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7,849 results for “Conservancy”
FIGURE 3 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 3. Habitats at collecting sites. a: Komba Forest (1860 m); b: Hana Wetland (2425 m); c: Bamboo Forest (2620 m).
FIGURE 37 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 37. Altitudinal variation in males of Neritius abyssinicus. Specimens from higher elevations (left) are significantly larger than those from lower altitudes (right) (Table 4) and are slightly differently coloured. Scale bar represents 1 cm.
FIGURE 32 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 32. Oxya hyla brachypterous form, Shorori wetland (1610 m), Ethiopia. Scale bar represents 1 cm.
FIGURE 4 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 4. Habitats at collecting sites. a: Shorori Wetland (1610 m); b: waterfall at Dembi Forest (1260 m); c: inside the bamboo forest at Bamboo Forest (2620 m).
FIGURE 35 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 35. Eyprepocnemis plorans ibandana, Dembi Forest (1260 m), Ethiopia. Scale bar represents 1 cm.
FIGURE 10 in Orthoptera (Insecta: Tettigonioidea, Pyrgomorphoidea, Acridoidea) of Kafa Biosphere Reserve, Bale Mountains National Park and other areas of conservation interest in Ethiopia
FIGURE 10. Anoedopoda lamellata, Bonga Village (1700 m), Ethiopia (same specimen). Scale bar represents 1 cm.
FIGURE 30 in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 30. Bayesian tree (TPM 2 uf + G) for Aegla species based on partial fragment of 16 S. Node numbers represent posterior probabilities (values <50 % are not shown), and divergence time in millions of years (my); * indicates the calibration points to molecular clock. The clade C proposed by Pérez-Losada et al. (2004) is highlighted in grey. The basin and sub-basin origin of the discussed species in this study are shown after the specific names.
FIGURE 24. A – L in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 24. A – L, proximal portion of fifth pereiopod showing coxa and sexual tube of long and narrow type. A – B, Aegla paulensis Schmitt, 1942 s. str., male topotype (MZUSP 34368). C – D, Aegla rosanae Campos Jr., 1998, male topotype (MZUSP 34369). E – F, Aegla vanini n. sp., male paratype (MZUSP 34372). G – H, Aegla japi n. sp., male paratype (MZUSP 34375). I – J, Aegla jaragua n. sp. male paratype (MZUSP 34378). K-L, Aegla jundiai n. sp., male paratype (MZUSP 13490). Bars: A – D, F – H, J = 200 µm; K, L = 100 µm; E, I = 500 µm.
FIGURE 8 in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 8. Types of Aegla Leach, 1820 male sexual tubes. A, long and narrow (A. lancinhas Bond-Buckup & Buckup in Santos et al., 2015, MZUSP 34403). B, short and wide (A. leptochela Bond-Buckup & Buckup, 1994, MZUSP 34491).
FIGURE 1 in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 1. Distribution of the species of Aegla in four main hydrographic basins of southern Brazil: Rio Grande, Rio Tietê (Upper Paraná system), Rio Paraíba do Sul and Ribeira de Iguape. Indications L 1 through L 7 refer to the locations mentioned under “ sampling area ” in the Material & Methods section.
Data for "Water (or the Lack Thereof), Management, and Conservation of an Endangered Desert Wetland Obligate, Lilaeopsis schaffneriana var. recurva"
<p>Raw and RData forms of data for "Water (or the Lack Thereof), Management, and Conservation of an Endangered Desert Wetland Obligate, <em>Lilaeopsis schaffneriana </em>var. <em>recurva". </em>Consists of six Excel files, with names corresponding to the type of data.</p> <ol> <li>field_ecology_data.xlsx </li> <li>experiment_randomization.xlsx </li> <li>experiment_entered_data.xlsx </li> <li>resilience_days_to_critical.xlsx </li> <li>resilience_experiment_data.xlsx </li> <li>resilience_leaf_density_data.xlsx </li> </ol> <p>Four RData files of the loaded Excel data, and one text file to explain the coding of the drought experiment data.</p>
A geometry preserving, conservative, mesh-to-mesh isogeometric interpolation algorithm for spatial adaptivity of the multigroup, second-order even-parity form of the neutron transport equation
<p>In this paper a method is presented for the application of energy-dependent spatial meshes applied to the multigroup, second-order, even-parity form of the neutron transport equation using Isogeometric Analysis (IGA). The computation of the inter-group regenerative source terms is based on conservative interpolation by Galerkin projection. The use of Non-Uniform Rational B-splines (NURBS) from the original computer-aided design (CAD) model allows for efficient implementation and calculation of the spatial projection operations while avoiding the complications of matching different geometric approximations faced by traditional finite element methods (FEM). The rate-of-convergence was verified using the method of manufactured solutions (MMS) and found to preserve the theoretical rates when interpolating between spatial meshes of different refinements. The scheme’s numerical efficiency was then studied using a series of two-energy group pincell test cases where a significant saving in the number of degrees-of-freedom can be found if the energy group with a complex variation in the solution is refined more than an energy group with a simpler solution function. Finally, the method was applied to a heterogeneous, seven-group reactor pincell where the spatial meshes for each energy group were adaptively selected for refinement. It was observed that by refining selected energy groups a reduction in the total number of degrees-of-freedom for the same total L2 error can be obtained.</p>
A cross-study transcriptional patient map of heart failure defines conserved multicellular coordination in cardiac remodeling
<p>Collection of auxiliary data to reproduce the results from "<strong>A cross-study transcriptional patient map of heart failure defines conserved multicellular coordination in cardiac remodeling</strong>". Source code is available at: https://github.com/saezlab/reheat2_pub<br><br>We provide processed data to facilitate access to the results, for the original count data, please see the associated manuscript for references to the original datasets. </p> <p> </p> <p> </p>
Data from: Area of habitat maps and validated occurrences for neotropical birds of conservation concern
<p>Understanding species distributions is essential for advancing bird conservation, especially in the rapidly changing landscapes of the Neotropics, where habitat loss and degradation are accelerating. Area of Habitat (AOH) maps offer valuable spatial tools for illustrating species distributions by highlighting potentially suitable habitats within their geographic range. In this study, we generated AOH maps for 713 neotropical bird species of conservation concern, which includes species listed as globally or nationally threatened, endemic, or with restricted ranges. Using primary biodiversity data and a structured geospatial workflow, we refined approximately 2.5 million occurrence records through a flagging process and validated 50,743 records manually.<strong> </strong>This unparalleled effort led to the creation of high-quality AOH maps, along with altitude-corrected Extent of Occurrence (EOO-DEM) and Inverse Distance Weighted (IDW) range maps. Our AOH maps significantly improved species distribution predictions for 82% of species, over EOO-DEM maps. The validated occurrences and AOH maps produced in this study have wide-ranging applications, providing a valuable basis for the development of new species distribution models and for evaluating species’ natural history, extinction risk, and habitat threats. They also support the identification of priority areas for strategic conservation investments. Importantly, these maps played a key role in systematic conservation planning analyses for the Conserva Aves initiative, which is facilitating the creation of more than 80 new protected areas across Latin America, safeguarding 2 million hectares and improving the management of an additional 2 million hectares (<a href="https://conserva-aves.org/">https://conserva-aves.org/</a>).</p>
Reassessing science communication for effective farmland biodiversity conservation.
<p>Data set and code for analysing a communication case study about biodiversity conservation and farming in the European decision-making environment. It includes: (1) a literature corpus, consisting of 5988 digital press releases and news texts, covering the period of 2015-2020, from 40 different organizations involved in European farming and food decision-making processes; (2) R code scripts for analysis and graphic representation.</p>
Fig. 5 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 5. Nonlinear multidimensional scaling of bird survey data pooled by point-transect. Vectors represent correlations between the ordination and habitat variables. Vectors and Pearson correlation coefficients are plotted for habitat variables with an r2> 0.200 for axis 1.
Fig. 4 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 4. Plots of (A) species and (B) individual rates (from Fig. 1) versus number of species listed by www.birdlife.org (Table 1) per habitat type.
Fig. 1 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 1. Map of forest occurrence in Borneo in 2005 (WWF-Malaysia, 2005) showing the localities of the Sarawak Planted Forest Project and Sabah Softwoods plantation.
Fig. 1 in Natural-Licks Use By Orangutans And Conservation Of Their Habitats In Bornean Tropical Production Forest
Fig. 1. Location maps of Deramakot Forest Reserve in Sabah, Malaysian Borneo (D1 to D4: natural-licks).
CONSERVATION BIOLOGY AND BEHAVIORAL ECOLOGY OF NOCTURNAL MAMMALS OF TAITA HILLS, KENYA
<p>Sound samples from PhD dissertation by Hanna Rosti</p><p>These sound samples include calls of following species</p><p>S1 Paragalago rondoensis, Saadani National Park, Tanzania, recorded by C. Hemp</p><p>S2 Paragalago orinus, Pugu Tanzania, recorded by A. Perkin</p><p>S3 Paragalago cocos, Shimba Hills National Reserve, Kenya, recorded by H. Rosti</p><p>S4 Paragalago zanzibaricus zanzibaricus, Zanzibar, Jozani, Tanzania, recorded by H. Rosti</p><p>S5 Paragalago zanzibaricus udzunwensis, Matundu, recorded by P. Honess</p><p>S6 Paragalago granti, Mdimba, Tanzania, recorded by S. Bearder</p><p>S7 Taita dwarf galago from Mbololo forest, Taita Hills, Kenya, recorded by H. Rosti</p><p>S8 Taita dwarf galago from Ngangao forest, Taita Hills, Kenya, recorded by H. Rosti</p><p>S9 Paragalago cocos, Diani Beach Kenya, recorded by H. Rosti</p><p>S10 Taita tree hyrax singing, Mbololo forest, Taita Hills, Kenya, recorded by H. Rosti</p><p>S11 Long 22 min recording of Taita tree hyrax singing, Mbololo forest, Taita Hills, Kenya, recorded by H. Rosti</p><p>S12 Rock hyrax song, Israel. Recorded by A. Ilany</p><p>S13 Strangled thwack from Taita Hills, Kenya, recorded by H. Rosti</p><p>S14 Dendrohyrax arboreus calls from Nanuyki, Kenia, recorded by H. Rosti</p><p>S15 Dendrohyrax dorsalis calls from Ostrava Zoo, Czechia, recorded by H. Rosti</p>
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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.