on size, depth, visibility, and trophic complexity, both juveniles from large lakes and small lakes preferred to visit large, trophically diverse lakes, which contained abundant food. Our results contrast with earlier findings, which show strict preference for lakes similar in size to the natal lake among young adults seeking to settle on a breeding lake. We suggest that NHPI is relaxed for juveniles, presumably because they select lakes that optimize short-term survival and growth. By characterizing NHPI during a poorly-studied life-stage, this study illustrates that NHPI can take different forms at different life stages.</p>
Distribution. Known from scattered localities in New Guinea, including the Central Range from Taritatu River E to Mt Dayman and the Torricelli Mts; possibly present across entire island of New Guinea in preferred habitat. It was found in Pleistocene archaeological sites on the Ayamaru Plateau, C Bird's Head (= Vogelkop), NW New Guinea. in Muridae
Distribution. Known from scattered localities in New Guinea, including the Central Range from Taritatu River E to Mt Dayman and the Torricelli Mts; possibly present across entire island of New Guinea in preferred habitat. It was found in Pleistocene archaeological sites on the Ayamaru Plateau, C Bird's Head (= Vogelkop), NW New Guinea.
Data from: Sundaic elephants prefer habitats on the periphery of protected areas
<p><span>1. </span><span>Protected Areas (PAs) are a cornerstone of global conservation strategies. PAs, however, are not equally effective for all threatened taxa, and it is important to understand taxa-specific effectiveness of PAs networks. </span></p> <p><span>2. </span><span>In this study we evaluate the role of the PAs network on the protection of Asian elephants (<em>Elephas maximus</em>) and their habitats in Southeast Asia's Sundaic region. Since Asian elephants tend to prefer secondary forests or forest gaps, </span><span>we predicted that PAs would not represent the species' preferred habitats.</span> <span>We conducted the most comprehensive analysis of Asian elephant space and habitat use to date through home range estimations and Step Selection Function analyses using over 600,000 GPS locations from 102 different elephants from Peninsular Malaysia and Borneo. </span></p> <p><span>3. </span><span>Our results revealed important similarities in the habitat use of elephants in both regions, with both females and males in Peninsular Malaysia and Sabah preferring secondary forest, forest gaps, and areas of regrowth and new plantations. </span></p> <p><span>4. </span><span>Our results supported our prediction that PAs do not represent Asian elephants' preferred habitats, since for most of the elephants, more than half of their ranges were outside PAs and the probability of selection values for both sexes in both geographical areas were lower inside than outside the PAs. </span></p> <p><span>5. </span><span>Synthesis and applications:</span><span> Our analysis suggests that conservation strategies need to acknowledge that the long-term survival of Asian elephants in the Sundaic region relies on our capacity to promote human-elephant coexistence at the boundaries of PAs. We advocate that Asian elephant conservation strategies should be based on the following three key points: 1) large PAs with core areas where elephants can find safety and potentially survive in the long term; 2) promoting connectivity among PAs using a system of wildlife corridors; and 3) effective human-elephant conflict management outside PAs. </span></p>
Data for Negros Bleeding-heart habitat preference assessment using GLMM
<p>Data for Negros Bleeding-heart habitat preference assessment using Generalised Linear Mixed Model. </p>
Fig. 1 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 1 Male adult Aradus brenskei, collected by Robin Van Heghe on 4.VII.2020 on a Fomes fomentarius infested poplar cultivar in Erpe-Mere © Theodoor Heijerman.
Fig. 5 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 5. Numbers of exposed individuals during the 20 days observation period at location 01. (Only on three occasions, adults were spotted in the morning. Each time, they had not moved since the evening before. The peak on 3.VI.2020 represents the appearance of seven larvae).
Fig. 20. Nutritional competition with Bolitophagus reticulatus, location 32 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 20. Nutritional competition with Bolitophagus reticulatus, location 32, Erpe-Mere, 25.VII.2020. © Brecht Verkempinck.
Fig. 22. Adult hanging under a fruitbody, location 4 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 22. Adult hanging under a fruitbody, location 4, Lede, 28.V.2020. © Brecht Verkempinck. Fig. 23. Mating, location 4, Lede, 3.VI.2020. © Brecht Verkempinck.
Fig. 2. Location 1 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 2. Location 1, Lede, 21.IV.2019. © Brecht Verkempinck. Fig. 3. Location 1, Lede, 07.V.2020. © Brecht Verkempinck.
Fig. 8 in The northernmost discovery of Aradus brenskei (Reuter, 1884) (Heteroptera: Aradidae). Considerations on the local distribution and the habitat preferences of this new Belgian species following a nine-months field survey
Fig. 8. Post-sunset inspection of habitat structures, Lede, location 44, 17.VIII.2020. © Brecht Verkempinck.
Fig. 2 in Distribution and habitat preferences of Galápagos ants (Hymenoptera: Formicidae)
Fig. 2. Relationship between ant species richness and island size within the Galápagos archipelago. Species or morphospecies with unknown origin have been excluded here. Size of islands as reported in SNELL et al. (1995).
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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