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1,723 results for “Alpine”

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Figure 3 in Non-breeding season records of the Alpine Leaf Warbler Phylloscopus occisinensis

Figure 3. Bayesian Inference phylogenetic trees based on COI (A) and Cytb (B) genes of collected samples and those downloaded from GenBank, with Yellow-streaked Warbler Phylloscopus armandii serving as an outgroup. Numbers on each node represent percent bootstrap values and posterior probabilities, respectively.

opencc-by-4.0Mar 2021View details →
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Fig. 8. a. – Humerocyrtis contraria n in New Middle Triassic Bell-Shaped Nassellarian Radiolaria From Alpine And Carpathian Areas

Fig. 8. a. – Humerocyrtis contraria n. sp., holotype, Rc4; b. – Humerocyrtis conica n. sp., holotype, Rc4. c. – Humerocyrtis jekeli n. sp., holotype, Rc2; e,?d.– Humerocyrtis undulata n. sp., Rc4: e – holotype. f – Humerocyrtis lahmi n. sp., holotype, Rc4. Scale bar of 50 µm is for all figures.

opencc-by-4.0Feb 2024View details →
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Figure 1 in Strong genetic difference of Eurasian perch Perca fluviatilis from two Alpine lakes used as founder populations for farming

Figure 1. – Maps of the studied lakes depicting sampling localities of Eurasian perch (Perca fluviatilis).

opencc-by-4.0Dec 2019View details →
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Figure 2 in Strong genetic difference of Eurasian perch Perca fluviatilis from two Alpine lakes used as founder populations for farming

Figure 2. – Bayesian clustering analysis of Eurasian perch population in Lake Geneva (LP1, LP2) and Lake Neuchâtel (NP1, NP2), during June 2012 (P1) and September 2012 (P2).

opencc-by-4.0Dec 2019View details →
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Figs 44-46 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 44-46 – Habitus of Rhizotrogus cicatricosus in life. 44, female from Italy, Scheggia e Pascelupo (photo courtesy of Maura Bocci); 45, male from Italy, Casola Valsenio (photo courtesy of Carlo Arrigo Casadio); 46, male from France, Ferrières-les-Verreries (photo courtesy of Titouen Roguet, fandefaune.free.fr).

opencc-by-4.0Dec 2022View details →
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Figs 13-14 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 13-14 – Comparison between elytra of fresh specimens of Rhizotrogus cicatricosus (13, from Casola Valsenio, Italy) and of R. tedeschii n. sp. (14, topotypical paratype). Photos were taken in the same lighting condition, to evidence the different the color of integument.

opencc-by-4.0Dec 2022View details →
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Figs 47-52 in Rhizotrogus tedeschii, a new species from the alpine zone of the Pollino Massif, southern Italy (Coleoptera: Scarabaeidae, Melolonthinae)

Figs 47-52 – Habitus and behaviour of Rhizotrogus tedeschii n. sp. in life. 47-48, males resting on low grasses; 49, two pairs mating at ground; 50, male trying to crawl beneath rocks following a female trail; 51-52, two different males trying to mate with the dry remains of a female (scavenger ants visible in Fig. 51). In Fig. 52, the female had been moved to a second site.

opencc-by-4.0Dec 2022View details →
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Alpine viper in changing climate: thermal ecology and prospects of a cold-adapted reptile in the warming Mediterranean

<p><span><span>In a rapidly changing thermal environment, reptiles are primarily dependent on in situ adaptation because of their limited ability to disperse and the restricted opportunity to shift their ranges or evolve. However, the rapid pace of climate change may surpass these adaptation capabilities or elevate energy expenditures. Therefore, understanding the variability in thermal traits at both individual and population scales is crucial, offering insights into reptiles' </span></span><span><span>vulnerability</span></span><span><span> to climate change. We studied the thermal ecology of the endangered Greek meadow viper (</span></span><span><span><em>Vipera graeca</em></span></span><span><span>), an endemic venomous snake of fragmented alpine-subalpine meadows above 1600 m of the Pindos mountain range in Greece and Albania,</span></span><span><span> </span></span><span><span>to assess its susceptibility to anticipated changes in </span></span><span><span><span>the</span></span></span><span><span> </span></span><span><span><span>alpine </span></span></span><span><span>thermal environment. We measured preferred body temperature in artificial thermal gradient, field body temperatures and the availability of environmental temperatures in five populations encompassing the entire geographic range of the species. </span></span><span><span>We found that the preferred body temperature (</span></span><span><span><em>T</em></span></span><sub><span><span><em>p</em></span></span></sub><span><span>) differed</span></span><span><span> </span></span><span><span><span>only</span></span></span><span><span> </span></span><span><span>between the northernmost and the southernmost populations </span></span><span><span>and increased with female body size but did not depend on sex or the gravidity status of females. </span></span><span><span><em>T</em></span></span><sub><span><span><em>p</em></span></span></sub><span><span> increased with latitude but was unaffected by the phylogenetic position of the populations. We also found high accuracy of thermoregulation in </span></span><span><span><em>V. graeca</em></span></span><span><span> populations and variation in the thermal quality of habitats throughout the range. The overall effectiveness of thermoregulation was high, indicating that </span></span><span><span><em>V. graeca</em></span></span><span><span> successfully achieves its target temperatures and exploits the thermal landscape. Current climatic conditions limit the activity period by an estimated 1278 hours per year, which is expected to increase considerably under future climate change. Restricted time available for thermoregulation, foraging and reproduction will represent a serious threat to the fitness of individuals and the persistence of populations in addition to habitat loss due to mining, tourism or skiing and habitat degradation due to overgrazing in the shrinking mountaintop habitats of</span></span><span><span><em> </em></span></span><span><span><em>V</em></span></span><span><span><em>. graeca</em></span></span><span><span>.</span></span></p>

opencc-by-4.0Jul 2024View details →
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Alpine grassland plant dataset

Open the record for dataset details and reuse information.

opencc-by-4.0Jul 2024View details →
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Figures 58-65 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 58-65 Male adult of Chaetocladius muttensis sp. n. 58–59, hypopygium, dorsal (58) and ventral with anal point and tergite IX removed (59); 60–61, virga, two aspects; 62, tergite IX and anal point in lateral view; 63, right gonostylus, lateral; 64, left gonostylus, distal part (dorsal); 65, anal point, gonocoxite, tergite IX and gonostylus in lateral view.

opencc-by-4.0Apr 2018View details →
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Figures 22-31 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 22-31 Male adult of Chaetocladius lencioniae sp. n.: 22, last flagellomere and preceding segment; 23, clypeus; 24, scutellum. Hypoygium: 25–26, dorsal (25) and ventral (26) with anal point and tergite IX removed; 27, virga; 28, anal point and tergite IX in lateral view; 29, left gonostylus, dorsal; 30, right gonostylus, ventral; 31, gonocoxite and gonostylus in lateral view.

opencc-by-4.0Apr 2018View details →
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Figures 14-21 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 14-21 Male adult of Chaetocladius spp. C. castellae sp. n. (paratype-1): 14–15, gonocoxite, lateral and dorsal; 16, gonostylus in dorsal view. C. castellae sp. n. (paratype-2): 17, hypopygium in dorsal view; 18, dorsal lamellae of tergite IX. C. insolitus: 19, gonostylus in dorsal view; 20, anal point and tergite IX in lateral view; 21, dorsal lamellae of tergite IX.

opencc-by-4.0Apr 2018View details →
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Figure 66 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figure 66 The Mutt stream valley with the Mutt glacier in the back and in the foreground station M4 (Photo, B. Lods-Crozet).

opencc-by-4.0Apr 2018View details →
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Figures 45-57 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 45-57 Male adult of Chaetocladius macunensis sp. n.: 45, palpomeres 2–3; 46, last flagellomere and the two preceding segments; 47, clypeus; 48, head, thorax and first abdominal segment; 49, antepronotum, left side; 50, tarsomeres 2–4 of PIII; 51, anal point and tergite IX in lateral view; 52–53, hypopygium, dorsal (52) and ventral with anal point and tergite IX removed (53); 54, virga; 55, left gonostylus, dorsal; 56, right gonostylus, lateral; 57, anal point, gonocoxite and gonostylus in lateral view.

opencc-by-4.0Apr 2018View details →
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Figure 68 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figure 68 Malaise trap set up at Immez Lake (Macun cirque, Eastern Alps, Swiss National Park, altitude 2616 m (photo J.L. Lods).

opencc-by-4.0Apr 2018View details →
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Figures 32-44 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 32-44 Male adult of Chaetocladius lodscrozetae sp. n.: 32–33, palpomeres 3–4 with sensilla clavata on palpomere 3; 34, last flagellomere; 35, clypeus; 36–37, hypopygium, dorsal (36) and ventral (37) with anal point and tergite IX removed; 38, virga, two aspects; 39, ventral view of inferior volsella; 40, anal point and tergite IX in lateral view; 41, left gonocoxite in lateral view; 42–44, gonostylus, lateral (42), dorsal (43) and dorso-lateral (44).

opencc-by-4.0Apr 2018View details →
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Figures 1-13 from: Moubayed-Breil J, Lods-Crozet B (2018) On the genus Chaetocladius s. str. Kieffer, 1911 from Switzerland with descriptions of five new relic species occurring in glacial alpine springs and streams (Diptera, Chironomidae). Alpine Entomology 2: 15-34. https://doi.org/10.3897/alpento.2.22759

Figures 1-13 Male adult of Chaetocladius spp. C. castellae sp. n.: 1, last flagellomere; 2, sensilla clavata on palpomere 3; 3, clypeus; 4, antepronotum, left side. C. muttensis sp. n.: 5, last flagellomere; 6, palpomere 3; 8, clypeus. C. insolitus: 7, apex of last flagellomere. Hypopygium of C. castellae sp. n.: 9, dorsal; 10, ventral with anal point and tergite IX removed; 11, dorsal lamellae of tergite IX; 12, anal point and tergite IX in lateral view; 13, left gonostylus in dorsal view.

opencc-by-4.0Apr 2018View details →
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Supplementary material 3 from: Gehrke B (2018) Staying cool: preadaptation to temperate climates required for colonising tropical alpine-like environments. PhytoKeys 96: 111-125. https://doi.org/10.3897/phytokeys.96.13353

Location of the tropical alpine-like climate regions in the Tropics :

opencc-zeroApr 2018View details →
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Supplementary material 1 from: Gehrke B (2018) Staying cool: preadaptation to temperate climates required for colonising tropical alpine-like environments. PhytoKeys 96: 111-125. https://doi.org/10.3897/phytokeys.96.13353

Detailed examples on how the coding was done :

opencc-zeroApr 2018View details →
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Figure 3 from: Gehrke B (2018) Staying cool: preadaptation to temperate climates required for colonising tropical alpine-like environments. PhytoKeys 96: 111-125. https://doi.org/10.3897/phytokeys.96.13353

Figure 3 Proportion of plant elements in tropical alpine regions based on generic distribution patterns according to Smith and Cleef (1988).

opencc-by-4.0Apr 2018View details →

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dandi-nwb
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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.

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OpenNeuro

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openneuro
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Last verified 2026-04-29Open record