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105 results for “Tenerife”

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zenodo32/100

Molino Cuevas Blancas, Tenerife.

Source: Objaverse 1.0 / Sketchfab

opencc-byFeb 2017View details →
zenodo32/100

Singing stones and Guanche rock art, Tenerife

Roque del Malpaso near Buzanada, Arona, Tenerife. This model shows a Guanche rock art panel (c.2m across) that is surrounded by singing stones. The volcanic rock has phonic properties and rings loudly when struck with a hammerstone. There are dozens of points on different rocks that have been struck and each location gives a different sound. These stones are located at the top of a dramatic craggy outcrop some 20m high; only a small area has been 3d modelled. Source: Objaverse 1.0 / Sketchfab

opencc-by-nc-1.0Mar 2016View details →
zenodo32/100

CUEVAS complex in Tenerife

Cuevas in Los Abrigos, Tenerife Source: Objaverse 1.0 / Sketchfab

opencc-byFeb 2022View details →
dryad32/100

Genetic data from the extinct giant rat from Tenerife (Canary Islands)

<p>Evolution of vertebrate endemics in oceanic islands follows a predictable pattern, known as the island rule, according to which gigantism arises in originally small-sized species and dwarfism in large ones. Species of extinct insular giant rodents are known from all over the world. In the Canary Islands, two examples of giant rats, <em>Canariomys bravoi </em>and <em>Canariomys tamarani</em>, endemic to Tenerife and Gran Canaria islands, respectively, disappeared soon after human settlement. The highly derived morphological features of these insular endemic rodents hamper the identification of their mainland relatives and the reconstruction of their evolutionary histories. We have retrieved partial mitochondrial (mtDNA) data from <em>C. bravoi</em> and used this information to explore its evolutionary history. The resulting dated phylogeny confidently places <em>C. bravoi</em> within the African grass rat clade (<em>Arvicanthis niloticus</em>). The estimated divergence time, 650,000 years ago, is roughly coincident with the onset of the Günz-Mindel interglacial stage. <em>C. bravoi</em> ancestors would have reached the island via passive rafting and then underwent a yearly increase of mean body mass calculated between 0.0015 g and 0.0023 g; this corresponds to fast evolutionary rates (in darwins [d], ranging from 7.09 d to 2.78 d) that are well above those observed for non-insular mammals.</p>

opencc-zeroNov 2021View details →
zenodo32/100

Subspecies and Distribution. B.b.barbastellusSchreber,1774—EuropefromIrelandandIberianPeninsulaEtoLaivia,Belarus,Ukraine,andtheCauca-sus;alsomajorMediterraneanIs,Moroc-co,andTurkey(Anatolia);possiblyextinctinBelgium,Netherlands,andNorway. B. b. guanchae Trujillo, Ibanez & Juste, 2002 — Canary Is (Tenerife and La Gomera). in Vespertilionidae

Subspecies and Distribution. B.b.barbastellusSchreber,1774—EuropefromIrelandandIberianPeninsulaEtoLaivia,Belarus,Ukraine,andtheCauca-sus;alsomajorMediterraneanIs,Moroc-co,andTurkey(Anatolia);possiblyextinctinBelgium,Netherlands,andNorway. B. b. guanchae Trujillo, Ibanez &amp; Juste, 2002 — Canary Is (Tenerife and La Gomera).

opennotspecifiedOct 2019View details →
zenodo32/100

Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles. in Vespertilionidae

Distribution. Madeira Archipelago (Madeira and Porto Santo) and W Canary Is (La Palma, La Gomera, El Hierro, and Tenerife). Individuals classified as Pipistrellus sp. from the Azores have been suggested to be Madeira Pipistrelles.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. R.a.aegyptiacusE.GeoffroySaint-Hilaire,1810—MiddleEastinSTurkey,Cyprus,WSyria,Lebanon,Israel,WJordan,andEgypt(NcoastandNileValley). R.a.arabicusJ.Anderson&deWinton,1902—ArabianPeninsula,SIran,andSWPakistan. R.a.leachiiA.Smith,1829—E&SAfrica,fromEthiopiatoSouthAfrica. R.a.princepsJuste &Ibanez,1993—-Principe1. R.a.tomensisJuste &Ibanez,1993—SaoToméI. R. a. unicolor]. E. Gray, 1870 — W Africa, from Senegal to WC Angola; also on Bioko I. Introduced during the 2000s in the Canary Is (Tenerife), but probably successfully eradicated and no longer present. in Pteropodidae

Subspecies and Distribution. R.a.aegyptiacusE.GeoffroySaint-Hilaire,1810—MiddleEastinSTurkey,Cyprus,WSyria,Lebanon,Israel,WJordan,andEgypt(NcoastandNileValley). R.a.arabicusJ.Anderson&amp;deWinton,1902—ArabianPeninsula,SIran,andSWPakistan. R.a.leachiiA.Smith,1829—E&amp;SAfrica,fromEthiopiatoSouthAfrica. R.a.princepsJuste &amp;Ibanez,1993—-Principe1. R.a.tomensisJuste &amp;Ibanez,1993—SaoToméI. R. a. unicolor]. E. Gray, 1870 — W Africa, from Senegal to WC Angola; also on Bioko I. Introduced during the 2000s in the Canary Is (Tenerife), but probably successfully eradicated and no longer present.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known. in Soricidae

Subspecies and Distribution. S.e.etruscusSavi,1822—EuropeandCaucasus;thissubspeciesprobablyalsoinTurkey(scatteredrecordsinW,N&amp;SC). S.e.bactrianusStroganov,1958—Tajikistan. S.e.madagascariensisCoquerel,1848—Madagascar. S.e.micronyxBlyth,1855—Himalayas. S.e.nanulaStroganov,1941—Uzbekistan. S.e.nudipesBlyth,1855—NEIndia. S. e. perrottetti Duvernoy, 1842 — S India. Also known from Tenerife I, many Mediterranean Is, North Africa, Arabia, Socotra I, and Central and South-east Asia, but subspecies involved not known.

opennotspecifiedJul 2018View details →
zenodo32/100

Grabados Rupestres Roque de Malpaso, Tenerife

Estación de grabados rupestres del Roque de Malpaso, Tenerife. Source: Objaverse 1.0 / Sketchfab

opencc-byFeb 2017View details →
zenodo32/100

tenerife

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opencc-by-4.0Jan 2019View details →
zenodo32/100

FIG. 2 in Patterns of insect ¯ower visitation in Lavandula buchii Webb (Lamiaceae), an endemic shrub of Tenerife (Canary Islands)

FIG. 2. Daily variation in the size of ¯ower display (A) and temporal distribution of insect visits (B) in Lavandula buchii. Shown are meansÔ 1 SE. Mean values of number of open ¯owers and visitation frequency were averaged for 10 plants. Visitation rates were pooled for the three insect species reported in Results.

opennotspecifiedNov 2000View details →
zenodo32/100

FIGURES 34‒39. Goja tenerife n in New Colombian Goja Navás (Psocodea: 'Psocoptera': Epipsocidae) with peculiar genitalia, and the first Goja with brachypterous male, from Oaxaca, Mexico

FIGURES 34‒39. Goja tenerife n. sp. Male. 34. Forewing. 35. Hindwing. 36. Front view of head. 37. Left paraproct and epiproct. 38. Hypandrium. 39. Phallosome. Scales in mm.

opennotspecifiedSep 2021View details →
zenodo32/100

FIGURE 8 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 8. Distribution of Rosa dumalis ssp. nov. teydensis showing type locality (yellow), records since 2000 (green) and before 2000 (blue) (adapted from Google Earth Pro, © 2021 Maxar Technologies / Grafcan).

opennotspecifiedJan 2023View details →
zenodo32/100

FIGURE 7 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 7. Rocky habitat of Rosa dumalis ssp. nov. teydensis within subalpine teydeginster shrub of the Cañadas del Teide, Tenerife (photo: A.-A. Weller)

opennotspecifiedJan 2023View details →
zenodo32/100

FIGURE 2 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 2. Leaflets and fruiting inflorescence of Rosa dumalis ssp. nov. teydensis. Pedicel length of the central flower only 3.2 mm (magnification: c. 2.5; photo: H. Reichert)

opennotspecifiedJan 2023View details →
zenodo32/100

FIGURE 3 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 3. Habitus of Rosa dumalis ssp. nov. teydensis. A: Shrub; B: flowering branch (photos: A.-A. Weller).

opennotspecifiedJan 2023View details →
zenodo32/100

FIGURE 1 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 1. Holotype of Rosa dumalis ssp. teydensis Weller &amp; H. Reichert (TFC 53.267) (photo: Herbario TFC)

opennotspecifiedJan 2023View details →
zenodo32/100

FIGURE 4 in On the identity of the Teyde dog-rose (Rosaceae): evidence for a new endemic taxon from Tenerife, Spain

FIGURE 4. Longitudinal section through the upper part of the fruit of Rosa dumalis ssp. teydensis showing the extremely wide and short orifice (diameter: 1.6 mm) (photo: H. Reichert)

opennotspecifiedJan 2023View details →
zenodo32/100

Rock art panel 2. Aripe, Tenerife

A photgrammerty model of a Guanche rock art panel near Aripe, Guia de Isora, Tenerife. The panel is dominated by deeply incised lines with occasional cross motifs. Source: Objaverse 1.0 / Sketchfab

opencc-by-nc-1.0Sep 2015View details →
dryad32/100

Data from: Matrix correspondence tests on the DNA phylogeny of the Tenerife lacertid elucidate both historical causes and morphological adaptation

Open the record for dataset details and reuse information.

publicJul 2009View details →

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