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272 results for “Central Andes”
Supplementary material 2 from: Ossowska EA, Moncada B, Kukwa M, Flakus A, Rodriguez-Flakus P, Olszewska S, Lücking R (2022) New species of Sticta (lichenised Ascomycota, lobarioid Peltigeraceae) from Bolivia suggest a high level of endemism in the Central Andes. MycoKeys 92: 131-160. https://doi.org/10.3897/mycokeys.92.89960
File S1
Supplementary material 3 from: Ossowska EA, Moncada B, Kukwa M, Flakus A, Rodriguez-Flakus P, Olszewska S, Lücking R (2022) New species of Sticta (lichenised Ascomycota, lobarioid Peltigeraceae) from Bolivia suggest a high level of endemism in the Central Andes. MycoKeys 92: 131-160. https://doi.org/10.3897/mycokeys.92.89960
Figure S1
Supplementary material 1 from: Ossowska EA, Moncada B, Kukwa M, Flakus A, Rodriguez-Flakus P, Olszewska S, Lücking R (2022) New species of Sticta (lichenised Ascomycota, lobarioid Peltigeraceae) from Bolivia suggest a high level of endemism in the Central Andes. MycoKeys 92: 131-160. https://doi.org/10.3897/mycokeys.92.89960
Table S1
Figure 4 from: Fernandez-Hilario R, Smith SD (2017) A new species of Saracha (Solanaceae) from the Central Andes of Peru. PhytoKeys 85: 31-43. https://doi.org/10.3897/phytokeys.85.12607
Figure 4 - Maximum likelihood phylogeny of Iochrominae (sensu Smith & Baum, 2006) showing placement of Saracha andina. The outgroups (Physalis peruviana, Leucophysalis grandiflora, Witheringia solanacea, Tubocapsicum anomalum, Cuatresia colombiana, and Larnax sachapapa) have been pruned from the tree. Bootstrap support (>70%) is indicated.
Figure 3 from: Fernandez-Hilario R, Smith SD (2017) A new species of Saracha (Solanaceae) from the Central Andes of Peru. PhytoKeys 85: 31-43. https://doi.org/10.3897/phytokeys.85.12607
Figure 3 - Saracha species. A Saracha punctata (R. Fernandez et al. 260; MOL) B Saracha quitensis (S. Smith 257; MO) C Saracha andina (P. Gonzáles et al. 3385; USM) D Saracha andina (R. Fernandez et al. 973; MOL) E Saracha punctata (R. Fernandez 998; MOL) F Saracha quitensis (S. Smith 257; MO) G Saracha andina (R. Fernandez et al. 973; MOL). Photos by: A, D, E, G Robin Fernandez; B, F Stacey Smith; C Paul Gonzáles.
Figure 1 from: Fernandez-Hilario R, Smith SD (2017) A new species of Saracha (Solanaceae) from the Central Andes of Peru. PhytoKeys 85: 31-43. https://doi.org/10.3897/phytokeys.85.12607
Figure 1 - Saracha andina. A Flowering branch B Flower in anthesis C Open corolla with the stamens D Gynoecium. From E. Pariente et al. 110 (MOL). Drawing by Eli Pariente.
Figure 2 from: Graham JG, Janovec JP (2016) A remarkable new species of Brunfelsia (Solanaceae) from the eastern Andes of Central Peru. PhytoKeys 75: 81-91. https://doi.org/10.3897/phytokeys.75.10759
Figure 2 - Inflorescences of Brunfelsia cabiesesiana. Left, cauline corymbiform inflorescences showing limb of corolla at anthesis. Right, stem with bracteate inflorescence branches.
Figure 6 from: Graham JG, Janovec JP (2016) A remarkable new species of Brunfelsia (Solanaceae) from the eastern Andes of Central Peru. PhytoKeys 75: 81-91. https://doi.org/10.3897/phytokeys.75.10759
Figure 6 - Two habit forms of Brunfelsia cabiesesiana found in the El Sira Mountains (drawing by JGG).
Figure 4 from: Graham JG, Janovec JP (2016) A remarkable new species of Brunfelsia (Solanaceae) from the eastern Andes of Central Peru. PhytoKeys 75: 81-91. https://doi.org/10.3897/phytokeys.75.10759
Figure 4 - Estivation of Brunfelsia cabiesesiana. A calyces in bud. (day 1–3) B emerging flower. (day 4–5) C petals unfold (day 6–7).
Figure 3 from: Graham JG, Janovec JP (2016) A remarkable new species of Brunfelsia (Solanaceae) from the eastern Andes of Central Peru. PhytoKeys 75: 81-91. https://doi.org/10.3897/phytokeys.75.10759
Figure 3 - Fruits of Brunfelsia cabiesesiana. Below, dried, dehiscent capsules with seeds. Above left, developing fruits.
Figure 2 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 2 Adult males of Alsodes from the new discovered localities. In parentheses the specific identification according to the phylogenetic analysis (Fig. 3), the snout-vent length (SVL) and code of the respective buccal mucosa sample are indicated. A. Vegas de Cisternas (A. hugoi, SVL = 68.3 mm, VC1m). B. Cajón de Plaza (undetermined, SVL = 54.8 mm, CP5m). C. Vegas de Andrade (A. hugoi, SVL = 57.2 mm, VA1m). D. Vegas de Miranda (A. hugoi, SVL = 56.3 mm, VM6m). E. Cajón Lagunitas (site 3) (A. hugoi, SVL = 71.7 mm, CLP3-5m). F. Lo Aguirre Chico (A. pehuenche, SVL = 52.0 mm, AgCh4m). Some populations are characterized by well-developed interdigital webbing in the hind feet (shown in the insets).
Figure 1 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 1 New and literature records of Alsodes from the Andes Range between 34°50' and 38°05'S. Yellow circles represent the new localities reported in this study; squares represent type localities. A. Andean localities of Alsodes of the literature between 34°50' and 38°05'S: the southernmost localities of A. montanus and A. tumultuosus, the type locality of A. hugoi, localities of A. pehuenche (within red box B, see map B) and the type locality of A. vittatus. There is a record of a putative new species related to A. nodosus in Pemehue (Alsodes sp. 1 of Blotto et al. 2013; not included in the map), presumably the same type locality of A. vittatus. Red boxes correspond to the three explored areas described in this study (maps B, C and D). B. Area explored during the first field campaign (Paso Pehuenche, Laguna del Maule and surroundings). All colored symbols correspond to localities of A. pehuenche: yellow circles correspond to new records; green circles and the square are all previously known localities of the species. The white circle is the place where no amphibian was found. C. Area and sites explored during the third field campaign (tributaries of the Guaiquivilo River). D. Area and sites explored during the second field campaign (surroundings of Laguna El Dial). See details of the localities and the populations discovered in Table 1. Orange lines represent the boundary between Chile and Argentina; thinner yellow lines indicate the boundaries of the administrative regions of Chile.
Figure 3 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 3 Bayesian consensus tree (50% majority-rule) showing the relationships of the new Andean populations of Alsodes. Representatives of the new populations are labeled in green (related to A. pehuenche) and red (related to A. hugoi) (see details of the new localities in Table 1). Note that specimens from Cajón de Plaza are distributed in both the red and green clades. Reference sequences of the type localities of A. pehuenche and A. hugoi are in bold. Numbers next to the nodes correspond to posterior probabilities (only values ≥ 0.95 of the more internal nodes are shown). The scale bar in the lower left corner represents the expected substitutions per site along the branches.
Figure 2 in On the oviposition of Homonota aff. darwinii in the Puna region of the Central Andes of Argentina
Figure 2. Homonota aff. darwinii oviposition in the Central Andes of Argentina. A) Laying of hatched eggs. B) Oviposition site for Egg 1. C) Oviposition site for Egg 2. D) Hatched and unhatched eggs. E) Homonota aff. darwinii embryo.
Dataset for AR article: New particle formation dynamics in the central Andes: contrasting urban and mountaintop environments
<p>Dataset for Article New particle formation dynamics in the central Andes:<br>contrasting urban and mountaintop environments (Aliaga et al. 2024; Aerosol research)</p> <p>It contains four key data files with clustered model output and measurement data from FLEXPART simulations and in situ observations. Details on each file are provided below:</p> <p>1. flx_clust20_alto.nc</p> <p> - Description: Contains clustered output from FLEXPART simulations at EAC site .</p> <p><br>2. flx_clust20_chc.nc</p> <p> - Description: Stores the clustered output from FLEXPART simulations at the CHC site.</p> <p><br>3. particle_number_size_dist.nc</p> <p> - Description: Provides particle number concentrations measured at CHC and EAC sites, utilizing instruments NAIS and DMPS.</p> <p><br>4. hourly_data.nc</p> <p> - Description: dataset with all relevant parameters, including meteorological variables, cloud fraction, chemical composition, and particle concentration across various sizes.</p> <p> </p>
FIGURE 8. Distribution map for Oressinoma sorina n in A new species of the enigmatic genus Oressinoma Doubleday from the Andes of central Peru (Lepidoptera: Nymphalidae, Satyrinae)
FIGURE 8. Distribution map for Oressinoma sorina n. sp. and Oressinoma sorata.
Figure 8 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 8. Egg clutches of Espadarana prosoblepon at different stages of development.
Figure 6 from: Lagomarsino LP, Santamaría-Aguilar D (2015) Two new species of Siphocampylus (Campanulaceae, Lobelioideae) from the Central Andes. PhytoKeys 58: 105-117. https://doi.org/10.3897/phytokeys.58.6973
Figure 6 - Closest relatives of Siphocampylus siberiensis, based on molecular phylogeny of Lagomarsino et al. (2014). A Flower of Siphocampylus boliviensis B Flower of Siphocampylus tunarensis C Flower of Siphocampylus tunicatus D Flower of Siphocampylus umbellatus E Habit of Siphocampylus tunarensis, shown with L. Lagomarsino F Habit of Siphocampylus tunicatus, shown with D. Santamaría-Aguilar. All photos taken in the field by L. Lagomarsino (A–D, F) and D. Santamaría-Aguilar (E). A L. Lagomarsino et al. 239 B, E L. Lagomarsino et al. 232 C, F L. Lagomarsino et al. 235 D L. Lagomarsino et al. 193.
Figure 3 from: Lagomarsino LP, Santamaría-Aguilar D (2015) Two new species of Siphocampylus (Campanulaceae, Lobelioideae) from the Central Andes. PhytoKeys 58: 105-117. https://doi.org/10.3897/phytokeys.58.6973
Figure 3 - Closest relatives of Siphocampylus antonellii, based on molecular phylogeny of Lagomarsino et al. (2014). A Flower of Siphocampylus veteranus B Flower of Siphocampylus actinothrix C Flower of Siphocampylus elfriedii D Cross-section of main stem of Siphocampylus veteranus, showing a much more robust habit than Siphocampylus antonellii, but similar wood structure. All photos taken in the field by L. Lagomarsino. A, D L. Lagomarsino et al. 388 B L. Lagomarsino et al. 403 C L. Lagomarsino et al. 387.
Figure 4 from: Lagomarsino LP, Santamaría-Aguilar D (2015) Two new species of Siphocampylus (Campanulaceae, Lobelioideae) from the Central Andes. PhytoKeys 58: 105-117. https://doi.org/10.3897/phytokeys.58.6973
Figure 4 - Siphocampylus siberiensis. A Flowering branch, showing the persistent leaf scars and developmental procession of distal flower at anthesis to basal capsular fruit B Flower in pistillate phase, including detail of sepal with pubescence C Corolla lobe detail, including marginal pubescence D Longitudinal section of a pistillate phase flower, showing the insertion of staminal tube to corolla, style and stigma as situated relative to the stamens, and bilocular ovary with axile placentation E Anther tube in staminate-phase flower F Capsule with lobes and ridges. Drawing by Bobbi Angel from the type.
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