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263 results for “Uplands”
FIGURE 3 in Phylogenetic relationships and description of a new upland species of Bent-toed Gecko (Cyrtodactylus Gray, 1827) of the C. sworderi complex from northeastern Peninsular Malaysia
FIGURE 3. Holotype (ZRC 2.6997) of Cyrtodactylus tebuensis sp. nov.
FIGURE 5 in A new species of upland Stream Toad of the genus Ansonia Stoliczka, 1870 (Anura: Bufonidae) from northeastern Peninsular Malaysia
FIGURE 5. Habitat of Ansonia lumut sp. nov. at Gunung Tebu, Terengganu.
FIGURE 2 in A new species of upland Stream Toad of the genus Ansonia Stoliczka, 1870 (Anura: Bufonidae) from northeastern Peninsular Malaysia
FIGURE 2. Live coloration of female paratype LSUHC 11211.
FIGURE 1 in The Family Baetidae (Insecta: Ephemeroptera) from Venezuelan Guayana's Uplands
FIGURE 1. Map. Sampling sites, Gran Sabana, Canaima National Park, Bolívar State, Venezuela.
Dataset for Prolonged storage of bound organic carbon in wetland but not upland soils: A 13C and 14C perspective
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Data from: Inter-specific variation in the potential for upland rush management advocated by agri-environment schemes to increase breeding wader densities
<p>Encroachment of rush Juncus spp. in the United Kingdom uplands poses a threat to declining wader populations due to taller, denser swards that can limit foraging and breeding habitat quality for some species. Rush management via cutting, implemented through agri-environment schemes (AESs), could thus increase wader abundance, but there is insufficient assessment and understanding of how rush management influences upland waders. Across two upland regions of England [South West Peak (SWP) and Geltsdale nature reserve, Cumbria], we surveyed waders over four visits in fields where rush was managed according to AES prescriptions (treatment; n = 21) and fields without rush management that were otherwise ecologically similar (control; n = 22) to assess how the densities of breeding wader pairs respond to rush management in the short-term. We find evidence for regional variation in the response of waders to rush management, with densities of Common Snipe Gallinago gallinago significantly higher in treatment than control fields in the SWP, but not Geltsdale. There were no statistically significant responses to treatment on densities of Eurasian Curlew Numenius arquata or Northern Lapwing Vanellus vanellus. The 95% confidence intervals for the treatment parameter estimates suggest that this may be due to limited statistical power in the case of Lapwing. For Curlew, however, any potential increases in densities are negligible. There was no evidence that variation in rush cover, which ranged from 10 to 70%, influenced densities of any of our three focal species. Our results suggest that rush management through AES prescriptions delivered in isolation of other interventions may not lead to general increases in breeding wader densities in the short-term, but benefits may arise in some situations due to regional and inter-specific variation in effectiveness. Rush management supported with interventions that improve soil conditions and thus food availability, or reduce predation pressure, may enable AES rush management to generate benefits. Additional research is required to maximise the potential benefits of rush management for each species through the development of prescriptions that tailor to individual species' optimum sward structure.</p>
Distribution. Kazakh uplands N, W & E in Ochotonidae
Distribution. Kazakh uplands N, W & E of Lake Balkash in E Kazakhstan.
Figures 2-3 from: de Lucena CA, Zaluski AB, de Lucena ZMS (2017) Astyanax taurorum a new species from dos Touros River, Pelotas River drainage, an upland southern Brazilian river (Characiformes: Characidae). Zoologia 34: 1-8. https://doi.org/10.3897/zoologia.34.e20174
Figures 2-3 - (2) Head depth as function of head length for Astyanax paris (y = -1.517 +(0.996X), R = 0.952, and Astyanax taurorum sp. nov. (y = -5·158+(1.037X), R = 0.932. Dotted lines, confidence interval of 95%; (3) Astyanax taurorum sp. nov. Posterodorsal region of head (lateral view, right side); EXS = Extrascapular, PTE = posttemporal, SCL = supracleithrum. White arrow indicates the hook on posterodorsal region of posttemporal bone (see text). Scale bar = 0.2 mm.
Figure 4 from: de Lucena CA, Zaluski AB, de Lucena ZMS (2017) Astyanax taurorum a new species from dos Touros River, Pelotas River drainage, an upland southern Brazilian river (Characiformes: Characidae). Zoologia 34: 1-8. https://doi.org/10.3897/zoologia.34.e20174
Figure 4 - Maxilla, premaxilla and dentary of Astyanax taurorum sp. nov., MCP 14370, paratype, 62.6 mm SL, lateral view of right side. Scale bar = 0.5 mm.
Figure 1 from: de Lucena CA, Zaluski AB, de Lucena ZMS (2017) Astyanax taurorum a new species from dos Touros River, Pelotas River drainage, an upland southern Brazilian river (Characiformes: Characidae). Zoologia 34: 1-8. https://doi.org/10.3897/zoologia.34.e20174
Figure 1 - Astyanax taurorum sp. nov., MCP 49468, 80,7 mm SL, holotype, tributary of dos Touros River, Rio Grande do Sul, Brazil.
Figures 5-6 from: de Lucena CA, Zaluski AB, de Lucena ZMS (2017) Astyanax taurorum a new species from dos Touros River, Pelotas River drainage, an upland southern Brazilian river (Characiformes: Characidae). Zoologia 34: 1-8. https://doi.org/10.3897/zoologia.34.e20174
Figures 5-6 - (5) Distribution of Astyanax taurorum sp. nov., white circle = type-locality. The symbol represents more than one locality; (6) stream tributary of dos Touros River, type locality of Astyanax taurorum sp. nov.
Figure 1 from: Costa WJEN, Amorim PF, Mattos JLO (2018) Diversity and conservation of seasonal killifishes of the Hypsolebias fulminantis complex from a Caatinga semiarid upland plateau, São Francisco River basin, northeastern Brazil (Cyprinodontiformes, Aplocheilidae). Zoosystematics and Evolution 94(2): 495-504. https://doi.org/10.3897/zse.94.29718
Figure 1 Bayesian phylogeny used to delimit species endemic to the upper Carnaíba de Dentro River drainage, inferred by using sequences of the mitochondrial gene cytochrome b, 416 bp. Posterior probability values below 95% are not depicted; asterisk above nodes represents maximum value of posterior probability (100 %); numbers before species names are catalogue numbers for voucher specimens.
Figure 4 from: Costa WJEN, Amorim PF, Mattos JLO (2018) Diversity and conservation of seasonal killifishes of the Hypsolebias fulminantis complex from a Caatinga semiarid upland plateau, São Francisco River basin, northeastern Brazil (Cyprinodontiformes, Aplocheilidae). Zoosystematics and Evolution 94(2): 495-504. https://doi.org/10.3897/zse.94.29718
Figure 4 Geographical distribution of species of the Hypsolebias J'-clade in the upper Carnaíba de Dentro River drainage (yellow, H.fulminantis; red, H.splendissimus; black, H.carlettoi) and H.shibattai (white); stars indicate type localities.
Figure 2 from: Costa WJEN, Amorim PF, Mattos JLO (2018) Diversity and conservation of seasonal killifishes of the Hypsolebias fulminantis complex from a Caatinga semiarid upland plateau, São Francisco River basin, northeastern Brazil (Cyprinodontiformes, Aplocheilidae). Zoosystematics and Evolution 94(2): 495-504. https://doi.org/10.3897/zse.94.29718
Figure 2 Hypsolebiassplendissimus Costa sp. n., live holotype, UFRJ 6909, male, 42.7 mm SL. Photograph by W.J.E.M. Costa.
Figure 3 from: Costa WJEN, Amorim PF, Mattos JLO (2018) Diversity and conservation of seasonal killifishes of the Hypsolebias fulminantis complex from a Caatinga semiarid upland plateau, São Francisco River basin, northeastern Brazil (Cyprinodontiformes, Aplocheilidae). Zoosystematics and Evolution 94(2): 495-504. https://doi.org/10.3897/zse.94.29718
Figure 3 Hypsolebiassplendissimus Costa sp. n., live paratype, UFRJ 6779, female, 28.5 mm SL. Photograph by W.J.E.M. Costa.
Fig. 1 in Association of Anagrus amazonensis Triapitsyn, Querino & Feitosa (Hymenoptera, Mymaridae) with aquatic insects in upland streams and floodplain lakes in central Amazonia, Brazil
Fig. 1. Sites where Anagrus amazonensis (Hymenoptera, Mymaridae), its hosts, and their associated plants were collected in Amazonas State, Brazil.
FIGURE 2 in A new Miconia (Melastomataceae: Miconieae) from upland rain forest of northwestern Guyana
FIGURE 2. Geographic distribution of Miconia angustidentata.
Data from: Inter-specific variation in the potential for upland rush management advocated by agri-environment schemes to increase breeding wader densities
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Data from: Generation of transcript assemblies and identification of single nucleotide polymorphisms from seven lowland and upland cultivars of switchgrass
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Upland grassland habitats and agri-environment schemes change soil microarthopod abundance
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Allen Brain Atlas
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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.