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168 results for “water conservation”

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zenodo40/100

FIG. 4 in The water mites of Madagascar (Acari, Hydrachnidia): a revised list completed by original material conserved at the Muséum national d'Histoire naturelle, Paris

FIG. 4. — Sigthoria nilotica (Nordenskiöld, 1905),; A, gnathosoma in lateral view; B, chelicera; C, palp in lateral view; D, fourth leg. Scale bar: 100 µm.

opencc-zeroDec 2004View details →
zenodo40/100

FIG. 5. — Moramangabates pauliani n. gen., n in The water mites of Madagascar (Acari, Hydrachnidia): a revised list completed by original material conserved at the Muséum national d'Histoire naturelle, Paris

FIG. 5. — Moramangabates pauliani n. gen., n. sp.; A, chelicera; B, palp in medial view; C, idiosoma, ventral view. Scale bar: 100 µm.

opencc-zeroDec 2004View details →
zenodo40/100

FIGURE 11 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 11 | Victoria cruziana (A) bud whole, (B) bud L.S., (C) bud from above, (D) first night flower, (E) first night flower L.S., (F) second night flower, (G) second night flower LTS, (H) habit, and (I) seed. (A–D,F,G) (photo LTS), (I) (CM) cultivated RBG Kew, (D,E) cultivated Denver Botanic Gardens (LTS).

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 10 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 10 | Victoria boliviana sp. nov. (A) bud whole, (B) bud L. S., (C) bud from above, (D) first night flower, (E) first night flower L. S., (F) second night flower, (G) second night flower L.S., (H) habit, and (I) seed. (A–G) (LTS), (I) (CM) cultivated RBG Kew, H (CM) Beni, Bolivia.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 9 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 9 | Victoria amazonica (A) bud whole, (B) bud L.S., (C) bud from above, (D) first night flower, (E) first night flower L.S., (F) second night flower, (G) second night flower LTS, (H) habit, and (I) seed. (A–H) (LTS) and (I) (CM) cultivated RBG Kew.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 7 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 7 | (A) Chronogram tree from StarBEAST2 representing molecular dating analysis of splits between V. amazonica, V. cruziana, and V. boliviana with confidence intervals highlighted. (B) Visual representation of plastid structure of V. boliviana assembled using GetOrganelle, with genomic locations of diagnostic characters indicated. Details of polymorphisms (indels) – in the context of multi plastid alignments – displayed within insets.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 5 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 5 | Victoria boliviana sp. nov. (A) habit, (B) abaxial leaf, (C) leaf rim profiles, (D) bud, whole and LS, (E) flower prickles, (F) first night flower, (G) second night flower, (H) carpellary appendages and tepal, staminode attachments; (I) ovule, whole and LS, (J) stamens, (K) seed. (All from material cultivated at RBG Kew). Illustration: Lucy T. Smith.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 6 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 6 | Victoria cruziana (A) habit, (B) abaxial leaf, (C) leaf rim profiles, (D) bud, whole and LS, (E) flower prickles, (F) first night flower, (G) second night flower, (H) carpellary appendages and tepal, staminode attachments; (I) ovule, whole and LS, (J) stamens, (K) seed. (A–E, G–K, cultivated at RBG Kew, F cult. Denver Botanic Gardens). Illustration: Lucy T. Smith.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 4 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 4 | Victoria amazonica (A) habit, (B) abaxial leaf, (C) leaf rim profiles, (D) bud, whole and LS, (E) flower prickles, (F) first night flower, (G) second night flower, (H) carpellary appendages and tepal, staminode attachments; (I) ovule, whole and LS, (J) stamens, (K) fruit, (L) seed. (All from material cultivated at RBG Kew). Illustration: Lucy T. Smith.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 1 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 1 | Wild populations of (A) Victoria amazonica (Peru, Loreto), (B) V. boliviana sp. nov. (Bolivia, Beni) and (C) V. cruziana (Argentina, Chaco). (Photo Credits: (A) Laurel Allen, iNaturalist ID 821386. (B) Carlos Magdalena. (C) Fernanda Alarcón, iNaturalist ID. 19516477).

opencc-by-4.0Jul 2022View details →
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FIGURE 3 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 3 | Line drawing comparing flower and seed morphology in: Victoria amazonica (A–C), V. boliviana sp. nov. (D–F), and V. cruziana (G–I); flower bud whole and in longitudinal section showing abaxial surface of outer tepals, bud profile, stigmatic chamber, carpellary appendage and prickle morphology; seeds. (cultivated at RBG Kew) Illustration: Lucy T Smith.

opencc-by-4.0Jul 2022View details →
zenodo40/100

FIGURE 2 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 2 | Flower morphology and terms, using a Victoria amazonica second-night flower in longitudinal section for reference (above) and a fully dissected flower (below). (A) Ovary, (B) stigmatic surface and stigmatic chamber, (C) locule and ovules, (D) floral apex, (E) outer tepals, (F) inner tepals, (G) outer staminodia, (H) stamens, (I) inner staminodia, (J) carpellary appendages. Illustration and photo: Lucy T. Smith.

opencc-by-4.0Jul 2022View details →
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FIGURE 8 in Revised Species Delimitation in the Giant Water Lily Genus Victoria (Nymphaeaceae) Confirms a New Species and Has Implications for Its Conservation

FIGURE 8 | Geographical context with population genomic and phylogenomic results. (A) Geographical coordinates of all Victoria samples used in analyses, where symbols are color-coded according to morphotype/species and symbol type denotes data source. (B) Phylogenomic representation of relationships between plastomes of 15 Victoria samples, with Nymphaea ampla as the outgroup and constructed using RAxML. (C) Principal component analysis of Victoria nuclear dataset in 16 individuals based on 229,281 genotype likelihoods obtained after skimming for a minor allele frequency (maf) threshold of 0.2.

opencc-by-4.0Jul 2022View details →
dryad36/100

Flying, nectar-loaded honey bees conserve water and improve heat tolerance by reducing wingbeat frequency and metabolic heat production

<p><span>Heat waves are becoming increasingly common due to climate change, making it crucial to identify and understand the capacities for insect pollinators, such as honey bees, to avoid overheating. We examined the effects of hot, dry air temperatures on the physiological and behavioral mechanisms that honey bees use to fly when carrying nectar loads, to assess how foraging is limited by overheating or desiccation. We found that flight muscle temperatures increased linearly with load mass at air temperatures of 20</span><span> or 30°C, but, remarkably, there was no change with increasing nectar loads at an air temperature of 40°C. Flying, nectar-loaded bees were able to avoid overheating at 40°C by reducing their flight metabolic rates and increasing evaporative cooling. At high body temperatures, bees apparently increase flight efficiency by lowering their wingbeat frequency and increasing stroke amplitude to compensate, reducing the need for evaporative cooling. However, even with reductions in metabolic heat production, desiccation likely limits foraging at temperatures well below bees' critical thermal maxima in hot, dry conditions.</span></p>

opencc-zeroJan 2024View details →
dryad36/100

Data from: Predicting habitat suitability and connectivity for management and conservation of urban wildlife: A real-time web application for grassland water voles

<ol> <li>Natural habitats in urban areas provide benefits for both humans and biodiversity. However, to achieve biodiversity gains we require new techniques to determine habitat suitability and ecological connectivity that will inform urban planning and development.</li> <li>Using an example of an urban population of water voles (<i>Arvicola amphibius</i>) we developed a habitat suitability model and a resistance-surface-based model of landscape connectivity to identify potential connectivity between areas of suitable habitat. We then updated the environmental variables according to new urban development plans and used our models to generate spatially explicit predictions of both habitat suitability and connectivity.</li> <li>To make models accessible to urban and conservation planners we developed an interactive mapping tool that provided users with a graphical user interface (GUI) to inform conservation planning for this species.</li> <li>The model found that habitat suitability for water voles was related to distance from key environmental variables, such as built-up areas and urban green spaces, while the connectivity model identified important corridors connecting areas of potential distribution for this species.</li> <li>Future development plans altered the potential spatial distribution of the water vole population, reducing the extent of suitable habitat in some core areas. The interactive mapping tool made available suitable habitat and connectivity maps for conservation managers to assess new planning applications and for the development of a conservation action plan for water voles.</li> <li>Synthesis and applications: We believe this approach provides a framework for future development of nature conservation tools that can be used by planners to inform ecological decision making, increase biodiversity and reduce human-wildlife conflict in urban environments.</li> </ol>

opencc-zeroJan 2022View details →
zenodo36/100

Fig. 6 in Evidence for cryptic diversity in the Neotropical water snake, Helicops angulatus (Linnaeus, 1758) (Dipsadidae, Hydropsini), with comments on its ecology, facultative reproductive mode, and conservation

Fig. 6. The lectotype of Natrix asper Wagler. Photos by Michael Franzen.

opencc-by-4.0Oct 2020View details →
zenodo36/100

Fig. 7 in Evidence for cryptic diversity in the Neotropical water snake, Helicops angulatus (Linnaeus, 1758) (Dipsadidae, Hydropsini), with comments on its ecology, facultative reproductive mode, and conservation

Fig. 7. The holotype of Helicops fumigatus Cope, 1868. Photo by Ned Gilmore.

opencc-by-4.0Oct 2020View details →
zenodo36/100

Fig. 4. NRM 17 in Evidence for cryptic diversity in the Neotropical water snake, Helicops angulatus (Linnaeus, 1758) (Dipsadidae, Hydropsini), with comments on its ecology, facultative reproductive mode, and conservation

Fig. 4. NRM 17, the holotype for Helicops angulatus. Photo courtesy of NRM.

opencc-by-4.0Oct 2020View details →
zenodo36/100

FIG. 9. — Wuria milloti n in The water mites of Madagascar (Acari, Hydrachnidia): a revised list completed by original material conserved at the Muséum national d'Histoire naturelle, Paris

FIG. 9. — Wuria milloti n. sp.,

opencc-zeroDec 2004View details →
zenodo36/100

FIG. 7. — Wuria milloti n in The water mites of Madagascar (Acari, Hydrachnidia): a revised list completed by original material conserved at the Muséum national d'Histoire naturelle, Paris

FIG. 7. — Wuria milloti n. sp.; A,, ventral view; B,, genital field. Scale bar: 100 µm.

opencc-zeroDec 2004View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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