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1,034 results for “HOT”
FIGURE 5 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 5. Sticta microcyphellata (holotype collection). A. Upper side of thallus. B. Lower side of thallus. C. Lower surface. D. Lower surface enlarged. E. Detail of lower tomentum and cyphellae. F. Apothecium. G. Microscopic section through thallus and cyphella. H. Microscopic section through thallus enlarged, showing lower tomentum. Scale in A–C = 10 mm, in D = 5 mm, in E and F = 1 mm, in G = 10 µm, in H = 50 µm.
FIGURE 6 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 6. Sticta papillata (A, Lücking 33370; B–E, holotype collection). A. Thallus in situ. B. Lower surface. C. Lower surface enlarged showing marginal cilia. D. Microscopic section through cyphella showing basal membrane with papillose cells. E. Microscopic section of differentiated upper cortex. Scale in A and B = 10 mm, in C = 5 mm, in D = 10 µm, in E = 30 µm.
FIGURE 4 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 4. Sticta maculofuliginosa (holotype collection). A. Thallus in situ. B. Thallus in herbarium. C. Lower surface. D. Lower surface enlarged. E. Maculate surface with laminal isidia. F. Laminal isidia enlarged. G. Microscopic section through thallus and cyphella. H. Microscopic section through thallus and isidium. Scale in A–D = 5 mm, in E and F = 1 mm, in G and H = 50 µm.
FIGURE 3 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 3. Sticta isidiokunthii (A and C–H, holotype collection; B, Lücking 33346). A–B. Thallus in situ. C. Upper and lower surface in the herbarium. D. Apothecia. E. Lower surface enlarged. F. Isidia enlarged. G. Detail of isidia. H. Microscopic section through thallus showing cyphella. Scale in A and B = 10 mm, in C–G = 5 mm, in H = 100 µm.
FIGURE 1 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 1. Sticta arachnofuliginosa (holotype collection). A. Upper lobe surface. B. Upper lobe surface enlarged. C. Lower surface enlarged. D. Isidia enlarged. E. Microscopic section of upper cortex and tomentum. Scale in A = 5 mm, in B = 0.7 mm, in C = 10 mm, in D = 1 mm, in E = 50 µm.
FIGURE 2 in Ten new species of Sticta and counting: Colombia as a hot spot for unrecognized diversification in a conspicuous macrolichen genus
FIGURE 2. Sticta arbuscula (holotype collection). A. Thallus. B. Lower surface. C. Upper surface enlarged. D. Lower surface enlarged. E. Laminal isidia enlarged. F. Marginal isidia enlarged. G. Microscopic section through cyphella. H. Microscopic section through cyphella enlarged, showing basal membrane with papillose cells. Scale in A and B = 10 mm, in C and D = 5 mm, in E = 1 mm, in F = 0.5 mm, in G = 50 µm, in H = 10 µm.
X-ray CT and MAPS data of Hot-dry rock
<p>These multiple scanning experiment image can be used to construct multi-scale multi component digital rock.</p>
FIGURE 3 in Arthrobotrys xiangyunensis, a novel nematode-trapping taxon from a hot-spring in Yunnan Province, China
FIGURE 3. Neighbor-joining tree generated based on beta-tubulin complete sequences of nematode-trapping fungi species. Bootstrap values were indicated on the branches. Neurospora crassa was set as outgroup. Scale bar at the bottom showed the tree length. M. = Monacrosporium, A. = Arthrobotrys, D. = Dactylella, Dac. = Dactylellina, Dre. = Drechslerella.
FIGURE 1 in Arthrobotrys xiangyunensis, a novel nematode-trapping taxon from a hot-spring in Yunnan Province, China
FIGURE 1. Arthrobotrys xiangyunensis (holotype). A–C. Conidiophores. D. Chlamydospores. E–H, J–N. Mature conidia. I. Adhesive network. Bars = 10μm.
FIGURE 2 in Arthrobotrys xiangyunensis, a novel nematode-trapping taxon from a hot-spring in Yunnan Province, China
FIGURE 2. Neighbor-joining tree generated based on ITS1, ITS2 and 5.8S rDNA complete sequences of nematode-trapping fungi species. Bootstrap values were indicated on the branches. Neurospora crassa was set as outgroup. Scale bar at the bottom showed the tree length. M. = Monacrosporium, A. = Arthrobotrys, D. = Dactylella, Dac. = Dactylellina, Dre. = Drechslerella.
FIGURE 3. Senegalia propinqua. A. Fertile branches. B in Senegalia propinqua (Leguminosae: Mimosoideae), a new species from the Yuanjiang dry-hot valley in south-central Yunnan Province, China
FIGURE 3. Senegalia propinqua. A. Fertile branches. B. Terminal raceme with leaf primordia (arrows) at base of peduncles. C. Head (showing elongated receptacle, and flowers with pale-coloured calyx and corolla). D. New shoot showing spathulate stipules (arrows) subtending emergent leaves, and stem with dark reddish brown glandular hairs in narrow grooves. E. Vegetative bud, and branchlet showing numerous lenticels and scattered prickles. F. Leaf (with petiole broken so that petiole gland not visible). G. Leaflets (lower surface) showing main veins close to and parallel with upper margin. H–J. Petiole glands (plane view). K–L. Petiole glands (side view). Photos. Lin Bai
FIGURE 2. Senegalia propinqua. A. Habit. B in Senegalia propinqua (Leguminosae: Mimosoideae), a new species from the Yuanjiang dry-hot valley in south-central Yunnan Province, China
FIGURE 2. Senegalia propinqua. A. Habit. B. Stems (inset: prickles scattered on mature branches). C. Branches. Photos. Lin Bai
FIGURE 1. Senegalia propinqua. A in Senegalia propinqua (Leguminosae: Mimosoideae), a new species from the Yuanjiang dry-hot valley in south-central Yunnan Province, China
FIGURE 1. Senegalia propinqua. A. Leaf showing numerous leaflets per pinnae and position of petiole gland (thick arrow) and rachis gland (thin arrow). B. Leaflets (upper surface—left and lower surface—right) showing indumentum, vernation and main vein close to upper margin. C. Flowering branch with oblongoid heads in axils of mature and immature (arrowed) leaves. D. Stipules (outer surface— left and inner surface—right). E. Branchlet with minute, straight patent hairs and scattered prickles. F. Petiole glands (side view). G. Petiole glands (plane view). H. Flower (calyx and corolla opened artificially to expose gynoecium and numerous, free stamens). I. Corolla (abaxially—upper and adaxially—lower). J. Gynoecium showing densely hirsute ovary. K. Stamen. Drawn by Ding Han Cui (South China Botanical Garden); A, B, D–K are based on holotype and isotype specimens (L. Bai & Q. Tian BLSC-029); C is based on H. Zhu-Ge 10424 (SWFC [barcode 00007548]).
Piloting Copilot and Codex: Hot Temperature, Cold Prompts, or Black Magic? - Data
<p>Generated programs from <a href="https://arxiv.org/abs/2210.14699">Piloting Copilot and Codex: Hot Temperature, Cold Prompts, or Black Magic?</a></p>
A comparative study on the polar cap hot patch and cold patch by using multi-instrument observations
<p>The support videos of paper<A comparative study on the polar cap hot patch and cold patch by using multi-instrument observations> is stored here. and will be updated if needed.</p>
Hot stops: Timing, pathways, and habitat selection of migrating Eastern Whip-poor-wills
<p>Although miniaturized data loggers allow new insights into avian migration, incomplete knowledge of basic patterns persists, especially for nightjars. Using GPS data loggers, this study examined migration ecology of the Eastern whip-poor-will (<em><span>Antrostomus vociferus</span></em><span>), across three</span> migration strategies: flyover, short-stay, and long-stay. <span>We documented migration movements, conducted hotspot analyses, quantified land cover within 1-km and 5-km buffers at used and available locations, and modeled habitat selection during migration. From 2018-2020 we captured breeding whip-poor-wills from three study sites in Massachusetts and programmed GPS tags to collect data during fall and spring migration periods. Across 19 individual males (nine of them with repeated years of data), GPS tags collected 479 </span>locations, where 30% were classified as flyover points, 33% as short-stays, and 37% as long-stay locations. We documented seasonal flexibility in migration duration, routes, and stopover locations among individuals and between years. Analyses identified hotspot clusters in fall and spring migration in the Sierra de Tamaulipas in Mexico. Land cover at used locations differed across location types at the 5-km scale, where closed forest cover increased and crop cover decreased for flyover, short-stay, and long-stay locations, and urban cover was lowest at long-stay locations. <span>D</span>iscrete choice modeling indicated that habitat selection by migrating whip-poor-wills differs depending on the scale and migration strategy. For example, at the 5-km scale birds avoided urban cover at long-stay locations and selected closed forest cover at short-stay locations. We suggest that w<span>hip-poor-wills may use land cover cues at large spatial scales, like 5-km, to influence rush or stay tactics during migration. </span></p>
77-47-Q184 Small Drill, Hot Springs Village, AK
Small Drill, Hot Springs Village, Port Moller, Alaska CAT# 77-47-Q216 Okada excavations HHQ, Level 4-1 Hot Springs 1C. 1300-1000 BCE The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
77-47-U49 Hafted Knife, Hot Springs Village
Hafted Knife, Hot Springs Village, Port Moller, Alaska CAT# 77-47-U49 Okada excavations HHU, Level 4B. Hot Springs 2B. 500-800 CE. The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
77-47-Q425 End Blade, Hot Springs Village
End Blade, Sanak Point Style, Hot Springs Village, Port Moller, Alaska CAT# 77-47-Q425 Okada excavations HHQ, Level 4-15 Hot Springs 1B. 1600-1300 BCE The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
77-47-Q314 Harpoon Fragment, Hot Springs Village
Harpoon Fragment, Hot Springs Village, Port Moller, Alaska CAT# 77-47-Q314 Okada excavations HHQ, Level 4-8 Hot Springs 1C. 1300-1000 BCE The Hot Springs site is a massive village on the shore of Port Moller, on the Alaska Peninsula side of the southern Bering Sea. It was excavated by several different teams over the last 100 years. The main occupations are from 2000 BCE-1000 BCE, and from 100 CE to 800 CE. The Hot Springs artifacts are presented as a result of the research conducted under grants NSF 0137756, NSF 1204020, NSF 1139266, and NSF 1321411. H. Maschner, Principal Investigator. Original digitizing work done at the IVL at Id. St. Univ. Subsequent processing completed at Global Digital Heritage. Source: Objaverse 1.0 / Sketchfab
ScienceDex guides
Understand access before you commit
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)
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.